Introduction The progression of mild hyperkalemia and the predictors of progression have not been well characterized. In this study we aimed to characterize the progression of hyperkalemia and identify the risk factors for hyperkalemia progression. Methods Adults with mild hyperkalemia (at least one serum potassium measure > 5.0 and <= 5.5 mEq/L) were identified using electronic medical records from the Research Action for Health Network (2012-2018). Progression to moderate-to-severe and progression to severe hyperkalemia were defined as the first occurrences of a serum potassium measure > 5.5 and > 6.0 mEq/L, respectively. Kaplan-Meier analyses were conducted to estimate progression rates for all patients and by pre-specified patient subgroups. Hazard ratios (HR) of moderate-to-severe and severe hyperkalemia progression were estimated using Cox models. Results Of 35,369 patients with mild hyperkalemia, 16.9% and 8.7% progressed to moderate-to-severe and severe hyperkalemia, respectively. Rates of hyperkalemia progression elevated with the severity of chronic kidney disease (CKD). The highest progression rates were seen in patients with CKD stage 5 (stage 5 vs. no CKD: moderate-to-severe, 50.2% vs. 12.0%; severe, 31.3% vs. 3.9%; p < 0.001). Higher progression rates were also observed in patients with heart failure, hypertension, and type II diabetes compared with patients without those conditions (all p < 0.001). The most prominent risk factors were CKD stage 5 (HR of progression to moderate-to-severe hyperkalemia, 3.32 [95% CI 3.03-3.64]; severe, 4.08 [3.55-4.69]), CKD stage 4 (2.19 [1.97-2.43], 2.28 [1.92-2.71]), CKD stage 3 (1.57 [1.46-1.68], 1.65 [1.46-1.87]), type I diabetes (1.37 [1.18-1.61], 1.54 [1.23-1.93]), and serum potassium (1.12 [1.10-1.15], 1.13 [1.10-1.17] per 0.1 mEq/L increase) (all p values < 0.05). Conclusion Hyperkalemia progression rates increased significantly with CKD stage and were also higher among patients with higher baseline potassium level, heart failure, hypertension, and diabetes.
机构:
HIGA San Martin CUCAIBA CRAI, Unidad Trasplante Organos, La Plata, ArgentinaHIGA San Martin CUCAIBA CRAI, Unidad Trasplante Organos, La Plata, Argentina
Cecilia Urena, Maria
Martin Ciappa, Julio
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HIGA San Martin CUCAIBA CRAI, Unidad Trasplante Organos, La Plata, ArgentinaHIGA San Martin CUCAIBA CRAI, Unidad Trasplante Organos, La Plata, Argentina
Martin Ciappa, Julio
Taylor, Marcelo
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HIGA San Martin CUCAIBA CRAI, Unidad Trasplante Organos, La Plata, ArgentinaHIGA San Martin CUCAIBA CRAI, Unidad Trasplante Organos, La Plata, Argentina
Taylor, Marcelo
Rodriguez, Segio
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HIGA San Martin CUCAIBA CRAI, Unidad Trasplante Organos, La Plata, ArgentinaHIGA San Martin CUCAIBA CRAI, Unidad Trasplante Organos, La Plata, Argentina
Rodriguez, Segio
Obregon, Liliana M.
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HIGA San Martin CUCAIBA CRAI, Unidad Trasplante Organos, La Plata, ArgentinaHIGA San Martin CUCAIBA CRAI, Unidad Trasplante Organos, La Plata, Argentina
Obregon, Liliana M.
Mir Sabato, German Alejo
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HIGA San Martin CUCAIBA CRAI, Unidad Trasplante Organos, La Plata, ArgentinaHIGA San Martin CUCAIBA CRAI, Unidad Trasplante Organos, La Plata, Argentina
机构:
Univ Texas SW Med Ctr Dallas, Dept Internal Med, Dallas, TX 75390 USAUniv Texas SW Med Ctr Dallas, Dept Internal Med, Dallas, TX 75390 USA
Palmer, Biff F.
Clegg, Deborah J.
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Cedars Sinai Med Ctr, Biomed Res Dept, Diabet & Obes Res Div, Beverly Hills, CA USAUniv Texas SW Med Ctr Dallas, Dept Internal Med, Dallas, TX 75390 USA
Clegg, Deborah J.
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION,
2015,
314
(22):
: 2405
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2406