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DDx for delirium / AMS

IS IT / MEATS



INTRACRANIAL


I nfection


S tructural/S eizure/S troke


I CH/I schemia


T rauma/T hrombus
_______________________
EXTRACRANIAL


M etabolic


E ndocrine/E nvironment


A noxia/A bnormal pCO2


T oxins/T ablets/T oo little (withdrawal)


pS ychiatric

Intubation preparation

STOP I C BARS
Suction
Tubes
Oxygenate
Prepare with Preload, Position, Pharmacy (drugs), Post-intubation plan
IV's
CO2 monitoring
Bougie & Blades
Alternate airway
Rescue airway
Surgical airway

Diagnosing the cause of an alarming ventilator

D - Dislodged tube
O - Obstructed tube (mucous plug, blood, kink)
P - Pneumothorax
E - Equipment failure (ventilator, tubing, etc)
S - Breath Stacking [breath] (Auto-PEEP)

CHF treatment

POND
Positive-pressure ventilation
Oxygen
Nitroglycerine
Diuretics

Ingestions that are not absorbed by activated charcoal

PHAILS
Pesticides
Hydrocarbons
Acids/Alkalis/Alcohols
Iron
Lead/Lithium
Solvents
Causes of anion-gap metabolic acidosis

KULT
Ketones
Uremia
Lactate
Toxins

Hydrocarbon additives that require GI decontamination

CHAMP
Camphor - seizures
Halogenated HC - dysrhythmias/hepatotoxicity
Aromatic HC - bone marrow suppression/cancer
Metals (arsenic, murcury & lead)
Pesticides - cholinergic crises/seizures/resp depression

Mass casualty triage protocol

Use the START (Simple Triage And Rapid Treatment) Protocol
Remember with ABCD
Use the START (Simple Triage And Rapid Treatment) Protocol
Remember with ABCD
PERC Rule

Apply if clinical gestalt = low risk for PE
HAD CLOTS
H - Hormone (estrogen) use
A - Age > 50
D - DVT or PE history (have they HAD CLOTS?)
C - Coughing blood
L - Leg swelling disparity
O - O2 sats < 95%
T - Tachycardia (>100bpm)
S - Surgery or Trauma (recent)

CATCH Rule - High Risk Criteria

WIGS

W - Worsening Headache
I - Irritability
G - GCS <15 2 hours after the injury
S - Suspected open/depressed skull #
CATCH Rule - Medium Risk Criteria

SDH

S - Skull #
D - Dangerous mechanism (MVC, fall >3ft or 5 stairs, bike accident without helmet)
H - Hematoma (boggy)

Causes of Seizure

STATUS EPILEPsy

S - alicylates / S eizure med noncompliance / S trychnine
T - ricyclic Antidepressants
A - VM / A cute hydrocephalus / A nticholinergics
T - rauma / T raumatic bleed (ICH, SDH)
U - remia (Renal Failure)
S - trychnine / S ugar (low glucose) / S epsis (meningitis)

E - lectrolytes (Hyponatremia, Hypocalcemia)
P - esticides
I - ctogenic foci (e.g. post TBI, post stroke)
L - ithium / L idocaine intoxication
E - clampsia / E tOH withdrawal
Psy - Psy chogenic Non-Epileptic Seizures (formerly known as ‘pseudo seizures’)

Signs of Delirium (for Confusion Assessment Method, CAM)
AIDA

A - cute and fluctuating
I - nattention
D - isorganized thinking - incoherent, rambling
A - ltered LOC - stuperous, agitated, hyper-alert, lethargic, drowsy
What is needed for a safe discharge plan?

No RISKS

R - oaming/wandering
I - mminent danger (falls/fire setting)
S - uicidal ideation
K - inship and relationship (abuse and/or supports)
S - afe driving, S ubstance misuse, S elf neglect

Diagnostic criteria of major depressive disorder

MDD classified as 5 or more of these symptoms occurring most days over a 2 week period along with a change in function. MUST have depressed mood or loss of interest/function.



SIGECAPS

S - leep
I - nterest
G - uilt
E - nergy
C - oncentration
A - ppetite
P - sychomotor slowing
S - uicidal ideation



Not a mixed episode, due to anxiety, caused by a general medical condition, or consistent with bereavement (<2 months from loss)

Approach to the Alarming Ventilator

D - Disconnect the patient from the ventilator +/- provide gentle pressure to the chest (assess for and treat breath Stacking and Equipment failure)
O - Oxygen (100%) and manual ventilation with a bag (check compliance by squeezing the bag: difficult bagging suggests Pneumothorax or Obstructed tube, very easy bagging suggests Dislodged tube or Equipment failure due to a deflated cuff)
T - Tube position/function (see if the tube has migrated to assess for Dislodged tube; pass a bougie or suction catheter through to see if the tube is Obstructed)
T - Tweak the vent (prevents breath Stacking by decreasing respiratory rate, decreasing tidal volume or decreasing inspiratory time)
S - Sonography (assess for pneumothorax, mainstem intubation, plugging)

Ottawa SAH Rule

A - Age > 40y
N - Neck pain/stiffness
T - Thunderclap onset

L - LOC
E - Exertion onset
a
F - Flexion decreased

Ring enhancing lesions on Head CT

MAGICAL DR

M - Metastatic lesions
A - Abscess / Parasite (Neurocysticercosis, Tapeworm)
G - GBM
I - Infarction
C - Contusion


A - Acute Disseminated Encephalomyelitis


L - Lymphoma



D - Demyelinating disease
R - Radiation necrosis

Anterior cord syndrome
Like a car - if it smashes the front the engine won't work (paralysis) but instruments/GPS will (soft touch and proprioception)

What are the NEXUS Criteria?

2 Exam
-Neurologic deficit
-Midline cervical tenderness

3 Credibility
-Normal GCS
-Not intoxicated
-No distracting injuries

Unstable C-Spine Fractures

Jefferson Bit Off A Hangman's Tit And Pinky

J efferson fracture (burst fracture of C1 seen on odontoid view)
B ilateral Facet Joint Dislocation (look for a step on the lateral, FLEXion mechanism)
O dontoid 2 or 3 (odontoid view neck or body fracture)
A tlanto-occipital / A xial dissociation (head detached with wide spinous process separation)
H angman's fracture (see break around the spinolaminar line at C2. HyperEXTENSION)
T eardrop (break of anteroinferior part of the spinal body, most often HyperFLEXion)


A ny fracture-dislocation


P osterior neural arch of C1

Approach to bradycardia

DIE!
Drugs (BB, CCB, Dig)
Infarction
Electrolytes (especially K!)
Rashes that start on the palms

Sifting Rocks Scabbed Emma's Hands
Siphylis
RMSF
Scabies
EM
Hand/foot/mouth (Coxsackie)

Rashes with a + Nikolsky sign

Stevie got scalded by TEN PV'd nickels
Steven-Johnson Syndrome
Staph Scalded Skin Syndrome
Toxic Epidermal Necrolisis (TEN)
Pemphigus vulgaruS (PV)
Nikolsky
Rashes with vesicle / bullae
Old man with BPPV fell into a pool of necrotizing gonorrhea
Bullous Pemphigoid / Pemphigus Vulgarus
Necrotizing fasciitis (hemmorhagic)
Gonorrhea (disseminated)

Rashes with petechiae / purpura

Henoch the Tick gave Meningitis to DICk the purple drug addict
Ricketsia (RMSF)
Meningococcemia
DIC (purpural fulminans)
Endocarditis

Exam findings of serotonin syndrome

CHARM
CNS dysffunction
Hyperthermia/Hyperreflexia
Autonomic dysfunction
Rigidity
Myoclonus

NOTE: NMS does NOT have myoclonus or hyperreflexia!!!

Depression symptoms

SIGECAPS
Sleep
Interest
Guilt
Energy
Concentration
Appetite
Psychomotor slowing
Suicidal Ideation

Suicidal ideation assessment

SADPERSONS scale correlates with the decision to admit to psychiatry. Does not predict risk of future suicidality.



S ex (male) - 1
A ge - 1
D epressed - 2
P revious attempt or psych care - 1
E thanol abuse or street drugs - 1
R ational thought (not) - 2
S eparated, widowed, divorced - 1
O rganized plan or serious attempt - 2
N o social support - 1
S tated future intent - 2



<6 - Outpatient


>6 - ED psych evaluation


>9 - Psych admission

Major and minor criteria for Rheumatic Fever. Treatment.

Jones criteria (requires evidence of strep infection + 2 major or 1 major/1 minor)



MAJOR


J - oints - polyarthritis of large joints (knees, elbows, wrist, ankles)


<3 - carditis (murmurs, effusions, cardiomegaly, CHF)


N - Nodules - subcutaneous on extensor surfaces (wrist, elbow, knees, spine)


E - Erythema marginatum (painless, non-pruritic)


S - Sydenham's Chorea



MINOR


F - Fever


A - Arthralgias


C - CRP


E - ESR


P - PR interval increased



Treatment


-Penicillin x 10 days or Benzathine penicillin 1million units IM; long-term prophylactic antibiotics


-Aspirin


-IVIg

Criteria for diagnosing Endocarditis

Duke's criteria ()


BE FIVER (+ if 2 major, 1 major 2 minor, 5 minor)



B - Blood cultures (2 positive with typical pathogens)


E - Echo lesions (vegetation, perivalve abscess, prosthetic valve dehisence, new regurgitation)



F - Fever (>38)


I - Immunologic (Roth, Osler, rheumatoid factor)


V - Vascular (Janeway, septic emboli, conjunctival hemorrhage)


E - eccentric blood culture (single positive culture unless organism does not cause IE) and echo (consistent with IE but do not meet criteria)


R - risk factors (IVDU, prosthetic valve)

San Francisco Syncope Rule

CHESS


CHF


Hematocrit <30%


ECG


SOB


Systolic BP <90

Dangerous ECG findings on an ECG of a patient with syncope

Prolonged QT


WPW


Brugada


HOCM


Ischemia

Causes of hyperacute T waves

Ischemia


Hyperkalemia


Pericarditis


LVH


LBBB


Benign early repolarization

Causes of tall R wave in v1

Posterior MI


RBBB
RVH


WPW type A


Children and adolescents


Dextrocardia

Causes of ST elevation on ECG

STEMI


Printzmetal's


LBBB


LVH


Pericarditis


Hyperkalemia


Brugada


PE


Celebral hemorrhage


Pacing


BER

How can VT be distinguished from SVT with aberrancy?

Brugada criteria (note: not good enough to use in real life):


1. Absence of any RS complexes in the chest leads
2. RS duration (measured from beginning of R to deepest part of S wave) greater than 100 msec
3. AV dissociation (often present but overlooked; may be best appreciated in inferior limb leads and V1-2)
4. Specific VT morphologic criteria

What are the common pacemaker malfunctions?

Failure to capture - lead displacement or break, block or battery


Oversensing - sensing T waves or extracardiac stimulus


Undersensing - poor lead connection or break, small amplitude, poor contact


Inappropriate rate - battery, response to atrial dysrhytmias

What is the code for pacemaker type?

Chamber paced - A, V, D


Champer sensed - A, V, D


Response to sensing - Inhibit pacing (V or A and V) or Trigger pacing (old)


Programming - simple, programmable, rate adaptive, communicating, none


Antitachy response - pace or shock

Complications of ICD and pacemaker placement

Infection of wound


Infection of pouch


Thrombophlebitics


Chronic thrombosis

Indications for a pacemaker

High level block:


-And symptomatic brady


-And asystole >3s (AFib pauses >5s)


-Following AV ablation


-With neuromuscular disease


-Intermittently with bi or trifascicular block


-With exercise


Indications for an ICD

1. Cardiac arrest from VF or VT not caused by a reversible event
2. Spontaneous sustained VT
3. Syncope of undetermined origin with inducable sustained VT or VF
4. Nonsustained VT with coronary artery disease, prior myocardial infarction, left ventricular dysfunction, and inducible VF

Etiology of Pericarditis

-Infectious (Viral, Bacterial, Fungal, Parasite, Rickettsia)


-Postinjury (Trauma, Surgery, Myocardial infarction, Radiation)


-Metabolic diseases (Uremia, Medications)
-Systemic diseases (Rheumatoid arthritis, Systemic lupus erythematosus, Sarcoidosis, Scleroderma, Dermatomyositis, Amyloidosis)


Tumors
Aortic dissection

List the hypertensive emergencies and their ideal treatment.

ACS - nitroglycerine, labetolol


Heart failure - nitroglycerine, furosemide


Dissection - esmolol & nitroprusside OR labetolol


Ischemic stroke - nicardipine, labetolol


Intracerebral hemorrhage - nicardipine, labetolol


Hypertensive encephalopathy - nicardipine, labetolol


Kidney injury - fenoldopam, nicardipine


Preeclampsia - magnesium and labetolol


Sympathetic crisis - phentolamine

What features distinguish orbital cellulitis from periorbital cellulitis?

Proptosis, opthalmoplegia, and visual changes (look for afferent pupillary defect secondary to increased IOP).

Differential diagnosis for a NAGMA

HARDUPS


Hyperalimentation / TPN


Acetazolamide


RTA


Diarrhea


Ureteral diversion


Pancreas


Spironolactone

Niacin deficiency

aka Vitamin B3 and results in Pellagra



4D’s:


Diarrhea


Dermatitis


Dementia


Death

Thiamine deficiency

aka vitamin B1



Wernicke's Encephalopathy- WACO: ataxia, confusion, opthalmoplegia


Korsakoff's Psychosis - irreversible short-term memory loss


Beri-beri - high output heart failure secondary to vasodilation and fistula formation

Cobalamin deficiency

aka vitamin B12



Megaloblastic anemia


Neurologic changes (paresthesias, ataxia, clonus, memory loss)


Psychiatric (depression, psychosis)



Folate looks the same except NO neurologic changes and it happens faster.

Causes of non-cardiogenic pulmonary edema

IS NOT THE HEART



I nhaled Toxins (Ammonia, Chlorine, Phosgene, Nitrous oxide)
S IRS / Sepsis / Septic Shock



N eurogenic (seizure, strangulation, trauma)
O verdose (Heroin, methadone, cocaine)
T hyrotoxicosis



T rauma
H eat (Smoke! Remember to also consider carbon monoxide!)
E lectrocution



H igh altitude pulmonary edema
E mbolism (Pulmonary Embolism, Acute Gas Embolism, Amniotic Fluid Embolism)
A SA toxicity
R eperfusion or Re-expansion pulmonary edema (or Rocky Mountain Spotted Fever*)
T ransfusion

Diagnostic criteria of Multiple Myeloma

-Monoclonal plasma cells or plasmacytoma in the bone marrow


-Monoclonal protein in blood or urine


-Organ dysfunction (CRAB criteria)


C - HyperCalcemia


R - Renal failure


A - Anemia


B - Bone damage (lesions or osteoporosis)

What cancers cause bone mets?

Painful Bones Kill These Suckers


Prostate


Breast


Kidney


Thyroid


Skin



Also Lungs

Hard signs of vascular injury

HARD Bruit



Hypotension


Arterial Bleed


Rapidly expanding hematoma


Deficit (pulse/neuro)


Bruit/thrill

Criteria to call a febrile seizure simple

6 months to 6 years


1 episode in 24 hours


Duration <15 minutes


Generalized


No neurological history

HELLP Syndrome

Hemolysis



Elevated


Liver enzymes



Low


Platelets

Kawasaki Disease criteria

Warm CREAM



Warm - fever >5 days


C - Conjunctivitis


R - Rash (erythematous, maculopapular, morbilliform)


E - Erythema of palms/soles with swelling


A - Adenopathy (cervical)


M - Mucous membranes (dry, red, strawberry tongue)

Tetrology of Fallot cardiac anomolies

-Boot shaped heart (Fall over your own Boots)


-Pulmonary hypertension, VSD, RVH, Overriding Aorta


-Ductal dependent lesion that crash after PDA closes (2-10 days, treat with PGE1 0.1mcg/kg/m)


Tet spells (knees to chest to increase SVR and O2 to decrease PVR)


Congenital Adrenal Hyperplasia abnormalities

21-hydroxylase deficiency


Low Na and High K


Virulized females, small penis in boys


Treat with glucose and hydrocortisone

Abuse fracture patterns

ANY in a child <1yo


Bucket


Corner**


Diaphysis of humerus, radius, femur, tibia (especially <3yo)


Rib**


Scapular**


Spinous process**


Sternum**


Skull (stellate)*


Vertebral*


Digits*


Multiple* or Bilateral


Different stages of healing*

Psychological signs of child sexual abuse

Very broad definition



Regression


Acting out


Sexualized behavior


Disclosure

The crashing neonate

THE MISFITS


T rauma / abuse


H eart disease / H ypothermia / H ypoxia


E ndocrine (CAH, hyperthyroid)


M etabolic (hypoglycemia, hyponatremia, hypocalcemia)


I nborn errors (ammonia)


S epsis (most common!)


F ormula mishaps


I ntestinal catastrophes (volvulus, NEC, diaphragmatic hernia)


T oxins (home remedies)


S eizures

Cyanotic heart disease

Increased lung markings


1-Truncus arteriosis


2-Transposition of the great arteries


5-Total anomalous venous return



Decreased lung markings


3-Tricuspid atresia / pulmonary atresia


4-Tetrology of Fallot


Congenital heart disease: Obstructive Lesions

Also happen with closure of the duct, but NOT cyanotic. Give them 0.1mcg/kg/m of PGE1



Coarctation of the aorta


Hypoplastic left heart syndrome


Interrupted aortic arch


Aortic stenosis (critical)

List some symptoms of lead poisoning

L - Lead lines


E - Encephalopathy


A - Anemia with basophilic stippling


D - Drop (wrist)

Outline the phases of iron poisoning

I GI effects (hemorrhagic GI effects) x 6 hours


II Quiscient x 12 hours


III Systemic (vasodilatory shock; hepatorenal dysfunction)


IV Liver failure


V Resolution (GI scarring, stomach obstruction)

Pelvic avulsion fractures (muscle attachments and bony anatomy)

Anticholinergic Toxidrome

Blind as a bat (Mydriasis)


Mad as a hatter (Altered mental status)


Red as a beet (vasodilation, flushed)


Hot as a hare (febrile)


Dry as a bone (no secretions/diaphoresis)


Bowel and bladder lose their tone


Heart runs alone (tachycardia)



Atropine, antihistamines, scopalamine, antipsychotics

Cholinergic Toxidrome

SLUDGE and the killer B's


Salivation


Lacrimation


Urination


Defication


Gastro upset


Emesis


Bradycardia, Bronchorrhea, Bronchospasm



Also mioisis and lethargy


Organophosphates, carbamates, mushrooms

Approach to CT Head

Blood Can Be Very Bad



Blood


Cisterns


Brain


Ventricles


Bone


Approach to CXR

ABCS



Airway


Breathing (lungs)


Cardiac (heart)


Skeleton and Soft tissues

Substances that are radioopaque on x-ray

CHIPES


Chloral hydrate


Hydrocarbons (especially halogenated ones)


Iron


Phenothiazines


Enteric coated


Solvents (some of them)

Associations with Ciguatera toxicity

Big fish (grouper, barracuda)


-Anticholinesterase (cholinergic) effects


-Gastroenteritis


-Hot/cold reversal of sensation or cold allodynia


-Teeth feel loose


-Brady / resp arrest


Treat with antihistamines (treat the itch), atropine, amitryptaline (allodynia), mannitol (controversial)

Associations with Scombroid

Poorly refrigerated fish (Tuna, mahi mahi)


Histidine in decomposing fish gets broken down into histamine


-Rapid flushing to head/face/torso


-Gastroenteritis

What is VATER Syndrome?

