Andriulli Angelo, Loperfido Silvano, Focareta Rosaria, Leo Pietro, Fornari Fabio, Garripoli Antonietta, Tonti Paolo, Peyre Sergio, Spadaccini Antonio, Marmo Riccardo, Merla Antonio, Caroli Alessandro, Forte Gian Battista, Belmonte Angelo, Aragona Giovanni, Imperiali Gianni, Forte Fabrizio, Monica Fabio, Caruso Nazario, Perri Francesco
Casa Sollievo della Sofferenza Hospital, IRCCS, San Giovanni, Rotondo, Italy.
Am J Gastroenterol. 2008 Dec;103(12):3011-8. doi: 10.1111/j.1572-0241.2008.02149.x.
The most effective schedule of proton pump inhibitor (PPI) administration following endoscopic hemostasis of bleeding ulcers remains uncertain.
Patients with actively bleeding ulcers and those with nonbleeding visible vessel or adherent clot were treated with epinephrine injection and/or thermal coagulation, and randomized to receive intravenous PPIs according to an intensive regimen (80 mg bolus followed by 8 mg/h as continuous infusion for 72 h) or a standard regimen (40 mg bolus daily followed by saline infusion for 72 h). After the infusion, all patients were given 20 mg PPI twice daily orally. The primary end point was the in-hospital rebleeding rate, as ascertained at the repeat endoscopy.
Bleeding recurred in 28 of 238 patients (11.8%) receiving the intensive regimen, and in 19 of 236 (8.1%) patients receiving the standard regimen (P= 0.18). Most rebleeding episodes occurred during the initial 72-h infusion: 18 (7.6%) and 19 events (8.1%) in the intensive and standard groups, respectively (P= 0.32). Mean units of blood transfused were 1.7 +/- 2.1 in the intensive and 1.5 +/- 2.1 in the standard regimen group (P= 0.34). The duration of hospital stay was <5 days for 88 (37.0%) and 111 patients (47.0%) in the intensive and standard groups (P= 0.03). There were fewer surgical interventions in the standard versus intensive regimen (1 vs 3). Five patients in each treatment group died.
Following endoscopic hemostasis of bleeding ulcers, standard-dose PPIs infusion was as effective as a high-dose regimen in reducing the risk of recurrent bleeding. (ClinicalTrials.gov number, NCT00374101).
内镜下止血治疗出血性溃疡后,质子泵抑制剂(PPI)给药的最有效方案仍不明确。
对活动性出血性溃疡患者以及有非出血性可见血管或附着血凝块的患者进行肾上腺素注射和/或热凝治疗,并随机分为两组,分别接受强化治疗方案(静脉推注80mg,随后以8mg/h持续输注72小时)或标准治疗方案(每日静脉推注40mg,随后输注生理盐水72小时)。输注结束后,所有患者每日口服20mg PPI两次。主要终点是重复内镜检查确定的院内再出血率。
接受强化治疗方案的238例患者中有28例(11.8%)出现再出血,接受标准治疗方案的236例患者中有19例(8.1%)出现再出血(P = 0.18)。大多数再出血事件发生在最初的72小时输注期间:强化组和标准组分别有18例(7.6%)和19例(8.1%)(P = 0.32)。强化组平均输血量为1.7±2.1单位,标准治疗方案组为1.5±2.1单位(P = 0.34)。强化组和标准组分别有88例(37.0%)和111例(47.0%)患者住院时间<5天(P = 0.03)。标准治疗方案与强化治疗方案相比,手术干预较少(1例对3例)。每个治疗组有5例患者死亡。
内镜下止血治疗出血性溃疡后,标准剂量PPI输注在降低再出血风险方面与高剂量方案同样有效。(ClinicalTrials.gov编号,NCT00374101)