Electrolyte abnormalities and severity, mortality, and resource utilization in U.S. cancer hospitalizations: National Inpatient Sample, 2018–2022.
Abstract
e23190 Background: Electrolyte abnormalities are common during cancer hospitalizations and are often managed as isolated disturbances. National data describing their association with inpatient physiologic severity, mortality, and resource utilization in oncology hospitalizations remain limited. Methods: A serial cross-sectional, hospitalization-level analysis of the 2018 to 2022 Healthcare Cost and Utilization Project National Inpatient Sample (NIS) was performed using discharge-level survey weighting with hospital clustering and stratification to generate nationally representative estimates. Adult hospitalizations with a principal diagnosis of malignancy were identified using ICD-10-CM codes C00 to C97 and D45 to D47. ICD-defined electrolyte abnormality phenotypes included hyponatremia (E87.1), hypercalcemia (E83.52), hypokalemia (E87.6), and hyperkalemia (E87.5), with a composite exposure capturing any electrolyte abnormality. Primary outcomes were All Patient Refined Diagnosis Related Group (APR-DRG) severity of illness subclass, with extreme inpatient severity defined as APR-DRG level 4. Secondary outcomes included in-hospital mortality, length of stay (LOS), and hospitalization cost. Survey-weighted multivariable models adjusted for demographics, payer, socioeconomic status, admission characteristics, cancer type, and hospital characteristics. Results: Among 961,848 unweighted cancer hospitalizations representing 4,809,239 hospitalizations nationally, any electrolyte abnormality occurred in 24.07%. Hyponatremia occurred in 11.12%, hypercalcemia in 2.85%, hypokalemia in 10.97%, and hyperkalemia in 4.13%. Hospitalizations with any electrolyte abnormality had higher mean APR-DRG severity than those without (3.13 vs 2.40), longer LOS (9.79 vs 5.77 days), and higher mean cost ($28,812 vs $21,146). Extreme inpatient severity occurred more frequently in hospitalizations with electrolyte abnormalities than without (5.88% vs. 2.69%). After adjustment, any electrolyte abnormality remained independently associated with higher inpatient severity (beta 0.51, 95% CI 0.50-0.52), increased odds of extreme severity (OR 2.37, 95% CI 2.29-2.45), and higher mortality (OR 1.91, 95% CI 1.86-1.96). Hyperkalemia showed the strongest associations with inpatient severity (beta 0.59, 95% CI 0.56-0.62), extreme severity (OR 3.01, 95% CI 2.79-3.25), and mortality (OR 3.29, 95% CI 3.02-3.58). Conclusions: Electrolyte abnormality phenotypes are common in U.S. cancer hospitalizations and are independently associated with substantially higher inpatient physiologic severity, mortality, and resource utilization. These findings support electrolyte abnormalities as markers of inpatient vulnerability that may inform risk stratification and operational planning in hospitalized oncology populations.
Article Details
Journal Info
Journal of Clinical Oncology
Lippincott Williams & Wilkins
Authors (5)
Jacob Everett
Department of Internal Medicine, Sunrise Health GME Consortium, Las Vegas, NV
Priam Chaganlal
Department of Internal Medicine - Sunrise Health GME Consortium, Las Vegas, NV
Daniel Thomas Jones
HCA Sunrise Health GME Consortium - MountainView Hospital, Las Vegas, NV
Kyaw Zin Thein
3Comprehensive Cancer Centers of Nevada, Division of Hematology and Medical Oncology, Las Vegas, United States
Pinak Shah
From Gagnon Cardiovascular Institute, Morristown Medical Center, Morristown, NJ (P.G.); Columbia University Medical Center/New York Presbyterian Hospital (A.S., R.T.H., M.B.L.), the Cardiovascular Research Foundation (D.J.C., R.T.H., B.R., M.B.L.), and Weill Cornell Medicine (B.R.), New York, and St. Francis Hospital and Heart Center, Roslyn (D.J.C.) — all in New York; University of Colorado Health, Medical Center of the Rockies, Loveland (J.B.O.); Laval University, Quebec, QC (P.P.), St. Paul’s Hospital, University of British Columbia, Vancouver (P.B., J.L.), and McMaster University, Hamilton, ON (T.S.) — all in Canada; Vanderbilt University Medical Center, Nashville (B.R.L., K.G.); Emory University, Atlanta (V.B.); the Division of Cardiovascular Medicine and Stanford Cardiovascular Institute, Stanford University, Stanford (W.F.F.), VA Palo Alto Health Care System, Palo Alto (W.F.F.), California Pacific Medical Center, San Francisco (D.V.D.), Cedars–Sinai Medical Center, Los Angeles (R.R.M.), and Edwards ...