Advance Care Planning for Adults With CKD: A Systematic Integrative Review

Background Recent clinical practice guidelines have highlighted the importance of advance care planning (ACP) for improving end-of-life care for people with chronic kidney disease (CKD). Study Design We conducted a systematic integrative review of the literature to inform future ACP practice and res...

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Veröffentlicht in:American journal of kidney diseases 2014-05, Vol.63 (5), p.761-770
Hauptverfasser: Luckett, Tim, PhD, Sellars, Marcus, PGDipPsych, Tieman, Jennifer, PhD, Pollock, Carol A., MBBS, FRACP, PhD, Silvester, William, MBBS, FRACP, Butow, Phyllis N., M Clin Psych, PhD, Detering, Karen M., MBBS, FRACP, MH Ethics, Brennan, Frank, MBBS, FRACP, Clayton, Josephine M., MBBS, FRACP, PhD
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container_end_page 770
container_issue 5
container_start_page 761
container_title American journal of kidney diseases
container_volume 63
creator Luckett, Tim, PhD
Sellars, Marcus, PGDipPsych
Tieman, Jennifer, PhD
Pollock, Carol A., MBBS, FRACP, PhD
Silvester, William, MBBS, FRACP
Butow, Phyllis N., M Clin Psych, PhD
Detering, Karen M., MBBS, FRACP, MH Ethics
Brennan, Frank, MBBS, FRACP
Clayton, Josephine M., MBBS, FRACP, PhD
description Background Recent clinical practice guidelines have highlighted the importance of advance care planning (ACP) for improving end-of-life care for people with chronic kidney disease (CKD). Study Design We conducted a systematic integrative review of the literature to inform future ACP practice and research in CKD, searching electronic databases in April 2013. Synthesis used narrative methods. Setting & Population We focused on adults with a primary diagnosis of CKD in any setting. Selection Criteria for Studies We included studies of any design, quantitative or qualitative. Interventions ACP was defined as any formal means taken to ensure that health professionals and family members are aware of patients’ wishes for care in the event they become too unwell to speak for themselves. Outcomes Measures of all kinds were considered of interest. Results 55 articles met criteria reporting on 51 discrete samples. All patient samples included people with CKD stage 5; 2 also included patients with stage 4. Seven interventions were tested; all were narrowly focused and none was evaluated by comparing wishes for end-of-life care with care received. One intervention demonstrated effects on patient and family outcomes in the form of improved well-being and anxiety following sessions with a peer mentor. Insights from qualitative studies that have not been used to inform interventions include the importance of instilling patient confidence that their advance directives will be enacted and discussing decisions about (dis)continuing dialysis therapy separately from “aggressive” life-sustaining treatments (eg, ventilation). Limitations Although quantitative and qualitative findings were integrated according to best practice, methods for this are in their infancy. Conclusions Research on ACP in patients with CKD is limited, especially intervention studies. Interventions in CKD should attend to barriers and facilitators at the levels of patient, caregiver, health professional, and system. Intervention studies should measure impact on compliance with patient wishes for end-of-life care.
