Center for Health Metrics and Evaluation, American Heart Association, 7272 Greenville Ave, Dallas, TX 75213, USA.
Center for Health Metrics and Evaluation, American Heart Association, 7272 Greenville Ave, Dallas, TX 75213, USA.
Heart Lung. 2021 Nov-Dec;50(6):788-793. doi: 10.1016/j.hrtlng.2021.06.004. Epub 2021 Jul 2.
Limited studies exist that describe diagnosis, treatment, and management experiences of patients with hypertrophic cardiomyopathy (HCM). This study's purpose is to characterize patient experiences related to symptom onset, diagnosis, symptom management, support from healthcare professionals, and impacts on daily living.
Semi-structured interviews were conducted using open-ended questions and question probes were conducted with adults aged ≥18 years diagnosed with HCM ≥1 year prior. Interview recordings were transcribed verbatim and inductive and deductive thematic analyses were performed.
A total of 32 interviews were conducted. The majority of participants were female (53.1%), aged ≥45 years (90.6%), white (96.9%), and non-Hispanic (96.9%). Participants with longer time to HCM diagnosis described having atypical HCM symptoms, denial of their own symptoms, and experiences of misdiagnoses. For HCM information and support, participants utilized personal healthcare professionals as well as non-medical resources. Participants described experiences of anxiety, denial, and upset feelings about their diagnosis, but also gratitude, acceptance, and increased mindfulness toward healthy habits. Individuals reported making changes in daily activities because of reduced physical capacity and making changes in lifestyle choices because of desire to be close to HCM specialists. Over time, participants also described becoming less fearful through utilization of available resources and treatment options.
The diverse but often challenging experiences of individuals with HCM suggest that increasing availability and utilization of HCM patient resources may be effective at reducing the unfavorable physical and psychological impacts of HCM. Common reports of misdiagnoses resulting in delayed HCM diagnosis also indicate a need for HCM-related educational opportunities for healthcare professionals.
目前仅有少量研究描述了肥厚型心肌病(HCM)患者的诊断、治疗和管理经验。本研究旨在描述与症状发作、诊断、症状管理、医疗专业人员支持以及对日常生活的影响相关的患者体验。
采用开放式问题进行半结构式访谈,并对年龄≥18 岁、确诊 HCM≥1 年的成年人进行问题探针访谈。访谈录音逐字转录,并进行归纳和演绎主题分析。
共进行了 32 次访谈。大多数参与者为女性(53.1%)、年龄≥45 岁(90.6%)、白人(96.9%)和非西班牙裔(96.9%)。诊断为 HCM 时间较长的参与者描述了非典型的 HCM 症状、否认自身症状以及误诊经历。在获取 HCM 信息和支持方面,参与者既利用了个人医疗保健专业人员,也利用了非医疗资源。参与者描述了对诊断的焦虑、否认和不安情绪,但也表达了感激、接受和对健康习惯的更多关注。由于身体能力下降,个人报告了日常生活活动的改变,由于希望接近 HCM 专家,也改变了生活方式选择。随着时间的推移,参与者还描述了通过利用现有资源和治疗选择来减少恐惧。
HCM 患者的经历多种多样但常常充满挑战,这表明增加 HCM 患者资源的可及性和利用率可能有助于减轻 HCM 的不利生理和心理影响。误诊导致诊断延迟的常见报告也表明需要为医疗保健专业人员提供与 HCM 相关的教育机会。