Abstract 5163

Introduction:

Hereditary Spherocytosis (HS) is one of the most common inherited hemolytic anemias. Many of them are autosomal dominant, being about 25% of the cases transmitted recessively.

Diagnostic of HS:

Classic testing for HS includes: Hematologic testing of red blood cell indices (RDW, MCHC, Reticulocyte count), peripheral blood smear (presence of spherocytes), osmotic fragility and Eosin-5-maleimide binding to band 3 and Rh-related proteins forms that may be used as screening tests for hereditary spherocytosis.

Objective:

Recently have been developed new parameters and information in the new automated hematology analyzer called DxH8008™ from Beckman Coulter as @MSCV (@Mean Sphered Cell Volume), @RSF, @MAF, @ LHD%. All this parameters may be used to create flagging for laboratory use only (LUO) or Research use only (RUO). The purpose of this study is to investigate the possible use or utility of this new information for the screening/flagging of Hereditary Spherocytosis. There are previous studies showing the possible benefit of using MCV minus @MSCV for the detection/flagging of cases with spherocytes.

Patient and Methods:

We have collected 28 patients with Hereditary Spherocytosis. All of them were confirmed by red cell morphology, osmotic fragility and Eosin-5-maleimide binding to band 3 and Rh-related proteins forms.

Table 1
Diagnosticn
NON BETA (control) 184 
HbH (alfa thalasemia intermedia) 129 
Alfa Thalassemia Heterozygous 48 
Beta Thalassemia Trait 30 
Hereditary Spherocytosis (study group) 28 
Iron Deficiency Anaemia 22 
Thalassemia intermedia (Beta-Thal Interm) 18 
microdrepanocitosi (Beta-S) 
Blackfan-Diamond Anemia 
Dyserithropoietic Anaemia type I (CDA I) 
Sickle cell anaemia 
Piruvate-Kinase deficiency 
IRIDA iron-refractory iron deficiency anemia 
Fanconi's Anaemia 
Dyserithropoietic Anaemia type II (CDA II) 
Hyporegenerative anemia 
Megaloblastic Anemia 
Piruvate-Kinase deficiency Splenectomized 
Hemoglobinopaty (Taybe) + α-thalassemia 
Hemoglobinopaty hyperunstable (Hb Cagliari) 
Hemoglobinopaty Koln 
Acute Lymphoblastic Leukemia (ALL) 
Pyropoikilocytosis 
Evans's Syndrome 
Diagnosticn
NON BETA (control) 184 
HbH (alfa thalasemia intermedia) 129 
Alfa Thalassemia Heterozygous 48 
Beta Thalassemia Trait 30 
Hereditary Spherocytosis (study group) 28 
Iron Deficiency Anaemia 22 
Thalassemia intermedia (Beta-Thal Interm) 18 
microdrepanocitosi (Beta-S) 
Blackfan-Diamond Anemia 
Dyserithropoietic Anaemia type I (CDA I) 
Sickle cell anaemia 
Piruvate-Kinase deficiency 
IRIDA iron-refractory iron deficiency anemia 
Fanconi's Anaemia 
Dyserithropoietic Anaemia type II (CDA II) 
Hyporegenerative anemia 
Megaloblastic Anemia 
Piruvate-Kinase deficiency Splenectomized 
Hemoglobinopaty (Taybe) + α-thalassemia 
Hemoglobinopaty hyperunstable (Hb Cagliari) 
Hemoglobinopaty Koln 
Acute Lymphoblastic Leukemia (ALL) 
Pyropoikilocytosis 
Evans's Syndrome 
Results:

Using ROC analysis, the best parameters differentiating the Hereditary Spherocytosis from the normals were: RET% (AUC 0. 996), MCV - @MSCV (AUC 0. 996), @MSCV (AUC 0. 969), RDW(AUC 0. 892), MCHC (AUC 0. 860), HGB (AUC 0. 787).

Using ROC analysis, the best parameters differentiating the Hereditary Spherocytosis from other anemias (excluding normals)were: MCV - @MSCV (AUC 0. 991), MCHC (AUC 0. 987), RET% (AUC 0. 857).

Disclosures:

Simon-Lopez:Beckman Coulter: @LHD, @MAF, @RSF, @LHD, @MAF, @RSF Patents & Royalties, Employment. Di Gaetano:Instrumentation Laboratory spa: Work for a distributor of Beckman Coulter Instruments in Italy Other. Galanello:Novartis: Research Funding, Speakers Bureau; Apopharma: Research Funding, Speakers Bureau; Ferrokin: Research Funding.

Author notes

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Asterisk with author names denotes non-ASH members.

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