AKA VACTERAL Association, these conditions occur together more commonly than would be expected otherwise


Vertebral anomolies


Anal atresia


Cardiac defects


Tracheo-esophogeal fistula


Esophageal atresia


Renal anomolies


Limb defects

DDx for febrile and altered mental status patients

SWEAT


Sepsis


Withdrawal


Endocrine (thyroid) & Environment (heat stroke)


Agitated delirium


Toxidromes (sympathimetic, anticholinergic, amphetamines, salicylates, SS, NMS, MH, strychnine, hallucinogens)

General approach to the intoxicated patient

ABCDDDEF


Airway


Breathing


Circulation


Dextrose


Decontamination


Diagnosis (ECG, VBG, acetaminophen, ASA, osmolality, EtOH)


Exposure (features of toxidrome)


Elimination (enhance it)


Find an antidote

TCA mechanisms of action

TCA


Thinker


1 – Indirect GABA antagonism (seizures)
2 – Serotonin reuptake inhibition (serotonin syndrome and agitated delirium)
3 – Norepinephrine reuptake inhibition (initial hypertension and agitated delirium)


Cardiac


4 - Na channel blockade in phase 0 of cardiac depolarization (wide QRS, impaired inotropy)
5 – K efflux blockade prolonging phase 3 of cardiac repolarization (long QT)
6 – Alpha-1 adrenergic blockade causing vasodilation (hypotension)


Anti


7 – Anticholinergic (delirium, seizures, sedation, coma, prolonged gastric emptying)
8 – Antihistamine (I don’t believe this causes any problems in OD)
9 – Antidepressant (this actually results from the Norepi/Serotonin reuptake inhibition, but it balances out the acronym!)

Sternbach's criteria for serotonin syndrome

Recent serotonergic med/med increase, no recent neuroleptics, no other cause, and 3 CAN features


Cognitive


-Agitation, Confusion, Delirium, Hypomania


Autonomic instability


-Tachy, HTN, shiver, diaphoresis, mydriasis, diarrhea


Neuromuscular activity


Fever, ataxia, tremor, hyperreflexia, myoclonus, muscular rigidity

Plants and animals containing cardiac glycosides

FLOWeRY BF


Foxglove


Lily of the valley


white Oleander


Weed of milk


Red squill


Yellow oleander



Bofo toad


Firefly


What are the indications for monitoring/admission after electrical injury?

Clinical


-Cardiac arrest, LOC, hypoxia, chest pain, suspected conductive injury, other injury requiring admission


ECG


-Abnormal or dysrhythmia has occurred


Risk factors


-Known CAD


-Risk factors for CAD

What is the feathering cutaneous burn caused by a lightning strike called?

Lictenburg figure

How do high voltage electrical injuries differ lightning injuries?

More often, high voltage electrical injury causes
-Muscle necrosis


-Rhabdomyolysis


-Compartment syndrome


-Kissing burns


-Mouth burns



But does not cause


-Lictenburg figures


-Karaunoparalysis

How do humans transfer heat?

Conduction - from a warmer to cooler object through direct physical contact


Convection - loss to circulating air and water molecules


Radiation - transferred by electromagnetic waves


Evaporation - conversion of liquid to gas

Contrast heat cramps, heat edema, heat syncope, prickly heat

Cramps - due to fluid replacement with hyptonic fluids


Edema - vasodilation causes pooling which leads to swelling


Syncope - vasodilation and dehydration lead to decreased CO and fainting


Prickly heat - obstruct the sweat pores, staph infection, vesicular rash - treat with chlorhexidine cream

What is the difference between classic and exertional heatstroke?

Classic is in older people with chronic disease in high temperatures, sweating is absent, rhabdo and ARF are rare, lactate is BAD



Exertional is in young people exerting themselves, sweating is common, rhabdo and ARF are common, and lactate is less bad

List the ways that a patient can be rewarmed from hypothemic states

Active external:


-Bair hugger, AV anastomosis, hot water immersion, heating pads, hot water bottles, radiant heat lamp, negative pressure rewarming


Active internal


-Humidified ventilation, warm IVF, thoracic bladder gastric myocardial or colonic lavage, peritoneal dialysis, ECMO +/- diathermy

Causes of syncope

P ressure (hypotensive causes)



A rrhythmias - Bradyarrhythmias, Tachyarrhythmia's (SVT, NSVT, A.F.), pacemaker malfunctions



S eizures



S ugar (hypo / hyperglycemia)



O utput (cardiac) - AS, PS, MS, IHSS, Cardiomyopathies, Atrial Myxoma, Cardiac Tamponade, Aortic Dissection, MI, CHF



O 2 (hypoxia) - PE, Pulm HTN, COPD exacerbation, CO poisoning



U nusual causes - Anxiety, Major depressive disorder, Panic disorder, Hyperventilation syndrome, Somatization disorder



T ransient Ischemic Attacks & Strokes, CNS dz's

Describe the Haddon matrix

Matrix to assess and modify factors related to injury



HAVE


Host


Agent


Vector/Environment



Before, during, and after injury

List 3 strategies used to decrease injuries

The E's



Education - teaching at risk populations how to prevent injury


Engineering - design safety into the environment (e.g. highway design)


Enforcement - of laws requiring safer behavior (e.g. seatbelts)

Hemiparesis ipsilateral to a pupil blown secondary to increased ICP

Kernohan's notch syndrome secondary to uncal herniation compressing the contralateral cerebral peduncle. It results in 'false localization'

Layers of the scalp and associated hemorrhage

SCALP


Skin


Connective Tissue (Caput succedaneum)


Aponeurosis galea


Loose areolar tissue (Subgaleal hematoma)


Periosteum (Cephalohematoma limited by sutures)

How can we assess for pseudosubluxation on pediatric c-spine x-rays?

Most commonly C2-C3


Look at spinolaminar (Swischuk's) line drawn from anterior cortex of the C1 to C3 spinous process. If the line is >2mm anterior to the anterior cortex of C2 suspect a posterior element fracture.

Differences in the pediatric versus adult airway

Anatomic differences in pediatric patients that change response to trauma

-Small size = more multitrauma


-Less protective fat/muscles = more internal organ injuries (liver, spleen, kidneys)


-Elastic chest wall = lung injury without #


-Open growth plates = different fracture patterns


-Large surface area = quicker hypothermia


-Faster metabolic rate = quicker desat, hypoglycemia


-Better at maintaining BP = tachy as only sign of shock


-Bigger head-to-body, thin skull, less myelin = more head injuries


-More elastic vertebral column = more SCIWORA


-Bigger head = higher fulcrum = C2-3 versus C6 injuries more common

Anatomic difference in pregnant patients that change response in trauma

Airway - more friable and edematous mucosa, lower esophageal sphincter tone, increased abdominal girth



Respiratory - higher RR = greater minute ventilation and lower CO2; higher diaphragm = lower FRC (quicker desat) and req's higher chest tube



Cardiac - Increased blood volume, tachycardia, decreased PVR, increased venous congestion/pressures, lots of blood to uterus, aortocaval compression when supine



Heme - dilutional and Fe-deficiency anemia; hypercoaguable



Abdomen - displaced contents; decreased sensitivity of exam for peritonitis; ALP doubles; decreased GB contractility (increased gallstones; weight gain



Nephro - bladder is extrapulvic after 12 weeks; decreased GFR; polyuria and hydropnephrosis due to bladder compression



MSK - widened pubic symphesis (4 -> 8mm)

How can we assess for atlanto-occipital dislocation on pediatric c-spine x-rays?

Use power's ratio (should be <1):


Basion to anterior cortex of C1 spinous process


Opisthion to posterior cortex of dens


 


Also Basion-Dens & Basion to posterior axillary line should be <12mm


 

Use power's ratio (should be <1):


Basion to anterior cortex of C1 spinous process


Opisthion to posterior cortex of dens



Also Basion-Dens & Basion to posterior axillary line should be <12mm


Tube sizes in pediatrics

Broselow tape


ETT = (age/4) + 4 (uncuffed - drop 0.5-1 size for a cuffed tube)


Chest tube = ETT size x 4


Foley / NG tube = ETT size x 2

Anatomic difference in elderly patients that change response in trauma

General - on medications


Cardiac - decreased reserve, can't increase HR


Pulmonary - decreased compliance and increased chest wall rigidity, brittle bones


Neurologic - brain atrophy increases mobility and shearing of bridging veins (SDH); dura is fused so less EDH


Derm - skin is thin and brittle, easier to lacerate and tear, forms ulcers quicker


MSK - osteopenia so increased fractures, decreased joint mobility, spinal stenosis

Approach to hyponatremia

Effects of typical antipsychotics

HOT DAMN



Fever


Dopamine receptor blockade


Alpha blockade


Muscarinic blockade


Na/K channel blockade (wide QRS and long QTc)

Addictions that can kill in withdrawl

ABBA


Alpha blockers (clonidine)


Benzo's


Barbiturates


Alcohol

Nicotinic stimulation effects

Monday - mydriasis


Tuesday - tachycardia


Wednesday - weakness


tHursday - hypertension


Friday - fasciculations


Saturday - seizures

Oxygen toxicity symptoms

VENTIAC


V ertigo


E uphoria


N ausea


T innitus


I mpaired judgement


A LOC (Altered LOC)


C onvulsions

Lake Louise criteria for AMS

Lake Louise criteria for HACE

Lake Louise criteria for HAPE

The TIMI Score

2 or more episodes of angina in past 24h


7 days history of ASA use



C AD (known and >50%)


A ge > 65


R isk factors (>3)


T roponin


S T changes

Predictors of difficult BVM

B eard


O bstructed / O bese / O SA


N eck stiffness / N eck mass


E xpecting (pregnant)


S tridor / S nores

Predictors of difficult intubation

L ook externally


E valuate 3-3-2


M allampati


O bstruction / O besity


N eck mobility (decreased)

Predictors of difficult cric

S urgery


H ematoma / H ave infection (abscess)


O besity


R adiation


T rauma / T umor

Predictors of difficult LMA

R estricted mouth opening


O bstruction


D istored airway anatomy


S tiff lungs / Neck

What are the lines of the cervical spine?

How do you assess for pseudosubluxation in the pediatric C-spine?

Swischuk's line (anterior arch of C1-C3 is within 2mm of C2)


 

Swischuk's line (anterior arch of C1-C3 is within 2mm of C2)


Cervical spine fracture mechanisms

All are flexion, except:



Vertical Compression - Burst & Jefferson



Extension - C1 neural arch, Hangman, Extension teardrop



Flexion-rotation - Unilateral facet, Rotary atlantoaxial

Sensory spinal levels

Motor spinal levels

Reflex spinal levels

Describe the motor deficit in central cord syndrome

It is MUDdy!



Motor > sensory


Upper > lower


Distal > proximal

Signs of aortic dissection on CXR

Wide CHAPPLA1N



Wide mediastinum (8cm AP, 6cm PA, >25% chest width at aortic knob)


C alcium sign


H emothorax


A ortic knob obscured


P aratracheal stripe widened


P leural cap


L eft mainstem bronchus depressed


A ortic window lost


1 st rib fracture


N G deviates to the right along with trachea

Occlusive and nonocclusive arterial injuries

Occlusive


-Transection


-Thrombosis


-Arterial spasm (reversible)



Nonocclusive


-Intimal flap


-Pseudoaneurysm


-AVM


-Compartment syndrome

Diagnostic aid for a migraine

Migraine is likely with two or more of the POUND criteria:


-P ounding


-hO urs lasts (4-72)


-U nilateral


-N ausea and vomiting


-D ebilitating

International Headache Society Migraine Definition

1 --> 4 to 72 hours



2 --> At least two of the following:


-Aggravation by or causing avoidance of routine physical activity


-Moderate or severe pain intensity


-Pulsating quality


-Unilateral location



3 --> During headache, at least one of the following:


-Nausea and/or vomiting


-Photophobia and phonophobia



4 --> Not attributed to another disorder



5 --> History of at least five attacks fulfilling above criteria

Causes of pancreatitis

I GET SMASHED


I diopathic



G allstones


E thanol


T umors (pancreas, ampula, choledochal)



S corpion stings


M icro - Bacterial (Mycoplasma, Camylobacter, TB), Viral (Mumps, Coxsackie, Rubella, Varicella, CMV, hepatitis, EBV), Parasites (ascaris, echinococcus)


A utoimmune (SLE, PAN, Crohn's)


S urgery / trauma


H yperlipidemia / H ypercalcemia (hyperparathyroid)


E mboli / ischemia


D rugs / toxins (azathioprine, estrogen, lasix, valproic acid, APAP, ASA, sulfonamides)

Types/causes of diarrhea

MMISO



M alabsorption (short gut, CF, IBD, celiac, lactose intolerant)


M otility (DM, neuromuscular, scleroderma)


I nflammatory - cellular damage causing secretion; can be hemorrhagic (enterohemorrhagic E Coli, Salmonella) or IBD, autoimmune, chemo


S ecretory (Toxin-mediated chloride secretion: Enterotoxic E Coli, Shigella, Salmonella, Vibrio, C Diff; does not decrease with fasting)


O smotic (altered gut flora from Noro or Rotavirus; ingestion of sorbitol or lactulose; decreases with fasting)

Top 5 causes of occult irritability in children

FAT SHIC



F racture


A buse


T esticular torsion



S urgical abdomen


H air tourniquet


I mproper feeding


C orneal abrasion / C olic

Dermatologic findings in pediatric seizures due to neurocutaneous disorders

Cafe au lait - Neurofibromatosis


Ash leave - Tuberous sclerosis


Port au Wine Staine - Sturge-Weber

Appearance assessment of the pediatric assessment triad

TICLS


Tone


Interactivity


Consolability


Look/gaze


Speech/cry

Lateral soft tissue x-ray findings of epiglottitis

AAA PBL on TV


A ir fluid level


A ryepiglottic fold swelling


A rytenoid swelling



P revertebral tissue swelling


B allooning of the hypopharynx


L oss of L ordosis



T humbprint epiglottis


V allecula obliteration

Approach to the striderous child

Supraglottic


-Congenital (Micrognathia, Macroglossia, Choanal atresia)


-Acquired (Retropharyngeal abscess, Epiglottitis)


Glottic


-Congenital (Laryngeal web, Vocal cord paralysis, Laryngeomalacia)


-Acquired (Laryngeal papilloma)


Subglottic


-Congenital (Subglottic stenosis, Hemangioma)


-Acquired (Croup, Subglottic stenosis)


Tracheal


-Congenital (Tracheomalacia, Tracheal stenosis, vascular ring)


-Acquired (Bacterial tracheitis, Foreign body)

Signs of retrobulbar hemorrhage and indications for lateral canthotomy

DIP A CONE (DIP is primary indications; A CONE is secondary)



D ecreased VA


I ncreased IOP (>40)


P roptosis



A fferent pupillary defect



C herry red macula


O pthalmoplegia


N erve head pallor


E ye pain

Medical treatment of increased IOP

ABCDPS


A lpha 2 agonist (Apraclonidine 1% - decrease production and increase outflow)


B eta blocker (Timolol 0.5% - decrease humor production)


C holinergic (Pilocarpine 1% - constricts pupil and opens trabecular meshwork)


D iuretic (Mannitol & Acetazolamide - decrease production)


P rostaglandins (Latanoprost - increase outflow)


S teroids (Prednisone acetate 1% - decrease inflammation)

Indications for referral to opthalmology of an eyelid laceration

The 5 L's



L id margin


L acrimal system


L evator or canthal tendons


L oss of tissue


L eaking of fat

DDx for sudden visual loss

Anatomic



Anterior chamber - hyphema, hypopiom, glaucoma


Iris/lens - lens dislocation, iritis


Posterior chamber - posterior vitreous detachment or hemorrhage


Retina - Retinal detachment, central venous occlusion, central arterial occlusion


Neuro-opthalmologic - pre-chiasm (optic neuritis due to ischemia/compression/toxin), chiasmal (tumor), post-chiasm (CVA, tumor, AVM, migraine), visual cortex (CVA)

Kanavel signs of flexor tenosynovitis

Fingers held in slight flexion


Fusiform (symmetrical) swelling


Pain to palpation of flexor tendon


Pain on passive extension

Hand motor testing

Radial nerve - wrist extension (triceps)


Posterior interosseous branch of the radial nerve - thumb extension



Median nerve - thumb opposition to fingers


Anterior interosseous branch of the median nerve - OK sign



Ulnar nerve - Froment's paper sign; finger abduction and adduction

Hand sensation testing

Radial nerve - dorsal 1st web space


Median nerve - volar tip of D2


Ulnar nerve - volar tip of D5

Back pain red flags

Infectious - fever, IVDU


Fracture - history of trauma


Cancer - weight loss, history of cancer


Cauda equina - urinary retention, fecal incontinence, saddle anesthesia



Nocturnal pain


Indications for lumbar spine x-rays

M alignancy


A ge (<18 or >50)



F ever


I mmunocompromised


N euro deficits (progressive)


D uration (>4-6 weeks)



W eight loss


I VDU


T rauma

Lines of the pelvis x-ray

One pill can kill

Alpha blocker (clonidine)


Antihyperglycemic agents


BB


Barbiturates


CCB


Digoxin



MAO-I


Methadone



Theophylline


TCA



Methyl salicylate


Toxic alcohol



Iron


Camphor


Lomotil

Drugs that cause seizures

WITH LA COPS


W ithdrawal / Wellbutrin


I NH


T heophylline / TCA
H ypoglycemic agents


L ithium / L ocal anesthetics / L ead


A nticholinergics


C holinergics / C amphor


O rganophosphates


P CP


S alicylates / Sympathomimetics

Drugs MDAC is appropriate for

Please Quit Drinking the AC Dummy


Phenobarb


Quinine


Dapsone


Theophylline / TCA (maybe)


ASA
Carbamezapine


Digoxin (maybe) / Dilantin (maybe)

Dialyzable drugs

BIT SLIME


B arbiturates


I soniazid


T heophylline



S alicylates


L ithium


I ctogenic drugs (Tegetrol, Valproate, Phenobarb)


M ethanol


E thylene glycol


D abigitran

Indications for reduction of a distal radius fracture

Step >1mm


Radial inclination <15 degrees (normal 22)


Volar tilt less than 0 degrees (normal 10-25)


Decreased radial height (normal 11mm, loss of 2mm relative to other side is short)

Clavicle fracture's requiring orthopedic consultation

The rule of 2's


>2 cm displacement


2 or more pieces


<2cm from either end of the clavicle


>2cm of shortening


2 good 2 be true

Shoulder dislocation techniques

Stimson - prone, arm hanging with weight x 20 minutes


Traction-countertraction - sheet under arm for countertraction, abducted arm


FARES - supine, slow abduction with flexion/extension until 90 degrees then external rotation


Milch - supine at 45 degrees, external rotation and abduction to 90/90 then longitudinal traction


Scapular manipulation - can be added to traction/countertraction and Stimson, rotate inferior tip medially


Cunningham - seated, shoulders adducted, elbow flexed with shoulder on provider shoulder, massage of bicep at mid-humeral level

Open fracture classification

Gustillo classification system


I - <1cm, clean, tx with 1st gen cephalosporin


II - >1cm, minimal soft tissue damage, tx with 1st gen cephalosporin


IIIa - significant soft tissue damage with adequate coverage, 1st gen cephalosporin and aminoglycoside (gentamicin)


IIIb - significant soft tissue damage with INadequate coverage, same tx as IIIa


IIIc - open # with vascular injury , same tx as IIIa



Add Pen G or Clinda if concern for anaerobes (farm injury) and Cipro if concern for salt water (pseudomonas)


Femoral nerve injury

Motor - weak knee extension, can't climb stairs or get up from sitting


Sensory - varies, most reliable superomedial to patella


Reflex - decreased patellar

Sciatic nerve injury

Motor - paralysis of hamstring (knee flexion) and all muscles below the knee


Sensory - posterior thigh and below the knee


Reflex - decreased Achilles tendon

Hip reduction techniques

Allis - patient supine with hip and knee flexed to 90 degrees, get on bed and provide vertical upward traction while someone holds the pelvis to the bed. Works for posterior and anterior-obturator (femoral head seen over obturator foramen).



