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Pulmonary arterial hypertension.

Mae M Centeno1

  • 1Heart Failure Program and Advanced Lung Disease Center, Baylor University Medical Center, 3500 Gaston Avenue, Dallas, TX 75246, USA. Mae.Centeno@Baylorhealth.edu

Critical Care Nursing Clinics of North America
|November 29, 2011
PubMed
Summary

Pulmonary arterial hypertension (PAH) necessitates lifelong treatment. Open discussions about therapy risks and benefits, alongside patient function and social support, are crucial for optimal management.

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