Free Systematic Review and Meta-Analysis Templates

Evidence synthesis infrastructure

The infrastructure problem in systematic review and meta-analysis

Trust in a systematic review rests on the path from question to conclusion. A reader should be able to follow the search, see why studies entered or left the review, inspect the extracted data, and understand how appraisal informed the analysis. Statistical skill cannot restore evidence that the team missed or decisions it failed to record.

Systematic reviews now form part of research infrastructure

Systematic reviews shape clinical guidance and public policy. They influence research priorities and technology assessment. Their reach also extends into education and environmental management, as well as decisions made inside organizations. Hoffmann and colleagues estimated that databases indexed 29,073 systematic reviews in 2019, almost 80 each day and more than twenty times the estimated number indexed in 2000.1 Volume changes the reach of an error. Once reviewers repeat a weak method across the literature, later researchers may build on the result without seeing the defect.

Authors earn authority through the methods they use and the record they provide. PRISMA 2020 asks them to explain why they conducted the review, describe what they did, and report what they found.4 Clear reporting cannot repair poor conduct. It gives readers enough information to judge the work for themselves.

Many decisive errors occur before analysis begins

Meta-analysis requires choices about effect measures and statistical models. Review teams must also address heterogeneity and publication bias. By that point, earlier decisions have shaped the evidence available for synthesis. A flawed search can omit eligible studies, while inconsistent screening can change the included evidence base. Unpiloted extraction introduces transcription or classification errors. If reviewers complete an appraisal without using it, a precise pooled estimate may carry more certainty than the evidence supports.

Salvador-Oliván and colleagues found errors in 92.7% of the published search strategies they examined. Many could reduce the retrieval of relevant studies.5 Rethlefsen and colleagues then studied the reproducibility of searches in 100 systematic reviews. One review provided enough information to reproduce all its database searches within the study’s prespecified tolerance. Among 453 individual searches, 4.9% reported all six assessed PRISMA-S elements.6

Critical appraisal creates a similar gap. Page and colleagues found that 70% of the biomedical systematic reviews they examined reported a formal assessment of risk of bias or study quality.7 The authors described the use of those assessments in analysis as uncommon. A review gains little from a risk-of-bias judgment that never reaches the analysis or interpretation.

The central methodological problem: a review team may finish a protocol, search strategy, screening record, extraction table, risk-of-bias assessment, and meta-analysis without creating a reproducible chain among them. If those links are missing, a reader cannot follow the path from the original question to the final conclusion.

Researchers must assemble a fragmented standards system

Evidence synthesis has a mature methodological system, but its guidance sits across separate standards and tools. PRISMA-P defines minimum reporting expectations for protocols.10 PRISMA-S specifies the information authors need to report a literature search with enough detail for another researcher to reproduce it.11 Review teams use structured instruments to judge risk of bias and GRADE to assess certainty in a body of evidence. PRISMA 2020 guides the report of a completed review.12134

Teams tend to encounter a standard when its form becomes due. That timing comes too late for some decisions. At manuscript submission, a reporting checklist may ask for information that nobody recorded during the review. A team may apply a risk-of-bias tool after extraction without deciding how the judgments will affect synthesis. The protocol may describe the intended methods, while later amendments remain undocumented. Valid components provide little protection when a team handles them as separate tasks.

Poor coordination costs time and labor. Borah and colleagues examined registered medical intervention reviews and reported a median interval of about 67 weeks from registration to publication. The projects also involved several contributors.8 That cohort covers one area of evidence synthesis, so the estimate does not extend to each discipline or review type. It does show how much work teams place at risk when methods, files, and responsibilities fall out of alignment. Chalmers and Glasziou identified further waste in research that remains unpublished or cannot answer a useful question.9

Review teams need a connected lifecycle

A systematic review works best as a sequence of linked decisions. The protocol records the plan before results appear and provides the reference point for later amendments. Search methods translate the question and eligibility criteria into retrievable concepts. During screening, reviewers apply those criteria to records and reports. They then create a traceable account of each included study during extraction. Reviewers use critical appraisal to decide how much confidence to place in the findings. During synthesis, the team combines evidence suited to the same analysis and assesses certainty before interpreting the result. Reporting completes the path from question to conclusion.

