EHR Analysis
Version Compatibility
Reference examples assume:
pyhealth 1.1.6+ (stable) or 2.0+ (latest, requires Python ≥ 3.12)
torch 2.0+
pandas 2.0+
Verify the runtime first:
- Python:
python -c "import pyhealth; print(pyhealth.__version__)"
- CLI:
pip show pyhealth
- If APIs differ between 1.x and 2.x, consult the installed docs and adapt the pattern accordingly.
Overview
Use this skill when the user needs to:
- load and structure EHR data from MIMIC-III, MIMIC-IV, eICU, OMOP-CDM, or a custom dataset
- define clinical prediction tasks such as mortality, readmission, length of stay, or drug recommendation
- train and evaluate deep learning or ML models on patient visit sequences
- apply medical code normalization, ontology mapping, or tokenization
- calibrate model outputs or generate post-hoc interpretability artifacts
When To Use This Skill
- the data source is a structured EHR database or tabular patient record export
- the task requires longitudinal patient visit sequences as model input
- the user needs benchmark-compatible evaluation metrics for clinical AI
- medical code systems (ICD, ATC, NDC, CPT, CCS) must be normalized or mapped before modeling
Quick Route
- Known EHR source (MIMIC, eICU, OMOP): load with a
pyhealth.datasets class, then set_task.
- Custom tabular data: wrap in
SampleBaseDataset, then follow the same pipeline.
- Code mapping only: use
pyhealth.medcode independently without the full pipeline.
- Evaluation only: use
pyhealth.metrics independently on existing predictions.
Progressive Disclosure
- Read
references/technical_reference.md for dataset branching rules, task schema details, model selection guidance, and calibration caveats.
- Read
references/commands_and_thresholds.md for concrete PyHealth code patterns, recommended thresholds, and output file conventions.
- Keep
SKILL.md as the main execution path and load reference files only when the task or failure mode needs the extra detail.
Default Rules
- Always use raw integer counts or visit-level code lists as model inputs; do not pre-aggregate before loading.
- Keep dataset loading, task definition, model training, and evaluation as separate, inspectable stages.
- Record dataset name, table selections, code mapping applied, task function, model class, and PyHealth version in every experiment.
- Favor reproducible train/val/test splits via
split_by_patient over random splits that can leak patient data.
Expected Inputs
- EHR source files or database dumps (MIMIC-III, MIMIC-IV, eICU, OMOP-CDM, or custom CSV/Parquet)
- table names to load (e.g.,
diagnoses_icd, procedures_icd, prescriptions)
- optional medical code mapping specifications
- task definition (predefined or custom)
- model architecture choice and training hyperparameters
Expected Outputs
results/model_checkpoint.pth
results/test_metrics.json
results/predictions.tsv
qc/dataset_stats.tsv
figures/calibration_curve.pdf
figures/feature_importance.pdf
Preferred Tools
pyhealth.datasets — MIMIC3Dataset, MIMIC4Dataset, eICUDataset, OMOPDataset, SampleBaseDataset
pyhealth.tasks — MortalityPrediction, ReadmissionPrediction, DrugRecommendation, LengthOfStayPrediction, and custom task functions
pyhealth.models — RNN, LSTM, GRU, Transformer, RETAIN, SafeDrug, GAMENet, AdaCare, ConCare, StageNet
pyhealth.trainer — Trainer
pyhealth.metrics — binary, multiclass, multilabel, fairness, interpretability metrics
pyhealth.medcode — InnerMap, CrossMap for ontology lookup and code mapping
pyhealth.tokenizer — Tokenizer for code-to-index transformations
pyhealth.calib — calibration and prediction set construction
Starter Pattern
from pyhealth.datasets import MIMIC3Dataset
from pyhealth.tasks import drug_recommendation_mimic3_fn
from pyhealth.datasets import split_by_patient, get_dataloader
from pyhealth.models import Transformer
from pyhealth.trainer import Trainer
# Step 1: load dataset
dataset = MIMIC3Dataset(
root="/path/to/mimic3/",
tables=["DIAGNOSES_ICD", "PROCEDURES_ICD", "PRESCRIPTIONS"],
code_mapping={"NDC": ("ATC", {"target_kwargs": {"level": 3}})},
)
# Step 2: define task
samples = dataset.set_task(task_fn=drug_recommendation_mimic3_fn)
# Step 3: split and build dataloaders
train_ds, val_ds, test_ds = split_by_patient(samples, [0.8, 0.1, 0.1])
train_loader = get_dataloader(train_ds, batch_size=32, shuffle=True)
val_loader = get_dataloader(val_ds, batch_size=32, shuffle=False)
test_loader = get_dataloader(test_ds, batch_size=32, shuffle=False)
# Step 4: initialize model
model = Transformer(
dataset=samples,
feature_keys=["conditions", "procedures"],
label_key="drugs",
mode="multilabel",
)
# Step 5: train
trainer = Trainer(model=model)
trainer.train(
train_dataloader=train_loader,
val_dataloader=val_loader,
epochs=50,
monitor="pr_auc_samples",
)
# Step 6: evaluate
metrics = trainer.evaluate(test_loader)
print(metrics)
Workflow
1. Validate dataset access and structure
Confirm the EHR source is accessible and the required tables are present. Inspect patient counts, visit counts, and code distributions before building tasks.
