Wilkinson, KA, Maokola, WM, Ngowi, BJ, Mahande, MJ, Todd, J, Robert, M and Msuya, SE. 2021. Impact of Isoniazid Preventive Therapy on Tuberculosis incidence among people living with HIV: A secondary data analysis using Inverse Probability Weighting of individuals attending HIV care and treatment clinics in Tanzania. S1 Dataset. [Online]. PLOS One. Available from: https://doi.org/10.1371/journal.pone.0254082.s001
Wilkinson, KA, Maokola, WM, Ngowi, BJ, Mahande, MJ, Todd, J, Robert, M and Msuya, SE. Impact of Isoniazid Preventive Therapy on Tuberculosis incidence among people living with HIV: A secondary data analysis using Inverse Probability Weighting of individuals attending HIV care and treatment clinics in Tanzania. S1 Dataset [Internet]. PLOS One; 2021. Available from: https://doi.org/10.1371/journal.pone.0254082.s001
Wilkinson, KA, Maokola, WM, Ngowi, BJ, Mahande, MJ, Todd, J, Robert, M and Msuya, SE (2021). Impact of Isoniazid Preventive Therapy on Tuberculosis incidence among people living with HIV: A secondary data analysis using Inverse Probability Weighting of individuals attending HIV care and treatment clinics in Tanzania. S1 Dataset. [Data Collection]. PLOS One. https://doi.org/10.1371/journal.pone.0254082.s001
Description
BACKGROUND: Information on how well Isoniazid Preventive Therapy (IPT) works on reducing TB incidence among people living with HIV (PLHIV) in routine settings using robust statistical methods to establish causality in observational studies is scarce. OBJECTIVES: To evaluate the effectiveness of IPT in routine clinical settings by comparing TB incidence between IPT and non-IPT groups. METHODS: We used data from PLHIV enrolled in 315 HIV care and treatment clinic from January 2012 to December 2016. We used Inverse Probability of Treatment Weighting to adjust for the probability of receiving IPT; balancing the baseline covariates between IPT and non-IPT groups. The effectiveness of IPT on TB incidence was estimated using Cox regression using the weighted sample. RESULTS: Of 171,743 PLHIV enrolled in the clinics over the five years, 10,326 (6.01%) were excluded leaving 161,417 available for the analysis. Of the 24,800 who received IPT, 1.00% developed TB disease whereas of the 136,617 who never received IPT 6,085 (4.98%) developed TB disease. In 278,545.90 person-years of follow up, a total 7,052 new TB cases were diagnosed. Using the weighted sample, the overall TB incidence was 11.57 (95% CI: 11.09–12.07) per 1,000 person-years. The TB incidence among PLHIV who received IPT was 10.49 (95% CI: 9.11–12.15) per 1,000 person-years and 12.00 (95% CI: 11.69–12.33) per 1,000 person-years in those who never received IPT. After adjusting for other covariates there was 52% lower risk of developing TB disease among those who received IPT compared to those who never received IPT: aHR = 0.48 (95% CI: 0.40–0.58, P<0.001).
Conclusion
IPT reduced TB incidence by 52% in PLHIV attending routine CTC in Tanzania. IPTW adjusted the groups for imbalances in the covariates associated with receiving IPT to achieve comparable groups of IPT and non-IPT. This study has added evidence on the effectiveness of IPT in routine clinical settings and on the use of IPTW to determine impact of interventions in observational studies.
Data capture method | Unknown | ||||
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Data Collection Period |
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Date (Date published in a 3rd party system) | 13 July 2021 | ||||
Language(s) of written materials | English |
Data Creators | Wilkinson, KA, Maokola, WM, Ngowi, BJ, Mahande, MJ, Todd, J, Robert, M and Msuya, SE |
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LSHTM Faculty/Department | Faculty of Epidemiology and Population Health > Dept of Population Health (2012- ) |
Participating Institutions | Kilimanjaro Christian Medical University College, Moshi, Tanzania, Mbeya University College of Health Sciences, Mbeya, Tanzania, Kilimanjaro Christian Medical University College, Moshi, Tanzania, London School of Hygiene & Tropical Medicine, London, United Kingdom, Mwenge Catholic University, Moshi, Tanzania |
Date Deposited | 13 Sep 2021 08:39 |
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Last Modified | 13 Sep 2021 08:42 |
Publisher | PLOS One |