doi_str_mv 10.1053/j.ajkd.2013.12.007
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Study Design We conducted a systematic integrative review of the literature to inform future ACP practice and research in CKD, searching electronic databases in April 2013. Synthesis used narrative methods. Setting &amp; Population We focused on adults with a primary diagnosis of CKD in any setting. Selection Criteria for Studies We included studies of any design, quantitative or qualitative. Interventions ACP was defined as any formal means taken to ensure that health professionals and family members are aware of patients’ wishes for care in the event they become too unwell to speak for themselves. Outcomes Measures of all kinds were considered of interest. Results 55 articles met criteria reporting on 51 discrete samples. All patient samples included people with CKD stage 5; 2 also included patients with stage 4. Seven interventions were tested; all were narrowly focused and none was evaluated by comparing wishes for end-of-life care with care received. One intervention demonstrated effects on patient and family outcomes in the form of improved well-being and anxiety following sessions with a peer mentor. Insights from qualitative studies that have not been used to inform interventions include the importance of instilling patient confidence that their advance directives will be enacted and discussing decisions about (dis)continuing dialysis therapy separately from “aggressive” life-sustaining treatments (eg, ventilation). Limitations Although quantitative and qualitative findings were integrated according to best practice, methods for this are in their infancy. Conclusions Research on ACP in patients with CKD is limited, especially intervention studies. Interventions in CKD should attend to barriers and facilitators at the levels of patient, caregiver, health professional, and system. Intervention studies should measure impact on compliance with patient wishes for end-of-life care.</description><identifier>ISSN: 0272-6386</identifier><identifier>EISSN: 1523-6838</identifier><identifier>DOI: 10.1053/j.ajkd.2013.12.007</identifier><identifier>PMID: 24434187</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>advance care planning (ACP) ; Advance Care Planning - organization &amp; administration ; advance directives ; Biological and medical sciences ; Chronic kidney disease (CKD) ; decision making ; end-of-life (EOL) care ; Humans ; Kidneys ; Medical sciences ; Nephrology ; Nephrology. Urinary tract diseases ; Nephropathies. Renovascular diseases. Renal failure ; palliative care ; patient-centered care ; Quality Indicators, Health Care ; Renal failure ; Renal Insufficiency, Chronic - therapy ; systematic integrative review ; Terminal Care - standards ; Urinary system involvement in other diseases. 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Study Design We conducted a systematic integrative review of the literature to inform future ACP practice and research in CKD, searching electronic databases in April 2013. Synthesis used narrative methods. Setting &amp; Population We focused on adults with a primary diagnosis of CKD in any setting. Selection Criteria for Studies We included studies of any design, quantitative or qualitative. Interventions ACP was defined as any formal means taken to ensure that health professionals and family members are aware of patients’ wishes for care in the event they become too unwell to speak for themselves. Outcomes Measures of all kinds were considered of interest. Results 55 articles met criteria reporting on 51 discrete samples. All patient samples included people with CKD stage 5; 2 also included patients with stage 4. Seven interventions were tested; all were narrowly focused and none was evaluated by comparing wishes for end-of-life care with care received. One intervention demonstrated effects on patient and family outcomes in the form of improved well-being and anxiety following sessions with a peer mentor. Insights from qualitative studies that have not been used to inform interventions include the importance of instilling patient confidence that their advance directives will be enacted and discussing decisions about (dis)continuing dialysis therapy separately from “aggressive” life-sustaining treatments (eg, ventilation). Limitations Although quantitative and qualitative findings were integrated according to best practice, methods for this are in their infancy. Conclusions Research on ACP in patients with CKD is limited, especially intervention studies. Interventions in CKD should attend to barriers and facilitators at the levels of patient, caregiver, health professional, and system. Intervention studies should measure impact on compliance with patient wishes for end-of-life care.</description><subject>advance care planning (ACP)</subject><subject>Advance Care Planning - organization &amp; administration</subject><subject>advance directives</subject><subject>Biological and medical sciences</subject><subject>Chronic kidney disease (CKD)</subject><subject>decision making</subject><subject>end-of-life (EOL) care</subject><subject>Humans</subject><subject>Kidneys</subject><subject>Medical sciences</subject><subject>Nephrology</subject><subject>Nephrology. Urinary tract diseases</subject><subject>Nephropathies. Renovascular diseases. Renal failure</subject><subject>palliative care</subject><subject>patient-centered care</subject><subject>Quality Indicators, Health Care</subject><subject>Renal failure</subject><subject>Renal Insufficiency, Chronic - therapy</subject><subject>systematic integrative review</subject><subject>Terminal Care - standards</subject><subject>Urinary system involvement in other diseases. 