2. Load data with pyhealth.datasets
Use the appropriate dataset class. Apply code mappings at load time so downstream tasks and models operate on a consistent vocabulary. Record which tables and mappings were used.
3. Define the clinical task
Choose a predefined task function or write a custom one. Confirm the input schema (feature keys and types) and output schema (label key and mode: binary, multiclass, or multilabel) match the clinical question.
4. Split patients and build dataloaders
Always split by patient, not by visit or row, to prevent patient-level data leakage. Use split_by_patient and get_dataloader from pyhealth.datasets.
5. Initialize and train the model
Select an architecture matched to the task and data size. Configure feature_keys, label_key, and mode explicitly. Use Trainer for training, validation monitoring, and checkpoint saving.
6. Evaluate and report
Compute task-appropriate metrics using pyhealth.metrics. For binary tasks report AUROC and AUPRC. For multilabel tasks report Jaccard and PR-AUC. Export a metrics JSON and a predictions TSV alongside the model checkpoint.
7. Calibrate and interpret where needed
Apply calibration from pyhealth.calib when predicted probabilities will be used for clinical decision support. Use pyhealth.interpret for feature-level or visit-level attribution when the use case requires explainability.
Output Artifacts
results/
├── model_checkpoint.pth
├── test_metrics.json
└── predictions.tsv
qc/
├── dataset_stats.tsv
└── split_summary.tsv
figures/
├── calibration_curve.pdf
└── feature_importance.pdf
Key Parameters
| Parameter |
Typical value |
Notes |
batch_size |
32 |
reduce for large visit sequences or memory-constrained environments |
epochs |
50 |
use early stopping via monitor metric |
monitor |
"pr_auc_samples" for multilabel; "roc_auc" for binary |
task-dependent |
split_by_patient ratios |
[0.8, 0.1, 0.1] |
always split by patient not by visit |
| code mapping level |
ATC level 3 for drug codes |
balance specificity and sparsity |
n_top_genes (HVG analog) |
N/A for EHR; use vocabulary filtering |
filter rare codes with min_count |
Quality Review
- Confirm patient count, visit count, and code vocabulary size before training.
- Verify that train, validation, and test sets have no overlapping patient IDs.
- Check class balance for binary and multiclass tasks before reporting metrics.
- Review calibration curves if predicted probabilities feed downstream clinical logic.
- Do not report only AUROC; include AUPRC especially for imbalanced clinical outcomes.
- Record dataset version, table selection, code mapping, task function, and model class for every experiment.
Anti-Patterns
- splitting by visit or row instead of by patient, causing data leakage
- using AUROC as the sole metric for rare clinical events
- applying code mappings inconsistently across train and test sets
- mixing raw codes and mapped codes in the same feature without documenting it
- reporting model results without checking data coverage for the target cohort
- treating predicted probabilities as calibrated without verification
Related Skills
Machine Learning For Omics
Multi-Omics Integration
Pathway Analysis
Reporting And Figure Export
Optional Supplements
pyhealth.medcode for standalone code mapping
pyhealth.calib for post-hoc calibration
pyhealth.interpret for interpretability
1---2name: ehr-analysis3description: End-to-end EHR predictive modeling pipeline with PyHealth, covering dataset loading, task definition, model training, evaluation, calibration, and clinical interpretation.4---5
6# EHR Analysis
7
8## Version Compatibility
9
10Reference examples assume:
11
12- `pyhealth` 1.1.6+ (stable) or 2.0+ (latest, requires Python ≥ 3.12)
13- `torch` 2.0+
14- `pandas` 2.0+
15
16Verify the runtime first:
17
18- Python: `python -c "import pyhealth; print(pyhealth.__version__)"`
19- CLI: `pip show pyhealth`
20- If APIs differ between 1.x and 2.x, consult the installed docs and adapt the pattern accordingly.
