Håkan Ashina1,2, David W Dodick3. 1. Danish Headache Center, Department of Neurology, Faculty of Health and Medical Sciences, Rigshospitalet Glostrup, University of Copenhagen, Copenhagen, Denmark. 2. Department of Neurorehabilitation/Traumatic Brain Injury, Rigshospitalet, Copenhagen, Denmark. 3. Department of Neurology, Mayo Clinic, Scottsdale, AZ, USA. dodick.david@mayo.edu.
Abstract
PURPOSE OF REVIEW: Post-traumatic headache is a common sequela of injury to the head and/or neck. Here, we review the current approach to pharmacologic management of post-traumatic headache and explore the therapeutic promise of targeting calcitonin gene-related peptide signaling to address unmet treatment needs. RECENT FINDINGS: The scarcity of data from controlled trials has left clinicians to rely on mainly expert opinion for the pharmacologic management of post-traumatic headache. The current view is that a phenotype-guided approach should be used, in which patients are treated according to the primary headache phenotype that their clinical features resemble the most (e.g. migraine, tension-type headache). Moreover, incremental advances are being made in the field that aim to identify possible cellular and molecular drivers of headache persistence. Calcitonin gene-related peptide has emerged as a key drug target which, in turn, has prompted novel insights on the potential importance of early initiation of pharmacologic treatment following the onset of post-traumatic headache. This, in turn, might prevent subsequent persistence and chronification of headache.
PURPOSE OF REVIEW: Post-traumatic headache is a common sequela of injury to the head and/or neck. Here, we review the current approach to pharmacologic management of post-traumatic headache and explore the therapeutic promise of targeting calcitonin gene-related peptide signaling to address unmet treatment needs. RECENT FINDINGS: The scarcity of data from controlled trials has left clinicians to rely on mainly expert opinion for the pharmacologic management of post-traumatic headache. The current view is that a phenotype-guided approach should be used, in which patients are treated according to the primary headache phenotype that their clinical features resemble the most (e.g. migraine, tension-type headache). Moreover, incremental advances are being made in the field that aim to identify possible cellular and molecular drivers of headache persistence. Calcitonin gene-related peptide has emerged as a key drug target which, in turn, has prompted novel insights on the potential importance of early initiation of pharmacologic treatment following the onset of post-traumatic headache. This, in turn, might prevent subsequent persistence and chronification of headache.
Authors: Håkan Ashina; Anna K Eigenbrodt; Tad Seifert; Alexandra J Sinclair; Ann I Scher; Henrik W Schytz; Mi Ji Lee; Roberto De Icco; Alan G Finkel; Messoud Ashina Journal: Lancet Neurol Date: 2021-06 Impact factor: 44.182
Authors: Håkan Ashina; Afrim Iljazi; Faisal M Amin; Messoud Ashina; Richard B Lipton; Henrik W Schytz Journal: J Headache Pain Date: 2020-11-19 Impact factor: 7.277
Authors: Håkan Ashina; Afrim Iljazi; Haidar M Al-Khazali; Thien Phu Do; Anna K Eigenbrodt; Eigil L Larsen; Amalie M Andersen; Kevin J Hansen; Karoline B Bräuner; Basit Ali Chaudhry; Casper E Christensen; Faisal Mohammad Amin; Henrik W Schytz Journal: J Headache Pain Date: 2022-10-17 Impact factor: 8.588