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4.6 Cross-Cutting Summary Table

TherapyBest efficacy evidenceResponder definition usedKey safety issueAvailability 2025–2026Australia
nVNS (gammaCore)eCH acute: ACT2 48% vs 6% attacks pain-free at 15 min, p<0.01. cCH acute: no effect (ACT2 5% vs 13%). cCH preventive: PREVA 40% vs 8.3% ≥50% respondersVaries: pain-free at 15 min; ≥50% attack reductionBenign. Perioral myokymia ~7%; no serious device-related AEsAvailable, electroCore commercially healthyYes — ARTG 355575, Medistar. Prescription/authorisation only. NO subsidy. Price unpublished
SPG stimulation (Pulsante)CH-1: 67.1% vs 7.4% pain relief at 15 min. CH-2: 62.5% vs 38.9%, OR 2.62, p=0.008. Registry: 65% therapeutic respondersAcute responder; ≥50% frequency reduction; “therapeutic responder” (either)81% facial sensory disturbance (mostly transient, some permanent); 5 SAEs in CH-1NOT AVAILABLE anywhere. Realeve holds FDA Breakthrough designation only; >700 patients stranded since 2019No pathway
ONSOpen-label 53–69% responders; L-ICON 59% at ≥50% for ≥half of 4.2 yrs. But ICON found 30% dose = 100% dose, and Fogh-Andersen 2026 found placebo > burst ONS (p=0.042)≥50% (ICON/L-ICON); ≥30% (Fogh-Andersen)72% ≥1 SAE over 4.2 yrs; 50% needed further surgery; no biological SAEs. Modern technique far better (0 lead migrations in 45 pts)Available — the only CE-marked invasive CH optionPerformed in Australia at some centres for refractory cases; no specific data retrieved
DBS posterior hypothalamus74.3% responders (78/105); frequency −70.1%; intensity −50.6%. Only RCT was negative≥50% improvement in frequency and/or intensity1 death (<1%); major complications 16.67%; haemorrhage 0.93–3%; irreversible dysarthria and diplopia reported; transient diplopia 22%~108 published cases in 22 yrs; handful of tertiary centres; EAN makes no recommendationNo realistic pathway
Trigeminal section/rhizotomy76% long-term full/near-complete relief (17 pts)Informal1 death, CSF leaks, meningitis, 2 patients needed surgery for corneal anaesthesia to prevent blindness; anaesthesia dolorosaHistoricalNot offered
Gamma knife77% initial response; 42% persisting“Meaningful pain reduction” (undefined)58% trigeminal sensory disturbance; 6% deafferentation pain; irreversibleEssentially abandonedNot offered
MVD73.3% initial ≥50% relief; 46.6% long-term; 87.5% of redo operations failed≥50% relief“Minimal” morbidity per authors; posterior fossa craniotomyHistorical for CH; retained for TN and possibly SUNCT/SUNARarely
GON blockade4/14 good, 5/14 moderate, 5/14 noneInformalMinimal, reversibleWidely used; counts towards EHF refractoriness criteriaYes, routinely

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