Automatic depletion with Spectra Optia allows a safe 16% reduction of red blood cell pack consumption in exchanged sickle cell anemia patients

被引:13
作者
Hequet, O. [1 ,2 ,3 ]
Poutrel, S. [4 ]
Connes, P. [5 ,6 ,7 ]
Revesz, D. [1 ]
Chelghoum, Y. [1 ]
Kebaili, K. [8 ]
Cannas, G. [4 ]
Gauthier, A. [8 ]
Guironnet-Paquet, A. [2 ,3 ]
Vocanson, M. [3 ]
Nicolas, J. F. [3 ]
Renoux, C. [5 ,6 ,9 ]
Raba, M. [10 ]
Cognasse, F. [2 ,11 ]
Bertrand, Y. [8 ]
Hot, A. [4 ]
Joly, P. [5 ,6 ,9 ]
机构
[1] Ctr Hosp Lyon Sud Pierre Benite, Etab Francais Sang Auvergne Rhone Alpes, Apheresis Unit, Pierre Benite, France
[2] Etab Francais Sang Auvergne Rhone Alpes, Sci Dept, St Etienne, France
[3] CIRI, Lab Allergol & Clin Immunol, Lyon, France
[4] Hosp Civils Lyon, Hop Edouard Herriot, Serv Med Interne, Ctr Reference Constitutif Syndromes Drepanocytair, Lyon, France
[5] Univ Claude Bernard Lyon 1, COMUE Lyon, Equipe Biol Vasc & Globule Rouge, EA7424,LIBM, Villeurbanne, France
[6] Lab Excellence Globule Rouge Labex GR Ex, Paris, France
[7] Inst Univ France, Paris, France
[8] Hosp Civils Lyon, Pediat Hematol, Inst Hematol & Oncol Pediat, Lyon, France
[9] Hosp Civils Lyon, Grp Hosp Est, Lab Biochim & Biol Mol Grand Est, Bron, France
[10] Ctr Hosp Lyon Sud, Etab Francais Sang Rhone Alpes, Distribut Unit, Pierre Benite, France
[11] Univ Lyon, GIMAP EA3064, St Etienne, France
关键词
CLINICAL COMPLICATIONS; ERYTHROCYTE-EXCHANGE; THERAPY; TRANSFUSION;
D O I
10.1111/trf.15188
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND Chronic red blood cell exchanges (RBCXs) are frequently used to prevent complications in patients with sickle cell anemia, but the scarcity of matched red blood cell packs (RBCPs) is a serious concern. The main goal of this study was to compare the number of RBCPs used during RBCXs between the Spectra Optia (SO) device (with the automatic depletion step) and the former Cobe Spectra (CSP) device. STUDY DESIGN AND METHODS The performances and safety of 300 SO sessions using the automatic depletion step (SO/DE) in 50 patients with sickle cell anemia under a chronic transfusion program over a 1-year period were prospectively analyzed. The numbers of RBCPs saved using this protocol compared to the SO device without depletion and to the CSP device were determined. RESULTS The SO/DE protocol appeared to be safe, as only 5% and 17% of the sessions were characterized by a significant decrease in blood pressure and increase in heart rate (grade 2 adverse events), respectively. Postapheresis hematocrit and fraction of cells remaining reached expected values. The SO/DE protocol required 16% fewer RBCPs compared to SO without depletion, allowing a mean saving of 12 RBCPs per patient and per year and 13% fewer compared to CSP device. Interestingly, the saving was more important for patients with high total blood volume and/or high preapheresis hematocrit. CONCLUSION The SO/DE protocol is an efficient, safe and cost-effective procedure for patients with sickle cell anemia under a chronic transfusion program.
引用
收藏
页码:1692 / 1697
页数:6
相关论文
共 25 条
[1]  
[Anonymous], 2009, NIH Publ
[2]   Sickle cell disease: Classification of clinical complications and approaches to preventive and therapeutic management [J].
Ballas, Samir K. .
CLINICAL HEMORHEOLOGY AND MICROCIRCULATION, 2018, 68 (2-3) :105-128
[3]   Short-Term Femoral Catheter Insertion: A Promising Alternative to Consistently Allow Long-Term Erythrocytapheresis Therapy in Children with Sickle Cell Anemia [J].
Billard, Marie ;
Combet, Sylvie ;
Hequet, Olivier ;
Kebaili, Kamila ;
Lorthois, Sylvie ;
Pondarre, Corinne .
JOURNAL OF PEDIATRICS, 2013, 162 (02) :423-426
[4]   Chronic red blood cell exchange to prevent clinical complications in sickle cell disease [J].
Cabibbo, S ;
Fidone, C ;
Garozzo, G ;
Antolino, A ;
Manenti, GO ;
Bennardello, F ;
Licitra, V ;
Calabrese, S ;
Costantino, F ;
Travali, S ;
Distefano, R ;
Bonomo, P .
TRANSFUSION AND APHERESIS SCIENCE, 2005, 32 (03) :315-321
[5]   Blood rheological abnormalities in sickle cell anemia [J].
Connes, Philippe ;
Renoux, Celine ;
Romana, Marc ;
Abkarian, Manouk ;
Joly, Philippe ;
Martin, Cyril ;
Hardy-Dessources, Marie-Dominique ;
Ballas, Samir K. .
CLINICAL HEMORHEOLOGY AND MICROCIRCULATION, 2018, 68 (2-3) :165-172
[6]   Haemolysis and abnormal haemorheology in sickle cell anaemia [J].
Connes, Philippe ;
Lamarre, Yann ;
Waltz, Xavier ;
Ballas, Samir K. ;
Lemonne, Nathalie ;
Etienne-Julan, Maryse ;
Hue, Olivier ;
Hardy-Dessources, Marie-Dominique ;
Romana, Marc .
BRITISH JOURNAL OF HAEMATOLOGY, 2014, 165 (04) :564-572
[7]   Inflammation in sickle cell disease [J].
Conran, Nicola ;
Belcher, John D. .
CLINICAL HEMORHEOLOGY AND MICROCIRCULATION, 2018, 68 (2-3) :263-299
[8]   ; Fluid therapy for septic shock resuscitation: which fluid should be used? [J].
Correa, Thiago Domingos ;
Rocha, Leonardo Lima ;
Souza Pessoa, Camila Menezes ;
Silva, Eliezer ;
Cesar de Assuncao, Murillo Santucci .
EINSTEIN-SAO PAULO, 2015, 13 (03) :462-468
[9]   Automated RBC exchange compared to manual exchange transfusion for children with sickle cell disease is cost-effective and reduces iron overload [J].
Dedeken, Laurence ;
Phu Quoc Le ;
Rozen, Laurence ;
El Kenz, Hanane ;
Huybrechts, Sophie ;
Devalck, Christine ;
Diallo, Safiatou ;
Heijmans, Catherine ;
Ferster, Alina .
TRANSFUSION, 2018, 58 (06) :1356-1362
[10]   Effectiveness of red blood cell exchange, partial manual exchange, and simple transfusion concurrently with iron chelation therapy in reducing iron overload in chronically transfused sickle cell anemia patients [J].
Fasano, Ross M. ;
Leong, Traci ;
Kaushal, Megha ;
Sagiv, Eyal ;
Luban, Naomi L. C. ;
Meier, Emily Riehm .
TRANSFUSION, 2016, 56 (07) :1707-1715