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https://hdl.handle.net/11499/57411
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DC Field | Value | Language |
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dc.contributor.author | Ufuk, Furkan | - |
dc.contributor.author | Yitik, Ahmet Yasin | - |
dc.contributor.author | Sarılar, Burak | - |
dc.contributor.author | Altınışık, Göksel | - |
dc.date.accessioned | 2024-06-29T13:49:32Z | - |
dc.date.available | 2024-06-29T13:49:32Z | - |
dc.date.issued | 2024 | - |
dc.identifier.issn | 0363-8715 | - |
dc.identifier.issn | 1532-3145 | - |
dc.identifier.uri | https://doi.org/10.1097/RCT.0000000000001577 | - |
dc.identifier.uri | https://hdl.handle.net/11499/57411 | - |
dc.description.abstract | Objective: The aims of this study were to assess the chest computed tomography (CT) findings in post-COVID-19 respiratory condition (rPCC) patients and compare the findings with asymptomatic participants (APs). It also aimed to evaluate the relationship between CT findings and pulmonary function tests (PFTs) in rPCC patients. Finally, it aimed to compare the quantitative chest CT findings and PFT results of patients with rPCC and APs. Methods: We retrospectively enrolled consecutive patients with rPCC who underwent unenhanced chest CT and PFTs between June 2020 and September 2022. In addition, a control group (APs) was prospectively formed and underwent nonenhanced chest CT and PFTs. The presence and extent of abnormalities in unenhanced chest CT images were evaluated qualitatively and semiquantitatively in a blinded manner. We used fully automatic software for automatic lung and airway segmentation and quantitative analyses. Results: Sixty-three patients with rPCC and 23 APs were investigated. Reticulation/interstitial thickening and extent of parenchymal abnormalities on CT were significantly greater in the rPCC group than in the control group (P = 0.001 and P = 0.004, respectively). Computed tomography extent score was significantly related to length of hospital stay, age, and intensive care unit stay (all Ps <= 0.006). The rPCC group also had a lower 85th percentile attenuation lung volume (P = 0.037). The extent of parenchymal abnormalities was significantly correlated with carbon monoxide diffusing capacity (r = -0.406, P = 0.001), forced vital capacity (FVC) (r = -0.342, P = 0.002), and forced expiratory volume in 1 second/FVC (r = 0.427, P < 0.001) values. Pulmonary function tests revealed significantly lower carbon monoxide diffusing capacity (P < 0.001), FVC (P = 0.036), and total lung capacity (P < 0.001) values in the rPCC group. Conclusions: The rPCC is characterized by impaired PFTs, a greater extent of lung abnormalities on CT, and decreased 85th percentile attenuation lung volume. Advanced age, intensive care unit admission history, and extended hospital stay are risk factors for chest CT abnormalities. | en_US |
dc.language.iso | en | en_US |
dc.publisher | Lippincott Williams & Wilkins | en_US |
dc.relation.ispartof | Journal of Computer Assisted Tomography | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | computed tomography | en_US |
dc.subject | post-acute COVID-19 syndrome | en_US |
dc.subject | respiratory function tests | en_US |
dc.subject | long COVID | en_US |
dc.subject | interstitial lung disease | en_US |
dc.title | Patients with post-covid-19 respiratory condition: chest computed tomography findings and pulmonary function tests and comparison with asymptomatic participants | en_US |
dc.type | Article | en_US |
dc.identifier.volume | 48 | en_US |
dc.identifier.issue | 3 | en_US |
dc.identifier.startpage | 415 | en_US |
dc.identifier.endpage | 423 | en_US |
dc.department | Pamukkale University | en_US |
dc.authorid | Ufuk, Furkan/0000-0002-8614-5387 | - |
dc.identifier.doi | 10.1097/RCT.0000000000001577 | - |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.authorscopusid | 56600861000 | - |
dc.authorscopusid | 57213174650 | - |
dc.authorscopusid | 58733772100 | - |
dc.authorscopusid | 56584711700 | - |
dc.authorwosid | Ufuk, Furkan/R-7366-2017 | - |
dc.identifier.pmid | 38213073 | en_US |
dc.identifier.scopus | 2-s2.0-85193309457 | en_US |
dc.identifier.wos | WOS:001223126700012 | en_US |
dc.institutionauthor | … | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.openairetype | Article | - |
item.cerifentitytype | Publications | - |
item.fulltext | No Fulltext | - |
item.grantfulltext | none | - |
item.languageiso639-1 | en | - |
crisitem.author.dept | 14.02. Internal Medicine | - |
crisitem.author.dept | 14.02. Internal Medicine | - |
crisitem.author.dept | 14.02. Internal Medicine | - |
crisitem.author.dept | 14.02. Internal Medicine | - |
Appears in Collections: | PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection Tıp Fakültesi Koleksiyonu WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection |
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