Data from the 1970s is not always relevant to the present day.

This discussion is about specific admission profiles tailored to the needs of consultants and clinical teams. It is not about running the same 18 channel SMA profile on every admission. The admission profile really consists of the tests which should be requested anyway on these patients. In terms of lab finance it is a better use of expensive manpower to measure amylase on every A&E admission for abdo pain than to find and reanalyse the sample for an add-on.

 

Mike Collins

BMS3

Biochemistry Automation

Norfolk & Norwich University Hospital

England

http://www.nnuh.nhs.uk/

 


From: Clinical biochemistry discussion list [mailto:[log in to unmask]] On Behalf Of John Doran (ABMU NHS Trust)
Sent: 26 September 2008 15:18
To: [log in to unmask]
Subject: Re: Admission tests

 

There was some similar data from Australia in the 1970's too. Why do we persist in trying to (re)invent the square wheel?

John

 

From: Clinical biochemistry discussion list [mailto:[log in to unmask]] On Behalf Of gordon challand
Sent: 26 September 2008 15:14
To: [log in to unmask]
Subject: Re: Admission tests

 

Dear Trevor

It is amazing how things tend to go full circle! More than 30 years ago Tom Whitehead's group did a careful study on the benefits associated with 'biochemical profiling' on admission (based I believe on the old Technicon 6-60 and 12-60 analyzers - a battery of some 18 analytes). They came to the conclusion that this increased rather than decreased average hospital stay, mainly owing to the need to investigate the 'unexpected abnormalities' which cropped up which required further investigation. There was no evidence to support your 'best opinion (which was then, and I believe still is widely accepted)!

with best wishes

Gordon Challand

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