define-variables
Literature-grounded variable operationalization for observational research. Turns a data dictionary + research question into a citation-backed table of exposure/outcome/covariate definitions, cutoffs, and DB variable mappings. Prevents ad-hoc phenotype definitions that invite rev
Install
npx skills add https://github.com/Aperivue/medsci-skills/tree/main/skills/define-variables
claude plugin marketplace add https://llmmart.ai/marketplace.json && claude plugin install aperivue-medsci-skills@llmmart
git clone https://github.com/Aperivue/medsci-skills.git
The skills CLI installs just this skill, for any of its supported agents. Claude Code installs the whole aperivue/medsci-skills collection as a plugin from our marketplace. Git is the plain clone.
Skill manifest
Define-Variables Skill
Purpose
Every observational study operationalizes abstract constructs (MASLD, CKD, emphysema, obesity, incidentaloma) into concrete rules against the available data dictionary. When that operationalization is invented ad-hoc from the dictionary alone, reviewers reject on construct validity regardless of downstream statistics.
This skill forces a literature-first pass: each variable is mapped to a canonical guideline/consensus definition, cross-checked against prior operationalizations in comparable cohorts, then mapped to available DB variables. Ad-hoc deviations are flagged explicitly and justified, not hidden.
Use it when:
- a study question is known and variables are being selected
- inclusion/exclusion criteria or phenotype definitions need citation backing
- a data dictionary has ambiguous or derived variables (eGFR formula, BMI class, liver steatosis criteria, etc.)
- a reviewer asked "why this cutoff?"
- a retrospective audit reveals drifted definitions across projects in the same cohort
Call after /design-study, before /write-protocol.
Communication Rules
- Communicate in the user's preferred language.
- All variable names, guideline names, cutoffs in English.
- Produce one artifact:
variable_operationalization.mdin the project root (or path the user specifies).
Inputs
- Research question (one sentence)
- Candidate variables — exposure, outcome, key covariates, eligibility filters
- Data dictionary path (xlsx / csv / markdown) OR explicit list of available DB columns
- Cohort type (e.g., health-screening, NHANES-like, claims, registry) — informs which prior-art cohort to compare against
Missing inputs → ask once, then proceed.
4-Tier Pipeline (DB codebook + token-efficient literature)
Tier 0 — DB codebook lookup (mandatory for DB-backed observational studies)
Trigger: project has a project.yaml::db.dictionary_path field pointing to a machine-readable codebook (xlsx/csv/markdown), OR user supplied a dictionary path in inputs. If neither, skip to Tier 1.
For every candidate DB variable — before touching literature — open the dictionary and record, verbatim, the sheet name, row number, and code→meaning mapping. This prevents the single most common observational-study error: assuming a column code (status == 0, grade == 4) means what it intuitively reads like, when the codebook says otherwise.
Concrete procedure per variable:
- Locate the variable in the dictionary by exact column name.
- Copy verbatim: the sheet title, row number, and full code→meaning mapping (or unit/range statement for continuous vars).
- Paste into the
Dict. sheet & row+Dict. verbatimcolumns of the operationalization table. - If the variable is not found, OR the codebook is silent on a specific code value, file a question to the DB owner / data steward. Do NOT infer from cross-tabs, do NOT guess, do NOT proceed with that variable until a verbatim answer exists.
Empirical checks (value distributions, cross-tabs with related columns) are useful for sanity testing after the verbatim codebook meaning is recorded — never as a substitute for it.
Project-level binding (recommended): commit a DICTIONARY_FIRST_POLICY.md at the project root (or shared-config path) capturing the canonical dictionary path + escalation contact. Cross-project rule template: ~/.claude/rules/dictionary-first.md.
Exit gate: check_dictionary_citations.py (or equivalent) PASS on the operationalization table before running Tier 1.
