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101 Cards in this Set

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How are the 2 kinds of CA staged?
i)NSCLC: TNM ii)SCLC: a)ltd: chest + supraclav nodes (no cervical or axillary). b)extensive: outside of ltd
How do you DX effusion? x3 What is thoracentesis good for? x2
i)CXR: blunted costophrenic angle. lateral decubitis is better for small effusions and if loculated vs free flowing ii)CT: better than CXR iii)thoracentesis: a)drains b)4 C's: chemistry (glucose/protein/LDH/pH); cytology; cell count (CBC w/diff); culture (gram)
how does IPF present and what is px? Who is it common in?
i)gradual onset of progressive dyspnea, nonprod cough. ii)very bad iii)men and smokers
How to DX bronchiectasis? x3
i)PFTs: obstructive ii)CT scan is study of choice iii)CXR nonsp but abnl. iv)bronchoscopy sometimes
How to dx for sarcoid? x4
Definitive dx: transbronchial BX: noncaseating granulomas. i)CXR: *bilat hilar lymphadenopathy ii)ACE is elevated iii)hypercalciuria/calcemia iv)Decr FEV1/FVC; decr lung vol; decr DLCO
How to treat empyema? x3
i)aggressive drainage of pleura and Abx ii)if severe and persistent, rib resect and open drainage
How to treat parapneunic effusion? uncomplicated vs complicated?
i)uncomp: Abx alone ii)compl: a)chest tube drainage b)intrapleural injection of thrombolytic agents(streptokinase) c)surgical lysis of adhesion
How to treat sarcoid?
i)most resolve on own ii)steroids if pt w/severe eye dz, heart block, serious lung dz iii)MTX if steroids refractory
How to treat tension pneumothorax? Why imp?
i)tension in pleural space not relieved->hemodynamic compromise (hypoxemia). ii)chest decompression w/large bore needle, then chest tube placement
Wha is cause of empyema? x2
i)usually untreated parapneumonic effusion (exudative). ii)other foci of infection like abscess or mediastinitis
What are 2 sxs of effusion? What are 3 signs?
i)a)dyspnea on exertion b)PND/orthopnea c)peripheral edema ii)a)dull to percussion b)decr breath sounds over effusion c)decr tactile fremitus
What are causes of bronchiectasis?x4
i)CF ii)infection iii)humoral immunodef (abnl lung defense) iv)airway obstruction
What are causes of exudative pleural effusion?x4
i)Malignancy (esp lung and breast). ii)bacterial pneumonia iii)PE iv)Collagen vasc dz
What are causes of tension pneumothorax? x3
i)mechanical ventilation w/ass'd barotrauma ii)CPR iii)trauma
What are clinical features of empyema? how to DX?
i)those of the underlying cause (ie pneumonia). ii)CXR and CT scan
What are clinical features of mediastinal mass? x5
i)cough (compressed bronchi/trachea) ii)CP iii)dysphagia iv)SVC syndrome v)compression of nerves (hoarse, Horners, hemidiaphragm paralysis via phrenic)
What are clinical features of tension pneumothorax? x4
i)hypotension: cardiac filling impaired due to compression of great veins ii)distended neck veins iii)decr breath on side collapsed; hyperresonance
What are complications of asthma? x3
i)status asthmaticus: no response to std meds ii)acute resp failure iii)pneumothorax, atelectasis, pneumomediastinum
What are secondary treatment options besides drugs for COPD? x3
i)O2 therapy: improves survival and quality of life in COPD and hypoxemia. It will decr pulm HTN and cor pulmonale b/c hypoxemia leads to that; need ABG to determine need for O2. ii)vaccinate against Strep pneum iii)SX: resect or xplant
What are signs of cor pulm?
i)loud P2, ii)paradoxical S2 split iii)EKG changes
What are signs of ILD? x3
i)rales at base ii)digital clubbing iii)signs of pulm HTN and cyanosis
What are Sxs of local invasion in lung cancer? x6
i)phrenic nerve palsy ii)hoarseness (Recurrent laryngeal) iii)Pancoast iv)Horner's v)malig effusion vi)SVC syndrome
What are sxs of pneumothorax? x2 What are signs? x4
A)i)ipsilateral CP, usually sudden ii)cough B)i)decr fremitus on that side ii)hyperresonance iii)decr breath sounds iv)mediastinal shift towards pneumothorax
What are symptoms of sarcoid for each system involved? What are systems involved (x5) and what is cause of death of sarcoid?
