Premedication and infusion reactions with infliximab: Results from a pediatric inflammatory bowel disease consortium

被引:78
作者
Jacobstein, DA
Markowitz, JE
Kirschner, BS
Ferry, G
Cohen, SA
Gold, BD
Winter, HS
Heyman, MB
Baldassano, RN
机构
[1] Childrens Hosp Philadelphia, Div Pediat Gastroenterol & Nutr, Philadelphia, PA 19104 USA
[2] Univ Chicago, Childrens Hosp, Sect Pediat Gastroenterol Hepatol & Nutr, Chicago, IL 60637 USA
[3] Texas Childrens Hosp, Baylor Coll Med, Div Pediat Gastroenterol & Nutr, Houston, TX 77030 USA
[4] Childrens Healthcare Atlanta, Childrens Ctr Digest Hlth Care, Atlanta, GA USA
[5] Emory Univ, Sch Med, Div Pediat Gastroenterol & Nutr, Atlanta, GA 30322 USA
[6] Massachusetts Gen Hosp Children, Pediat Gastroenterol Unit, Boston, MA USA
[7] Univ Calif San Francisco, Childrens Hosp, Div Pediat Gastroenterol Hepatol & Nutr, San Francisco, CA 94143 USA
关键词
Crohn's disease; inflammatory bowel disease; infliximab; infusion reactions;
D O I
10.1097/01.MIB.0000158166.88238.ea
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: Infusion reactions (IRs) are the most common adverse events associated with the use of infliximab for inflammatory bowel disease (IBD). Antipyretics, antihistamines, and corticosteroids have been used to prevent the development of IRs, but their efficacy is not known. We studied the proportion of pediatric patients receiving infliximab for IBD that developed IRs and the potential effects of premedication on IR. Methods: Uniformly collected data from a cohort of pediatric patients with IBD) enrolled between January 2000 and May 2003 at 6 pediatric centers were analyzed. Data were retrospectively reviewed and analyzed. Results: A total of 1652 infusions given to 243 patients in 6 centers was analyzed. Overall, 60 IRs were recorded in 40 patients (3.6%0 of infusions, 16.5% of patients). Thirty-three of 243 patients received premedication before the first IR (group 1). Two hundred ten patients did not receive premedication until the development of IRs, if at all (group 2). IRs were more common among patients in group 1 than in group 2 (12/33 versus 28/210 P < 0.0 1). Of the 28 patients in group 2 with IRs, 10 began receiving premedication with each subsequent infusion, 12 continued without premedications, and 6 had no further infusions recorded. Two of 10 who began receiving premedication had a subsequent IR versus 6 of 12 who did not receive premedication (P = 0. 15). Conclusions: IRs occur in a small proportion of infusions among pediatric patients receiving infliximab for IBD. Premedication does not seem to prevent the development of IRs; however, once an IR has occurred, premedication may be indicated to prevent subsequent IRs.
引用
收藏
页码:442 / 446
页数:5
相关论文
共 13 条
[1]   Influence of immunogenicity on the long-term efficacy of infliximab in Crohn's disease [J].
Baert, F ;
Noman, M ;
Vermeire, S ;
Van Assche, G ;
D'Haens, G ;
Carbonez, A ;
Rutgeerts, P .
NEW ENGLAND JOURNAL OF MEDICINE, 2003, 348 (07) :601-608
[2]   The incidence and management of infusion reactions to infliximab: A large center experience [J].
Cheifetz, A ;
Smedley, M ;
Martin, S ;
Reiter, M ;
Leone, G ;
Mayer, L ;
Plevy, S .
AMERICAN JOURNAL OF GASTROENTEROLOGY, 2003, 98 (06) :1315-1324
[3]   Efficacy and safety of repeated infliximab infusions for Crohn's disease: 1-year clinical experience [J].
Cohen, RD .
INFLAMMATORY BOWEL DISEASES, 2001, 7 :S17-S22
[4]   The safety profile of infliximab in patients with Crohn's disease: The Mayo Clinic experience in 500 patients [J].
Colombel, JF ;
Loftus, EV ;
Tremaine, WJ ;
Egan, LJ ;
Harmsen, WS ;
Schleck, CD ;
Zinsmeister, AR ;
Sandborn, WJ .
GASTROENTEROLOGY, 2004, 126 (01) :19-31
[5]   Infusion reactions to infliximab in children and adolescents: frequency, outcome and a predictive model [J].
Crandall, WV ;
Mackner, LM .
ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 2003, 17 (01) :75-84
[6]   Infliximab Retreatment in adults and children with Crohn's disease: Risk factors for the development of delayed severe systemic reaction [J].
Kugathasan, S ;
Levy, MB ;
Saeian, K ;
Vasilopoulos, S ;
Kim, JP ;
Prajapati, D ;
Emmons, J ;
Martinez, A ;
Kelly, KJ ;
Binion, DG .
AMERICAN JOURNAL OF GASTROENTEROLOGY, 2002, 97 (06) :1408-1414
[7]   Efficacy and tolerance of infliximab in children and adolescents with Crohn's disease [J].
Lamireau, T ;
Cézard, JPC ;
Dabadie, A ;
Goulet, O ;
Lachaux, A ;
Turck, D ;
Maurage, C ;
Morali, A ;
Sokal, E ;
Belli, D ;
Stoller, J ;
Cadranel, S ;
Ginies, JL ;
Viola, S ;
Huet, FD ;
Languepin, J ;
Lenaerts, C ;
Bury, F ;
Sarles, J .
INFLAMMATORY BOWEL DISEASES, 2004, 10 (06) :745-750
[8]   Human antichimeric antibody in children and young adults with inflammatory bowel disease receiving infliximab [J].
Miele, E ;
Markowitz, JE ;
Mamula, P ;
Baldassano, RN .
JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION, 2004, 38 (05) :502-508
[9]   Infliximab for the treatment of fistulas in patients with Crohn's disease [J].
Present, DH ;
Rutgeerts, P ;
Targan, S ;
Hanauer, SB ;
Mayer, L ;
van Hogezand, RA ;
Podolsky, DK ;
Sands, BE ;
Braakman, T ;
DeWoody, KL ;
Schaible, TF ;
van Deventer, SJH .
NEW ENGLAND JOURNAL OF MEDICINE, 1999, 340 (18) :1398-1405
[10]   Infliximab for Crohn's disease in clinical practice at the mayo clinic: The first 100 patients [J].
Ricart, E ;
Panaccione, R ;
Loftus, EV ;
Tremaine, WJ ;
Sandborn, WJ .
AMERICAN JOURNAL OF GASTROENTEROLOGY, 2001, 96 (03) :722-729