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225 Cards in this Set

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Define transudates and causes?

<25g/l protein


-due to changes in hydrostatic or oncotic P


-heart/liver/renal failure


-hypoalbuminaemia


-pertinoeal dialysis



Define exudates and causes?

>35g/l protein


-due to inflammation causing inc capillary permeability


-malignancy


-pneumonia, TB, mesothelioma


-RA, SLE


-pancreatitis

What about protein between 25 and 35g/l?

LIGHTS criteria


exudate if:


-pleural fluid divided by serum protein >0.5


-pleural LDH divided by serum LDH > 0.6


-pleural LDH > 2/3 of normal serum LDH



Examination findings of pleural effusion?

tracheal devation (away)


stony dull percussion


bronchial breathing over effusion


diminished breath sounds and expansion

What other characteristics of aspirated pleural fluid are you interested in?

ph - <7.2 = infection


glucose - <3.3 in empyema, RA, lupus, TB, malignancy


amylase - raised in pancreatitis, malignancy


cytology - ?malignancy

Describe SIADH?

Important cause of hyponatraemia


-urine Na>20 and osmolality >100 in the presence of plasma Na<125 and low plasma osmolality


-WITHOUT hypovolaemia, oedema or diuretics

Causes of SIADH?

malignancy - lung, pancreas, prostate, lymphoma


CNS - stroke, subarachnoid/subdural haemorrhage, head injury, abscess


respiratory - TB, pneumonia


drugs - opiates, SSRIs, carbamazepine, morphine

Treatment of SIADH?

treat cause then resrict fluid


-slow infusion saline + loop diuretic


-demeclocycline to reduce responsiveness to ADH if refractory

Presentation of hyponatraemia?

anorexia, nausea and malaise >> headache, confusion, weakness, seizures

Causes of hyponatraemia without dehydration?

nephrotic syndrome


HF


LF


cirrhosis

Causes of hyponatraemia with dehydration and high urinary Na?

addisons


RF


diuretics

Type 1 respiratory failure causes?

pneumonia, pulmnary oedema, PE, asthma, emphysema, fibrosis


>>give high flow O2

Type 2 respiratory failure causes?

VQ mismatch WITH alveolar hypoventilation


-resp disease: asthma, COPD, end stage fibrosis


-reduced drive: sedatives, CNS tumour


-thoracic wall disease


>>>give 24% O2

Resp failure presentation?

type 1 - agitation


type 2 - drowsiness, bounding pulse, tachycardia

Examination findings of pneumona?

dull percussion

bronchial breathing


inspiratory crackles


inc tactile vocal fremitus

Describe CURB65?

determines severity of CAP


-confusion


-urea>7


-RR>30


-BP <60syst or >90diast


-aged over 65

Management of CAP?

non severe - amoxicillin for 7 days


severe - IV coamoxiclav + clarithromycin

Management of hospital acquired pneumonia?

IV aminoglycoside (ie gentamicin) + penicillin

Define COPD?

progressive airflow obtruction that isnt fully reversible and doesnt change over months

Examination findings in COPD?

hyperinflation


dec expansion


hyperressonant percussion


if cor pulmonale > rraised JVP + pitting oedema

CXR findings in COPD?

flat hemidiaphgragm


large central PA


dec peripheral vascular markings


bullae

Differentiate between pink puffer and blue bloater?

pink puffer if emphysema primary pathology


-breathless but not cyanosed


-progresses to type 1 failure


blue bloater if chronic bronchitis


-cyanosed but not breathless


-progresses to cor pulmonale but relies on hypoxic drive

Treatment of COPD?

1. b-agonist or ipatropium


2. long acting antimuscarinic ie tiotropium


3. LABA + corticosteroids

Define bronchiectasis?

irreversible dilation of bronchi predisposing to finfection


- post infection ie pneumonia, TB, measles


-aspergillosis


-obstruction


-CF

Examination findings in bronchiectasis?

usual resp symptoms


+ haemoptysis, weight loss, clubbing,


-coarse inspiratory creps

CXR findings in bronchiectasis?

dilated bronchi with thickened walls (TRAMLINES)


cystic structures



Management of bronchiectasis?

postural drainage


antibiotics


immunisation


lobectomy if only 1 lobe

Define CF?

