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Saturday, June 13

Literature

Comparing bridging drug therapy approaches prior to balloon pulmonary angioplasty in patients with chronic thromboembolic pulmonary hypertension: a prospective analysis from the national UK CURATE registry.

Evidence suggests dual therapy with phosphodiesterase-5 inhibitor and endothelin receptor antagonist provided superior hemodynamic improvements compared to monotherapy in adult CTEPH patients bridging to balloon pulmonary angioplasty. Signal observed for 40% increase in cardiac index and 39% reduction in pulmonary vascular resistance with dual therapy versus more modest improvements with PDE5i or riociguat monotherapy, without increased periprocedural complications. Worth noting this real-world registry data demonstrates efficacy of combination pulmonary hypertension therapies in the CTEPH population.

PDE5i and ERA dual therapy was associated with greater haemodynamic improvement than monotherapy with PDE5i or riociguat, without differences in complication rates.

Relevance: Study comparing bridging PH medical therapies (PDE5i, ERA dual therapy, riociguat) in chronic thromboembolic pulmonary hypertension before balloon angioplasty. Directly relevant to pulmonary hypertension research interest; however, focuses on adult CTEPH rather than pediatric congenital heart disease. Some drugs discussed (sildenafil is a PDE5i, similar mechanism) relate to profile formulary.

PMID: 42259581Open heart(Journal Article)
Literature

Pulmonary Arterial Hypertension Associated With Calcitonin Gene-Related Peptide Antagonist Therapy for Migraine: A Case Series.

Signal observed for potential pulmonary arterial hypertension development in three adult patients receiving CGRP-targeted migraine therapies, with markedly elevated pulmonary vascular resistance noted in all cases. Evidence suggests two patients improved after discontinuation of CGRP therapy and initiation of PAH treatment, though temporal association does not establish causality. Worth noting the biological plausibility given CGRP's role as an endogenous pulmonary vasodilator and experimental evidence of worsening pulmonary hypertension with CGRP blockade.

Clinicians should remain vigilant for cardiopulmonary symptoms in patients receiving CGRP-targeted therapies.

Relevance: Case series describing pulmonary arterial hypertension associated with CGRP antagonist therapy. Pulmonary hypertension is a stated research interest; however, the article focuses on adult patients with migraine-related PAH rather than pediatric congenital heart disease or the specific diagnoses in the profile.

PMID: 42264575Chest(Case Reports)