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一种带有局部麻醉注射口的新型男性导尿管在减轻导尿管相关性膀胱不适方面的疗效:一项随机对照研究。

Efficacy of a novel urinary catheter for men with a local anesthetic injection port for catheter-related bladder discomfort: a randomized controlled study.

机构信息

Department of Anesthesiology, Niigata University Graduate School of Medical and Dental Sciences, 1-757 Asahimachi-dori, Chuo-ku, Niigata, 951-8510, Japan.

出版信息

J Anesth. 2020 Oct;34(5):688-693. doi: 10.1007/s00540-020-02807-6. Epub 2020 Jun 4.

DOI:10.1007/s00540-020-02807-6
PMID:32500201
Abstract

PURPOSE

The NMOC-3WAY catheter is a novel urinary catheter for men that can be used to inject a local anesthetic into the urethra. We sought to assess whether the injection of a local anesthetic into the urethra via the NMOC-3WAY catheter would reduce catheter-related bladder discomfort (CRBD) after endovascular aneurysm repair (EVAR).

METHODS

Adult male patients who underwent elective EVAR for abdominal aortic aneurysms were randomly assigned to the 2% lidocaine group and the normal saline group (control group). CRBD was evaluated at 0, 1, 2, 4, and 6 h after surgery. The primary outcome was the incidence of CRBD at 0 h after surgery.

RESULTS

Data for 37 patients (19 in the lidocaine group and 18 in the control group) were analyzed. CRBD was observed at 0 h in six patients (31.6%; mild, n = 5; moderate, n = 1) in the lidocaine group and in five patients (27.8%; mild, n = 1; moderate, n = 3; severe, n = 1) in the control group. The control group showed a tendency to have severe CRBD at 0 h, although there was no significant difference in either the incidence (P = 0.80) or severity (P = 0.21) of CRBD between the two groups.

CONCLUSION

Our results suggest that the use of the NMOC-3WAY catheter for the injection of 2% lidocaine into the urethra does not reduce the incidence of CRBD immediately after EVAR. However, it may reduce moderate or severe CRBD that may lead to postoperative distress and agitation.

摘要

目的

NMOC-3WAY 导尿管是一种新型男性导尿管,可将局部麻醉剂注入尿道。我们旨在评估通过 NMOC-3WAY 导尿管向尿道内注射局部麻醉剂是否会降低血管内腹主动脉瘤修复(EVAR)后与导管相关的膀胱不适(CRBD)。

方法

接受择期 EVAR 治疗腹主动脉瘤的成年男性患者被随机分配到 2%利多卡因组和生理盐水组(对照组)。术后 0、1、2、4 和 6 小时评估 CRBD。主要结局是术后 0 小时的 CRBD 发生率。

结果

分析了 37 例患者的数据(利多卡因组 19 例,对照组 18 例)。在利多卡因组中,有 6 例(31.6%;轻度,n=5;中度,n=1)在 0 小时观察到 CRBD,对照组中有 5 例(27.8%;轻度,n=1;中度,n=3;严重,n=1)。尽管两组间 CRBD 的发生率(P=0.80)或严重程度(P=0.21)无显著差异,但对照组在 0 小时时出现严重 CRBD 的趋势。

结论

我们的结果表明,使用 NMOC-3WAY 导尿管向尿道内注射 2%利多卡因并不能降低 EVAR 后即刻 CRBD 的发生率。然而,它可能会减轻可能导致术后不适和躁动的中度或重度 CRBD。

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