护理人员报告的患有威廉姆斯综合症的儿童和成人的护理障碍。

IF 1.5 Q4 GENETICS & HEREDITY Journal of Community Genetics Pub Date : 2024-08-01 Epub Date: 2024-05-22 DOI:10.1007/s12687-024-00707-w
Elizabeth W Barnhardt, Marilee Martens, Rebecca Andridge, Jennifer Walton
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引用次数: 0

摘要

威廉姆斯综合症(WS)患者可能会遇到各种医疗、行为和教育方面的问题。本研究的主要目的是评估威廉姆斯综合症患者的医疗障碍,主要使用医疗障碍问卷(BCQ),并评估各种人口统计学因素是否与这些障碍相关。我们利用威廉姆斯综合症协会研究登记处分发了一份 REDCap 调查表。美国 319 名威廉姆斯综合症患者的照顾者填写了 BCQ。在 BCQ 中,得分越低表示护理障碍越多。年龄越小,语用和技能两个分量表的得分就越低,而收入水平越低、与了解 WS 的医疗服务提供者的距离越远,BCQ 的总分就越低。
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Caregiver-reported barriers to care for children and adults with Williams Syndrome.

Individuals with Williams syndrome (WS) may experience a variety of medical, behavioral, and educational concerns. The primary objective of this study was to assess barriers to health care for patients with WS, primarily using the Barriers to Care Questionnaire (BCQ), and to assess whether various demographic factors are correlated with these barriers. A REDCap survey was distributed using the Williams Syndrome Association Research Registry. 319 caregivers of individuals with WS in the United States completed the BCQ. On the BCQ, lower scores indicate more barriers to care. Younger age was associated with lower scores for both the pragmatics and the skills subscales while lower income levels and increased distances to providers knowledgeable about WS were consistently associated with lower total BCQ scores.

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来源期刊
Journal of Community Genetics
Journal of Community Genetics GENETICS & HEREDITY-
CiteScore
3.30
自引率
5.30%
发文量
54
期刊介绍: The Journal of Community Genetics is an international forum for research in the ever-expanding field of community genetics, the art and science of applying medical genetics to human communities for the benefit of their individuals. Community genetics comprises all activities which identify persons at increased genetic risk and has an interest in assessing this risk, in order to enable those at risk to make informed decisions. Community genetics services thus encompass such activities as genetic screening, registration of genetic conditions in the population, routine preconceptional and prenatal genetic consultations, public education on genetic issues, and public debate on related ethical issues. The Journal of Community Genetics has a multidisciplinary scope. It covers medical genetics, epidemiology, genetics in primary care, public health aspects of genetics, and ethical, legal, social and economic issues. Its intention is to serve as a forum for community genetics worldwide, with a focus on low- and middle-income countries. The journal features original research papers, reviews, short communications, program reports, news, and correspondence. Program reports describe illustrative projects in the field of community genetics, e.g., design and progress of an educational program or the protocol and achievement of a gene bank. Case reports describing individual patients are not accepted.
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