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A Conceptual Framework and Key Research Questions in Educational Needs of Blood and Marrow Transplantation Patients, Caregivers, and Families.
Schoemans, Helene M; Finn, Laura; Foster, Jackie; Roche-Green, Alva; Bevans, Margaret; Kullberg, Susan; Lee, Everett; Sargeant, Cindy; Schatz, Barry A; Scheeler, Kristin; Shaw, Bronwen E; Shereck, Evan; Murphy, Elizabeth A; Burns, Linda J; Schmit-Pokorny, Kim.
Afiliación
  • Schoemans HM; Department of Hematology, University Hospital Leuven and KU Leuven, Leuven, Belgium. Electronic address: helene.schoemans@uzleuven.be.
  • Finn L; Division of Hematology and Bone Marrow Transplant, Ochsner Health System, New Orleans, Louisiana.
  • Foster J; National Marrow Donor Program/Be The Match, Minneapolis, Minnesota.
  • Roche-Green A; Department of Family and Palliative Medicine, Mayo Clinic, Jacksonville, Florida.
  • Bevans M; Office of Research on Women's Health, National Institutes of Health, Bethesda, Maryland.
  • Kullberg S; Minneapolis, Minnesota.
  • Lee E; Dallas, Texas.
  • Sargeant C; Woodbine, Maryland.
  • Schatz BA; Cancer Center Administration, Loyola University Chicago, Chicago, Illinois.
  • Scheeler K; Information Resource Center, The Leukemia & Lymphoma Society, Rye Brook, New York.
  • Shaw BE; Center for Blood and Marrow Transplant Research and the Medical College of Wisconsin, Milwaukee, Wisconsin.
  • Shereck E; Department of Pediatrics, Oregon Health & Science University, Portland, Oregon.
  • Murphy EA; National Marrow Donor Program/Be The Match, Minneapolis, Minnesota.
  • Burns LJ; National Marrow Donor Program/Be The Match, Minneapolis, Minnesota; Center for International Blood and Marrow Transplant Research, Minneapolis, Minnesota.
  • Schmit-Pokorny K; Nebraska Medicine, Omaha, Nebraska.
Biol Blood Marrow Transplant ; 25(7): 1416-1423, 2019 07.
Article en En | MEDLINE | ID: mdl-30796997
Patient, caregiver, and family education and support was 1 of 6 key areas of interest identified by the National Marrow Donor Program/Be The Match 2-year project to prioritize patient-centered outcomes research (PCOR) goals for the blood and marrow transplantation (BMT) community. PCOR focuses on research to help patients and their caregivers make informed decisions about health care. Therefore, each area of interest was assigned to a working group with broad representation, including patients, caregivers, and clinicians. Each working group was charged with identifying gaps in knowledge and making priority recommendations for critical research to fill those gaps. The report from this working group presents a conceptual framework to address gaps in knowledge regarding patient and caregiver education in BMT and recommendations for priority research questions on this topic.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Médula Ósea / Familia / Educación del Paciente como Asunto / Trasplante de Médula Ósea / Cuidadores / Evaluación del Resultado de la Atención al Paciente Tipo de estudio: Guideline / Prognostic_studies Límite: Female / Humans / Male Idioma: En Revista: Biol Blood Marrow Transplant Asunto de la revista: HEMATOLOGIA / TRANSPLANTE Año: 2019 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Médula Ósea / Familia / Educación del Paciente como Asunto / Trasplante de Médula Ósea / Cuidadores / Evaluación del Resultado de la Atención al Paciente Tipo de estudio: Guideline / Prognostic_studies Límite: Female / Humans / Male Idioma: En Revista: Biol Blood Marrow Transplant Asunto de la revista: HEMATOLOGIA / TRANSPLANTE Año: 2019 Tipo del documento: Article