American Society of Hirudotherapy

Drug-discovery frontier · Evidence-first

A drug-discovery frontier, hidden in leech biology.

440+ bioactive proteins make up the medicinal-leech secretome — three have already become FDA-approved anticoagulant drugs (lepirudin, bivalirudin, desirudin), and most remain scientifically uncharted. The American Society of Hirudotherapy curates 141 years of evidence, verifies every citation, and opens the field to clinicians, researchers, and partners.

Peer-reviewed research · Independent 501(c)(3) · 1,400+ publications · 71 authoritative sources · 30 documented safety events

How we work · How we grade evidence · Editorial methodology

FDA-cleared device indication framingClinical knowledge infrastructure

141

Years of leech-derived science

From Haycraft 1884 → Markwardt 1957 → Bivalirudin 2000

440+

Characterized salivary proteins

Liu et al. 2019 · expanded 2025

78%

Microsurgical flap salvage rate

Whitaker et al. 2012 · n=277 systematic review

HOW WE EVALUATE EVIDENCE

GRADE framework · ASH evidence tiers · open research questions.

We distinguish FDA-cleared indications from off-label applications on every page. We acknowledge what we don't yet know — 42 open research questions catalogued. We are a 501(c)(3) nonprofit with a public conflict-of-interest policy and a transparent correction log.

Read our editorial methodology

What we do

Safe institutional adoption

A ten-phase Implementation Playbook covering stakeholder alignment, clinical protocols, pharmacy workflow, nursing training, infection prevention, quality metrics, billing, and regulatory compliance — synthesizing best practice from leading microsurgical centers.

Read the playbook

Practitioner training & education

A five-level educational framework from medical-student survey through reconstructive-microsurgery fellowship and continuing medical education. Competencies, learning objectives, assessment methods, faculty resources.

See the curriculum

Research leadership

1,400+ indexed publications. 71 authoritative external sources mapped. 42 open research questions identified. 30 milestones across 141 years documented. 12 breakthrough horizons mapped.

Open the research library

U.S. medicinal leech supply

A public-benefit infrastructure project focused on biosecurity, chain-of-custody documentation, antimicrobial resistance surveillance, and domestic-source resilience for the world's third-most-prescribed living medical device.

Read the proposal

Where 141 years of evidence meets the next decade of breakthrough medicine.

FDA-cleared indications are explicit on every clinical page. Investigational and off-label uses are clearly labeled. Read our editorial methodology for our evidence-grading framework.

This website provides educational information and does not constitute medical advice, diagnosis, or treatment recommendations. Medicinal leech therapy carries clinically meaningful risks and should be performed only by qualified clinicians under institutionally approved protocols. FDA 510(k) clearance for medicinal leeches is limited to specific indications; investigational and off-label discussions are labeled accordingly. For patient-specific guidance, consult a qualified healthcare provider.

American Society of Hirudotherapy — Living Medicine, Modern Science