Stimson - patient prone with one leg hanging off of the bed, flex hip and knee to 90 degrees, vertical downward traction while someone holds the pelvis/pushes down on the femoral head.



Whistler - patient supine, arm under knee of dislocated hip with arm on opposite knee (both legs flexed at the hip/knee) to use opposite leg as a fulcrum. A modification of this is the Captain Morgan with your leg under the patient's knee instead of your hand.

Kocher criteria to distinguish septic arthritis from transient synovitis

With 0-4 criteria the likelihood is: 2%, 9.5%, 35%, 73%, 93%


-Non weight bearing


-ESR >40


-WBC >12


-Fever > 38.5


CRP >20 is also predictive

Ottawa Knee Rule

Get x-rays if:


Age >55


Inability to transfer weight 4 times at time of injury OR in ED


Inability to flex to 90 degrees


Patellar tenderness


Fibular head tenderness

How do you assess for patella alta / baja?

Blumensaat's line or Insall-Salvati ratio (patella length should be <0.8 of patellar tendon length; if not patella alta)


 

Blumensaat's line or Insall-Salvati ratio (patella length should be <0.8 of patellar tendon length; if not patella alta)


Ottawa Ankle Rule

Applied to acute ankle injuries with malleolar pain (not hindfoot, forefoot, upper fibula)


-Pain to posterior edge of the lateral malleolus from its distal part and 6cm proximal


-Pain to the posterior edge of the medial malleolus from its distal part and 6cm proximal


-Unable to weight bear 4 steps immediately after the injury and in the ED

Ottawa Foot Rule

-Pain over the navicular bone


-Pain to the base of the 5th metatarsal


-Unable to weight bear 4 steps immediately after the injury and in the ED

How do you calculate Boehler's angle?

A = Posterior tuberosity


B = Apex of posterior facet


C = Apex of anterior process

A = Posterior tuberosity


B = Apex of posterior facet


C = Apex of anterior process

Bones at high risk of AVN

-Head of femur (Legg-Calve-Perthes syndrome in children generally 4-10yo)


-Scaphoid


-Lunate (Kienbock's disease)


-Talus


-Navicular (Kohler's disease)


-Second metatarsal

DDx for non-accidental trauma in children (fractures and bruising)

-Osteogenesis Imperfecta


-Rickets


-Scurvy


-Menkes' Kinky Hair Syndrome


-Hypervitaminosis A


-Hypoparathyroidism


-Congenital Syphilis


-Pathologic fractures


-Birth fractures



-Metaphyseal cupping & spurring (normal variant - bilateral, diaphyseal, smooth)


-Periosteal new bone formation (normal variant - especially to the femur)



-Cultural practices (Cupping, Coining, Spooning)


-Bleeding disorders (hemophilia, vWD, HSP)


-Mongolian spots


-Hemangioma


-'Tattooing'



-ITP


-HSP


-Secondary syphilis

Diagnostic criteria for staph toxic shock syndrome

DR FrOH (NO culture needed)


D esquamation of the skin (begins during recovery phase after 1-2 weeks;


R ash (blanching, macular, erythematous, NOT itchy, fades before desquamation)



F ever (>38.9)


r


O rgan systems (>3/7 involved: CNS, mucous membranes, GI, renal, hepatic, heme, MSK)


H ypotension (sBP < 90 or < 5th percentile in children)

Diagnostic criteria for strep toxic shock syndrome

You going to the strep SHO?



S erology (isolation from a sterile [definite] or nonsterile [non-definite] site)


H ypotension (sBP<90 or <5th percentile)


O rgan systems (>2/6 involved: Renal, Heme, Liver, Lung, Rash, Soft tissue necrosis)

Determining capacity

C ommunication


U nderstanding


R easoning


V alues


E mergency


S urrogate

When can implied consent be assumed

-Patient is unable to express their preferences (CURV)


-Immediate action is required (E)


-No surrogate decision maker (S)

Signs of Lithium toxicity

SNAP MUD


S eizures


N /V/D


A taxia


P arkinsonian



M yoclonus


U MN


D elirium/D ecreased LOC

Infections requiring airborne precautions

Respiratory TB


Varicella (chickenpox and disseminated zoster)


Measles


SARS
Smallpox


+/- Ebola and TB (during aerosolizing procedures)

AIDS-defining illnesses

Heme


-CD4<200



Malignancies


-Kaposi's Sarcoma


-Lymphoma


-Cervical cancer (invasive)



Neuro


-HIV-associated encephalopathy


-Progressive multifocal leukoencephalopathy


-Toxoplasmosis of brain



Fungal infection


-Candida (esophageal or pulmonary)


-Histoplasmosis


-Cryptococcus


-Coccidiomycosis



Protozoa infection


-PJP pneumonia


-Isosporiasis


-Toxoplasma gondii


-Cryptosporidium



Viral


-HSV (persistent, pneumonia, esophagitis)


-CMV (except spleen/liver/lymphatics)



Bacterial infection


-Tuberculosis


-Mycobacterium avium complex


-Salmonella sepsis


-Recurrent bacterial infections

SIRS

HR > 90


RR < 20 OR PaCO2 <32


T < 36 OR > 38


WBC <4 OR >12 OR >10% bands

Definition of ARDS

As per the 2012 Berlin Definition


-Respiratory symptoms started or worsened acutely with the last week


-PaCO2 / FiO2 ratio 200-300 = mild, 100-200 = moderate, <100 = severe


-Bilateral pulmonary infiltrates (CXR or CT)


-Not in cardiac failure / no fluid overload


Malaria: Organism, Vector, Incubation, Presentation, Complications, Diagnosis, Treatment

-Organism: Plasmodium Falciparum is most dangerous (also Ovale, Vivax, Malariae)


-Vector: Female anopheles mosquito


-Incubation: 8-28 days


-Presentation: Fever in the returning traveler, anemia, constitutional (weak, dizzy, N/V/D, lethargy, myalgia, arthralgia, CP, abd pain, SOB)


-Complications: cerebral/seizures, ARDS, ARI, DIC, anemia, acidosis, hypoglycemia


-Diagnosis: Thin and thick peripheral blood smears q8-12h x 3d


-Treatment: Chloroquine if sensitive; otherwise quinine & doxycycline

Lyme disease: Organism, Vector, Incubation, Presentation, Diagnosis, Complications, Treatment

-Organism: Borrelia Borgdorferi (spirochete)


-Vector: Ixodes Tick


-Incubation: Tick must attach long enough to become engorged (>48 hours)


-Presentation: 1st stage erythema migrans & flu-like symptoms/HA; 2nd stage 4 weeks later with fluctuating meningoencephalitis/bilat Bells palsy, conduction block/pericarditis, arthritis, eye inflammation; 3rd stage lasting >1y with fatigue syndrome and arthritis


-Diagnosis: Tick bite, IgM+ from 3-6 weeks, IgG+ >1 month (send both)


-Complications: Can get Jarisch-Herxheimer reaction when tx started


-Treatment: prophylax within 72h in endemic areas if adult tick on for >36h - use Doxy 200mg x1; treat with Doxy 200mg BID x 28d

Rocky-Mountain Spotted Fever: Organism, Vector, Incubation, Presentation, Diagnosis, Complications, Treatment

-Organism: Rickettsia Rickettsii


-Vector: Rocky Mountain Wood Tick


-Presentation: Sudden onset fever followed by N/V/abd pain/HA. Gets into vessels and releases tPA & vWF causing microthrombi and vascular permeability. Petechiae develop on wrists/hands then spread inward. Also cardiac (AVB, myocarditis), pulmonary (ARDS), neurologic (meningismis, transient deficits due to microinfarcts), renal (microinfarcts), heme (DIC).


-Diagnosis: Serology not positive for 1/52 but req'd for conclusive Dx. Skin bx at 4-10 days.


-Complications: Death due to renal failure then ARDS/DIC in 25% if not treated


-Treatment: Doxycycline

Things that shift the oxygen-hemoglobin dissociation curve

CADETS turn right and fall down


(right shift and decreased oxygen affinity)


C - CO2


A - Acid


D - 2,3 DPG


E - Exercise


T - Temperature


S - Sickled Hb S

Diagnostic criteria for delerium

4 criteria:


-Inability to focus/Inattention


-Fluctuating course


-Cognitive deficit (memory, disorientation, language) or perceptual disturbance not caused by dementia


-Evidence that it is caused by a medical condition, ingestion, or withdrawl

Diagnostic criteria for dementia

1 - Memory impairment AND


2 - One of aphasia, apraxia, agnosia, impairment in executive functioning


-Causing significant impairment


-NOT due to delerium

Treatment of active TB

RIPE (side effects) x 9 months!


R ifampin (orange body fluid)


I soniazid (INH injures nerves and hepatocytes)


P yrazinomide


E thambutol (E=eyes - optic neuritis; can't distinguish red/green)

Treatment for hyperkalemia

C BIG K Drop



C alcium



B eta agonist / B icarbonate


I nsulin


G lucose



K ayexalate



D iuretics (Furosemide)


R - R enal dialysis


o


p

GBS: Cause, Presentation, Diagnosis, Complications, Treatment

Cause: idiopathic, often secondary to Campylobacter, Mycoplasma, CMV or EBV - results in antibodies to nerves



Presentation: progressive ascending symmetric weakness and areflexia; Miller-Fischer variant starts centrally (areflexia, ataxia, opthalmoplegia with III/IV/VI affected). Also has autonomic dysfunction (tx brady with atropine; use short acting for hypertension, fluids for hypotension)



Diagnosis: CSF elevated protein, normal glucose and WBC



Complications: respiratory compromise req'ing intubation if FVC <20ml/kg or NIF <30mL/kg



Treatment: IVIg or plasmaphoresis

Myasthenia Gravis: Cause, Presentation, Diagnosis, Complications, Treatment

Cause: Antibodies to post-synaptic ACh receptors (take spots & destroy them)



Presentation: Ptosis, Diplopia, Dysarthria, Dysphagia, Blurred vision with spared pupils, resp failure. Treated patients can present with cholinergic crisis.



Diagnosis: Tensilon test, ice to eyes, NIF (<15 intubate)/FVC (<15 intubate); check for anti-AChR antibodies



Treatment: Plasma exchange or IVIg (neostigmine and/or thymectomy for chronic); intubate with cisatracurium (Hoffman degradation)

DDx of bulbar neuropathy

-Myasthenia gravis


-Lambert-Eaton myasthenic syndrome


-ALS


-Miller-Fisher variant GBS


-Elapidae (coral snake) or Hydraphidae (sea snake) envenomation


-Botulism


-Lyme disease


-Organophosphate poisoning


-Congenital syndrome


-Penicillamine toxicity

How can Tick Paralysis and GBS be distinguished?

-Both generally ascending paralysis


-Finding/not finding an Ixodes tick attached


-Tick paralysis has pupillary dilation while GBS does not

Gram stain results of bacteria

Staph: Gram+ cocci in singles, doubles, tetrads or clusters


Strep: Gram+ paired diplococci (other strep in pairs/chains)


Listeria: Gram+ single or chains


Moraxella caterrhalis: Gram- diplococci


Neisseria: Gram- paired diplococci


H Flu: Gram- coccobacilli


E Coli: Gram- rods


Pseudomonas: Gram- rods

Angina Classification

Canadian Cardiovascular Society


I - No limitation of ordinary activity


II - Mild limitation. Symptoms at >1-2 blocks or >1 flight of stairs.


III - Moderate limitation. Symptoms at <1-2 blocks or <1 flight of stairs.


IV - Severe limitation. Symptoms at rest.

Definition of stable angina

Predictable


Transient (<15m)


Reproducible with activity


Relieved with rest/nitro

Definition of acute MI

-Rise and fall of troponin with: ischemic symptoms, Q waves, ST/T changes, coronary artery intervention


-Pathological evidence

Types of myocardial infarction

I - ischemia due to a primary coronary event (plaque rupture or dissection)


II - supply-demand ischemia


III - sudden cardiac death with symptoms of MI


IV - MI with coronary instrumentation


V - MI with CABG

At risk for an atypical presentation of MI

Aunt Jemima with dementia


-Elderly


-Diabetic (from all the syrup)


-Non-white


-Female


-Dementia


-Hyperlipidemia (from all the sausages)



Also: No prior history of MI, history of stroke, /CHF, no family history

Liver transplant criteria in acetaminophen-induced and non-acetaminophen-induced fulminant hepatic failure (King's College criteria)

Acetaminophen induced


pH <7.3 or lactate >3 after 12h of resuscitation


Lactate >3.5 after 4h of resuscitation



OR all 3 of:


-Cr >300


-INR >6.5


-Grade 3-4 hepatic encephalopathy



Non-acetaminophen induced


INR >6.5



OR 3/5 of:


J aundice >1 week prior to encephalopathy


A ge <10 or >40


N on-A non-B hepatitis


E tiology: indeterminate or drug reaction


B ilirubin >300mmol/L


I NR >3.5

Sgarbossa Criteria

In setting of LBBB, the criteria for calling AMI is >3 points:


>1mm concordant STE (OR 25, 5 points)


>1mm STD in v1, v2, v3 (OR 6, 3 points)


>5mm discordant STE (OR 4.3, 2 points)



Also look at ST (baseline to T) / S (top of S to baseline) ratio <-0.25


Classification of AMI severity

Killip classes


1 no failure


2 crackles, S3, elevated JVP


3 frank pulmonary edema


4 cardiogenic shock, hypotension, vasoconstriction (oligurea & cyanosis)

What are the target times for ACS?

Door


Data (10m)


Decision


Drug (lytic 30m, PCI 90m in center)

What is the Ashman phenomenom?

-Seen in supraventricular tachyarrhythmias (generally AFib)


-Long R-R interval (has long refractory period) followed by a short R-R interval results in part of the right bundle being refractory


-Get a RBBB waveform that looks like a PVC

Mechanisms for arrhythmias

-Increased automaticity (ischemia, electrolytes, drugs)


-Reentry (req's 2 conduction pathways with different responsiveness and conduction speed)


-Triggered (early afterpolarizations in brady/long QTc; treat by increasing HR vs late afterpolarizations in tachy/increased Ca; treat by slowing HR and decreasing Ca)

Antiarrhythmic types/actions

Some Buggers Kill Cats



S odium channel blocker (a block fast, b block inactivated phase, c block both) - procainamide/TCA/cocaine, lidocaine/phenytoin, flecainide/dilantin


B eta blocker - propranolol/esmolol


K potassium channel blocker - amiodarone/sotalol


C alcium channel blocker (slow) - verapamil/diltiazam

How does Digoxin work?

1 - Blocks Na/K ATPase leading to increased intracellular Ca++ (increased inotropy, tachyarrhythmias)


2 - Increases vagal tone (anti-arrhythmic, bradyarrhythmias)

Non-compensatory pause vs compensatory pause

Non-compensatory pause: sinus node is reset and beat following the aberrant beat occurs at the same R-R interval as it would have if it came after a regular beat.



Compensatory pause: sinus node is NOT reset. One sinus beat is not conducted (meets refractory AVN) and the next is. The next beat comes after exactly 2x the standard R-R interval.

DDx for irregular SVT

-AFib


-MAT


-Atrial flutter/tachy with variable conduction


-Parasystole


-Extrasystoles

Contraindications to ED Cardioversion of AFib

1 - Lasted > 48 hours


2 - Rheumatic heart disease


3 - Mechanical valve


4 - History of stroke/TIA

Risk stratification for AFib - who needs anticoagulation?

CHADS2


C HF


H ypertension


A ge > 75


D iabetes


S troke before (worth 2 points)



0 = ASA; 1 = ASA or anticoagulant (anticoagulant preferred); 2 = anticoagulant

Strong predictors of VT in a rapid wide-complex tachycardia

-AV Dissociation


-Fusion beats


-Capture beats


-QRS >0.14


-Extreme left axis



Brugada and Griffith criteria are too unreliable for use and likely cause harm

Congenital vs Adult Torsades

Congenital: precipitated by tachycardia, catacholamine excess, and delayed afterpolarization, treat with beta blockers, associated with Romano-Ward syndrome and Jervall & Lange Nielson syndrome



Adult: precipitated by bradycardia, early afterpolarization, treat with beta agonists, associated with drugs

Drugs that prolong QT

Antidysrhythmics Ia, Ic, III: procainamide, propafenone, amiodarone


Antibiotics: azithromycin, ciprofloxacin


Antipsychotics: haloperidol


Antiemetics: ondansetron, metoclopramide


Anticonvulsants:


Antihistamines:


Antifungals:


Antimalarials: chloroquine


Antidepressants: TCA, citalopram


Analgesia: Methadone



Also, hypoCa, hypoMg, hypoK

Effect and indications for use of a magnet on a pacemaker

Changes a standard pacemaker to VOO mode and turns off defibrillation in an ICD/pacemaker



-Atrial tachycardia with rapid ventricular rate


-Runaway pacemaker (re-entry tachycardia)


-Bradycardia due to oversensing

Causes of ICD malfunction

Frequent shocks


-Shocking SVT


-Oversensing T waves


-Having frequent VF/VT (hypoK, hypoMg, Ischemia, drug-induced)



Inadequate shocks (dizzy/syncope)


-Undersensing VT


-Shocks not strong enough


-Inadequate backup pacing for brady



Cardiac arrest


-Likely VF did not respond to defibrillation


-May have not detected VF (change parameters)

Anemia differential approach

Decreased production


-Lack of stimulation (renal disease, chronic disease)


-Unfunctional marrow (infiltrative disease: amyloid, metastasis; marrow disorders: aplastic, myelofibrosis; blood cancers: lymphoma, leukemia; tox: heavy metals, clozapine)


-Lack components (B12, Folate, Fe)



Increased destruction


-Intravascular (mechanical: prosthetics and microangiopathic DIC/TTP; transfusion reaction: ABO, antibodies; defects: G6PD, sickling)


-Extravascular (abnormal RBC: spherocytosis, thalassemia)

Causes of sideroblastic anemia

Impaired production of porphoryn; leads to anemia and excess Fe in RBC's (Fe ring in sideroblasts)



-Toxins: Lead, Alcohol & INH


-Premalignant condition in elderly (often get AML)


-Malignancy


-RA


-Pyridoxime deficiency

Paroxysmal nocturnal hemglobinuria

Definition - Stem cell defect with abnormal sensitivity of RBCs, neutrophils and platelets to complement


Diagnosis - Get hemosiderinurea, low RBC/Plt/Neutrophils, chronic hemolysis


-Luekocyte alkanine phosphatase levels are elevated


-Complications: thrombosis of arteries and hepatic vein. Also MUST transfuse with WASHED RBC's or compliment on them will lead to lysis.

