Key result
A home-based strategy for transitioning patients with pulmonary arterial hypertension from bosentan to macitentan or ambrisentan was well tolerated, with 0 process-related adverse events among 92 patients.
Why the study?
Does a home-based drug-transitioning approach safely facilitate switching from bosentan to newer endothelin receptor antagonists in patients with PAH?
Observational (n=92)
No
Does a home-based drug-transitioning approach safely facilitate switching from bosentan to newer endothelin receptor antagonists in patients with PAH?
A home-based, nurse-led strategy for transitioning PAH patients between endothelin receptor antagonists appears safe and feasible, avoiding unnecessary hospital visits.
BACKGROUND: Newer endothelin receptor antagonists (ERAs) used to treat patients with pulmonary arterial hypertension (PAH) are associated with fewer drug-drug interactions than bosentan and require less monitoring. This, combined with a pharmacokinetic basis for improved efficacy, means there may be a clinical rationale for changing therapies. However, this can be challenging and few data on its safety in patients with PAH are available. AIMS: At the Royal Free Hospital in London, UK, home-based medication transitioning has been standard practice since 2009 to avoid unnecessary hospital visits for patients, unless there is a clinical imperative. In this audit of standard practice we evaluated the consequences of adopting such a strategy when transitioning PAH patients between ERA therapies. METHODS AND RESULTS: Using a Clinical Nurse Specialist-led, home-based transitioning strategy, 92 patients with PAH were transitioned from bosentan to macitentan or ambrisentan. Observational data were analysed retrospectively. The majority of patients were female with PAH associated with connective tissue disease and their ERA was changed in the hope of improving efficacy. The process was well tolerated with no adverse events associated with the process. Seventeen patients died during the study (macitentan, n = 5; ambrisentan, n = 12). None of the deaths was considered related to ERA treatment. The majority of patients remained clinically stable, based on WHO functional class and exercise capacity. CONCLUSION: An established home-based transitioning strategy can be adopted safely for patients with PAH changing ERA therapies. Most patients remained stable and the therapy change was well tolerated.
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Dawson et al. (2018) conducted an observational in Pulmonary arterial hypertension (n=92). Home-based medication transitioning strategy was evaluated on Safety and tolerability (adverse events). A home-based strategy for transitioning patients with pulmonary arterial hypertension from bosentan to macitentan or ambrisentan was well tolerated, with 0 process-related adverse events among 92 patients.
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