Pander Jan, Termorshuizen Fabian, de Lange Dylan W, Beekman-Hendriks Wendy, Lanfermeijer Josien, Bakhshi-Raiez Ferishta, Dongelmans Dave A
AstraZeneca BV, PO Box 93015, 2509 AA, Den Haag, The Netherlands.
National Intensive Care Evaluation (NICE) Foundation, Postbus 23640, 1100 EC, Amsterdam, The Netherlands.
Infect Dis Ther. 2025 Apr;14(4):881-888. doi: 10.1007/s40121-025-01122-5. Epub 2025 Mar 14.
The corona virus disease 19 (COVID-19) pandemic has presented a global health challenge, and several consecutive variants of the severe acute respiratory syndrome-corona virus-2 (SARS-CoV-2) virus have been dominant. Previous studies highlighted decreased mortality rates during the predominance of the omicron variant; however, severely immunocompromised individuals remained at high risk due to limited vaccine response. This study aims to compare mortality rates during the omicron period between immunocompromised and non-immunocompromised patients in intensive care units (ICUs) in The Netherlands.
Utilizing data from the Dutch National Intensive Care Evaluation (NICE) registry, this study analyzed ICU admissions due to COVID-19 from February 2022 to December 2023. Patients were categorized as immunocompromised based on recorded immunologic insufficiencies or associated conditions. A historical cohort of viral pneumonia patients from 2017 to 2019 was used for comparison. Logistic regression analyses, adjusted for age, gender, body-mass index (BMI), and acute physiology and chronic health evaluation IV (APACHE-IV) mortality risk, compared in-hospital and ICU mortality and length of stay between groups. A sensitivity analysis excluded early omicron period admissions to assess the consistency of findings.
Among 1491 patients admitted to the ICU due to COVID-19, 29.5% were immunocompromised, showing significantly higher in-hospital adjusted odds ratio (OR = 1.56, 95% CI 1.20-2.04) and ICU mortality (OR = 1.64, 95% CI 1.25-2.17) compared to non-immunocompromised patients. The historical cohort exhibited lower mortality rates for immunocompromised individuals compared to the COVID-19 cohort. Sensitivity analysis confirmed these trends, with slight attenuation of odds ratios.
Immunocompromised patients admitted to the ICU due to COVID-19 during the omicron period had higher mortality than non-immunocompromised patients. Additionally, immunocompromised patients with COVID-19 had higher mortality than immunocompromised patients with other viral pneumonias. Our results provide additional evidence that COVID-19 is still a significant health concern to immunocompromised individuals, which warrants specific and effective measures to protect this vulnerable group.
2019年冠状病毒病(COVID-19)大流行带来了全球健康挑战,严重急性呼吸综合征冠状病毒2(SARS-CoV-2)病毒的几个连续变种一直占据主导地位。先前的研究强调了在奥密克戎变种占主导期间死亡率有所下降;然而,由于疫苗反应有限,严重免疫功能低下的个体仍然处于高风险之中。本研究旨在比较荷兰重症监护病房(ICU)中免疫功能低下和非免疫功能低下患者在奥密克戎时期的死亡率。
利用荷兰国家重症监护评估(NICE)登记处的数据,本研究分析了2022年2月至2023年12月因COVID-19入住ICU的患者情况。根据记录的免疫功能不全或相关疾病,将患者分类为免疫功能低下。使用2017年至2019年病毒性肺炎患者的历史队列作为对照。在对年龄、性别、体重指数(BMI)和急性生理学与慢性健康状况评估IV(APACHE-IV)死亡风险进行调整后,通过逻辑回归分析比较了两组患者的院内死亡率、ICU死亡率和住院时间。一项敏感性分析排除了奥密克戎早期入住ICU的患者,以评估研究结果的一致性。
在1491例因COVID-19入住ICU的患者中,29.5%为免疫功能低下患者,与非免疫功能低下患者相比,其院内调整后的优势比(OR = 1.56,95%可信区间1.20 - 2.04)和ICU死亡率(OR = 1.64,95%可信区间1.25 - 2.17)显著更高。与COVID-19队列相比,历史队列中免疫功能低下个体的死亡率较低。敏感性分析证实了这些趋势,优势比略有下降。
在奥密克戎时期因COVID-19入住ICU的免疫功能低下患者的死亡率高于非免疫功能低下患者。此外,患有COVID-19的免疫功能低下患者的死亡率高于患有其他病毒性肺炎的免疫功能低下患者。我们的结果提供了额外的证据,表明COVID-19仍然是免疫功能低下个体的一个重大健康问题,这需要采取具体有效的措施来保护这一弱势群体。