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经颅磁刺激对肠易激综合征直肠敏感性的影响:一项随机、安慰剂对照的初步研究。

Effect of transcranial magnetic stimulation on rectal sensitivity in irritable bowel syndrome: a randomized, placebo-controlled pilot study.

机构信息

INSERM U1073, CIC Rouen University Hospital, Rouen, France.

出版信息

Colorectal Dis. 2014 Mar;16(3):O104-11. doi: 10.1111/codi.12450.

Abstract

AIM

Repetitive transcranial magnetic stimulation (rTMS) applied to the motor cortex can induce analgesic effects in patients with chronic pain syndromes through its effect on central pain-modulatory systems. Our aim was to evaluate the effect of rTMS on rectal sensitivity in irritable bowel syndrome (IBS) patients.

METHOD

In this randomized, sham-controlled, proof-of concept trial, 21 IBS patients (11 women and 10 men; mean age 44.0 ± 12.6 years) were randomized, using a double-blind crossover protocol, to active or sham rTMS for 5 days of treatment. The primary outcome was the increase in the pressure pain threshold after rTMS. Secondary outcomes were the changes in maximum tolerated rectal volume, rectal compliance and average pain intensity between baseline and the end of the treatments.

RESULTS

There were no statistically significant differences between active and sham rTMS in terms of an increase in the pressure pain threshold, maximum tolerated volume and rectal compliance at the end of the treatments compared with baseline. However, in the subgroup of patients with the most marked rectal hypersensitivity, the volume threshold was significantly improved by active, but not by sham, rTMS (P = 0.03). Patients experienced a significant improvement in pain regardless of the type of stimulation.

CONCLUSION

This pilot study failed to demonstrate any benefit of rTMS on our primary end-point. However, the effect of rTMS on rectal tolerated volume in the most hypersensitive patients was encouraging enough to plan more powered studies.

摘要

目的

经颅重复磁刺激(rTMS)作用于运动皮层,可通过对中枢疼痛调节系统的影响,在慢性疼痛综合征患者中产生镇痛效果。我们的目的是评估 rTMS 对肠易激综合征(IBS)患者直肠敏感性的影响。

方法

在这项随机、假刺激对照、概念验证试验中,21 例 IBS 患者(11 名女性和 10 名男性;平均年龄 44.0±12.6 岁)采用双盲交叉方案随机分为 rTMS 治疗组或假刺激组,每组 5 天。主要终点是 rTMS 后压力痛阈的增加。次要终点是治疗结束时与基线相比最大耐受直肠容量、直肠顺应性和平均疼痛强度的变化。

结果

与基线相比,治疗结束时,无论是压力痛阈、最大耐受容量还是直肠顺应性,rTMS 治疗组与假刺激组之间均无统计学差异。然而,在直肠高敏性最明显的患者亚组中,rTMS 治疗组(而非假刺激组)的容积阈值显著改善(P=0.03)。无论刺激类型如何,患者的疼痛均显著改善。

结论

这项初步研究未能证明 rTMS 对我们的主要终点有任何益处。然而,rTMS 对最敏感患者直肠耐受容量的影响令人鼓舞,足以计划进行更多的研究。

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