Spectrochimica acta. Part B, Atomic spectroscopy·2021
Evaluating a thyroid function testing strategy, this study found that discretionary thyroid stimulating hormone (TSH) testing after total plasma thyroxine (tT4) measurement had similar abnormal rates whether lab-initiated or clinician-initiated. This suggests the testing strategy is effective for diagnosing hypothyroidism.
Area of Science:
Endocrinology
Clinical Chemistry
Diagnostic Medicine
Background:
Thyroid function testing is crucial for diagnosing thyroid disorders.
Primary hypothyroidism diagnosis often involves measuring thyroid stimulating hormone (TSH) and total plasma thyroxine (tT4).
Evaluating the effectiveness of diagnostic strategies is essential for optimizing patient care and resource allocation.
Purpose of the Study:
To retrospectively evaluate a thyroid function testing strategy involving discretionary thyroid stimulating hormone (TSH) assay after initial total plasma thyroxine (tT4) measurement.
To assess the diagnostic yield of TSH testing in relation to primary hypothyroidism diagnosis.
To compare TSH assay initiation by laboratory versus clinician/pathologist.
Main Methods:
Retrospective analysis of 14,641 tT4 and 6,887 TSH assays over a two-year period.
Categorization of TSH assays based on initiation source (laboratory, clinician, pathologist).
Analysis of TSH values in relation to tT4 levels and clinical information.
Main Results:
The percentage of elevated TSH values (over 5 mU/l) was comparable between laboratory-initiated (29%) and clinician/pathologist-initiated requests (23.2% and 23.6%).
Among patients with tT4 below 100 nmol/l without TSH requests, 5.3% had elevated TSH values.
A significant proportion of abnormal TSH results could be explained by unsubmitted clinical information.
Conclusions:
The discretionary TSH testing strategy following tT4 measurement demonstrates similar diagnostic utility regardless of request initiation.
The current strategy appears effective for identifying primary hypothyroidism.
Improved communication of clinical information to the laboratory could further refine TSH assay interpretation.