Tier 1 — Canonical index lookup (no API calls)
Check references/common_definitions.md (shipped with skill) for the variable. Covers high-frequency constructs:
- Liver: MASLD (AASLD 2023), MetALD (AASLD 2023), MAFLD (2020), NAFLD (legacy), ALD, viral hepatitis (AASLD 2022/2024 HBV, AASLD-IDSA HCV)
- Metabolic: T2DM (ADA 2024), prediabetes (ADA 2024), metabolic syndrome (IDF 2009 / NCEP ATP III / K-NCEP), obesity/BMI (WHO Asian 2004 + WHO global), HTN (ACC/AHA 2017 + JNC-8), dyslipidemia (NCEP ATP III, 2023 AHA/ACC)
- Renal: CKD (KDIGO 2024), eGFR formulas (CKD-EPI 2021 race-free, MDRD legacy), incidental renal mass (ACR 2018 white paper, Bosniak 2019)
- Pulmonary: COPD (GOLD 2024), emphysema imaging (Fleischner 2015)
- CV: CAC scoring (Agatston 1990, MESA percentiles), CAD risk (2018 ACC/AHA cholesterol, PREVENT 2023)
- Cancer: gastric cancer H. pylori (Maastricht VI 2022), thyroid nodule (ACR TI-RADS 2017), gallbladder polyp (European 2022 joint guideline)
- Imaging incidentalomas: adrenal (ACR 2023), pancreas (ACR 2017), renal (ACR 2018), thyroid (ACR 2017)
If the variable hits Tier 1, record: guideline, year, canonical cutoff, BibTeX key. Done — no /search-lit call.
Tier 2 — Targeted /search-lit (focused queries only)
For variables NOT in Tier 1, OR when subgroup justification is needed (Asian-specific cutoff, pediatric, young-adult, pregnancy, etc.), call /search-lit with one query per variable — not a general sweep. Query pattern:
"{construct} definition {cohort type} {subgroup qualifier}"
e.g., "obstructive sleep apnea prevalence Korean health screening cohort"
Cap: 5 queries per session. Stop early if first 1-2 papers converge on the same definition.
Tier 3 — Verification
Before finalizing, run /verify-refs on the accumulated BibTeX to confirm every citation exists in PubMed/CrossRef. Ad-hoc choices (no canonical source found) must be flagged Ad-hoc: yes and justified with 1-2 sentences — never hidden.
Output Template
Write to {project_root}/variable_operationalization.md using templates/variable_operationalization.md. Required structure:
Header: research question, cohort type, date, author
Operationalization table — one row per variable:
| Variable | Role | Dict. sheet & row | Dict. verbatim | Canonical source | Definition | Cutoff | DB vars | Implementation | Ad-hoc? |
Role: exposure / outcome / covariate / eligibilityDict. sheet & row: e.g.5-1.복부초음파 r12— mandatory if a DB dictionary existsDict. verbatim: full code→meaning string copied from the dictionary — mandatory same conditionCanonical source: BibTeX key (e.g.,@rinella2023_aasld_masld)Definition: one line, verbatim from guideline where possibleCutoff: numeric + unitsDB vars: exact dictionary column names usedImplementation: SQL/pandas-style pseudocode (e.g.,bmi>=25 & (b_tg>=150 | b_hdl<40))Ad-hoc?: yes/no. If yes, justification below table
Ad-hoc justifications — for each yes row
Mapping gaps — variables in the protocol with no DB equivalent; list proxy / omit / request decisions
References — BibTeX block
Non-Goals
- Statistical analysis →
/analyze-stats - Manuscript drafting →
/write-paper - Data cleaning / missingness →
/clean-data - Sample size →
/calc-sample-size
Pipeline Position
intake-project → design-study → search-lit → define-variables → write-protocol → analyze-stats → write-paper
^^^^^^^^^^^^^^^
/orchestrate should insert this skill between /search-lit and /write-protocol for any observational cohort or registry study.
Anti-Hallucination
Every variable definition, cutoff, and era anchor must be grounded in a verified source — a clinical guideline, a peer-reviewed paper with DOI, or an established registry data dictionary. Never invent a phenotype threshold from the model's prior; if the source is unknown, mark the row Ad-hoc: yes and require user confirmation before it propagates into /write-protocol or /analyze-stats. When citing papers to justify a cutoff, verify the citation via /search-lit or /verify-refs — do not carry references from memory alone. The output table must carry explicit source, year, and guideline_version columns so downstream skills can re-verify.
Failure Modes to Avoid
- Ad-hoc DB code interpretation (the single most costly observational-study error). Interpreting a column value (
status == 0,grade == 4) by its surface reading without consulting the codebook. Tier 0 exists specifically to prevent this. Distinguish from Failure #1: Tier 0 says "once you've picked the DB column, quote the codebook verbatim before using its values." Failure #1 says "don't pick DB columns before picking definitions from literature." Both rules co-exist. - Dictionary-first framing — starting from what columns exist, then picking a definition that matches. Always flip: definition first, then map.
