Measuring the quality of patient-provider relationships in serious illness : a scoping review

Article indépendant

WASSEF, Karen | MA, Kristine | DURIEUX, Brigitte N. | BROWN, Tyler L. | PALADINO, Joanna | THORNE, Sally | SANDERS, Justin J.

BACKGROUND: People affected by serious illness face several threats to their well-being: physical symptoms, psychological distress, disrupted social relations, and spiritual/existential crises. Relationships with clinicians provide a form of structured support that promotes shared decision-making and adaptive stress coping. Measuring relationship quality may improve quality assessment and patient care outcomes. However, researchers and those promoting quality improvement lack clear guidance on measuring this. AIM: To identify and assess items from valid measures of patient-provider relationship quality in serious illness settings for guiding quality assessment. DESIGN: Scoping review. DATA SOURCES: We identified peer-reviewed, English-language articles published from 1990 to 2023 in CINAHL, Embase, and PubMed. Eligible articles described the validation of measures assessing healthcare experiences of patient populations characterized by serious illness. We used Clarke et al.'s theory of relationship quality to assess relationship-focused items. RESULTS: From 3868 screened articles, we identified 101 publications describing 47 valid measures used in serious illness settings. Measures assessed patients and other caregivers. We determined that 597 of 2238 items (26.7%) related to relationships. Most measures (n = 46) included items related to engaging the patient as a whole person. Measures evaluated how providers promote information exchange (n = 35), foster therapeutic alliance (n = 35), recognize and respond to emotion (n = 27), and include patients in care-related decisions (n = 23). Few instruments (n = 9) assessed patient self-management and navigation. CONCLUSIONS: Measures include items that assess patient-provider relationship quality in serious illness settings. Researchers may consider these for evaluating and improving relationship quality, a patient-centered care and research outcome.

http://dx.doi.org/10.1177/02692163251315304

Voir la revue «PALLIATIVE MEDICINE»

Autres numéros de la revue «PALLIATIVE MEDICINE»

Consulter en ligne

Suggestions

Du même auteur

Measuring the quality of patient-provider rel...

Article | WASSEF, Karen | PALLIATIVE MEDICINE

BACKGROUND: People affected by serious illness face several threats to their well-being: physical symptoms, psychological distress, disrupted social relations, and spiritual/existential crises. Relationships with clinicians provid...

Psychosocial correlates of death anxiety in a...

Article | BROWN, Tyler L. | Psycho-oncology | n°1 | vol.34

OBJECTIVES: Individuals living with advanced cancer commonly experience death anxiety, which refers to the distressing thoughts or feelings associated with awareness of one's mortality. Deriving an overview of existing literature ...

Psychosocial correlates of death anxiety in a...

Article indépendant | BROWN, Tyler L. | Psycho-oncology | n°1 | vol.34

OBJECTIVES: Individuals living with advanced cancer commonly experience death anxiety, which refers to the distressing thoughts or feelings associated with awareness of one's mortality. Deriving an overview of existing literature ...

De la même série

Posttraumatic growth in palliative care setti...

Article indépendant | AUSTIN, Philip D. | PALLIATIVE MEDICINE | n°2 | vol.38

BACKGROUND: Posttraumatic growth refers to positive psychological change following trauma. However, there is a need to better understand the experience of posttraumatic growth in the palliative care setting as well as the availabi...

Long-term bereavement outcomes in family memb...

Article indépendant | LAPENSKIE, Julie | PALLIATIVE MEDICINE | n°2 | vol.38

Background: Severe grief is highly distressing and prevalent up to 1 year post-death among people bereaved during the first wave of COVID-19, but no study has assessed changes in grief severity beyond this timeframe. Aim: Understa...

Understanding the extent to which PROMs and P...

Article indépendant | HOWARD, Faith D. | PALLIATIVE MEDICINE | n°2 | vol.38

BACKGROUND: Older people with severe frailty are nearing the end of life but their needs are often unknown and unmet. Systematic ways to capture and measure the needs of this group are required. Patient reported Outcome Measures (...

The perspectives of people with dementia and ...

Article indépendant | MONNET, Fanny | PALLIATIVE MEDICINE | n°2 | vol.38

BACKGROUND: Advance care planning has been defined in an international consensus paper, supported by the European Association for Palliative Care. There are concerns that this definition may not apply to dementia. Moreover, it is ...

Revised European Association for Palliative C...

Article indépendant | SURGES, Séverine M. | PALLIATIVE MEDICINE | n°2 | vol.38

BACKGROUND: The European Association for Palliative Care (EAPC) acknowledges palliative sedation as an important, broadly accepted intervention for patients with life-limiting disease experiencing refractory symptoms. The EAPC the...

Chargement des enrichissements...