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

This pathway guides clinicians in best practices for screening and treatment for adolescents presenting to the Emergency Department and Primary Care sites who might be at risk for sexually transmitted infections.

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 end of life care pathway is a detailed plan of the essential steps in end of life care for the deceased child.

This pathway should be used to guide the screening, assessment, and care planning for patients with known or suspected non-traumatic pancreatitis in an emergency or inpatient setting.

This pathway should be used to guide the health screening, evaluation and management of patients presenting with concerns for the mpox virus.