Ch 7 delta F508 mutation causing defective Cl secretion + inc Na absorption


>>inc mucous viscosity

CF presentation?

bronchiectasis


steatorrhoea


clubbing


gallstones


nasal polyps


meconium ileus



Investigations for CF?

immunoreactive trypsinogen (heel prick)


sweat test - Na+Cl>60


CXR - hyperinflation, exaggerated bronchial markings


USS - fatty liver, cirrhosis

Describe interstital lung disease?

umbrella term


-commonest idiopathic pulmnary fibrosis aka UIP


-also hypersensitivty pneumonitis, sarcoidosis, asbestosis etc


*BASAL WITH HONEYCOMBING ON CT

What is Meigs syndrome?


ascites


pleural effusion


benign ovarian tumour

Describe vocal resonance?

Normal = muffled 99


Inc = clearly audible as in consolidation


Dec = effusion or pneumothorax

Describe surgical emphysema?

air trapped in subcut tissues


-rice crispy noise


-due to pneumothorax, post drain insertion, post surgery,


-usually benign

Describe Wernickes ?

thiamine deficiency causing confusion, ataxia (wide gait) + opthalmoplegia (nystagmus etc)


-focal areas of brain damage


-progresses to korsakoffs

Describe korsakoffs?

hypothalamic damage and cerebral atrophy due to thiamine deficiency


-causes dec ability to make new memories, confabulation, lack of insight + apathy

Describe aminoglycosides?

great for pseudomonas


-has to be IV/IM or nebulised

Describe types of lung cancer?

80% non small cell associated with smoking


-adenocarcinoma slow growing


-large cell rapidly growing

Describe APTT?

normal 25-38 secs


-aim to increase to 1.5-2.5x in heparin therapy

Describe percussion notes?

dull in collapse or consolidation


hyperresonant - hyperinflation/air


stony dull - effusion

Causes of clubbing?

Cyanotic heart disease


Lung disease


UC/Crohns


Biliary cirrhosis


Birth defect


Infective endocarditis


Neoplasm esp hodgkins


GI malasbsorption

Describe ECG leads?

2,3+avf = inferior


v1+v2 = septal


1, avl, v5+v6 = lateral


v3+v4 = anterior

When would you do a CABG?

if 3 vessel disease - RCA + both branches of left


OR left main branch


OR 2 vessel disease involving LAD

Describe process of CABG?

LIMA connected to LAD


great saphenous grafted from ascending aorta to below blockage


-LIMA lasts 25yrs, veins 10-15yrs, stents 5yrs


-use radials if VV as dont want to use both LIMAs

Describe tissue v mechanical valves?

Tissue valves only last 10-15 yrs but dont require warfarin


-mechanical valves if <65yrs

Describe main cause of aortic stenosis?

senile calcification but can be congenital bicuspid valve



Examination findings in aortic stenosis?

LV heave

aortic thrill


ejection systolic murmur radiating to carotids

ECG findings in aortic stenosis?

p mitrale


poor R wave progression


LBBB


LVH pattern

CXR findings in aortic stenosis?

LVH


post stenotic dilation of ascending aorta

Diagnosis of aortic stenosis?

ECHO to estimate gradient across valve


-severe if >50mmHg and valve <1cm


NB if symptomatic 2-3yr survival without treatment

Describe aortic regurgiation?

acute - IE, aortic dissection,


chronic - congen, CT disorders, marfans, HT



Examination findings in aortic regurgitation?

collapsing pulse


displaced apex


high pitched diastolic murmur - heard expiration sitting forward

Management of aortic regurgitation?

reduce BP and ECHO every 6-12 months


-surgery if worsens prior to significant LV dysfunction

Describe mitral stenosis?

usually due to Rheumatic fever



Examination findings in mitral stenosis?

malar flush due to CO2 retention


low volume pulse


AF


opening snap


rumbling mid-disastolic murmur - expiration on left side

ECG findings in mitral stenosis?

