The quality of laboratory aspects of troponin testing in clinical practice guidelines and consensus documents needs
Kristin M Aakre1, Michel R Langlois2, Julian H Barth3
1Laboratory of Clinical Biochemistry, Haukeland University Hospital, Bergen, Norway; The Norwegian Clinical Chemistry EQA Program, Bergen, Norway; The European Federation of Clinical Chemistry and Laboratory Medicine and European Union of Medical Specialists joint working group on Guidelines.
Insights
Clinical practice guidelines often lack standardized information on troponin testing for acute coronary syndrome diagnosis. This study highlights the need for updated guidelines addressing analytical and biological issues in troponin assays.
Area of Science:
- Clinical Chemistry
- Laboratory Medicine
- Cardiology
Background:
- Standardizing laboratory test descriptions in clinical practice guidelines (CPGs) is crucial for consistent patient care.
- The European Federation of Laboratory Medicine (EFLM) and Union of European Medical Specialists (UEMS) proposed a checklist for this purpose.
Purpose of the Study:
- To evaluate existing CPGs for chest pain and acute coronary syndrome diagnosis against the EFLM-UEMS checklist.
- To identify gaps and inconsistencies in the reporting of troponin assays within these guidelines.
Main Methods:
- A systematic review of nine CPGs or consensus documents published between 2011 and 2013.
- Evaluation of these documents using the standardized checklist for laboratory investigations.
Main Results:
- CPGs frequently discuss troponin testing for acute coronary syndrome but provide variable and vague information.
- Key checklist items are often omitted or outdated, particularly regarding analytical quality goals for high-sensitivity assays and potential interferences.
- Inconsistencies can lead to diagnostic uncertainty.
Conclusions:
- Current CPGs require updates to accurately reflect analytical and biological aspects of troponin assays.
- Recommendations are provided for improved analytical quality goals to enhance diagnostic accuracy in CPGs.
Objective:
The European Federation of Laboratory Medicine (EFLM) and the Union of European Medical Specialists (UEMS) joint Working Group on guidelines recently proposed a checklist to help standardize the description of laboratory investigations in clinical practice guidelines (CPG).
Methods:
Nine CPGs or consensus documents published from 2011 to 2013 describing the investigation of chest pain, diagnosis of acute coronary syndrome, or myocardial infarction were evaluated against the published checklist.
Results:
Clinical use of troponin analysis are commonly dealt with but the publications present variable, vague and sometimes conflicting information regarding this laboratory test being very much relied on upon making a diagnosis of acute coronary syndrome. Most of the laboratory related checklist items are not considered or need to be updated e.g. suggested analytical quality goals are not applicable for the high sensitive assays and important interferences that may lead to false positive or negative diagnoses are commonly not mentioned.
Conclusion:
The current paper sums up important analytical and biological issues related to troponin assays and gives suggestions for analytical quality goals that could be included in CPG's.
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