Opioide bei chronischem Kreuzschmerz
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  • 作者:F. Petzke ; P. Welsch ; P. Klose ; R. Schaefert ; C. Sommer ; PD Dr. W. H?user
  • 关键词:Systematische übersichtsarbeit ; Metaanalyse ; Opioide ; Chronischer Rückenschmerz ; Systematic review ; Meta ; analysis ; Opioids ; Chronic low back pain
  • 刊名:Der Schmerz
  • 出版年:2015
  • 出版时间:February 2015
  • 年:2015
  • 卷:29
  • 期:1
  • 页码:60-72
  • 全文大小:840 KB
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  • 刊物类别:Medicine
  • 刊物主题:Medicine & Public Health
    Pain Medicine
    Anesthesiology
    Chiropractic Medicine
    Psychotherapy
  • 出版者:Springer Berlin / Heidelberg
  • ISSN:1432-2129
文摘
Background The efficacy and safety of opioid therapy in chronic low back pain (CLBP) is under debate. We updated a recent systematic review on the efficacy and safety of opioids in CLBP. Methods We screened MEDLINE, Scopus and the Cochrane Central Register of Controlled Trials (CENTRAL) up until October?2013, as well as reference sections of original studies and systematic reviews of randomized controlled trials (RCTs) of opioids in CLBP. We included double-blind randomized placebo-controlled studies of at least 4?weeks duration. Using a random effects model, absolute risk differences (RD) were calculated for categorical data and standardized mean differences (SMD) for continuous variables. Results We included 12?RCTs with 17?treatment arms and 4375?participants. Median study duration was 12?(4-6)?weeks. Of the 17?treatment arms, seven?(41.2-) used oxycodone; four?(23.6-) tramadol; buprenorphine and oxymorphone were each used in two?(11.8-) and hydromorphone and tapentadol each in one?(5.8-). The results for studies with parallel/cross-over design were as follows (with 95- confidence interval, CI): opioids were superior to placebo in reducing pain intensity (SMD??-.29 [?-.37,??-.21], p--.0001; six studies with 2896?participants). Opioids were superior to placebo in 50- pain reduction (RD?0.05 [0.01,?0.10], p--.01; two studies with 1492?participants; number needed to benefit (NNTB)?19 [95-?CI?10-07]). Opioids were not superior to placebo in reports of much or very much improved pain (RD?0.16 [?-.01,?0.34], p--.07; two studies with 1153?participants). Opioids were superior to placebo in improving physical functioning (SMD??-.22 [?-.31,??-.12], p--.0001; four studies with 1895?participants). Patients dropped out less frequently with opioids than with placebo due to lack of efficacy (RD??-.10 [?-.16,??-.04], p--.001; five studies with 3168?participants; NNTB?10?[8-3]). Patients dropped out more frequently with opioids than with placebo due to adverse events (RD?0.12 [0.05,?0.19], p--.0007; six studies with 2910?participants; number needed to harm (NNTH)?7?[95-?CI?6-]). There was no significant difference between opioids and placebo in terms of the frequency of serious adverse events or deaths. Conclusion Opioids were superior to placebo in terms of efficacy and inferior in terms of tolerability. Opioids and placebo did not differ in terms of safety during the study period. The conclusion on the safety of opioids compared to placebo is limited by the low number of serious adverse events and deaths. Short-term and intermediate-term opioid therapy may be considered in selected CLBP patients. The English full-text version of this article is freely available at SpringerLink (under “Supplemental-.

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