Encapsulated bacteria

SSome Nasty Killers Have Capsular Protection



S trep pneumoniae


S almonella typhi


N eisseria meningitidis


K lebsiella pneumoniae


H aemophilus influenzae


C ryptococcus neoformans


P seudomonas aeruginosa


Equipment required for a neonatal resuscitation

Be prepared for baby WOBLIS



W armer / polyethylene bag - all babies


O xygen (blended) - for persistent hypoxia


B ag and mask - if HR<100, gasping, apnea give 40-60 bpm with PPV


L aryngoscope and ETT - for meconium suctioning, ineffective/prolonged BVM, chest compressions


I ncubator for transport


S uction

Does the baby need resuscitation?

Term?


Breathing or crying?


Muscle tone?



If yes, no resuscitation needed

Neonatal CPR

CPR is indicated if the infant's HR is <60bpm despite 30s of adequate PPV.



Chest compression rate is 90/minute


Breathing rate is 30/minute (q 3 chest compressions)


Epinephrine is used if HR <60bpm after 30s of CPR (dose 0.1-0.3mL/kg of 1:10,000 epi IV)

When should an infant not be resuscitated?

-<23 weeks


-<400g birth weight


-Anencephaly


-Known chromosomal abnormalities incompatible with life (trisomy 13 or 18)


-Stop resuscitation at 10m if there has been no HR or respiratory effort

Causes of ascending paralysis

Goes BOTTOM VP



G BS



B uckthorn / B-virus (Herpes Simiae)


O rganophosphate


T ick paralysis


T oxic neuropathies (DM, EtOH, B-vitamin deficiencies, Buckthorn)


M etabolic (hyperkalemic periodic paralysis)



V iral (Rabies, CNS VZV/CMV, West Nile)


P olio

Causes of hemolytic anemia (low haptoglobin, high LDH)

Intrinsic:


-Enzymes (Pyruvate Kinase or G6PD)


-Membrane (Spherocytosis, Elliptocytosis, PNH)


-Heme (Thallasemia, Sickle Cell)



Extrinsic


-Mechanical (Microangiopathic - DIC/TTP/HUS/Vasculitis/Preeclampsia)


-Other (valves, march)


-Immunologic


--> Alloimmune (ABO IgM intravasc / Rh IgG extravasc)


--> Autoimmune (Reticular neoplasms [CML, CLL, lymphoma, myeloma], Inflammatory (SLE/RA/PAN/UC), Drugs (quinine, quinidine, methyldopa, PCN/cephalosporins, sulfa), Infectious (CMV/EBV/Mycoplasma/Coxsackie/Hepatitis), Thyroid,



Environmental (hyperthermia, brown recluse bites, freshwater drowning, burns, snakes, malaria)



Abnormal sequestration (hypersplenism)

Pentad of TTP

CRAFTY



C NS changes (fluctuating seizures, paresthesias, altered LOC)


R enal failure (ARI, hematuria, proteinuria)


A nemia (microangiopathic hemolytic with schistocytes)


F ever


T hrombocytopenia (Plts 10-50)

Erythema nodosum

BELTY SLIPS


B ehcets


E strogen


L ofgran's


T B


Y = V iral (#2)



S trep (#1)


L ymphoma (NHL) and Leukemia


I BD


P CN


S ulpha

Define and give a DDx for ALTE

ALTE is an acute, unexpected change in an infant's breathing (apnea or gagging), appearance (color change), or behavior (loss of muscle tone) that frightens the observer. Prevalence peaks at 10-12 weeks but can occur in children <1yo.



-Neuro - Seizures/Hydrocephalus


-Cardiac - Arrhythmia, Congenital heart disease


-Respiratory tract infection (Pertussis, RSV)


-GI - GERD (Sandifer syndrome)


-Metabolic - Hypoglycemia, inborn errors of metabolism, hyponatremia


-Sepsis - pneumonia, UTI


-Heme - anemia


-NAT


-Factitious illness


-Toxins

HUS vs TTP vs DIC

HUS


-Caused by Shiga toxin of O157:H7


-Renal symptoms predominate


-Consumptive (elevated DDimer decreased haptoglobin but normal LDH)


-Children with bloody diarrhea


-Plasmapheresis ineffective



TTP


-Caused by lack of ADAMTS13 (? autoimmune) not cleaving vWF precursor


-Neuro symptoms predominate


-Adults


-Non-consumptive (normal DDimer/Haptoglobin/fibrinogen but elevated LDH)


-Schistocytes


-Treat with plasmaphoresis or plasma exchange



DIC


-Consumptive: low fibrinogin and fibrin levels; high DDimer


-Bleeding and clotting at the same time; ultimately bleed when factors gone


-Schistocytes, anemia, thrombocytopenia


-Caused by multiple underlying disorders

Treatment options in patients with vWD

1 - Tranexamic acid or Aminocaproic acid (plasmin inhibitors - 5g po/iv)


2 - DDAVP (releases vWF and F8 from endothelium - 0.3mcg/kg SC/IV or 1.5mg nasal spray x 2)


3 - Humate-P F8 concentrate (need to ensure it has enough vWF)


4 - Cryoprecipitate (not recommended due to potential for viral transmission)

Describe how factors should be replaced in Hemophilia A and B

Can empirically use 15-20mL/kg FFP (40mL/kg replaces 100% of all factors).


-Cryo contains F8. DDAVP releases F8


-Cryo-poor plasma contains F9.


-aF7 bypasses both



Generally use F8 & F9 concentrate, respectively.


Give 0.5IU/kg/% activity needed for F8


Give 1IU/kg/% activity needed for F9



INITIAL goals: Mild ~30%, Moderate ~50%, Life-threatening >90%; repeat dosing needed for F8 (q8-12h) and F9 (q18-24h)


-Minor bruising/lacerations - 40%


-Dental work /severe epistaxis/renal/deep lac - 50%


-Deep muscle (e.g. iliopsoas)/CNS/Throat/GI/major surgery - 80-100%

Bleeding reversal agents for Aspirin, Clopidogrel, Ticegralor, Warfarin, UFH, LMWH, Dabigatran, Rivaroxaban, Apixaban, t-PA/lytic

Aspirin: DDAVP for minor, platelets for major



Clopidogrel/Ticegralor: DDAVP for minor, platelets for major



Warfarin: Depends. Hold if not bleeding. Hold + vit K po if have time. Hold + vit K IV + FFP (15mL/kg or 2-4U) OR PCC 50IU/kg



UFH: Protamine sulfate 1mg per 100U



LMWH: Protamine sulfate 1mg per 1mg



Dabigatran: PCC 50IU/kg, try FEIBA, vitamin K, Tranexamic acid (1g IV), dialysis (only 33% protein bound); send TT (thrombin time to confirm cause)



Rivaroxaban/Apixaban: PCC 50IU/kg; try tranexamic acid (1g IV), NO dialysis; send anti-Xa level to confirm cause



t-PA/thrombolytic: FFP 2U q6h x 4; Cryoprecipitate x 10U; Tranexamic Acid 1g; Platelets 1 adult; DDAVP 0.3mcg/kg IV; Protamine to reverse any heparin; treat ICP; be prepared to treat seizures

Causes of heart failure

HEART FAILED


H ypertension


E ndocarditis / E nvironment (heat wave


A nemia


R heumatic heart disease


T hyrotoxicosis



F ailure to take meds


A rrhythmia


I nfection / I schemia / I nfarction


L ung (COPD, PE, Pneumonia)


E ndocrine (Pheochromocytoma / Hyperaldosteronism)


D ietary indiscretions (salt / fluid)

Heart failure classes

NYHA Functional classes for CHF


I - Asymptomatic with ordinary physical activity


II - Symptomatic with ordinary physical activity


III - Symptomatic with less than ordinary physical activity


IV - Symptomatic at rest

Organisms responsible for endocarditis

Staph aureus (especially in right sided / IVDU)


Strep viridans


Strep bovis (association with GI malignancies)


Enterococcus (add vanco and watch for resistance)



HACEK - haemophilus atrophilus, actinobacilus, cardiobacterium hominus, eikenella corrdons, kingella kingae (often chronic IE, hard to culture)



Immunocompromised fungal - Candida/Aspirgillus

ECG changes of pericarditis and how are they different than MI

1 - PR depression and diffuse STE (hours to days)


2 - Normalization of ST segments and flattening of T waves


3 - Deep, symmetrical T wave inversion


4 - ECG reverts to normal (sometimes T waves remain inverted)



Different than MI: non-anatomic pattern, concave up, no Q waves, no dynamic worsening

Distinguishing murmur of AS vs HOCM

AS is more likely to have insufficiency on top of other findings.



Valsalva (increased intrathoracic pressure decreases pre and afterload) - HCM louder and AS quieter



Squat (increased SVR increases pre and afterload) - HCM quieter and AS louder

Prognostic factors for pancreatitis

Ranson criteria (on admission) - mortality for 1-2 = 1%; 3-4 = 15%; 5 = 50%



Non-gallstone / Gallstone


A GALL


A ge >55yo / >70yo



G lucose >11 / >12


A ST >250 / >250


L DH >350 / >400


L eukocytes >16 / >18



BISAP score



Urea > 8.92


Impaired mental status


>2 SIRS criteria


Age >60


Pleural effusion

Transfer to a burn center

-Partial thickness burn 10% BSA (2nd degree)


-Any 3rd degree burn


-Burns to face, hands, feet, genitalia, perinium, joints


-Electrical burn (including lightning)


-Chemical burn


-Inhalational burn


-Pre-existing medical conditions that complicate management


-Children at a location that can not care for children


-Cocomitent burn and trauma where the burn is the greatest danger


-Burn injury in patients requiring social, emotional, rehabilitative intervention

Dive injuries

On descent


-Ear barotrauma (inner, middle, external)


-Mask squeeze (facial barotrauma)


-Sinus barotrauma



At depth


-Oxygen toxicity


-Contaminated gases


-Hypothermia


-Nitrogen narcosis



On ascent


-Alternobaric vertigo


-AGE


-Pneumothorax/ Pneumomediastinum/ Pulmonary hemorrhage


-GI barotrauma


-Barodontalgia

Dive injuries requiring a recompression chamber

-AGE


-DCS I and II


-Contaminated gases (CO)

Arterial embolism vs thrombosis

Embolism


-Source of emboli


-Sharp demarcation (no collaterals)



Thrombosis


-History of claudication


-Contralateral findings of partial occlusion


-Diffuse atherosclerosis (lots of collaterals)

Causes of CVL obstruction

Complete


-Clots


-Precipitant


-Mechanical obstruction



Withdrawl


-Against vessel wall


-Vein thrombosis


-Fibrin sheath


-Ball-valve thrombus



Intermittent


-Pinching between clavicle and 1st rib

Well's DVT Criteria

DImPLES and the 3 C's (-2 points if an alternative diagnosis is as likely) - Likely if 2 or more



D VT previously


I mmobilization (paralysis, plaster)


P ain (along deep venous system)


L eg swelling (entire leg)


P itting edema (to only the affected leg)


S urgery (last 3m)



C ancer (palliative or treated in past 6m)


C alf swelling (>3cm circumference difference


C ollateral veins (visible and nonvaricose)

Well's PE Criteria

Likely if 4 or more



D VT signs and symptoms


A lternative less likely


M alignancy


P revious P E/DVT


H emoptysis


I mmobilization


hR > 100

Contraindications for fibrinolytic in STEMI and PE

1-Dissection?



Stroke


2-Prior ICH?


3-Ischemic stroke in last 3m?



Bleed


4-Known vascular lesion? (AVM)


5-Known intracelebral neoplasm?


6-Significant head/facial trauma in last 3m?



Can't Clot


7-Active bleeding


8-Bleeding diatheses?

Gas laws (Pascal, Boyle, Charles, Dalton, Henry)

Pascal - Pressure on a fluid is transmitted equally throughout


Boyle - P1V2 = P2V2


Charles - V1/T1 = V2/T2


Dalton - Pt = P1 + P2 + P3 ...


Henry - The amount of gas dissolved in a liquid (solubility) is proportional to the partial pressure of that gas above the liquid

Reasons to modify the dose of adenosine

-Patient weight (obese, pediatrics), need more or less


-Heart transplant (don't use it)


-Methylxanthines (theophylline) stimulates receptors, need more


-Carbamezapine, needs less


-Dipyradamole prevents breakdown, needs less


-CVL delivery, need less

Causes of priapism

Medical conditions


-Sickle cell


-Leukemia


-Spinal cord injury


-G6PD deficiency


-Thalassemia



Medications


-ED - papaverine and PGE-1


-Phosphodiesterase inhibitors - sildenafil


-Antipsychotics - chlorpromazine, clozapine


-Antidepressants - SSRI's - trazodone


-HTN - HCTZ


-Mood/convulsant - Valproic acid


-Recreational - alcohol, cocaine, amphetamines, heroin

Toxic levels: ASA, APAP, Iron, Digoxin, Lithium, Methanol, Ethylene Glycol, TCA

ASA


Dose: 200mg/kg dose


Level: Acute >7mmol/L; Chronic >3.5mmol/L



APAP


Dose: 200mg/kg/24h dose; >150mg/kg/d for 48h; >100mg/kg/d for 72h


Level: >1000mmol/L



Iron


Dose: 20-40mg/kg (mild); 40-60mg/kg (mod); >60mg/kg (severe)


Level: >90mmol/L



Digoxin


Dose: 0.1mg/kg


Level: >19mmol/L acute; >12mmol/L chronic



Lithium


Level: >4mmoL/L acute; >2.5mmoL/L chronic



Methanol


Dose: 0.15mL/kg


Level: >6mmol/L toxic; >15mmol/L HD



Ethylene Glycol


Dose: 0.2mL/kg


Level: >3mmol/L toxic; >8mmol/L HD



TCA


Dose: >5mg/kg

Contrast Dilated, Hypertrophic, Restrictive, Takotsubo, Peripartum Cardiomyopathies (cause, treatment)

Dilated: Mostly idiopathic but caused by ethanol, smoking, HTN, pregnancy, infection (myocarditis). Treated with pre and afterload reduction (ACEi, diuretics, PPV)



Hypertrophic: Caused by HOCM, AS, CAD, HTN. Treated with afterload reduction (BB). Must maintain preload!



Restrictive: Caused by amyloidosis, sarcoidosis, hemochromatosis, scleroderma, radiation, glycoven-storage diseases (Fabry/Gaucher). Treat underlying cause. Optimize preload (fluids).



Takotsubo: Caused by ? stress hormones. Treat as MI (indistinguishable from anterior STEMI) then BB and ACEi until recovery.



Peripartum: Caused by pregnancy (3 months before delivery to 6 months after). Treat afterload (hydralazine/labetolol until delivery, ACEi/BB after), preload (nitro), and contractility (digoxin) until recovery.

Arteriosclerosis obliterans vs Thromboangiitis obliterans

Arteriosclerosis: blue toe syndrome, claudication, ischemic rest pain in an elderly (>50) vasculopath (DM, smoker, HTN, cholesterol). Requires intervention if they have pain at rest. Can have distal ulcers.



Thromboangiitis: aka Buerger's disease, get painful erythematous nodules and decreased pulse in peripheral arteries. Only most commonly in male smokers 20-40yo and cure is stopping smoking completely.

Distinguish vasogenic skin ulcers

Arterial - distal to ankle, shiny, hairless, unswollen skin and thick nails. Less painful when dependent.



Venous - proximal to ankle, ++ swelling, weaping. Less painful when elevated.



Neurotrophic - sites of repeated trauma that they don't feel. Heels, toes, plantar surface. Not painful.



Hypertensive - on lateral malleolus, hemorrhagic bleb becomes an ulcer. Very painful.

Vascular complications of IV drug use

AV fistula and pseudoaneurysms (from 'hitting pink')



Unilateral hand edema (obliteration of superficial venous circulation)



Distal ischemia (severe burning pain distal to injections; possibly FB, talc, precipitate - nothing works to fix it; can need amputation)



Infected pseudoaneurysm (infected mass after hitting artery, reason that we assess abcesses for pulsatility)

Extensive ileofemoral DVT: Names and diagnosis

Phlegmasia Cerulia Dolens - swollen, congested, painful, cyanotic leg due to iliofemoral occlusion. Treat with thrombectomy.



Phlegmasia Alba Dolens - painful white leg secondary to arterial spasm that results from iliofemoral occlusion. Looks like arterial occlusion. Worse then cerulia. Treat with thrombectomy.

APGAR Score

A ppearance (pink, acrocyanosis, cyanosis)


P ulse (>100, <100, absent)


G rimace (sneeze/cough/pull away, grimace, no response)


A ctivity (active, arms/legs flexed, limp)


R espirations (good crying, weak cry, absent)

Diagnosis and management of oncologic emergencies: febrile neutropenia, SVC syndrome, Tumor lysis syndrome, Hyperviscosity syndrome, Hypercalcemia

Febrile neutropenia: Temp >38.3 (x1) or 38.0 (x1h) with ANC<1 or expected <0.5 (biggest drop 5-10 days post chemo). NO rectal temps. Treat with Tazocin x 14d if stable + vanco/gent if not stable.



SVC syndrome: Present with periorbital edema, plethora, facial swelling, arm swelling, dyspnea. Diagnose with CT. Treat with radiation/chemo or stent (stent best).



Tumor lysis syndrome: See hyperkalemia, hyperphosphatemia, hyperuricemia, hypocalcemia. Treat with IVF +/- urinary alkalinization if acidic +/- dialysis. Can also try rasburicase with consultations. Allopurinol can prevent but not treat.



Hyperviscosity syndrome: Lab can't run tests. Happens with MM, Waldenstrom's Macroglobulinemia, Leukemia. Present with CNS/vision changes. Treat with exchange transfusion, plasma/leukopheresis.



Hypercalcemia: Due to mets or parthyroid-like hormone. Treat with hydration, furosemide, bisphosphonates, calcitonin.

Indications for dialysis in tumor lysis syndrome

Phosphate >3.2


Potassium >6


Uric acid >590


Creatinine >880


Volume overload


Symptomatic hypocalcemia

Synovial fluid interpretation (Color, Viscosity, WBC/mm3, Differential, Culture)

Special tests for the shoulder (Jobe, Drop arm, Neer's, Hawkin's, Painful arc, Lift off, Lift off lag, Yergason's, Speed's)

Supraspinatus


Jobe's: 90 degrees abd, 30 degrees anterior to coronal plane, internally rotated/pronated - weakness or pain = supraspinatus involvement.


