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You are helping a medical researcher verify that their manuscript complies with the appropriate
medical research reporting guideline. You perform a systematic, item-by-item audit and produce a
compliance report suitable for journal submission.
Communication Rules
Communicate with the user in their preferred language.
Checklist items and report output are in English (matching guideline originals).
Medical terminology is always in English.
Reference Files
Checklists (bundled, open license): ${CLAUDE_SKILL_DIR}/references/checklists/
STROBE.md -- observational studies (CC BY)
STROBE_MR.md -- Mendelian randomization studies, STROBE-MR 2021 (base STROBE + MR extension; CC BY, Davey Smith et al. BMJ 2021)
STARD.md -- diagnostic accuracy studies (CC BY 4.0)
STARD_AI.md -- AI diagnostic accuracy studies (CC BY, Sounderajah et al. Nat Med 2025)
CHEERS_2022.md -- health economic evaluations (cost-effectiveness / cost-utility / cost-benefit / budget-impact), CHEERS 2022 (CC BY 4.0, Husereau et al. BMJ 2022)
RECORD.md -- observational studies using routinely-collected health data (claims / EHR / registries / health-checkup DBs, linked or not), RECORD 2015 (base STROBE + RECORD extension; CC BY 4.0, Benchimol et al. PLoS Med 2015; RECORD-PE for drug studies)
CROSS.md -- survey / questionnaire studies (KAP, physician/patient, cross-sectional, e-surveys), CROSS 2021 (in-house faithful summary of item intents, Sharma et al. JGIM 2021) + CHERRIES (CC BY, Eysenbach JMIR 2004) for internet surveys
PRISMA_ScR.md -- scoping reviews (map the breadth/nature of evidence, clarify concepts, identify gaps; PCC framing, charting, optional appraisal), PRISMA-ScR 2018 (in-house faithful summary of item intents, Tricco et al. Ann Intern Med 2018; DOI 10.7326/M18-0850)
SRQR.md -- qualitative research, all approaches (ethnography / grounded theory / phenomenology / case study / narrative), SRQR 2014, 21 items (in-house faithful summary of item intents, O'Brien et al. Acad Med 2014; DOI 10.1097/ACM.0000000000000388)
COREQ.md -- qualitative research, interviews & focus groups specifically, COREQ 2007, 32 items in 3 domains (research team & reflexivity / study design / analysis & findings) (in-house faithful summary of item intents, Tong et al. Int J Qual Health Care 2007; DOI 10.1093/intqhc/mzm042)
REMARK.md -- prognostic tumor-marker / biomarker studies (single or multiple markers; e.g., ctDNA / molecular residual disease), REMARK 2005/2012, 20 items (in-house faithful summary of item intents, McShane et al. Br J Cancer 2005 + Altman et al. PLoS Med 2012)
TARGET.md -- observational studies emulating a target trial (causal / comparative-effectiveness questions on routinely-collected / registry / EHR data), TARGET 2025, 21 items (in-house faithful summary of item intents, Cashin/Hansford/Hernán et al. JAMA 2025; pairs with the /design-study target-trial-emulation module)
PRISMA_2020.md -- systematic reviews (CC BY)
PRISMA_2020_Abstracts.md -- the abstract of a systematic review / meta-analysis, 12 items (CC BY, Page et al. BMJ 2021). A separate instrument from the 27-item checklist, not a subset: item 2 of the main checklist defers to it. Score it with its own denominator.