i)constitutional sxs: malaise, fever, wt loss. ii)lungs: dry cough, dyspnea. iii)skin: erythema nodosum iv)eyes: ant uveitis v)heart: arrhythmia or sudden death vi)arthralgias
What are the 6 types of ILD? What are exs of each?
i)Environmental lung dz: silicosis, asbestosis ii)Granulomatous ILD: sarcoid; wegener's; Churg Strauss iii)Aveolar filling dz: goodpastures iv)hypersensitivity lung dz: hypersen pneumonitis; eosino pneumonitis v)drug induced; vi)misc: IPF; ARDS; ILD ass'd w/CT disorders
What are the causes of elevated pleural fluid amylase? x3
i)esophaeal rupture ii)pancreatitis iii)malignancy
What do you give for acute exacerbation in COPD?
1st: B agon/anticholin->systemic steroids and ABX. Give O2 to keep O2>90%. Use Noninvasive PPV to help in acute exacerbations. Intubate and mech ventilate if these don't stabilizeDon't give B block in acute COPD or asthma exacerbations.
what is a risk factor for COPD besides smoking, A1AT, and environment
asthma
What is Churg Strauss Syndrome? how does it present x3? What are its ass'n for DX? How to treat?
i)vasculitis w/asthma ii)a)pulm infiltrates b)rash c)eosinophilia. iii)a)blood eosinophilia b)P-Anca iv)steroids
What is clinical pic of Eaton Lambert Syndrome x3
i)paresthesias ii)decr DTR iii)prox muscle weakness/fatigability
What is COP? How to treat?
i)inflamm lung dz w/similar clinical and radiographic features to infectious pneumonia. ii)resistant to Abx but treat w/steroids. iii)ass'd w/virus, meds, CT dz
What is defn of chronic bronchitis? Of emphysema?
i)CB: clinical dx; chronic cough w/sputum for 3 mo/year for 2 years. ii)pathologic dx; permanent enlargement distal to TB due to destruction of alveolar walls
What is defn of ILD?
inflamm process of alveolar wall leading to fibroelastic prolif and collagen deposition->get distorted architecture, fibrosis, impaired gas xchange
What is diff b/w parapneumonic effusion vs empyema?
parapneumonic is uninfected transudative effusion; empyema is infected parapneumonic effusion
What is goodpastures due to and what does it lead to? How does it present? How does it get DXd? How to treat?
i)autoimmune IgG to glom and alveolar BM (T2HS). ii)hemorrhagic pneumonitis and glomnephritis iii)present w/hemoptysis and dyspnea iv)anti-GBM Igs v)plasmapheresis, cyclophos, steroid
What is histiocytosis X? What is ass'n? What are findings x4?
i)chronic interstitial pneumonia caused by abnl prolif of histiocytes ii)smoking iii)a)dyspnea, b)nonprod cough, c)spon pneumothorax, d)DI
What is hypersensitivity pneumonitis? What is hallmark finding? What does the acute form present as and what is treatment?
i)inhaled antigenic agent->immune mediated pneumonitis->chronicity=restrictive lung dz. ii)IgG and IgA to inhaled Ag (can have Ig w/o dz tho) iii)flu like feature w/pulm infiltrates on CXR. iv)removal and steroids
What is longterm tx of mod asthma? severe?
i)mod: daily inhaled steroid OR cromolyn, methylxanthine, or antileukotriene. ii)high dose steroid OR long acting B agonist OR methylxanthine and PO steroid
What is most common cause of mediastinal mass? What is most common according to location? x2 for each
i)metastatic CA (esp lung). ii)a)ant: thyroid, teratogenic tumor b)Middle: lung Ca; lymphoma c)posterior: neurogenic; esophageal mass
what is path of panlobular emphysema? Who gets it? Where in lungs?
i)prox and distal acini ii)a1AT def iii)lung bases
What is pathophys of exudative effusion?x2
i)incr permeability of pleura ii)decr lymphatic flow bc damage to pleural membranes or vasculature (inflamm/malig)
What is pathophys of tension pneumo and what happens?
i)tissue around opening into pleural space is a flap->air in pleural space. ii)collapses opposite lung
What is precipitant of bronchiectasis? x2 What happens?x2
i)infection in patient w/airway obstruction; b) impaired defense or drainage. ii)a)permanent, abnl dilation and destruction of bronchial walls b)cilia are damaged
What is primary spontaneous pneumothorax? What is it due to? How are the resp reserves?
