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开腹治疗后的长期结局:功能与生活质量。

Long Term Outcome After Open Abdomen Treatment: Function and Quality of Life.

作者信息

Theodorou Alexis, Jedig Agnes, Manekeller Steffen, Willms Arnulf, Pantelis Dimitrios, Matthaei Hanno, Schäfer Nico, Kalff Jörg C, von Websky Martin W

机构信息

Department of General, Visceral, Thoracic and Vascular Surgery, University Hospital Bonn, Bonn, Germany.

Department of General-, Visceral- and Thoracic Surgery, Bundeswehr Central Hospital, Koblenz, Germany.

出版信息

Front Surg. 2021 Mar 29;8:590245. doi: 10.3389/fsurg.2021.590245. eCollection 2021.

DOI:10.3389/fsurg.2021.590245
PMID:33855043
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8039509/
Abstract

Open abdomen treatment (OAT) is widely accepted to manage severe abdominal conditions such as peritonitis and abdominal compartment syndrome but can be associated with high morbidity and mortality. The main risks in OAT are (1) entero-atmospheric fistula (EAF), (2) failure of primary fascial closure, and (3) incisional hernias. In this study, we assessed the long-term functional outcome after OAT to understand which factors impacted most on quality of life (QoL)/daily living activities and the natural course after OAT. After a retrospective analysis of 165 consecutive OAT patients over a period of 10 years (2002-2012) with over 65 clinical parameters that had been performed at our center (1), we initiated a prospective structured follow-up approach. All survivors were invited for a clinical follow-up. Forty complete datasets including clinical and social follow-up with SF-36 scores were available for full analysis. The patients were dominantly male (75%) with a median age of 52 years. Primary fascial closure (PC) was achieved in 9/40 (23%), while in 77% a planned ventral hernia (PVH) approach was followed. A total of 3/4 of the PVH patients underwent a secondary-stage abdominal wall reconstruction (SSR), but 2/3 of these reconstructed patients developed recurrent hernias. Fifty-five percent of the patients with PC developed an incisional hernia, while 20% of all patients developed significant scarring (Vancouver Scar Score >8). Scar pain was described by 15% of the patients as "moderate" [Visual Analog Scale (VAS) 4-6] and by 10% as "severe" (VAS > 7). While hernia presence, PC or PVH, and scarring showed no impact on QoL, male sex and especially EAF formation significantly reduced QoL. Despite many advantages, OAT was associated with relevant mortality and morbidity, especially in the early era before the implementation of a structured concept at our center. Follow-up revealed that hernia incidence after OAT and secondary reconstruction were high and that 25% of patients qualifying for a secondary reconstruction either did not want surgery or were unfit. Sex and EAF formation impacted significantly on QoL, which was lower than in the general population. With regard to hernia incidence, new strategies such as prophylactic mesh implantation upon fascial closure should be discussed analogous to other major abdominal procedures.

摘要

开放腹部治疗(OAT)被广泛用于处理诸如腹膜炎和腹腔间隔室综合征等严重腹部疾病,但可能伴有较高的发病率和死亡率。OAT的主要风险包括:(1)肠-气瘘(EAF),(2)一期筋膜关闭失败,以及(3)切口疝。在本研究中,我们评估了OAT后的长期功能结局,以了解哪些因素对生活质量(QoL)/日常生活活动影响最大以及OAT后的自然病程。在对我院10年期间(2002 - 2012年)连续165例OAT患者进行回顾性分析后(我院进行了超过65项临床参数评估),我们启动了一项前瞻性结构化随访研究。邀请所有幸存者进行临床随访。共有40份完整数据集,包括临床和社会随访以及SF - 36评分,可用于全面分析。患者以男性为主(75%),中位年龄为52岁。40例患者中有9例(23%)实现了一期筋膜关闭(PC),而77%的患者采用了计划性腹疝(PVH)治疗方法。PVH患者中有3/4接受了二期腹壁重建(SSR),但这些重建患者中有2/3出现了复发性疝。PC患者中有55%发生了切口疝,所有患者中有20%出现了明显的瘢痕形成(温哥华瘢痕评分>8)。15%的患者将瘢痕疼痛描述为“中度”[视觉模拟评分(VAS)4 - 6],10%的患者描述为“重度”(VAS>7)。虽然疝的存在、PC或PVH以及瘢痕形成对QoL没有影响,但男性性别尤其是EAF的形成显著降低了QoL。尽管有许多优点,但OAT仍伴有相关的死亡率和发病率,尤其是在我院实施结构化概念之前的早期阶段。随访显示,OAT和二期重建后的疝发病率很高,有资格进行二期重建的患者中有25%要么不想手术要么不适合手术。性别和EAF的形成对QoL有显著影响,QoL低于一般人群。关于疝发病率,应类似于其他主要腹部手术讨论在筋膜关闭时进行预防性网片植入等新策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/706b/8039509/4a6e5bc5e097/fsurg-08-590245-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/706b/8039509/7e61f1c7c9ce/fsurg-08-590245-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/706b/8039509/cb8dd9786e86/fsurg-08-590245-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/706b/8039509/a8ecb9604d29/fsurg-08-590245-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/706b/8039509/4a6e5bc5e097/fsurg-08-590245-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/706b/8039509/7e61f1c7c9ce/fsurg-08-590245-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/706b/8039509/cb8dd9786e86/fsurg-08-590245-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/706b/8039509/a8ecb9604d29/fsurg-08-590245-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/706b/8039509/4a6e5bc5e097/fsurg-08-590245-g0004.jpg

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