ABIM Pulmonary flashcards
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- COPD spirometric criterion
- Persistent airflow obstruction is defined by a post-bronchodilator FEV1/FVC ratio below 0.70, confirming COPD in a patient with compatible symptoms and exposure history.
- Asthmatic bronchodilator response
- A reversible airway obstruction is defined as an increase in FEV1 of at least 12 percent and at least 200 mL after inhaling a short-acting bronchodilator.
- Alpha-1 antitrypsin deficiency clues
- Consider testing in early-onset emphysema, basilar-predominant disease, family history, or unexplained liver disease; serum alpha-1 antitrypsin level is the initial test.
- COPD oxygen target
- In COPD patients at risk for hypercapnia, titrate supplemental oxygen to a saturation of 88 to 92 percent to avoid worsening carbon dioxide retention.
- Usual interstitial pneumonia pattern
- High-resolution CT shows peripheral, basal-predominant reticulation, honeycombing, and traction bronchiectasis with minimal ground-glass opacity; this pattern supports a diagnosis of idiopathic pulmonary fibrosis.
- IPF disease-slowing drugs
- Nintedanib and pirfenidone slow the rate of forced vital capacity decline in idiopathic pulmonary fibrosis; immunosuppressive regimens are harmful and should not be used.
- Sarcoidosis BAL finding
- Bronchoalveolar lavage often shows a CD4 to CD8 ratio greater than 3.5, supporting sarcoidosis, although the diagnosis requires compatible clinical, radiographic, and histologic findings.
- Massive pulmonary embolism
- Pulmonary embolism with sustained hypotension or shock is massive; treat with systemic thrombolysis or surgical or catheter embolectomy rather than anticoagulation alone.
- CTEPH screening test
- Chronic thromboembolic pulmonary hypertension should be evaluated with a ventilation-perfusion scan, which is more sensitive than CT pulmonary angiography for detecting chronic thromboembolic disease.
- Pulmonary arterial hypertension definition
- Pulmonary arterial hypertension requires mean pulmonary artery pressure above 20 mm Hg, pulmonary vascular resistance at least 3 Wood units, and pulmonary artery wedge pressure 15 mm Hg or less.
- Berlin ARDS oxygenation categories
- ARDS is mild at a PaO2/FiO2 ratio of 200 to 300, moderate at 100 to 200, and severe below 100, all measured with positive end-expiratory pressure at least 5 cm H2O.
- Lung-protective ventilation
- Use tidal volume of 6 mL per kg predicted body weight and target plateau pressure of 30 cm H2O or less to reduce mortality in acute respiratory distress syndrome.
- NIV for COPD exacerbation
- Noninvasive ventilation reduces intubation and mortality in COPD exacerbation with respiratory acidosis, typically when pH is 7.25 to 7.35 and hypercapnia is present.
- Obstructive sleep apnea criterion
- Obstructive sleep apnea is diagnosed when the apnea-hypopnea index is at least 5 with compatible symptoms, or at least 15 regardless of symptoms.
- Obesity hypoventilation syndrome
- Obesity hypoventilation syndrome is defined by body mass index at least 30, awake PaCO2 above 45 mm Hg, and sleep-disordered breathing after excluding other causes of hypoventilation.
- Adaptive servo-ventilation caution
- Adaptive servo-ventilation is contraindicated in patients with heart failure and ejection fraction 45 percent or less because it increases mortality in central sleep apnea.
- Latent tuberculosis treatment
- Preferred regimens for latent tuberculosis include four months of daily rifampin or nine months of daily isoniazid; alternatives depend on resistance, age, and liver disease.
- Pneumocystis prophylaxis threshold
- Start trimethoprim-sulfamethoxazole prophylaxis for Pneumocystis jirovecii when CD4 count falls below 200 cells per microliter in HIV infection.
- Empyema pleural fluid
- Pleural fluid that is frank pus, or has pH below 7.20, glucose below 60 mg/dL, or LDH above 1000 IU/L, indicates empyema and requires drainage.
- CURB-65 variables
- CURB-65 scores confusion, urea above 7 mmol/L, respiratory rate at least 30, blood pressure low, and age 65 or older to stratify community-acquired pneumonia.
- SCLC paraneoplastic syndrome
- Small cell lung cancer commonly causes SIADH with hyponatremia and, less often, Cushing syndrome from ectopic ACTH; squamous cell carcinoma more often causes hypercalcemia.
- EGFR inhibitor indication
- Advanced non-small cell lung cancer with an activating EGFR mutation is treated with an EGFR tyrosine kinase inhibitor such as osimertinib, which improves response and survival.
- Solitary pulmonary nodule follow-up
- For a solid nodule 6 to 8 mm in a low-risk patient, guidelines recommend initial follow-up CT at 6 to 12 months, with subsequent intervals based on stability.
- Light criteria exudate
- Pleural fluid is an exudate if protein ratio exceeds 0.5, LDH ratio exceeds 0.6, or pleural LDH exceeds two-thirds the upper limit of normal serum LDH.
- Tension pneumothorax management
- Tension pneumothorax is a clinical diagnosis requiring immediate needle decompression followed by tube thoracostomy; do not delay for chest radiography.
- Chylothorax laboratory finding
- Pleural fluid triglyceride above 110 mg/dL supports chylothorax, usually from thoracic duct disruption by trauma, surgery, lymphoma, or malignancy.
- Asbestosis radiographic features
- Asbestosis causes lower-lobe-predominant interstitial fibrosis and often pleural plaques; it increases risk of mesothelioma and lung cancer, with a long latency.
- Silicosis classic pattern
- Silicosis produces upper-lobe-predominant nodules and eggshell calcification of hilar lymph nodes; it also increases susceptibility to tuberculosis.
- Beryllium sensitization test
- Beryllium lymphocyte proliferation testing supports chronic beryllium disease, which causes noncaseating granulomas and interstitial lung disease in exposed workers.
- ALS noninvasive ventilation
- Noninvasive ventilation improves survival and quality of life in amyotrophic lateral sclerosis when forced vital capacity falls below 50 percent or nocturnal hypoventilation develops.
- Myasthenic crisis respiratory failure
- Myasthenic crisis causes neuromuscular respiratory failure with weak cough and falling vital capacity; treat with plasma exchange or intravenous immunoglobulin and avoid aminoglycosides.
- Kyphoscoliosis pulmonary function
- Severe kyphoscoliosis produces restrictive physiology with reduced vital capacity and total lung capacity, often with preserved DLCO until late disease.