Niveen Salama, Omnia Y. Abd El Dayem, Doaa Shaltout, M. Nassim
{"title":"地中海贫血......哪些人需要接受筛查?","authors":"Niveen Salama, Omnia Y. Abd El Dayem, Doaa Shaltout, M. Nassim","doi":"10.21608/cupsj.2023.238929.1106","DOIUrl":null,"url":null,"abstract":": Background: Thalassemia carrier rate in Egypt is as high as 9-10%. The first step to eradicate thalassemia is to define population at risk. Aim of the work: to define the high risk population to be screened for thalassemia. Subjects and Methods: This observational cross-sectional study included children aged between 1 and 16 years presenting with microcytic anemia to Cairo university Children Hospitals from the period between March and September 2022. Children with hemoglobin <10mg/dL and mean red blood corpuscle volume (MCV) <70fl were included in the study. Complete blood count, serum ferritin, and hemoglobin electrophoresis were done. Results : Out of a total of 180 patients, 120 patients (66.7%) had iron deficiency anemia, 2 patients (1.1%) had alpha thalassemia, and 14 patients (7.7%) had beta thalassemia, 14 (7.7%) patients had thalassemia trait, 3 (1.67%) had sickle thalassemia, 7 (3.88%) had combined iron deficiency anemia (IDA) and thalassemia, and 20 (11.1%) required further investigations. Patients were divided according to MCV into 3 groups MCV<60, 60-65, >65. There was no significant difference in the diagnosis between the three groups. Conclusion : 22 % of children with MCV < 70 fl were found to have an inherited hemolytic anemia. Children with MCV <70 should be screened for thalassemia.","PeriodicalId":153483,"journal":{"name":"Pediatric Sciences Journal","volume":"BC-19 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-11-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Thalassemia...Who is to be screened?\",\"authors\":\"Niveen Salama, Omnia Y. Abd El Dayem, Doaa Shaltout, M. Nassim\",\"doi\":\"10.21608/cupsj.2023.238929.1106\",\"DOIUrl\":null,\"url\":null,\"abstract\":\": Background: Thalassemia carrier rate in Egypt is as high as 9-10%. The first step to eradicate thalassemia is to define population at risk. Aim of the work: to define the high risk population to be screened for thalassemia. Subjects and Methods: This observational cross-sectional study included children aged between 1 and 16 years presenting with microcytic anemia to Cairo university Children Hospitals from the period between March and September 2022. Children with hemoglobin <10mg/dL and mean red blood corpuscle volume (MCV) <70fl were included in the study. Complete blood count, serum ferritin, and hemoglobin electrophoresis were done. Results : Out of a total of 180 patients, 120 patients (66.7%) had iron deficiency anemia, 2 patients (1.1%) had alpha thalassemia, and 14 patients (7.7%) had beta thalassemia, 14 (7.7%) patients had thalassemia trait, 3 (1.67%) had sickle thalassemia, 7 (3.88%) had combined iron deficiency anemia (IDA) and thalassemia, and 20 (11.1%) required further investigations. Patients were divided according to MCV into 3 groups MCV<60, 60-65, >65. There was no significant difference in the diagnosis between the three groups. Conclusion : 22 % of children with MCV < 70 fl were found to have an inherited hemolytic anemia. Children with MCV <70 should be screened for thalassemia.\",\"PeriodicalId\":153483,\"journal\":{\"name\":\"Pediatric Sciences Journal\",\"volume\":\"BC-19 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-11-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Pediatric Sciences Journal\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.21608/cupsj.2023.238929.1106\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pediatric Sciences Journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.21608/cupsj.2023.238929.1106","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
: Background: Thalassemia carrier rate in Egypt is as high as 9-10%. The first step to eradicate thalassemia is to define population at risk. Aim of the work: to define the high risk population to be screened for thalassemia. Subjects and Methods: This observational cross-sectional study included children aged between 1 and 16 years presenting with microcytic anemia to Cairo university Children Hospitals from the period between March and September 2022. Children with hemoglobin <10mg/dL and mean red blood corpuscle volume (MCV) <70fl were included in the study. Complete blood count, serum ferritin, and hemoglobin electrophoresis were done. Results : Out of a total of 180 patients, 120 patients (66.7%) had iron deficiency anemia, 2 patients (1.1%) had alpha thalassemia, and 14 patients (7.7%) had beta thalassemia, 14 (7.7%) patients had thalassemia trait, 3 (1.67%) had sickle thalassemia, 7 (3.88%) had combined iron deficiency anemia (IDA) and thalassemia, and 20 (11.1%) required further investigations. Patients were divided according to MCV into 3 groups MCV<60, 60-65, >65. There was no significant difference in the diagnosis between the three groups. Conclusion : 22 % of children with MCV < 70 fl were found to have an inherited hemolytic anemia. Children with MCV <70 should be screened for thalassemia.