# PRISMA 2020 — Systematic Review Report Template ## Purpose Template for writing a systematic review report following PRISMA 2020 (Page et al., 2021). All 27 PRISMA items are mapped to their corresponding sections. Use alongside `references/systematic_review_toolkit.md` for detailed guidance. **Reference**: Page et al. (2021). The PRISMA 2020 statement: an updated guideline for reporting systematic reviews. BMJ, 372, n71. https://doi.org/10.1136/bmj.n71 --- ## Title [PRISMA Item 1] **[Full title identifying the report as a systematic review, meta-analysis, or both]** Example: "The Effect of [Intervention] on [Outcome] in [Population]: A Systematic Review and Meta-Analysis" --- ## Abstract [PRISMA Item 2] ### Background [1-2 sentences on context and why the review was done] ### Objectives [Research question(s), ideally structured as PICOS] ### Data Sources [Databases searched and dates of last search] ### Study Selection [Eligibility criteria in brief] ### Data Extraction and Synthesis [Methods used for data extraction, risk of bias, and synthesis] ### Results [Number of studies included, key findings, effect estimates with CIs, certainty of evidence] ### Limitations [Key limitations of the evidence and/or the review process] ### Conclusions [General interpretation and implications] ### Registration [Protocol registration number and repository] **Keywords**: [3-5 keywords] --- ## 1. Introduction ### 1.1 Rationale [PRISMA Item 3] [Describe the rationale for the review in the context of existing knowledge. Address:] - What is the problem or question? - What is already known (with references to existing reviews)? - Why is this review needed (e.g., no existing review, existing review outdated, conflicting evidence)? ### 1.2 Objectives [PRISMA Item 4] [Provide an explicit statement of the question(s) using PICOS:] - **Population**: [target population] - **Intervention/Exposure**: [intervention or exposure of interest] - **Comparator**: [comparison group] - **Outcome(s)**: [primary and secondary outcomes] - **Study Design**: [eligible study designs] --- ## 2. Methods ### 2.1 Eligibility Criteria [PRISMA Item 5] | Criterion | Include | Exclude | |-----------|---------|---------| | Study design | [e.g., RCTs, quasi-experimental] | [e.g., case reports, editorials] | | Population | [describe] | [describe] | | Intervention | [describe] | [describe] | | Comparator | [describe] | [describe] | | Outcome | [describe] | [describe] | | Time frame | [e.g., published 2014-2024] | [before cutoff] | | Language | [e.g., English] | [other] | | Setting | [describe] | [describe] | ### 2.2 Information Sources [PRISMA Item 6] [List all databases and other sources searched, with dates of coverage and last search date:] | Source | Date Range | Last Searched | |--------|-----------|---------------| | [Database 1] | [start]-[end] | [date] | | [Database 2] | [start]-[end] | [date] | | [Other sources: reference lists, expert contact, grey literature] | — | [date] | ### 2.3 Search Strategy [PRISMA Item 7] [Present the complete search strategy for at least one database. Include all search terms, Boolean operators, and any filters applied.] **[Database Name] Search Strategy**: ``` #1 [search block 1 - Population terms] #2 [search block 2 - Intervention terms] #3 [search block 3 - Outcome terms] #4 #1 AND #2 AND #3 #5 #4 with filters: [date, language, document type] ``` [Search strategies for other databases are available in Appendix A.] ### 2.4 Selection Process [PRISMA Item 8] [Describe the study selection process:] - Number of reviewers at each stage - How independence was maintained - How disagreements were resolved - Software used (e.g., Covidence, Rayyan) - Pilot testing of screening criteria ### 2.5 Data Collection Process [PRISMA Item 9] [Describe methods for extracting data from reports:] - Data extraction form (developed, piloted) - Number of extractors and independence - Process for resolving discrepancies - How missing data were handled (e.g., contacted authors) ### 2.6 Data Items [PRISMA Item 10] [List all variables for which data were sought:] | Category | Variables | |----------|----------| | Study-level | Authors, year, country, design, setting, funding | | Participants | N, age, gender, diagnosis/condition, attrition | | Intervention | Type, duration, frequency, fidelity | | Outcomes | Definition, measurement tool, time points | | Results | Effect sizes, CIs, p-values, raw data | ### 2.7 Study Risk of Bias Assessment [PRISMA Item 11] [Describe