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

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 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.

The suspected traumatic spinal cord injury clinical pathway outlines the care plan for assessment and treatment of spinal cord injury in the emergency department and ICU.

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.