Weil Clara, Tene Lilac, Chodick Gabriel, Fallach Noga, Ansari Wajeeha, Distelman-Menachem Tal, Maor Yasmin
Maccabi Institute for Research and Innovation, Maccabi Healthcare Services, Tel Aviv 6812509, Israel.
Pfizer Inc., New York, NY 10017, USA.
J Clin Med. 2024 Oct 12;13(20):6091. doi: 10.3390/jcm13206091.
Nirmatrelvir-ritonavir was granted emergency use authorization in Israel in January 2022 to treat high-risk patients with mild-to-moderate COVID-19. The aim of the study was to assess the association between nirmatrelvir-ritonavir treatment and COVID-19-related hospitalization and healthcare resource utilization (HCRU) in a country with a high level of vaccinations compared to patients who were offered treatment and declined. The Maccabi Healthcare Services dataset was used to identify high-risk SARS-CoV-2-positive adults from January to February 2022 who received nirmatrelvir-ritonavir within 5 days of symptom onset (treatment group) or who were offered nirmatrelvir-ritonavir treatment and declined it (reference group). COVID-19-related hospitalizations and all-cause mortality and HCRU within 30 days were compared between treatment and reference groups using inverse probability of treatment weighting. Treatment and reference groups included 3460 (median age, 68.4 years) and 1654 (70.2 years) patients, respectively. Patients with ≥1 dose of COVID-19 vaccine accounted for 89.5% (treatment group) and 72.1% (reference group) of the total. Treatment was associated with a lower risk of COVID-19-related hospitalization (adjusted OR, 0.59 [95% CI, 0.41,0.83]). Results were similar by age group (18-64/≥65 years) and among patients with/without vaccination in the prior 180 days. There were 11 (0.3%) versus 11 (0.7%) deaths in the treatment and reference groups, respectively. Treated patients had lower inpatient HCRU and greater less intensive outpatient HCRU (e.g., telemedicine and emergency room visits). Nirmatrelvir-ritonavir treatment was associated with a reduced risk of COVID-19-related hospitalization and a shift to less intensive outpatient HCRU. Comparison with a reference group of nirmatrelvir-ritonavir-eligible patients who declined treatment enabled an unbiased outcome assessment. Real-world data gathered during the Omicron BA.1 variant wave of COVID-19 in Israel support the continued use of nirmatrelvir-ritonavir for high-risk adults of all ages, regardless of previous vaccinations.
2022年1月,奈玛特韦-利托那韦在以色列获得紧急使用授权,用于治疗轻至中度新冠病毒病(COVID-19)的高危患者。本研究的目的是评估在一个疫苗接种率较高的国家,与接受奈玛特韦-利托那韦治疗但拒绝治疗的患者相比,奈玛特韦-利托那韦治疗与COVID-19相关住院及医疗资源利用(HCRU)之间的关联。利用马卡比医疗服务数据集,识别出2022年1月至2月期间症状出现5天内接受奈玛特韦-利托那韦治疗的高危严重急性呼吸综合征冠状病毒2(SARS-CoV-2)阳性成年人(治疗组),以及被提供奈玛特韦-利托那韦治疗但拒绝治疗的患者(参照组)。采用治疗权重的逆概率方法,比较治疗组和参照组30天内COVID-19相关住院、全因死亡率及HCRU情况。治疗组和参照组分别纳入3460例(中位年龄68.4岁)和1654例(70.2岁)患者。接种≥1剂COVID-19疫苗的患者分别占治疗组总数的89.5%和参照组总数的72.1%。治疗与COVID-19相关住院风险较低相关(校正比值比,0.59[95%置信区间,0.41,0.83])。按年龄组(18 - 64岁/≥65岁)以及过去180天内接种/未接种疫苗的患者分层,结果相似。治疗组和参照组分别有11例(0.3%)和11例(0.7%)死亡。接受治疗的患者住院HCRU较低,强度较低的门诊HCRU(如远程医疗和急诊就诊)较多。奈玛特韦-利托那韦治疗与COVID-19相关住院风险降低以及向强度较低的门诊HCRU转变相关。与拒绝治疗的符合奈玛特韦-利托那韦治疗条件的患者参照组进行比较,能够进行无偏倚的结果评估。在以色列奥密克戎BA.1变异株流行期间收集的真实世界数据支持继续对所有年龄段的高危成年人使用奈玛特韦-利托那韦,无论其既往是否接种过疫苗。