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Exploring patient-borne costs and wait times for obstructive sleep apnea (OSA) care among rural and urban adults 探讨农村和城市成人阻塞性睡眠呼吸暂停(OSA)治疗的患者负担费用和等待时间
IF 0.8 Q3 RESPIRATORY SYSTEM Pub Date : 2023-01-02 DOI: 10.1080/24745332.2022.2156936
Duaa Fatima, W. Tsai, J. Corrigan, I. Ogah, A. Ip-Buting, H. Sharpe, C. Laratta, P. Peller, S. Pendharkar
Abstract RATIONALE: Geography is an increasingly recognized barrier to the diagnosis and treatment of chronic diseases, yet no prior studies have investigated its influence on the patient-borne burden of obstructive sleep apnea (OSA) care. OBJECTIVE: We aimed to determine if wait times and costs of OSA care differ between rural and urban adults. METHODS: We conducted a secondary analysis of data from a prospective cohort study comparing OSA treatment outcomes among urban and rural adults. Participants were recruited at the time of continuous positive airway pressure (CPAP) initiation for uncomplicated OSA. Residential postal codes were translated into geographic census areas to classify participants as urban (community size > 100,000) or rural. Participants were administered a questionnaire exploring wait times and costs of OSA care at baseline and three months. RESULTS: We enrolled 242 participants (100 rural). Twenty-six percent of respondents waited at least six months to seek medical attention for possible OSA, with no difference between groups. Wait times for diagnosis and treatment were three months or less for 91 and 93% of respondents, respectively. However, rural respondents experienced longer delays from first assessment to diagnosis and from diagnosis to treatment. Fewer individuals with rural residence were supported by government funding for diagnostic testing or CPAP. Rural participants more commonly reported additional appointment-related costs and greater total costs of care. CONCLUSION: Rural patients experience longer wait times and a greater financial burden for OSA care. The findings of this study will inform the development of novel models of OSA care sensitive to the needs of unique populations.
理由:地理位置越来越被认为是慢性疾病诊断和治疗的障碍,但尚未有研究调查其对阻塞性睡眠呼吸暂停(OSA)护理患者负担的影响。目的:我们旨在确定OSA治疗的等待时间和费用在农村和城市成年人之间是否存在差异。方法:我们对来自一项前瞻性队列研究的数据进行了二次分析,比较了城市和农村成年人的OSA治疗结果。参与者是在开始持续气道正压通气(CPAP)治疗无并发症OSA时招募的。住宅邮政编码被翻译成地理普查区域,将参与者分为城市(社区规模> 10万)和农村。研究人员对参与者进行问卷调查,了解在基线和三个月时OSA治疗的等待时间和费用。结果:我们招募了242名参与者(100名农村参与者)。26%的受访者至少等了6个月才寻求可能的阻塞性睡眠呼吸暂停的医疗救助,这在两组之间没有差异。91%的应答者和93%的应答者等待诊断和治疗的时间分别为三个月或更短。然而,农村应答者从首次评估到诊断以及从诊断到治疗的延误时间较长。很少有农村居民得到政府资助进行诊断检测或CPAP。农村参与者更普遍地报告了额外的预约相关费用和更高的护理总费用。结论:农村患者接受OSA治疗的等待时间更长,经济负担更大。这项研究的结果将为开发对特殊人群需求敏感的OSA护理新模式提供信息。
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引用次数: 0
Linkage of administrative and compensation databases for work-related asthma surveillance in Ontario: A proof of concept study 安大略省与工作有关的哮喘监测的行政和补偿数据库的联系:概念研究的证明
IF 0.8 Q3 RESPIRATORY SYSTEM Pub Date : 2023-01-02 DOI: 10.1080/24745332.2022.2161025
M. MacKinnon, K. Barrick, L. Lévesque, G. Liss, S. Tarlo, M. Lougheed
Abstract RATIONALE: Approximately 15% of all asthma cases are work-related and eligible for workers’ compensation in Ontario. However, compensation rates of work-related asthma (WRA) are far less than predicted, making it difficult to estimate the prevalence of the disease. OBJECTIVES We aimed to estimate prevalence of compensated WRA in Ontario; profile the pattern of compensated WRA by demographic, temporal and geographic factors; and demonstrate the potential for database linkage to monitor rates of compensated WRA cases. METHODS Compensated WRA claims data were linked to asthma cases in the Institute of Clinical Evaluative Sciences (ICES) asthma database via encrypted health card numbers. WRA claims between April 1998 and March 2002 were accessed from: i) the Ontario Workplace Safety and Insurance Board (WSIB) Occupational Disease Information Surveillance System (ODISS); and ii) a University of Toronto research database (RD) created by abstracting the same WSIB ODISS claim files. MAIN RESULTS: The estimated prevalence of WRA among individuals with asthma in the asthma database was less than 1% compared to an expected prevalence of 15-20%. Sensitivity of the Asthma database for including individuals with asthma with WRA was very good but differed significantly based on claims category (p < 0.001) compared to the RD as the gold standard. CONCLUSIONS Our findings suggest WRA is severely under-reported. Approximately 11-15% of compensated WRA claims are not captured by the asthma database. Factors accounting for discordance between databases should be explored in order for administrative data linkage to be used to monitor the rates of compensated WRA cases in Ontario.
