Impact of Adding a Rapid PCR-Based Blood Culture Identification Panel to the Antimicrobial Stewardship Program of Patients with Febrile Neutropenia in a Peruvian Referral Hospital

Author:

Pérez-Lazo Giancarlo12ORCID,del Valle-Mendoza Juana3,Sandoval-Ahumada Roxana4,Soto-Febres Fernando2,Castillo-Córdova Raúl2,Zárate-Tantaleán Melissa4,Morales-Castillo Liliana4,Páucar-Miranda Celia Joanna4,Altamirano-Molina Milagros5ORCID,Pacheco-Modesto Iván5,Ruiz de Somocurcio-Cruzado Claudia5,Arana-Jurado Denis5,del Villar-Alarcón Carmen5,Vargas-Castro Olga5,Díaz-Bardales Carol5,Guerrero-Arismendiz Bruno5,Eyzaguirre-Zapata Renee5,Aguilar-Luis Miguel Angel3ORCID,Martins-Luna Johanna3ORCID,Silva-Caso Wilmer3

Affiliation:

1. Escuela de Medicina, Universidad César Vallejo, Piura 20001, Peru

2. Division of Infectious Diseases, Guillermo Almenara Irigoyen National Hospital-EsSalud, Lima 15033, Peru

3. Centro de Investigación e Innovación de la Facultad de Ciencias de la Salud, Universidad Peruana de Ciencias Aplicadas, Lima 15023, Peru

4. Clinical Pathology Department, Guillermo Almenara Irigoyen National Hospital-EsSalud, Lima 15033, Peru

5. Clinical Hematology Service, Guillermo Almenara Irigoyen National Hospital-EsSalud, Lima 15033, Peru

Abstract

The addition of Biofire® FilmArray® Blood Culture Identification panel 2 (BCID2) to the antimicrobial stewardship program (ASP) could improve outcomes in bloodstream infections (BSI) of patients with febrile neutropenia (FN). A pre- and post-quasi-experimental single-center study was conducted at a reference hospital in Peru. Three groups were considered: patients with BSI before ASP intervention (control group), patients with BSI after ASP intervention (group 1), and patients with BSI after ASP intervention plus BCID2 PCR Panel implementation (group 2). Overall, 93 patients were identified (32 control, 30 group 1, 31 group 2). The median time to effective therapy was significantly shorter in group 2 compared to group 1 and control group, respectively (3.75 vs. 10 h, p = 0.004; 3.75 vs. 19 h, p < 0.001). No significant differences in terms of relapse of bacteremia, in-hospital mortality (all cause), and 30-day-all-cause hospital readmission between the three study periods were found. The appropriateness of empirical antimicrobial use, adding or change, and the following de-escalation or discontinuation was significant when the two intervention periods were compared with the control group (p < 0.001). In addition to the lack of local studies documenting the microbiological profile of FN episodes, adding syndromic panels-based testing could allow for the consolidation of ASP strategies.

Funder

Investigator Sponsored Research (ISR)-Pfizer

Publisher

MDPI AG

Subject

Pharmacology (medical),Infectious Diseases,Microbiology (medical),General Pharmacology, Toxicology and Pharmaceutics,Biochemistry,Microbiology

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