Other pulm dx Flashcards

objectives

1
Q

Pulmonary embolism

A
  • Pulmonary Thromboembolism: passage of a clot from the venous system that lodges in a pulmonary artery
    • Venous thromboembolism (VTE) is the third MC CV illness
    • Symptoms: variable
      • MC dyspnea followed by pleuritic CP, symptoms of DVT and cough
      • Sudden death can occur
      • PE: tachypnea and tachycardia
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2
Q

PE gold standard Dx

A
  • Gold standard: catheter-based pulmonary angiography but this is RARELY used
    • For pts where interventional therapy is indicated bc it can combine interventions for clot lysis and diagnosis in one scan
    • This will tell you yes or no regardless of how costly/invasive. Not first line a lot!
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3
Q

PE dx

A
  • Combo of pretest probability, D-dimer, definitive diagnostic imaging, spiral CT pulm angiography (CTPA) and less commonly ventilation perfusion scanning
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4
Q

PE pre-test, wells score

A
  • To determine pretest: Wells Score
    • 0-2 pts- low risk
    • 3-6 pts – moderate risk
    • over 6 pts- high risk of PE
      • Criteria: suspected dvt 3, alternate dx 3, tachycardia1.5 , post-surgery/disabled in last 4 wks 1.5, previous dvt/pe 1.5, hemoptysis 1 , malignancy past 6 months 1 (causes hypercoag state)
    • For modified wells score: what is used now!
      • Over 4, PE is likely
      • Under 4, PE is unlikely
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5
Q

PE d-dimer

A
  • D-Dimer testing: to r/u PE w/unlikely PE pts……………… (TO EXCLUDE PE)
    • You will order this first if PE is unlikely
    • D-dimers are degradation products of crosslinked fibrin that reflects ongoing activation of hemostatic and thrombolytic system.
    • Elevated D-dimer should prompt further testing with diagnostic imaging > 500
      • Healthy individuals have a minimal d-dimer
      • You CANNOT make a dx of a PE using only d-dimer because you can get false positives (higher w/pregnancy/trauma/surgery/over 50)
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6
Q

PE CTPA

A
  • CTPA: First choice diagnostic imaging modality; if PE is likely, get a CTPA- also called CT w/PE protocol
    • What is the process? 90% sensitive test
      • Images acquired when pt is holding their breath during pulmonary arterial enhancement phase after IV contrast injection.
      • The PE will appear as a filling defect in the opacificed pulmonary artery
        • You can also use this to disclose causes of hypoxemia
      • Use on pts with moderate to high risk of PE! Not for low risk pts
  • If the CTPA is inconclusive and cannot confirm or deny PE, then you need more testing.
    • V/Q scan, contrast pulmonary angiography, US, MRI pulmonary angiography
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7
Q

When to consider using Lung V/Q scan: gamma camera (doesn’t use iodine contrast) for PE

A
  • Nuclear Medicine scan with radiopharm (IV and inhalation) that creates an image of air and blood flow patterns in lungs
  • Use when CTPA is contraindicated such as with renal insufficiency and hx of severe contrast allergy or if CTPA is inconclusive
    • You compare ventilation to perfusion and look for mismatches to indicate PE.
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8
Q

CXR for PE

A
  • nonspecific as well
    • When ordering CXR, you are looking for alternative causes to the pts symptoms.
    • Nonspecific abnormalities are common on CXR for PE but many have normal CXR
    • Possible signs: not common though
      • Hampton’s Hump: shallow, hump-shaped opacity in the periphery of the lung, with its base against the pleural surface and hump towards the hilum
        • Pulmonary infarction
    • Westermark’s sign: demonstration of a sharp cut-off of pulmonary vessels with distal hypoperfusion in a segmental distribution within the lung
      • “less whiteness” aka less vasculature
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9
Q

EKG for PE

A
  • EKG for PE: nonspecific as well
  • Sometimes: S1Q3 pattern
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10
Q

USPSTF recommendations regarding screening for lung cancer

A
  • Lung cancer is MCC of cancer death in both genders
    • 90% due to smoking
    • Symptoms:
      • Dyspnea, non-productive cough, hemoptysis, pleuritic CP, hoarseness (if presses on laryngeal nerve), pleural effusion, wt loss ~~> advanced disease
    • Screening:
      • Do not use CXR for SCREENING. They do not reduce mortality.
      • CT screening offered to:
        • Smoker and former smokers 55-74 yo with more than 30 pack-years
          • Annual low dose CT scanning
      • NOT for pts:
        • Less than 30 pack-years, outside ages, w/severe comorbidities that could dec ability to cure it or limit life
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11
Q

techniques utilized to diagnose and stage lung cancer to include CT scanning, PET scanning, bronchoscopy with endobronchial ultrasound (EBUS)-directed biopsy, and transthoracic needle biopsy.

