ACE Report Cover
Pain and function improved with Hyalgan in treatment of knee OA in the Asian population
Translate this  ACE Report Translate this  ACE Report Translate this  ACE Report
言語
Download Download Download
ダウンロード
Cite this Report Cite this Report Cite this Report
引用
Add to Favorites Add to Favorites Add to Favorites Remove from Favorites Remove from Favorites Remove from Favorites
+ お気に入り
Translate this  ACE Report Translate this  ACE Report Translate this  ACE Report
言語
Download Download Download
ダウンロード
Cite this Report Cite this Report Cite this Report
引用
Add to Favorites Add to Favorites Add to Favorites Remove from Favorites Remove from Favorites Remove from Favorites
+ お気に入り
BMC Musculoskelet Disord

OSTEOARTHRITIS

Intra-articular injections of sodium hyaluronate (Hyalgan) in osteoarthritis of the knee. a randomized, controlled, double-blind, multicenter trial in the Asian population.

OrthoEvidence Journal (OE Journal) - ACE Report

OE Journal. 2013;1(18):20

. 2011 ;():.

200 patients were randomized to investigate the efficacy of sodium hyaluronate in the treatment of knee osteoarthritis in the Asian population. Patients were allocated to receive 5 weekly intra-articular (i.a.) injections of Hyalgan or saline placebo, and were followed-up for 20 weeks afterward. The results indicated that patients who were treated with i.a. sodium hyaluronate experienced significantly improved pain and function compared to those treated with placebo saline solution.


出版資金提供の詳細 +
資金提供:
Industry funded
スポンサー:
Hyalgan is kindly provided by Fidia Farmaceutici SpA and Med Pharma Co., Ltd.
コンフリクト:
None disclosed

バイアスのリスク

7.5/10

報告基準

15/20

脆弱性指数

N/A

Was the allocation sequence adequately generated?

Was allocation adequately concealed?

Blinding Treatment Providers: Was knowledge of the allocated interventions adequately prevented?

Blinding Outcome Assessors: Was knowledge of the allocated interventions adequately prevented?

Blinding Patients: Was knowledge of the allocated interventions adequately prevented?

Was loss to follow-up (missing outcome data) infrequent?

Are reports of the study free of suggestion of selective outcome reporting?

Were outcomes objective, patient-important and assessed in a manner to limit bias (ie. duplicate assessors, Independent assessors)?

Was the sample size sufficiently large to assure a balance of prognosis and sufficiently large number of outcome events?

Was investigator expertise/experience with both treatment and control techniques likely the same (ie.were criteria for surgeon participation/expertise provided)?

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。

2/4

Randomization

3/4

Outcome Measurements

4/4

Inclusion / Exclusion

2/4

Therapy Description

4/4

Statistics

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?

Common primary treatment of knee osteoarthritis usually consists of simple analgesics, but when pain can no longer be effectively reduced, a therapy of nonsteroidal anti-inflammatory drugs (NSAIDs) is adopted. Although NSAIDs possess well documented pain relief and anti-inflammatory effects, serious gastrointestinal side-effects have been reported with their use. A preferential alternative to NSAIDs has been intra-articular injections of sodium hyaluronate (Hyalgan), but despite extensive research on a worldwide scale, only one study has been dedicated to investigating the efficacy of such treatment in an Asian population.

主な研究課題は何ですか?

Did 5 weekly intra-articular injections of 20-mg/2mL sodium hyaluronate effectively reduce pain compared to 2mL of placebo saline solution, when measured after 25 weeks from the beginning of therapy?

研究の特徴 +
人口:
200 patients diagnosed with knee osteoarthritis based on American College of Rheumatology (ACR) criteria (knee pain with at least one of the following conditions: >50 years old, crepitus, or morning stiffness <30 minutes in duration). (n=176 completed follow-up)
介入:
Hyalgan group: Patients received intra-articular injection of sodium hyaluronate (20-mg/2mL) once a week for 5 weeks. (n=88 completed follow-up)
比較:
Placebo group: Patients received intra-articular injection of saline placebo (2mL) once a week for 5 weeks. (n=88 completed follow-up)
アウトカム:
Primary outcome was pain reduction on a 100-mm visual analog scale (VAS) during the 50-foot walking test. Secondary outcomes were pain, stiffness, and function through subsections of the Western Ontario McMaster Universities Arthritis Index (WOMAC), time required to complete the 50-foot walking test, synovial effusion volume of the knee, patient and investigator subjective scoring of effectiveness (scale 1 to 6), and acetaminophen consumption.
方法:
RCT, Double Blind, Multicenter, Placebo-controlled, Prospective
時間:
Evaluation was conducted at baseline, 5 weeks (ie. end of injections), 13 and 25 weeks.

