Book Open Access
<?xml version='1.0' encoding='utf-8'?> <resource xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns="http://datacite.org/schema/kernel-4" xsi:schemaLocation="http://datacite.org/schema/kernel-4 http://schema.datacite.org/meta/kernel-4.1/metadata.xsd"> <identifier identifierType="DOI">10.5281/zenodo.4722674</identifier> <creators> <creator> <creatorName>Mohamad Adam Bujang</creatorName> <nameIdentifier nameIdentifierScheme="ORCID" schemeURI="http://orcid.org/">0000-0001-6231-4062</nameIdentifier> <affiliation>Clinical Research Centre, Sarawak General Hospital, Institute for Clinical Research, NIH</affiliation> </creator> </creators> <titles> <title>Patient Registry Data for Research: A Basic Practical Guide</title> </titles> <publisher>Zenodo</publisher> <publicationYear>2021</publicationYear> <subjects> <subject>Patient Registry</subject> <subject>Disease Registry</subject> <subject>Clinical Research</subject> <subject>Medical Registry</subject> <subject>Research Data</subject> <subject>Biostatistics</subject> </subjects> <dates> <date dateType="Issued">2021-04-27</date> </dates> <language>en</language> <resourceType resourceTypeGeneral="Book"/> <alternateIdentifiers> <alternateIdentifier alternateIdentifierType="url">https://zenodo.org/record/4722674</alternateIdentifier> </alternateIdentifiers> <relatedIdentifiers> <relatedIdentifier relatedIdentifierType="DOI" relationType="IsVersionOf">10.5281/zenodo.4722673</relatedIdentifier> <relatedIdentifier relatedIdentifierType="URL" relationType="IsPartOf">https://zenodo.org/communities/crc_icr_nih</relatedIdentifier> </relatedIdentifiers> <rightsList> <rights rightsURI="https://creativecommons.org/licenses/by-nc/4.0/legalcode">Creative Commons Attribution Non Commercial 4.0 International</rights> <rights rightsURI="info:eu-repo/semantics/openAccess">Open Access</rights> </rightsList> <descriptions> <description descriptionType="Abstract"><p>Analysis of patient data can be a complicated and challenging process, especially when the data involve many subjects and many variables. A patient registry is a database that organizes collecting the important set of data on a list of identifiable individuals for a specific disease. This type of data usually has tons of data and hundreds of different variables. Thus, the approach to conducting research by using a patient registry database will be more complicated than the other types of dataset. Since the handling of patient registry data is a challenging task, the authors have come out with this book to become a guideline for the statisticians, medical officers and scientists for them to refer as a handbook whenever they need to use patient registry data for their research.</p></description> </descriptions> </resource>
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