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局部麻醉下的环形电切术(LEEP):在质量保证计划下对435例后续病例的回顾性分析。

Loop electrosurgical excision procedure (LEEP) under local anesthesia: a retrospective analysis of 435 subsequent cases under a quality assurance program.

作者信息

Binder Ulrike, Wenzl Alice, Lafleur Judith, Tempfer Clemens, Hefler Lukas

机构信息

Karl Landsteiner Institute of Gynaecological Surgery and Oncology, Schultestrasse 1, 4020, Linz, Austria.

Ordensklinikum Linz and Konventhospital Barmherzige Brueder, Seilerstaette 2-4, Linz, Austria.

出版信息

Arch Gynecol Obstet. 2025 May 23. doi: 10.1007/s00404-025-08060-0.

Abstract

PURPOSE

The aim of this study is to analyze a quality assurance program regarding the switch from loop electrosurgical excision procedure (LEEP) in general anesthesia (GA) to local anesthesia (LA) regarding patients' perioperative pain levels, patients´ satisfaction, as well as resection margins.

METHODS

We performed a single-center retrospective analysis of our quality assurance program including all patients undergoing LEEP at the Department of Obstetrics and Gynecology, Ordensklinikum Linz and Konventhospital Barmherzige Brueder Linz, from January 2021 to June 2024. 435 patients were questioned postoperatively after being treated with LEEP in LA regarding the perioperative pain as measured by a numeric rating scale (NRS) and patients' satisfaction. Clinical data were collected from the patients' electronic chart to investigate further parameters.

RESULTS

Mean perioperative pain levels were stated as 1.3 (1.9). Five perioperative complications were reported. In seven out of 435 cases (1.6%) an inpatient readmission or a revision surgery under GA had to be performed. A R0 resection rate of 81.4% could be achieved. In 9.7% and 8.3% a R1 resection rate was reported on the ectocervix and on the endocervix, respectively. 95.3% of patients would choose LEEP in LA as their preferred method of anesthesia for a possible subsequent surgical LEEP procedure.

CONCLUSIONS

Our study showed that the implementation of LEEP in LA was successful at our department as a new standard of care, resulting in a high R0 resection status and a high level of patients' satisfaction. We encourage physicians and organizations to switch from GA to LA when performing LEEP for cervical dysplasia.

摘要

目的

本研究旨在分析一项质量保证计划,该计划涉及从全身麻醉(GA)下的环形电切术(LEEP)转换为局部麻醉(LA),内容包括患者围手术期疼痛水平、患者满意度以及切除边缘情况。

方法

我们对质量保证计划进行了单中心回顾性分析,纳入了2021年1月至2024年6月期间在林茨奥登斯klinikum妇产科和林茨慈善兄弟会康文特医院接受LEEP治疗的所有患者。435例患者在接受LA下的LEEP治疗后,就围手术期疼痛(采用数字评分量表[NRS]测量)和患者满意度接受了术后询问。从患者电子病历中收集临床数据以调查其他参数。

结果

围手术期平均疼痛水平为1.3(1.9)。报告了5例围手术期并发症。在435例病例中有7例(1.6%)需要进行住院再入院治疗或在GA下进行翻修手术。R0切除率可达81.4%。分别有9.7%和8.3%的患者在外宫颈和宫颈管内报告为R1切除率。95.3%的患者会选择LA下的LEEP作为后续可能的手术LEEP程序的首选麻醉方法。

结论

我们的研究表明,在我们科室将LA下的LEEP作为一种新的护理标准实施是成功的,导致了高R0切除状态和高水平的患者满意度。我们鼓励医生和医疗机构在对宫颈发育异常进行LEEP手术时从GA转换为LA。

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