Volume 14, Issue 6 pp. 1199-1206
ORIGINAL ARTICLE

Arteriovenous fistula creation for hypoxia after single ventricle palliation: A single-institution experience and literature review

Andrew D. Spearman MD

Corresponding Author

Andrew D. Spearman MD

Department of Pediatrics, Division of Cardiology, Medical College of Wisconsin, Milwaukee, Wisconsin

Correspondence

Andrew D. Spearman, Department of Pediatrics, Division of Cardiology, Medical College of Wisconsin, 9000 West Wisconsin Avenue, Milwaukee, WI 53226.

Email: [email protected]

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Steven J. Kindel MD

Steven J. Kindel MD

Department of Pediatrics, Division of Cardiology, Medical College of Wisconsin, Milwaukee, Wisconsin

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Ronald K. Woods MD, PhD

Ronald K. Woods MD, PhD

Department of Surgery, Division of Pediatric Cardiovascular Surgery, Medical College of Wisconsin, Milwaukee, Wisconsin

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Salil Ginde MD

Salil Ginde MD

Department of Pediatrics, Division of Cardiology, Medical College of Wisconsin, Milwaukee, Wisconsin

Department of Internal Medicine, Division of Cardiology, Medical College of Wisconsin, Milwaukee, Wisconsin

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First published: 01 August 2019
Citations: 7

Abstract

Background

Hypoxia is a common and sometimes severe morbidity of single ventricle congenital heart disease (CHD). Creation of an arteriovenous fistula (AVF) is occasionally performed for patients after superior or total cavopulmonary connection (SCPC or TCPC) in an attempt to improve oxygen saturations. Despite previous reports, AVF creation is a rare palliation with inadequately defined benefits and risks. We sought to determine changes in peripheral oxygen saturation (SpO2) and risk of adverse event after AVF creation in children with single ventricle CHD at our institution.

Methods

We conducted a retrospective chart review of patients with a history of single ventricle palliation and history of surgical AVF creation who were seen at our tertiary care center from 1996 to 2017.

Results

A total of seven patients were included in our study. SpO2 for the overall cohort did not significantly increase after AVF creation (pre-AVF 79.1 ± 6.9%, post-AVF 82.7 ± 6.0% [P = .23]). SpO2 trended up for large shunts (>5 mm) (pre-AVF 75.0 ± 7.6%, post-AVF 84.0 ± 5.3% [P = .25]). SpO2 did not improve for small shunts (≤5 mm) (pre-AVF 82.3 ± 6.5%, post-AVF 81.0 ± 8.5% [P = .50]). The 12-month overall and transplant-free survival were 85.7% and 71.4%, respectively. Freedom from AVF-related complication (cephalic edema, thrombotic occlusion) was 51.4% at 12 months.

Conclusion

Palliative AVF creation for patients with single ventricle CHD and hypoxia does not universally improve SpO2 and is prone to early complications. Despite a lack of durable benefit and known risks, AVF creation remains a reasonable palliation for a subset of patients after SCPC who are not candidates for TCPC, or potentially as a bridge to heart transplantation.

CONFLICT OF INTEREST

The authors declare that they have no conflict of interest with the contents of this article.

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