ABSTRACT
Background
Craniofacial pain (CFP) poses a burden on patients and health care systems. It is hypothesized that ketamine, an N-methyl-d-aspartate (NMDA) receptor antagonist, can reverse central sensitization associated with causation and propagation of CFP. This systematic review aims to assess the role of ketamine for CFP.
Methods
Databases were searched for studies published up to September 26, 2022, investigating the efficacy of ketamine for adults with CFP. Primary outcome was the change in pain intensity at 60 min postintervention. Two reviewers screened and extracted data. Registration with PROSPERO was performed (CRD42020178649).
Results
Twenty papers (six randomized controlled trials [RCTs], 14 observational studies) including 670 patients were identified. Substantial heterogeneity in terms of study design, population, dose, route of administration, treatment duration, and follow-up was noted. Bolus dose ranged from 0.2–0.3 mg/kg (intravenous) to 0.4 mg/kg (intramuscular) to 0.25–0.75 mg/kg (intranasal). Ketamine infusions (0.1–1 mg/kg/h) were given over various durations. Follow-up was short in RCTs (from 60 min to 72 h) but longer in observational studies (up to 18 months). Ketamine by bolus treatment failed to reduce migraine intensity but had an effect by reducing intensity of aura, cluster headache (CH), and trigeminal neuralgia. Prolonged ketamine infusions showed sustainable reduction of migraine intensity and frequency of CH attacks, but the quality of the evidence is low.
Conclusion
Current evidence remains conflicting on the efficacy of ketamine for CFP owing to low quality and heterogeneity across studies. Ketamine infusions are suggested to provide sustained improvement, possibly because of prolonged duration and higher dosage of administration. RCTs should focus on the dose–response relationship of prolonged ketamine infusions on CFP.
KEYWORDS: craniofacial pain, headache, migraine, cluster headache, trigeminal neuralgia, trigeminal neuropathy, ketamine, chronic pain
RÉSUMÉ
Contexte: La douleur crânio-faciale représente un fardeau pour les patients et les systèmes de soins de santé. L’hypothèse a été émise que la kétamine, un antagoniste du récepteur N-méthyl-D-aspartate (NMDA), peut inverser la sensibilisation centrale associée à la causalité et à la propagation de la douleur crânio-faciale. Cette revue systématique vise à évaluer le rôle de la kétamine dans la douleur crânio-faciale.
Méthodes: Les bases de données ont été consultées pour y repérer les études publiées jusqu’au 26 septembre 2022 qui portaient sur l’efficacité de la kétamine chez les adultes atteints de douleur crânio-faciale. Le critère de jugement principal était le changement de l’intensité de la douleur 60 minutes après l’intervention. Deux évaluateurs ont examiné et extrait les données. L’inscription auprès de PROSPERO a été réalisée (CRD42020178649).
Résultats: Vingt articles (six essais contrôlés randomisés, 14 études observationnelles) incluant 670 patients ont été répertoriées. Une hétérogénéité considérable en matière de devis d’étude, de population, de dose, de voie d’administration, de durée du traitement et de suivi a été notée. La dose bolus variait de 0,2 à 0,3 mg/kg (voie intraveineuse) à 0,4 mg/kg (voie intramusculaire) et à 0,25-0,75 mg/kg (voie intranasale). Les perfusions de kétamine (0,1-1 mg/kg/h) étaient administrées sur différentes durées. Le suivi était court dans les études contrôllées randomisées (de 60 min à 72 h) mais plus long dans les études observationnelles (jusqu’à 18 mois). La kétamine par traitement bolus n’a pas réussi à réduire l’intensité de la migraine mais a eu un effet en réduisant l’intensité de l’aura, la céphalée en grappe et la névralgie du trijumeau. Les perfusions de kétamine prolongées ont montré une réduction durable de l’intensité de la migraine et la fréquence des crises de CH, mais la qualité des données probantes est faible.
Conclusions: Les données probantes actuelles demeurent contradictoires sur l’efficacité de la kétamine pour la douleur crânio-faciale en raison de la faible qualité et de l’hétérogénéité des études. Il est suggéré que les perfusions de kétamine procurent une amélioration soutenue, peut-être en raison de leur durée prolongée et de leur posologie d’administration plus élevée. Les essais contrôlés randomisés devraient se concentrer sur la relation dose-réponse des perfusions prolongées de kétamine sur la douleur crâno-faciale.
Introduction
Description of the Condition
Craniofacial pain (CFP) is common, with a lifelong incidence of 96%, and poses a significant burden on patients’ quality of life and the health care system.1–4 Despite the availability of a variety of treatment modalities, many patients experience unsatisfactory pain relief and/or adverse effects from existing pharmacological interventions or cannot afford expensive treatments.3,5
It is hypothesized that CFP syndromes share a mechanism of central sensitization as a cause for pain. Central sensitization is characterized by an increase in neuronal excitability secondary to repetitive stimulation of the nociceptive C-fibers in the trigeminocervical complex and the brain, which is mediated by the activation of N-methyl-d-aspartate (NMDA) receptors.6–8 Activation of the NMDA receptors plays a major role in ongoing pain, opioid-induced hyperalgesia, and mood dysregulation, and it is considered the principal receptor involved in the phenomena of central sensitization and “wind-up,” resulting in hyperalgesia, allodynia, and spontaneous pain.9,10 This central sensitization can be reversed by blockade of these receptors by noncompetitive NMDA antagonists such as ketamine.6,7,10,11
Ketamine is a chemical derivative of phencyclidine with analgesic, dissociative, and psychomimetic properties.12 Its primary mechanism of action is as a noncompetitive antagonist of the NMDA receptors residing in the central nervous system.10,13 Ketamine is a versatile drug that can be administered via many routes, including intravenous (IV) and intramuscular (IM) but also oral, intranasal, inhalation, topical, and rectal, rendering it an easy agent for out-of-hospital care. It can be given as a single bolus or infusion or a combination of both. Although its potency is comparable to that of opioids, ketamine has a much better safety profile and is less likely to lead to development of tolerance. Possible adverse effects of ketamine include hypertension and tachycardia, hallucinations, and hepatic toxicity with chronic exposure.14
Ketamine has successfully been used in the treatment of complex chronic pain states such as complex regional pain syndrome and neuropathic pain,11 but its therapeutic role in CFP has not been completely established. Therefore, the objective of this systematic review was to evaluate the efficacy of ketamine for the treatment of CFP and examine its effects on pain-associated domains.
Methods
Registration
This systematic review was conducted according to the recommendations of the Cochrane Collaboration and was reported as per the Preferred Reporting Items for Systematic Reviews and Meta-Analysis (PRISMA) guidelines. The protocol of this systematic review was registered with PROSPERO (ID CRD42020178649).
Data Sources and Search Strategy
We conducted a comprehensive search of the literature from inception to February 1, 2020. Updated searches were conducted over the same databases and clinical trial registries on November 3, 2020, and September 26, 2022, with the assistance of a medical information specialist (M.E.).
The following databases were searched: Embase (1947–), MEDLINE (1946–), MEDLINE ePubs, In-Process and Other Non-Indexed Citations, Cochrane Database of Systematic Reviews (2005–), Cochrane Central Register of Controlled Trials (1991–), and PubMed-NOT-MEDLINE. We also searched Web of Science Core Collection (1900–; Clarivate Analytics) and Scopus (1960–; Elsevier). Clinical trial registries, ClinicalTrials.Gov, and the World Health Organization International Clinical Trials Registry Platform were searched to identify trials.
We restricted our search to human subjects with moderate-to-severe pain. For Embase, MEDLINE, Cochrane CENTRAL, and Scopus, both controlled vocabulary terms (Embase-Emtree; MEDLINE-MeSH) and text word searching were conducted for each of the following segments: (“ketamine” or related synonyms) AND (“headache” or “migraine” or “cluster headache” or “facial pain” or “short-lasting unilateral neuralgiform headache attacks with conjunctival injection and tearing (SUNCT)” or “short-lasting unilateral neuralgiform headache attacks with cranial autonomic symptoms (SUNA)” or “trigeminal neuralgia” or “trigeminal autonomic cephalalgia (TAC)” or “occipital neuralgia” or “cephalalgia” or other related terms). The most recent Ovid Medline search strategy and the MEDLINE search strategy are provided in Appendix 1.
Inclusion/Exclusion Criteria
The studies were screened for eligibility based on title, abstract, and subsequently full manuscript. Studies were included if they met the selection criteria as listed below.
Population
This review included studies of human subjects ≥18 years of age with a CFP (primary headache or neuropathic facial pain) diagnosis that fit the criteria of the International Classification of Headache Disorders third edition.15 Studies that investigated effects of ketamine on a mixed population of patients with pain for which data on CFP could not be extracted separately were excluded. No restrictions were put in terms of chronicity, frequency, or duration of the attack. An initial restriction of including participants with only moderate-to-severe pain was waived at the start of the title screening process because of fear of selection bias.
