4.6 Article

Is Erythrocyte Sedimentation Rate Necessary for the Initial Diagnosis of Giant Cell Arteritis?

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LIFE-BASEL
卷 13, 期 3, 页码 -

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MDPI
DOI: 10.3390/life13030693

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giant cell arteritis; biomarkers; C-reactive protein; platelet count; erythrocyte sedimentation rate; diagnostic test accuracy; sequential biomarker analysis

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Giant cell arteritis (GCA) is an ophthalmological emergency that requires prompt treatment. A study investigated the diagnostic value of platelet count, C-reactive protein (CRP), and erythrocyte sedimentation rate (ESR) in patients with suspected GCA. The results showed that platelet count and CRP can be used for initial evaluation without waiting for ESR, allowing faster decision-making.
Giant cell arteritis (GCA) is an ophthalmological emergency that can be difficult to diagnose and prompt treatment is vital. We investigated the sequential diagnostic value for patients with suspected GCA using three biochemical measures as they arrive to the clinician: first, platelet count, then C-reactive protein (CRP), and lastly, erythrocyte sedimentation rate (ESR). This retrospective cross-sectional study of consecutive patients with suspected GCA investigated platelet count, CRP, and ESR using diagnostic test accuracy statistics and odds ratios (ORs) in a sequential fashion. The diagnosis was established by experts at follow-up, considering clinical findings and tests including temporal artery biopsy. A total of 94 patients were included, of which 37 (40%) were diagnosed with GCA. Compared with those without GCA, patients with GCA had a higher platelet count (p < 0.001), CRP (p < 0.001), and ESR (p < 0.001). Platelet count demonstrated a low sensitivity (38%) and high specificity (88%); CRP, a high sensitivity (86%) and low specificity (56%); routine ESR, a high sensitivity (89%) and low specificity (47%); and age-adjusted ESR, a moderate sensitivity (65%) and moderate specificity (65%). Sequential analysis revealed that ESR did not provide additional value in evaluating risk of GCA. Initial biochemical evaluation can be based on platelet count and CRP, without waiting for ESR, which allows faster initial decision-making in GCA.

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