Characterizing the Language Used to Discuss Death in Family Meetings for Critically Ill Infants

Author:

Barlet Margaret H.1,Barks Mary C.2,Ubel Peter A.134,Davis J. Kelly2,Pollak Kathryn I.5,Kaye Erica C.6,Weinfurt Kevin P.5,Lemmon Monica E.57

Affiliation:

1. Duke University School of Medicine, Durham, North Carolina

2. Margolis Center for Health Policy, Duke University, Durham, North Carolina

3. Fuqua School of Business, Duke University, Durham, North Carolina

4. Sanford School of Public Policy, Duke University, Durham, North Carolina

5. Department of Population Health Sciences, Duke University School of Medicine, Durham, North Carolina

6. Department of Oncology, St Jude Children’s Research Hospital, Memphis, Tennessee

7. Department of Pediatrics, Duke University School of Medicine, Durham, North Carolina

Abstract

ImportanceCommunication during conversations about death is critical; however, little is known about the language clinicians and families use to discuss death.ObjectiveTo characterize (1) the way death is discussed in family meetings between parents of critically ill infants and the clinical team and (2) how discussion of death differs between clinicians and family members.Design, Setting, and ParticipantsThis longitudinal qualitative study took place at a single academic hospital in the southeast US. Patients were enrolled from September 2018 to September 2020, and infants were followed up longitudinally throughout their hospitalization. Participants included families of infants with neurologic conditions who were hospitalized in the intensive care unit and had a planned family meeting to discuss neurologic prognosis or starting, not starting, or discontinuing life-sustaining treatment. Family meetings were recorded, transcribed, and deidentified before being screened for discussion of death.Main Outcomes and MeasuresThe main outcome was the language used to reference death during family meetings between parents and clinicians. Conventional content analysis was used to analyze data.ResultsA total of 68 family meetings involving 36 parents of 24 infants were screened; 33 family meetings (49%) involving 20 parents (56%) and 13 infants (54%) included discussion of death. Most parents involved in discussion of death identified as the infant’s mother (13 [65%]) and as Black (12 [60%]). Death was referenced 406 times throughout the family meetings (275 times by clinicians and 131 times by family members); the words die, death, dying, or stillborn were used 5% of the time by clinicians (13 of 275 references) and 15% of the time by family members (19 of 131 references). Four types of euphemisms used in place of die, death, dying, or stillborn were identified: (1) survival framing (eg, not live), (2) colloquialisms (eg, pass away), (3) medical jargon, including obscure technical terms (eg, code event) or talking around death with physiologic terms (eg, irrecoverable heart rate drop), and (4) pronouns without an antecedent (eg, it). The most common type of euphemism used by clinicians was medical jargon (118 of 275 references [43%]). The most common type of euphemism used by family members was colloquialism (44 of 131 references [34%]).Conclusions and RelevanceIn this qualitative study, the words die, death, dying, or stillborn were rarely used to refer to death in family meetings with clinicians. Families most often used colloquialisms to reference death, and clinicians most often used medical jargon. Future work should evaluate the effects of euphemisms on mutual understanding, shared decision-making, and clinician-family relationships.

Publisher

American Medical Association (AMA)

Subject

General Medicine

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