a)primary: no DZ (healthy peeps); due to rupture of sublpleural bleb at apex->collapsed lung. Pts have suff resp reserve.
what are causes of 2ndary (complicated)pneumothorax? x4
b)secondary (complicated): complication of lung dz (usually COPD; asthma, ILD, TB). Life threatening b/c Lack of pulmonary reserve
What is Wegener's charaterized by? Where does it affect x3? What are manifestations x3? How to DX x2? how to treat?
i)necrotizing granulomatous vasculitis ii)vessels of lung, kidney, upper airway iii)a)upper/lower RTI; b)glomneph; c)pulm nodules. iv)tissue BX. C-ANCA. v)steroids and immunosuppressants
What local invasive/paraneoplastic sxs is SCLC ass'd w/? x4 Sq CC? x4
i)Eaton Lambert; SVC; SIADH; ACTH secretion ii)SqCC: Pancoast; PTH pr; long bone pain
What nerves does Pancoast affect? What are the sxs? x3
i)C8 and T1-2. ii)a)pain in arm b)weakness in arm b/c brachial plexus c)Horner's ass'n
What tests should be performed for lung cancer DX? x3 How are each imp?
i)CXR: most imp radio study for DX: if stable for 2 years, benign. ii)CT scan: for staging (see mets and mediastinal lympadenopathy). iii)Needle BX: SCLC vs NSCLC
Which procedures do you always need CXR b/c of traumatic pneumothorax?
i)Central line ii)thoracentesis iii)transthoracic needle aspiration
What kinds of test if dyspnea? x10
i)Hx/PE w/VS. ii)pulse oximetry iii)ABG: a)If O2 sat low on pulsimetry b)hypercarbia suspected c)evaluate for acid base abnl iv)CXR: pneumothorax, effusion, infiltrates for ILD/pneumonia v)CBC: anemia, infection vi)EKG: IHD or ventricular hypertrophy vii)echo: evaluate CHF or valves viii)PFTs: if above are nl or ostructive lung dz suspect ix)VQ and spiral CT for PE x)FB aspiration=bronchoscope
What are 2 causes of pulm HTN? 2 exs of each
i)postcapillary causes: incr left side of heart->incr pulm venous pressure. MS, LV dysfcn. ii)mixed cap and precap causes: dz of lung parenchyma or pulm vessels (all obstructive and parenchymal dz). COPD, ILD
What are complications of ARDS? x3
i)permanent lung injury: honeycomb lung or scarred. ii)pneumothorax or pneumomediastinum due to mech ventilation: barotrauma due to hi press mech ventilation iii)nosocomial pneumonia b/c of ventilation. iv)line ass'd infections: central lines and pulm A catheters(line sepsis), urinary catheter (uti), nasal tube (sinus infection)
What is gold std to DX PE? Other 4 tests that are good? What are they good for?
i)pulm angiography: definitive dx or exclusion but invasive: last resort if serious case (unstable, risk of anticoag high, other test not good). ii)Spiral CT: best noninvasive test; C/I w/RF b/c of contrast. Good for small clots but not for peripheral. iii)VQ scan: if spiral is C/I; good sensitivity and treat w/Heparin. If intermediate result and high clinical suspicion, pulm angio. iv)D dimer: Sn; if normal results w/low suspicion, then PE is unlikely
How to treat cor pulm? x3
i)treat underlying d/o* ii)diuretics cautiously b/c pts might be preload dependent iii)apply O2 longterm if pt hypoxic
How to DX pulm HTN? x2
i)EKG: RVH->rt axis deviation and rt atrial abnl ii)echo: dilated pulm A; abnl movement of IV septum (b/c incr rt ventricular vol); rt heart cath=incr pulm A pressure
How to treat hemoptysis x3?
i)treat underlying cause ii)suppress cough if aggravates hemoptysis iii)correct bleeding diathesis (but anticoag is tx for PE)
What is presentation of pulm aspiration?x3
i)may develop acute resp distress w/no apparent cause or later develops resp dysfcn: cough, SOB, fever, tachypnea, frothy sputum. ii)obstruction w/wheezing iii)+/- fever
How to DX respir failure? x4 What are mech for differential?
