Why the study?
Does pulmonary thromboendarterectomy improve clinical and hemodynamic outcomes in patients with chronic thromboembolic pulmonary hypertension?
Does pulmonary thromboendarterectomy improve clinical and hemodynamic outcomes in patients with chronic thromboembolic pulmonary hypertension?
Pulmonary thromboendarterectomy for chronic thromboembolic pulmonary hypertension provides significant hemodynamic and symptomatic improvements with acceptable early and long-term mortality.
Supports PTE hemodynamic benefit in CTEPH; leaves open safety and efficacy in larger prospective cohorts.
BACKGROUND: We present our 12-year experience of pulmonary thromboendarterectomy in patients with chronic thromboembolic pulmonary hypertension. MATERIALS AND METHODS: Between January 1999 and March 2011, 16 patients underwent pulmonary thromboendarterectomy. Eleven patients (69%) were classified as functional class III or IV based on the New York Heart Association (NYHA) classification. Seven patients had a history of inferior vena cava filter insertion, and 5 patients showed coagulation disorders. Pulmonary thromboendarterectomy was performed during total circulatory arrest with deep hypothermia in 14 patients. RESULTS: In-hospital mortality and late death occurred in 2 patients (12.5%) and 1 patient (6.3%), respectively. Extracorporeal membrane oxygenation support was required in 4 patients who developed severe hypoxemia after surgery. Thirteen of the 14 survivors have been followed up for 54 months (range, 2 to 141 months). The pulmonary arterial systolic pressure and cardiothoracic ratio on chest radiography was significantly decreased after surgery (76±26 mmHg vs. 41±17 mmHg, p=0.001; 55%±8% vs. 48%±3%, p=0.003). Tricuspid regurgitation was reduced from 2.1±1.1 to 0.7±0.6 (p=0.007), and the NYHA functional class was also improved to I or II in 13 patients (81%). These symptomatic and hemodynamic improvements maintained during the late follow-up period. CONCLUSION: Pulmonary thromboendarterectomy for chronic thromboembolic pulmonary hypertension shows good clinical outcomes with acceptable early and long term mortality.
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Oh et al. (2013) studied this question.
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