Intervention
The intervention was defined as bolus/infusion administration of ketamine of any dose or administration type (IV, IM, subcutaneous, intranasal, epidural, sublingual, rectal, oral). Studies in a perioperative setting and/or with mixed combinations of ketamine with another drug were excluded. There was no limit on the duration of treatment or number of treatments.
Comparator
Comparators included no treatment, placebo treatment, or conventional medical management, which could include pharmacological, physical, psychological, and/or interventional therapies.
Outcome
The primary outcome was the change in intensity of pain assessed on a numeric rating scale (NRS)/visual analog scale (VAS) at 60 min after the intervention. Secondary outcomes included (1) positive response (defined as a reduction in pain score by ≥30% from baseline at 60 min after the intervention) and effect of ketamine infusion on (2) pain intensity (NRS/VAS) at any time after the intervention up to 6 months posttreatment, (3) adverse effects, (4) functional outcome, (5) quality of life, (6) mood, and (7) patient satisfaction. The threshold of >30% pain relief has been demonstrated to constitute clinically meaningful improvement.16 The initial restriction of 6 months’ follow-up time was extended to 18 months at the time of data collection.
Study Selection Process
All citations were independently screened on title and abstract for eligibility by two reviewers (Y.H. and P.K.) as per the inclusion criteria. Covidence17 was used as a systematic review management tool. Papers of interest were then full-text screened. Of the selected papers, data were independently extracted by two reviewers (T.M. and M.P.). Any disagreement was resolved through discussion with the senior author (P.K.).
Data Extraction
The reference data, populations, and outcomes were extracted from the articles into prespecified tables on a standardized data collection form in Word that was pilot tested before use. Extracted data for each study included general characteristics (publication year, design, number of arms), patient characteristics (number, demographics, and sample size), clinical information (diagnosis, duration, pain intensity), details of intervention and comparator (dose and administration regimen), data on primary and secondary outcomes of interest, follow-up time points, and adverse effects.
Assessment of Quality as Risk of Bias
Two review authors (Y.H. and M.P.) independently assessed the risk of bias for randomized controlled trials using the Cochrane Risk of Bias tool 2.0.18 Any disagreement was resolved through discussion with the senior author (P.K.). The Robins-I was used to assess the risk of bias in observational studies.19 For case reports/case series, the Quality Appraisal Tool for Case Series was used.20
Data Synthesis and Analysis
We narratively synthesized the characteristics of all studies that met inclusion criteria. Study characteristics and treatment details were summarized. For continuous data, means (or medians) and standard deviations (or interquartile ranges or ranges) were extracted. No meta-analysis was performed because of the heterogeneity of data, low quality, and small sample sizes of included studies.
Results
Search Results
A total of 2080 unique articles were retrieved from all searches, of which 1956 were excluded at the screening stage. During the initial search, 72 full texts were assessed for eligibility, of which 14 papers were deemed to meet all eligibility criteria for inclusion in this review (Figure 1). During the following searches, 9 additional full texts were selected and assessed, of which 6 papers met all eligibility criteria for inclusion in this review (Figure 2).
Figure 1.
PRISMA flow diagram.
Figure 2.
PRISMA flow diagram for updated systematic reviews.
The 20 papers included in our review, reporting on 670 patients in total, included the following studies: Six randomized controlled trials (RCTs)21–26 and 14 observational studies, of which 5 were prospective cohort studies,27–31 3 were retrospective cohort studies,32–34 3 were case series,35–37 and 3 were case reports, were included38–40 (Tables 1 and 2).
Table 1.
Characteristics of studies included in the systematic review: participants, interventions, comparators, and outcome measures.
Study (patient n) | Participants: Age, gender, diagnosis, duration of pain | Intervention, route, and dose | Comparator, route, and dose | Outcomes measured |
---|---|---|---|---|
RCTs | ||||
Rabben et al.21 (n = 30) Crossover trial |
Mean age (range): 57.6 years (29–89) F/M: 26/4 Diagnosis: Trigeminal neuropathy Mean duration of symptoms (range): 6 years (0.5–20) Baseline NRS ≥ 25/100 |
Week 1: One injection of IM K 0.4 mg/kg + midazolam 0.05 mg/kg Week 2: One injection of IM pethidine 1.0 mg/kg + midazolam 0.05 mg/kg Week 3: Oral K 4 mg/kg QHS × 3 days |
Week 1: One injection of IM pethidine 1.0 mg/kg + midazolam 0.05 mg/kg Week 2: One injection of IM K 0.4 mg/kg + midazolam 0.05 mg/kg Week 3: Placebo × 3 days |
Primary: NRS Secondary: Adverse effects |
Afridi et al.23 (n = 18) |
Mean age (range): 35 years K vs. 39 years C (18–55) F/M: 14/4 F: 77.8% K vs. 77.8% C Diagnosis: Migraine with aura Mean number of migraine-years: 14.6 years K vs. 21.9 years C Mean duration of aura (range): 30 h (18–72) K vs. 13 h (6–31) C Mean number of attacks per year: 21.7 K vs. 22.4 C Severity score without treatment: 9.5 K vs. 11 C |
Intranasal K: One dose 25 mg (for three attacks) No treatment for three attacks |
Intranasal midazolam: One dose 2 mg (for three attacks) No treatment for three attacks |
Primary: Duration of aura attack Secondary: Severity of aura attack |
Etchinson et al.25 (n = 34) |
Mean age (SD): 38.5 years (13.75) K vs. 30.5 (8.3) C (range 18–65 years) F/M: 26/8 F: 81% K vs. 72% C Diagnosis: Migraine without or with aura Headache duration >24 h: 31% K vs. 33% C Migraine without aura: 47% K vs. 50% C Migraine with aura: 33% K vs. 17% C Probable migraine without aura: 13% K vs. 17% C Probable migraine with aura: 7% K vs. 17% C Baseline severe pain intensity: 88% K vs. 67% C |
IV K 0.2 mg/kg; one dose | IV NS, equivalent amount in mL to IV K; one dose | Primary: Between-group difference in NRS score reduction from baseline to 30 min Secondary: Functional disability scores, categorical pain scores, pain, rescue medication, patient satisfaction, SERSDA side effects |
Zitek et al.24 (n = 54) |
Mean age (SD): 32.3 years (10.3) K vs. 37.4 years (10.4) C (range 18–65) Diagnosis: Primary headache at ER admission F/M: 38/16 F: 82.6% K vs. 78.3% C Mean (SD) baseline VAS: 77.8 (14.6) K vs. 78.3 (17.7) C Mean (SD) baseline VAS anxiety: 37.8 (35.7) K vs. 46.1 (36.4) C Mean (SD) baseline VAS nausea: 47.1 (33.0) K vs. 47.6 (35.2) C |
K 0.3 mg/kg IV (diluted in 5 mL NS) + ondansetron 4 mg IV (diluted in 2 mL NS) | Prochlorperazine 10 mg IV (diluted in 5 mL NS) + diphenhydramine 25 mg IV (diluted in 2 mL NS) | Primary: Between-group mean VAS difference at 60 min Secondary: Changes in VAS pain at other FU times, admission rate, side effects, rescue medication use, patient satisfaction |
