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硝唑尼特治疗重度轮状病毒腹泻的效果:随机双盲安慰剂对照试验

Effect of nitazoxanide for treatment of severe rotavirus diarrhoea: randomised double-blind placebo-controlled trial.

作者信息

Rossignol Jean-François, Abu-Zekry Mona, Hussein Abeer, Santoro M Gabriella

机构信息

Romark Institute for Medical Research, Tampa, Florida 33607, USA.

出版信息

Lancet. 2006 Jul 8;368(9530):124-9. doi: 10.1016/S0140-6736(06)68852-1.

Abstract

BACKGROUND

Rotavirus is a leading cause of morbidity and mortality in children younger than 5 years, but there is no effective treatment. We assessed the activity of nitazoxanide, a broad-spectrum anti-infective drug, against rotavirus in cell culture and in a clinical trial in paediatric patients hospitalised with severe rotavirus diarrhoea.

METHODS

We did a randomised double-blind placebo-controlled trial in 50 children admitted to the Cairo University Children's Hospital between June 15 and Aug 23, 2005, with severe rotavirus diarrhoea. 38 children aged 5 months to 7 years (median age 11 months) with rotavirus as the sole identified cause of gastroenteritis were enrolled in the clinical study. Patients were randomly assigned either 7.5 mg/kg nitazoxanide as an oral suspension or placebo twice a day for 3 days, and all remained in hospital for 7 days after start of treatment. The primary endpoint was time from first dose to resolution of illness, and analysis was by modified intention-to-treat. This study is registered with ClinicalTrials.gov, number NCT00302640.

FINDINGS

Survival analysis showed that the median time to resolution of illness was 31 h (IQR 22-73) for the nitazoxanide-treated group compared with 75 h (51-124) for the placebo group (p=0.0137). No significant adverse events were reported.

INTERPRETATION

A 3-day course of nitazoxanide significantly reduced the duration of rotavirus disease in hospitalised paediatric patients. These results are encouraging, and might lead us to think about new approaches to managing rotavirus disease in children.

摘要

背景

轮状病毒是5岁以下儿童发病和死亡的主要原因,但尚无有效治疗方法。我们评估了广谱抗感染药物硝唑尼特在细胞培养以及在一项针对因严重轮状病毒腹泻住院的儿科患者的临床试验中对轮状病毒的活性。

方法

2005年6月15日至8月23日期间,我们在开罗大学儿童医院对50名因严重轮状病毒腹泻入院的儿童进行了一项随机双盲安慰剂对照试验。38名年龄在5个月至7岁(中位年龄11个月)、轮状病毒为唯一确定的胃肠炎病因的儿童被纳入临床研究。患者被随机分配接受7.5mg/kg硝唑尼特口服混悬液或安慰剂,每日两次,共3天,且所有患者在开始治疗后均住院7天。主要终点是从首剂给药到疾病缓解的时间,分析采用改良意向性分析。本研究已在ClinicalTrials.gov注册,注册号为NCT00302640。

结果

生存分析显示,硝唑尼特治疗组疾病缓解的中位时间为31小时(IQR 22 - 73),而安慰剂组为75小时(51 - 124)(p = 0.0137)。未报告显著不良事件。

解读

硝唑尼特3天疗程显著缩短了住院儿科患者轮状病毒疾病的病程。这些结果令人鼓舞,可能会促使我们思考儿童轮状病毒疾病管理的新方法。

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