Post-exposure prophylaxis in leprosy (PEOPLE): a cluster randomised trial - Institut Pasteur de Madagascar
Article Dans Une Revue The Lancet global health Année : 2024

Post-exposure prophylaxis in leprosy (PEOPLE): a cluster randomised trial

Andriamira Randrianantoandro
  • Fonction : Auteur
Sofie Marijke Braet
  • Fonction : Auteur
Abdallah Baco
  • Fonction : Auteur
Aboubacar Mzembaba
  • Fonction : Auteur
Zahara Salim
  • Fonction : Auteur
Mohammed Amidy
  • Fonction : Auteur
Saverio Grillone
  • Fonction : Auteur
Nissad Attoumani
  • Fonction : Auteur
Sillahi Halifa Grillone
  • Fonction : Auteur
Maya Ronse
  • Fonction : Auteur
Hanitra Harinjatovo
  • Fonction : Auteur
Rian Snijders
  • Fonction : Auteur
Carolien Hoof
  • Fonction : Auteur
Achilleas Tsoumanis
  • Fonction : Auteur
Tahinamandranto Rasamoelina
  • Fonction : Auteur
Paul Corstjens
  • Fonction : Auteur
Nimer Ortuno-Gutierrez
  • Fonction : Auteur
Annemieke Geluk
  • Fonction : Auteur
Emmanuelle Cambau
  • Fonction : Auteur
Bouke Catharina de Jong
  • Fonction : Auteur

Résumé

Background Post-exposure prophylaxis (PEP) using single-dose rifampicin reduces progression from infection with Mycobacterium leprae to leprosy disease. We compared effectiveness of different administration modalities, using a higher (20 mg/kg) dose of rifampicin-single double-dose rifampicin (SDDR)-PEP.

Methods

We did a cluster randomised study in 16 villages in Madagascar and 48 villages in Comoros. Villages were randomly assigned to four study arms and inhabitants were screened once a year for leprosy, for 4 consecutive years. All permanent residents (no age restriction) were eligible to participate and all identified patients with leprosy were treated with multidrug therapy (SDDR-PEP was provided to asymptomatic contacts aged ≥2 years). Arm 1 was the comparator arm, in which no PEP was provided. In arm 2, SDDR-PEP was provided to household contacts of patients with leprosy, whereas arm 3 extended SDDR-PEP to anyone living within 100 m. In arm 4, SDDR-PEP was offered to household contacts and to anyone living within 100 m and testing positive to anti-phenolic glycolipid-I. The main outcome was the incidence rate ratio (IRR) of leprosy between the comparator arm and each of the intervention arms. We also assessed the individual protective effect of SDDR-PEP and explored spatial associations. This trial is registered with ClinicalTrials.gov, NCT03662022, and is completed. Findings Between Jan 11, 2019, and Jan 16, 2023, we enrolled 109 436 individuals, of whom 95 762 had evaluable followup data. Our primary analysis showed a non-significant reduction in leprosy incidence in arm 2 (IRR 0•95), arm 3 (IRR 0•80), and arm 4 (IRR 0•58). After controlling for baseline prevalence, the reduction in arm 3 became stronger and significant (IRR 0•56, p=0•0030). At an individual level SDDR-PEP was also protective with an IRR of 0•55 (p=0•0050). Risk of leprosy was two to four times higher for those living within 75 m of an index patient at baseline.

Interpretation SDDR-PEP appears to protect against leprosy but less than anticipated. Strong spatial associations were observed within 75 m of index patients. Targeted door-to-door screening around index patients complemented by a blanket SDDR-PEP approach will probably have a substantial effect on transmission.

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Dates et versions

hal-04729751 , version 1 (10-10-2024)

Identifiants

Citer

Epco Hasker, Younoussa Assoumani, Andriamira Randrianantoandro, Stéphanie Ramboarina, Sofie Marijke Braet, et al.. Post-exposure prophylaxis in leprosy (PEOPLE): a cluster randomised trial. The Lancet global health, 2024, 12 (6), pp.e1017-e1026. ⟨10.1016/S2214-109X(24)00062-7⟩. ⟨hal-04729751⟩
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