Effectiveness of COVID-19 vaccines in a large European hemodialysis cohort.

COVID-19 SARS-CoV-2 effectiveness hemodialysis mRNA vaccines viral-carrier vaccines

Journal

Frontiers in nephrology
ISSN: 2813-0626
Titre abrégé: Front Nephrol
Pays: Switzerland
ID NLM: 9918469487906676

Informations de publication

Date de publication:
2022
Historique:
received: 06 09 2022
accepted: 17 10 2022
medline: 7 9 2023
pubmed: 7 9 2023
entrez: 7 9 2023
Statut: epublish

Résumé

Hemodialysis patients have high-risk of severe SARS-CoV-2 infection but were unrepresented in randomized controlled trials evaluating the safety and efficacy of COVID-19 vaccines. We estimated the real-world effectiveness of COVID-19 vaccines in a large international cohort of hemodialysis patients. In this historical, 1:1 matched cohort study, we included adult hemodialysis patients receiving treatment from December 1, 2020, to May 31, 2021. For each vaccinated patient, an unvaccinated control was selected among patients registered in the same country and attending a dialysis session around the first vaccination date. Matching was based on demographics, clinical characteristics, past COVID-19 infections and a risk score representing the local background risk of infection at vaccination dates. We estimated the effectiveness of mRNA and viral-carrier COVID-19 vaccines in preventing infection and mortality rates from a time-dependent Cox regression stratified by country. In the effectiveness analysis concerning mRNA vaccines, we observed 850 SARS-CoV-2 infections and 201 COVID-19 related deaths among the 28110 patients during a mean follow up of 44 ± 40 days. In the effectiveness analysis concerning viral-carrier vaccines, we observed 297 SARS-CoV-2 infections and 64 COVID-19 related deaths among 12888 patients during a mean follow up of 48 ± 32 days. We observed 18.5/100-patient-year and 8.5/100-patient-year fewer infections and 5.4/100-patient-year and 5.2/100-patient-year fewer COVID-19 related deaths among patients vaccinated with mRNA and viral-carrier vaccines respectively, compared to matched unvaccinated controls. Estimated vaccine effectiveness at days 15, 30, 60 and 90 after the first dose of a mRNA vaccine was: for infection, 41.3%, 54.5%, 72.6% and 83.5% and, for death, 33.1%, 55.4%, 80.1% and 91.2%. Estimated vaccine effectiveness after the first dose of a viral-carrier vaccine was: for infection, 38.3% without increasing over time and, for death, 56.6%, 75.3%, 92.0% and 97.4%. In this large, real-world cohort of hemodialyzed patients, mRNA and viral-carrier COVID-19 vaccines were associated with reduced COVID-19 related mortality. Additionally, we observed a strong reduction of SARS-CoV-2 infection in hemodialysis patients receiving mRNA vaccines.

Sections du résumé

Background UNASSIGNED
Hemodialysis patients have high-risk of severe SARS-CoV-2 infection but were unrepresented in randomized controlled trials evaluating the safety and efficacy of COVID-19 vaccines. We estimated the real-world effectiveness of COVID-19 vaccines in a large international cohort of hemodialysis patients.
Methods UNASSIGNED
In this historical, 1:1 matched cohort study, we included adult hemodialysis patients receiving treatment from December 1, 2020, to May 31, 2021. For each vaccinated patient, an unvaccinated control was selected among patients registered in the same country and attending a dialysis session around the first vaccination date. Matching was based on demographics, clinical characteristics, past COVID-19 infections and a risk score representing the local background risk of infection at vaccination dates. We estimated the effectiveness of mRNA and viral-carrier COVID-19 vaccines in preventing infection and mortality rates from a time-dependent Cox regression stratified by country.
Results UNASSIGNED
In the effectiveness analysis concerning mRNA vaccines, we observed 850 SARS-CoV-2 infections and 201 COVID-19 related deaths among the 28110 patients during a mean follow up of 44 ± 40 days. In the effectiveness analysis concerning viral-carrier vaccines, we observed 297 SARS-CoV-2 infections and 64 COVID-19 related deaths among 12888 patients during a mean follow up of 48 ± 32 days. We observed 18.5/100-patient-year and 8.5/100-patient-year fewer infections and 5.4/100-patient-year and 5.2/100-patient-year fewer COVID-19 related deaths among patients vaccinated with mRNA and viral-carrier vaccines respectively, compared to matched unvaccinated controls. Estimated vaccine effectiveness at days 15, 30, 60 and 90 after the first dose of a mRNA vaccine was: for infection, 41.3%, 54.5%, 72.6% and 83.5% and, for death, 33.1%, 55.4%, 80.1% and 91.2%. Estimated vaccine effectiveness after the first dose of a viral-carrier vaccine was: for infection, 38.3% without increasing over time and, for death, 56.6%, 75.3%, 92.0% and 97.4%.
Conclusion UNASSIGNED
In this large, real-world cohort of hemodialyzed patients, mRNA and viral-carrier COVID-19 vaccines were associated with reduced COVID-19 related mortality. Additionally, we observed a strong reduction of SARS-CoV-2 infection in hemodialysis patients receiving mRNA vaccines.

Identifiants

pubmed: 37675035
doi: 10.3389/fneph.2022.1037754
pmc: PMC10479614
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1037754

Informations de copyright

Copyright © 2022 Bernardo, Carioni, Stuard, Kotanko, Usvyat, Kovarova, Arkossy, Bellocchio, Tupputi, Gervasoni, Winter, Zhang, Zhang, Ponce and Neri.

