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Anesthesia for Potts Shunt in a Child with Severe Refractory Idiopathic Pulmonary Arterial Hypertension
Ashley Eggers1, Gregory J Latham, Jeremy Geiduschek
1From the Departments of *Anesthesiology and Pain Medicine, †Pediatric Cardiology, and ‡Pediatric Cardiovascular Surgery, Seattle Children's Hospital, University of Washington, Seattle, Washington.
Insights
A surgical Potts shunt offers a promising rescue therapy for children with severe pulmonary arterial hypertension, potentially improving quality and duration of life by creating Eisenmenger physiology.
Area of Science:
- Pediatric Cardiology
- Cardiovascular Surgery
- Anesthesiology
Background:
- Childhood idiopathic pulmonary arterial hypertension (IPAH) is a severe, progressive condition.
- Atrial septostomy is a bridge to lung transplantation for refractory cases.
- Surgical Potts shunt is an emerging alternative rescue therapy.
Observation:
- This report details the anesthetic management for a pediatric patient undergoing a surgical Potts shunt.
- The procedure converts the patient to Eisenmenger physiology.
- Unique intraoperative anesthetic considerations are highlighted.
Findings:
- The surgical Potts shunt is a novel intervention for end-stage pulmonary arterial hypertension in children.
- Initial outcomes suggest promising results for this rescue therapy.
- Anesthetic management requires careful attention to unique physiological changes.
Implications:
- The Potts shunt may offer improved quality and duration of life for pediatric patients with pulmonary arterial hypertension.
- This technique provides a potential alternative to lung transplantation.
- Further research into anesthetic protocols is warranted for this procedure.
Abstract:
Childhood idiopathic pulmonary arterial hypertension is a progressive and fatal disease. When pulmonary artery pressures become suprasystemic and refractory to medical management, atrial septostomy can be recommended for bridging patients to lung transplantation. Recently, a surgical Potts shunt has been recommended as an alternative rescue therapy, and initial outcome data are promising. The placement of a Potts shunt converts the child to Eisenmenger physiology, which is anticipated to provide an improved quality and duration of life. We present the first description of anesthetic management of a child undergoing surgical Potts shunt for pulmonary arterial hypertension and summarize the multiple, unique intraoperative considerations.
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