E. Liozon et al., Risk factors of developing irreversible cranial ischemic complications in giant cell arteritis. A prospective study of 178 cases, REV MED IN, 22(1), 2001, pp. 30-41
Purpose. - To search for risk factors of developing irreversible cranial is
chemic complications (ICIC) in patients with giant cell arteritis (GCA) and
to explore whether two subsets of patients (high risk and low risk of deve
loping ICIC) can be defined.
Methods. - One-hundred seventy-eight consecutive patients with temporal art
eritis (149 biopsy-proven) were diagnosed and followed up in a department o
f Internal Medicine between 1976 and 1999. The patients were separated into
two groups, according to the presence or absence of ICIC, with comparison
of 17 clinical and biological parameters prospectively recorded for each pa
tient using a pre-established comprehensive questionnaire.
Results. - ICIC occurred in 25 patients (14%), with amaurosis in 22 cases.
Suggestive symptoms and/or signs of temporal arteritis were present in 92%
of the patients, lasting 50 days (median) before the onset of ICIC. Forty-t
hree patients (24%) complained of transient visual ischemic symptoms (TVIS)
, which preceded acute blindness in 11 cases. A multivariate logistic regre
ssion, from which 28 cases with upper limb artery involvement were excluded
for technical reasons (no CCII in any case, thus predicting perfectly the
lack of ischemic risk, P = 0.02), indicated that the only independent varia
bles associated with the ischemic risk were: a history of TVIS (P = 0.05),
the lack of signs of polymyalgia rheumatica (PMR; P = 0.02), lower blood le
vels of fibrinogen (P = 0.024) and higher mean blood platelets levels (P =
0.006). However, these five variables predicted only 30% of the variability
of the model. Sensitivity, specificity, positive and negative predictive v
alues of the model reached respectively 36, 96, 64 and 88%. Overall, 86% of
the cases were correctly classified with respect to the ischemic risk.
Conclusion. - The rate of ICIC should be reduced by an earlier recognition
of the usual signs of temporal arteritis. Several independent risk factors
of ICIC have been identified. However, the logistic model failed to predict
accurately the ischemic risk in 14% of the cases, indicating that as yet u
nrecognised factors probably exist that play a role in the occurrence of IC
IC. Nevertheless, regarding the strong association between platelet levels
and ICIC, patients with thrombocytosis should receive initially both cortic
osteroids and antiplatelet agents. (C) 2001 Editions scientifiques et medic
ales Elsevier SAS.