AF


P mitrale


RVH



CXR findings in mitral stenosis?

left atrial enlargement


double right heart border


pulmonary oedema



Management of mitral stenosis?

rate control if AF


warfarin


diuretics


then consider balloon valvuloplasty or replacement

Describe mitral prolapse?

displacement of abnormal thick mitral valve into LA during systole


commonest valvular abnormality


-alone or with ASD, PDA, cardiomyopathy, turners, marfans, OI etc


-asymptomatic or atypical chest pain + palpitations

Diagnosis + management of mitral prolapse?

midsystolic click +/- late systolic murmur


-echo to diagnose


-b-blockers, surgery if severe


NB found in 5% of population

Define an aortic aneurysm?

any dilation >50% original diameter


-true if involve all 3 layers


-pseudo if blood collecting in adventitia outer layer ie after trauma


-present in 3% of >50s

Presentation of ruptured abdominal aneurysm?

intermittent/continuous abdo pain radiating to back, iliac fossa or groins


-1 in 3 will reach hospital


-only repaired if >5.5cm


-operative mortality 5%

Normal BP?

140/90 but 150/90 IN >80S

1st line treatment for HT?

<55 = ACEI


>55 or afrocaribean = CCB

Further treatment for HT?

2. Add other - ACEI or CCB(dipines)


3. Add thiazide


4. consider b-blocker

When would you use an ARB?

if ACEI intolerant


diabetic nephropathy


LVH


HF


post-MI

Contraindications to CCBs?

HF


heart block

Examination findings of DVT?

warm


tender


pitting oedema (mild normal following surgery or immobility

How do you evaluate a suspected DVT?

WELLS CRITERIA


-if moderate risk do D-dimer then USS


-if high risk USS straight awa


NB D-dimer not helpful if on warfarin or post-op

Treatment of DVT?

rivaroxaban for 3 months

compression stockings for 2 years to prevent post thrombotic syndrome

What are brown skin pigmentations esp on legs?

haemosiderin deposits


-seen in venous insufficiency and haemochromatosis, elderly

What is POTS?

postural tachycardia syndrome


-dizziness, faints, palpitations


-following growth spurt, viral, systemic disase


-diagnosed if HR inc of 30bmp after 10 mins standing

Describe hiatus hernia?

protrusion of upper stomach through diaphragm


-most often due to obesity presenting with GORD


-Ba swallow to diagnose


>>weight loss + symptomatic relief

What is Bence-Jones protein associated with?

myeloma


-they are free Ig light chains filtered by kidneys

Define pulse pressure?

difference between systolic and diastolic BP


-<40 indicates poor heart function


->60 predicts heart problems + athersclerosis

Describe MAP?

MAP = CO x TPR


- estimate = systolic + 2xdiastolic / 3


-should be 70-110mmHg


-aka perfusion pressure of organs


-<60 = shock

What is high take off?

large T waves NOT ST elevation

Describe haematocrit?

45% for men, 40% women


-low in anaemia, bleeding, leukaemia


-high in CHD, cor pulmonale, hypoxia, polycthaemia vera

Elevated lactate?

usually tissue hypoperfusion


-but also shock, alcohol, cocaine, seizures, excercise, thiamine deficiency, LF etc

Normal CRP?

less than 10

What is PCP?

pneumocystis pneumonia


-yeast like fungus that is main opportunistic lung infection in immunocomprimised

PA v AP film?

PA standard - standing


-cant comment on heart size on AP

Xray penetration?

vertebrae should just be visible behind heart

Describe an air bronchogram?

dark bronchi being made visible by white opacification of surrounding alveoli


- due to pulm oedema, consolidation etc

Describe CCBs?

rate limiting ie verapamil and non-rate limiting eg amlodipine

- vasodilate and reduce BP

Name a drug METABOLISED by the kidney?

insulin

Describe cockroft-gault formula?

