The use of a brief 5-item measure of family satisfaction as a critical quality indicator in advanced cancer care : a multisite comparison

Article indépendant

ORNSTEIN, Katherine A. | PENROD, Joan | SCHNUR, Julie B. | SMITH, Cardinale B. | TERESI, Jeanne A. | GARRIDO, Melissa M. | MCKENDRICK, Karen | SIU, Albert L. | MEIER, Diane E. | MORRISON, R. Sean

Background: Although family satisfaction is recognized as a critical indicator of quality for patients with advanced cancer, it is rarely assessed as part of routine clinical care. Measurement burden may be one barrier to widespread use of family satisfaction measures. Objective: The goal of this study was to test the ability of a new, brief 5-item measure of family satisfaction with care to accurately capture differences across hospital settings. Design: Using data from the Palliative Care for Cancer Patients study, a prospective study of 1979 patients and caregivers, the authors used multivariate regression analysis to detect significant differences across five sites. Settings: Hospitalized patients with advanced cancer and their caregivers Methods: they used both the shortened 5-item version of the FAMCARE scale (previously developed using Item Response Theory) and the original 20-item FAMCARE to measure family satisfaction. Results: On the 5-item FAMCARE, sites ranged from mean scores of 5.5–6.9 out of a possible high score of 10. Family members at one care site (n = 783) were significantly (p < 0.05) less satisfied with their care than family members at four other care sites. The original 20-item measure failed to differentiate satisfaction levels between all hospital sites. Discussion: Variability in family satisfaction with advanced cancer care across hospital settings can be more sensitively detected using a brief 5-item questionnaire versus longer measures. The development of less lengthy and burdensome measures for monitoring family satisfaction, which are still valid, can facilitate routine assessments to maintain and promote high-quality care across care settings.

http://dx.doi.org/10.1089/jpm.2016.0442

Voir la revue «JOURNAL OF PALLIATIVE MEDICINE, 20»

Autres numéros de la revue «JOURNAL OF PALLIATIVE MEDICINE»

Consulter en ligne

Suggestions

Du même auteur

The use of a brief 5-item measure of family s...

Article indépendant | ORNSTEIN, Katherine A. | JOURNAL OF PALLIATIVE MEDICINE | n°7 | vol.20

Background: Although family satisfaction is recognized as a critical indicator of quality for patients with advanced cancer, it is rarely assessed as part of routine clinical care. Measurement burden may be one barrier to widespre...

Service availability in assisted living and o...

Article | ALDRIDGE, Melissa D. | JOURNAL OF PALLIATIVE MEDICINE | n°11 | vol.24

Background: Community-based residential settings (e.g., assisted living facilities and retirement communities), are increasing, where vulnerable older adults are living as they age and die. Despite prevalent serious illness, funct...

Service availability in assisted living and o...

Article indépendant | ALDRIDGE, Melissa D. | JOURNAL OF PALLIATIVE MEDICINE | n°11 | vol.24

Background: Community-based residential settings (e.g., assisted living facilities and retirement communities), are increasing, where vulnerable older adults are living as they age and die. Despite prevalent serious illness, funct...

De la même série

Feasibility of a palliative care intervention...

Article indépendant | VERMA, Manisha | JOURNAL OF PALLIATIVE MEDICINE | n°3 | vol.36

Background: Patients with hepatocellular cancer (HCC) are at risk for poor quality of life (QoL) and high symptom burden, coupled with limited treatment options. Palliative care (PC) can play an important role in reducing the suff...

"You suffer from being interested" : a tribut...

Article indépendant | MILLER, Pringl | JOURNAL OF PALLIATIVE MEDICINE | n°12 | vol.31

I met Hank during my palliative medicine fellowship after his nurse Cynthia paged me to request a consult for existential suffering. When reviewing Hank's electronic medical record, it became evident he was dying and averse to spe...

Top ten tips palliative care clinicians shoul...

Article indépendant | CHUNG, Jenny E. | JOURNAL OF PALLIATIVE MEDICINE | n°1 | vol.27

As of 2019, there are 4.2 million Filipino Americans (FAs) and 1.9 million Korean Americans (KAs) in the United States, largely concentrated in New York, California, Texas, Illinois, and Washington. In both populations, similar to...

Interventions for family caregivers of patien...

Article indépendant | ALSHAKHS, Sulaiman | JOURNAL OF PALLIATIVE MEDICINE | n°1 | vol.27

There is a need for understanding the breadth of interventions for caregivers of individuals receiving hospice care at home, given the important role caregivers play in caring and the negative outcomes (e.g., depression) associate...

Associations between measures of disability a...

Article indépendant | CHANG, Victoria A. | JOURNAL OF PALLIATIVE MEDICINE | n°1 | vol.27

Background: The modified Rankin Scale (mRS), which measures degree of disability in daily activities, is the most common outcome measure in stroke research. Quality of life (QoL), however, is impacted by factors other than disabil...

Chargement des enrichissements...