Safety and efficacy of personalised versus standard dosing of linezolid in patients with sepsis (SePkLin): a pragmatic, multicentre, randomised, controlled and superiority clinical trial protocol
Cristina Mondelo-García,
Irene Zarra-Ferro,
Anxo Fernández-Ferreiro,
Antonio Pose-Reino,
Luis Valdés,
Manuel Taboada-Muñiz,
Ana Estany-Gestal,
Teresa Cabaleiro,
Enrique Bandín-Vilar,
Eva Rial-Pensado,
Ana Castro-Balado,
Iria Varela-Rey,
Francisco Cajade-Pascual,
María Teresa Rodríguez-Jato,
María Teresa Rey-Rilo,
Jorge Arca-Suárez,
María Sandra Albiñana-Pérez,
Pedro Rascado-Sedes,
Gema Barbeito-Castiñeiras,
Álvaro Mena de Cea,
Enrique Alemparte-Pardavila,
SePkLin Study Group
Affiliations
Cristina Mondelo-García
2 Pharmacy Department, University Clinical Hospital of Santiago de Compostela, Santiago de Compostela, Spain
Irene Zarra-Ferro
1 FarmaCHUSLab Group, Health Research Institute of Santiago de Compostela, Santiago de Compostela, Spain
Anxo Fernández-Ferreiro
1 FarmaCHUSLab Group, Health Research Institute of Santiago de Compostela, Santiago de Compostela, Spain
Antonio Pose-Reino
9 Internal Medicine Department, University Clinical Hospital of Santiago de Compostela (CHUS), Santiago de Compostela, Spain
Luis Valdés
10 Pneumology Department, University Clinical Hospital of Santiago de Compostela (CHUS), Santiago de Compostela, Spain
Manuel Taboada-Muñiz
11 Department of Anaesthesia and Critical Care, University Clinical Hospital of Santiago de Compostela, Santiago de Compostela, Spain
Ana Estany-Gestal
3 Research Methodology Unit, Health Research Institute of Santiago de Compostela, Santiago de Compostela, Spain
Teresa Cabaleiro
3 Research Methodology Unit, Health Research Institute of Santiago de Compostela, Santiago de Compostela, Spain
Enrique Bandín-Vilar
1 FarmaCHUSLab Group, Health Research Institute of Santiago de Compostela, Santiago de Compostela, Spain
Eva Rial-Pensado
3 Research Methodology Unit, Health Research Institute of Santiago de Compostela, Santiago de Compostela, Spain
Ana Castro-Balado
1 FarmaCHUSLab Group, Health Research Institute of Santiago de Compostela, Santiago de Compostela, Spain
Iria Varela-Rey
1 FarmaCHUSLab Group, Health Research Institute of Santiago de Compostela, Santiago de Compostela, Spain
Francisco Cajade-Pascual
1 FarmaCHUSLab Group, Health Research Institute of Santiago de Compostela, Santiago de Compostela, Spain
María Teresa Rodríguez-Jato
2 Pharmacy Department, University Clinical Hospital of Santiago de Compostela, Santiago de Compostela, Spain
María Teresa Rey-Rilo
4 Department of Anaesthesiology and Perioperative Care, University Clinical Hospital of A Coruña (CHUAC), A Coruña, Spain
Jorge Arca-Suárez
5 Microbiology Department and Health Research Insitute A Coruña (INIBIC), University Clinical Hospital of A Coruña (CHUAC), A Coruña, Spain
María Sandra Albiñana-Pérez
7 Pharmacy Department, University Clinical Hospital of A Coruña (CHUAC), A Coruña, Spain
Pedro Rascado-Sedes
8 Intensive Care Department, University Clinical Hospital of Santiago de Compostela (CHUS), Santiago de Compostela, Spain
Gema Barbeito-Castiñeiras
12 Department of Microbiology, University Clinical Hospital of Santiago de Compostela, Santiago de Compostela, Spain
Álvaro Mena de Cea
13 Service of Infectious Internal Medicine, University Clinical Hospital of A Coruña, A Coruña, Spain
Enrique Alemparte-Pardavila
14 Intensive Care Unit, University Clinical Hospital of A Coruña (CHUAC), A Coruña, Spain
SePkLin Study Group
15 Consellería de Sanidade e o Servizo Galego de Saúde, Santiago de Compostela, Spain
Introduction Linezolid is a broadly used antibiotic to treat complicated infections caused by gram-positive bacteria. Therapeutic drug monitoring of linezolid concentrations is recommended to maximise its efficacy and safety, mainly haematological toxicity. Different pharmacokinetic/pharmacodynamic targets have been proposed to improve linezolid exposure: the ratio of the area under the concentration–time curve during a 24-hour period to minimum inhibitory concentration (MIC) between 80 and 120; percentage of time that the drug concentration remains above the MIC during a dosing interval greater than 85% and the trough concentration between 2 and 7 mg/L. This clinical trial aims to evaluate the safety, efficacy and the clinical and economic utility of personalised dosing of linezolid using Bayesian forecasting methods to attain pharmacokinetic/pharmacodynamic targets, known as model-informed precision dosing.Methods and analysis This is a pragmatic, multicentre, randomised, parallel, controlled, phase IV and low intervention trial. Participants will be randomly assigned 1:1 to each group (n=346 per group). Control group will receive the standard dose of linezolid. Intervention group will receive personalised dosage of linezolid based on pharmacokinetic–pharmacodynamic adjustments. The primary outcome will be the incidence of thrombocytopenia in both groups.Ethics and dissemination This protocol was approved by the Ethical Committee of the Investigation with Medicines of Galicia (code 2022/140) and authorised by the Spanish Agency for Medicines and Medical Devices. The trial is implemented in accordance with the Declaration of Helsinki and the international ethical and scientific quality standard, the Good Clinical Practice. The results will be published in peer-reviewed journals.Trial registration number EudraCT registration code: 2022-000144-30.