Population pharmacokinetic analysis of teicoplanin in paediatric patients, including those receiving continuous kidney replacement therapy: a prospective cohort study
- Autores
- Butragueño Laiseca, Laura; García Orueta, Gastón; Riva, Natalia; Trocóniz, Iñaki F.; Fernández, Sarah N.; Camacho Vicente, Verónica; Padilla, Belén; Slöcker, María; Santiago, María José
- Año de publicación
- 2025
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Objectives: Teicoplanin is a commonly used antibiotic in critically ill children. However, teicoplanin dosing is ofteninaccurate, especially in children undergoing continuous kidney replacement therapy (CKRT). This study aimsto develop a population pharmacokinetic (PK) model to optimize teicoplanin dosing in critically ill children, includingthose on CKRT.Methods: Data from 26 critically ill children (12 with CKRT) receiving the standard dosing regimen were analysed.In total, 172 teicoplanin concentration measurements from plasma, pre- and post-filter ports were modelled simultaneouslyusing NONMEM 7.4. Simulations were conducted to assess the target attainment (Cmin = 10 mg/L andAUC24/MIC > 800 h) of the current standard dosing regimen and of different alternative dosing regimens.Results: A two-compartment model was selected. Weight significantly affected renal clearance and volume ofdistribution of the central compartment, while filter surface area affected haemofilter clearance. Only 16 patients(59%) achieved a Cmin of >10 mg/L with the standard dosing regimen, and only 1 achieved the targetAUC/MIC. Based on simulation results, 3 × 15 mg/kg q12h + 10 mg/kg q24h (CKRT) and 3 × 15 mg/kg q12h +15 mg/kg q24h (no CKRT) could be better alternative regimens.Conclusions: This population model is a good proof of concept to develop modelling approaches that could helpin an individualized dosing approach that needs to be adopted in critically ill paediatric patients. The standardpaediatric dosage for teicoplanin could be insufficient for optimal exposure, and higher doses may benefit bothCKRT and non-CKRT patients.
Fil: Butragueño Laiseca, Laura. Universidad de Navarra. Facultad de Farmacia y Nutricion.; España
Fil: García Orueta, Gastón. Universidad de Navarra. Facultad de Farmacia y Nutricion.; España
Fil: Riva, Natalia. Universidad de Navarra. Facultad de Farmacia y Nutricion.; España. Gobierno de la Ciudad de Buenos Aires. Hospital de Pediatría "Juan P. Garrahan"; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Trocóniz, Iñaki F.. Universidad de Navarra. Facultad de Farmacia y Nutricion.; España
Fil: Fernández, Sarah N.. Universidad de Navarra. Facultad de Farmacia y Nutricion.; España
Fil: Camacho Vicente, Verónica. Universidad de Navarra. Facultad de Farmacia y Nutricion.; España
Fil: Padilla, Belén. Universidad de Navarra. Facultad de Farmacia y Nutricion.; España
Fil: Slöcker, María. Universidad de Navarra. Facultad de Farmacia y Nutricion.; España
Fil: Santiago, María José. Universidad de Navarra. Facultad de Farmacia y Nutricion.; España - Materia
-
PEDIATRICS
TEICOPLANIN - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
- Repositorio
.jpg)
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/266327
Ver los metadatos del registro completo
| id |
CONICETDig_1aecd9ca1eeafe47de3877b3392ed1a9 |
|---|---|
| oai_identifier_str |
oai:ri.conicet.gov.ar:11336/266327 |
| network_acronym_str |
CONICETDig |
| repository_id_str |
3498 |
| network_name_str |
CONICET Digital (CONICET) |
| spelling |
