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医疗报告结构与来源检查

整理病例、诊断、试验和研究报告的文档结构,使用本地检查工具核对来源事实与报告字段,结果供专业人员审阅。

开源精选医疗业务39 个文件50,135 Stars浏览次数 2K-Dense-AI/scientific-agent-skills MIT版本 a1043ef
开始使用

适用环境:Requires Python 3.11+ for optional dependency-free local scripts. No credentials or network needed for data processing; network access is needed only to review current public guidance.

输入资料
获准使用且符合原文范围的资料 经过核查的来源事实与报告类型 阅读本节完整说明
交付内容
结构化报告草稿 来源与文档检查记录 阅读本节完整说明
  1. 获取完整包,保留配套文件的目录结构。
  2. 按照原文准备所需工具、依赖与输入资料。
  3. 阅读对应使用步骤与输入输出说明,在自己的环境中验证结果。

使用提示摘自原文,配套文件保留来源版本;实际运行条件以各包说明为准。

正文

获取原文件

references/case_report_guidelines.md

Current source

The official CARE site continues to identify the 2013 CARE Checklist as the core checklist. The 2017 explanation and elaboration supplies rationale and examples. CARE is reporting guidance for case reports; it does not authorize record access, establish consent, prove de-identification, or replace journal instructions.

Thirteen checklist headings

Preserve the official structure:

  1. title;
  2. key words;
  3. abstract;
  4. introduction;
  5. patient information;
  6. clinical findings;
  7. timeline;
  8. diagnostic assessment;
  9. therapeutic intervention;
  10. follow-up and outcomes;
  11. discussion;
  12. patient perspective;
  13. informed consent.

Use the official checklist and explanation for subitems. The local validator checks only that all headings have an allowed status and verified fact references; it does not judge clinical accuracy or CARE adherence.

Safe use

  • Begin with assets/case_report_template.json.
  • Use de-identified source facts, not copied charts or free-text records.
  • Keep direct identifiers and contact details out of the draft manifest.
  • Represent chronology with relative study/case offsets when authorized and scientifically adequate; do not alter chronology to disguise conflicts.
  • Preserve diagnostic and therapeutic statements as attributed facts from authorized records. Do not independently diagnose, rationalize treatment, or recommend care.
  • Attribute the patient perspective to an authorized source; never invent a quote.
  • Keep uncertainty, missing follow-up, adverse outcomes, and limitations visible.
  • Do not claim novelty until an accountable author has reviewed the literature.
  • Avoid causal or general treatment claims from a single case.

CARE includes informed consent as an item, but a template cannot obtain or verify consent.

  • Record only a consent status verified by the responsible human reviewer.
  • Do not create a stock statement asserting that consent was obtained.
  • Consent for publication and HIPAA de-identification are separate questions.
  • De-identification does not necessarily remove all re-identification risk, particularly for rare conditions, small communities, images, unusual timelines, or distinctive combinations.
  • Journal, institution, law, ethics-board policy, and circumstances involving minors, deceased persons, or persons unable to consent require qualified review.

Fail-closed statuses

Each CARE item uses one of:

  • verified_present — supported by one or more verified source-fact IDs;
  • not_applicable_with_rationale — a qualified reviewer supplied a recorded rationale;
  • missing — blocks structural readiness;
  • conflict — source records disagree and human resolution is required.

The consent item cannot be waived by the script. A missing or unresolved consent status blocks publication handoff.

Qualified review

Before any journal handoff, accountable authors and the appropriate clinical, privacy/legal, and institutional reviewers must verify:

  • source accuracy and chronology;
  • consent and authorization;
  • privacy and image/metadata handling;
  • terminology and clinical interpretation;
  • discussion claims and citations;
  • conflicts, limitations, and adverse outcomes;
  • the target journal’s current instructions.

A structural result of STRUCTURE_COMPLETE_REVIEW_REQUIRED is not permission to submit.

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