Evidence map›Paper›PMID 29373574›Full record

ArticlePloS one2018

Loss to follow-up before and after initiation of antiretroviral therapy in HIV facilities in Lilongwe, Malawi.

Hannock Tweya, Ikwo Kitefre Oboho, Salem T Gugsa, Sam Phiri, Ethel Rambiki, Rebecca Banda, Johnbosco Mwafilaso, Chimango Munthali, Sundeep Gupta, Moses Bateganya and 1 more

Abstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 68 papers, 6 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
68citing papers in PubMed, 6 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

68 citing papers in PubMed, 6 syntheses or guidelines pooled it.

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8 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Hannock TweyaThe International Union Against Tuberculosis and Lung Disease, Paris, France.
Ikwo Kitefre ObohoDivision of Global HIV and Tuberculosis (DGHT), Center for Global Health, Centers for Disease Control and Prevention (CDC), Atlanta, Georgia, United States of America.
Salem T GugsaLighthouse Trust, Lilongwe, Malawi.
Sam PhiriLighthouse Trust, Lilongwe, Malawi.
Ethel RambikiBwaila Hospital, Ministry of Health, Lilongwe, Malawi.
Rebecca BandaLighthouse Trust, Lilongwe, Malawi.
Johnbosco MwafilasoLighthouse Trust, Lilongwe, Malawi.
Chimango MunthaliBaobab Health Trust, Lilongwe, Malawi.
Sundeep GuptaDivision of Global HIV and Tuberculosis (DGHT), Center for Global Health, Centers for Disease Control and Prevention (CDC), Lilongwe, Malawi.
Moses BateganyaDivision of Global HIV and Tuberculosis (DGHT), Center for Global Health, Centers for Disease Control and Prevention (CDC), Atlanta, Georgia, United States of America.
Alice MaidaDivision of Global HIV and Tuberculosis (DGHT), Center for Global Health, Centers for Disease Control and Prevention (CDC), Lilongwe, Malawi.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionAlthough several studies have explored factors associated with loss to follow-up (LTFU) from HIV care, there remains a gap in understanding how these factors vary by setting, volume of patient and patients' demographic and clinical characteristics. We determined rates and factors associated with LTFU in HIV care Lilongwe, Malawi.

methodsWe conducted a retrospective cohort study of HIV-infected individuals aged 15 years or older at the time of registration for HIV care in 12 ART facilities, between April 2012 and March 2013. HIV-positive individuals who had not started ART (pre-ART patients) were clinically assessed to determine ART eligibility at registration and during clinic follow-up visits. ART-eligible patients were initiated on triple antiretroviral combination. Study data were abstracted from patients' cards, facility ART registers or electronic medical record system from the date of registration for HIV care to a maximum follow-up period of 24 months. Descriptive statistics were undertaken to summarize characteristics of the study patients. Separate univariable and multivariable poisson regression models were used to explore factors associated with LTFU in pre-ART and ART care.

resultsA total of 10,812 HIV-infected individuals registered for HIV care. Of these patients, 1,907 (18%) and 8,905 (82%) enrolled in pre-ART and ART care, respectively. Of the 1,907 pre-ART patients, 490 (26%) subsequently initiated ART and were included in both the pre-ART and ART analyses. The LTFU rates among patients in pre-ART and ART care were 48 and 26 per 100 person-years, respectively. Of the 9,105 ART patients with reasons for starting ART, 2,451 (27%) were initiated on ART because of pregnancy or breastfeeding (Option B+) status. Multivariable analysis showed that being ≥35 years and female were associated with decreased risk of LTFU in the pre-ART and ART phases of HIV care. However, being in WHO clinical stage 3 (adjusted risk ratio (aRR) 1.35, 95% confidence interval (CI): 1.20-1.51) and stage 4 (aRR 1.87, 95% CI: 1.62-2.18), body mass index ≤ 18.4 (aRR 1.24, 95% CI: 1.11-1.39) at ART initiation, poor adherence to clinic appointments (aRR 4.55, 95% CI: 4.16-4.97) and receiving HIV care in rural facilities (aRR 2.32, 95% CI: 1.94-2.87) were associated with increased risk of LTFU among ART patients. Being re-initiated on ART once (aRR 0.20, 95% CI: 0.17-0.22), more than once (aRR 0.06, 95% CI: 0.05-0.07), and being enrolled at a low-volume facility (aRR 0.25, 95% CI: 0.20-0.30) were associated with decreased risk of LTFU from ART care.

conclusionA sizeable proportion of ART LTFU occurred among women enrolled during pregnancy or breast-feeding. Non- compliance to clinic and receiving ART in a rural facility or high-volume facility were associated with increased risk of LTFU from ART care. Developing effective interventions that target high-risk subgroups and contexts may help reduce LTFU from HIV care.

Indexed as

Lost to Follow-UpAdolescentAdultAgedAnti-HIV AgentsCohort StudiesFemaleFollow-Up StudiesHIV InfectionsHumansMalawiMaleMiddle AgedPatient CompliancePregnancyPregnancy Complications, InfectiousAnti-HIV Agents

Identifiers

PMID29373574
PMCPMC5786288

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.