首页> 外文期刊>Hemoglobin: International Journal for Hemoglobin Research >Secular trends in the national and provincial births of new thalassemia cases in Iran from 2001 to 2006
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Secular trends in the national and provincial births of new thalassemia cases in Iran from 2001 to 2006

机译:2001年至2006年伊朗新发地中海贫血病例的国家和省级出生的长期趋势

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Thalassemia is one of the genetic diseases for which there are only a few successful prevention protocols. In this study, we aimed to analyze data for thalassemia newborns in a period of 6 years to find out the geographical distribution of cases, the "high-risk" provinces in Iran, the causes of thalassemia newborn cases, the coverage rate of the prevention programs and the limitations of the thalassemia registration system. To further our aim, an analytic cross-sectional study was designed at the Iranian Blood Transfusion Organization (IBTO), Tehran, Iran. A questionnaire was then prepared to gather data from each of the 30 provincial centers to find out the number and causes of thalassemia births. Furthermore, another questionnaire, to be completed by the physicians in charge, was aimed at gathering data from all 207 thalassemia care centers. We then performed a stratified analysis of the frequency of distributions; the associations among the existing variables were evaluated using the χ or Fisher's exact tests at a 5.0% significance level. According to the findings, from 2001-2006, a total of 2091 thalassemia patients were born. The main causes were: the at-risk couples not using prenatal diagnosis (PND), marriages before the commencement of Iranian prevention plans, unregistered marriages based on religious conventions, among foreign citizens and the existence of some test errors. The causes of birth for 284 (13.6%) of new cases were not documented. There was a statistically significant difference between the five high-risk provinces regarding the proportional causes of thalassemia newborns [Pearson χ = 4.549; degree of freedom (df) = 8, p value = 0.0001]. Although the plan succeeded in avoiding the annual birth of 826 new cases on average, there is continuing concern that more than 300 new cases were born every year during 2001-2006 and new prevention strategies need to be put into practice. It is highly recommended that focus be put on factors persistently causing the birth of new cases, especially in high-risk areas in which the success rates are lower than 50.0%.
机译:地中海贫血是一种遗传疾病,只有少数几种成功的预防措施。在这项研究中,我们旨在分析6年期间地中海贫血新生儿的数据,以了解病例的地理分布,伊朗“高危”省份,地中海贫血新生儿病例的成因,预防的覆盖率方案和地中海贫血注册系统的局限性。为了进一步实现我们的目标,在伊朗德黑兰的伊朗输血组织(IBTO)设计了横断面分析研究。然后准备了一份调查表,以收集来自30个省中心的数据,以了解地中海贫血的出生数量和原因。此外,另一份由负责医师填写的问卷旨在收集所有207个地中海贫血护理中心的数据。然后,我们对分布频率进行了分层分析。使用χ或Fisher精确检验以5.0%的显着性水平评估现有变量之间的关联。根据调查结果,从2001年至2006年,共有2091名地中海贫血患者出生。主要原因是:未使用产前诊断(PND)的高风险夫妇,伊朗预防计划开始之前的婚姻,基于宗教习俗的未登记婚姻,外国公民之间的婚姻以及某些测试错误的存在。 284例(13.6%)的新病例的出生原因尚未记录。在五个高危省份之间,地中海贫血新生儿的比例成因在统计上有显着差异[Pearsonχ= 4.549;自由度(df)= 8,p值= 0.0001]。尽管该计划成功地避免了平均826例每年的新出生,但仍然令人担忧的是,在2001-2006年期间,每年有300多例新出生,需要采取新的预防策略。强烈建议将重点放在持续导致新病例诞生的因素上,特别是在成功率低于50.0%的高风险地区。

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