pyhealth

name	pyhealth
description	Python library for healthcare ML on EHR data: process MIMIC-III/IV, eICU, OMOP-CDM; encode medical codes (ICD, ATC, NDC); build patient-level datasets; train Transformer, RETAIN, GRASP, MedBERT for mortality, drug recommendation, readmission, diagnosis prediction. Alternatives: FIDDLE (preprocessing), clinical-longformer (clinical NLP), ehr-ml (embeddings).
license	BSD-3-Clause

PyHealth

Overview

PyHealth provides an end-to-end pipeline for healthcare ML on EHR data: data loading → medical code processing → patient-level dataset construction → model training → evaluation. It natively supports MIMIC-III, MIMIC-IV, eICU-CRD, and OMOP-CDM structured databases, and handles the idiosyncratic data formats of each. Medical codes (ICD-9, ICD-10, ATC, NDC, SNOMED) are organized in a hierarchical code system that supports code-level embedding and cross-ontology mapping. Pre-built tasks — mortality prediction, drug recommendation, readmission, length-of-stay, diagnosis code prediction — can be instantiated in a few lines. Custom tasks follow a standardized interface.

When to Use

• Training clinical outcome prediction models (mortality, readmission, LOS) from MIMIC-III or MIMIC-IV
• Building drug recommendation or drug interaction prediction models using ATC code hierarchy
• Processing OMOP-CDM formatted data from institutional EHR systems for ML
• Using pretrained clinical models (RETAIN, GRASP, MedBERT) as baselines on healthcare benchmarks
• Constructing patient visit sequences with temporal structure for RNN/Transformer models
• Evaluating clinical prediction models with appropriate metrics (AUROC, AUPRC, F1, Jaccard)
• Use FIDDLE for pure EHR preprocessing without ML; use clinical-longformer for clinical note NLP

Prerequisites

• Python packages: pyhealth, torch, pandas, scikit-learn
• Data requirements: MIMIC-III/IV CSV files (requires PhysioNet credentialing), eICU, or OMOP-CDM database
• MIMIC access: request at physionet.org (free; requires CITI training, ~1 week)

pip install pyhealth torch pandas scikit-learn
# Download MIMIC-III: https://physionet.org/content/mimiciii/
# Download MIMIC-IV: https://physionet.org/content/mimiciv/

Quick Start

from pyhealth.datasets import MIMIC3Dataset

# Load MIMIC-III (specify path to downloaded CSV files)
dataset = MIMIC3Dataset(
    root="path/to/mimic-iii/",
    tables=["DIAGNOSES_ICD", "PRESCRIPTIONS", "PROCEDURES_ICD"],
    code_mapping={"ICD9CM": "CCSCM"},  # map ICD-9 codes to CCS multi-level
    dev=True,  # dev=True uses 1% of data for fast testing
)

print(f"Patients: {dataset.stat()['num_patients']}")
print(f"Visits: {dataset.stat()['num_visits']}")

Core API

Module 1: Dataset Loading

Load MIMIC-III, MIMIC-IV, eICU, and OMOP-CDM datasets.

from pyhealth.datasets import MIMIC3Dataset, MIMIC4Dataset, eICUDataset

# MIMIC-III
mimic3 = MIMIC3Dataset(
    root="data/mimic-iii/",
    tables=["DIAGNOSES_ICD", "PRESCRIPTIONS", "PROCEDURES_ICD", "LABEVENTS"],
    code_mapping={"ICD9CM": "CCSCM", "NDC": "ATC3"},  # standardize codes
    dev=False,
)
stats = mimic3.stat()
print(f"MIMIC-III: {stats['num_patients']} patients, {stats['num_visits']} visits")

# MIMIC-IV
mimic4 = MIMIC4Dataset(
    root="data/mimic-iv/",
    tables=["diagnoses_icd", "prescriptions", "procedures_icd"],
    code_mapping={"ICD10CM": "CCSCM"},
    dev=True,
)

