Gastroenterology and Endoscopy Unit, Cardinal Massaja Hospital, Asti, Italy.
Department of Clinical and Experimental Medicine, University of Sassari, Sassari, Italy.
Dig Dis Sci. 2018 Nov;63(11):3105-3111. doi: 10.1007/s10620-018-4988-5. Epub 2018 Feb 26.
Although chronically constipated patients usually respond to medical treatment, there is a subgroup with scarce/no response, generally labeled as refractory or intractable. However, whether this lack of response is real or due to ancillary causes (suboptimal dosage, lack of compliance etc.) is unknown.
To see whether a pharmacologic test (bisacodyl colonic intraluminal infusion during manometric assessment) may predict the therapeutic outcome.
Data of patients undergoing 24/h colonic manometry for severe intractable constipation in whom the bisacodyl test (10 ml of drug dissolved into saline and injected through the more proximal recording port) had been carried out were retrieved and analysed, and correlations with the therapeutic outcome made.
Overall, charts from 38 patients (5 men) were available; of these, only 21% displayed naive high-amplitude propagated contractions (average, less than 2/24 h), mostly meal-induced, during the recordings. A bisacodyl response was present in 31.6% patients, with a mean number of events of 1.8 per patient. After bisacodyl testing, 47.3% patients underwent intensive medical treatment, 44.7% surgery (medical failures), and 8% transanal irrigation, a procedure employed to treat refractory patients. The presence of naive propulsive contractions significantly correlated with the response to bisacodyl infusion (p < 0.0001), and with a favourable outcome to intensive medical treatment (p < 0.0001).
The bisacodyl test may be clinically useful to better categorize constipated patients erroneously labelled as intractable and to exclude true colonic inertia, thus avoiding surgery in more than 30% of these subjects.
虽然慢性便秘患者通常对药物治疗有反应,但有一小部分患者反应不佳甚至无反应,通常被标记为难治性或顽固性。然而,这种无反应是真实存在的,还是由于辅助原因(剂量不足、不遵医嘱等)尚不清楚。
观察药物试验(测压时直肠腔内给予比沙可啶)是否可以预测治疗效果。
回顾性分析了 38 例(5 例男性)因严重难治性便秘行 24 小时结肠测压且行比沙可啶试验(10ml 药物溶于生理盐水,通过近端记录端口注入)的患者资料,分析其与治疗效果的相关性。
共 38 例患者(5 例男性)的图表可供分析;其中,只有 21%的患者在记录期间表现出无高幅传播收缩(平均每 24 小时少于 2 次),且主要与进餐相关。31.6%的患者出现比沙可啶反应,平均每人 1.8 次。比沙可啶试验后,47.3%的患者接受强化药物治疗,44.7%的患者接受手术(药物治疗失败),8%的患者接受经肛门灌洗,这一操作用于治疗难治性患者。存在原发性推进性收缩与比沙可啶输注反应(p<0.0001)以及强化药物治疗的良好效果(p<0.0001)显著相关。
比沙可啶试验可能有助于更好地对被错误标记为难治性的便秘患者进行分类,并排除真正的结肠动力不足,从而避免对这些患者中超过 30%的患者进行手术。