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先天性心脏病手术患儿术后乳糜胸

Post-Operative Chylothorax in Children Undergoing Congenital Heart Surgery.

作者信息

Ahmed Mehnaz Atiq

机构信息

Pediatric Cardiology, Department of Pediatrics, Liaquat National Hospital, Karachi, PAK.

出版信息

Cureus. 2021 Mar 10;13(3):e13811. doi: 10.7759/cureus.13811.

Abstract

Chylothorax is a rare postoperative complication of congenital heart surgery. It has high morbidity with increased hospital stay and cost of treatment. Damage to the thoracic duct, disruption of accessory lymphatic vessels, and increased venous pressure exceeding that in the thoracic duct have been proposed as the possible causes of chylothorax after surgery for congenital heart disease. Prompt diagnose with early initiation of treatment will reduce the duration of drainage. Staged treatment is the general principle in managing this serious complication. Loss of chyle leads to volume, nutritional and electrolyte depletion, immunological deficiencies and hematological complications. Identifying the underlying cause and addressing it is crucial to definitive management.

摘要

乳糜胸是先天性心脏病手术后一种罕见的并发症。其发病率高,会延长住院时间并增加治疗费用。胸导管损伤、附属淋巴管破裂以及静脉压升高超过胸导管内压力,被认为是先天性心脏病手术后发生乳糜胸的可能原因。及时诊断并尽早开始治疗可缩短引流时间。分阶段治疗是处理这一严重并发症的一般原则。乳糜流失会导致容量、营养和电解质消耗、免疫缺陷及血液学并发症。确定潜在病因并加以解决对明确治疗至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f389/8038894/25c8e212cf4b/cureus-0013-00000013811-i01.jpg

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