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78 Cards in this Set

  • Front
  • Back
R lobes vs L lobes
Each lobe = %fxn
Each lung ___ segments
Gas xchange @___ branches
Alveolar ducts @___ branches
Sacs @ ____ branches
- Right = 3 lobes (55%)
- Left = 2 lobes (45%)
- Each lobe = 20% lung fnx
- Each lung = 10 segments
- gas exchange starts @ 17 branches
- alveolar duct @ 20 branches
- sacs @23 branches = most gas exchange
4 types of cells in the lungs
type 1- Gas exchange alveolar cells
tyep 2- produce surfactant
Primary cells- macrophages
associated endothelial cells
A/a gradient
A-a Gradient: Alveolus : arteriole
- Capacity of lungs to oxygenate blood – difference btwn alveolar and arterial O2.
Higher A-a gradient = worse Px. Normal gradient is 7-14.
Understand how change in atmosphere or CO2 will change the PaO2 equation
Decreased atmospheric pressure drops it
increased CO2 in lungs will drop it (its a ratio, when CO2 goes up O2 HAS to go down.
V/Q
Volume of Air to a section
Flow of blood to a section
ideal is 1 but higher vent at top and higher Q at bottom makes natural inequality
High = lots of air - little blood (PE possibly)
Low = Little air- lots of blood (leads to SHUNT)
Blood pH evaluations
- Low pH= Acidosis – caused by High PaCO2, lactic acidosis, Kidney dz, toxins
- High pH = Alkalosis – caused by Low PaCo2, met alkalosis, hyperventilation
define
FVC
FEV1
- FVC: forced VC (expired)
- FEV1: forced expired in 1sec
FEV1/FVC: <70 = obstruction
- low in Obstructive lung dz.
Lung Volume and associated diseases indicators
Lung Volumes
- high: emphysema
- normal/high: asthma/CB
- low: restrictive lung dz
Diffusing Capacity and diseases
Diffusing capacity – how well O2 getting into blood
(↓ in emphysema; fibrotic lung dz)
- Low: emphysema; restrictive lung dzs
- normal: asthma/CB
Obstructive lung disease Pulmonary Function tests:
low Fev1/FVC <70%
High volume
Low diffusing Capacity
Asthma has >12% bronchodilation response
Restrictive lung disease Pulmonary Function tests
Normal to increased FEV1/FVC
Low volume
Low difusing capacity
What are the Obstructive lung disease?
Restrictive?
Asthma, COPD, CF
Pulm Fibrosis, Sarcoidosis, Neromm dz, Pulmonary Edema
Effects of surgery on lung function
- More risk = ab/thoracic surgery: sig effects post op
- less risk = surgery on limbs: not ass w/ Δ in lung fnx, but may predispose to other pulm complications
- ↓ lung vol; poor cough due to sedation/pain meds; immobility; post op infxns; COPD exacerbation: gets worse (death 5% - not uncom)
considering VQ inequality what is a Zero Q? What is a Zero V?
Q is called dead space- O2 supplement will help
V is called Shung- O2 will not help.
What are the 4 mechanisms of hypoxia?
COPD or Asthma (V/Q inequality)
ARDS or Aspiration
Hypoventilation (decreased central dirve or ability to ventilate)
Pulmonary Fibrosis (diffusion defects)
Diffuse interstitial lung disease clinical
SX: SOB w normal activity, NonProdCough
CXR: diffuse linear or Nodular scarring prominent @bases
PFT: Dec Vol, Diffusing Capacity, FEV1/FEV is Normal
TX:
Sarcoidosis Lung disease Clinical
SX: 20-40yo, US-black, SOB, Cough, Rash, Iritis, noncaseating granulomas on multiple organs (liver, bone, heart, erythema nodosum
CXR: Hilar LN enlargement w/ no-caseating Gran.
PFT: Dec Vol, Diffusing Capacity, FEV1/FEV is Normal
TX: Corticosteroids, Methotrexate (diabetics who can't tolerate corticosteroids)
Idiopathic Pulmonary Fibrosis Clinical
SX: 60-70yo Only lungs involved, Crackles, Clubbing of digits, cough
CXR: Honeycombing, bronchiectasis, reticular opacities
biopsy shows normal tissue next to abnormal w/o transition
PFT:
TX: "no proven therapy," Transplant
What is the most common cause of decrease in lung volume with no change in diffusion capcaity?
Obesitay!
What neuromuscular diseases can cause Restrictive lung diseases/
ALS
Myasthenia Gravis
What are the two features of Asthma and the appropriate Tx?
1- airway bronchospasm (hyperactivity >12%): Bronchodilators
2- Airway inflammation and mucus: corticosteroids
What are the sings of poor control in an asthmatic?