Population pharmacokinetic analysis of teicoplanin in paediatric patients, including those receiving continuous kidney replacement therapy: a prospective cohort studyButragueño Laiseca, LauraGarcía Orueta, GastónRiva, NataliaTrocóniz, Iñaki F.Fernández, Sarah N.Camacho Vicente, VerónicaPadilla, BelénSlöcker, MaríaSantiago, María JoséPEDIATRICSTEICOPLANINhttps://purl.org/becyt/ford/3.2https://purl.org/becyt/ford/3Objectives: Teicoplanin is a commonly used antibiotic in critically ill children. However, teicoplanin dosing is ofteninaccurate, especially in children undergoing continuous kidney replacement therapy (CKRT). This study aimsto develop a population pharmacokinetic (PK) model to optimize teicoplanin dosing in critically ill children, includingthose on CKRT.Methods: Data from 26 critically ill children (12 with CKRT) receiving the standard dosing regimen were analysed.In total, 172 teicoplanin concentration measurements from plasma, pre- and post-filter ports were modelled simultaneouslyusing NONMEM 7.4. Simulations were conducted to assess the target attainment (Cmin = 10 mg/L andAUC24/MIC > 800 h) of the current standard dosing regimen and of different alternative dosing regimens.Results: A two-compartment model was selected. Weight significantly affected renal clearance and volume ofdistribution of the central compartment, while filter surface area affected haemofilter clearance. Only 16 patients(59%) achieved a Cmin of >10 mg/L with the standard dosing regimen, and only 1 achieved the targetAUC/MIC. Based on simulation results, 3 × 15 mg/kg q12h + 10 mg/kg q24h (CKRT) and 3 × 15 mg/kg q12h +15 mg/kg q24h (no CKRT) could be better alternative regimens.Conclusions: This population model is a good proof of concept to develop modelling approaches that could helpin an individualized dosing approach that needs to be adopted in critically ill paediatric patients. The standardpaediatric dosage for teicoplanin could be insufficient for optimal exposure, and higher doses may benefit bothCKRT and non-CKRT patients.Fil: Butragueño Laiseca, Laura. Universidad de Navarra. Facultad de Farmacia y Nutricion.; EspañaFil: García Orueta, Gastón. Universidad de Navarra. Facultad de Farmacia y Nutricion.; EspañaFil: Riva, Natalia. Universidad de Navarra. Facultad de Farmacia y Nutricion.; España. Gobierno de la Ciudad de Buenos Aires. Hospital de Pediatría "Juan P. Garrahan"; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Trocóniz, Iñaki F.. Universidad de Navarra. Facultad de Farmacia y Nutricion.; EspañaFil: Fernández, Sarah N.. Universidad de Navarra. Facultad de Farmacia y Nutricion.; EspañaFil: Camacho Vicente, Verónica. Universidad de Navarra. Facultad de Farmacia y Nutricion.; EspañaFil: Padilla, Belén. Universidad de Navarra. Facultad de Farmacia y Nutricion.; EspañaFil: Slöcker, María. Universidad de Navarra. Facultad de Farmacia y Nutricion.; EspañaFil: Santiago, María José. Universidad de Navarra. Facultad de Farmacia y Nutricion.; EspañaOxford University Press2025-03info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/266327Butragueño Laiseca, Laura; García Orueta, Gastón; Riva, Natalia; Trocóniz, Iñaki F.; Fernández, Sarah N.; et al.; Population pharmacokinetic analysis of teicoplanin in paediatric patients, including those receiving continuous kidney replacement therapy: a prospective cohort study; Oxford University Press; Journal of Antimicrobial Chemotherapy; 80; 3; 3-2025; 868-8750305-7453CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://academic.oup.com/jac/article/80/3/868/7974752info:eu-repo/semantics/altIdentifier/doi/10.1093/jac/dkaf012info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2026-08-25T14:38:32Zoai:ri.conicet.gov.ar:11336/266327instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982026-08-25 14:38:32.39CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
| dc.title.none.fl_str_mv |
Population pharmacokinetic analysis of teicoplanin in paediatric patients, including those receiving continuous kidney replacement therapy: a prospective cohort study |
| title |
Population pharmacokinetic analysis of teicoplanin in paediatric patients, including those receiving continuous kidney replacement therapy: a prospective cohort study |
| spellingShingle |
Population pharmacokinetic analysis of teicoplanin in paediatric patients, including those receiving continuous kidney replacement therapy: a prospective cohort study Butragueño Laiseca, Laura PEDIATRICS TEICOPLANIN |
| title_short |
Population pharmacokinetic analysis of teicoplanin in paediatric patients, including those receiving continuous kidney replacement therapy: a prospective cohort study |
