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新冠后综合征患者的临床及影像特征与肺功能测试的相关性

Association of clinical and imaging characteristics with pulmonary function testing in patients with Long-COVID.

作者信息

Zhao Lin-Mei, Lancaster Andrew C, Patel Ritesh, Zhang Helen, Duong Tim Q, Jiao Zhicheng, Lin Cheng Ting, Healey Terrance, Wright Thaddeus, Wu Jing, Bai Harrison X

机构信息

Department of Radiology and Radiological Science, Johns Hopkins University School of Medicine, Baltimore, MD, USA.

Department of Radiology, Xiangya Hospital, Central South University, Changsha, Hunan, China.

出版信息

Heliyon. 2024 May 22;10(11):e31751. doi: 10.1016/j.heliyon.2024.e31751. eCollection 2024 Jun 15.

DOI:10.1016/j.heliyon.2024.e31751
PMID:38845871
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11153179/
Abstract

PURPOSE

The purpose of this study is to identify clinical and imaging characteristics associated with post-COVID pulmonary function decline.

METHODS

This study included 22 patients recovering from COVID-19 who underwent serial spirometry pulmonary function testing (PFT) before and after diagnosis. Patients were divided into two cohorts by difference between baseline and post-COVID follow-up PFT: Decline group (>10 % decrease in FEV1), and Stable group (≤10 % decrease or improvement in FEV1). Demographic, clinical, and laboratory data were collected, as well as PFT and chest computed tomography (CT) at the time of COVID diagnosis and follow-up. CTs were semi-quantitatively scored on a five-point severity scale for disease extent in each lobe by two radiologists. Mann-Whitney U-tests, T-tests, and Chi-Squared tests were used for comparison. P-values <0.05 were considered statistically significant.

RESULTS

The Decline group had a higher proportion of neutrophils (79.47 ± 4.83 % vs. 65.45 ± 10.22 %; p = 0.003), a higher absolute neutrophil count (5.73 ± 2.68 × 10/L vs. 3.43 ± 1.74 × 10/L; p = 0.031), and a lower proportion of lymphocytes (9.90 ± 4.20 % vs. 21.21 ± 10.97 %; p = 0.018) compared to the Stable group. The Decline group also had significantly higher involvement of ground-glass opacities (GGO) on follow-up chest CT [8.50 (4.50, 14.50) vs. 3.0 (1.50, 9.50); p = 0.032] and significantly higher extent of reticulations on chest CT at time of COVID diagnosis [6.50 (4.00, 9.00) vs. 2.00 (0.00, 6.00); p = 0.039] and follow-up [5.00 (3.00, 13.00) vs. 2.00 (0.00, 5.00); p = 0.041]. ICU admission was higher in the Decline group than in the Stable group (71.4 % vs. 13.3 %; p = 0.014).

CONCLUSIONS

This study provides novel insight into factors influencing post-COVID lung function, irrespective of pre-existing pulmonary conditions. Our findings underscore the significance of neutrophil counts, reduced lymphocyte counts, pulmonary reticulation on chest CT at diagnosis, and extent of GGOs on follow-up chest CT as potential indicators of decreased post-COVID lung function. This knowledge may guide prediction and further understanding of long-term sequelae of COVID-19 infection.

摘要

目的

本研究旨在确定与新冠后肺功能下降相关的临床和影像学特征。

方法

本研究纳入了22例从新冠中康复的患者,这些患者在诊断前后接受了系列肺量计肺功能测试(PFT)。根据新冠后随访PFT与基线的差异,将患者分为两个队列:下降组(FEV1下降>10%)和稳定组(FEV1下降≤10%或改善)。收集了人口统计学、临床和实验室数据,以及新冠诊断和随访时的PFT和胸部计算机断层扫描(CT)。两名放射科医生根据每个肺叶疾病范围的五点严重程度量表对CT进行半定量评分。采用曼-惠特尼U检验、T检验和卡方检验进行比较。P值<0.05被认为具有统计学意义。

结果

与稳定组相比,下降组中性粒细胞比例更高(79.47±4.83%对65.45±10.22%;p = 0.003),绝对中性粒细胞计数更高(5.73±2.68×10/L对3.43±1.74×10/L;p = 0.031),淋巴细胞比例更低(9.90±4.20%对21.21±10.97%;p = 0.018)。下降组在随访胸部CT上磨玻璃影(GGO)的累及程度也显著更高[8.50(4.50,14.50)对3.0(1.50,9.50);p = 0.032],在新冠诊断时胸部CT上网状影的范围显著更高[6.50(4.00,9.00)对2.00(0.00,6.00);p = 0.039],随访时也更高[5.00(3.00,13.00)对2.00(0.00,5.00);p = 0.041]。下降组的ICU入院率高于稳定组(71.4%对13.3%;p = 0.014)。

结论

本研究为影响新冠后肺功能的因素提供了新的见解,无论既往是否存在肺部疾病。我们的研究结果强调了中性粒细胞计数、淋巴细胞计数减少、诊断时胸部CT上的肺网状影以及随访胸部CT上GGO的范围作为新冠后肺功能下降潜在指标的重要性。这些知识可能有助于预测和进一步了解新冠病毒感染的长期后遗症。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/36e0/11153179/5293504550ac/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/36e0/11153179/b2a058eedb37/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/36e0/11153179/5be539b99a9b/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/36e0/11153179/a45846274f4d/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/36e0/11153179/5293504550ac/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/36e0/11153179/b2a058eedb37/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/36e0/11153179/5be539b99a9b/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/36e0/11153179/a45846274f4d/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/36e0/11153179/5293504550ac/gr4.jpg

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