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Key articles and guidelines in the management of pulmonary arterial hypertension: 2011 update. | LitMetric

AI Article Synopsis

  • Pharmacotherapeutic strategies for managing pulmonary arterial hypertension (PAH) have significantly evolved over the past decade, shifting from the older terminology of primary PAH to accommodate distinct forms of the disease.
  • Treatment options now include medications like prostacyclin analogues, endothelin receptor antagonists, and phosphodiesterase inhibitors, alongside traditional therapies such as diuretics, while combination therapies are becoming standard due to their documented effectiveness.
  • The role of pharmacists in PAH management is expanding beyond dispensing medications to include improving patient access, providing counseling, and potentially participating in future drug development and specialized patient management programs.

Article Abstract

Pharmacotherapeutic approaches for the management of pulmonary arterial hypertension (PAH) have expanded greatly in the last 10 years. Pulmonary arterial hypertension is a relatively rare disease and is associated with myriad disease processes. The older term for PAH, primary PAH, has been changed to represent these differences and to distinguish it from postcapillary PAH associated with left-sided heart failure. Limitations in evaluating treatment approaches for PAH include its rarity, the small number of patients included in clinical trials, and issues regarding the use of placebo-controlled trials in a disease with such a high mortality rate if left untreated. Management options include the use of prostacyclin and prostacyclin analogues, endothelin receptor antagonists, and phosphodiesterase inhibitors, as well as traditional background therapy with diuretics, digoxin, calcium channel blockers, and warfarin. Numerous drugs are under investigation to evaluate their possible roles in management. Combination therapy is increasingly becoming a standard approach to therapy, with mounting literature to document effectiveness. Current or emerging roles for the pharmacist in the management of PAH largely involves ensuring access to drug therapy, facilitating specialty pharmacy dispensing, and providing patient counseling. Newer roles may include future drug development, optimized use of investigational drugs, and specialized disease management programs. This compilation includes a series of articles identifying important literature in cardiovascular pharmacotherapy. This bibliography focuses on pharmacotherapeutic management of pulmonary arterial hypertension (PAH). Most of the cited works present the results of significant human clinical studies that have shaped the management of patients with PAH. Limited primary literature is available for some topics, so in addition, consensus documents prepared by expert panels are reviewed. This compilation may serve as a teaching tool, reference resource, or update of the literature for pharmacy clinicians, physicians, and students.

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Source
http://dx.doi.org/10.1002/j.1875-9114.2012.01105.xDOI Listing

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