American Society of Hirudotherapy

Protocol Version Registry

A reference record showing how every educational protocol document carries a version, a last-reviewed date, a next-review date, and a defined review cycle.

Educational reference infrastructureNot authorized clinical orders

The American Society of Hirudotherapy maintains a registry of educational reference protocol documents. The registry exists so that institutions can see, at a glance, which version of a reference document they are reading, when it was last reviewed, when it is next scheduled for review, and where it sits in the review cycle.

Every document in the registry is an educational reference. It is written to help institutions, educators, and clinicians understand how a topic is structured and documented — not to issue instructions. Each reference protocol must be adapted to local context and formally approved by the receiving institution before it is used. The registry records governance metadata; it does not authorize care.

What every protocol document carries

To be listed in the registry, a reference protocol document must carry four pieces of governance metadata. These fields make the document auditable and let any reader judge how current it is.

Version

A unique version identifier (for example v2.1) so readers and institutions can cite exactly which edition they relied on.

Last reviewed

The date the document last completed a full editorial and evidence review, so currency is transparent.

Next review

The date the document is next scheduled for review, so readers know when content will be re-examined.

Status

Where the document sits in its review cycle: current, in review, review due, or superseded by a newer version.

The review cycle

Every reference protocol document follows a defined, repeating review cycle. On a fixed cadence — and sooner if new evidence or a regulatory change warrants it — each document is re-examined, its metadata is updated, and a new version is issued where the content changes.

1

Scheduled review

Each document carries a next-review date. When that date arrives, the document enters review and its status changes accordingly.

2

Evidence and editorial re-examination

Reviewers check the content against current evidence, regulatory references, and editorial standards, and record what changed.

3

New version and dates

A new version identifier is assigned, the last-reviewed date is set to the review date, and a new next-review date is scheduled. The prior version is marked superseded.

4

Out-of-cycle updates

If new evidence or a regulatory change is material, a document can be reviewed and re-versioned before its scheduled date rather than waiting for the next cycle.

Illustrative registry

The table below illustrates the structure of the registry. The rows are illustrative placeholders that show the columns and field formats — they are not a live published schedule. Each row records a document, its version, its last-reviewed date, its next-review date, and its status in the review cycle.

Illustrative placeholders — not a live schedule and not authorized clinical orders.
Document (illustrative)VersionLast reviewedNext reviewStatus
Reference protocol — venous congestion adjunct (educational)v2.1March 2025March 2027Current
Reference protocol — documentation and consent templatev1.4November 2024November 2026Current
Reference protocol — contraindication screening checklistv3.0January 2025January 2027In review
Reference protocol — device handling and storage guidancev1.2June 2023June 2025Review due
Reference protocol — adverse-event reporting outlinev2.0August 2024August 2026Current
Reference protocol — early draft (replaced)v0.9February 2022n/aSuperseded

Why versioned review matters for institutions

Versioned, dated review is reference infrastructure that institutions can rely on. It lets a hospital, clinic, or training program answer practical governance questions without guesswork.

Auditability

A version and review date let an institution cite exactly which edition of a reference informed its own locally approved documents.

Currency

A next-review date makes it clear when content is scheduled to be re-examined, so institutions are not relying on material of unknown age.

Change tracking

Superseding old versions with new ones creates a clear record of how reference content has evolved over time.

Local accountability

Because each document is a versioned reference, the institution that adopts it can record which version it reviewed and approved for local use.

Reference protocols require local approval

These are educational reference protocols. They require local adaptation and formal approval by the receiving institution before use. They are not authorized clinical orders and do not constitute medical advice. Nothing in this registry describes a cure or a guaranteed treatment outcome; clinical decisions remain the responsibility of qualified clinicians acting under local governance.

Related Resources

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.