Barriers to and facilitators for implementing quality improvements in palliative care - results from a qualitative interview study in Norway

被引:64
作者
Sommerbakk, Ragni [1 ,2 ,3 ]
Haugen, Dagny Faksvag [1 ,2 ,4 ]
Tjora, Aksel [5 ]
Kaasa, Stein [1 ,2 ,6 ,7 ]
Hjermstad, Marianne Jensen [1 ,2 ,8 ]
机构
[1] Norwegian Univ Sci & Technol, NTNU, European Palliat Care Res Ctr PRC, Dept Canc Res & Mol Med,Fac Med, POB 8905, N-7491 Trondheim, Norway
[2] Univ Trondheim Hosp, St Olavs Hosp, POB 8905, N-7491 Trondheim, Norway
[3] Univ Trondheim Hosp, St Olavs Hosp, Canc Clin, Trondheim, Norway
[4] Haukeland Hosp, Reg Ctr Excellence Palliat Care, Bergen, Norway
[5] Norwegian Univ Sci & Technol, Dept Sociol & Polit Sci, Trondheim, Norway
[6] Oslo Univ Hosp, Dept Oncol, Oslo, Norway
[7] Univ Oslo, Oslo, Norway
[8] Oslo Univ Hosp, Dept Oncol, Reg Ctr Excellence Palliat Care, Oslo, Norway
来源
BMC PALLIATIVE CARE | 2016年 / 15卷
关键词
Palliative care; End-of-life; Barrier; Facilitator; Quality improvement; Implementation strategy; Organization of care; Cancer; Dementia; Norway; DEMENTIA; RECOMMENDATIONS; INTERVENTIONS; PERSONNEL; PATIENT; HOSPICE;
D O I
10.1186/s12904-016-0132-5
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
Background: Implementation of quality improvements in palliative care (PC) is challenging, and detailed knowledge about factors that may facilitate or hinder implementation is essential for success. One part of the EU-funded IMPACT project (IMplementation of quality indicators in PAlliative Care sTudy) aiming to increase the knowledge base, was to conduct national studies in PC services. This study aims to identify factors perceived as barriers or facilitators for improving PC in cancer and dementia settings in Norway. Methods: Individual, dual-participant and focus group interviews were conducted with 20 employees working in different health care services in Norway: two hospitals, one nursing home, and two local medical centers. Thematic analysis with a combined inductive and theoretical approach was applied. Results: Barriers and facilitators were connected to (1) the innovation (e.g. credibility, advantage, accessibility, attractiveness); (2) the individual professional (e.g. motivation, PC expertise, confidence); (3) the patient (e.g. compliance); (4) the social context (e.g. leadership, culture of change, face-to-face contact); (5) the organizational context (e.g. resources, structures/facilities, expertise); (6) the political and economic context (e.g. policy, legislation, financial arrangements) and (7) the implementation strategy (e.g. educational, meetings, reminders). Four barriers that were particular to PC were identified: the poor general condition of patients in need of PC, symptom assessment tools that were not validated in all patient groups, lack of PC expertise and changes perceived to be at odds with staff's philosophy of care. Conclusion: When planning an improvement project in PC, services should pay particular attention to factors associated with their chosen implementation strategy. Leaders should also involve staff early in the improvement process, ensure that they have the necessary training in PC and that the change is consistent with the staff's philosophy of care. An important consideration when implementing a symptom assessment tool is whether or not the tool has been validated for the relevant patient group, and to what degree patients need to be involved when using the tool.
引用
收藏
页数:17
相关论文
共 46 条
[1]   The importance of key personnel and active management for successful implementation of computer-based technology in palliative care:: Results from a qualitative study [J].
Andre, Beate ;
Ringdal, Gerd Inger ;
Loge, Jon H. ;
Rannestad, Toril ;
Kaasa, Stein .
CIN-COMPUTERS INFORMATICS NURSING, 2008, 26 (04) :183-189
[2]   Work culture among healthcare personnel in a palliative medicine unit [J].
Andre, Beate ;
Sjovold, Endre ;
Rannestad, Toril ;
Holmemo, Marte ;
Ringdal, Gerd I. .
PALLIATIVE & SUPPORTIVE CARE, 2013, 11 (02) :135-140
[3]  
Andre Beate, 2009, Palliat Support Care, V7, P57, DOI 10.1017/S147895150900008X
[4]   World Medical Association Declaration of Helsinki Ethical Principles for Medical Research Involving Human Subjects [J].
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2013, 310 (20) :2191-2194
[5]  
[Anonymous], 2013, DEF PALL CAR
[6]  
Bero LA, 1998, BMJ-BRIT MED J, V317, P465
[7]   The spiritual dimension of hospice: The secularization of an ideal [J].
Bradshaw, A .
SOCIAL SCIENCE & MEDICINE, 1996, 43 (03) :409-419
[8]  
Braun V, 2006, QUAL RES PSYCHOL, V3, DOI [DOI 10.1191/1478088706QP063OA, 10.1191/1478088706qp063oa]
[9]  
Bruera E, 1991, J Palliat Care, V7, P6
[10]   Designing and evaluating complex interventions to improve health care [J].
Campbell, Neil C. ;
Murray, Elizabeth ;
Darbyshire, Janet ;
Emery, Jon ;
Farmer, Andrew ;
Griffiths, Frances ;
Guthrie, Bruce ;
Lester, Helen ;
Wilson, Phil ;
Kinmonth, Ann Louise .
BMJ-BRITISH MEDICAL JOURNAL, 2007, 334 (7591) :455-459