The Cochrane Handbook organizes review methods around this lifecycle. Its chapters connect planning with study selection, then carry the work through data collection, appraisal, synthesis, interpretation, and reporting.18 PRISMA 2020 has a narrower purpose: it guides authors in reporting a completed review. Conduct methods and quality assessment require other guidance. Teams must design and document their methodological decisions before they write the final manuscript.4

  • Pre-specificationRecord analytical and eligibility decisions before their consequences are known.
  • TraceabilityLink each study and extracted value to its source. Record exclusions and amendments.
  • Methodological continuityUse the output from one stage as a controlled input for the next.
  • Transparent interpretationInterpret findings in light of risk of bias and uncertainty. Account for heterogeneity and applicability.

Infrastructure must support expert judgment

Templates and checklists can make reasoning visible. Logs preserve decisions across a long project. These tools create false confidence when they display completed forms without recording the judgments behind them. Reviewers must decide whether studies have enough clinical comparability for synthesis and whether an appraisal instrument fits the research question. They must interpret statistical heterogeneity in context, regardless of what an automated output reports.

With well-designed infrastructure, the review team addresses each question at the appropriate stage and records the answer in a consistent form. Assumptions remain visible. Each new decision retains its connection to the evidence that supports it. Researchers in different fields may choose different question frameworks or databases. They may also require different appraisal instruments, synthesis methods, and reporting extensions. The need for a traceable chain does not change.

Review teams build a defensible synthesis through decisions they plan, document, check, and connect from the start. A final table or forest plot shows one part of that work. Readers need the complete record to judge the quality of the synthesis.

Research infrastructure

Systematic review and meta-analysis resource hubs

Free templates, workbooks, and protocols for every phase of evidence synthesis. Select a lifecycle stage below to access the specialized hub and download the current methodologies. Dr. Robat.

1. Systematic Review Protocol Planning and Registration

Protocol

Turn a research idea into a defensible, pre-specified review plan. Frame the question, establish eligibility criteria, document every planned method, and prepare a PRISMA-P aligned protocol for PROSPERO or OSF registration.

Systematic review project starter kit

Set up a reproducible review workspace, folder structure, file-naming system, project checklist, and data-management foundation before the search begins.

Systematic review timeline and milestone planner

Sequence protocol, searching, screening, extraction, appraisal, synthesis, and reporting with owners, dependencies, realistic milestones, and progress checks.

Protocol amendment and deviation log

Record what changed after protocol approval or registration, when it changed, why it changed, who approved it, and how the change affects analysis and reporting.

2. Systematic Review Search Strategy and Study Identification

Search

Build a reproducible systematic review search strategy from eligibility criteria to an auditable study‑identification record. Includes concept planning, database syntax, peer review, grey literature, deduplication, and PRISMA‑S documentation.

Systematic review search strategy template

Systematic review search documentation: capture review scope, concept decisions, source coverage, controlled vocabulary, free‑text terms, platform translations, testing results, PRESS feedback, executed searches, deduplication methods, updates, and PRISMA‑S reporting details.

Systematic review boolean search planning worksheet

Use this Boolean search worksheet to assemble concepts, synonyms, operators, phrases, truncation and proximity syntax before translating searches across platforms.

Grey literature search checklist and log for systematic reviews

Use this grey literature search checklist and log for systematic reviews to plan and record searches of registries, repositories, organizational websites.

3. Systematic Review Screening, Study Selection and PRISMA Flow Diagram

Screening

PRISMA 2020 study selection: build and apply eligibility criteria consistently, preserve decision evidence, and produce reconciled study‑selection records for reporting.

PRISMA 2020 flow diagram generator

Produce verified PRISMA 2020 flow counts: reconcile records, reports and studies, select the correct template family.

Systematic review screening form and eligibility Criteria

Study selection screening: translate protocol criteria into operational rules and preserve independent title, abstract, and full‑text decisions.

Full-Text exclusion reasons log for systematic reviews

Record one primary exclusion reason per report, preserve supporting evidence, and maintain counts that reconcile with your PRISMA flow diagram.

4. Systematic Review Data Extraction and Data Management

Data Extraction

Systematic review data extraction: design and pilot extraction forms, define study‑characteristics fields, document missing data and author queries, and preserve every transformation and verification decision.

Systematic review data extraction form template

Design and pilot forms, define study‑characteristics fields, document missing data, author queries, and preserve transformation and verification decisions.

Study characteristics table template

Systematic review data extraction: define the row unit and comparison fields needed to describe studies without mixing study, arm, and outcome levels.