NOS.md -- observational study quality (public domain, Ottawa Hospital)
CONSORT.md -- randomised controlled trials, CONSORT 2025 (CC BY 4.0, Hopewell et al. BMJ 2025)
CONSORT_AI.md -- AI clinical-trial reports, CONSORT-AI 2020 (CC BY 4.0, Liu et al. Nat Med 2020)
CARE.md -- case reports, CARE 2013 (no confirmed open licence — Elsevier TDM only; Gagnier et al. J Clin Epidemiol 2014)
SPIRIT.md -- clinical trial protocols, SPIRIT 2025 (CC BY 4.0, Chan et al. BMJ 2025)
SPIRIT_AI.md -- AI clinical-trial protocols, SPIRIT-AI 2020 (CC BY 4.0, Cruz Rivera et al. Nat Med 2020)
CLAIM_2024.md -- AI/ML in clinical imaging, CLAIM 2024 Update (RSNA open access, Tejani et al. Radiol Artif Intell 2024)
DECIDE_AI.md -- early-stage clinical evaluation of AI decision-support systems, DECIDE-AI 2022 (educational summary, CC BY-NC, Vasey et al. Nat Med 2022)
MI_CLEAR_LLM.md -- LLM accuracy studies in healthcare (CC BY-NC 4.0, Park et al. KJR 2024; 2025 update)
SQUIRE_2.md -- quality improvement in healthcare/education (no open licence — Crossref returns none; Ogrinc et al. BMJ Qual Saf 2016)
CLEAR.md -- radiomics studies (CC BY 4.0, Kocak et al. Insights Imaging 2023)
MOOSE.md -- meta-analysis of observational studies (Stroup et al. JAMA 2000)
GRRAS.md -- reliability and agreement studies (Kottner et al. J Clin Epidemiol 2011)
ROBINS_E.md -- non-randomised exposure studies risk of bias (CC BY-NC-ND 4.0, Higgins et al. Environ Int 2024)
ROBIS.md -- risk of bias in systematic reviews (Whiting et al. J Clin Epidemiol 2016)
ROB_ME.md -- risk of bias due to missing evidence in meta-analysis (no open licence — BMJ TDM policy only; Page et al. BMJ 2023)
PROBAST_AI.md -- prediction model risk of bias, updated for AI/ML (Moons et al. BMJ 2025)
COSMIN_RoB.md -- reliability/measurement error risk of bias (Mokkink et al. BMC Med Res Methodol 2020)
RoB_NMA.md -- risk of bias in network meta-analysis (Lunny et al. 2024)
AMSTAR2.md -- quality of systematic reviews (Shea et al. BMJ 2017)
PRISMA_P.md -- systematic review protocols (Shamseer et al. BMJ 2015)
SWiM.md -- synthesis without meta-analysis reporting (Campbell et al. BMJ 2020)
GATHER.md -- health-estimate / burden-of-disease modeling studies (GBD and GBD-satellite, comparative-risk / population-attributable-fraction, cause-of-death and prevalence/incidence estimation, with or without forecasts), GATHER 2016 (in-house faithful summary; CC BY, Stevens et al. Lancet 2016;388:e19-23 / PLoS Med 2016;13(6):e1002056). Pairs with /analyze-statsreferences/analysis_guides/burden_decomposition_forecasting.md for the analytic methods.
Fail-fast contract: if a routed guideline has no vendored checklist file, the skill does not silently construct items from memory. It halts with a MISSING_CHECKLIST_CONTRACT_VIOLATION and surfaces the gap. A from-memory assessment is allowed only with the explicit --allow-from-memory opt-in, and that report must be clearly labelled NON-AUTHORITATIVE. See Step 2 and scripts/check_checklist_exists.py.
Critical-item floor: ${CLAUDE_SKILL_DIR}/references/critical_item_floor.md -- the small set of non-waivable items per study type (presence outranks the headline %), plus the AI/radiomics methodological-quality / risk-of-bias instruments (PROBAST+AI, METRICS/RQS, APPRAISE-AI) kept distinct from their reporting counterparts. Loaded in Step 4f.
Workflow
Step 0: Existing-checklist staleness pre-check
If a checklist already exists for this project (qc/reporting_checklist.json or a prior .md report), verify it targets the current manuscript before reusing it — a checklist generated against an older version carries stale section/line references and a stale version label that a reviewer who cross-checks will catch:
A non-zero exit means the existing checklist is stale (older target_version, changed source_sha256, different target_manuscript) or pre-dates the version contract — regenerate it against the current manuscript (Steps 1–5) rather than reusing it. Every report you generate must carry the target_manuscript / target_version / source_sha256 fields (Part A header + Part D JSON) so this check works next round.
Step 1: Select Guideline
Determine the appropriate reporting guideline. Auto-detect from the manuscript type or accept
user specification.