- Cutoff drift — using a different cutoff than the cited guideline without justification (e.g., BMI≥23 cited as WHO Asian while text says ≥25).
- Mixing eras — 2020 MAFLD criteria with 2023 MASLD criteria in the same analysis. Pick one and note why.
- Silent ad-hoc — introducing a novel cutoff without the
Ad-hoc: yesflag. - Sweep-style /search-lit — running a generic lit search instead of one focused query per gap variable. Wastes tokens and buries the signal.
- Dose/duration structural-missingness — operationalizing a dose/duration covariate (pack-years, cessation-years, alcohol grams/week) anchored to a categorical exposure (smoking status, alcohol use) without specifying what the reference level (never-smoker, never-drinker) does to the dose. A never-smoker's pack-years is a structural zero, not a missing value; conflating the two collapses the analytic sample under complete-case modeling and lets MICE fabricate a non-zero dose for the unexposed. Operationalize it explicitly — add a row with
Role = covariateandImplementation = "IF status == 'never' THEN dose = 0 ELSE measured_value"— and adjust on the categorical status variable, reserving the continuous dose for an exposed-only secondary analysis./clean-data(categorical-implied-zero flag) and/analyze-stats("Covariate Pitfalls") enforce this downstream.
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.
Files (medsci-skills)
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references
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common_definitions.md 7.2 KB
# Canonical Definitions Index (Tier 1) Curated index of high-frequency phenotype/variable definitions for observational research. Each entry gives the authoritative source, year, cutoff, BibTeX key stub, and DOI. **Always quote the cutoff verbatim** — do not paraphrase. Update cadence: review annually or when a major guideline revision drops. --- ## Hepatology ### MASLD (Metabolic dysfunction-associated Steatotic Liver Disease) - **Source**: Rinella et al., AASLD multi-society Delphi consensus, *Hepatology* 2023 - **Definition**: Hepatic steatosis (imaging/histology) + ≥1 cardiometabolic risk factor, no other identifiable cause - **Cardiometabolic criteria (≥1 of 5)**: - BMI ≥25 kg/m² (≥23 for Asian populations) OR WC >94 cm (M) / >80 cm (F) - FPG ≥100 mg/dL OR 2h-PG ≥140 OR HbA1c ≥5.7% OR T2DM OR T2DM treatment - BP ≥130/85 OR antihypertensive treatment - TG ≥150 mg/dL OR lipid-lowering treatment - HDL ≤40 (M) / ≤50 (F) mg/dL OR lipid-lowering treatment - **BibTeX**: `@rinella2023_aasld_masld` - **DOI**: 10.1097/HEP.0000000000000520 ### MetALD - **Source**: Same AASLD 2023 consensus - **Definition**: MASLD criteria + moderate alcohol (M 140–350 g/wk, F 70–210 g/wk) - **BibTeX**: `@rinella2023_aasld_masld` ### ALD (Alcohol-associated Liver Disease) - **Source**: AASLD 2023 consensus + Crabb et al., AASLD practice guidance 2020 - **Definition**: Steatosis + alcohol >350 g/wk (M) / >210 g/wk (F) - **BibTeX**: `@crabb2020_aasld_ald`, `@rinella2023_aasld_masld` ### MAFLD (legacy, 2020) - **Source**: Eslam et al., international expert consensus, *J Hepatol* 2020 - **BibTeX**: `@eslam2020_mafld` - **Note**: Superseded by MASLD (2023) — use only for backwards comparability. ### HBV chronic infection - **Source**: Terrault et al., AASLD 2022/2018 guidance - **Definition**: HBsAg positive ≥6 months - **BibTeX**: `@terrault2018_aasld_hbv` ### HCV chronic infection - **Source**: AASLD-IDSA HCV guidance (latest rolling update at hcvguidelines.org) - **Definition**: Anti-HCV positive + HCV RNA detectable - **BibTeX**: `@aasld_idsa_hcv_guidance` ### Liver fibrosis non-invasive scores - **FIB-4**: Sterling et al. 2006. Cutoffs <1.3 exclude advanced fibrosis (<65 y); <2.0 (≥65 y). >2.67 rule-in. `@sterling2006_fib4` - **NFS (NAFLD fibrosis score)**: Angulo et al. 2007. `@angulo2007_nfs` --- ## Metabolic / Endocrine ### Type 2 Diabetes - **Source**: ADA Standards of Care in Diabetes — 2024, *Diabetes Care* - **Definition (any ONE)**: - FPG ≥126 mg/dL - 2h-PG ≥200 mg/dL on 