肺血栓内膜切除术
医学
血栓性
慢性血栓栓塞性肺高压
肺动脉高压
心脏病学
内科学
外科
血栓形成
作者
Hakan Akbayrak,Hayrettin Tekümit
出处
期刊:Cardiovascular journal of South Africa : official journal for Southern Africa Cardiac Society [and] South African Society of Cardiac Practitioners
日期:2019-02-28
卷期号:30 (1): e4-e6
被引量:2
标识
DOI:10.5830/cvja-2018-052
摘要
Chronic thromboembolic pulmonary hypertension (CTEPH) is a potentially correctable cause of secondary pulmonary hypertension. Surgical treatment remains the primary treatment for patients with CTEPH. Pulmonary thromboendarterectomy (PEA) with deep hypothermic circulatory arrest is the standard and recommended surgical technique for the treatment of these patients. The prevalence of CTEPH after an acute pulmonary thromboembolism (PTE) has been found in various studies to be between 0.6 and 8.8%. Mortality rates in elective PEA cases with CTEPH are reported to be between 1.9 and 4.5%. We report on a 50-year-old female patient with combined inherited thrombophilia, including protein C and protein S deficiencies, who was diagnosed with CTEPH and was successfully treated with pulmonary thromboendarterectomy.
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