Key result
PEA is associated with ~3 mmHg lower mPAP than BPA, despite similar exercise capacity improvements.
Why the study?
Comparisons of hemodynamic and functional outcomes between pulmonary endarterectomy and balloon pulmonary angioplasty in CTEPH patients are scarce.
Does pulmonary endarterectomy compared to balloon pulmonary angioplasty improve hemodynamics and functional capacity in patients with chronic thromboembolic pulmonary hypertension?
Cohort (n=82)
No
Does pulmonary endarterectomy compared to balloon pulmonary angioplasty improve hemodynamics and functional capacity in patients with chronic thromboembolic pulmonary hypertension?
Absolute Event Rate: 28% vs 31%
While pulmonary endarterectomy provides greater reductions in pulmonary pressures than balloon pulmonary angioplasty in CTEPH patients, both treatments yield similar improvements in short-term exercise capacity.
Comparable functional gains after PEA or BPA support individualized selection in CTEPH; leaves open long-term outcome differences pending randomized trials.
The treatment of choice for chronic thromboembolic pulmonary hypertension (CTEPH) is pulmonary endarterectomy (PEA). Balloon pulmonary angioplasty (BPA) is an emerging option for inoperable patients. Comparisons of the hemodynamic and functional outcome between these treatments are scarce. In this single‐center observational cohort study, we compared hemodynamics by right heart catheterization and peak oxygen consumption before and 5 months (±14 days) after either PEA or BPA. Comprehensive evaluation and selection for PEA or BPA was performed by an expert CTEPH team. Fourty‐two and fourty consecutive patients were treated with PEA or BPA, respectively. Demographics were similar between groups. Both PEA and BPA significantly reduced mean pulmonary artery pressure (from 46 ± 11 mmHg at baseline to 28 ± 13 mmHg at follow‐up; p < 0.001 and from 43 ± 12 mmHg to 31 ± 9 mmHg; p < 0.001) and pulmonary vascular resistance (from 686 ± 347 dyn s cm−5 at baseline to 281 ± 197 dyn s cm−5 at follow‐up; p < 0.001 and from 544 ± 322 dyn s cm−5 to 338 ± 180 dyn s cm−5; p < 0.001), with significantly lower reductions for both parameters in the former group. However, cardiopulmonary exercise testing revealed no significant between group differences in exercise capacity. Diffusion capacity for carbon monoxide at baseline was the only follow‐up predictor for peak VO2. In our study, PEA reduced pulmonary pressures more than BPA did, but similar improvements were observed for exercise capacity. Thus, while long term data after BPA is lacking, BPA treated CTEPH patients can expect physical gains in line with PEA.
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Ravnestad et al. (2023) conducted a cohort in chronic thromboembolic pulmonary hypertension (CTEPH) (n=82). Pulmonary endarterectomy (PEA) vs. Balloon pulmonary angioplasty (BPA) was evaluated on mean pulmonary artery pressure at 5 months. Pulmonary endarterectomy reduced mean pulmonary artery pressure more than balloon pulmonary angioplasty (to 28 vs 31 mmHg), but both treatments yielded similar improvements in exercise capacity.
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