Kearns Thérèse M, Speare Richard, Cheng Allen C, McCarthy James, Carapetis Jonathan R, Holt Deborah C, Currie Bart J, Page Wendy, Shield Jennifer, Gundjirryirr Roslyn, Bundhala Leanne, Mulholland Eddie, Chatfield Mark, Andrews Ross M
Menzies School of Health Research, Charles Darwin University, Darwin, Australia.
James Cook University, Townsville, Australia.
PLoS Negl Trop Dis. 2015 Oct 30;9(10):e0004151. doi: 10.1371/journal.pntd.0004151. eCollection 2015 Oct.
Scabies is endemic in many Aboriginal and Torres Strait Islander communities, with 69% of infants infected in the first year of life. We report the outcomes against scabies of two oral ivermectin mass drug administrations (MDAs) delivered 12 months apart in a remote Australian Aboriginal community.
Utilizing a before and after study design, we measured scabies prevalence through population census with sequential MDAs at baseline and month 12. Surveys at months 6 and 18 determined disease acquisition and treatment failures. Scabies infestations were diagnosed clinically with additional laboratory investigations for crusted scabies. Non-pregnant participants weighing ≥15 kg were administered a single 200 μg/kg ivermectin dose, repeated after 2-3 weeks if scabies was diagnosed, others followed a standard alternative algorithm.
We saw >1000 participants at each population census. Scabies prevalence fell from 4% at baseline to 1% at month 6. Prevalence rose to 9% at month 12 amongst the baseline cohort in association with an identified exposure to a presumptive crusted scabies case with a higher prevalence of 14% amongst new entries to the cohort. At month 18, scabies prevalence fell to 2%. Scabies acquisitions six months after each MDA were 1% and 2% whilst treatment failures were 6% and 5% respectively.
Scabies prevalence reduced in the six months after each MDA with a low risk of acquisition (1-2%). However, in a setting where living conditions are conducive to high scabies transmissibility, exposure to presumptive crusted scabies and population mobility, a sustained reduction in prevalence was not achieved.
Australian New Zealand Clinical Trial Register (ACTRN-12609000654257).
疥疮在许多原住民和托雷斯海峡岛民社区呈地方性流行,69%的婴儿在出生后第一年内感染。我们报告了在澳大利亚一个偏远原住民社区相隔12个月进行的两次口服伊维菌素大规模药物给药(MDA)治疗疥疮的结果。
采用前后对照研究设计,我们通过在基线和第12个月进行连续MDA的人口普查来测量疥疮患病率。在第6个月和第18个月的调查确定了疾病感染情况和治疗失败情况。疥疮感染通过临床诊断,并对结痂性疥疮进行额外的实验室检查。体重≥15 kg的非孕妇参与者单次服用200 μg/kg伊维菌素剂量,若诊断为疥疮,则在2 - 3周后重复给药,其他参与者遵循标准的替代方案。
每次人口普查我们观察了超过1000名参与者。疥疮患病率从基线时的4%降至第6个月时的1%。在基线队列中,患病率在第12个月升至9%,这与确定接触一例疑似结痂性疥疮病例有关,在该队列的新入组者中患病率更高,为患14%。在第18个月,疥疮患病率降至2%。每次MDA后6个月的疥疮感染率分别为1%和2%,而治疗失败率分别为6%和5%。
每次MDA后的6个月内疥疮患病率降低,感染风险较低(1 - 2%)。然而,在生活条件有利于疥疮高传播性、接触疑似结痂性疥疮和人口流动的环境中,患病率并未持续降低。
澳大利亚和新西兰临床试验注册中心(ACTRN - 12609000654257)。