SARS-CoV-2 viremia but not respiratory viral load is associated with respiratory complications in patients with severe COVID-19

被引:0
|
作者
Chen, Lingye [1 ]
Olson, Lyra B. [2 ]
Naqvi, Ibtehaj A. [3 ]
Sullenger, Bruce A. [3 ]
Que, Loretta G. [1 ]
Denny, Thomas N. [1 ,4 ]
Kraft, Bryan D. [1 ]
机构
[1] Duke Univ, Sch Med, Dept Med, Durham, NC 27710 USA
[2] Duke Univ, Dept Pharmacol & Canc Biol, Duke Med Scientist Training Program, Sch Med, Durham, NC 27710 USA
[3] Duke Univ, Sch Med, Dept Surg, Durham, NC 27710 USA
[4] Duke Univ, Sch Med, Duke Human Vaccine Inst, Durham, NC 27710 USA
来源
BMC PULMONARY MEDICINE | 2024年 / 24卷 / 01期
关键词
COVID-19; COVID-19 nucleic acid testing; Pneumonia; Ventilator-associated pneumonia; Respiration; artificial; Biomarkers/blood; PNEUMONIA;
D O I
10.1186/s12890-024-03183-7
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Background Severe COVID-19 carries a high morbidity and mortality. Previous studies have shown an association between COVID-19 severity and SARS-CoV-2 viral load (VL). We sought to measure VL in multiple compartments (urine, plasma, lower respiratory tract) in patients admitted to the intensive care unit (ICU) with severe COVID-19 pneumonia and correlate with clinical outcomes. Methods Plasma, urine, and endotracheal aspirate (ETA) samples were obtained on days 1, 3, 7, 14, and 21 from subjects admitted to the ICU with severe COVID-19. VL was measured via reverse transcriptase polymerase chain reaction. Clinical data was collected from the electronic health record. Grouped comparisons were performed using Student's t-test or 1-way ANOVA. Linear regression was used to correlate VL from different compartments collected at the same time. Logistic regression was performed to model ventilator-freedom at 28 days as a function of peak plasma VL. Results We enrolled 57 subjects with severe COVID-19 and measured VL in plasma (n = 57), urine (n = 25), and ETA (n = 34). Ventilator-associated pneumonia developed in 63% of subjects. 49% of subjects were viremic on study day 1. VL in plasma and ETA both significantly decreased by day 14 (P < 0.05), and the two were weakly correlated on study day 1 (P = 0.0037, r(2) = 0.2343) and on all study days (P < 0.001, r(2) = 0.2211). VL were not detected in urine. While no associations were observed with peak ETA VL, subjects with higher peak plasma VL experienced a greater number of respiratory complications, including ventilator-associated pneumonia and fewer ventilator-free and hospital-free days. There was no association between VL in either plasma or ETA and mortality. In viremic patients, plasma VL was significantly lower in subjects that were ICU-free and ventilator-free (P < 0.05), with trends noted for hospital-freedom, ventilator-associated pneumonia, and survival to discharge (P < 0.1). By logistic regression, plasma VL was inversely associated with ventilator-freedom at 28 days (odds ratio 0.14, 95% confidence interval 0.02-0.50). Conclusions Elevated SARS-CoV-2 VL in the plasma but not in the lower respiratory tract is a novel biomarker in severe COVID-19 for respiratory complications.
引用
收藏
页数:8
相关论文
共 50 条
  • [41] Musculoskeletal symptoms in SARS-CoV-2 (COVID-19) patients
    Cipollaro, Lucio
    Giordano, Lorenzo
    Padulo, Johnny
    Oliva, Francesco
    Maffulli, Nicola
    JOURNAL OF ORTHOPAEDIC SURGERY AND RESEARCH, 2020, 15 (01)
  • [42] Recovery in patients with SARS-CoV-2 associated respiratory failure
    Kohlbrenner, Dario
    Kuhn, Manuel
    Stuessi-Helbling, Melina
    Spielmanns, Marc
    Nordmann, Yves
    Clarenbach, Christian F.
    EUROPEAN RESPIRATORY JOURNAL, 2021, 58
  • [43] Circulation of Non-SARS-CoV-2 Respiratory Pathogens and Coinfection with SARS-CoV-2 Amid the COVID-19 Pandemic
    Uhteg, Katharine
    Amadi, Adannaya
    Forman, Michael
    Mostafa, Heba H.
    OPEN FORUM INFECTIOUS DISEASES, 2022, 9 (03):
  • [44] Evaluation of SARS-CoV-2 in Tears of Patients with Moderate to Severe COVID-19
    Arora, Ritu
    Goel, Ruchi
    Kumar, Sumit
    Chhabra, Mohit
    Saxena, Sonal
    Manchanda, Vikas
    Pumma, Palak
    OPHTHALMOLOGY, 2021, 128 (04) : 494 - 503
  • [45] SARS-CoV-2 Viral Load, IFNλ Polymorphisms and the Course of COVID-19: An Observational Study
    Amodio, Emanuele
    Pipitone, Rosaria Maria
    Grimaudo, Stefania
    Immordino, Palmira
    Maida, Carmelo Massimo
    Prestileo, Tullio
    Restivo, Vincenzo
    Tramuto, Fabio
    Vitale, Francesco
    Craxi, Antonio
    Casuccio, Alessandra
    JOURNAL OF CLINICAL MEDICINE, 2020, 9 (10) : 1 - 9
  • [46] Is Higher Viral Load in SARS-CoV-2 Associated with Death?
    Faico-Filho, Klinger Soares
    Passarelli, Victor Cabelho
    Bellei, Nancy
    AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE, 2020, 103 (05) : 2019 - 2021
  • [47] Impact of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) in the Nervous System: Implications of COVID-19 in Neurodegeneration
    Rodriguez, Myosotys
    Soler, Yemmy
    Perry, Marissa
    Reynolds, Jessica L.
    El-Hage, Nazira
    FRONTIERS IN NEUROLOGY, 2020, 11
  • [48] Covid-19 Ontology Engineering-Knowledge Modeling of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2)
    Sherimon, Vinu
    Sherimon, P. C.
    Mathew, Renchi
    Kumar, Sandeep M.
    Nair, Rahul, V
    Shaikh, Khalid
    Al Ghafri, Hilal Khalid
    Al Shuaily, Huda Salim
    INTERNATIONAL JOURNAL OF ADVANCED COMPUTER SCIENCE AND APPLICATIONS, 2020, 11 (11) : 117 - 123
  • [49] Coinfection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and influenza virus during the COVID-19 pandemic
    Delsuz Rezaee
    Somaye Bakhtiari
    Farid Azizi Jalilian
    Amin Doosti-Irani
    Fatemeh Torkaman Asadi
    Nastaran Ansari
    Archives of Virology, 2023, 168
  • [50] Coinfection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and influenza virus during the COVID-19 pandemic
    Rezaee, Delsuz
    Bakhtiari, Somaye
    Jalilian, Farid Azizi
    Doosti-Irani, Amin
    Asadi, Fatemeh Torkaman
    Ansari, Nastaran
    ARCHIVES OF VIROLOGY, 2023, 168 (02)