地中海贫血患者生活质量的移动应用程序部署:叙述性综述

Afifah Ayu, S. Mulyono
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引用次数: 0

摘要

地中海贫血是遗传自父母的遗传性溶血性贫血。由于红细胞不能形成血红蛋白而发生。从而导致地中海贫血患者终生接受输血治疗。该移动应用程序包含地中海贫血的详细信息,地中海贫血患者及其家人可以轻松访问这些信息,以保持地中海贫血患者的生活质量。本文献综述的目的是确定应用于地中海贫血患者生活质量的移动应用程序的有效性。本次准备使用的方法是通过在线数据库的电子搜索,即:Google Scholar Science Direct,PROQUEST。写作的标准是2018-2022年的全文和出版物。研究搜索发现有10篇文章被提取出来。所获得的结果是,地中海贫血患者生活质量的移动应用程序具有积极的反应,需要动态开发。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mobile App Deployment for Quality-of-Life Patient with Thalassemia: A narrative review
Thalassemia is a hereditary hemolytic anemia disease that is inherited from parents. Occurs due to the inability of red blood cells to form hemoglobin. Thus causing thalassemia patients to undergo transfusion therapy for life. The mobile application contains detailed information about thalassemia that can be easily accessed by thalassemia patients and their families aiming to maintain the quality of life of patients with thalassemia. The purpose of this literature review is to determine the effectiveness of mobile applications applied to the quality of life of patients thalassemia. The method used in this preparation is by electronic search of online databases, namely: Google Scholar Science Direct, PROQUEST. The criteria for writing are full text and publications in 2018-2022. Research search found 10 articles had been extracted. The results obtained are mobile applications for the quality of life of patients with thalassemia have a positive response and dynamically need to be developed.
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