重要な知見は?

  • Pain (VAS) on the 50 foot walking test was reduced from 45.15mm to 21.53mm (baseline to week 25) in the placebo group and 47.85mm to 17.00mm in the Hyalgan group. The difference in pain at week 25 (P=0.035) and the overall reduction of pain (0.002) were statistically significant, favoring the Hyalgan group.
  • Pain and function, as assessed by WOMAC subscales, was significantly reduced with sodium hyaluronate compared to the placebo (P=0.0050 and 0.0038, respectively). Significance was detected by week 5 and carried through for the remainder of the study.
  • Although WOMAC stiffness scores were generally more improved in the Hyalgan group, there was no significant difference in this outcome between groups for the duration of the study.
  • Both groups achieved slight reduction from baseline 50-foot walking test, with no significant difference.
  • No difference was observed in the amount of synovial fluid of the knee between treatment groups.
  • Patient and investigator rating of therapy effectiveness did not significantly differ between groups.
  • There was no difference in acetaminophen consumption between groups for the duration of the study.
最も覚えておくべきことは?

The 5-injection administration of 20-mg/mL sodium hyaluronte provided improved pain (100-mm and WOMAC subscale) and function (WOMAC subscale) compared to saline placebo in an Asian population. Difference was detected after 5 weeks and held through to the end of the study at 25 weeks.

それが私の患者ケアにどのように影響するか?

The results of this study support the use of sodium hyaluronate for the treatment of knee osteoarthritis in the Asian population. For a more robust understanding of the efficacy of Hyalgan in the Asian population, future studies should consider outcomes in the long-term and employ Minimum Important Differences (MIDs).

免責事項

このページに記載されている内容は、情報提供のみを目的としたものであり、専門的な医療アドバイス、診断、治療の代わりとなるものではありません。治療が必要な場合は、必ず医師の診断を仰ぐか、最寄りの救急外来を受診してください。このページに記載されている内容に関して個人が表明した意見、信念、見解は、OrthoEvidenceの意見、信念、見解を反映するものではありません。

0の4 月間無料記事のロック解除
今月の無料記事閲覧数が4件に達しました。

週1.99ドルからOrthoEvidenceにアクセスできます。

最新のエビデンスにアクセスしてください。いつでもキャンセルできます。
  • 整形外科における最新のインパクトのあるランダム化比較試験とシステマティックレビューの批判的評価
  • Journal of Bone and Joint Surgeryとのコラボレーション、国際的に著名な外科医へのインタビュー、整形外科ニュースやトピックに関する座談会など、OrthoEvidenceポッドキャストコンテンツへのアクセス
  • 週2回発行されるエビデンスに基づくニュースレター、The Pulseの購読。
Upgrade
Close Dialog
おかえりなさい
パスワードをお忘れですか?
今すぐ無料トライアルを開始

あなたのアカウントは
OrthoEvidenceへの無料アクセスが含まれます。


または
パスワードをお忘れですか?

または
Eメールをご確認ください

入力されたメールアドレスにアカウントが存在する場合、パスワードリセットのメールが送信されます。メールが届かない場合は、迷惑メールフォルダをご確認ください。

その他のサポート サポートチームまでご連絡ください。.

この機能を有効にするにはログインしてください

この機能にアクセスするには、有効なOrthoEvidenceアカウントにログインする必要があります。ログインするか、無料トライアルアカウントを作成してください。

ACEレポートを翻訳

OrthoEvidenceは、多言語でコンテンツにアクセスできるようにするため、第三者の翻訳サービスを利用しています。正確性を確保するためにあらゆる努力をしていますが、翻訳が必ずしも完璧ではない可能性があることにご注意ください。

引用方法 ACE Report

OrthoEvidence. Pain and function improved with Hyalgan in treatment of knee OA in the Asian population. OE Journal. 2013;1(18):20. Available from: https://myorthoevidence.com/AceReport/Show/pain-and-function-improved-with-hyalgan-in-treatment-of-knee-oa-in-the-asian-population

引用のコピー
この機能を有効にするにはログインしてください

この機能にアクセスするには、有効なOrthoEvidenceアカウントにログインする必要があります。ログインするか、無料トライアルアカウントを作成してください。

プレミアム会員機能

この機能にアクセスするには、OrthoEvidenceのプレミアムアカウントにログインする必要があります。

共有 ACE Report