Signs of Poor Control: *RULE OF 2s
- must use “rescue” meds >2x/week
- nighttime awakening due to breathing >2x/month
- do NOT do elective surgery if poor control
Define Status Asthmaticus
Status Asthmaticus: severe asthmatic episode that is NOT responsive to repeated tx w/ usual inhaled medications (probably due to mucus) (if doesn’t improve w/ 2nd admin of meds w/ 5 min btwn admin – seek medical help)
Treatment for SEVERE asthma
Severe:
-1st inhaled corticosteroids (Flovent/Pulmacort)
*when above doesn’t control, use combo:
-2nd inhaled long acting bronchodilator (don’t use by themselves)
- Leukotriene receptor antagonist (Singulaire)
- Anti Ig E tx (Zolaire) – injxn 2/week – serious
- oral steroids (prednisone)
What is the most important way to prevent the onset of progression of COPD?
Smokin Cessation
compare Sx of CB and Emphysema
CB is an inflammatory problem around the airways
Emphysema is actual destruction of the lung tissue without inflammation or cough (remember the antitrypsin thingy bob)
COPD Severity is indicated by Spirometry (FEV in particular), What are the 5 stages?
-Remember that to have any Obstructive dusease has to have a FEV1/FEV ration of?
Ratio will always be <70%
0- FEV is normal = at risk of COPD
1- Mild: FEV >80
2- Mod: FEV 50-80
3- Sev: FEV 30-50
4- Very bad: FEV <30 or Pao2 hypoxic w FEV < 50
what are the factors influencing survival in COPD?
BODE (doesn't bode well for them)
B-BMI
O- degree of obstruction (FEV1)
D- dyspnea level: how SOB
E- Exercise capacity (6min walk-how far can you go?)
Drugs used in COPD:
(BAD!)
Brochodilators
- B2 agonists (albuterol, salmeterol (long acting))
-Anticholinergic (Ipratroprium, Tiotroprium (LA))
-Methylxanthine (theophyline)
Anti Inflammatories
-Inhaled Steroids: Fluticasone, Budesonide
Dual Action Tx:
-Albut + Ipratrop
-Bude + Form
-Flut + Salm
What is the step-wise approach to tx of COPD?
Bronchodilators O2 tx  exercise training/Rehab
- Dyspnea ↓ & exercise tolerance ↑
*Smoking cessation is KEY; reg use of inhaled meds; flu & pneumonia vaccines; reg exercise; good nutrition/ wt control; rapid tx of exacerbations
Tell me about CysticFibrosis
genetic dz (m/c fatal auto recessive among caucasion pops (1 in 2000-3000 live births)
*Usual sxs: (mainly found in childhood)
Sx of Cystic Fibrosis
Mainly found in childhood, Persistent Pulmonary infection (pseudomonas), Pancreatic insufficiency, Elevated sweat chlroine test
Pulmonary:
-Persistent productive cough
-Airflow obstruction
-bronchiectasis
Physical finding:
-wheezing
-clubbing
Other Sx:
-Sinus dz (sinusitis or polyps)
-Pancreatif insufficiency with malabsorption
-Infertility
Tx of Cystic Fibrosis Lung disorders
- tx & prevention of respiratory infxns
- reg respiratory therapy to clear airway secretions
- lung transplant for severe lung dz
Common Cold
SX: not localized, fever, malaise w/o lymphadenopathy, mild sore throat
TX: Tylenol, Cepastat/Benadryl for sore throat
Influenza
SX: Prominent Fever, Malaise, myalgia everywhere, non-specific runny eyes/nose, scratchy throat, seasonal
Dx: Nasopharyngeal swab
Tx: in first 2 days- Tamiflu 75mg BIDx 5 days
-post 2 days sx releif
Acute Pharyngitis
SX: Beefy Red pharynx w/ purulence, Fever, Anterior Cervical Lymphadenopathy
Dx: Usually Strep- Rapid strep test, ASO titer
TX: Amoxicillin or Ampicillin
Mono
SX: Dull white grey exudate, possible hepatosplenomeg, POST cervical adenopathy
Dx: monospot/CBC (atypical lymphs)
TX: Amoxicillin Ampicillin
- if causes rash- give corticosteroids
Sinusitis
SX: Facial pain due to Sinus ostial obstruction
Acute: <4wks
-following URI (opportunistic Pathogens)
-Noninfectious: Polyps, irritants, tumor, (any obstruction)
TX: Empric: Narrow spectrum antibiotics (Amox, TMP, SMX)
- if >7days w/ purulence give Ampicillin/sulbactim or augmentin or oxyquinolone.
