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Patient registry data for research: a basic practical guide

Bujang, Mohamad Adam and Ang, Swee Hung and Tg Abu Bakar Sidik, Tg Mohd Ikhwan and Adnan, Tassha Hilda and Sa'at, Nadiah and Hon, Yoon Khee and Alan Fong, Yean Yip and Ab Rahman, Jamalludin and Shah, Shamsul Azhar (2021) Patient registry data for research: a basic practical guide. Institute for Clinical Research, National Institute of Health, Ministry of Health Malaysia, Selangor, Malaysia. ISBN 9781005767600

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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 e-book/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.

Item Type: Book
Additional Information: 3297/89261
Uncontrolled Keywords: patient registry data, statistics, research, practical guide
Subjects: H Social Sciences > H Social Sciences (General) > H62 Study and teaching. Research
H Social Sciences > HA Statistics
H Social Sciences > HA Statistics > HA154 Statistical data
Kulliyyahs/Centres/Divisions/Institutes (Can select more than one option. Press CONTROL button): Kulliyyah of Medicine > Department of Community Medicine (Effective: 1st January 2011)
Kulliyyah of Medicine
Depositing User: nur hakimah a manan
Date Deposited: 19 May 2021 09:55
Last Modified: 19 May 2021 09:55
URI: http://irep.iium.edu.my/id/eprint/89261

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