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Risk Factors for Permanent Visual Loss in Biopsy-proven Giant Cell Arteritis: A Study of 339 Patients. | LitMetric

Risk Factors for Permanent Visual Loss in Biopsy-proven Giant Cell Arteritis: A Study of 339 Patients.

J Rheumatol

From the Department of Internal Medicine, Le centre hospitalier et universitaire (CHU) Limoges, Limoges, France.E. Liozon, MD, Department of Internal Medicine, CHU Limoges; F. Dalmay, PhD, Department of Internal Medicine, CHU Limoges; F. Lalloue, PhD, Department of Internal Medicine, CHU Limoges; G. Gondran, MD, Department of Internal Medicine, CHU Limoges; H. Bezanahary, MD, Department of Internal Medicine, CHU Limoges; A.L. Fauchais, MD, PhD, Department of Internal Medicine, CHU Limoges; K.H. Ly, MD, PhD, Department of Internal Medicine, CHU Limoges.

Published: July 2016

AI Article Synopsis

  • - The study aimed to identify risk factors for permanent visual loss (PVL) in patients diagnosed with giant cell arteritis (GCA) over nearly 40 years, analyzing clinical and laboratory data from 339 patients.
  • - Key predictors for increased risk of PVL included older age, previous transient visual symptoms, and jaw claudication, while fever and rheumatic symptoms were associated with a significantly lower risk of visual loss.
  • - The findings indicate that clinical observations are crucial for estimating visual ischemic risk in GCA patients, emphasizing the necessity of prompt glucocorticoid treatment, as no patients were found to be entirely free of risk for visual loss.

Article Abstract

Objective: To determine the risk factors for permanent visual loss (PVL) in patients with biopsy-proven giant cell arteritis (GCA) and the usefulness of the factors in clinical practice.

Methods: From 1976 through 2015, the clinical charts and laboratory results of 339 patients with biopsy-proven GCA were recorded prospectively at the time of diagnosis. We used multivariable logistic regression analysis to determine which of 24 pretreatment characteristics were associated with PVL.

Results: Visual ischemic manifestations occurred in 108 patients, including PVL in 53 (16%), bilaterally in 15 patients (28%). The independent predictors associated with an increased risk of PVL were age (OR 1.06, 95% CI 1.01-1.12, p = 0.01), a history of transient visual ischemic symptoms (OR 2.62, 95% CI 1.29-5.29, p < 0.01), and jaw claudication (OR 2.11, 95% CI 1.09-4.10, p = 0.03). The presence of fever (OR 0.30, 95% CI 0.14-0.64, p < 0.01) and rheumatic symptoms (OR 0.23, 95% CI 0.10-0.57, p = 0.001) were associated with a markedly reduced risk of developing visual loss (3.7% if features were both present). No laboratory variables were independently associated with PVL.

Conclusion: The visual ischemic risk of untreated GCA can be readily estimated upon simple clinical findings, but not laboratory variables. However, we did not identify a subgroup of patients carrying no risk of developing visual loss. Glucocorticoid treatment remains, therefore, urgent for any patient with a high clinical suspicion index.

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Source
http://dx.doi.org/10.3899/jrheum.151135DOI Listing

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