Benish et al.22 (n = 53; 27/26) |
Age (range): 31 years (25–42) K vs. 35 years (27–43) C (range 18–65 years) F/M: 37/16 F: 73.1% K vs. 66.7% C Diagnosis: Primary headache at ER admission Hx of migraine: 84.6% K vs. 81.5% C Mean (SD) baseline VAS: 73.5 (17.5) K vs. 74.5 (16.2) C Self-reported pain severity of >5/10 |
IV: 1000 mL NaCl + intranasal K: First dose 0.75 mg/kg Repeat dose: 0.25 mg/kg |
IV: 1000 NS + 10 mg metoclopramide + 25 mg diphenhydramine + intranasal NS |
Primary: Pain intensity at 30 mins Secondary: Rescue medication, side effects, hospital admission, return to care within 72 h, patient satisfaction |
Sarvari et al.26 (n = 140) |
Age: 41.6 ± 16.6 years F/M: 75/65 F: 55.3% K vs. 52.9% C Diagnosis: Primary headache (migraine, tension, and CH) Hx of headache: 67% K vs. 49% C Self-reported pain severity of ≥4/10 Mean (SD) baseline VAS: 8.0 (1.1) K vs. 9.0 (0.7) C (P < 0.05) |
IV: 1000 mL NaCl + intranasal K: 0.75 mg/kg (maximum 75 mg) | IV: 30 mg ketorolac + intranasal NS (0.015 mL/kg, maximum 1.5 mL) | Primary: Pain intensity at 60 min Secondary: Side effects, vital signs |
Observational studies | ||||
Mathisen et al.28 (n = 7) P |
Age range: 42–79 years F/M: 7/0 Diagnosis: Trigeminal neuropathy Duration: 1–21 years Baseline pain score: Severe |
Bolus of IV/IM 0.4–1 mg/kg ± infusion of 0.25–0.5 mg/kg/30’ | N/A | Primary: Pain intensity Secondary: Adverse effects |
Rabben and Øye27 (n = 17) P |
Age (range): 32–88 years F/M: 13/4 Diagnosis: Neuropathic orofacial pain Duration: 6 months–28 years Baseline pain score: NP |
Bolus of IM K 0.4 mg/kg with 0.05 mg/kg midazolam, followed by 3 days of oral K 4 mg/kg QHS | N/A | Primary: Pain intensity Secondary: Adverse events |
Granata et al.29 (n = 29) P |
Mean age (SD): 44 years (NP) F/M: 2/27 Diagnosis: chronic or episodic CH Duration: 1–18 years Frequency of attacks: 2–8/day Episodic/chronic CH: 16/13 Baseline pain score: NP |
IV infusion 0.5 mg/kg over 1 h, every 2 weeks. In total one to four treatments | N/A | Primary: Attack frequency Secondary: Attack intensity, responder rate |
Pomeroy et al.30 (n = 77) R |
Mean age (range): 40.6 years (16–65) F/M: 57/20 Diagnosis: CM: 63/77 NDPH: 14/77 MOH: 37/77 Median baseline pain score: 7.1 |
Mean length of ketamine infusion: 4.8 days (range 2–9) Mean K rate: 0.53 mg/kg/h (range 0.08–1.25) |
N/A | Primary: Responder rate Secondary: Adverse events |
Schwenk et al.31 (n = 61) R |
Mean age (range): 42.4 years (20–65) F/M: 17/44 Diagnosis: Migraine: 59/61 (96.7%) CH: 2/61 (3.3%) Mean (SD) baseline pain score: 7.5 (0.2) |
5-day IV infusion of 1 mg/kg/h max Mean length of infusion: 5.1 days (SD 0.1) Mean weight: 85.4 (SD 0.6) mg/h Mean infusion rate: 43.7 mg/h (SD 4.2) |
N/A | Primary: Pain intensity; secondary: responder rate, adverse events |
Petersen et al.30 (n = 23; 20/3) |
Age: 49 (27–59) vs. 53 (30, 60) F/M: 5/15 vs. 2/1 Diagnosis: CCH Mean duration (years): 19 vs. 15 Median (range) baseline pain score: 10 (7–10) vs. 8 (7, 10) |
Intranasal K 15 mg/dose; given every 6 min. Five doses max | Patient with CCH with no attack | Primary: >50% NRS reduction at 15 min after first dose Secondary: >50% NRS reduction at 30 min; effect on autonomic symptoms, rescue medication, adverse events |
Schwenk et al.33 (n = 6) Pilot P |
Age: 20–55 years F/M: 3/3 Diagnosis: Refractory chronic migraine Mean baseline pain score: 7.5 ± 2.2 C vs. 7.4 ± 1.4 K |
5-day IV infusion K 1 mg/kg/h max Mean maximum K infusion rate on day 5: 72.5 ± 10.4 mg/h |
5-day IV infusion IV lidocaine: 1 mg/min (max 4 mg/min) Mean lidocaine infusion rate on day 4: 2.5 ± 0.7 mg/min |
Primary: Pain intensity Secondary: Rescue medications, side effects |
Ray et al.34 N = 83 (33/50) R |
Mean age: 42.9 ± 16.2 C vs. 42.2 ± 13.9 K F/M: 69/14 F/M: 78% C vs. 90.9% K Diagnosis: Migraine: 77/83 NDPH: 3/83 SUNCT: 2/83 CH: 1/83 Mean baseline VAS Migraine: 44.1 Mean number of previously failed preventative medications: 5.8 ± 3.8 C vs. 8.7 ± 4.1 K (P = 0.013) Mean number of comorbidities: 2.8 ± 2.5 C vs. 4.1 ± 2.9 (P = 0.024) |
IV infusions: K started at 7 mg/h, max of 24 mg/h Mean duration: 5.1 (1.5) days |
IV infusions: lidocaine: 2 mg/h mean duration: 6.2 (2.4) days |
Primary: 50% or more reduction in pain intensity at the end of infusion Secondary: 30-day readmission, side effects |
Case series/case reports | ||||
Kaube et al.35 (n = 11) |
Age range: 18–47 years F/M: 5/1 Diagnosis: FHM Baseline pain score: Severe |
Intranasal K 25 mg; one dose at commencement of migraine aura 25 attacks were treated |
N/A | Primary: Aura intensity Secondary: Time to cessation of aura, duration of aura, severity of motor deficit, presence or absence of visual hemifield disturbance and dysphagia, progression from one system to another |
Lauritsen et al.36 (n = 6) |
Median age (range): 36.5 (29–54) F/M: 5/1 Diagnosis: Chronic migraine without aura Median age at migraine onset (range): 17 years (8–29) Median duration of illness (range): 17 years (12–46) Mean number of failed acute migraine treatments (range): 18 (14–26) Mean baseline pain score: 9.5/10 |
IV K infusion of 0.1 mg/kg/h, increased by 0.1 mg/kg/h every 3–4 h as tolerated until the pain score of 3/10 was achieved, maintained for 8 h | N/A | Primary: Pain intensity Target end point: Achievement of VAS ≤3/10 for at least 8 h, timing of target point |
Moisset et al.38 (n = 2) |
45-year-old male Diagnosis: Chronic intractable CH Duration: 6 years, 6 attacks/day 28 years old male Diagnosis: CCH Duration: 6 years, 1–7 attacks/day |
IV infusion 0.5 mg/kg over 2 h + MgSO4 IV infusion 3000 mg over 30 min | N/A | Primary: Attack frequency |
Aggarwal39 (n = 1) |
58-year-old male Diagnosis: SUNCT Duration: 6 years, 100 attacks/day |
SC K infusion 6 mg/h × 6 days followed by SL 25 mg TID | N/A | Primary: Attack frequency Secondary: Medication use |
Moisset et al.37 (n = 17) |
Mean age (range): 35.2 ± 8.1 years (23–50) F/M: 3/14 Diagnosis: CCH Duration: 6.6 ± 4.3 years Mean number of daily attacks: 4.3 ± 2.4 |
IV K infusion 0.5 mg/kg × 2 h + MgSO4 3 g | N/A | Primary: Number of daily attacks day 7 Secondary: Percentage of responders, adverse events, vital signs |
Shiiba et al.40 (n = 1) |
56-year-old male Diagnosis: SUNCT |
IV K 0.4 mg/kg × 1 h × 7 days, then twice/month, then once/month | N/A | Primary: Attack frequency Secondary: Attack intensity, side effects |
C = comparator; (C)CH = (chronic) cluster headache; CM = chronic migraine; ER = emergency room; FHM = familial hemiplegic migraine; FU = follow-up; Hx = history; K = ketamine; MgSO4 = magnesium sulfate; N/A = not applicable; NaCl = sodium chloride; NDPH = new daily persistent headache; NP = not provided; NS = normal saline; q = every; QHS = at bedtime; SC = subcutaneous; SERSDA = Side Effects Rating Scale for Dissociative Anesthetics; SL = sublingual; TID = three times daily; P = prospective; R = retrospective.
Table 2.
Characteristics of studies included in the systematic review: Follow-up times, outcomes, and adverse effects.
