Patient- and family-centered care “is an innovative approach to the planning, delivery, and evaluation of health care that is grounded in a mutually beneficial partnership among patients, families, and providers that recognizes the importance of the family in the patient’s life.”1 Similarly, family partnerships in pediatric palliative care (PPC) research represent an innovative approach to the planning, delivery, and evaluation of research that is grounded in mutually beneficial relationships that recognize the importance of the family caregiver perspective. The goal of partnered research or study teams is to synthesize the unique perspectives of family caregivers, clinicians, regulatory representatives, and researchers to strengthen research design and implementation. This is accomplished by each unique stakeholder speaking from their own perspective, contributing what they know, and working together to integrate perspectives. The process of moving from just inviting family caregivers to be research subjects to actually engaging with family caregivers as partners...
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July 2021
Family Partnerships|
July 01 2021
Family Caregiver Partnerships in Palliative Care Research Design and Implementation Available to Purchase
Meaghann S. Weaver, MD, MPH, FAAP;
aDivision of Palliative Care, Department of Pediatrics, Children’s Hospital and Medical Center, Omaha, Nebraska
bNational Center for Ethics in Healthcare, Washington, District of Columbia
Address correspondence to Meaghann S. Weaver, MD, MPH, FAAP, Hand in Hand/Division of Pediatric Palliative Care, Children’s Hospital and Medical Center, 8200 Dodge St, Omaha, NE 68198. E-mail: [email protected]
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Lori Wiener, PhD, DCSW;
Lori Wiener, PhD, DCSW
cPediatric Oncology Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, Maryland
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Michelle M. Moon, DO;
dParent, Division of Hospice and Palliative Medicine, Department of Internal Medicine, School of Medicine, University of Nevada, Reno, Nevada
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Bruce Gordon, MD, FAAP;
Bruce Gordon, MD, FAAP
eDepartment of Pediatrics, College of Medicine, University of Nebraska Medical Center, Omaha, Nebraska
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Katherine Patterson Kelly, PhD, RN;
Katherine Patterson Kelly, PhD, RN
fDepartment of Nursing Science, Professional Practice and Quality, Children's National Hospital and Department of Pediatrics, School of Medicine and Health Sciences, George Washington University, Washington, District of Columbia
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Pamela S. Hinds, PhD, RN, FAAN
Pamela S. Hinds, PhD, RN, FAAN
fDepartment of Nursing Science, Professional Practice and Quality, Children's National Hospital and Department of Pediatrics, School of Medicine and Health Sciences, George Washington University, Washington, District of Columbia
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*
Parent author
Address correspondence to Meaghann S. Weaver, MD, MPH, FAAP, Hand in Hand/Division of Pediatric Palliative Care, Children’s Hospital and Medical Center, 8200 Dodge St, Omaha, NE 68198. E-mail: [email protected]
POTENTIAL CONFLICT OF INTEREST: The authors have no conflicts of interest relevant to this article to disclose.
FINANCIAL DISCLOSURE: The authors have indicated they have no financial relationships relevant to this article to disclose.
Pediatrics (2021) 148 (1): e2020049403.
Article history
Accepted:
April 07 2021
Citation
Meaghann S. Weaver, Lori Wiener, Michelle M. Moon, Bruce Gordon, Katherine Patterson Kelly, Pamela S. Hinds; Family Caregiver Partnerships in Palliative Care Research Design and Implementation. Pediatrics July 2021; 148 (1): e2020049403. 10.1542/peds.2020-049403
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