Improving Recognition of Fracture Risk in People with Human Immunodeficiency Virus: Performance and Model Contribution of Two Common Risk Assessment Tools

弗雷克斯 医学 置信区间 队列 髋部骨折 内科学 人口 队列研究 前瞻性队列研究 骨质疏松症 人类免疫缺陷病毒(HIV) 脆弱性 物理疗法 骨质疏松性骨折 骨矿物 家庭医学 环境卫生 化学 物理化学
作者
Pilar Vizcarra,Ana Moreno,María Jesús Vivancos,Alba García,Ricardo Pelazas González,Félix Gutiérrez,Diana Corona Mata,Pepa Galindo,Sònia Calzado,José Luis Casado
出处
期刊:Aids Patient Care and Stds [Mary Ann Liebert]
卷期号:37 (1): 11-21 被引量:1
标识
DOI:10.1089/apc.2022.0183
摘要

Current guidelines recommend screening people with HIV (PWH) for bone disease using predictive tools developed for the general population, although data on PWH are scarce. In this study, we assessed the performance of FRAX and QFracture scoring systems to predict the occurrence of fragility fractures in a prospective cohort of 17,671 adults with human immunodeficiency virus (HIV) included in the HIV/AIDS research network (CoRIS) in Spain. The survival estimates of fragility fractures during follow-up were calculated and FRAX and QFracture scores were computed at cohort inclusion. For both tools, discriminatory measures and the observed-to-expected (O/E) ratios were assessed. During a follow-up time of 42,411.55 person-years, 113 fragility fractures were recorded. Areas under the curve were 0.66 [95% confidence interval (95% CI) 0.61–0.71] for FRAX and 0.67 (95% CI 0.62–0.73) for QFracture for major osteoporotic fractures, and 0.72 (95% CI 0.57–0.88) and 0.81 (95% CI 0.68–0.95) for hip fracture, respectively. The O/E was 1.67 for FRAX and 5.49 for QFracture for major osteoporotic fractures, and 11.23 for FRAX and 4.87 for QFracture for hip fractures. Moreover, O/E raised as the risk increased for both tools and in almost all age groups. When using the recommended assessment thresholds, <6% and 10% of major osteoporotic and hip fractures would have been identified, respectively. In conclusion, FRAX and QFracture displayed acceptable discrimination, although both tools significantly underestimated the risk of fragility fractures in PWH. The recommended assessment thresholds may not be appropriate for this population as they were unable to identify individuals with fragility fractures during follow-up.
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