Literature DB >> 28679172

Potts shunt in children with pulmonary arterial hypertension: institutional experience.

Sergey V Gorbachevsky1, Anton A Shmalts1, Irina Y Barishnikova1, Sergey B Zaets1.   

Abstract

OBJECTIVES: Since 2004, different techniques for the Potts shunt have been used in patients with incurable pulmonary arterial hypertension. However, the experience with these interventions in a single institution is limited. We present our series of Potts shunts in children with pulmonary arterial hypertension.
METHODS: Eight patients with suprasystemic pulmonary arterial hypertension (pulmonary artery-to-aorta mean pressure ratio of 1.39 ± 0.30) had a Potts shunt at the median age of 13.5 months. Six patients were followed up for 2-32 (median 17) months after the operation.
RESULTS: In all cases, the Potts shunt caused a decrease in arterial blood oxygen saturation at the lower extremities and was the genesis of the arterial blood oxygen saturation gradient between the upper and lower extremities (10.5 ± 1.8% at discharge). Postoperative echocardiography revealed flattening of the ventricular septum as well as a decrease in the right ventricle-to-left ventricle end-diastolic diameter ratio from 1.36 ± 0.14 preoperatively to 0.99 ± 0.22 at discharge (P = 0.010). The 2 patients with the highest preoperative pulmonary artery-to-aorta mean pressure ratio (1.79-1.86) died during the early postoperative period from repeated pulmonary hypertension crises and uncontrolled hypoxaemia. There were no deaths during the follow-up period. The paediatric functional class of the patients improved from IIIb-IV to I-II, syncopal episodes no longer persisted and the weight deficit decreased from 21.8 ± 7.5% preoperatively to 11.5 ± 5.9% at the latest follow-up examination (P = 0.004). The arterial blood oxygen saturation gradient between the upper and lower extremities and the right ventricle-to-left ventricle end-diastolic diameter ratio were the same as they were while the patients were in the hospital.
CONCLUSIONS: Our limited experience demonstrates that the Potts shunt lowers suprasystemic pulmonary hypertension to the systemic level, limits manifestations of right-sided heart failure and improves the overall functional status of the patients.
© The Author 2017. Published by Oxford University Press on behalf of the European Association for Cardio-Thoracic Surgery. All rights reserved.

Entities:  

Keywords:  Eisenmenger syndrome; Potts shunt; Pulmonary arterial hypertension

Mesh:

Year:  2017        PMID: 28679172     DOI: 10.1093/icvts/ivx209

Source DB:  PubMed          Journal:  Interact Cardiovasc Thorac Surg        ISSN: 1569-9285


  4 in total

1.  Potts shunt as an effective palliation for patients with end stage pulmonary arterial hypertension.

Authors:  Prashant Bobhate; Smruti Ranjan Mohanty; Kamlesh Tailor; Shankar Kadam; Tanuja Karande; Keyoor Bhavsar; Hari Bipin Katanna; Suresh Rao; Snehal Kulkarni
Journal:  Indian Heart J       Date:  2021-01-06

2.  Pediatric Pulmonary Hypertension: Definitions, Mechanisms, Diagnosis, and Treatment.

Authors:  Devashis Mukherjee; Girija G Konduri
Journal:  Compr Physiol       Date:  2021-06-30       Impact factor: 8.915

3.  Pulmonary-to-Systemic Arterial Shunt to Treat Children With Severe Pulmonary Hypertension.

Authors:  R Mark Grady; Matthew W Canter; Fei Wan; Anton A Shmalts; Ryan D Coleman; Maurice Beghetti; Rolf M F Berger; Maria J Del Cerro Marin; Scott E Fletcher; Russel Hirsch; Tilman Humpl; D Dunbar Ivy; Edward C Kirkpatrick; Thomas J Kulik; Marilyne Levy; Shahin Moledina; Delphine Yung; Pirooz Eghtesady; Damien Bonnet
Journal:  J Am Coll Cardiol       Date:  2021-08-03       Impact factor: 27.203

4.  Potts anastomosis in children with severe pulmonary arterial hypertension and atrial septal defect.

Authors:  Alice Capel; Marilyne Lévy; Isabelle Szezepanski; Sophie Malekzadeh-Milani; Pascal Vouhé; Damien Bonnet
Journal:  ESC Heart Fail       Date:  2020-11-20
  4 in total

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