Drop arm test: passive abduction to 90 degrees. If can't be maintained, possible large supraspinatus tear.



Supraspinatus/Impingement


Neer's: Hand stabilizing scapula, passive flexion to 180 degrees. Pain towards 180 degrees indicates impingement.


Hawkin's: imagine a hawk being held on an arm (90-90 flexion at shoulder/elbow) then internally rotate and see if there is pain. Indicates impingement.



Subacromial bursitis


Painful arc: Abduction with pain from 70-100 degrees indicates subacromial bursitis.



Subscapularis


Lift off test: assess for tear by putting internally rotated hand on back, holding elbow, and getting patient to lift off.


Lift off lag: assess for rupture by doing same but passively lifting off and seeing if patient can maintain.



Biceps


Yergason's sign: Flex elbow to 90 and have patient try to supinate against resistance. Pain is positive.


Speed's test: Extend elbow and supinate forearm. Flex shoulder against resistance. Pain is positive.


Types of hypersensitivity reactions

ACID


I A naphylaxis - IgE-mediated degranulation of mast cells and basophils


II C ytotoxic - IgG mediated complex fixation


III I mmune complex - IgG or IgM antigen-antibody complex deposition


IV D elayed - T cell mediated

Causes of cavitating lesions

CAVITY


C ancer (metastasis)


A utoimmune (Wegener's granulomatosis, Rheumatoid Arthritis)


V ascular (emboli, infarction)


I nfection (TB, MRSA, SA, Klebsiella, Fungal)


T rauma (pneumatocele)


Y outh (congenital things; bronchogenic cyst)


Treatment of common Tinea (capitis/barbae, kereon, versicolour, unguinum, pedis, other)

Tinea capitis/barbae: Itraconazole 250mg po od x 4/52; Selenium Sulphide shampoo 2x weekly



Kerion: As per tinea, plus Keflex 500mg po qid (if infected) and Prednisone 1mg/kg/d x 1/52



Tinea versicolour (Malassezia Furfur): Selenium Suphide shampoo (q monthly for prophylaxis) +/- Fluconazole 400mg po x 1



Tinea unguinum: Penlac (antifungal painted on nail) trial; Ketoconazole 200mg po od x 6 months +/- surgical nail removal



Tinea pedis: Clotrimazole 1% bid x 6 weeks



Tinea (other areas): Clotrimazole 1% bid x 3 weeks

Treatment of candidiasis (Thrush, Cutaneous, Vulvovaginal)

Thrush: Adults Nystatin (100,000U/kg) swish and spit 5mL po qid until resolved x 1/52. Infants the same but 'paint the mouth' qid x 7 days. Fluconazole if immunocompromised.



Cutaneous: Dry regularly, zinc oxide prn, 1% hydrocortisone prn, Nystatin (100,000U/kg) cream bid-qid OR Clotrimazole 1% qid x 6/52. Can also use Fluconazole 100mg od x 2/52.



Vulvovaginal: Clotrimazole intravaginal OTC. Can also use Fluconazole 150mg po x 1.

Indications for emergent decompression of a subdural hematoma

-Midline shift >5mm


->1cm thick


-GCS decreased by 2 or more since the time of the injury


-Fixed dilated pupils


-ICP >20mmHg

Define SIDS, apnea, pathological apnea, apnea of infancy, apnea of prematurity, periodic breathing

SIDS: sudden infant death in a child without historical, physical, laboratory, or postmortem findings that explain the death. Peaks at 3-5 months (90% <6 months)



Apnea: cessation of air flow (central, obstructive, mixed)



Pathologic apnea: apnea lasting >20s with bradycardia, cyanosis, hypotonia



Apnea of infancy: pathologic apnea with no identifiable cause



Apnea of prematurity: pathologic apnea associated with pre-term delivery (generally resolves by 37 weeks)



Periodic breathing: breathing pattern with 3 or more pauses each lasting >3s with 20s of normal breathing surrounding them.

Gout vs Pseudogout (crystals, risks, treatment)

Gout


-Negatively birefringent needle urate crystals


-Risks: obesity, DM, HTN, diuretics, alcohol, meat, seafood, beer, legumes


-Treat: allopurinal (production), probenacid (excretion) chronically; colchicine 1.2/0.6/0.6, NSAIDS, steroids acutely



Pseudogout


-Positively birefringent rhomboid calcium pyrophosphate crystals


-Risks: hyperparathyroid, hypothyroid, hypoMg, hypoPO4, Wilson's, Hemochromatosis


-Treat: As for gout except steroids > NSAIDs/Colchicine; also treat underlying cause but does not affect course.

What is Still's disease? Treatment?

Multisystem inflammatory disorder characterized by fever, arthritis, sore throat, myalgias, pericarditis, hepatitis, splenomegaly, and salmon colored rash that occurs ONLY with the fever.



Treat with NSAIDs, Steroids, IVIg

What are the seronegative spondyloarthropathies?

-They are RF NEGATIVE and HLA B27 POSITIVE . Generally involve the axial skeleton (not extremities)



PAIRS -


P soriatic arthritis (affects smaller joints, sausage fingers and psoriasis)


A nkylising spondylitis (males, back pain, sacroiliitis, bamboo spine)


I nflammatory bowel disease


R eiters syndrome / reactive arthritis (post GU chlamydia or GI shigella, salmonella, campylobacter, yersinia infection)


Medial and lateral epicondylitis

Medial - Pitcher's/Golfer's Elbow


-Flex wrist then try to pronate against resistance - pain to medial epicondyle



Lateral - Tennis


-Extend and supinate wrist then try to flex against resistance - pain to the lateral epicondyle (Cozun test)



Both - treat with rest, RICE, PT

Criteria for the diagnosis of lupus

Require 4/11


ANA is quite sensitive (good rule-out); anti-DS-DNA & anti-Sm are quite specific (good rule-in)



-Malar rash


-Discoid rash


-Oral ulcers


-Photosensitivity



-Nonerosive polyarthritis



-Serositis (pericardial or pleural effusion)


-Renal disorder (nephrotic or nephritic)


-Neurologic disorder (seizures or psychosis nos)


Hematologic disorder (low Hb, WBC, platelets)



-Immunologic disorder (anti-dsdna, anti-sm, LAC, anticardiolpin, false + syphilis serology)


-Positive ANA

Drugs that cause drug-induced lupus

Cardiac: procainamide, amiodarone


HTN: hydralazine, methyldopa


Antimalarial: quinidine


Antimicrobial: nitrofurantoin, penicillin, INH, sulfonamides, tetracycline


Anticonvulsant: phenytoin


Antithyroid: PTU


Antipsychotic: lithium, chlorpromazine


Gout: allopurinol

Diagnostic criteria for giant cell arteritis

If you have 2 treat and get biopsy, if you have 3 just treat.



1 - >50yo


2 - new onset localized headache


3 - ESR >50


4 - abnormal biopsy with mononuclear infiltration or granulomatous inflammation

Vasculitis classification and key features

Large vessel:


-Takasayu's - pulseless disease, renovascular hypertension


-Giant cell - temporal artery headache, amaerosus fugax



Medium vessel:


-Polyarteritis nodosa - mostly CNS/GI necrotizing arteritis, no venous involvement, non-granulomatous, palpable purpura, hypergammaglobulinemia, ANCA negative


-Buerger's disease - aka thromboangiitis obliterans, 20-40yo male smokers, painful dark phlebitis migrans nodules


-Kawasaki disease - Warm CREAM, pediatrics



Small vessel


-Goodpasture's - anti-GBM antibody +, alveolar hemorrhage, glomerulonephritis (RPGN). c-ANCA negative (unlike Wegener's)


-Microscopic polyangitis - alveolar hemorrhage, glomerulonephritis, nerve involvement. NOT granulomatous (unlike Wegener's). p-ANCA+ (unlike Goodpasture's)


-Wegener's granulomatosis - necrotizing granulomatous with upper resp (sinusitis, otitis, ulcers, tracheal stenosis), lower resp (bilat nodular infiltrates with cavitation), renal (RPGN), can have multiple other sx's, c-ANCA +


-Churg-Strauss - asthma attacks, allergic rhinitis, eosinophilia. Constrictive pericarditis.


-Behcet's - uveitis (also optic neuritis, iritis), apthous ulcers, genital ulcers.


-HSP - IgA mediated hypersensitivity vasculitis mostly in <20yo. Fever, lower extremity palpable purpura, abd pain (occasionally intussusception), glomerulonephritis, arthralgias.



Treatment for all is a combo of steroids, plasmapheresis, cyclophosphamide

What is serum sickness (pathophys, cause, presentation, treatment)?

-Type III hypersensitivity response with immune-complex complement fixation in vessel walls.


-Associated with penicillin, sulpha, NSAIDs


-Get erythema to fingers/toes, then urticaria, lymphadenopathy, arthralgias, constitutional symptoms 7-21 days after exposure.


-Give steroids if severe

DDx for target lesions

Pityriasis rosea (herald patch with salmon colored central clearing)


Tinea corporis (very well defined)


Erythema multiforme (dark center, clearing, dark halo)


Urticaria (raised, migratory)


Erythema marginatum (dark center, clearing, dark halo similar to multiforme but there is only 1 and it is much bigger)


Secondary syphilis


MRSA risk factors

J ail



S ports


H omeless / H ealthcare


I VDU


R esidence


C rowded

Antibiotics effective against MRSA

Clindamycin


Septra


Doxycycline



Vancomycin


Linezolid


Cefepime


Ceftobiprole



Daptomycin


Tigecycline

Measles vs Rubella

Both present with viral exanthems and should get MMR


-Measles is highly contagious and classically presents with cough, coryza, conjunctivitis, and Koplic spots. Treat with Ig. Measles rash starts on hand and feet.


-Rubella presents with rash, fever and lymphadenopathy with a rash that goes face to trunk.

Treatment of pediculitis (lice) and scabies

Both


-Simultaneously treat the patient, sexual partners, family members, clothing, furniture and homes


-Clothes should be washed in hot water and dried in a hot dryer. Other things can be frozen for 5 days.



Lice


-Permethrin (Nix) 1% shampoo for 10m on day 1 and 8 while avoiding conditioner for 2 weeks



Scabies


-Permethrin 5% cream applied for 8-14h on day 1 and 8

Syphilis (Stages, Diagnosis, Treatment)

Stages


-Primary - painless chancre (papule -> 1cm ulcer) with painless lymphadenopathy


-Secondary - 6 weeks to 6 months post-exposure, symmetrical non-pruritic macular/papular rash to palms and soles, can have condyloma lata around genitals, fatigue, lymphadenopathy, exanthem, myalgia, pharyngitis


-Latent - Nil


-Tertiary - gummas, granulomatous ulcerative lesions on skin, liver, bones, brain



Treatment


-VDRL is positive after primary syphilis. Used for screening (false positives in SLE, thyroiditis, lymphoma, post-vaccine, mycoplasma, mono, hepatitis, measles, malaria, pregnancy)


-FTA used for diagnosis (flouresence treponomal antibody test)



Treatment


-Primary & secondary: Benzathine penicillin 2.4 million U IM; VDRL goes non-reactive after ~12 months


-Persistent or tertiary: treat weekly


-Watch for Jerisch Herscheimer reaction

Pemphigus vulgaris vs bullous pemphigoid

PV


-Autoimmune reaction affecting patients 50-60yo generally on penicillamine, captopril or rifampim


-Present with oral bullae -> painful ulcers then skin bullae -> painful ulcers


-Diagnose with history, + Nikolski sign, + Tzank smear


-Treat with high dose prednisone (100-300mg/d), immunosuppresants, plasmapheresis



BP


-IgG autoimmune reaction of those ~65yo. Less sick than PV.


-Present with tense, fluid-filled blisters and a negative Nikolski sign. Mucous membrane involvement is possible but less frequent than PV.


-Treat with prednisone and other immunosuppresants for 2-5 years and it generally resolves.

Canadian C-Spine Rule

Indications for dialysis in renal failure

AEIOU



A cidosis / A lkalosis (note: HCO3 can precipitate tetany/convulsions in the setting of hypoCa)


E lectrolyte abnormalities (HyperK, HyperMg, HyperCa - MM)


I ngestions that are dialyzable


O verload of fluid (CHF, pulmonary edema, severe HTN)


U remia (pericarditis, N/V, lethargy)

Bacteria causing UTI's

KEEPPSSS



K lebsiella (institutionalized, newborns)


E nterococcus (institutionalized)


E coli (>80% of UTI's)


P roteus (3-11yo)


P seudomonas


S taphylococcus saprophyticus (can be normal skin flora in perineum)


S erratia


S almonella

UTI treatment length

Uncomplicated lower tract - 3 days with nitrofurantoin, cefixime, cipro, septra



Complicated lower tract - 7 days (diabetes, sickle cell, immunocompromised) with cefixime, cipro, septra



Pregnancy lower tract - 10 days with cefixime or nitrofurantoin (avoid near term due to hemolytic anemia) or septra (avoid near term due to hemolytic anemia, jaundice, kernicterus)



Upper tract - 10-14 days with cefixime or ceftriaxone

Types of kidney stones and causes

Calcium oxalate 75% - excess calcium (milk alkali syndrome, high dietary intake, antacids, increased PTH). Oxalate increases in radiation enteritis, IBD, and ethylene glycol ingestion.



Struvite 15% - infection with urea-splitting organisms (pseudomonas, proteus, klebsiella, staph)



Hyperuricemia 10% - gout, tumor lysis syndrome, hematologic malignancies. they are radioluscent.



Cysteine 1% - inborn error of metabolism



Struvite, urate, and cysteine stones can form staghorn calculi.

5 locations of urinary obstruction

Renal calyx


UPJ (uretopelvic junction)


Pelvic brim


UVJ (uretovesicular junction)


Vesicular orifice

Acute scrotal pain / swelling differential and physical exam features

Pain


-Testicular torsion - negative cremasteric reflex


-Torsion of the testicular appendage (appendix testis or appendix epididymis) - blue dot sign


-Epididymitis - Prehn's sign


-Trauma


-Orchitis


-Testicular tumor WITH hemorrhage (normally tumor is not painful)


-Inguinal hernia (if incarcerated/strangulated)



Swelling


-Varicocele (bag of worms)


-Ideopathic scrotal edema


-Hydrocele



Causes of varicocele

Venous varicocities of spermatic veins (bag of worms)



-Right spermatic vein -> IVC - generally caused by IVC compression or thrombosis


-Left spermatic vein -> left renal vein - generally caused by RCC

Approach to priapism

Determine low (painful) or high (not painful) flow



Treatment of low flow


->4h duration requires treatment


-Noninvasive tx - walk up stairs (decrease flow to penis), ice packs, compress


-PO treatment - terbutaline 5-10mg PO (beta agonist)


-Analgesia with dorsal nerve block


-Aspiration of cavernosum


-Injection of alpha agonist (phenylephrine) or methylene blue


-Sicklers get O2 and hydration as well



Treatment of high flow


-Angiography, surgical shunt, if painful can do block

Causes of false positive hematuria

Myoglobin


Porphyria


Bilirubinuria



Meds


-Nitrofurantoin


-Rifampin


-Chloroquine/Hydroxychloroquine


-Iodine bromide



Foods


-Food coloring


-Beets


-Rhubarb


-Berries

Nephrotic vs Nephritic syndrome

Nephrotic - HALEH


H ypoalbuminea


A lbuminurea (>3.5g/d proteinuria)


L ipiduria


E dema


H yperlipidemia (and clotting - produce increased clotting factors)



Nephritic - PHAROH


P roteinuria (<3.5g/d)


H ematuria (micro or macroscopic)


A zotemia (increased urea/Cr)


R BC casts


O liguria (<400mL/d)


H ypertension

Causes of amenorrhea

-Hypothalamic - exercise, stress, anorexia, hypothalamic tumor, GnRH deficiency



-Pituitary - primary hypopituitarism, Sheehan syndrome, pituitary tumor



-Ovarian dysfunction - PCOS, gonadal dysgenesis (Turner's), menopause, radiation/chemo



-Endocrine - Hyperprolactinemia, hyper/hypothyroidism, Cushing's, hyperandrogenism (PCOS)



-Obstruction - imperforate hymen, cervical stenosis

Definition and causes of menorrhagia and metrorrhagia

Menorrhagia is prolonged (>7d) or heavy (>80cc) bleeding



Metrorrhagia is bleeding at irregular intervals (e.g. between periods



Non-structural (COTIPE)


C oagulopathy


O vulatory dysfunction (ovulation, anovulation, exogenous steroids)


I atrogenic (OCP) / I nfectious (endometritis, cervicitis, vaginitis)


P regnancy (implantation, ectopic, abortion, molar)


E ndometriosis


E ndocrine (Cushing's)



Structural (PLAMT)


P olyps


L eiomyoma


A denomyosis


M alignancy (Endometrial / Cervical / Ovarian cancer)


T rauma (sexual abuse, foreign body)

Treatment of unstable (stable) uterine bleeding

-Premarin 25mg IV q4-6h until bleeding stops along with an antiemetic (2.5mg PO bid-qid - follow up with progesterone for normal withdrawal bleeding OR 5-4-3-2-1 regular OCP's/day then 1 pill x 7 days, then 4 day period and restart)


-Tranexamic acid 1g IV (1g PO tid-qid while menstrating)


-Intrauterine foley to tamponade bleeding


-OR - D&C / Hysterectomy

Causes of false BhCG test

False positive


-Post-menopausal (usually <10)


-Abortion (x 60 days)


-BhCG secreting tumor (hydratiform mole)


-Exogenous source (e.g. to induce ovulation)


-Incomplete abortion, abortion with 2nd fetus, abortion with heterotopic ectopic



False negative


-Dilute urine early in gestation

DDx for hematuria (>5RBC / hpf)

Hematological/Cardiac


-Sickle cell (infarcts)


-Coagulopathy


-Endocarditis



Renal


-Glomerular - primary glomerulonephritis (post-strep) or secondary glomerulonephritis (HUS, TTP, SLE, PAN, PAN, Wegener's, Goodpastures)


-Nonglomerular - trauma, pyelonephritis, AIN, RCC, infarct, AVM, Polycystic Kidneys, Exercise



Postrenal


-Ureter - stone, TCC


-Bladder - trauma, TCC, cystitis


-Prostate - prostatitis, BPH, prostate cancer


-Urethra - Foley, urethritis



False


-Myoglobin


-Menstration


-Traumatic cath


-Drugs (rifampin, nitrofurantoin, chloroquine/hydroxychloroquine)


-Feeds (beets, berries, food coloring)

DDx for proteinuria

Glomerular (can be >10g/d)


-Nephrotic syndrome, minimal change disease, membranous GN, focal segmental glomerulosclerosis, Post-strep GN, IgA nephropathy



Tubular (generally <2g/d)


-UTI


-AIN


-Sickle cell



Overflow


-Multiple myeloma, Waldenstrom's macroglobulinemia, Amyloidosis



Other


-Orthostatic proteinuria


-Pregnancy


-Exertion, stress


What is ATN and its diagnostic criteria?

