Advance care planning for patients with cancer in the palliative phase in Dutch general practices

2018 ◽  
Vol 36 (5) ◽  
pp. 587-593 ◽  
Author(s):  
Daisy J M Ermers ◽  
Karin J H van Bussel ◽  
Marieke Perry ◽  
Yvonne Engels ◽  
Henk J Schers

Abstract Background Advance care planning (ACP) is a crucial element of palliative care. It improves the quality of end-of-life care and reduces aggressive and needless life-prolonging medical interventions. However, little is known about its application in daily practice. This study aims to examine the application of ACP for patients with cancer in general practice. Methods We performed a retrospective cohort study in 11 general practices in the Netherlands. Electronic patient records (EPRs) of deceased patients with colorectal or lung cancer were analysed. Data on ACP documentation, correspondence between medical specialist and GP, and health care use in the last year of life were extracted. Results Records of 163 deceased patients were analysed. In 74% of the records, one or more ACP items were registered. GPs especially documented patients’ preferences for euthanasia (58%), palliative sedation (46%) and preferred place of death (26%). Per patient, GPs received on average six letters from medical specialists. These letters mainly contained information regarding medical treatment and rarely ACP items. In the last year of life, patients contacted the GP over 30 times, and 51% visited the emergency department at least once, of whom 54% in the last month. Conclusions Registration of ACP items in GPs’ EPRs appeared to be limited. ACP elements were rarely subject of communication between primary and secondary care, which may impact the continuity of patient care during the last year of life. More emphasis on registration of ACP items and better exchange of information regarding patients’ preferences are needed.

2021 ◽  
Author(s):  
Yvonne A.C. Bekker ◽  
A. Suntjens ◽  
Y. Engels ◽  
H. Schers ◽  
Gert P. Westert ◽  
...  

Abstract BackgroundAdvance Care Planning (ACP) enables physicians to align healthcare with patients wishes, reduces burdensome life-prolonging medical interventions, and potentially improves the quality of life of patients in the last phase of life. However, little objective information is available about the extent to which structured ACP conversations are held in general practice. Our aim was to examine the documentation of ACP for patients with cancer, organ failure and multimorbidity in medical records (as a proxy for ACP application) in Dutch general practice. MethodsWe chose a retrospective medical record study design in seven primary care facilities. Medical records of 119 patients who died non-suddenly (55 cancer, 28 organ failure and 36 multimorbidity) were analysed. Other variables were: general characteristics, data on ACP documentation, correspondence between medical specialist and GP, and healthcare utilization in the last two years of life. ResultsIn 65% of the records, one or more ACP items was registered. Most often documented were aspects regarding euthanasia (35%), the preferred place of care and death (29%) and concerns and hopes towards the future (29%). Median timing of the first ACP conversation was 126 days before death. ACP was more often documented in patients with cancer (84%) than in those with organ failure (57%) or multimorbidity (42%) (p = 0,000). Patients with cancer had the most frequent (median 3 times, inter-quartile range (IQR) 2-5), and extensive (median 5 items, IQR 2-7) ACP consultations. ConclusionDocumentation of ACP items in medical records by GPs is present, but incomplete, especially in patients with multimorbidity or organ failure. We recommend more attention for, and documentation of ACP in daily practice in order to start anticipatory conversations in time, and to address the needs of all people living with advanced conditions in primary care.


2020 ◽  
Vol 23 (10) ◽  
pp. 1335-1341 ◽  
Author(s):  
Cara L. McDermott ◽  
Ruth A. Engelberg ◽  
James Sibley ◽  
Mohamed L. Sorror ◽  
J. Randall Curtis

2015 ◽  
Vol 5 (Suppl 2) ◽  
pp. A24.3-A24
Author(s):  
Jan Schildmann ◽  
C Bausewein ◽  
Tanja Krones ◽  
A Simon ◽  
ST Simon ◽  
...  

