Craniocervical flexion test in patients with migraine: Discriminative validity and accuracy
Fecha
2021
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Wiley
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Objectives: To evaluate the discriminative validity and provide a clinical cut-off
of the
craniocervical flexion test (CCFT) in migraineurs stratified by the report of neck pain,
headache-related
disability and neck disability.
Methods: Fifty women without headache and 102 women with migraine were
recruited by convenience from a local tertiary care setting. Migraine diagnosis
followed the International Classification of Headache Disorders. All volunteers
underwent the CCFT. Patients with migraine answered the Migraine Disability
Assessment (MIDAS) and Neck Disability Index (NDI) questionnaires. Discriminative
validity was verified by group comparison, and the clinical cut-off
was obtained and
classified according to the diagnostic accuracy of the CCFT.
Results: The CCFT presented discriminative validity for comparing control (median
= 28, IQR = 6) with migraine (median = 26, IQR = 4, P = .01) and migraine with
neck pain (median = 26, IQR = 4, P = .01), but not among the migraine subtypes with
disability by migraine or neck pain-related
disability on the MIDAS and NDI. The diagnostic
accuracies were classified between poor and not discriminating with the area
under the receiver operating characteristic curve ranging from 57% to 69% and non-acceptable
values of sensitivity, specificity and positive and negative likelihood ratios.
Conclusion: The CCFT can discriminate asymptomatic controls from migraine patients
with and without neck pain. However, it cannot discriminate patients with migraine
according to their pain-related
disability. Also, the CCFT does not offer an
optimal cut-off
value in migraine patients adequate to clinical practice.
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Rodrigues A, Florencio LL, Martins J, Bragatto MM, Fernández-de-Las-Penãs C, Dach F, Bevilaqua-Grossi D. Craniocervical flexion test in patients with migraine: Discriminative validity and accuracy. Int J Clin Pract. 2021 Jul;75(7):e14248. doi: 10.1111/ijcp.14248. Epub 2021 May 1. PMID: 33884715.
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