硬膜外类固醇注射与患有神经根病的老年人的骨折发生率。

IF 5.1 1区 医学 Q1 ENDOCRINOLOGY & METABOLISM Journal of Bone and Mineral Research Pub Date : 2024-09-30 DOI:10.1093/jbmr/zjae162
Huifeng Yun, Ye Liu, Jeffrey R Curtis, Kenneth Saag, Gia D'Erasmo, Katherine Haseltine, Emily M Stein
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引用次数: 0

摘要

硬膜外类固醇注射(ESI)是治疗根性背痛的一种常见且通常有效的方法。虽然口服糖皮质激素会增加骨折的发生率,但人们对ESI后的骨折风险知之甚少。本研究调查了接受过 ESI 和没有接受过 ESI 的人的骨折发生率。我们假设,接受 ESI 会增加骨质疏松性骨折,尤其是椎体骨折的发生率。我们使用 2005-2018 年 5% 的医疗保险数据,通过暴露密度采样(EDS),按照年龄、性别和根性疼痛诊断月份,将接受过≥1 次 ESI 的根性疼痛患者与未接受过 ESI 的患者(非 ESI)进行 1:10 匹配。根据多个数据维度的前 500 个协变量计算出的高维倾向得分 (HDPS),ESI 和非 ESI 患者进行了 1:1 匹配。骨折是通过有效的 ICD-9/10 诊断代码确定的。按组别计算骨折发生率(IR),并使用 Cox 回归法比较危险比(HR)。通过 EDS 确定了符合资格标准的 25 062 名 ESI 患者和 221 735 名非 ESI 患者。平均年龄为 76 岁(74% 为女性)。在接受过 ESI 治疗的患者中,有 2296 例骨折,IR 为 49.1(95% CI:47.2-51.2)/1000 人年。在未接受ESI治疗的患者中,有11 917人发生骨折,IR值为35.2(95% CI:34.5-35.8)。接受ESI治疗的患者在典型的骨质疏松部位发生骨折的风险更大,根据EDS计算,HR为1.39(95% CI为1.33-1.46),根据HDPS计算,HR为1.32(1.12-1.54);发生脊椎骨折的风险更大,根据EDS计算,HR为1.54(1.45-1.64),根据HDPS计算,HR为1.69(1.38-2.07)。接受较多累积 ESI 剂量(1 年内≥3 次)的患者在随访的前 6 个月内发生骨折的风险较高。老年人接触 ESI 会增加骨折风险,这表明 ESI 可能会对骨骼产生持久的有害影响。有必要进一步研究降低这一人群骨折风险的策略。
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Epidural Steroid Injections and Fracture Incidence Among Older Individuals with Radiculopathy.

Epidural steroid injections (ESIs) are a common and often effective treatment for radicular back pain. While oral glucocorticoids increase fracture incidence, little is known regarding fracture risk after ESI. This study investigated the incidence of fractures among individuals who received ESI and those who did not. We hypothesized that ESI exposure would be associated with an increased incidence of osteoporotic fracture and specifically vertebral fractures. Using 2005-2018 5% Medicare data, individuals with radicular pain who had ≥1 ESI and those who did not (non-ESI) were matched 1:10 by age, sex, and month of radicular pain diagnosis using exposure density sampling (EDS). Using a high-dimensional propensity score (HDPS) calculated based on the top 500 covariates across multiple data dimensions, ESI and non-ESI individuals were matched 1:1. Fractures were identified using validated ICD-9/10 diagnosis codes. Fracture incidence rate (IR) was calculated by group, and hazard ratios (HR) compared using Cox regression. 25 062 ESI patients and 221 735 non-ESI patients who met eligibility criteria were identified using EDS. Mean age was 76 years (74% female). Among ESI-treated individuals, there were 2296 fractures, IR 49.1 (95% CI: 47.2-51.2) per 1000 person years. For non-ESI individuals, there were 11 917 fractures, IR 35.2 (95% CI: 34.5-35.8). Individuals who received ESI had a greater hazard of fracture at typical osteoporotic sites, HR 1.39 (95% CI 1.33-1.46) by EDS and 1.32 (1.12-1.54) by HDPS, and greater hazard of vertebral fracture, 1.54 (1.45-1.64) by EDS and 1.69 (1.38-2.07) by HDPS. Patients who received greater cumulative ESI doses (≥3 in 1 year) had a higher risk of fractures within the first six months of follow-up. ESI exposure in older individuals is associated with an increased risk of fracture, suggesting there may be lasting detrimental skeletal effects of ESI. Further research into strategies to reduce fracture risk in this population is warranted.

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来源期刊
Journal of Bone and Mineral Research
Journal of Bone and Mineral Research 医学-内分泌学与代谢
CiteScore
11.30
自引率
6.50%
发文量
257
审稿时长
2 months
期刊介绍: The Journal of Bone and Mineral Research (JBMR) publishes highly impactful original manuscripts, reviews, and special articles on basic, translational and clinical investigations relevant to the musculoskeletal system and mineral metabolism. Specifically, the journal is interested in original research on the biology and physiology of skeletal tissues, interdisciplinary research spanning the musculoskeletal and other systems, including but not limited to immunology, hematology, energy metabolism, cancer biology, and neurology, and systems biology topics using large scale “-omics” approaches. The journal welcomes clinical research on the pathophysiology, treatment and prevention of osteoporosis and fractures, as well as sarcopenia, disorders of bone and mineral metabolism, and rare or genetically determined bone diseases.
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