A
  • To diagnosis:

Imaging: use imaging to optimize selection of biopsy site and preferred modality to get sample.

  • CXR (PA and lat) is first line imaging choice
  • Eventually, every pt should get a CT of chest and upper abdomen to evaluate extent of

Primary tumor and potential spread to liver and adrenal glands

  • Pet scan can be used sometimes to evaluate mediastinal LN involvement if sx is option

Tissue biopsy: the cancer diagnosis is based on pathologic evaluation of cytologic of histopathologic specimens

  • Cytology: get from thoracentesis or sputum cytology
    • More protein and more LDH will be present
    • Malignancy will most likely be unilateral
  • Bronchoscopy w/biopsy: if malignancy is more centrally located
    • Bronchoscopy w/EBUS-directed biopsy is common due to high diagnostic accuracy for getting central primary tumor and most mediastinal LN
      • EBUS: used to dx lung cancer, lung infections, enlarged LN/masses in chest
        • Uses US with scope to visualize airway wall and structures that guides transbronchial needle aspiration samples (termed TBNA)
          • Helpful for biopsy; localizes what’s just outside of bronchi
        • Minimally invasive
          • For squamous cell carcinomas- you can see this a lot since they lie in the bronchi
  • Transthoracic needle biopsy (TTNB) : peripheral
    • Can obtain tissue for accurate diagnosis of peripheral lung nodules/masses
      • May use CT and US to guide
        • CT is MC
        • Complications: pneumothorax is MC and hemoptysis
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12
Q

Two major tests for latent TB

A
  • TST and IGRA
    • Evaluates cell- mediated Immunity
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13
Q

Latent: LTBI- no symptoms

A
  • Clinical diagnosis established by demonstrating prior TB infection and excluding active TB disease
  • Latent symptoms: positive TST and positive IGRA, negative sputum smear, stable calcified granulomas
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14
Q

Active TB: latent can become active especially when become immunocompromised

A
  • Five classic symptoms: cough of 3 weeks, hemoptysis, wt loss, fever, night sweats
  • Infectious, positive TST, positive IGRA, abnormal findings
    • Culturing sputum for growth of m. tb + staining acid-fast
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15
Q

PPD testing: also known as TST

A
  • Once you place it, make sure you see a Intradermal bleb.
  • Measure longest horizontal diameter in mm of raised/induration reaction 48-72 hours
    • Not erythema/redness
    • Only record in mm. do not record as positive or negative
  • Positive: measurement + pt’s pretest probability
    • <5 HIV w/close contact to active contagious case
    • >5 immunocompromised, + CXR
    • Healthcare workers: > 10 mm
    • Health ppl > 15 mm
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16
Q

IGRA

A
  • These are blood tests (T spot or quantiferon- TB gold in tube)
    • Will measure T cell release of IG following stimulation by antigens of M.TB
    • One visit, expensive, more specific, same sensitivity as ppd
    • They cannot distinguish active vs latent
  • BCG vaccines do not affect these. You can give this test to pts who received the bcg vaccine and can get a diagnosis
    • Foreign pts
17
Q

Dx of active

A
  • Clinical symptoms (cough > 2-3 wks, lymphadenopathy, fevers, night sweat, wt loss) + epidemiology factors (hx of dz, known exposure, residence/travel to high incidence areas)
  • Definite dx via isolating mycobacterium tuberculosis from bodily secretion or tissue
  • CXR in active:
    • Focal infiltration of upper lobes (apical/posterior mc) or lower lobes (apical/superior)
    • Can be unilateral or bilateral
    • Cavitation may be present, inflammation, tissue destruction -> fibrosis
  • Enlargement of hilar and mediastinal LN
18
Q

PE dx flow chart

A