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Opioid-sparing effect, but limited analgesic efficacy, with preop gabapentinoids in THA
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ARTHROPLASTY

The efficacy of preoperative administration of gabapentin/pregabalin in improving pain after total hip arthroplasty: a meta-analysis

OrthoEvidence Journal (OE Journal) - ACE Report

OE Journal. 2022;10(10):9 BMC Musculoskelet Disord. 2016 Aug 30;17(1):373

寄稿者

Y Mao L Wu W Ding

Seven randomized controlled trials were included in this meta-analysis evaluating the efficacy and safety of preoperative gabapentin and pregabalin for postoperative analgesia following total hip arthroplasty. In all studies, gabapentin and/or pregabalin were compared to either placebo or no intervention. Pooled results demonstrated significantly lower cumulative morphine consumption with gabapentin compared to control up to 24 hours after surgery, and with pregabalin compared to control up to 48 hours after surgery. In contrast, pooled pain scores at rest or on mobilization did not demonstrate significantly lower scores with either gabapentin or pregabalin compared to control. In fact, pain scores during mobilization after 48 hours were significantly higher among gabapentin groups compared to control groups.


出版資金提供の詳細 +
資金提供:
Not Reported
コンフリクト:
None disclosed

バイアスのリスク

5.5/10

報告基準

16/20

脆弱性指数

N/A

Were the search methods used to find evidence (original research) on the primary question or questions stated?

Was the search for evidence reasonably comprehensive?

Were the criteria used for deciding which studies to include in the overview reported?

Was the bias in the selection of studies avoided?

Were the criteria used for assessing the validity of the included studies reported?

Was the validity of all of the studies referred to in the text assessed with use of appropriate criteria (either in selecting the studies for inclusion or in analyzing the studies that were cited)?

Were the methods used to combine the findings of the relevant studies (to reach a conclusion) reported?

Were the findings of the relevant studies combined appropriately relative to the primary question that the overview addresses?

Were the conclusions made by the author or authors supported by the data and or analysis reported in the overview?

How would you rate the scientific quality of this evidence?

はい = 1

不確実=0.5

無関係 = 0

いいえ = 0

報告基準評価では、著者が出版物内で試験の方法論的特徴や試験特性を報告する際の透明性を評価します。評価は以下の5つのカテゴリーに分類されます。

4/4

Introduction

4/4

Accessing Data

3/4

Analysing Data

4/4

Results

1/4

Discussion

Detsky AS, Naylor CD, O'Rourke K, McGeer AJ, L'Abbé KA. J Clin Epidemiol. 1992;45:255-65

Fragility Indexは、重要な所見の解釈を助けるツールで、結果の強さの尺度を提供します。Fragility Indexは、その所見が有意でなくなるために、二項対立の結果に追加する必要がある連続した事象の数を表します。数値が小さいほど弱い所見を表し、数値が大きいほど強い所見を表します。

なぜ今この研究が必要なのですか?

One of the most important areas of research regarding perioperative treatment of patients undergoing total hip arthroplasty is postoperative analgesia. Patient-controlled analgesia with opioids remains a standard method of analgesia, although the undesirable side-effects of opioids have led to an emphasis on trying to limit their administration to only rescue analgesia and improve primary treatment. Gabapentinoids, such as gabapentin and pregabalin, have been suggested as medications with possible analgesic efficacy in these patients.

主な研究課題は何ですか?

What are the efficacy and safety profiles of preoperative gabapentin and pregabalin, compared to control, for analgesia following total hip arthroplasty?

