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

被引:1
|
作者
Campbell, Patrick O. [1 ,2 ]
Bauro, Temea [3 ]
Rimon, Erei [3 ]
Timeon, Eretii [3 ]
Bland, Caitlin [4 ]
Ioteba, Nabura [5 ]
Douglas, Nicholas M. [2 ,6 ,7 ]
Cunanan, Arturo [8 ,9 ]
Chambers, Stephen T. [1 ]
机构
[1] Univ Otago, Dept Pathol & Biomed Sci, Christchurch 8011, New Zealand
[2] Christchurch Hosp, Dept Infect Dis, Canterbury 8011, New Zealand
[3] Govt Republ Kiribati Minist Hlth & Med Serv, POB 268, Tarawa, Kiribati
[4] Univ Otago, Otago Med Sch, Christchurch 8011, New Zealand
[5] Pasifika Med Assoc, Christchurch 8011, New Zealand
[6] Univ Otago, Dept Med, Christchurch 8011, New Zealand
[7] Charles Darwin Univ, Menzies Sch Hlth Res, Div Global & Trop Hlth, Darwin, NT 0811, Australia
[8] Culion Sanat & Gen Hosp, Dept Hlth, Culion 5315, Philippines
[9] Div Programmes Dis Control, Manila 1003, Philippines
关键词
leprosy; feasibility studies; single-dose rifampicin; Mycobacterium leprae; household contacts; post-exposure prophylaxis;
D O I
10.3390/tropicalmed9030058
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
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.
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页数:11
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