Comparison of Centor and McIsaac scores in primary care: a meta-analysis over multiple thresholds

Brian H Willis1, Dyuti Coomar1, Mohammed Baragilly1

  • 1Institute of Applied Health Research, University of Birmingham, Birmingham.

Insights

Centor and McIsaac scores offer fair, equivalent performance in diagnosing group A beta-haemolytic streptococcus (GABHS) pharyngitis. A score of ≤0 may effectively rule out GABHS infection, but further tests are needed to confirm positive cases.

Area of Science:

  • Infectious Diseases
  • Diagnostic Accuracy
  • Primary Care Medicine

Background:

  • Group A beta-haemolytic streptococcus (GABHS) pharyngitis is common in primary care.
  • Centor and McIsaac scores are clinical prediction rules used to estimate GABHS likelihood.
  • A direct meta-analysis comparing these scores was previously lacking.

Purpose of the Study:

  • To conduct a meta-analysis comparing the diagnostic accuracy of Centor and McIsaac scores for GABHS in primary care patients with pharyngitis.
  • To evaluate the performance of these scores across multiple thresholds.

Main Methods:

  • A meta-analysis of diagnostic test accuracy studies was performed.
  • Studies were identified through comprehensive database searches (MEDLINE, EMBASE, PsycINFO) from 1980-2019.
  • Data from 10 Centor and 8 McIsaac score studies were synthesized using summary receiver operating characteristic (SROC) curves and calibration analysis.

Main Results:

  • The area under the SROC curve for the McIsaac score was 0.7052 and for the Centor score was 0.6888.
  • Statistical analysis indicated no significant difference in performance between the two scores (P=0.419).
  • Both scores exhibited poor calibration, suggesting limitations in accurately predicting positive GABHS cases.

Conclusions:

  • Centor and McIsaac scores demonstrate fair and comparable diagnostic discrimination for GABHS.
  • The findings suggest that a Centor or McIsaac score of ≤0 may be useful for ruling out GABHS infection.
  • Poor calibration necessitates the use of additional point-of-care tests for confirming GABHS diagnoses.
Abstract

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