# eICU
eicu = eICUDataset(
    root="data/eicu/",
    tables=["diagnosis", "medication", "treatment"],
    dev=True,
)
print(f"eICU loaded: {eicu.stat()}")

# Explore dataset structure
patient_id = list(mimic3.patients.keys())[0]
patient = mimic3.patients[patient_id]
print(f"Patient {patient_id}: {len(patient.visits)} visits")

for visit in patient.visits[:2]:
    print(f"  Visit {visit.visit_id}:")
    print(f"    Diagnoses: {visit.get_code_list('CCSCM')[:5]}")
    print(f"    Medications: {visit.get_code_list('ATC3')[:3]}")

Module 2: Task Construction

Convert raw datasets into ML-ready task datasets.

from pyhealth.tasks import mortality_prediction_mimic3_fn
from pyhealth.datasets import SampleDataset

# Mortality prediction task
# Each sample: patient's visit history → binary mortality label
mortality_dataset = SampleDataset(
    dataset=mimic3,
    task_fn=mortality_prediction_mimic3_fn,
)

print(f"Task: mortality prediction")
print(f"Samples: {len(mortality_dataset)}")

# Inspect a sample
sample = mortality_dataset[0]
print(f"Sample keys: {list(sample.keys())}")
print(f"Conditions (ICD codes): {sample['conditions'][:3]}")
print(f"Drugs (ATC codes): {sample['drugs'][:3]}")
print(f"Label (mortality): {sample['label']}")

# Custom task: 30-day readmission prediction
def readmission_30day_fn(patient):
    """Custom task function: predict 30-day readmission after discharge."""
    samples = []
    for i, visit in enumerate(patient.visits[:-1]):
        next_visit = patient.visits[i + 1]
        # Compute days between discharge and next admission
        days_gap = (next_visit.encounter_time - visit.discharge_time).days
        label = int(days_gap <= 30)

        samples.append({
            "visit_id": visit.visit_id,
            "patient_id": patient.patient_id,
            "conditions": visit.get_code_list("CCSCM"),
            "drugs": visit.get_code_list("ATC3"),
            "procedures": visit.get_code_list("ICD9PROC"),
            "label": label,
        })
    return samples

readmission_dataset = SampleDataset(dataset=mimic3, task_fn=readmission_30day_fn)
print(f"Readmission samples: {len(readmission_dataset)}")
pos_rate = sum(s["label"] for s in readmission_dataset) / len(readmission_dataset)
print(f"Positive rate (30-day readmission): {pos_rate:.2%}")

Module 3: Medical Code Systems

Work with ICD, ATC, NDC, and other hierarchical medical code systems.

from pyhealth.medcode import InnerMap

# ICD-9-CM diagnosis codes
icd9 = InnerMap.load("ICD9CM")
code = "428.0"  # Heart failure, unspecified
print(f"Code: {code}")
print(f"Description: {icd9.lookup(code)}")
print(f"Ancestors: {icd9.get_ancestors(code)}")
print(f"Children: {icd9.get_children(code)[:5]}")

# ATC drug classification
atc = InnerMap.load("ATC")
drug_code = "A10BA02"  # Metformin
print(f"\nATC: {drug_code}")
print(f"Drug: {atc.lookup(drug_code)}")
print(f"L1 class: {atc.get_ancestors(drug_code)}")

# Cross-ontology code mapping
from pyhealth.medcode import CrossMap

# Map NDC (drug product codes) to ATC level 3
ndc_to_atc = CrossMap.load("NDC", "ATC3")
ndc_code = "0069-2587-30"  # example NDC
atc3_codes = ndc_to_atc.map(ndc_code)
print(f"NDC {ndc_code} → ATC3: {atc3_codes}")

# Map ICD-9 to ICD-10
icd9_to_icd10 = CrossMap.load("ICD9CM", "ICD10CM")
icd10 = icd9_to_icd10.map("428.0")
print(f"ICD-9 428.0 → ICD-10: {icd10}")

Module 4: Model Training

Train pre-implemented clinical ML models.

