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Systematic Review Protocol
Retrospective Public Protocol Pack (OSF-ready) — PRISMA 2020 & AMSTAR 2 aligned
1. Registration & Administrative Information [PRISMA #24, AMSTAR #2]
| Review Title | Network Meta-Analysis of IL-17 and IL-23 Pathway Biologics (Guselkumab, Risankizumab, Ixekizumab, Secukinumab, Bimekizumab) vs Placebo + Active Comparators in Moderate-to-Severe Plaque Psoriasis: Expanded Phase 3 RCT Network on OR Scale |
| Protocol Version | v15.0 (Living Protocol — auto-updating) |
| Protocol Freeze Date | 2026-03-10 |
| Protocol Registration | Immutable timestamp via GitHub commit history at github.com/mahmood726-cyber/rapidmeta-finerenone. Each protocol amendment is a separate commit; the freeze date above corresponds to the most recent protocol-affecting commit. For external registration (PROSPERO / OSF) on submission-bound topics, see the per-topic Submission Cockpit. Per ICMJE 2023, GitHub commit hash + timestamp constitutes a verifiable pre-registration record equivalent to PROSPERO for tracking outcome / eligibility / analysis-plan changes. |
| Last Substantive Amendment | 2026-03-10 |
| Planned Update Frequency | Continuous (living review); formal snapshot at each new trial publication |
| Funding Source | No external funding (independent academic review) |
| Conflicts of Interest | None declared |
| Contributor Roles (CRediT) | MA — Conceptualization, Methodology, Data Curation, Writing (Original Draft & Review & Editing), Supervision. Per ICMJE 2023: human author takes full responsibility for accuracy and integrity of the work, including all AI-assisted components. |
| AI Assistance Disclosure | AI tools (Claude / Anthropic) provided: (a) automated audit tooling implementation (internal-consistency, fragility-index, PI-gap, GRIM/Benford, AACT cross-check, PMID DataBankList verification), (b) statistical module implementation (REML+HKSJ primary with DerSimonian-Laird sensitivity pooling, node-splitting, Doi/LFK, comparison-adjusted funnel, CINeMA-lite, POTH, Q-decomposition, contribution matrix), (c) initial drafts of summary text subject to human verification. AI is NOT listed as an author per ICMJE 2023; AI cannot take responsibility for a manuscript. All AI-generated content was reviewed and verified by the human author. The audit/extraction infrastructure is open-source at the GitHub repository for independent verification. |
2. Review Question — PICO Framework [PRISMA #3, AMSTAR #1]
| Population | |
| Intervention | |
| Comparator | |
| Primary Outcome | |
| Secondary Outcomes | All-cause mortality; renal composite (eGFR decline, ESKD, renal death); individual MACE components; hyperkalemia |
| Subgroup Plan |
3. Eligibility Criteria [PRISMA #5–6, AMSTAR #3]
| Criterion | Inclusion | Exclusion |
|---|---|---|
| Study Design | Randomized controlled trials (RCTs), parallel or crossover | Non-randomized, observational, single-arm, case series |
| Phase | Phase III or IV | Phase I/II (including IIa/IIb), PK/PD, dose-finding, bioequivalence, first-in-human |
| Participants | Mod-severe plaque psoriasis | Healthy volunteers, paediatric, animal/in-vitro |
| Intervention | Systemic biologic as primary experimental drug | Systemic biologic as background only; open-label extensions without comparator |
| Comparator | Placebo, sham, or standard of care | Active comparator without placebo arm |
| Outcomes | ≥1 primary dermatology efficacy endpoint (PASI response, IGA 0/1, EASI improvement, or NRS) with extractable data | Biomarker-only, PK-only, no event data |
| Publication | Published or registered; any language | Pre-2015; duplicate cohorts; editorials, letters, reviews |
| Follow-up | ≥12 weeks (primary outcome assessment) | <12 weeks or acute/single-dose studies |
4. Information Sources & Search Strategy [PRISMA #7–8, AMSTAR #4–5]
| Database | Search String / API Query | Type |
|---|---|---|
| ClinicalTrials.gov | https://clinicaltrials.gov/api/v2/studies?query.intr=empagliflozin+OR+dapagliflozin+OR+sacubitril+AND+heart+failure+reduced&pageSize=100&filter.overallStatus=COMPLETED | Registry (API v2) |
| PubMed (Europe PMC) | hfref quadruple therapy AND (TITLE:randomized OR PUB_TYPE:"Randomized Controlled Trial" OR PUB_TYPE:"Clinical Trial") AND SRC:MED | Bibliographic (REST) |
| OpenAlex | search=hfref quadruple therapy&filter=concepts.id:C71924100&per_page=50 | Bibliographic (REST) |
| Reference Check | Backward citation search: built-in landmark database cross-checked against API returns | Manual supplement |
NCT-ID exact match → PubMed dbCrossReferenceList linkage → NCT pattern extraction from abstract → fuzzy title dedup (normalized alphanumeric). Enrichment: abstracts, authors, journal metadata merged from PubMed into registry stubs. All 3 fetches run in parallel via Promise.allSettled.
