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The decomposition approach involved four stages that serially introduced (a) the binary marker for reporting any hospital episodes in the year prior to baseline, (b) the binary marker for whether post-baseline hospitalizations for ACSCs occurred, (c) the fifteen covariates, and finally, (d) the propensity score adjustment for potential selection bias.
Note that these AHRs were adjusted for the binary marker for reporting any hospital episodes in the year prior to baseline, the binary marker for whether post-baseline hospitalizations for ACSCs occurred, the fifteen covariates, and the propensity score adjustment for potential selection bias.
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The CESD-8 was transformed into markers for reporting two or more symptoms, or for not having been asked these items, vs. the reference category of reporting none or only one of the symptoms.
Here we present a standard developed by the Genomic Standards Consortium GSCC) for reporting marker gene sequences the minimum information about a marker gene sequence (MIMARKS).
As the evaluation of candidate prognostic markers is often limited by inadequate study design and analyses, formal recommendations for reporting tumour marker prognostic studies (REMARK) have now been agreed upon (McShane et al, 2005).
Our study was conducted and reported according to Reporting recommendations for tumor marker prognostic studies (REMARK) criteria for reporting tumor biomarker prognostic studies [ 23].
Reporting of plasma OPN measurements and analysis was completed using the National Cancer Institute and European Organization for Research and Treatment of Cancer recommendations for reporting tumour marker prognostic studies (McShane et al, 2006).
We used published guidelines for reporting tumor marker studies and quality metrics for evaluating studies to include in the cancer-related meta-analyses [ 9, 11].
We have adhered to the REMARK [ 47] recommendations for reporting tumour marker studies as these criteria create a coherent and transparent framework for the reporting a wider range of study designs [see Supplementary table S7 in Additional file 3].
Guidelines for reporting tumor markers (REMARK) were used as outlined (see Additional file 1: Table S1).
Guidelines for reporting tumor markers (REMARK) [ 17] were used, as outlined in Additional file 1.
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