from pyhealth.models import Transformer, RETAIN
from pyhealth.datasets import split_by_patient, get_dataloader
import torch

# Train/val/test split (patient-level, no leakage)
train_ds, val_ds, test_ds = split_by_patient(mortality_dataset, [0.7, 0.1, 0.2])

train_loader = get_dataloader(train_ds, batch_size=32, shuffle=True)
val_loader   = get_dataloader(val_ds,   batch_size=64, shuffle=False)
test_loader  = get_dataloader(test_ds,  batch_size=64, shuffle=False)

print(f"Train: {len(train_ds)} | Val: {len(val_ds)} | Test: {len(test_ds)}")

# Transformer model for EHR sequence modeling
model = Transformer(
    dataset=mortality_dataset,
    feature_keys=["conditions", "drugs", "procedures"],
    label_key="label",
    mode="binary",        # binary classification
    embedding_dim=128,
    num_heads=4,
    num_layers=2,
    dropout=0.1,
)

print(f"Model parameters: {sum(p.numel() for p in model.parameters()):,}")

# RETAIN: Reverse Time Attention model (interpretable clinical ML)
retain_model = RETAIN(
    dataset=mortality_dataset,
    feature_keys=["conditions", "drugs"],
    label_key="label",
    mode="binary",
    embedding_dim=64,
)

Module 5: Training and Evaluation

from pyhealth.trainer import Trainer

trainer = Trainer(
    model=model,
    metrics=["pr_auc", "roc_auc", "f1"],  # PR-AUC, ROC-AUC, F1
)

trainer.train(
    train_dataloader=train_loader,
    val_dataloader=val_loader,
    epochs=20,
    optimizer_params={"lr": 1e-3},
    weight_decay=1e-5,
    monitor="pr_auc",           # early stopping metric
    monitor_criterion="max",
    load_best_model_after_train=True,
)

# Evaluate on test set
results = trainer.evaluate(test_loader)
print("Test results:")
for metric, value in results.items():
    print(f"  {metric}: {value:.4f}")

Module 6: Drug Recommendation

Predict which drugs a patient should receive based on visit history.

from pyhealth.tasks import drug_recommendation_mimic3_fn
from pyhealth.models import GAMENet
from pyhealth.datasets import SampleDataset, split_by_patient, get_dataloader

# Drug recommendation task
drug_dataset = SampleDataset(
    dataset=mimic3,
    task_fn=drug_recommendation_mimic3_fn,
)

train_ds, val_ds, test_ds = split_by_patient(drug_dataset, [0.7, 0.1, 0.2])

# GAMENet: graph-augmented memory network for drug recommendation
gamenet = GAMENet(
    dataset=drug_dataset,
    feature_keys=["conditions", "procedures"],
    label_key="drugs",
    mode="multilabel",     # recommend multiple drugs per visit
    embedding_dim=64,
)

train_loader = get_dataloader(train_ds, batch_size=16, shuffle=True)

trainer = Trainer(model=gamenet, metrics=["jaccard", "f1", "prauc"])
trainer.train(train_dataloader=train_loader,
              val_dataloader=get_dataloader(val_ds, 32),
              epochs=30, monitor="jaccard")
print("Drug recommendation model trained")

Key Concepts

Patient-Visit-Event Hierarchy

PyHealth organizes EHR data as Patient → Visit → medical codes. Each Visit contains timestamped events across multiple tables (diagnoses, medications, procedures, labs). ML models see each patient as a sequence of visits, each visit as a set of medical codes, capturing temporal disease progression.

Code Mapping and Standardization

Raw EHR codes (ICD-9, NDC) are highly specific and numerous. PyHealth's code_mapping parameter automatically converts them to coarser ontologies (CCSCM has ~260 categories vs. ~15,000 ICD-9 codes), reducing vocabulary size and enabling transfer between datasets.

