{"id":23677,"date":"2023-04-13T04:37:00","date_gmt":"2023-04-12T20:37:00","guid":{"rendered":"http:\/\/csccm.org.cn\/?p=23677"},"modified":"2023-04-13T05:50:35","modified_gmt":"2023-04-12T21:50:35","slug":"lancet-infect-dis%e5%8f%91%e8%a1%a8%e8%ae%ba%e6%96%87%ef%bc%9a%e7%9c%9f%e5%ae%9e%e4%b8%96%e7%95%8c%e4%b8%ad%e5%a5%88%e7%8e%9b%e7%89%b9%e9%9f%a6-%e5%88%a9%e6%89%98%e9%82%a3%e9%9f%a6%e5%af%b9%e6%96%b0","status":"publish","type":"post","link":"https:\/\/csccm.org.cn\/?p=23677","title":{"rendered":"[Lancet Infect Dis\u53d1\u8868\u8ff0\u8bc4]\uff1a\u771f\u5b9e\u4e16\u754c\u4e2d\u5948\u739b\u7279\u97e6-\u5229\u6258\u90a3\u97e6\u5bf9\u65b0\u51a0\u75c5\u6bd2BA.4\u548cBA.5\u5965\u5bc6\u514b\u620e\u53d8\u5f02\u682a\u7684\u6709\u6548\u6027"},"content":{"rendered":"\n<p>COMMENT|<a href=\"https:\/\/www.thelancet.com\/journals\/laninf\/onlinefirst\">ONLINE FIRST<\/a><\/p>\n\n\n\n<h1 class=\"wp-block-heading\">Real-world effectiveness of nirmatrelvir\u2013ritonavir against BA.4 and BA.5 omicron SARS-CoV-2 variants<\/h1>\n\n\n\n<h3 class=\"wp-block-heading\"><span style=\"font-size: revert;\">Carlos K H Wong<\/span>, <a style=\"font-size: revert;\" href=\"mailto:carlosho@hku.hk\"><\/a><span style=\"font-size: revert;\">Kristy T K Lau, Gabriel M Leung<\/span><\/h3>\n\n\n\n<h3 class=\"wp-block-heading\">Lancet Infect Dis Published: February 10, 2023<\/h3>\n\n\n\n<h3 class=\"wp-block-heading\">DOI:<a href=\"https:\/\/doi.org\/10.1016\/S1473-3099(23)00056-7\">https:\/\/doi.org\/10.1016\/S1473-3099(23)00056-7<\/a><\/h3>\n\n\n\n<p id=\"para10\">Over the past year of the COVID-19 pandemic, populations worldwide have been facing the constant threat of the SARS-CoV-2 omicron variant and its sublineages, and the high transmissibility and substantial immune evasion properties of the variants have contributed to considerable numbers of hospitalisations and deaths. Nevertheless, with the increasing availability and access to novel oral antiviral drugs (eg, nirmatrelvir\u2013ritonavir and molnupiravir) and hybrid immunity induced by infection and COVID-19 prime-boost vaccines, the risk of progression to severe disease, hospitalisation, or death has reduced.<\/p>\n\n\n\n<p id=\"para20\">In&nbsp;<em>The Lancet Infectious Diseases<\/em>, Neil R Aggarwal and colleagues<a href=\"https:\/\/www.sciencedirect.com\/science\/article\/pii\/S1473309923000567#bib1\"><sup>1<\/sup><\/a>&nbsp;reported the real-world use of nirmatrelvir\u2013ritonavir among high-risk outpatients with COVID-19 during the omicron BA.2 and BA.2.12.1 (from March 26 to June 18, 2022) and BA.4 and BA.5 (from June 19 to Aug 25, 2022) waves in Colorado, USA. This retrospective cohort study used nirmatrelvir\u2013ritonavir order in the non-hospitalised setting as the time of exposure, and designated the SARS-CoV-2 positive test date as the index date (assumed to be 1 day before the recorded nirmatrelvir\u2013ritonavir order date if the positive test date was missing). After propensity-score matching, 7168 patients treated with nirmatrelvir\u2013ritonavir and 9361 untreated controls were included for analysis. Outpatient use of nirmatrelvir\u2013ritonavir was associated with significantly reduced odds of 28-day all-cause hospitalisation (adjusted odds ratio 0.45, 95% CI 0\u00b733\u20130\u00b762), the primary outcome of this study. Such clinical benefit was consistently observed during both omicron BA.2 and BA.2.12.1 and BA.4 and BA.5 predominant periods. Treatment with nirmatrelvir\u2013ritonavir was also associated with significantly reduced odds of 28-day all-cause mortality. Additionally, reduced odds of emergency department visits after nirmatrelvir\u2013ritonavir administration were observed among patients who were treated, compared with their untreated counterparts, suggesting that clinically significant rebound requiring urgent medical care was not observed more frequently among users of oral antivirals.<\/p>\n\n\n\n<p id=\"para30\">This study has provided timely information on the effectiveness of nirmatrelvir\u2013ritonavir against different sublineages of the omicron SARS-CoV-2 variant in a population with high COVID-19 vaccination coverage (over 78% of patients had received at least one dose, and over 57% had been boosted). Although several meta-analyses concluded similar reductions in the risk of hospitalisation or death with nirmatrelvir\u2013ritonavir use, the studies included were primarily done during the predominance of the delta variant (the pivotal EPIC-HR trial) or omicron BA.1 and BA.2 (most observational studies);<a href=\"https:\/\/www.sciencedirect.com\/science\/article\/pii\/S1473309923000567#bib2\">2<\/a>,&nbsp;<a href=\"https:\/\/www.sciencedirect.com\/science\/article\/pii\/S1473309923000567#bib3\">3<\/a>,&nbsp;<a href=\"https:\/\/www.sciencedirect.com\/science\/article\/pii\/S1473309923000567#bib4\">4<\/a>&nbsp;hence, this study by Aggarwal and colleagues has added information on the real-world use of nirmatrelvir\u2013ritonavir against omicron BA.4 and BA.5 sublineages, which are prevailing in some parts of the world. Another preprint cohort study has identified similar protection against hospitalisation and death with nirmatrelvir\u2013ritonavir use during a period characterised by the growth of omicron BA.5, yet its effectiveness appeared to have attenuated slightly compared with the pre-BA.5 period.