Auto-detection mapping:
Study Type
Primary Guideline
AI Extension
Observational study
STROBE
--
Mendelian randomization study
STROBE-MR (base STROBE + MR extension)
--
Health economic evaluation (cost-effectiveness / cost-utility / cost-benefit / budget-impact)
CHEERS 2022
--
Observational study using routinely-collected data (claims / EHR / registry / health-checkup DB)
RECORD (base STROBE + RECORD extension; RECORD-PE for drug studies)
--
Survey / questionnaire study (KAP, physician/patient, cross-sectional, e-survey)
CROSS (+ CHERRIES for internet surveys)
--
Scoping review (maps breadth/nature of evidence, clarifies concepts, identifies gaps — not a focused effectiveness/accuracy question)
SRQR (all qualitative approaches); COREQ (interviews/focus groups specifically)
--
Randomized controlled trial
CONSORT 2025
CONSORT-AI
Diagnostic accuracy study
STARD 2015
STARD-AI
Prediction model (development/validation)
TRIPOD
TRIPOD+AI
Polygenic (risk) score prediction study
PGS-RS (with TRIPOD / TRIPOD+AI)
--
Prognostic tumor-marker / biomarker study (single or multiple markers; e.g., ctDNA / molecular residual disease)
REMARK (pair with STROBE for the observational-design items; TRIPOD / TRIPOD+AI if a prognostic model is developed)
--
Causal / comparative-effectiveness question emulated on observational data (treatment vs treatment, screening vs none, drug A vs B on registry / EHR / claims data)
TARGET (pair with the /design-study target-trial-emulation module for design; RECORD / STROBE for the routinely-collected-data items)
--
Health-estimate / burden-of-disease modeling study (GBD or GBD-satellite, comparative-risk / population-attributable-fraction, cause-of-death or prevalence/incidence estimation, with or without forecasts)
GATHER (pair with /analyze-stats burden-decomposition-forecasting guide for the analytic layer)
--
Systematic review / meta-analysis
PRISMA 2020
PRISMA 2020 for Abstracts (run on the abstract, scored separately)
DTA systematic review / meta-analysis
PRISMA-DTA
PRISMA 2020 for Abstracts (run on the abstract, scored separately)
Meta-analysis of observational studies
MOOSE
PRISMA 2020 (use both)
Risk of bias (DTA studies)
QUADAS-3 (current recommended version)
QUADAS-2 only when appraising or reproducing a review that used it
Risk of bias (RCTs)
RoB 2
--
Risk of bias (non-randomised intervention studies)
ROBINS-I
--
Risk of bias (non-randomised exposure studies)
ROBINS-E
--
Risk of bias (comparative DTA studies)
QUADAS-C
QUADAS-3 (use both; apply the E&E's adaptation — see Using QUADAS-C with QUADAS-3 in QUADAS3.md)
Risk of bias (prediction models)
PROBAST
PROBAST+AI
Risk of bias (systematic reviews)
ROBIS
AMSTAR 2
Risk of bias (missing evidence in MA)
ROB-ME
--
Risk of bias (network meta-analysis)
RoB NMA
--
Risk of bias (measurement properties)
COSMIN RoB
--
Quality assessment (observational)
NOS
--
Case report
CARE
--
Study protocol
SPIRIT 2025
SPIRIT-AI
Animal study
ARRIVE 2.0
--
AI/ML study in clinical imaging
CLAIM 2024
--
Study using a large language model (develop/fine-tune/prompt/evaluate an LLM)
TRIPOD-LLM
MI-CLEAR-LLM (use alongside when LLM accuracy is an outcome)
Early-stage / live clinical evaluation of an AI decision-support system (human factors, workflow, safety)
DECIDE-AI
--
LLM accuracy evaluation in healthcare
MI-CLEAR-LLM
STARD-AI or CLAIM 2024 (use alongside)
Reliability / agreement study
GRRAS
--
SR protocol
PRISMA-P
--
Synthesis without meta-analysis
SWiM
PRISMA 2020 (use both)
Quality of systematic reviews
AMSTAR 2
ROBIS
Radiomics study
CLEAR
CLAIM 2024 (if deep learning component)
Educational / QI study
SQUIRE 2.0
--
Generative AI images ARE the study object (realism / real-vs-synthetic reader study / model-vs-model quality)
(no single guideline -- assemble)
see decision aid below
QUADAS-3 has two protocol-stage phases, and this skill usually runs too late for them.
Phase 1 (state the synthesis question) and phase 2 (define the ideal test accuracy trial
each judgement is made against) are review-level and belong in the protocol, alongside the
review-specific guidance for answering each signalling question. Reaching them for the first
time during manuscript QC means writing the comparator after seeing the results.
