Tabari Azin, Golpayegani Goli, Tabari Azadeh, Saedi Babak, Mahdkhah Aydin, Amali Amin, Jazinizadeh Saber, Sahebi Leyla, Saffarzadeh Negin, Sadrehosseini Seyed Mousa
Department of Otolaryngology-Head and Neck Surgery, Otorhinolaryngology Research Center, Imam Khomeini Hospital Complex, Tehran University of Medical Sciences, Keshavarz Blvd, Tehran, Iran.
Department of Radiology, Massachusetts General Hospital and Harvard Medical School, Boston, MA USA.
Indian J Otolaryngol Head Neck Surg. 2022 Oct;74(Suppl 2):2894-2899. doi: 10.1007/s12070-021-02507-x. Epub 2021 Mar 12.
To perform a quantitative olfactory test in positive COVID19 RT-PCR admitted patients and asymptomatic ones, to evaluate the association between hyposmia and disease severity. This is a Cross sectional study. Ninety-one patients including 68 inpatients and 23 asymptomatic healthcare workers with positive COVID-19 RT-PCRs. Methods: Demographics and clinical characteristics were collected. Iran Smell Identification Test (IR-SIT), a highly accurate 6-odorant test was used to evaluate the reliability of self-reported hyposmia and determine the correlation of the measured olfactory dysfunction with disease severity. Twenty-two of 91 patients (24%) reported hyposmia, while 41/91 (45%) patients had measurable olfactory dysfunction (IR-SIT score 1-4, < 0.05). Mean age of the 68 inpatients and 23 asymptomatic patients were 43.97 ± 16.13 years; M:F 43:25, and 43.87 ± 12.76 years; M:F 8:15 respectively. Of 68 patients, 20 were graded as severe, and 48/68 had mild course of disease. IR-SIT detected hyposmia in 80% of patients with severe disease, and 50% with mild disease, respectively. The risk of disease severity was significantly increased for patients with olfactory dysfunction and was detected 4 times higher when compared to patients with mild disease (OR 4, 95% CI: 1.166-13.728, = 0.028). Olfactory Dysfunction was present in 80% of patients with severe course. The risk of disease severity is significantly increased with olfactory dysfunction in admitted patients.
对新冠病毒逆转录聚合酶链式反应(RT-PCR)检测呈阳性的住院患者及无症状感染者进行定量嗅觉测试,以评估嗅觉减退与疾病严重程度之间的关联。这是一项横断面研究。91名患者,包括68名住院患者和23名新冠病毒RT-PCR检测呈阳性的无症状医护人员。方法:收集人口统计学和临床特征。使用伊朗嗅觉识别测试(IR-SIT),这是一种高度准确的6种气味测试,用于评估自我报告的嗅觉减退的可靠性,并确定所测量的嗅觉功能障碍与疾病严重程度的相关性。91名患者中有22名(24%)报告有嗅觉减退,而41/91(45%)的患者存在可测量的嗅觉功能障碍(IR-SIT评分1-4,<0.05)。68名住院患者和23名无症状患者的平均年龄分别为43.97±16.13岁;男:女为43:25,以及43.87±12.76岁;男:女为8:15。68名患者中,20名被评为重症,48/68患有轻症。IR-SIT分别在80%的重症患者和50%的轻症患者中检测到嗅觉减退。嗅觉功能障碍患者的疾病严重程度风险显著增加,与轻症患者相比,检测到的风险高4倍(比值比4,95%置信区间:1.166-13.728,P=0.028)。80%的重症患者存在嗅觉功能障碍。住院患者中,嗅觉功能障碍会显著增加疾病严重程度的风险。