Schutz Kobi L, Fancourt Nicholas, Chang Anne B, Morris Peter, Buckley Rachel, Biancardi Edwina, Roberts Kathryn, Cush James, Heraganahally Subash, McCallum Gabrielle B
Child Health Division, Menzies School of Health Research, Charles Darwin University, Darwin, NT, Australia.
School of Nursing, Charles Darwin University, Darwin, NT, Australia.
Front Pediatr. 2023 Apr 28;11:1184303. doi: 10.3389/fped.2023.1184303. eCollection 2023.
Bronchiectasis is increasingly being recognized to exist in all settings with a high burden of disease seen in First Nations populations. With increasing numbers of pediatric patients with chronic illnesses surviving into adulthood, there is more awareness on examining the transition from pediatric to adult medical care services. We undertook a retrospective medical chart audit to describe what processes, timeframes, and supports were in place for the transition of young people (≥14 years) with bronchiectasis from pediatric to adult services in the Northern Territory (NT), Australia.
Participants were identified from a larger prospective study of children investigated for bronchiectasis at the Royal Darwin Hospital, NT, from 2007 to 2022. Young people were included if they were aged ≥14 years on October 1, 2022, with a radiological diagnosis of bronchiectasis on high-resolution computed tomography scan. Electronic and paper-based hospital medical records and electronic records from NT government health clinics and, where possible, general practitioner and other medical service attendance were reviewed. We recorded any written evidence of transition planning and hospital engagement from age ≥14 to 20 years.
One hundred and two participants were included, 53% were males, and most were First Nations people (95%) and lived in a remote location (90.2%). Nine (8.8%) participants had some form of documented evidence of transition planning or discharge from pediatric services. Twenty-six participants had turned 18 years, yet there was no evidence in the medical records of any young person attending an adult respiratory clinic at the Royal Darwin Hospital or being seen by the adult outreach respiratory clinic.
This study demonstrates an important gap in the documentation of delivery of care, and the need to develop an evidence-based transition framework for the transition of young people with bronchiectasis from pediatric to adult medical care services in the NT.
支气管扩张症在各种环境中越来越多地被认识到存在,在原住民人群中疾病负担很高。随着越来越多患有慢性病的儿科患者存活至成年,人们越来越意识到要审视从儿科医疗服务向成人医疗服务的过渡。我们进行了一项回顾性病历审核,以描述澳大利亚北领地(NT)患有支气管扩张症的年轻人(≥14岁)从儿科服务过渡到成人服务的过程、时间框架和支持措施。
参与者来自2007年至2022年在北领地皇家达尔文医院对因支气管扩张症接受调查的儿童进行的一项更大规模的前瞻性研究。如果年轻人在2022年10月1日年满≥14岁,且在高分辨率计算机断层扫描上有支气管扩张症的放射学诊断,则纳入研究。对电子和纸质医院病历以及北领地政府健康诊所的电子记录,并在可能的情况下,对全科医生和其他医疗服务就诊记录进行了审查。我们记录了从≥14岁到20岁期间过渡计划和医院参与的任何书面证据。
纳入了102名参与者,53%为男性,大多数是原住民(95%),居住在偏远地区(90.2%)。9名(8.8%)参与者有某种形式的过渡计划记录或从儿科服务出院的记录。26名参与者已年满18岁,但病历中没有证据表明任何年轻人曾在皇家达尔文医院的成人呼吸科诊所就诊或接受成人外展呼吸科诊所的诊治。
本研究表明在医疗服务提供的记录方面存在重要差距,并且需要为北领地患有支气管扩张症的年轻人从儿科医疗服务过渡到成人医疗服务制定一个基于证据的过渡框架。