Understanding How Software Can Support the Needs of Family Caregivers for Patients with Severe Conditions

In this paper, we report an extensive analysis that we performed in two scenarios where the care relation between doctor and patients are mediated by the relatives of the patients: Pediatric Palliative Care (PPC) and Nursing Homes (NH). When the patients are children or very old adults in the end of life, the provision of care often involve a family caregiver as the main point of contact for the health service. PPC and NH are characterized by emotional complexity, since incurable diseases expose the family caregivers to heavy careload and human distress. In this paper, we discuss our findings with a novel perspective, focusing on: information, coordination and social challenges that arise by dealing with such contexts, the existing technology as it is appropriated today to cope with them, and what we, as software researchers, can do to develop the right solutions.

[1]  Madhu C. Reddy,et al.  Proceedings of the companion publication of the 17th ACM conference on Computer supported cooperative work & social computing , 2014 .

[2]  D. Baker,et al.  Deficits in communication and information transfer between hospital-based and primary care physicians: implications for patient safety and continuity of care. , 2007, JAMA.

[3]  Karen Davis,et al.  Taking the pulse of health care systems: experiences of patients with health problems in six countries. , 2005, Health affairs.

[4]  Philip W. Brickner,et al.  There's No Place Like Home: Place and Care in an Ageing Society , 2016 .

[5]  John Zimmerman,et al.  Opportunities to support parents in managing their children's health , 2008, CHI Extended Abstracts.

[6]  Ji Ruan,et al.  Enhancing Patient-Centered Palliative Care with Collaborative Agents , 2010, 2010 IEEE/WIC/ACM International Conference on Web Intelligence and Intelligent Agent Technology.

[7]  L. E. Lassiter,et al.  The Chicago Guide to Collaborative Ethnography , 2005 .

[8]  Steven J. Taylor Introduction to qualitative research methods , 1975 .

[9]  C. Adair,et al.  Continuity of care: a multidisciplinary review , 2003, BMJ : British Medical Journal.

[10]  Jooyoung Cheon,et al.  Family-centered end-of-life care in the ICU. , 2013, Journal of gerontological nursing.

[11]  T. Bodenheimer Coordinating care--a perilous journey through the health care system. , 2008, The New England journal of medicine.

[12]  Jody Hoffer Gittell,et al.  Impact of relational coordination on job satisfaction and quality outcomes: a study of nursing homes , 2008 .

[13]  Jody Hoffer Gittell,et al.  Coordination between formal providers and informal caregivers. , 2007, Health care management review.

[14]  E. Wagner The role of patient care teams in chronic disease management , 2000, BMJ : British Medical Journal.

[15]  Aparecido Fabiano Pinatti de Carvalho,et al.  Collaboration and coordination in the context of informal care (CCCiC 2014) , 2014, CSCW Companion.

[16]  B. Carter,et al.  Pediatric palliative care: current evidence and evidence gaps. , 2015, The Journal of pediatrics.

[17]  S. Savage,et al.  The impact of caring on caregivers' mental health: a review of the literature. , 2004, Australian health review : a publication of the Australian Hospital Association.

[18]  Claus Bossen,et al.  CareCoor: Augmenting the coordination of cooperative home care work , 2013, Int. J. Medical Informatics.