75g OGTT - HbA1c ≥6.5% - Classic hyperglycemia symptoms + random PG ≥200 - Physician diagnosis OR antidiabetic medication - **BibTeX**: `@ada2024_standards` - **DOI**: 10.2337/dc24-S002 ### Prediabetes - **Source**: ADA 2024 - **Definition**: FPG 100–125 OR 2h-PG 140–199 OR HbA1c 5.7–6.4% ### Metabolic Syndrome - **Source**: IDF 2009 harmonized (Alberti et al., *Circulation*) — ≥3 of 5 criteria - **Criteria**: - WC (ethnicity-specific: Asian M ≥90, F ≥80 cm) - TG ≥150 OR treatment - HDL <40 (M) / <50 (F) OR treatment - BP ≥130/85 OR antihypertensive treatment - FPG ≥100 OR T2DM treatment - **BibTeX**: `@alberti2009_idf_harmonized` - **DOI**: 10.1161/CIRCULATIONAHA.109.192644 ### Obesity (BMI) - **WHO global**: Overweight ≥25, obese ≥30 kg/m². `@who2000_obesity` - **WHO Asian (2004, *Lancet*)**: Overweight ≥23, obese ≥25. `@who2004_asian_bmi` - **Korean Society for the Study of Obesity (KSSO) 2022**: Same 23/25 thresholds. `@ksso2022_obesity` ### Hypertension - **ACC/AHA 2017**: ≥130/80 = stage 1. `@whelton2017_accaha_htn` - **JNC-8 / ESC (legacy)**: ≥140/90. `@james2014_jnc8` - **Pick one explicitly** — do not mix. ### Dyslipidemia - **Source**: 2018 AHA/ACC/multi-society cholesterol guideline; 2023 update - **BibTeX**: `@grundy2019_aha_cholesterol` --- ## Renal ### CKD - **Source**: KDIGO 2024 CKD guideline, *Kidney Int* - **Definition**: eGFR <60 mL/min/1.73m² OR markers of kidney damage (ACR ≥30 mg/g etc.) ≥3 months - **Staging**: G1–G5 by eGFR; A1–A3 by albuminuria - **BibTeX**: `@kdigo2024_ckd` ### eGFR formulas - **CKD-EPI 2021 (race-free)** — *NEJM* 2021, Inker et al. `@inker2021_ckdepi2021`. Current KDIGO-recommended. - **CKD-EPI 2009** — legacy, race-based. `@levey2009_ckdepi` - **MDRD** — obsolete for clinical use; still seen in older datasets. `@levey2006_mdrd` ### Incidental Renal Mass - **Source**: ACR White Paper 2018 (Herts et al., *JACR*) - **Cutoffs**: <1 cm too small to characterize; ≥1 cm workup per size/attenuation; growth >5 mm/y concerning - **BibTeX**: `@herts2018_acr_renal` - **DOI**: 10.1016/j.jacr.2017.10.028 ### Bosniak Classification (cystic renal mass) - **Source**: Silverman et al., *Radiology* 2019 update - **BibTeX**: `@silverman2019_bosniak` --- ## Pulmonary ### COPD - **Source**: GOLD 2024 Report - **Definition**: Post-bronchodilator FEV1/FVC <0.70 + compatible symptoms/exposure - **Severity (GOLD 1–4)** by FEV1% predicted: ≥80 / 50–79 / 30–49 / <30 - **BibTeX**: `@gold2024` ### Emphysema (imaging) - **Source**: Fleischner Society 2015 statement (Lynch et al., *Radiology*) - **CT pattern classification**: centrilobular (trace/mild/moderate/confluent/advanced destructive), paraseptal, panlobular - **BibTeX**: `@lynch2015_fleischner_emphysema` - **DOI**: 10.1148/radiol.2015141579 --- ## Cardiovascular ### CAC (Coronary Artery Calcium) - **Agatston method**: Agatston et al., *JACC* 1990. `@agatston1990` - **MESA percentiles** (age/sex/race): McClelland et al. 2015. `@mcclelland2015_mesa` - **Categories**: 0 / 1–99 / 100–399 / ≥400 (widely used) ### ASCVD risk - **Pooled Cohort Equations**: 2013 ACC/AHA. `@goff2014_pce` - **PREVENT (2023)**: AHA new risk calculator, Khan et al., *Circulation*. `@khan2023_prevent` --- ## Oncology / Imaging incidentalomas ### Thyroid nodule - **ACR TI-RADS 2017**: Tessler et al., *JACR*. `@tessler2017_tirads` ### Gallbladder polyp - **European joint guideline 2022**: Foley et al., *Eur Radiol*. `@foley2022_gb_polyp` ### Adrenal incidentaloma - **ACR 2023 white paper**: Mayo-Smith et al. `@mayosmith2023_acr_adrenal` - **ESE 2023 clinical**: Fassnacht et al., *Eur J Endocrinol*. `@fassnacht2023_ese_adrenal` ### Pancreatic cystic lesion - **ACR 2017 white paper**: Megibow et al., *JACR*. `@megibow2017_acr_pancreas` ### H. pylori / gastric - **Maastricht VI / Florence Consensus 2022**: Malfertheiner et al., *Gut*. `@malfertheiner2022_maastricht6` --- ## Alcohol exposure ### Standard drink (Korea) - 1 drink ≈ 10 g ethanol (KNHANES; KCDC standard-drink definition) - ALD cutoffs above use grams/week, not drinks/week — convert when operationalizing. ### AUDIT-C / AUDIT - Bush et al. 1998; Saunders et al. 1993. `@bush1998_auditc`, `@saunders1993_audit` --- ## How to extend this file 1. Add a new subsection under the appropriate organ/domain. 