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		<property:AnnShortSummary rdf:datatype="http://www.w3.org/2001/XMLSchema#string">IPrA 2017 panel on "Talking about dying" by Ruth Parry and Marco Pino</property:AnnShortSummary>
		<property:AnnShortTitle rdf:datatype="http://www.w3.org/2001/XMLSchema#string">IPrA2017 Death talk</property:AnnShortTitle>
		<property:AnnText rdf:datatype="http://www.w3.org/2001/XMLSchema#string">Marco Pino: m.pino@lboro.ac.uk

Ruth Parry: ruth.parry@nottingham.ac.uk

This panel brings together studies that take an interactional approach
to death as a topic in conversation. How do people talk about dying?
What norms and constraints inform their practices for initiating,
managing, and closing off conversations about dying? Our panel
specifically focuses on occasions where people are demonstrably
orienting to the death of one of the parties to the interaction (or
someone close to them) as a relevant matter or concern within the
interaction; at the same time, it takes a broad approach in terms of
how death can become relevant for the participants – as a topic for
the conversation or as a relevant concern within specific action
sequences and activities (e.g. making plans for future care).

This line of inquiry is timely given increasing
cultural and political trends – or even pressures – that encourage
individuals to discuss, think about, and make preparations for their
own dying. These trends are underpinned by assumptions that death is
not discussed enough (due to cultural taboo) and that this has
negative repercussions in terms of missed opportunities to prepare for
one’s end. Health professionals have been called upon to encourage
patients to discuss dying and communicate their wishes about the care
and support they want for their end of life. There is evidence that
both healthcare professionals and patients regard talk about death as
important, but at the same time difficult to initiate. Conversation
analytic studies showed that death is a special topic insofar as
people orient to distinctive interactional norms for initiating,
managing, and terminating discussions about death. Holt’s (1993) study
on how people announce the death of a mutual acquaintance in informal
telephone conversations shows that people recurrently follow talk
about death with more positive commentaries within “bright side
sequences”. Studies on healthcare interactions (in HIV counselling,
oncology, and palliative medicine) show that professionals regularly
hold off introducing death as a topic and instead subtly cue patients
to death in ways that give them opportunities to be the fist to
introduce death as a focus for the conversation (Peräkylä, 1995;
Lutfey and Maynard, 1998; Pino, Parry et al., 2016).

This panel extends these lines of inquiry by
bringing together studies on recorded episodes of interaction where
participants demonstrably treat the death of one of the parties to the
interaction (or someone close to them) as a relevant topic or concern
within the conversation. The studies focus on how death is managed as
a conversational topic (how people initiate, progress and terminate
it, or sometimes only allude to, or even avoid it) as well as the
various action sequences and interactional activities within which (or
related to which) death is a demonstrably relevant concern (e.g.
investigating and assessing the patient’s emotional wellbeing relative
to the prospect of dying; making plans for end of life care).

We welcome studies that employ a rigorous analytic
process based on participants’ interaction-internal displayed
understandings of each other actions.

References

Holt E. The structure of death announcements. Text. 1993;13(2):189-212.

Lutfey K, Maynard DW. Bad news in oncology: How physician and patient
talk about death and dying without using those words. Social
Psychology Quarterly. 1998;61(4):321-41.

Peräkylä A. AIDS counselling: Institutional interaction and clinical
practice. Cambridge: Cambridge University Press; 1995.

Pino M., Parry R., Land V., Faull C., Feathers L., Seymour J. Engaging
terminally ill patients in end of life talk: How experienced
palliative medicine doctors navigate the dilemma of promoting
discussions about dying. Plos ONE 11(5). 2016.</property:AnnText>
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