Motaze Nkengafac Villyen, Nwachukwu Chukwuemeka, Humphreys Eliza
Centre for Development of Best Practices in Health (CDBPH), Yaoundé Central Hospital, Yaoundé, Cameroon.
Cochrane South African, South African Medical Research Council, Cape Town, South Africa.
Pan Afr Med J. 2018 Apr 9;29:208. doi: 10.11604/pamj.2018.29.208.15240. eCollection 2018.
Seventy percent of an estimated 10 million children less than five years of age in developing countries die each year of acute respiratory infections, diarrhoea, measles, malaria, malnutrition or a combination of these conditions. Children living with Human immunodeficiency virus (HIV) are at risk of diarrhoea because of drug interactions with antiretroviral therapy and bottle feeding. This may be aggravated by malnutrition and other infectious diseases which are frequent in children living with HIV. Objective: to evaluate treatment interventions for diarrhoea in HIV infected and exposed children.
A comprehensive search was conducted on 02 June 2016 to identify relevant studies for inclusion. We included randomised controlled trials of HIV infected or exposed children under 15 years of age with diarrhoea. Two authors independently selected studies for inclusion, assessed risk of bias (RoB) and extracted data using a pre-designed data extraction form.
We included two studies (Amadi 2002 and Mda 2010) that each enrolled 50 participants. The RoB was assessed as low-risk for both included studies. There was no difference in clinical cure and all-cause mortality between nitazoxanide and placebo for cryptosporidial diarrhoea in Amadi 2002. In Mda 2010, there was a reduction in duration of hospitalisation in the micronutrient supplement group (P < 0.005) although there was no difference in all-cause mortality.
There is low certainty evidence on the effectiveness of nitazoxanide for treating cryptosporidial diarrhoea and micronutrient supplementation in children with diarrhoea. Adequately powered trials are needed to assess micronutrients and nitazoxanide, as well as other interventions, for diarrhoea in HIV-infected and-exposed children.
在发展中国家,估计有1000万5岁以下儿童,其中70%每年死于急性呼吸道感染、腹泻、麻疹、疟疾、营养不良或这些病症的某种组合。感染人类免疫缺陷病毒(HIV)的儿童因抗逆转录病毒疗法的药物相互作用和奶瓶喂养而有腹泻风险。这可能因营养不良和HIV感染儿童中常见的其他传染病而加剧。目的:评估针对感染HIV和暴露于HIV的儿童腹泻的治疗干预措施。
于2016年6月2日进行了全面检索,以确定纳入的相关研究。我们纳入了15岁以下感染或暴露于HIV且患有腹泻的儿童的随机对照试验。两位作者独立选择纳入研究,评估偏倚风险(RoB)并使用预先设计的数据提取表提取数据。
我们纳入了两项研究(阿马迪2002年和姆达2010年),每项研究招募了50名参与者。两项纳入研究的RoB均被评估为低风险。在阿马迪2002年的研究中,硝唑尼特和安慰剂治疗隐孢子虫腹泻的临床治愈率和全因死亡率没有差异。在姆达2010年的研究中,微量营养素补充组的住院时间缩短(P<0.005),尽管全因死亡率没有差异。
关于硝唑尼特治疗隐孢子虫腹泻和腹泻儿童补充微量营养素的有效性,证据的确定性较低。需要进行有足够效力(样本量)的试验来评估微量营养素、硝唑尼特以及其他干预措施对感染HIV和暴露于HIV儿童腹泻的疗效。