Effect of patient-delivered household contact tracing and prevention for tuberculosis: A household cluster-randomised trial in Malawi

dc.contributor.authorKaswaswa K.
dc.contributor.authorMacPherson P.
dc.contributor.authorKumwenda M.
dc.contributor.authorMpunga J.
dc.contributor.authorThindwa D.
dc.contributor.authorNliwasa M.
dc.contributor.authorMwapasa M.
dc.contributor.authorOdland J.
dc.contributor.authorTomoka T.
dc.contributor.authorChipungu G.
dc.contributor.authorMukaka M.
dc.contributor.authorCorbett E.L.
dc.contributor.otherMahidol University
dc.date.accessioned2023-06-18T18:05:23Z
dc.date.available2023-06-18T18:05:23Z
dc.date.issued2022-09-01
dc.description.abstractBackground Household contact tracing provides TB screening and TB preventive therapy (TPT) to contacts at high risk of TB disease. However, it is resource intensive, inconvenient, and often poorly implemented. We investigated a novel model aiming to improve uptake. Methods Between May and December 2014, we randomised patient with TB who consented to participate in the trial to either standard of care (SOC) or intervention (PACTS) arms. Participants randomised to PACTS received one screening/triage tool (adapted from WHO integrated management of adolescent and adult illnesses [IMAI] guidelines) and sputum pots for each reported household contact. The tool guided participants through symptom screening; TPT (6-months of isoniazid) eligibility; and sputum collection for contacts. Patients randomised to SOC were managed in accordance with national guidelines, that is, they received verbal instruction on who to bring to clinics for investigation using national guidelines. Main outcome and measures The primary outcome was the proportion of adult contacts receiving treatment for TB within 3 months of randomisation. Secondary outcomes were the proportions of child contacts under age 5 years (U5Y) who were commenced on, and completed, TPT. Data were analyzed by logistic regression with random effects to adjust for household clustering. Results Two hundred and fourteen index TB participants were block-randomized from two sites (107 PACTS, reporting 418 contacts; and 107 SOC, reporting 420 contacts). Overall, 62.8% of index TB participants were HIV-positive and 52.1% were TB culture-positive. 250 otherwise eligible TB patients declined participation and 6 households (10 PACTS, 6 SOC) were lost to follow-up and were not included in the analysis. By three months, nine contacts (PACTS: 6, [1.4%]; SOC: 3, [0.7%]) had TB diagnosed, with no difference between groups (adjusted odds ratio [aOR]: 2.18, 95% CI: 0.60-7.95). Eligible PACTS contacts (37/96, 38.5%) were more likely to initiate TPT by 3-months compared to SOC contacts (27/101, 26.7%; aOR 2.27, 95% CI: 1.04-4.98). U5Y children in the PACTS arm (47/81 58.0%) were more likely to have initiated TPT before the 3-month visit compared to SOC children (36/89, 41.4%; aOR: 2.31, 95% CI: 1.05-5.06). Conclusions and relevance A household-centred patient-delivered symptom screen and IPT eligibility assessment significantly increased timely TPT uptake among U5Y children, but did not significantly increase TB diagnosis. This model needs to be optimized for acceptability, given low participation, and investigated in other low resource settings.
dc.identifier.citationPLoS ONE Vol.17 No.9 September (2022)
dc.identifier.doi10.1371/journal.pone.0269219
dc.identifier.eissn19326203
dc.identifier.pmid36074775
dc.identifier.scopus2-s2.0-85137656540
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/86479
dc.rights.holderSCOPUS
dc.subjectMultidisciplinary
dc.titleEffect of patient-delivered household contact tracing and prevention for tuberculosis: A household cluster-randomised trial in Malawi
dc.typeArticle
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85137656540&origin=inward
oaire.citation.issue9 September
oaire.citation.titlePLoS ONE
oaire.citation.volume17
oairecerif.author.affiliationKamuzu University of Health Sciences
oairecerif.author.affiliationFaculty of Tropical Medicine, Mahidol University
oairecerif.author.affiliationMalawi-Liverpool-Wellcome Trust Clinical Research Programme
oairecerif.author.affiliationLondon School of Hygiene & Tropical Medicine
oairecerif.author.affiliationUiT Norges Arktiske Universitet
oairecerif.author.affiliationLiverpool School of Tropical Medicine
oairecerif.author.affiliationNuffield Department of Medicine
oairecerif.author.affiliationMalawi National TB Control Programme

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