Eduardo Maia Martins Pereira , Patrícia Viana , Rodrigo Araujo Monteiro da Silva , Pedro Furlan Silott , Sara Amaral
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Sensitivity and trial-sequential analyses were performed to assess inconsistencies and weight type I and II errors, and estimate the required information size of the samples for all end points.</div></div><div><h3>Results</h3><div>Sixteen randomized controlled trials (1220 patients) were included. Compared with LA alone, dexmedetomidine was associated with prolonged (1) motor block duration (MD: 65.01 minutes, <em>P</em> < .001), (2) sensory block duration (MD: 81.94 minutes, <em>P</em> < .001), (3) reduced intraocular pressure (MD: –2.6 mm Hg, <em>P</em> < .001), and (4) decreased need for supplemental injections (RR: 0.44, <em>P</em> = .007). In addition, dexmedetomidine showed (5) longer time to analgesic request (MD: 97.15 minutes, <em>P</em> < .001) and (6) increased surgeon satisfaction (RR: 1.52, <em>P</em> = .01). Sensitivity analyses and trial-sequential analyses were consistent across all end points, and the required information size was achieved for most end points, indicating that pooled analyses were reliable and sample sizes were sufficient.</div></div><div><h3>Conclusions</h3><div>Compared with LA alone, dexmedetomidine significantly prolonged sensory and motor block duration and the time to the first analgesic request; moreover, it decreased intraocular pressure and the need for supplemental injections, while increasing surgeon satisfaction.</div></div>","PeriodicalId":7568,"journal":{"name":"American Journal of Ophthalmology","volume":null,"pages":null},"PeriodicalIF":4.1000,"publicationDate":"2024-07-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Efficacy of Dexmedetomidine as an Adjuvant to Local Anesthetics in Peribulbar Block: A Meta-analysis With Trial-Sequential Analysis\",\"authors\":\"Eduardo Maia Martins Pereira , Patrícia Viana , Rodrigo Araujo Monteiro da Silva , Pedro Furlan Silott , Sara Amaral\",\"doi\":\"10.1016/j.ajo.2024.07.011\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Purpose</h3><div>To assess the role of dexmedetomidine as an adjuvant to local anesthetics (LA) in enhancing the duration and quality of peribulbar blocks for ophthalmic surgeries.</div></div><div><h3>Design</h3><div>Systematic review with meta-analysis and trial sequential analysis.</div></div><div><h3>Methods</h3><div>We systematically searched MEDLINE, Embase, and Cochrane for randomized controlled trials involving adult patients undergoing ophthalmic surgery under peribulbar block, comparing LA alone vs LA + dexmedetomidine. Risk ratios (RR) and mean differences (MD) with 95% confidence intervals were computed using a random-effects model. Sensitivity and trial-sequential analyses were performed to assess inconsistencies and weight type I and II errors, and estimate the required information size of the samples for all end points.</div></div><div><h3>Results</h3><div>Sixteen randomized controlled trials (1220 patients) were included. Compared with LA alone, dexmedetomidine was associated with prolonged (1) motor block duration (MD: 65.01 minutes, <em>P</em> < .001), (2) sensory block duration (MD: 81.94 minutes, <em>P</em> < .001), (3) reduced intraocular pressure (MD: –2.6 mm Hg, <em>P</em> < .001), and (4) decreased need for supplemental injections (RR: 0.44, <em>P</em> = .007). In addition, dexmedetomidine showed (5) longer time to analgesic request (MD: 97.15 minutes, <em>P</em> < .001) and (6) increased surgeon satisfaction (RR: 1.52, <em>P</em> = .01). 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引用次数: 0
摘要
目的:评估右美托咪定作为局麻药(LA)的辅助用药在提高眼科手术中眼周阻滞的持续时间和质量方面的作用:设计:系统综述、荟萃分析和试验序列分析我们系统检索了 MEDLINE、Embase 和 Cochrane 中涉及接受眼科手术周围阻滞的成人患者的随机对照试验 (RCT),比较了单独使用 LA 与 LA + 右美托咪定的效果。采用随机效应模型计算了风险比 (RR) 和平均差 (MD) 以及 95% 置信区间 (CI)。进行了敏感性分析和试验序列分析(TSA),以评估不一致性、II型和II型误差的权重,并估算所有终点所需的样本信息量:结果:共纳入了 16 项 RCT(1,220 名患者)。与单用 LA 相比,右美托咪定可延长(1)运动阻滞持续时间(MD 65.01 分钟,pC):与单独使用 LA 相比,右美托咪定可明显延长感觉和运动阻滞持续时间以及首次要求镇痛的时间;降低眼压和补充注射的需要,同时提高外科医生的满意度。
Efficacy of Dexmedetomidine as an Adjuvant to Local Anesthetics in Peribulbar Block: A Meta-analysis With Trial-Sequential Analysis
Purpose
To assess the role of dexmedetomidine as an adjuvant to local anesthetics (LA) in enhancing the duration and quality of peribulbar blocks for ophthalmic surgeries.
Design
Systematic review with meta-analysis and trial sequential analysis.
Methods
We systematically searched MEDLINE, Embase, and Cochrane for randomized controlled trials involving adult patients undergoing ophthalmic surgery under peribulbar block, comparing LA alone vs LA + dexmedetomidine. Risk ratios (RR) and mean differences (MD) with 95% confidence intervals were computed using a random-effects model. Sensitivity and trial-sequential analyses were performed to assess inconsistencies and weight type I and II errors, and estimate the required information size of the samples for all end points.
Results
Sixteen randomized controlled trials (1220 patients) were included. Compared with LA alone, dexmedetomidine was associated with prolonged (1) motor block duration (MD: 65.01 minutes, P < .001), (2) sensory block duration (MD: 81.94 minutes, P < .001), (3) reduced intraocular pressure (MD: –2.6 mm Hg, P < .001), and (4) decreased need for supplemental injections (RR: 0.44, P = .007). In addition, dexmedetomidine showed (5) longer time to analgesic request (MD: 97.15 minutes, P < .001) and (6) increased surgeon satisfaction (RR: 1.52, P = .01). Sensitivity analyses and trial-sequential analyses were consistent across all end points, and the required information size was achieved for most end points, indicating that pooled analyses were reliable and sample sizes were sufficient.
Conclusions
Compared with LA alone, dexmedetomidine significantly prolonged sensory and motor block duration and the time to the first analgesic request; moreover, it decreased intraocular pressure and the need for supplemental injections, while increasing surgeon satisfaction.
期刊介绍:
The American Journal of Ophthalmology is a peer-reviewed, scientific publication that welcomes the submission of original, previously unpublished manuscripts directed to ophthalmologists and visual science specialists describing clinical investigations, clinical observations, and clinically relevant laboratory investigations. Published monthly since 1884, the full text of the American Journal of Ophthalmology and supplementary material are also presented online at www.AJO.com and on ScienceDirect.
The American Journal of Ophthalmology publishes Full-Length Articles, Perspectives, Editorials, Correspondences, Books Reports and Announcements. Brief Reports and Case Reports are no longer published. We recommend submitting Brief Reports and Case Reports to our companion publication, the American Journal of Ophthalmology Case Reports.
Manuscripts are accepted with the understanding that they have not been and will not be published elsewhere substantially in any format, and that there are no ethical problems with the content or data collection. Authors may be requested to produce the data upon which the manuscript is based and to answer expeditiously any questions about the manuscript or its authors.