Botulinum Toxin Improves Quality of Life and Clinical Outcomes in Pediatric Defecation Disorders.

IF 2.9 3区 医学 Q1 CLINICAL NEUROLOGY Neurogastroenterology and Motility Pub Date : 2025-06-01 Epub Date: 2025-02-17 DOI:10.1111/nmo.70005
Trevor A Davis, Ashlyn Turner, Carrie Wilson, Jinli Wang, Shannon Joerger, Elizabeth C Utterson, Baddr A Shakhsheer
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Abstract

Objective: To elucidate the effect of internal anal sphincter (IAS) botox as an adjunct to standard treatment for disordered defecation (DD), defined by the inability to effectively evacuate stool from the rectum resulting in constipation, on patient/caregiver quality of life (QoL) metrics in association with corresponding clinical outcomes.

Methods: Consecutive children undergoing IAS botox for DD completed surveys at baseline, two weeks, and three months post-procedure. Time points included assessment of clinical symptoms (Rome IV Questionnaire), QoL (Pediatric Quality of Life Inventory [PedsQL]), and caregiver well-being/family functioning (PedsQL-Family Impact Module [PedsQL-FIM]).

Results: Of 60 participants, the median age was 7 years (IQR 4-10), with 34 (56.7%) males and 32 (53.3%) first-time Botox recipients. The median onset of positive effect after Botox was 6 days (IQR 3-14), while the median loss of effect was 70 days (IQR 39-83). Compared to baseline, by 3 months there was a lower chance of meeting Rome IV criteria for functional constipation in first-time recipients (RR 0.73, 95% CI: 0.58-0.91; p = 0.005). This remained significant after adjusting for any bowel regimen change during the 3-month period following Botox (OR 0.33, 95% CI: 0.13-0.74; p = 0.012). Regarding QoL, there was significant improvement in total PedsQL score at both 2-weeks (11.79 point improvement, 95% CI: 6.36-17.22; p < 0.0001) and 3 months (13.97 point improvement, 95% CI: 8.47-19.47; p < 0.0001) from baseline for first-time recipients, while improvement was only observed at 2 weeks for prior recipients (6.67 point improvement, 95% CI: 0.65-12.69; p = 0.030). First-time recipients demonstrated significant improvements in total PedsQL-FIM score at both 2 weeks (9.33 point improvement, 95% CI: 3.77-14.89; p = 0.001) and 3 months (11.57 point improvement, 95% CI: 5.94-17.20; p < 0.0001) from baseline.

Conclusion: Our findings establish far-reaching benefits of IAS botox primarily for first-time recipients, both clinically and psychosocially, suggesting that appropriate incorporation into the treatment paradigm may globally enhance outcomes in children with DD.

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肉毒杆菌毒素改善儿童排便障碍的生活质量和临床结果。
目的:阐明内肛门括约肌(IAS)肉毒杆菌毒素作为排便障碍(DD)标准治疗的辅助治疗对患者/护理人员生活质量(QoL)指标的影响,这些指标与相应的临床结果相关。排便障碍是指无法有效地将粪便从直肠排出导致便秘。方法:连续接受IAS肉毒杆菌毒素治疗DD的儿童在基线、2周和3个月后完成调查。时间点包括评估临床症状(Rome IV Questionnaire)、QoL(儿科生活质量量表[PedsQL])和照顾者幸福感/家庭功能(PedsQL-家庭影响模块[PedsQL- fim])。结果:在60名参与者中,中位年龄为7岁(IQR 4-10),其中34名(56.7%)男性和32名(53.3%)首次接受肉毒杆菌注射。肉毒杆菌注射后出现积极效果的中位时间为6天(IQR 3-14),而效果丧失的中位时间为70天(IQR 39-83)。与基线相比,到3个月时,首次接受治疗的患者达到功能性便秘的罗马IV标准的机会较低(RR 0.73, 95% CI: 0.58-0.91;p = 0.005)。在肉毒杆菌注射后的3个月期间,调整了任何肠道方案的改变后,这一结果仍然显著(OR 0.33, 95% CI: 0.13-0.74;p = 0.012)。关于生活质量,两周PedsQL总分均有显著改善(改善11.79分,95% CI: 6.36-17.22;结论:我们的研究结果确立了IAS肉毒杆菌素的深远益处,主要是针对首次接受治疗的患者,无论是临床还是心理社会,这表明将IAS肉毒杆菌素适当纳入治疗模式可能会在全球范围内提高DD儿童的预后。
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来源期刊
Neurogastroenterology and Motility
Neurogastroenterology and Motility 医学-临床神经学
CiteScore
7.80
自引率
8.60%
发文量
178
审稿时长
3-6 weeks
期刊介绍: Neurogastroenterology & Motility (NMO) is the official Journal of the European Society of Neurogastroenterology & Motility (ESNM) and the American Neurogastroenterology and Motility Society (ANMS). It is edited by James Galligan, Albert Bredenoord, and Stephen Vanner. The editorial and peer review process is independent of the societies affiliated to the journal and publisher: Neither the ANMS, the ESNM or the Publisher have editorial decision-making power. Whenever these are relevant to the content being considered or published, the editors, journal management committee and editorial board declare their interests and affiliations.
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