5. Study Selection Process [PRISMA #16, AMSTAR #5–7]
| Stage 1: Auto-Screening | RCT relevance classifier (keyword + publication type scoring, 0–100). Auto-exclude <25. App location: Screening tab |
| Stage 2: Title/Abstract | Two-reviewer adjudication workflow with rationale note and second-review confirmation (I = propose include, E = propose exclude, C = second confirmation, N/P = navigate). App location: Screening tab |
| Stage 3: Source Verification | Verify eligibility and endpoint fit against CT.gov records plus PubMed/OpenAlex abstracts; no full-text extraction in the locked constrained-source workflow. App location: Extraction tab |
| Conflict Resolution | Re-review with exclusion reason recorded in audit log. PRISMA flow auto-generated. |
| PRISMA Flow Diagram | Auto-computed from search/screening counts. App location: Report tab → PRISMA section |
6. Data Collection & Extraction [PRISMA #10, AMSTAR #6]
| Data Item | Details | App Location |
|---|---|---|
| Study identifiers | NCT ID, PMID, DOI, first author, year | Extraction → Data Entry |
| Participants | N randomized per arm, age, sex distribution, indication, baseline eGFR | Extraction → Demographics |
| Intervention details | Systemic biologic dose/regimen, trial phase, treatment duration | Extraction → Data Entry |
| Outcome events | 2×2 table: Events(Tx), N(Tx), Events(Ctrl), N(Ctrl); continuity correction 0.5 for zero cells | Extraction → Data Entry |
| Risk of Bias | RoB 2 domains D1–D5, each rated Low/Some/High | Extraction → Risk of Bias |
| Source evidence | Verbatim extracts from ClinicalTrials.gov records and PubMed/OpenAlex abstracts with source citations | Extraction → Evidence panels |
7. Risk of Bias Assessment [PRISMA #11–12, AMSTAR #9]
| Domain | Signalling Questions (RoB 2) | App Location |
|---|---|---|
| D1: Randomization | Sequence generation, allocation concealment | Extraction → RoB (click to cycle) |
| D2: Deviations | Blinding, ITT adherence, co-interventions | Extraction → RoB (click to cycle) |
| D3: Missing Data | Completeness, attrition handling, sensitivity for missing | Extraction → RoB (click to cycle) |
| D4: Measurement | Outcome assessment blinding, adjudication committees | Extraction → RoB (click to cycle) |
| D5: Selective Reporting | Pre-registered endpoints, protocol deviations | Extraction → RoB (click to cycle) |
| Presentation | Traffic-light summary table (per-study) + stacked horizontal bar chart (per-domain) | Analysis → Charts #16, Extraction → RoB |
8. Synthesis & Statistical Methods [PRISMA #13, AMSTAR #11–12]
| Method | Specification | App Location |
|---|---|---|
| Effect Measure | Primary analysis uses risk ratio (RR) for binary endpoints (PASI 90, PASI 75, IGA 0/1, EASI-75) or mean difference (MD) for continuous symptom scores. Hazard ratios are not applicable to dermatology response-rate endpoints assessed at fixed timepoints; odds ratios retained for sensitivity analysis. | Analysis → Stats |
| Pooling Model | REML random-effects, HKSJ-adjusted (inverse-variance weighting) | Analysis → Forest (#1) |
| CI Adjustment | Hartung-Knapp-Sidik-Jonkman (HKSJ); t-distribution with df = k−1 | Analysis → Stats |
| Prediction Interval | t-distribution, df = k−1 (Cochrane Handbook v6.5) | Analysis → Stats |
| Heterogeneity | Cochran Q (p-value), I² (%), τ² (DL estimator) | Analysis → Stats |
| Subgroup Analysis | By pre-specified subgroup; Q-between test for interaction | Analysis → Subgroup (#2) |
| Cumulative MA | Sequential addition by year; monitoring evidence accrual | Analysis → Cumulative (#3) |
| Leave-One-Out | Influence analysis: remove each study, re-pool | Analysis → LOO (#5) |
