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| Chemical pathology |
1 Department of Clinical Biochemistry, Royal Infirmary Edinburgh, Room S6114, Level 2, 51 Little France Crescent, Edinburgh EH16 4SA, UK
2 Clinical Chemistry Department, Queens Hospital, Belvedere Road, Burton upon Trent, Staffordshire, DE13 0RB, UK
3 Department of Chemical Pathology, Guys and St Thomass Hospital, 5th Floor, North Wing, Lambeth Palace Road, London SE1 7EH, UK
Correspondence to:
Dr P J Twomey
Department of Clinical Biochemistry, Royal Infirmary Edinburgh, Room S6114 Level 2, 51 Little France Crescent, Edinburgh EH16 4SA, UK; taptwomey@aol.com
Keywords: information technology; analytical variation; chronic management; intra-individual variation; screening
| The first 150 words of the full text of this article appear below. |
Medicine is continuously changingscreening tools, diagnostic assays, and new medications and treatment modalities are rapidly being developed. However, in this age of super fast computers, one question that is not often asked is whether healthcare professionals are making the most of the currently available patient data? Chronic conditions such as diabetes mellitus, hypertension, and dyslipidaemia are increasing in prevalence at an alarming rate. At the same time, treatment guidelines are evolving and the audit of treatment targets is now being instituted as an objective means of measuring quality. However, there is relatively little research into the examination of the effects of such targets for individual patients as opposed to patient populations. We have previously shown that the effect of individual risk factor variation on screening for coronary heart disease can be considerable.1 So, how can we rationally overcome this variability in the monitoring of chronic clinical conditions? As
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