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Changes in Cerebral Oxygenation during Transfusion Therapy.
Hakim, Mumin; Tumin, Dmitry; Martin, David P; Samora, Walter; Beebe, Allan C; Klamar, Jan E; Hodge, Ashley B; Tobias, Joseph D.
Afiliación
  • Hakim M; Departments of Anesthesiology and Pain Medicine, Nationwide Children's Hospital, Columbus, Ohio.
  • Tumin D; Departments of Anesthesiology and Pain Medicine, Nationwide Children's Hospital, Columbus, Ohio.
  • Martin DP; Departments of Anesthesiology and Pain Medicine, Nationwide Children's Hospital, Columbus, Ohio.; Department of Anesthesiology, The Ohio State University, Columbus, Ohio.
  • Samora W; Department of Orthopedic Surgery, Nationwide Children's Hospital, Columbus, Ohio.
  • Beebe AC; Department of Orthopedic Surgery, Nationwide Children's Hospital, Columbus, Ohio.
  • Klamar JE; Department of Orthopedic Surgery, Nationwide Children's Hospital, Columbus, Ohio.
  • Hodge AB; The Heart Center at Nationwide Children's Hospital, Columbus, Ohio.
  • Tobias JD; Departments of Anesthesiology and Pain Medicine, Nationwide Children's Hospital, Columbus, Ohio.; Department of Anesthesiology, The Ohio State University, Columbus, Ohio.
J Extra Corpor Technol ; 48(4): 173-178, 2016 12.
Article en En | MEDLINE | ID: mdl-27994257
ABSTRACT
This study assesses the effects of transfusion of autologous or allogeneic blood on cerebral and tissue oxygenation during spinal surgery. Packed red blood cell transfusions are indicated to improve oxygen delivery to tissues. There are limited data demonstrating changes in tissue oxygenation with blood administration. Tissue (deltoid) and cerebral oxygenation were monitored using near-infrared spectroscopy during spinal surgery in patients. As indicated, cell saver or allogeneic blood was administered. Tissue and cerebral oxygenation were recorded before and after transfusion. The study enrolled 50 patients, 33 of whom (17 males and 16 females) received allogeneic blood (n = 8) or autologous blood (n = 25). Patients ranged in age from 9 to 19 years (14.0 ± 2.3 years) and in weight from 16.8 to 122.7 kg (54.6 ± 25.7 kg). Tissue oxygenation increased from 83 ± 9 (pretransfusion) to 86 ± 7 at the end of transfusion (p = .002) and remained at the same level (86 ± 7) in the post-transfusion period. Cerebral oxygenation increased from 76 ± 8 (pretransfusion) to 84 ± 8 at the end of transfusion (p < .001) and remained at 84 ± 8 in the post-transfusion period. Changes in tissue and cerebral oxygenation were similar between cell saver and allogeneic blood and between starting hemoglobin value <8 gm/dL and starting hemoglobin ≥8 gm/dL. In conclusion, although both cerebral and tissue oxygenation increased during the administration of either allogeneic or autologous blood, the clinical impact was likely limited given the high initial tissue and cerebral oxygenation values. No differences were noted between autologous (cell saver) and allogeneic blood or based on the starting hemoglobin value.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Oxígeno / Fusión Vertebral / Transfusión de Sangre Autóloga / Encéfalo / Pérdida de Sangre Quirúrgica / Recuperación de Sangre Operatoria Tipo de estudio: Clinical_trials / Observational_studies Límite: Adolescent / Adult / Child / Female / Humans / Male Idioma: En Revista: J Extra Corpor Technol Año: 2016 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Oxígeno / Fusión Vertebral / Transfusión de Sangre Autóloga / Encéfalo / Pérdida de Sangre Quirúrgica / Recuperación de Sangre Operatoria Tipo de estudio: Clinical_trials / Observational_studies Límite: Adolescent / Adult / Child / Female / Humans / Male Idioma: En Revista: J Extra Corpor Technol Año: 2016 Tipo del documento: Article