基本原理:大约15%的哮喘病例与工作有关,在安大略省有资格获得工人赔偿。然而,与工作有关的哮喘(WRA)的补偿率远低于预期,因此难以估计该疾病的患病率。目的:我们旨在估计安大略省代偿性WRA的患病率;按人口、时间和地理因素分析补偿型WRA的格局;并展示了数据库连接的潜力,以监测WRA补偿案件的比率。方法补偿的WRA索赔数据通过加密的健康卡号与临床评估科学研究所(ICES)哮喘数据库中的哮喘病例相关联。1998年4月至2002年3月期间WRA索赔的资料来自:i)安大略省工作场所安全和保险委员会职业病信息监测系统;ii)多伦多大学研究数据库(RD),通过对相同的WSIB ODISS索赔文件进行抽象而创建。主要结果:哮喘数据库中哮喘患者中WRA的估计患病率低于1%,而预期患病率为15-20%。与RD作为金标准相比,哮喘数据库对纳入患有WRA的哮喘患者的敏感性非常好,但基于索赔类别存在显著差异(p < 0.001)。结论:我们的研究结果表明WRA被严重低估。大约11% -15%的WRA赔偿索赔未被纳入哮喘数据库。应当探讨造成数据库之间不一致的因素,以便利用行政数据联系来监测安大略省得到补偿的WRA案件的比率。
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引用次数: 0
Respiratory manifestations of long COVID 长冠状病毒的呼吸道表现
IF 0.8 Q3 RESPIRATORY SYSTEM Pub Date : 2023-01-02 DOI: 10.1080/24745332.2022.2156407
A. Kouri, Samir Gupta
Abstract As we near the third year of the COVID-19 pandemic, greater attention is now being paid to the potential long-term consequences of SARS-CoV-2 in the hundreds of millions of people infected globally. A syndrome termed “long COVID” has emerged, which predominantly manifests as persistent fatigue, dyspnea, chest pain, and cognitive dysfunction following acute infection. The incidence of long COVID is in the range of 15% based on current best evidence, and symptoms are likely a result of several different pathophysiological mechanisms including multi-organ injury from acute infection, systemic viral persistence, immune dysregulation, and/or autoimmunity. Pulmonary symptoms represent a significant component of long COVID, and there is a growing body of research describing the epidemiology, risk factors, physiology, and radiology of the respiratory manifestations of long COVID. In this clinical review, we examine the most recent evidence relating to “respiratory long COVID,” discuss how innovative technologies such as Xenon-129 gas transfer magnetic resonance imaging (MRI) and respiratory oscillometry are helping to elucidate its unique pathophysiology, and consider the role of preventative strategies and possible treatments such as adapted pulmonary rehabilitation. The burden of respiratory long COVID is likely to continue to grow, and all healthcare professionals who care for patients with respiratory disease must prepare for this emerging chronic condition. This will require increased resources from healthcare decision makers, inventive approaches to healthcare delivery, further research, and the same spirit of collaboration that has enabled the many success stories to date in the global effort against COVID-19.
