Sleep Center, Division of Pulmonary and Sleep Medicine, Children's Hospital of Philadelphia, Philadelphia, PA, USA; Department of Child and Adolescent Psychiatry and Behavioral Sciences, Children's Hospital of Philadelphia, Philadelphia, PA, USA; Department of Psychiatry, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Mixed Methods Research Lab, Department of Family Medicine and Community Health, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Sleep Med. 2023 Jul;107:179-186. doi: 10.1016/j.sleep.2023.04.022. Epub 2023 Apr 28.
BACKGROUND/OBJECTIVE: While positive airway pressure (PAP) is an efficacious intervention for the treatment of obstructive sleep apnea syndrome (OSAS) in children with Down syndrome (DS), implementation and consistent use can be difficult. Caregiver perspectives and experiences using PAP are described with the aim of informing clinical practice.
Qualitative semi-structured phone interviews were conducted with 40 caregivers (i.e., mothers) of children with DS and OSAS treated with PAP for at least 6 months. Content analysis was used to identify themes associated with adherence and non-adherence.
Respondents indicated variability in caregiver experience with the adoption of PAP and observed benefits of PAP. Varied experiences were attributed to several themes including accessing supplies, interactions with the medical team and equipment company, and patients' unique needs and behaviors, including the child's willingness and ability to adapt to PAP, sensory sensitivities, keeping the mask on all night, and differences in daytime behavior. Many families reported that desensitization with a reward system and trust within the caregiver-patient relationship were helpful. Caregiver suggestions for improving PAP adherence for families of children with DS included improving communication with the medical team and medical equipment company, emphasizing patience, using visual supports, and social support and education for extended family.
Although family experiences varied, several actionable strategies by both the medical team and families emerged for improving the experience of and adherence to PAP in children with DS.
背景/目的:虽然气道正压通气(PAP)是治疗唐氏综合征(DS)儿童阻塞性睡眠呼吸暂停综合征(OSAS)的有效干预措施,但实施和持续使用可能存在困难。本研究旨在描述照顾者使用 PAP 的观点和经验,为临床实践提供信息。
对 40 名接受 PAP 治疗至少 6 个月的 DS 和 OSAS 儿童的照顾者(即母亲)进行了定性半结构式电话访谈。采用内容分析法识别与依从性和不依从性相关的主题。
受访者表示,照顾者在采用 PAP 方面的经验存在差异,并观察到 PAP 的益处。不同的经验归因于几个主题,包括获取用品、与医疗团队和设备公司的互动以及患者的独特需求和行为,包括孩子对 PAP 的意愿和适应能力、感觉敏感性、整夜戴口罩以及日间行为的差异。许多家庭报告说,通过奖励系统脱敏和照顾者与患者之间的信任关系很有帮助。改善 DS 儿童家庭 PAP 依从性的建议包括改善与医疗团队和医疗设备公司的沟通、强调耐心、使用视觉支持以及为大家庭提供社会支持和教育。
尽管家庭的经验存在差异,但医疗团队和家庭都提出了一些可行的策略,以改善 DS 儿童对 PAP 的使用体验和依从性。