Ferro Mark A, Lipman Ellen L, Van Lieshout Ryan J, Timmons Brian, Shanahan Lilly, Gorter Jan Willem, Georgiades Kathy, Boyle Michael
School of Public Health and Health Systems, University of Waterloo, Waterloo, Ontario.
Department of Psychiatry and Behavioural Neurosciences, McMaster University, Hamilton, Ontario.
J Can Acad Child Adolesc Psychiatry. 2021 May;30(2):104-115. Epub 2021 May 1.
This manuscript serves to provide an overview of the methods of the Multimorbidity in Children and Youth across the Life-course (MY LIFE) study, profile sample characteristics of the cohort, and provide baseline estimates of multimorbidity to foster collaboration with clinical and research colleagues across Canada.
MY LIFE is comprised of 263 children (2-16 years) with a physical illness recruited from McMaster Children's Hospital, their primary caregiving parent, and their closest-aged sibling. Participants are followed with data collection at recruitment, 6, 12, and 24 months which includes structured interviews, self-reported measures, and biological samples and occur in a private research office or at participants' homes. Post-COVID-19, data collection transitioned to mail and telephone surveys.
At recruitment, children were 9.4 (4.2) years of age and 52.7% were male. The mean duration of their physical illness was 4.5 (4.1) years; 25% represent incident cases (duration <1 year). Most (69.7%) had healthy body weight and intelligence in the average range (73.5%). Overall, 38.2% of children screened positive for ≥1 mental illness according to parent report (24.8% screened positive based on child self-report). Compared to 2016 Census data, the MY LIFE cohort overrepresents families of higher socioeconomic status.
Multimorbidity is common among children and these baseline data will serve to measure relative changes in the mental health of children with physical illness over time. MY LIFE will provide new information for understanding multimorbidity among children, though underrepresentation of lower socioeconomic families may have implications for the generalizability of findings.
本手稿旨在概述儿童和青少年全生命周期多重疾病(MY LIFE)研究的方法,描述该队列的样本特征,并提供多重疾病的基线估计,以促进与加拿大各地临床和研究同事的合作。
MY LIFE研究招募了263名患有身体疾病的儿童(2至16岁)、他们的主要照顾父母以及年龄最接近的兄弟姐妹,这些儿童来自麦克马斯特儿童医院。在招募时、6个月、12个月和24个月时对参与者进行数据收集,包括结构化访谈、自我报告测量和生物样本采集,数据收集在私人研究办公室或参与者家中进行。在新冠疫情之后,数据收集转变为邮寄和电话调查。
招募时,儿童的年龄为9.4(4.2)岁,52.7%为男性。他们身体疾病的平均持续时间为4.5(4.1)年;25%为新发病例(病程<1年)。大多数(69.7%)儿童体重健康,智力处于平均水平(73.5%)。总体而言,根据家长报告,38.2%的儿童筛查出≥1种精神疾病呈阳性(根据儿童自我报告,24.8%筛查呈阳性)。与2016年人口普查数据相比,MY LIFE队列中社会经济地位较高的家庭占比过高。
多重疾病在儿童中很常见,这些基线数据将用于衡量患有身体疾病的儿童心理健康随时间的相对变化。MY LIFE研究将为了解儿童多重疾病提供新信息,尽管社会经济地位较低的家庭代表性不足可能会影响研究结果的普遍性。