Does palliative care utilization facilitate conversion to hospice care? : a qualitative study of the "soft no"

Article indépendant

SPENCER, Karen Lutfey | MRIG, Emily Hammad | TALAIE, Ariana Kobra

BACKGROUND: Facilitating patient conversion to hospice at end of life is a prominent clinical concern. Enrollment in outpatient palliative care services is often assumed to encourage seamless transition to hospice care, but this has not been demonstrated. Moreover, decisions to convert from palliative care to hospice are generally treated as dichotomous, thus hampering our ability to understand decision processes. OBJECTIVE: To examine medical decision-making among patients who are prospectively evaluating whether to convert from palliative care to hospice. DESIGN: Qualitative case study, using in-depth interviews and constant comparative method. SETTING/PATIENTS: Terminally ill patients currently enrolled in outpatient palliative care services (N = 26) and their caregivers (N = 16), selected purposely for maximum variation in condition and personal background. MEASUREMENTS: Themes identified in qualitative in-depth interviews. RESULTS: Patients rarely refused hospice outright but more often postponed using a "soft no," in which they neither accepted nor overtly refused hospice. Justifications patients and caregivers offered for why hospice was not needed (yet) appeared in these themes: (1) not seeing the value added of hospice, (2) assuming the timing is premature, and (3) relying on extensive health-related support networks that justify or endorse continuation of active care. CONCLUSIONS: Despite assumptions to the contrary, benefits associated with utilization of outpatient palliative care services have the potential to incentivize the delay of hospice in some cases. Clinical interactions with outpatient palliative care patients should consider the influence of these broad social support systems when discussing hospice options.

http://dx.doi.org/10.1177/1049909119900640

Voir la revue «The American journal of hospice and palliative care, 37»

Autres numéros de la revue «The American journal of hospice and palliative care»

Consulter en ligne

Suggestions

Du même auteur

Political economy of hope as a cultural facet...

Article indépendant | MRIG, Emily Hammad | Social science and medicine | vol.200

A growing body of social science literature is devoted to describing processes of biomedicalization. The issue of biomedicalization is especially relevant for individuals suffering from end-stage cancer and hoping that aggressive ...

Political economy of hope as a cultural facet...

Article indépendant | MRIG, Emily Hammad | Social science and medicine | vol.200

A growing body of social science literature is devoted to describing processes of biomedicalization. The issue of biomedicalization is especially relevant for individuals suffering from end-stage cancer and hoping that aggressive ...

Does palliative care utilization facilitate c...

Article indépendant | SPENCER, Karen Lutfey | The American journal of hospice and palliative care | n°9 | vol.37

BACKGROUND: Facilitating patient conversion to hospice at end of life is a prominent clinical concern. Enrollment in outpatient palliative care services is often assumed to encourage seamless transition to hospice care, but this h...

De la même série

Life story themes : a qualitative analysis of...

Article indépendant | SKINNER, Shannon | The American journal of hospice and palliative care | n°9 | vol.366

OBJECTIVE: To identify common themes and topics that patients nearing the end of life want to discuss when sharing their life stories. METHODS: Twenty audio-recorded transcripts of open-ended interviews of patients cared for by a ...

Students' experiences with death and dying pr...

Article indépendant | TALWALKAR, Jaideep S. | The American journal of hospice and palliative care | n°11 | vol.366

BACKGROUND: Personal experiences with death and dying are common among medical students, but little is known about student attitudes and emotional responses to these experiences. Our objectives were to ascertain matriculating medi...

Managing end of life care for the critically ...

Article indépendant | BASS, Kathryn | The American journal of hospice and palliative care | n°1 | vol.42

Background: Navigating medical care at the end of life can be a challenging experience for patients. There are also significant resource burdens, including intensive care unit (ICU) admissions, accompanying terminal illness. For a...

End-of-life care for patients with end-stage ...

Article indépendant | RIVERA, Frederick Berro | The American journal of hospice and palliative care | n°1 | vol.41

Heart failure (HF) is a chronic, debilitating condition associated with significant morbidity, mortality, and socioeconomic burden. Patients with end-stage HF (ESHF) who are not a candidate for advanced therapies will continue to ...

Hospice patients' end-of-life dreams and visi...

Article indépendant | RABITTI, Elisa | The American journal of hospice and palliative care | n°1 | vol.41

When conscious, about 50% to 60% of hospice patients report a "visitation" by someone who is not there while they dream or are awake: a phenomenon known as End-of-Life Dreams and Visions (ELDVs). Since the dying process is frequen...

Chargement des enrichissements...