Aim
Mitral valve transcatheter edge-to-edge repair (TEER) is a minimally invasive treatment option for patients with severe symptomatic mitral regurgitation who are at increased risk for cardiac surgery and are receiving optimal medical therapy. Little is known about patients’ perspectives of their journey of care, including their experiences leading up to treatment, and their early recovery period. The aim of this study was to explore patients’ experiences of their journey to TEER and their perspectives on their early recovery.
Methods and results
We conducted a qualitative study using interpretive description. A purposive sample of 12 patients, 3 to 6 months post TEER procedure, were recruited from a tertiary hospital. The median age was 79 years and 7 were male and 5 were female. Data collection included semi-structured interviews via the telephone. Data analysis followed an iterative process and utilized thematic analysis. There were four central themes highlighting the experiences of the patients leading up to their procedure: (1) escalating challenges with everyday life; (2) plummeting losses; (3) choosing and readiness to proceed with TEER; and (4) the long and uncertain wait. The theme improved health status highlights the experiences of patients in their early recovery.
Conclusion
Patients’ experiences of waiting for TEER are complex and involve multifaceted challenges related to their worsening cardiac symptoms and navigating the health care system. Care pathways must be in place to provide continuity of care and support.
Funding Acknowledgements
Type of funding sources: Foundation. Main funding source(s): Heart & Stroke Foundation (Canada)
Background
Shared decision-making (SDM) is endorsed by multiple guidelines to help clinicians and patients achieve a high-quality treatment decision that integrates patients’ priorities, preferences and values. Patient decision aids (PDAs) are evidence-based tools designed to support the process of SDM. There is a gap in knowledge translation to facilitate the adoption of guideline recommendations for the treatment of aortic stenosis (AS).
Rationale: There is strong evidence of improved outcomes associated with SDM; in contrast, implementation research is needed to address the pressing question of "how to do SDM". Therefore, the SEEK-AS study aims to plan and evaluate the implementation of a PDA for AS to facilitate the integration of SDM in the treatment of valvular heart disease.
Study Design: We will present the design of a prospective multi-method implementation study of a novel set of paper-based and individualised web-based PDAs for AS. We aim to explore diverse perspectives and uncover barriers and enablers to investigate the "real-world" implementation of the PDAs. The study prioritises patient and family engagement, and is informed by the Ottawa Model for Research Use (OMRU) conceptual model to guide the sequential objectives: (1) select and tailor implementation strategies in four distinct healthcare organisations, across diverse patient and clinician populations to develop distinct implementation blueprints, and (2) evaluate the implementation of the PDAs across health care organisations and users. Data collection will include a series of in-depth focus group and individual interviews with patients treated with different modalities and multidisciplinary clinicians using content analysis organised under the OMRU levels (innovation, potential adopters, and practice environment; objectives 1 and 2), and patient and clinician surveys using outcomes mapped to OMRU levels and patient/clinician levels (objective 2).
Anticipated Research Output: We will present the stakeholder engagement plan and patient engagement strategies. The findings of the study will include the identification of barriers and facilitators of regional implementation, and provide evidence to guide the successful adoption of PDAs to help shift the culture of care from clinician-driven to patient-centred and improve the care of patients with valvular heart disease.
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