Sina Grape , Kariem El-Boghdadly , Cécile Jaques , Eric Albrecht
{"title":"神经阻滞氢吗啡酮的疗效和安全性:系统回顾和荟萃分析与试验序列分析。","authors":"Sina Grape , Kariem El-Boghdadly , Cécile Jaques , Eric Albrecht","doi":"10.1016/j.jclinane.2024.111664","DOIUrl":null,"url":null,"abstract":"<div><h3>Study objective</h3><div>Neuraxial hydromorphone provides postoperative pain relief. However, the magnitude of this effect and the optimal dose remain unknown. The objective of this study is to clarify these uncertainties.</div></div><div><h3>Design</h3><div>Systematic review and meta-analysis with trial sequential analysis.</div></div><div><h3>Setting</h3><div>Postoperative recovery area and ward, up to 24 h.</div></div><div><h3>Patients</h3><div>Any patient undergoing any type of surgery or being in labor.</div></div><div><h3>Interventions</h3><div>Neuraxial hydromorphone versus control.</div></div><div><h3>Measurements</h3><div>Our primary outcome was rest pain score (analogue scale, 0–10) at 24 h according to route of administration (epidural versus spinal) and type of surgery (orthopedic versus other). Secondary outcomes included rest pain score at 0–4 and 8–12 h; rates of postoperative nausea and vomiting, and pruritus at 24 h.</div></div><div><h3>Main results</h3><div>Six trials, including 436 patients, were identified. Rest pain score at 24 postoperative hours was significantly reduced in the hydromorphone group, with a mean difference (95 %CI) of −0.4 (−0.8 to −0.1), I<sup>2</sup> = 74 %, <em>p</em> = 0.01. Neuraxial hydromorphone did not increase postoperative nausea and vomiting (risk ratio [95 %CI]: 1.2 [0.8–1.8], I<sup>2</sup> = 27 %, <em>p</em> = 0.47), but increases pruritus (risk ratio [95 %CI]: 3.1 [1.6–5.9], I<sup>2</sup> = 0 %, <em>p</em> = 0.0005). The quality of evidence was very low for our primary and secondary outcomes. In conclusion, there is very low level of evidence that neuraxial hydromorphone provides effective analgesia after surgery or labor, at the expense of an increased rate of pruritus. The improvement in pain scores appears to be clinically insignificant. With only six trials published over a period of 30 years, we were unable to perform a meta-regression.</div></div><div><h3>Conclusions</h3><div>If neuraxial hydromorphone is to be used regularly, trials focusing on the optimal dose and side-effects should be performed before widely administering this medication into the neuraxial space.</div><div>More trials focusing on the optimal dose and side-effects should be performed before widely administering this medication into the neuraxial space.</div></div>","PeriodicalId":15506,"journal":{"name":"Journal of Clinical Anesthesia","volume":"99 ","pages":"Article 111664"},"PeriodicalIF":5.0000,"publicationDate":"2024-10-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Efficacy and safety of neuraxial hydromorphone: A systematic review and meta-analysis with trial sequential analysis\",\"authors\":\"Sina Grape , Kariem El-Boghdadly , Cécile Jaques , Eric Albrecht\",\"doi\":\"10.1016/j.jclinane.2024.111664\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Study objective</h3><div>Neuraxial hydromorphone provides postoperative pain relief. However, the magnitude of this effect and the optimal dose remain unknown. The objective of this study is to clarify these uncertainties.</div></div><div><h3>Design</h3><div>Systematic review and meta-analysis with trial sequential analysis.</div></div><div><h3>Setting</h3><div>Postoperative recovery area and ward, up to 24 h.</div></div><div><h3>Patients</h3><div>Any patient undergoing any type of surgery or being in labor.</div></div><div><h3>Interventions</h3><div>Neuraxial hydromorphone versus control.</div></div><div><h3>Measurements</h3><div>Our primary outcome was rest pain score (analogue scale, 0–10) at 24 h according to route of administration (epidural versus spinal) and type of surgery (orthopedic versus other). Secondary outcomes included rest pain score at 0–4 and 8–12 h; rates of postoperative nausea and vomiting, and pruritus at 24 h.</div></div><div><h3>Main results</h3><div>Six trials, including 436 patients, were identified. Rest pain score at 24 postoperative hours was significantly reduced in the hydromorphone group, with a mean difference (95 %CI) of −0.4 (−0.8 to −0.1), I<sup>2</sup> = 74 %, <em>p</em> = 0.01. Neuraxial hydromorphone did not increase postoperative nausea and vomiting (risk ratio [95 %CI]: 1.2 [0.8–1.8], I<sup>2</sup> = 27 %, <em>p</em> = 0.47), but increases pruritus (risk ratio [95 %CI]: 3.1 [1.6–5.9], I<sup>2</sup> = 0 %, <em>p</em> = 0.0005). The quality of evidence was very low for our primary and secondary outcomes. In conclusion, there is very low level of evidence that neuraxial hydromorphone provides effective analgesia after surgery or labor, at the expense of an increased rate of pruritus. The improvement in pain scores appears to be clinically insignificant. With only six trials published over a period of 30 years, we were unable to perform a meta-regression.