Study (patient n) | Follow-up time points | Results: Primary outcome | Results: Secondary outcomes | Adverse effects |
---|---|---|---|---|
Randomized controlled trials | ||||
Rabben21 (n = 30) |
IM protocol: q1h for first day and at day 3 Oral protocol: 3 days |
K superior At 60 min: pain relief with K > C: n = 9/26 VAS compared to baseline at 60 min: 63.2% ± 24.3 K vs. 76.9% ± 21.9 C (P < 0.02) Long-lasting (>12 h) pain relief with K > C: n = 8/26 Oral K: 5/8 long-lasting responders to IM K reported pain relief with oral K |
N/A | K: Nausea, n = 2 (7.7%); dizziness, n = 18 (69.2%); sedation, n = 18 (69.2%); blurred vision, n = 16 (61.5%); xerostomia, n = 16 (61.5%); feelings of insobriety, n = 25 (96.1%); altered hearing, n = 4 (15.4%); hallucinations, n = 6 (23.1%) C: Nausea, n = 5 (19.2%); dizziness, n = 17 (65.4%); sedation, n = 14 (53.8%); blurred vision, n = 5 (19.2%); xerostomia, n = 17 (65.4%); feelings of insobriety, n = 12 (46.1%); altered hearing, n = 1 (3.8%); hallucinations, n = 0 Oral group: Adverse effects only in patients not asleep within 30 min of administration |
Afridi23 (n = 18) |
FU after six aura-attacks (three treated with intranasal K/midazolam, three treated with placebo) |
K superior Duration of attacks: 3 h (2–46) shorter in K vs. placebo; 3 h (0–15) shorter in M vs. placebo |
Severity of attack: K vs. placebo: difference was 1.5 (−0.5 to 2.5) on the clinical severity scale, suggesting baseline attack worse than treated attack M vs. placebo: difference was −0.5 (−0.7 to 1.5), suggesting that the attack was no different on treatment |
K: 5 subjects described feelings of unreality, euphoria or mild giddiness Midazolam: 4 subjects reported transient sedation or giddiness |
Etchinson25 (n = 34) |
At 30 and 60 min |
No statistically significant difference between groups Between-group median NRS difference at 30 min: 1.0 (IQR 0, 2.25; P = 0.0215) K vs. 2.0 (IQR 0, 3.75; P = 0.0034); ESD −1.0 (−2, 1.0), P = 0.5035 |
Mean categorical pain score change from baseline at 30 min: 0.56 (95% CI 0.44–0.68) K vs. 0.72 (95% CI 0.61–0.83) C; ESD 0.16 (95% CI −0.85–0.53) Mean functional disability score change from baseline at 30 min: 0.44 (95% CI 0.32–0.56) K vs. 0.39 (95% CI 0.30–0.48) C; ESD −0.05 (−0.59, 0.69) Patient satisfaction at 60 min: 62% K vs. 72% C Patient desires same treatment in the future: 62% K vs. 44% C Rescue medication requested at 30 min: 69% K vs. 78% C |
SERSDA for generalized discomfort: Greater in K arm at baseline (P = 0.0247) and at 30 min (P = 0.008) SERSDA for fatigue: Greater in K arm at 60 min (P = 0.0216) No significant difference in side effect severity at 30 min between K and placebo arms 88% of K subjects had Ramsay score = 2 at 30 min |
Zitek24 (n = 54) |
At 15, 30, 45, and 60 min |
Comparator superior Mean VAS score at 60 min: 34.3 K vs. 14.8 C; MD −19.5 (−37.8 to −1.3, P = 0.03) |
Mean VAS score at 15 min: 38.7 K vs. 50.9 C; MD 12.2 (95% CI −6.2 to 30.7) Mean VAS score at 30 min: 45.8 K vs. 31.8 C; MD −14.1 (−31.1 to 3.0) Mean VAS score at 45 min: 39.8 K vs. 22.2 C; MD −17.6 (−35.7 to 0.59) Requirement for rescue medications: 47.8% K vs. 28.6% C; MD 19.2% (95% CI −7.1 to 45.6) Admission to hospital: 8.7% K vs. 3.6% C; MD 5.1% (95% CI −8.3 to 18.5) Satisfaction at FU (scale 0–10): 4.9 K vs. 8.3 C; MD 3.4 (95% CI 1.2–5.6) Headache at FU: 50% K vs. 30% C; MD 20% (95% CI −10.6 to 50.6) |
Development of subjective restlessness: 13.0% K vs. 10.7% C; MD 2.3% (95% CI −15.6 to 20.2) Vomiting during collection period: 13.0% K vs. 7.1% C; MD 5.9% (95% CI −10.9 to 22.7) Patient withdrawal from study: K group: n = 2; prochlorperazine group: n = 1 |
Benish22 (n = 53;27/26) |
In ED: at 15, 30, 60 min After ED: at 48–72 h post-ED discharge |
No statistically significant difference between groups Mean VAS at 30 min: C 22.2 (SD 24) vs. K 29 (SD 21.6); ESD 6.8 (95% CI: −5.8 to 19.4) |
Median VAS score at discharge: C 2 (range 0–4) vs. K 1 (range 0–4) ESD 0 (−1 to 1) Median VAS score at 72 h: C 0 (range 0–0) vs. K 0 (range 0–0); ESD (0–0) Required second dose: C 11.5% vs. K 51.9% Rescue medication: C 30.8% (14.3–51.8) vs. K 22.2% (8.6–42.3); ESD −8.5 (−33.2–16.1) Required admission for headache: C 11.5% (3.2–29.8) vs. K 3.7 (0.0–19.8); ESD −7.3 (−22.5 to 6.9) Returned to ED within 72 h: C 11.5 (3.2–29.8) vs. K 0 (0–14.8); ESD −11.5 (−24.1 to 1.0 In control arm, 80.8% received ketorolac and 26.9% received DXM Patient satisfaction: C 9 (8–10) vs. K 9 (7–10); ESD (−1 to 1) |
Adverse event rate: 66.7% (CI 46–83.5%) K vs. 65.4% (95% CI 44.3–82.8) C |
Sarvari26 (n = 140) |
At 30, 60, and 120 min |
K superior At 60 min: Mean VAS K < C: K 2.07 ± 0.2 vs. C 2.42 ± 0.7 (P < 0.001) |
At 30 min: Mean VAS K < C: K 3.47 ± 0.5 vs. C 4.98 ± 0.7 (P < 0.001) At 120 min: Mean VAS K = C: K 1.10 ± 0.3 vs. 1.00 ± 0.0 |
Dizziness: K 11 (15.71%) vs. C 2 (2.86%), P = 0.009 Nausea: K 8 (11.43%) vs. C 2 (2.86%), P = 0.049 Heart rate rising: K 28 (40%) vs. C 11 (15.71%), P = 0.001 Blood pressure rising: K 9 (12.86%) vs. C 23 (32.86%), P = 0.005 |
Observational studies | ||||
Mathisen,28 (n = 7) P |
q15min until 80 min posttreatment |
No change Two patients: Pain-free for 1 day posttreatment One patient: Pain-free for 3 days posttreatment Four patients: No treatment effect |
N/A | Blurred vision, 6 (85.7%); altered hearing, 4 (57.1%); dizziness, 7 (100%); illusions, 4 (57.1%); dreams, 3 (42.9%); hallucinations, 3 (42.9%) All side effects subsided 30 min after treatment |
Rabben,27 (n = 17) P |
30 min after IM dose 1 day after oral dose |
Improved IM K: 4/17 patients: no analgesia; 7/17: <60 min: analgesia (not quantified); 6/17: > 60 min: mean pain reduction 80% Oral K: 5/13: no analgesia Responders to IM also responded to oral dose |
N/A | IM K: 17/17 had some level of side effects: sedation, blurry vision, dry mouth. 4/17 dropped out due to side effects Oral K: 4/13 |
Granata,29 (n = 29) P |
At 18 months |
Improved CCH: 7/13: complete resolution of attacks for 3–18 months. Onset: 1–2 weeks after final treatment; 4/13: no improvement; 1/13: excluded due to spontaneous symptom improvement before intervention Episodic CH: 16/16: complete cessation of attack |
CCH: 1/13: partial responder: HA decreased in intensity K significantly shortened subsequent episodes for all patients |
1/29: Dissociation 1/29: Hypotension 2/29: Bradycardia 29/29: Moderate-to-severe fatigue after infusion lasting up to 24 h |
Pomeroy,32 (n = 77) R |
At end of infusion At 1 month |
Improved NDPH: Acute responders: 8/14, MD 4.25 (95% CI 2.59–5.91, P < 0.0005) Sustained responders: 4/6, MD 2.5 (95% CI 0.91–4.09, P < 0.0154) CM: Acute responders: 47/63, MD 4.628 (95% CI 3.99–5.27, P < 0.0001) Sustained responders: 11/36, MD 2.136 (95% CI 0.91–3.37, P < 0.0031) |
N/A | Adverse events common: 66/77 28/77 diplopia, 19/77 confusion, 16/77 hallucinations, 9/77 dysarthria, 9/77 dizziness, 7/77 vivid dreams, 7/77 sedation, 6/77 unsteady gait, 5/77 worsened nausea, 1/77 nonepileptic seizure, 1/77 transaminitis, 1/77 suicidiality, 2/77 fall Most events stopped after stop infusion |
Schwenk,31 (n = 61) R |
At discharge At 30 and 90 days |
Improved Mean NRS: 7.5 (SD 0.2) vs. 3.4 (SD 0.3) (baseline vs. discharge), P < 0.001 |
Baseline NRS: 7.8 (SD 0.23) immediate responder vs. 6.8 (SD 0.64) nonresponder Posttreatment NRS: 2.6 (SD 0.28) immediate responder vs. 6.6 (SD 0.68) nonresponder, P < 0.01 Mean time to lowest NRS: 4.56 h First FU at 38.1 days (SD 4.7): 21/52 (40%): sustained response; 30/51 (58%): no longer response; 1/51: no immediate response but pain relief at 1 month Second FU 101.3 days (SD 8.8): 19/49 (39%) sustained response No significant difference in age/sex between responders vs. nonresponders |
Immediate responders: 53/61 nystagmus; 31/61 sedation; 23/61 N/V; 23/61 blurred vision; 17/61 hallucinations; 8/61 vivid dreams No significant difference in adverse effects |
Petersen,30 (n = 23; 20/3) Proof of Concept |
At 1, 3, 6, 30, 60, 120, 180 min At 1–2 weeks |
Improved At 15 min: Mean difference 1.1 (95% CI: −0.6 to 2.7, P = 0.188); 4/20 patients >50% pain relief |
At 30 min: Mean difference: 4.3 (95% CI: 2.4–6.2, P > 0.001) Complete relief for 8/20 patients (timing not known) 6/20: no relief 50% of patients preferred K over oxygen/sumatriptan |
