Cardiovascular disease risk after a SARS-CoV-2 infection: A systematic review and meta-analysis

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Cardiovascular disease risk after a SARS-CoV-2 infection: A systematic review and meta-analysis. / Romero Starke, Karla; Kaboth, Pauline; Rath, Natalie; Reissig, David; Kaempf, Daniel; Nienhaus, Albert; Seidler, Andreas.

In: J INFECTION, Vol. 89, No. 3, 09.2024, p. 106215.

Research output: SCORING: Contribution to journalSCORING: Review articleResearch

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Romero Starke, K, Kaboth, P, Rath, N, Reissig, D, Kaempf, D, Nienhaus, A & Seidler, A 2024, 'Cardiovascular disease risk after a SARS-CoV-2 infection: A systematic review and meta-analysis', J INFECTION, vol. 89, no. 3, pp. 106215. https://doi.org/10.1016/j.jinf.2024.106215

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Bibtex

@article{ec942663cf3c427b8c8b54299bcb71df,
title = "Cardiovascular disease risk after a SARS-CoV-2 infection: A systematic review and meta-analysis",
abstract = "OBJECTIVES: To our knowledge, there is no systematic review examining CVD risks after a SARS-CoV-2 infection over time, while also taking into account disease severity. All evidence on the risk for pulmonary embolism (PE), myocardial infarction (MI), ischaemic stroke (IS), haemorrhagic stroke (HS), and arterial thrombosis following infection was evaluated.METHODS: The protocol was registered with PROSPERO. We searched Pubmed, Embase, MedRxiv and screened the titles/abstracts and full texts. We extracted the included studies, assessed their quality, and estimated pooled risks by time after infection and according to disease severity.RESULTS: Risks were highest in the acute phase [PE: 27.1 (17.8-41.10); MI: 4.4 (1.6-12.4); stroke: 3.3 (2.1-5.2); IS: 5.6 (2.1-14.8); HS: 4.0 (0.1-326.2)] compared to the post-acute phase [PE: 2.9 (2.6-3.3); MI: 1.4 (1.1-1.9); stroke: 1.4 (1.0-2.0); IS: 1.6 (0.9-2.7)]. Highest risks were observed after infection confirmation, dropping during the first month post-infection (e.g. PE: RR(7 days) = 31; RR(1 month) = 8.1). A doubled risk was still observed until 4.5 months for PE, one month for MI and two months for IS. Risks decreased with decreasing disease severity.CONCLUSIONS: Because of increased risk of CVD outcomes, management of persons who survived a severe SARS-CoV-2 infection is required, especially during the first nine months post-infection.",
author = "{Romero Starke}, Karla and Pauline Kaboth and Natalie Rath and David Reissig and Daniel Kaempf and Albert Nienhaus and Andreas Seidler",
note = "Copyright {\textcopyright} 2024 The Author(s). Published by Elsevier Ltd.. All rights reserved.",
year = "2024",
month = sep,
doi = "10.1016/j.jinf.2024.106215",
language = "English",
volume = "89",
pages = "106215",
journal = "J INFECTION",
issn = "0163-4453",
publisher = "W.B. Saunders Ltd",
number = "3",

}

RIS

TY - JOUR

T1 - Cardiovascular disease risk after a SARS-CoV-2 infection: A systematic review and meta-analysis

AU - Romero Starke, Karla

AU - Kaboth, Pauline

AU - Rath, Natalie

AU - Reissig, David

AU - Kaempf, Daniel

AU - Nienhaus, Albert

AU - Seidler, Andreas

N1 - Copyright © 2024 The Author(s). Published by Elsevier Ltd.. All rights reserved.

PY - 2024/9

Y1 - 2024/9

N2 - OBJECTIVES: To our knowledge, there is no systematic review examining CVD risks after a SARS-CoV-2 infection over time, while also taking into account disease severity. All evidence on the risk for pulmonary embolism (PE), myocardial infarction (MI), ischaemic stroke (IS), haemorrhagic stroke (HS), and arterial thrombosis following infection was evaluated.METHODS: The protocol was registered with PROSPERO. We searched Pubmed, Embase, MedRxiv and screened the titles/abstracts and full texts. We extracted the included studies, assessed their quality, and estimated pooled risks by time after infection and according to disease severity.RESULTS: Risks were highest in the acute phase [PE: 27.1 (17.8-41.10); MI: 4.4 (1.6-12.4); stroke: 3.3 (2.1-5.2); IS: 5.6 (2.1-14.8); HS: 4.0 (0.1-326.2)] compared to the post-acute phase [PE: 2.9 (2.6-3.3); MI: 1.4 (1.1-1.9); stroke: 1.4 (1.0-2.0); IS: 1.6 (0.9-2.7)]. Highest risks were observed after infection confirmation, dropping during the first month post-infection (e.g. PE: RR(7 days) = 31; RR(1 month) = 8.1). A doubled risk was still observed until 4.5 months for PE, one month for MI and two months for IS. Risks decreased with decreasing disease severity.CONCLUSIONS: Because of increased risk of CVD outcomes, management of persons who survived a severe SARS-CoV-2 infection is required, especially during the first nine months post-infection.

AB - OBJECTIVES: To our knowledge, there is no systematic review examining CVD risks after a SARS-CoV-2 infection over time, while also taking into account disease severity. All evidence on the risk for pulmonary embolism (PE), myocardial infarction (MI), ischaemic stroke (IS), haemorrhagic stroke (HS), and arterial thrombosis following infection was evaluated.METHODS: The protocol was registered with PROSPERO. We searched Pubmed, Embase, MedRxiv and screened the titles/abstracts and full texts. We extracted the included studies, assessed their quality, and estimated pooled risks by time after infection and according to disease severity.RESULTS: Risks were highest in the acute phase [PE: 27.1 (17.8-41.10); MI: 4.4 (1.6-12.4); stroke: 3.3 (2.1-5.2); IS: 5.6 (2.1-14.8); HS: 4.0 (0.1-326.2)] compared to the post-acute phase [PE: 2.9 (2.6-3.3); MI: 1.4 (1.1-1.9); stroke: 1.4 (1.0-2.0); IS: 1.6 (0.9-2.7)]. Highest risks were observed after infection confirmation, dropping during the first month post-infection (e.g. PE: RR(7 days) = 31; RR(1 month) = 8.1). A doubled risk was still observed until 4.5 months for PE, one month for MI and two months for IS. Risks decreased with decreasing disease severity.CONCLUSIONS: Because of increased risk of CVD outcomes, management of persons who survived a severe SARS-CoV-2 infection is required, especially during the first nine months post-infection.

U2 - 10.1016/j.jinf.2024.106215

DO - 10.1016/j.jinf.2024.106215

M3 - SCORING: Review article

C2 - 38971381

VL - 89

SP - 106215

JO - J INFECTION

JF - J INFECTION

SN - 0163-4453

IS - 3

ER -