Improving care experiences for patients and caregivers at end of life : a systematic review

Article indépendant

QUIGLEY, Denise D. | MCCLESKEY, Sara G.

Background: End-of-life care is increasing as the US population ages. Approaches to providing high-quality end-of-life care vary across setting, diseases, and populations. Several data collection tools measure patient and/or caregiver care experiences at end of life and can be used for quality improvement. Previous reviews examined palliative care improvements or available measures but none explicitly on improving care experiences. We reviewed literature on improving patient and/or caregiver end-of-life care experiences. Design: We searched U.S. English-language peer-reviewed and grey literature after 2000 on adult end-of-life care experiences. We followed the Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines for quantitative studies, Enhancing Transparency in Reporting the Synthesis of Qualitative Research approach for qualitative studies, and Assessment of Multiple Systematic Reviews tool for the literature reviews. Setting: Palliative and hospice care. Population: Full-text abstraction of 84 articles, identifying 16 articles. Measures: Patient and/or caregiver end-of-life care experiences (captured through administrative data or direct report). Results: Articles examined palliative care experiences across settings; none studied hospice care experiences. Patients and/or caregivers assessed overall care experiences, clinician–staff interactions, provider communication, respect and trust, timeliness of care, spiritual support, caregiver knowledge of care plans, or bereavement support. Efforts aimed at improving end-of-life care experiences are limited and show mixed results. Conclusions: Literature on improving patient and/or caregiver end-of-life care experiences is emerging and focused on palliative care experiences. Evidence on improving hospice care experiences is lacking. Research on strategies for improving end-of-life care experiences should go beyond overall care experiences to include specific aspects of palliative and hospice care experiences.

http://dx.doi.org/10.1177/1049909120931468

Voir la revue «The American journal of hospice and palliative care, 38»

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

Consulter en ligne

Suggestions

Du même auteur

Improving care experiences for patients and c...

Article | QUIGLEY, Denise D. | The American journal of hospice and palliative care | n°1 | vol.38

Background: End-of-life care is increasing as the US population ages. Approaches to providing high-quality end-of-life care vary across setting, diseases, and populations. Several data collection tools measure patient and/or careg...

Improving care experiences for patients and c...

Article indépendant | QUIGLEY, Denise D. | The American journal of hospice and palliative care | n°1 | vol.38

Background: End-of-life care is increasing as the US population ages. Approaches to providing high-quality end-of-life care vary across setting, diseases, and populations. Several data collection tools measure patient and/or careg...

Palliative care and infection management at e...

Article | TARK, Aluem | PALLIATIVE MEDICINE | n°5 | vol.34

BACKGROUND: Infections are common occurrences at end of life that are associated with high rates of morbidity and mortality among frail elderly individuals. The problem of infections in nursing homes has led to a subsequent overus...

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...