Azathioprine in paediatric inflammatory bowel disease: an Italian multicentre survey

被引:37
作者
Barabino, A
Torrente, F
Ventura, A
Cucchiara, S
Castro, M
Barbera, C
机构
[1] IRCCS G Gaslini, Genoa, Italy
[2] Royal Free Hosp, London NW3 2QG, England
[3] Univ Trieste, IRCCS Burlo Garofolo, Trieste, Italy
[4] Univ Roma La Sapienza, Rome, Italy
[5] IRCCS Bambino Gesu, Rome, Italy
[6] Univ Turin, Turin, Italy
关键词
D O I
10.1046/j.1365-2036.2002.01269.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Aim: To assess the efficacy and safety of azathioprine in a paediatric population with inflammatory bowel disease. Patients and methods: One hundred and twenty-three Italian children treated with azathioprine were studied retrospectively. The treatment duration and causes of its discontinuation, side-effects and variation in corticosteroid dose were assessed. Results: The mean age at inflammatory bowel disease diagnosis was 9.8 +/- 3.6 years, and at the start of azathioprine therapy 11.8 +/- 4.3 years. The mean duration of treatment was 19 +/- 16 months. Fifty patients (41%) stopped treatment due to surgery (12%), prolonged remission (11%), non-response (7%), severe side-effects (7%) and poor compliance (3%). Of the 73 patients (59%) remaining on azathioprine, 11 had never been treated with corticosteroids, 27 were able to stop them and 35 were still on a very low daily dose (91% < 0.3 mg/kg). The difference in the daily corticosteroid dose between the beginning of azathioprine treatment (1 +/- 0.6 mg/kg) and the conclusion of the study (0.18 +/- 0.16 mg/kg) was statistically significant. Side-effects were recorded in 48 of the 123 patients (39%), but only eight required discontinuation of azathioprine. Conclusions: Azathioprine was efficacious in 70% of patients, but ineffective in 20% and induced severe toxicity in 7%. Corticosteroids were stopped or markedly reduced in 62% of patients, but they were never given in 9%.
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页码:1125 / 1130
页数:6
相关论文
共 26 条
[1]   Long-term follow-up of patients with Crohn's disease treated with azathioprine or 6-mercaptopurine [J].
Bouhnik, Y ;
Lemann, M ;
Mary, JY ;
Scemama, G ;
Tai, R ;
Matuchansky, C ;
Modigliani, R ;
Rambaud, JC .
LANCET, 1996, 347 (8996) :215-219
[2]  
COLONNA T, 1994, AM J GASTROENTEROL, V89, P362
[3]   LONG-TERM NEOPLASIA RISK AFTER AZATHIOPRINE TREATMENT IN INFLAMMATORY BOWEL-DISEASE [J].
CONNELL, WR ;
KAMM, MA ;
DICKSON, M ;
BALKWILL, AM ;
RITCHIE, JK ;
LENNARDJONES, JE .
LANCET, 1994, 343 (8908) :1249-1252
[4]   BONE-MARROW TOXICITY CAUSED BY AZATHIOPRINE IN INFLAMMATORY BOWEL-DISEASE - 27 YEARS OF EXPERIENCE [J].
CONNELL, WR ;
KAMM, MA ;
RITCHIE, JK ;
LENNARDJONES, JE .
GUT, 1993, 34 (08) :1081-1085
[5]   Utilisation of erythrocyte 6-thioguanine metabolite levels to optimise azathioprine therapy in patients with inflammatory bowel disease [J].
Cuffari, C ;
Hunt, S ;
Bayless, T .
GUT, 2001, 48 (05) :642-646
[6]   6-Mercaptopurine metabolism in Crohn's disease: Correlation with efficacy and toxicity [J].
Cuffari, C ;
Theoret, Y ;
Latour, S ;
Seidman, G .
GUT, 1996, 39 (03) :401-406
[7]   Pharmacogenomics and metabolite measurement for 6-mercaptopurine therapy in inflammatory bowel disease [J].
Dubinsky, MC ;
Lamothe, S ;
Yang, HY ;
Targan, SR ;
Sinnett, D ;
Théorêt, Y ;
Seidman, EG .
GASTROENTEROLOGY, 2000, 118 (04) :705-713
[8]   AZATHIOPRINE COMBINED WITH PREDNISOLONE OR MONOTHERAPY WITH PREDNISOLONE IN ACTIVE CROHNS-DISEASE [J].
EWE, K ;
PRESS, AG ;
SINGE, CC ;
STUFLER, M ;
UEBERSCHAER, B ;
HOMMEL, G ;
ZUMBUSCHENFELDE, KHM .
GASTROENTEROLOGY, 1993, 105 (02) :367-372
[9]  
GREENSTEIN AJ, 1992, CANCER-AM CANCER SOC, V69, P1119
[10]  
GREENSTEIN AJ, 1985, CANCER, V56, P2914, DOI 10.1002/1097-0142(19851215)56:12<2914::AID-CNCR2820561232>3.0.CO