4.6 Article

Spatio-temporal analysis of leprosy risks in a municipality in the state of Mato Grosso-Brazilian Amazon: results from the leprosy post-exposure prophylaxis program in Brazil

期刊

INFECTIOUS DISEASES OF POVERTY
卷 11, 期 1, 页码 -

出版社

BMC
DOI: 10.1186/s40249-022-00943-7

关键词

Leprosy; Epidemiological profile; Contact tracing; Spatial analysis; Poverty; Surveillance

资金

  1. Brazilian MoH (UFMT-TED) [100/2020]

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This study analyzed the spatio-temporal changes in the distribution of index cases and co-prevalent cases among contacts of leprosy patients during a leprosy post-exposure prophylaxis program. The results showed that the distribution of the disease was partly explained by poverty indicators and that the program influenced the spatial dynamic of the disease. The study highlights the importance of systematic contact surveillance for leprosy elimination.
Background: Leprosy post-exposure prophylaxis (LPEP) with single dose rifampicin (SDR) can be integrated into different leprosy control program set-ups once contact tracing has been established. We analyzed the spatio-temporal changes in the distribution of index cases (IC) and co-prevalent cases among contacts of leprosy patients (CP) over the course of the LPEP program in one of the four study areas in Brazil, namely the municipality of Alta Floresta, state of Mato Grosso, in the Brazilian Amazon basin. Methods: Leprosy cases were mapped, and socioeconomic indicators were evaluated to explain the leprosy distribution of all leprosy cases diagnosed in the period 2016-2018. Data were obtained on new leprosy cases [Notifiable diseases information system (Sinan)], contacts traced by the LPEP program, and socioeconomic variables [Brazilian Institute of Geography and Statistics (IBGE)]. Kernel, SCAN, factor analysis and spatial regression were applied to analyze changes. Results: Overall, the new case detection rate (NCDR) was 20/10 000 inhabitants or 304 new cases, of which 55 were CP cases among the 2076 examined contacts. Changes over time were observed in the geographic distribution of cases. The highest concentration of cases was observed in the northeast of the study area, including one significant cluster (Relative risk = 2.24; population 27 427, P-value < 0.001) in an area characterized by different indicators associated with poverty as identified through spatial regression (Coefficient 3.34, P-value = 0.01). Conclusions: The disease distribution was partly explained by poverty indicators. LPEP influences the spatial dynamic of the disease and results highlighted the relevance of systematic contact surveillance for leprosy elimination.

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