Adverse event rate: 85% Most common: dizziness, light-headedness, nausea/vomiting, paresthesias |
Schwenk,33 (n = 6) Pilot P |
At end of treatment At 1 month |
Improved Lidocaine: Mean NRS by end of hospitalization/treatment (day 5) for lidocaine: 4.7 ± 2.8 (P ≤ 0.05) Mean NRS at postdischarge visit at 28 ± 8 days after treatment for lidocaine: 7.0 ± 1.4 (P > 0.05) K: Mean NRS at baseline for K: 7.4 ± 1.4 Mean NRS by end of hospitalization/treatment (day 5) for K: 3.7 ± 2.3 (p ≤ .05) Mean NRS at postdischarge visit at 4.1 ± 7 days after treatment for K: 7.2 ± 1.7 (P > 0.05) Mean NRS decrease K > C: K −3.7 vs. C −2.8 (P ≤ 0.05) |
No serious adverse events for K or C Lidocaine: 4/6 experienced transient adverse events (1 with bradycardia/junctional heart rhythm and nausea, 1 hallucinations and blurry vision, 1 nausea and blurry vision, 1 insomnia) K: 6/6 experienced adverse events including hallucinations, nightmares, vivid dreams, blurry vision, and nausea/vomiting |
|
Ray,34 N = 83 (33/50) R |
At end of infusion At 4 weeks |
Improved Migraine cohort (n = 77): n = 45 C vs. n = 32 K Responder: 23/45 (51.1%) after 4.5 ± 0.5 days C vs. 11/32 (34.4%) after 3.4 ± 0.5 days K Pain-free: 14/45 (31.1%) after 6.2 ± 2.4 days C vs. 5/32 (15.6%) after 5.1 ± 1.5 days K Mean VAS percentage (SD) reduction: 53% (39.3) C vs. 31.6% (41.3) K NDPH cohort (n = 3): n = 2 C vs. n = 1 K Responder: 2/2 C vs. 0/1 K Pain-free: 0/2 C vs. 0/1 K |
Migraine cohort (n = 77): 30-day readmission: 3/45 (6.7%) C vs. 1/32 (3.1%) K NDPH cohort (n = 3): 30-day readmission: 0/2 C vs. 0/1 K |
K: Anxiety/agitation/dizziness,3%; confusion, 6.1%; paresthesias, 12.1%; hallucinations, 6.1%; psychogenic seizure, 3% C: Anxiety/agitation, 8%; dizziness, 6%; arrhythmia, 4%; hypotension, 6%; confusion, 2%; paresthesias, 2%; rash, 2%; nausea, 2% |
Case series/case reports | ||||
Kaube,35 (n = 11) |
q15min following onset of aura until cessation |
Improved 5/11 patients: Improvement in aura symptoms using K for all attacks 6/11 patients: No benefit |
2/11 patients: Improvement in headache severity | 6/11 patients: Feelings of alienation and mild ataxia |
Lauritsen,36 (n = 6) |
At end of infusion |
Improved All patients achieved the target end point (VAS ≤3/10 for at least 8 h) |
Mean time (range) to target end point: 44 h (12–82) Mean (range) K infusion rate at pain relief end point: 0.34 mg/kg/h (0.12–0.42) |
One patient experienced a brief dissociative experience; resolved with reduction in infusion rate |
Moisset,38 (n = 2) |
At 6 weeks |
Improved Patient 1: Complete resolution of attacks until 6 weeks Patient 2: 50% decrease in attack frequency for 6 weeks |
N/A | None |
Aggarwal,39 (n = 1) |
At 3 months |
Improved Attack-free for 3 months At 3 months: Slight recurrence in attacks, managed with temporary increase in SL K |
D/C other medications (pregabalin, tapentadol, lamotrigine, amitriptyline) | No reported side effects |
Moisset,37 (n = 17) |
At 7 days |
Improved Mean number of daily attacks decreased from 4.3 ± 2.4 to 1.3 ± 1.0, MD −2.75 (95% CI −4.0 to −1.75, P < 0.001) |
Time to analgesic effect: 1 to 6 days (median = 3 days) Length of analgesic effect: 2 to 68 weeks (median = 4 weeks) Responders: 13/17 (76.5%, 95% CI 56.3–96.6) Full resolution: 7/17 |
Transient sedation: 7/17 (41.2%) No patients experienced hallucinations No debilitating sedation 1 h after end of infusion No bradycardia or high blood pressure |
Shiiba,40 (n = 1) |
At end of infusion At 3 months |
Improved No SUNCT pain attacks for 3 months after treatment |
No side effects | None |
C = comparator; (C)CH = (chronic) cluster headache; CI = confidence interval; CM = chronic migraine; D/C = discontinued; DXM = dexamethasone; ED = emergency department; ESD = effect size difference; FU = follow-up; HA = headache; IQR = interquartile range; K = ketamine; M = midazolam; MD = mean difference; N/V = nausea and vomiting; SERSDA = Side Effects Rating Scale for Dissociative Anesthetics; SL = sublingual; P = prospective; R = retrospective; Comparator = prochlorperazine + diphenhydramine.
Risk of Bias for Included Studies
The results for assessment of the risk of bias for the included RCTs are listed in Appendix 3. The overall risk of bias was deemed to have “some concerns” for two of the RCTs24,25 and “high risk of bias” for the remaining four RCTs.21–23,26 The risk of bias assessment of the included nonrandomized trials showed one study of low risk of bias,30 one study of moderate risk of bias,33 two studies deemed to have a serious risk for bias,27,32,34 and two studies that demonstrated a critical risk of bias28,29,31 (Appendix 4). The quality of the two case series was moderate35,36 and one was of high quality37 (Appendix 5).
Study Characteristics
Demographic and clinical characteristics of the 670 patients reported in the 20 included studies are summarized in Table 1. The use of ketamine for the treatment of primary headache was discussed in 17 studies (n = 616), including 5 RCTs22–26 and 12 observational studies (6 nonrandomized trials29–34 and 6 case series/case reports).35–40 Three studies (n = 54) reported the use of ketamine for treatment of neuropathic facial pain, including 1 RCT21 and 2 prospective observational studies.27,28
Primary Headaches
Demographics and Pain Profiles of Participants in the Included Studies
We found five RCTs including 299 patients with primary headaches: migraine, tension-type headaches, and cluster headaches (63% females, 18–65 years) (Table 1).22–26 Baseline pain intensity ranged from VAS of 56/100 to 95/100.22,24–26
We found 12 observational studies including 317 patients (50% females) with the following diagnoses: chronic migraine (CM; n = 222), cluster headache (CH)–episodic (n = 17) or chronic (CCH; n = 57), short-lasting unilateral neuralgiform headache with conjunctival injection and tearing (SUNCT; n = 4), medication overuse headache (MOH; n = 37), and new daily persistent headache (NDPH; n = 17).29–40 Baseline pain intensity was moderate to severe in all observational studies. The duration of headache history was only provided in 3 studies.23,30,37
Details of the Ketamine Treatment
Route of Administration and Dosing
Treatment with a single23–26,31 or double22 or five30 boluses of ketamine was investigated in seven papers. Five papers (three RCTs, one cohort study, one case series; n = 245) looked into the effect of and intranasal bolus of ketamine compared to midazolam,23 diphenhydramine,22 ketorolac,26 or no comparator.30,35 Bolus dose ranged from 0.25 to 0.75 mg/kg. Ketamine was administered as an IV bolus in two RCTs.24,25 Bolus dose ranged from 0.2 to 0.3 mg/kg and comparators were placebo25 or prochlorperazine with diphenhydramine.24
The effect of IV ketamine infusions was reported in ten observational studies (including 283 patients).29,31–34,37,40 Patient population in these studies was mixed and included patients with CM and CH. Infusions were given over dosages ranging from 0.1 to 1 mg/kg/h over various durations (ranging from a single 1-h infusion up to infusions for up to 6 h on nine consecutive days). Two studies had a comparator (lidocaine).31,34
Duration of Follow-Up
The follow-up time in the RCTs ranged from 60 min25,26 to 72 h posttreatment,22,24 with one additional trial specifying only that follow-up occurred for six consecutive migraine attacks.23 The follow-up time for the observational studies was longer, ranging from immediately posttreatment,30,34–36 to 1 week,37 1 month,31,32 3 months,33,38–40 and 18 months29 after treatment.
Outcome
Impact on Migraine Pain Intensity
Four studies (all RCTs) investigated the analgesic effect of ketamine bolus treatment on migraine intensity,22,24–26 and five studies (all observational studies) investigated ketamine infusions.31–36
Of the four RCTs investigating the analgesic efficacy of ketamine bolus treatment, only one RCT demonstrated superiority of ketamine compared to the comparator (ketorolac), providing significant pain relief up to 2 h posttreatment.26 The three other RCTs failed to demonstrate superiority of ketamine compared to placebo, metoclopramide, or midazolam22,23,25 (Table 2).
