Tixagevimab-cilgavimab for preventing breakthrough COVID-19 in dialysis patients: a prospective study.

IF 3.9 2区 医学 Q1 UROLOGY & NEPHROLOGY Clinical Kidney Journal Pub Date : 2024-10-18 eCollection Date: 2024-11-01 DOI:10.1093/ckj/sfae309
Sarinya Boongird, Thatsaphan Srithongkul, Sethanant Sethakarun, Jackrapong Bruminhent, Sasisopin Kiertiburanakul, Arkom Nongnuch, Chagriya Kitiyakara, Suchai Sritippayawan
{"title":"Tixagevimab-cilgavimab for preventing breakthrough COVID-19 in dialysis patients: a prospective study.","authors":"Sarinya Boongird, Thatsaphan Srithongkul, Sethanant Sethakarun, Jackrapong Bruminhent, Sasisopin Kiertiburanakul, Arkom Nongnuch, Chagriya Kitiyakara, Suchai Sritippayawan","doi":"10.1093/ckj/sfae309","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>The effectiveness of tixagevimab-cilgavimab as pre-exposure prophylaxis (PrEP) against breakthrough coronavirus disease 2019 (COVID-19) in dialysis patients remains uncertain due to limited data.</p><p><strong>Methods: </strong>In this multicenter prospective study, we enrolled vaccinated dialysis patients and divided them into two groups: a tixagevimab-cilgavimab group (received a 150 mg/150 mg intramuscular dose of tixagevimab-cilgavimab) and a control group (age-matched patients not receiving tixagevimab-cilgavimab). The primary outcome was the breakthrough COVID-19 rate at 6 months, whereas secondary outcomes included COVID-19-related hospitalization, intensive care unit admission, endotracheal intubation and mortality. The safety of tixagevimab-cilgavimab was assessed.</p><p><strong>Results: </strong>Two hundred participants were enrolled, with equal numbers in each group (<i>n</i> = 100 each). Baseline characteristics were comparable between groups, except for a higher number of COVID-19 vaccine doses in the tixagevimab-cilgavimab group [median (IQR) 4 (3-5) vs. 3 (3-4); <i>P</i> = .01]. At 6 months, the breakthrough COVID-19 rates were comparable between the tixagevimab-cilgavimab (17%) and control (15%) groups (<i>P</i> = .66). However, the median (IQR) time to diagnosis of breakthrough infections tended to be longer in the tixagevimab-cilgavimab group [4.49 (2.81-4.98) vs 1.96 (1.65-2.91) months; <i>P</i> = .08]. Tixagevimab-cilgavimab significantly reduced COVID-19-related hospitalization rates (5.9% vs 40.0%; <i>P</i> = .02) among participants with breakthrough infections. All tixagevimab-cilgavimab-related adverse events were mild.</p><p><strong>Conclusion: </strong>The use of tixagevimab-cilgavimab as PrEP in vaccinated dialysis patients during the Omicron surge did not prevent breakthrough infections but significantly reduced COVID-19-related hospitalizations. Further research should prioritize alternative strategies.</p>","PeriodicalId":10435,"journal":{"name":"Clinical Kidney Journal","volume":"17 11","pages":"sfae309"},"PeriodicalIF":3.9000,"publicationDate":"2024-10-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11558061/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinical Kidney Journal","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1093/ckj/sfae309","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/11/1 0:00:00","PubModel":"eCollection","JCR":"Q1","JCRName":"UROLOGY & NEPHROLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Background: The effectiveness of tixagevimab-cilgavimab as pre-exposure prophylaxis (PrEP) against breakthrough coronavirus disease 2019 (COVID-19) in dialysis patients remains uncertain due to limited data.

Methods: In this multicenter prospective study, we enrolled vaccinated dialysis patients and divided them into two groups: a tixagevimab-cilgavimab group (received a 150 mg/150 mg intramuscular dose of tixagevimab-cilgavimab) and a control group (age-matched patients not receiving tixagevimab-cilgavimab). The primary outcome was the breakthrough COVID-19 rate at 6 months, whereas secondary outcomes included COVID-19-related hospitalization, intensive care unit admission, endotracheal intubation and mortality. The safety of tixagevimab-cilgavimab was assessed.