Missing data contact log and request templates

Plan precise systematic review author queries, document the correspondence, and preserve how additional information changed the analytical record.

5. Risk of Bias Assessment and Critical Appraisal Tools for Systematic Reviews

RoB

PRISMA 2020 study selection: build and apply eligibility criteria consistently, preserve decision evidence, and produce reconciled study‑selection records for reporting.

Risk-of-bias tool selection decision aid for systematic reviews

Systematic review appraisal: select an instrument that fits your review question, evidence type, study design, and intended inference.

Risk-of-bias decision and reviewer consensus log for systematic reviews

Bias assessment: preserve independent judgments, supporting quotations, reviewer disagreements, consensus reasoning and justified overrides.

Critical appraisal findings summary template for systematic reviews

Risk of bias assessment: document domain concerns, supporting quotes, synthesis impact, sensitivity, and reporting without composite score

6. Meta-analysis Methods, Effect Sizes and Forest Plots

Meta-analysis

Apply structured worksheets and checklists to document effect‑measure decisions, analysis‑model assumptions and the quality control of forest plots produced in validated statistical software.

Effect size selection worksheet for meta-Analysis

Document the outcome type, construct, measurement scale, direction, candidate effect measure, compatibility assumptions, software output and rationale.

Meta-analysis model selection and reporting checklist

Document common‑effect or random‑effects assumptions, estimator, confidence‑interval method, heterogeneity handling, sensitivity plans, software, reporting decisions.

Forest plot interpretation and quality-control checklist

Verify effect direction, scale, labels, confidence intervals, study weights, pooled estimates, subgroups, heterogeneity, prediction intervals.

7. Meta-analysis heterogeneity, sensitivity analysis and publication bias

Heterogeneity

Interpret heterogeneity, sensitivity-analysis, and small-study-effect outputs produced in validated software. Use structured worksheets and logs to document assumptions, compare analyses, and report uncertainty without treating any statistic as an automatic verdict.

Meta-analysis heterogeneity interpretation worksheet

Record Q, I², tau-squared, confidence or prediction intervals, clinical diversity, methodological diversity, and an evidence-based interpretation from validated software output.

Meta-analysis sensitivity analysis planning and results log

Pre-specify alternative assumptions and exclusions, record sensitivity and leave-one-out outputs from validated software, and document whether conclusions remain robust.

Funnel plot and small-study effects interpretation checklist

Record applicability conditions, study count, effect measure, visual features, test output from validated software, alternative explanations, and cautious conclusions about asymmetry.

8. GRADE certainty of evidence and Summary of Findings

Certainty

Move from synthesized effects to transparent certainty judgments. Assess GRADE domains for each critical outcome, explain every rating decision, build Summary of Findings tables, and connect evidence to recommendations without collapsing judgment into a score.

GRADE Summary of Findings table template

Present relative and absolute effects, participant counts, certainty judgments, and concise explanations in a clear manuscript-ready table.

GRADE certainty of evidence assessment worksheet

Work through risk of bias, inconsistency, indirectness, imprecision, publication bias, upgrading factors, and support for every outcome-level judgment.

GRADE Evidence-to-Decision framework template

Translate evidence into recommendations by documenting benefits, harms, values, resources, equity, acceptability, and feasibility without collapsing judgment into a score.

9. PRISMA 2020 reporting and systematic review publication

Reporting

Turn a completed review into a transparent, publication-ready research report. Apply PRISMA 2020 across the manuscript, abstract, figures, tables, and supplementary files while preserving consistency between the protocol, analyses, results, and conclusions.

PRISMA 2020 checklist and compliance tracker

Map every PRISMA 2020 item to the exact manuscript section, page, figure, table, or supplement where it is reported.

Systematic review manuscript template

Draft a coherent title, introduction, methods, results, discussion, declarations, and supplementary package around PRISMA 2020 reporting expectations.

Systematic review abstract template and PRISMA checklist

Build a structured, journal-ready abstract and verify it against PRISMA for Abstracts without omitting essential methods or results.

10. Types of systematic reviews and evidence-synthesis designs

Typology

Match the review method to the decision the evidence must support. Compare purposes, question structures, eligibility logic, search expectations, synthesis options, reporting standards, and updating requirements across major review types.

Choose your review type

Use a guided decision tool to distinguish systematic, scoping, rapid, umbrella, and living reviews from the purpose and structure of the research question.