| Bayesian RE | Grid approximation (200 τ × 300 μ); half-normal prior on τ; posterior OR + CrI + P(OR<1) | Analysis → Posterior (#11) |
| Meta-Regression | WLS on log-OR; covariates: Year, Phase, Indication; Knapp-Hartung SE; permutation p (1000x) | Analysis → Meta-Reg (#12) |
| Fragility Index | Walsh method: sequential single-arm event modification until significance flips | Analysis → Stats |
| NNT / Clinical Utility | NNT = 1 / ARR; curve across baseline risk range | Analysis → NNT (#8) |
9. Publication Bias Assessment [PRISMA #14–15, AMSTAR #15]
| Method | Specification | App Location |
|---|---|---|
| Visual | Contour-enhanced funnel plot with significance regions (p < 0.01/0.05/0.10) | Analysis → Funnel (#9) |
| Statistical | Egger's weighted regression test: intercept ≠ 0 (k ≥ 3 required) | Analysis → Egger (#15) |
| Correction | Duval-Tweedie trim-and-fill (L0 estimator); imputed studies shown as open circles on funnel | Analysis → Stats chip |
| Sensitivity | Copas-style sensitivity (heuristic rank-reweighting, not Copas-Shi MLE): ρ sweep −0.99 to 0 (34 steps); classify Robust/Sensitive | Analysis → Copas (#13) |
| Power | RIS formula with D² diversity; conditional power curve (next-study N 100–2000) | Analysis → Power (#14) |
10. Certainty of Evidence [PRISMA #22, AMSTAR #14]
| GRADE Domain | Criteria for Downgrading | App Location |
|---|---|---|
| Risk of Bias | ≥50% studies rated Some Concerns or High on any domain | Report → GRADE |
| Inconsistency | I² ≥ 50% or prediction interval crosses null | Report → GRADE |
| Indirectness | Population, intervention, or outcome mismatch with review question | Report → GRADE |
| Imprecision | CI crosses MID (OR = 0.80 or 1.25) or optimal information size not met | Report → GRADE |
| Publication Bias | Egger p < 0.10, asymmetric funnel, Copas sensitivity, trim-fill k0 > 0 | Report → GRADE |
| Supplementary | Bayesian P(OR < 1), Information Fraction (RIS), Summary of Findings table | Report → SoF table |
11. AMSTAR 2 Critical Domains Compliance
| # | AMSTAR 2 Item | Critical? | How Addressed |
|---|---|---|---|
| 1 | PICO components for research question | No | Section 2 above |
| 2 | Protocol registered before commencement | No | Retrospective public protocol pack prepared on March 10, 2026; this tab is the living internal protocol |
| 4 | Comprehensive literature search strategy | Yes | Section 4: 3 databases + reference check; search strings visible |
| 7 | List of excluded studies with justifications | Yes | Screening tab: excluded with auto/manual reason |
| 9 | Satisfactory RoB assessment technique | Yes | Section 7: Cochrane RoB 2, 5 domains |
| 11 | Appropriate meta-analytical methods | Yes | Section 8: DL RE + HKSJ, R/Python cross-validated |
| 13 | RoB impact on results considered | Yes | GRADE domain 1, Extraction → RoB tab |
| 15 | Publication bias assessment | Yes | Section 9: Funnel + Egger + Trim-Fill + Copas |
12. Reporting & Dissemination [PRISMA #23–27, AMSTAR #16]
| Reporting Guideline | PRISMA 2020 (27-item checklist auto-generated as CSV) |
| Export Formats | CSV (study data), JSON (full state), R validation script, Python validation script, PRISMA checklist CSV, HTML standalone report |
| Data Integrity | SHA-256 data seal (cryptographic fingerprint) on every report; version timeline with delta alerts |
| Cross-Validation | R (metafor) and Python (scipy) scripts included for independent replication of pooled OR, CI, τ² |
| Patient Mode | Plain-language summary with traffic-light visual; hides technical statistics for lay audiences |
Search History Log [PRISMA #8]
No searches recorded yet. Run an acquisition from the Search tab to log results here.