2020 ◽  
Vol 29 (13-14) ◽  
pp. 2069-2082
Author(s):  
Anne Kuusisto ◽  
Jenni Santavirta ◽  
Kaija Saranto ◽  
Päivi Korhonen ◽  
Elina Haavisto

Author(s):  
Manali I. Patel ◽  
Sana Khateeb ◽  
Tumaini Coker

Introduction: Advance care planning and symptom screening among patients with cancer require team-based approaches to ensure that these services are equitably and appropriately delivered. In several organizations across the United States, we trained and employed lay health workers (LHWs) to assist with delivering these services for patients with cancer. The aim of this study was to understand LHWs’ views on delivering these services. Methods: We conducted semi-structured interviews with 22 LHWs in 6 US-based clinical cancer care settings in 4 large cities. We recorded, transcribed, and analyzed interviews using the constant comparative method of qualitative analysis. Results: Participants noted the importance of their role in assisting with the delivery of advance care planning (ACP) and symptom screening services. Participants noted the importance of developing relationships with patients to engage openly in ACP and symptom screening discussions. Participants reported that ongoing training provided skills and empowered them to discuss sensitive issues with patients and their caregivers. Participants described challenges in their roles including communication with oncology providers and their own emotional well-being. Participants identified solutions to these challenges including formal opportunities for introduction with oncology clinicians and staff and grievance sessions with LHWs and other team members. Discussion: LHWs from several organizations endorsed the importance of their roles in ensuring the delivery of ACP and proactive symptom screening. LHWs noted challenges and specific solutions to improve their effectiveness in delivering these important services to patients after their diagnosis of cancer.


2019 ◽  
Vol 37 (4) ◽  
pp. 519-524
Author(s):  
Jolien J Glaudemans ◽  
Dick L Willems ◽  
Jan Wind ◽  
Bregje D Onwuteaka Philipsen

Abstract Background Using advance care planning (ACP) to anticipate future decisions can increase compliance with people’s end-of-life wishes, decrease inappropriate life-sustaining treatment and reduce stress, anxiety and depression. Despite this, only a minority of older people engage in ACP, partly because care professionals lack knowledge of approaches towards ACP with older people and their families. Objective To explore older people’s and their families’ experiences with ACP in primary care. Methods We conducted qualitative, semi-structured, face-to-face interviews with 22 older people (aged >70 years, v/m: 11/11), with experience in ACP, and eight of their family members (aged 40–79 years, f/m: 7/1). Transcripts were inductively analysed using a grounded theory approach. Results We distinguished three main themes. (i) Openness and trust: Respondents were more open to ACP if they wanted to prevent specific future situations and less open if they lacked trust or had negative thoughts regarding general practitioners’ (GPs’) time for and interest in ACP. Engaging in ACP appeared to increase trust. (ii) Timing and topics: ACP was not initiated too early. Quality of ACP seemed to improve if respondents’ views on their current life and future, a few specific future care scenarios and expectations and responsibilities regarding ACP were discussed. (iii) Roles of family: Quality of ACP appeared to improve if family was involved in ACP. Conclusions Quality and accessibility of ACP may improve if GPs and nurses involve family, explain GPs’ interest in ACP and discuss future situations older people may want to prevent, and views on their current life and future.


JAMA Oncology ◽  
2015 ◽  
Vol 1 (5) ◽  
pp. 601 ◽  
Author(s):  
Amol K. Narang ◽  
Alexi A. Wright ◽  
Lauren H. Nicholas

Blood ◽  
2018 ◽  
Vol 132 (Supplement 1) ◽  
pp. 4842-4842
Author(s):  
Kelly Marie Trevino ◽  
Peter Martin ◽  
Sarah C. Rutherford ◽  
Chrystal Marte ◽  
Daniel Jie Ouyang ◽  
...  