21
22
23## Overview
24
25Use this skill when the user needs to:
26
27- load and structure EHR data from MIMIC-III, MIMIC-IV, eICU, OMOP-CDM, or a custom dataset
28- define clinical prediction tasks such as mortality, readmission, length of stay, or drug recommendation
29- train and evaluate deep learning or ML models on patient visit sequences
30- apply medical code normalization, ontology mapping, or tokenization
31- calibrate model outputs or generate post-hoc interpretability artifacts
32
33## When To Use This Skill
34
35- the data source is a structured EHR database or tabular patient record export
36- the task requires longitudinal patient visit sequences as model input
37- the user needs benchmark-compatible evaluation metrics for clinical AI
38- medical code systems (ICD, ATC, NDC, CPT, CCS) must be normalized or mapped before modeling
39
40## Quick Route
41
42- Known EHR source (MIMIC, eICU, OMOP): load with a `pyhealth.datasets` class, then `set_task`.
43- Custom tabular data: wrap in `SampleBaseDataset`, then follow the same pipeline.
44- Code mapping only: use `pyhealth.medcode` independently without the full pipeline.
45- Evaluation only: use `pyhealth.metrics` independently on existing predictions.
46
47## Progressive Disclosure
48
49- Read `references/technical_reference.md` for dataset branching rules, task schema details, model selection guidance, and calibration caveats.
50- Read `references/commands_and_thresholds.md` for concrete PyHealth code patterns, recommended thresholds, and output file conventions.
51- Keep `SKILL.md` as the main execution path and load reference files only when the task or failure mode needs the extra detail.
52
53## Default Rules
54
55- Always use raw integer counts or visit-level code lists as model inputs; do not pre-aggregate before loading.
56- Keep dataset loading, task definition, model training, and evaluation as separate, inspectable stages.
57- Record dataset name, table selections, code mapping applied, task function, model class, and PyHealth version in every experiment.
58- Favor reproducible train/val/test splits via `split_by_patient` over random splits that can leak patient data.
59
60## Expected Inputs
61
62- EHR source files or database dumps (MIMIC-III, MIMIC-IV, eICU, OMOP-CDM, or custom CSV/Parquet)
63- table names to load (e.g., `diagnoses_icd`, `procedures_icd`, `prescriptions`)
64- optional medical code mapping specifications
65- task definition (predefined or custom)
66- model architecture choice and training hyperparameters
67
68## Expected Outputs
69
70- `results/model_checkpoint.pth`
71- `results/test_metrics.json`
72- `results/predictions.tsv`
73- `qc/dataset_stats.tsv`
74- `figures/calibration_curve.pdf`
75- `figures/feature_importance.pdf`
76
77## Preferred Tools
78
79- `pyhealth.datasets` — MIMIC3Dataset, MIMIC4Dataset, eICUDataset, OMOPDataset, SampleBaseDataset
80- `pyhealth.tasks` — MortalityPrediction, ReadmissionPrediction, DrugRecommendation, LengthOfStayPrediction, and custom task functions
81- `pyhealth.models` — RNN, LSTM, GRU, Transformer, RETAIN, SafeDrug, GAMENet, AdaCare, ConCare, StageNet
82- `pyhealth.trainer` — Trainer
83- `pyhealth.metrics` — binary, multiclass, multilabel, fairness, interpretability metrics
84- `pyhealth.medcode` — InnerMap, CrossMap for ontology lookup and code mapping
85- `pyhealth.tokenizer` — Tokenizer for code-to-index transformations
86- `pyhealth.calib` — calibration and prediction set construction
87
88## Starter Pattern
89
90```python
91from pyhealth.datasets import MIMIC3Dataset
92from pyhealth.tasks import drug_recommendation_mimic3_fn
93from pyhealth.datasets import split_by_patient, get_dataloader
94from pyhealth.models import Transformer
95from pyhealth.trainer import Trainer
96
97# Step 1: load dataset
98dataset = MIMIC3Dataset(
99 root="/path/to/mimic3/",
100 tables=["DIAGNOSES_ICD", "PROCEDURES_ICD", "PRESCRIPTIONS"],
101 code_mapping={"NDC": ("ATC", {"target_kwargs": {"level": 3}})},
102)
103
104# Step 2: define task
105samples = dataset.set_task(task_fn=drug_recommendation_mimic3_fn)
106
107# Step 3: split and build dataloaders
108train_ds, val_ds, test_ds = split_by_patient(samples, [0.8, 0.1, 0.1])
109train_loader = get_dataloader(train_ds, batch_size=32, shuffle=True)
110val_loader = get_dataloader(val_ds, batch_size=32, shuffle=False)
111test_loader = get_dataloader(test_ds, batch_size=32, shuffle=False)
112
113# Step 4: initialize model
114model = Transformer(
115 dataset=samples,
116 feature_keys=["conditions", "procedures"],
117 label_key="drugs",
118 mode="multilabel",
119)
120
121# Step 5: train
122trainer = Trainer(model=model)
123trainer.train(
124 train_dataloader=train_loader,
125 val_dataloader=val_loader,
126 epochs=50,
127 monitor="pr_auc_samples",
128)
129
130# Step 6: evaluate
131metrics = trainer.evaluate(test_loader)
132print(metrics)
133```
134
135## Workflow
136
137### 1. Validate dataset access and structure
138
139Confirm the EHR source is accessible and the required tables are present. Inspect patient counts, visit counts, and code distributions before building tasks.
