Klinge Mette W, Haase Anne Mette, Rolighed Nanna Sutter, Krogh Klaus, Scott Mark, Schlageter Vincent, Mark Esben Bolvig, Nandhra Gursharan Kaur, Drewes Asbjørn Mohr, Loedrup Anders Bergh
Department of Hepatology and Gastroenterology, Aarhus University Hospital, 8200 Aarhus N, Denmark.
Blizard Institute, Queen Mary University of London, London E1 4NS, UK.
J Clin Med. 2024 Nov 25;13(23):7127. doi: 10.3390/jcm13237127.
Chronic nausea and vomiting (N/V) disorders are common in clinical practice. Our primary aim was to compare total and segmental gastrointestinal transit times as well as gastric contraction patterns in patients with chronic N/V syndrome to those of healthy volunteers (HVs). In the patient group, our secondary aim was to explore how symptoms and motility patterns were affected by a serotonin HT receptor agonist (Prucalopride). Patients with chronic N/V syndrome and HVs underwent baseline assessment of regional gastrointestinal (GI) motility/transit using the Motilis 3D-Transit system. Patients were then treated with Prucalopride 2 mg daily for 28 days, with the 3D-transit examination repeated within 10-20 days after treatment onset. Two self-administered questionnaires (the Gastrointestinal Symptom Rating Scale [GSRS] and Gastroparesis Cardinal Symptom Index [GCSI]) were used to assess patients' symptoms. A total of 19 patients (13 F; median age 25 years (IQR 22-39) and 55 HVs (25 F; median age 28 (24-35) were included. At baseline, no differences in regional GI transit times were found between groups. However, patients had a significantly lower gastric contraction amplitude than HVs (9 mmHg (IQR 8-11) vs. 12 (10-15: < 0.001). In response to Prucalopride treatment, gastric emptying time was reduced from a median of 3.1 h to 1.6 h ( < 0.005). Further, the GCSI was significantly reduced from GCSI 3.0 (IQR 2.3-3.7) at baseline to GCSI 1.9 (IQR 1.3-3.2) with Prucalopride. Patients with chronic N/V syndrome have significantly lower gastric contraction amplitude than HVs and may symptomatically benefit from prokinetics. They do not, however, have evidence of panenteric dysmotility.
慢性恶心和呕吐(N/V)障碍在临床实践中很常见。我们的主要目的是比较慢性N/V综合征患者与健康志愿者(HV)的全胃肠道和节段性胃肠道转运时间以及胃收缩模式。在患者组中,我们的次要目的是探讨5-羟色胺HT受体激动剂(普芦卡必利)如何影响症状和运动模式。慢性N/V综合征患者和HV使用Motilis 3D-Transit系统进行区域胃肠道(GI)运动/转运的基线评估。然后患者接受每日2 mg普芦卡必利治疗28天,并在治疗开始后10 - 20天内重复进行3D转运检查。使用两份自我管理问卷(胃肠道症状评分量表[GSRS]和胃轻瘫主要症状指数[GCSI])评估患者症状。共纳入19例患者(13例女性;中位年龄25岁(四分位间距22 - 39))和55例HV(25例女性;中位年龄28(24 - 35))。基线时,两组之间区域胃肠道转运时间无差异。然而,患者的胃收缩幅度明显低于HV(9 mmHg(四分位间距8 - 11)对12(10 - 15):<0.001)。对普芦卡必利治疗的反应是,胃排空时间从中位3.1小时减少到1.6小时(<0.005)。此外,GCSI从基线时的GCSI 3.0(四分位间距2.3 - 3.7)显著降低至使用普芦卡必利时的GCSI 1.9(四分位间距1.3 - 3.2)。慢性N/V综合征患者的胃收缩幅度明显低于HV,可能在症状上从促动力药中获益。然而,他们没有全肠道运动障碍的证据。