Evidence Acquisition
Multi-Source: ClinicalTrials.gov + PubMed + OpenAlex
Search Strings Used
https://clinicaltrials.gov/api/v2/studies?query.intr=empagliflozin+OR+dapagliflozin+OR+sacubitril+AND+heart+failure+reduced&pageSize=100&filter.overallStatus=COMPLETED
hfref quadruple therapy AND (TITLE:randomized OR PUB_TYPE:"Randomized Controlled Trial" OR PUB_TYPE:"Clinical Trial") AND SRC:MED
search=hfref quadruple therapy&filter=concepts.id:C71924100&per_page=50
Saved Search Log
No searches recorded yet.
PRISMA-NMA Flow Diagram
Extraction & Source Verification
Interactive truth capture with highlighted registry denominators.
Outcome-Switching Audit (registry vs paper)
Cochrane RoB-2 (per-domain traffic light)
Study Characteristics
| Trial | Year | Phase | Indication | N (Tx) | N (Ctrl) | ER Tx% | ER Ctrl% | RoB |
|---|
ER = Event Rate. Values extracted from registry records — verify against published manuscripts before finalizing.
Precision Analytics Suite
1. Forest Plot (Fixed/Random Effects)
1b. Dose-Response Curves (drug-stratified linear fits)
2. Subgroup Synthesis
3. Cumulative Meta-Analysis
4. Cumulative Z-Curve Analysis
5. Leave-One-Out Sensitivity
6. L'Abbe Plot (Event Incidence)
7. Galbraith Plot (Heterogeneity Check)
8. Clinical Utility (NNT Curve)
9. Funnel Plot (Publication Bias)
10. Baujat Plot (Influence x Heterogeneity)
11. Bayesian Posterior Density
12. Meta-Regression
13. Copas Sensitivity Curve
14. Conditional Power Curve
15. Egger's Regression Plot
16. Risk of Bias Summary
17. Sensitivity Analysis Panel
18. Influence & Outlier Diagnostics
What does this mean for you?
This is a summary for general understanding. Always discuss with your healthcare provider.
9. Quality Appraisal (RoB 2.0)
WebR: Validate with R in Your Browser
Not loadedRuns metafor::rma() directly in your browser via WebAssembly. No server needed. First load installs R + metafor (~20-40s).
10. Evidence Summary (GRADE)
TruthCert R-Metafor Script (DL Model)
Reference Cross-Validation
Scientific Synthesis
Generating Visual Abstract & PRISMA Diagram...
HFrEF Drug Comparison NMA
Multi-source meta-analysis of landmark RCTs
Auto-Generated Manuscript Text
Click "Generate Output" to create manuscript text.
Waiting Room Summary
For general understanding only. Discuss treatment decisions with your healthcare provider.
PRISMA 2020 Flow Diagram
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Duplicates / Ineligible
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The hfref quadruple therapy Evidence
A quantitative synthesis of landmark randomized trials.
Confidence Interval Comparison
Visual comparison of estimation methods on the odds ratio scale. The pooled point estimate is identical; interval widths differ by method.
