Key result
Ten commercial procalcitonin immunoassays demonstrated highly significant correlation (r=0.918-0.997, p<0.001) but highly variable bias (±0.2% to ±38.6%) and limited agreement at clinical thresholds.
Why the study?
This study was designed to verify the comparability of procalcitonin values among 10 different commercial immunoassays.
Observational (n=176)
Yes
Effect estimate: Correlation coefficients 0.918 to 0.997
p-value: p=<0.001
Despite acceptable correlation among 10 commercial PCT immunoassays, limited agreement at clinical decision thresholds, especially at lower concentrations, may jeopardize the clinical value of the biomarker.
PCT variability across assays warrants result interpretation caution; leaves open standardization needs for clinical and research use.
Background This two-center study was designed to verify comparability of procalcitonin (PCT) values among 10 different commercial immunoassays. Methods A total number of 176 routine lithium-heparin plasma samples were divided in identical aliquots and simultaneously analyzed with 10 different PCT immunoassays, including Kryptor BRAHMS PCT sensitive, Abbott Architect BRAHMS PCT, Beckman Coulter Access PCT (on Access and DXI), BioMérieux Vidas BRAHMS PCT, Diasorin Liaison BRAHMS PCT, Fujirebio Lumipulse G BRAHMS PCT, Roche BRAHMS PCT (on Cobas E801), Diazyme PCT (on Roche Cobas C702) and SNIBE Maglumi PCT. Results Highly significant correlation was always found across multiple comparisons, with correlation coefficients comprised between 0.918 and 0.997 (all p < 0.001). Bland and Altman plots analysis revealed highly variable bias among immunoassays, ranging between ±0.2% and ±38.6%. Diazyme PCT on Roche Cobas C702 and SNIBE Maglumi PCT displayed the larger overestimation, whilst PCT values were underestimated by Cobas BRAHAMS PCT. The agreement was always >80% (all p < 0.001), but varied largely across multiple comparisons, ranging between 90%-99% at 0.1 μg/L, 81%-99% at 0.25 μg/L, 83%-100% at 0.5 μg/L, 94%-100% at 2.0 μg/L and 90%-99% at 10 μg/L, respectively. The larger disagreement was observed comparing Diazyme PCT and Maglumi PCT with the other methods. Conclusions Although we found acceptable correlation among 10 commercial PCT immunoassays, the limited agreement at clinical decision thresholds remains a major issue, especially at lower end of PCT concentration, thus potentially contributing to jeopardize the clinical value of this biomarker.
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Lippi et al. (2019) reported an observational. 10 commercial procalcitonin (PCT) immunoassays was evaluated on Comparability of procalcitonin (PCT) values (Correlation coefficients 0.918 to 0.997, p=<0.001). Ten commercial procalcitonin immunoassays demonstrated highly significant correlation (r=0.918-0.997, p<0.001) but highly variable bias (±0.2% to ±38.6%) and limited agreement at clinical thresholds.
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