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Left Atrial Stenosis Induced Pulmonary Venous Arterialization and Group 2 Pulmonary Hypertension in Rat
Published on: November 18, 2018
[Pulmonary hypertension associated with lung disease]
Michael Halank1, Katarina E Zeder2,3, Natascha Sommer4,5
1Universitätsklinikum Carl Gustav Carus an der TU Dresden, Med. Klinik I, Bereich Pneumologie, Dresden, Deutschland.
Pulmonary hypertension (PH) often accompanies lung diseases, with severe cases indicating a poor prognosis. Prompt referral to PH clinics and individualized therapy are crucial for managing severe PH in lung disease patients.
Area of Science:
- Cardiology
- Pulmonology
- Internal Medicine
Context:
- Lung diseases and hypoventilation syndromes frequently present with pulmonary hypertension (PH).
- PH is hemodynamically defined by mean pulmonary arterial pressure (PAPm) >20 mmHg, pulmonary arterial wedge pressure (PAWP) ≤15 mmHg, and pulmonary vascular resistance (PVR) ≤5 Wood units (WU).
- Both non-severe (PVR ≤5 WU) and severe (PVR >5 WU) PH are associated with unfavorable prognoses.
Purpose:
- To outline diagnostic and therapeutic recommendations for PH associated with lung diseases.
- To identify risk factors for pulmonary arterial hypertension (PAH) and chronic thromboembolic pulmonary hypertension (CTEPH).
- To guide the management of severe PH in patients with COPD and interstitial lung disease.
Summary:
- Early identification of risk factors for PAH and CTEPH is recommended when PH is suspected.
- Patients with suspected severe PH or risk factors should be promptly referred to a PH outpatient clinic.
- Personalized therapy, including PH-specific drugs and inhaled treprostinil, should be considered for severe PH in lung disease patients, with specific criteria for COPD and interstitial lung disease.
Impact:
- Improved diagnostic pathways for PH in lung disease patients.
- Timely referral and intervention for patients with severe PH.
- Personalized treatment strategies to improve outcomes for patients with lung disease-related PH.
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