加拿大阿尔伯塔省新冠肺炎大流行对肺移植护理获取和服务提供影响的患者和提供者观点的解释性描述

IF 0.9 Q3 SURGERY
Journal of Transplantation Pub Date : 2025-05-22 eCollection Date: 2025-01-01 DOI:10.1155/joot/6850873
Katelyn Brehon, Pam Hung, Maxi Miciak, Rhea Varughese, Kieran Halloran, Kadija Perreault, Paul E Ronksley, Michael K Stickland, Jason Weatherald, Douglas P Gross, Grace Y Lam
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引用次数: 0

摘要

背景:COVID-19大流行影响了为慢性肺病患者提供卫生服务的方式。据我们所知,在加拿大阿尔伯塔省的背景下,尚未探讨COVID-19大流行期间肺移植患者及其提供者对获得护理和服务的看法。我们的目标是探讨LT患者和提供者对COVID-19大流行对医疗保健获取和服务提供的影响的观点。方法:我们采用解释性描述,一种定性方法,最终目的是为临床实践中的决策和行动提供信息。面谈是以虚拟方式进行的,并逐字保密地记录下来。数据生成和分析同时进行。Braun和Clarke提出了反身性主题分析的六个阶段。采用了提高调查结果的严谨性和可信度的策略。结果:共完成17次访谈,其中患者8次,提供者9次。产生了四个关键主题:(1)“COVID-19筑起了一道关系之墙;”(2)“决定如何提供医疗服务是一件复杂的事情;”(3)“平衡供需”;(4)“在全球大流行期间免疫功能低下的独特代价。”大流行影响了LT患者的社会关系,特别是通过使用虚拟护理。有几个因素阻碍了肝移植患者获得护理。提供者与会者强调,大流行期间移植数量减少,导致移植手术积压。对COVID-19的恐惧意味着一些LT患者不愿寻求医疗服务,导致后期健康后果。尽管明显缺乏可用的服务,但仍确定这一人群需要心理健康服务。与会者强调,由于检测和治疗不再那么容易获得,目前针对这一人群的COVID-19资源存在缺口。结论:总之,提供者参与者在他们所面临的情况下尽了最大努力为LT患者提供高质量的护理。然而,尽管患者参与者总体上了解情况,但由于COVID-19大流行,LT护理受到了影响。对这一人群的护理通常需要亲自进行,但由于肝移植患者免疫功能低下的性质,这一建议存在细微差别。卫生系统领导人可以利用我们的研究结果来实施从大流行中吸取的教训,并继续改善对不断增长的LT人口的服务。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
An Interpretive Description of Patient and Provider Perspectives on the Impact of the COVID-19 Pandemic on Lung Transplant Care Access and Service Delivery in Alberta, Canada.

Background: The COVID-19 pandemic impacted how health services were delivered for patients with chronic pulmonary conditions. To our knowledge, perceptions of patients with lung transplant (LT) and their providers on access to care and service delivery during the COVID-19 pandemic have not been explored in our context of Alberta, Canada. Our objective was to explore LT patient and provider perspectives on the impact of the COVID-19 pandemic on healthcare access and service delivery. Methods: We used interpretive description, a qualitative approach with the end-goal of informing decisions and actions in clinical practice. Interviews were conducted virtually and confidentially transcribed verbatim. Data generation and analysis occurred concurrently. Analysis was informed by Braun and Clarke's six phases of reflexive thematic analysis. Strategies to enhance rigor and trustworthiness of the findings were utilized. Results: We completed 17 interviews: 8 with patients and 9 with providers. Four key themes were generated: (1) "COVID-19 created a relational wall;" (2) "Determining how care should be delivered was a juggling act;" (3) "Balancing supply and demand;" and (4) "The unique costs of being immunocompromised during a global pandemic." The pandemic impacted social relationships for LT patients, especially through the use of virtual care. Several factors hindered access to care for LT patients. Provider participants highlighted how there were less transplants during the pandemic which created a backlog in transplant surgeries. Fear of COVID-19 meant that some LT patients were hesitant to seek healthcare services, resulting in later-term health consequences. A need for mental health services was identified among this population despite an apparent lack of available services. Participants highlighted the gap in COVID-19 resources that now exists for this population since testing and treatments are no longer as readily available. Conclusions: In conclusion, provider participants did the best that they could with the circumstances they faced to provide high-quality care to LT patients. However, while patient participants were generally understanding of circumstances, LT care suffered as a result of the COVID-19 pandemic. Care for this population generally needs to be in-person, but there is nuance surrounding this recommendation due to LT patients' immunocompromised nature. Health system leaders can leverage our findings to implement learnings from the pandemic and continue to improve services for the ever-growing LT population.

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