Rajzbaum Gerald, Jakob Franz, Karras Dimitrios, Ljunggren Osten, Lems Willem F, Langdahl Bente L, Fahrleitner-Pammer Astrid, Walsh J Bernard, Gibson Anthony, Tynan Aodán J, Marin Fernando
Hôpital St Joseph, Paris, France.
Curr Med Res Opin. 2008 Feb;24(2):377-84. doi: 10.1185/030079908x261087.
The European Forsteo Observational Study (EFOS) study was primarily designed to assess fracture incidence, degree of pain, health-related quality of life (HRQoL) and compliance in women prescribed teriparatide in a community setting. This report describes the design of the study and characteristics of the patients at entry.
At entry, 1645 postmenopausal women with a diagnosis of osteoporosis and about to initiate teriparatide treatment were enrolled in eight European countries. Baseline data were collected on demographic characteristics, medical and osteoporosis history, disease status, prior use of medications and HRQoL.
The mean (standard deviation [SD]) age of patients was 71.5 (8.4) years, lumbar spine bone mineral density (BMD) T-score was -3.3 (1.2), the mean number of previous fractures reported after 40 years of age was 2.9 (2.0), 70% had two or more vertebral deformities and 91.7% were pre-treated with bisphosphonates. HRQoL, evaluated by the health state value (HSV) (median: 0.59, Q1; Q3: 0.08; 0.71) and visual analogue scale (VAS) (median 50.0, Q1; Q3: 35.0; 69.0) status of the European quality of life questionnaire (EQ-5D) was poor. Extreme problems were reported by 31% of patients for the pain/discomfort dimension, mobility was limited in 69% and anxiety/depression was reported by 57% of patients. Chronic or intermittent back pain was reported by 91% of patients, which occurred every day or almost every day within the last month in 66% of patients.
The post-menopausal women prescribed teriparatide were severely osteoporotic, with a high fracture risk and poor HRQoL, despite previous therapy for osteoporosis. Moderate to severe back pain was very common.
欧洲福善美观察性研究(EFOS)主要旨在评估在社区环境中接受特立帕肽治疗的女性的骨折发生率、疼痛程度、健康相关生活质量(HRQoL)和依从性。本报告描述了该研究的设计及入组患者的特征。
入组时,1645名诊断为骨质疏松症且即将开始特立帕肽治疗的绝经后女性在8个欧洲国家入组。收集了关于人口统计学特征、医疗和骨质疏松症病史、疾病状态、既往用药情况及HRQoL的基线数据。
患者的平均(标准差[SD])年龄为71.5(8.4)岁,腰椎骨密度(BMD)T值为-3.3(1.2),40岁后报告的既往骨折平均次数为2.9(2.0)次,70%的患者有两处或更多椎体畸形,91.7%的患者曾接受双膦酸盐治疗。通过欧洲生活质量调查问卷(EQ-5D)的健康状态值(HSV)(中位数:0.59,第一四分位数;第三四分位数:0.08;0.71)和视觉模拟量表(VAS)(中位数50.0,第一四分位数;第三四分位数:35.0;69.0)评估的HRQoL较差。31%的患者在疼痛/不适维度报告有极端问题,69%的患者活动受限,57%的患者报告有焦虑/抑郁。91%的患者报告有慢性或间歇性背痛,其中66%的患者在过去一个月内每天或几乎每天都出现背痛。
尽管此前曾接受骨质疏松症治疗,但接受特立帕肽治疗的绝经后女性骨质疏松严重,骨折风险高且HRQoL差。中度至重度背痛非常常见。