在 COVID-19 大流行期间,地诺单抗的按时用药量迅速恢复,但仍未达到最佳水平

IF 3.4 Q2 ENDOCRINOLOGY & METABOLISM
JBMR Plus Pub Date : 2024-04-09 DOI:10.1093/jbmrpl/ziae027
Anna M Rzepka, Angela M Cheung, Sandra Kim, Tara Gomes, Suzanne M Cadarette
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引用次数: 0

摘要

摘要 在骨质疏松症治疗中,每 6 个月及时服用一次地诺单抗对于避免停用或延迟服用地诺单抗后出现多发性椎体骨折的风险至关重要。本研究旨在估算 COVID-19 大流行对地诺单抗用药时间的直接和长期影响。我们利用安大略省药物福利数据确定了居住在社区的老年人(≥66 岁),他们应在 2016 年 1 月至 2020 年 12 月期间接受地诺单抗治疗。我们完成了一项间断时间序列分析,以估计 COVID-19 大流行(2020 年 3 月)对每月按时服用地诺单抗剂量(183 +/-30 d)比例的影响。分析按使用者类型进行了分层:第二次服药到期的患者(新使用者)、第三次或第四次服药的患者(中间使用者)或≥5 次服药的患者(成熟使用者)。在其他分析中,我们考虑了居住在疗养院的患者、改用其他骨质疏松症药物的患者,并报告了截至 2022 年 2 月的趋势。我们研究了 148 554 名患者(90.9% 为女性,平均 [SD] 年龄为 79.6 [8.0] 岁),他们接受了 648 221 次地诺单抗治疗。大流行前按时治疗的平均比例在社区中保持稳定,但因使用者类型而异:新使用者占 64.9%,中级使用者占 72.3%,高级使用者占 78.0%。我们发现,在大流行开始时,所有用户类型的按时服药比例立即出现整体下降:-17.8%(95% CI,-19.6,-16.0)。在疗养院,大流行前各类用户的按时治疗比例相似(平均 83.5%),但在大流行开始时略有下降:-3.2%(95% CI,-5.0,-1.2)。到 2020 年 10 月,按时服药率已恢复到大流行前的水平,且未受到转换疗法的影响。尽管截至 2022 年 2 月,按时给药情况保持稳定,但社区中仍有约四分之一的患者没有按时接受地诺单抗治疗。总之,虽然大流行对地诺单抗剂量的干扰是暂时的,但按时治疗的水平仍未达到最佳。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
On-time denosumab dosing recovered rapidly during the COVID-19 pandemic, yet remains suboptimal
Abstract Timely administration of denosumab every 6 mo is critical in osteoporosis treatment to avoid multiple vertebral fracture risk upon denosumab discontinuation or delay. This study aimed to estimate the immediate and prolonged impact of the COVID-19 pandemic on the timing of denosumab doses. We identified older adults (≥66 yr) residing in the community who were due to receive denosumab between January 2016 and December 2020 using Ontario Drug Benefit data. We completed an interrupted time-series analysis to estimate the impact of the COVID-19 pandemic (March 2020) on the monthly proportion of on-time denosumab doses (183 +/−30 d). Analyses were stratified by user type: patients due for their second dose (novice users), third or fourth dose (intermediate users), or ≥5th dose (established users). In additional analyses, we considered patients living in nursing homes, switching to other osteoporosis drugs, and reported trends until February 2022. We studied 148 554 patients (90.9% female, mean [SD] age 79.6 [8.0] yr) receiving 648 221 denosumab doses. The average pre-pandemic proportion of on-time therapy was steady in the community, yet differed by user type: 64.9% novice users, 72.3% intermediate users, and 78.0% established users. We identified an immediate overall decline in the proportion of on-time doses across all user types at the start of the pandemic: −17.8% (95% CI, −19.6, −16.0). In nursing homes, the pre-pandemic proportion of on-time therapy was similar across user types (average 83.5%), with a small decline at the start of the pandemic: −3.2% (95% CI, −5.0, −1.2). On-time therapy returned to pre-pandemic levels by October 2020 and was not impacted by therapy switching. Although on-time dosing remains stable as of February 2022, approximately one-fourth of patients in the community do not receive denosumab on-time. In conclusion, although pandemic disruptions to denosumab dosing were temporary, levels of on-time therapy remain suboptimal.
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来源期刊
JBMR Plus
JBMR Plus Medicine-Orthopedics and Sports Medicine
CiteScore
5.80
自引率
2.60%
发文量
103
审稿时长
8 weeks
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