2. Cite the authoritative guideline/consensus (not a secondary review). 3. Quote the cutoff exactly — include units. 4. Provide BibTeX key stub + DOI. 5. If multiple competing guidelines exist (e.g., HTN 130 vs 140), list both and note "pick one explicitly." 6. Commit with message: `define-variables: add {construct} canonical definition ({guideline year})`.
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templates
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variable_operationalization.md 3.3 KB
# Variable Operationalization — {{PROJECT_SHORT_TITLE}} - **Research question**: {{ONE_SENTENCE_Q}} - **Cohort**: {{COHORT_NAME_TYPE}} (e.g., Institutional Health Screening Cohort, retrospective) - **Author**: {{AUTHOR_NAME}} - **Last updated**: {{YYYY-MM-DD}} - **Upstream artifacts**: `design_study.md`, `search_lit_results.md` (if present) ## Operationalization table | # | Variable | Role | Dict. sheet & row | Dict. verbatim | Canonical source | Definition | Cutoff | DB vars | Implementation | Ad-hoc? | |---|----------|------|-------------------|----------------|------------------|------------|--------|---------|----------------|---------| | 1 | {{var}} | exposure | `{{sheet}} r{{N}}` | `{{code→meaning verbatim from dictionary}}` | @bibkey | verbatim from guideline | value + units | `col_a, col_b` | `col_a>=X & col_b==Y` | no | | 2 | {{var}} | outcome | `{{sheet}} r{{N}}` | `{{verbatim}}` | @bibkey | ... | ... | ... | ... | no | | 3 | {{var}} | covariate | `{{sheet}} r{{N}}` | `{{verbatim}}` | @bibkey | ... | ... | ... | ... | yes | | 4 | {{var}} | eligibility | `{{sheet}} r{{N}}` | `{{verbatim}}` | @bibkey | ... | ... | ... | ... | no | Roles: `exposure` / `outcome` / `covariate` / `eligibility` **Dict. sheet & row / Dict. verbatim (mandatory for DB-backed projects)**: - Citation format example (categorical): sheet = `{{dictionary_sheet}}`, row = `r{{N}}`, verbatim = `0={{meaning}}, 1={{meaning}}, ...` (copied exactly from the codebook). - **Mandatory** for observational studies that have a data dictionary (e.g., NHIS, KNHANES, UK Biobank, institutional EMR / health-screening registries) — it cannot be left blank. Record the project-level policy in `DICTIONARY_FIRST_POLICY.md` (or a shared config) in the repo. - For a code value not specified in the dictionary → hold off filling that row until you have asked the DB owner / data steward and received an answer. - Self-evident continuous variables such as BMI/SBP may be marked `dict: n/a (continuous)`. The cutoff still requires a canonical source. ## Ad-hoc justifications For each row flagged `Ad-hoc: yes`, document: ### {{variable_name}} - **Why no canonical source**: e.g., no guideline for this subgroup; novel combination of existing criteria - **Chosen rule**: precise cutoff / logic - **Sensitivity plan**: alternative cutoff to test in sensitivity analysis - **Reviewer-facing justification**: 1-2 sentences that will appear in Methods ## Mapping gaps Variables defined in the protocol but NOT directly available in the DB: | Protocol variable | DB status | Decision | |-------------------|-----------|----------| | {{name}} | not available | proxy with `...` / request from DB owner / drop | ## References ```bibtex @article{rinella2023_aasld_masld, author = {Rinella, Mary E and others}, title = {A multisociety {Delphi} consensus statement on new fatty liver disease nomenclature}, journal = {Hepatology}, year = {2023}, doi = {10.1097/HEP.0000000000000520} } % add one entry per cited canonical source ``` ## Verification log - [ ] Tier 1 lookups documented (guideline year, cutoff quoted) - [ ] Tier 2 `/search-lit` queries logged (query string + papers retained) - [ ] Tier 3 `/verify-refs` passed (0 unverified citations) - [ ] No silent ad-hoc — every deviation flagged and justified
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SKILL.md 11 KB
