Successful bosentan and nonnucleoside reverse transcriptase inhibitor-based therapy in a patient with acquired immunodeficiency syndrome and pulmonary arterial hypertension

Pharmacotherapy. 2010 Apr;30(4):139e-44e. doi: 10.1592/phco.30.4.422.

Abstract

Pulmonary arterial hypertension (PAH), which can be a complication of human immunodeficiency virus (HIV) infection, is characterized by increased pulmonary arterial pressure and peripheral vascular resistance, subsequently leading to right heart failure. In HIV-infected patients, the management of PAH is challenging given the potential drug interactions between PAH-specific vasodilators and antiretroviral drugs. We describe a 51-year-old female with acquired immunodeficiency syndrome (AIDS) and HIV-associated PAH. She was treated with the oral endothelin receptor antagonist bosentan while taking a nevirapine (a nonnucleoside reverse transcriptase inhibitor)-based antiretroviral regimen. Due to concerns about potential drug interactions with the antiretroviral therapy, her nevirapine plasma concentration, as well as CD4(+) cell count and viral load, were continuously monitored. We observed no interaction between bosentan and nevirapine during a 4-year period. To our knowledge, this report is the first to demonstrate successful, long-term coadministration of bosentan and a nonnucleoside reverse transcriptase inhibitor.

Publication types

  • Case Reports

MeSH terms

  • Acquired Immunodeficiency Syndrome / drug therapy*
  • Acquired Immunodeficiency Syndrome / genetics
  • Arteries
  • Bosentan
  • Drug Interactions / genetics
  • Female
  • HIV Infections / drug therapy*
  • HIV Infections / genetics
  • Humans
  • Hypertension / drug therapy*
  • Hypertension / genetics
  • Hypertension, Pulmonary / drug therapy*
  • Hypertension, Pulmonary / genetics
  • Middle Aged
  • Nevirapine / therapeutic use
  • Plasma / chemistry
  • Reverse Transcriptase Inhibitors / therapeutic use*
  • Sulfonamides / therapeutic use
  • Viral Load

Substances

  • Reverse Transcriptase Inhibitors
  • Sulfonamides
  • Nevirapine
  • Bosentan