If they are missing, say so as a limitation rather than reconstructing them — and route the
protocol work to /meta-analysis Phase 1. Phases 3–6 are what a QC pass can genuinely run.
Rules:
If the study involves AI/ML, always apply the AI extension in addition to the base guideline.
Exception — TRIPOD: TRIPOD+AI 2024 (Collins et al., BMJ 2024) is a complete rewrite, not an addendum to TRIPOD 2015 (Moons et al., Ann Intern Med 2015). For non-AI prediction models, use TRIPOD 2015 only. For AI/ML prediction models, use TRIPOD+AI 2024 only. Do NOT apply both simultaneously.
STARD-AI (Sounderajah et al., Nat Med 2025) extends STARD 2015 with 14 new and 4 modified items (40 total). For AI diagnostic accuracy studies, use STARD-AI (which incorporates all STARD 2015 items). Do NOT apply both STARD 2015 and STARD-AI simultaneously — STARD-AI supersedes STARD 2015 for AI studies.
TRIPOD-LLM (Gallifant et al., Nat Med 2025) is the reporting guideline for studies that develop, fine-tune, prompt, or evaluate a large language model for a clinical/biomedical task. It extends the TRIPOD family (TRIPOD 2015 → TRIPOD+AI 2024 → TRIPOD-LLM 2025); name the base instrument and the extension and cite each. It is modular — task-specific items (Annotation, Prompting, Summarization, Instruction-tuning) are N/A when that component is absent. Use TRIPOD-LLM for LLM studies in place of TRIPOD+AI; pair with MI-CLEAR-LLM when LLM accuracy is an evaluated outcome. The vendored checklist is an educational summary (own-words paraphrase of item intent); complete the official instrument for a submission checklist.
MI-CLEAR-LLM is a supplementary checklist (8 item categories in the 2025 update; the 2024 original had 6), not a standalone reporting guideline. Always pair it with the study's primary guideline (e.g., STARD-AI for AI diagnostic accuracy, CLAIM for imaging AI). Apply MI-CLEAR-LLM whenever the study evaluates LLM accuracy as an outcome — do NOT apply it merely because the manuscript was written with LLM assistance. Its scope is LLM accuracy studies (including VLMs interpreting images); it does not apply at study level to studies where a generative model produces the images under study (see next bullet).
Generative-AI images as the study object (a generative model synthesizes images and the study evaluates their realism, controllability, real-vs-synthetic distinguishability, or model-vs-model quality) has no single dominant checklist. Assemble: CLAIM 2024 (imaging-AI umbrella; model-development items N/A when commercial models are used as-is) + FUTURE-AI traceability + MI-CLEAR-LLM transparency items only (prompt/model/version/params/runs — for generation provenance, not study-level compliance) on the generator side; STARD-AI (for real-vs-synthetic detection) + GRRAS (reader reliability) + MRMC reporting on the evaluation side. Map applicable items and cite base + extension; never claim wholesale compliance. Full decision aid: ${CLAUDE_SKILL_DIR}/references/genai_image_study_object_decision_aid.md.
If multiple guidelines apply (e.g., a diagnostic accuracy study that is also an AI study), check against all relevant guidelines and merge into one report.
If the user requests a specific guideline, use that one regardless of auto-detection.
Step 2: Load Checklist
Run the fail-fast guard first for every guideline you intend to apply:
Exit 0 → the vendored checklist exists; read it from
${CLAUDE_SKILL_DIR}/references/checklists/ and proceed.
Exit 1 (MISSING_CHECKLIST_CONTRACT_VIOLATION) → the guideline is routed
but no checklist file is vendored. Do not construct items from memory.
Halt, report the violation to the user, and stop unless they explicitly
opt in (next bullet).
Exit 2 (UNKNOWN_GUIDELINE) → the name is not recognised; confirm the
correct guideline with the user.
No silent fallback. A from-memory checklist is permitted only when the
user explicitly accepts it — re-run the guard with --allow-from-memory
(exit 0 + a NON-AUTHORITATIVE warning). In that case the output report MUST
carry a prominent banner that the assessment was constructed from model
knowledge and is not backed by a vendored checklist, and submission_safe
must not be asserted on its basis.
