'I'll be in a safe place': A qualitative study of the decisions taken by people with advanced cancer to seek emergency department care

TY - JOUR

T1 - 'I'll be in a safe place'

T2 - A qualitative study of the decisions taken by people with advanced cancer to seek emergency department care

AU - Henson, Lesley A.

AU - Higginson, Irene J.

AU - Daveson, Barbara A.

AU - Ellis-Smith, Clare

AU - Koffman, Jonathan

AU - Morgan, Myfanwy

AU - Gao, Wei

PY - 2016/11

Y1 - 2016/11

N2 - Objective: To explore the decisions of people with advanced cancer and their caregivers to seek emergency department (ED) care, and understand the issues that influence the decision-making process. Design: Cross-sectional qualitative study incorporating semistructured patient and caregiver interviews. Methods: Between December 2014 and July 2015, semistructured interviews were conducted with 18 people with advanced cancer, all of whom had recently attended the ED of a large university teaching hospital located in south-east London; and six of their caregivers. Interviews were audio recorded, transcribed verbatim and analysed using a constant comparative approach. Padgett and Brodsky's modified version of the 'Behavioral Model of Health Services Use' was used as a framework to guide the study. Results: Issues influencing the decision-making process included: (1) disease-related anxiety - those with greater anxiety related to their cancer diagnosis interpreted their symptoms as more severe and/or requiring immediate attention; (2) prior patterns of health-seeking behaviour - at times of crisis participants defaulted to previously used services; (3) feelings of safety and familiarity with the hospital setting - many felt reassured by the presence of healthcare professionals and monitoring of their condition; and, (4) difficulties accessing community healthcare services - especially urgently and/or out-of-hours. Conclusions: These data provide healthcare professionals and policymakers with a greater understanding of how systems of care may be developed to help reduce ED visits by people with advanced cancer. In particular, our findings suggest that the number of ED visits could be reduced with greater end-of-life symptom support and education, earlier collaboration between oncology and palliative care, and with increased access to community healthcare services.

AB - Objective: To explore the decisions of people with advanced cancer and their caregivers to seek emergency department (ED) care, and understand the issues that influence the decision-making process. Design: Cross-sectional qualitative study incorporating semistructured patient and caregiver interviews. Methods: Between December 2014 and July 2015, semistructured interviews were conducted with 18 people with advanced cancer, all of whom had recently attended the ED of a large university teaching hospital located in south-east London; and six of their caregivers. Interviews were audio recorded, transcribed verbatim and analysed using a constant comparative approach. Padgett and Brodsky's modified version of the 'Behavioral Model of Health Services Use' was used as a framework to guide the study. Results: Issues influencing the decision-making process included: (1) disease-related anxiety - those with greater anxiety related to their cancer diagnosis interpreted their symptoms as more severe and/or requiring immediate attention; (2) prior patterns of health-seeking behaviour - at times of crisis participants defaulted to previously used services; (3) feelings of safety and familiarity with the hospital setting - many felt reassured by the presence of healthcare professionals and monitoring of their condition; and, (4) difficulties accessing community healthcare services - especially urgently and/or out-of-hours. Conclusions: These data provide healthcare professionals and policymakers with a greater understanding of how systems of care may be developed to help reduce ED visits by people with advanced cancer. In particular, our findings suggest that the number of ED visits could be reduced with greater end-of-life symptom support and education, earlier collaboration between oncology and palliative care, and with increased access to community healthcare services.

U2 - 10.1136/bmjopen-2016-012134

DO - 10.1136/bmjopen-2016-012134

M3 - Article

AN - SCOPUS:84994536187

SN - 2044-6055

VL - 6

JO - BMJ Open

JF - BMJ Open

IS - 11

M1 - e012134

ER -