Faculty of Health, University of Canberra, 11 Kirinari St, Bruce, ACT, 2617, Australia.
Research Institute for Sport and Exercise, University of Canberra, 11 Kirinari St, Bruce, ACT, 2617, Australia.
BMC Musculoskelet Disord. 2021 Dec 20;22(1):1048. doi: 10.1186/s12891-021-04935-w.
Greater trochanteric pain syndrome (GTPS) is a musculoskeletal condition which can cause disability and reduce quality of life. However, limited evidence is available on the long-term outcomes of people with GTPS. Our aims were to determine the long-term prevalence of GTPS; to calculate the proportion of people with GTPS who had developed hip osteoarthritis (OA); and to determine the level of function and quality of life, 11-years after initial GTPS diagnosis.
A prospective 11-year natural history study. Two groups [GTPS group (n = 24), asymptomatic control (ASC) group (n = 20)] were evaluated at baseline, 12-months and 11-years. At 11-years all participants completed the modified Harris Hip Score (mHHS), Oswestry Disability Index (ODI) and Assessment of Quality-of-Life questionnaire. At 11-year follow-up 20/24 GTPS and 19/20 ASC participants were clinically assessed for GTPS and hip OA, completed the 10 metre-walk-test, timed up and go, and hip abduction and external rotation strength testing.
At 11-year follow-up 45.0% of GTPS participants had GTPS compared to 5.3% of ASC participants (p = 0.008), OR [95% CI]: 10.19 [1.95, 104.3], and 35.0% of GTPS participants were clinically diagnosed with hip OA compared to none of the ASC participants (p = 0.002), OR [95% CI]: 21.6, [2.3, 2898.0]. GTPS participants reported more pain and disability than ASC participants via the ODI, mean difference [95% CI]: 6.1 [0.7, 11.6] but not the modified Harris Hip Score, mean difference [95% CI]: -3.3 [-10.3, 3.7]. Both groups had similar levels of quality of life and measures of function.
GTPS is a chronic condition: people with GTPS at baseline had twice the odds of being clinically diagnosed with GTPS or hip OA than the control group at 11-years. Further, there appears to be a temporal relationship between GTPS and the development of hip OA. This finding highlights the need to identify effective treatments that address the underlying impairments associated with GTPS. Pain and function results varied depending on the assessment tools used. Between group differences in quality of life seen at baseline are not found at the 11-year follow-up. The small sample size means the results must be considered with caution.
Level II Natural history Study.
大转子疼痛综合征(GTPS)是一种肌肉骨骼疾病,可导致残疾和降低生活质量。然而,关于 GTPS 患者的长期预后结果的证据有限。我们的目的是确定 GTPS 的长期患病率;计算患有髋骨关节炎(OA)的 GTPS 患者比例;并确定初始 GTPS 诊断 11 年后的功能和生活质量水平。
一项前瞻性 11 年自然史研究。两组[GTPS 组(n=24),无症状对照组(ASC)组(n=20)]在基线、12 个月和 11 年时进行评估。在 11 年时,所有参与者都完成了改良 Harris 髋关节评分(mHHS)、Oswestry 残疾指数(ODI)和生活质量评估问卷。在 11 年随访时,20/24 名 GTPS 和 19/20 名 ASC 参与者进行了 GTPS 和髋 OA 的临床评估,完成了 10 米步行测试、计时起身和走、髋关节外展和外旋力量测试。
在 11 年随访时,45.0%的 GTPS 参与者患有 GTPS,而 ASC 参与者为 5.3%(p=0.008),比值比(OR)[95%置信区间]:10.19 [1.95,104.3],35.0%的 GTPS 参与者被临床诊断为髋 OA,而 ASC 参与者均无此诊断(p=0.002),OR [95%置信区间]:21.6,[2.3,2898.0]。GTPS 参与者通过 ODI 报告的疼痛和残疾比 ASC 参与者多,平均差异[95%置信区间]:6.1 [0.7,11.6],但改良 Harris 髋关节评分没有差异,平均差异[95%置信区间]:-3.3 [-10.3,3.7]。两组的生活质量和功能水平相似。
GTPS 是一种慢性疾病:在基线时患有 GTPS 的患者在 11 年时被临床诊断为 GTPS 或髋 OA 的可能性是对照组的两倍。此外,GTPS 和髋 OA 的发展之间似乎存在时间关系。这一发现强调了需要确定有效的治疗方法,以解决与 GTPS 相关的潜在损伤。疼痛和功能结果因所使用的评估工具而异。基线时两组之间的生活质量差异在 11 年随访时并未发现。样本量小意味着结果必须谨慎考虑。
II 级 自然史研究。