Use of capillary blood to diagnose hereditary spherocytosis

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We studied 31 children with hemolytic anemia, or with positive family history for hereditary spherocytosis (HS), to assess the reliability of capillary blood samples for the diagnosis. HS was diagnosed in 20 patients. Cryohemolysis (CH) was positive in 94% and eosin-5'-maleimide flow cytometry...

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Autor principal: Crisp, R.L
Otros Autores: Solari, L., Gammella, D., Schvartzman, G.A, Rapetti, M.C, Donato, H.
Formato: Capítulo de libro
Lenguaje:Inglés
Publicado: 2012
Materias:
OSMOSIS
Acceso en línea:Registro en Scopus
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Biblioteca Central Dr. Luis F. Leloir (FCEN) de Universidad de Buenos Aires
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024 7 |2 cas  |a bilirubin, 18422-02-1, 635-65-4; Composite Resins; Eosine Yellowish-(YS), 17372-87-1; eosin maleimide, 76296-42-9; flowable hybrid composite 
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100 1 |a Crisp, R.L. 
245 1 0 |a Use of capillary blood to diagnose hereditary spherocytosis 
260 |c 2012 
270 1 0 |m Crisp, R.L.; División Hematología Clínica, Departamento de Medicina, Hospital Nacional Alejandro Posadas, Fernandez de Enciso 4602, 1419 Buenos Aires, Argentina; email: reneecrisp@gmail.com 
506 |2 openaire  |e Política editorial 
504 |a Crisp, R.L., Solari, L., Vota, D., A prospective study to assess the predictive value for hereditary spherocytosis using five laboratory tests (cryohemolysis test, eosin-5'-maleimide flow cytometry, osmotic fragility test, autohemolysis test, and SDS-PAGE) on 50 hereditary spherocytosis families in Argentina (2011) Ann Hematol, 90, pp. 625-634 
504 |a Won, D.I., Suh, J.S., Flow cytometric detection of erythrocyte osmotic fragility (2009) Cytometry Part B, 76 B, pp. 135-141 
504 |a Burman, D., Congenital spherocytosis in infancy (1958) Arch Dis Child, 33, pp. 335-351 
504 |a Schroter, W., Kashnitz, E., Diagnosis of hereditary spherocytosis in newborn infants (1983) J Pediatr, 103, pp. 460-466 
504 |a Grace, R.F., Lux, S.E., Disorders of the red cell membrane. (2009) Hematology of infancy and childhood, pp. 659-838. , Orkin SH, Nathan DG, Ginsburg D, Fisher DE, Lux SE, editors. Philadelphia: WB Sanders 
504 |a Stamey, C.C., Diamond, L.K., Congenital hemolytic anemia in the newborn (1957) Am J Dis Child, 94, pp. 616-624 
504 |a Pinto, L., Iolascon, A., Miraglia del Giudice, E., The Italian pediatric survey on hereditary spherocytosis (1995) Int J Pediatr Hematol Oncol, 2, pp. 43-47 
504 |a Saada, V., Cynober, T., Brossard, Y., Incidence of hereditary spherocytosis in a population of jaundiced neonates (2006) Pediatr Hematol Oncol, 23, pp. 387-397 
504 |a Berardi, A., Lugli, L., Ferrari, F., Kernicterus associated with hereditary spherocytosis and UGT1A1 promoter polymorphism (2006) Biol Neonat, 90, pp. 243-246 
504 |a Sgro, M., Campbell, D., Shah, V., Incidence and causes of severe neonatal hyperbilirubinemia in Canada (2006) CMAJ, 175, pp. 587-590 
504 |a Christensen, R.D., Henry, E., Hereditary spherocytosis in neonates with hyperbilirubinemia (2010) Pediatrics, 125, pp. 120-125 
504 |a Mariani, M., Barcellini, W., Vercellati, C., Clinical and hematologic features of 300 patients affected by hereditary spherocytosis grouped according to the type of the membrane protein defect (2008) Haematologica, 93, pp. 1310-1317 
