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Evidence Synthesis & Systematic Review Support for Medical Librarians

Accelerate systematic reviews with AI-powered evidence screening and data extraction

3.5(6 reviews)
100+ downloads
Updated Nov 2026

What You Can Do

Streamline your systematic reviews by using Claude to screen abstracts against inclusion criteria, extract structured data from full texts, and synthesize findings across studies. Reduce manual screening time by 60-80% while maintaining rigorous documentation of your review methodology. Claude becomes your collaborative partner throughout the entire evidence synthesis workflow, from protocol planning to final data synthesis.

Features

Automated Abstract Screening

Screen hundreds of abstracts against PICOS criteria and inclusion/exclusion rules in minutes, with documented rationale for each decision

Structured Data Extraction

Extract and standardize data fields from research papers—study design, population, interventions, outcomes, results—in consistent table formats

Quality & Risk of Bias Assessment

Evaluate methodological rigor using Cochrane RoB 2, GRADE, or JBI frameworks with supporting evidence and bias domain ratings

Findings Synthesis & Organization

Organize study findings thematically, identify patterns across diverse designs, and generate strength-of-evidence statements

PRISMA Protocol & Documentation

Generate systematic review protocol checkpoints, flow diagrams, and registration-ready documentation for PROSPERO

Decision Audit Trail

Maintain transparent logs of all screening decisions and extraction rules, supporting reproducibility and methods sections

Bibliography & Citation Integration

Work with RIS, BibTeX, and JSON formats to ingest reference lists and maintain study-level metadata throughout review

Example Output

Example 1: Abstract Screening Summary

PubMed IDTitleDecisionRationale
38214567Metformin and cardiovascular outcomes in type 2 diabetesINCLUDERCT design, population ≥18y with T2D, intervention: metformin, outcome: CV events
38156234Insulin glargine in geriatric patientsEXCLUDEPopulation: geriatric (age cutoff specified ≥60), intervention: insulin not metformin
38091456Effects of GLP-1 agonists on HbA1cUNCLEARIntervention partially overlaps (combinotherapy with metformin). Needs full-text review.

Example 2: Data Extraction Table

Study IDDesignNMean AgeInterventionDurationPrimary OutcomeEffect Sizep-valueFunding
Adams2022RCT45058.3yMetformin 1g BID24 monthsHbA1c reduction1.2% (95% CI: 0.9–1.5%)<0.001NIH

Example 3: Risk of Bias Summary

Bias DomainRisk LevelEvidenceRating
Selection biasLowRandomization sequence generated by computer, allocation concealment used✓
Performance biasSome concernsSingle-blind design; patients aware of intervention⚠
Detection biasLowOutcome assessors blinded to allocation✓
Overall RiskLowMost domains low risk; performance bias acceptableIncluded in meta-analysis

What's Included

  • Screening Workflow Templates: Pre-built decision trees for PICOS frameworks, Cochrane Consumers and Communication criteria, and custom inclusion rules
  • Data Extraction Schemas: Customizable templates for RCTs, cohort studies, qualitative research, and diagnostic accuracy studies with field validation
  • Critical Appraisal Tools: Integration with Cochrane Risk of Bias 2, GRADE assessments, JBI checklists, and CASP instruments
  • Synthesis Prompts & Frameworks: Guided prompts for thematic synthesis, narrative reviews, vote-counting meta-analysis, and complex interventions
  • Documentation & Reporting Templates: PRISMA 2020 checklist, PROSPERO registration scaffold, flow diagram data, and supplementary tables ready for publication
  • Quality Control Workflows: Prompts for inter-rater reliability checks, consistency verification across screeners, and duplicate-study detection

Who It's For

  • Medical Librarians
  • Clinical Research Scientists
  • Evidence Synthesis Coordinators
  • Healthcare Policy & Guidelines Developers
  • Graduate Students & Doctoral Researchers

Best For

  • Accelerating initial abstract screening at scale
  • Standardizing data extraction across diverse study types
  • Conducting methodological quality assessments
  • Organizing complex syntheses with multiple outcomes
  • Generating PRISMA-compliant documentation

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