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Efficacy of Adductor Canal Block on Medial Knee Pain in Patients with Knee Osteoarthritis: A Randomized Single-Blind Placebo-Controlled Study.
Kim, Ki-Yong; Huh, Yool-Gang; Ma, Sang Hyeok; Yoon, Jong Hyeon; Jeong, Kil-Yong; Park, Do Young; Yoon, Seung-Hyun.
Afiliación
  • Kim KY; Department of Physical Medicine and Rehabilitation, Ajou University Medical Center, Suwon 16499, Republic of Korea.
  • Huh YG; Department of Physical Medicine and Rehabilitation, Ajou University Medical Center, Suwon 16499, Republic of Korea.
  • Ma SH; Department of Physical Medicine and Rehabilitation, Ajou University Medical Center, Suwon 16499, Republic of Korea.
  • Yoon JH; Department of Physical Medicine and Rehabilitation, Ajou University Medical Center, Suwon 16499, Republic of Korea.
  • Jeong KY; Department of Physical Medicine and Rehabilitation, Ajou University Medical Center, Suwon 16499, Republic of Korea.
  • Park DY; Department of Orthopedic Surgery, Ajou University Medical Center, Suwon 16499, Republic of Korea.
  • Yoon SH; Department of Physical Medicine and Rehabilitation, Ajou University Medical Center, Suwon 16499, Republic of Korea.
Article en En | MEDLINE | ID: mdl-36430138
ABSTRACT

BACKGROUND:

This study aimed to confirm the efficacy of ultrasound-guided adductor canal block (ACB) as a treatment option for medial knee pain caused by knee osteoarthritis (KOA).

METHODS:

In total, 31 participants with medial knee pain due to KOA were randomized to either the ACB (ultrasound-guided ACB, n = 15) or placebo group (1 mL of 1% lidocaine, n = 16). The primary outcome was a numerical rating scale (NRS) for knee pain intensity comparing before and 4 weeks after injection. The secondary outcomes were the Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC), average daily number of analgesics consumed, average daily opioid consumption, and Timed Up and Go (TUG) test results before and 4 weeks after injection.

RESULTS:

Participants' baseline characteristics were not significantly different between the groups, except for age. At 4 weeks post-injection, the NRS score in the ACB group significantly improved compared to that in the placebo group (p = 0.009). However, the WOMAC, average daily number of analgesics consumed, average daily opioid consumption, and TUG test results did not show significant differences.

CONCLUSION:

ACB can be an effective treatment for reducing medial knee pain in patients with KOA.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Osteoartritis de la Rodilla Tipo de estudio: Clinical_trials Límite: Humans Idioma: En Revista: Int J Environ Res Public Health Año: 2022 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Osteoartritis de la Rodilla Tipo de estudio: Clinical_trials Límite: Humans Idioma: En Revista: Int J Environ Res Public Health Año: 2022 Tipo del documento: Article