Varni James W, Limbers Christine A, Burwinkle Tasha M
Department of Pediatrics, College of Medicine, Department of Landscape Architecture and Urban Planning, College of Architecture, Texas A&M University, 3137 TAMU, College Station, TX 77843-3137, USA.
Health Qual Life Outcomes. 2007 Jan 3;5:1. doi: 10.1186/1477-7525-5-1.
The last decade has evidenced a dramatic increase in the development and utilization of pediatric health-related quality of life (HRQOL) measures in an effort to improve pediatric patient health and well-being and determine the value of healthcare services. The emerging paradigm shift toward patient-reported outcomes (PROs) in clinical trials has provided the opportunity to further emphasize the value and essential need for pediatric patient self-reported outcomes measurement. Data from the PedsQL DatabaseSM were utilized to test the hypothesis that children as young as 5 years of age can reliably and validly report their HRQOL.
The sample analyzed represented child self-report age data on 8,591 children ages 5 to 16 years from the PedsQL 4.0 Generic Core Scales DatabaseSM. Participants were recruited from general pediatric clinics, subspecialty clinics, and hospitals in which children were being seen for well-child checks, mild acute illness, or chronic illness care (n = 2,603, 30.3%), and from a State Children's Health Insurance Program (SCHIP) in California (n = 5,988, 69.7%).
Items on the PedsQL 4.0 Generic Core Scales had minimal missing responses for children as young as 5 years old, supporting feasibility. The majority of the child self-report scales across the age subgroups, including for children as young as 5 years, exceeded the minimum internal consistency reliability standard of 0.70 required for group comparisons, while the Total Scale Scores across the age subgroups approached or exceeded the reliability criterion of 0.90 recommended for analyzing individual patient scale scores. Construct validity was demonstrated utilizing the known groups approach. For each PedsQL scale and summary score, across age subgroups, including children as young as 5 years, healthy children demonstrated a statistically significant difference in HRQOL (better HRQOL) than children with a known chronic health condition, with most effect sizes in the medium to large effect size range.
The results demonstrate that children as young as the 5 year old age subgroup can reliably and validly self-report their HRQOL when given the opportunity to do so with an age-appropriate instrument. These analyses are consistent with recent FDA guidelines which require instrument development and validation testing for children and adolescents within fairly narrow age groupings and which determine the lower age limit at which children can provide reliable and valid responses across age categories.
在过去十年中,儿科健康相关生活质量(HRQOL)测量方法的开发和应用显著增加,旨在改善儿科患者的健康和福祉,并确定医疗服务的价值。临床试验中向患者报告结局(PROs)的新兴范式转变为进一步强调儿科患者自我报告结局测量的价值和基本需求提供了机会。利用来自儿童生活质量量表数据库(PedsQL DatabaseSM)的数据来检验以下假设:年仅5岁的儿童能够可靠且有效地报告其HRQOL。
所分析的样本代表了来自儿童生活质量量表4.0通用核心量表数据库(PedsQL 4.0 Generic Core Scales DatabaseSM)中8591名5至16岁儿童的自我报告年龄数据。参与者招募自普通儿科诊所、专科诊所和医院,这些机构中儿童因健康检查、轻度急性疾病或慢性病护理前来就诊(n = 2603,占30.3%),以及来自加利福尼亚州的州儿童健康保险计划(SCHIP)(n = 5988,占69.7%)。
儿童生活质量量表4.0通用核心量表上的项目,对于年仅5岁的儿童,缺失回答极少,这支持了其可行性。在各个年龄亚组中,包括年仅5岁的儿童,大多数儿童自我报告量表超过了组间比较所需的最低内部一致性信度标准0.70,而各个年龄亚组的总量表得分接近或超过了分析个体患者量表得分所建议的0.90的信度标准。利用已知群体法证明了结构效度。对于每个儿童生活质量量表和汇总得分,在各个年龄亚组中,包括年仅5岁的儿童,健康儿童在HRQOL方面(更好的HRQOL)比患有已知慢性健康状况的儿童表现出统计学上的显著差异,大多数效应量处于中等到大效应量范围。
结果表明,年仅5岁年龄亚组的儿童在有机会使用适合其年龄的工具时,能够可靠且有效地自我报告其HRQOL。这些分析与美国食品药品监督管理局(FDA)最近的指南一致,该指南要求在相当狭窄的年龄组内对儿童和青少年进行工具开发和效度测试,并确定儿童能够在各个年龄类别中提供可靠且有效回答的最低年龄限制。