Is testing for inherited coagulation inhibitor deficiencies in young stroke patients worthwhile?

M Amiri1, J W Schmidley, L M Fink

  • 1Department of Neurology, University of Arkansas for Medical Sciences and Central Arkansas Veterans Healthcare System, Mail Stop 500, 4301 West Markham, 72205, Little Rock, AR, USA.

Insights

Testing for inherited coagulation inhibitor deficiencies like protein C, protein S, and antithrombin III is unlikely to be beneficial in young stroke patients without a clear family or medical history suggesting such disorders.

Area of Science:

  • Neurology
  • Hematology
  • Genetics

Background:

  • Cerebral infarcts in young adults can have various causes.
  • Inherited thrombophilias are potential risk factors for arterial ischemic stroke.
  • Screening for coagulation inhibitor deficiencies is considered in specific patient populations.

Purpose of the Study:

  • To evaluate the diagnostic yield of laboratory testing for inherited deficiencies of protein C, protein S, and antithrombin III.
  • To assess the hypothesis that such testing is low in young patients (<50 years) with first arterial ischemic cerebral infarcts and no suggestive family or medical history.

Main Methods:

  • A cohort of 55 patients under age 50 with a first arterial ischemic cerebral infarct was studied.
  • Systematic laboratory investigation for deficiencies in protein C, protein S, and antithrombin III was performed.

Main Results:

  • No deficiencies in protein C or antithrombin III were identified in the study cohort.
  • One patient exhibited a deficiency in protein S, deemed likely acquired rather than inherited.

Conclusions:

  • The laboratory search for inherited deficiencies of protein C, protein S, and antithrombin III yields limited results in young stroke patients lacking clinical indicators of a prothrombotic state.
  • Routine screening for these specific inherited coagulation disorders may not be cost-effective in this patient group.
Abstract

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