Literature DB >> 28429629

Developing indicators of appropriate and inappropriate end-of-life care in people with Alzheimer's disease, cancer or chronic obstructive pulmonary disease for population-level administrative databases: A RAND/UCLA appropriateness study.

Robrecht De Schreye1, Dirk Houttekier1, Luc Deliens1,2, Joachim Cohen1.   

Abstract

BACKGROUND: A substantial amount of aggressive life-prolonging treatments in the final stages of life has been reported for people with progressive life-shortening conditions. Monitoring appropriate and inappropriate end-of-life care is an important public health challenge and requires validated quality indicators. AIM: To develop indicators of appropriate and inappropriate end-of-life care for people with cancer, chronic obstructive pulmonary disease or Alzheimer's disease, measurable with population-level administrative data.
DESIGN: modified RAND/UCLA appropriateness method. SETTING/PARTICIPANTS: Potential indicators were identified by literature review and expert interviews and scored in a survey among three panels of experts (one for each disease group). Indicators for which no consensus was reached were taken into group discussions. Indicators with consensus among the experts were retained for the final quality indicator sets.
RESULTS: The final sets consist of 28 quality indicators for Alzheimer's disease, 26 quality indicators for cancer and 27 quality indicators for chronic obstructive pulmonary disease. The indicator sets measure aspects of aggressiveness of care, pain and symptom treatment, specialist palliative care, place of care and place of death and coordination and continuity of care.
CONCLUSION: We developed a comprehensive set of quality indicators of appropriate and inappropriate end-of-life care in people with Alzheimer's disease, cancer or chronic obstructive pulmonary disease, to be used in population-level research. Our focus on administrative healthcare databases limits us to treatment and medication, excluding other important quality aspects such as communication, which can be monitored using complementary approaches. Nevertheless, our sets will enable an efficient comparison of healthcare providers, regions and countries in terms of their performance on appropriateness of end-of-life care.

Entities:  

Keywords:  Alzheimer’s disease; Quality indicator; appropriate; chronic obstructive pulmonary disease; end of life care; neoplasms

Mesh:

Year:  2017        PMID: 28429629     DOI: 10.1177/0269216317705099

Source DB:  PubMed          Journal:  Palliat Med        ISSN: 0269-2163            Impact factor:   4.762


  17 in total

1.  Dementia diagnosis in the hospital and outcomes among patients with advanced dementia documented in the Minimum Data Set.

Authors:  Cassandra L Hua; Kali S Thomas; Jennifer N Bunker; Pedro L Gozalo; Emmanuelle Bélanger; Susan L Mitchell; Joan M Teno
Journal:  J Am Geriatr Soc       Date:  2021-11-19       Impact factor: 5.562

2.  Palliative care is increasing, but curative care is growing even faster in the last months of life.

Authors:  Scott Murray; Jordi Amblàs
Journal:  Br J Gen Pract       Date:  2021-08-26       Impact factor: 6.302

3.  Dementia and Early Do-Not-Resuscitate Orders Associated With Less Intensive of End-of-Life Care: A Retrospective Cohort Study.

Authors:  Elizabeth A Luth; Cynthia X Pan; Martin Viola; Holly G Prigerson
Journal:  Am J Hosp Palliat Care       Date:  2021-01-20       Impact factor: 2.500

4.  Association between palliative care and healthcare outcomes among adults with terminal non-cancer illness: population based matched cohort study.

Authors:  Kieran L Quinn; Therese Stukel; Nathan M Stall; Anjie Huang; Sarina Isenberg; Peter Tanuseputro; Russell Goldman; Peter Cram; Dio Kavalieratos; Allan S Detsky; Chaim M Bell
Journal:  BMJ       Date:  2020-07-06

5.  Socioeconomic position and use of healthcare in the last year of life: A systematic review and meta-analysis.

Authors:  Joanna M Davies; Katherine E Sleeman; Javiera Leniz; Rebecca Wilson; Irene J Higginson; Julia Verne; Matthew Maddocks; Fliss E M Murtagh
Journal:  PLoS Med       Date:  2019-04-23       Impact factor: 11.069

6.  Influence of health interventions on quality of life in seriously ill children at the end of life: a systematic review protocol.

Authors:  Veerle E Piette; Joachim Cohen; Luc Deliens; Nele Pauwels; Jutte van der Werff Ten Bosch; Kim Beernaert
Journal:  Syst Rev       Date:  2019-07-11

7.  Documentation of older people's end-of-life care in the context of specialised palliative care: a retrospective review of patient records.

Authors:  M Sjöberg; A-K Edberg; B H Rasmussen; I Beck
Journal:  BMC Palliat Care       Date:  2021-06-24       Impact factor: 3.234

8.  Inappropriate end-of-life cancer care in a generalist and specialist palliative care model: a nationwide retrospective population-based observational study.

Authors:  Manon S Boddaert; Chantal Pereira; Jeroen Adema; Kris C P Vissers; Yvette M van der Linden; Natasja J H Raijmakers; Heidi P Fransen
Journal:  BMJ Support Palliat Care       Date:  2020-12-22       Impact factor: 4.633

9.  Quality indicators for responsible use of medicines: a systematic review.

Authors:  Kenji Fujita; Rebekah J Moles; Timothy F Chen
Journal:  BMJ Open       Date:  2018-07-16       Impact factor: 2.692

10.  Adequate, questionable, and inadequate drug prescribing for older adults at the end of life: a European expert consensus.

Authors:  Lucas Morin; Marie-Laure Laroche; Davide L Vetrano; Johan Fastbom; Kristina Johnell
Journal:  Eur J Clin Pharmacol       Date:  2018-06-23       Impact factor: 2.953

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.