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Infant Malnutrition/Failure to Thrive (FTT) Clinical Pathway — Inpatient
The Infant Malnutrition (Failure to Thrive) Pathway provides a consistent approach to caring for infants with malnutrition on the General Pediatrics service in the inpatient setting.
Clinical Pathway for Pancreatic Enzyme Replacement Therapy (PERT) in Children with or at Risk for Exocrine Pancreatic Insufficiency (EPI)
Guidelines for evaluating patients suspected to have exocrine pancreatic insufficiency and initiating/optimizing pancreatic enzyme replacement therapy.
Inflammatory Bowel Disease with Iron Deficiency and Anemia Clinical Pathway — All Settings
Clinical Care Pathway for screening, management and follow up of iron deficiency and anemia among patients with Inflammatory Bowel Disease.
Double Volume Exchange Transfusion Clinical Pathway — ICU
This pathway should be used to guide the management of infants requiring a double volume exchange transfusion
Gastroenteritis Clinical Pathway — Inpatient
The Gastroenteritis Pathway is intended to guide inpatient evaluation and management of dehydration secondary to gastroenteritis in the pediatric patient.
Jeune Syndrome/Chest Wall Hypoplasia, VEPTR Implantation Clinical Pathway — PICU and Inpatient
Pre-op and post-op care for patients with Jeunes Syndrome/Chest Wall Hypoplasia treated at CHOP for insertion of a Vertical Expandable Prosthetic Titanium Rib (VEPTR)
Infant Malnutrition Clinical Pathway — Outpatient Specialty Care and Primary Care
The Infant Malnutrition (Failure to Thrive) Pathway provides a consistent approach to caring for infants at risk for malnutrition in the outpatient setting.
Partial Volume Exchange Transfusion, Clinical Pathway, ICU
This pathway should be used to guide the management of infants requiring a Partial Volume Exchange Transfusion (PVET). Most common reasons for PVET include severe chronic anemia or Polycythemia/Hyperviscosity syndrome.
Emergency Department and Inpatient Mitochondrial Clinical Pathway
This pathway guides the ED and inpatient care for patients of any age with Genetically confirmed, Primary (Definite) Mitochondrial Disease or Suspected Mitochondrial Disease.
Acute Pulmonary Embolism Clinical Pathway — Emergency Department, ICU and Inpatient
This pathway will guide the evaluation and treatment of a pediatric patient with a suspected acute pulmonary embolism/embolus.