69 A Population-based Study of Parent-reported Health Outcomes at Preschool Age of Children Born Very Preterm

IF 1.8 4区 医学 Q2 PEDIATRICS Paediatrics & child health Pub Date : 2023-09-01 DOI:10.1093/pch/pxad055.069
Sydney MacDonald, Satvinder Ghotra, Alexandra Stratas, Marsha Campbell-Yeo, Anne Synnes, Prakesh Shah, Navjot Sandila
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Abstract

Abstract Background Most existing literature on health status (HS) and health-related quality of life (HRQL) of preterm survivors focuses on late childhood, adolescent, and adult age, with only a small body of data on preschool age children. Little is known about the relationship between parent-reported HS outcomes and standardized neurodevelopmental outcomes measured in preterm survivors at preschool age. Objectives To present parent-reported HS outcomes at 36 months of age in a population-based cohort of very preterm survivors and compare parent-reported subjective outcomes to standardized neurodevelopmental outcomes measured by clinicians at the same age. Design/Methods Infants <31 weeks’ gestation born between April 2014 and June 2016 were prospectively followed through the Perinatal Follow-Up Program and enrolled in a population-based database. HS was measured using the Health Status Classification System for Pre-School Children questionnaire, completed by parents when children reached 36 months’ age. At the same age, neurological examination and standardized developmental assessments were completed by clinicians, using the Bayley Scales of Infant and Toddler Development – III to determine neurodevelopmental impairment (NDI). NDI was categorized as none, “mild”, or “significant" (moderate or severe cerebral palsy, Bayley-III <70, blind or required hearing aid). Inter-rater reliability between the physician and parent scores was assessed using Cohen’s weighted kappa coefficient. Results Of 118 children included, there were 47 and 71 children born in <28 and ≥28 weeks’ gestational age, respectively. At 36 months’ age, 73.7% had a parental health concern, mild in >50% and severe in only 8.5%. The most affected HS attributes were language (46.6%) and self-care (39.0%). Nearly 75% of the participants did not meet the criteria for NDI. Of 11 (9.3%) children with significant NDI at 36 months’ age, all parents reported moderate (36.4%) or severe (63.6%) health concerns. Conversely, of 26 (22%) children with parents reporting moderate to severe health concerns, 11 (42.3%) met the criteria for significant NDI (Table 1). Weighted Kappa coefficient was 0.33 (CI=0.20,0.046). Conclusion Most parents expressed at least one concern for their preschool-aged child born preterm. Despite high parental concern, most children did not meet the criteria for NDI via clinician assessment. Overall, there was fair agreement between parental concerns and clinician-reported outcomes.
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一项基于人群的极早产儿童学龄前父母报告健康结果的研究
背景大多数关于早产儿幸存者健康状况(HS)和健康相关生活质量(HRQL)的现有文献集中在儿童期晚期、青春期和成年期,只有一小部分关于学龄前儿童的数据。关于父母报告的HS结果与学龄前早产儿幸存者的标准化神经发育结果之间的关系,我们知之甚少。目的:在一个以人群为基础的早产儿幸存者队列中,研究36月龄时父母报告的HS结果,并将父母报告的主观结果与临床医生在相同年龄时测量的标准化神经发育结果进行比较。设计/方法2014年4月至2016年6月期间出生的孕31周的婴儿通过围产期随访计划进行前瞻性随访,并纳入基于人群的数据库。HS采用学前儿童健康状况分类系统问卷进行测量,问卷由家长在儿童年满36个月时填写。在同一年龄,由临床医生完成神经学检查和标准化发育评估,使用Bayley婴幼儿发育量表- III来确定神经发育障碍(NDI)。NDI分为无、“轻度”和“显著”(中度或重度脑瘫,贝利氏综合征(Bayley-III) 70,失明或需要助听器)。医师和家长评分间的信度采用科恩加权卡帕系数进行评估。结果118例患儿中,28周和≥28周出生的分别有47例和71例。在36个月大时,73.7%的婴儿有父母健康问题,轻度的占50%,重度的只有8.5%。受影响最大的HS属性是语言(46.6%)和自我护理(39.0%)。近75%的参与者不符合NDI的标准。在11名(9.3%)36月龄时出现严重NDI的儿童中,所有父母都报告了中度(36.4%)或重度(63.6%)健康问题。相反,在26名(22%)父母报告有中度至重度健康问题的儿童中,11名(42.3%)符合显著NDI标准(表1)。加权Kappa系数为0.33 (CI=0.20,0.046)。结论大多数家长对学龄前早产儿至少表达了一种担忧。尽管家长高度关注,但通过临床医生评估,大多数儿童不符合NDI的标准。总的来说,父母的担忧和临床医生报告的结果是相当一致的。
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来源期刊
Paediatrics & child health
Paediatrics & child health 医学-小儿科
CiteScore
2.10
自引率
5.30%
发文量
208
审稿时长
>12 weeks
期刊介绍: Paediatrics & Child Health (PCH) is the official journal of the Canadian Paediatric Society, and the only peer-reviewed paediatric journal in Canada. Its mission is to advocate for the health and well-being of all Canadian children and youth and to educate child and youth health professionals across the country. PCH reaches 8,000 paediatricians, family physicians and other child and youth health professionals, as well as ministers and officials in various levels of government who are involved with child and youth health policy in Canada.
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