Evidence map›Paper›PMID 18398473›Full record

ArticlePloS one2008

Late entry to HIV care limits the impact of anti-retroviral therapy in The Netherlands.

Colette Smit, Timothy B Hallett, Joep Lange, Geoff Garnett, Frank de Wolf

Abstract read
In one paragraph

Article in PloS one, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
–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

18 citing papers in PubMed.

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  17. Late presentation for human immunodeficiency virus care in the United States and Canada.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2010
    Article
  18. Article
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

5 authors.

Colette SmitHIV Monitoring Foundation Amsterdam, Amsterdam, The Netherlands. Colette.Smit@amc.uva.nl
Timothy B Hallett
Joep Lange
Geoff Garnett
Frank de Wolf

Funding

Medical Research CouncilWellcome Trust
6 · The paper itself

Abstract

objectiveTo explain differences in survival in the first three years of combination anti-retroviral therapy (cART) between HIV treatment centres in The Netherlands. METHODOLOGY/PRINCIPAL

findingsWe developed a mathematical simulation model, parameterised using data from the ATHENA cohort that describes patients entering care, being monitored and starting cART. Three scenarios were used to represent three treatment centres with widely varying mortality rates on cART that were differentiated by: (i) the distribution of CD4 counts of patients entering care; (ii) the age distribution of patients entering care; (iii) the average rate of monitoring the patients not on cART. At the level of the treatment centre, the fraction of Dutch MSM dying in the first three years of treatment ranged from 0% to 8%. The mathematical model captured the large variation in observed mortality between the three treatment centres. Manipulating the age-distribution of patients or the frequency of monitoring did not affect the model predictions. In contrast, when the same national average distribution of CD4 count at entry was used in all the scenarios, the variation in predicted mortality between all centres was diminished. CONCLUSIONS/SIGNIFICANCE: Patients entering care with low CD4 counts appears to be the main source of variation in the mortality rates between Dutch treatment centres. Recruiting HIV-infected individuals to care earlier could lead to substantial improvements in cART outcomes. For example, if patients were to present with at least 400 CD4 cells/mm(3), as they do already in some centres, then our model predicts that the mortality in the first three years of cART could be reduced by approximately 20%.

Indexed as

AdultAnti-HIV AgentsAnti-Retroviral AgentsCD4-Positive T-LymphocytesCell CountCohort StudiesHealth Services AccessibilityHIV InfectionsHumansMaleModels, TheoreticalNetherlandsRiskTime FactorsTreatment OutcomeAnti-HIV AgentsAnti-Retroviral Agents

Identifiers

PMID18398473
PMCPMC2276315

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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.