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    Bronchiectasis Medical Slides

    Generate publication-quality bronchiectasis lecture slides in 30 seconds. AI-powered content structured for clinical education.

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    Why teach Bronchiectasis?

    Bronchiectasis prevalence has increased by 40% over the past decade, affecting approximately 350-566 per 100,000 adults. Post-infectious causes remain most common globally, though idiopathic bronchiectasis accounts for 30-50% of cases in developed countries. The 2017 ERS guidelines provide the framework for etiological workup, and the Bronchiectasis Severity Index (BSI) guides risk stratification and management intensity.

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    01HRCT Diagnosis: Signet Ring Sign, Lack of Tapering, and Visibility Within 1 cm of Pleura
    02Etiological Workup: Immunoglobulins, ABPA, CF Testing, PCD, and Alpha-1 Antitrypsin
    03Vicious Cycle Hypothesis: Infection, Inflammation, Structural Damage, and Impaired Clearance
    04Airway Clearance: Oscillatory PEP, Active Cycle Breathing, and Postural Drainage Techniques
    05Long-Term Macrolide Therapy: EMBRACE, BAT, and BLESS Trial Evidence
    06Exacerbation Management: Sputum Culture-Guided Antibiotics and Pseudomonas Eradication
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    Bronchiectasis Presentation FAQ

    What etiological workup should be presented in bronchiectasis teaching?

    Present the ERS 2017 minimum workup: immunoglobulins (IgG, IgA, IgM — immunodeficiency in 2-8%), specific antibody responses, ABPA screen (total IgE, Aspergillus-specific IgE/IgG — ABPA in 1-10%), sputum culture (including mycobacteria), and consider: CF testing (sweat chloride + CFTR genetics, especially if age <40), alpha-1 antitrypsin level, ciliary function testing, autoimmune panel. Up to 30-50% remain idiopathic despite comprehensive evaluation.

    How should long-term macrolide evidence be presented?

    Present the three landmark trials: EMBRACE (azithromycin 500 mg 3x/week reduced exacerbations, NZ), BAT (azithromycin 250 mg daily reduced exacerbations by 70%, Netherlands), BLESS (erythromycin 400 mg twice daily reduced exacerbations, Australia). Common findings: approximately 50% reduction in exacerbation frequency. Key considerations: screen for NTM before starting (risk of macrolide resistance), ECG for QTc prolongation, hearing assessment, liver function monitoring. ERS recommends for ≥3 exacerbations/year.

    What Pseudomonas management strategy should be covered?

    Present the significance: Pseudomonas colonization is associated with 3-fold increased mortality and accelerated lung function decline. Eradication protocol at first isolation: IV anti-pseudomonal antibiotics or inhaled colistin/tobramycin for 2-4 weeks. Chronic Pseudomonas: long-term inhaled antibiotics (nebulized colistin, tobramycin, or aztreonam in 28-day on/off cycles). Reference RESPIRE 1 and 2 trials for inhaled ciprofloxacin dry powder. BSI scoring guides treatment intensity.

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