Fig. — DerSimonian-Laird (standard), Hartung-Knapp-Sidik-Jonkman (adjusted), and Prediction Interval estimates
Publication-Quality Forest Plot
Annotated forest plot with trial-level statistics and weight contributions. Suitable for manuscript figures.
Fig. — Forest plot of hfref quadruple therapy vs placebo for MACE composite (random-effects, DL estimator)
Summary of Findings
| Outcome | No. Trials | Total N | Effect (OR) | 95% CI | I² | GRADE |
|---|
SoF table follows GRADE Working Group recommendations. Verify values against R validation script output.
Evidence Guardian
Release-style validation for a constrained-source pairwise review: search coverage, dual-review status, endpoint harmonization, and sparse-evidence risks.
Validation Checks
Constraint Ledger
Recommendations
Reviewer Concordance
Generate a report to summarize documented dual-review coverage, reviewer-pair activity, and adjudication load.
Screening & Extraction
Reviewer Pair Activity
| Pair | Screen | Extract | Total |
|---|---|---|---|
| No concordance pairs rendered yet. | |||
Recommendations
CT.gov Evidence Delta
Generate a report to audit CT.gov results coverage, protocol/SAP attachment coverage, endpoint bridging against registered primaries, and publication-without-results watchlist signals.
Registry Checks
Recommendations
| Trial | Scope | Registered Primary | Current Endpoint | CT.gov / Docs | Publication | Delta Signal |
|---|---|---|---|---|---|---|
| No CT.gov evidence delta rendered yet. | ||||||
Published Meta Benchmark
Generate a report to compare the current pooled estimate against published hfref quadruple therapy pooled analyses.
| Comparator | Year | Trials | N | Measure | Estimate | 95% CI | Alignment |
|---|---|---|---|---|---|---|---|
| No benchmark rendered yet. | |||||||
Benchmarks use a locked local comparator database of published hfref quadruple therapy pooled analyses.
PRISMA 2020 Flow Diagram (SVG)
Auto-Generated Manuscript Draft
GRADE Evidence Profile (Summary of Findings)
Cumulative Evidence Over Time
Quality Assurance (18 Automated Checks)
Living Update Log
Reproducibility Artifact
Frozen analysis fingerprint linking search scope, included trials, pooled result, threat ledger, and data seal.
Network Meta-Analysis
Indirect comparisons via connected treatment network
Treatment Network
League Table (All Pairwise Comparisons)
Live Re-pool from Raw 2×2 (verifier)
Re-pools the trial-level raw event counts in realData using REML random-effects + HKSJ + Cochrane v6.5 prediction interval (tk-1).
Compare the pooled estimate (cyan diamond) vs the published headline (gold dashed). Per-trial rows show the
back-transformed RR with 95% CI and RE weight.
Treatment Rankings (P-Score)
Consistency Assessment (Node-Splitting)
Network Consistency (NMA Pro Transplant)
NMA-Pro-style direct/indirect node-splitting with Fisher-combined global inconsistency test (Dias et al. 2010 back-calculation). Star networks (every comparison via a common reference) trigger an explicit transitivity-only disclosure since no closed loops exist to test consistency by node-splitting.
ROB-NMA + Transitivity (Cochrane 2025)
Lunny 2025 BMJ ROB-NMA tool (17 items, 3 domains) with auto-prefill from existing modules + transitivity effect-modifier balance per Brignardello-Petersen 2023 GRADE-NMA Article 5 / Lasch 2025 Res Synth Methods.
Bias & Certainty (Tier 2 Transplants)
Small-study-effects (Doi plot + LFK index, Furuya-Kanamori 2018), comparison-adjusted funnel (Chaimani & Salanti 2012), and per-pairwise certainty (CINeMA, Nikolakopoulou 2020). Tools chosen for k<10 networks where Egger's test is underpowered.
NMA Scientific Output
Auto-Generated NMA Manuscript Text
Click "Run NMA" to generate Methods + Results text describing this network.
PRISMA-NMA Checklist Items
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Text separate from figures
Supplementary (submittable)
Supplementary material (auto-generated)