Gather context from the full document before starting the item-by-item assessment.
Step 4: Assess Each Item
For every checklist item, determine:
Status
Criteria
PRESENT
The item is fully addressed with sufficient detail.
PARTIAL
The item is mentioned or partially addressed but lacks required detail.
MISSING
The item is not found anywhere in the manuscript.
N/A
The item does not apply to this particular study (justify why).
For each item, record:
Status: PRESENT / PARTIAL / MISSING / N/A
Location: Section name and paragraph or approximate position (e.g., "Methods, paragraph 3")
Notes: What was found (if PRESENT/PARTIAL) or what should be added (if MISSING)
What is appraised is the source paper's reporting — never your convenience in using it. This
holds for every instrument here, reporting checklists and risk-of-bias / quality tools alike, and it
is easiest to lose in a systematic review, where you read each paper in order to extract from it.
An item asking "are the results clearly reported?" is not asking "were they reported in the unit my
pool needs".
A reviewer scoring a case-series quality tool marked four papers down on the outcome-reporting item
because their analysis unit did not match the pool's — treatment-level results against a
patient-level denominator. A second assessor's correction was one sentence, that is a limit of our
extraction, not a defect in their reporting, and all four scores went back up. Single-scorer
appraisal is where this happens, because there is nobody to say it.
So: if a downgrade's stated reason turns on a denominator, an analysis unit, a subgroup you needed
and they did not report separately, or a format you could not parse, it is an extraction note, not
a scoring reason. Record it in a separate extraction-note column and restore the score.
Both belong in the table. An extraction limitation is a real constraint on your synthesis and often
belongs in your limitations paragraph — it just is not evidence about the paper being appraised, and
folding it into the score makes the appraisal unreproducible: another assessor with a different pool
would score the same paper differently.
Step 4b: Section Boundary Check
In addition to checklist items, verify that:
Results section contains only factual findings: no interpretation, no "why" explanations,
no prior literature comparisons, no evaluative adjectives without numbers.
Discussion section does not introduce new data not presented in Results.
Flag any boundary violation as a separate finding in Part C Action Items with the label
[BOUNDARY].
Applies to: systematic reviews, meta-analyses, and intervention studies with
prospective registration (PRISMA 2020, PRISMA-DTA, PRISMA-P, MOOSE, CONSORT, SPIRIT).
Why this step exists: the registration identifier is a single checklist item and can
pass Step 4 even when the manuscript is internally inconsistent about when the
registration or its amendments occurred relative to the analysis. An undisclosed
post-hoc amendment is a common rejection trigger.
Five audit items (summary): (1) registration identifier present in Methods, Abstract,
and cover letter; (2) initial registration date precedes — or is explicitly disclosed as
post-dating — the extraction milestone; (3) amendment dates appear in Methods, the
described change is visible in Methods, analysis was re-run if amendment post-dates the
lock, and no amendment post-dates submission; (4) cross-artifact agreement between
Methods and the registry record (PROSPERO PDF, ClinicalTrials.gov export) — silent
discrepancy is a finding; (5) retrospective-registration disclosure paragraph when
evidence suggests post-extraction filing.
Registration-ID format gate: a PROSPERO ID is CRD42 + 9 digits = 14 characters
(^CRD42\d{9}$, e.g. CRD42024500001). Run grep -oE 'CRD42[0-9]+' manuscript.md and
assert each match is 14 characters long; a 15-character ID (a stray inserted digit) is a
transcription error logged as [REGISTRATION-TIMING] (fixable_by_ai: false — verify against
the live PROSPERO record, do not guess the correct digit).
Flagging: any failure is logged in Part C Action Items with label
[REGISTRATION-TIMING]. fixable_by_ai: false when reconciliation requires an external
amendment filing; true only when the fix is a Methods-text insertion of a date already
disclosed elsewhere. Part D JSON includes a registration_timing object
(registry, id, initial_registration_date, amendments[], timing_consistency, findings[]).
Applies to: systematic reviews and meta-analyses using PRISMA 2020 / PRISMA-DTA /
PRISMA-P. Triggers when Item 16a (flow diagram) is PRESENT.