140 - age x weight x costant / serum creatinine

HT drugs to beware of in renal disease?

b-blockers


thiazine diuretics


K-sparing diuretics CONTRAINDICATED


*also metformin

Describe use of loop diuretics?

mainly HF causing pulm/peripheral oedema


-can cause hypo K/Ca/Na/Mg


-NOT with aminoglycosides or digoxin

Describe use of K-sparing diuretics?

adjunct to diuretics in HT or HF


-can cause hyperkalaemia or hyponatraemia

Differentiate between restrictive and obstructive lung disease?

Obstructive - cant get air out


-eg asthma, COPD, bronchiectasis, CF




Restrictive - cant get air in


-eg ILD, sarcoidsosis, obesity


-both FVC + FEV1 reduced q

Management of non-severe and severe CAP?

non-severe - amoxicillin


severe - co-amoxiclav + clari if atypical or fluclox if staph

Management of hospital acquired pneumonia?

if <4 days from admission treat as CAP


non severe - amoxicillin


Severe - coamoxiclav +/- gentamicin

Describe SARS?

severe acute respiratory distress syndrome


-contagious pneumonia due to coronavirus


-fevers,chills, rigors, myalgia, dry cough, dec WCC


-can lead to resp failure + ARDS


-1-50% mortality


-supportive treatment only

Presentation of bronchiectasis?

copious puruluent sputum


intermittent haemoptysis


persistent ough

Treatment of bronchiectasis?

postural drainage


antibiotics



Presentation of CF?

cough


wheeze


bronchiectasis


pneumothorax


haemoptysis


cor pulmonale


meconium ileus


rectal prolapse


>>cyanosis, clubbing, coarse crackles

Investigations for lung cancer?

sputum + pleural fluid cytology


FNA


CT


radinuclide bone scan

Management of different types of lung cancer?

non small cell - excision if peripheral + no mets, chemo +/- radiotherapy


small cell - nearly always disseminated at presentation


- may respond to chemo but usually relapse


- palliative radiotherapy for bronchial or SVC obstruction


- median survival 3 months ,1-1.5yrs with treatment

Describe stages of lung cancer?

Stage 4 - any mets


Stage 3b if nodes on contralateral side

Define asthma?

bronchial smooth muscle spasm , mucosal inflammation and inc mucous

Signs of asthma/

hyperinflated chest


hyperresonant percussion


dec air entry


usually DEC CO2 unless severe

Treatment pathway for asthma?

1. SABA ie salbutamol


2. Inhaled corticosteroid ie beclometasone


3. LABA ie salmeterol


4. Higher dose beclometasone OR LRA ie montelukast


5. Oral prednisolone

Treatment acute asthma?

1. salbutamol 5mg nebs with O2


2. hydrocontrisone 100mg IV OR pred


3. O2 if sats <92


4.salbutamol neb every 15 mins + ecg


5.ipatropium neb


6.MgSo4

Define components of COPD?


chronic bronchitis - productive cough on most days for 3 months for 2yrs


emphysema - enlarged air spaces distal to terminal bronchioles with alveolar wall destruction

Management of COPD?


1. inhlated antimuscarinic eg tiotropium or b2 agonist


2.LABA + corticosteroids


3. steroid terial

Management of acute COPD?


1. salbutamol nebs + ipratropium


2. 24-28% O2 if sats <88


3. iV STEROIDS


4. Antibiotics if inection


5. IV aminophylline

Define ARDS?

inflammation causing inc capillary permeability,pulm oedema + multi organ failure


-direct injury or secondary to systemic illness

Signs of hypercapnia?


headache


peripheral vasodilation


bounding pulse


tremor/flap


confusion


drowsiness

Differentiating type 1 + 2 resp failure managamenet?


type 1 - 35-60% O2


type 2 - start at 24% O2 but if causes PCO2 rise then consider NIVPP

Describe types of o2 therapy?


