Ganesh Aravind, Rosentreter Ryan E, Chen Yushi, Mehta Rahul, McLeod Graham A, Wan Miranda W, Krett Jonathan D, Mahjoub Yasamin, Lee Angela S, Schwartz Ilan S, Richer Lawrence P, Metz Luanne M, Smith Eric E, Hill Michael D
Departments of Clinical Neurosciences (Ganesh, McLeod, Wan, Krett, Mahjoub, Lee, Metz, Smith, Hill), Community Health Sciences (Ganesh, Smith, Hill), Medicine (Rosentreter, Hill) and Radiology (Hill), University of Calgary Cumming School of Medicine; The Hotchkiss Brain Institute (Ganesh, Metz, Smith, Hill) and The Mathison Centre for Mental Health Research & Education (Ganesh), University of Calgary, Calgary, Alta.; Departments of Dentistry (Chen) and Medicine (Mehta, Schwartz), Faculty of Medicine and Dentistry, University of Alberta; Department of Pediatrics (Richer), Faculty of Medicine and Dentistry, College of Health Sciences, University of Alberta; and Women and Children's Health Research Institute (Richer), University of Alberta, Edmonton, Alta.
CMAJ Open. 2023 Aug 8;11(4):E696-E705. doi: 10.9778/cmajo.20220248. Print 2023 Jul-Aug.
Various neurologic manifestations have been reported in patients with COVID-19, mostly in retrospective studies of patients admitted to hospital, but there are few data on patients with mild COVID-19. We examined the frequency and persistence of neurologic/neuropsychiatric symptoms in patients with mild COVID-19 in a 1-year prospective cohort study, as well as assessment of use of health care services and patient-reported outcomes.
Participants in the Alberta HOPE COVID-19 trial (hydroxychloroquine v. placebo for 5 d), managed as outpatients, were prospectively assessed 3 months and 1 year after their positive test result. They completed detailed neurologic/neuropsychiatric symptom questionnaires, the telephone version of the Montreal Cognitive Assessment (T-MoCA), the Kessler Psychological Distress Scale (K10) and the EuroQol EQ-5D-3L (measure of quality of life). Close informants completed the Mild Behavioural Impairment Checklist (MBI-C) and the Informant Questionnaire on Cognitive Decline in the Elderly. We also tracked use of health care services and neurologic investigations.
The cohort consisted of 198 participants (87 female [43.9%] median age 45 yr, interquartile range 37-54 yr). Of the 179 participants with symptom assessments, 139 (77.6%) reported at least 1 neurologic symptom, the most common being anosmia/dysgeusia (99 [55.3%]), myalgia (76 [42.5%]) and headache (75 [41.9%]). Forty patients (22.3%) reported persistent symptoms at 1 year, including confusion (20 [50.0%]), headache (21 [52.5%]), insomnia (16 [40.0%]) and depression (14 [35.0%]); 27/179 (15.1%) reported no improvement. Body mass index (BMI), a history of asthma and lack of full-time employment were associated with the presence and persistence of neurologic/neuropsychiatric symptoms; female sex was independently associated with both (presence: odds ratio [OR] adjusted for age, race, BMI, history of asthma and neuropsychiatric history 5.04, 95% confidence interval [CI] 1.58 to 16.10). Compared to participants without persistent symptoms, those with persistent symptoms had more hospital admissions and family physician visits, and worse MBI-C scores and less frequent independence for instrumental activities at 1 year (83.8% v. 97.8%, = 0.005). Patients with any or persistent neurologic symptoms had worse psychologic distress (K10 score ≥ 20: adjusted OR 12.1, 95% CI 1.4 to 97.2) and quality of life (median EQ-5D-3L visual analogue scale rating 75 v. 90, < 0.001); 42/84 (50.0%) had a T-MoCA score less than 18 at 3 months, as did 36 (42.9%) at 1 year. Participants who reported memory loss were more likely than those who did not report such symptoms to have informant-reported cognitive-behavioural decline (1-yr MBI-C score ≥ 6.5: adjusted OR 15.0, 95% CI 2.42 to 92.60).
Neurologic/neuropsychiatric symptoms were commonly reported in survivors of mild COVID-19, and they persisted in 1 in 5 patients 1 year later. Symptoms were associated with worse participant- and informant-reported outcomes. ClinicalTrials.gov, no. NCT04329611.
新型冠状病毒肺炎(COVID-19)患者中已报告了各种神经系统表现,大多来自对住院患者的回顾性研究,但关于轻症COVID-19患者的数据较少。我们在一项为期1年的前瞻性队列研究中,研究了轻症COVID-19患者神经系统/神经精神症状的发生频率和持续情况,以及对医疗服务利用情况和患者报告结局的评估。
阿尔伯塔省HOPE COVID-19试验(羟氯喹啉与安慰剂治疗5天)的参与者作为门诊患者进行管理,在其检测结果呈阳性后的3个月和1年进行前瞻性评估。他们完成了详细的神经系统/神经精神症状问卷、蒙特利尔认知评估电话版(T-MoCA)、凯斯勒心理困扰量表(K10)和欧洲五维健康量表EQ-5D-3L(生活质量测量量表)。亲密知情者完成了轻度行为损害检查表(MBI-C)和老年人认知功能下降知情者问卷。我们还跟踪了医疗服务利用情况和神经系统检查。
该队列由198名参与者组成(87名女性[43.9%],中位年龄45岁,四分位间距37 - 54岁)。在179名有症状评估的参与者中,139名(77.6%)报告了至少1种神经系统症状,最常见的是嗅觉减退/味觉障碍(99名[55.3%])、肌痛(76名[42.5%])和头痛(75名[41.9%])。40名患者(22.3%)在1年后报告有持续症状,包括意识模糊(20名[50.0%])、头痛(21名[52.5%])、失眠(16名[40.0%])和抑郁(14名[35.0%]);179名中有27名(15.1%)报告无改善。体重指数(BMI)、哮喘病史和非全职工作与神经系统/神经精神症状的出现和持续有关;女性与之独立相关(出现:调整年龄、种族、BMI、哮喘病史和神经精神病史后的比值比[OR]为5.04,95%置信区间[CI]为1.58至16.10)。与无持续症状的参与者相比,有持续症状的参与者有更多的住院次数和家庭医生就诊次数,1年后MBI-C评分更差,工具性活动的独立频率更低(83.8%对97.8%,P = 0.005)。有任何或持续神经系统症状的患者心理困扰更严重(K10评分≥20:调整后的OR为12.1,95% CI为1.4至97.2),生活质量更差(EQ-5D-3L视觉模拟量表评分中位数75对90,P < 0.001);84名中有42名(50.0%)在3个月时T-MoCA评分低于18分,1年时为36名(42.9%)。报告有记忆丧失的参与者比未报告此类症状的参与者更有可能出现知情者报告的认知行为下降(1年MBI-C评分≥6.5:调整后的OR为15.0,95% CI为2.42至92.60)。
轻症COVID-19幸存者中常见神经系统/神经精神症状,1年后五分之一的患者症状仍持续存在。这些症状与患者及知情者报告的更差结局相关。ClinicalTrials.gov,编号NCT04329611。