Key result
Balloon pulmonary angioplasty is associated with a ~9 mmHg reduction in mPAP among CTEPH patients.
Why the study?
Not all patients with chronic thromboembolic pulmonary hypertension are eligible for pulmonary endarterectomy, and some experience recurrence of pulmonary hypertension after PEA.
Does balloon pulmonary angioplasty improve hemodynamics and functional capacity in patients with chronic thromboembolic pulmonary hypertension?
Observational (n=15)
No
Does balloon pulmonary angioplasty improve hemodynamics and functional capacity in patients with chronic thromboembolic pulmonary hypertension?
Absolute Event Rate: 32.1% vs 41.1%
p-value: p=<0.001
Balloon pulmonary angioplasty is a safe and effective treatment that improves hemodynamics and functional capacity in inoperable CTEPH patients and those with residual pulmonary hypertension after PEA.
Balloon pulmonary angioplasty was associated with hemodynamic improvement in CTEPH; extends observational data but leaves open randomized confirmation before practice change.
BACKGROUND: The treatment of choice for chronic thromboembolic pulmonary hypertension (CTEPH) is pulmonary endarterectomy (PEA). However, not all patients are eligible for PEA, and some patients experience recurrence of pulmonary hypertension even after PEA. METHODS: Patients who underwent balloon pulmonary angioplasty (BPA) between December 2015 and April 2017 were enrolled from the Samsung Medical Center CTEPH registry. Enrolled patients underwent right heart catheterization, echocardiography, and 6-minute walk distance (6MWD) at baseline, 4 and 24 weeks after their first BPA session. We compared clinical and hemodynamic parameters at the baseline and last BPA session. RESULTS: Fifty-two BPA sessions were performed in 15 patients, six of whom had a history of PEA. BPA resulted in improvements in World Health Organization (WHO) functional class (2.9 ± 0.8 to 1.7 ± 0.6, P = 0.002), 6MWD (387.0 ± 86.4 to 453.4 ± 64.8 m, P = 0.01), tricuspid annular plane systolic excursion (14.1 ± 3.6 to 15.6 ± 4.3 mm, P = 0.03) and hemodynamics, including a decline in mean pulmonary artery pressure (41.1 ± 13.1 to 32.1 ± 9.5 mmHg, P < 0.001) and in pulmonary vascular resistance (607.4 ± 452.3 to 406.7 ± 265.4 dyne.sec.cm⁻⁵, P = 0.01) but not in cardiac index (2.94 ± 0.79 to 2.96 ± 0.93 L/min/m², P = 0.92). Six cases of complications were recorded, including two cases of reperfusion injury. CONCLUSION: BPA might be a safe and effective treatment strategy for both inoperable CTEPH patients and patients with residual pulmonary hypertension after PEA.
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Kwon et al. (2017) conducted an observational in Chronic Thromboembolic Pulmonary Hypertension (n=15). Balloon Pulmonary Angioplasty vs. Baseline was evaluated on Mean pulmonary artery pressure (mmHg) (p=<0.001). Balloon pulmonary angioplasty significantly improved hemodynamics in patients with chronic thromboembolic pulmonary hypertension, reducing mean pulmonary artery pressure from 41.1 to 32.1 mmHg.
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