Literature DB >> 29025150

Collection and determinants of patient reported outcome measures in haemodialysis patients in Scotland.

A Nimmo1, S Bell2, C Brunton3, J Campbell4, A Doyle5, B MacKinnon6, R K Peel7, S Robertson8, I Shilliday9, E Spalding10, J P Traynor4,6, W Metcalfe11,6.   

Abstract

BACKGROUND/
INTRODUCTION: Patient reported outcome measures (PROMs) can evaluate the quality of health in patients with established renal failure. There is limited experience of their use within national renal registries. AIM: To describe the Scottish Renal Registry's (SRR) experience of collecting PROMS in the haemodialysis population and correlate PROMS to demographic and clinical parameters.
DESIGN: Retrospective observational cross-sectional study.
METHODS: Haemodialysis patients in Scotland were invited to complete the KDQOL™-36 questionnaire on the day of the annual SRR census in 2015 and 2016. Questionnaires were linked to census demographic and clinical variables.
RESULTS: In 2016, 738 questionnaires were linked to census data (39% of prevalent haemodialysis population). Response rates differed with age (≥ 65 years 42%, < 65 years 36%) [χ2P = 0.006]; duration of renal replacement therapy (<1 year 46%, ≥1 < 5 years 38%, ≥ 5 years 33%) [χ2P = 0.002] and social class (Scottish Index of Multiple Deprivation (SIMD) Class 1 32%, Class 2 41%, Class 3 40%, Class 4 48%, Class 5 40%) [χ2P < 0.001]. There were significant differences in PROMs with age, SIMD quintile and primary renal diagnosis. Achieving a urea reduction ratio of >65% and dialysing through arteriovenous access were associated with significantly higher PROMs. PROMs were not affected by haemoglobin or phosphate concentration. DISCUSSION/
CONCLUSIONS: Routine collection of PROMs is feasible and can identify potentially under-recognized and treatable determinants to quality of life. The association between attaining recommended standards of care and improved PROMs is striking. Individual and population-wide strategies are required to improve PROMs.
© The Author 2017. Published by Oxford University Press on behalf of the Association of Physicians. All rights reserved. For Permissions, please email: journals.permissions@oup.com

Entities:  

Mesh:

Year:  2018        PMID: 29025150     DOI: 10.1093/qjmed/hcx180

Source DB:  PubMed          Journal:  QJM        ISSN: 1460-2393


  7 in total

1.  Patient-reported outcome measures as a new application in the Swedish Renal Registry: health-related quality of life through RAND-36.

Authors:  Agneta A Pagels; Maria Stendahl; Marie Evans
Journal:  Clin Kidney J       Date:  2019-07-25

2.  Incorporating patient-reported outcomes (PROs) into dialysis policy: Current initiatives, challenges, and opportunities.

Authors:  Ebele M Umeukeje; Devika Nair; Rachel B Fissell; Kerri L Cavanaugh
Journal:  Semin Dial       Date:  2020-01       Impact factor: 3.455

Review 3.  Outcomes after kidney transplantation, let's focus on the patients' perspectives.

Authors:  Yiman Wang; Jaapjan D Snoep; Marc H Hemmelder; Koen E A van der Bogt; Willem Jan W Bos; Paul J M van der Boog; Friedo W Dekker; Aiko P J de Vries; Yvette Meuleman
Journal:  Clin Kidney J       Date:  2021-01-20

4.  Patient-reported outcome measures: selection of a valid questionnaire for routine symptom assessment in patients with advanced chronic kidney disease - a four-phase mixed methods study.

Authors:  Esmee M van der Willik; Yvette Meuleman; Karen Prantl; Giel van Rijn; Willem Jan W Bos; Frans J van Ittersum; Hans A J Bart; Marc H Hemmelder; Friedo W Dekker
Journal:  BMC Nephrol       Date:  2019-09-02       Impact factor: 2.388

5.  Patient-reported outcome measures in hemodialysis patients: results of the first multicenter cross-sectional ePROMs study in France.

Authors:  Abdallah Guerraoui; Mathilde Prezelin-Reydit; Anne Kolko; Marie Lino-Daniel; Charlotte Dumas de Roque; Pablo Urena; Philippe Chauveau; Catherine Lasseur; Julie Haesebaert; Agnes Caillette-Beaudoin
Journal:  BMC Nephrol       Date:  2021-10-30       Impact factor: 2.388

6.  The role of kidney registries in expediting large-scale collection of patient-reported outcome measures for people with chronic kidney disease.

Authors:  Sabine N van der Veer; Cecile Couchoud; Rachael L Morton
Journal:  Clin Kidney J       Date:  2021-03-16

7.  Routinely measuring symptom burden and health-related quality of life in dialysis patients: first results from the Dutch registry of patient-reported outcome measures.

Authors:  Esmee M van der Willik; Marc H Hemmelder; Hans A J Bart; Frans J van Ittersum; Judith M Hoogendijk-van den Akker; Willem Jan W Bos; Friedo W Dekker; Yvette Meuleman
Journal:  Clin Kidney J       Date:  2020-02-03
  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.