Acute Tubular Necrosis


-Death of the tubular epithelium of the kidney


-Generally caused by toxins (HHS, rhabdo, hemolysis, aminoglycosides, contrast) and hypoperfusion (shock)


-See FENa >1%, Urine Na >40

Requirements for the use of methotrexate in an ectopic pregnancy

-Patient is hemodynamically stable


-Tubal mass is <3.5cm


-No FHR


-No signs of rupture (FF)


-BhCG <1200-5000

Shoulder dystocia: problem, risk factors, diagnosis, treatment

Problem: vertical (rather than oblique) shoulder orientation of fetus (sacropubic)



Risk factors: maternal obesity, DM; fetal macrosomia; pregnancy post-date, prolonged 2nd stage



Diagnosis: can not deliver either shoulder, turtle sign



Treatment: HELPER


H elp (obs, anesthesia, neonatal)


E pisiotomy (oblique) / E mpty bladder


L egs flexed (McRoberts maneuver)


P ressure suprapublically to push the anterior shoulder down and to the side


E nter vagina (Rubin - post most accessible shoulder toward fetal chest; Woods - rotate 180 degrees Rubin plus spin the opposite hip the other direction)


R emove posterior arm (grab hand and sweep arm across the chest and deliver it with the shoulder; can have humerus and brachial plexus injury)



Other:


-Break the babies clavicle


-Symphesotomy


BLS Termination of Resuscitation

No defibrillation by AED


No ROSC prehospital


Not witnessed by EMS

ALS Termination of Resuscitation

No defibrillation


No ROSC prehodpitsl


Not witnessed by EMS


Not witnessed by bystanders


No bystander CPR

Risk factors for death due to asthma

Asthma history


-Intubation/ICU admission for asthma


-Hospitalized 2 or more times in past year


-To ED 3 or more times in past year


-Hospitilization/ED visit in past month


->2 MDI canisters of B-agonist/month


-Using or withdrawing from corticosteroids


-Difficulty perceiving asthma severity/symptoms



Social history


-Low socioeconomic status


-Psychosocial problems


-Illicit drug use (especially cocaine/heroin)



Comorbidities


-Cardiovascular disease


-Chronic lung disease


-Psychiatric disease

Definition and classification of COPD

Irreversible, progressive airway destruction secondary to an abnormal inflammatory response.



Chronic bronchitis: productive cough for >3 months in the past 2 years; high pCO2


Emphysema: destruction of the lung parenchyma due to imbalance of elastase/antielastase from inflammation; low pCO2 (breath a lot to maintain pO2)



4 classes in the Gold Classification - all have FEV1/FVC < 70%


I Mild FEV1>80%; no symptoms


II Moderate FEV1<80%; AECOPD and SOBOE


III Severe FEV1 <50%; affects QoL


IV Very Severe FEV1 <30%; R heart failure


4

Define AECOPD. What decreases mortality in COPD?

An acute Exacerbation of COPD is characterized by the Antonisen criteria: 1) increased dyspnea, 2) sputum production, or 3) sputum purulence. Generally need 2/3 to treat.



Mortality in COPD is decreased by 1) quitting smoking and 2) chronic oxygen therapy

Indications for intubation and mechanical ventilation?

-Respiratory arrest


-Decreased LOC despite maximal therapy


-Cardiovascular instability


-NIPPV failure or unable to use (exclusion criteria)


-Severe dyspnea


-Severe tachypnea


-Life-threatening hypoxia


-Severe acidosis / hypercapnea


-Severe illness requiring respiratory support

Complications of posterior nasal packing

B radycardia
A sphyxia / Aspiration / Arrest
D ysrhythmia
N ecrosis of mucosa, palate / Nasorespiratory reflex
O titis Media
S hock (Toxic Shock)
E ustachian tube dysfunction

Distinguish epiglottitis, peritonsillar abscess, retropharyngeal abscess

Lingual tonsillitis - hot potato voice, pain on tongue depression, scalloped anterior valecula



Epiglottitis - hyoid tenderness and muffled (not hoarse) voice, sniffing position



Peritonsillar abscess - hot potato voice, drooling, hallitosis, trismus, inferomedially displaced tonsil



Parapharyngeal abscess - same as peritonsillar except can have Horner's and oral/nasal/aural bleeding from carotid.



Retropharyngeal abscess - supine with head extended, neck pain, meningismus, cri du canard (duck quack voice)

Complications of deep space infections of the posterior pharynx

Airway compromise


Mediastinitis


Pericarditis


Pneumonia


Empyema


Lemierre's syndrome (jugular vein thrombophlebitis)


Horner's (sympathetic chain)


Carotid artery erosion or pseudoaneurysm


Cavernous sinus thrombosis


Mastoiditis


Otitis


Meningitis


Brain abscess

How does O2 increase the speed of PTx resolution?

Decreases the partial pressure in the blood and as per Henry's gas law this results in the N2 from the PTx being resorbed more quickly into circulation. It increases resorbtion from 1-2%/d to 4-8%/d

How do you calculate the size of a PTx in %?

((A x B x C)/3) x 10%

((A + B + C)/3) x 10%

What are light's criteria?

Distinguishes between exudative and transudative effusion



Exudative have at least one of:


Pleural fluid >2/3 of upper level of normal serum LDH


Pleural LDH/serum LDH >0.6


Pleural protein/serum protein >0.5



Highly sensitive, less specific for exudate

Causes of miscarraige

Two main:


-Chromosomal anomolies


-Uterine malformations (leiomyoma, bifid uterus, uterine scarring, cervical incompetence)



Other:


-Increased maternal/paternal age


-Low pre-pregnancy BMI


-History of miscarriage


-History of vaginal bleeding


-Maternal stress


-Increased parity


-Autoimmune disease


-Endocrine disorders (DM)


-Maternal infections


-Maternal toxin ingestion (cocaine, EtOH)

Categories of hypertension in pregnancy

Hypertension in pregnancy: >140/90


Preeclampsia: A disorder of pregnancy characterized by hypertension and proteinuria during pregnancy that is thought to be due to endothelial dysfunction



Types of hypertension in pregnancy


Chronic hypertension: dx'd before 20 weeks


Gestational hypertension: dx'd after 20 weeks and no proteinuria


Pre-eclampsia with chronic hypertension: proteinuria (>300mg/24h) and BP >160/110 in a patient with known hypertension


Pre-eclampsia: proteinuria (>300mg/24h) and BP >140/90

Amniotic fluid embolism: pathophysiology, major causes, presentation

Pathophysiology: release of amniotic fluid into the circulation causing an anaphylactoid reaction



Causes: labor, amniocentesis, uterine manipulation (version), placental separation. Can also occur during miscarriage/abortion and spontaneously.



Presentation: hypoxemia due to plugging of pulmonary vessels, cardiovascular collapse, non-cardiogenic pulmonary edema, DIC



Treatment: aggressive ventilatory and hemodynamic support. Plasma exchange to remove cytokines. Delivery of fetus.

Diagnostic algorithm for PE in pregnancy

If leg symptoms -> compression U/S (treat if pos)


If no leg symptoms or U/S neg -> CXR


If CXR clear -> V/Q scan


If V/Q inconclusive -> CTPE


If CXR abnormal -> CTPE


If CTPE neg -> stop


Hyperemesis gravidarum: definition, onset,

Definition: emesis that causes starvation metabolism with weight loss, dehydration, ketonuria, and ketonemia



Onset: 6-20 weeks



Pathyphys: unsure, associated with increased B-hCG, molar pregnancy, and multiple gestation



Management: fluid rehydration, enteral nutrition, diclectin (doxylamine and B6) up to 8 tabs/d then gravol then zofran/maxeran then methylprednisone

What is a teratogen? What characteristics of a drug increase its ability to cross the placenta?

Any chemical, pharmacologic, environmental or mechanical agent that can cause deviant or disruptive development of the conceptus



Characteristics that increase crossing the placenta


Size (small), ionization (uncharged), protein binding (free drug), pKa (weak organic acids get caught in fetal base-ness), lipid solubility (more soluble)

List 10 teratogens

Heavy metals/toxins: Lead, CO, Iodine


Anticoagulant: Warfarin


Antiarrhythmics: Amiodarone, Quinine


Anti-inflammatories: NSAIDs, misoprostol


Antiepileptics: Phenytoin, VPA, carbamazepine


Chemotherapeutics Busulfan, methotrexate, thalidomide


Anti-hypertensives: ACEI, ARBs


Dermatologic: Retinoic acid derivatives


Androgens/Estrogens: OCP, HRT, diethylstilbestrol


Antipsychotics: Lithium


Drugs of Abuse: EtOH, cocaine


Antibiotics: Erythromycin, tetracycline,


aminoglycosides

Distinguish true labor from false labor

True labor


-cyclic uterine contractions of increasing frequency, duration, and strength


-cervical dilation


-bloody show



False labor (Braxton-Hicks contractions)


-no cervical dilation or effacement


-intact membranes


-do not escalate in frequency, duration or strength


-not sensed by external monitors

What is assessed on pelvic exam in true labor? How can fontanelles be distinguished?

Cervical dilation, cervical effacement, presenting part, station of presenting part, orientation of presenting part



The anterior fontanelle has 4 sutures while the posterior fontanelle has 3. OA is the most common presentation.

Steps to breech delivery

-Get a C-section instead


-Call obstetrics


-Monitors


-Rule-out prolapsed cord


-Open pelvis (knees wide)


-Episiotomy


-When abdomen is through pull out 10-15cm of cord to try to avoid it getting trapped


-Grasp neonate by the pelvis and direct face/abdomen away from the symphysis


-Keep the next flexed forward (do not let it extend!! Causes spinal cord injury)


Umbilical cord prolapse: diagnosis and treatment

Diagnosis: see the cord on pelvic, suddenly non-reassuring FHR



Treatment: emergency C-section, mother in knee to chest position with head down, fingers elevate presenting part, Foley to install 500-750 cc of fluid into bladder, replace cord above the presenting part

Uterine prolapse: risk factors, diagnosis and treatment

Risk factors:


-Primip


-Oxytocin use


-fundal implantation


-forceful traction on umbilical cord


-MgSO4 use



Diagnosis


-Severe abdominal pain


-Visualization of the uterus at the os or in the introitus



Treatment


-Do NOT remove the placenta while the uterus is out


-Give tocolytics (terbutaline, MgSO4, halogenated anesthetics to relax the uterine ring


-Replace uterus


-Then start oxytocin

DDx for diffuse wheeze

Pulmonary


-Lower airway


o Congenital: CF, Bronchopulmonary dysplasia


o Trauma: FB, Aspiration


o Infectious: Pneumonia, Bronchiolitis, COPD


o Inflammatory: Anaphylaxis


o Vascular: PE


o Degenerative: Sarcoidosis


-Upper airway


o Congenital: Vascular ring


o Trauma: FB, Caustic ingestion


o Infectious: Epiglottitis, Croup, Retropharyngeal abscess


o Inflammatory: Anaphylaxis, Angioedema


o Neoplastic


o Vascular ring


Extra-pulmonary


-CHF


-ARDS

Asthma severity classifications

PEFR


Mild >70% predicted


Moderate 40-70% predicted


Severe <40% predicted


Life threatening <25%

Side effects of steroids

SHORT TERM


o Insomnia


o Mood alterations or Psychosis


o GI upset


o Increased appetite/weight gain


o Fluid retention


o Hyperglycemia


o Hypokalemia



LONG TERM


o Hyperglycemia


o Osteoporosis


o Thin skin, easy bruising, poor wound healing


o Rare: HTN, PUD, AVN, Allergic reaction


o Adrenal suppression if > 4 courses/year

Soft signs of arterial injury in neck trauma

FOAHHDDS
F ocal neuro deficit
O ropharnygeal blood
A irleak from chest tube
Hemoptysis / Hematemesis
H ematoma (non-expansive)
D ysphagia / Dysphonia
D yspnea
Subcutaneous Air (or mediastinal Air)

Risk factors for primary and secondary PTx

Primary:


-Tall, skinny, male smokers with Marfan's and Mitral valve prolapse at altitude



Secondary:


-Airway: cystic fibrosis, asthma, COPD


-Infectious: TB, PJP, lung abscess, necrotizing


-Interstitial: sarcoid, fibrosis, pneumoconioses, tuberous sclerosis


-Neoplasm: primary or metastatic


-Miscellaneous: endometriosis, pulmonary infarction

When is a diagnostic thoracentesis indicated?

Unexplained pleural effusions



Pneumonic and parapneumonic effusions


-Pneumonia with a parapneumonic effusion >10mm wide on decubitus films


-Loculated pleural effusion


-Thickened pleural core



Diagnosis of a possible malignancy

Indications for bicarbonate therapy

-pH <7.1


-HCO3 <12


-Refractory hypotension (to pressors)


-TCA toxicity


-ASA toxicity


-Phenobarb overdose


-Ethylene glycol and methanol ingestion



Empiric dose is 1 mEq/kg with 1/2 as a bolus and 1/2 over 4 hours

How can bicarbonate cause a paradoxical intracranial acidosis? Other complications?

Paradoxical CNS acidosis


-HCO3 diffuses over the BBB slowly


-HCO3 in the plasma is converted by carbonic anhydrase to CO2 which is then blown off to decrease pH


-This CO2 can diffuse quickly over the BBB decreasing the CNS pH


-With the improved pH the RR is decreased increasing CO2 which again crosses the BBB



Other complications


-Hypernatremia


-Hyperosmolarity


-Hypocalcemia


-Hypokalemia

Metabolic alkalosis: causes

Causes: hypovolemia, hypokalemia, hypochloremia



DDx:


-Volume contracted (saline responsive, urine Cl<10): Vomiting, diarrhea, NG suction, diuretics


-Normal or expanded volume (saline unresponsive, urine Cl>10): primary hyperaldosteronism (Conn's, CAH), secondary hyperaldosteronism (CHF, cirrhosis, nephrotic syndrome, Cushing's, Barter's, Licorice, ectopic ACTH)


-Other: milk-alkali syndrome, citrate, nonparathyroid hypercalcemia



Treatment


-Saline responsive: fluid and acetazolamide


-Saline resistant: replace K and spironolactone (aldosterone antagonist)

K - symptoms of hyperkalemia and hypokalemia

Hyperkalemia:


-CVS: dysrhythmias (heart block, WCT, sine wave pattern)


-CNS: muscle cramps, weakness, paralysis, paresthesias



Hypokalemia (sloooow muscles):


-CNS: lethargy, depression, irratibility, confusion, paresthesias, decreased reflexes, weakness


-CVS: dysrhythmias (heart blocks, AF)


-GI: N/V, ileus


-MSK: myalgias, rhabdo, weakness

Na - symptoms of hypernatremia and hyponatremia

Hypernatremia:


-General: fatigue, malaise, anorexia, N/V


-CNS: seizures, AMS, coma


-MSK: twitching, hyperreflexia, clonus, tremor


-Skin: dry and doughy



Hyponatremia:


-Nonspecific: nausea, malaise, anorexia


-CNS: HA, AMS, decreased LOC, seizures, focal neural deficits


-MSK: cramps, weakness


Definition of DKA

Due to a lack of insulin and increase in glucagon leading to hyperglycemia, osmotic diuresis, and ketoacidosis.



Glucose >13.9mmol/L (peds <11)


pH <7.3


HCO3 <18 (peds <15)


Serum or urine ketones

How does iodide bolus affect thyroid hormone production?

2 possible effects:



Wolff-Chaikoff effect: excess iodide inhibits ion trapping, thyroglobin iodination, and blocks the release of thyroid hormone



Jod-Basedow effect: in patients with Graves or multinodular goiter who are iodine deficient it can induce hyperthyroidism

Thyroid storm: cause, precipitants, and treatment

Cause: increased T3/T4 over a prolonged period of time increases B receptors and sympathetic surge activates them all at once.



Precipitants:


-Trauma (burns, surgery, thyroid trauma)


-Vascular (MI, CVA, PE, CHF)


-Toxicologic (Iodine, radiocontrast, hormone ingestion, amiodarone, stopping therapy, ASA, chemo, pseudoephedrine, OP's)


-Sepsis


-Metabolic: hypo or hyperglycemia


-Pregnancy


-Psych: mania, emotional crisis



Treatment:


-Decrease hormone production with PTU 1g po


-Decrease release of preformed hormone with Saturated Solution of Potassium Iodide (SSKI) 5 drops 1h after PTU; Li works too


-Beta blockade with propranolol 1-2mg IV q15m


-Prevent T4->T3 conversion with hydrocortisone 100mg IV


-Prevent enterohepatic circulation with cholestyramine


-Prevent entry of thyroid hormone into cell with L-Carnitine


-Supportive care with cooling, benzos, acetaminophen


-Remove thyroid hormones with plasmapheresis, dialysis, plasma exchange


-Treat precipitant


-Admit to ICU


-Thyroid surgery or ablation

Myxedema coma: cause, precipitants, and treatment

Cause: severe longstanding hypothyroidism with a precipitant



Precipitants:


-Trauma, burns


-Vascular: CVA, GIB, MI


-Toxicologic: lithium/iodide (decrease release), narcotics, benzo's, barbiturates


-Metabolic: hypoglycemia, hyponatremia, hypoxia, DKA, hypercapnea


-Cold exposure



Treatment


-ABC's - note macroglossia/mucosal swelling


-IVF - watch Na and glucose (often need to be added)


-Thyroid hormone - T4 if old/cardiac hx (T4 300-500ug IV bolus); T3 if young (T3 10-20ug IV bolus). Can also give a bit of each.


-Hydrocortisone 100mg IV


-Rewarming


-Treat precipitant

Treatment of upper and lower esophageal foreign body

Upper:


-Magill forceps / Glidescope


-Foley


-Bougienage


-Endoscopy



Lower:


-Pop


-Glucagon


-Maxeran


-Nifedipine


-SL nitro


-Midazolam sedation


-Endoscopy

Indications for immediate endoscopy of an esophageal foreign body

-Complete obstruction (unable to handle secretions)


-Respiratory distress (FB in esophagus can compress trachea)


-Sharp objects


-Impacted for 24 hours


-Coins in the proximal esophagus


-Alkaline button batteries


-Failure of medical treatment


-Coins in children <2yo (relative)

Complications of esophageal FB's

-Abscess


-Tracheo-esophageal fistula


-Aorto-enteric fistula


-Perforation and mediastinitis / pneumothorax / pneumomediastinum

Indications for immediate removal of a foreign body in the stomach

>2.5cm wide


>5cm long


Sharp


Toxic (e.g. lead)


>3-4 weeks impaction



90% of objects that make it to the stomach make it all the way through. If past the pylorus things can generally be left alone (then require surgery rather than endoscopy). Remove if hasn't moved in 3-4 weeks.

Indications for surgery to remove a foreign body in the small intestines

>99% of these pass without problem



-Hasn't moved for >7 days


-Hasn't passed in >4 weeks


->1 industrial strength magnet (not a fridge magnet)

Grades and treatment of hepatic encephalopathy

Grades


I - Depression, irritability, disordered sleep, mild cognitive dysfunction


II - Lethargy, disorientation, asterixis


III - Somnolence, disorientation, confused speech


IV - Coma



Treatment


-Stop all sedatives / CNS depressants


-Correct hypokalemia (allows ammonia to be excreted renally)


-Remove GI protein (treat bleed, decrease protein intake, treat constipation)


-Give lactulose 30mL qid (becomes lactic acid and traps NH4+ and decreases transport time)


-Flagyl or Clarithromycin to kill NH3 producing gut flora


-Acarbose to decrease NH3 production


-MARS

How does lactulose correct hepatic encephalopathy? What are other treatments?