Abstract Introduction. The prognosis of an aggressive lymphoma can change significantly after disease progression following first line treatment, with the chance of cure changing from likely to unlikely. This sudden shift creates a unique context for illness understanding and advance care planning (ACP). Yet, research on illness understanding and ACP has focused primarily on patients with solid tumors rather than hematologic malignancies, a notable gap given the relationship between ACP and receipt of care consistent with patient preferences. In this study, we examined illness understanding, rates of ACP engagement, and reasons for lack of ACP engagement in patients with recurrent aggressive B-cell lymphomas. Methods. Patients (n=27, Table 1) with aggressive B-cell lymphomas that progressed after first or second line treatment were recruited from an urban academic medical center. Self-report measures of illness understanding (i.e., aggressiveness, terminality, curability) and ACP (i.e., discussions of care preferences, completion of advance directives) were administered over the telephone by trained study staff. Frequency and descriptive statistics were used to examine sample characteristics, illness understanding, and rates of ACP. Results. Over two-thirds of the sample described their illness as aggressive (n=18, 69.2%) but less than one-third reporting being terminally ill (n=8, 29.6%) and having incurable disease (n=6, 22.2%). The majority of the sample had a healthcare proxy (HCP; n=22, 81.5%; Table 2). Reasons for not designating a HCP included that patients were considering whom to choose (n=2, 7.4%), had not thought about it (n=2, 7.4%), and did not know the definition of a HCP (n=1, 3.7%). Two-thirds of the sample (n=17, 65.4%) had not completed a living will. Of those who completed a living will, 22.2% (n=2) selected comfort measures only, 22.2% (n=2) selected limited medical interventions, and 11.1% (n=1) selected no limitations on medical interventions. Almost half of patients who completed a living will (n=4, 44.4%) did not know their documented care preference and 14.5% (n=4) of the total sample did not know the definition of a living will. Over one-third of patients (n=10, 37%) had not decided about their DNR status and 11.1% (n=3) did not have a DNR order because they wanted resuscitation to be attempted. Reasons for not making a DNR decision included that patients did not know the definition of a DNR order (n=3, 11.1%), had not thought about it (n=3, 11.1%), were considering whether they wanted a DNR order (n=1, 3.7%), and other (n=3, 11.1%). Less than half of the sample (n=12, 44.4%) reported writing down or talking to someone about the care they would like to receive should they become critically ill. Of those patients who discussed their care preferences, only 11.1% (n=3) discussed their preferences with a healthcare provider. Conclusions. Our findings identify several issues that require potential intervention and validation. Many patients with recurrent aggressive lymphoma do not accurately understand their prognosis. Research identifying the causes of this gap (e.g., information is not provided, information is provided using language the patient cannot understanding, patients' emotions interfere with understanding) will inform the development of targeted interventions to improve patient understanding. Longitudinal research on illness understanding and strategies for improving illness understanding will be particularly important for patients with aggressive lymphoma due to the sudden change in prognosis as the disease progresses. Additionally, research on strategies to promote discussion of patients' EOL care wishes with their oncologist/care team is needed, particularly in light of evidence that these discussions facilitate receipt of care consistent with patients' preferences. Further, patients with aggressive lymphoma may benefit from basic information on and assistance in completion of a living will and DNR order. Given that most patients with recurrent aggressive lymphoma will die of their disease, our study highlights the need for greater prioritization of and support for patient education on the nature of aggressive lymphoma and completion of advanced directives. Disclosures Martin: Seattle Genetics: Consultancy; Gilead: Consultancy; Janssen: Consultancy; AstraZeneca: Consultancy; Kite: Consultancy; Bayer: Consultancy. Leonard:Genentech/Roche: Consultancy; AstraZeneca: Consultancy; Novartis: Consultancy; Karyopharm: Consultancy; United Therapeutics: Consultancy; Celgene: Consultancy; Pfizer: Consultancy; Juno: Consultancy; ADC Therapeutics: Consultancy; Biotest: Consultancy; BMS: Consultancy; Sutro: Consultancy; Gilead: Consultancy; Bayer: Consultancy; MEI Pharma: Consultancy.


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