Common Workflows

Workflow 1: Full Mortality Prediction Pipeline

from pyhealth.datasets import MIMIC3Dataset, SampleDataset, split_by_patient, get_dataloader
from pyhealth.tasks import mortality_prediction_mimic3_fn
from pyhealth.models import Transformer
from pyhealth.trainer import Trainer

# 1. Load data
dataset = MIMIC3Dataset(
    root="data/mimic-iii/",
    tables=["DIAGNOSES_ICD", "PRESCRIPTIONS", "PROCEDURES_ICD"],
    code_mapping={"ICD9CM": "CCSCM", "NDC": "ATC3"},
    dev=True,
)

# 2. Build task dataset
task_ds = SampleDataset(dataset, task_fn=mortality_prediction_mimic3_fn)
print(f"Samples: {len(task_ds)}, Positive rate: {sum(s['label'] for s in task_ds)/len(task_ds):.2%}")

# 3. Split
train_ds, val_ds, test_ds = split_by_patient(task_ds, [0.7, 0.1, 0.2])

# 4. Model
model = Transformer(
    dataset=task_ds,
    feature_keys=["conditions", "drugs"],
    label_key="label",
    mode="binary",
    embedding_dim=128,
)

# 5. Train
trainer = Trainer(model=model, metrics=["pr_auc", "roc_auc"])
trainer.train(
    train_dataloader=get_dataloader(train_ds, 32, shuffle=True),
    val_dataloader=get_dataloader(val_ds, ),
    epochs=,
    monitor=,
)


results = trainer.evaluate(get_dataloader(test_ds, ))
()
()

Workflow 2: Model Comparison Benchmark

from pyhealth.models import Transformer, RETAIN, MedBERT
from pyhealth.trainer import Trainer
from pyhealth.datasets import get_dataloader
import pandas as pd

models = {
    "Transformer": Transformer(task_ds, ["conditions", "drugs"], "label", "binary"),
    "RETAIN":      RETAIN(task_ds, ["conditions", "drugs"], "label", "binary"),
}

results_list = []
for name, model in models.items():
    trainer = Trainer(model=model, metrics=["pr_auc", "roc_auc", "f1"])
    trainer.train(
        train_dataloader=get_dataloader(train_ds, 32, shuffle=True),
        val_dataloader=get_dataloader(val_ds, 64),
        epochs=10,
        monitor="pr_auc",
    )
    test_results = trainer.evaluate(get_dataloader(test_ds, 64))
    test_results["model"] = name
    results_list.append(test_results)
    print(f"{name}: PR-AUC={test_results['pr_auc']:.4f}, ROC-AUC={test_results['roc_auc']:.4f}")

results_df = pd.DataFrame(results_list).set_index("model")
results_df.to_csv("model_comparison.csv")
print(results_df)

Key Parameters

Parameter	Module/Class	Default	Range / Options	Effect
tables	MIMIC3Dataset	—	list of MIMIC table names	Which EHR tables to load; more tables = richer features, slower load
code_mapping	MIMIC3Dataset	{}	{"ICD9CM": "CCSCM"}	Maps raw codes to standardized ontologies
dev	MIMIC3Dataset	False	True/False	True uses 1% of data for fast development
feature_keys	All models	—	list of code type strings	Which medical code types to use as model input
embedding_dim	Transformer, RETAIN	128	64–512	Hidden size for code and patient embeddings
num_heads	Transformer	4	1–16	Multi-head attention heads (must divide embedding_dim)
num_layers	Transformer	2	1–6	Number of Transformer encoder layers
dropout	All models	0.1	0–0.5	Dropout rate for regularization
mode	All models	—	"binary", "multiclass", "multilabel"	Prediction task type
monitor	Trainer.train	"loss"	"pr_auc", "roc_auc", "f1"	Metric for early stopping and model selection

Best Practices

1. Always use split_by_patient, never random split: Splitting by visit (random) causes data leakage — the same patient can appear in train and test sets across different visits. PyHealth's split_by_patient ensures strict patient-level separation.

