Clinical Pathways Search Results

Clinical Care Pathway for screening, management and follow up of iron deficiency and anemia among patients with Inflammatory Bowel Disease.

This pathway provides guidance for identifying neonates symptomatic at or near the time of birth from Hypoxic-Ischemic Encephalopathy (HIE) who may be eligible whole body cooling.

This pathway should be used to guide the management of infants requiring a double volume exchange transfusion

This pathway guides care of patients in the Emergency Department and inpatient units coming to the General Operating Rooms and radiologic procedures under Anesthesia/sedation.

This pathway guides the care of children who present with onset of flaccid weakness in one or more extremities +/- bulbar/cranial nerve findings without other clear cause. 

The PICU central diabetes insipidus pathway provides guidance for the care of patients with known or suspected central diabetes insipidus requiring ICU care.

The unprovoked seizure clinical pathway outlines the steps to standardize the ED clinical assessment, evaluation and recommend Neurology follow-up for healthy children presenting with new onset unprovoked seizure(s).

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.

This pathway guides the ED and inpatient care for patients of any age with Genetically confirmed, Primary (Definite) Mitochondrial Disease or Suspected Mitochondrial Disease.

This pathway will guide the evaluation and treatment of a pediatric patient with a suspected acute pulmonary embolism/embolus.