Approach to pulmonary hypertension

Curr Rheumatol Rep. 2000 Dec;2(6):517-23. doi: 10.1007/s11926-000-0030-x.

Abstract

Until recently, many physicians considered pulmonary hypertension a rare and esoteric condition that is difficult to diagnose and nearly impossible to treat. However, pulmonary hypertension can complicate a variety of relatively common diseases and, with the development of new and effective therapies, there is a need for greater awareness of this condition. Pulmonary hypertension should be considered when patients present with unexplained shortness of breath, chest pain, or syncope. The usual delay of 1 to 2 years between onset of symptoms and diagnosis underscores the importance of considering pulmonary hypertension in the differential diagnosis of patients who present with atypical cardiorespiratory symptoms.

Publication types

  • Review

MeSH terms

  • Anticoagulants / administration & dosage
  • Cardiac Catheterization
  • Cardiotonic Agents / administration & dosage
  • Causality
  • Diuretics / administration & dosage
  • Echocardiography
  • Female
  • Follow-Up Studies
  • Humans
  • Hypertension, Pulmonary / diagnosis*
  • Hypertension, Pulmonary / drug therapy
  • Hypertension, Pulmonary / epidemiology*
  • Male
  • Pregnancy
  • Pregnancy Complications, Cardiovascular / mortality
  • Radiography, Thoracic
  • Respiratory Function Tests
  • Risk Assessment
  • Risk Factors
  • Survival Rate

Substances

  • Anticoagulants
  • Cardiotonic Agents
  • Diuretics