Volume 65, Issue 9 e27225
REVIEW

Pediatric superior vena cava syndrome: An evidence-based systematic review of the literature

Fadi Nossair

Corresponding Author

Fadi Nossair

Division of Oncology, CHOC Children's, Orange, California

Division of Hematology, CHOC Children's, Orange, California

Department of Pediatrics, University of California–Irvine, Irvine, California

Correspondence

Fadi Nossair, CHOC Children's, 1201 W La Veta Ave, Orange, CA 92868.

Email: [email protected]

Search for more papers by this author
Peter Schoettler

Peter Schoettler

Department of Pediatrics, University of California–Irvine, Irvine, California

Department of Pediatrics, CHOC Children's, Orange, California

Search for more papers by this author
Joanne Starr

Joanne Starr

Division of Cardiothoracic Surgery, CHOC Children's, Orange, California

Search for more papers by this author
Anthony K. C. Chan

Anthony K. C. Chan

Thrombosis and Atherosclerosis Research Institute, Hamilton, Ontario, Canada

Department of Pediatrics, McMaster University, Hamilton, Ontario, Canada

Search for more papers by this author
Ivan Kirov

Ivan Kirov

Division of Oncology, CHOC Children's, Orange, California

Department of Pediatrics, University of California–Irvine, Irvine, California

Search for more papers by this author
Bosco Paes

Bosco Paes

Department of Pediatrics, McMaster University, Hamilton, Ontario, Canada

Search for more papers by this author
Arash Mahajerin

Arash Mahajerin

Division of Hematology, CHOC Children's, Orange, California

Department of Pediatrics, University of California–Irvine, Irvine, California

Search for more papers by this author
First published: 21 May 2018
Citations: 35

Abstract

Superior vena cava syndrome (SVCS) results in vascular, respiratory, and neurologic compromise. A systematic search was conducted to determine the prevalence of pediatric SVCS subtypes and identify clinical characteristics/treatment strategies that may influence overall outcomes. Data from 101 case reports/case series (142 patients) were analyzed. Morbidity (30%), mortality (18%), and acute complications (55%) were assessed as outcomes. Thrombosis was present in 36%, with multi-modal anticoagulation showing improved outcome by >50% (P = 0.004). Infant age (P = 0.04), lack of collaterals (P = 0.007), acute complications (P = 0.005), and clinical presentation may have prognostic utility that could influence clinical decisions and surveillance practices in pediatric SVCS.

CONFLICT OF INTEREST

The authors declare no conflict of interest.

The full text of this article hosted at iucr.org is unavailable due to technical difficulties.