研究の特徴 +
データソース:
MEDLINE, EMBASE, PubMed, the Cochrane Central Register of Controlled Trials, Web of Science, and Google were searched for relevant articles published up to January 2016. Reference lists of identified articles were also hand search for any additional studies possibly missed by the electronic search.
索引用語:
Search terms included: "gabapentin", "pregabalin", "pain control", "total hip arthroplasty", "total hip replacement", "THA" and "THR".
研究の選択:
Eligibility criteria included: a randomized controlled trial design; patients were scheduled for total hip arthroplasty; patients were allocated to an intervention group, consisting of treatment with either preoperative gabapentin or pregabalin, and a control group, consisting of either placebo treatment or no treatment; and reported at least one of the following outcomes: visual analog scale for pain, morphine consumption, or incidence of either pruritus, dizziness, or nausea. Study search and selection was performed independently by two reviewers, with disagreements resolved through discussion with a third reviewer. A total of 7 RCTs, with data sampled from 769 patients, were selected for final inclusion.
データ抽出:
Data extraction was performed independently by two reviewers, with disagreement resolved by discussion and consensus.
データ統合:
Statistical analyses were performed using Stata software (Stata 12.0). Continuous outcomes were expressed as mean differences (MD), and dichotomous outcomes as relative risks (RR), both with 95% confidence intervals. Heterogeneity was assessed using the I-squared (I^2) statistic, with values >50% considered indicative of significant statistical heterogeneity.

重要な知見は?

  • Pooled cumulative morphine consumption was significantly lower among gabapentin groups compared to control after 24h (MD -2.65 [95%CI -3.67, -1.63]; p<0.001) but not 48h (MD 0.00 [95%CI -7.69, 7.69]; p=1.000), while it was significantly lower for pregabalin compared to control after both 24 (MD -19.42 [95%CI -11.72, -3.93]; p<0.001) and 48h (MD -33.02 [95%CI -45.86, -20.19]; p<0.001).
  • VAS pain at rest and at 24h did not significantly differ between gabapentin and control (MD 0.32 [95%CI -0.03, 0.67]; p=0.076), and pregabalin and control (MD -3.05 [95%CI -11.63, 5.53]; p=0.486). VAS pain at rest was significantly higher with gabapentin compared to control after 48h (MD 0.41 [95%CI 0.00-0.81]; p=0.049).
  • VAS pain with mobilization between gabapentin and control did not significantly differ after 24h (MD 0.72 [95%CI -0.23, 1.66]), and was significantly higher among gabapentin groups after 48h (MD 1.90 [95%CI 0.04-3.75]; p=0.045). No significant difference in VAS pain with mobilization between pregabalin and control was observed after 24h (MD -0.78 [95%CI -6.91, 5.35]; p=0.803).
  • No significant difference between gabapentin/pregabalin groups overall and control groups was observed in the incidences of vomiting (RR 0.95 [95%CI 0.47-1.92]), dizziness (RR 0.82 [95%CI 0.51-1.33]), or pruritus (RR 0.89 [95%CI 0.57-1.39]). A significantly lower incidence of nausea was observed with gabapentin/pregabalin groups compared to control (RR 0.49 [95%CI 0.27-0.92]).
最も覚えておくべきことは?

In total hip arthroplasty, an opioid-sparing effect was observed with preoperative gabapentin up to 24 hours after surgery, and with preoperative pregabalin up to 48 hours after surgery. However, neither treatment provided a significant benefit compared to the control group for pain at rest or on movement. In contrast, pooled pain scores during movement were actually higher in gabapentin groups compared to control groups after 48 hours.

それが私の患者ケアにどのように影響するか?

While there may be a short-term reduction in opioid requirement with the use of either gabapentin or pregabalin following total hip arthroplasty, these interventions do not appear to significantly reduce short-term pain scores in patients. Therefore, their role in postoperative analgesia following total hip arthroplasty should be scrutinized based on the currently available data. It is important to note limitations of the available body of evidence, as only 2-3 studies were available to separately assess the efficacy and safety of gabapentin and pregabalin each indicating the need to further large randomized controlled trials.

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引用方法 ACE Report

OrthoEvidence. Opioid-sparing effect, but limited analgesic efficacy, with preop gabapentinoids in THA. OE Journal. 2022;10(10):9. Available from: https://myorthoevidence.com/AceReport/Show/

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