--- name: define-variables description: > Literature-grounded variable operationalization for observational research. Turns a data dictionary + research question into a citation-backed table of exposure/outcome/covariate definitions, cutoffs, and DB variable mappings. Prevents ad-hoc phenotype definitions that invite reviewer rejection. Bridges /search-lit output into /write-protocol Methods. triggers: variable definition, phenotype definition, operationalization, cutoff justification, inclusion criteria, case definition, grouping criteria, literature-grounded definition, canonical definition, 변수 정의, 정의 근거 tools: Read, Write, Edit, Bash, Grep, Glob model: inherit --- # Define-Variables Skill ## Purpose Every observational study operationalizes abstract constructs (MASLD, CKD, emphysema, obesity, incidentaloma) into concrete rules against the available data dictionary. When that operationalization is invented ad-hoc from the dictionary alone, reviewers reject on construct validity regardless of downstream statistics. This skill forces a **literature-first** pass: each variable is mapped to a canonical guideline/consensus definition, cross-checked against prior operationalizations in comparable cohorts, then mapped to available DB variables. Ad-hoc deviations are flagged explicitly and justified, not hidden. Use it when: - a study question is known and variables are being selected - inclusion/exclusion criteria or phenotype definitions need citation backing - a data dictionary has ambiguous or derived variables (eGFR formula, BMI class, liver steatosis criteria, etc.) - a reviewer asked "why this cutoff?" - a retrospective audit reveals drifted definitions across projects in the same cohort Call after `/design-study`, before `/write-protocol`. ## Communication Rules - Communicate in the user's preferred language. - All variable names, guideline names, cutoffs in English. - Produce one artifact: `variable_operationalization.md` in the project root (or path the user specifies). ## Inputs 1. **Research question** (one sentence) 2. **Candidate variables** — exposure, outcome, key covariates, eligibility filters 3. **Data dictionary path** (xlsx / csv / markdown) OR explicit list of available DB columns 4. **Cohort type** (e.g., health-screening, NHANES-like, claims, registry) — informs which prior-art cohort to compare against Missing inputs → ask once, then proceed. ## 4-Tier Pipeline (DB codebook + token-efficient literature) ### Tier 0 — DB codebook lookup (mandatory for DB-backed observational studies) **Trigger**: project has a `project.yaml::db.dictionary_path` field pointing to a machine-readable codebook (xlsx/csv/markdown), OR user supplied a dictionary path in inputs. If neither, skip to Tier 1. For every candidate DB variable — **before** touching literature — open the dictionary and record, verbatim, the sheet name, row number, and code→meaning mapping. This prevents the single most common observational-study error: assuming a column code (`status == 0`, `grade == 4`) means what it intuitively reads like, when the codebook says otherwise. Concrete procedure per variable: 1. Locate the variable in the dictionary by exact column name. 2. Copy verbatim: the sheet title, row number, and full code→meaning mapping (or unit/range statement for continuous vars). 3. Paste into the `Dict. sheet & row` + `Dict. verbatim` columns of the operationalization table. 