Why this step exists: the flow diagram is a single checklist item and can pass Step 4
visually while still containing arithmetic errors (records screened ≠ identified − duplicates;
sought-for-retrieval ≠ screened − excluded) or text↔figure number disagreements. Senior
MA reviewers commonly require strict PRISMA 2020 diagram conformance and explicit body↔
figure number agreement; reviewers who detect these mismatches lose confidence in the
study's data integrity immediately.
Four arithmetic checks:
records screened = records identified − duplicates removed
records sought-for-retrieval = records screened − records excluded (screening)
reports retrieved = sought − reports not retrieved
studies included = reports assessed for eligibility − reports excluded (with reasons)
Two cross-reference checks:
Body text PRISMA numbers (e.g., "315 records identified, 122 duplicates removed,
186 records screened") match Figure 1 box labels 1:1.
Reasons for exclusion (Methods + Figure legend) agree on counts and category names.
Procedure:
Run the deterministic implementation first — it performs steps 1, 4, 5, and 6 below
automatically (same keyword regex, the four arithmetic equations, the body↔figure
cross-reference) and writes qc/prisma_figure_audit.json:
Exit 1 = an arithmetic or cross-reference MISMATCH (log a Part C Action Item labelled
[PRISMA-FIGURE], fixable_by_ai: false — the author must reconcile the numbers); exit
2 = missing/unparsable input. The manual algorithm below documents exactly what the
script checks and is the fallback when Figure 1 numbers live only in a PNG/SVG that must
be transcribed by hand:
Extract numbers from Figure 1 source — preferred order: (a) analysis/figures/Figure1_PRISMA.md
markdown manifest, (b) caption text in manuscript.md, (c) PPTX text run if .pptx
exists, (d) manual entry from PNG/SVG.
Cross-check analysis/figures/_figure_manifest.md (produced by /make-figures):
verify that the row whose Type = prisma (or Type = prisma-dta) points at the same
file path used as the audit source, and that the row's Critic field is yes or
partial (not no). A missing manifest row, mismatched path, or Critic = no flag
logs [MANIFEST-XREF] (advisory) — the arithmetic check still runs against the source
identified in step 2. Skip this sub-step if _figure_manifest.md does not exist (older
projects).
Run 4 arithmetic checks; emit PRESENT / MISSING / MISMATCH per equation.
Run 2 cross-reference checks; emit PRESENT / MISSING / MISMATCH per number.
Output qc/prisma_figure_audit.json and a short table.
Flagging: any MISMATCH or arithmetic failure logs a Part C Action Item with label
[PRISMA-FIGURE]. fixable_by_ai: false (numbers must be reconciled by the author).
Cross-cutting: integrates with ~/.claude/rules/numerical-safety.md (PRISMA 5-way
consistency: text ↔ Figure ↔ extraction CSV ↔ analysis script ↔ supplementary).
Step 4e: Reporting-Framework Naming Audit
Applies to: any manuscript that invokes an AI/extension reporting framework
(PROBAST+AI, STARD-AI, TRIPOD+AI, TRIPOD-LLM, CONSORT-AI, SPIRIT-AI, PRISMA-DTA, QUADAS-C).
Why this step exists: a base reporting tool and its extension are distinct instruments
with separate citations (manuscript-style-classical §14). Step 1 routes to the right
checklist but does not police how the framework is named in prose. The recurring failures
are: invoking an extension without ever naming or citing the base instrument it extends;
mixing +AI and -AI hyphenation for one family within a single document; coining item
labels like "12-AI"; and waving at "recent guidance" instead of naming the framework.
Verdicts:BASE_MISSING (extension used, base instrument never named standalone) is a
Major and logs [FRAMEWORK-NAMING] in Part C with fixable_by_ai: true (insert the base
name + its citation). HYPHEN_MIX, CITE_MISSING, SELF_COINED_LABEL, and VAGUE_GUIDANCE
are Minor (fixable_by_ai: true). Part D JSON includes a framework_naming object mirroring
the script's claims[].
Step 4f: Critical-item floor cross-check
Applies to: every guideline assessment for which the floor defines a row (load and
check only those; do not invent a floor for an unlisted guideline). After the item-by-item
table, load ${CLAUDE_SKILL_DIR}/references/critical_item_floor.md and check the small set
of non-waivable items for this study type. A MISSING critical item is surfaced as a
Critical gap and becomes the report's headline regardless of the overall percentage —
a high percentage with a missing critical item (undefined reference standard, no
leakage-controlled partition, calibration absent for a prediction model, an unreconciled
flow diagram) is not "broadly acceptable."
