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The Effect of COVID-19 Vaccine in Patients with Immune Thrombocytopenia
Background: Immune thrombocytopenia (ITP) is an acquired autoimmune disorder against platelets characterized by a low platelet count and increased bleeding risk. ITP is likely to rise from defective immune tolerance in addition to a triggering event, such as vaccination. COVID-19 vaccination is asso...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society of Hematology. Published by Elsevier Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8701596/ https://www.ncbi.nlm.nih.gov/pubmed/34157077 http://dx.doi.org/10.1182/blood-2021-146529 |
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author | Visser, Chantal Swinkels, Maurice van Werkhoven, Erik D. Croles, F. Nanne Noordzij, Heike Eefting, Matthijs Last-Koopmans, Suzanne M. Idink, Cecile Westerweel, Peter E. Santbergen, Bart Jobse, Pieter A. Baboe, Fazil Consortium, Recovac-IR Levin, Mark-David Kruip, Marieke J.H.A. Jansen, A.J. Gerard |
author_facet | Visser, Chantal Swinkels, Maurice van Werkhoven, Erik D. Croles, F. Nanne Noordzij, Heike Eefting, Matthijs Last-Koopmans, Suzanne M. Idink, Cecile Westerweel, Peter E. Santbergen, Bart Jobse, Pieter A. Baboe, Fazil Consortium, Recovac-IR Levin, Mark-David Kruip, Marieke J.H.A. Jansen, A.J. Gerard |
author_sort | Visser, Chantal |
collection | PubMed |
description | Background: Immune thrombocytopenia (ITP) is an acquired autoimmune disorder against platelets characterized by a low platelet count and increased bleeding risk. ITP is likely to rise from defective immune tolerance in addition to a triggering event, such as vaccination. COVID-19 vaccination is associated with a small increased risk of development of de novo ITP. In patients historically diagnosed with ITP, relapse of thrombocytopenia after COVID-19 vaccination has been described. However, the precise platelet dynamics in previously diagnosed ITP patients after COVID-19 vaccination is unknown Aims: To investigate the effect of the COVID-19 vaccine on platelet count, the occurrence of severe bleeding complications and necessity of rescue medication in patients historically diagnosed with ITP. Methods: Platelet counts of ITP patients and healthy controls were collected immediately before, 1 and 4 weeks after the first and second vaccination. Linear mixed effects modelling was applied to analyse platelet count dynamics over time. Results: We included 218 ITP patients (50.9% women) with a mean (SD) age of 58 (17) years and 200 healthy controls (60.0% women) with a mean (SD) age of 58 (13) years. Healthy controls and ITP patients had similar baseline characteristics (Table 1). 201/218 (92.2%)ITP patients received the mRNA-1273 vaccine, 16/218 (7.3%) the BNT162b vaccine and 1/218 (0.46%) the Vaxzevria vaccine. All healthy controls received the mRNA-1273 vaccine. Fifteen (6.8%) patients needed rescue medication (Table 1). Significantly more ITP patients who needed rescue medication were on ITP treatment prior COVID-19 vaccination compared to patients without exacerbation (56.2% (7/16) vs 27.4% (55/202), p=0.016). We found a significant effect of vaccination on platelet count over time in both ITP patients and healthy controls (Figure 1A). Platelet counts of ITP patients decreased 7.9% between baseline and 4 weeks after second vaccination (p=0.045). Rescue medication and prior treatment significantly increased platelet count over time (p=0.042 and p=0.044). Healthy controls decreased 4.5% in platelet count (p<0.001) between baseline and 4 weeks after second vaccination. There was no significant difference in platelet count between ITP patients and healthy controls (p=0.78) (Figure 2). IPT patients with a baseline platelet count of >150x10 (9)/L had a significant decrease of platelet count 4 weeks after second vaccination compared to baseline (median platelet count (IQR) 205 (94) vs 203 x10 (9)/L (109) p=0.001). No significant decrease was seen in ITP patients with a baseline platelet count <150 x10 (9)/L. Median (IQR) platelet counts were similar between patients with and without exacerbation, except for 4 weeks after second vaccination (112 (105) vs 45 x 10 (9)/L (70), p=0.025) (Figure 1B). No significant effect was observed over time in ITP patients with rescue medication (p=0.478) (Figure 1C). In ITP patients without rescue medication, COVID-19 vaccination had a significant effect over time (p=0.001), especially 1 week after second vaccination (Figure1B). Of the 15 patients who needed rescue medication, 8/15 patients (53.3%) received rescue medication within 4 weeks after first vaccination and 4/15 (26.67%) needed rescue medication after the first as well as after the second vaccination. 