i)ABGs: a)hypoxemia=VQ mismatch, shunt, hypoventilation. b)hypercapnia: hypoventilation c)pH: Resp acidosis w/hypercapnia, unless chronic b/c have compensation. ii)CXR or CT iii)CBC and metabolic iv)if cardiogenic edema: get cardiac enzymes
What structures are necessary for maintaining normal respiration? x6 what are 2 causes for each?
i)CNS depression or insult: drugs, stroke ii)neuromuscular dz: MG, ALS iii)upper airway: obstruction; paralysis. iv)thorax and pleura: mechanical restriction->kyphoscoliosis, hemothorax. v)CV/blood: a)CHF, b)valve dz, c)PE, d)anemia vi)lower airways/alveoli: a)asthma, b)COPD, c)ARDS
How is ventilation monitored? How is oxygenation monitored? How are each changed?
i)ventilation: by PaCO2, and to decr PaCO2, need to incr RR or incr TV (minute vent=RRxVT. ii)Oxygenation: by O2 sat and PaO2: decr PaO2 by decr FIO2 or PEEP. Ventilation and oxygenation are unrelated
What does hypoxemia lead to? What does hypercapnia (and resp acidosis) lead to?
i)irrevers damage to organs (esp CNS and CV system). ii)leads to dyspnea and vasodilation of cerebral vessels: incr ICP, H/A, papilledema, coma
How to dx PPH (4)? What is best test?
i)cardiac cath is best ii)CXR: large central PA; enlarged RV; clear lung fields. iii)PFTs=restrictive iv)EKG: rt axis deviation and RVH
What is defn of acute resp failure? (gen defn and the criteria (x2))
i)Gen: happens when there is inadequate O2 of blood or inadeq ventilation (lose CO2)or both. ii)a)hypoxia: PaO2<60mmHg and PaCO2 >50mmHg. b)hypercapnia: PCO2>50mmHg
What ABG does hypoventilation lead to? Diffusion impairment? What are causes of hypercapnic respiratory failure? x3
i)hypercapnia w/2ndary hypoxemia. ii)hypoxemia w/o hypercapnia. iii)sepsis, DKA, hyperthermia
What are complications of mech vent? x5
i)anxiety and discomfort: need Benzos for sedation; opioids for analgesia. ii)tracheal secretions: need suction iii)hypotension: incr intrathoracic pressures->decr venous return iv)tracheomalacia: softened tracheal cartilage. v)GI effects: ulcers and cholestasis v)ET doesn't prevent aspiration
What is DDX for hemoptysis? x7
i)*bronchitis ii)lung CA iii)TB iv)bronchiectasis v)pneumonia vi)Good pastures vii)PE w/pulm infarct
How to evaluate pt w/hypoxemia?
1st: elevated or non elevated PaCO2? i)nonelevated: A-a grad->if not, then low FIO2; if elev: give O2 and if not better, then shunt (vs VQ mismatch). ii)if elevated: hypoventilation->if Aa grad incr, then another mech is also present like shunt or VQ.
What are clinical features of cor pulm? x4
i)cyanosis and digital clubbing ii)parasternal lift iii)RVH iv)polycythemia if COPD is cause
What are key parameters in mech vent? x4
i)Minute vent (RRxTV): adjust to achieve baseline PCO2. Lower TV for COPD and ARDS. 10-12 br/min is good. ii)FIO2: start at 100% and titrate down when PO2 is >60 or O2sat 90%; If FIO2 .5 can't give good PO2, then add PEEP or CPAP (supports PO2 at lower FIO2). iii)Insp:Exp ratio: if incr time in insp, then decr time in exp (1:2 is good ratio). iv)PEEP: pos press maintained at end of passive exhalation to keep alveoli open. Used in ARDS
How to DX pulm aspiration? WHat is seen?
CXR: infiltrates like pneumonia. atelectasis and local areas of collapse may be present
What are 3 dx modalities of ARDS? What do they show?
i)CXR: diffuse b/l pulm infiltrates: diuresis improves and vol o/l worsens CXR, but CXR doesn't say if ARDS has improved. ii)ABG: PaO2<60; initial resp alkalosis PaCO2<40, but becomes acidotic. If septic, then may have met acidosis iii)PCWP: indir IV vol status->differentiates from cardiogenic (PCWP <18)
What are the 3 info you need for mech of hypoxemia?
