{"title":"Analysis of hemoglobin electrophoresis results and physicians investigative practices in Saudi Arabia.","authors":"Syed Riaz Mehdi, Badr Abdullah Al Dahmash","doi":"10.4103/0971-6866.120829","DOIUrl":null,"url":null,"abstract":"<p><strong>Background and objectives: </strong>Riyadh and central province falls in a moderate prevalent zone of hemoglobinopathies in Saudi Arabia. However, it has been observed that the physicians working in Saudi Arabia invariably advise all cases of anemia for hemoglobin electrophoresis (HE). The present work was carried out to study the yield of the HE in Riyadh and the investigative practices of the physicians advising HE.</p><p><strong>Settings and design: </strong>The study was carried out in the hospitals of King Saud University from 2009 to 2011 in order to assess the yield of HE in referred cases of clinical anemia.</p><p><strong>Materials and methods: </strong>A total of 1073 cases divided in two groups of males and females had undergone complete blood count and red blood cell morphology. Cellulose acetate HE was performed and all the positive results were reconfirmed on the high performance liquid chromatography (HPLC). The results were analyzed for the type of hemoglobinopathies. For statistical analysis Statistical Package for Social Sciences 15 version (SPSS Inc., Chicago, IL, USA) was used.</p><p><strong>Results: </strong>A total of 405 males and 668 females blood samples were included in the present study. 116 (28.5%) males and 167 (25%) females showed an abnormal pattern on HE. The incidence of beta thalassemia trait was higher in females while sickle cell trait was predominantly seen in males. Red cell indices were reduced considerably in thalassemias, but were unaffected in sickle cell disorders, except those which had concurrent alpha trait. The total yield of HE was 26.6% which was much less than expected.</p><p><strong>Conclusion: </strong>The physicians are advised to rule out iron deficiency and other common causes of anemia before investigating the cases for hemoglobinopathies, which employs time consuming and expensive tests of HE and HPLC.</p>","PeriodicalId":88516,"journal":{"name":"Indian journal of human genetics","volume":"19 3","pages":"337-41"},"PeriodicalIF":0.0000,"publicationDate":"2013-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.4103/0971-6866.120829","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Indian journal of human genetics","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4103/0971-6866.120829","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1
Abstract
Background and objectives: Riyadh and central province falls in a moderate prevalent zone of hemoglobinopathies in Saudi Arabia. However, it has been observed that the physicians working in Saudi Arabia invariably advise all cases of anemia for hemoglobin electrophoresis (HE). The present work was carried out to study the yield of the HE in Riyadh and the investigative practices of the physicians advising HE.
Settings and design: The study was carried out in the hospitals of King Saud University from 2009 to 2011 in order to assess the yield of HE in referred cases of clinical anemia.
Materials and methods: A total of 1073 cases divided in two groups of males and females had undergone complete blood count and red blood cell morphology. Cellulose acetate HE was performed and all the positive results were reconfirmed on the high performance liquid chromatography (HPLC). The results were analyzed for the type of hemoglobinopathies. For statistical analysis Statistical Package for Social Sciences 15 version (SPSS Inc., Chicago, IL, USA) was used.
Results: A total of 405 males and 668 females blood samples were included in the present study. 116 (28.5%) males and 167 (25%) females showed an abnormal pattern on HE. The incidence of beta thalassemia trait was higher in females while sickle cell trait was predominantly seen in males. Red cell indices were reduced considerably in thalassemias, but were unaffected in sickle cell disorders, except those which had concurrent alpha trait. The total yield of HE was 26.6% which was much less than expected.
Conclusion: The physicians are advised to rule out iron deficiency and other common causes of anemia before investigating the cases for hemoglobinopathies, which employs time consuming and expensive tests of HE and HPLC.
背景和目的:利雅得和中部省属于沙特阿拉伯血红蛋白病的中度流行区。然而,据观察,在沙特阿拉伯工作的医生总是建议所有贫血病例进行血红蛋白电泳(HE)。目前的工作是为了研究利雅得HE的产量和医生建议HE的调查实践而进行的。背景与设计:本研究于2009 - 2011年在沙特国王大学各医院开展,目的是评估临床贫血转诊病例的HE产率。材料与方法:对1073例患者进行全血细胞计数和红细胞形态学检查,分为男女两组。对醋酸纤维素进行HE分析,所有阳性结果在高效液相色谱(HPLC)上得到再次确认。结果分析血红蛋白病的类型。统计分析使用statistical Package For Social Sciences 15 version (SPSS Inc., Chicago, IL, USA)。结果:本研究共纳入男性血样405份,女性血样668份。男性116例(28.5%),女性167例(25%)HE表现异常。β -地中海贫血性状在女性中发生率较高,而镰状细胞性状在男性中占主导地位。红细胞指数在地中海贫血中显著降低,但在镰状细胞疾病中不受影响,除了那些同时具有α性状的疾病。HE的总收率为26.6%,远低于预期。结论:在检查血红蛋白病病例之前,建议医生排除缺铁和其他常见的贫血原因,这需要耗费时间和昂贵的HE和HPLC检测。