Page 57 - PATIENT REGISTRY DATA FOR RESEARCH: A Basic Practical Guide
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(NORM), National Suicide Registry Malaysia (NSRM), National Database on Children and

               Adolescent with Diabetes (DiCARE), and many more. All the registries aim to recruit


               patients at a national level, which are initiated by hospitals and Ministry of Health Malaysia.

               (Please see Appendix 1).


                       Finally, this book concludes with a summary which provides a recommended

               step-by-step guide of the flow of this procedure (as presented in Figure 5.1) and also a


               structured checklist (as presented in Table 5.1) that can be very useful for guiding and

               facilitating a statistician for conducting research by using data obtained from a patient


               registry database.
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