Department of Internal Medicine, St. Antonius Hospital, Utrecht/Nieuwegein, The Netherlands.
Department of Internal Medicine, Leiden University Medical Centre, Leiden, The Netherlands.
Int J Obes (Lond). 2022 Nov;46(11):2000-2005. doi: 10.1038/s41366-022-01204-1. Epub 2022 Aug 19.
A fixed 6 mg dexamethasone dose for 10 days is the standard treatment for all hospitalised COVID-19 patients who require supplemental oxygen. Yet, the pharmacokinetic properties of dexamethasone can lead to diminishing systemic dexamethasone exposure with increasing body mass index (BMI). The present study examines whether this translates to overweight and obesity being associated with worse clinical outcomes, defined as ICU admission or in hospital death, in COVID-19 patients treated with fixed-dose dexamethasone.
We conducted a single centre retrospective cohort study in COVID-19 patients who were admitted to a non-ICU ward and were treated with dexamethasone (6 mg once daily for a maximum of ten days) between June 2020 and January 2021. Univariable and multivariable logistic regression analyses were conducted to assess the association between BMI-categories and an unfavourable clinical course (ICU admission and/or in hospital death). Analyses were adjusted for age, comorbidities, inflammatory status, and oxygen requirement at admission. For reference, similar analyses were repeated in a cohort of patients hospitalised before dexamethasone was introduced (March 2020 through May 2020).
In patients treated with dexamethasone (n = 385) an unfavourable clinical course was most prevalent in patients with normal weight (BMI < 25) compared to patients with overweight (BMI 25-30) and patients with obesity (BMI ≥ 30) with percentages of 33, 26 and 21% respectively. In multivariable analyses, there was no association between BMI-category and an unfavourable clinical course (respectively with aORs of 0.81 (0.43-1.53) and 0.61 (0.30-1.27) with normal weight as reference). In the reference cohort (n = 249) the opposite was observed with an unfavourable clinical course being most prevalent in patients with overweight (39% vs 28%; aOR 2.17 (0.99-4.76)). In both cohorts, CRP level at admission was higher and lymphocyte count was lower in patients with normal weight compared to patients with obesity.
Overweight and obesity are not associated with an unfavourable clinical course in COVID-19 patients admitted to a non-ICU ward and treated with 6 mg dexamethasone once daily.
对于所有需要补充氧气的住院 COVID-19 患者,固定剂量的 6 毫克地塞米松治疗 10 天是标准治疗方法。然而,地塞米松的药代动力学特性可能导致随着体重指数(BMI)的增加,全身地塞米松暴露量减少。本研究旨在探讨超重和肥胖是否与 COVID-19 患者接受固定剂量地塞米松治疗后的临床结局恶化有关,定义为 ICU 入院或住院死亡。
我们进行了一项单中心回顾性队列研究,纳入了 2020 年 6 月至 2021 年 1 月期间入住非 ICU 病房并接受地塞米松(每天 6 毫克,最多 10 天)治疗的 COVID-19 患者。采用单变量和多变量逻辑回归分析评估 BMI 类别与不良临床病程(ICU 入院和/或住院死亡)之间的关系。分析调整了年龄、合并症、炎症状态和入院时的氧需求。作为参考,在引入地塞米松之前(2020 年 3 月至 2020 年 5 月)住院的患者队列中重复了类似的分析。
在接受地塞米松治疗的患者(n=385)中,与正常体重(BMI<25)相比,超重(BMI 25-30)和肥胖(BMI≥30)患者的不良临床病程更为常见,分别为 33%、26%和 21%。多变量分析显示,BMI 类别与不良临床病程之间无关联(分别为正常体重的 OR 值为 0.81(0.43-1.53)和 0.61(0.30-1.27))。在参考队列(n=249)中,观察到相反的情况,不良临床病程最常见于超重患者(39% vs 28%;OR 2.17(0.99-4.76))。在两个队列中,与肥胖患者相比,入院时 CRP 水平较高,淋巴细胞计数较低。
在入住非 ICU 病房并接受每日 6 毫克地塞米松治疗的 COVID-19 患者中,超重和肥胖与不良临床病程无关。