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Lean body weight dosing avoids excessive systemic exposure to proton pump inhibitors for children with obesity.
Shakhnovich, V; Abdel-Rahman, S; Friesen, C A; Weigel, J; Pearce, R E; Gaedigk, A; Leeder, J S; Kearns, G L.
Afiliação
  • Shakhnovich V; Department of Pediatrics, University of Missouri Kansas City School of Medicine, Kansas City, MO, USA.
  • Abdel-Rahman S; Division of Clinical Pharmacology, Toxicology and Therapeutic Innovation, The Childrens Mercy Hospital, Kansas City, MO, USA.
  • Friesen CA; Division of Gastroenterology, Hepatology and Nutrition, The Childrens Mercy Hospital, Kansas City, MO, USA.
  • Weigel J; Department of Pediatrics, University of Missouri Kansas City School of Medicine, Kansas City, MO, USA.
  • Pearce RE; Division of Clinical Pharmacology, Toxicology and Therapeutic Innovation, The Childrens Mercy Hospital, Kansas City, MO, USA.
  • Gaedigk A; Department of Pediatrics, University of Missouri Kansas City School of Medicine, Kansas City, MO, USA.
  • Leeder JS; Division of Gastroenterology, Hepatology and Nutrition, The Childrens Mercy Hospital, Kansas City, MO, USA.
  • Kearns GL; Department of Pediatrics, University of Missouri Kansas City School of Medicine, Kansas City, MO, USA.
Pediatr Obes ; 14(1)2019 01.
Article em En | MEDLINE | ID: mdl-30257076
ABSTRACT

BACKGROUND:

Children with obesity are more likely to suffer gastroesophageal reflux disease, requiring acid-suppression therapy with proton pump inhibitors (PPIs) and no guidelines regarding dosing.

OBJECTIVE:

To prospectively evaluate lean-body-weight-based (LBW) dosing of the PPI pantoprazole for children with and without obesity.

METHODS:

Methods:

Sixty-two children (6-17 years) received a one-time oral dose of liquid pantoprazole (1.2 mg kg-1 LBW). Plasma pantoprazole concentrations were measured at 10 time points over 8 h and pharmacokinetic (PK) profiles generated using non-compartmental techniques, in order to compare PK parameters of interest between children with and without obesity, while accounting for CYP2C19 genotype.

RESULTS:

Adjusted for milligram-per-kilogram total body weight (TBW) pantoprazole received, apparent drug clearance (CL/F) was reduced 50% in children with vs. without obesity (p=0.03). LBW-based dosing compensated for this reduction in CL/F (p = 0.15).

CONCLUSION:

To achieve comparable systemic PPI exposures for children with and without obesity, we recommend using LBW, rather than TBW-based dosing for pantoprazole.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Peso Corporal / Refluxo Gastroesofágico / Inibidores da Bomba de Prótons / Obesidade Infantil / Pantoprazol Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Peso Corporal / Refluxo Gastroesofágico / Inibidores da Bomba de Prótons / Obesidade Infantil / Pantoprazol Idioma: En Ano de publicação: 2019 Tipo de documento: Article