Clinical Pathways Search Results

Guidelines for evaluating patients suspected to have exocrine pancreatic insufficiency and initiating/optimizing pancreatic enzyme replacement therapy.

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

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

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 provides guidance for the care of patients at baseline risk for malnutrition and/or unlikely to consume adequate caloric intake by mouth within 3 days of admission to the ICU.

This pathway guides the diagnosis of Somatic Symptom and Related Disorders (SSRD) where the history/physical of a patient’s chief complaint does not align with known organic medical causes.

This pathway guides the care for children in the ED, ICU or inpatient setting with signs and symptoms of UGI bleeding

The ileocolic intussusception clinical pathway is a detailed care plan that outlines the necessary steps in treating a healthy child with suspected ileocolic intussusception without a pathologic lead point in the emergency department.

The hyperbilirubinemia pathway is a standard approach to initial evaluation, treatment, and management of infants with hyperbilirubinemia from birth through 21 days of life.

The pathway is intended to guide inpatient evaluation and management of malnutrition, weight loss and eating disorders through nutritional rehabilitation in the adolescent patient