Lansoprazole in children: pharmacokinetics and efficacy in reflux oesophagitis

被引:38
作者
Faure, C
Michaud, L
Shaghaghi, EK
Popon, M
Laurence, M
Mougenot, JF
Hankard, R
Navarro, J
Jacqz-Aigrain, E
机构
[1] Hop Robert Debre, Serv Gastroenterol Pediat, F-75019 Paris, France
[2] Hop Jeanne de Flandre, Pediat Clin, Unite Gastroenterol Hepatol & Nutr, Lille, France
[3] Hop Robert Debre, Lab Pharmacol Pediat & Pharmacogenet, F-75019 Paris, France
[4] Hop Robert Debre, Ctr Invest Clin, F-75019 Paris, France
关键词
D O I
10.1046/j.1365-2036.2001.01076.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: Data on the proton pump inhibitor lansoprazole in paediatric patients are limited. Aim: To investigate the pharmacokinetics, optimal dosage and efficacy of lansoprazole in paediatric patients. Methods: A 24-h gastric pH recording and a pharmacokinetic study were performed after 7 days of lansoprazole, 17 mg/m(2) in 23 patients with reflux oesophagitis (median age, 3.5 years). Response was defined as pH > 3 for > 65% of the recording. The dosage was doubled in non-responders. Patients with no response on day 14 were excluded. Responders underwent endoscopy after 4 weeks on the response-inducing dosage; abnormal findings led to a repeat endoscopy after four additional weeks. Results: Nine patients responded to 17 mg/m(2) and six to 30.3 mg/m(2). On day 7, time with pH > 3 was significantly correlated with the area under the plasma concentration-time curve (P = 0.003). The area under the plasma concentration-time curve was significantly greater in the nine responders to 17 mg/m(2) than in the 14 other patients. Pharmacokinetic parameters were similar in responders and non-responders to the higher dose. After 4 weeks, oesophagitis was healed in 80% of responders. Adverse events occurred in three patients and required treatment discontinuation in one. Conclusions: Lansoprazole is effective and safe in children. The optimal starting dosage is 30 mg/m(2) or 1.4 mg/kg.
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页码:1397 / 1402
页数:6
相关论文
共 18 条
[1]  
Andersson T, 2000, AM J GASTROENTEROL, V95, P3101
[2]   LANSOPRAZOLE - A REVIEW OF ITS PHARMACODYNAMIC AND PHARMACOKINETIC PROPERTIES AND ITS THERAPEUTIC EFFICACY IN ACID-RELATED DISORDERS [J].
BARRADELL, LB ;
FAULDS, D ;
MCTAVISH, D .
DRUGS, 1992, 44 (02) :225-250
[3]  
DESVARANNES SB, 1994, ALIMENT PHARM THERAP, V8, P309
[4]   Pharmacokinetics and absolute bioavailability of lansoprazole [J].
Gerloff, J ;
Mignot, A ;
Barth, H ;
Heintze, K .
EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY, 1996, 50 (04) :293-297
[5]  
Gremse D., 2000, JPGN, V31, pS39
[6]  
Gunasekaran T., 2000, JPGN, V31, pS97
[7]  
Gupta S. K., 2000, JPGN, V31, pS97
[8]   Omeprazole for treatment of chronic erosive esophagitis in children:: A multicenter study of efficacy, safety, tolerability and dose requirements [J].
Hassall, E ;
Israel, D ;
Shepherd, R ;
Radke, M ;
Dalväg, A ;
Sköld, B ;
Junghard, O ;
Lundborg, P .
JOURNAL OF PEDIATRICS, 2000, 137 (06) :800-807
[9]   LANSOPRAZOLE, A NOVEL BENZIMIDAZOLE PROTON PUMP INHIBITOR, AND ITS RELATED-COMPOUNDS HAVE SELECTIVE ACTIVITY AGAINST HELICOBACTER-PYLORI [J].
IWAHI, T ;
SATOH, H ;
NAKAO, M ;
IWASAKI, T ;
YAMAZAKI, T ;
KUBO, K ;
TAMURA, T ;
IMADA, A .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1991, 35 (03) :490-496
[10]   DETERMINATION OF LANSOPRAZOLE AND 5 METABOLITES IN PLASMA BY HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY [J].
KAROL, MD ;
GRANNEMAN, GR ;
ALEXANDER, K .
JOURNAL OF CHROMATOGRAPHY B-BIOMEDICAL APPLICATIONS, 1995, 668 (01) :182-186