Tixagevimab-cilgavimab for preventing breakthrough COVID-19 in dialysis patients: a prospective study
dc.contributor.author | Boongird S. | |
dc.contributor.author | Srithongkul T. | |
dc.contributor.author | Sethakarun S. | |
dc.contributor.author | Bruminhent J. | |
dc.contributor.author | Kiertiburanakul S. | |
dc.contributor.author | Nongnuch A. | |
dc.contributor.author | Kitiyakara C. | |
dc.contributor.author | Sritippayawan S. | |
dc.contributor.correspondence | Boongird S. | |
dc.contributor.other | Mahidol University | |
dc.date.accessioned | 2024-11-26T18:11:50Z | |
dc.date.available | 2024-11-26T18:11:50Z | |
dc.date.issued | 2024-11-01 | |
dc.description.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. | |
dc.identifier.citation | Clinical Kidney Journal Vol.17 No.11 (2024) | |
dc.identifier.doi | 10.1093/ckj/sfae309 | |
dc.identifier.eissn | 20488513 | |
dc.identifier.issn | 20488505 | |
dc.identifier.scopus | 2-s2.0-85209642953 | |
dc.identifier.uri | https://repository.li.mahidol.ac.th/handle/20.500.14594/102180 | |
dc.rights.holder | SCOPUS | |
dc.subject | Medicine | |
dc.title | Tixagevimab-cilgavimab for preventing breakthrough COVID-19 in dialysis patients: a prospective study | |
dc.type | Article | |
mu.datasource.scopus | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85209642953&origin=inward | |
oaire.citation.issue | 11 | |
oaire.citation.title | Clinical Kidney Journal | |
oaire.citation.volume | 17 | |
oairecerif.author.affiliation | Siriraj Hospital | |
oairecerif.author.affiliation | Faculty of Medicine Ramathibodi Hospital, Mahidol University | |
oairecerif.author.affiliation | Bhumirajanagarindra Kidney Institute |