Nasal cannula - preferred by patient, allows 1-4L/24-40% O2


Face masks imprecise so not in hypercapnia or type 2


Venturi mask most precise + colour coded


Non rebreathing mask - 60-90% O2

Presentation of PE?


pleuritic pain


haemoptysis


dizziness


syncope


cyanosis


hypotension


pleural rub/effusion

Investigations for PE?


D-dimer only if low probability


CXR - low circulation in affected segement, dilated PA, partial collapse, small effusion, wedge shaped opacities

ECG in PE?

normal or RBBB

Treatment of PE?


O2 + morphine


-immediate thrombolysis if severe


-start heparin


-colloids if syst <90


-noradrenaline


-if still low systolic then thrombolysis


-warfarin for 3 months

Presentation of pneumothorax?


sudden onset dysnpnoa + pleuritic pain


reduced expansion


hyperressonant percussion

Briefly define transudate and exudate causes?


Transudate - inc venous P or hypoproteinaemia


Exudate - leaking capillaries due to infection/inflammation or malignancy

CXR in pleural effusion?


blunt costophrenic angles


shadows with concave upper borders

Presence of neutrophils in pleural fluid?


parapneumonic


PE

Presence of lymphocytes in pleural fluid?


malignancy


TB


RA


SLE


Sarcoidosis

Describe sarcoidosis?


multisystem granulomatous dirsorder of unkown cause


-adults 20-40yo


-acute form presents with erythema nodosum + polyarthralgia and resolves spontaneously

Pulmonary presentation of sarcoidosis?


bilateral hilar lymphadenopathy


fibrosis


pulmonary infiltrates


dry cough


progressive dynspnoea


chest pain

Extra-pulmonary presentation of sarcoidsosi?


Skin


Arthritis


Respiratory


Calcium


Orbit


Interstitial fibrosis


Deranged Liver + kidney

Treatment of sarcoidosis?


NSAIDS


prednsiolone reducing over 1 yr


-80% cure

Causes of bilateral hilar lymphadenopathy?


sarcoidosis


TB


malignancy

Describe interstitial lung disease?


umbrella term for diffuse lung parenchyma disease


-most commonly idiopathic pulmonary fibrosis


-3 categories: known causes, systemic disorder or idiopathic

Presentation of ILD?

dynspnoea


non productive paroxysmal cough (outbursts)


restrictive spirometry

Causes of upper zone fibrotic shadowing on CXR?


TB


extrinsic allergic albeolitis


sarcoidosis

Causes of lower zone fibrotic shadowing on CXR?


idiopathic pulmonary fibrosis


asbestosis

Presentation of idiopathic pulmonary fibrosis?


dry cough


malaise


weight loss


arthralgia


cyanosis


clubbing


fine creps


-ANA +Ve in 30%


-lower zone shadows


-honeycombing if advanced

Treatment of idiopathic pulmonary fibrosis?


O2, rehab, opiates, pallatiative


-50% 5YS

Presentation of asbestosis?


progressive dysnpnoea


clubbing


fine crackles


pleural plaques


-risk of mesothelioma

Describe malignant mesothelioma?


usually pleura


-90% have previous asbestos exposure


-latency up to 45yrs

Presentation of malignant mesothelioma?

dysnpnoea


weight loss


clubbing


recurrent pleural effusions


pleural thickening


bloody pleural fluid


>>>chemo can improve survival

Describe cor pulmonale?


RHF due to chronic pulmonary arterial HT

Causes of cor pulmonale?


lung - COPD, bronchiectasis, severe asthma


vascular - PHT, ARDS, sickle cell, emboli


thoracic cage - kyphosis, scoliosis


neuromuscular


hypoventilation - apnoea,

Presentation of cor pulmonale?

raised JVP


RV heave


hepatomegaly


oedema


fatigue


-secondary polycythaemia


-graham steel murmur of pulm regurg


-pansystolic murmur of tricsuspid regurg

ECG in cor pulmonale?


p pulmonale - p >2.5mm in inf leads indicating RA enlargement


right axis deviation


RVH/strain

Treatment of cor pulmonale?

treat underlying cause


-diuretics, K-sparing if necessary


-venesection if haematocrit >55


>>50% 5YS

Describe types of chest pain?


constricting - angina, oes spasm


sharp - pleura or pericardium


dull/crushing - MI

Describe aortic dissection pain?


instantaneous


tearing


interscapular

Pain eased by leaning forward?

pericarditis

Describe antiplatelets?