Scoping review protocol template and PRISMA-ScR checklist

Plan a focused scoping review around population, concept, and context, then map protocol and reporting decisions to JBI guidance and PRISMA-ScR.

Rapid review protocol template

Document stakeholder priorities, time-saving adaptations, search limits, screening methods, synthesis choices, and certainty implications without hiding methodological shortcuts.

11. Network meta-analysis, HEOR and market access evidence synthesis

HEOR

Adapt rigorous evidence synthesis to health technology assessment, payer, reimbursement, and comparative-effectiveness decisions. Plan systematic literature reviews, indirect comparisons, and network meta-analysis around decision-relevant populations, comparators, outcomes, and submission requirements.

Network meta-analysis assumptions checklist

Appraise network geometry, similarity, transitivity, consistency, effect modifiers, heterogeneity, and model reporting before interpreting indirect or mixed comparisons.

Indirect treatment comparison appraisal checklist and evidence table

Identify the common comparator, structure the evidence network, record estimates produced in validated software, and appraise transitivity, consistency, relevance, and credibility without calculating effects.

HEOR systematic literature review protocol template

Plan an HTA and market-access evidence review with decision scope, databases, grey literature, comparators, outcomes, evidence tables, governance, and update rules.

12. Patient-reported outcomes and COSMIN measurement science

PROMS

Select, appraise, extract, and synthesize patient-reported outcome measures without treating instrument scores as interchangeable. Apply COSMIN principles to content validity, measurement properties, feasibility, interpretability, and risk of bias.

COSMIN risk of bias checklist navigation guide

Identify the relevant official COSMIN standards and document design and statistical considerations for each measurement-property study without automating the final judgment.

PROMs measurement-property data extraction form

Extract instrument characteristics, populations, administration details, validity, reliability, responsiveness, interpretability, and feasibility consistently.

Patient-reported outcome measure comparison worksheet

Compare candidate instruments by construct, population, language, respondent burden, content validity, measurement quality, interpretability, feasibility, and intended use without issuing an automatic selection.

13. Professional Practice in Evidence Synthesis

Professional

Explore evidence-synthesis careers, professional competencies, responsible AI practice, teaching, consulting, leadership and decision support.

Careers in Evidence Synthesis: Roles, Skills and Professional Pathways

Explore evidence-synthesis roles, competency expectations and professional pathways across academic, healthcare, policy, HTA, industry and consulting settings.

Evidence Synthesis Professional Competency and Career Roadmap

Map your evidence-synthesis competencies, identify development gaps and plan next steps across methodology, communication, AI literacy and professional practice.

Professional Evidence Synthesis in the Age of AI: Skills, Accountability and Human Judgment

Examine the skills, accountability, validation responsibility and human judgment required for professional evidence synthesis in an AI-enabled field.

From isolated tasks to a defensible evidence system

A trustworthy evidence synthesis is not created by one decisive step. It is the cumulative product of a prespecified question, a reproducible search, transparent selection decisions, structured data collection, method-appropriate appraisal, justified synthesis, and complete reporting. Weakness at one stage can alter every stage that follows. For this reason, reporting standards and methodological guidance are most useful when they operate as a connected system rather than as documents consulted only before submission.4101118

Structured worksheets, logs, checklists, and interpretation aids can make that system operational. Their scientific value lies in making assumptions, judgments, changes, and unresolved uncertainties visible at the point where they arise. They do not convert a judgment into a mechanical answer, and they do not make every method appropriate for every review. A risk-of-bias instrument still requires domain-specific reasoning. A certainty assessment still requires explicit judgments across the relevant domains. An Evidence-to-Decision framework still requires decision makers to consider benefits, harms, values, resources, equity, acceptability, and feasibility in context.121314

The same boundary applies to automation and artificial intelligence. Machine-learning systems can prioritize records and support semi-automated screening, but evidence of efficiency does not transfer scientific responsibility from the review team to the tool.1920 Reviewers must still define the task, verify outputs against source records, examine errors, document how the system was used, and retain accountability for every consequential decision. The defensible model is therefore assisted work with traceable human oversight, not unsupervised substitution.

This lifecycle is transferable across fields because its organizing questions are general: What decision is being informed? Which evidence is eligible? How will that evidence be found, appraised, synthesized, and communicated? The answers are not universal. They depend on the review purpose, study designs, outcomes, disciplinary conventions, and decision context. A common infrastructure should preserve those differences while ensuring that the reasoning behind them can be inspected.

