Platelet-rich plasma injection for the treatment of ankle osteoarthritis: a systematic review and meta-analysis.
足関節変形性関節症に対する多血小板血漿注射:系統的レビューとメタ分析 (機械翻訳の邦題)
記録の確認項目
- 研究デザイン
- メタ分析
- 対象
- ヒト
- 出版年
- 2023
- 出典
- doi.org
- 抄録の表示
- 表示あり
- 出版状態
- 有効な記録
- 状態確認日
- 2026/08/17
- 収集日
- 2026/08/04
- 鮮度
- 確認期限内
- 確認段階
- 自動処理
- 記録状態
- 公開
日本語要約(機械生成)
足関節変形性関節症に対する多血小板血漿注射の有効性を評価するため、2023年1月までにPubMedとScopusで検索し、無作為化比較試験または観察研究を対象に系統的レビューとメタ分析を行った。184例の足関節変形性関節症患者(うち132例に多血小板血漿注射)を含む5研究(無作為化比較試験1件、前後比較研究4件)を解析した。その結果、注射前と比較して12週時点で疼痛スコア(視覚アナログ尺度)と機能スコアが有意に改善した。しかし、改善の程度は先行の無作為化比較試験におけるプラセボ効果と同程度であり、治療効果を証明するには大規模な無作為化比較試験が必要である。登録番号:PROSPERO CRD42022297503。
この要約は公開抄録のみを根拠にAIが機械的に生成したものです。正確な内容は原文を確認してください。
抄録
Background: Platelet-rich plasma (PRP) injection for ankle osteoarthritis (OA) treatment showed contradictory results. This review was aimed to pool individual studies which assessed the efficacy of PRP for ankle OA treatment.Methods: This study was conducted following the preferred report items of systematic review and meta-analysis guideline. PubMed and Scopus were searched up to January 2023. Meta-analysis, or individual randomised controlled trial (RCT), or observational studies were included if they involved ankle OA with aged ≥ 18 years, compared before-after receiving PRP, or PRP with other treatments, and reported visual analog scale (VAS) or functional outcomes. Selection of eligible studies and data extraction were independently performed by two authors. Heterogeneity test using Cochrane Q test and the I2-statistic were assessed. Standardised (SMD) or unstandardised mean difference (USMD) and 95% confidence interval (CI) were estimated and pooled across studies.Results: Three studies from meta-analysis and two individual studies were included, which consisted of one RCT and four before-after studies with 184 ankle OAs and 132 PRP. The average age was 50.8-59.3 years, and 25-60% of PRP injected cases were male. The number of primary ankle OA was accounted to 0-100%. When compared to before treatment, PRP significantly reduced VAS and functional score at 12 weeks with pooled USMD of - 2.80, 95% CI - 3.91, - 2.68; p < 0.001 (Q = 82.91, p < 0.001; I2 96.38%), and pooled SMD of 1.73, 95% CI 1.37, 2.09; p < 0.001 (Q = 4.87, p = 0.18; I2 38.44%), respectively.Conclusion: PRP may beneficially improve pain and functional scores for ankle OA in a short-term period. Its magnitude of improvement seems to be similar to placebo effects from the previous RCT. A large-scale RCT with proper whole blood and PRP preparation processes is required to prove treatment effects. Trial registration PROSPERO number CRD42022297503.
MeSH
DOI 10.1186/s13018-023-03828-z
PMID 37208754
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