COX inhibitors - aspiring


ADP receptor antagonists - clopidogrel if aspirin intolerant

Describe antiocoagulants?


warfarin - for AF + mechanical valves


LMWH


Xa inhibitors eg apixiban

Describe action of b-blockers?

antagonist symp nervous system


-b1>dec pulse by dec SA firing


-b2 > peripheral vasoconstriction + bronchoconstriction


-propanolol non-selective but bisoprolol b1 selective

Side effects of b-blockers?

headache


erectile dysfunction


nightmares


lethargy

Describe CCBs?

promotes coronary + peripheral vasodilation


-dihydropyridines ie amylodipine


-non-dihydropyridines ie verapamil rate limiting

Side effects of CCBs?

flushes


headaches


diuretic unresponsive oedema


NOT in heart block

Decribe digoxin?

use to slow pulse in fast AF


-weak positive iontrope so inc strength of contractions

Describe statins?

HMG-CoA reductase inhibitor that synthesis cholesterol


-causes muscle aches, abdo discomfort

Side effects of ACEI?

DRY COUGH


hypotension


taste disturbance

What is decubitus angna?

precipitated by lying flat

ECG in angina?

may be normal


ST depression, flat/inverted T-waes


-exclude anaemia, DM, lipids, thyrotoxicosis

Management of angina?

statin if cholesterol >4


spirin


b-blocker


nitrate


CCBs if b-blockef contraindicated



Describe a silent infarct?

syncope


epigastric pain


vomiting


hypotension


pulmonray oedema


*common in elderly or diabetics

ECG following MI?

tall T-waves


ST elevation


new LBBB


t-wave inversion + q-waves developing in following days

Describe cardiac enzymes?

troponin T+I - peaks at 24-48hrs


CK-MB peaks at 24hrs


-both take 3 hrs to rise

Prehospital/immediate management of MI?

aspirin 300mg chewed


GTN


morphine


metoclopramide

Management of stemi?

PCI if within 120 mins


fibrinolysis otherwise



Management of nstemi?

LMWH


b-blocker

Complications of MI?

arrhythmias


heart block


mitral regurgitation


VSD


pericarditis

Treatment of bradycardia?

atropine if rate <40

Describe SVT?

narrow complex tachycardia


-DC cardioversion if acute otherwise identify rhythm


-if needed give adenosine to cause transient block + convert to sinus rhythm


-then b-blocker

Describe VT?

broad complex tachycardia with HR>100


-amiodarone


-shock if necessary

Describe first degree heart block?

PR interval >200ms


-no treatment required

Describe second degree heart block?

Mobitz I - progressive PR elongation until non-conducted P-wave


- doesnt usually require treatment


Mobitz II - constant PR interval with intermittend non-conducted P-wave


- always sinister so pace


- due to bundle of His

Describe third degree heart block?

complete AV node dissociation


-ventricular escape rhythm with no relation to atrial rhythm/rate


-pacemaker

Describe WPW syndrome?

tachycardia due to congenital accessory conduction pathways between atria + ventricles


-short PR interval, wide QRS


-delta upstroke at start of Qrs


-presents with SVT


>>Ablation

Describe ventricular ectopics?

commonest post-MI arrhythmia


-due to electrical instability with risk of VF


-if >10/min consider amiodarone

Describe torsades du pointes?

looks like VF but is VT with varying axis


-due to increased QT interval which is side effect of antiarrhythmic so consider stopping


-give Mg SO4

Describe AF/Flutter?

chaotic electrical rhythm with AV node responding intermittently thus irregular ventricular rate


-CO drops by 10-20%


-main risk is embolic stroke

Presentation of AF/flutter?

chest pain, palpitations, dynspnoea, faint


-irregularly irregular pulse


-absent p-waves + irregular QRS complexes

Treatment of acute AF?

