地中海贫血症患者的家庭筛查和提供地中海贫血症预防知识教育的效果

Rameez Iqbal, Sidrah, Asfahan Akhtar, Kiran Memon, Muhammad Rahil Khan, Muhammad Anique, Kiran Aamir, Aamir Ramzan
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引用次数: 0

摘要

目的确定 Beta 型地中海贫血症患者家庭中的携带者,并确定预防地中海贫血症教育的效果。方法:观察-横断面研究从 2021 年 9 月 1 日至 2022 年 3 月 31 日的 6 个月内,在获得知情书面同意后,对 73 名地中海贫血症患者及其家属进行了观察-横断面研究。这项研究采用非概率、方便抽样的方式,在海德拉巴/贾姆索罗 LUMHS 病理科和诊断与研究实验室进行。数据通过 SPSS 21.0 进行分析:患者的平均年龄为 17.34 + 7.32 岁。52%的参与者为男性,平均年龄为 15.23 + 9.67 岁;48%的参与者为女性,平均年龄为 13.48 + 5.7 岁。大多数患者每两周输血一次,占 42.8%,32.9%的患者每月输血一次。每两个月输血的患者最少。87.70%的患者父母为近亲结婚。地中海贫血患者兄弟姐妹的血红蛋白电泳模式显示,4.1%的患者患有重型地中海贫血,32.8%的患者患有轻型地中海贫血,63%的患者血红蛋白电泳模式正常。地中海贫血患者兄弟姐妹的平均血红蛋白为 09.23 + 3.65 mg/dl,平均 MCV 为 63.86 + 8.41 mg/dl。结论研究发现,约三分之二的家庭有地中海贫血的阳性病史,约四分之一的患者有输血史。教育课程有效地提高了地中海贫血症患者的相关知识。关键词地中海贫血症、携带者、家族史、教育意识的有效性
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Family Screening of Thalassemic Patients and Effectiveness of Education in Providing Knowledge about Prevention of Thalassemia
Objective: To identify the carriers in the families of Beta Thalassemia patients and to determine the effectiveness of education about the prevention of thalassemia. Methods: The Observational - Cross-Sectional study was carried out in 6 months from 01-09-2021 to 31-03-2022 on a sample of 73 thalassemia patients and their families, after taking informed written consent. This study was conducted via non-probability, convenient sampling and was carried out at the Department of Pathology & Diagnostic and Research Laboratory - LUMHS Hyderabad/Jamshoro. The data was analyzed via SPSS 21.0 Results: The mean age of patients was found to be 17.34 + 7.32 years. 52% of participants were males with mean age of 15.23 + 9.67 years and 48% participants were females with mean age of 13.48 + 5.7 years. Most of the patients were having fortnightly blood transfusion i.e. 42.8% followed by 32.9% patients with monthly transfusion. Bi-monthly transfusion were found to be least reported. Consanguineous marriage among parents was found in 87.70% of patients. Hb electrophoresis pattern among siblings of thalassemia patients showed 4.1% occurrence of thalassemia major and 32.8% occurrence of thalassemia minor while 63% patients were found to be having normal electrophoresis pattern. The mean hemoglobin was found to be 09.23 + 3.65 mg/dl among siblings of thalassemia patients with 63.86 + 8.41 mg/dl mean MCV. Conclusion: The study found out that the around 2/3rd of the families were having positive history of thalassemia with around 1/4th of the patients had history of blood transfusion. The educational session was found to effective in improving the knowledge regarding the thalassemia. Keywords: Thalassemia, carriers, family history, effectiveness of educational awareness
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