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Internal Medicine Resident Lecture  - PowerPoint Presentation

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Internal Medicine Resident Lecture  - PPT Presentation

Michael Forte MD  Pulmonary and Critical Care  4623 Overview  Bronchiectasis  Sarcoidosis  Pulmonary Vasculitis and Hemorrhage  Bronchiectasis  Bad syndrome irreversible airway dilation and destruction of bronchi and inadequate clearance of mucous and pooling of secretions  ID: 1041907

normal examination year chronic examination normal chronic year symptoms cough biopsy dah lung physical evaluated chest patients question bilateral

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1. Internal Medicine Resident Lecture Michael Forte MD Pulmonary and Critical Care 4/6/23

2. Overview... Bronchiectasis Sarcoidosis Pulmonary Vasculitis and Hemorrhage 

3. Bronchiectasis Bad syndrome – irreversible airway dilation and destruction of bronchi and inadequate clearance of mucous and pooling of secretions Recurrent infections, inflammatory response Major divide CF versus non CF bronchiectasisSymptoms- cough, sputum, recurrent infections, foul smelling sputum, hemoptysis, dyspnea, weight loss  Common pathogens H flu, PSA, Strep PNA, Staph Aureus 

4. Spiral of Death

5. Etiologies 

6. Diagnosis Classic symptoms plus HRCT findings 3 major classifications : cylindrical, varicose, cystic Tram track sign (lack of tapers, 1-1.5 x size of vessel), signet ring sign, string of pearls 

7. CT images 

8. Location Clues 

9. Investigations/Workup PFT- usually obstructionHRCTCBCSputum cultures and AFBRF/ANA/Autoimmune workup ImmunoglobulinsAlpha 1Sweat chloride Aspergillus antibodies RFHIVBronchoscopy

10. Treatment Treat underlying etiology No specific therapies approved for NCFBBronchodilators ICS etc Airway clearance most important Mucolytics Dornase alpha/pulmozyme --NOHTS/mannitol/NAC?Suppressive abx? Especially inhaled abx PSA? macrolides -- frequent exabations?Longer courses of abx for acute exacerbation 

11. Sarcoidosis Chronic granulomatous disease of unclear etiology Must rule out exposure to beryllium, WTC works and interferon therapy can show same pathological findings Disease of young patients. Scandanaivan countries and African Americans F>MSmall fraction hereditySome association with HLA genes 

12. Presentation

13. Clinical Findings Constitutional symptoms are commonWeight loss, fever, night sweats etc Cough, wheezing, dyspnea, pleurisy PFT- obstruction, restriction or both +methacholine challenge FVC and DLCO most important to monitor disease progression 

14. Labs and Imaging Hypercalcemia, hypercalcuria ACE levelsBAL lymphocytosis with >cd4/cd8 ratioCXR nonspecificCT classic findings adenopathy +/-nodules Will be PET +, not usually helpfulECG, ECHO, CMR

15. Classic CT

16. Diagnosis / PathNo lab diagnosis Bronchoscopy of biopsy showing noncaseating granuloma in absense of fungal and AFB TBBXEBUS Endobronchial disease 

17. TreatmentSpontaneous remissions occur and prognosis is based on the initial radiographicstage:1 55–90% of patients with Stage I disease2 40–70% with Stage II disease310–20% with Stage III disease4 0% with Stage IV diseaseThe course of the disease is usually dictated within 18–24 months of onset.Patients with worsening symptoms, worsening forced vital capacity and/or DLCO, or worsening lung fibrosis should receive therapy. Extrathoracic abnormalities also play a role in deciding whether treatment should be initiated ie cardiac sarcoid, hypercalcemia etc 

18. Drugs

19. Pulmonary Vasculitis Small vessel vasculitis, systemic and necrotizing This group of diseases includes granulomatosis with polyangiitis(GPA), microscopic polyangiitis (MPA), and eosinophilic granulomatosis with polyangiitis (EGPA). Frequent occurrence of ANCA is pathognomonic, but not required for diagnosis. More than half of patients with these vasculitides haveANCA positivity as well as predominant pulmonary symptoms.

20. Breakdown

21. Treatment

22. Anti GBM

23. DAHDAH is characterized by diffuse hemorrhage into the alveolar spaces. Hemoptysis may be absent in up to 30% of patients. Progressive dyspnea and hypoxemia leadsto respiratory failure. Chest radiograph typically shows diffuse alveolar infiltrate sbilaterally. Reduced and/or declining hemoglobin (iron-deficiency) is also seen.Coagulopathy and thrombocytopenia can predispose to alveolar hemorrhage.

