Pharmacotherapeutical options in inflammatory bowel disease: an update

被引:32
作者
Kho, YH [1 ]
Pool, MO
Jansman, FGA
Harting, JW
机构
[1] Isala Klin, Dept Internal Med, Zwolle, Netherlands
[2] Isala Klin, Dept Clin Pharm, Zwolle, Netherlands
来源
PHARMACY WORLD & SCIENCE | 2001年 / 23卷 / 01期
关键词
Crohn's disease; inflammatory bowel disease; medical treatment; ulcerative colitis;
D O I
10.1023/A:1011268302386
中图分类号
R9 [药学];
学科分类号
1007 [药学];
摘要
Chronic inflamatory bowel disease (IBD) refers to two diseases: Crohn's disease (CD) and ulcerative colitis (UC). The etiology of IBD remains unknown. The understanding of the pathogenesis has expanded greatly over the last decade. The combination of genetic risk factors, abnormalities in the immune system, vascular and neural factors, and random environmental factors may all play an important role. Most treatments currently in use have multiple action. The choice of appropriate medical treatment is determined by the status (inductive or maintenance therapy) and severity of the disease and the potential for toxicity. Despite the variety of medical therapies available for the treatment of IBD, none is ideal. Ongoing research into the well-established drugs, as well as novel agents with more precise targets, may contribute to an optimal therapy of IBD in the near future. In this paper the current (5-aminosalicylates, glucocorticosteroids, thioguanine derivatives, methotrexate, cyclosporin and infliximab) as well as some of the new (mycophenolate mofetil and thalidomide) therapeutic options are reviewed.
引用
收藏
页码:17 / 21
页数:5
相关论文
共 43 条
[1]
NON-STEROIDAL ANTI-INFLAMMATORY DRUG-INDUCED DISEASE IN THE DISTAL ILEUM AND LARGE BOWEL [J].
AABAKKEN, L ;
OSNES, M .
SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY, 1989, 24 :48-55
[2]
The pill: safe sex and Crohn's disease? [J].
Alstead, EM .
GUT, 1999, 45 (02) :165-166
[3]
Andus T, 2000, HEPATO-GASTROENTEROL, V47, P29
[4]
Inflammatory bowel disease approaching the 3rd millennium: pathogenesis and therapeutic implications? [J].
Ardizzone, S ;
Bollani, S ;
Manzionna, G ;
Porro, GB .
EUROPEAN JOURNAL OF GASTROENTEROLOGY & HEPATOLOGY, 1999, 11 (01) :27-32
[5]
Antibodies to tumour necrosis factor α as treatment for Crohn's disease [J].
Bell, S ;
Kamm, MA .
LANCET, 2000, 355 (9207) :858-860
[6]
Bjorkman David, 1998, American Journal of Medicine, V105, p17S, DOI 10.1016/S0002-9343(98)00276-9
[7]
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
[8]
A PLACEBO-CONTROLLED, DOUBLE-BLIND, RANDOMIZED TRIAL OF CYCLOSPORINE THERAPY IN ACTIVE CHRONIC CROHNS-DISEASE [J].
BRYNSKOV, J ;
FREUND, L ;
RASMUSSEN, SN ;
LAURITSEN, K ;
DEMUCKADELL, OS ;
WILLIAMS, N ;
MACDONALD, AS ;
TANTON, R ;
MOLINA, F ;
CAMPANINI, MC ;
BIANCHI, P ;
RANZI, T ;
DIPALO, FQ ;
MALCHOWMOLLER, A ;
THOMSEN, OO ;
TAGEJENSEN, U ;
BINDER, V ;
RIIS, P .
NEW ENGLAND JOURNAL OF MEDICINE, 1989, 321 (13) :845-850
[9]
A CONTROLLED DOUBLE-BLIND-STUDY OF AZATHIOPRINE IN THE MANAGEMENT OF CROHNS-DISEASE [J].
CANDY, S ;
WRIGHT, J ;
GERBER, M ;
ADAMS, G ;
GERIG, M ;
GOODMAN, R .
GUT, 1995, 37 (05) :674-678
[10]
Crohn's disease severity in familial and sporadic cases [J].
Carbonnel, F ;
Macaigne, G ;
Beaugerie, L ;
Gendre, JP ;
Cosnes, J .
GUT, 1999, 44 (01) :91-95