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- W2691144196 abstract "Chronic thromboembolic pulmonary hypertension (CTEPH) is a rare but life‐threatening complication of acute pulmonary embolism (PE). This entity is the consequence of a persistent obstruction of the pulmonary arteries and progressive vascular remodeling. Some patients with CTEPH do not have a history of classic pulmonary embolism symptoms. The diagnostic process to detect CTEPH should include ventilation‐perfusion scintigraphy, which has a high sensitive and negative predictive value (nearly 100%) and CT angiography demonstrating typical features of CTEPH (occlusion of pulmonary arteries, mosaic perfusion or intraluminal bands or webs). Patients suspected of having CTEPH must be referred to an experienced center in order to complete the diagnostic workup (right‐heart catheterization and pulmonary angiography) and determine the best treatment. Pulmonary endarterectomy (PEA) remains the treatment of choice for CTEPH and is associated with excellent long‐term results and a highly curative rate. Patients with inoperable CTEPH are given medical and interventional modalities." @default.
- W2691144196 created "2017-06-30" @default.
- W2691144196 creator A5087472789 @default.
- W2691144196 date "2017-06-21" @default.
- W2691144196 modified "2023-10-03" @default.
- W2691144196 title "Surgical Management of Chronic Pulmonary Embolism" @default.
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- W2691144196 doi "https://doi.org/10.5772/67708" @default.
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