Abstract: TH-PO630
Association Between CKD Progression and Heart Failure: A Retrospective Cohort Study
Session Information
- Hypertension and CVD: Epidemiology, Risk Factors, Prevention
November 03, 2022 | Location: Exhibit Hall, Orange County Convention Center‚ West Building
Abstract Time: 10:00 AM - 12:00 PM
Category: Hypertension and CVD
- 1502 Hypertension and CVD: Clinical‚ Outcomes‚ and Trials
Authors
- Leon Mantilla, Silvia Juliana, Seven Oaks General Hospital, Winnipeg, Manitoba, Canada
- Whitlock, Reid, Seven Oaks General Hospital, Winnipeg, Manitoba, Canada
- Bohm, Clara, University of Manitoba Max Rady College of Medicine, Winnipeg, Manitoba, Canada
- Komenda, Paul, University of Manitoba Max Rady College of Medicine, Winnipeg, Manitoba, Canada
- Rigatto, Claudio, University of Manitoba Max Rady College of Medicine, Winnipeg, Manitoba, Canada
- Tangri, Navdeep, University of Manitoba Max Rady College of Medicine, Winnipeg, Manitoba, Canada
Background
Heart failure (HF) and chronic kidney disease (CKD) are strongly interlinked through multifaceted inter-organ cross-talk that increase the risk of the co-existence of both conditions. HF and CKD separately and in combination, are associated with high symptom burden, mortality risk and increased healthcare costs. We sought to determine if heart failure is a risk factor for adverse renal outcomes and death in patients with CKD and to quantify the magnitude of its effect.
Methods
We conducted a retrospective cohort study using administrative health data from Manitoba, Canada. We included all adults (≥ 18 years) with prevalent CKD (as defined by KDIGO using CDK-EPI eGFR <60 mL/min/1.73 m2 and/or proteinuria for over 3 months) between January 1st, 2007, and Jan 1st, 2018. We identified a subgroup of patients with HF at baseline. We examined the association of interim HF event (as time-dependent exposure) with study outcomes using time-dependent Cox models adjusted for demographics, comorbidities, eGFR, UACR, and medications (e.g., RAASi, beta blockers). The primary composite outcome was ≥ 40% decline in estimated glomerular filtration rate (eGFR), renal replacement therapy (chronic dialysis or kidney transplant), or all-cause mortality: DD40 events.
Results
Of the 18,880 prevalent CKD, 3,650 (19%) had history of HF at baseline. The mean eGFR was 51 ± 26 mL/min/1/.73m2 and the median UACR was 6.20 mg/mmol (IQR: 1.4 - 32.4). There were 4,546 (24%) patients with at least 1 interim HF event, with a median time to first interim HF event of 1.9 years. In time-dependent analysis, those with HF at baseline had a higher risk of DD40 events as well as its components after an interim HF event compared to those without interim HF events adjusted HR for DD40 (aHR): 1.98; 95%CI: 1.81-2.17. Similarly, in those without HF at baseline, interim HF hospitalization was associated with higher risk of DD40 events compared to those without interim HF events (aHR: 1.59; 95%CI: 1.50-1.69).
Conclusion
Interim heart failure is associated with an increased risk of a composite outcome of all-cause mortality, ESKD, and ≥ 40% decline in eGFR in patients with CKD irrespective of history of HF. These findings strongly support efforts to optimize treatment for primary and secondary prevention of heart failure hospitalizations in patients with CKD.
Funding
- Private Foundation Support