Improved pulmonary function and exercise tolerance despite persistent pulmonary fibrosis over 1 year after severe COVID-19 infection

被引:1
|
作者
McGroder, Claire F. [1 ]
Salvatore, Mary M. [2 ]
D'Souza, Belinda M. [2 ]
Hoffman, Eric A. [3 ]
Baldwin, Matthew R. [1 ]
Garcia, Christine Kim [1 ,4 ,5 ,6 ]
机构
[1] Columbia Univ, Med Pulm Allergy & Crit Care Med, Irving Med Ctr, New York, NY USA
[2] Columbia Univ, Med Ctr, New York, NY USA
[3] Univ Iowa, Carver Coll Med, Radiol Med Biomed Engn, Iowa City, IA USA
[4] Columbia Univ, Precis Med Initiat, New York, NY 10032 USA
[5] Columbia Univ, Ctr Precis Med & Genom, New York, NY USA
[6] Columbia Univ, Irving Med Ctr, Med Pulm Crit Care Med, New York, NY 10027 USA
关键词
COVID-19; interstitial fibrosis; clinical epidemiology; imaging/CT MRI; respiratory measurement; viral infection; OUTCOMES;
D O I
10.1136/thorax-2023-220370
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
We conducted a prospective single-centre cohort study of 104 multi-ethnic severe COVID-19 survivors from the first wave of the pandemic 15 months after hospitalisation. Of those who were assessed at 4 and 15 months, improvement of ground glass opacities correlated with worsened fibrotic reticulations. Despite a high prevalence of fibrotic patterns (64%), pulmonary function, grip strength, 6 min walk distance and frailty normalised. Overall, dyspnoea, cough and exhaustion did not improve and were not correlated with pulmonary function or radiographic fibrosis at 15 months, suggesting non-respiratory aetiologies. Monitoring persistent, and often subclinical, fibrotic interstitial abnormalities will be needed to determine their potential for future progression.
引用
收藏
页码:472 / 475
页数:4
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