Abstract

IntroductionAlthough many terminally ill people are admitted to an intensive care unit (ICU) at the end of life, their care is often inadequate because of poor communication by physicians and lack of patient- and family-centred care. The aim of this systematic literature review was to describe physician-related barriers to adequate communication within the team and with patients and families, as well as barriers to patient- and family-centred decision-making, towards the end of life in the ICU. We base our discussion and evaluation on the quality indicators for end-of-life care in the ICU developed by the Robert Wood Johnson Foundation Critical Care End-of-Life Peer Workgroup.MethodFour electronic databases (MEDLINE, Embase, CINAHL and PsycINFO) were searched, using controlled vocabulary and free text words, for potentially relevant records published between 2003 and 2013 in English or Dutch. Studies were included if the authors reported on physician-related and physician-reported barriers to adequate communication and decision-making. Barriers were categorized as being related to physicians’ knowledge, physicians’ attitudes or physicians’ practice. Study quality was assessed using design-specific tools. Evidence for barriers was graded according to the quantity and quality of studies in which the barriers were reported.ResultsOf 2,191 potentially relevant records, 36 studies were withheld for data synthesis. We determined 90 barriers, of which 46 were related to physicians’ attitudes, 24 to physicians’ knowledge and 20 to physicians’ practice. Stronger evidence was found for physicians’ lack of communication training and skills, their attitudes towards death in the ICU, their focus on clinical parameters and their lack of confidence in their own judgment of their patient’s true condition.ConclusionsWe conclude that many physician-related barriers hinder adequate communication and shared decision-making in ICUs. Better physician education and palliative care guidelines are needed to enhance knowledge, attitudes and practice regarding end-of-life care. Patient-, family- and health care system–related barriers need to be examined.Electronic supplementary materialThe online version of this article (doi:10.1186/s13054-014-0604-z) contains supplementary material, which is available to authorized users.

Highlights

  • Many terminally ill people are admitted to an intensive care unit (ICU) at the end of life, their care is often inadequate because of poor communication by physicians and lack of patient- and family-centred care

  • We conclude that many physician-related barriers hinder adequate communication and shared decision-making in ICUs

  • The following are the specific research questions we sought to answer in this systematic literature review: (1) What are the physician-related and physician-reported barriers to communication within the team and with patients and families in end-of-life care in the ICU according to the 10 Quality indicator (QI) for communication within the team and with patients and families in end-of-life care in the ICU, as developed by the Robert Wood Johnson Foundation (RWJF)? (2) What are the physician-related and physician-reported barriers to patient- and family-centred decision-making in end-of-life care in the ICU according to the 13 QIs for patient- and family-centred decision-making in end-of-life care in the ICU, as developed by the RWJF?

Read more

Summary

Introduction

Many terminally ill people are admitted to an intensive care unit (ICU) at the end of life, their care is often inadequate because of poor communication by physicians and lack of patient- and family-centred care. The aim of this systematic literature review was to describe physician-related barriers to adequate communication within the team and with patients and families, as well as barriers to patient- and family-centred decision-making, towards the end of life in the ICU. The conclusion of the SUPPORT study investigators in 1995 was that many patients in ICUs receive unwanted life-sustaining treatments and insufficient palliative care at the end of their lives [2]. Continuing life-sustaining treatments without clinical improvement causes suffering to patients and deprives them and their families of palliative care, deprives them and their families of honest prognostic information, and reduces patients’ time to prepare for dying and their families’ time to prepare for bereavement [4,6]

Objectives
Methods
Results
Discussion
Conclusion
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.