Le SIDA en Afrique subsaharienne (serveur d'exploration)

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Loss to programme between HIV diagnosis and initiation of antiretroviral therapy in sub-Saharan Africa: Systematic review and meta-analysis

Identifieur interne : 001F12 ( Pmc/Corpus ); précédent : 001F11; suivant : 001F13

Loss to programme between HIV diagnosis and initiation of antiretroviral therapy in sub-Saharan Africa: Systematic review and meta-analysis

Auteurs : Catrina Mugglin ; Janne Estill ; Gilles Wandeler ; Nicole Bender ; Matthias Egger ; Thomas Gsponer ; Olivia Keiser

Source :

RBID : PMC:3895621

Abstract

Objectives

To assess the proportion of patients lost to programme (died, lost to follow-up, transferred-out) between HIV diagnosis and start of antiretroviral therapy (ART) in sub-Saharan Africa, and determine factors associated with loss to programme.

Methods

Systematic review and meta-analysis. We searched PubMed and EMBASE databases for studies in adults. Outcomes were the percentage of patients dying before starting ART, the percentage lost to follow-up, the percentage with a CD4 cell count, the distribution of first CD4 counts and the percentage of eligible patients starting ART. Data were combined using random-effects meta-analysis.

Results

29 studies from sub-Saharan Africa including 148,912 patients were analysed. 6 studies covered the whole period from HIV diagnosis to ART start. Meta-analysis of these studies showed that of 100 patients with a positive HIV test, 72 (95% CI 60–84) had a CD4 cell count measured, 40 (95% CI 26–55) were eligible for ART and 25 (95% CI 13–37) started ART. There was substantial heterogeneity between studies (p<0.0001). Median CD4 cell count at presentation ranged from 154 cells/μl to 274 cells/μl. Patients eligible for ART were less likely to become lost to programme (25% versus 54%, p<0.0001) but eligible patients were more likely to die (11% versus 5%, p<0.0001) than ineligible patients. Loss to programme was higher in men, in patients with low CD4 cell counts and low socio-economic status, and in recent time periods.

Conclusions

Monitoring and care in the pre-ART time period needs improvement, with greater emphasis on patients not yet eligible for ART.


Url:
DOI: 10.1111/j.1365-3156.2012.03089.x
PubMed: 22994151
PubMed Central: 3895621

Links to Exploration step

PMC:3895621

Le document en format XML

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<sec id="S1">
<title>Objectives</title>
<p id="P1">To assess the proportion of patients lost to programme (died, lost to follow-up, transferred-out) between HIV diagnosis and start of antiretroviral therapy (ART) in sub-Saharan Africa, and determine factors associated with loss to programme.</p>
</sec>
<sec id="S2">
<title>Methods</title>
<p id="P2">Systematic review and meta-analysis. We searched PubMed and EMBASE databases for studies in adults. Outcomes were the percentage of patients dying before starting ART, the percentage lost to follow-up, the percentage with a CD4 cell count, the distribution of first CD4 counts and the percentage of eligible patients starting ART. Data were combined using random-effects meta-analysis.</p>
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<title>Results</title>
<p id="P3">29 studies from sub-Saharan Africa including 148,912 patients were analysed. 6 studies covered the whole period from HIV diagnosis to ART start. Meta-analysis of these studies showed that of 100 patients with a positive HIV test, 72 (95% CI 60–84) had a CD4 cell count measured, 40 (95% CI 26–55) were eligible for ART and 25 (95% CI 13–37) started ART. There was substantial heterogeneity between studies (p<0.0001). Median CD4 cell count at presentation ranged from 154 cells/μl to 274 cells/μl. Patients eligible for ART were less likely to become lost to programme (25% versus 54%, p<0.0001) but eligible patients were more likely to die (11% versus 5%, p<0.0001) than ineligible patients. Loss to programme was higher in men, in patients with low CD4 cell counts and low socio-economic status, and in recent time periods.</p>
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<title>Conclusions</title>
<p id="P4">Monitoring and care in the pre-ART time period needs improvement, with greater emphasis on patients not yet eligible for ART.</p>
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<name>
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<on-behalf-of>for IeDEA Southern Africa</on-behalf-of>
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Division of International and Environmental Health, Institute of Social and Preventive Medicine (ISPM), University of Bern, Bern, Switzerland</aff>
<aff id="A2">
<label>2</label>
Infectious Diseases Clinic, University Hospital Bern, Bern, Switzerland</aff>
<aff id="A3">
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School of Public Health and Family Medicine, University of Cape Town, Cape Town, South Africa</aff>
<author-notes>
<corresp id="FN1">Corresponding authors: Olivia Keiser and Catrina Mugglin, Institute of Social and Preventive Medicine (ISPM), University of Bern, Finkenhubelweg 11, CH-3012 Bern, Switzerland. Phone +41 31 631 35 15; Fax +41 31 631 35 20;
<email>okeiser@ispm.unibe.ch</email>
,
<email>catrina.mugglin@gmail.com</email>
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<pmc-comment>elocation-id from pubmed: 10.1111/j.1365-3156.2012.03089.x</pmc-comment>
<abstract>
<sec id="S1">
<title>Objectives</title>
<p id="P1">To assess the proportion of patients lost to programme (died, lost to follow-up, transferred-out) between HIV diagnosis and start of antiretroviral therapy (ART) in sub-Saharan Africa, and determine factors associated with loss to programme.</p>
</sec>
<sec id="S2">
<title>Methods</title>
<p id="P2">Systematic review and meta-analysis. We searched PubMed and EMBASE databases for studies in adults. Outcomes were the percentage of patients dying before starting ART, the percentage lost to follow-up, the percentage with a CD4 cell count, the distribution of first CD4 counts and the percentage of eligible patients starting ART. Data were combined using random-effects meta-analysis.</p>
</sec>
<sec id="S3">
<title>Results</title>
<p id="P3">29 studies from sub-Saharan Africa including 148,912 patients were analysed. 6 studies covered the whole period from HIV diagnosis to ART start. Meta-analysis of these studies showed that of 100 patients with a positive HIV test, 72 (95% CI 60–84) had a CD4 cell count measured, 40 (95% CI 26–55) were eligible for ART and 25 (95% CI 13–37) started ART. There was substantial heterogeneity between studies (p<0.0001). Median CD4 cell count at presentation ranged from 154 cells/μl to 274 cells/μl. Patients eligible for ART were less likely to become lost to programme (25% versus 54%, p<0.0001) but eligible patients were more likely to die (11% versus 5%, p<0.0001) than ineligible patients. Loss to programme was higher in men, in patients with low CD4 cell counts and low socio-economic status, and in recent time periods.</p>
</sec>
<sec id="S4">
<title>Conclusions</title>
<p id="P4">Monitoring and care in the pre-ART time period needs improvement, with greater emphasis on patients not yet eligible for ART.</p>
</sec>
</abstract>
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<kwd>sub-Saharan Africa</kwd>
<kwd>mortality</kwd>
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</kwd-group>
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</front>
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