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Automatic depletion with Spectra Optia allows a safe 16% reduction of red blood cell pack consumption in exchanged sickle cell anemia patients.
Hequet, O; Poutrel, S; Connes, P; Revesz, D; Chelghoum, Y; Kebaili, K; Cannas, G; Gauthier, A; Guironnet-Paquet, A; Vocanson, M; Nicolas, J F; Renoux, C; Raba, M; Cognasse, F; Bertrand, Y; Hot, A; Joly, P.
Afiliação
  • Hequet O; Établissement Français du Sang Auvergne-Rhône-Alpes, Apheresis unit, Centre Hospitalier Lyon Sud Pierre Bénite, France.
  • Poutrel S; Scientific Department, Établissement Français du Sang Auvergne-Rhône-Alpes, Saint-Etienne, France.
  • Connes P; Laboratory of Allergology and Clinical Immunology, CIRI, Lyon, France.
  • Revesz D; Centre de référence constitutif des syndromes drépanocytaires majeurs, des thalassémies et des autres maladies de l'érythropoïèse, Service de Médecine interne, Hôpital Edouard Herriot, Hospices Civils de Lyon, Lyon, France.
  • Chelghoum Y; Laboratoire Interuniversitaire de Biologie de la Motricité (LIBM) EA7424, Equipe "Biologie vasculaire et du globule rouge", Université Claude Bernard Lyon 1, COMUE Lyon, Villeurbanne, France.
  • Kebaili K; Laboratoire d'Excellence sur le globule rouge (Labex GR-Ex), Paris, France.
  • Cannas G; Institut Universitaire de France, Paris, France.
  • Gauthier A; Établissement Français du Sang Auvergne-Rhône-Alpes, Apheresis unit, Centre Hospitalier Lyon Sud Pierre Bénite, France.
  • Guironnet-Paquet A; Établissement Français du Sang Auvergne-Rhône-Alpes, Apheresis unit, Centre Hospitalier Lyon Sud Pierre Bénite, France.
  • Vocanson M; Hospices Civils de Lyon, Pediatric Hematology, Institut d'Hematologie et d'Oncologie Pédiatrique, Lyon, France.
  • Nicolas JF; Centre de référence constitutif des syndromes drépanocytaires majeurs, des thalassémies et des autres maladies de l'érythropoïèse, Service de Médecine interne, Hôpital Edouard Herriot, Hospices Civils de Lyon, Lyon, France.
  • Renoux C; Hospices Civils de Lyon, Pediatric Hematology, Institut d'Hematologie et d'Oncologie Pédiatrique, Lyon, France.
  • Raba M; Scientific Department, Établissement Français du Sang Auvergne-Rhône-Alpes, Saint-Etienne, France.
  • Cognasse F; Laboratory of Allergology and Clinical Immunology, CIRI, Lyon, France.
  • Bertrand Y; Laboratory of Allergology and Clinical Immunology, CIRI, Lyon, France.
  • Hot A; Laboratory of Allergology and Clinical Immunology, CIRI, Lyon, France.
  • Joly P; Laboratoire Interuniversitaire de Biologie de la Motricité (LIBM) EA7424, Equipe "Biologie vasculaire et du globule rouge", Université Claude Bernard Lyon 1, COMUE Lyon, Villeurbanne, France.
Transfusion ; 59(5): 1692-1697, 2019 05.
Article em En | MEDLINE | ID: mdl-30747440
ABSTRACT

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.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transfusão de Eritrócitos / Eritrócitos / Anemia Falciforme Tipo de estudo: Observational_studies Limite: Adolescent / Adult / Child / Female / Humans / Male Idioma: En Revista: Transfusion Ano de publicação: 2019 Tipo de documento: Article País de afiliação: França

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transfusão de Eritrócitos / Eritrócitos / Anemia Falciforme Tipo de estudo: Observational_studies Limite: Adolescent / Adult / Child / Female / Humans / Male Idioma: En Revista: Transfusion Ano de publicação: 2019 Tipo de documento: Article País de afiliação: França