2. Use dev=True during development: MIMIC-III contains ~46,000 patients. Loading the full dataset takes minutes; dev mode loads ~460 patients in seconds. Switch to dev=False only for final training runs.

3. Apply code mapping to standardize across datasets: Raw ICD-9 codes have ~15,000 unique values; CCSCM reduces this to ~260 clinically meaningful groups. This dramatically reduces model vocabulary and enables meaningful code embeddings, especially important for small datasets.

4. Evaluate with PR-AUC alongside ROC-AUC: Clinical datasets are typically highly imbalanced (e.g., 10% mortality rate). PR-AUC is more informative than ROC-AUC for imbalanced tasks — a model that predicts all negatives achieves ROC-AUC ~0.5 but PR-AUC approaching the positive rate (~0.1).

Common Recipes

Recipe: Export Patient Embeddings

import torch
from pyhealth.datasets import get_dataloader
import numpy as np

model.eval()
embeddings = []
labels = []

with torch.no_grad():
    for batch in get_dataloader(test_ds, batch_size=64):
        # Get patient-level representation (before classification head)
        hidden = model.get_patient_representation(batch)
        embeddings.append(hidden.cpu().numpy())
        labels.append(batch["label"].numpy())

embeddings = np.concatenate(embeddings, axis=0)
labels = np.concatenate(labels, axis=0)
np.save("patient_embeddings.npy", embeddings)
np.save("patient_labels.npy", labels)
print(f"Embeddings: {embeddings.shape}")

Recipe: Class-Imbalance Handling with Weighted Sampler

import torch
from torch.utils.data import WeightedRandomSampler
from pyhealth.datasets import get_dataloader

# Compute class weights for imbalanced mortality prediction
labels = [sample["label"] for sample in train_ds]
pos = sum(labels)
neg = len(labels) - pos
weights = [1.0/neg if l == 0 else 1.0/pos for l in labels]
sampler = WeightedRandomSampler(weights, num_samples=len(weights), replacement=True)

# Use sampler in dataloader
balanced_loader = torch.utils.data.DataLoader(
    train_ds, batch_size=32, sampler=sampler,
    collate_fn=train_ds.collate_fn
)
print(f"Balanced loader: {len(balanced_loader)} batches")

Troubleshooting

Problem	Cause	Solution
FileNotFoundError on dataset load	Wrong root path or missing MIMIC CSV files	Verify root contains the correct CSV files; list contents with ls data/mimic-iii/*.csv
KeyError for code type in feature_keys	Code type not loaded or mapping failed	Ensure tables includes the required table and code_mapping maps to the expected ontology
All samples have label=0 in task dataset	Task function logic error or data issue	Print task_fn(patient) on a single patient; check label derivation logic
Memory error loading full MIMIC	Large dataset; insufficient RAM	Use dev=True during development; use chunked loading or reduce tables list
ROC-AUC ~0.5 on test set	Severe class imbalance causing trivial predictor	Use WeightedRandomSampler; report PR-AUC instead; lower classification threshold
CUDA out of memory during training	Batch size too large	Reduce batch_size from 32 to 8 or 16; use gradient accumulation
Code mapping returns empty list	Code not found in cross-map	Check code format (e.g., ICD-9 with decimal vs. without); try InnerMap.load("ICD9CM").lookup(code)

Related Skills

• statsmodels-statistical-modeling — logistic regression baselines for clinical outcome prediction
• scikit-learn-machine-learning — traditional ML baselines (random forest, gradient boosting) on PyHealth features
• clinical-decision-support-documents — translating clinical ML model outputs to decision support tools

References

• PyHealth documentation — API reference, tutorials, and task descriptions
• PyHealth paper: Zhao et al. (2021), arXiv — library design and benchmark tasks
• MIMIC-III paper: Johnson et al. (2016), Nature Scientific Data — dataset description
• MIMIC-IV paper: Johnson et al. (2023), Nature Scientific Data — updated dataset
• RETAIN paper: Choi et al. (2016), NeurIPS — interpretable clinical prediction model
• PyHealth GitHub — source code and examples