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This document provides structured forms for data abstraction related to articles discussing care coordination and systematic reviews. It includes questions designed to evaluate the article's relevance,
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How to fill out Appendix B: Sample Data Abstraction Forms

01
Gather required patient data.
02
Review the case definitions for the data you need to collect.
03
Open the Appendix B form and identify the sections to fill.
04
Enter the patient's demographic information in the appropriate fields.
05
Document clinical information as per the guidelines provided.
06
Fill in any laboratory results or imaging studies relevant to the case.
07
Input treatment details and outcomes based on the patient’s medical history.
08
Ensure all entries are legible and accurate.
09
Review the completed form for completeness and consistency.
10
Submit the form to the designated authority for processing.

Who needs Appendix B: Sample Data Abstraction Forms?

01
Researchers conducting clinical studies.
02
Healthcare professionals involved in data collection.
03
Persons coordinating quality assurance programs.
04
Regulatory agencies requiring standardized data reporting.
05
Organizations compiling health statistics and reports.
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Appendix B: Sample Data Abstraction Forms are standardized templates used to collect and organize specific data from various sources, providing a structured format for researchers or organizations to record information.
Organizations or individuals conducting research or evaluations that require standardized data collection protocols are typically required to file Appendix B: Sample Data Abstraction Forms.
To fill out Appendix B: Sample Data Abstraction Forms, follow the guidelines provided in the instructions, complete each section accurately with the relevant data, and ensure all necessary fields are filled before submission.
The purpose of Appendix B: Sample Data Abstraction Forms is to facilitate the systematic collection and reporting of data, ensuring consistency and accuracy in the information gathered for analysis.
The information that must be reported includes participant demographics, data related to the research subject, specific measurements, and any relevant outcomes as defined by the data collection protocol.
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