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Population Pharmacokinetics of Doxycycline in Children.
Thompson, Elizabeth J; Wu, Huali; Melloni, Chiara; Balevic, Stephen; Sullivan, Janice E; Laughon, Matthew; Clark, Kira M; Kalra, Rohit; Mendley, Susan; Payne, Elizabeth H; Erinjeri, Jinson; Gelber, Casey E; Harper, Barrie; Cohen-Wolkowiez, Michael; Hornik, Christoph P.
Afiliación
  • Thompson EJ; Department of Pediatrics, Duke University Medical Center, Durham, NC, USA.
  • Wu H; Duke Clinical Research Institute, Durham, NC, USA.
  • Melloni C; Duke Clinical Research Institute, Durham, NC, USA.
  • Balevic S; Department of Pediatrics, Duke University Medical Center, Durham, NC, USA.
  • Sullivan JE; Duke Clinical Research Institute, Durham, NC, USA.
  • Laughon M; University of Louisville, Norton Children's Hospital, Louisville, KY, USA.
  • Clark KM; University of North Carolina, Chapel Hill, NC, USA.
  • Kalra R; Department of Pediatrics, Oregon Health & Science University, Portland, OR, USA.
  • Mendley S; Ann & Robert H. Lurie Children's Hospital, Chicago, IL, USA.
  • Payne EH; University of Maryland School of Medicine, Baltimore, MD, USA.
  • Erinjeri J; The Emmes Company, LLC, Rockville, MD, USA.
  • Gelber CE; The Emmes Company, LLC, Rockville, MD, USA.
  • Harper B; The Emmes Company, LLC, Rockville, MD, USA.
  • Cohen-Wolkowiez M; Duke Clinical Research Institute, Durham, NC, USA.
  • Hornik CP; Department of Pediatrics, Duke University Medical Center, Durham, NC, USA.
Antimicrob Agents Chemother ; 63(12)2019 09 09.
Article en En | MEDLINE | ID: mdl-31548185
Doxycycline is a tetracycline-class antimicrobial labeled by the United States (U.S.) Food and Drug Administration for children >8 years of age for many common childhood infections. Doxycycline is not labeled for children ≤8 years of age, due to the association between tetracycline class antibiotics and tooth staining, although doxycycline may be used off-label in severe conditions. Accordingly, there is a paucity of pharmacokinetic (PK) data to guide dosing in children 8 years and younger. We leveraged opportunistically-collected plasma samples after intravenous (IV) and oral doxycycline doses received per standard of care to characterize the PK of doxycycline in children of different ages, and evaluated the effect of obesity and fasting status on PK parameters.We developed a population PK model of doxycycline using data collected from 47 patients 0-18 years of age, including 14 participants ≤8 years. We developed a 1 compartment PK model and found doxycycline clearance to be 3.32 L/h/70 kg and volume to be 96.8 L/70kg for all patients; comparable to values reported in adults. We estimated a bioavailability of 89.6%, also consistent with adult data. Allometrically scaled clearance and volume of distribution did not differ between children 2 to ≤8 years of age and children >8 to ≤18 years of age, suggesting that younger children may be given the same per kg dosing. Obese and fasting status were not selected for inclusion in the final model. Additional doxycycline PK samples collected in future studies may be used to improve model performance and maximize its clinical value.

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Antimicrob Agents Chemother Año: 2019 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Antimicrob Agents Chemother Año: 2019 Tipo del documento: Article País de afiliación: Estados Unidos
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