O2


emergency cardiovesion or IV amiodarone

Treatment of chronic AF?

RATE CONTROL + anticoag


-rhythm control with cardioversion or flecainide only needed if symptompatic, CCF, young etc

Types of HF?

systolic if problem with contraction leading to <40% ejection fraction


- due to IHD, MI


diastolic failure if inability to relax properly


- due to constrictive pericarditis, tamponade, HT

Presentation of LV failure?

SOB, fatigue, orthopnoea


paroxysmal noctural dyspnoea


nocturnal cough


weight loss

Presentation of RV failure?

peripheral oedema


ascies


nausea


epistaxis


**due to LVF, pulmonary stenosis or lung disease

Define congestive HF?

heart not pumping enough blood out to meet bodys demands

Describe high output HF?

rarer


-normal or inc CO>circulatory overloads>HF


-anaemia, pregnancy, hyperthyroid, pagets

Diagnosis of HF?

FRAMINGHAM CRITERIA (2 major or 1 major+2minor)

Presentation of HF?

cool peripheries


cyanosis


low BP


narrow pulse pressure


pulsus alternans (weak + Strong)


RV heave



CXR in HF?

perihilar batwing shadowing (consolidation)


fluid in fissures


Kerley B lines - thickened interlobular septae, horizontal lines at periphery




Alveolar oedema (batwings)


kerley B lines


Cardiomegaly


Dilated upper lobe vessels


Effusion

Management of HF?

1. Diuretics eg frusomide


2. ACEI


3. B-blocker


4. spironolactone


5. digoxin


6. vasodilators

Describe natriuretic peptides?

ANP -inc urine + Na


BNP - closely related to LV pressure


*released in MI + LV dysfunction


-act to dec renal Na absorption + preload

Describe natriurtic peptides in HF?

plasma BNP >100 diagnoses HF from other causes of dyspnoea

What is malignant hypertension?

sudden rise in bp to systolic>200 with bilateral retinal haemorrhages + exudate


-causes organ damage


-90% 1Y mortality untreated

Causes of secondary HT?

Renal


Endocrine - cushings, conns, acromegaly, hyperparathyroid


pregnancy


steroids



Describe rheumatic fever?

pharyngeal infection with b-haemolytic strep triggering rheumatic fever 2-4wks later


-5-15y/o


-antibody reacts with valves causing damage - 70% mitral, 40% aortic

Presentation of mitral stenosis?

fatigue, palpitations etc


malar flush


low vol pulse


AF


mid-disatolic murmur


P-mitrale

Presentation of mitral prolapse?

asymptomatic or atypical chest pain + palpitations


-midsystolic click


-commonest valvular abnoramlity

Presentation of aortic stenosis?

narrow pulse pressure


apex heave


LV heave


aortic thrill


ejection systolic murmur



Presentation of aortic regurgitation?

acute due to IE or trauma


-orthopnoea


-collapsing pulse


-wide pulse P



Presentation of tricuspid regurgitation?

hepatic pain on exertion


ascites


oedema


pulsatile hepatomegaly


jaundice


*due to PHT, Rh fever, IE, ASD

Describe pulmonary stenosis?

usually congenital - turners, noonans, williams


-oedema


-ascites


-RV heave


-ejection click


>>valvuloplasty or valvotomy

Describe CABG?

LIMA attached to LAD from origin at subclavian


long saphenous used to bypass blockage elsewhere

Presentation of infective endocarditis?

fever + new mumur - IE until proven otherwise


-acute so presents wwith HF +/- emboli


-subacute if prosthetic valve


-usually staph aureus

Causes of IE?

staph aureus


strep viridans

IE presentation?