24. DAH etiology 

25. DAH Diagnosis BRONCHOSCOPY—DAH from any cause is best confirmed by bronchoalveolar lavage (BAL). The serial lavage aliquots will be gradually more hemorrhagic, confirming the alveolar origin of the blood. Hemosiderin-ladenmacrophages (demonstrated by Prussian blue staining) are also characteristically found in BAL fluid from patients with DAH, In the absence of active hemorrhage, > 20% of hemosiderin-laden macrophages in the BAL seals diagnosis 

26. DAH BAL

27. DAH management Pulse dose steroids -- ?evidencePlasma exchange Cyclophosphamide Rituxumab Not RCT but favoring lower steroid now ?need for plasma exchange 

28. Question 1A 54-year-old man is evaluated for a 2-year history of chronic productive cough. He has intermittent wheezing, shortness of breath with exertion, and nasal congestion.On physical examination, vital signs are normal. Bibasilar crackles are present. Cardiac examination is normal.CT scan of the chest shows cylindrical bronchiectasis of bilateral lower lobes.Which of the following is the most appropriate diagnostic test to perform next?A Bronch BALB Serum Immunoglobulins C Measurement of IgG response to pneumococcal immunizationD Nasal Ciliary Biopsy 

29. Question 2A 23-year-old woman is evaluated for chronic cough. She reports several episodes of chronic bronchitis as a child and persistent cough productive of thick purulent sputum since childhood. She also has chronic nasal congestion and chronic diarrhea. Medications are albuterol and glucocorticoid inhalers and benzonatate as needed.On physical examination, vital signs are normal; oxygen saturation  is 96% with the patient breathing ambient air. BMI is 18. Lung examination reveals bilateral diffuse crackles. The remainder of the examination is normal.Complete blood count and immunoglobulin levels are normal.Chest CT scan shows bilateral upper-lobe-predominant bronchiectasis with luminal filling.Spirometry shows an FEV1  of 68% of predicted.Which of the following is the most likely diagnosis?A ABPAB Alpha 1C CFD IgA Def

30. Question 3A 72-year-old woman is evaluated for exacerbation of bronchiectasis symptoms over the past 3 days. Chronic productive cough has worsened in frequency and severity, and her sputum has increased in amount, become thicker, and changed in color from white to dark yellow. She has been using albuterol and hypertonic saline nebulization with a positive expiratory pressure device three times daily since her symptoms increased.On physical examination, vital signs are normal. Lung examination reveals bibasilar crackles. There is no accessory muscle use.Prior sputum cultures have grown Pseudomonas aeruginosa and Haemophilus parainfluenzae.Chest radiograph reveals chronic interstitial markings but no acute change.Which of the following is the most appropriate treatment?A AzithroB Dornase AlphaC Prednisone D Cipro

31. Question 4A 31-year-old man is evaluated following an abnormal finding on a chest radiograph obtained as a part of pre-employment screening. He is a lifelong nonsmoker with no history of dust exposure. His medical history is unremarkable, and he has no known respiratory or constitutional symptoms.The vital signs and physical examination are normal.Spirometry is normal.Chest radiograph reveals bilateral symmetric hilar prominence with clear lung fields.Interferon-γ release assay is normal.Which of the following is the most appropriate managementA Bronch with biopsy and EBUSB MTXC Prednisone D Observation E Bone marrow biopsy 

32. Question 5 A 58-year-old man is evaluated in the hospital for new-onset heart failure after presenting with palpitations, light-headedness, and progressive dyspnea. Medical history includes hypertension, dyslipidemia, and pulmonary sarcoidosis.On physical examination, blood pressure is 110/70 mm Hg and pulse rate is 70/min and irregular. Oxygen saturation is 96% with the patient breathing ambient air. The central venous pressure is elevated. An S3 is present, but the lungs are clear to auscultation.An ECG demonstrates frequent premature ventricular contractions and left bundle branch block. Frequent three- to five-beat runs of nonsustained monomorphic ventricular tachycardia are noted on telemetry.An echocardiogram demonstrates a dilated left ventricle, with an ejection fraction of 39%. Regional wall motion abnormalities include hypokinesis of the inferobasal and mid-anterolateral left ventricular walls. A coronary angiogram demonstrates no obstructive coronary artery disease.Which of the following is the most appropriate next step in management?A Amiodarone B CMRC Endomyocardial biopsy D ICD

33. Question 6A 67-year-old woman is evaluated in the hospital for malaise, fatigue, arthralgia, and rash of 8 weeks' duration; dry cough and sinus congestion of 6 weeks' duration; and painless eye redness and dyspnea that began several days ago.On physical examination, temperature is 38.2 °C (100.8 °F), blood pressure is 122/76 mm Hg, pulse rate is 104/min, respiration rate is 24/min, and oxygen saturation  is 92% with the patient breathing ambient air. Bilateral, localized ocular injection is seen. Scattered rhonchi are heard on lung auscultation, and petechiae and purpura are visible on the legs.

34. Q 6 A kidney biopsy, B skin biopsy, C lung biopsy, D Sinus biopsy

35. Thank you for your attention