随着COVID-19大流行即将进入第三个年头,人们越来越关注SARS-CoV-2对全球数亿感染者的潜在长期影响。一种被称为“长冠”的综合征已经出现,其主要表现为急性感染后的持续疲劳、呼吸困难、胸痛和认知功能障碍。根据目前的最佳证据,长冠状病毒病的发病率在15%左右,症状可能是几种不同的病理生理机制的结果,包括急性感染引起的多器官损伤、全身病毒持续存在、免疫失调和/或自身免疫。肺部症状是新冠肺炎的重要组成部分,越来越多的研究描述了新冠肺炎的流行病学、危险因素、生理学和影像学表现。在这篇临床综述中,我们研究了与“呼吸性长冠状病毒”相关的最新证据,讨论了氙-129气体转移磁共振成像(MRI)和呼吸振荡测量等创新技术如何帮助阐明其独特的病理生理学,并考虑了预防策略和可能的治疗方法(如适应性肺康复)的作用。呼吸道疾病的负担可能会继续增加,所有照顾呼吸道疾病患者的医疗保健专业人员都必须为这种新出现的慢性疾病做好准备。这将需要卫生保健决策者提供更多资源,采用创新的卫生保健提供方法,开展进一步研究,并发扬迄今在全球抗击COVID-19努力中取得许多成功的合作精神。
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引用次数: 0
Bronchoscopy during the COVID-19 pandemic: A Canadian Thoracic Society Position Statement update COVID-19大流行期间的支气管镜检查:加拿大胸科学会立场声明更新
IF 0.8 Q3 RESPIRATORY SYSTEM Pub Date : 2022-11-14 DOI: 10.1080/24745332.2022.2137317
Simon A. Houston, Yusing Gu, T. Vandemoortele, Elaine Dumoulin, Ashley-Mae E. Gillson, C. Tyan, L. Sakr, G. Bendiak, Anne V Gonzalez, M. Fortin
adivision of respirology, Qeii-Halifax infirmary, department of Medicine, dalhousie university, Halifax, nova scotia, Canada; bdivision of respiratory Medicine, department of Medicine, university of Montreal, Montreal, Québec, Canada; cdivision of respiratory Medicine, Cumming school of Medicine, university of Calgary, Calgary, alberta, Canada; ddivision of pulmonary Medicine, department of Medicine, university of alberta, edmonton, alberta, Canada; edivision of respirology, Critical Care and sleep Medicine, university of saskatchewan, saskatoon, saskatchewan, Canada; fdivision of respirology, Jewish General Hospital, department of Medicine, McGill university, Montreal, Québec, Canada; gsection of respiratory Medicine, alberta Children’s Hospital, department of pediatrics, university of Calgary, Calgary, alberta, Canada; hdivision of respiratory Medicine, department of Medicine, McGill university Health Centre, Montreal, Québec, Canada; idivision of respirology, institut universitaire de cardiologie et de pneumologie de Québec, department of Medicine, université laval, Québec, Québec, Canada
加拿大新斯科舍省哈利法克斯达尔豪斯大学医学院哈利法克斯医院呼吸内科;b蒙特利尔大学医学系呼吸内科,加拿大蒙特利尔;加拿大阿尔伯塔省卡尔加里市卡尔加里大学卡明医学院呼吸内科;加拿大艾伯塔省埃德蒙顿市阿尔伯塔大学医学系肺内科;加拿大萨斯喀彻温省萨斯卡通萨斯喀彻温大学呼吸学、重症监护和睡眠医学部;加拿大魁北克蒙特利尔麦吉尔大学犹太总医院内科呼吸内科;加拿大阿尔伯塔省卡尔加里市卡尔加里大学阿尔伯塔儿童医院儿科呼吸内科;加拿大魁北克蒙特利尔麦吉尔大学保健中心医学系呼吸内科;加拿大魁魁省魁魁省拉瓦尔大学医学院魁魁省心脏病与肺病研究所呼吸学分科
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引用次数: 0
President’s message 总统的消息
IF 0.8 Q3 RESPIRATORY SYSTEM Pub Date : 2022-11-14 DOI: 10.1080/24745332.2022.2117471
R. Leigh
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引用次数: 0
President’s message 总统的消息
IF 0.8 Q3 RESPIRATORY SYSTEM Pub Date : 2022-11-02 DOI: 10.1080/24745332.2022.2139578
R. Leigh
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引用次数: 0
Canadian Tuberculosis Standards 8th edition: What’s new? And what’s next? 加拿大结核病标准第8版:有什么新内容?接下来呢?
