Oral Sodium Chloride in the Prevention of Contrast-Associated Acute Kidney Injury in Elderly Outpatients: The PNIC-Na Randomized Non-Inferiority Trial

Author:

Suárez Carantoña Cecilia12ORCID,Escobar Cervantes Carlos3ORCID,Fabregate Martín1ORCID,López Rodríguez Mónica12ORCID,Bara Ledesma Nuria1,Soto Pérez-Olivares Javier45ORCID,Ruiz Ortega Raúl Antonio12,López Castellanos Genoveva12,Olavarría Delgado Andreina5,Blázquez Sánchez Javier5,Gómez del Olmo Vicente12,Moralejo Martín Myriam1,Pumares Álvarez María Belén1,Sánchez Gallego María de la Concepción1,Llàcer Pau12ORCID,Liaño Fernando6,Manzano Luis12ORCID

Affiliation:

1. Internal Medicine Department, Hospital Universitario Ramón y Cajal, IRYCIS, CTRA M-607 Colmenar Viejo, Km 9.10, 28034 Madrid, Spain

2. Faculty of Medicine and Health Sciences, Universidad de Alcalá (UAH), Pl. de San Diego, s/n, 28801 Alcalá de Henares, Spain

3. Cardiology Department, Hospital Universitario La Paz, IdiPaz, P.º de la Castellana, 261, 28046 Madrid, Spain

4. Centro de Innovación en Tecnología para el Desarrollo Humano, Universidad Politécnica de Madrid (itdUPM), Av. Complutense s/n, 28040 Madrid, Spain

5. Radiology Department, Hospital Universitario Ramón y Cajal, IRYCIS, CTRA M-607 Colmenar Viejo, Km 9.10, 28034 Madrid, Spain

6. Department of Nephrology, Hospital Universitario Ramón y Cajal, IRYCIS, CTRA M-607 Colmenar Viejo, Km 9.10, 28034 Madrid, Spain

Abstract

Objective: We aimed to test the non-inferiority of oral versus intravenous hydration in the incidence of contrast-associated acute kidney injury (CA-AKI) in elderly outpatients undergoing a contrast-enhanced computed tomography (CE-CT) scan. Methods: PNIC-Na (NCT03476460) is a phase-2, single-center, randomized, open-label, non-inferiority trial. We included outpatients undergoing a CE-CT scan, >65 years having at least one risk factor for CA-AKI, such as diabetes, heart failure, or an estimated glomerular filtration rate (eGFR) of 30–59 mL/min/1.73 m². Participants were randomized (1:1) to oral sodium-chloride capsules or intravenous hydration. The primary outcome was an increase in serum creatinine >0.3 mg/dL or a reduction in eGFR >25% within 48 h. The non-inferiority margin was set at 5%. Results: A total of 271 subjects (mean age 74 years, 66% male) were randomized, and 252 were considered for the main analysis (per-protocol). A total of 123 received oral hydration and 129 intravenous. CA-AKI occurred in 9 (3.6%) of 252 patients and 5/123 (4.1%) in the oral-hydration group vs. 4/129 (3.1%) in the intravenous-hydration group. The absolute difference between the groups was 1.0% (95% CI −4.8% to 7.0%), and the upper limit of the 95% CI exceeded the pre-established non-inferiority margin. No major safety concerns were observed. Conclusion: The incidence of CA-AKI was lower than expected. Although both regimens showed similar incidences of CA-AKI, the non-inferiority was not shown.

Funder

Spanish Health Ministry

Publisher

MDPI AG

Subject

General Medicine

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