Seppänen Anna-Veera, Sauvegrain Priscille, Draper Elizabeth S, Toome Liis, El Rafei Rym, Petrou Stavros, Barros Henrique, Zimmermann Luc J I, Cuttini Marina, Zeitlin Jennifer
Université de Paris, CRESS, Obstetrical Perinatal and Pediatric Epidemiology Research Team, EPOPé, INSERM, INRA, 75004, Paris, France.
Sorbonne Université Collège Doctoral, 75005, Paris, France.
Pediatr Res. 2021 Mar;89(4):1004-1012. doi: 10.1038/s41390-020-01120-y. Epub 2020 Sep 18.
Follow-up of very preterm infants is essential for reducing risks of health and developmental problems and relies on parental engagement. We investigated parents' perceptions of post-discharge healthcare for their children born very preterm in a European multi-country cohort study.
Data come from a 5-year follow-up of an area-based cohort of births <32 weeks' gestation in 19 regions from 11 European countries. Perinatal data were collected from medical records and 5-year data from parent-report questionnaires. Parents rated post-discharge care related to their children's preterm birth (poor/fair/good/excellent) and provided free-text suggestions for improvements. We analyzed sociodemographic and medical factors associated with poor/fair ratings, using inverse probability weights to adjust for attrition bias, and assessed free-text responses using thematic analysis.
Questionnaires were returned for 3635 children (53.8% response rate). Care was rated as poor/fair for 14.2% [from 6.1% (France) to 31.6% (Denmark)]; rates were higher when children had health or developmental problems (e.g. cerebral palsy (34.4%) or epilepsy (36.9%)). From 971 responses, 4 themes and 25 subthemes concerning care improvement were identified.
Parents' experiences provide guidance for improving very preterm children's post-discharge care; this is a priority for children with health and developmental problems as parental dissatisfaction was high.
In a European population-based very preterm birth cohort, parents rated post-discharge healthcare as poor or fair for 14.2% of children, with a wide variation (6.1-31.6%) between countries. Dissatisfaction was reported in over one-third of cases when children had health or developmental difficulties, such as epilepsy or cerebral palsy. Parents' free-text suggestions for improving preterm-related post-discharge healthcare were similar across countries; these focused primarily on better communication with parents and better coordination of care. Parents' lived experiences are a valuable resource for understanding where care improvements are needed and should be included in future research.
对极早产儿进行随访对于降低健康和发育问题风险至关重要,且依赖于家长的参与。在一项欧洲多国队列研究中,我们调查了家长对其极早产儿出院后医疗保健的看法。
数据来自对11个欧洲国家19个地区孕周小于32周的基于地区的出生队列的5年随访。围产期数据从医疗记录中收集,5年数据从家长报告问卷中收集。家长对与其孩子早产相关的出院后护理进行评分(差/一般/好/优秀),并提供改进的自由文本建议。我们使用逆概率权重分析与差/一般评分相关的社会人口学和医学因素,以调整失访偏倚,并使用主题分析评估自由文本回复。
共收回3635名儿童的问卷(回复率为53.8%)。14.2%的护理被评为差/一般[从6.1%(法国)到31.6%(丹麦)];当儿童有健康或发育问题时(如脑瘫(34.4%)或癫痫(36.9%)),该比例更高。从971份回复中,确定了4个主题和25个子主题关于护理改进。
家长的经历为改善极早产儿出院后护理提供了指导;对于有健康和发育问题的儿童,这是一个优先事项,因为家长的不满程度很高。
在一个基于欧洲人群的极早产出生队列中,14.2%的儿童家长将出院后医疗保健评为差或一般,各国之间差异很大(6.1%-31.6%)。当儿童有健康或发育困难,如癫痫或脑瘫时,超过三分之一的病例报告有不满。各国家长关于改善早产相关出院后医疗保健的自由文本建议相似;这些主要集中在与家长更好的沟通和更好的护理协调上。家长的实际经历是了解需要改进护理之处的宝贵资源,应纳入未来研究。