i)PaCO2 level ii)Aa gradient iii)response to supplemental O2
What are causes of ARDS? x5
i)sepsis* (pneum, urosepsis, wound infect). ii)aspiration iii)trauma iv)pancreatitis v)intracranial HTN
What are DX studies for hemoptysis x3
i)CXR: indicates pathogenesis: opacity b/c of pulm infarct; granuloma, irreg mass. Does not exclude CA or PE. ii)fiberoptic bronchoscopy: used even if CXR normal if suspect CA. Or can localize site of bleeding. iii)CT chest: complement to bronchoscopy or substitute if C/I to bronchoscopy
What is pathophys of PE? x2
i)emboli block some of pulm vasculature->incr pulm A p; PVR; RVP. If large, can get cor pulm. ii)Get incr dead space w/ventilation but no perfusion->hypoxemia and hypercarbia cause tachypnea and tachycardia; if large->SOB.
What is pathophysiology of ARDS? x4. What kinds of PFT is seen?
i)*Widespread shunting of blood w/no improvement w/100% O2. Due to atelectasis, collapse of alveoli, surfactant dysfcn. ii)Interstitial edema and alveolar collapse due to incr lung fluid->stiff lungs, incr Aa grad, ineff gas xchange (same effects as cardiogenic pulm edema, but diff cause: cardio is b/c of HSP, whereas ARDS is incr cap permeability). iii)decr pulm compliance: incr WoB. iv)incr dead space: b/c of obstruction and destroyed pulm cap bed. v)Low VC, Low FRC
How to treat ARDS?x5
i)give O2; sat>90% ii)mech ventilate w/PEEP: opens alveoli and decr shunt iii)fluid manage: low IV vol (PCWP 12-15) but if septic, need more fluid. iv)tube feed nutrition v)treat the cause
What are the 4 kinds of ventilator settings?
i)Assisted controlled ventilation(resp failure): pt can go over determined rate but not under, and every breath over delivers predetermined tidal vol. ii)SIMV(failure and weaning): breath over the determined rate but the TV not determined; if not breathing, the ventilator gives predetermined breath. iii)CPAP(wean): Pos pressure delivered continously but pt breaths on own. Used to assess if pt can breath on own. Use PEEP or pressure support iv)PressSupportVent (wean): pressure delivered in response to initiated breath to enhance resp efforts. Can add PEEP
What are clinical features of sarcoid lung? x3
i)incr WoB: dyspnea, tachycard, tachypnea. ii)progressive hypoxemia: not helped by O2 iii)pt diff to ventilate b/c of high peak airway pressures b/c stiff, noncompliant lungs
What are the sxs of PE? x3 Signs? x3
i)a)Dyspnea b)pleuritic CP c)cough ii)a)tachypnea b)rales c)tachycardia. 1/3 of PE pts have signs and sxs of DVT
What are adv to PEEP? x3 What are disadv?x2
A)i)incr lung compliance and oxygenation: improves gas xchange. ii)prevents alv collapse and atelectasis B)i)barotrauma->pneumothorax. ii)low CO b/c decr venous return, esp if hypovolemic. This is b/c PEEP (like any pos intrathoracic pressure) lowers venous return and incr Pulm VR.
What is pathophysio of shunt? What are causes x3?
i)Little ventilation in perfused areas (b/c collapsed or fluid filled alveoli)->venous blood shunted to arterial side w/o O2. ii)a)atelectasis b)fluid build up: pnemonia or edema c)congenital dz causing rt to left flow
What are 5 risk factors for DVT/PE?
i)malignancy ii)hypercoag states iii)CHF iv)nephrotic syndrome v)trauma or SX
How to DX cor pulm? x3
i)CXR: enlarged RA, RV, pulm A's. ii)EKG: rt axis deviation and RVH; "P pulmonale" (peaked P waves). iii)echo: RV dilated w/nl LV size and fcn (to exclude LV cause)
What is TX of pulm aspiration?
i)If see aspiration: a)ABCs b)O2 c)supportive ii)if aspiration pneumonia suspected, give ABx (don't give prophylactically if aspirate) iii)prevention: keep head elevated, NG tube to decompress stomach
What are the 6 pathophysiologic of pulm HTN causes? 2 exs of each?
