This article examines clinical data management from a research context. It describes the experience of the authors' in the collation and analysis of computerized general practice records. In particular, the authors' examine some of the issues associated with obtaining consent, data deidentification, data quality, ownership, data value, and cost.
AndersonJGComputer-based ambulatory information systems: Recent developments. J Ambulatory Care Manage.2000;23(2):53–63.
3.
WalkerDBeilbyJMarleyJChamberlainNDuszynskiKRavetJFrankOHenningRZaninovichLBuckleyBQuayEMacIsaacP.Facing the future—clinical systems used for epidemiological research. [CD-ROM]. In: WalkerJWhettonSWiseMStarkK, eds HIC-99. Proceedings of the 7th Health Informatics Conference; 1999.Hobart, Australia: Health Informatics Society of Australia; 1999:333.
4.
MacIsaacP.Royal Australian College of General Practitioners. The Computer Assisted Practice Project 1986–1988: Final Report.Melbourne, Australia: Royal Australian College of General Practitioners, 1989.
5.
Royal Australian College of General Practitioners.Code of Practice for the Management of Health Information in General Practice.Melbourne, Australia: Royal Australian College of General Practitioners; 1998.
Commonwealth Department of Health and Aged Care.Personal Health Information in General Practice.Canberra, Australia: Australian Government Printing Service; 1998.
National Health and Medical Research Council.National Statement on Ethical Conduct in Research Involving Humans.Canberra, Australia: Commonwealth of Australia; 1999:vii.
11.
National Health and Medical Research Council.Epidemiological Research. In National Statement on Ethical Conduct in Research Involving Humans.Canberra, Australia: Commonwealth of Australia; 1999:40–42.
12.
National Health and Medical Research Council.NHMRC Guidelines Under Section 95 of the Privacy Act, 1988.Canberra, Australia: Australian Government Printing Service; 1988.
13.
Australian Pharmaceutical Advisory Council.APAC Privacy Principles for Programs Involving Use of Medication Data to Promote Quality Use of Medicines.Canberra, Australia: Australian Government Printing Service; 1996.
14.
MortensenC.Ethical issues: Australian national pharmaco-epidemiological database seminar 1996. Aust Pres.1997;20(Suppl 2):36–40.
15.
Australian Pharmaceutical Advisory Council.Principle 8 of the APAC Privacy Principles for Programs Involving Use of Medication Data to Promote Quality Use of Medicines.Canberra, Australia: Australian Government Printing Service; 1996.
16.
Commonwealth Department of Health and Aged Care.General Practice Data Model & Core Data Set Specification Project.Canberra, Australia: Australian Government Printing Service; 1999.
17.
Commonwealth Department of Health and Aged Care.Final Report of the General Practice Coding Jury.Canberra, Australia: Australian Government Printing Service; 2000.
18.
LambertsHWoodM, eds. ICPC, International Classification of Primary Care.Oxford: Oxford Medical Publications; 1987:201.
19.
BrittH.International Classification of Primary Care Plus Extensions (ICPC+).Sydney, Australia: University of Sydney; 1999.
National Electronic Health Records Taskforce.A Health Information Network for Australia.Canberra, Australia: Australian Government Printing Service, 2000:183–187.
22.
SilvermanBWSome Aspects of the Spline Smoothing Approach to Non-parametric Regression Curve Fitting. J Royal Stat Soc Series B.1985;47:1–52.
23.
ThompsonSGBarberJAHow should cost in pragmatic randomised trials be analysed?Br Med J.2000;320:1197–2000.