The final product of evidence synthesis is therefore more than a manuscript or a pooled estimate. It is an accountable path from a question to a conclusion, with enough documentation for readers to understand what was done, why it was done, and where uncertainty remains. From Florence Nightingale’s use of statistics to make preventable harm visible to Archie Cochrane’s call for organized, periodically updated critical summaries, the durable aim has been the same: evidence should be made usable for decisions without concealing the judgments on which those decisions depend.2218

The practical standard is simple: structure the work, preserve the audit trail, verify every consequential output, and state uncertainty with the same care used to state the result.
Methodological questions

Frequently asked questions

What is included in this systematic review and meta-analysis resource architecture?

It organizes 39 flagship resources across 13 lifecycle-ordered hubs. Each hub groups three practical assets, such as planning worksheets, reporting checklists, decision logs, data-collection forms, or interpretation aids. The assets support consistent work and documentation, but they do not replace the governing methodological standards or expert judgment.

Which systematic review resource hub should I use first?

For a new review, begin with protocol planning and registration, then move through searching, screening, data extraction, appraisal, synthesis, certainty assessment, and reporting. If a review is already underway, enter at the relevant stage but first check whether the necessary upstream decisions were prespecified and documented.1018

What is the difference between a systematic review and a meta-analysis?

A systematic review is a structured process for identifying, selecting, appraising, and synthesizing evidence in relation to a defined question. Meta-analysis is a statistical method for combining compatible quantitative estimates and may be one component of a systematic review. A systematic review does not require meta-analysis when studies, outcomes, or effect measures cannot be combined defensibly.18

What is the difference between a systematic review and a scoping review?

A systematic review usually addresses a focused question and seeks a methodologically justified synthesis of the eligible evidence. A scoping review usually maps the extent, characteristics, concepts, or gaps in a broader body of literature. Critical appraisal can be included in a scoping review when it serves the review purpose, but it is not mandatory in every scoping review. The choice should follow the objective of the review, not the preferred label.21

Are these evidence synthesis resources only for health and medicine?

No. The lifecycle can be applied in health, education, social science, environmental research, policy, business, and other fields. However, field-agnostic does not mean method-identical. The question framework, information sources, eligibility rules, appraisal instrument, synthesis method, and reporting standard must be selected for the evidence and decision context.

Can AI complete a systematic review or meta-analysis without human oversight?

No. AI and machine-learning tools can assist bounded tasks, such as prioritizing records for screening, but they do not remove the need for methodological expertise, source verification, error checking, transparent documentation, and accountable human decisions. Any use of automation should be reported clearly enough for readers to understand what the tool did and how its outputs were verified.1920

