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Trigeminal autonomic cephalalgias: diagnostic and therapeutic developments
Peter J Goadsby1, Elisabetta Cittadini, Brian Burns
1Headache Group, Department of Neurology, University of California, San Francisco, San Francisco California 94143-0114, USA. peter.goadsby@ucsf.edu
Current Opinion in Neurology
|May 3, 2008
Summary
Recent research on trigeminal autonomic cephalalgias, including cluster headache and SUNCT/SUNA, highlights distinct attack patterns and the critical role of accurate diagnosis for effective, targeted treatments.
Area of Science:
- Neurology
- Headache Medicine
Background:
- Trigeminal autonomic cephalalgias (TACs) are a group of primary headache disorders characterized by unilateral head pain associated with cranial autonomic features.
- Key TACs include cluster headache, paroxysmal hemicrania, short-lasting unilateral neuralgiform headache attacks with conjunctival injection and tearing (SUNCT/SUNA), and hemicrania continua.
Purpose of the Study:
- To review and summarize recent research advancements in the diagnosis and treatment of TACs.
- To differentiate the clinical characteristics of various TAC syndromes.
Main Methods:
- Literature review of recent studies on trigeminal autonomic cephalalgias.
- Comparative analysis of attack duration, frequency, and phenotypic features across different TACs.
Main Results:
- Cluster headache: Longest attack duration, low frequency.
- Paroxysmal hemicrania: Intermediate duration and frequency.
- SUNCT/SUNA: Shortest duration, highest frequency.
- Hemicrania continua: Continuous pain with autonomic exacerbations.
- Accurate diagnosis is crucial due to highly selective and effective treatment responses.
Conclusions:
- Significant progress has been made in understanding and managing TACs.
- Neurologists should be aware of the latest diagnostic criteria and therapeutic strategies for these debilitating headache disorders.