Fever


Roth spots - retinal haemorrhages


Oslers nodes


Murmur


Janeway lesions


Anaemia


Nail haemorrhages


Emboli

Describe oslers nodes and janeway lesions?

Oslers - painful red raised lesions on hands + feet


Janeway lesions - small non-tender erythematous, haemorrhagic or nodular lesions on palms or soles

Investigations of IE?

blood cultures - x3 from 3 different sites


normochromic normocytic anaemia


neutrophilia


microscopic haematuria


long PR interval on ECG


>>>DUKES CRITERIA TO DIAGNOSE

Management of native IE??

blind - amoxicillin + gentamicin


staph - fluclox IV for >4wks

Management of prosthetic IE?

blind - vanc, gentamicin + rifampicin


staph - flucox, rifamp + gentamicin 6 wks

Cause of acute myocarditis?

viral


bacterial


drugs - cyclophosph, herceptin, penicillin

Presentation of acute myocarditis?

fatigue, fever, palpitations


-Twave inversion


+ve troponin


>>supportive treatment + treat cause > recovery or HF



What is dilated cardiomyopathy?

dilated flabby heart of unkown cause


-associated with alcohol, viral, autoimmune

Presentation of dilated cardiomyopathy?

pulmonary oedema


RVF


AF


displaced apex


mitral/tricuspid reurgitation


jaundice


hepatomegaly


ascites

Treatment of dilated cardiomyopathy?

bed rest


diuretics


ACEI


anticoag


-40% 2Y mortality

Describe hypertrophic cardiomyopathy?

LV outflow obstruction from asymmetric septal hypertrophy


-leading cause of sudden cardiac death in young


-AD but 50% sporadic

Presentation of hypertrophic cardiomyopathy?

systolic thrill or harsh ejection systolic murmur


angina, dyspnoea, palpitations



ECG in hypertrophic cardiomyopathy?

LVH


T-wave inversion


AF


WPW


ventricular ectopic

Management of hypertrophic cardiomyopathy?

b-blockers for symptoms


anticoag


implantable defib


-6%mortality per yr if <14yrs, 2.5% if >14yrs

Describe restrictive cardiomyopathy?

rigid ventricle walls causing impaired fillng


- central chest pain worse on inspiration or lying flat

Causes of resrictiv cardiomyopathy?

amyloidosis


haemachromatosis


sarcoidosis


scleroderma

Causes of acute pericarditis?

viral


bacteria


post MI (Dresslers syndrome)


drugs - penicillin etc


RA


SLA


radiotherapy

Presentation of acute pericarditis?

central chest pain worse on inspiration + lying flat, relieved by sittng forward


pericardial friction rub


-concave/saddle shaped ST segment elevation on ECG`

Management of acute pericarditis?

treat cause + analgesia


-steroids


-15-40% recurr

Describe pericardial effusion?

fluid acculumation in pericardial sac


-same causes as pericarditis

Presentation of pericardial effusion?

dysnpnoea, raised jvp


-bronchial breathing L-base


-Ewarts sign - dull percussion left lower lung


-low volatage QRS on ECG


-echo free zone around heart on echo

Treatment of pericardial effusion?

treat cause


-pericardiocentesis to diagnose or therapeutic

Describe constrictive pericarditis?

heart encased in rigid pericardium


-often unknown cause or after any pericarditis



Presentation of constrictive pericarditis?

raised JVP


kussmauls sign - raised JVP on inspiration


quiet heart sounds


hepatosplenomegaly


ascites


small heart on CXR


>>>> surgical excision

What is cardiac tamponade?

pericardial fluid accumulation > raised pressure > poor filling > dec cardiac output



Causes of cardiac tamponade?

any pericarditis


warfarin


trans-septal puncture during cardiac catheterisation

Presentation of cardiac tamponde?

inc bulse, dec BP


pulsus paradox


raised JVP


kussmauls sign


low voltage QRS

What is Becks triad?

Distant heart sounds


Distended jugular veins


Decreased BP