Lactulose is converted to lactic acid, acidifying the bowel contents. This converts ammonia (NH3) to ammonium (NH4+) and its positive charge keeps it trapped in the lumen.



Remove other sources of protein (e.g. NG for GIB, protein-restricted diet)


Clarithromycin or Flagyl (alter gut flora to decrease ammonia production)


Acarbose (changes bacterial activity to decrease ammonia)

What is the SAAG? How is it interpreted?

SAAG = serum-ascites albumin gradient (serum albumin - ascites albumin)


This replaces the distinction between transudate/exudate



SAAG<11 = inflammation or decreased oncotic pressure (Carcinomatosis, TB, Pancreatic or biliary ascites, nephrotic syndrome)


SAAG>11 = portal hypertension (Cirrhosis, Alcoholic hepatitis, portal-vein thrombosis, Budd Chiari, liver mets)

Diagnosis of SBP. Differentiating primary versus secondary bacterial peritonitis

Diagnosis:


-PMN >250 cells/mm3


-Positive culture


-Ascites fluid pH <7.34 or a gap between blood pH of >0.10



Primary:


-Protein <10


-Prior SBP


-Bili >42mmol/L


-Platelets <98


-Single bacteria cultured



Secondary:


-Protein >10


-Glucose <2.8


-LDH > upper limit of normal serum LDH


-Multiple types of bacteria cultured

The triad and tetrad of ascending cholangitis

Charcot's triad:


-Fever


-Jaundice


-RUQ pain



Raynaud's pentad:


-Charcot's triad plus altered mental status and shock (hypotension/tachycardia)

Sonographic findings of an abnormal TV ultrasound

-BhCG >3000 and no gestational sac


-Gestational sac >13mm and no yolk sac


->5mm crown rump length and no fetal heart tones


-No fetal heart tones after 10-12 weeks


-Gestational sac >25mm and no fetus

Risk factors for ectopic pregnancy

PMHx - PID, previous ectopic or abortion, tubal surgery, infertility, abnormal anatomy


Patient factors - smoker, age


Pregnancy factors - has IUD, embryo transfer fertility treatments

What is a molar pregnancy? What are the types? How does it present

-Disordered proliferation of chorionic villi



Two types:


-Complete hydatidiform mole: absence of fetal tissue


-Incomplete hydatidiform mole (much less common): fetal tissue with focal trophoblastic hyperplasia


-Can also get choriocarcinoma (responds well to chemo, can metastasize)



Presentation


-Hyperemesis gravidarum


-Crazy high BhCG


-Snowstorm U/S

Numbness or pain to the outer side of the thigh associated with pregnancy or obesity

-Meralgia paresthetica


-Due to compression of the lateral femoral cutaneous nerve of the thigh as it passes the inguinal ligament

Cause and treatment of postpartum hemorrhage

Cause:


Tissue - retained products, accreta (placental villi adhere to myometrium) / increta (enter the myometrium) /percreta (through the myometrium) make more likely


Tone - diagnosis of exclusion


Trauma - perineal tears, vulva/vaginal epithelium trauma


Thrombin - vWD, coagulopathy, DIC



Treatment


Uterine massage


Repair lacerations


Remove products of conception


Oxytocin - run 40U/1L fast; 10U IM


Misoprostol (PGE1) - 800-1000mcg PR


Hemabate (PGFalpha) - 250mcg IM


Pack uterus


Foley in uterus


Embolize vessels


D&C


Hysterectomy

Types of lactic acidosis

A - tissue hypoxia


B1 - systemic disorders (DM, renal insufficiency, leukemia, sepsis)


B2 - substance associated (biguanides, methanol, salicylates, INH)


B3 - heritable metabolic disease

Risk factors, presentation, and treatment of cerebral edema in DKA

Risk factors


-New onset diabetes


-Children <5yo


-Extremely ill on presentation


-Treated with HCO3


-Excessive fluid replacement


-Rapidly dropping serum osmolality



Presentation


-HA


-Behavioral changes


-Incontinence


-Seizures


-Autonomic (BP and temp)


Then coma, respiratory arrest, death



Treatment


-Mannitol 1-2g/kg over 15m


-Decrease IVF and insulin rate


-Intubate, hyperventilate, CT head



NB - cause is unknown - ? idiogenic osmoles

4 characteristics that determine the toxicity of a hydrocarbon

•Viscosity
•Volatility
•Side chains (halogenated)
•Surface tension

Diagnostic criteria of HHS

Glucose >33


Sosm >320


pH >7.3


HCO3 >15

Complications of long-term DM

Infection (immunocompromised secondary to decreased neutrophil and lymphocyte activity)


Diabetic foot


Insulin allergy (must go desensitization or change type)


Cutaneous manifestations (diabetic dermopathy, dermal hypersensitivity at injection sites as well as hypo or hypertrophy, acanthosis nigrans, necrobiosis lipoidica diabeticoricum, xanthoma diabeticorum)


Macrovascular complications (CAD, CVD, PVD)


Microvascular complications (Nephropathy, Retinopathy, Neuropathy)

Causes of rhabdomyolysis

Traumatic


-Crush


-Compartment syndrome


-Excessive exertion



Non-traumatic (relate to lack of ATP)


-Electrolytes (HypoK or HypoP)


-Ischemia


-Congenital ATP deficiency due to inborn errors of metabolism


-Environmental (electrical injury, heat stroke, hypothermia, rattle snake bite)


-Endocrine (pheochromocytoma, DKA, HHS, hypo/hyperthermia)


-Toxin (SS, NMS, statins, alcohol)


-Infections (all types)


-Seizures


-Rheumatic (polymyositis, dermatomyositis, Sjogren's)

Thyroid diseases

Hyperthyroid


-Graves (TSH receptor antibodies)


-Toxic multinodular goiter (multiple overactive and big areas, can cause SVC syndrome)


-Toxic adenoma


-Acute thyroiditis (gland is tender)


--> Autoimmune (Hashimoto's antibody to thyroid peroxidase; Postpartum; Sporadic)


--> Infectious (De Quervian's viral; suppurative bacterial)


--> Drug induced (amiodarone, iodine, interferon, lithium)


-Pituitary adenoma


-Gestational trophoblastic / germ cell tumors (create TSH-like hormone)



Hypothyroid


-Hypothalamic and pituitary underactivity (tumors, Sheehan's, amyloidosis, sarcoidosis, radiation)


-Late thyroiditis (as per above)


-Iatrogenic (thyroidectomy, ablation, lithium, iodine, amiodarone)


-Congenital (causes cretinism)


Primary versus secondary adrenal dysfunciton

Primary is a disease of the gland itself and affects all 3 functions (glucocorticoids, mineralocorticoids, androgens)


-See hyperpigmentation, hyperkalemia, hyponatremia, salt craving, and acidosis from the lack of aldosterone / excess ACTH



Secondary is a disease of the pituitary and does NOT affect mineralocorticoids (regulated by the RAAS)


-Still get hyponatremia, but it is due to increased ADH



Both


-Hypotension


-Depression, delerium, HA, abdominal pain, emesis, hypoglycemia, hyponatremia (differnet reasons), hypercalcemia, fevers, ARF

Steroid equivalency (hydrocortisone, prednisone, methylprednisolone, dexamethasone)

Hydrocortisone = 1


Prednisone/Prednisolone = 4


Methylprednisolone = 5


Dexamethasone = 25

Esophageal narrowings and risk factors for obstruction / dysphagia

Narrowings


-Upper esophageal sphincter (cricopharyngeus)


-Aortic arch


-Left mainstem bronchus


-Lower esophageal sphincter



Causes of obstruction / dysphagia



Poor dentition (they don't chew)



Intrinsic


-Esophageal carcinoma


-Shatzki's ring


-Peptic stricture


-Esophageal web



Extrinsic


-Cardiomegaly


-Aortic aneurysms or anomylous right subclavian


-Goiter


-Mediastinal tumor


-Enlarged lymph nodes


-Zenker's diverticulum



Neuromuscular (Neuro - head trauma, brain tumor, CVA, Alzheimer's, Parkinsons, MS, ALS, Myesthenia; Muscular - achalasia, scleroderma)



Toxic (Lead or EtOH)



Infectious (Bacteria - diptheria, botulism, syphilis, tetany OR Viral - rabies, polio)

What is Mackler's triad? How can the problem be diagnosed?

Suggests esophageal rupture



-Subcutaneous emphysema


-Chest pain


-Vomiting



Diagnose with contrast study. Use gastrograffin if no risk of aspiration (safer but less sensitive test; pneumonitis if aspirated) THEN barium (worse inflammatory response through perforation). Try CT if normal or unsafe to do.

Contributors to thte development of GERD and evidence-based ways to get rid of it

-Decreased sphincter tone (anticholinergics, caffeine, benzo's, nicotine, nitrates, peppermint, chocolate, estrogen, progesterone)


-Decreased esophageal motility (DM, achalasia, scleroderma)


-Increased intraabdominal pressure (pregnancy, obesity)


-Decreased gastric emptying (anticholinergic, diabetic gastroparesis, outlet obstruction)



Evidence-based treatments: weight loss and bed elevation

Eradication treatment for H Pylori

Triple:


Clarithromycin 500bid / Amoxicillin 1000bid OR Metronidazole 500bid/ PPI x 10-14d



OR



Quadruple:


Bismuth subsalicylate (pepto-bismol) 525qid / metronidazole 250qid / Tetracycline 500qid / PPI x 10-14d

Poor predictors of outcome in upper esophageal bleed

Components of the Rockall score



Age >60


Heart failure


Ischemic heart disease


Renal failure


Liver failure


Metastatic cancer


Gastric cancer


Vigorous bleeding

DDx for transaminitis

-Structural:


o Inflammatory/ Autoimmune/ Infiltrative: autoimmune hepatitis (PBS, PSC), NASH (? d/t insulin resistance), amyloid


o Vascular: Budd-Chiari (thrombosis of hepatic veins or IVC/SVC), portal vein thrombosis, ischemia, CHF


o Congen/Degen: neonatal hepatitis


-Toxicology: acetaminophen, EtOH, INH, iron, phenytoin, ecstasy (autoimmune hepatitis)


-Infection:


o Viral: HAV, HBV, HCV, HDV, HGV, EBV, CMV


o Protazoan: amoeba


o Toxoplasmosis


o Associated with bacterial sepsis


-Metabolic: Wilson’s disease (copper overload), Reye’s syndrome, hemochromatosis


-Pregnancy: Fatty liver of pregnancy


-GI: gallstones, strictures, cholangitis, biliary/pancreatic cancer, annular pancreas (obstructive causes)

Hepatitis serology

Hep A


-For acute infection send HAV IgM


-For chronic infection send HAV IgG



Hep B


-For acute infection send HBV sAg and HBV cAb IgM


-For chronic infection send HBV cAb IgG


-For vaccine immunity send HBV sAb



Hep C


-HCV Ab

Hepatitis post-exposure prophylaxis

A: HAIg to unvaccinated close personal contacts, childcare workers/attendees (people who wipe their bum), similar food-borne source in last 2/52



B: HBIg to:


-unvaccinated / low titer recipients exposed to source that is HBV sAg + OR high risk


-neonates with HBV sAg + mothers



C: N/A

Signs of cholecystitis on ultrasound

-Stones / biliary sludge


-Wall thickening (2-4mm)


-Distension of GB (>4cm wide or 10cm long)


-Pericholecystic fluid


-Air in the GB wall (emphysematous or gangrenous cholecystitis)


-Murphy's sign (sonographic)

Treatment of hyponatremia with focal neurologic symptoms, seizure, or coma. Complication of rapid correction.

Hypertonic (3%) saline 100mL over 10m then 100mL over the next hour (approximately 3mL/kg total)



After this aim to correct by 0.5mEq/L/h if chronic, 1mEq/L/h is okay if acute



Complication: central pontine myelinolysis

Causes, diagnosis and treatment of SIADH

Lung masses


-Cancer, pneumonia, TB, abscess


CNS disorders


-Infection (meningitis, abscess), mass (subdural, postop, CVA)


Drugs


-Thiazides, narcotics, oral hypoglycemic agents, barbiturates, neoplastic agents, vasopressin



Diagnosis - low Sosm (<280), high Uosm (>100) with no other explanation



Treatment - water restriction, treat cause

Causes of hypercalcemia and hypocalcemia

Hypercalcemia


-Increased intake (Ca supplements, milk-alkali)


-Decreased losses (HCTZ)


-Bone resorption (primary hyperparathyroidism, parathyroid-like hormone from small cell lung tumor, lytic bone lesions)


-OD - estrogens, vitamin A, vitamin D, Lithium


-Endocrine - hyperthyroid, adrenal insufficiency


-Granulomatous disorders (activate macrophages that convert vit D to make active) - sarcoid, TB, coccidiomycosis, histoplasmosis



Hypocalcemia


-Hypoparathyroidism (congenital, maternal, thyroid surgery)


-Tox (EtOH, chemo)


-Hyperphosphatemia, tumor-lysis syndrome

Ca - symptoms and treatment of hypercalcemia and hypocalcemia

Hypercalcemia


-CNS - AMS, ataxia, fatigue


-CVS - HTN, short QT, brady, STE


-GI - N/V, anorexia, ileus, constipation


-Renal - polyuria, dehydration, nephrolithiasis


Treatment - IVF, zaledronic acid, calcitonin, steroids, lasix, underlying cause



Hypocalcemia


-Neuromuscular - paresthesias, tetany (Chvostek's, Trousseau's)


-CV - long QT, hypotension, brady, arrest


-Resp - bronchspasm, laryngospasm


-Psych/CNS - confusion, psychosis, dementia, depression, anxiety, irritability


Treatment - asymptomatic CaCO3 1-4g/d po, stable CaGluc 10mL IV, unstable CaCl4 10mL IV

Conditions that can cause a false positive lipase result (not pancreatitis)

Many false positives at standard cutoff. Quite specific at 5x standard level, but down to 60% sensitivity. 2x cutoff is best for maximal sensitivity/specificity.



-Cholecystitis


-Bowel obstruction


-Peritonitis


-Duodenal ulcer


-DKA


-Trauma


-Post ERCP


-Idiopathic

x-ray and ultrasound findings of pancreatitis

x-ray


-Pleural effusion


-Pancreatic calcification


-Free air (? due to perf'd something)


-Ileus


-ARDS



Ultrasound


-Occasionally can see CBD stone and/or enlarged hepatic duct (suggesting distal obstruction)

Causes of simple and closed loop SBO

Top 3:


-Adhesions


-Hernias


-Cancer



Intrinsic - congenital, IBD, radiation enteritis, cancer, intussusception, hematoma



Extrinsic - hernias, adhesions, volvulus, compressing tumors, abscesses, hematomas



Intraluminal - FB, gallstones, bezoar, barium, ascaris

X-ray signs of intussusception

Crescent sign


Target sign


Abdominal mass (no air in one area - usually RUQ) / No liver edge sign


Air fluid levels (SBO)


Dilated loops of bowel (SBO)



NOTE: In adults (as opposed to children) you do not want to reduce this with enema as it is often caused by cancer and this can result in seeding

X-ray signs of mechanical SBO, closed loop obstruction, ileus. Normal measurements of bowel.

Mechanical


-Dilated proximal loops and flattened distal loops


-Sharply angulated or step-ladder loops of small bowel


-Multiple air-fluid levels


-'String of pearls' (pockets of gas trapped in the plicae semicircularis when the bowel is full of fluid)



Closed-loop


-Coffee bean sign (U-shaped bowel loop also seen in sigmoid volvulus)


-Pseudotumor sign (fluid filled loop resembling a mass)



Ileus


-Dilated loops throughout the entire bowel including the colon


-Dilation less prominent


-Air fluid levels less prominent



Bowel measurements:


-Small 3cm


-Large 6cm


-Cecum 9cm

Causes of mesenteric ischemia and risk factors

-Arterial embolism ~50% - mostly SMA (CAD, valvular disease, AF, aneurysms, dissections, coronary angiography) - needs embolectomy


-Arterial thrombosis >15% - mostly SMA and have h/o abdominal angina (elderly, PVD, hypertension) - needs revascularization, heparin


-Venous thrombosis <15% (same risk factors as DVT/hypercoaguability; Factor V Leiden most common) - needs heparain, thromboplasty


-Non-occlusive - 20% (all shock states, cocaine, vasopressors; >50yo)



Lactate is highly sensitive


CT angiography is most helpful diagnostic test; Angiography is gold standard and early angiography decreases death

Modified Alverado score, WBC/CRP, U/S and CT for Appy

Alverado score


History: Migratory RLQ pain, Anorexia, N/V


PE: T>37.5, RLQ tender (2 points), Rebound tenderness, Leukocytosis (2 points)



WBC<10 and CRP<12 have a -LR of 0.09 (very sensitive) but less helpful in peds.



U/S 75-95% sensitive, 85-95% specific - operator dependent but 1st choice for kids/women - see non-compressible, thick-walled (>2mm), dilated (>6mm), thickened mesentary, pain with compression, appendicolith



CT 95% sensitivity and specificity

Rome III criteria for IBD

Recurrent abdominal pain/discomfort for at least 3d in the past 3m associated with 2/3 of:


-Improvement with defecation


-Onset associated with a change in stool frequency


-Onset associated with a change in stool appearance

Causes of large bowel obstruction

1 - Colorectal cancer


2 - Volvulus


3 - Diverticulitis


4 - Extrinsic compression from mets



Also:


Abscess, stricture due to chronic ischemia, fecal impaction, IBD, CF, Hirschsprung's, body packers/stuffers, Ogilvie's (pseudo-obstruction)

AXR findings of large bowel obstruction

Distended colon


Air-fluid levels


Cecal dilation >12cm has increased risk of perforation

Volvulus types, risk factors, x-ray findings

Gastric: hiatal hernia, either between 40 and 50yo or <1yo. Often have diaphragmatic defects, gastric ulcer or cancer, adhesions, paralyzed diaphragm. Can't pass NG tube!!



Cecal: pregnancy, 'coffee bean sign' pointing to LUQ, also can have air-fluid levels in the small bowel, paucity of colonic gas. Treatment surgical.



Sigmoid: elderly, psych/neuro disease, institutionalized, constipation, high fiber diet, 'coffee bean sign' pointing to RUQ, bird's beak contrast. Treatment endoscopic detorsion or surgery.