In stark contrast, all of the five observational ketamine infusion studies (n = 233) reported significant pain improvement at the end of the infusion period.31–34,36 Infusions of solely ketamine were given for 8 h36 to 5 days in a row.32,33 In two studies, the effect of multiday ketamine infusion was compared to multiday lidocaine infusion.31,34 In the studies with lidocaine as a comparator, both groups were associated with significant pain reduction at the end of the infusion as compared to baseline, although the difference between groups was significant in favor of lidocaine in one study34 and in favor of ketamine in the other study.31
Only three out of five papers reported long-term outcomes. Two studies noted a positive effect up to 132 and 3 months.33 In the third paper, patients had returned back to their baseline pain at 1-month follow-up.31
Impact on Aura Attack during Migraine
Only one RCT investigated the effect of ketamine and midazolam on length and severity of aura compared to placebo.23 The severity of the aura was significantly improved by ketamine compared to placebo. However, both agents were equally effective in reducing the median duration of the attack compared to placebo. In a case series of 11 patients with familial hemiplegic migraine treated with 25 mg intranasal ketamine, 5 patients experienced an improvement of aura duration and severity for all 14 attacks treated. Three patients experienced a return of aura symptoms after initial improvement.35
Impact on Pain Relief and Attack Frequency of TAC Headaches
All seven studies including patients with TAC (n = 76) reported a resolution or reduction in the attack frequency after ketamine treatment. An immediate but short-lasting effect was noted after bolus treatment30 and an immediate to sustained effect was noted after ketamine infusion.29,34,37–40 Patients were reported to have more than a 50% reduction in attack frequency for 6 weeks38 to complete resolution of attacks for 6 weeks34,37,38 up to 3 months.39,40
Effect on Pain-Associated Domains (Functional Outcome, Sleep, Quality of Life)
Only one RCT reported on the effect of ketamine on pain-associated domains. No significant difference in functional disability scores (rated on a 4-point scale), measured 30 min posttreatment, between the IV ketamine bolus and placebo groups was identified.25
Patient Preference/Satisfaction
Only three papers reported on patient satisfaction and/or preference for ketamine versus the comparator using an NRS.22,24,25 In only one study was a significant difference identified, in favor of prochlorperazine.24
Impact of Ketamine on Intake of Pain Medication
A few studies commented on change in use of rescue medication during or following ketamine treatment. Although not statistically significant, two RCTs demonstrated that a smaller proportion of patients in the ketamine group needed rescue medication during the infusion compared to the comparator.22,25 Two case series mentioned a reduction in dose and/or discontinuation of analgesics following ketamine infusion, but further details were not provided.38,39
Adverse Effects and Complications of Ketamine Infusion
Approximately 70% of patients across all studies experienced side effects related to ketamine infusions; however, most were mild and resolved with decreased rate or ending the ketamine infusion. Side effects included dizziness, sedation, and blurred vision’ One patient’s ketamine infusion was stopped because the patient experienced suicidal thoughts32 and one patient preferred to stop ketamine because of the side effects.33 One additional patient developed an asymptomatic elevation in liver enzymes.32 None of the patients needed to be hospitalized because of intolerable side effects such as feelings of insobriety, confusion, nausea and vomiting, hallucinations, and tachycardia.
Facial Pain
Demographics and Pain Profiles of Participants in the Included Studies
Of three studies including 54 patients (85% females, 29–89 years), one crossover RCT (n = 30)21 and one small observational study (n = 7)28 examined the use of ketamine for patients with trigeminal neuropathy. Another small observational study (n = 17) included patients with neuropathic orofacial pain (not specified).27 Baseline pain intensity was moderate to severe21,28 or not provided.27 The duration of pain ranged from 6 months to 28 years.
Details and Outcome of Ketamine Treatment
In the three studies, all patients received a single bolus of ketamine 0.4 mg/kg. One study compared ketamine to IM pethidine 1 mg/kg.21 In two studies, the bolus treatment was followed by 4 days of oral ketamine.21,27 Follow-up duration was short in these studies and ranged from 60 min after ketamine IM bolus21,27,28 to 3 days after oral treatment.21,27 Ketamine demonstrated a significant immediate improvement of facial pain in two studies for the duration of follow-up (3 days).21,27 It was noted that those responding to IM ketamine also reported pain relief with oral ketamine.21,27 The adverse events profile was similar as reported in the primary headache studies.
Discussion
Despite recent evolutions in pharmacological and interventional management of patients with CFP, many patients continue to experience a significant reduction in quality of life, thereby imposing a significant burden on the health care system. We therefore conducted this systematic review to evaluate the evidence on the role of ketamine for patients with headache and/or facial pain.
Impact on Headache and Facial Pain
Although we evaluated 5 RCTs and 12 observational studies, evidence remains conflicting on the efficacy of ketamine for treatment of primary headaches. This is likely due to the limited study quality, moderate to high risk of study bias, confounding and substantial heterogeneity across studies in terms of study design, patient populations, details of ketamine treatment, and (lack of) follow-up. Only 2 of the 5 RCTs demonstrated a significant immediate effect of ketamine on the intensity of pain and aura of migraine relief in the emergency room,23,26 and the remaining RCTs failed to demonstrate a significant effect of ketamine on headache intensity compared to various comparators. On the other hand, all observational studies demonstrated a significant reduction in migraine pain intensity and duration, as well as decreased frequency and intensity of CH attacks immediately postintervention that lasted for up to 3 months postinfusion. The difference in these findings may be explained as follows. First, it may be attributed to the shorter administration times and/or lower dose of ketamine bolus treatment in the RCTs, because nearly all observational studies explored single-/multiple-day ketamine infusions. The typical doses for chronic pain IV ketamine treatment are 0.2 to 0.75 mg/kg (bolus), 0.5 to 2 mg/kg/h (infusion), 0.1 to 0.5 mg/kg for IM administration, and 0.2 to 1 mg/kg for intranasal administration, which is higher than what was administrated in the RCTs.10 A high dosage and extended administration (infusions) of ketamine have been associated with better pain relief in patients with chronic pain.41 Similar conclusions were made in the consensus guidelines on the use of IV ketamine infusions for chronic pain.10 Future research in patients with primary headache should therefore focus on investigating the effect of high-dose and repeated administration of ketamine in a randomized controlled setting. Second, most RCTs had a mixed patient population, including patients with acute and chronic headache of migraine, cluster, and MOH types, which increased study heterogeneity, potentially affecting the outcome. Lastly, the 5 papers that did show a positive outcome of ketamine bolus treatment investigated patients solely with TAC, and bolus treatment failed in studies on patients with chronic migraine. This difference in outcome could be explained by a difference in pathophysiology, where TAC is driven by changes in the sphenopalatine ganglion, which potentially is more susceptible for the ketamine effect.
The evidence on ketamine for neuropathic facial pain is scarce but appears promising. Intramuscular ketamine was associated with significant improvement in two out of three studies on patients with trigeminal neuropathy,21 and a tendency for continued pain relief with oral ketamine after initial IV/IM treatment was also noted.21,27 This treatment option of oral ketamine should be further explored because this could be a valuable therapy for patients in remote areas with limited access to health care facilities.
Effect on Pain-Associated Domains
Although the International Classification of Headache Disorders third edition diagnostic criteria for CFP are widely accepted and recommended,42 a majority of the papers did not mention use of this validated instrument for diagnosis. This is a weakness that needs to be addressed to avoid misclassification bias and improve generalizability of the study results. Though a handful of studies examined patient satisfaction/preference and the need for rescue medications, most papers in this review did not mention use of validated tools to evaluate the effect of ketamine on pain-associated domains (sleep, mood, quality of life) in addition to its analgesic efficacy. This is surprising because the importance of evaluating pain-related domains in clinical and research settings is established, and validated tools to evaluate these domains are available.43 Ketamine has been demonstrated to have an effect on sleep and mood and could therefore potentially improve patients’ quality of life even if pain intensity is unchanged.44,45
Safety
It is widely accepted that ketamine is associated with adverse psychomimetic, cardiovascular, and gastrointestinal effects resulting from its activity on a variety of substrate receptors including NMDA, acetylcholine, opioid, monoamine, and histamine.10 The incidence of reported ketamine-induced side effects in the included papers was high regardless of type of administration or dose and only included psychomimetic effects. Most side effects were mild and resolved after decreasing the dose or ending treatment. Although central nervous system effects appear to be dose dependent when ketamine is used in anesthetic doses, the evidence is not as clear for subanesthetic regimens, beyond a yet-to-be-determined threshold.10 In our review, no clear difference was noted in the incidence of side effects when comparing high to low doses. Most patients experienced hallucinations, which resolved after cessation of treatment, and one patient experienced suicidal thoughts. Based on the America Psychiatric Association44 guidelines on the use of ketamine, a history of psychosis is a contraindication for administration of subanesthetic IV ketamine.
