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Research · 04 of 06

HIV-associated pulmonary arterial hypertension: survival improved, but only 64% got targeted therapy at diagnosis

In people with HIV and confirmed PAH, refer to a pulmonary hypertension centre to consider targeted therapy.

Design
Systematic review and meta-analysis of 12 cohorts
Population
537 people with right heart catheterisation-confirmed HIV-associated PAH (1986 to 2021)
Primary outcome
Presentation, treatment use and survival over time
Effect
64% received PAH-targeted therapy at diagnosis; survival improved over three decades

This systematic review and meta-analysis pooled 12 cohorts of right heart catheterisation-confirmed HIV-associated pulmonary arterial hypertension, with 537 patients spanning 1986 to 2021.

The condition presented with severe haemodynamics and advanced functional limitation. Only 64% received PAH-targeted therapy at diagnosis. Survival improved progressively over three decades alongside increasing use of such therapy.

The abstract does not give effect sizes, and the improvement over time may reflect better antiretroviral therapy, earlier diagnosis and other changes beyond PAH drugs. The authors say the findings support considering contemporary combination PAH therapy in people with HIV.

  • Consider pulmonary hypertension in people with HIV and unexplained breathlessness.
  • Confirm the diagnosis by right heart catheterisation before labelling PAH.
  • Do not leave confirmed PAH untreated; discuss targeted therapy with a PH centre.
  • Antiretroviral therapy continues alongside PAH therapy; check interactions.

Why it matters

A third of patients in the pooled cohorts did not receive targeted therapy at diagnosis, which is a gap clinicians can close.

Don't overread it

Pooled observational cohorts spanning 35 years cannot attribute improved survival to any single therapy.

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