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微创与传统主动脉瓣置换术的出血比较。

Bleeding in minimally invasive versus conventional aortic valve replacement.

机构信息

Department of Cardiothoracic Surgery, Karolinska University Hospital, Stockholm, SE-17176, Sweden.

Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.

出版信息

J Cardiothorac Surg. 2024 Jun 21;19(1):349. doi: 10.1186/s13019-024-02667-1.

Abstract

BACKGROUND

Observational studies have shown reduced perioperative bleeding in patients undergoing minimally invasive, compared with full sternotomy, aortic valve replacement. Data from randomized trials are conflicting.

METHODS

This was a Swedish single center study where adult patients with aortic stenosis, 100 patients were randomly assigned in a 1:1 ratio to undergo either minimally invasive (ministernotomy) or full sternotomy aortic valve replacement. The primary outcome was severe or massive bleeding defined by the Universal Definition of Perioperative Bleeding in adult cardiac surgery (UDPB). Secondary outcomes included blood product transfusions, chest tube output, re-exploration for bleeding, and several other clinically relevant events.

RESULTS

Out of 100 patients, three patients randomized to ministernotomy were intraoperatively converted to full sternotomy (none was bleeding-related). Three patients (6%) in the full sternotomy group and 3 patients (6%) in the ministernotomy group suffered severe or massive postoperative bleeding according to the UDPB definition (p = 1.00). Mean chest tube output during the first 12 postoperative hours was 350 (standard deviation (SD) 220) ml in the full sternotomy group and 270 (SD 190) ml in the ministernotomy group (p = 0.08). 28% of patients in the full sternotomy group and 36% of patients in the ministernotomy group received at least one packed red blood cells transfusion (p = 0.39). Two patients in each group (4%) underwent re-exploration for bleeding.

CONCLUSIONS

Minimally invasive aortic valve replacement did not result in less bleeding-related outcomes compared to full sternotomy.

CLINICAL TRIAL REGISTRATION

http://www.

CLINICALTRIALS

gov . Unique identifier: NCT02272621.

摘要

背景

观察性研究表明,与完全胸骨切开术相比,微创主动脉瓣置换术可减少围手术期出血。随机试验的数据存在冲突。

方法

这是一项瑞典单中心研究,100 例主动脉瓣狭窄的成年患者以 1:1 的比例随机分配接受微创(小胸骨切开术)或完全胸骨切开术主动脉瓣置换术。主要结局是根据成人心脏手术围手术期出血的通用定义(UDPB)定义的严重或大量出血。次要结局包括输血量、胸腔引流管引流量、因出血再次探查以及其他一些临床相关事件。

结果

100 例患者中,3 例随机分配至小胸骨切开术的患者术中转为完全胸骨切开术(均与出血无关)。根据 UDPB 定义,完全胸骨切开组有 3 例(6%)和小胸骨切开组有 3 例(6%)患者发生严重或大量术后出血(p=1.00)。完全胸骨切开组术后 12 小时内胸腔引流管引流量平均为 350(标准差 220)ml,小胸骨切开组为 270(标准差 190)ml(p=0.08)。完全胸骨切开组 28%的患者和小胸骨切开组 36%的患者至少接受了 1 次红细胞悬液输注(p=0.39)。每组各有 2 例患者(4%)因出血再次探查。

结论

微创主动脉瓣置换术并未导致与完全胸骨切开术相比出血相关结局减少。

临床试验注册

http://www.clinicaltrials.gov。独特标识符:NCT02272621。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9910/11191138/81c0e006f95a/13019_2024_2667_Fig1_HTML.jpg

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