YuukiAS Clinical Report Writing
Safety Boundary
Use this skill for drafting and structuring medical documentation. Do not assert diagnosis, causality, guideline compliance, or regulatory status without current source verification and user-provided facts.
Workflow
- Classify report type: case report, diagnostic report, clinical trial/SAE/CSR document, SOAP note, H&P, discharge summary, or consultation note.
- Confirm privacy constraints and remove identifiers before analysis or drafting.
- Read the relevant checklist for report type, then verify any clinical guideline, CARE/CONSORT/STROBE/ICH statement, or disease fact against current sources.
- Draft with clear separation between user-provided data, interpretation, missing data, and literature-backed context.
- Keep required sections only; avoid copying long generic checklists into the output.
- Validate de-identification, consent language, source dates, and limits of interpretation.
References
- Read
references/source-notes.mdbefore citing guidelines, regulatory standards, or clinical facts. - Read
references/clinical-report-checklist.mdfor report-type routing and de-identification checks. - Read
references/legacy-full-skill.mdonly for detailed legacy templates, CARE checklist text, and LaTeX formatting patterns.
Validation
- All patient facts are either supplied by the user or explicitly marked missing.
- All current clinical claims are dated and sourced.
- The report includes review/sign-off language when used for clinical or regulatory contexts.