Orally administered ranitidine plasma concentrations before and after biliopancreatic diversion in morbidly obese patients

被引:8
作者
Cossu, ML [1 ]
Caccia, S [1 ]
Coppola, M [1 ]
Fais, E [1 ]
Ruggiu, M [1 ]
Fracasso, C [1 ]
Nacca, A [1 ]
Noya, G [1 ]
机构
[1] Univ Sassari, Clin Chirurg Gen, Cattedra Chirurg Urgenza, I-07100 Sassari, Italy
关键词
morbid obesity; biliopancreatic diversion; ranitidine plasma concentrations;
D O I
10.1381/096089299765553728
中图分类号
R61 [外科手术学];
学科分类号
摘要
Background: Patients undergoing biliopancreatic diversion (BPD) may develop gastric ulcers, particularly within the first postoperative year. The prophylactic use of antisecretory compounds at the usual therapeutic doses, mainly conventional H-2-receptor antagonists such as ranitidine, may reduce the incidence of this complication, which occurs in similar to 5% of patients after BPD. Methods: The authors measured the plasma concentrations of ranitidine (300 mg orally) in obese patients, before and 8 months after BPD, and in control subjects of normal weight. The study included 11 obese patients undergoing BPD (age 45 +/- 14 years; preoperative and postoperative weights 124 +/- 21 and 92 +/- 11 kg) and 10 normal-weight subjects (age 37 +/- 13 years, weight 67 +/- 9 kg). Results: Postoperative ranitidine plasma concentrations showed only minor differences from preoperative levels, with slightly higher maximum concentrations occurring sooner. The mean area under the curve was on the average 30% higher than preoperatively. All parameters, however, were similar to those in control subjects. Conclusions: BPD per se does not greatly affect the pharmacokinetic behavior of ranitidine, and therefore a conventional dosage regimen appears adequate for the prophylaxis and therapy of gastric ulcers associated with this operation.
引用
收藏
页码:36 / 39
页数:4
相关论文
共 11 条
[1]  
Adami, 1991, Obes Surg, V1, P293
[2]   RANITIDINE KINETICS IN NORMAL SUBJECTS [J].
CHAU, NP ;
ZECH, PY ;
POZET, N ;
HADJAISSA, A .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 1982, 31 (06) :770-774
[3]  
COSSU ML, 1996, INT J OBESITY, V20, P133
[4]   PHARMACOKINETICS OF RANITIDINE IN MORBIDLY OBESE WOMEN [J].
DAVIS, RL ;
QUENZER, RW ;
BOZIGIAN, HP ;
WARNER, CW .
DICP-THE ANNALS OF PHARMACOTHERAPY, 1990, 24 (11) :1040-1043
[5]   SITE-DEPENDENT SMALL-INTESTINAL ABSORPTION OF RANITIDINE [J].
GRAMATTE, T ;
ELDESOKY, E ;
KLOTZ, U .
EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY, 1994, 46 (03) :253-259
[6]   DETERMINATION OF RANITIDINE IN RAT PLASMA AND BRAIN BY HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY [J].
GUISO, G ;
FRACASSO, C ;
CACCIA, S ;
ABBIATI, A .
JOURNAL OF CHROMATOGRAPHY-BIOMEDICAL APPLICATIONS, 1987, 413 :363-369
[7]   Pharmacokinetic optimisation in the treatment of gastro-oesophageal reflux disease [J].
Hatlebakk, JG ;
Berstad, A .
CLINICAL PHARMACOKINETICS, 1996, 31 (05) :386-406
[8]   Biliopancreatic diversion for treatment of morbid obesity: Experience in 50 cases [J].
Noya, G ;
Cossu, ML ;
Coppola, M ;
Tonolo, G ;
Angius, MF ;
Fais, E ;
Ruggiu, M .
OBESITY SURGERY, 1998, 8 (01) :61-66
[9]  
PEDEN NR, 1979, LANCET, V2, P199
[10]   Biliopancreatic obesity eighteen years [J].
Scopinaro, N ;
Gianetta, E ;
Adami, GF ;
Friedman, D ;
Traverse, E ;
Marinari, GM ;
Cuneo, S ;
Vitale, B ;
Ballari, F ;
Colombini, M ;
Baschieri, G ;
Bachi, V .
SURGERY, 1996, 119 (03) :261-268