Acute and chronic complication profiles among patients with chronic kidney disease in Alberta, Canada: a retrospective observational study.


Journal

BMC nephrology
ISSN: 1471-2369
Titre abrégé: BMC Nephrol
Pays: England
ID NLM: 100967793

Informations de publication

Date de publication:
29 Jul 2024
Historique:
received: 05 06 2023
accepted: 20 07 2024
medline: 31 7 2024
pubmed: 31 7 2024
entrez: 30 7 2024
Statut: epublish

Résumé

Chronic kidney disease (CKD) poses a substantial burden to individuals, caregivers, and healthcare systems. CKD is associated with higher risk for adverse events, including renal failure, cardiovascular disease, and death. This study aims to describe comorbidities and complications in patients with CKD. We conducted a retrospective observational study linking administrative health databases in Alberta, Canada. Adults with CKD were identified (April 1, 2010 and March 31, 2019) and indexed on the first diagnostic code or laboratory test date meeting the CKD algorithm criteria. Cardiovascular, renal, diabetic, and other comorbidities were described in the two years before index; complications were described for events after index date. Complications were stratified by CKD stage, atherosclerotic cardiovascular disease (ASCVD), and type 2 diabetes mellitus (T2DM) status at index. The cohort included 588,170 patients. Common chronic comorbidities were hypertension (36.9%) and T2DM (24.1%), while 11.4% and 2.6% had ASCVD and chronic heart failure, respectively. Common acute complications were infection (58.2%) and cardiovascular hospitalization (24.4%), with rates (95% confidence interval [CI]) of 29.4 (29.3-29.5) and 8.37 (8.32-8.42) per 100 person-years, respectively. Common chronic complications were dyslipidemia (17.3%), anemia (14.7%), and hypertension (11.1%), with rates (95% CI) of 11.9 (11.7-12.1), 4.76 (4.69-4.83), and 13.0 (12.8-13.3) per 100 person-years, respectively. Patients with more advanced CKD, ASCVD, and T2DM at index exhibited higher complication rates. Over two-thirds of patients with CKD experienced complications, with higher rates observed in those with cardio-renal-metabolic comorbidities. Strategies to mitigate risk factors and complications can reduce patient burden.

Sections du résumé

BACKGROUND BACKGROUND
Chronic kidney disease (CKD) poses a substantial burden to individuals, caregivers, and healthcare systems. CKD is associated with higher risk for adverse events, including renal failure, cardiovascular disease, and death. This study aims to describe comorbidities and complications in patients with CKD.
METHODS METHODS
We conducted a retrospective observational study linking administrative health databases in Alberta, Canada. Adults with CKD were identified (April 1, 2010 and March 31, 2019) and indexed on the first diagnostic code or laboratory test date meeting the CKD algorithm criteria. Cardiovascular, renal, diabetic, and other comorbidities were described in the two years before index; complications were described for events after index date. Complications were stratified by CKD stage, atherosclerotic cardiovascular disease (ASCVD), and type 2 diabetes mellitus (T2DM) status at index.
RESULTS RESULTS
The cohort included 588,170 patients. Common chronic comorbidities were hypertension (36.9%) and T2DM (24.1%), while 11.4% and 2.6% had ASCVD and chronic heart failure, respectively. Common acute complications were infection (58.2%) and cardiovascular hospitalization (24.4%), with rates (95% confidence interval [CI]) of 29.4 (29.3-29.5) and 8.37 (8.32-8.42) per 100 person-years, respectively. Common chronic complications were dyslipidemia (17.3%), anemia (14.7%), and hypertension (11.1%), with rates (95% CI) of 11.9 (11.7-12.1), 4.76 (4.69-4.83), and 13.0 (12.8-13.3) per 100 person-years, respectively. Patients with more advanced CKD, ASCVD, and T2DM at index exhibited higher complication rates.
CONCLUSIONS CONCLUSIONS
Over two-thirds of patients with CKD experienced complications, with higher rates observed in those with cardio-renal-metabolic comorbidities. Strategies to mitigate risk factors and complications can reduce patient burden.

Identifiants

pubmed: 39080608
doi: 10.1186/s12882-024-03682-z
pii: 10.1186/s12882-024-03682-z
doi:

Types de publication

Journal Article Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

244

Informations de copyright

© 2024. The Author(s).

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Auteurs

David C W Lau (DCW)

Division of Endocrinology and Metabolism, Department of Medicine, University of Calgary Cumming School of Medicine, Calgary, AB, Canada.

Eileen Shaw (E)

Medlior Health Outcomes Research Ltd, Suite 300 - 160 Quarry Park Blvd. SE, Calgary, AB, Canada. eileen.shaw@medlior.com.

Suzanne McMullen (S)

Medlior Health Outcomes Research Ltd, Suite 300 - 160 Quarry Park Blvd. SE, Calgary, AB, Canada.

Tara Cowling (T)

Medlior Health Outcomes Research Ltd, Suite 300 - 160 Quarry Park Blvd. SE, Calgary, AB, Canada.

Kelcie Witges (K)

Medlior Health Outcomes Research Ltd, Suite 300 - 160 Quarry Park Blvd. SE, Calgary, AB, Canada.

Efrat L Amitay (EL)

Boehringer Ingelheim International GmbH, Ingelheim am Rhein, Germany.

Dominik Steubl (D)

Boehringer Ingelheim International GmbH, Ingelheim am Rhein, Germany.
Department of Nephrology, Hospital rechts der Isar, Technical University Munich, Munich, Germany.

Louis P Girard (LP)

Division of Nephrology, Department of Medicine, University of Calgary Cumming School of Medicine, Calgary, AB, Canada.

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