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基于人群的队列研究中皮质类固醇的使用与带状疱疹风险的关系。

Corticosteroid Use and Risk of Herpes Zoster in a Population-Based Cohort.

机构信息

School of Population Health, University of New South Wales, Sydney, NSW, Australia.

National Centre for Epidemiology and Population Health, Australian National University, Canberra, Australia; The Sax Institute, Sydney, NSW, Australia.

出版信息

Mayo Clin Proc. 2021 Nov;96(11):2843-2853. doi: 10.1016/j.mayocp.2021.05.029.

Abstract

OBJECTIVE

To examine the relationship between corticosteroid use and herpes zoster risk.

METHODS

With data from a large cohort of adults (the 45 and Up Study) recruited between 2006 and 2009 and linked to health data sets, the effect of corticosteroid use on zoster risk was analyzed by Cox proportional hazards models, adjusting for age, sex, and other characteristics.

RESULTS

During 602,152 person-years (median, 7.36 years) of follow-up, there were 20,048 new systemic corticosteroid users and 6294 incident herpes zoster events among 94,677 participants (zoster incidence, 11.0 per 1000 person-years). Compared with nonusers, the risk of zoster was 59% higher in those using systemic corticosteroids (adjusted hazard ratio [aHR], 1.59; 95% CI, 1.48 to 1.71) and greater with higher cumulative doses: aHR of 1.32 (95% CI, 1.17 to 1.48), 1.74 (95% CI, 1.55 to 1.95), and 1.80 (95% CI, 1.61 to 2.02) for use of less than 500 mg, 500 mg to less than 1000 mg, and 1000 mg or more prednisolone equivalents, respectively (P value for trend, <.001). Compared with nonusers, zoster risk increased significantly (aHR, 6.00; 95% CI, 4.85 to 7.42) in the month after a single prescription of systemic corticosteroids and returned to levels similar to those in nonusers by the third month after dispensing (aHR, 0.91; 95% CI, 0.49 to 1.69).

CONCLUSION

Practitioners should be alert to the increased risk of zoster among patients taking systemic corticosteroids. Given the significant morbidity from zoster, particularly in older adults, these findings support judicious prescribing of corticosteroids, including using as low a dose and as short a course as possible.

摘要

目的

探讨皮质类固醇使用与带状疱疹风险之间的关系。

方法

利用一项大型成人队列研究(45 and Up 研究)的数据(该研究于 2006 年至 2009 年间招募参与者,并与健康数据进行了关联),采用 Cox 比例风险模型分析了皮质类固醇使用对带状疱疹风险的影响,调整了年龄、性别和其他特征。

结果

在 602152 人年(中位数为 7.36 年)的随访期间,94677 名参与者中有 20048 名新的全身性皮质类固醇使用者和 6294 例带状疱疹事件(带状疱疹发病率为 11.0/1000 人年)。与非使用者相比,全身性皮质类固醇使用者的带状疱疹风险增加了 59%(调整后的风险比[HR],1.59;95%CI,1.48 至 1.71),且累积剂量越高风险越大:使用皮质类固醇剂量小于 500mg、500mg 至小于 1000mg 和 1000mg 或更多泼尼松龙等效剂量的 HR 分别为 1.32(95%CI,1.17 至 1.48)、1.74(95%CI,1.55 至 1.95)和 1.80(95%CI,1.61 至 2.02)(趋势检验 P 值<0.001)。与非使用者相比,单次处方全身性皮质类固醇后,带状疱疹风险显著增加(HR,6.00;95%CI,4.85 至 7.42),在配药后第三个月,风险恢复到与非使用者相似的水平(HR,0.91;95%CI,0.49 至 1.69)。

结论

医生应警惕接受全身性皮质类固醇治疗的患者带状疱疹风险增加。鉴于带状疱疹发病率较高,特别是在老年人中,这些发现支持合理处方皮质类固醇,包括使用尽可能低的剂量和尽可能短的疗程。

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