Amerikanische Gesellschaft für Hirudotherapie

Functional Dyspepsia (Investigational Adjunct)

Investigational adjunct for functional dyspepsia (Rome IV criteria); H. pylori eradication when positive, proton pump inhibitors, prokinetics, and tricyclic antidepressants remain evidence-based.

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

Patienten-Zusammenfassung

Ist dies FDA-zugelassen fuer diese Anwendung?
Not FDA-cleared for functional dyspepsia. FDA cleared medicinal leeches only for venous congestion in microsurgical reconstruction (K040187, June 2004). Use for functional dyspepsia is investigational.
Welche Evidenz existiert?
Tier C (investigational). Only anecdotal reports; there are no randomized controlled trials. Evidence-based therapy for functional dyspepsia per ACG guidelines: test-and-treat for Helicobacter pylori (urea breath test or stool antigen, eradicate if positive), proton pump inhibitor trial, low-dose tricyclic antidepressant (amitriptyline 10-25 mg) for postprandial distress, prokinetics (metoclopramide short-course, itopride), and psychological therapies (cognitive-behavioral therapy, gut-directed hypnotherapy) for refractory cases. Alarm features require upper endoscopy.
Hauptrisiken
  • Bleeding from bite sites for 6 to 24 hours after detachment
  • Bruising and tenderness over the upper abdomen
  • Local skin infection or, rarely, Aeromonas infection
  • Allergic reaction to leech saliva (uncommon)
  • Trigger of nausea or worsening dyspeptic symptoms
  • Risk of missed underlying gastric ulcer, malignancy, or H. pylori infection
  • Delay of proton pump inhibitor or H. pylori eradication therapy
  • Substitution for low-dose tricyclic antidepressant or psychological therapy in refractory cases
Wer dies nicht in Betracht ziehen sollte
  • Patients with alarm features (unintentional weight loss, anemia, dysphagia, persistent vomiting, hematemesis, melena, palpable mass)
  • Patients who have not been tested for Helicobacter pylori
  • Patients with active peptic ulcer disease or gastric malignancy
  • Patients on anticoagulants, with hemophilia, or with severe anemia
  • Pregnant patients
  • Patients who have not tried proton pump inhibitor for 4-8 weeks
Was Sie Ihren Kliniker fragen sollten
  • Have I been tested for Helicobacter pylori (urea breath test or stool antigen)?
  • Have I had upper endoscopy if I have any alarm features?
  • Have I tried a proton pump inhibitor for 4-8 weeks?
  • Am I a candidate for low-dose tricyclic antidepressant (amitriptyline 10-25 mg)?
  • Have I been offered cognitive-behavioral therapy or gut-directed hypnotherapy?
  • What evidence specifically supports leech therapy for functional dyspepsia?
  • What is the cost and is it covered by insurance? (typically not covered)
Wann dringende medizinische Versorgung suchen
  • Vomiting blood or coffee-ground material (possible upper GI bleeding)
  • Passing black tarry stools (possible GI bleeding)
  • Unintentional weight loss, anemia, or dysphagia (alarm features — endoscopy needed)
  • Severe abdominal pain (possible peptic ulcer perforation)
  • Persistent vomiting or inability to keep down food
  • Spreading redness, warmth, pus, or red streaks (cellulitis)
  • Fever above 38.0 C / 100.4 F or chills
  • Hives, facial or tongue swelling, throat tightness, or breathing difficulty

Was dies NICHT bedeutet

  • This is NOT FDA-cleared for functional dyspepsia.
  • Anecdotal reports do NOT establish efficacy versus H. pylori eradication, proton pump inhibitor, or low-dose tricyclic antidepressant.
  • It does NOT replace upper endoscopy when alarm features are present.
  • It does NOT substitute for evidence-based pharmacologic and psychological therapy.
  • It does NOT distinguish functional dyspepsia from peptic ulcer disease or gastric malignancy.

Clinical Profile

Category
gastrointestinal
ICD-10
K30
Safety tier
medium

Evidence Summary

Functional dyspepsia (Rome IV) is epigastric pain or postprandial distress syndrome without identifiable structural or biochemical cause, after upper endoscopy and H. pylori testing. Evidence-based stepwise management is H. pylori eradication when positive, proton pump inhibitor trial (4-8 weeks), prokinetics (acotiamide where available, or metoclopramide short-term with cardiac caution), low-dose tricyclic antidepressants for refractory pain-predominant disease, and dietary modification. Hypnotherapy and cognitive behavioral therapy have RCT support. No published controlled trials of hirudotherapy exist for functional dyspepsia. Epigastric or upper-abdominal placement has been mentioned in Russian traditional-medicine literature without efficacy data and without consideration of bleeding risk in patients on aspirin or anticoagulants.

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.)

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
  • Untreated H. pylori infection (treat first)
  • Active peptic ulcer disease or upper GI bleeding
  • Aspirin, NSAID, or anticoagulant use
  • Suspected gastric malignancy on endoscopy
  • Prior gastric surgery or bariatric procedure

Related Conditions

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Functional Dyspepsia (Investigational Adjunct) — Hirudotherapy Evidence | ASH