Suppr超能文献

慢性肺栓塞的外科治疗

Surgical management of chronic pulmonary embolism.

作者信息

Sabiston D C, Wolfe W G, Oldham H N, Wechsler A S, Crawford F A, Jones K W, Jones R H

出版信息

Ann Surg. 1977 Jun;185(6):699-712. doi: 10.1097/00000658-197706000-00013.

Abstract

The clinical course of most patients with pulmonary embolism is one of gradual resolution with re-establishment of flow in the pulmonary arteries. In a small but definite group of patients, the emboli do not resolve and a state of chronic pulmonary embolism ensues. The primary thrombotic process in the systemic venous system may persist, and in some instances may be unrecognized. Such patients experience recurrent showers of emboli which may ultimately occlude a large part of the pulmonary arterial circulation with development of severe respiratory insufficiency. Six patients with this syndrome are described, and in each there was a history of dyspnea, cyanoiss, and exercise intolerance associated with a low arterial PO2, right ventricular hypertrophy, and pulmonary hypertension. Pulmonary scans and arteriograms demonstrated that more than half of the major pulmonary arteries were occluded and, in addition, smaller vessels were also obstructed. Pulmonary embolectomy was performed in each patient. Five of the 6 obtained a highly gratifying response, including relief of the dyspnea and cyanosis, an increase in arterial PO2, and a decrease in pulmonary arterial pressure. In each of the five in whom improvement occurred, the back-bleeding from the pulmonary artery at the time of embolectomy was quite good. In the sixth patient, the back-bleeding was very poor, and despite embolectomy, the vessel thrombosed postoperatively with no improvement in the patient's clinical course. Follow-up studies in these patients range up to 8 years with demonstration of continued patency of the pulmonary arteries as well as continued improvement in clinical symptoms and in the arterial PO2.

摘要

大多数肺栓塞患者的临床病程是逐渐缓解,肺动脉血流得以重建。在一小部分但确切存在的患者群体中,栓子不会溶解,继而会发展为慢性肺栓塞状态。体静脉系统的原发性血栓形成过程可能持续存在,在某些情况下可能未被识别。这类患者会反复出现栓子,最终可能导致大部分肺动脉循环阻塞,并发严重的呼吸功能不全。本文描述了6例患有此综合征的患者,每例患者均有呼吸困难、发绀和运动不耐受的病史,同时伴有动脉血氧分压降低、右心室肥厚和肺动脉高压。肺部扫描和动脉造影显示,超过半数的主要肺动脉被阻塞,此外,较小的血管也有阻塞。每位患者均接受了肺动脉血栓切除术。6例患者中有5例获得了非常满意的疗效,包括呼吸困难和发绀缓解、动脉血氧分压升高以及肺动脉压降低。在病情改善的5例患者中,血栓切除术时肺动脉的回血情况良好。在第6例患者中,回血情况很差,尽管进行了血栓切除术,但术后血管仍发生血栓形成,患者的临床病程无改善。对这些患者的随访研究长达8年,结果显示肺动脉持续通畅,临床症状和动脉血氧分压持续改善。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a271/1396238/f3ed320251a0/annsurg00377-0092-a.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验