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奈玛特韦/利托那韦片的临床疗效评价:文献综述。

Clinical Effectiveness of Ritonavir-Boosted Nirmatrelvir-A Literature Review.

机构信息

FG Verkehrssystemplanung und Verkehrstelematik, Technische Universität Berlin, 10623 Berlin, Germany.

Zuse Institute Berlin, Takustraße 7, 14195 Berlin, Germany.

出版信息

Adv Respir Med. 2024 Jan 18;92(1):66-76. doi: 10.3390/arm92010009.

Abstract

Nirmatrelvir/Ritonavir is an oral treatment for mild to moderate COVID-19 cases with a high risk for a severe course of the disease. For this paper, a comprehensive literature review was performed, leading to a summary of currently available data on Nirmatrelvir/Ritonavir's ability to reduce the risk of progressing to a severe disease state. Herein, the focus lies on publications that include comparisons between patients receiving Nirmatrelvir/Ritonavir and a control group. The findings can be summarized as follows: Data from the time when the Delta-variant was dominant show that Nirmatrelvir/Ritonavir reduced the risk of hospitalization or death by 88.9% for unvaccinated, non-hospitalized high-risk individuals. Data from the time when the Omicron variant was dominant found decreased relative risk reductions for various vaccination statuses: between 26% and 65% for hospitalization. The presented papers that differentiate between unvaccinated and vaccinated individuals agree that unvaccinated patients benefit more from treatment with Nirmatrelvir/Ritonavir. However, when it comes to the dependency of potential on age and comorbidities, further studies are necessary. From the available data, one can conclude that Nirmatrelvir/Ritonavir cannot substitute vaccinations; however, its low manufacturing cost and easy administration make it a valuable tool in fighting COVID-19, especially for countries with low vaccination rates.

摘要

尼马瑞韦/利托那韦是一种用于治疗轻度至中度 COVID-19 病例的口服药物,这些病例存在疾病严重恶化的高风险。本文进行了全面的文献回顾,总结了尼马瑞韦/利托那韦降低疾病严重程度风险的现有数据。本文重点关注包含尼马瑞韦/利托那韦组与对照组比较的出版物。研究结果可以总结如下:当 Delta 变体占主导地位时的数据表明,对于未接种疫苗、未住院的高危人群,尼马瑞韦/利托那韦将住院或死亡的风险降低了 88.9%。当 Omicron 变体占主导地位时的数据发现,各种疫苗接种状态下的相对风险降低了:住院的风险降低了 26%至 65%。区分未接种疫苗和接种疫苗个体的论文一致认为,未接种疫苗的患者从尼马瑞韦/利托那韦治疗中获益更多。然而,当涉及到潜在获益与年龄和合并症的相关性时,还需要进一步的研究。从现有数据可以得出结论,尼马瑞韦/利托那韦不能替代疫苗接种;然而,其低廉的制造成本和易于管理使其成为抗击 COVID-19 的一种有价值的工具,尤其是在疫苗接种率较低的国家。

相似文献

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Nirmatrelvir combined with ritonavir for preventing and treating COVID-19.奈玛特韦/利托那韦片用于 COVID-19 的预防和治疗。
Cochrane Database Syst Rev. 2023 Nov 30;11(11):CD015395. doi: 10.1002/14651858.CD015395.pub3.

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