4. If the variable is not found, OR the codebook is silent on a specific code value, file a question to the DB owner / data steward. Do NOT infer from cross-tabs, do NOT guess, do NOT proceed with that variable until a verbatim answer exists. Empirical checks (value distributions, cross-tabs with related columns) are useful for sanity testing **after** the verbatim codebook meaning is recorded — never as a substitute for it. Project-level binding (recommended): commit a `DICTIONARY_FIRST_POLICY.md` at the project root (or shared-config path) capturing the canonical dictionary path + escalation contact. Cross-project rule template: `~/.claude/rules/dictionary-first.md`. **Exit gate**: `check_dictionary_citations.py` (or equivalent) PASS on the operationalization table before running Tier 1. ### Tier 1 — Canonical index lookup (no API calls) Check `references/common_definitions.md` (shipped with skill) for the variable. Covers high-frequency constructs: - Liver: MASLD (AASLD 2023), MetALD (AASLD 2023), MAFLD (2020), NAFLD (legacy), ALD, viral hepatitis (AASLD 2022/2024 HBV, AASLD-IDSA HCV) - Metabolic: T2DM (ADA 2024), prediabetes (ADA 2024), metabolic syndrome (IDF 2009 / NCEP ATP III / K-NCEP), obesity/BMI (WHO Asian 2004 + WHO global), HTN (ACC/AHA 2017 + JNC-8), dyslipidemia (NCEP ATP III, 2023 AHA/ACC) - Renal: CKD (KDIGO 2024), eGFR formulas (CKD-EPI 2021 race-free, MDRD legacy), incidental renal mass (ACR 2018 white paper, Bosniak 2019) - Pulmonary: COPD (GOLD 2024), emphysema imaging (Fleischner 2015) - CV: CAC scoring (Agatston 1990, MESA percentiles), CAD risk (2018 ACC/AHA cholesterol, PREVENT 2023) - Cancer: gastric cancer H. pylori (Maastricht VI 2022), thyroid nodule (ACR TI-RADS 2017), gallbladder polyp (European 2022 joint guideline) - Imaging incidentalomas: adrenal (ACR 2023), pancreas (ACR 2017), renal (ACR 2018), thyroid (ACR 2017) If the variable hits Tier 1, record: guideline, year, canonical cutoff, BibTeX key. Done — no `/search-lit` call. ### Tier 2 — Targeted `/search-lit` (focused queries only) For variables NOT in Tier 1, OR when subgroup justification is needed (Asian-specific cutoff, pediatric, young-adult, pregnancy, etc.), call `/search-lit` with **one query per variable** — not a general sweep. Query pattern: ``` "{construct} definition {cohort type} {subgroup qualifier}" e.g., "obstructive sleep apnea prevalence Korean health screening cohort" ``` Cap: 5 queries per session. Stop early if first 1-2 papers converge on the same definition. ### Tier 3 — Verification Before finalizing, run `/verify-refs` on the accumulated BibTeX to confirm every citation exists in PubMed/CrossRef. Ad-hoc choices (no canonical source found) must be flagged `Ad-hoc: yes` and justified with 1-2 sentences — never hidden. ## Output Template Write to `{project_root}/variable_operationalization.md` using `templates/variable_operationalization.md`. Required structure: 1. **Header**: research question, cohort type, date, author 2. **Operationalization table** — one row per variable: | Variable | Role | Dict. sheet & row | Dict. verbatim | Canonical source | Definition | Cutoff | DB vars | Implementation | Ad-hoc? | - `Role`: exposure / outcome / covariate / eligibility - `Dict. sheet & row`: e.g. `5-1.복부초음파 r12` — mandatory if a DB dictionary exists - `Dict. verbatim`: full code→meaning string copied from the dictionary — mandatory same condition - `Canonical source`: BibTeX key (e.g., `@rinella2023_aasld_masld`) - `Definition`: one line, verbatim from guideline where possible - `Cutoff`: numeric + units - `DB vars`: exact dictionary column names used - `Implementation`: SQL/pandas-style pseudocode (e.g., `bmi>=25 & (b_tg>=150 | b_hdl<40)`) - `Ad-hoc?`: yes/no. If yes, justification below table 3. **Ad-hoc justifications** — for each yes row 4. **Mapping gaps** — variables in the protocol with no DB equivalent; list proxy / omit / request decisions 5. **References** — BibTeX block ## Non-Goals - Statistical analysis → `/analyze-stats` - Manuscript drafting → `/write-paper` - Data cleaning / missingness → `/clean-data` - Sample size → `/calc-sample-size` ## Pipeline Position ``` intake-project → design-study → search-lit → define-variables → write-protocol → analyze-stats → write-paper ^^^^^^^^^^^^^^^ ``` `/orchestrate` should insert this skill between `/search-lit` and `/write-protocol` for any observational cohort or registry study. ## Anti-Hallucination Every variable definition, cutoff, and era anchor must be grounded in a verified source — a clinical guideline, a peer-reviewed paper with DOI, or an established registry data dictionary. Never invent a phenotype