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Urinary tract diseases</topic><topic>Nephropathies. Renovascular diseases. Renal failure</topic><topic>palliative care</topic><topic>patient-centered care</topic><topic>Quality Indicators, Health Care</topic><topic>Renal failure</topic><topic>Renal Insufficiency, Chronic - therapy</topic><topic>systematic integrative review</topic><topic>Terminal Care - standards</topic><topic>Urinary system involvement in other diseases. Miscellaneous</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Luckett, Tim, PhD</creatorcontrib><creatorcontrib>Sellars, Marcus, PGDipPsych</creatorcontrib><creatorcontrib>Tieman, Jennifer, PhD</creatorcontrib><creatorcontrib>Pollock, Carol A., MBBS, FRACP, PhD</creatorcontrib><creatorcontrib>Silvester, William, MBBS, FRACP</creatorcontrib><creatorcontrib>Butow, Phyllis N., M Clin Psych, PhD</creatorcontrib><creatorcontrib>Detering, Karen M., MBBS, FRACP, MH Ethics</creatorcontrib><creatorcontrib>Brennan, Frank, MBBS, FRACP</creatorcontrib><creatorcontrib>Clayton, Josephine M., MBBS, FRACP, PhD</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>American journal of kidney diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Luckett, Tim, PhD</au><au>Sellars, Marcus, PGDipPsych</au><au>Tieman, Jennifer, PhD</au><au>Pollock, Carol A., MBBS, FRACP, PhD</au><au>Silvester, William, MBBS, FRACP</au><au>Butow, Phyllis N., M Clin Psych, PhD</au><au>Detering, Karen M., MBBS, FRACP, MH Ethics</au><au>Brennan, Frank, MBBS, FRACP</au><au>Clayton, Josephine M., MBBS, FRACP, PhD</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Advance Care Planning for Adults With CKD: A Systematic Integrative Review</atitle><jtitle>American journal of kidney diseases</jtitle><addtitle>Am J Kidney Dis</addtitle><date>2014-05-01</date><risdate>2014</risdate><volume>63</volume><issue>5</issue><spage>761</spage><epage>770</epage><pages>761-770</pages><issn>0272-6386</issn><eissn>1523-6838</eissn><abstract>Background Recent clinical practice guidelines have highlighted the importance of advance care planning (ACP) for improving end-of-life care for people with chronic kidney disease (CKD). Study Design We conducted a systematic integrative review of the literature to inform future ACP practice and research in CKD, searching electronic databases in April 2013. Synthesis used narrative methods. Setting &amp; Population We focused on adults with a primary diagnosis of CKD in any setting. Selection Criteria for Studies We included studies of any design, quantitative or qualitative. Interventions ACP was defined as any formal means taken to ensure that health professionals and family members are aware of patients’ wishes for care in the event they become too unwell to speak for themselves. Outcomes Measures of all kinds were considered of interest. Results 55 articles met criteria reporting on 51 discrete samples. All patient samples included people with CKD stage 5; 2 also included patients with stage 4. Seven interventions were tested; all were narrowly focused and none was evaluated by comparing wishes for end-of-life care with care received. One intervention demonstrated effects on patient and family outcomes in the form of improved well-being and anxiety following sessions with a peer mentor. Insights from qualitative studies that have not been used to inform interventions include the importance of instilling patient confidence that their advance directives will be enacted and discussing decisions about (dis)continuing dialysis therapy separately from “aggressive” life-sustaining treatments (eg, ventilation). Limitations Although quantitative and qualitative findings were integrated according to best practice, methods for this are in their infancy. Conclusions Research on ACP in patients with CKD is limited, especially intervention studies. Interventions in CKD should attend to barriers and facilitators at the levels of patient, caregiver, health professional, and system. Intervention studies should measure impact on compliance with patient wishes for end-of-life care.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>24434187</pmid><doi>10.1053/j.ajkd.2013.12.007</doi><tpages>10</tpages></addata></record>
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subjects advance care planning (ACP)
Advance Care Planning - organization & administration
advance directives
Biological and medical sciences
Chronic kidney disease (CKD)
decision making
end-of-life (EOL) care
Humans
Kidneys
Medical sciences
Nephrology
Nephrology. Urinary tract diseases
Nephropathies. Renovascular diseases. Renal failure
palliative care
patient-centered care
Quality Indicators, Health Care
Renal failure
Renal Insufficiency, Chronic - therapy
systematic integrative review
Terminal Care - standards
Urinary system involvement in other diseases. Miscellaneous
title Advance Care Planning for Adults With CKD: A Systematic Integrative Review
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