Education and implementation of home spirometry in an adolescent cystic fibrosis population

IF 2.2 4区 医学 Q3 RESPIRATORY SYSTEM
Sarah Schaffer, Abigail Strang, Ambika Shenoy, Dawn Selhorst, Aaron Chidekel
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Abstract

Background

Lung function in individuals with cystic fibrosis (CF) is closely monitored as an objective marker of clinical status. The COVID-19 pandemic shifted our ability to assess individuals from in-person to remote monitoring using telehealth. As part of efforts to monitor individuals remotely during this time, this study describes the process of education and implementation of home spirometry in an adolescent CF population at Nemours Children's Hospital in Wilmington, Delaware, USA. In addition, this study reviews the ability of adolescents with CF to produce reliable, consistent, and accurate results using home spirometry.

Methods

This was a quality-improvement study over a 9-month period at a single CF center. Home spirometers were supplied by the CF Foundation to 40 adolescents with CF. An educational curriculum was used for initial training on the device by a dedicated CF respiratory therapist. After training, participants reported spirometry results weekly until reliable technique was established. Once reliable technique was achieved, participants reported results monthly. Results were retrospectively reviewed to determine accuracy and consistency. The percentages of patients who were able to achieve reliable, consistent, and accurate results were recorded as well as the need for additional training or other reasons for inability to produce ongoing results.

Results

Home spirometers were distributed to 40 adolescents. Out of these 40 participants, 35 (88%) completed initial training; 29 (83%) sent at least one set of results, and 24 (60%) established reliable technique after an average of 5 weekly attempts. When home spirometer results were retrospectively reviewed, 83% (20/24) were deemed accurate in comparison to spirometry completed in clinic, and 83% (20/24) showed consistency between efforts sent.

Conclusion

Home spirometry, when properly implemented with structured education and active participant engagement, has potential to provide meaningful data and feedback to CF care teams. Implementation of this process requires substantial resources and active participation from an adolescent population who are at higher risk for non-adherence. Future studies are needed to determine the impact of home spirometry on clinical outcomes and reliability over time and to address barriers to consistent and enduring engagement in the adolescent population.

青少年囊性纤维化患者家庭肺活量测定的教育和实施。
背景:囊性纤维化(CF)患者的肺功能作为临床状态的客观标志物受到密切监测。新冠肺炎大流行将我们评估个人的能力从住院转变为使用远程医疗进行远程监测。作为在此期间远程监测个体的努力的一部分,本研究描述了美国特拉华州威尔明顿Nemours儿童医院青少年CF人群中家庭肺活量测定的教育和实施过程。此外,本研究还回顾了CF青少年使用家庭肺活计得出可靠、一致和准确结果的能力。方法:这是一项在单个CF中心进行的为期9个月的质量改进研究。CF基金会为40名CF青少年提供了家庭肺活量计。专门的CF呼吸治疗师使用教育课程对该设备进行了初步培训。训练后,参与者每周报告肺活量测定结果,直到建立可靠的技术。一旦实现了可靠的技术,参与者每月报告结果。对结果进行回顾性审查,以确定准确性和一致性。记录了能够获得可靠、一致和准确结果的患者百分比,以及需要额外培训或其他无法产生持续结果的原因。结果:家庭肺活量计被分配给40名青少年。在这40名参与者中,35人(88%)完成了初步培训;29人(83%)发送了至少一组结果,24人(60%)在平均每周5次尝试后建立了可靠的技术。当对家庭肺活量计的结果进行回顾性审查时,与临床完成的肺活量测定相比,83%(20/24)的结果被认为是准确的,83%(2000/24)的结果显示所做努力的一致性。结论:如果通过结构化的教育和积极的参与者参与正确实施家庭肺活量测定,有可能为CF护理团队提供有意义的数据和反馈。这一进程的实施需要大量资源和不遵守的风险较高的青少年群体的积极参与。未来的研究需要确定家庭肺活量测定对临床结果和可靠性的影响,并解决青少年群体持续和持久参与的障碍。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Respiratory Medicine and Research
Respiratory Medicine and Research RESPIRATORY SYSTEM-
CiteScore
2.70
自引率
0.00%
发文量
82
审稿时长
50 days
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