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符合条件的新冠病毒肺炎患者中奈玛特韦/利托那韦使用不足。

Underutilization of nirmatrelvir/ritonavir in eligible COVID-19 patients.

作者信息

de Arpe Celia Fortea, Homen Reynaldo, Valls-Carbó Adrian, Barrado Julia, Olmos-Mata Carolina, Pérez-Somarriba Juncal, Muñoz-Gomez Ana, Núñez-Orantos Maria Jose, Cabello-Clotet Noemí, Estrada Vicente

机构信息

Hospital Clinico San Carlos, Madrid, Spain.

Centro de investigación biomédica en red en enfermedades infecciosas (CIBERINFEC), Madrid, Spain.

出版信息

Eur J Clin Microbiol Infect Dis. 2025 Jun 13. doi: 10.1007/s10096-025-05150-4.

DOI:10.1007/s10096-025-05150-4
PMID:40512249
Abstract

Nirmatrelvir/ritonavir (NMV/r) might reduce the risk of hospitalization or death due to SARS-CoV2. Indirect data suggest that antiviral use among non-hospitalized patients is low. The aim of the study is to determine the number of patients admitted for COVID-19 who met the criteria to receive NMV/r prior to admission but did not receive it. We analyzed clinical data from electronic medical records of 132 patients who were hospitalized due to Covid-19 from August to November 2023. Among the 88 patients eligible for NMV/r before hospitalization, only 3.8% received it, even though 24.3% had previous contact with the healthcare system. Among those who were eligible for treatment, a potential drug interaction was identified in 80.6%; NMV/r was contraindicated in only ten cases (11.3%) due to a serious interaction, as it was deemed impossible to stop or alter it. Of the patients who did not receive treatment, three died from Covid-19, while there were no deaths in the treatment group. Our data confirm that many patients who could benefit from early treatment with NMV/r are not receiving it. This limited use may be linked to missed opportunities to prevent hospitalization and mortality from Covid-19.

摘要

奈玛特韦/利托那韦(NMV/r)可能会降低因严重急性呼吸综合征冠状病毒2(SARS-CoV2)导致的住院或死亡风险。间接数据表明,非住院患者中抗病毒药物的使用比例较低。本研究的目的是确定因新型冠状病毒肺炎(COVID-19)入院的患者中,那些在入院前符合接受NMV/r标准但未接受该治疗的患者数量。我们分析了2023年8月至11月因COVID-19住院的132例患者的电子病历临床数据。在88例住院前符合使用NMV/r条件的患者中,尽管有24.3%的患者此前曾与医疗系统接触,但只有3.8%的患者接受了该治疗。在符合治疗条件的患者中,80.6%的患者存在潜在药物相互作用;由于严重相互作用被认为无法停用或改变,仅10例(11.3%)患者禁忌使用NMV/r。在未接受治疗的患者中,有3例死于COVID-19,而治疗组无死亡病例。我们的数据证实,许多本可从NMV/r早期治疗中获益的患者并未接受该治疗。这种有限的使用可能与错过预防COVID-19住院和死亡的机会有关。

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Underutilization of nirmatrelvir/ritonavir in eligible COVID-19 patients.符合条件的新冠病毒肺炎患者中奈玛特韦/利托那韦使用不足。
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本文引用的文献

1
Low antiviral uptake of nirmatrelvir/ritonavir and molnupiravir in adult patients with COVID-19 in Taiwan in 2022.2022 年台湾成年 COVID-19 患者对奈玛特韦/利托那韦和莫努匹韦的抗病毒药物使用率较低。
J Glob Health. 2024 Nov 8;14:05032. doi: 10.7189/jogh.14.05032.
2
Nirmatrelvir for Vaccinated or Unvaccinated Adult Outpatients with Covid-19.奈玛特韦片/利托那韦片组合包装用于新冠病毒感染的成年门诊患者(接种或未接种疫苗)。
N Engl J Med. 2024 Apr 4;390(13):1186-1195. doi: 10.1056/NEJMoa2309003.
3
Real-world effectiveness of molnupiravir and nirmatrelvir plus ritonavir against mortality, hospitalisation, and in-hospital outcomes among community-dwelling, ambulatory patients with confirmed SARS-CoV-2 infection during the omicron wave in Hong Kong: an observational study.
奥密克戎变异株流行期间香港社区居住、活动的经实验室确诊的 2 型严重急性呼吸综合征冠状病毒 2 感染患者中莫努匹韦和奈玛特韦/利托那韦对比死亡率、住院率和住院结局的真实世界疗效:一项观察性研究。
Lancet. 2022 Oct 8;400(10359):1213-1222. doi: 10.1016/S0140-6736(22)01586-0.
4
Oral Nirmatrelvir for High-Risk, Nonhospitalized Adults with Covid-19.奈玛特韦片/利托那韦片组合包装口服药用于伴有进展为重症高风险因素的 COVID-19 门诊患者。
N Engl J Med. 2022 Apr 14;386(15):1397-1408. doi: 10.1056/NEJMoa2118542. Epub 2022 Feb 16.