Coutant Régis, Tauber Maithé, Demaret Béatrice, Henocque Robin, Brault Yves, Montestruc François, Chassany Olivier, Polak Michel
Department of Pediatric Endocrinology and Diabetology, Reference Center for Rare Pituiatry Diseases, University Hospital of Angers, Angers, France.
Reference Center for the Prader-Willi syndrome and other rare obesities with feeding disorders (PRADORT), Children Hospital, CHU Toulouse, Toulouse, France.
Endocr Connect. 2023 Mar 28;12(4). doi: 10.1530/EC-22-0464. Print 2023 Apr 1.
The objective of this study was to describe in a real-life setting the treatment burden and adherence and quality of life (QOL) of children treated with daily injections of growth hormone and their relationship with treatment duration.
This non-interventional, multicenter, cross-sectional French study involved children aged 3-17 years treated with daily growth hormone injections.
Based on a recent validated dyad questionnaire, the mean overall life interference total score (100 = most interference) was described, with treatment adherence and QOL, using the Quality of Life of Short Stature Youth questionnaire (100 = best). All analyses were performed according to treatment duration prior to inclusion.
Among the 275/277 analyzed children, 166 (60.4%) had only growth hormone deficiency (GHD). In the GHD group, the mean age was 11.7 ± 3.2 years; median treatment duration was 3.3 years (interquartile range 1.8-6.4). The mean overall life interference total score was 27.7 ± 20.7 (95% CI (24.2; 31.2)), with non-significant correlation with treatment duration (P = 0.1925). Treatment adherence was good (95.0% of children reported receiving >80% of planned injections over the last month); it slightly decreased with treatment duration (P = 0.0364). Children's overall QOL was good (81.5 ± 16.6 and 77.6 ± 18.7 according to children and parents, respectively), but subscores of the coping and treatment impact domains were <50. Similar results were observed in all patients independently of the condition requiring treatment.
This real-life French cohort confirms the treatment burden of daily growth hormone injections, as previously reported in an interventional study.
本研究的目的是在现实生活环境中描述接受每日生长激素注射治疗的儿童的治疗负担、依从性和生活质量(QOL),以及它们与治疗持续时间的关系。
这项非干预性、多中心、横断面的法国研究纳入了年龄在3至17岁、接受每日生长激素注射治疗的儿童。
基于最近一份经过验证的二元问卷,使用矮小青年生活质量问卷(满分100分,分数越高越好)描述了平均总体生活干扰总分(满分100分,分数越高干扰越大),以及治疗依从性和生活质量。所有分析均根据纳入前的治疗持续时间进行。
在275/277名接受分析的儿童中,166名(60.4%)仅有生长激素缺乏(GHD)。在GHD组中,平均年龄为11.7±3.2岁;治疗持续时间中位数为3.3年(四分位间距1.8 - 6.4年)。平均总体生活干扰总分是27.7±20.7(95%置信区间(24.2; 31.2)),与治疗持续时间无显著相关性(P = 0.1925)。治疗依从性良好(95.0%的儿童报告在过去一个月内接受了超过计划注射量的80%);依从性随治疗持续时间略有下降(P = 0.0364)。儿童的总体生活质量良好(儿童自评分为81.5±16.6,家长评分为77.6±18.7),但应对和治疗影响领域的子分数<50。在所有患者中,无论需要治疗的病情如何,均观察到类似结果。
这个法国现实生活队列证实了每日生长激素注射的治疗负担,正如之前在一项干预性研究中所报道的那样。