COVID-19患者不同临床严重程度组别中嗅觉和味觉功能障碍的发生率

S. I. Vento, I. Taskila, J. Martola, L. Kuusela, G. Kurdo, A. Lyly, J. Hästbacka
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摘要

背景:关于 COVID-19 急性期重症患者长期嗅觉和味觉障碍的研究十分有限。我们的研究旨在评估和比较危重、重度或轻度 COVID-19 患者的心理物理测试和自我报告的嗅觉和味觉障碍,并在急性期后 6 个月的随访中对三组患者的恢复情况进行比较。方法:这项前瞻性对照研究共有 227 名参与者,其中包括 72 名接受过重症监护室(ICU)治疗的患者、53 名接受过肺部或传染病病房(WARD)治疗的患者、48 名曾患 COVID-19 的家庭隔离患者(HOME),以及 54 名无 COVID-19 病史的患者(对照组)。所有参与者均在急性期后六个月前往复诊诊所进行嗅觉筛查,并接受大脑、嗅球和鼻窦部位的磁共振成像(MRI)检查。在复诊前,参与者收到了一份有关嗅觉和味觉功能的问卷。在急性期后的中位数 502.5 天时,我们发出了一份补充问卷,其中包括幻嗅和副嗅以及味觉恢复等问题。结果:我们发现,在嗅觉和味觉功能障碍的发生率、恢复情况、幻嗅或旁嗅的发生率方面,各组之间没有明显的统计学差异。不同研究组和对照组在半客观嗅觉表现方面没有明显的统计学差异。所有患者和对照组的嗅球体积均正常。鼻旁窦粘膜增厚的情况很少见。结论:我们发现,在为期六个月的随访中,COVID-19 的三个严重程度组别与对照组在主观或半客观嗅觉和味觉方面均无差异。
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Prevalence of smell and taste dysfunction in different clinical severity groups of COVID-19 patients
BACKGROUND: Studies on the long-term prevalence of smell and taste impairment concerned with severe disease in the acute phase of COVID-19 are limited. The aim of our study was to assess and compare psychophysical testing and self-reported smell and taste disturbances and recovery between three patient groups suffering from critical, severe, or mild COVID-19 in a follow-up at six-months after the acute phase. METHODOLOGY: The prospective controlled study of 227 participants comprised 72 intensive-care-unit-treated (ICU-treated), 53 pulmonology- or infectious-diseases-ward-treated (WARD-treated), and 48 home-isolated patients (HOME) with preceding COVID-19, and 54 individuals with no history of COVID-19 (CONTROL). All participants visited a follow-up clinic for a sense-of-smell screening and underwent Magnetic Resonance Imaging (MRI) of the brain, olfactory bulbs and sinonasal area at six months after acute disease. Before the follow-up visit, the participants received a questionnaire concerning smell and taste function. We sent a supplementary questionnaire including questions about phantosmia and parosmia and taste recovery at a median of 502.5 days after the acute phase. RESULTS: We found no statistically significant differences between the groups in the incidence of smell and taste dysfunction, recovery, or the occurrence of parosmia or phantosmia. There were no statistically significant differences in semi-objective smell performance across the different study groups and controls. The olfactory bulb volume was normal in all patients and controls. Mucosal thickening in paranasal sinuses was rare. CONCLUSIONS: We found no difference in a six-month follow-up in the subjective or semi-objective senses of smell and taste between three severity groups of COVID-19 and controls.
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