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Effectiveness of adding additional tests and/or comments to laboratory reports in a patient population, referred by general practitioners to the clinical chemistry laboratory.

Recruiting
Conditions
As the procedure involves the inspection of all (abnormal) reports by a laboratory specialist, all related diseases will be subject to this investigation.
Registration Number
NL-OMON23047
Lead Sponsor
Dr. Wytze P. OosterhuisArts Klinische Chemie, EpidemioloogAtrium Medisch Centrum ParkstadKlinische ChemiePostbus 44466401 CX Heerlen
Brief Summary

/A

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Not specified
Target Recruitment
400
Inclusion Criteria

The study will be restricted to those cases, in which abnormal test results require additional testing and/or comments, according to the laboratory specialist.

Exclusion Criteria

Cases in which there is substantial risk for the patient and normally (following the existing protocol) the lab would either send an urgent fax message to the practice or the laboratory specialist would directly make a telephone call to the general practitioner.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
In every case where a report with comments is generated (both in control and study groups), the following data will be collected:<br /><br>1. Following laboratory reports;<br /> <br>2. Following treatments, referrals;<br /> <br>3. Other additional diagnostic procedures and patient data from the general practitioner.
Secondary Outcome Measures
NameTimeMethod
A panel (consisting of medical specialists) will be asked to answer the following questions:<br /> <br>1. How useful were the additional tests and comments for the patient?;<br /><br>2. What was the benefit for the patient in terms of health improvement?;<br /> <br>3. Was the treatment adequate in the control group, without additional information reported to the general practitioner? This will be graded from negative to positive.
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