直肠内加热利多卡因凝胶和前列腺周围神经阻滞在经直肠超声引导前列腺活检中疼痛控制的比较:一项随机对照非劣效性试验

IF 2.7 2区 医学 Q2 UROLOGY & NEPHROLOGY
Hoon Jang , Hee Nam Moon , Jung Im Kim , Sang Rak Bae , Chang Hee Han , Bong Hee Park
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引用次数: 0

摘要

研究加热利多卡因凝胶(IRLAH)直肠内局部麻醉在经直肠超声(TRUS)引导下前列腺活检患者镇痛方面是否不劣于前列腺周围神经阻滞(PNB)。方法我们对100名参与者进行了随机对照非劣效性试验,这些参与者在2019年8月至2020年7月期间接受了系统TRUS引导的12核心前列腺活检。这些参与者被随机分为一组,接受20 mL加热(40°C)2%利多卡因凝胶(n=50)或PNB(n=50。主要结果是在4个时间点的0–10视觉模拟量表(VAS)上的疼痛评分,非劣效性界限为1;VAS-1:在局部麻醉应用期间;VAS-2:探针插入期间;VAS-3:活检期间;VAS-4:手术后30分钟。次要结果包括手术期间和手术后的并发症。结果IRLAH组(0.1)与PNB组(2.33)相比,符合VAS-1平均得分的非劣效性和优效性标准(P<;0.001),因为两组之间的差异(95%置信区间[CI])为−2.23(−2.66至−1.79),并且95%置信区间的上限均低于预先指定的非劣性界限且低于零。平均VAS-3评分的差异(95%CI)为0.3(-0.38至0.98),95%CI的上限没有超过预定义的非劣效性界限,表明IRLAH是非劣效的(IRLAH组,3.44;PNB组,3.14)。此外,VAS-2和VAS-4的疼痛评分也显示为非劣效。并发症没有显著差异。结论在TRUS引导的前列腺活检中,IRLAH是一种无创且不劣于PNB的疼痛控制替代方案,不会增加并发症的风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Comparison of intrarectal heated lidocaine gel and periprostatic nerve block for pain control in transrectal ultrasound-guided prostate biopsy: A randomized controlled non-inferiority trial

Comparison of intrarectal heated lidocaine gel and periprostatic nerve block for pain control in transrectal ultrasound-guided prostate biopsy: A randomized controlled non-inferiority trial

Comparison of intrarectal heated lidocaine gel and periprostatic nerve block for pain control in transrectal ultrasound-guided prostate biopsy: A randomized controlled non-inferiority trial

Background

To investigate whether intrarectal local anesthesia with heated lidocaine gel (IRLAH) is non-inferior to periprostatic nerve block (PNB) for reducing pain in patients undergoing transrectal ultrasound (TRUS)-guided prostate biopsy.

Methods

We performed a randomized controlled non-inferiority trial with 100 participants who underwent systematic TRUS-guided, 12-core prostate biopsy from August 2019 to July 2020. These participants were randomly assigned to a group receiving intrarectal local anesthesia with 20 mL of heated (40°C) 2% lidocaine gel (n = 50) or PNB (n = 50). The primary outcome was a pain score on a 0–10 visual analogue scale (VAS) at four time points with the non-inferiority margin of 1; VAS-1: during local anesthesia application; VAS-2: during probe insertion; VAS-3: during biopsy; VAS-4: 30 minutes after the procedure. The secondary outcome included complications during and after the procedure.

Results

The IRLAH group (0.1) met non-inferiority as well as superiority criteria for mean VAS-1 score vs. the PNB group (2.33) (P < 0.001), as the difference (95% confidence interval [CI]) between the two groups was −2.23 (−2.66 to −1.79) and the upper bound of the 95% CI were both below the prespecified non-inferiority margin and below zero. For mean VAS-3 score, the difference (95% CI) was 0.3 (−0.38 to 0.98) and the upper bound of the 95% CI did not exceed the predefined non-inferiority margin indicating that IRLAH was non-inferior (IRLAH group, 3.44; PNB group, 3.14). Also, non-inferiority was shown for pain scores at VAS-2 and VAS-4. There were no significant differences in complications.

Conclusion

IRLAH is a noninvasive and non-inferior alternative to PNB for pain control in TRUS-guided prostate biopsy without increased risk of complications.

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来源期刊
Prostate International
Prostate International Medicine-Urology
CiteScore
4.40
自引率
26.70%
发文量
40
审稿时长
35 days
期刊介绍: Prostate International (Prostate Int, PI), the official English-language journal of Asian Pacific Prostate Society (APPS), is an international peer-reviewed academic journal dedicated to basic and clinical studies on prostate cancer, benign prostatic hyperplasia, prostatitis, and ...
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