AI Article Synopsis

  • The study aimed to assess the prevalence of classic and non-calf intermittent claudication (IC) in patients without known atherosclerotic disease and their effectiveness in detecting peripheral arterial disease (PAD).
  • A total of 1,487 outpatients, primarily with diabetes or a higher cardiovascular risk, were evaluated using the Edinburgh Claudication Questionnaire and diagnostic ankle-brachial index (ABI) testing.
  • The findings showed that both types of IC had similar accuracy for detecting PAD, suggesting that integrating the questionnaire into patient evaluations could enhance PAD diagnosis, but confirmation with ABI is essential.

Article Abstract

Objectives: To evaluate the prevalence of both non-calf intermittent claudication (IC) and classic IC in patients with no known atherosclerotic disease, and their accuracy to detect peripheral arterial disease (PAD).

Design: Cross sectional, observational study conducted at 96 internal medicine services.

Materials And Methods: 1487 outpatients with no known atherosclerotic disease, and either diabetes or a SCORE risk estimation of at least 3% were enrolled. IC was assessed using the Edinburgh Claudication Questionnaire and PAD was confirmed by an ankle-brachial index (ABI) <0.9.

Results: Overall, 7.2% met criteria of classic and 5.8% of non-calf IC. PAD was diagnosed in 393 cases (26.4%). In these PAD patients, 17.8% exhibited classic and 13.2% non-calf IC. Both calf and non-calf IC had similar overall accuracy for detecting PAD. Considering both categories as a whole, the sensitivity of IC to predict a low ABI was 31% and the specificity 93%.

Conclusions: Non-calf IC is comparable to classic IC for the diagnosis of PAD in patients with no known arterial disease. The systematic implementation of Edinburgh Claudication Questionnaire could be a valuable call-to-action to improve clinical evaluation of PAD, bearing in mind that PAD detected by either non-calf or classic IC must be confirmed by ABI testing.

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Source
http://dx.doi.org/10.1016/j.ejim.2008.12.019DOI Listing

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