-if narrow is uneffective give Levoflox
otitis Externa
Swimmer's ear: Crusty goodness
Cause- usually pseudomonas, sometimes staph
TX: Ciprofloxacin drops w/debridement
Otitis Media
Usually Bacterial infx following viral URI
Tx: Amox or no Amox w/ tylenol
Recurrent Otitis Media
> 4 in 1 yr or
3 in 6 months
Tx: bata lactam antibiotics
- possibly maintenance w/ TMP/SMX; possible myrinotomy tube
- 1 dose daily of TMP
Serous Otitis Media
Serous otitis media:
Usually goes away on its own but slowly
consider antibiotics and/or myringotyomy tubes if sig hearing loss/effusion > 3 mo – conductive
Chronic Otitis Media
Chronic otitis media:
-recurrent purulent drainage w/ a chronic TM perforation; usually requires mastoidectomy & tympanoplasty
- usually pseudomonas – resistant to many txs
Laryngitis:
inflammation of the larynx
nearly always viral
Tx: Don't talk
Epiglottitis
Epiglottitis: potentially fatal
- usually H. influenza
- pools of saliva around epiglottis; narrowed opening – intense wheezing (stridor)
- lateral neck films; cherry red epiglottis w/ fiberoptic rhino-laryngoscopy (visualize thru nose)

Hospitalization/ICU possible tracheostomy
Tx: Ampicillin/sulbactam or (2nd/3rd generation cephalosporin
- Hib vaccine – prophylaxis
- (↓ incidence)
Acute Bronchitis
SX: cough w/ sputum production- purulent or foamy, no fever, occasional rhoncus
Dx: absence of abnormality on CXR
TX: quinalone (especially in pt with COPD)
Sever Bronchitis
Acute with
1- increased amount of sputum
2- change in color of sputum
3- increased SOB
4- FEVER
TX: Z-pac with possible tx of bronchospasm
Pleurisy
*inflammation involving surface of lung
- 1⁰ sxs: chest pain, worse w/ inspiration
-lasts about a month
- usually viral
- tx: sxs – DOC = NSAIDs; narcotics in severe cases
- Terrible terrible = corticosteroids
What are the general sx of pneumonia?
Cough
Fever/Chills
dyspnea
Malaise/sepsis
Confusion in elderly
What are the general physical findings of Pneumonia?
Fever and Tachycardia
Tachypnea
Crackles, sometimes wheezes or absent breath sounds
Fremitus/egophony w/ consolidaiton
What are the 5 causes of pneumonia
Bacterial +: Strep Pneumonia, -: Klebsiella, Psuedomonas
Fungal: Cocci, Histoplasmosis, Blastomycosis, Aspergillis
Mycobacterium: TB, Avium intercellulare
Viral: RSV, Adeno, Flu
Atypical: Chlamydia, mycoplasma
Community Acquired Pneumonia 2 types
Previously healthy outpatient- Gram+, Atypical, Viral, Fungal w/ low mortality
Older (>65) or w/ cardiopulm dz: add G-, aspiration, higher mortality
Hospital Acquired Pneumonias severity types
Floor: most common is S. Pnuemonia with mortality of 5-20%
ICU: S. Pneumonia w/ MRSA. Mortality of 25-30%
- add in Pneumocystis in unsuspected HIV patient
Pathogens in Immunocompromised Pt
Bact: Pseudomonas, Nocardia
Fungal: coccidiomycosis, Aspergillis,
Mycobacterium
Viral (CMV)
Protozoal
--- all have a poor prognosis
Clinical signs of severe pneumonia
hypoxia w/ SOB, SaO2<92%
Tachycardia
Hypotension (indicates septic shock)
Walking pneumonia that lasts a long time is mainly caused by
any atypical pathogen
TX for more severely ill Pneumonia Pt
Initial empiric coverage w/ mutliple antibiotics for a variety of pathogens
-Ceftriaxone 2gIV daily w/ Levoflox 750mg orally
Tx for mildly ill Pneumonia Pt
Moderately?
Empiric Macrolide - Erythromycin
Quinolone
Pt comes in with mild non productive cough, cxr reveals infiltrates in RUL. What is the suspicion?
What is the Tx?
First- pneumonia, second cocci, 3rd maybe TB or Viral. So while you are waiting for all your cultures to come back what do you treat him with?” Azythromycin: covers typical and atypicals- place to start.
Latent TB definition
Dx?
Tx?
Not active disease aquired previously -NOT infx
DX: manitoux intradermal injection of PPD +=+
TX: DOC is Isoniazid and B6 50mg for 9 mo
-Isoniazid resistant: Rifampin 300mg for 4 mo
Increased risk for TB?
prisoners, nursing home, hospital/health workers; Indian reserve
- rate of hospital workers as high as 50%
Define Active TB
Dx?
