임상 데이터 분석 자동화: 병원 데이터 내보내기에서 논문 초안까지 파이프라인

발행: (2026년 3월 28일 PM 06:31 GMT+9)
3 분 소요
원문: Dev.to

Source: Dev.to

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The input problem

A typical clinical data export looks like this:

PatientID | Age | Sex | HbA1c | SBP | DBP | eGFR | Dx | AdmDate   | DisDate   | Status
001       | 67  | M   | 8.2   | 145 | 92  |      | T2DM | 2024-01-15 | 01/25/2024 | alive
002       | 54  | F   |       | 128 | 78  | 85   | 2型糖尿病 | 20240203   | 2024-02-10 | 
003       | -5  | M   | 7.1   | 300 | 85  | 92   | type 2 DM | 2024-03-01 | 2024-03-08 | dead

Notice: three different date formats in the same column, the same diagnosis coded three different ways, an obviously wrong age, a systolic BP that is likely a data‑entry error, missing values that could mean “not tested” or “not recorded,” and mixed languages. This variability is typical for clinical exports.

The analysis pipeline

Raw export (CSV/XLSX)

├─ Structure detection
│   └─ row = patient? visit? wide? long?

├─ Data cleaning
│   ├─ Date format standardization
│   ├─ Coding unification ("T2DM" = "2型糖尿病" = "type 2 DM")
│   ├─ Outlier flagging (SBP=300, Age=-5)
│   └─ Missing value classification (not tested vs not recorded)

├─ Variable typing
│   ├─ Continuous (age, HbA1c, eGFR)
│   ├─ Categorical (sex, diagnosis, comorbidities)
│   └─ Time‑to‑event (survival time + censoring status)

├─ Statistical analysis (Python execution)
│   ├─ Baseline table with per‑variable test selection
│   ├─ Regression (logistic / Cox / linear / Poisson)
│   ├─ Survival analysis (KM + log‑rank)
│   └─ Diagnostic evaluation (ROC + AUC)

└─ Output generation
    ├─ Formatted tables (baseline, regression results)
    ├─ Figures (KM curves, ROC curves, forest plots)
    └─ Manuscript sections (methods + results)

Key technical decisions

  • Python execution, not LLM computation. Statistics must be verifiable. The LLM writes the interpretation; scipy, statsmodels, and lifelines compute the numbers.
  • Clinical variable lookup. Recognizing “SBP” as systolic blood pressure enables domain‑aware outlier detection (e.g., flag 300 mmHg as likely error) rather than relying solely on statistical outlier methods.
  • Assumption checking. Every statistical test includes prerequisite verification—normality for parametric tests, events‑per‑variable for logistic regression, proportional hazards for Cox models. Running analysis without these checks is the #1 reason clinical papers get sent back by reviewers.

The baseline table problem

Generating Table 1 (baseline characteristics) sounds simple but requires per‑variable logic:

for variable in dataset:
    if is_categorical(variable):
        # n (%), chi‑square or Fisher's exact
    elif is_normal(variable):
        # mean ± SD, t‑test or ANOVA
    elif is_skewed(variable):
        # median (IQR), Mann‑Whitney or Kruskal‑Wallis

The tricky part is automating the normality decision and handling edge cases (e.g., small cell counts triggering Fisher’s exact test instead of chi‑square).

Stack

  • Next.js + Vercel
  • Claude API for text generation
  • Python chain for statistical computation
  • Export formats: PDF / DOCX / LaTeX / ZIP
  • 7 output languages

What I’m still figuring out

  • Better heuristics for distinguishing “not tested” vs “not recorded” missing values
  • Automated detection of wide vs long format in longitudinal datasets
  • Handling mixed‑language clinical notes in the same dataset

If you’ve worked on similar problems—clinical data pipelines, automated statistical analysis, or structured document generation from data—I’d love to compare notes.

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