Medical evidence methods · Study selection
How to select studies for a systematic review: deduplication and PRISMA flow
Organise selection decisions into a reviewable PRISMA count table Requested outputs / delivery goal: A selection-ledger structure, a PRISMA count-checking table and items awaiting adjudication.
Specify eligibility criteria first, retain deduplication and screening decisions, then link different reports of the same study. Build the PRISMA diagram from actual records, not by drawing boxes and inventing numbers.
This guide concerns selection and counting, not a complete review protocol, search design, risk-of-bias assessment or meta-analysis. PRISMA 2020 is reporting guidance, not quality certification; literature counts are not participant counts.
Sources are official PRISMA materials and Cochrane Handbook Chapter 4. For Cochrane intervention reviews, at least two people independently make final full-text eligibility decisions, with disagreement procedures defined in advance. Duplicate independent initial screening is desirable, not mandatory in that chapter. Other reviews should state arrangements under their applicable guidance and protocol.
A concrete task with RigorMed
Organise selection decisions into a reviewable PRISMA count table
These are suggested task inputs and outputs to request, not a new execution, a customer outcome or a guarantee of completion.
Materials to provide: Prespecified eligibility criteria, sourced search records, actual deduplication, initial screening and full-text decisions, and exclusion reasons.
Requested outputs / delivery goal: A selection-ledger structure, a PRISMA count-checking table and items awaiting adjudication.
An example request
Distinguish records, reports and studies. Using the actual decisions I provide, organise a selection ledger and PRISMA count-checking table, listing conflicts and missing reasons. Do not perform independent screening that has not been done on my behalf.
What still needs review
This is not a completed systematic review, independent dual screening or meta-analysis. Original-text decisions and disagreement resolution remain the responsibility of the designated reviewers.
Four steps from search results to included studies
Prespecify the question and eligibility rules
Before screening, define population, intervention or exposure, comparator, outcomes, design and necessary date or language limits. Explain restrictions, reviewer roles and disagreement procedures. Pilot the rules on a small set; retain unclear records rather than excluding them automatically because an abstract omits information.
Deduplicate records without losing provenance
Save databases, complete searches, dates, export batches and identifiers. Check duplicate candidates using DOI, PMID, title, authors and year; retain merge mappings and sources. A preprint, conference abstract and journal article may be different reports of one study, not disposable duplicates.
Separate initial screening, retrieval and full-text assessment
Screen titles and abstracts, seek potentially eligible full texts, then apply the prespecified rules. Distinguish reports not retrieved from reports read and found ineligible. Log stage, decision, reason, reviewer, date and resolved disagreements; an AI summary is not a final eligibility assessment.
Link reports to studies and reconcile the flow
Use registration numbers, locations, dates, populations and methods to link reports; retain their additional information. Count records, reports and studies separately. Neither one article per study nor a participant-flow counting scheme can be assumed.
A reconciled synthetic PRISMA example
Assume a new review used only databases and registers, removed only duplicates before screening, and mapped each retained candidate record to one report sought. All numbers are synthetic teaching data: no real search or review was conducted.
| Stage | Unit | Count |
|---|---|---|
| Identified | Records | 1000 |
| Duplicates removed before screening | Records | 200 |
| Title/abstract screening | Records | 800 |
| Excluded at initial screening | Records | 680 |
| Sought for retrieval | Reports | 120 |
| Not retrieved | Reports | 8 |
| Assessed for eligibility | Reports | 112 |
| Excluded after full-text assessment | Reports | 92 |
| Reports of included studies | Reports | 20 |
| Included | Studies | 18 |
Reconcile stages: 1000 − 200 = 800; 800 − 680 = 120; 120 − 8 = 112; 112 − 92 = 20. Linking the 20 included reports identifies 18 studies; subtraction alone cannot establish that linkage. Other sources, automated removals or an updated review need the appropriate official template and separately documented branches.
Trace exclusion reasons; balanced counts do not prove absence of bias
Synthetic primary full-text exclusion reasons are wrong population (40), design (20), intervention or exposure (18), and prespecified time range (14): 40 + 20 + 18 + 14 = 92. These are teaching counts, not universal thresholds. Retain every applicable reason, but count one primary reason using a prespecified hierarchy; never subtract the same report twice.
The 8 unretrieved reports are not 8 assessed, ineligible studies. Disclose retrieval attempts and non-retrieval, and assess possible implications. Reconciled counts do not establish comprehensive searching, unbiased selection or suitability for pooling effects.
Six checks before reporting the flow
Check real screening records, not merely the drawing:
- Were eligibility rules, reviewers and disagreement procedures prespecified?
- Are search sources, dates, strategies and duplicate mappings retained?
- Are initial exclusions, non-retrieval and full-text exclusions separate?
- Can exclusion decisions be traced to rules, original texts and records?
- Are multiple reports linked correctly and counted separately from studies?
- Do text, supplements and diagram agree, without confusing literature with participants?
Automation may assist organisation and flagging, but disclose its actual use, human decisions and verification. Software checks do not replace review authors’ responsibility.
Frequently asked questions
Does deduplication leave the number of studies?
No. Records can refer to the same report, and one study can have several reports. Deduplicate records, assess full-text eligibility, link studies and preserve each counting unit.
Can an unavailable full text be excluded as ineligible?
Non-retrieval alone does not establish assessed ineligibility. Report it separately and document attempts. Judge eligibility only under the protocol and verifiable materials; preserve uncertainty when evidence is insufficient.
Does a completed PRISMA diagram permit meta-analysis?
No. Extract and verify data, assess risk of bias, evaluate comparability and define synthesis methods under the protocol. The diagram neither authorises statistical computation nor establishes valid conclusions.
Verified sources
The official sources below were checked on 2026-10-03 / RigorMed: 2026-10-13. Access conditions and update dates are rechecked before publication.
- PRISMA official: 2020 reporting guidance
Reporting guidance is not quality certification.
- PRISMA official: 2020 flow diagrams
Choose the template for new or updated reviews and actual sources.
- Cochrane Handbook: Chapter 4, searching and selecting studies
Section 4.6; independent dual full-text decisions are described in the intervention-review context.
Start with a specific task
Organise selection decisions into a reviewable PRISMA count table
Bring legally usable materials and this page's example request to the workspace. Check the pre-execution material and credit notices before confirming, then review the resulting outputs.
