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首页> 外文期刊>Gut: Journal of the British Society of Gastroenterology >Combined versus sequential diuretic treatment of ascites in non-azotaemic patients with cirrhosis: results of an open randomised clinical trial.
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Combined versus sequential diuretic treatment of ascites in non-azotaemic patients with cirrhosis: results of an open randomised clinical trial.

机译:非固氮型肝硬化患者腹水联合利尿剂和序贯利尿剂治疗:一项开放随机临床试验的结果。

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OBJECTIVE: The aim of the study was to compare sequential versus combined diuretic therapy in patients with cirrhosis, moderate ascites and without renal failure. DESIGN: One hundred patients were randomly assigned to the two diuretic treatments. The sequential treatment provided potassium canrenoate at the initial dose of 200 mg/day, then increased to 400 mg/day. Non-responders were treated with 400 mg/day of potassium canrenoate and furosemide at an initial dose of 50 mg/day, then increased to 150 mg/day. The combined treatment provided the initial dose of 200 mg/day of potassium canrenoate and 50 mg/day of furosemide, then increased to 400 mg/day and 150 mg/day, respectively. RESULTS: Most patients who received sequential treatment responded to potassium canrenoate alone (19% to 200 mg/day and 52.63% to 400 mg/day, respectively). Most patients who received the combined treatment responded to the first two steps (40% to the first step and 50% to the second, ie, 400 mg/day of potassium canrenoate plus 100 mg/day of furosemide). Adverse effects (38% vs 20%, p<0.05), in particular, hyperkalaemia (18% vs 4%, p<0.05), were more frequent in patients who received sequential therapy. As a consequence, the per cent of patients who resolved ascites without changing the effective diuretic step was higher in those who received the combined treatment (56% vs 76%, p<0.05). CONCLUSIONS: The combined diuretic treatment is preferable to the sequential one in the treatment of moderate ascites in patients with cirrhosis and without renal failure. NCT00741663. This work is an open randomised clinical trial.
机译:目的:本研究的目的是比较有肝硬化,中度腹水且无肾功能衰竭患者的序贯和联合利尿剂治疗。设计:将一百例患者随机分配至两种利尿剂治疗。序贯治疗以200 mg / day的初始剂量提供了肾上腺素钾,然后增加至400 mg / day。无反应者以50 mg / day的初始剂量用400 mg / day的松果酸钾和呋塞米治疗,然后增加至150 mg / day。联合治疗提供了200 mg /天的松果酸钾和50 mg /天的速尿初始剂量,然后分别增加到400 mg /天和150 mg /天。结果:大多数接受序贯治疗的患者对单独的鸟氨酸钾有反应(分别为19%至200 mg /天和52.63%至400 mg /天)。接受联合治疗的大多数患者对前两个步骤有反应(第一步占40%,第二步占50%,即400毫克/天的坎瑞诺酸钾加100毫克/天的速尿)。在接受序贯治疗的患者中,不良反应(38%vs 20%,p <0.05)尤其是高钾血症(18%vs 4%,p <0.05)更为常见。结果,在接受联合治疗的患者中,在不改变有效利尿步骤的情况下解决腹水的患者比例更高(56%比76%,p <0.05)。结论:在不伴有肾功能衰竭的肝硬化患者中,腹水合并中度腹水的治疗要优于顺序利尿剂。 NCT00741663。这项工作是一项开放的随机临床试验。

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