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Examining the Real-Life Journey of Individuals and Families Affected by Single-Ventricle Congenital Heart Disease.
Mery, Carlos M; Well, Andrew; Taylor, Kate; Carberry, Kathleen; Colucci, José; Ulack, Christopher; Zeiner, Adam; Mizrahi, Michelle; Stewart, Eileen; Dillingham, Christine; Cook, Taylor; Hartounian, Arotin; McCullum, Elizabeth; Affolter, Jeremy T; Van Diest, Heather; Lamari-Fisher, Alexandra; Chang, Stacey; Wallace, Scott; Teisberg, Elizabeth; Fraser, Charles D.
Afiliación
  • Mery CM; Texas Center for Pediatric and Congenital Heart Disease UT Health Austin/Dell Children's Medical Center Austin TX.
  • Well A; Department of Surgery and Perioperative Care The University of Texas at Austin Dell Medical School Austin TX.
  • Taylor K; Texas Center for Pediatric and Congenital Heart Disease UT Health Austin/Dell Children's Medical Center Austin TX.
  • Carberry K; Department of Surgery and Perioperative Care The University of Texas at Austin Dell Medical School Austin TX.
  • Colucci J; Value Institute for Health and Care The University of Texas at Austin Dell Medical School and McCombs School of Business Austin TX.
  • Ulack C; Texas Center for Pediatric and Congenital Heart Disease UT Health Austin/Dell Children's Medical Center Austin TX.
  • Zeiner A; Department of Surgery and Perioperative Care The University of Texas at Austin Dell Medical School Austin TX.
  • Mizrahi M; Value Institute for Health and Care The University of Texas at Austin Dell Medical School and McCombs School of Business Austin TX.
  • Stewart E; Design Institute for Health The University of Texas at Austin Dell Medical School and College of Fine Arts Austin TX.
  • Dillingham C; Value Institute for Health and Care The University of Texas at Austin Dell Medical School and McCombs School of Business Austin TX.
  • Cook T; Design Institute for Health The University of Texas at Austin Dell Medical School and College of Fine Arts Austin TX.
  • Hartounian A; Texas Center for Pediatric and Congenital Heart Disease UT Health Austin/Dell Children's Medical Center Austin TX.
  • McCullum E; Department of Surgery and Perioperative Care The University of Texas at Austin Dell Medical School Austin TX.
  • Affolter JT; Texas Center for Pediatric and Congenital Heart Disease UT Health Austin/Dell Children's Medical Center Austin TX.
  • Van Diest H; Department of Pediatrics The University of Texas at Austin Dell Medical School Austin TX.
  • Lamari-Fisher A; Texas Center for Pediatric and Congenital Heart Disease UT Health Austin/Dell Children's Medical Center Austin TX.
  • Chang S; Design Institute for Health The University of Texas at Austin Dell Medical School and College of Fine Arts Austin TX.
  • Wallace S; Design Institute for Health The University of Texas at Austin Dell Medical School and College of Fine Arts Austin TX.
  • Teisberg E; Texas Center for Pediatric and Congenital Heart Disease UT Health Austin/Dell Children's Medical Center Austin TX.
  • Fraser CD; Department of Surgery and Perioperative Care The University of Texas at Austin Dell Medical School Austin TX.
J Am Heart Assoc ; 12(5): e027556, 2023 03 07.
Article en En | MEDLINE | ID: mdl-36802928
Background The lifetime journey of patients with single-ventricle congenital heart disease is characterized by long-term challenges that are incompletely understood and still unfolding. Health care redesign requires a thorough understanding of this journey to create and implement solutions that improve outcomes. This study maps the lifetime journey of individuals with single-ventricle congenital heart disease and their families, identifies the most meaningful outcomes to them, and defines significant challenges in the journey. Methods and Results This qualitative research study involved experience group sessions and 1:1 interviews of patients, parents, siblings, partners, and stakeholders. Journey maps were created. The most meaningful outcomes to patients and parents and significant gaps in care were identified across the life journey. A total of 142 participants from 79 families and 28 stakeholders were included. Lifelong and life-stage specific journey maps were created. The most meaningful outcomes to patients and parents were identified and categorized using a "capability (doing the things in life you want to), comfort (experience of physical/emotional pain/distress), and calm (experiencing health care with the least impact on daily life)" framework. Gaps in care were identified and classified into areas of ineffective communication, lack of seamless transitions, lack of comprehensive support, structural deficiencies, and insufficient education. Conclusions There are significant gaps in care during the lifelong journey of individuals with single-ventricle congenital heart disease and their families. A thorough understanding of this journey is a critical first step in developing initiatives to redesign care around their needs and priorities. This approach can be used for people with other forms of congenital heart disease and other chronic conditions. Registration URL: https://www.clinicaltrials.gov; Unique identifier: NCT04613934.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Corazón Univentricular / Cardiopatías Congénitas Tipo de estudio: Diagnostic_studies / Prognostic_studies / Qualitative_research Límite: Humans Idioma: En Revista: J Am Heart Assoc Año: 2023 Tipo del documento: Article Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Corazón Univentricular / Cardiopatías Congénitas Tipo de estudio: Diagnostic_studies / Prognostic_studies / Qualitative_research Límite: Humans Idioma: En Revista: J Am Heart Assoc Año: 2023 Tipo del documento: Article Pais de publicación: Reino Unido