IF 0.8 Q3 RESPIRATORY SYSTEM Pub Date : 2022-11-02 DOI: 10.1080/24745332.2022.2133030
D. Menzies
On World Tuberculosis (TB) Day 2022, the 8th edition of the Canadian Tuberculosis Standards (at: https://www.tandfonline.com/toc/ucts20/6/sup1) was published by the Canadian Thoracic Society in collaboration with Association of Medical Microbiology and Infectious Disease (AMMI) Canada and the support of the Public Health Agency of Canada. Written by a large and diverse group from across Canada, with expertise in clinical, epidemiologic, pathogenetic, microbiologic and public health aspects of TB, and with important input from community partners, notably from indigenous communities, the TB standards is intended to provide comprehensive and practical guidance for front line providers. After decades of neglect between 1970 and 2000, the last 20 years has seen a surge in new diagnostics, new treatments, and new control strategies for TB. These advances are reflected in the new TB Standards, with major changes in recommendations in many sections. See Table 1 for a summary of some of the most important changes. However, these advances have not yet impacted TB rates—which have barely changed over the last two decades—globally1 and in Canada.2 In fact, as detailed in the first chapter of the Standards, the number of persons diagnosed with TB disease each year in Canada has increased over the last 3 years.2 Clearly, new diagnostics, treatments and strategies are needed, not only as recommendations but in practice. For the diagnosis of TB disease, rapid molecular tests can be used3—to accelerate detection of the disease, and are recommended for the rapid identification of drug resistant strains—such that appropriate and effective therapy can be started promptly. The technology has been available for close to a decade, but implementation has been slow due to cost considerations. Given the risks to patients,4 increased transmission5 and high costs to health systems of delayed or missed diagnoses, the investment to implement these rapid and highly accurate tests seems modest. Isoniazid (INH) has been the mainstay of TB prevention since the first edition of the TB Standards in 1970. Although the long duration (of 6 to 12 months), and potential for serious, even fatal hepato-toxicity were major drawbacks, the evidence for alternate regimens was slow in arriving. However, two rifamycin based regimens have undergone rigorous evaluations in randomized trials and are now recommended as first line regimens for TB prevention.6 One regimen is 4 months daily Rifampin (RIF) (4 R), which has significantly better completion, fewer severe adverse events and noninferior efficacy for TB prevention, compared to 9 months INH (9H) in adults7,8 and children.9 The other is 3 months once weekly INH & Rifapentine (3HP), which has better completion and less hepato-toxicity, and noninferior efficacy compared to 6H or 9H in adults10–12 and children.13 The fact that 3HP has only 12 doses seems appealing, but a drawback is that each dose must be directly observed14; this is not feasible