Tx?
evidence of TB most often multiplying in lungs or extrapulm site- INFXous
DX: Sptutum AFB smear and culture x3, occasional bronchoscopy
TX: 4drug combo: Isoniazid +b6, Rifampin, Pyrazinamide, Ethambutol for 2 months
-then Isoniazid, B6 and Rifampin for 4 months
NOTE: Need to report to state: skin test all contacts
Primary TB
first exposure- Not INFXous
SX: cough, minor sx for 2-4wks
DX: Central infiltrates on CXR
TX: prevent
Secondary TB
"Reactivated"- INFXous
SX: Cough w/ hemoptysis, fever and Nightsweats, Fatigue
DX: peripheral and apical CXR infiltrates, Hilar adenopathy
Ghon's complex
Secondary TB course of infection
Infection -> granuloma -> m/o remains viable, but sequestered -> dz may “reactivate” & begin growing
- may experience complications of pneumonia and tubercles in organs: Kindeys, Brains, Bones's
what is a key source of false + TB tests?
Pt who received CBG vaccine
PE risk factors
• recent surgery (knee/hip); trauma; immobilization (also travel, prego, obesity) anything that leads to stasis of blood.
• cancer (hypercoagulability state – also Estrogen (birth control), prego, obesity, genetic/acquired thombophilia – ATIII/Protein C/S def; Factor V Leiden; SLE)
• Prior hx of DVT or PE
• smoking; air embolism (air in IV needle); amniotic fluid embolism, placenta previa (placenta separates before baby is born)
3 primary presentations of PE:
1. Pleuritic pain – esp w/ deep breath; abrupt – infarcts part of lung – see wedge on CXR; /hemoptysis – (generally after acute event) = 65%
2. isolated dyspnea = 22%
3. Circulatory collapse – SOB = 8%
DX of DVT
*US of LE*; spiral CT; d-dimer
PE prophylactic TX
• prophylactic tx w/ lose dose heparin in high risk pts: low dose hep post op, then 4-6 weeks of Coumadin following arthroplasty
EKG signs of PE
• EKG: cor pulmonle w/ RAD; increased p wave amplitude in lead II; large S wave in lead I; ST depression in lead II; large W wave w/ t wave inversion in III
What is the most useful test in DX PE?
D Dimer
PE treatment course
• Initial tx = Heparin
• If unstable pt – consider thrombolytic therapy (TPA) or surgical embolectomy, someone who is hemodynamically really compromised.
• Long term tx = Warfarin (Coumadin) – 1st episode: 6 months of therapy; 2nd episode: Lifelong therapy; if pt has predisposing factor: Lifelong therapy
• Filter in subclavian vein to IVC to catch clot
Risks for Lung Cancers
Risk- 90% - smokers/ex
- women- 15-20% nonsmokers
- ↑ risk w/ Carcinogens (asbestos/air pollution); 2nd hand smoke, fam hx of lung cancer
Signs of possible lung cancer
- Cough m/c sx; Hemoptysis (centrally located m/c); wheeze, SOB, dysphagia (compression of esophagus); wt loss (unexplained);
chest discomfort (impinge bvs - 2⁰ to growth);
- **signs of metastatic dz (liver, bone, brain, adrenal glands, could mimic CVA/seizure) – lung cancer is usually aggressive & met is common
5 common types of lung cancer
Adenocarcinoma- m/c peripheral
SCC- Smoker Central Cancer
Small Cell Carcinoma- Agressive, rarely tx w/ surgery, smoker
Large Cell Carcinoma- less common, peripheral
BAC- NOT related to smoking, slow, looks like infiltrate pneumonia, multifocal
Lung Cancer Tumor Staging
Staging: (*3 & 4 m/c dx since we usually “catch” these lung cancers late – no surgery is usually performed do to LN involvement & metastasis)
1 – small (3 cm) No involvement of LN (N0)
2 – larger, possible hilar LN involvement (N1)- can be resected
3 – mediastinal LN involvement (N2)- no longer resectable
4 – Metastatic dz
Lung cancer Dx, TX, Px?
DX: • Routine CT scans in select grps w/ cig smoking hx may ↓ mortality ;
• screening bronchoscopy w/ autoaluorescence (blue light will show up brown where neoplastic cells are located)
TX: • for NON-small cell lung cancers – surgery is the only tx that offers significant chance @ long term survival (<5yrs)
• Surgery @ stages 1 & 2, but many not be able to do if pt has comorbitity – COPD, etc.; not recommended @ stage 3.
PX: • even in Stage 1 – 1/3 pts still die w/in 5 yrs (relapse even w/ surgery);
• survival in stage 4: <2 yrs