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

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.

This pathway provides guidance for the care of all patients who have sustained a traumatic injury with risk to life or limb. Patients with recognized life threatening injuries are classified as Trauma Level One or Trauma Level Two and require initial evaluation and resuscitation in the Trauma Bay.

This pathway is intended for Emergency Department patients requiring procedural sedation who are healthy or those with mild systemic disease that is well controlled.

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.