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    Pulmonary Hypertension Medical Slides

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

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    Why teach Pulmonary Hypertension?

    Pulmonary hypertension was redefined in 2022 by the 6th World Symposium with a lowered mPAP threshold from ≥25 to >20 mmHg, reflecting evidence that mPAP 21-24 mmHg confers increased mortality. PAH (Group 1) has a prevalence of 15-50 per million and untreated median survival of 2.8 years. Teaching PH requires systematic classification across the five WHO groups, hemodynamic assessment, and understanding of targeted combination therapy strategies.

    Sample Lecture Slides

    What AI generates for Pulmonary Hypertension

    Enter “Pulmonary Hypertension” and SlideCraft generates a complete lecture deck with slides like these.

    01WHO Classification: Five Groups with Updated 2022 Hemodynamic Definitions
    02Right Heart Catheterization: mPAP, PAWP, PVR, and Pre-/Post-Capillary Differentiation
    03Diagnostic Algorithm: Echocardiography Screening to RHC Confirmation
    04PAH-Targeted Therapy: Prostacyclin, ERA, and PDE5i Combination Strategy (AMBITION Trial)
    05Risk Stratification: ESC/ERS Low-Intermediate-High Risk Assessment Framework
    06Group 2 and Group 3 PH: HFpEF-Associated and Lung Disease-Associated Management
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    Pulmonary Hypertension Presentation FAQ

    How should the 2022 hemodynamic definition changes be presented?

    Present the updated 6th WSPH (2022) definitions: PH is now mPAP >20 mmHg (previously ≥25 mmHg), pre-capillary PH adds PVR >2 WU (previously >3 WU), post-capillary PH requires PAWP >15 mmHg. Combined pre- and post-capillary PH: PAWP >15 mmHg AND PVR >2 WU. Emphasize the clinical significance — patients with mPAP 21-24 mmHg have increased mortality in multiple registries, justifying earlier identification.

    What PAH-targeted therapy trials should be referenced?

    Present the combination therapy evidence: AMBITION trial (2015) — upfront ambrisentan + tadalafil reduced clinical failure by 50% versus monotherapy, establishing initial combination as standard of care. GRIPHON (selexipag reduced morbidity/mortality by 40%), SERAPHIN (macitentan reduced morbidity/mortality by 45%), and REPLACE trial (switching PDE5i to riociguat in inadequate responders). Current strategy: upfront double combination (ERA + PDE5i) with escalation to triple therapy including prostacyclin pathway.

    How should risk stratification guide treatment decisions in teaching?

    Present the ESC/ERS risk stratification using WHO functional class, 6-minute walk distance (>440 m low risk), BNP/NT-proBNP levels, right atrial area and pericardial effusion on echo, hemodynamics (CI, RAP, SvO2). Low risk: maintain therapy. Intermediate risk: consider escalation. High risk: escalate to parenteral prostacyclin, refer for transplant evaluation. Reference the COMPERA and French registry data validating this framework.

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