Knowledge Base Policy

ChatIBD answers questions using retrieval grounded in a curated knowledge base of clinical sources, rather than from the open-ended memory of a general language model. This policy sets out how sources are selected, sourced, versioned, and retired, so that every source in the corpus is either core IBD guidance from a recognised body or carries a recorded reason it changes IBD management.

Our aim is a corpus that is bounded, explainable, and auditable: not "everything that might be relevant", but a defined set of sources whose inclusion can be justified and whose gaps are stated honestly rather than left silent.

Last Updated: 9 July 2026

What the knowledge base contains

The knowledge base holds the professional sources used to ground ChatIBD's answers. These fall into two tiers:

  • Core sources — IBD-specialist guidance from recognised authorities.
  • Adjacent sources — non-IBD-guideline material admitted only where it changes how IBD is managed, such as vaccination guidance, medicines safety alerts, and the product labels (Summaries of Product Characteristics, or SmPCs) of co-prescribed drugs.

Research datasets, ethics-study materials, general website content, and user chat content are not part of the retrieval knowledge base and are governed separately.

Two questions we ask of every source

Each source is assessed on two independent questions, recorded separately:

  • Eligibilityshould this source be in scope?
  • Sourcing and licensingcan we lawfully store, index, and reuse it?

A source can be eligible but not lawfully sourceable. Keeping these separate means such a gap is logged honestly ("in scope, not indexed for licensing reasons") rather than appearing as though the material simply does not exist.

Generally, an eligible source is one that is published by a recognised professional, academic, regulatory, or medicines-information body; is date-stamped and attributable to a publisher; and is available in a stable format suitable for citation and review.

Core sources: recognised IBD guidance

A core source is admitted if either:

  1. It is published by a recognised IBD guidance body — for example BSG, ECCO, ESPGHAN, ACG, AGA, or GETECCU. Recognising a body does not automatically admit everything it publishes; each document is still assessed on its own merits.
  2. A named clinical reviewer admits it with a recorded rationale — preserving legitimate specialist judgement for high-quality sources outside the list above, while keeping every such decision explainable and attributable.

Each core source records its grade — guideline, consensus/position statement, or review — because these carry different authority, and formal guidelines should outweigh narrative reviews where sources disagree.

Adjacent sources: the management-change gate

A non-IBD-guideline source is eligible only where the material it contains changes IBD management. It must satisfy at least one of the following, each backed by a citable source:

  • Interaction with an IBD therapy — an actionable pharmacological interaction (dose change, avoid, or monitor). For example, allopurinol with a thiopurine.
  • Peri-procedural implication — it changes management around endoscopy or surgery. For example, anticoagulants before endoscopy, or GLP-1 agonists and aspiration risk under sedation.
  • Effect on disease activity — it can precipitate, worsen, or mimic IBD activity. For example, NSAIDs triggering a flare, or checkpoint-inhibitor colitis.
  • Change to preventive care driven by immunosuppression or IBD therapy — vaccination, infection screening, or malignancy surveillance altered by IBD treatment. For example, live-vaccine contraindications under biologics or thiopurines, and pre-biologic TB and hepatitis B screening.

Prevalence alone is not a criterion. That a condition or medicine is common among IBD patients does not, by itself, admit a source. Without this line the corpus would expand without limit into general cardiology, endocrinology, and beyond. How common something is affects only how we prioritise work — never whether a source is in scope.

Co-prescribed drug labels (SmPCs)

As IBD patients are increasingly co-prescribed non-IBD medicines, ChatIBD indexes the official product labels of a curated set of drugs relevant to IBD care. A drug's label is included only where co-prescribing it changes IBD management, through one of the mechanisms above.

We source labels from the European Medicines Agency's centrally authorised products, which carry clean reuse terms. As a consequence, some nationally authorised medicines — for example mesalazine and NSAIDs — are recognised as in scope but their labels are not indexed, because we cannot currently license those national sources. This is a structural sourcing limit, not an oversight.

Where a label is not indexed, ChatIBD will say so rather than imply the medicine is safe, irrelevant, or unknown. The indexed set is deliberately capped to keep it maintainable, and the model discloses which product and indication a label came from.

Jurisdiction and precedence

Sources span jurisdictions (for example UK, EU, US). Each source records a jurisdiction tag, and:

  • Current UK and local guidance is the default frame for answers.
  • Adjacent and foreign-jurisdiction sources are supplementary and must not silently override core UK guidance.
  • Where the basis of an answer is a source from another jurisdiction, ChatIBD discloses that jurisdiction — a US safety alert answering a UK question is identified as US.

Superseded and conflicting guidance

  • Superseded guidance is marked as such and removed from active retrieval unless there is a documented reason to retain it; a replacement is added where available.
  • Conflicting guidance is retained where each source is authoritative and current. Rather than hiding disagreement, ChatIBD is designed to present it, applying precedence by jurisdiction, recency, and document grade.

What we exclude

  • Patient forum and social-media content.
  • Unattributed or undated content.
  • Superseded guidance, unless deliberately retained and clearly marked.
  • Promotional material, unless used solely as clearly identified product information and reviewed for bias.
  • Sources that cannot be lawfully stored or indexed.
  • Adjacent sources that fail the management-change gate.

Review and change control

  • Sources pass through a single intake step that records the reason for inclusion, publisher, jurisdiction, licensing status, and a currency check before they are added.
  • The corpus is reviewed on a regular cadence, and immediately after any significant user-reported error or superseding publication.
  • Material changes to the corpus — additions, removals, and updates — are recorded in an internal change log with the reason, approver, and impact.

Feedback

If you believe an important source is missing, out of date, or incorrectly cited, please tell us. User feedback is reviewed as part of the process above, and clinically significant reports are escalated for review.

For queries about this policy, contact us at contact@chatibd.com.