SCI journal selection assistant for meta-analysis and systematic review papers. Use this skill when the user has completed or is completing a meta-analysis a...
数据分析
Hcc Meta Ai
试用AI-assisted meta-analysis workflow for hepatocellular carcinoma comparative effectiveness research. Six-element prompt framework covering full pipeline from...
它能做什么
AI-assisted meta-analysis workflow for hepatocellular carcinoma comparative effectiveness research. Six-element prompt framework covering full pipeline from literature screening to data extraction. Published skill accompanying the validated methodology paper.
技能文档
HCC Meta-Analysis AI Skill
Overview
This skill implements a standardized, AI-assisted meta-analysis workflow for comparing treatment efficacy in hepatocellular carcinoma (HCC). It follows a six-element prompt architecture (Role–Objective–Skills–Constraints–Workflow–Output) validated across two independent clinical questions with three large language models.
The workflow covers the full meta-analysis pipeline:
- Literature screening (fuzzy → precise → supplementation)
- Full-text eligibility determination
- Newcastle–Ottawa Scale (NOS) quality appraisal
- Structured baseline data extraction
- Clinical outcome data extraction
Validation: Benchmarked against dual-independent manual review across two HCC projects with GPT-5.2, GPT-4o, and DeepSeek V3.1. Best-performing models achieved >95% accuracy at most stages with >80% total time reduction.
When to Use
- Conducting a meta-analysis comparing two HCC treatments
- Need rapid evidence synthesis for HCC therapeutic comparison
- Want to standardize the AI-assisted review process across projects
- Teaching or replicating the validated AI meta-analysis methodology
Six-Element Prompt Framework
Every prompt in this workflow follows a standardized six-element structure:
| Element | Purpose | Example |
|---|---|---|
| Role | Defines AI's academic persona | "You are a clinical epidemiologist specializing in HCC..." |
| Objective | States the specific task goal | "Screen titles for studies comparing treatment A vs B..." |
| Skills | Lists required capabilities | "Identify medical terms, apply synonym rules, extract structured data" |
| Constraints | Sets methodological boundaries | "Apply NOS scoring rules strictly; mark missing data as NA" |
| Workflow | Specifies step-by-step execution | "Read title → check for intervention terms → classify" |
| Output | Defines structured output format | "Output as JSON table with fields: PMID, Decision, Reason" |
Workflow Stages
Stage 1: Literature Screening
Three sub-stages with escalating cognitive demands:
-
Fuzzy Screening — Title-level keyword matching
- Batch 100 records per query
- Check for presence of target disease + intervention terms
- Template:
scripts/01-fuzzy-screening.md
-
Precise Screening — Abstract-level multi-constraint reasoning
- Evaluate title + abstract against inclusion criteria
- Requires comparison of two interventions with reported outcomes
- Template:
scripts/02-precise-screening.md
-
Literature Supplementation — Citation tracing from full texts
- Upload PDFs of included studies
- Extract reference lists; flag potentially missed eligible studies
- Template:
scripts/03-literature-supplement.md
Stage 2: Full-Text Eligibility Determination
Full-text comprehension and multi-criteria decision-making:
- Study population (primary HCC confirmed)
- Direct comparison of two target treatments
- ≥1 clinical outcome reported
- Original study design (prospective/retrospective cohort, case-control, RCT)
- Data separable by treatment group
- Sample size ≥10
- Template:
scripts/04-eligibility.md
Stage 3: NOS Quality Appraisal
Structured scoring across three domains:
- Selection (4 items, max 4 pts): representativeness, non-exposed cohort, exposure ascertainment, outcome absent at baseline
- Comparability (1 item, max 2 pts): confounder control
- Outcome (3 items, max 3 pts): assessment objectivity, follow-up duration, follow-up completeness
- Template:
scripts/05-nos-scoring.md
Stage 4: Baseline Data Extraction
Structured extraction of study characteristics and patient demographics:
- Core fields: author, year, design, treatment groups, sample size, age, sex, tumor characteristics, follow-up, laboratory values
- Topic-specific extensions (see references)
- Template:
scripts/06-baseline-extraction.md
Stage 5: Outcome Data Extraction
Structured extraction of clinical endpoints:
- 1–5 year overall survival (OS), recurrence-free survival (RFS)
- Local tumor progression, distant recurrence, technical success
- Complication rates and subtypes
- Template:
scripts/07-outcome-extraction.md
Disease-Agnostic Design
The six-element scaffold is independent of specific diseases. To adapt this workflow for a different disease:
- Replace disease terminology in
references/terminology.json - Swap intervention names in each prompt template
- Adjust topic-specific extraction fields in baseline/outcome templates
- Keep the core logical structure intact
For HCC specifically, the pre-configured terminology and extraction fields in references/ are ready to use.
Platform
A web-based platform for deploying and sharing this workflow is available at: http://8.149.142.6/metaexp/
References
- Full methodology: see accompanying manuscript
- Supplementary prompt details: S1 (Project 1 prompts), S2 (Project 2 prompts)
- Terminology database:
references/terminology.json
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