Acute Postoperative Pain Due to Dental Extraction in the Adult Population: A Systematic Review and Network Meta-analysis

Author:

Miroshnychenko A.1,Ibrahim S.2,Azab M.2ORCID,Roldan Y.1,Martinez J.P.D.1,Tamilselvan D.2,He L.2,Little J.W.3,Urquhart O.4ORCID,Tampi M.5,Polk D.E.6ORCID,Moore P.A.6,Hersh E.V.7,Claytor B.8,Carrasco-Labra A.9,Brignardello-Petersen R.1

Affiliation:

1. Department of Health Research Methods, Evidence and Impact, McMaster University, Hamilton, Ontario, Canada

2. Faculty of Health Sciences, McMaster University, Hamilton, Ontario, Canada

3. Division of Oral and Craniofacial Health Sciences, Adams School of Dentistry, Chapel Hill, NC, USA

4. ADA Science and Research Institute, Chicago, Illinois, USA

5. Department of Cariology, University of Michigan School of Dentistry, Ann Arbor, MI, USA

6. Department of Dental Public Health, University of Pittsburgh, Pittsburgh, PA, USA

7. Department of Oral Surgery and Pharmacology, University of Pennsylvania, Philadelphia, PA, USA

8. N.C. Caring Dental Professionals, Aberdeen, NC, USA

9. Department of Preventative and Restorative Sciences, University of Pennsylvania, Philadelphia, PA, USA

Abstract

This study compares the effectiveness of pharmacological treatments to develop guidelines for the management of acute pain after tooth extraction. We searched Medline, EMBASE, CENTRAL, and US Clinical Trials registry on November 21, 2020. We included randomized clinical trials (RCTs) of participants undergoing dental extractions comparing 10 interventions, including acetaminophen, nonsteroidal anti-inflammatory drugs (NSAIDs), opioids, and combinations to placebo. After duplicate screening and data abstraction, we conducted a frequentist network meta-analysis for each outcome at 6 h (i.e., pain relief, total pain relief [TOTPAR], summed pain intensity difference [SPID], global efficacy rating, rescue analgesia, and adverse effects). We assessed the risk of bias using a modified Cochrane RoB 2.0 tool and the certainty of evidence using the Grading of Recommendations, Assessment, Development, and Evaluation approach. We implemented the analyses in RStudio version 3.5.3 and classified interventions from most to least beneficial or harmful. We included 82 RCTs. Fifty-six RCTs enrolling 9,095 participants found moderate- and high-certainty evidence that ibuprofen 200 to 400 mg plus acetaminophen 500 to 1,000 mg (mean difference compared to placebo [MDp], 1.68; 95% confidence interval [CI], 1.06–2.31), acetaminophen 650 mg plus oxycodone 10 mg (MDp, 1.19; 95% CI, 0.85–1.54), ibuprofen 400 mg (MDp, 1.31; 95% CI, 1.17–1.45), and naproxen 400–440 mg (MDp, 1.44; 95% CI, 1.07–1.80) were most effective for pain relief on a 0 to 4 scale. Oxycodone 5 mg, codeine 60 mg, and tramadol 37.5 mg plus acetaminophen 325 mg were no better than placebo. The results for TOTPAR, SPID, global efficacy rating, and rescue analgesia were similar. Based on low- and very low-certainty evidence, most interventions were classified as no more harmful than placebo for most adverse effects. Based on moderate- and high-certainty evidence, NSAIDs with or without acetaminophen result in better pain-related outcomes than opioids with or without acetaminophen (except acetaminophen 650 mg plus oxycodone 10 mg) or placebo.

Funder

u.s. food and drug administration

Publisher

SAGE Publications

Subject

General Dentistry

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3