非妊娠期局部麻醉或sedo镇痛下输尿管支架置入术

J. Gabriel, M. Quraishi, B. Osman, L. Shafik, Abraham Gabriel, G. Watson, S. Mackie
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Around 1,460 papers were systematically screened for inclusion.ResultsSeventeen studies were identified; one randomised controlled trials (RCT), four non-randomised com-parative studies, and 12 case-series describing LAUSI. The 17 studies encompassed a total of some 1545 LAUSI. The clinical indications were similar to those for GAUSI. Successful LAUSI rate ranged from 71-98.9% in studies overall, with a pooled mean success rate of 89.3% overall (86.8% in LA only, 91.75% in LA ± sedoanalgesia). The tolerability of a LAUSI patient across 14 studies had a pooled mean rate of 91.8% (88.6% in LA only, 95% in LA ± sedoanalgesia). The procedure time was reported in seven studies, and it ranged from 5.35±0.87 to 65.0±27.5 minutes. The four comparative studies showed no difference in complication rates between LAUSI and GAUSI. 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引用次数: 1

摘要

背景与目的描述妊娠外输尿管局部麻醉支架置入(LAUSI)的相关证据,这是一种通常在全身麻醉(GAUSI)下进行的手术,因为它从未成为系统综述的主题。材料和方法对Medline、EMBASE、PubMed、AMED、BNI、EMCARE、HMIC和PsycINFO数据库进行了系统回顾,根据系统回顾和荟萃分析(PRISMA)指南的首选报告项目,围绕技术、患者人口统计学、环境、使用的LA±sedo镇痛药类型、膀胱镜和透视镜使用、患者耐受性和疼痛、疗效、并发症和成本效益,检查已发表的证据。大约1460篇论文被系统筛选纳入。结果共纳入17项研究;1项随机对照试验(RCT)、4项非随机对照研究和12个描述LAUSI的病例系列。这17项研究共涉及约1545个LAUSI。临床适应症与GAUSI相似。所有研究的LAUSI成功率为71-98.9%,总体平均成功率为89.3%(仅LA为86.8%,LA±sedo镇痛为91.75%)。在14项研究中,LAUSI患者的耐受性汇总平均率为91.8%(仅LA为88.6%,LA±sedo镇痛为95%)。7项研究报告了手术时间,范围为5.35±0.87至65.0±27.5分钟。四项比较研究显示LAUSI和GAUSI的并发症发生率无差异。报告成本效益的所有五项研究均显示LAUSI优于GAUSI。结论slausi是一种安全、有效、经济的替代GAUSI的方法,但未得到充分利用。需要以随机对照试验的形式进行进一步的研究,以正式确定其在泌尿科医生中的地位和可接受性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Primary Ureteric Stent Insertion Under Local Anaesthetic or Sedoanalgesia in Non-pregnancy
Background and ObjectiveTo characterise the evidence surrounding local anaesthetic ureteric stent insertion (LAUSI) in contexts outside of pregnancy, a procedure typically performed under general anaesthetic (GAUSI), as it has never been the subject of a systematic review.Materials and MethodsA systematic review of the Medline, EMBASE, PubMed, AMED, BNI, EMCARE, HMIC and PsycINFO databases was conducted to examine the published evidence in line with the Preferred Reporting Items of Systematic Review and Meta-analyses (PRISMA) guidelines surrounding the technique, patient demographics, setting, type of LA± sedoanalgesia used, cystoscopy and fluoroscopy usage, patient tolerability and pain, efficacy, complications and cost-effectiveness. Around 1,460 papers were systematically screened for inclusion.ResultsSeventeen studies were identified; one randomised controlled trials (RCT), four non-randomised com-parative studies, and 12 case-series describing LAUSI. The 17 studies encompassed a total of some 1545 LAUSI. The clinical indications were similar to those for GAUSI. Successful LAUSI rate ranged from 71-98.9% in studies overall, with a pooled mean success rate of 89.3% overall (86.8% in LA only, 91.75% in LA ± sedoanalgesia). The tolerability of a LAUSI patient across 14 studies had a pooled mean rate of 91.8% (88.6% in LA only, 95% in LA ± sedoanalgesia). The procedure time was reported in seven studies, and it ranged from 5.35±0.87 to 65.0±27.5 minutes. The four comparative studies showed no difference in complication rates between LAUSI and GAUSI. All five studies reporting on cost-effectiveness showed LAUSI to be superior to GAUSI.ConclusionsLAUSI is a safe, effective, and cost-effective alternative to GAUSI, which is underutilised. Further research in the form of RCTs is required to formally establish its place and acceptability amongst urologists.
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