照顾者感知唐氏综合症退行性障碍的诊断和护理障碍。

IF 1.7 4区 生物学 Q3 GENETICS & HEREDITY
Anya Alag, Nicole A Nishimori, Lilia Kazerooni, Maeve C Lucas, David J Huh, Mariam M Yousuf, Saba Jafarpour, Cathy Franklin, Eileen A Quinn, Jonathan D Santoro
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引用次数: 0

摘要

唐氏综合症退行性障碍(DSRD)是一种罕见的影响21三体患者的神经精神疾病。对dsd患者的护理障碍尚未进行研究。本研究旨在探讨人口统计学、社会经济和地理因素如何影响dsd患者获得诊断、检测和治疗。一个横断面的,在线的,REDCap调查被用来询问患有dsd的个体的照顾者。符合条件的护理人员回答了有关人口统计学、临床特征和诊断和治疗障碍的问题。采用R软件进行统计学分析,采用χ2、Mann-Whitney U和Kruskal-Wallis H检验。共有397名参与者入组,其中大多数来自美国(74%)。诊断障碍(58.1%)、治疗障碍(52.6%)、转诊障碍(52.0%)和检测障碍(39.4%)普遍存在。主要障碍包括医生不熟悉dsd和缺乏当地专家。诊断、检测和治疗的旅行距离很大,14.7%的人为了诊断而旅行超过500英里,有些人需要国际旅行。影响诊断和治疗延误的因素包括家庭收入、地区和人口变量。收入越高,诊断时间越短(p = 0.004),治疗时间越短(p = 0.004)
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Caregiver Perceived Barriers to Diagnosis and Care in Down Syndrome Regression Disorder.

Down Syndrome Regression Disorder (DSRD) is a rare neuropsychiatric condition affecting individuals with Trisomy 21. Barriers to care for DSRD patients have not been studied. This research aimed to explore how demographic, socioeconomic, and geographic factors influence access to diagnosis, testing, and treatment for individuals with DSRD. A cross-sectional, online, REDCap survey was utilized to query caregivers of individuals with DSRD. Eligible caregivers answered questions regarding demographics, clinical features, and barriers to diagnosis and treatment. Statistical analysis was performed using R software, employing χ2, Mann-Whitney U, and Kruskal-Wallis H tests. A total of 397 participants were enrolled, most from the US (74%). Barriers to diagnosis (58.1%), treatment (52.6%), referral (52.0%), and testing (39.4%) were prevalent. Key barriers included physician unfamiliarity with DSRD and a lack of local specialists. Travel distances for diagnosis, testing, and treatment were significant, with 14.7% traveling over 500 miles for diagnosis and some requiring international travel. Factors influencing delays in diagnosis and treatment included household income, region, and demographic variables. Higher income was associated with shorter time to diagnosis (p = 0.004) and treatment (p < 0.001). Race, income, maternal education, and setting influenced delays in diagnosis. Delays in treatment were influenced by ethnicity, income, and location. This large international survey of caregivers of individuals with DSRD elucidates perceived barriers to accessing diagnosis, testing, and treatment, with demographic factors such as socioeconomic status and geography influencing these challenges. The directionality of these effects and their impact on clinical care and outcomes will be a logical basis for additional studies. Further studies are needed to explore these barriers in greater depth and assess their impact on healthcare outcomes.

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来源期刊
CiteScore
3.50
自引率
5.00%
发文量
432
审稿时长
2-4 weeks
期刊介绍: The American Journal of Medical Genetics - Part A (AJMG) gives you continuous coverage of all biological and medical aspects of genetic disorders and birth defects, as well as in-depth documentation of phenotype analysis within the current context of genotype/phenotype correlations. In addition to Part A , AJMG also publishes two other parts: Part B: Neuropsychiatric Genetics , covering experimental and clinical investigations of the genetic mechanisms underlying neurologic and psychiatric disorders. Part C: Seminars in Medical Genetics , guest-edited collections of thematic reviews of topical interest to the readership of AJMG .
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