Results: Two hundred participants were enrolled, with equal numbers in each group (n = 100 each). Baseline characteristics were comparable between groups, except for a higher number of COVID-19 vaccine doses in the tixagevimab-cilgavimab group [median (IQR) 4 (3-5) vs. 3 (3-4); P = .01]. At 6 months, the breakthrough COVID-19 rates were comparable between the tixagevimab-cilgavimab (17%) and control (15%) groups (P = .66). However, the median (IQR) time to diagnosis of breakthrough infections tended to be longer in the tixagevimab-cilgavimab group [4.49 (2.81-4.98) vs 1.96 (1.65-2.91) months; P = .08]. Tixagevimab-cilgavimab significantly reduced COVID-19-related hospitalization rates (5.9% vs 40.0%; P = .02) among participants with breakthrough infections. All tixagevimab-cilgavimab-related adverse events were mild.

Conclusion: The use of tixagevimab-cilgavimab as PrEP in vaccinated dialysis patients during the Omicron surge did not prevent breakthrough infections but significantly reduced COVID-19-related hospitalizations. Further research should prioritize alternative strategies.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
预防透析患者突破性 COVID-19 的 Tixagevimab-cilgavimab 前瞻性研究。
背景:由于数据有限,透析患者使用替沙吉单抗-西格维单抗作为暴露前预防疗法(PrEP)预防2019年突破性冠状病毒病(COVID-19)的效果仍不确定:在这项多中心前瞻性研究中,我们招募了已接种疫苗的透析患者,并将其分为两组:替沙吉单抗-替加维单抗组(接受150毫克/150毫克的替沙吉单抗-替加维单抗肌肉注射剂量)和对照组(未接受替沙吉单抗-替加维单抗的年龄匹配患者)。主要结果是6个月时的COVID-19突破率,次要结果包括与COVID-19相关的住院、入住重症监护室、气管插管和死亡率。此外,还对tixagevimab-cilgavimab的安全性进行了评估:共招募了 200 名参与者,每组人数相等(n = 100)。除了替沙吉单抗-西利加维单抗组接种 COVID-19 疫苗的次数较多外(中位数(IQR)4 (3-5) vs. 3 (3-4);P = .01),各组的基线特征具有可比性。6个月时,tixagevimab-cilgavimab组(17%)和对照组(15%)的COVID-19突破率相当(P = .66)。然而,tixagevimab-cilgavimab 组诊断突破性感染的中位(IQR)时间往往更长[4.49 (2.81-4.98) vs 1.96 (1.65-2.91) 个月;P = .08]。在出现突破性感染的参与者中,Tixagevimab-cilgavimab能显著降低COVID-19相关的住院率(5.9% vs 40.0%; P = .02)。所有与tixagevimab-cilgavimab相关的不良事件都很轻微:结论:在Omicron激增期间,在接种疫苗的透析患者中使用tixagevimab-cilgavimab作为PrEP并不能预防突破性感染,但却能显著减少与COVID-19相关的住院治疗。进一步的研究应优先考虑替代策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Clinical Kidney Journal
Clinical Kidney Journal Medicine-Transplantation
CiteScore
6.70
自引率
10.90%
发文量
242
审稿时长
8 weeks
期刊介绍: About the Journal Clinical Kidney Journal: Clinical and Translational Nephrology (ckj), an official journal of the ERA-EDTA (European Renal Association-European Dialysis and Transplant Association), is a fully open access, online only journal publishing bimonthly. The journal is an essential educational and training resource integrating clinical, translational and educational research into clinical practice. ckj aims to contribute to a translational research culture among nephrologists and kidney pathologists that helps close the gap between basic researchers and practicing clinicians and promote sorely needed innovation in the Nephrology field. All research articles in this journal have undergone peer review.
期刊最新文献
Correction. Liver safety of tolvaptan in patients with autosomal dominant polycystic kidney disease: interim data from a post-authorization safety study. Integrated, person-centred care for patients with complex cardiovascular disease, diabetes mellitus and chronic kidney disease: a randomized trial. Adding biomarker change information to the kidney failure risk equation improves predictive ability for dialysis dependency in eGFR <30 ml/min/1.73 m2. The Emboless® venous chamber efficiently reduces air bubbles: a randomized study of chronic hemodialysis patients.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1