Switch from systemic steroids to budesonide in steroid dependent patients with inactive Crohn's disease

被引:82
作者
Cortot, A [1 ]
Colombel, JF
Rutgeerts, P
Lauritsen, K
Malchow, H
Hämling, J
Winter, T
Van Gossum, A
Persson, T
Pettersson, E
机构
[1] Hop Claude Huriez, Gastroenterol Serv, F-59037 Lille, France
[2] Katholieke Univ Leuven Hosp, Dept Gastroenterol, Louvain, Belgium
[3] Odense Univ Hosp, Dept Med Gastroenterol, DK-5000 Odense, Denmark
[4] Stadt Krankenhaus Leverkusen, Med Klin 2, Leverkusen, Germany
[5] Krankenhaus Tabea, Hamburg, Germany
[6] Groote Schuur Hosp, Dept Gastroenterol, ZA-7925 Cape Town, South Africa
[7] Hop Erasme, Gastroenterol Serv, Brussels, Belgium
[8] AstraZeneca R&D, Clin Res & Dev, Lund, Sweden
关键词
budesonide; Crohn's disease; steroid dependent; prednisolone;
D O I
10.1136/gut.48.2.186
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background-Steroid dependent patients with Crohn's disease are at high risk of developing glucocorticosteroid induced side effects. Aims-We switching budesonide ((Entocort) in prednisolone/prednisone dependent patients with inactive Crohn's disease affecting the ileum and/or ascending colon. Patients-Steroid dependent patients with a Crohn's disease activity index less than or equal to 200 were included. Methods-In a double blind multicentre trial, 120 patients were randomly assigned to receive budesonide 6 mg once daily or placebo. Prednisolone was tapered to zero during the first 4-10 weeks and budesonide or placebo was given concomitantly and for a further 12 weeks. Relapse was defined as an index >200 and an increase of 60 points from baseline or withdrawal due to disease deterioration. Results-After one and 13 weeks without prednisolone, relapse rates were 17% and 32%, respectively, in the budesonide group, and 41% and 65% in the placebo group (95% confidence intervals for the difference in percentages -41%, -8% and -51%, -16%; p=0.004 and p<0.001, respectively). The number of glucocorticosteroid side effects was reduced by 50% by switching from prednisolone and was similar in the budesonide and placebo groups. Basal plasma cortisol increased in both groups. Conclusions-The majority of patients with steroid dependent ileocaecal Crohn's disease may be switched to budesonide controlled ileal release capsules 6 rug without relapse, resulting in a sharp decrease in glucocorticosteroid side effects similar to placebo, and with an increase in plasma cortisol levels.
引用
收藏
页码:186 / 190
页数:5
相关论文
共 20 条
  • [1] BEST WR, 1976, GASTROENTEROLOGY, V70, P439
  • [2] Brattsand R., 1990, Can J Gastroenterol, V4, P407
  • [3] Oral budesonide is as effective as oral prednisolone in active Crohn's disease
    Campieri, M
    Ferguson, A
    Doe, W
    Persson, T
    Nilsson, LG
    Malchow, H
    Prantera, C
    Mani, V
    OMorain, C
    Selby, W
    Pallone, F
    diPietralata, MM
    Sjodahl, R
    Florin, T
    Smith, P
    Bianchi, P
    Lofberg, R
    Rutgeerts, P
    Smallwood, R
    Lamers, HW
    TasmanJones, C
    Hunter, JO
    Hodgson, H
    Danielsson, A
    Lee, FI
    Piacitelli, G
    Giovanni, S
    Ellis, A
    Weir, DG
    [J]. GUT, 1997, 41 (02) : 209 - 214
  • [4] Colombel JF, 1999, GASTROENTEROLOGY, V116, pA689
  • [5] Feagan B, 1997, GASTROENTEROLOGY, V112, pA970
  • [6] METHOTREXATE FOR THE TREATMENT OF CROHNS-DISEASE
    FEAGAN, BG
    ROCHON, J
    FEDORAK, RN
    IRVINE, EJ
    WILD, G
    SUTHERLAND, L
    STEINHART, AH
    GREENBERG, GR
    GILLIES, R
    HOPKINS, M
    HANAUER, SB
    MCDONALD, JWD
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1995, 332 (05) : 292 - 297
  • [7] Oral budesonide as maintenance treatment for Crohn's disease: A placebo-controlled, dose-ranging study
    Greenberg, GR
    Feagan, BG
    Martin, F
    Sutherland, LR
    Thomson, ABR
    Williams, N
    Nilsson, LG
    Persson, T
    [J]. GASTROENTEROLOGY, 1996, 110 (01) : 45 - 51
  • [8] ORAL BUDESONIDE FOR ACTIVE CROHNS-DISEASE
    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
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1994, 331 (13) : 836 - 841
  • [9] Gross V, 1997, GASTROENTEROLOGY, V112, pA987
  • [10] A NEW MEASURE OF HEALTH-STATUS FOR CLINICAL-TRIALS IN INFLAMMATORY BOWEL-DISEASE
    GUYATT, G
    MITCHELL, A
    IRVINE, EJ
    SINGER, J
    WILLIAMS, N
    GOODACRE, R
    TOMPKINS, C
    [J]. GASTROENTEROLOGY, 1989, 96 (03) : 804 - 810