在2022年世界防治结核病日,加拿大胸科学会与加拿大医学微生物学和传染病协会合作,在加拿大公共卫生署的支持下,出版了第八版加拿大结核病标准(网址:https://www.tandfonline.com/toc/ucts20/6/sup1)。结核病标准由来自加拿大各地的一个庞大而多样化的小组编写,具有结核病的临床、流行病学、病原学、微生物学和公共卫生方面的专业知识,并得到社区合作伙伴,特别是土著社区的重要投入,旨在为一线提供者提供全面和实用的指导。在1970年至2000年期间被忽视了几十年之后,过去20年出现了结核病的新诊断方法、新治疗方法和新控制战略的激增。这些进展反映在新的结核病标准中,许多章节的建议发生了重大变化。参见表1对一些最重要更改的总结。然而,这些进步尚未影响到结核病发病率——在过去二十年中,全球和加拿大的结核病发病率几乎没有变化。事实上,正如标准第一章所详述的那样,加拿大每年被诊断患有结核病的人数在过去三年中有所增加显然,不仅需要作为建议,而且需要在实践中采用新的诊断方法、治疗方法和策略。对于结核病的诊断,可以使用快速分子检测来加速疾病的发现,并建议用于快速识别耐药菌株,以便及时开始适当和有效的治疗。这项技术已有近十年的历史,但由于成本方面的考虑,实施进展缓慢。考虑到延误或漏诊给患者带来的风险、传播的增加以及卫生系统的高昂成本,实施这些快速和高度准确的检测的投资似乎不多。自1970年《结核病标准》第一版以来,异烟肼(INH)一直是预防结核病的主要手段。虽然持续时间长(6至12个月)和潜在的严重甚至致命的肝毒性是主要的缺点,但替代方案的证据来得很慢。然而,两种基于利福霉素的方案在随机试验中经过了严格的评估,现在被推荐为预防结核病的一线方案一种方案是每日4个月的利福平(RIF) (4r),与成人和儿童的9个月INH (9H)相比,它具有明显更好的完成度,更少的严重不良事件和非劣效的结核病预防效果另一种是3个月,每周一次的INH和利福喷丁(3HP),在成人10 - 12和儿童中,与6H或9H相比,它具有更好的完成性和更少的肝毒性,并且疗效不逊色3HP只有12剂似乎很吸引人,但缺点是每次剂量都必须直接观察14;这并非在所有情况下都可行。由对所有结核病药物敏感的生物体引起的结核病的推荐治疗方案保持不变最近一项使用高剂量利福喷丁和氟喹诺酮的研究表明,与目前6个月的标准相比,4个月的治疗是足够的。然而,由于担心毒性增加,在获得更多关于其安全性的数据之前,加拿大尚未推荐该方案。然而,耐药结核病的治疗已经通过引入新的或重新利用的药物,包括新一代氟喹诺酮类药物(莫西沙星或左氧氟沙星)、利奈唑胺、氯法齐明和贝达喹啉而发生了转变。虽然很少有随机试验,但对许多观察性研究的个体患者数据的分析表明,使用这些药物治疗耐多药(MDR)结核病可大幅降低死亡率,提高治愈率。因此,新的结核病标准建议采用这些药物的全口服治疗方案,取代长期使用阿米卡星等注射药物治疗耐多药结核病18此外,现在建议将氟喹诺酮类药物作为耐药结核病治疗的一部分,耐药结核病18是加拿大和全球最常见的耐药结核病形式。1,19但是,执行这些新建议将具有挑战性。在加拿大,许多新近推荐的结核病预防或结核病治疗方案需要的药物尚未获得加拿大卫生部的监管批准。这些药物包括利福喷丁、贝达喹啉和氯法齐明。尽管有充分的证据表明它们治疗这些疾病的有效性和安全性,包括证据表明这些药物大大优于目前在加拿大批准用于相同疾病的药物,尽管它们是世界卫生组织强烈推荐的
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引用次数: 1
“Not just the asthma”: Understanding the acute asthma experiences of adult women with asthma presenting to the emergency department through photovoice “不只是哮喘”:通过影像语音了解到急诊科就诊的成年女性哮喘患者的急性哮喘经历
IF 0.8 Q3 RESPIRATORY SYSTEM Pub Date : 2022-10-26 DOI: 10.1080/24745332.2022.2133756
L. Krebs, N. Hill, C. Villa‐Roel, P. McLane, B. Rowe, Samir Gupta
Abstract Rationale: Asthma is a common reason for emergency department (ED) presentation. Few studies have explored the experiences of adults during asthma exacerbation, particularly those that necessitate ED care. Objectives: This study explored adults experiences during asthma exacerbation. Methods: A photovoice study was conducted. ED patients presenting for asthma care between the ages of 17-55 years were eligible for the study and recruited in the ED. Participants had 3-4 weeks to take photographs and subsequently completed a one-on-one photo-elicitation interview. Interviews were audio recorded, transcribed and thematically analyzed. Measurements and Main Results: Six patients agreed to participate; 2 were lost to follow-up. One primary theme emerged. Specifically, the role of hope and fear, including the tension between them, in their experience of their condition. Hope and fear permeated all aspects of experience, including the following subthemes: 1) participants adopting the roles of advocate and expert, 2) frustration with their health state, 3) loss of freedom and subsequent feelings of failure, 4) barriers to accessing health care, and 5) “good” and “bad” ED care. Asthma was an ever-present consideration in participants lives during times of “good asthma control” and times of exacerbation. Conclusions: Participants’ focus on the roles of hope and fear, both in the ED and beyond, suggests that openly acknowledging and addressing these emotional aspects as a part of the ED interaction could result in a better care experience for some patients. Seeing the whole person as more than their symptoms and sharing decision-making may help clinicians to provide care that supports hopefulness.