Strengths and Limitations
We found one other systematic review on the efficacy of ketamine for headaches, with evidence found in RCTs that were primarily focused on bolus administration of ketamine for acute headache pain relief.46 The authors concluded that the benefit of ketamine for headache treatment is unclear but that long-term follow-up and different ketamine dosages in patients with chronic pain should be explored. Therefore, our systematic review attempted to take a closer look at the larger amount of evidence in observational trials that focused on ketamine infusions. Our review demonstrated that prolonged ketamine infusions can indeed significantly and sustainably reduce migraine intensity and frequency of CH attacks. This provides promising evidence, and this temporal and dose-dependent relationship should be further explored in new high-quality trials. To our knowledge, no attempt has been made to systematically gather evidence regarding the effects of ketamine on facial pain.
This review has several limitations. Most of the studies included in this review reported observational data, with inherent high risk of confounding and bias. Further, the heterogeneity across papers was substantial, with large differences in dosing, duration and route of administration, and comparators, which made comparison challenging and precluded a meta-analysis. Lastly, this review did not assess the long-term benefits and harms of ketamine for the treatment of CFP owing to lack of data in the literature.
A high-quality placebo-controlled RCT investigating the effect and safety of high-dose and/or prolonged ketamine infusion treatment on refractory headache pain and pain-associated domains would be the logical next step to investigate ketamine’s potential in the treatment of CFP. Recent systematic reviews and meta-analyses of this evidence show that infusions of ketamine 1 mg/kg/h are associated with greater and sustained pain relief compared to one-off bolus and low-dose infusion regimens.10 However, adverse effects of ketamine are common and could limit dose escalation, and the potential long-term risks of repeated administration of high doses of ketamine need to be further investigated.
Conclusions
Current evidence on the efficacy of ketamine for treatment of CFP remains conflicting, precluding the ability to make any recommendations. This is likely due to the limited study quality, moderate to high risk of study bias, and substantial heterogeneity across studies in terms of study design, patient populations, details of ketamine treatment, and (lack of) follow-up. Ketamine bolus treatment showed significant reduction of migraine aura severity, TAC intensity and frequency, and trigeminal neuropathic pain but failed to reduce migraine intensity or duration. The included observational trials suggest that ketamine infusion treatment has an immediate and sustained benefit on headache pain intensity, possibly because of the prolonged duration of treatment and higher dose of administration. Most papers failed to evaluate the effect of ketamine on pain-associated domains. RCTs are required that focus on the dose–response relationship and immediate and long-term effects of prolonged ketamine treatment on CFP and pain-associated domains.
Supplementary Material
Disclosure Statement
YH received the Early Career Investigator Pain Research Grant from the Canadian Pain Society for the KetHead study “A Multi-Center Randomized Controlled Trial of Efficacy and Safety of Intravenous Ketamine for Chronic Daily Headaches: The KetHead Study.” All other authors have no conflicts of interest to report.
Authorship Statement
Study conception and design: YH and ME; drafting of the article: YH and MP; research into, design of, and execution of database search strategies: ME; management and curation of database results, write-up of search methodology; ME; data acquisition, analysis, and interpretation: YH, TM, MP, PK; review and editing of manuscript: all authors.
Supplementary Material
Supplemental data for this article can be accessed online at https://doi.org/10.1080/24740527.2023.2210167.
References
- 1.Stovner LJ, Hagen K, Jensen R, Katsarava Z, Lipton RB, Scher AI, Steiner TJ, Zwart J-A.. The global burden of headache: a documentation of headache prevalence and disability worldwide. Cephalalgia. 2007;27:193–17. doi: 10.1111/j.1468-2982.2007.01288.x. [DOI] [PubMed] [Google Scholar]
- 2.Ananthan S, Benoliel R. Chronic orofacial pain. J Neural Transm (Vienna). 2020. Apr;127(4):575–88. doi: 10.1007/s00702-020-02157-3. [DOI] [PubMed] [Google Scholar]
- 3.Burch RC, Loder S, Loder E, Smitherman TA. The prevalence and burden of migraine and severe headache in the United States: updated statistics from government health surveillance studies. Headache. 2015;55(1):21–34. doi: 10.1111/head.12482. [DOI] [PubMed] [Google Scholar]
- 4.Stokes M, Becker WJ, Lipton RB, Sullivan SD, Wilcox TK, Wells L, Manack A, Proskorovsky I, Gladstone J, Buse DC, et al. Cost of health care among patients with chronic and episodic migraine in Canada and the USA: results from the International Burden of Migraine Study (IBMS). Headache. 2011. Jul-Aug;51(7):1058–77. doi: 10.1111/j.1526-4610.2011.01945.x. [DOI] [PubMed] [Google Scholar]
- 5.Bendtsen L, Zakrzewska JM, Heinskou TB, Hodaie M, Leal PRL, Nurmikko T, Obermann M, Cruccu G, Maarbjerg S. Advances in diagnosis, classification, pathophysiology, and management of trigeminal neuralgia. Lancet Neurol. 2020. Sep;19(9):784–96. doi: 10.1016/S1474-4422(20)30233-7. [DOI] [PubMed] [Google Scholar]
- 6.Chichorro JG, Porreca F, Sessle B. Mechanisms of craniofacial pain. Cephalalgia. 2017. Jun;37(7):613–26. doi: 10.1177/0333102417704187. [DOI] [PubMed] [Google Scholar]
- 7.Hoffmann J, Storer RJ, Park J-W, Goadsby PJ. N-Methyl-d-aspartate receptor open-channel blockers memantine and magnesium modulate nociceptive trigeminovascular neurotransmission in rats. Eur J Neurosci. 2019;50:2847–59. doi: 10.1111/ejn.14423. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8.Hoffmann J, Baca SM, Akerman S. Neurovascular mechanisms of migraine and cluster headache. J Cereb Blood Flow Metab. 2019. Apr;39(4):573–94. doi: 10.1177/0271678X17733655. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Cohen SP, Liao W, Gupta A, Plunkett A. Ketamine in pain management. Adv Psychosom Med. 2011;30:139–61. [DOI] [PubMed] [Google Scholar]
- 10.Cohen SP, Bhatia A, Bhaskar A, Schwenk ES, Wasan AD, Hurley RW, Viscusi ER, Narouze S, Davis FN, Ritchie EC, et al. Consensus guidelines on the use of intravenous ketamine infusions for chronic pain from the American Society of Regional Anesthesia and Pain Medicine, the American Academy of Pain Medicine, and the American Society of Anesthesiologists. Reg Anesth Pain Med. 2018;43(5):521–46. doi: 10.1097/AAP.0000000000000808. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 11.Orhurhu V, Orhurhu MS, Bhatia A, Cohen SP. Ketamine infusions for chronic pain: a systematic review and meta-analysis of randomized controlled trials. Anesth Analg. 2019;129:241–54. doi: 10.1213/ANE.0000000000004185. [DOI] [PubMed] [Google Scholar]
- 12.Adams HA. Mechanisms of action of ketamine. Anaesthesiol Reanim. 1998;23:60–63. [PubMed] [Google Scholar]
- 13.Orser BA, Pennefather PS, MacDonald JF. Multiple mechanisms of ketamine blockade of N-methyl-D-aspartate receptors. Anesthesiology. 1997;86:903–17. doi: 10.1097/00000542-199704000-00021. [DOI] [PubMed] [Google Scholar]
- 14.Zanos P, Moaddel R, Morris PJ, Riggs LM, Highland JN, Georgiou P, Pereira EFR, Albuquerque EX, Thomas CJ, Zarate CA Jr, et al. Ketamine and ketamine metabolite pharmacology: insights into therapeutic mechanisms. Pharmacol Rev. 2018. Jul;70(3):621–60. doi: 10.1124/pr.117.015198. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 15.Headache classification committee of the International Headache Society (IHS) the international classification of headache disorders, 3rd edition. Cephalalgia. 2018. Jan;38(1):1–211. doi: 10.1177/0333102417738202. [DOI] [PubMed] [Google Scholar]
- 16.Farrar JT, Young JP Jr, LaMoreaux L, Werth JL, Poole RM. Clinical importance of changes in chronic pain intensity measured on an 11-point numerical pain rating scale. Pain. 2001;94:149–58. doi: 10.1016/S0304-3959(01)00349-9. [DOI] [PubMed] [Google Scholar]