the risk of bias assessment:] - Tool(s) used: [RoB 2 for RCTs / ROBINS-I for non-randomized / other] - Domains assessed - Number of assessors and independence - How results were used in the synthesis ### 2.8 Effect Measures [PRISMA Item 12] [Specify the effect measure(s) for each outcome:] | Outcome | Type | Effect Measure | Justification | |---------|------|---------------|---------------| | [Outcome 1] | Continuous | SMD (Hedges' g) | Different scales across studies | | [Outcome 2] | Binary | RR | Incidence data | ### 2.9 Synthesis Methods [PRISMA Items 13a-13f] **13a. Eligibility for synthesis**: [Criteria for grouping studies into each synthesis] **13b. Data preparation**: [Methods to prepare data, e.g., converting SE to SD, handling multi-arm studies] **13c. Tabulation/visualization**: [Methods for displaying individual study and synthesis results, e.g., forest plots, summary tables] **13d. Synthesis approach**: [Statistical model and software] - Model: [Fixed-effect / Random-effects (DerSimonian-Laird / REML)] - Software: [R metafor / RevMan / Stata] - OR if narrative: [SWiM approach, vote counting, effect direction plot] **13e. Heterogeneity exploration**: [Methods used] - Subgroup analyses: [pre-specified subgroups and rationale] - Meta-regression: [covariates tested, if applicable] **13f. Sensitivity analyses**: [Planned sensitivity analyses] 1. Leave-one-out analysis 2. Excluding high risk of bias studies 3. Fixed-effect vs. random-effects comparison 4. [Other analyses] ### 2.10 Reporting Bias Assessment [PRISMA Item 14] [Methods to assess publication bias:] - Funnel plot (visual inspection) - Statistical test: [Egger's / Peter's / trim-and-fill] - Comparison of protocol to published reports ### 2.11 Certainty Assessment [PRISMA Item 15] [Framework used to assess certainty of evidence:] - GRADE approach - Factors assessed: risk of bias, inconsistency, indirectness, imprecision, publication bias - Rating up factors (for observational studies): large effect, dose-response, plausible confounding --- ## 3. Results ### 3.1 Study Selection [PRISMA Item 16a, 16b] #### PRISMA Flow Diagram ``` ┌─────────────────────────────────────────────────────┐ │ IDENTIFICATION │ ├─────────────────────────────────────────────────────┤ │ Records identified from databases (n = ) │ │ Database 1 (n = ) │ │ Database 2 (n = ) │ │ Database 3 (n = ) │ │ Records identified from other sources (n = ) │ │ Reference lists (n = ) │ │ Expert recommendations (n = ) │ └──────────────────────┬──────────────────────────────┘ │ ┌──────────────────────▼──────────────────────────────┐ │ Records removed before screening: │ │ Duplicate records (n = ) │ │ Records marked ineligible by automation (n = ) │ │ Records removed for other reasons (n = ) │ └──────────────────────┬──────────────────────────────┘ │ ┌──────────────────────▼──────────────────────────────┐ │ SCREENING │ ├─────────────────────────────────────────────────────┤ │ Records screened (n = ) │ │ Records excluded (n = ) │ └──────────────────────┬──────────────────────────────┘ │ ┌──────────────────────▼──────────────────────────────┐ │ Reports sought for retrieval (n = ) │ │ Reports not retrieved (n = ) │ └──────────────────────┬──────────────────────────────┘ │ ┌──────────────────────▼──────────────────────────────┐ │ Reports assessed for eligibility (n = ) │ │ Reports excluded, with reasons (n = ) │ │ Reason 1 (n = ) │ │ Reason 2 (n = ) │ │ Reason 3 (n = ) │ └──────────────────────┬──────────────────────────────┘ │ ┌──────────────────────▼──────────────────────────────┐ │ INCLUDED │ ├─────────────────────────────────────────────────────┤ │ Studies included in review (n = ) │ │ Reports of included studies (n = ) │ │ Studies in quantitative synthesis (n = ) │ └─────────────────────────────────────────────────────┘ ``` [PRISMA Item 16b: Cite studies that appeared to meet inclusion criteria but were excluded, with reasons.] ### 3.2 Study Characteristics [PRISMA Item 17] **Table: Characteristics of Included Studies** | Study | Country | Design | Population (N) | Intervention | Comparator | Outcome(s) | Follow-up | Funding | |-------|---------|--------|----------------|-------------|-----------|------------|-----------|---------| | Author1 (Year) | [country] | [design] | [N] | [intervention] | [comparator] | [outcomes] | [duration] | [source] | | Author2 (Year) | ... | ... | ... | ... | ... | ... | ... | ... | ### 3.3 Risk of Bias in Studies [PRISMA Item 18] **Table: Risk of Bias Summary (Traffic-Light)** | Study | D1 | D2 | D3 | D4 | D5 | Overall | |-------|----|----|----|----|----|---------| | Author1 (Year) | [L/S/H] | [L/S/H] | [L/S/H] | [L/S/H] | [L/S/H] | [L/S/H] | | Author2 (Year) | ... | ... | ... | ... | ... | ... | L = Low risk, S = Some concerns, H = High risk [Narrative summary of risk of bias findings across studies] ### 3.4 Results of Individual Studies [PRISMA Item 19] **Table: Individual Study Results** | Study | Outcome | Effect Estimate | 95% CI | p-value | Weight | |-------|---------|----------------|--------|---------|--------| | Author1 (Year) | [outcome] | [estimate] | [lower, upper] | [p] | [%] | | Author2 (Year) | ... | ... | ... | ... | ... | ### 3.5 Results of Syntheses [PRISMA Items 20a-20d] #### Primary Outcome: [Name] **20a. Study characteristics**: [Brief summary of contributing studies' characteristics and risk of bias] **20b. Pooled result**: - Pooled effect: [estimate] (95% CI: [lower, upper]) - Statistical significance: Z = [value], p = [value] - Heterogeneity: I² = [value]% (95% CI: [lower, upper]), Q = [value] (df = [n], p = [value]), tau² = [value] - Prediction interval: [lower, upper] **Forest Plot**: [Insert or reference forest plot] **20c. Heterogeneity investigation**: - Subgroup analyses: [results] - Meta-regression: [results, if conducted] **20d. Sensitivity analyses**: 1. Leave-one-out: [results — did any single study substantially change the estimate?] 2. Excluding high-risk studies: [revised estimate] 3. Fixed vs. random effects: [comparison] #### Secondary Outcome(s): [Name] [Repeat structure above for each secondary outcome] ### 3.6 Reporting Biases [PRISMA Item 21] [Report assessments of publication bias:] - Funnel plot: [description of symmetry/asymmetry] - Statistical test: [result] - Trim-and-fill: [adjusted estimate, if applicable] - Other assessments: [protocol-outcome comparison] ### 3.7 Certainty of Evidence [PRISMA Item 22] **GRADE Summary of Findings Table** | Outcome | Studies (n) | Participants (N) | Effect (95% CI) | Certainty | Rationale | |---------|------------|-------------------|-----------------|-----------|-----------| | [Outcome 1] | [n] | [N] | [estimate (CI)] | [High/Moderate/Low/Very Low] | [Reasons for up/downgrading] | | [Outcome 2] | [n] | [N] | [estimate (CI)] | [level] | [reasons] | --- ## 4. Discussion [PRISMA Item 23] ### 4.1 Summary of Evidence [Provide a general interpretation of the results in the context of other evidence. Address:] - Main findings for each outcome - How findings compare to previous reviews - Consistency of findings across studies ### 4.2 Limitations **Limitations of the evidence**: - [e.g., risk of bias across studies, inconsistency, indirectness, imprecision] **Limitations of the review process**: - [e.g., language restrictions, database coverage, inability to contact authors] ### 4.3 Implications **For practice**: - [What practitioners should do based on these findings] **For research**: - [Gaps identified, recommended future study designs] **For policy**: - [Policy implications, if applicable] --- ## 5. Other Information ### 5.1 Registration and Protocol [PRISMA Item 24] [Provide registration information and link to protocol:] - Registry: [e.g., PROSPERO] - Registration number: [number] - Protocol URL: [link] - Deviations from protocol: [describe any deviations and rationale] ### 5.2 Support [PRISMA Item 25] [Describe sources of support:] - Financial: [funding sources and grant numbers] - Non-financial: [e.g., institutional support, access to databases] - Role of funder: [describe any role of funders in the review] ### 5.3 Competing Interests [PRISMA Item 26] [Declare competing interests of all authors] ### 5.4 Availability of Data and Materials [PRISMA Item 27] [Report availability of:] - [ ] Data extraction forms - [ ] Extracted data from included studies - [ ] Analysis code - [ ] List of excluded studies with reasons - [ ] PRISMA checklist (completed) --- ## Appendices ### Appendix A: Full Search Strategies [Complete search strategies for all databases] ### Appendix B: Excluded Studies with Reasons | Study | Reason for Exclusion | |-------|---------------------| | [citation] | [reason] | ### Appendix C: PRISMA 2020 Checklist [Completed PRISMA 2020 checklist with page/section numbers for each item] | Item # | Checklist Item | Reported on Page/Section | |--------|---------------|-------------------------| | 1 | Title | [page] | | 2 | Abstract | [page] | | ... | ... | ... | | 27 | Availability | [page] |