140
141### 2. Load data with `pyhealth.datasets`
142
143Use the appropriate dataset class. Apply code mappings at load time so downstream tasks and models operate on a consistent vocabulary. Record which tables and mappings were used.
144
145### 3. Define the clinical task
146
147Choose a predefined task function or write a custom one. Confirm the input schema (feature keys and types) and output schema (label key and mode: binary, multiclass, or multilabel) match the clinical question.
148
149### 4. Split patients and build dataloaders
150
151Always split by patient, not by visit or row, to prevent patient-level data leakage. Use `split_by_patient` and `get_dataloader` from `pyhealth.datasets`.
152
153### 5. Initialize and train the model
154
155Select an architecture matched to the task and data size. Configure `feature_keys`, `label_key`, and `mode` explicitly. Use `Trainer` for training, validation monitoring, and checkpoint saving.
156
157### 6. Evaluate and report
158
159Compute task-appropriate metrics using `pyhealth.metrics`. For binary tasks report AUROC and AUPRC. For multilabel tasks report Jaccard and PR-AUC. Export a metrics JSON and a predictions TSV alongside the model checkpoint.
160
161### 7. Calibrate and interpret where needed
162
163Apply calibration from `pyhealth.calib` when predicted probabilities will be used for clinical decision support. Use `pyhealth.interpret` for feature-level or visit-level attribution when the use case requires explainability.
164
165
166## Output Artifacts
167
168```text
169results/
170├── model_checkpoint.pth
171├── test_metrics.json
172└── predictions.tsv
173qc/
174├── dataset_stats.tsv
175└── split_summary.tsv
176figures/
177├── calibration_curve.pdf
178└── feature_importance.pdf
179```
180
181
182## Key Parameters
183
184| Parameter | Typical value | Notes |
185|---|---|---|
186| `batch_size` | `32` | reduce for large visit sequences or memory-constrained environments |
187| `epochs` | `50` | use early stopping via `monitor` metric |
188| `monitor` | `"pr_auc_samples"` for multilabel; `"roc_auc"` for binary | task-dependent |
189| `split_by_patient` ratios | `[0.8, 0.1, 0.1]` | always split by patient not by visit |
190| code mapping level | ATC level 3 for drug codes | balance specificity and sparsity |
191| `n_top_genes` (HVG analog) | N/A for EHR; use vocabulary filtering | filter rare codes with `min_count` |
192
193
194## Quality Review
195
196- Confirm patient count, visit count, and code vocabulary size before training.
197- Verify that train, validation, and test sets have no overlapping patient IDs.
198- Check class balance for binary and multiclass tasks before reporting metrics.
199- Review calibration curves if predicted probabilities feed downstream clinical logic.
200- Do not report only AUROC; include AUPRC especially for imbalanced clinical outcomes.
201- Record dataset version, table selection, code mapping, task function, and model class for every experiment.
202
203## Anti-Patterns
204
205- splitting by visit or row instead of by patient, causing data leakage
206- using AUROC as the sole metric for rare clinical events
207- applying code mappings inconsistently across train and test sets
208- mixing raw codes and mapped codes in the same feature without documenting it
209- reporting model results without checking data coverage for the target cohort
210- treating predicted probabilities as calibrated without verification
211
212## Related Skills
213
214- `Machine Learning For Omics`
215- `Multi-Omics Integration`
216- `Pathway Analysis`
217- `Reporting And Figure Export`
218
219## Optional Supplements
220
221- `pyhealth.medcode` for standalone code mapping
222- `pyhealth.calib` for post-hoc calibration
223- `pyhealth.interpret` for interpretability