i)passive type: resistance to pulm venous drainage (no dz in pulm vasc bed): MS, LVF. ii)hyperkinetic type: high pulm blood flow (L-R cardiac shunts). VSD, ASD. iii)obstructive type: resistance to flow thru large pulm A's->PE, stenosis of pulm A. iv)obliterative type: resistance to flow thru small pulm vessels (arterioles) due to some parenchymal inflamm leading to fibrosis; PPH, Coll Vasc Dz. v)vasoconstrictive type: resistance to flow due to hypoxia induced vasoconstriction; chronic hypoxemia causes, COPD. vi)increased intrathoracic pressure: mech vent w/PEEP, COPD. vii)increased blood viscosity: P vera
What is TX for PE? x5
i)O2 for hypoxemia ii)Heparin immediately if suspicious->1.5-2.5 aPTT; C/I: active bleeding, uncontrolled HTN, recent stroke, HIT. iii)Warfarin to INR 2-3 x3-6 mths. (lifelong if hypercoag state or malignancy). iv)thrombolytics: a)massive PE who are unstable b)evidence of RHF (they reverse it). v)IVC filter: if C/I anticoag; current complication w/anticoag; pt w/low pulm reserve who may die
What are 2 types of Noninvasive pos pressure ventilation-NPPV? What is diff? What is the indication of NPPV? Who does it work best in? What must be intact to use it--if not, then use what
i)CPAP vs BIPAP. BIPAP has diff insp and expir pressures. ii)pt in impending resp failure to avoid intubation and mech ventilation. iii)hypercarbic resp failure (esp COPD). iv)a)neuro intact b)awake and cooperative c)can protect airway. v)intubate and mechanical ventilation
What are 3 causes of pulm aspiration and which lung does it go to?
i)a)acidic gastric contents: damaging to lungs b)aspiration of oropharyngeal flora c)FB/fluid aspiration. ii)rt lung b/c of more straight (lower segments of upper lobe and upper seg of lower lobe)
What is Cor pulmonale? What are 4 causes?
i)rt sided LVH 2ndary to HTN (RVH 2ndary to pulm htn). Not due to causes of pulm HTN 2ndary to L sided dz. ii)a)COPD* b)recurrent PE c)ILD d)asthma
What are 2 causes of pulm aspiration?
i)GERD ii)Neuromuscular dz
What is ARDS? what is the primary mechanism? Is it a primary dz?
i)diffuse inflamm process (not only infectious) involving both lungs. ii)neutrophil activation in systemic or pulmonary circulations. iii)2ndary to other conditions causing widespread inflamm process.
What are reasons for mech ventilation? x5
i)impaired or reduced level of consciousness w/inability to protect airway (absent gag or cough reflexes) ii)metabolic acidosis (can't hyperventilate). iii)resp muscle fatigue iv)significant hypoxemia (<70mmHg) or hypercapnia (PaCO2>50). v)resp acidosis (pH<7.2) w/hypercapnia
What are the 2 types of acute respiratory failure? What are their causes? What are the pathophys of each?
i)hypoxemic respiratory failure: a)low PaO2 w/PaCO2 low or normal (O2 sat <90%). b)cause: dz process of lung (ARDS, severe pneumonia, edema). c)VQ mismatch; shunt. ii)Hypercarbic (ventilatory) respiratory failure (failure of alveolar ventilation). a)decr in minute ventilation or incr in dead space->CO2 retention and get hypoxemia. b)cause: lung dz (COPD, asthma, bronchitis). c)or NM dz, resp fatigue (hypervent in DKA)
ow to treat PPH? x3
i)1st do vasodilator trial: inhaled NO, IV adenosine or oral CCBii)pulm vasodilaters: IV prostacyclin; CCBs. iii)warfarin w/INR around 2 iv)lung xplant
What tests tell you that you can you treat PE w/anticoag? x3. What tests r/o PE x3?
i)a)intraluminal filling defects on helical CT+suspicion b)DVT dx'd w/U/S+suspicion. c)pos pulm angiogram: proves PE. ii)a)low probability VQ scan+low suspicion b)Neg pulm angiogram (definite). c)Neg D dimer+low suspicion
How to treat resp failure? x4
i)treat underlying d/o (bronchodilate, steroids, Abx, etc). ii)Give O2: a)hypoxemic failure->lowest [O2] b/c of possible O2 tox w/radicals. b)hypercarbic: give some O2, tho hx says hypoxia drives breathing, so that the pt can get worse (esp COPD). iii)NPPV:conscious pts who can breath iv)may need intubation and ventilation w/resp failure
What are other sources of emboli to lungs besides thrombus? x5
i)fat embolism (bone) ii)amniotic fluid embolism: during or after deliver iii)air embolism: trauma to thorax; indwelling lines. iv)septic embolism (IVDU) v)schistosomiasis