Assessing the prevalence of unmet need for genetic counseling in Canada and exploring associations with sociodemographic factors

IF 3.7 2区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Kennedy Borle, Jehannine Austin, Larry D. Lynd
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Abstract

Understanding the prevalence and distribution of unmet need for genetic counseling (GC) can help inform health human resource planning. It is known that not all patients who could benefit from GC are currently accessing it, however, the prevalence of unmet need in Canada is unknown. Using a cross-sectional design, we surveyed 1160 Canadians to estimate the prevalence and distribution of unmet need for GC. The survey included measures of unmet need (NSGC Pathways Tool), personal utility (PrU), capability (ICECAP-A), distrust in healthcare (Revised Health Care System Distrust Scale) and demographic variables. A market research company (Leger Opinion Panel) was used for recruitment. We used descriptive statistics to estimate prevalence and multivariable regression to explore factors associated with unmet need. We found that 39% of respondents (457/1160) had unmet need for GC and 68% of this unmet need was unperceived. In the multivariable regression analysis, unmet need for GC was more likely in individuals who: had a mental health condition, were younger ( $$\le$$ 45 yo), reported higher personal utility, and lower levels of capability (all p < 0.05 in multivariable analysis). There is a high prevalence of unmet need for GC in Canada and individuals experiencing other challenges to accessing healthcare may also be more likely to have unmet need for GC.
评估加拿大未满足的遗传咨询需求的流行程度,并探索其与社会人口因素的关系。
了解遗传咨询(GC)未满足需求的流行程度和分布,有助于为卫生人力资源规划提供信息。众所周知,目前并非所有可能受益于GC的患者都在使用它,然而,加拿大未满足需求的患病率尚不清楚。使用横断面设计,我们调查了1160名加拿大人,以估计未满足GC需求的患病率和分布。该调查包括未满足需求(NSGC途径工具)、个人效用(PrU)、能力(ICECAP-A)、对医疗保健的不信任(修订的医疗保健系统不信任量表)和人口变量的测量。聘请了一家市场调查公司(Leger Opinion Panel)。我们使用描述性统计来估计患病率,并使用多变量回归来探索与未满足需求相关的因素。我们发现39%的受访者(457/1160)对GC的需求未得到满足,而这些未得到满足的需求中有68%未被察觉。在多变量回归分析中,未满足的GC需求更可能发生在以下人群中:有精神健康状况、年轻(≤45岁)、报告较高的个人效用和较低的能力水平
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
European Journal of Human Genetics
European Journal of Human Genetics 生物-生化与分子生物学
CiteScore
9.90
自引率
5.80%
发文量
216
审稿时长
2 months
期刊介绍: The European Journal of Human Genetics is the official journal of the European Society of Human Genetics, publishing high-quality, original research papers, short reports and reviews in the rapidly expanding field of human genetics and genomics. It covers molecular, clinical and cytogenetics, interfacing between advanced biomedical research and the clinician, and bridging the great diversity of facilities, resources and viewpoints in the genetics community. Key areas include: -Monogenic and multifactorial disorders -Development and malformation -Hereditary cancer -Medical Genomics -Gene mapping and functional studies -Genotype-phenotype correlations -Genetic variation and genome diversity -Statistical and computational genetics -Bioinformatics -Advances in diagnostics -Therapy and prevention -Animal models -Genetic services -Community genetics
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