McGuire Molly F, Vakulenko-Lagun Bella, Millis Michael B, Almakias Roi, Cole Earl P, Kim Harry K W
Department of Orthopedic Research, Scottish Rite for Children, Dallas, Texas, USA.
Department of Statistics, University of Haifa, Haifa, Israel.
Bone Jt Open. 2022 May;3(5):404-414. doi: 10.1302/2633-1462.35.BJO-2021-0185.R1.
Perthes' disease is an uncommon hip disorder with limited data on the long-term outcomes in adulthood. We partnered with community-based foundations and utilized web-based survey methodology to develop the Adult Perthes Survey, which includes demographics, childhood and adult Perthes' disease history, the University of California Los Angeles (UCLA) Activity Scale item, Short Form-36, the Hip disability and Osteoarthritis Outcome Score, and a body pain diagram. Here we investigate the following questions: 1) what is the feasibility of obtaining > 1,000 survey responses from adults who had Perthes' disease using a web-based platform?; and 2) what are the baseline characteristics and demographic composition of our sample?
The survey link was available publicly for 15 months and advertised among support groups. Of 1,505 participants who attempted the Adult Perthes survey, 1,182 completed it with a median timeframe of 11 minutes (IQR 8.633 to 14.72). Participants who dropped out were similar to those who completed the survey on several fixed variables. Participants represented 45 countries including the USA (n = 570; 48%), UK (n = 295; 25%), Australia (n = 133; 11%), and Canada (n = 46; 4%). Of the 1,182 respondents, 58% were female and the mean age was 39 years (SD 12.6).
Ages at onset of Perthes' disease were < six years (n = 512; 43%), six to seven years (n = 321; 27%), eight to 11 years (n = 261; 22%), and > 11 years (n = 76; 6%), similar to the known age distribution of Perthes' disease. During childhood, 40% (n = 476) of respondents had at least one surgery. Bracing, weightbearing restriction, and absence of any treatment varied significantly between USA and non-USA respondents (p < 0.001, p = 0.002, and p < 0.001, respectively). As adults, 22% (n = 261) had at least one total hip arthroplasty, and 30% (n = 347) had any type of surgery; both more commonly reported among women (p = 0.002).
While there are limitations due to self-sampling, our study shows the feasibility of obtaining a large set of patient-reported data from adults who had childhood Perthes' from multiple countries. Cite this article: 2022;3(5):404-414.
佩特兹病是一种罕见的髋关节疾病,关于其成年后的长期预后数据有限。我们与社区基金会合作,采用基于网络的调查方法开发了成人佩特兹病调查问卷,内容包括人口统计学信息、儿童期和成年期佩特兹病病史、加利福尼亚大学洛杉矶分校(UCLA)活动量表项目、简短健康调查问卷-36、髋关节残疾和骨关节炎结果评分以及身体疼痛图。在此,我们研究以下问题:1)使用基于网络的平台从患有佩特兹病的成年人中获得1000份以上调查问卷回复的可行性如何?2)我们样本的基线特征和人口构成是怎样的?
调查问卷链接公开了15个月,并在支持小组中进行宣传。在1505名尝试成人佩特兹病调查问卷的参与者中,1182人完成了调查,中位用时为11分钟(四分位间距8.633至14.72)。在几个固定变量方面,退出的参与者与完成调查的参与者相似。参与者来自45个国家,包括美国(n = 570;48%)、英国(n = 295;25%)、澳大利亚(n = 133;11%)和加拿大(n = 46;4%)。在1182名受访者中,58%为女性,平均年龄为39岁(标准差12.6)。
佩特兹病发病年龄小于6岁的有512人(43%),6至7岁的有321人(27%),8至11岁的有261人(22%),大于11岁的有76人(6%),与已知的佩特兹病年龄分布相似。在儿童期,40%(n = 476)的受访者至少接受过一次手术。在美国和非美国受访者之间,支具治疗、负重限制和未接受任何治疗的情况差异显著(分别为p < 0.001、p = 0.002和p < 0.001)。成年后,22%(n = 261)的人至少接受过一次全髋关节置换术,30%(n = 347)的人接受过任何类型的手术;女性报告的比例更高(p = 0.002)。
尽管由于自我抽样存在局限性,但我们的研究表明从多个国家患有儿童期佩特兹病的成年人中获取大量患者报告数据是可行的。引用本文:2022;3(5):404 - 414。