3/15 (20.0%) patients needed rescue medication after the second vaccination. In the total ITP population, 5/218 (2.2%) experienced a WHO grade 2-4 bleeding complication and 3/218 (1.4%) needed platelet transfusion. 4/5 (80%) bleedings occurred before the second vaccination. One of these patients had fatal varices bleeding, although platelet count was normal. Conclusion: COVID-19 vaccination has a significant effect on platelet count in ITP patients and healthy controls. In 6.8% of ITP patients rescue medication was needed and in 2.2% of ITP patients a WHO grade 2-4 bleeding occurred. The majority of rescue medication was given and the majority bleeding complications occurred in the 4 weeks after the first vaccination. Our results demonstrate that close monitoring of platelet count after COVID-19 vaccination is important in patients historically diagnosed with ITP. [Figure: see text] DISCLOSURES: Westerweel: Pfizer: Consultancy; BMS / Celgene: Consultancy; Incyte: Consultancy; Novartis: Research Funding. Levin: Roche, Janssen, Abbvie: Other: Travel Expenses, Ad-Board. Kruip: Bayer: Honoraria, Research Funding; Daiichi Sankyo: Research Funding. Jansen: Novartis: Consultancy, Other: Travel, Accommodations, Expenses; Advisory Board Novartis: Membership on an entity's Board of Directors or advisory committees; 3SBIO, Novartis: Other: Travel, accomodations, expenses. |
format | Online Article Text |
id | pubmed-8701596 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Society of Hematology. Published by Elsevier Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-87015962021-12-28 The Effect of COVID-19 Vaccine in Patients with Immune Thrombocytopenia Visser, Chantal Swinkels, Maurice van Werkhoven, Erik D. Croles, F. Nanne Noordzij, Heike Eefting, Matthijs Last-Koopmans, Suzanne M. Idink, Cecile Westerweel, Peter E. Santbergen, Bart Jobse, Pieter A. Baboe, Fazil Consortium, Recovac-IR Levin, Mark-David Kruip, Marieke J.H.A. Jansen, A.J. Gerard Blood 311.Disorders of Platelet Number or Function: Clinical and Epidemiological Background: Immune thrombocytopenia (ITP) is an acquired autoimmune disorder against platelets characterized by a low platelet count and increased bleeding risk. ITP is likely to rise from defective immune tolerance in addition to a triggering event, such as vaccination. COVID-19 vaccination is associated with a small increased risk of development of de novo ITP. In patients historically diagnosed with ITP, relapse of thrombocytopenia after COVID-19 vaccination has been described. However, the precise platelet dynamics in previously diagnosed ITP patients after COVID-19 vaccination is unknown Aims: To investigate the effect of the COVID-19 vaccine on platelet count, the occurrence of severe bleeding complications and necessity of rescue medication in patients historically diagnosed with ITP. Methods: Platelet counts of ITP patients and healthy controls were collected immediately before, 1 and 4 weeks after the first and second vaccination. Linear mixed effects modelling was applied to analyse platelet count dynamics over time. Results: We included 218 ITP patients (50.9% women) with a mean (SD) age of 58 (17) years and 200 healthy controls (60.0% women) with a mean (SD) age of 58 (13) years. Healthy controls and ITP patients had similar baseline characteristics (Table 1). 