For AI/ML and radiomics manuscripts, also confirm the chosen methodological-quality /
risk-of-bias instrument (PROBAST+AI, METRICS/RQS, APPRAISE-AI) and its non-waivable
concerns — a fully reported paper can still be at high risk of bias. For radiomics, the
fuller METRICS breakdown (9 categories / 30 weighted items) is in
${CLAUDE_SKILL_DIR}/references/appraisal_tools/METRICS.md (an appraisal reference, not a counted
reporting checklist). Keep these distinct
from the reporting counterparts (CLEAR, DECIDE-AI), which route through the normal checklist
flow. Do not assert a numeric journal desk-reject threshold; the hard signals are a missing
critical item and the journal's own required elements.
Step 5: Generate Report
Produce a structured compliance report in four parts.
This report is an internal working audit — it carries auto-fix annotations, a
machine-readable JSON block (compliance_pct, fixable_by_ai, …), and Action Items. It is
NOT the official reporting checklist a journal expects (that is the blank guideline form with
Item | Recommendation | Reported in page/section, which the authors fill in). Never submit
this report as the submission checklist. So that the file is self-identifying and cannot be
reused by filename into a later submission package, the report MUST begin with this banner as
its very first line:
<!-- INTERNAL AUDIT — NOT FOR SUBMISSION. This is the /check-reporting working
report, not the official journal checklist. Do not upload to a submission portal. -->
(/sync-submission's check_checklist_dump_leak gate also catches this dump if it ever lands in
a submission directory — but the banner is what makes it catchable.)
The four parts — literal templates in ${CLAUDE_SKILL_DIR}/references/report_templates.md:
Part A — Summary. Header (manuscript file, version token, guideline, date), the
PRESENT/PARTIAL/MISSING/N-A count table, and overall compliance. The headline is the critical
items (Step 4f), not the percentage: report {present}/{total} and name every missing
critical item with the section it belongs in.
Part B — Item-by-item checklist. One row per item: # | Section | Item | Status | Location | Notes.
Part C — Action items (MISSING and PARTIAL only), ordered by: items most journals enforce
strictly (ethics approval, registration, sample size) → items in Methods (easiest to fix) →
everything else.
Part D — Machine-readable JSON, appended as a fenced block. MUST be present under
--json or when called from /write-paper Phase 7, which parses it.
JSON field contract (the part other skills depend on — get these right):
action_items — MISSING and PARTIAL only; PRESENT and N/A are excluded.
fixable_by_ai — true when the fix inserts or expands text using information already in the
manuscript or inferable from it; false when it needs external facts the author alone holds
(registration number, IRB approval number, protocol details).
suggested_fix — concrete draft text, insertable as written.
source_sha256 — first 12 hex chars of the SHA-256 of the manuscript bytes, so a stale report
cannot be silently attributed to a newer manuscript.
Read on demand:
File
Read it when
Cost if read blindly
references/report_templates.md
you have finished the audit and are writing the report
~1,900 tokens of pure output format — it informs no part of the assessment itself
Assessment Standards
Be Strict
PARTIAL means the item is mentioned but lacks specificity. For example:
"We used appropriate statistical tests" = PARTIAL (which tests?)
"We used the Mann-Whitney U test for continuous variables and Fisher's exact test for categorical variables" = PRESENT
A vague reference does not count as PRESENT. The detail level must match what the guideline expects.
Be Specific in Suggestions
For MISSING items, provide a draft sentence the user can insert.
For PARTIAL items, point to the exact gap and suggest specific additions.
Reference the specific manuscript section where the addition should go.
Common Gaps to Watch For
These items are frequently missing in medical manuscripts:
Study registration number (CONSORT, PRISMA, STARD)
Registration / amendment date consistency (PRISMA 2020, PRISMA-DTA, CONSORT, SPIRIT) — run Step 4c whenever a registration identifier is present
AI-specific: commercial interests and data/code availability (STARD-AI)
Power-aware framing of a null result (STROBE 16a / 18 / 20) — for an observational study whose headline is a non-significant association, a flat "X was not associated with Y" overreads the data when the analysis is not powered to exclude a clinically meaningful effect. Mark item 18/20 PARTIAL unless the manuscript states the precision as an exclusion (e.g., "the 95% CI excluded an eGFR difference larger than ~1.7") or reports a minimum detectable effect — "no effect" vs "could not exclude an effect of size X" are different claims, and a negative conclusion needs the latter.
