Venous Thromboembolism Clinical Trial
Official title:
Systematic Review and Meta-Analysis of Venous Thromboembolism Risk Assessment Models in Hospitalized Medical Patients
A systematic review and meta analysis will be performed of risk assessment models for Venous thromboembolism ("VTE" including pulmonary embolism "PE" and deep venous thrombosis "DVT")in hospitalized medical patients. The goal of this study is to evaluate whether the incidence of VTE is lower in patients that are evaluated with a risk assessment model and treated with thromboprophylaxis for their assigned level of risk.
Venous thromboembolism ("VTE" including pulmonary embolism "PE" and deep venous thrombosis
"DVT") is associated with significant morbidity and mortality. Only about half of eligible
hospitalized medical patients receive appropriate thromboprophylaxis. Understanding VTE risk
factors predictive of VTE among hospitalized medical patients may promote superior
thromboprophylaxis. To date a systematic review of VTE risk assessment strategies among
hospitalized medical patients, and a meta-analysis reporting the rate of VTE among patient
groups at varying levels of risk for VTE does not exist.
The investigators will use the Preferred Reporting Items for Systematic reviews and
Meta-Analyses (PRISMA) checklist for reporting systematic reviews and meta-analyses to
develop this systematic review and meta-analysis.
The investigators will perform a systematic review of the literature and report VTE risk
assessment models that have been derived and validated among hospitalized medical patients.
The investigators will perform a meta-analysis of studies that report a rate of VTE among
patients identified as being at elevated risk for VTE and those that are not. The
investigators pre-specify that they are going to analyze the prospective and retrospective
studies captured by the literature search in two ways. First, the investigators will perform
an analysis that groups both prospective and retrospective studies together. The
investigators will also perform an analysis that separates out the prospective and
retrospective studies. While this will decrease our sample size (and thus power), this
approach may allow us to identify any bias or confounding present due to the retrospective
study design and then control for it. Notably confirmation that both retrospective and
prospective studies identified the same findings would enhance the clinical usefulness of
our findings.
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