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This document outlines the use of SRTR (Scientific Registry of Transplant Recipients) program-specific reporting tools, detailing their complementary roles in policymaking and patient care. It covers various aspects such as data sources, reporting formats for diverse audiences, analysis methods for incomplete data, and adjusting outcomes based on risk factors. Additionally, it reviews the advantages of using SRTR data over self-reported data, timelines for reports, and specific criteria for evaluating center performance. This guide is essential for improving transplant outcomes through informed decision-making.
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SRTR Products and Responsibilities Inferential Analyses to Support Policymaking and Patient Care
Program-Specific Reporting Different Formats for Different Audiences
Different Audiences, Different Questions: Different Statistics and Interpretations
Why Don’t We Have 1-Year Survival for Last Month’s Transplants?
Incomplete Data and Lost to Follow-UpSolution 1: Censored Data Methods
Incomplete Data and Lost to Follow-UpSolution 2: Extra Ascertainment
How Many Kidney Programs Have Better Outcomes for ECD than for SCD?
The Importance of AdjustmentCenter SizeLength of Follow-UpCase Mix
Center X Transplants More Older Recipients Than National Average