Experimental activation of the sphenopalatine ganglion provokes cluster-like attacks in humans. (July 2013)

• Record Type: Journal Article
• Authors: Schytz, Henrik W; Barløse, Mads; Guo, Song; Selb, Juliette; Caparso, Anthony; Jensen, Rigmor; Ashina, Messoud
• Is Part Of: Cephalalgia. Volume 33:Number 10(2013)
• Page Start: 831
• Page End: 841
• Publication Date: 2013-07
• Subjects: Cluster headache -- neurostimulation -- sphenopalatine ganglion -- headache model -- autonomic nervous system; Headache -- Periodicals; 616.8491
• DOI: 10.1177/0333102413476370
• Languages: English
• ISSNs: 0333-1024

Abstract

Background: High frequency (HF) stimulation of the sphenopalatine ganglion (SPG) is an emerging abortive treatment for cluster headache (CH) attacks. HF SPG stimulation is thought to exert its effect by physiologically blocking parasympathetic outflow. We hypothesized that low frequency (LF) SPG stimulation may activate the SPG, causing increased parasympathetic outflow and thereby provoking cluster attacks in CH patients. Methods: In a double-blind randomized cross-over study, seven CH patients implanted with an SPG neurostimulator were randomly allocated to receive HF or LF stimulation for 3 min on 2 separate days. We recorded headache characteristics and autonomic symptoms during and after stimulation. Results: Six patients completed the study. Three out of six patients (50%) reported ipsilateral cluster-like attacks during or within 30 min of LF SPG stimulation. These cluster-like attacks were all successfully treated with the therapeutic HF SPG stimulation. One out of six reported a cluster-like attack with 3 min HF SPG stimulation, which was also successfully treated with continued HF therapeutic SPG stimulation. Discussion: LF SPG stimulation may induce cluster-like attacks with autonomic features, which can subsequently be treated by HF SPG stimulation. Efferent parasympathetic outflow from the SPG may initiate autonomic symptoms and activate trigeminovascular sensory afferents, which may initiate the onset of pain associated with CH.