201/218 (92.2%)ITP patients received the mRNA-1273 vaccine, 16/218 (7.3%) the BNT162b vaccine and 1/218 (0.46%) the Vaxzevria vaccine. All healthy controls received the mRNA-1273 vaccine. Fifteen (6.8%) patients needed rescue medication (Table 1). Significantly more ITP patients who needed rescue medication were on ITP treatment prior COVID-19 vaccination compared to patients without exacerbation (56.2% (7/16) vs 27.4% (55/202), p=0.016). We found a significant effect of vaccination on platelet count over time in both ITP patients and healthy controls (Figure 1A). Platelet counts of ITP patients decreased 7.9% between baseline and 4 weeks after second vaccination (p=0.045). Rescue medication and prior treatment significantly increased platelet count over time (p=0.042 and p=0.044). Healthy controls decreased 4.5% in platelet count (p<0.001) between baseline and 4 weeks after second vaccination. There was no significant difference in platelet count between ITP patients and healthy controls (p=0.78) (Figure 2). IPT patients with a baseline platelet count of >150x10 (9)/L had a significant decrease of platelet count 4 weeks after second vaccination compared to baseline (median platelet count (IQR) 205 (94) vs 203 x10 (9)/L (109) p=0.001). No significant decrease was seen in ITP patients with a baseline platelet count <150 x10 (9)/L. Median (IQR) platelet counts were similar between patients with and without exacerbation, except for 4 weeks after second vaccination (112 (105) vs 45 x 10 (9)/L (70), p=0.025) (Figure 1B). No significant effect was observed over time in ITP patients with rescue medication (p=0.478) (Figure 1C). In ITP patients without rescue medication, COVID-19 vaccination had a significant effect over time (p=0.001), especially 1 week after second vaccination (Figure1B). Of the 15 patients who needed rescue medication, 8/15 patients (53.3%) received rescue medication within 4 weeks after first vaccination and 4/15 (26.67%) needed rescue medication after the first as well as after the second vaccination. 3/15 (20.0%) patients needed rescue medication after the second vaccination. In the total ITP population, 5/218 (2.2%) experienced a WHO grade 2-4 bleeding complication and 3/218 (1.4%) needed platelet transfusion. 4/5 (80%) bleedings occurred before the second vaccination. One of these patients had fatal varices bleeding, although platelet count was normal. Conclusion: COVID-19 vaccination has a significant effect on platelet count in ITP patients and healthy controls. In 6.8% of ITP patients rescue medication was needed and in 2.2% of ITP patients a WHO grade 2-4 bleeding occurred. The majority of rescue medication was given and the majority bleeding complications occurred in the 4 weeks after the first vaccination. Our results demonstrate that close monitoring of platelet count after COVID-19 vaccination is important in patients historically diagnosed with ITP. [Figure: see text] DISCLOSURES: Westerweel: Pfizer: Consultancy; BMS / Celgene: Consultancy; Incyte: Consultancy; Novartis: Research Funding. Levin: Roche, Janssen, Abbvie: Other: Travel Expenses, Ad-Board. Kruip: Bayer: Honoraria, Research Funding; Daiichi Sankyo: Research Funding. Jansen: Novartis: Consultancy, Other: Travel, Accommodations, Expenses; Advisory Board Novartis: Membership on an entity's Board of Directors or advisory committees; 3SBIO, Novartis: Other: Travel, accomodations, expenses. American Society of Hematology. Published by Elsevier Inc. 2021-11-23 2021-12-24 /pmc/articles/PMC8701596/ /pubmed/34157077 http://dx.doi.org/10.1182/blood-2021-146529 Text en Copyright © 2021 American Society of Hematology. Published by Elsevier Inc. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | 311.Disorders of Platelet Number or Function: Clinical and Epidemiological Visser, Chantal Swinkels, Maurice van Werkhoven, Erik D. Croles, F. Nanne Noordzij, Heike Eefting, Matthijs Last-Koopmans, Suzanne M. Idink, Cecile Westerweel, Peter E. Santbergen, Bart Jobse, Pieter A. Baboe, Fazil Consortium, Recovac-IR Levin, Mark-David Kruip, Marieke J.H.A. Jansen, A.J. Gerard The Effect of COVID-19 Vaccine in Patients with Immune Thrombocytopenia |
title | The Effect of COVID-19 Vaccine in Patients with Immune Thrombocytopenia |
title_full | The Effect of COVID-19 Vaccine in Patients with Immune Thrombocytopenia |
title_fullStr | The Effect of COVID-19 Vaccine in Patients with Immune Thrombocytopenia |
title_full_unstemmed | The Effect of COVID-19 Vaccine in Patients with Immune Thrombocytopenia |
title_short | The Effect of COVID-19 Vaccine in Patients with Immune Thrombocytopenia |
title_sort | effect of covid-19 vaccine in patients with immune thrombocytopenia |
topic | 311.Disorders of Platelet Number or Function: Clinical and Epidemiological |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8701596/ https://www.ncbi.nlm.nih.gov/pubmed/34157077 http://dx.doi.org/10.1182/blood-2021-146529 |
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