</div></div><div><h3>Conclusions</h3><div>If neuraxial hydromorphone is to be used regularly, trials focusing on the optimal dose and side-effects should be performed before widely administering this medication into the neuraxial space.</div><div>More trials focusing on the optimal dose and side-effects should be performed before widely administering this medication into the neuraxial space.</div></div>\",\"PeriodicalId\":15506,\"journal\":{\"name\":\"Journal of Clinical Anesthesia\",\"volume\":\"99 \",\"pages\":\"Article 111664\"},\"PeriodicalIF\":5.0000,\"publicationDate\":\"2024-10-22\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Clinical Anesthesia\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0952818024002939\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"ANESTHESIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Clinical Anesthesia","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0952818024002939","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ANESTHESIOLOGY","Score":null,"Total":0}
Efficacy and safety of neuraxial hydromorphone: A systematic review and meta-analysis with trial sequential analysis
Study objective
Neuraxial hydromorphone provides postoperative pain relief. However, the magnitude of this effect and the optimal dose remain unknown. The objective of this study is to clarify these uncertainties.
Design
Systematic review and meta-analysis with trial sequential analysis.
Setting
Postoperative recovery area and ward, up to 24 h.
Patients
Any patient undergoing any type of surgery or being in labor.
Interventions
Neuraxial hydromorphone versus control.
Measurements
Our primary outcome was rest pain score (analogue scale, 0–10) at 24 h according to route of administration (epidural versus spinal) and type of surgery (orthopedic versus other). Secondary outcomes included rest pain score at 0–4 and 8–12 h; rates of postoperative nausea and vomiting, and pruritus at 24 h.
Main results
Six trials, including 436 patients, were identified. Rest pain score at 24 postoperative hours was significantly reduced in the hydromorphone group, with a mean difference (95 %CI) of −0.4 (−0.8 to −0.1), I2 = 74 %, p = 0.01. Neuraxial hydromorphone did not increase postoperative nausea and vomiting (risk ratio [95 %CI]: 1.2 [0.8–1.8], I2 = 27 %, p = 0.47), but increases pruritus (risk ratio [95 %CI]: 3.1 [1.6–5.9], I2 = 0 %, p = 0.0005). The quality of evidence was very low for our primary and secondary outcomes. In conclusion, there is very low level of evidence that neuraxial hydromorphone provides effective analgesia after surgery or labor, at the expense of an increased rate of pruritus. The improvement in pain scores appears to be clinically insignificant. With only six trials published over a period of 30 years, we were unable to perform a meta-regression.
Conclusions
If neuraxial hydromorphone is to be used regularly, trials focusing on the optimal dose and side-effects should be performed before widely administering this medication into the neuraxial space.
More trials focusing on the optimal dose and side-effects should be performed before widely administering this medication into the neuraxial space.
期刊介绍:
The Journal of Clinical Anesthesia (JCA) addresses all aspects of anesthesia practice, including anesthetic administration, pharmacokinetics, preoperative and postoperative considerations, coexisting disease and other complicating factors, cost issues, and similar concerns anesthesiologists contend with daily. Exceptionally high standards of presentation and accuracy are maintained.
The core of the journal is original contributions on subjects relevant to clinical practice, and rigorously peer-reviewed. Highly respected international experts have joined together to form the Editorial Board, sharing their years of experience and clinical expertise. Specialized section editors cover the various subspecialties within the field. To keep your practical clinical skills current, the journal bridges the gap between the laboratory and the clinical practice of anesthesiology and critical care to clarify how new insights can improve daily practice.