Déclaration de conflit d'intérêts

AB, PC, SS, LU, VK, OA, FB, AT, FG, AW, YZ, PP and LN are employees of Fresenius Medical Care. PK and HZ are employees of the Renal Research Institute, a wholly owned subsidiary of Fresenius Medical Care. LU and PK have share options/ownership in Fresenius Medical Care. PK, HZ, LU are inventors on patents in the field of dialysis. PK receives honorarium from UpToDate and HS Talks, and is on the Editorial Board of Blood Purification, Frontiers in Nephrology, Kidney and Dialysis, and Kidney and Blood Pressure Research.

Références

J Nephrol. 2001 Nov-Dec;14 Suppl 4:S94-100
pubmed: 11798154
Psychol Methods. 2010 Sep;15(3):234-49
pubmed: 20822250
Can J Kidney Health Dis. 2019 Apr 29;6:2054358119839080
pubmed: 31065378
Clin J Am Soc Nephrol. 2022 Jun;17(6):843-850
pubmed: 35649718
Clin J Am Soc Nephrol. 2021 Jul;16(7):1073-1082
pubmed: 34031181
Clin J Am Soc Nephrol. 2008 Sep;3(5):1526-33
pubmed: 18701615
J Am Soc Nephrol. 2022 Apr;33(4):839-849
pubmed: 35264455
Nat Rev Nephrol. 2013 May;9(5):255-65
pubmed: 23507826
Kidney360. 2020 Dec 09;2(2):263-269
pubmed: 35373027
J Am Soc Nephrol. 2022 Jan;33(1):49-57
pubmed: 34789546
Am J Kidney Dis. 2021 May;77(5):748-756.e1
pubmed: 33465417
Lancet. 2021 Jan 9;397(10269):99-111
pubmed: 33306989
N Engl J Med. 2021 Jun 10;384(23):2187-2201
pubmed: 33882225
Methods Inf Med. 2004;43(1):83-8
pubmed: 15026844
Blood Purif. 2007;25(3):221-8
pubmed: 17377376
Contrib Nephrol. 2002;(137):293-9
pubmed: 12101968
J Am Soc Nephrol. 2020 Nov;31(11):2517-2521
pubmed: 33077614
J Am Soc Nephrol. 2021 Dec 1;32(12):3208-3220
pubmed: 34588184
JAMA. 2021 Jul 6;326(1):35-45
pubmed: 34037666
Int J Environ Res Public Health. 2021 Sep 16;18(18):
pubmed: 34574664
Kidney Int. 2021 Jun;99(6):1496-1498
pubmed: 33887318
BMJ. 2021 Aug 20;374:n1943
pubmed: 34417165
Nature. 2020 Oct;586(7830):589-593
pubmed: 32785213
Sci Rep. 2021 Apr 20;11(1):8562
pubmed: 33879826
Nature. 2020 Aug;584(7821):430-436
pubmed: 32640463
Nephrol Dial Transplant. 2021 Aug 27;36(9):1709-1716
pubmed: 33999200
N Engl J Med. 2021 Feb 4;384(5):403-416
pubmed: 33378609
Clin J Am Soc Nephrol. 2021 Jul;16(7):1037-1042
pubmed: 33824157
Kidney Int. 2021 Jun;99(6):1470-1477
pubmed: 33774082
Sci Rep. 2019 Mar 25;9(1):5041
pubmed: 30911040
Stat Sci. 2010 Feb 1;25(1):1-21
pubmed: 20871802
N Engl J Med. 2020 Dec 31;383(27):2603-2615
pubmed: 33301246
Kidney Int. 2020 Dec;98(6):1530-1539
pubmed: 32810523

Auteurs

Ana Paula Bernardo (AP)

Fresenius Medical Care Portugal / Nephrocare Portugal, Vila Nova de Gaia, Portugal.
Unit for Multidisciplinary Research in Biomedicine (UMIB), Institute of Biomedical Sciences Abel Salazar (ICBAS), Porto University, Oporto, Portugal.

Paola Carioni (P)

Fresenius Medical Care Italia SpA, Palazzo Pignano, Italy.

Stefano Stuard (S)

Fresenius Medical Care Deutschland GmbH, Bad Homburg, Germany.

Peter Kotanko (P)

Renal Research Institute, New York, NY, United States.
Icahn School of Medicine at Mount Sinai, New York, NY, United States.

Len A Usvyat (LA)

Fresenius Medical Care, Waltham, MA, United States.

Vratislava Kovarova (V)

Fresenius Medical Care Deutschland GmbH, Bad Homburg, Germany.

Otto Arkossy (O)

Fresenius Medical Care Deutschland GmbH, Bad Homburg, Germany.

Francesco Bellocchio (F)

Fresenius Medical Care Italia SpA, Palazzo Pignano, Italy.

Antonio Tupputi (A)

Fresenius Medical Care Italia SpA, Palazzo Pignano, Italy.

Federica Gervasoni (F)

Fresenius Medical Care Italia SpA, Palazzo Pignano, Italy.

Anke Winter (A)

Fresenius Medical Care Deutschland GmbH, Bad Homburg, Germany.

Yan Zhang (Y)

Fresenius Medical Care Deutschland GmbH, Bad Homburg, Germany.

Hanjie Zhang (H)

Renal Research Institute, New York, NY, United States.

Pedro Ponce (P)

Fresenius Medical Care Portugal / Nephrocare Portugal, Lisboa, Portugal.

Luca Neri (L)

Fresenius Medical Care Italia SpA, Palazzo Pignano, Italy.

Classifications MeSH