Oral decontamination with colistin plus neomycin in solid organ transplant recipients colonized by multidrug-resistant Enterobacterales: a multicentre, randomized, controlled, open-label, parallel-group clinical trial. (June 2021)
- Record Type:
- Journal Article
- Title:
- Oral decontamination with colistin plus neomycin in solid organ transplant recipients colonized by multidrug-resistant Enterobacterales: a multicentre, randomized, controlled, open-label, parallel-group clinical trial. (June 2021)
- Main Title:
- Oral decontamination with colistin plus neomycin in solid organ transplant recipients colonized by multidrug-resistant Enterobacterales: a multicentre, randomized, controlled, open-label, parallel-group clinical trial
- Authors:
- Fariñas, Maria Carmen
González-Rico, Claudia
Fernández-Martínez, Marta
Fortún, Jesús
Escudero-Sanchez, Rosa
Moreno, Asunción
Bodro, Marta
Muñoz, Patricia
Valerio, Maricela
Montejo, Miguel
Nieto, Javier
Ruiz-San Millan, Juan Carlos
Casafont-Morencos, Fernando
Martinez-Martínez, Luis
Fariñas-Álvarez, Concepción
Armiñanzas, Carlos
Arnaiz de las Revillas, Francisco
Calvo, Jorge
Cuadrado, Antonio
Flor, Virginia
Fábrega, Emilio
Gozalo, Mónica
Illaro, Aitziber
Rodrigo, Emilio
Fernández, Ana
Graus, Javier
Martin Dávil, Pilar
Martínez, Adolfo
Ruiz Garbajosa, Patricia
Sánchez-Díaz, Ana M.
Linares, Laura
Cofan, Frederic
Marco, Francesc
Navasa, Miquel
Aranzamendi, Maitane
Blanco, María José
Agnelli Bento, Caroline
Machado, Marina
Olmedo, María
Rincón Sanz, Cristina
Rodríguez Ferrero, María Luisa
Sánchez Cámara, Luis Alberto
Vicente-Rangel, Teresa
Gracia-Ahufinger, Irene
Rodríguez, Fernando
Torre-Cisneros, Julián
Páez Vega, Aurora
Aguadov, José María
Chaves, Fernando
Resino, Elena
… (more) - Abstract:
- Abstract: Objectives: To evaluate the efficacy of oral colistin-neomycin in preventing multidrug-resistant Enterobacterales (MDR-E) infections in solid organ transplant (SOT) recipients. Methods: Multicentre, open-label, parallel-group, controlled trial with balanced (1:1) randomization in five transplant units. SOT recipients were screened for MDR-E intestinal colonization (extended-spectrum β-lactamase or carbapenemase producing) before transplantation and +7 and + 14 days after transplantation and assigned 1:1 to receive treatment with colistin sulfate plus neomycin sulfate for 14 days (decolonization treatment (DT) group) or no treatment (no decolonization treatment (NDT) group). The primary outcome was diagnosis of an MDR-E infection. Safety outcomes were appearance of adverse effects, mainly diarrhoea, rash, nausea and vomiting. Patients were monitored weekly until 30 days after treatment. Intention-to-treat analysis was performed. Results: MDR-E rectal colonization was assessed in 768 SOT recipients; 105 colonized patients were included in the clinical trial, 53 receiving DT and 52 NDT. No significant decrease in the risk of infection by MDR-E was observed in the DT group (9.4%, 5/53) compared to the NDT group (13.5%, 7/52) (relative risk 0.70; 95% confidence interval 0.24–2.08; p 0.517). Four patients (5.6%), three (5.6%) in the DT group and one (1.9%) in the NDT group, developed colistin resistance. Twelve patients (22.7%) in the DT group had diarrhoea, eightAbstract: Objectives: To evaluate the efficacy of oral colistin-neomycin in preventing multidrug-resistant Enterobacterales (MDR-E) infections in solid organ transplant (SOT) recipients. Methods: Multicentre, open-label, parallel-group, controlled trial with balanced (1:1) randomization in five transplant units. SOT recipients were screened for MDR-E intestinal colonization (extended-spectrum β-lactamase or carbapenemase producing) before transplantation and +7 and + 14 days after transplantation and assigned 1:1 to receive treatment with colistin sulfate plus neomycin sulfate for 14 days (decolonization treatment (DT) group) or no treatment (no decolonization treatment (NDT) group). The primary outcome was diagnosis of an MDR-E infection. Safety outcomes were appearance of adverse effects, mainly diarrhoea, rash, nausea and vomiting. Patients were monitored weekly until 30 days after treatment. Intention-to-treat analysis was performed. Results: MDR-E rectal colonization was assessed in 768 SOT recipients; 105 colonized patients were included in the clinical trial, 53 receiving DT and 52 NDT. No significant decrease in the risk of infection by MDR-E was observed in the DT group (9.4%, 5/53) compared to the NDT group (13.5%, 7/52) (relative risk 0.70; 95% confidence interval 0.24–2.08; p 0.517). Four patients (5.6%), three (5.6%) in the DT group and one (1.9%) in the NDT group, developed colistin resistance. Twelve patients (22.7%) in the DT group had diarrhoea, eight related to treatment (15.0%); one patient (1.8%) developed skin rash and another (1.8%) nausea and vomiting. Two patients (3.8%) in the NDT group developed diarrhoea. Conclusions: DT does not reduce MDR-E infections in SOT. Colistin resistance and adverse effects such as diarrhoea are a potential issue that must be taken seriously. … (more)
- Is Part Of:
- Clinical microbiology and infection. Volume 27:Number 6(2021)
- Journal:
- Clinical microbiology and infection
- Issue:
- Volume 27:Number 6(2021)
- Issue Display:
- Volume 27, Issue 6 (2021)
- Year:
- 2021
- Volume:
- 27
- Issue:
- 6
- Issue Sort Value:
- 2021-0027-0006-0000
- Page Start:
- 856
- Page End:
- 863
- Publication Date:
- 2021-06
- Subjects:
- Enterobacterales -- Infections -- Multiresistance -- Rectal colonization -- Solid organ transplantation
Medical microbiology -- Periodicals
Diagnostic microbiology -- Periodicals
Communicable diseases -- Periodicals
Infection -- Periodicals
616.01 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1469-0691 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1016/j.cmi.2020.12.016 ↗
- Languages:
- English
- ISSNs:
- 1198-743X
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3286.305520
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