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MOH NMA Liu 2025

Network meta-analysis comparing efficacy of different strategies on medication-overuse headache

Year of Publication: 2025

Authors: Koonalintip P, Yamutai S, Setthawatcharawanich S, ..., Wakerley BR

Journal: The Journal of Headache and Pain

Citation: Koonalintip et al. The Journal of Headache and Pain (2025) 26:43

Link: https://doi.org/10.1186/s10194-025-01982-9


Clinical Question

Which treatment strategy—withdrawal, prevention (oral, anti-CGRP, botulinum toxin), education, neurostimulation, or combinations—is most effective at reducing monthly headache days in patients with medication-overuse headache?

Bottom Line

Combination therapies—particularly abrupt withdrawal + oral prevention + greater occipital nerve block, and restriction + oral prevention + anti-CGRP(R) therapy—are the most effective initial strategies for medication-overuse headache. Oral prevention, anti-CGRP(R) therapies, and botulinum toxin all significantly reduce monthly headache days with similar efficacy as monotherapies. Abrupt withdrawal alone is insufficient and should not be used in isolation.

Major Points

  • Combination of abrupt withdrawal + oral prevention + greater occipital nerve block (W+P+Nb) produced the largest reduction in monthly headache days: MD -10.6 (95% CI: -15.03 to -6.16) vs control
  • Restriction + oral prevention + anti-CGRP(R) therapy (R+P+A) also highly effective: MD -8.47 (95% CI: -12.78 to -4.15)
  • Headache prevention strategies—oral prevention, anti-CGRP(R) therapies, and botulinum toxin—each significantly reduced monthly headache days, with no single agent superior to the others
  • Abrupt withdrawal alone (W) was NOT effective: MD -2.77 (95% CI: -5.74 to 0.20)—no significant difference from control
  • Greater reduction in headache frequency may lower MOH relapse risk, supporting use of more effective combination regimens as first-line therapy
  • Findings support combination therapies—especially those incorporating anti-CGRP(R) or nerve blocks—as initial treatment options for MOH

Design

Study Type: Systematic review and network meta-analysis of randomized controlled trials

Randomization:

Enrollment Period: Studies published 2006 to 2023; literature search through December 2024

Follow-up Duration: Most studies (81.25%) reported outcomes at 8–16 weeks; three extended to 24 weeks; outcomes standardized to 12 weeks where possible

Centers: 0

Countries: Iran, Denmark, Multicenter, Norway, Turkey, Brazil, Netherlands, Italy, United States

Sample Size: 3000

Analyzed: 3000

Analysis: Random-effects network meta-analysis using mean difference (MD) and SD as effect size; treatments ranked by p-scores (0 = least effective, 1 = most effective); pairwise meta-analyses with random-effects model; netmeta package in RStudio; heterogeneity assessed by I² (≥50%) and τ² (>0.1)

Registration: PROSPERO CRD42024620487


Inclusion Criteria

  • Adults ≥18 years
  • Meeting ICHD-2, ICHD-3, or ICHD-3 beta criteria for MOH, OR primary headache disorder with medication overuse defined by ICHD frequency criteria
  • Randomized controlled trial design
  • Compared withdrawal strategies, headache prevention, additional education, and/or bridging neurostimulation (alone or in combination)
  • Reported reduction in monthly headache or migraine frequency at 2–6 months post-intervention or 6 months post-education sessions
  • Published in English

Exclusion Criteria

  • Studies that did not control for each component of strategies outlined in protocol (e.g., comparing abrupt withdrawal + education vs abrupt withdrawal alone without controlling for prevention)
  • Non-randomized studies
  • Non-English publications

Arms

FieldControlAbrupt withdrawal (W)Oral prevention (P)Botulinum toxin (B)Anti-CGRP(R) therapy (A)Withdrawal + oral prevention (W+P)Withdrawal + botulinum toxin (W+B)Withdrawal + nerve block (W+Nb)Withdrawal + education (W+E)Restriction + oral prevention (R+P)Restriction + education (R+E)Withdrawal + oral prevention + nerve block (W+P+Nb)Withdrawal + oral prevention + education (W+P+E)Restriction + oral prevention + anti-CGRP(R) (R+P+A)
N00000000000000
InterventionReference comparator (no active treatment / placebo)Abrupt withdrawal of overused acute medicationOral migraine preventive medication (topiramate, valproate, beta-blockers, amitriptyline, candesartan, others)OnabotulinumtoxinA injection (100U or 155U)Anti-CGRP or anti-CGRP receptor monoclonal antibody (e.g., galcanezumab 120 mg SC monthly)Abrupt withdrawal combined with oral preventive medicationAbrupt withdrawal combined with botulinum toxin injectionAbrupt withdrawal combined with greater occipital nerve block (lidocaine ± triamcinolone)Abrupt withdrawal combined with additional educational/behavioral sessionsRestriction of overused medication combined with oral preventive medicationRestriction of overused medication combined with educational sessionsAbrupt withdrawal + oral preventive + greater occipital nerve block with 2% lidocaine and triamcinoloneAbrupt withdrawal + oral preventive + 12-week education program (6 sessions)Restriction of overused medication + oral preventive + anti-CGRP(R) therapy
Duration8–24 weeks8–24 weeks8–24 weeks12 weeks24 weeks8–24 weeks12 weeks8 weeks8 weeks12 weeks8 weeks12 weeks24 weeks post-education12 weeks

Outcomes

OutcomeTypeControlInterventionHR / OR / RRP-value
Reduction in monthly headache days (MHDs) compared to control, derived from network meta-analysis combining direct and indirect evidencePrimaryReference (MD = 0)W+P+Nb: MD -10.6; R+P+A: MD -8.47; W alone: MD -2.77 (NS)
Secondary
Secondary
Secondary

Subgroup Analysis

Network includes 15 studies and 12 strategies with control as reference; two closed loops in network. Risk of bias assessed using Cochrane RoB 2.0 tool; publication bias assessed via funnel plot.


Criticisms

  • Significant clinical and methodological heterogeneity across included studies (variability in patient populations, intervention types, and follow-up duration)
  • Diagnostic criteria for MOH varied (ICHD-2 vs ICHD-3 vs ICHD-3 beta), evolving over the study period
  • Two studies included participants with primary headache + medication overuse rather than strict MOH
  • Outcome measurement timepoints varied (8–24 weeks); standardization to 12 weeks not always possible
  • Limited number of studies per node in network may reduce precision of indirect comparisons
  • Only English-language publications included, raising potential publication/language bias
  • Anti-CGRP(R) and botulinum toxin had limited number of contributing trials

Based on: MOH NMA Liu 2025 (The Journal of Headache and Pain, 2025)

Authors: Koonalintip P, Yamutai S, Setthawatcharawanich S, ..., Wakerley BR

Citation: Koonalintip et al. The Journal of Headache and Pain (2025) 26:43

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