Vasculitis & polymyalgia rheumatica

Comparison of four clinical risk prediction models for the diagnosis of giant cell arteritis: results from the ongoing PREDICT-GCA study

RMD OpenPublished Diagnostic accuracy study

Authors' conclusion

Clinical prediction models for the diagnosis of GCA differ in their diagnostic accuracy. Clinically relevant discordances of individual risk prediction are common.

Study context

Population
Patients enrolled in the ongoing prospective PREDICT giant cell arteritis (GCA) study, all undergoing temporal artery biopsy plus detailed clinical and sonographic workupanalysed
Participants
70 patients
Comparison
Four clinical prediction rules for GCA: Ing et al model, Southend GCA Probability Score, Bhavsar-Khalidi Score, PREDICT score
Outcome
Diagnostic accuracy (2×2 contingency tables and ROC analysis) vs final diagnosis based on 6-month follow-up (ambiguous cases judged by independent expert panel)
Follow-up
6 months
Methodological detailsprospective, ongoing
  • Prospective
  • Ongoing

Performance

As reported in the abstract

Diagnostic accuracy (AUC, NPV)
Test or modelAUCNPV
Ing et al model0.8486.7%
Southend GCA Probability Score0.7478.6%
Bhavsar-Khalidi Score0.7573.7%
PREDICT score0.7077.8%

AUC

Ing et al model0.84
Southend GCA Probability Score0.74
Bhavsar-Khalidi Score0.75
PREDICT score0.70

NPV

Ing et al model86.7%
Southend GCA Probability Score78.6%
Bhavsar-Khalidi Score73.7%
PREDICT score77.8%

Further findings

Clinically significant discordance in risk categorisation (low vs non-low risk by different scores)

Patients with discordant categorisation
37.5%
Discordant patients less frequently had clinical symptoms and signs of cranial GCA (all p<0.01)
Rate of visual impairment did not differ from patients with consistent risk estimation

Original publication

Comparison of four clinical risk prediction models for the diagnosis of giant cell arteritis: results from the ongoing PREDICT-GCA study. RMD Open. Published 25 September 2026. doi:10.1136/rmdopen-2026-006932

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