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首页> 外文期刊>Alimentary pharmacology & therapeutics. >Randomised clinical trial: High-dose vs. standard-dose proton pump inhibitors for the prevention of recurrent haemorrhage after combined endoscopic haemostasis of bleeding peptic ulcers
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Randomised clinical trial: High-dose vs. standard-dose proton pump inhibitors for the prevention of recurrent haemorrhage after combined endoscopic haemostasis of bleeding peptic ulcers

机译:随机临床试验:大剂量与标准剂量质子泵抑制剂预防出血性消化性溃疡合并内镜止血后的复发性出血

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Background The optimal dosage of intravenous proton pump inhibitors (PPIs) for the prevention of peptic ulcer rebleeding remains unclear. Aim To compare the rebleeding rate of high-dose and standard-dose PPI use after endoscopic haemostasis. Methods A total of 201 patients with bleeding ulcers undergoing endoscopic treatment with epinephrine injection and heater probe thermocoagulation were randomised to receive a high-dose regimen (80 mg bolus, followed by pantoprazole 8 mg/h infusion, n = 100) or a standard-dose regimen (pantoprazole 40 mg bolus daily, n = 101). After 72 h, all patients were given 40 mg pantoprazole daily orally for 27 days. Results There were no statistical differences in mean units of blood transfused, length of hospitalisation 5 days, surgical or radiological interventions and mortality within 30 days between two groups. Bleeding recurred within 30 days in six patients [6.2%, 95% confidence interval (CI) 1.3-11.1%] in the high-dose group, as compared to five patients (5.2%, 95% CI 0.6-9.7%) in the standard-dose group (P = 0.77). The stepwise Cox regression analysis showed end-stage renal disease, haematemesis, chronic obstructive pulmonary disease (hazard ratio: 37.15, 10.07, 9.12, 95% CI: 6.76-204.14, 2.07-49.01, 1.66-50.00 respectively) were independent risk factors for rebleeding and Helicobacter pylori infection was associated with lower risk of rebleeding (hazard ratio: 0.20, 95% CI: 0.04-0.94). Conclusions Following combined endoscopic haemostasis of bleeding ulcers, co-morbidities, haematemesis and H. pylori Status, but not PPI dosage, are associated with rebleeding (.ID: NCT00709046).
机译:背景技术用于预防消化性溃疡再出血的静脉内质子泵抑制剂(PPI)的最佳剂量仍不清楚。目的比较内镜止血后大剂量和标准剂量PPI的再出血率。方法总共201例接受内镜肾上腺素注射和加热器探针热凝治疗的出血性溃疡患者随机接受大剂量方案(80毫克推注,然后输注pan托拉唑8毫克/小时,n = 100)或标准剂量-剂量方案(pan托拉唑每天40毫克推注,n = 101)。 72小时后,所有患者每天口服40 mg潘托拉唑,治疗27天。结果两组之间的平均输血单位,5天住院时间,手术或放射学干预措施以及30天内死亡率之间无统计学差异。高剂量组中有6例患者[6.2%,95%置信区间(CI)1.3-11.1%]在30天内复发,相比之下,高剂量组有5例患者(5.2%,95%CI 0.6-9.7%)出现出血。标准剂量组(P = 0.77)。逐步Cox回归分析显示终末期肾脏疾病,呕血,慢性阻塞性肺疾病(危险比:分别为37.15、10.07、9.12、95%CI:6.76-204.14、2.07-49.01、1.66-50.00)是以下因素的独立危险因素再出血和幽门螺杆菌感染与再出血风险降低相关(危险比:0.20,95%CI:0.04-0.94)。结论内镜止血合并溃疡止血后,合并出血,合并症,呕血和幽门螺杆菌状态(而非PPI剂量)与出血有关(ID:NCT00709046)。

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