| title_full |
Population pharmacokinetic analysis of teicoplanin in paediatric patients, including those receiving continuous kidney replacement therapy: a prospective cohort study |
| title_fullStr |
Population pharmacokinetic analysis of teicoplanin in paediatric patients, including those receiving continuous kidney replacement therapy: a prospective cohort study |
| title_full_unstemmed |
Population pharmacokinetic analysis of teicoplanin in paediatric patients, including those receiving continuous kidney replacement therapy: a prospective cohort study |
| title_sort |
Population pharmacokinetic analysis of teicoplanin in paediatric patients, including those receiving continuous kidney replacement therapy: a prospective cohort study |
| dc.creator.none.fl_str_mv |
Butragueño Laiseca, Laura García Orueta, Gastón Riva, Natalia Trocóniz, Iñaki F. Fernández, Sarah N. Camacho Vicente, Verónica Padilla, Belén Slöcker, María Santiago, María José |
| author |
Butragueño Laiseca, Laura |
| author_facet |
Butragueño Laiseca, Laura García Orueta, Gastón Riva, Natalia Trocóniz, Iñaki F. Fernández, Sarah N. Camacho Vicente, Verónica Padilla, Belén Slöcker, María Santiago, María José |
| author_role |
author |
| author2 |
García Orueta, Gastón Riva, Natalia Trocóniz, Iñaki F. Fernández, Sarah N. Camacho Vicente, Verónica Padilla, Belén Slöcker, María Santiago, María José |
| author2_role |
author author author author author author author author |
| dc.subject.none.fl_str_mv |
PEDIATRICS TEICOPLANIN |
| topic |
PEDIATRICS TEICOPLANIN |
| purl_subject.fl_str_mv |
https://purl.org/becyt/ford/3.2 https://purl.org/becyt/ford/3 |
| dc.description.none.fl_txt_mv |
Objectives: Teicoplanin is a commonly used antibiotic in critically ill children. However, teicoplanin dosing is ofteninaccurate, especially in children undergoing continuous kidney replacement therapy (CKRT). This study aimsto develop a population pharmacokinetic (PK) model to optimize teicoplanin dosing in critically ill children, includingthose on CKRT.Methods: Data from 26 critically ill children (12 with CKRT) receiving the standard dosing regimen were analysed.In total, 172 teicoplanin concentration measurements from plasma, pre- and post-filter ports were modelled simultaneouslyusing NONMEM 7.4. Simulations were conducted to assess the target attainment (Cmin = 10 mg/L andAUC24/MIC > 800 h) of the current standard dosing regimen and of different alternative dosing regimens.Results: A two-compartment model was selected. Weight significantly affected renal clearance and volume ofdistribution of the central compartment, while filter surface area affected haemofilter clearance. Only 16 patients(59%) achieved a Cmin of >10 mg/L with the standard dosing regimen, and only 1 achieved the targetAUC/MIC. Based on simulation results, 3 × 15 mg/kg q12h + 10 mg/kg q24h (CKRT) and 3 × 15 mg/kg q12h +15 mg/kg q24h (no CKRT) could be better alternative regimens.Conclusions: This population model is a good proof of concept to develop modelling approaches that could helpin an individualized dosing approach that needs to be adopted in critically ill paediatric patients. The standardpaediatric dosage for teicoplanin could be insufficient for optimal exposure, and higher doses may benefit bothCKRT and non-CKRT patients. Fil: Butragueño Laiseca, Laura. Universidad de Navarra. Facultad de Farmacia y Nutricion.; España Fil: García Orueta, Gastón. Universidad de Navarra. Facultad de Farmacia y Nutricion.; España Fil: Riva, Natalia. Universidad de Navarra. Facultad de Farmacia y Nutricion.; España. Gobierno de la Ciudad de Buenos Aires. Hospital de Pediatría "Juan P. Garrahan"; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina Fil: Trocóniz, Iñaki F.. Universidad de Navarra. Facultad de Farmacia y Nutricion.; España Fil: Fernández, Sarah N.. Universidad de Navarra. Facultad de Farmacia y Nutricion.; España Fil: Camacho Vicente, Verónica. Universidad de Navarra. Facultad de Farmacia y Nutricion.; España Fil: Padilla, Belén. Universidad de Navarra. Facultad de Farmacia y Nutricion.; España Fil: Slöcker, María. Universidad de Navarra. Facultad de Farmacia y Nutricion.; España Fil: Santiago, María José. Universidad de Navarra. Facultad de Farmacia y Nutricion.; España |
