A Real-World Data Observational Analysis of the Impact of Liposomal Amphotericin B on Renal Function Using Machine Learning in Critically Ill Patients

Author:

Sacanella Ignasi1,Esteve-Pitarch Erika1ORCID,Guevara-Chaux Jessica23,Berrueta Julen24ORCID,García-Martínez Alejandro24,Gómez Josep5,Casarino Cecilia6,Alés Florencia27,Canadell Laura1ORCID,Martín-Loeches Ignacio8ORCID,Grau Santiago910ORCID,Candel Francisco Javier1112ORCID,Bodí María21314ORCID,Rodríguez Alejandro21314ORCID

Affiliation:

1. Department of Pharmacy, Hospital Universitari Joan XXIII, 43005 Tarragona, Spain

2. Department of Critical Care, Hospital Universitari Joan XXIII, 43005 Tarragona, Spain

3. Postgrado Medicina Crítica y Cuidado Intensivo, Facultad de Medicina, Fundación Universitari Ciencias de la Salud, Distrito Especial, Cra. 54 No.67A-80, Bogotá 111221, Colombia

4. Tarragona Health Data Research Working Group (THeDaR), 43005 Tarragona, Spain

5. Technical Secretary’s Department, Hospital Universitari Joan XXIII, 43005 Tarragona, Spain

6. Department of Pharmacy, Hospital de Pediatría Garrahan, Buenos Aires C1245, Argentina

7. Internal Medicine Department, Hospital Dr. Alejandro Gutiérrez, Venado Tuerto S2600, Argentina

8. Department of Intensive Care Medicine, Multidisciplinary Intensive Care Research Organization (MICRO), St James’ Hospital, D08 NHY1 Dublin, Ireland

9. Department of Pharmacy, Hospital del Mar, 08003 Barcelona, Spain

10. Department of Medicine, Pompeu Fabra University, 08003 Barcelona, Spain

11. Clinical Microbiology & Infectious Diseases Department, Hospital Clínico Universitario San Carlos, 28040 Madrid, Spain

12. San Carlos Hospital Health Research Institute (IdISSC & IML), 28040 Madrid, Spain

13. Faculty of Medicine, Pere Virgili Health Research Institute, Rovira i Virgili University, 43005 Tarragona, Spain

14. Centre for Biomedical Research Network Respiratory Diseases (CIBERES), 43005 Tarragona, Spain

Abstract

Background: Liposomal amphotericin B (L-AmB) has become the mainstay of treatment for severe invasive fungal infections. However, the potential for renal toxicity must be considered. Aims: To evaluate the incidence of acute kidney injury (AKI) in critically ill patients receiving L-AmB for more than 48 h. Methods: Retrospective, observational, single-center study. Clinical, demographic and laboratory variables were obtained automatically from the electronic medical record. AKI incidence was analyzed in the entire population and in patients with a “low” or “high” risk of AKI based on their creatinine levels at the outset of the study. Factors associated with the development of AKI were studied using random forest models. Results: Finally, 67 patients with a median age of 61 (53–71) years, 67% male, a median SOFA of 4 (3–6.5) and a crude mortality of 34.3% were included. No variations in serum creatinine were observed during the observation period, except for a decrease in the high-risk subgroup. A total of 26.8% (total population), 25% (low risk) and 13% (high risk) of patients developed AKI. Norepinephrine, the SOFA score, furosemide (general model), potassium, C-reactive protein and procalcitonin (low-risk subgroup) were the variables identified by the random forest models as important contributing factors to the development of AKI other than L-AmB administration. Conclusions: The development of AKI is multifactorial and the administration of L-AmB appears to be safe in this group of patients.

Publisher

MDPI AG

Reference21 articles.

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