Soykan I, Sarosiek I, McCallum R W
Division of Gastroenterology, Hepatology, and Nutrition, University of Virginia Health Sciences Center, Charlottesville, USA.
Am J Gastroenterol. 1997 Jun;92(6):976-80.
Our aim was to determine whether domperidone could improve the symptoms of patients with gastroparesis, accelerate gastric emptying, and enhance quality of life.
Seventeen patients (13 women, 4 men; mean age 42.9 yr) with documented gastroparesis were evaluated. A baseline gastric emptying study was performed using an isotope-labeled solid meal and a follow-up study was repeated > or =6 months after initiating domperidone therapy. The severity of nausea, vomiting, abdominal pain, and bloating were obtained at baseline and at 6-month intervals and were graded from 0 to 5 (0 = none, 5 = most severe). Also, the number of hospital admissions were noted during the study period. Patients were asked to assess their overall health status and quality of life and were begun on domperidone 20 mg q.i.d. On average, patients received domperidone for 23.3 months (range 6-48 months). Domperidone doses ranged from 40 to 120 mg daily during the study period.
Gastroparesis symptom scores were reduced from 4.1 +/- 0.22 (mean +/- SEM) to 1.3 +/- 0.2, and hospital admissions were decreased significantly during the study compared with before domperidone therapy (p < 0.05). At baseline, patients had a 87.3 +/- 3.71% retention of a solid meal at 2 hours compared with a 57.2 +/- 5.04% retention during domperidone therapy (p < 0.05). Domperidone treatment enhanced the quality of life in 88% of patients. The mean prolactin level was 58.9 pg/ml during the study and three patients reported gynecomastia.
Chronic domperidone treatment in patients with gastroparesis significantly reduced GI symptoms and hospitalizations, enhanced quality of life, and accelerated gastric emptying of a solid meal to a normal rate. Domperidone successfully treats gastroparesis on a long-term outcome basis and has an excellent safety profile.
我们的目的是确定多潘立酮是否能改善胃轻瘫患者的症状、加速胃排空并提高生活质量。
对17例有胃轻瘫记录的患者(13例女性,4例男性;平均年龄42.9岁)进行评估。使用同位素标记的固体餐进行基线胃排空研究,并在开始多潘立酮治疗后≥6个月重复进行随访研究。在基线时以及每隔6个月获取恶心、呕吐、腹痛和腹胀的严重程度,并从0到5进行分级(0=无,5=最严重)。此外,记录研究期间的住院次数。要求患者评估其总体健康状况和生活质量,并开始服用多潘立酮20毫克,每日4次。平均而言,患者接受多潘立酮治疗23.3个月(范围6 - 48个月)。研究期间多潘立酮剂量范围为每日40至120毫克。
胃轻瘫症状评分从4.1±0.22(平均值±标准误)降至1.3±0.2,与多潘立酮治疗前相比,研究期间住院次数显著减少(p<0.05)。基线时,患者在2小时时固体餐的潴留率为87.3±3.71%,而在多潘立酮治疗期间为57.2±5.04%(p<0.05)。多潘立酮治疗使88%的患者生活质量得到提高。研究期间平均催乳素水平为58.9皮克/毫升,3例患者报告有男性乳房发育。
对胃轻瘫患者进行长期多潘立酮治疗可显著减轻胃肠道症状和住院次数,提高生活质量,并将固体餐的胃排空加速至正常速率。多潘立酮在长期治疗结果方面成功治疗胃轻瘫,且具有良好的安全性。