理由:哮喘是急诊科(ED)就诊的常见原因。很少有研究探讨成人在哮喘发作期间的经历,特别是那些需要ED护理的人。目的:本研究探讨成人在哮喘发作期间的经历。方法:采用光声法。年龄在17-55岁之间接受哮喘治疗的ED患者符合研究条件,并在ED中招募。参与者有3-4周的时间拍照,随后完成一对一的照片激发访谈。采访录音,转录和主题分析。测量和主要结果:6例患者同意参与;2例失访。一个主要的主题出现了。具体来说,希望和恐惧的作用,包括它们之间的紧张关系,在他们的经历中。希望和恐惧渗透在经历的各个方面,包括以下分主题:1)参与者扮演倡导者和专家的角色,2)对自己的健康状况感到沮丧,3)失去自由和随后的失败感,4)获得医疗保健的障碍,以及5)“好”和“坏”急诊科护理。在“良好的哮喘控制”时期和恶化时期,哮喘是参与者生活中始终存在的考虑因素。结论:参与者对希望和恐惧的角色的关注,无论是在急诊科还是其他地方,都表明公开承认和处理这些情感方面作为急诊科互动的一部分,可能会给一些患者带来更好的护理体验。看到整个人不仅仅是他们的症状和分享决策可以帮助临床医生提供支持希望的护理。
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引用次数: 0
History of asthma in Canada 加拿大哮喘史
IF 0.8 Q3 RESPIRATORY SYSTEM Pub Date : 2022-10-20 DOI: 10.1080/24745332.2022.2130840
D. Cockcroft
Abstract Asthma prevalence in Canada is high and, at least until recently, has been rising. Deaths from asthma have been gradually declining with a small but significant transient increase between about 1975 and 1995, most likely due to the inappropriate use of inhaled ß2 agonists leading to under-treatment with anti-inflammatory agents. Canada has been at the forefront of development of asthma treatments and asthma guidelines. Expressing the spectrum of asthma severity as a continuum rather than a series of steps is unique to the Canadian asthma guidelines. Other Canadian contributions include major participation in GINA, measurement of AHR, measurement of induced sputum cell counts, developments in aerosol science including large volume spacer devices, measurement of asthma quality of life and investigations into occupational asthma.
加拿大的哮喘患病率很高,至少直到最近,患病率一直在上升。哮喘死亡人数逐渐下降,大约在1975年至1995年期间出现了短暂的小幅但显著的增长,很可能是由于吸入ß2激动剂使用不当导致抗炎药治疗不足。加拿大一直处于哮喘治疗和哮喘指南发展的前沿。将哮喘严重程度的谱表示为一个连续体而不是一系列步骤是加拿大哮喘指南的独特之处。加拿大的其他贡献包括主要参与GINA, AHR的测量,诱导痰细胞计数的测量,气溶胶科学的发展,包括大容量间隔装置,哮喘生活质量的测量和职业性哮喘的调查。
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引用次数: 1
Acute fibrinous and organizing pneumonia following the COVID-19 mRNA-1273 vaccine COVID-19 mRNA-1273疫苗后急性纤维性肺炎和组织性肺炎
IF 0.8 Q3 RESPIRATORY SYSTEM Pub Date : 2022-08-29 DOI: 10.1080/24745332.2022.2111998
S. Nevison, David Hwang, A. Oikonomou, L. Fidler
Abstract A 57-year-old man developed respiratory symptoms 72 hours after receiving his third dose of the COVID-19 mRNA-1273 vaccine and underwent computed tomography (CT) chest imaging. This showed new diffuse subpleural and peribronchovascular nodular opacities with reverse halo sign. Laboratory investigations demonstrated an eosinophil count of 0.8 x 10E9/L and unremarkable connective tissue disease screen. Bronchoscopy with lavage and transbronchial biopsies demonstrated lymphocytic alveolitis without evidence of infection and histopathology consistent with acute fibrinous and organizing pneumonia (AFOP). He was treated with corticosteroids resulting in resolution of symptoms and CT findings. We present radiographic and histopathologic findings of AFOP following COVID-19 mRNA-1273 vaccination.
一名57岁男性在接种第三剂COVID-19 mRNA-1273疫苗72小时后出现呼吸道症状,并接受了CT胸部成像。显示新的弥漫性胸膜下和支气管血管周围结节性混浊伴反晕征。实验室检查显示嗜酸性粒细胞计数为0.8 x 10E9/L,结缔组织疾病筛查不明显。支气管镜检查伴灌洗和经支气管活检显示淋巴细胞性肺泡炎,无感染证据,组织病理学符合急性纤维性和组织性肺炎(AFOP)。他接受了皮质类固醇治疗,症状和CT表现得到缓解。我们报告了COVID-19 mRNA-1273疫苗接种后AFOP的放射学和组织病理学结果。
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引用次数: 0
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Canadian Journal of Respiratory, Critical Care, and Sleep Medicine
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