土耳其黑海地区一个省婚前血红蛋白病筛查项目结果:三年经验。

Postgraduate medicine Pub Date : 2023-11-01 Epub Date: 2024-01-10 DOI:10.1080/00325481.2023.2285726
Sule Ozdemır, Muhammet Ali Oruc, Bahadır Yazıcıoglu, Sibel Turkan
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引用次数: 0

摘要

目的:血红蛋白病是一个全球性的公共卫生问题,死亡率和发病率高,治疗费用昂贵。通过血红蛋白病筛查试验可以减少和预防疾病。这是可能的,以确定携带者血红蛋白病筛查程序应用在世界上许多国家和土耳其。本研究旨在评估在基层医疗机构开展的全国婚前血红蛋白病筛查计划的结果。方法:采用流行病学和横断面研究方法。回顾性评估了2019年1月1日至2021年12月31日在三星婚前血红蛋白病筛查项目范围内检查的电泳结果。年龄,性别,筛查年份和血红蛋白病筛查结果从记录中获得。结果:接受血红蛋白病筛查方案筛查的52338人的中位年龄为29.0(16.0 ~ 86.0)岁。接受筛查的患者中约有54.1% (n = 28,309)是女性,而2020年的筛查人数最少(n = 15,765(30.1%))。筛查结果显示,β-地中海贫血(β-thal)性状发生率为1.37% (n = 676), HbS异常发生率为0.04% (n = 20)。β-thal性状出现频率在2020年(1.5%)高于其他年份(p = 0.029)。对结果进行性别分析时,HbS异常的女性比例(3.7%)显著高于其他男性(p = 0.017)。结论:本研究介绍了土耳其北部国家血红蛋白病筛查计划的结果,发现β-thal和异常HbS率较低。获得的数据将有助于监测血红蛋白病疾病和评估当前计划的有效性在未来。它将使决策者能够实施政策变化并优先考虑新项目。
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Premarital hemoglobinopathy screening program results of a province in the Black Sea region of Turkey: three years' experience.

Objectives: Hemoglobinopathies are a global public health problem with high mortality and morbidity and very expensive treatment. Disease can be reduced and prevented with hemoglobinopathy screening tests. It is possible to identify carriers with the hemoglobinopathy screening program applied in many countries of the world and in Turkey. This study aims to evaluate the results of the national premarital hemoglobinopathy screening program carried out in primary healthcare institutions.

Methods: The research is of epidemiological and cross-sectional type. Electrophoresis results examined within the scope of the premarital hemoglobinopathy screening program in Samsun between 1 January 2019 and 31 December 2021 were evaluated retrospectively. Age, gender, year of screening, and hemoglobinopathy screening results were obtained from the records. In the statistical analysis of the data, p < 0.05 was accepted.

Results: The median age of 52,338 people screened under the hemoglobinopathy screening program was 29.0 (16.0-86.0) years. About 54.1% (n = 28,309) of those who were screened were female, and it was found that the least screening was done in 2020 (n = 15,765 (30.1%)). As a result of the screening, the frequency of the β-thalassemia (β-thal) trait was 1.37% (n = 676), the frequency of the abnormal HbS was 0.04% (n = 20). The frequency of β-thal trait was statistically significantly higher in 2020 (1.5%) compared to other years (p = 0.029). When the results were analyzed by gender, the rate of women with abnormal HbS (3.7%) was significantly higher than the others (p = 0.017).

Conclusions: This study presents the results of the national hemoglobinopathy screening program in Northern Turkey and the β-thal and the abnormal HbS rates were found to be low. The data obtained will be useful in monitoring hemoglobinopathy disorders and evaluating the current program's effectiveness in the future. It will allow decision-makers to implement policy changes and prioritize new programs.

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