Single-Dose Rifampicin Leprosy Chemoprophylaxis for Household Contacts in Kiribati: An Audit of a Combined Retrospective and Prospective Approach

Author:

Campbell Patrick O.12ORCID,Bauro Temea3,Rimon Erei3,Timeon Eretii3,Bland Caitlin4,Ioteba Nabura5,Douglas Nicholas M.267ORCID,Cunanan Arturo89,Chambers Stephen T.1

Affiliation:

1. Department of Pathology and Biomedical Science, University of Otago, Christchurch 8011, New Zealand

2. Department of Infectious Diseases, Christchurch Hospital, Te Whatu Ora Waitaha, Canterbury 8011, New Zealand

3. Government of the Republic of Kiribati Ministry of Health and Medical Services, Tarawa P.O. Box 268, Kiribati

4. Otago Medical School, University of Otago, Christchurch 8011, New Zealand

5. Pasifika Medical Association, Christchurch 8011, New Zealand

6. Department of Medicine, University of Otago, Christchurch 8011, New Zealand

7. Division of Global and Tropical Health, Menzies School of Health Research, Charles Darwin University, Darwin, NT 0811, Australia

8. Department of Health, Culion Sanatorium and General Hospital, Culion 5315, Philippines

9. Division of Programmes for Disease Control, Manila 1003, Philippines

Abstract

Kiribati is a Pacific Island nation with a widely dispersed population and one of the highest rates of leprosy worldwide. Single-dose rifampicin post-exposure prophylaxis (SDR-PEP) of leprosy contacts has reduced new case detection rates in controlled trials. In 2018, an SDR-PEP programme was introduced in Kiribati that included screening and chemoprophylaxis of household contacts of leprosy cases retrospectively (2010–2017) and prospectively (2018–2022). We conducted a retrospective audit to determine the comprehensiveness, timeliness and feasibility of the SDR-PEP programme. Overall, 13,641 household contacts were identified (9791 in the retrospective and 3850 in the prospective cohort). In the retrospective cohort, 1044 (11%) contacts were absent, 403 (4%) were ineligible for SDR, and 42 new cases were detected (0.4%) Overall, SDR coverage was 84.7%. In the prospective cohort, 164 (4%) contacts were absent, 251 (7%) were ineligible for SDR, and 23 new cases were diagnosed (0.6%). Overall, SDR coverage was 88.1%. Across both cohorts, there were 23 SDR refusals. The median time to SDR administration was 220 days (IQR 162–468) and 120 days (IQR 36–283) for the retrospective and prospective cohorts, respectively. SDR was readily accepted in both cohorts. The new case detection rate (0.5%) is consistent with that in other studies. Overall SDR coverage in both the retrospective and prospective phases met programmatic expectations.

Funder

Health Research Council of New Zealand

Publisher

MDPI AG

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