threshold from the model's prior; if the source is unknown, mark the row `Ad-hoc: yes` and require user confirmation before it propagates into `/write-protocol` or `/analyze-stats`. When citing papers to justify a cutoff, verify the citation via `/search-lit` or `/verify-refs` — do not carry references from memory alone. The output table must carry explicit `source`, `year`, and `guideline_version` columns so downstream skills can re-verify. ## Failure Modes to Avoid 0. **Ad-hoc DB code interpretation** (the single most costly observational-study error). Interpreting a column value (`status == 0`, `grade == 4`) by its surface reading without consulting the codebook. Tier 0 exists specifically to prevent this. Distinguish from Failure #1: Tier 0 says "once you've picked the DB column, quote the codebook verbatim before using its values." Failure #1 says "don't pick DB columns before picking definitions from literature." Both rules co-exist. 1. **Dictionary-first framing** — starting from what columns exist, then picking a definition that matches. Always flip: definition first, then map. 2. **Cutoff drift** — using a different cutoff than the cited guideline without justification (e.g., BMI≥23 cited as WHO Asian while text says ≥25). 3. **Mixing eras** — 2020 MAFLD criteria with 2023 MASLD criteria in the same analysis. Pick one and note why. 4. **Silent ad-hoc** — introducing a novel cutoff without the `Ad-hoc: yes` flag. 5. **Sweep-style /search-lit** — running a generic lit search instead of one focused query per gap variable. Wastes tokens and buries the signal. 6. **Dose/duration structural-missingness** — operationalizing a dose/duration covariate (pack-years, cessation-years, alcohol grams/week) anchored to a categorical exposure (smoking status, alcohol use) without specifying what the *reference level* (never-smoker, never-drinker) does to the dose. A never-smoker's pack-years is a structural zero, not a missing value; conflating the two collapses the analytic sample under complete-case modeling and lets MICE fabricate a non-zero dose for the unexposed. Operationalize it explicitly — add a row with `Role = covariate` and `Implementation = "IF status == 'never' THEN dose = 0 ELSE measured_value"` — and adjust on the categorical **status** variable, reserving the continuous **dose** for an exposed-only secondary analysis. `/clean-data` (categorical-implied-zero flag) and `/analyze-stats` ("Covariate Pitfalls") enforce this downstream. ## 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. -
skill.yml 1.4 KB
schema_version: 2 name: define-variables layer: C owner_domain: variable_operationalization maturity: official when_to_use: "Turn a data dictionary + research question into a citation-backed table of exposure/outcome/covariate definitions, cutoffs, and DB variable mappings." when_NOT_to_use: "Drafting Methods prose (use write-protocol/write-paper); finding literature (use search-lit)." inputs: - "data dictionary" - "research question" - "candidate literature" outputs: - "variable operationalization table (definitions, cutoffs, DB mappings)" side_effects: - writes_project_artifacts downstream_consumers: - write-protocol - analyze-stats forbidden_actions: - define_phenotype_without_dictionary_citation - invent_cutoff_without_literature_source # v2.1 quality card purpose: "Produce a literature-grounded, dictionary-cited operationalization table that prevents ad-hoc phenotype definitions." safety_boundaries: - "Every DB variable interpretation quotes the data dictionary verbatim (dictionary-first)." - "Cutoffs cite a canonical literature source; unsupported definitions are flagged, not invented." known_limitations: - "Quality depends on a complete data dictionary; silent dictionary gaps block definitions." - "No standalone demo; output is reviewed against the dictionary and sources." validation_commands: - "cross-check each row's dictionary citation against the source dictionary" evidence_surface: manual_workflow
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