Literature DB >> 26274351

Comparative evaluation of the depletion-red cell exchange program with the Spectra Optia and the isovolemic hemodilution-red cell exchange method with the COBE Spectra in sickle cell disease patients.

Pascale Poullin1, Frederick Sanderson2, Emmanuelle Bernit3, Marion Brun2, Yael Berdah4, Catherine Badens5.   

Abstract

BACKGROUND: This study aims to compare in patients with sickle cell disease (SCD), the technical performance and packed red blood cell unit consumption between the automated depletion/Red Blood Cell exchange (RBCx) program (Spectra Optia Apheresis System) with the isovolemic hemodilution (IHD)/RBCx procedure (COBE Spectra Apheresis System) in a routine clinical setting.
METHODS: We retrospectively reviewed the data of 23 patients treated between October 2010 and August 2013 who underwent repeated RBCx on both apheresis systems for preventive indications. Each patient was their own control and had undergone two procedures on each system, totaling 46 sessions per group. On Spectra Optia, we performed the automated depletion/RBCx program. For COBE Spectra, we used a modified IHD/RBCx protocol. All patients had an initial 250 mL depletion offset by a 5% albumin prior to the exchange procedure, for the respective device, with leucodepleted Rh/Kell compatible and cross-matched RBC packs.
RESULTS: All procedures were well tolerated except three mild febrile nonhemolytic reactions. Postprocedure hemoglobin S (HbS), fraction of cells remaining (FCR), procedure duration and processed blood and anticoagulant volumes were comparable in the two groups. However, the RBCx volume was significantly higher for the Spectra Optia group (+71 mL, P = 0.01), with no significant difference in the number of RBC units used.
CONCLUSIONS: Technical performance and packed RBC unit consumption were not compromised when switching from the COBE Spectra IHD/RBCx protocol to the depletion/RBCx protocol on the Spectra Optia. Tolerability was equal for both protocols. J. Clin. Apheresis 31:429-433, 2016.
© 2015 Wiley Periodicals, Inc. © 2015 Wiley Periodicals, Inc.

Entities:  

Keywords:  COBE Spectra; Spectra Optia; erythrocytapheresis; isovolemic hemodilution; red blood cell exchange; sickle-cell disease

Mesh:

Year:  2015        PMID: 26274351     DOI: 10.1002/jca.21422

Source DB:  PubMed          Journal:  J Clin Apher        ISSN: 0733-2459            Impact factor:   2.821


  4 in total

Review 1.  Sickle cell disease: when and how to transfuse.

Authors:  Jo Howard
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2016-12-02

2.  Reversal of a rheologic cardiomyopathy following hematopoietic stem cell transplantation for sickle cell disease.

Authors:  Vandana Sachdev; Matthew Hsieh; Neal Jeffries; Anna Noreuil; Wen Li; Stanislav Sidenko; Hwaida Hannoush; Emily Limerick; Delon Wilson; John Tisdale; Courtney Fitzhugh
Journal:  Blood Adv       Date:  2019-10-08

3.  Comparative efficacy in red blood cell exchange transfusions with different apheresis machines in patients with sickle cell disease.

Authors:  Nurhilal Buyukkurt; Ilknur Kozanoğlu; Asli Pan Korur; Suheyl Asma; Mahmut Yeral; Soner Solmaz; Fatih Kandemir; Cigdem Gereklioglu; Cagla Sariturk; Can Boga; Hakan Ozdogu
Journal:  Indian J Hematol Blood Transfus       Date:  2017-11-07       Impact factor: 0.900

4.  Procedural adverse events in pediatric patients with sickle cell disease undergoing chronic automated red cell exchange.

Authors:  Jenna Wade; Marianne E M Yee; Kirk A Easley; Shannon Pahz; Hailly Butler; Patricia E Zerra; Cassandra D Josephson; Ross M Fasano
Journal:  Transfusion       Date:  2022-01-24       Impact factor: 3.157

  4 in total

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