Confounder-selection rationale, not "adjust for everything that differs" (STROBE 16a explicitly asks which confounders were adjusted for and why) — flag a kitchen-sink adjustment set chosen because variables differ in Table 1. The Methods must give a causal rationale (DAG / prior literature) and must not adjust for a mediator or consequence of the outcome (over-adjustment, e.g. serum uric acid in an eGFR model); both an unjustified inclusion and an unjustified omission are item-16a gaps.
PRISMA Cascade Arithmetic Auto-Verify
PRISMA 2020 flow diagrams chain a cascade of subtractions (database
records → after dedup → title/abstract screened → full-text reviewed →
included in synthesis). Off-by-one errors in the prose cascade are a
high-frequency reviewer red flag (e.g., 151 + 108 + 39 + 1 + 1 + 4 = 304 followed by a prose summary "305" four lines later).
When PRISMA 2020 or PRISMA-DTA is selected and round-by-round
screening TSV artifacts are available, run the cascade auto-verify:
Reads the round TSVs and counts INCLUDE / EXCLUDE / MAYBE
decisions per round.
Computes the cascade arithmetic from raw decisions (no prose).
Optionally grep the manuscript for matching stage-count claims and
emits per-stage drift when the prose disagrees.
Treat any manuscript_drift entry as a P0 blocker — fix the prose to
match the computed cascade and re-run.
Submission Checklist Export
Many journals require a filled reporting checklist to be submitted alongside the manuscript.
When the user asks for a submission-ready checklist, format the output as:
Page numbers should be filled in by the user after final formatting. Use section names as placeholders.
Skill Interactions
When
Call
Purpose
During manuscript writing
/write-paper Phase 7
Final compliance check
Need to add Methods text
/write-paper Phase 3
Draft missing Methods content
Need statistical details
/analyze-stats
Generate missing statistical reporting
Need flow diagram
/make-figures
Generate CONSORT/STARD/PRISMA diagram
Error Handling
If the manuscript file cannot be read, ask the user for the correct path.
If the study type is ambiguous, ask the user to confirm before selecting a guideline.
If a checklist item is genuinely unclear in its applicability, mark as N/A with justification.
This is a pre-screening tool. Always remind the user that final compliance should be verified by all co-authors and ideally by a methodologist.
Language
Checklist content and compliance report: English
Communication with user: Match user's preferred language
Medical terms: English only
Anti-Hallucination
Never fabricate references. All citations must be verified via /search-lit with confirmed DOI or PMID. Mark unverified references as [UNVERIFIED - NEEDS MANUAL CHECK].
Never invent clinical definitions, diagnostic criteria, or guideline recommendations. If uncertain, flag with [VERIFY] and ask the user.
Never fabricate numerical results — compliance percentages, scores, effect sizes, or sample sizes must come from actual data or analysis output.
If a reporting guideline item, journal policy, or clinical standard is uncertain, state the uncertainty rather than guessing.
Gates
Gate
Severity
Trigger
Action on fail
Mandatory items present
ENFORCED at submission
< 100% of guideline-mandatory items marked PRESENT
Auto-fix MISSING items where text exists; otherwise route to /write-paper Phase 7 for re-draft
flow numbers don't sum (e.g., screened ≠ included + excluded), or in-text counts mismatch flow diagram
HALT; reconcile against extraction artifacts
Optional items (e.g., supplementary AI declarations)
ADVISORY
< 80% of optional items present
warn; user accepts
Cross-reporting-guideline routing (study type → guideline)
ENFORCED
study type undeclared or guideline missing
Ask user; do not silently default
Global-rule references
Some passages in this skill cite a path of the form ~/.claude/rules/<name>.md. Those are the
maintainer's personal global rules, kept outside this repository. They are not shipped with
this skill and will not exist on your machine; they appear only as provenance for where a
convention came from. If one of them looks like it is standing in for an instruction you actually
need, that is a bug — please open an issue, because the instruction belongs here.