<a href=\"https:\/\/www.sciencedirect.com\/science\/article\/pii\/S1473309923000567#bib5\"><sup>5<\/sup><\/a>&nbsp;Two more observational studies showed similar clinical benefits of early nirmatrelvir\u2013ritonavir use in outpatients with COVID-19 against various omicron sublineages, including BA.4 and BA.5; however, the results were not stratified to confirm the oral antiviral effectiveness against BA.4 and BA.5.<a href=\"https:\/\/www.sciencedirect.com\/science\/article\/pii\/S1473309923000567#bib6\">6<\/a>,&nbsp;<a href=\"https:\/\/www.sciencedirect.com\/science\/article\/pii\/S1473309923000567#bib7\">7<\/a><\/p>\n\n\n\n<p id=\"para40\">Acknowledging the absence of a SARS-CoV-2 positive test date for the majority of their patients treated with nirmatrelvir\u2013ritonavir, Aggarwal and colleagues<a href=\"https:\/\/www.sciencedirect.com\/science\/article\/pii\/S1473309923000567#bib1\"><sup>1<\/sup><\/a>&nbsp;did a sensitivity analysis using a 3-day difference between the oral antiviral order date and assumed positive test date, and obtained similar results. Notably, symptom duration before the nirmatrelvir\u2013ritonavir order date was also not available, and the missingness of these data might preclude accurate interpretation of the findings in relation to the optimal timing of oral antiviral initiation, as evidence has shown that late receipt of nirmatrelvir\u2013ritonavir (&gt;5 days after symptom onset) was associated with a considerable decrease in treatment effectiveness against hospitalisation and death.<a href=\"https:\/\/www.sciencedirect.com\/science\/article\/pii\/S1473309923000567#bib7\"><sup>7<\/sup><\/a><\/p>\n\n\n\n<p id=\"para50\">At the time of writing, emerging and recombinant variants of omicron continue to pose an imminent threat to public health, especially XBB.1.5 and BQ.1.1, which have even greater immune evasion capabilities than BA.5. While in-vitro evidence has shown susceptibility of BQ.1.1 and XBB to remdesivir, molnupiravir, and nirmatrelvir similar to omicron BA.2 and BA.5,<a href=\"https:\/\/www.sciencedirect.com\/science\/article\/pii\/S1473309923000567#bib8\"><sup>8<\/sup><\/a>&nbsp;real-world studies are needed to evaluate relative effectiveness in different populations and health-care settings. This need is particularly relevant in the assessment of cost-effectiveness for different therapeutic strategies and their prioritisation for various patient populations, as the number needed to treat to prevent one case of severe COVID-19 might also increase in view of the growing population immunity.<a href=\"https:\/\/www.sciencedirect.com\/science\/article\/pii\/S1473309923000567#bib5\">5<\/a>,&nbsp;<a href=\"https:\/\/www.sciencedirect.com\/science\/article\/pii\/S1473309923000567#bib9\">9<\/a>&nbsp;Further research is needed to investigate the COVID-19 rebound phenomenon and its associated clinical consequences among oral antiviral users and non-users infected with emerging or recombinant variants, as higher incidences of COVID-19 rebound infections and symptoms after nirmatrelvir\u2013ritonavir treatment have been observed in a patient cohort with omicron BA.5 patient cohort compared with a cohort with BA.2.12.1.<a href=\"https:\/\/www.sciencedirect.com\/science\/article\/pii\/S1473309923000567#bib10\"><sup>10<\/sup><\/a>&nbsp;Finally, active pharmacovigilance programmes and monitoring of any viral mutations that might confer resistance to existing antivirals remain crucial.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>COMMENT|ONLINE FIRST Real-world effectiveness of nirmat [&hellip;]<\/p>\n","protected":false},"author":3,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[24,23],"tags":[],"_links":{"self":[{"href":"https:\/\/csccm.org.cn\/index.php?rest_route=\/wp\/v2\/posts\/23677"}],"collection":[{"href":"https:\/\/csccm.org.cn\/index.php?rest_route=\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/csccm.org.cn\/index.php?rest_route=\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/csccm.org.cn\/index.php?rest_route=\/wp\/v2\/users\/3"}],"replies":[{"embeddable":true,"href":"https:\/\/csccm.org.cn\/index.php?rest_route=%2Fwp%2Fv2%2Fcomments&post=23677"}],"version-history":[{"count":2,"href":"https:\/\/csccm.org.cn\/index.php?rest_route=\/wp\/v2\/posts\/23677\/revisions"}],"predecessor-version":[{"id":23679,"href":"https:\/\/csccm.org.cn\/index.php?rest_route=\/wp\/v2\/posts\/23677\/revisions\/23679"}],"wp:attachment":[{"href":"https:\/\/csccm.org.cn\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=23677"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/csccm.org.cn\/index.php?rest_route=%2Fwp%2Fv2%2Fcategories&post=23677"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/csccm.org.cn\/index.php?rest_route=%2Fwp%2Fv2%2Ftags&post=23677"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}