Laboratorio Satelite Iquitos, Asociación Benéfica Prisma, Área de Investigaciones Biomédicas, Calle Ramirez Hurtado Nº 622, Iquitos, Peru.
Division of Infectious Diseases and International Health, Department of Internal Medicine, University of Virginia, MR-6 Rm 2207, 345 Crispell Dr, Charlottesville, VA, 22908, USA.
BMC Infect Dis. 2022 Jun 7;22(1):528. doi: 10.1186/s12879-022-07494-0.
Deworming programs aimed at reducing morbidity and mortality from geohelminth infections are common in many countries where these infections are endemic, but data demonstrating increasing levels of resistance to albendazole and mebendazole are causes for concern. Studies to evaluate the clinical efficacy of deworming programs are critical to maintain high infection control goals.
We propose to assess the clinical efficacy of Peruvian national guidelines for deworming programs in a prospective observational study conducted in the Amazon River basin area near Iquitos, Peru. Major outcomes to be evaluated include (1) albendazole resistance of intestinal helminths (trichuriasis, ascariasis, hookworm), and (2) frequency of reinfection with intestinal helminths 4 months after treatment with albendazole. Children ages 2-11 years from the Belén District of Iquitos will be identified based on a community census. Following parental informed consent, demographic data, weight, and height will be recorded and a stool specimen for parasitological exam by direct observation and Kato-Katz concentration method, and helminthic egg counts will be collected prior to administration of albendazole, following Peruvian national guidelines. Follow-up stool specimens examined in the same manner will be collected at 20 days, 90 days, and 100 days following initial administration of albendazole, and based on parasites found repeat treatment will be administered in accordance with national guidelines. Real-time multiplex qPCR will be performed on helminth positive samples collected prior to initial deworming and on helminth-positive specimens detected on day 15-20. A total sample size of 380 participants was calculated based on total population in the target group and prevalence estimates of helminth infections and clinical resistance based on recent data.
Data from observational clinical efficacy studies are important to guide geohelminth infection control programs. Trial registration https://www.researchregistry.com/ . Identification number: researchregistry7736; Registered retrospectively March 13, 2022; https://www.researchregistry.com/browse-the-registry#home/registrationdetails/622e024cf06132001e3327bf/.
在许多寄生虫病流行的国家,旨在降低土源性蠕虫感染发病率和死亡率的驱虫方案较为常见,但阿苯达唑和甲苯达唑耐药水平不断上升的数据令人担忧。评估驱虫方案临床疗效的研究对于维持高感染控制目标至关重要。
我们拟在秘鲁亚马逊河流域伊基托斯附近进行一项前瞻性观察性研究,评估秘鲁国家驱虫方案指南的临床疗效。主要评估结果包括:(1)肠道蠕虫(鞭虫病、蛔虫病、钩虫病)的阿苯达唑耐药性;(2)服用阿苯达唑治疗 4 个月后肠道蠕虫再感染的频率。伊基托斯贝伦区年龄在 2-11 岁的儿童将根据社区普查确定。在获得家长知情同意后,记录人口统计学数据、体重和身高,并按照秘鲁国家指南,采集粪便样本进行寄生虫直接镜检和加藤厚涂片检查,并进行粪便虫卵计数。驱虫前,将按照秘鲁国家指南采集粪便样本进行阿苯达唑治疗。初次服药后第 20 天、90 天和 100 天,将采用相同方法采集粪便样本进行随访。根据寄生虫检出情况,按照国家指南重复治疗。采用实时多重 qPCR 检测驱虫前的阳性样本和第 15-20 天的阳性样本。根据目标人群的总人数以及最近的数据估计的寄生虫感染和临床耐药的流行率,计算出 380 名参与者的总样本量。
观察性临床疗效研究的数据对于指导土源性蠕虫感染控制方案非常重要。试验注册网址:https://www.researchregistry.com/ 。识别号:researchregistry7736;注册日期:2022 年 3 月 13 日,注册方式:回溯注册;https://www.researchregistry.com/browse-the-registry/#home/registrationdetails/622e024cf06132001e3327bf/。