ORAL BUDESONIDE FOR ACTIVE CROHNS-DISEASE

被引:473
作者
GREENBERG, GR
FEAGAN, BG
MARTIN, F
SUTHERLAND, LR
THOMSON, ABR
WILLIAMS, CR
NILSSON, LG
PERSSON, T
BAIN, V
CHERRY, R
FEDORAK, R
LALOR, E
SHERBANIUK, R
YACYSHYN, B
KIERDEKIS, P
BAILEY, R
MEYER, D
FREEMAN, H
DAWS, P
HOLLAND, S
BUYTENDORP, M
WHITTAKER, S
CHANG, A
SUTHERLAND, L
HERSHFIELD, N
MACCANNELL, K
MEDDING, J
PRICE, L
SHAFFER, E
RACICOT, N
BASS, S
BRIDGES, R
BLUSTEIN, P
LAY, T
VANROSENDAAL, G
WATSON, M
WILLIAMS, CN
VANZANTEN, V
LEDDIN, D
FALKENHAM, J
TANTON, R
HUMAN, P
TURNBALL, G
SCHEP, G
WOOLNOUGH, J
DALLAIRE, C
ROSSEAU, B
BERNARD, F
DUBE, R
PARE, P
机构
[1] UNIV TORONTO,DEPT MED,TORONTO,ON,CANADA
[2] UNIV WESTERN ONTARIO,DEPT MED,LONDON,ON,CANADA
[3] UNIV WESTERN ONTARIO,DEPT EPIDEMIOL & BIOSTAT,LONDON,ON,CANADA
[4] UNIV MONTREAL,DEPT MED,MONTREAL H3C 3J7,PQ,CANADA
[5] UNIV CALGARY,DEPT MED,CALGARY,AB,CANADA
[6] UNIV ALBERTA,DEPT MED,EDMONTON,AB,CANADA
[7] DALHOUSIE UNIV,DEPT MED,HALIFAX,NS,CANADA
[8] ASTRO DRACO AB,DEPT CLIN RES & DEV,LUND,SWEDEN
[9] ASTRO DRACO AB,DEPT BIOSTAT & DATA PROC,LUND,SWEDEN
[10] UNIV ALBERTA HOSP,EDMONTON,AB,CANADA
[11] ROYAL ALEXANDRA HOSP,EDMONTON,AB,CANADA
[12] UNIV BRITISH COLUMBIA HOSP,VANCOUVER,BC,CANADA
[13] VICTORIA GEN HOSP,HALIFAX,NS,CANADA
[14] ST PAULS HOSP,VANCOUVER,BC,CANADA
[15] FOOTHILLS PROV GEN HOSP,CALGARY,AB,CANADA
[16] CALGARY GEN HOSP,CALGARY,AB,CANADA
[17] HALIFAX INFIRM,HALIFAX,NS,CANADA
[18] CAMP HILL HOSP,HALIFAX,NS,CANADA
[19] UNIV LAVAL,QUEBEC CITY,PQ,CANADA
[20] HOP ST FRANCOIS ASSISE,QUEBEC CITY,PQ,CANADA
[21] HOP HOTEL DIEU,QUEBEC CITY,PQ,CANADA
[22] MCGILL UNIV,JEWISH GEN HOSP,MONTREAL,PQ,CANADA
[23] MONTREAL GEN HOSP,MONTREAL,PQ,CANADA
[24] ROYAL VICTORIA HOSP,MONTREAL,PQ,CANADA
[25] MCMASTER UNIV,HLTH SCI CTR,HAMILTON,ON,CANADA
[26] UNIV MANITOBA,WINNIPEG,MB,CANADA
[27] ST BONIFACE GEN HOSP,WINNIPEG,MB,CANADA
[28] UNIV MONTREAL,HOP MAISON NEUVE ROSEMONT,MONTREAL,PQ,CANADA
[29] HOP ST LUC,MONTREAL,PQ,CANADA
[30] CARLETON UNIV,OTTAWA CIVIC HOSP,OTTAWA,ON,CANADA
[31] UNIV SASKATCHEWAN,ROYAL UNIV HOSP,SASKATOON,SK,CANADA
[32] PASQUA HOSP,REGINA,SK,CANADA
[33] UNIV TORONTO,MT SINAI HOSP,TORONTO M5G 1X5,ON,CANADA
[34] ST MICHAELS HOSP,TORONTO,ON,CANADA
[35] SUNNYBROOK MED CTR,TORONTO,ON,CANADA
[36] TORONTO GEN HOSP,TORONTO,ON,CANADA
[37] WOMENS COLL HOSP,TORONTO,ON,CANADA
[38] UNIV WESTERN ONTARIO HOSP,LONDON,ON,CANADA
[39] ST JOSEPHS HOSP,HAMILTON,ON,CANADA
[40] UNIV BRITISH COLUMBIA,VICTORIA GEN HOSP,VICTORIA,BC,CANADA
[41] HALIFAX INFIRM,HALIFAX,NS,CANADA
[42] ASTRA PHARMA CANADA,TORONTO,ON,CANADA
关键词
D O I
10.1056/NEJM199409293311303
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background. Corticosteroids are the most efficacious drugs for inducing remission in active Crohn's disease, but their benefits are frequently offset by serious side effects. Budesonide is a corticosteroid with high topical antiinflammatory activity but low systemic activity because of extensive hepatic metabolism. We investigated the efficacy and safety of an oral controlled-ileal-release preparation of budesonide in patients with active Crohn's disease involving the ileum or ileum and proximal colon. Methods. In a double-blind, multicenter trial, 258 patients were randomly assigned to receive placebo or one of three doses of budesonide - 3, 9, or 15 mg daily. The primary outcome measure was clinical remission, as defined by a score of 150 or less on the Crohn's disease activity index. Results. After eight weeks of treatment, remission occurred in 51 percent of the patients in the group receiving 9 mg of budesonide (95 percent confidence interval, 39 to 63 percent), 43 percent of those receiving 15 mg (95 percent confidence interval, 31 to 55 percent), and 33 percent of those receiving 3 mg (95 percent confidence interval, 21 to 44 percent), as compared with 20 percent of those receiving placebo (P < 0.001, P = 0.009, and P = 0.13, respectively). Improvements in the quality of life, as measured by the patients' responses to the inflammatory bower disease questionnaire, parallelled these remission rates. Location of disease, prior surgical resection, and previous use of corticosteroids did not affect the outcome. A total of 119 patients (46 percent) were withdrawn from the study before the trial ended, 96 because of insufficient therapeutic effects, 13 because of adverse reactions, and 10 because of noncompliance. Budesonide caused a dose-related reduction in basal and corticotropin-stimulated plasma cortisol concentrations but was not associated with clinically important corticosteroid-related symptoms or other toxic effects. Conclusions. In an eight-week trial, an oral controlled-release preparation of budesonide at an optimal daily dose of 9 mg was well tolerated and effective against active Crohn's disease of the ileum and proximal colon.
引用
收藏
页码:836 / 841
页数:6
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