Sociedad Americana de Hirudoterapia

Chronic Migraine Prophylaxis (≥15 Headache Days/Month)

Investigational adjunct for chronic migraine (≥15 days/month, ≥8 migrainous) refractory to two preventive classes; distinct from episodic migraine.

Tier C — InvestigationalInvestigacionalLast updated: 2026-05-26 · Reviewed by ASH Editorial Board

Resumen para el Paciente

¿Está esto autorizado por FDA para este uso?
Not FDA-cleared for chronic migraine prophylaxis. FDA cleared medicinal leeches only for venous congestion in microsurgical reconstruction (K040187, 2004). Use here is investigational.
¿Qué evidencia existe?
Tier C (investigational). There are no published controlled trials of leech therapy for chronic migraine prophylaxis. Evidence-based options include FDA-approved CGRP monoclonal antibodies (erenumab, fremanezumab, galcanezumab, eptinezumab) with strong RCT support, FDA-approved onabotulinumtoxinA for chronic migraine (PREEMPT trials), topiramate, propranolol or other beta-blockers, amitriptyline, venlafaxine, and behavioral therapies (CBT, biofeedback). Acute therapy: triptans, gepants, ditans, NSAIDs. Avoidance of medication-overuse headache is critical.
Riesgos principales
  • Bleeding from each bite site for 6 to 24 hours after detachment
  • Bruising over the temporal or periorbital region for 5 to 10 days
  • Local skin or, rarely, Aeromonas hydrophila infection
  • Allergic reaction to leech saliva (uncommon)
  • TRIGGER RISK: many migraine patients have specific triggers; placement may precipitate attacks
  • Worsening of migraine for 1 to 3 days following sessions
  • Delay of FDA-approved CGRP monoclonal antibodies, onabotulinumtoxinA, topiramate, propranolol
  • Placebo response masking medication-overuse headache or secondary causes
Quién no debería considerar esto
  • Patients with red-flag headache features (sudden onset, neurological deficits, fever, immunosuppression, age over 50 new-onset)
  • Patients with medication-overuse headache who need analgesic detoxification first
  • Patients who have not tried CGRP monoclonal antibodies, onabotulinumtoxinA, topiramate, propranolol, or other RCT-supported preventives
  • Patients with active dermatitis or broken skin at planned placement sites
  • Patients on anticoagulants, with hemophilia, or with severe anemia
  • Pregnant patients (migraine prevention strategy is different in pregnancy)
Qué preguntar a su clínico
  • Have I tried CGRP monoclonal antibodies (erenumab, fremanezumab, galcanezumab, eptinezumab) or gepants?
  • Am I a candidate for onabotulinumtoxinA (Botox) using the PREEMPT protocol for chronic migraine?
  • Have I tried topiramate, propranolol, amitriptyline, or other RCT-supported preventives at adequate doses?
  • Am I using acute therapy more than 10 to 15 days per month (medication-overuse headache risk)?
  • Have I tried CBT, biofeedback, lifestyle modification, sleep optimization, and trigger management?
  • Why is leech therapy being considered given highly effective FDA-approved options for migraine?
  • What is the practitioner's plan if I have a migraine attack during or after a session?
Cuándo buscar atención urgente
  • Thunderclap (worst-of-life) headache (possible subarachnoid hemorrhage - 911)
  • Headache with fever, stiff neck, photophobia, or altered mental status (possible meningitis)
  • Headache with focal neurological deficit, persistent vision change, speech difficulty, or seizure
  • Jaw claudication, scalp tenderness, or vision change in age over 50 (possible giant cell arteritis)
  • Migraine with aura lasting more than 1 hour, or atypical aura
  • Bleeding from a bite site lasting more than 24 hours
  • Hives, facial or throat swelling, or breathing difficulty

Qué NO significa esto

  • This is not FDA-cleared for migraine prophylaxis.
  • No controlled trials support efficacy; FDA-approved CGRP monoclonal antibodies and onabotulinumtoxinA have transformed chronic migraine treatment.
  • It does not replace evidence-based prevention with the strongest RCT support.
  • Medication-overuse headache must be addressed first if present.
  • Migraine triggers vary by patient - placement may precipitate rather than prevent attacks.

Clinical Profile

Category
neurological
ICD-10
G43.701, G43.711, G43.719, G43.A0, G43.A1
Safety tier
low

Evidence Summary

Chronic migraine is defined per ICHD-3 as ≥15 headache days/month for ≥3 months with ≥8 migrainous features. Preventive options include topiramate, propranolol, candesartan, onabotulinumtoxinA, and CGRP-targeted therapies (erenumab, fremanezumab, galcanezumab). Medication-overuse headache must be ruled out and addressed first. No controlled clinical trial or published prophylaxis series of leech therapy for chronic migraine has been reported; any use is investigational and mechanistic only, with no comparator-controlled data to support it.

Treatment specifics

How many leeches, where they are placed, how long a session lasts, and whether to repeat are clinical decisions made by a qualified provider under institutional protocol — not something to self-administer. Discuss the specifics with a clinician experienced in medicinal leech therapy. (Clinicians: switch the audience selector in the top bar to “Clinician” to view protocol detail.)

Key Trials

  1. Bahramsoltani M et al. (2020), n=22

Contraindications

  • Active anticoagulant therapy (warfarin INR >2.0, DOACs, heparin)
  • Hemophilia or other bleeding disorder
  • Severe anemia (Hb <10 g/dL)
  • Active bacteremia or sepsis
  • Known hypersensitivity to leech salivary proteins
  • Pregnancy (relative — first/third trimester)
  • Immunocompromised state with severe neutropenia
  • Medication-overuse headache without prior taper
  • Secondary headache from undiagnosed cause
  • Current ergot or triptan overuse

Related Conditions

Este sitio web proporciona información educativa y no constituye consejo médico, diagnóstico ni recomendaciones de tratamiento. La terapia con sanguijuelas medicinales conlleva riesgos clínicamente significativos y debe ser realizada únicamente por profesionales calificados bajo protocolos aprobados institucionalmente. La autorización 510(k) de la FDA para sanguijuelas medicinales se limita a indicaciones específicas; las discusiones sobre uso investigativo y fuera de indicación se señalan correspondientemente. Para orientación médica específica, consulte a un profesional de salud calificado.

Chronic Migraine Prophylaxis (≥15 Headache Days/Month) — Hirudotherapy Evidence | ASH