The Efficacy of Botulinum Toxin A Injection in Pelvic Floor Muscles in Chronic Pelvic Pain Patients: A Double-Blinded Randomised Controlled Trial.
Abstract
[OBJECTIVE] To evaluate and compare the efficacy and safety of Botulinum Toxin A (BTA) injections versus placebo injections, combined with pelvic floor muscle therapy (PFMT), in women with chronic pelvic pain (CPP).
[DESIGN] Randomised, double-blinded clinical trial (January 2020-April 2023).
[SETTING] This multicentre study was conducted at four hospitals in the Netherlands.
[POPULATION AND SAMPLE] Ninety-four women with CPP and increased pelvic floor muscle tone despite previous PFMT, were enrolled.
[METHODS] Participants received either BTA injections (100 units) or placebo injections into the pelvic floor muscle, followed by four PFMT sessions.
[MAIN OUTCOMES AND MEASURES] Primary outcomes included the number of women with at least a 33% reduction in pain and those reporting (very) much improvement of their pain. Secondary outcomes covered quality of life and pelvic floor function. Follow-up visits were scheduled at 4, 8, 12, and 26 weeks post-treatment. Mixed models for repeated measurements were used for analysis.
[RESULTS] A 33% reduction or more in average pain score was reported by 15 participants (33%) after BTA treatment and 9 participants (20%) after placebo treatment (odd ratio placebo/BTA 1.88; 95% CI 0.72-4.90, p = 0.19). In both groups, 8 women (17%) reported their improvement as (very) much better (odd ratio placebo/BTA 0.947; 95% CI 0.32-2.80, p = 0.92). Pelvic floor resting activity decreased significantly after BTA treatment compared to placebo (p = 0.001).
[CONCLUSION] The results from this study do not support the use of BTA injections in the management of CPP in women.
[DESIGN] Randomised, double-blinded clinical trial (January 2020-April 2023).
[SETTING] This multicentre study was conducted at four hospitals in the Netherlands.
[POPULATION AND SAMPLE] Ninety-four women with CPP and increased pelvic floor muscle tone despite previous PFMT, were enrolled.
[METHODS] Participants received either BTA injections (100 units) or placebo injections into the pelvic floor muscle, followed by four PFMT sessions.
[MAIN OUTCOMES AND MEASURES] Primary outcomes included the number of women with at least a 33% reduction in pain and those reporting (very) much improvement of their pain. Secondary outcomes covered quality of life and pelvic floor function. Follow-up visits were scheduled at 4, 8, 12, and 26 weeks post-treatment. Mixed models for repeated measurements were used for analysis.
[RESULTS] A 33% reduction or more in average pain score was reported by 15 participants (33%) after BTA treatment and 9 participants (20%) after placebo treatment (odd ratio placebo/BTA 1.88; 95% CI 0.72-4.90, p = 0.19). In both groups, 8 women (17%) reported their improvement as (very) much better (odd ratio placebo/BTA 0.947; 95% CI 0.32-2.80, p = 0.92). Pelvic floor resting activity decreased significantly after BTA treatment compared to placebo (p = 0.001).
[CONCLUSION] The results from this study do not support the use of BTA injections in the management of CPP in women.
추출된 의학 개체 (NER)
| 유형 | 영어 표현 | 한국어 / 풀이 | UMLS CUI | 출처 | 등장 |
|---|---|---|---|---|---|
| 시술 | botulinum toxin
|
보툴리눔독소 주사 | dict | 2 | |
| 약물 | CPP
→ chronic pelvic pain
|
scispacy | 1 | ||
| 약물 | [MAIN OUTCOMES AND
|
scispacy | 1 | ||
| 약물 | [RESULTS] A
|
scispacy | 1 | ||
| 약물 | BTA
→ Botulinum Toxin A
|
scispacy | 1 | ||
| 질환 | Pelvic Pain
|
C0030794
Pelvic Pain
|
scispacy | 1 | |
| 질환 | pain
|
C0030193
Pain
|
scispacy | 1 | |
| 질환 | Pelvic Floor Muscles
|
scispacy | 1 | ||
| 질환 | BTA
→ Botulinum Toxin A
|
scispacy | 1 | ||
| 기타 | Botulinum Toxin A
|
scispacy | 1 | ||
| 기타 | pelvic floor muscle
|
scispacy | 1 | ||
| 기타 | women
|
scispacy | 1 | ||
| 기타 | CPP
→ chronic pelvic pain
|
scispacy | 1 | ||
| 기타 | BTA injections
|
scispacy | 1 | ||
| 기타 | pelvic floor
|
scispacy | 1 |
MeSH Terms
Humans; Female; Botulinum Toxins, Type A; Double-Blind Method; Pelvic Pain; Pelvic Floor; Adult; Chronic Pain; Neuromuscular Agents; Injections, Intramuscular; Middle Aged; Treatment Outcome; Netherlands; Quality of Life; Pain Measurement
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