Please use this identifier to cite or link to this item: http://ir.mu.ac.ke:8080/jspui/handle/123456789/3345
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dc.contributor.authorMwangi, Ann W.-
dc.contributor.authorSiika, Abraham-
dc.date.accessioned2020-08-05T09:21:00Z-
dc.date.available2020-08-05T09:21:00Z-
dc.date.issued2017-
dc.identifier.urihttp://ir.mu.ac.ke:8080/jspui/handle/123456789/3345-
dc.description.abstractThe timing of antiretroviral therapy (ART) initiation for HIV and tuberculosis (TB) co-infected patients needs to be considered carefully. CD4 cell count can be used to guide decision making about when to initiate ART. Evidence from recent randomized trials and observational studies generally supports early initiation but does not provide information about effects of initiation time on a continuous scale. In this paper, we develop and apply a highly flexible structural proportional hazards model for characterizing the effect of treatment initiation time on a survival distribution. The model can be fitted using a weighted partial likelihood score function. Construction of both the score function and the weights must accommodate censoring of the treatment initiation time, the outcome, or both. The methods are applied to data on 4903 individuals with HIV/TB co-infection, derived from electronic health records in a large HIV care program in Kenya. We use a model formulation that flexibly captures the joint effects of ART initiation time and ART duration using natural cubic splines. The model is used to generate survival curves corresponding to specific treatment initiation times; and to identify optimal times for ART initiation for subgroups defined by CD4 count at time of TB diagnosis. Our findings potentially provide ‘higher resolution’ information about the relationship between ART timing and mortality, and about the differential effect of ART timing within CD4 subgroupsen_US
dc.language.isoenen_US
dc.publisherWileyen_US
dc.subjectAntiretroviral therapyen_US
dc.subjectElectronic health records;en_US
dc.subjectInformative censoringen_US
dc.subjectInverse weightingen_US
dc.subjectMarginal structural modelen_US
dc.subjectTime-varying confoundersen_US
dc.titleModeling the causal effect of treatment initiation time on survival: Application to HIV/TB Co-infectionen_US
dc.typeArticleen_US
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