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. 2013 Jul 24;11(1):12.
doi: 10.1186/1478-7954-11-12.

A comparison of missing data procedures for addressing selection bias in HIV sentinel surveillance data

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A comparison of missing data procedures for addressing selection bias in HIV sentinel surveillance data

Marie Ng et al. Popul Health Metr. .

Abstract

Background: Selection bias is common in clinic-based HIV surveillance. Clinics located in HIV hotspots are often the first to be chosen and monitored, while clinics in less prevalent areas are added to the surveillance system later on. Consequently, the estimated HIV prevalence based on clinic data is substantially distorted, with markedly higher HIV prevalence in the earlier periods and trends that reveal much more dramatic declines than actually occur.

Methods: Using simulations, we compare and contrast the performance of the various approaches and models for handling selection bias in clinic-based HIV surveillance. In particular, we compare the application of complete-case analysis and multiple imputation (MI). Several models are considered for each of the approaches. We demonstrate the application of the methods through sentinel surveillance data collected between 2002 and 2008 from India.

Results: Simulations suggested that selection bias, if not handled properly, can lead to biased estimates of HIV prevalence trends and inaccurate evaluation of program impact. Complete-case analysis and MI differed considerably in their ability to handle selection bias. In scenarios where HIV prevalence remained constant over time (i.e. β = 0), the estimated β^1 derived from MI tended to be biased downward. Depending on the imputation model used, the estimated bias ranged from -1.883 to -0.048 in logit prevalence. Furthermore, as the level of selection bias intensified, the extent of bias also increased. In contrast, the estimates yielded by complete-case analysis were relatively unbiased and stable across the various scenarios. The estimated bias ranged from -0.002 to 0.002 in logit prevalence.

Conclusions: Given that selection bias is common in clinic-based HIV surveillance, when analyzing data from such sources appropriate adjustment methods need to be applied. The results in this paper suggest that indiscriminant application of imputation models can lead to biased results.

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Figures

Figure 1
Figure 1
Examples of simulated data with high, medium and low degree of selection bias. Each line indicates the simulated HIV prevalence of a unique site.
Figure 2
Figure 2
HIV prevalence trend and number of ANC sites in 6 Indian States.

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References

    1. WHO. Towards universal access: scaling up priority HIV/AIDS interventions in the health sector. Geneva; 2010. (progress report 2010).
    1. UNAIDS. Scaling up access to HIV prevention, treatment, care and support: the next steps. 2006.
    1. UNAIDS. AIDS epidemic update: special report on HIV prevention. 2005.
    1. Gouws E, Mishra V, Fowler TB. Comparison of adult HIV prevalence from national population-based surveys and antenatal clinic surveillance in countries with generalised epidemics: implications for calibrating surveillance data. Sex Transm Infect. 2008;84:i17–i23. doi: 10.1136/sti.2008.030452. - DOI - PMC - PubMed
    1. Walker N, Garcia-Calleja JM, Heaton L, Asamoah-Odei E, Poumerol G, Lazzari S, Ghys PD, Schwartländer B, Stanecki KA. Epidemiological analysis of the quality of HIV sero-surveillance in the world: how well do we track the epidemic? AIDS. 2001;15:1545–1554. doi: 10.1097/00002030-200108170-00012. - DOI - PubMed

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