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Effects of Botulinum Toxin Landmark-Guided Intra-articular Injection in Subjects With Knee Osteoarthritis.
Hsieh, Lin-Fen; Wu, Chia-Wei; Chou, Ching-Chieh; Yang, Sai-Wei; Wu, Shih-Hui; Lin, Yi-Jia; Hsu, Wei-Chun.
Afiliação
  • Hsieh LF; Department of Physical Medicine and Rehabilitation, Shin Kong Wu Ho-Su Memorial Hospital, Taipei, Taiwan, Republic of China; School of Medicine, Fu Jen Catholic University, New Taipei City, Taiwan, Republic of China(∗).
  • Wu CW; Department of Physical Medicine and Rehabilitation, Shin Kong Wu Ho-Su Memorial Hospital, Taipei, Taiwan, Republic of China(†).
  • Chou CC; Neuromuscular Research Laboratory, Department of Physical Therapy, Chang Gung University, Tao-Yuan, Taiwan, Republic of China(‡).
  • Yang SW; Department of Biomedical Engineering, National Yang-Ming University, No. 155, Section 2, Li-Nong Street, Taipei, Taiwan, Republic of China(§). Electronic address: swyang@ym.edu.tw.
  • Wu SH; Department of Physical Medicine and Rehabilitation, Cardinal Tien Hospital, Taipei, Taiwan, Republic of China(‖).
  • Lin YJ; Graduate Institute of Biomedical Engineering, National Taiwan University of Science and Technology, Taipei, Taiwan, Republic of China(¶).
  • Hsu WC; Graduate Institute of Biomedical Engineering, National Taiwan University of Science and Technology, Taipei, Taiwan, Republic of China; National Defense Medical Center, Taipei, Taiwan, Republic of China(#).
PM R ; 8(12): 1127-1135, 2016 12.
Article em En | MEDLINE | ID: mdl-27210235
ABSTRACT

BACKGROUND:

Increasing evidence has suggested that botulinum toxin A (BoNT/A) can inhibit the release of selected neuropeptide transmitters from primary sensory neurons. Thus, intra-articular (IA) injection therapies with BoNT/A may reduce pain in patients with knee osteoarthritis (OA).

OBJECTIVE:

To investigate the effects of landmark-guided IA injection of BoNT/A on patients with knee OA.

DESIGN:

A prospective randomized controlled trial.

SETTING:

A rehabilitation clinic of a private teaching hospital. PATIENTS A total of 46 patients with symptomatic knee OA (mostly Kellgren-Lawrence grade 2-3).

METHODS:

The patients were randomly assigned to 1 of the following groups BoNT/A group (BoNT/A injection; n = 21) or control group (education only; n = 20). The patients in the BoNT/A group received an IA injection of 100 units of BoNT/A into the affected knee. MAIN OUTCOME

MEASURES:

The short-term (1 week posttreatment) and long-term (6 months posttreatment) effects were evaluated using a pain visual analogue scale (VAS) and questionnaires concerning functional status, including the Lequesne and Western Ontario and McMaster Universities (WOMAC) indexes.

RESULTS:

The between-group comparison revealed significant differences with regard to the pain VAS score at 1 week (P < .001) and at 6 months (P = .001) posttreatment. Similar findings for the between-group comparison were observed for the WOMAC and Lequesne indexes at 6 months (P < .05) posttreatment. The pain VAS score in the BoNT/A group significantly decreased from 5.05 ± 1.12 (pretreatment) to 2.89 ± 1.04 at 1 week (P < .001) and 3.45 ± 1.70 at 6 months posttreatment (P < .001) but not in the control group (P = .476).

CONCLUSIONS:

The IA injection of BoNT/A provided pain relief and improved functional abilities in patients with knee OA in both the short- and long-term follow-up. LEVEL OF EVIDENCE I.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Osteoartrite do Joelho Tipo de estudo: Clinical_trials / Observational_studies / Qualitative_research Limite: Humans Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Osteoartrite do Joelho Tipo de estudo: Clinical_trials / Observational_studies / Qualitative_research Limite: Humans Idioma: En Ano de publicação: 2016 Tipo de documento: Article