- 17.Covidence systematic review software, Veritas Health Innovation. Melbourne, Australia. www.covidence.org. [Google Scholar]
- 18.Sterne JAC, Savovic J, Page MJ, Elbers RG, Blencowe NS, Boutron I, Cates CJ, Cheng H-Y, Corbett MS, Eldridge SM, et al. RoB 2: a revised tool for assessing risk of bias in randomised trials. BMJ. 2019;366:l4898. doi: 10.1136/bmj.l4898. [DOI] [PubMed] [Google Scholar]
- 19.Sterne JAC, Hernán MA, Reeves BC, Savovic J, Berkman ND, Viswanathan M, Henry D, Altman DG, Ansari MT, Boutron I, et al. ROBINS-I: a tool for assessing risk of bias in non-randomized studies of interventions. BMJ. 2016;355:i4919. doi: 10.1136/bmj.i4919. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 20.Moga C, Guo B, Schopflocher D, Harstall C. Development of a quality appraisal tool for case series using a modified Delphi technique. Edmonton (Canada): Institute of Health Economics; 2012. [Google Scholar]
- 21.Rabben T, Skjelbred P, Oye I. Prolonged analgesic effect of ketamine, an N-methyl-D-aspartate receptor inhibitor, in patients with chronic pain. J Pharmaol Exp Ther. 1999;289:1060–66. [PubMed] [Google Scholar]
- 22.Benish T, Villalobos D, Love S, Casmaer M, Hunter CJ, Summers SM, April MD. The THINK (Treatment of headache with intranasal ketamine) trial: a randomized controlled trial comparing intranasal ketamine with intravenous metoclopramide. J Emerg Med. 2019. Mar;56(3):248–57. doi: 10.1016/j.jemermed.2018.12.007. [DOI] [PubMed] [Google Scholar]
- 23.Afridi SK, Giffin NJ, Kaube H, Goadsby PJ. A randomized controlled trial of intranasal ketamine in migraine with prolonged aura. Neurology. 2013;80:642–47. doi: 10.1212/WNL.0b013e3182824e66. [DOI] [PubMed] [Google Scholar]
- 24.Zitek T, Gates M, Pitotti C, Bartlett A, Patel J, Rahbar A, Forred W, Sontgerath JS, Clark JM. A comparison of headache treatment in the emergency department: prochlorperazine versus ketamine. Ann Emerg Med. 2018. Mar;71(3):369–77. doi: 10.1016/j.annemergmed.2017.08.063. [DOI] [PubMed] [Google Scholar]
- 25.Etchinson A, Bos L, Ray M, McAllister K, Mohammed M, Park B, Phan A, Heitz C. Low-dose ketamine does not improve migraine in the emergency department: a randomized placebo-controlled trial. West J Emerg Med. 2018. Nov;19(6):952–60. doi: 10.5811/westjem.2018.8.37875. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 26.Sarvari HR, Baigrezaii H, Nazarianpirdosti M, Meysami A, Safari-Faramani R. Comparison of the efficacy of intranasal ketamine versus intravenous ketorolac on acute non-traumatic headaches: a randomized double-blind clinical trial. Head Face Med. 2022. Jan 3;18(1):1. doi: 10.1186/s13005-021-00303-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 27.Rabben T, Øye I. Interindividual differences in the analgesic response to ketamine in chronic orofacial pain. Eur J Pain. 2001;5(3):233–40. doi: 10.1053/eujp.2001.0232. [DOI] [PubMed] [Google Scholar]
- 28.Mathisen LC, Skjelbred P, Skoglund LA, Oye I. Effect of ketamine, an NMDA receptor inhibitor, in acute and chronic orofacial pain. Pain. 1995. May;61(2):215–20. doi: 10.1016/0304-3959(94)00170-J. [DOI] [PubMed] [Google Scholar]
- 29.Granata L, Niebergall H, Langner R, Agosti R, Sakellaris L. Ketamin i. v. zur Behandlung von Clusterkopfschmerz: eine Beobachtungsstudie [Ketamine i. v. for the treatment of cluster headaches: an observational study]. Schmerz. 2016. Jun;30(3):286–88. German. doi: 10.1007/s00482-016-0111-z. PMID: 27067225. [DOI] [PubMed] [Google Scholar]
- 30.Petersen AS, Pedersen AS, Barloese MCJ, Holm P, Pedersen O, Jensen RH, Snoer AH. Intranasal ketamine for acute cluster headache attacks-results from a proof-of-concept open-label trial. Headache. 2022. Jan;62(1):26–35. doi: 10.1111/head.14220. [DOI] [PubMed] [Google Scholar]
- 31.Schwenk ES, Torjman MC, Moaddel R, Lovett J, Katz D, Denk W, Lauritsen C, Silberstein SD, Wainer IW. Ketamine for refractory chronic migraine: an observational pilot study and metabolite analysis. J Clin Pharmacol. 2021. Nov;61(11):1421–29. doi: 10.1002/jcph.1920. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 32.Pomeroy JL, Marmura MJ, Nahas SJ, Viscusi ER. Ketamine infusions for treatment refractory headache. Headache. 2017;57:276–82. doi: 10.1111/head.13013. [DOI] [PubMed] [Google Scholar]
- 33.Schwenk ES, Dayan AC, Rangavajjula A, Torjman MC, Hernandez MG, Lauritsen CG, Silberstein SD, Young W, Viscusi ER. Ketamine for refractory headache: a retrospective analysis. Reg Anesth Pain Med. 2018. Nov;43(8):875–79. doi: 10.1097/AAP.0000000000000827. [DOI] [PubMed] [Google Scholar]
- 34.Ray JC, Cheng S, Tsan K, Hussain H, Stark RJ, Matharu MS. Intravenous lidocaine and ketamine infusions for headache disorders: a retrospective cohort study. Front Neurol. 2022. Mar;9(13):842082. doi: 10.3389/fneur.2022.842082. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 35.Kaube H, Herzog J, Käufer T, Dichgans M, Diener HC. Aura in some patients with familial hemiplegic migraine can be stopped by intranasal ketamine. Neurology. 2000. Jul 12;55(1):139–41. doi: 10.1212/wnl.55.1.139. PMID: 10891926. [DOI] [PubMed] [Google Scholar]
- 36.Lauritsen C, Mazuera S, Lipton RB, Ashina S. Intravenous ketamine for subacute treatment of refractory chronic migraine: a case series. J Headache Pain. 2016. Dec;17(1):106. doi: 10.1186/s10194-016-0700-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 37.Moisset X, Giraud P, Meunier E, Condé S, Périé M, Picard P, Pereira B, Ciampi de Andrade D, Clavelou P, Dallel R. Ketamine-magnesium for refractory chronic cluster headache: a case series. Headache. 2020. Nov;60(10):2537–43. doi: 10.1111/head.14005. [DOI] [PubMed] [Google Scholar]
- 38.Moisset X, Clavelou P, Lauxerois M, Dallel R, Picard P. Ketamine infusion combined with magnesium as a therapy for intractable chronic cluster headache: report of two cases. Headache. 2017. Sep;57(8):1261–64. doi: 10.1111/head.13135. [DOI] [PubMed] [Google Scholar]
- 39.Aggarwal A. Ketamine as a potential option in the treatment of short-lasting unilateral neuralgiform headache attacks with conjunctival injection and tearing. Natl Med J India. 2019. Mar-Apr;32(2):86–87. doi: 10.4103/0970-258X.275347. [DOI] [PubMed] [Google Scholar]
- 40.Shiiba S, Sago T, Kawabata K. Pain relief in short-lasting unilateral neuralgiform headache with conjunctival injection and tearing syndrome with intravenous ketamine: a case report. Acta Neurol Taiwan. 2021. Mar;30(1):35–38. [PubMed] [Google Scholar]
- 41.Maher DP, Chen L, Mao J. Intravenous ketamine infusions for neuropathic pain management: a promising therapy in need of optimization. Anesth Analg. 2017;124:661–74. doi: 10.1213/ANE.0000000000001787. [DOI] [PubMed] [Google Scholar]
- 42.Ashina S, Olesen J, Lipton RB. How well does the ICHD 3 (Beta) help in real-life migraine diagnosis and management? Curr Pain Headache Rep. 2016. Dec;20(12):66. doi: 10.1007/s11916-016-0599-z. [DOI] [PubMed] [Google Scholar]
- 43.Dworkin RH, Turk DC, Farrar JT, Haythornthwaite JA, Jensen MP, Katz NP, Kerns RD, Stucki G, Allen RR, Bellamy N, et al. Core outcome measures for chronic pain clinical trials: IMMPACT recommendations. Pain. 2005;113(1–2):9–19. doi: 10.1016/j.pain.2004.09.012. [DOI] [PubMed] [Google Scholar]
- 44.Sanacora G, Frye MA, McDonald W, Mathew SJ, Turner MS, Schatzberg AF, Summergrad P, Nemeroff CB, American Psychiatric Association (APA) Council of Research Task Force on Novel Biomarkers and Treatments . A consensus statement on the use of ketamine in the treatment of mood disorders. JAMA Psychiatry. 2017. Apr 1;74(4):399–405. doi: 10.1001/jamapsychiatry.2017.0080. [DOI] [PubMed] [Google Scholar]
- 45.Song B, Zhu JC. Mechanisms of the rapid effects of ketamine on depression and sleep disturbances: a narrative review. Front Pharmacol. 2021. Dec;14(12):782457. doi: 10.3389/fphar.2021.782457. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 46.Chah N, Jones M, Milord S, Al-Eryani K, Enciso R. Efficacy of ketamine in the treatment of migraines and other unspecified primary headache disorders compared to placebo and other interventions: a systematic review. J Dent Anesth Pain Med. 2021. Oct;21(5):413–29. doi: 10.17245/jdapm.2021.21.5.413. [DOI] [PMC free article] [PubMed] [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.