Crohn's versus colitis

Crohn's affects mouth to anus / Colitis large colon and rectum only



Crohn's commonly found in terminal ileum and colon / Colitis starts at rectum and moves proximally



Crohn's is transmural / Colitis is superficial mucosa



Crohn's has skip lesions / Colitis is continuous



Crohn's gets primary sclerosing cholangitis / Colitis gets colon cancer

Extra-intestinal manifestations of IBD

ULCERATIVE


U rinary stones


L iver cirrhosis / sclerosing cholangitis


C holelithiasis


E rythema nodosum / erythema multiforme / pyoderma gangrenosum


R etardation of growth


A rthralgias / arthritis / ankylosing spondylitis


T hrombophlebitis


I atrogenic (steroids)


V itamin deficiency


E yes (uveitis, episcleritis)



Also pulmonary fibrosis

Intestinal manifestations of IBD

COLITIS


C ancer


O bstruction


L eakage / perf


I ron deficiency


T oxic megacolon


I nanition (wasting)


S tricture



Also: abscess, fistula

What is toxic megacolon? What causes it? What's the treatment?

Inflammation of the smooth muscles of the colon leads to dilation and perforation if untreated. Patients look toxic and have dilated colon on AXR (>6cm).



Often due to infection (C Diff gets po vanco or po/iv flagyl; other gets ceftriaxone/flagyl), IBD (gets tazo and steroids), antimotility agents (anticholinergic or opioid - stop them). May need OR.

What is required to prove negligence in a malpractice suit?


-Health care provider has a duty of care


-That duty of care is breached by breaking the standard of care


-The patient is harmed


-There is a direct link between the breach and the harm

Mimics appendicitis


Backpacker's diarrhea


Raw/undercooked poultry


Associated with GBS


Diarrhea and seizures


Associated with Reiter's


Raw oysters/shellfish


Prolonged diarrhea


Dysentry without fever


Fried rice


GI and neuro


Cold allodynia / hot/cold reversal


Worse after EtOH ingestion


Mayo/potato salad


Eggs

Mimics appendicitis: campylobacter and yersinia


Backpacker's diarrhea: giardia lamblia, campylobacter


Raw/undercooked poultry: campylobacter


Associated with GBS: campylobacter


Diarrhea and seizures: shigella


Associated with Reiter's: salmonella


Raw oysters/shellfish: vibrio parahemolyticus, plesiomonas


Prolonged diarrhea: yersinia, aeromonas, parasite


Dysentry without fever: e coli O157:H7


Fried rice: bacillus cereus (toxin mediated)


GI and neuro: ciguatera toxin


Cold allodynia / hot/cold reversal: ciguatera toxin


Worse after EtOH ingestion: ciguatera toxin


Mayo/potato salad: staph aureus


Eggs: salmonella

Bacterial causes of diarrhea; antibiotic treatment

CSS Yalk Constantly - So Believe Every Child Vomiting And Pooping



C ampylobacter


S higella - treat dysenteriae for public health


S almonella - treat typhi and all food handlers for public health


Y ersinia


C lostridium jejuni


S taph aureus (toxins)


B acillus cereus (toxins)


E coli (toxins)


C difficile and perfringins (toxins)


V ibrio cholera (toxins) and parahemolyticus


A eromonas


P lesiomonas



Toxin-producing generally do not respond to antibiotics



Antibiotics for severe infectious diarrhea with no evidence of HUS with cultures pending - children cefixime/azithro x 3-14d; adults cipro x 3-14d

Causes of free fluid in the abdomen

-Blood


-Urine


-Peritoneal dialysis fluid


-Ascites


> Liver disease - cirrhosis, alcoholic hepatitis, portal vein thrombosis, Budd-Chiari, liver mets (SAAG>11)


> Abdominal or ovarian malignancies / carcinomatosis (SAAG<11)


> TB peritonitis (SAAG<11)


> Pancreatitis (SAAG<11)


> Nephrotic syndrome (SAAG<11)


> CHF


> Hemodialysis

Internal hemorrhoid classification and treatment

1st degree - sense of fullness, no prolapse, medical management


2nd degree - prolapse during defecation and spontaneously reduce, medical management


3rd degree - prolapse spontaneously and during bowel movement, reduce spontaneously, medical or surgical management


4th degree - permanent prolapse with risk of thrombosis, surgical repair

Medical and surgical hemorrhoid treatment

Medical: WASH


W arm water


A nalgesia (topical nifedipine, lidocaine for external; internal controversial)


S tool softeners


H igh fiber diet



Surgical: sclerotherapy, hemorrhoidectomy, banding

What is the anal fissure triad? Treatment?

Deep ulcer


Sentinal pile (hypertrophic edematous skin tag)


Enlarged anal papilla



Treatment with WASH (warm water, analgesia with nitro/lidocaine/nifedepine, stool softeners, high fiber diet) as per hemorrhoids.

Types of rectal abscess

Supralevator (high and deep)


Intersphincteric (internal, above pectinate line)


Ischiorectal (lateral)


Perianal

-Supralevator (high and deep)


-Intersphincteric (internal, above pectinate line)


-Ischiorectal (lateral; may be able to drain in ED - controversial)


-Perianal and Perirectal (only ones we'd drain in ED)



Always tx with tetanus; Abx if DM/ immunocompromised/ valvular disease

Causes of fecal incontinence

Pediatric


-Congenital (meningocele, myelomeningocele, spina bifida)


-Post-op imperforate anus


-Sexual abuse



-Neuro (demential, spinal cord injury, autonomic neuropathy from DM, pedental nerve damage from surgery/obstetrics, Hirshsprung's)


-Trauma to sphincter


-Mass (colorectal cancer, foreign body, hemorrhoids, fecal impaction)


-Medical (rectal prolapse, diarrhea, IBD, laxatives)

Gastroenteritis bugs that require treatment

1) Culture positive, 2) immunocompromised, and 3) not improving



Also:


-Shigella dysentariae (even if asymptomatic - public health)


-Yersinia (even if asymptomatic - public health)


-Salmonella typhi in food handlers, healthcare workers, severe colitis, <3m/o, >50yo


-Bacillus anthracis


-C difficile


-Giardia Lambia


-Entamoeba histolytica

When can anti-diarrheal medications be given?

AVOID in <2yo and those with fever or dysentery (blood +/- pus or mucous)



Consider in patients with severe symptoms along with antibiotics

Diarrhea history - key questions

Travel - parasites


Antibiotics - c diff


Ingestions - food poisoning


Well-water - parasites


Infectious contacts - virulent bacteria


Pets at home - salmonella

DDx for bilateral CNVII palsy

Gosh, bilateral CNVII isn't just B2E2LLS3



GBS (Millar-Fischer variant)
Basilar Skull # / Bacterial Meningitis
EBV / CMV


Ethylene glycol toxicity
Lyme
Leukemia
Sarcoidosis / Syphillis / Sarcoma, Kaposi’s

Characteristics of self-induced knife wounds

-Multiple superficial incisions to trunk/arms/face


-Multiple superficial stabs to trunk/arms/face


-Parallel incisions on the non-dominant side of the body in close proximety to each other


-Sparing of sensitive areas


-Linear or curved incisions toward the hand inflicting the wound


-Intact clothing covering the wound


-Evidence of similar prior wounds

Types of abuse

3 categories:


-Domestic


-Institutional


-Self



Multiple types


-Physical


-Emotional


-Sexual


-Neglect


-Abandonment


-Financial


-Factitious disease (Munchausen's by proxy)

Risk factors for child abuse

Child


-Premature


-Difficult temperament


-Developmental delay or chronic medical condition


-Social isolation



Caregiver


-EtOH or substance abuse***


-Abused as a child


-Intimate partner violence


-Mental illness


-Single parent



Demographic


-Low SES


-Ethnic minority

Shaken baby syndrome; imaging studies

-Generally <1yo; can be <3yo


-No evidence of impact


-SDH and SAH


-On fundoscopy see retinal hemorrhages (>75%), papilledema due to increased ICP



CT is better for SAH, imaging of intracranial injuries, easier to perform. MRI is better if subacute/chronic, deel cerebral injuries, extraaxial fluid, smaller SDH's

Historical indicators of child abuse

-Magical injuries


-Inconsistent story


-Inconsistent with childhood development (can't bruise if can't cruise; 3 week-old 'rolling' off of a table)


-Unexplained delay in seeking care


-History does not explain the injury

Risk factors for HIV transmission via sexual intercourse

Victim


-Anal > vaginal


-Coexisting STD's or genital lesions


-Trauma evident


-Ejaculate on mucous membranes


-Cervical ectopy


-Active menstration


-Currently pregnant



Assailant


-Foreskin


-Primary infection


-Late stage infection


-Viral load in genital tract


-STI's or genital lesions


-Not on HAART


-Multiple offenders


-Incarcerated, homosexual, bisexual

Risk factors for interpersonal violence

Victim


-Demographics (<35yo, female, immigrant, separated or divorced)


-Environment (low SES, homeless, previous exposure to violent caretakers)


-History (disabled, previous physical or sexual assault)



Perpetrator


-Demographics (young)


-Societal (low income, unemployed, low SES, low academic achievement, criminal behavior)


-Psych (low self-esteem, personality disorder, emotional dependence, insecure)


-Substance abuse


-History (abused as a child, violence in family of origin, history of TBI)

Medical problems on DDx with interperesonal violence

-Depression, PTSD, suicidal ideation


-Headaches


-Stress-related illnesses


-EtOH / substance abuse


-Trauma in pregnancy


-Chronic pain


-STI/HIV

Historical indicators of elder abuse

Implausible mechanism of injury


Inconsistent history between patient and caregiver


Delay to presentation



Unexplained injuries


Elder being called 'accident prone'


Past history of frequent injuries



Noncompliance with meds, appointments, directions


Caregiver does not know patient's history/meds


Caregiver answers all questions


Caregiver/patient reluctant to give answers



Strained patient/caregiver interactions


Poor living situation

Diagnostic criteria for a manic episode

Manic episodes are characterized by a >2 week period with elevated/irritable mood and >3 of the following



GST PAID


G randiosity


S leep (decreased)


T alkative



P leasurable activities / P ainful consequences


A ctivity


I deas (flight of)


D istractable



Is not mixed, causes marked impairment or requires hospitalization, not due to a general medical condition.

Anxiety definitions: Anxiety, Panic attack, Agoraphobia, Social phobia, Phobia, OCD, Generalized anxiety, PTSD, acute stress disorder

-Anxiety: a specific unpleasurable state of tension that forewarns the presence of danger (uneasiness stems from the anticipation of some imminent danger, the source of which is unknown or unrecognized)



-Panic attack: discrete period of sudden onset of intense apprehension, often associated with feelings of impending doom



-Agoraphobia: Anxiety about place or situations from which escape might be difficult (fear of being along in public places).



-Panic disorder with agoraphobia: Pts have recurrent unexpected panic attack and become fearful of situations where they might occur



-Specific phobia: irrational fear of something that is perceived as dangerous (normal in children)



-Social phobia: anxiety d/t social or performance situations



-Obsessive-Compulsive Disorder: Obsessions → stress or anxiety which is relieved by a compulsive behaviour



-Generalized anxiety disorder: persistent, excessive anxiety or worry for > 6 months



-Post-traumatic stress disorder: Heightened arousal and avoidance of stimulus following a significant traumatic exposure



-Acute stress disorder: similar to PTSD occurring immediately in the aftermath of an extremely traumatic event

Predictors of organic anxiety disorders

Predictors


-Onset after 35yo


-Lack of childhood, personal, or family history of anxiety/phobias


-Lack of avoidance behavior


-Absence of live events that would exacerbate anxiety


-Poor response to anxiolyticsiD

Disorders that can manifest as anxiety

Substance abuse: sympathomimetics (caffeine, amphetamine, cocaine), hallucinogens (LSD, PCP, Ecstasy, marijuana)


Withdrawl: depressants (benzos, barbiturates, EtOH)


Cardiac: arrhythmias, mitral valve prolapse


Endocrine: hypo/hyperthyroid, hypoglycemia, pheochromocytoma, hyperadrenocortism


Resp: asthma, PE


Medications: alpha agonists, theophylline, corticosteroids, thyroid hormone

What is somatization disorder?

Somatization disorder


-Unexplained physical symptoms beginning before 30yo


-At least 4 sites of pain, 2 GI symptoms, 1 reproductive/sexual symptom, 1 neurologic symptom


-Not explained by another medical condition


-Not intentionally feigned/produced



Risk factors


-Women, low SES, alcoholism, addictions, poor education, interpersonal problems

What is conversion disorder?

-A somatoform disorder


-Sudden onset of a single symptom not under the patient's control and often associated with la belle indifference


-Generally neurological (motor: tremors, paralysis, pseudoseizures, aphonia, ataxia; sensory: anesthesia, blindness, tunnel vision)


-Often a psychiatric coping mechanism

What is somatization? List the somatoform disorders.

Somatization


The unconscious experience and communication of psychological distress through physical symptoms.



-Somatization disorder


-Conversion disorder


-Pain disorder


-Hypochondriasis

What is hypochondriasis? DDx for it? Treatment?

4 key features:


-Symptoms are more than the organic disease that is evident


-Fear of disease and conviction that one is sick


-Preoccupied with their body


-Persistent and unsatisfying pursuit of medical care



DDx


-Endocrine (hyperparathyroid, thyroid disorders, Addison's, insulinoma, panhypuitarism), MS, porphyria, Lupus, Wilson's disease, Myesthenia Gravis, GBS, Uremia



Treatment


-Reassurance, legitimize, share diagnostic uncertianty, assure ongoing care, avoid drugs that cause dependency, come up with realistic treatment goals focused on symptom control, arrange single-physician follow-up

Compare factitious disorder, Munchausen's Syndrome, Munchausen's syndrome by proxy, Malingering,

Factitious disorder: symptoms and signs produced or feigned in the absence of external symptoms to take on the sick role, IS a mental disorder, unmarried educated women <40yo with healthcare background.



Munchausen's: a form of factitious disorder, wide variety of illnesses with intent of gaining hospital admission, hospital shoppers, believe they are very important, initially praise care -> become disruptive -> rage and AMA



Munchausen's by proxy: a form of factitious disorder where illness produced/feigned in a child. Persistent presentations with symptoms that stop when perperator is removed. Parents work in healthcare. Notify protective services and consult psych for mother.



Malingering: Malingerers ARE motivated by external incentives! Assume somatization unless otherwise proven. Often medicolegal context, discrepancy between findings and disability, poor cooperation, antisocial behavior. Don't want to get better; gaming the system.

Diagnosis of schizophrenia

>2 of these symptoms for >1 month


-Delusions (if delusions bizarre counts as 2)


-Hallucinations (if running commentary counts as 2)


-Disorganized speech


-Disorganized or catatonic behavior


-Negative features (avolition, poverty of speech, flat affect)



As well as:


-Sharp deterioration


-Disturbance for >6 months (with prodrome)


-Other causes ruled out

Complications of neuroleptic use and treatment

-Orthostatic hypotension - alpha blockade, give fluids


-Acute dystonia - cholinergic, treat with anticholinergic benztropine (cogentin) 1-2mg IV/IM +/- benadryl


-Akathisia - motor restlessness, decrease dose or try beta-blocker


-Parkinsonism - can be indistinguishable from Parkinson's, tends to resolve over time, decrease dose or start parkinson's meds


-Tardive dyskinesia - occurs over years, bad, choreathetoid movements (tongue, grimace, writhing), no known treatments, try switching to atypical or benzo's


-NMS

Symptoms (in order) of NMS, medications that cause it, treatment

MR HA


altered M ental status (agitated or catatonic)


R igidity (lead pipe, tremor)


H yperthermia


A utonomic instability



Medications: typical and atypical antipsychotics, lithium, Parkinson's medications, maxeran



Treatment: Benzo's, stop neuroleptics, bromocriptine/dantroline/amantidine, cool, ICU, electroconvulsive therapy (Seriously? Seriously??)

Simple vs complex skull fracture

Simple:


-Linear not crossing suture lines


-<2mm of separation



Complex:


-Linear crossing suture lines


->2mm of separation


-Stellate


-Comminuted


-Depressed


-Compound


-Diastatic

Triad of shaken baby syndrome

-Subdural hematoma


-Cerebral edema


-Retinal hemorrhages

DDx for retinal hemorrhages

-Vaginal delivery (resolve in 10-14 days)


-Bleeding disorders


-AV malformations


-Meningitis


-Severe accidental head injury

Physical exam signs of sexual abuse

-Unexplained vulvar bruising


-Hemorrhage


-Hymenal or vulvar tears


-Loss of hymen out to the margin of the vagina


-Signs of STI's (gonorrhea, chlamydia, hsv2, syphilis, trichomonas)



Can get HPV, HSV1, Gardnerella vaginosis, Hepatitis B/D and AIDS without assault.

Bronchiolitis treatments

-Oxygen - yes if hypoxic



-IVF - yes if dehydrated



-Beta agonists - not generally recommended (perhaps 10% responders, atopic people more likely)



-Steroids - no



-Epinephrine - some bad evidence that it can help prevent hospitalization, but not enough evidence to use it



-Epi and steroids together - may be a synergistic response, but more evidence needed. NOT recommended.



-Nebulized hypertonic saline - evidence moving towards its use, but it is still not in the guidelines

Inadequate view of prevertebral soft tissue in children

-View taken on EXpiration


-Flexed or neutral (rather than extended) neck

Esophageal button battery - mechanisms of injury

-Current from the battery forming a circuit


-Release of hydroxide


-Pressure necrosis due to esophageal foreign body

What are the goals / indications of PSA?

Analgesia


Anxiolysis


Sedation


Immobility


Amnesia

Crisis vs psychiatric emergency

Crisis: acute emotional upset arising from situational or developmental problems that results in temporary inability to cope



Psychiatric emergency: acute behavioral disturbance related to severe mental or emotional instability or dysfunction requiring medical intervention

HEADSS social history

H ome


E ducation


A fter school


D rugs


S exual history


S uicidal thoughts/attempts

Mental status exam

Appearance


Attitude


Behavior


Mood


Affect (appropriateness, lability, eye contact)


Orientation (date/time/place)


Speech


Thought process (disorganized)


Thought content (delusions)


Perceptions (hallucinations)


Cognition (memory, content of thought, preoccupations, coherent speech, ability to reason, insight, judgement)


Insight


Judgement


Suicidal ideation


Homicidal ideation


Capacity (CURVES)


Substance dependence

WITHDraw IT



W ithdrawal


I nterest or Important activities neglected


T olerance


H arm to physical and psychosocial are known but they continue to use


D esire to cut down, control it



I ntended time, amount exceeded


T ime spent too much

Pediatric vs adult bones

-Thicker and more stable periosteum


-Faster healing with less immobilization


-Better remodeling capability and vascularity


-Growth plates weaker than ligaments


-More porous and pliable

Toddler's fracture characteristics

-Minimal or no history of trauma


-Red flags for NAT are: more transverse fracture with an associated fibular injury


-Generally 9m to 3y of age


-On physical exam spiral oblique axial load provokes pain (put axial load and twist ankle)


-Generally treat with an above knee backslab - sometimes don't need anything.

Seven pulmonary complications of pneumonia

-Pleural effusion / empyema


-Pneumothorax


-Lung abscess


-Bronchopleural fistula


-Necrotizing pneumonia


-Pneumatocele


-Acute respiratory failure

How long are these pediatric rashes congagious for? (varicella, rubella, measles, parvovirus)

-Varicella - 2 days before until lesions are all crusted over


-Rubella - 1-2 weeks before they present with rash


-Measles - 5 days before and 4 days after


-Parvovirus - a week before until the rash starts