Race, presenting signs and symptoms, use of carotid artery imaging, and appropriateness of carotid endarterectomy.

Published

Journal Article

BACKGROUND AND PURPOSE: We sought to determine whether there are racial differences in use of carotid artery imaging after controlling for clinical factors and to ascertain racial differences in presenting signs and symptoms and overall appropriateness for carotid endarterectomy (CE). METHODS: We performed a retrospective cohort study of 803 patients older than 45 years, hospitalized between 1991 and 1994 at any of 4 Veterans Affairs Medical Centers, with a discharge diagnosis of transient ischemic attack or ischemic stroke. Clinical data were abstracted from the medical record, including presenting symptoms, diagnostic test results, and use of surgical procedures. Appropriateness for CE was determined according to RAND criteria. RESULTS: Black patients were more likely than white patients to present with stroke (78% versus 55%) but less likely to present with transient ischemic attack (22% versus 45%; P=0.001). There was no racial difference in medical comorbidity or preoperative risk. Black patients were less likely to have an imaging study of their carotid arteries (67% versus 79%; P=0.001). Race remained an independent predictor of imaging after adjustment for clinical factors (odds ratio=1.50; 95% CI, 1.06 to 2.13). Because of higher prevalence of significant carotid artery stenosis, whites were significantly more likely than blacks to be assessed as appropriate candidates for surgery with the use of RAND criteria (18% versus 4%; P=0.001). CONCLUSIONS: Use of carotid artery imaging, a critical step in determining eligibility for CE, is influenced by the patient's race after controlling for clinical presentation. Adjustment for appropriateness of CE reduces but does not eliminate the importance of race.

Full Text

Duke Authors

Cited Authors

  • Oddone, EZ; Horner, RD; Sloane, R; McIntyre, L; Ward, A; Whittle, J; Passman, LJ; Kroupa, L; Heaney, R; Diem, S; Matchar, D

Published Date

  • July 1999

Published In

Volume / Issue

  • 30 / 7

Start / End Page

  • 1350 - 1356

PubMed ID

  • 10390306

Pubmed Central ID

  • 10390306

International Standard Serial Number (ISSN)

  • 0039-2499

Language

  • eng

Conference Location

  • United States