clinical-reports
Write clinical reports with compliance validation
Also available from: K-Dense-AI
Healthcare professionals need to create accurate, regulation-compliant clinical documentation but struggle with complex guidelines and verification. This skill provides CARE-compliant case report templates, HIPAA de-identification checks, and validation tools for clinical trial documents.
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Using "clinical-reports". Create a clinical case report for a 65-year-old patient with atypical pneumonia presentation
Expected outcome:
- Case Report Template Generated
- Structure: Title, Abstract, Introduction, Patient Information, Clinical Findings, Timeline, Diagnostic Assessment, Therapeutic Interventions, Follow-up and Outcomes, Discussion, Informed Consent Statement
- Validation: 12 CARE checklist items identified
- Note: Remember to remove all HIPAA identifiers before publication
Using "clinical-reports". Check this discharge summary for HIPAA compliance
Expected outcome:
- HIPAA De-identification Check Complete
- Found 3 potential identifier types: Names, Dates, Geographic data
- Example locations flagged for review
- Recommendation: Replace names with 'the patient', use approximate dates
Security Audit
Low RiskLegitimate clinical documentation skill. All 589 static findings are false positives caused by pattern detection on medical documentation content. The skill contains 8 Python scripts for local text processing and validation. No network calls, no external command execution, no credential access, no obfuscated code.
Risk Factors
⚡ Contains scripts (3)
📁 Filesystem access (2)
🌐 Network access
⚙️ External commands
🔑 Env variables
Quality Score
What You Can Build
Publish case reports
Create CARE-compliant case reports for medical journal submission with proper de-identification
Document trial safety
Write SAE reports and clinical study reports meeting ICH-E3 and FDA regulatory requirements
Standardize documentation
Generate consistent radiology, pathology, and laboratory reports using professional templates
Try These Prompts
Generate a clinical case report template for a patient with [condition]. Include sections for introduction, patient information, clinical findings, diagnostic assessment, treatment, and follow-up.
Check my clinical case report for HIPAA compliance. Identify any of the 18 protected health information identifiers that need to be removed or modified.
Create a serious adverse event report template for a clinical trial participant. Include all required elements for regulatory submission.
Generate a SOAP note template for a [follow-up/initial] visit. Include subjective, objective, assessment, and plan sections with placeholders.
Best Practices
- Always verify de-identification before sharing or publishing any clinical document
- Obtain and document informed consent before creating case reports for publication
- Use the validation scripts to check compliance before regulatory submission
Avoid
- Publishing clinical documents without removing all 18 HIPAA identifiers
- Skipping the informed consent documentation step for case reports
- Submitting clinical trial reports without validating against ICH-E3 structure
Frequently Asked Questions
Is this skill compatible with all electronic health record systems?
What are the word count requirements for case reports?
Does this skill integrate with reference management tools?
Is patient data stored or transmitted anywhere?
What do I do if HIPAA identifiers are detected?
How does this compare to other medical writing tools?
Developer Details
File structure