504 |a Crisp, R., Solari, L., Gammela, D., Use of capillary blood to perform the eosin-5'-maleimide flow cytometry (EMA-FC) test: Results are comparable to venous blood (2010) Haematologica, 95, p. 700. , abs 1808 
504 |a Warang, P., Gupta, M., Kedar, P., Flow cytometric osmotic fragility - An effective screening approach for red cell membranopathies (2011) Cytometry Part B, 80 B, pp. 186-1190 
504 |a Crisp, R., Solari, L., Gammela, D., Flow cytometric osmotic fragility (FC-OF) can replace the traditional osmotic fragility (OF) test? Preliminary results (2010) Haematologica, 95, p. 703. , abs. 1816 
520 3 |a We studied 31 children with hemolytic anemia, or with positive family history for hereditary spherocytosis (HS), to assess the reliability of capillary blood samples for the diagnosis. HS was diagnosed in 20 patients. Cryohemolysis (CH) was positive in 94% and eosin-5'-maleimide flow cytometry in 90% of them, whereas flow cytometric osmotic fragility was positive in 94%. Capillary blood sampling showed to be useful for the diagnosis. Simultaneous use of these three tests allows confirming diagnosis in 100% of patients. The use of very small blood volumes (300μl) allows an earlier diagnosis in neonates and small infants. © 2012 Wiley Periodicals, Inc.  |l eng 
593 |a División Hematología Clínica, Departamento de Medicina, Hospital Nacional Alejandro Posadas, Buenos Aires, Argentina 
593 |a Laboratorio de Análisis Biológicos, Departamento de Química Biológica, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Buenos Aires, Argentina 
593 |a Consultorios de Hematología Infantil, Buenos Aires, Argentina 
593 |a Laboratorio de Citometría, Departamento de Diagnóstico, Hospital Nacional Alejandro Posadas, Buenos Aires, Argentina 
593 |a Seccion Hematología/Oncología, Hospital Municipal del Niño de San Justo, San Justo, Buenos Aires, Argentina 
690 1 0 |a CAPILLARY BLOOD 
690 1 0 |a FLOW CYTOMETRY 
690 1 0 |a HEREDITARY SPHEROCYTOSIS 
690 1 0 |a HYPERTONIC CRYOHEMOLYSIS 
690 1 0 |a NEONATAL ANEMIA 
690 1 0 |a OSMOTIC FRAGILITY 
690 1 0 |a BILIRUBIN 
690 1 0 |a ARTICLE 
690 1 0 |a BILIRUBIN BLOOD LEVEL 
690 1 0 |a BLOOD GROUP ABO INCOMPATIBILITY 
690 1 0 |a BLOOD SAMPLING 
690 1 0 |a BLOOD SMEAR 
690 1 0 |a BLOOD VOLUME 
690 1 0 |a CAPILLARY BLOOD 
690 1 0 |a CHILD 
690 1 0 |a CLINICAL ARTICLE 
690 1 0 |a CRYOHEMOLYSIS 
690 1 0 |a EARLY DIAGNOSIS 
690 1 0 |a ERYTHROCYTE DISORDER 
690 1 0 |a FAMILY HISTORY 
690 1 0 |a FLOW CYTOMETRY 
690 1 0 |a HEMOLYSIS 
690 1 0 |a HEMOLYTIC ANEMIA 
690 1 0 |a HEREDITARY SPHEROCYTOSIS 
690 1 0 |a HUMAN 
690 1 0 |a INFANT 
690 1 0 |a NEWBORN HEMOLYTIC DISEASE 
690 1 0 |a PRESCHOOL CHILD 
690 1 0 |a PRIORITY JOURNAL 
690 1 0 |a RETICULOCYTE COUNT 
690 1 0 |a SCHOOL CHILD 
690 1 0 |a ANEMIA, HEMOLYTIC 
690 1 0 |a BLOOD SPECIMEN COLLECTION 
690 1 0 |a CAPILLARIES 
690 1 0 |a CHILD 
690 1 0 |a CHILD, PRESCHOOL 
690 1 0 |a COMPOSITE RESINS 
690 1 0 |a EOSINE YELLOWISH-(YS) 
690 1 0 |a FREEZING 
690 1 0 |a HEMATOLOGIC TESTS 
690 1 0 |a HEMOLYSIS 
690 1 0 |a HUMANS 
690 1 0 |a INFANT 
690 1 0 |a INFANT, NEWBORN 
690 1 0 |a OSMOTIC FRAGILITY 
690 1 0 |a SENSITIVITY AND SPECIFICITY 
690 1 0 |a SPHEROCYTOSIS, HEREDITARY 
650 1 7 |2 spines  |a OSMOSIS 
700 1 |a Solari, L. 
700 1 |a Gammella, D. 
700 1 |a Schvartzman, G.A. 
700 1 |a Rapetti, M.C. 
700 1 |a Donato, H. 
773 0 |d 2012  |g v. 59  |h pp. 1299-1301  |k n. 7  |p Pediatr. Blood Cancer  |x 15455009  |t Pediatric Blood and Cancer 
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