Prevalence and Association of Pruritus and Its Current Treatment During the First Year of Dialysis: A DOMESTICO Study.


Journal

Kidney360
ISSN: 2641-7650
Titre abrégé: Kidney360
Pays: United States
ID NLM: 101766381

Informations de publication

Date de publication:
16 Oct 2024
Historique:
received: 05 07 2024
accepted: 03 10 2024
medline: 25 10 2024
pubmed: 25 10 2024
entrez: 25 10 2024
Statut: aheadofprint

Résumé

Pruritus is common in dialysis patients and associated with impaired health-related quality of life (HRQoL) and sleep disturbances. Its pathophysiology remains unclear resulting in limited treatment options and lack of treatment guidelines. The exact trajectory of pruritus after dialysis initiation nor the state of current medical treatment has been studied. Incident dialysis patients (n=1438), included in the Dutch nOcturnal and hoME dialysis Study To Improve Clinical Outcomes (DOMESTICO), were studied. Outcome parameters were prevalence of pruritus, severity of pruritus and the use of antipruritic medication, repeatedly measured during the first year of dialysis. Associations between treatment, pruritus and quality of life were longitudinally studied using linear mixed models. The prevalence of pruritus ranged from 50.5% to 56.6% during the first year of dialysis. Throughout the year approximately 35% experienced persistent pruritus and 40% fluctuating pruritus. During follow-up 21.5% to 26.5% received medical treatment for pruritus. Emollients were associated with more severe pruritus (adjusted β = 0.31, 95% CI 0.15; 0.48), the remaining treatments did not show any association. Pruritus was significantly associated with lower physical and mental HRQoL (adjusted β = -2.04, 95% CI -2.78; -1.30 and β = -1.73, 95% CI -2.51; -0.94, respectively), irrespective of treatment. During the first year of dialysis, pruritus is highly prevalent, predominantly fluctuating, and associated with impaired HRQoL. The minority of patients received medical treatment; in our study current treatment was not associated with an improvement of pruritus. These results highlight the need for more awareness among clinicians and for the development of effective treatment options.

Sections du résumé

BACKGROUND BACKGROUND
Pruritus is common in dialysis patients and associated with impaired health-related quality of life (HRQoL) and sleep disturbances. Its pathophysiology remains unclear resulting in limited treatment options and lack of treatment guidelines. The exact trajectory of pruritus after dialysis initiation nor the state of current medical treatment has been studied.
METHODS METHODS
Incident dialysis patients (n=1438), included in the Dutch nOcturnal and hoME dialysis Study To Improve Clinical Outcomes (DOMESTICO), were studied. Outcome parameters were prevalence of pruritus, severity of pruritus and the use of antipruritic medication, repeatedly measured during the first year of dialysis. Associations between treatment, pruritus and quality of life were longitudinally studied using linear mixed models.
RESULTS RESULTS
The prevalence of pruritus ranged from 50.5% to 56.6% during the first year of dialysis. Throughout the year approximately 35% experienced persistent pruritus and 40% fluctuating pruritus. During follow-up 21.5% to 26.5% received medical treatment for pruritus. Emollients were associated with more severe pruritus (adjusted β = 0.31, 95% CI 0.15; 0.48), the remaining treatments did not show any association. Pruritus was significantly associated with lower physical and mental HRQoL (adjusted β = -2.04, 95% CI -2.78; -1.30 and β = -1.73, 95% CI -2.51; -0.94, respectively), irrespective of treatment.
CONCLUSIONS CONCLUSIONS
During the first year of dialysis, pruritus is highly prevalent, predominantly fluctuating, and associated with impaired HRQoL. The minority of patients received medical treatment; in our study current treatment was not associated with an improvement of pruritus. These results highlight the need for more awareness among clinicians and for the development of effective treatment options.

Identifiants

pubmed: 39453829
doi: 10.34067/KID.0000000615
pii: 02200512-990000000-00506
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Fresenius Medical Care Deutschland GmbH, ZonMw, Nierstichting, Baxter Nederland, Dirinco, AstraZeneca, Cablon Medical, Eurocept Homecare, Novartis, CSL Vifor, Bayer, Alnylam Pharmaceuticals

Informations de copyright

Copyright © 2024 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Society of Nephrology.

Auteurs

Thomas S van Lieshout (TS)

Department of Nephrology, Amsterdam UMC location Vrije Universiteit Amsterdam, Amsterdam, Research institute Amsterdam Cardiovascular Sciences, the Netherlands.
Department of Internal Medicine, Northwest Clinics, Alkmaar, the Netherlands.
Amsterdam Cardiovascular Sciences, Diabetes and Metabolism, Amsterdam, the Netherlands.

Esmee Driehuis (E)

Department of Nephrology, Amsterdam UMC location Vrije Universiteit Amsterdam, Amsterdam, Research institute Amsterdam Cardiovascular Sciences, the Netherlands.
Department of Nephrology and Hypertension, University Medical Center Utrecht, Utrecht, the Netherlands.

Alferso C Abrahams (AC)

Department of Nephrology and Hypertension, University Medical Center Utrecht, Utrecht, the Netherlands.

Violette de Ruijter (V)

Department of Nephrology, Amsterdam UMC location Vrije Universiteit Amsterdam, Amsterdam, Research institute Amsterdam Cardiovascular Sciences, the Netherlands.

Sanne J de Lange (SJ)

Department of Nephrology and Hypertension, University Medical Center Utrecht, Utrecht, the Netherlands.

Anna A Bonenkamp (AA)

Department of Nephrology, Amsterdam UMC location Vrije Universiteit Amsterdam, Amsterdam, Research institute Amsterdam Cardiovascular Sciences, the Netherlands.
Department of Internal Medicine, Jeroen Bosch Hospital, 's Hertogenbosch, the Netherlands.

An S De Vriese (AS)

Division of Nephrology and Infectious Diseases, AZ Sint-Jan Brugge-Oostende AV, Brugge, Belgium.
Department of Internal Medicine, Ghent University, Ghent, Belgium.

Robin Wm Vernooij (RW)

Department of Nephrology and Hypertension, University Medical Center Utrecht, Utrecht, the Netherlands.
Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands.

Patrick M J H Kemperman (PMJH)

Department of Dermatology, Amsterdam University Medical Center (UMC), Amsterdam, The Netherlands.
Department of Dermatology, Dijklander Hospital, Purmerend, The Netherlands.

Thomas Rustemeyer (T)

Department of Dermatology, Amsterdam University Medical Center (UMC), Amsterdam, The Netherlands.

Frans J van Ittersum (FJ)

Department of Nephrology, Amsterdam UMC location Vrije Universiteit Amsterdam, Amsterdam, Research institute Amsterdam Cardiovascular Sciences, the Netherlands.
Amsterdam Cardiovascular Sciences, Diabetes and Metabolism, Amsterdam, the Netherlands.

Erik L Penne (EL)

Department of Internal Medicine, Northwest Clinics, Alkmaar, the Netherlands.

Brigit C van Jaarsveld (BC)

Department of Nephrology, Amsterdam UMC location Vrije Universiteit Amsterdam, Amsterdam, Research institute Amsterdam Cardiovascular Sciences, the Netherlands.
Amsterdam Cardiovascular Sciences, Diabetes and Metabolism, Amsterdam, the Netherlands.
Nephrocare Diapriva Dialysis Center, Amsterdam, the Netherlands.

Classifications MeSH