诊断和管理初级状动力障碍症及其在美国的影响:一个迷你回顾
M Castillo1, E Freire1, V I Romero1
1School of Medicine, Universidad San Francisco de Quito, Quito, Ecuador.
Frontiers in pediatrics
|September 25, 2023
概括
拉丁美洲缺乏初级状动力障碍 (PCD) 诊断和治疗指南. 本次审查强调了与北美和欧洲相比,诊断工具和治疗可访问性的差异.
科学领域:
- 医学研究 医学研究
- 遗传学 是一个遗传学.
- 公共卫生 公共卫生
背景情况:
- 初级状动力障碍 (PCD) 是一种罕见的遗传疾病,由于状动力受损,导致严重的健康问题.
- 目前的诊断方法包括高速视频显微镜,氧化测量和遗传检测,但没有单一的确定的测试存在.
- 特别是拉丁美洲,PCD管理缺乏标准化指导方针.
研究的目的:
- 为了突出拉丁美洲PCD缺乏标准化的诊断和治疗指南.
- 将北美和欧洲PCD指南与拉丁美洲的诊断工具和治疗方法的可访问性进行比较.
主要方法:
- 对北美,欧洲和拉丁美洲的文学进行了全面的审查.
- 疾病信息被收集并组织成表格,拉丁美洲的管理信息从病例报告中推断出来.
- 从5,774个出版物中,确定了15篇符合纳入标准的文章 (PCD管理,同行评审,美洲).
主要成果:
- 没有发现拉丁美洲PCD的特定临床指南.
- 在许多拉丁美洲国家,北美和欧洲指南中推的诊断工具和治疗方法并不容易获得.
- 资源和研究有限,导致拉丁美洲缺乏PCD指导方针.
结论:
- 在拉丁美洲,PCD流行,研究和建议的记录不足,这可能是由于经济因素.
- 对于拉丁美洲PCD患者来说,有限的诊断测试是显著的不利因素.
- 建议使用PICADAR评分作为在低收入环境中对PCD的潜在查工具.
关键词:
厄瓜多尔 厄瓜多尔 厄瓜多尔 是一个拉丁美洲 拉丁美洲 拉丁美洲皮卡达尔 (PICADAR) 是什么意思西里亚西里亚是什么意思纤维病变 (ciliopathy) 是一种纤维病变.卡塔基纳综合症 (Kartagener Syndrome) 是一个更多相关视频
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