04250nas a2200493 4500000000100000008004100001260001600042653002400058653003300082653003100115653005700146653003000203653001800233653004600251653002200297653002200319653002100341100001300362700001300375700001500388700001100403700001300414700001100427700001100438700001000449700001200459700001200471700001400483700001500497700001100512700001500523700001100538700001400549700001500563700001500578700001300593700001300606245014500619856015300764300001100917490000700928520280700935022001403742 2022 d bElsevier BV10aInfectious Diseases10aPsychiatry and Mental health10aGeriatrics and Gerontology10aPublic Health, Environmental and Occupational Health10aObstetrics and Gynecology10aHealth Policy10aPediatrics, Perinatology and Child Health10aInternal Medicine10aalbendazole (ALB)10aivermectin (IVM)1 aThean LJ1 aRomani L1 aEngelman D1 aWand H1 aJenney A1 aMani J1 aPaka J1 aCua T1 aTaole S1 aSilai M1 aAshwini K1 aSahukhan A1 aKama M1 aTuicakau M1 aKado J1 aParnaby M1 aCarvalho N1 aWhitfeld M1 aKaldor J1 aSteer AC00aPrevention of bacterial complications of scabies using mass drug administration: A population-based, before-after trial in Fiji, 2018–2020 uhttps://www.sciencedirect.com/science/article/pii/S2666606522000487/pdfft?md5=964fa4819f1def2722c2d2f016a12f17&pid=1-s2.0-S2666606522000487-main.pdf a1004330 v223 a

Background

Scabies is an important predisposing factor of impetigo which can lead to serious bacterial complications. Ivermectin-based mass drug administration can substantially reduce scabies and impetigo prevalence in endemic settings, but the impact on serious bacterial complications is not known.

Methods

We conducted a before-after trial in the Northern Division of Fiji (population: 131,914) of mass drug administration for scabies control. Prospective surveillance was conducted from 2018 to 2020. Mass drug administration took place in 2019, involving two doses of oral ivermectin or topical permethrin, delivered alongside diethylcarbamazine and albendazole for lymphatic filariasis. The primary outcomes were incidence of hospitalisations with skin and soft tissue infections, and childhood invasive infections and post-streptococcal sequelae. Secondary outcomes included presentations to primary healthcare with skin infections and community prevalence of scabies and impetigo.

Findings

The incidence of hospitalisations with skin and soft tissue infections was 17% lower after the intervention compared to baseline (388 vs 467 per 100,000 person-years; incidence rate ratio 0.83, 95% CI, 0.74 to 0.94; P = 0.002). There was no difference in incidence of childhood invasive infections and post-streptococcal sequelae. Incidence of primary healthcare presentations with scabies and skin infections was 21% lower (89.2 vs 108 per 1000 person-years, incidence rate ratio, IRR 0.79, 95% CI, 0.78 to 0.82). Crude community prevalence of scabies declined from 14.2% to 7.7% (cluster-adjusted prevalence 12.5% to 8.9%; prevalence ratio 0.71, 95% CI, 0.28 to 1.17). Cluster-adjusted prevalence of impetigo declined from 15.3% to 6.1% (prevalence ratio 0.4, 95% CI, 0.18 to 0.86).

Interpretation

Mass drug administration for scabies control was associated with a substantial reduction in hospitalisations for skin and soft tissue infections.

 a2666-6065