ACE Report Cover
Addition of epinephrine to popliteal nerve block does not extend analgesia in ankle fusion
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

FOOT & ANKLE

The effects of adding epinephrine to ropivacaine for popliteal nerve block on the duration of postoperative analgesia: a randomized controlled trial
Verified
This report has been verified by one or more authors of the original publication.

OrthoEvidence Journal (OE Journal) - ACE Report

OE Journal. 2015;3(19):7 BMC Anesthesiol. 2015 Jul 10;15:100

38 patients patients scheduled for ankle fusion and/or subtalar fusion under continuous popliteal sciatic nerve block were randomized to receive 30 mL ropivacaine (0.75%) with or without the addition of epinephrine (5 ug/mL). The purpose of the study was to determine how the duration of postoperative analgesia was affected by the addition of epinephrine, as measured by the time elapsed from poplitear catheter placement until the time of first request for postoperative analgesia via patient controlled analgesia. Results indicated that the duration of postoperative analgesia was not significantly increased with the addition of epinephrine to ropivacaine for continuous popliteal nerve block.


出版資金提供の詳細 +
資金提供:
Non-Industry funded
スポンサー:
Internal funds from the department of Anaesthesiology, Sint Maartenskliniek, Nijmegen, The Netherlands.
コンフリクト:
None disclosed

バイアスのリスク

8/10

報告基準

19/20

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。

3/4

Randomization

4/4

Outcome Measurements

4/4

Inclusion / Exclusion

4/4

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?

Peripheral nerve block is often used for analgesia in ankle surgery. While the choice of local anaesthetic agent used in popliteal nerve blocks impacts efficacy, it has been suggested that so too does the addition of epinephrine. The theory behind the addition of epinephrine to local anaesthetic is to reduce local plasma concentration via vasoconstriction and slow absorption, thereby increasing the duration of analgesia. The current literature was limited in relation to this treatment, and thus the present study was conducted.

主な研究課題は何ですか?

In ankle and subtalar fusion under popliteal nerve block, how does time to first request for postoperative anaglesia compare between blocks performed with 30 mL ropivacaine (0.75%), with and without the addition of epinephrine?

研究の特徴 +
人口:
38 patients (18 years of age or older) scheduled for ankle fusion and/or subtalar fusion under continuous popliteal sciatic nerve block. All patients received paracetamol 1000mg orally 3x/day and etoricoxib 90mg orally once/day, starting on the morning of surgery for at least 7 days. Patient controlled analgesia (PCA) (GemStar, Hospira Inc) was used for postoperative analgesia, with bolus doses of 10mL ropivacaine 0.2% and 15 minute lock out time, and max dose of 30mL/4hours. If patients still needed pain medication, they received morphine 0.1-0.15 mg/kg every 4 hours subcutaneously (30 completed follow-up).
介入:
ROPI-EPI group: received ultrasound guided continuous popliteal nerve block with 30 mL ropivacaine (0.75%) with epinephrine (5 ug/mL) (n=18, 15 completed follow-up, Mean age: 56 +/- 11, 9M/6F).
比較:
ROPI group: received ultrasound guided continuous popliteal nerve block with 30 mL ropivacaine (0.75%) without epinephrine (n=20, 15 completed follow-up, Mean age: 61 +/- 7, 8M/7F).
アウトカム:
The primary outcome measure was the duration of postoperative analgesia defined as the time to first request for postoperative analgesia (TTFR) via PCA, where TTFR was defined as the time elapsed from t=0 (placement of popliteal catheter) until the time of first request. Secondary outcomes included the onset of sensory and motor block, and Numeric Rating Scale (NRS) score for pain at rest and during movement. Sensory block, as well as motor function of the tibial (plantar flexion foot) and peroneal nerve (dorsal flexion of the foot), were scored on a three point scale (0=absent, 1=partial, 2=complete).
方法:
RCT, prospective, double-blinded, single-centered.
時間:
Outcomes were assessed immediately, at 24h, and at 48h postoperatively.

重要な知見は?

  • Median [interquartile range] TTFR for postoperative analgesia was 463 [300-1197] min in the ROPI group and 830 [397-1128] min in the ROPI-EPI group; the difference between groups in TTFR was not statistically significant (p=0.56).
  • There was no significant difference noted between groups in terms of NRS rest at 24 h (p=0.70), NRS movement at 24 h (p=0.47), NRS max during 24 h (p=0.17), or NRS satisfaction with the block (p=0.08).
  • In the ROPI group, 4 patients received complete block in tibial sensory, 10 in tibial motor, 12 in peroneal sensory, and 11 in peroneal motor. In the ROPI-EPI group, 9 patients received complete block in tibial sensory, 9 in tibial motor, 11 in peroneal sensory, and 10 in peroneal motor.
  • No patients displayed signs of local anesthetic toxicity or inadvertent intravascular injection of epinephrine.
最も覚えておくべきことは?

Duration of postoperative analgesia, as measured by the time to first request for postoperative analgesia, was not significantly increased via the addition of epinephrine to ropivacaine for popliteal nerve block in ankle and/or subtalar fusion. Additionally, no significant differences were noted in any clinical outcome between the group receiving epinephrine and the group that did not.

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 indicate that the addition of epinephrine to ropivacaine treatment in popliteal nerve block may not significantly increase the duration of postoperative analgesia. Further high quality evidence, including larger sample sizes, is required before firm decisions regarding the use of epinephrine in this treatment are made in the clinical field.

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. Addition of epinephrine to popliteal nerve block does not extend analgesia in ankle fusion. OE Journal. 2015;3(19):7. Available from: https://myorthoevidence.com/AceReport/Show/addition-of-epinephrine-to-popliteal-nerve-block-does-not-extend-analgesia-in-ankle-fusion

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