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A Double-Blind Placebo Randomized Controlled Trial of Minocycline to Reduce Pain After Carpal Tunnel and Trigger Finger Release.
Curtin, Catherine M; Kenney, Debbie; Suarez, Paola; Hentz, Vincent R; Hernandez-Boussard, Tina; Mackey, Sean; Carroll, Ian R.
Afiliación
  • Curtin CM; Department of Surgery, Palo Alto VA, Palo Alto, CA; Division of Plastic Surgery, Department of Surgery, Stanford University, Palo Alto, CA. Electronic address: curtincatherine@yahoo.com.
  • Kenney D; Department of Orthopedic Surgery, Stanford University, Palo Alto, CA.
  • Suarez P; Department of Surgery, Stanford University, Palo Alto, CA.
  • Hentz VR; Department of Surgery, Palo Alto VA, Palo Alto, CA; Division of Plastic Surgery, Department of Surgery, Stanford University, Palo Alto, CA.
  • Hernandez-Boussard T; Department of Surgery, Stanford University, Palo Alto, CA.
  • Mackey S; Division of Pain Management, Department of Anesthesiology, Stanford University, Palo Alto, CA.
  • Carroll IR; Division of Pain Management, Department of Anesthesiology, Stanford University, Palo Alto, CA.
J Hand Surg Am ; 42(3): 166-174, 2017 Mar.
Article en En | MEDLINE | ID: mdl-28259273
ABSTRACT

PURPOSE:

Minocycline is a microglial cell inhibitor and decreases pain behaviors in animal models. Minocycline might represent an intervention for reducing postoperative pain. This trial tested whether perioperative administration of minocycline reduced time to pain resolution (TPR) after standardized hand surgeries with known prolonged pain profiles carpal tunnel release (CTR) and trigger finger release (TFR).

METHODS:

This double-blinded randomized controlled trial included patients undergoing CTR or TFR under local anesthesia. Before surgery, participants recorded psychological and pain measures. Participants received oral minocycline, 200 mg, or placebo 2 hours prior to procedure, and then 100 mg of minocycline or placebo 2 times a day for 5 days. After surgery, participants were called daily assessing their pain. The primary end point of TPR was when participants had 3 consecutive days of 0 postsurgical pain. Futility analysis and Kaplan-Meier analyses were performed.

RESULTS:

A total of 131 participants were randomized and 56 placebo and 58 controls were analyzed. Median TPR for CTR was 3 weeks, with 15% having pain more than 6 weeks. Median TPR for TFR was 2 weeks with 18% having pain more than 6 weeks. The overall median TPR for the placebo group was 2 weeks (10% pain > 6 weeks) versus 2.5 weeks (17% pain > 6 weeks) for the minocycline group. Futility analysis found that the likelihood of a true underlying clinically meaningful reduction in TPR owing to minocycline was only 3.5%. Survival analysis found minocycline did not reduce TPR. However, subgroup analysis of those with elevated posttraumatic distress scores found the minocycline group had longer TPR.

CONCLUSIONS:

Oral administration of minocycline did not reduce TPR after minor hand surgery. There was evidence that minocycline might increase length of pain in those with increased posttraumatic stress disorder symptoms. TYPE OF STUDY/LEVEL OF EVIDENCE Therapeutic I.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Dolor Postoperatorio / Síndrome del Túnel Carpiano / Trastorno del Dedo en Gatillo / Dolor Crónico Tipo de estudio: Clinical_trials / Prognostic_studies Límite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Año: 2017 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Dolor Postoperatorio / Síndrome del Túnel Carpiano / Trastorno del Dedo en Gatillo / Dolor Crónico Tipo de estudio: Clinical_trials / Prognostic_studies Límite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Año: 2017 Tipo del documento: Article