Evidence map›Paper›PMID 28827063›Full record

ArticleJournal of pain and symptom management2017

Beyond Simple Planning: Existential Dimensions of Conversations With Patients at Risk of Dying From Heart Failure.

Valerie Marie Schulz, Allison M Crombeen, Denise Marshall, Joshua Shadd, Kori A LaDonna, Lorelei Lingard

Open access · bronzeAbstract readMulticenter Study
In one paragraph

Article in Journal of pain and symptom management, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
2.2field-weighted citation impact, top 12% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 27 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Observational
  5. Article
  6. Article
  7. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Valerie Marie SchulzSchulich School of Medicine and Dentistry, University of Western Ontario, London, Ontario, Canada; Centre for Education Research and Innovation, McMaster University, Hamilton, Ontario, Canada; Department of Anesthesia & Perioperative Medicine, practicing in Palliative Care, McMaster University, Hamilton, Ontario, Canada. Electronic address: valerie.schulz@lhsc.on.ca.
Allison M CrombeenSchulich School of Medicine and Dentistry, University of Western Ontario, London, Ontario, Canada; Department of Family Medicine, McMaster University, Hamilton, Ontario, Canada.
Denise MarshallDepartment of Family Medicine, Division of Palliative Care, McMaster University, Hamilton, Ontario, Canada.
Joshua ShaddDepartment of Family Medicine, Division of Palliative Care, McMaster University, Hamilton, Ontario, Canada.
Kori A LaDonnaSchulich School of Medicine and Dentistry, University of Western Ontario, London, Ontario, Canada; Centre for Education Research and Innovation, McMaster University, Hamilton, Ontario, Canada.
Lorelei LingardSchulich School of Medicine and Dentistry, University of Western Ontario, London, Ontario, Canada; Centre for Education Research and Innovation, McMaster University, Hamilton, Ontario, Canada; Department of Medicine, McMaster University, Hamilton, Ontario, Canada.
Western University · CAMcMaster University · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

contextDespite the recent promotion of communication guides to improve decision making with patients nearing the end of their lives, these conversations remain challenging. Deeper and more comprehensive understanding of communication barriers that undermine discussions and decisions with patients at risk of dying from heart failure (HF) is vital for informing communication in health care.

objectivesTo explore experiences and perspectives of patients with advanced HF, their caregivers, and providers, regarding conversations for patients at risk of dying from HF.

methodsFollowing Research Ethics Board approval, index patients with advanced HF (New York Heart Association III or IV) and consenting patient-identified care team members were interviewed. A team sampling unit was formed when the patient plus at least two additional team members participated in interviews. Team members included health professionals (e.g., cardiologist, family physician, HF nurse practitioner, social worker, and specialists, such as respirologist, nephrologist, palliative care physician), family caregivers (e.g., daughter, spouse, roommate, close friend), and community members (e.g., minister, neighbor, regular taxi driver). Our data set included 209 individual interviews clustered into 50 team sampling units at five sites from three Canadian provinces. Key informants, identified as practicing experts in the field, reviewed our initial findings with attention to relevance to practice as a form of triangulation. Iterative data collection and analysis followed constructivist grounded theory procedures with sensitizing concepts drawn from complexity theory. To ensure confidentiality, all participants were given a pseudonym.

resultsParticipants' reports of their perceptions and experiences of conversations related to death and dying suggested two main dimensions of such conversations: instrumental and existential. Instrumental dimensions included how these conversations were planned and operationalized as well as the triggers and barriers to these discussions. Existential dimensions of these conversations included evasive maneuvers, powerful emotions, and the phenomenon of death without dying. Existential dimensions appeared to have a basis in issues of mortality and could strongly influence conversations related to death and dying.

conclusionConversations for patients at risk of dying from HF have both instrumental and existential dimensions, in which routines and relationships are inseparable. Our current focus on the instrumental aspects of these conversations is necessary but insufficient. The existential dimensions of conversations related to death are profound and may explain why these conversations have struggled to achieve their desired effect. To improve this communication, we need to also attend to existential dimensions, particularly in terms of their impact on the occurrence of these conversations, the nature of relationships and responses within these conversations, and the fluidity of meaning within these conversations.

Indexed as

CommunicationAttitude to DeathExistentialismHealth PersonnelHeart FailureHumansInterviews as TopicPalliative CarePatient Care TeamTerminal CareDeath and dying conversationsemotionend-of-life conversations for heart failureexistentialmortality salience

Identifiers

PMID28827063
PMCPMC5651176
OpenAlexW2742908089

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.