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References

  1. Hoffmann F, Allers K, Rombey T, Helbach J, Hoffmann A, Mathes T, et al. Nearly 80 systematic reviews were published each day: observational study on trends in epidemiology and reporting over the years 2000-2019. J Clin Epidemiol. 2021;138:1-11. doi:10.1016/j.jclinepi.2021.05.022
  2. Ioannidis JPA. The mass production of redundant, misleading, and conflicted systematic reviews and meta-analyses. Milbank Q. 2016;94(3):485-514. doi:10.1111/1468-0009.12210
  3. Centre for Reviews and Dissemination. PROSPERO: international prospective register of systematic reviews. York: University of York; 2024. Available from: https://www.crd.york.ac.uk/prospero/
  4. Page MJ, McKenzie JE, Bossuyt PM, Boutron I, Hoffmann TC, Mulrow CD, et al. The PRISMA 2020 statement: an updated guideline for reporting systematic reviews. BMJ. 2021;372:n71. doi:10.1136/bmj.n71
  5. Salvador-Oliván JA, Marco-Cuenca G, Arquero-Avilés R. Errors in search strategies used in systematic reviews and their effects on information retrieval. J Med Libr Assoc. 2019;107(2):210-221. doi:10.5195/jmla.2019.567
  6. Rethlefsen ML, Brigham TJ, Price C, Moher D, Bouter LM, Kirkham JJ, et al. Systematic review search strategies are poorly reported and not reproducible: a cross-sectional metaresearch study. J Clin Epidemiol. 2024;166:111229. doi:10.1016/j.jclinepi.2023.111229
  7. Page MJ, Shamseer L, Altman DG, Tetzlaff J, Sampson M, Tricco AC, et al. Epidemiology and reporting characteristics of systematic reviews of biomedical research: a cross-sectional study. PLoS Med. 2016;13(5):e1002028. doi:10.1371/journal.pmed.1002028
  8. Borah R, Brown AW, Capers PL, Kaiser KA. Analysis of the time and workers needed to conduct systematic reviews of medical interventions using data from the PROSPERO registry. BMJ Open. 2017;7(2):e012545. doi:10.1136/bmjopen-2016-012545
  9. Chalmers I, Glasziou P. Avoidable waste in the production and reporting of research evidence. Lancet. 2009;374(9683):86-89. doi:10.1016/S0140-6736(09)60329-9
  10. Moher D, Shamseer L, Clarke M, Ghersi D, Liberati A, Petticrew M, et al. Preferred reporting items for systematic review and meta-analysis protocols (PRISMA-P) 2015 statement. Syst Rev. 2015;4(1):1. doi:10.1186/2046-4053-4-1
  11. Rethlefsen ML, Kirtley S, Waffenschmidt S, Ayala AP, Moher D, Page MJ, et al. PRISMA-S: an extension to the PRISMA statement for reporting literature searches in systematic reviews. Syst Rev. 2021;10(1):39. doi:10.1186/s13643-020-01542-z
  12. Sterne JAC, Savović J, Page MJ, Elbers RG, Blencowe NS, Boutron I, et al. RoB 2: a revised tool for assessing risk of bias in randomised trials. BMJ. 2019;366:l4898. doi:10.1136/bmj.l4898
  13. Guyatt GH, Oxman AD, Schünemann HJ, Tugwell P, Knottnerus A. GRADE guidelines: 1. Introduction, GRADE evidence profiles and summary of findings tables. J Clin Epidemiol. 2011;64(4):383-394. doi:10.1016/j.jclinepi.2010.04.026
  14. Alonso-Coello P, Schünemann HJ, Moberg J, Brignardello-Petersen R, Akl EA, Davoli M, et al. GRADE Evidence to Decision (EtD) frameworks: a systematic and transparent approach to making well informed healthcare choices. 1: Introduction. BMJ. 2016;353:i2016. doi:10.1136/bmj.i2016
  15. Tricco AC, Lillie E, Zarin W, O’Brien KK, Colquhoun H, Levac D, et al. PRISMA extension for scoping reviews (PRISMA-ScR): checklist and explanation. Ann Intern Med. 2018;169(7):467-473. doi:10.7326/M18-0850
  16. Hutton B, Salanti G, Caldwell DM, Chaimani A, Schmid CH, Cameron C, et al. The PRISMA extension statement for reporting of systematic reviews incorporating network meta-analyses of health care interventions: checklist and explanations. Ann Intern Med. 2015;162(11):777-784. doi:10.7326/M14-2385
  17. Gagnier JJ, Lai J, Mokkink LB, Terwee CB. COSMIN reporting guideline for studies on measurement properties of patient-reported outcome measures. Qual Life Res. 2021;30(8):2197-2218. doi:10.1007/s11136-021-02822-4
  18. Higgins JPT, Thomas J, Chandler J, Cumpston M, Li T, Page MJ, Welch VA, editors. Cochrane Handbook for Systematic Reviews of Interventions. Version 6.5 (updated 2024). Cochrane; 2024. Available from: https://www.cochrane.org/authors/handbooks-and-manuals/handbook/current
  19. van de Schoot R, de Bruin J, Schram R, Zahedi P, de Boer J, Weijdema F, et al. An open source machine learning framework for efficient and transparent systematic reviews. Nat Mach Intell. 2021;3:125-133. doi:10.1038/s42256-020-00287-7
  20. Chai KEK, Lines RLJ, Gucciardi DF, Ng L. Research Screener: a machine learning tool to semi-automate abstract screening for systematic reviews. Syst Rev. 2021;10(1):93. doi:10.1186/s13643-021-01635-3
  21. Munn Z, Peters MDJ, Stern C, Tufanaru C, McArthur A, Aromataris E. Systematic review or scoping review? Guidance for authors when choosing between a systematic or scoping review approach. BMC Med Res Methodol. 2018;18(1):143. doi:10.1186/s12874-018-0611-x
  22. Office for Statistics Regulation. Nightingale’s example shines a light on the importance of accessible and transparent statistics. 2020 May 12. Available from: https://osr.statisticsauthority.gov.uk/blog/nightingales-example-shines-a-light-on-the-importance-of-accessible-and-transparent-statistics/