| description |
Objectives: Teicoplanin is a commonly used antibiotic in critically ill children. However, teicoplanin dosing is ofteninaccurate, especially in children undergoing continuous kidney replacement therapy (CKRT). This study aimsto develop a population pharmacokinetic (PK) model to optimize teicoplanin dosing in critically ill children, includingthose on CKRT.Methods: Data from 26 critically ill children (12 with CKRT) receiving the standard dosing regimen were analysed.In total, 172 teicoplanin concentration measurements from plasma, pre- and post-filter ports were modelled simultaneouslyusing NONMEM 7.4. Simulations were conducted to assess the target attainment (Cmin = 10 mg/L andAUC24/MIC > 800 h) of the current standard dosing regimen and of different alternative dosing regimens.Results: A two-compartment model was selected. Weight significantly affected renal clearance and volume ofdistribution of the central compartment, while filter surface area affected haemofilter clearance. Only 16 patients(59%) achieved a Cmin of >10 mg/L with the standard dosing regimen, and only 1 achieved the targetAUC/MIC. Based on simulation results, 3 × 15 mg/kg q12h + 10 mg/kg q24h (CKRT) and 3 × 15 mg/kg q12h +15 mg/kg q24h (no CKRT) could be better alternative regimens.Conclusions: This population model is a good proof of concept to develop modelling approaches that could helpin an individualized dosing approach that needs to be adopted in critically ill paediatric patients. The standardpaediatric dosage for teicoplanin could be insufficient for optimal exposure, and higher doses may benefit bothCKRT and non-CKRT patients. |
| publishDate |
2025 |
| dc.date.none.fl_str_mv |
2025-03 |
| dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
| format |
article |
| status_str |
publishedVersion |
| dc.identifier.none.fl_str_mv |
http://hdl.handle.net/11336/266327 Butragueño Laiseca, Laura; García Orueta, Gastón; Riva, Natalia; Trocóniz, Iñaki F.; Fernández, Sarah N.; et al.; Population pharmacokinetic analysis of teicoplanin in paediatric patients, including those receiving continuous kidney replacement therapy: a prospective cohort study; Oxford University Press; Journal of Antimicrobial Chemotherapy; 80; 3; 3-2025; 868-875 0305-7453 CONICET Digital CONICET |
| url |
http://hdl.handle.net/11336/266327 |
| identifier_str_mv |
Butragueño Laiseca, Laura; García Orueta, Gastón; Riva, Natalia; Trocóniz, Iñaki F.; Fernández, Sarah N.; et al.; Population pharmacokinetic analysis of teicoplanin in paediatric patients, including those receiving continuous kidney replacement therapy: a prospective cohort study; Oxford University Press; Journal of Antimicrobial Chemotherapy; 80; 3; 3-2025; 868-875 0305-7453 CONICET Digital CONICET |
| dc.language.none.fl_str_mv |
eng |
| language |
eng |
| dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/url/https://academic.oup.com/jac/article/80/3/868/7974752 info:eu-repo/semantics/altIdentifier/doi/10.1093/jac/dkaf012 |
| dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
| eu_rights_str_mv |
openAccess |
| rights_invalid_str_mv |
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
| dc.format.none.fl_str_mv |
application/pdf application/pdf |
| dc.publisher.none.fl_str_mv |
Oxford University Press |
| publisher.none.fl_str_mv |
Oxford University Press |
| dc.source.none.fl_str_mv |
reponame:CONICET Digital (CONICET) instname:Consejo Nacional de Investigaciones Científicas y Técnicas |
| reponame_str |
CONICET Digital (CONICET) |
| collection |
CONICET Digital (CONICET) |
| instname_str |
Consejo Nacional de Investigaciones Científicas y Técnicas |
| repository.name.fl_str_mv |
CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas |
| repository.mail.fl_str_mv |
dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar |
| _version_ |
1874774366082826240 |
| score |
13.364332 |