Volume 50, Issue 2 pp. 354-356
Brief Report

Pinch-off syndrome in patients with sickle cell disease receiving erythrocytapheresis

Rachelle Nuss MD

Corresponding Author

Rachelle Nuss MD

Department of Pediatric Hematology, The Children's Hospital and the University of Colorado at Denver Health Sciences Center, Denver, Colorado

Colorado Sickle Cell Treatment and Research Center, University of Colorado at Denver Health Sciences Center, Denver, Colorado

1056 E. 19th Ave. Box B-115, Denver, CO 80218.===Search for more papers by this author
Laura Cole RN

Laura Cole RN

Colorado Sickle Cell Treatment and Research Center, University of Colorado at Denver Health Sciences Center, Denver, Colorado

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Tuan Le MD

Tuan Le MD

Department of Pathology, The Children's Hospital, Denver, Colorado

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Edmund Orsini MD

Edmund Orsini MD

Department of Pathology, The Children's Hospital, Denver, Colorado

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Roger Harned MD

Roger Harned MD

Department of Radiology, The Children's Hospital and the University of Colorado at Denver Health Sciences Center, Denver, Colorado

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First published: 07 November 2006
Citations: 3

Abstract

A 6-year-old female with homozygous sickle cell disease had a central venous access device (CVAD) placed to facilitate chronic erythrocytapheresis. Erythrocytapheresis was ineffective due to the rare pinch-off syndrome causing communication between the dual lumen tubing. Awareness of and monitoring for the pinch-off syndrome is indicated in people with sickle cell disease and a CVAD for chronic erythrocytapheresis. Pediatr Blood Cancer 2008;50:354–356. © 2006 Wiley-Liss, Inc.

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