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Evidence-Based Laboratory reportingto clinicians

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RIMeL / IJLaM 2008; 4 (Suppl.)

112

Ricevuto: 03-09-2008 Pubblicato on-line: 13-10-2008

Corrispondenza a: Dott. Davide Giavarina, Laboratorio di Chimica clinica ed Ematologia, Ospedale Civile San Bortolo, Via Rodolfi n. 37, 36100 Vicenza, Italia. E-mail: davide.giavarina@ulssvicenza.it

Evidence-Based Laboratory reporting to clinicians

D. Giavarina

Clinical Pathology Dept., San Bortolo Hospital, Vicenza, Italy

The difference between an ‘Information’ and a ‘notice’

lies in the former’s ability to remove or significantly reduce someone’s uncertainty about something. In Laboratory Medicine, you have to know exactly how to ask a clinical question, i.e. what are you looking for, in order to get a plausible answer. A test result, the same test result, is going to get completely different information depending on the clinical context where you decided to order it, namely for screening or diagnosis rather than for monitoring or fol- low up. The first step in Evidence Based Laboratory Me- dicine is asking an answerable clinical question, e.g. using a popular tool as the Fagan’s nomogram you have to get some clinical (pre-test) information in order to evaluate the post-test probability. As a laboratory physician you must understand the clinical question; the other way round, cli- nicians must be aware of the more relevant pre-analytical, analytical and post-analytical issues. How the laboratory reports its results is paramount for clinicians to understand their real meaning. A typical Laboratory report is made of a list of figures sided by reference intervals, set to dimen- sion the biological signal. Common practice and profes- sional standards such as ISO 15189 and CPA UK both suggest the application of appropriate comments, accu- racy indicators, quality specifications, decision levels based upon biological variation or expert advice. Further im- provements of Lab reports are expected adding infor- mation on pre-analytical issues, such as serum indices of hemolysis, lipemia and jaundice, managing analytical infor- mation about tests and their performance, add on testing

(reflex), autoverification (faster reporting of results under

defined conditions) delta checks or range checks (helping

in detection of possible erroneous results), abnormality

flags (high, low, critical results), correlation to other rele-

vant results (both electronic and manual), interpretative

comments, computerized decision supports (artificial in-

telligence). All suitable tools to generate added valuable

clinical information in order to modify behavioral habits

and favor a more efficient and appropriate use of lab test

results. Unfortunately evidence supporting the clinical

advantage of these tools are still fair. Most often added

information derives from previous experience and is con-

sensus-based. Sometimes local or national regulations and

reccomandations from professional bodies help defining

a more evidence based approach but up to now a clear

benefit to the patient from an interpretative comment or

by data on test accuracy has never been proved, even thou-

gh the single physician likes to receive advice. In a survey

about the order of multiple coagulation tests whose resul-

ts were reported also by narrative interpretation, Laposata

et al could demonstrate time savings and/or improved

diagnostic workups in 80% of cases. While documenting

clinician’s needs is of importance, we still lack evidence

that answering these needs will get improved clinical ou-

tcome fot the patient. In summary, Laboratory physicians

are well aware that translational knowledge goes far beyond

the analytical quality and a sound laboratory report will

play a major role in the patient-centered healthcare of the

near future.

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