Long COVID-19 syndrome associated with Omicron XBB.1.5 infection: a case report.
Long COVID-19 syndrome associated with Omicron XBB.1.5 infection: a case report.
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DOI:
10.1590/0074-02760230069
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发表时间:
2023
影响因子:
2.8
通讯作者:
Brasil, Patricia
中科院分区:
文献类型:
--
作者:
Espindola, Otavio;Resende, Paola C.;Guaraldo, Lusiele;Calvet, Guilherme Amaral;Fuller, Trevon L.;Penetra, Stephanie Lema Suarez;Santos, Heloisa Ferreira Pinto;Pina-Costa, Anielle;da Silva, Michele Fernanda Borges;Moraes, Isabella Campos Vargas;Medeiros, Fernando;Whitworth, Jimmy;Smith, Christopher;Nielsen-Saines, Karin;Siqueira, Marilda M.;Brasil, Patricia
There is interest in lingering non-specific symptoms after severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection, referred to as Long coronavirus disease 2019 (Long COVID-19). It remains unknown whether the risk of Long COVID-19 is associated with pre-existing comorbidities or initial COVID-19 severity, including infections due to new Omicron lineages which predominated in 2023. The aim of this case report was to characterize the clinical features of acute XBB.1.5 infection followed by Long COVID-19. We followed a 73-year old female resident of Rio de Janeiro with laboratory-confirmed SARS-CoV-2 during acute infection and subsequent months. The SARS-CoV-2 lineage was determined by genome sequencing. The participant denied comorbidities and had completed a two-dose vaccination schedule followed by two booster doses eight months prior to SARS-CoV-2 infection. Primary infection by viral lineage XBB.1.5. was clinically mild, but the participant subsequently reported persistent fatigue. This case demonstrates that Long COVID-19 may develop even after mild disease due to SARS-CoV-2 in fully vaccinated and boosted individuals without comorbidities. Continued monitoring of new SARS-CoV-2 lineages and associated clinical outcomes is warranted. Measures to prevent infection should continue to be implemented including development of new vaccines and antivirals effective against novel variants.
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影响因子:
8.8
作者:
通讯作者:
--
DOI:
10.1016/j.jcv.2023.105500
发表时间:
2023-08
期刊:
Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology
影响因子:
--
作者:
Klein EY;Fall A;Norton JM;Eldesouki RE;Abdullah O;Han L;Yunker M;Mostafa HH
通讯作者:
Mostafa HH
DOI:
10.1016/s1473-3099(21)00703-9
发表时间:
2022-04
期刊:
The Lancet. Infectious diseases
影响因子:
--
作者:
Soriano JB;Murthy S;Marshall JC;Relan P;Diaz JV;WHO Clinical Case Definition Working Group on Post-COVID-19 Condition
通讯作者:
WHO Clinical Case Definition Working Group on Post-COVID-19 Condition
影响因子:
33.9
作者:
Ma, Kevin C.;Shirk, Philip;Lambrou, Anastasia S.;Hassell, Norman;Zheng, Xiao-yu;Payne, Amanda B.;Ali, Akilah R.;Batra, Dhwani;Caravas, Jason;Chau, Reina;Cook, Peter W.;Howard, Dakota;Kovacs, Nicholas A.;Lacek, Kristine A.;Lee, Justin S.;MacCannell, Duncan R.;Malapati, Lakshmi;Mathew, Sandra;Mittal, Neha;Nagilla, Roopa R.;Parikh, Rishika;Paul, Prabasaj;Rambo-Martin, Benjamin L.;Shepard, Samuel S.;Sheth, Mili;Wentworth, David E.;Winn, Amber;Hall, Aron J.;Silk, Benjamin J.;Thornburg, Natalie;Kondor, Rebecca;Scobie, Heather M.;Paden, Clinton R.
通讯作者:
Paden, Clinton R.
影响因子:
120.7
作者:
Thaweethai, Tanayott;Jolley, Sarah E.;Foulkes, Andrea S.
通讯作者:
Foulkes, Andrea S.