Adverse effects of intravenous immunoglobulin therapy in 56 patients with autoimmune diseases

被引:88
作者
Sherer, Y
Levy, Y
Langevitz, P
Rauova, L
Fabrizzi, F
Shoenfeld, Y [1 ]
机构
[1] Chaim Sheba Med Ctr, Dept Med B, IL-52621 Tel Hashomer, Israel
[2] Chaim Sheba Med Ctr, Autoimmune Dis Res Unit, IL-52621 Tel Hashomer, Israel
[3] Tel Aviv Univ, Sackler Fac Med, IL-69978 Tel Aviv, Israel
关键词
autoimmune disease; intravenous immunoglobulin; adverse effects; viral safety;
D O I
10.1159/000056085
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Objective: To test the adverse effects and viral safety of intravenous immunoglobulin (IVIg) use in autoimmune diseases. Methods: Fifty-six patients with various autoimmune diseases who were treated with one to six IVIg courses were evaluated for the presence of adverse effects following IVIg therapy and were screened before a nd after the treatment for the presence of serum human immunodeficiency virus antibodies, hepatitis C virus antibodies, and hepatitis B surface antigen. Results: Among the 56 patients, 20 (36%) had at least one adverse effect following at least one of the treatment courses. These included headache, low-grade fever, chills, anemia, low-back pain, transient hypotension, nausea, intensified perspiration, and superficial and deep vein thromboses. Whereas the presence of adverse effect to IVIg was unrelated to either the clinical response to the treatment or to the nature of the autoimmune disease, the occurrence of an adverse effect in the first treatment course was significantly associated with a greater chance for an adverse effect in the subsequent courses. No transmission of any of the three viral agents examined could be detected. Conclusions: Although IVIg use in autoimmune diseases is associated with adverse effects in about one third of the patients, these effects are usually mild and transient. Patients who develop adverse effects during the first treatment course may be at increased risk of adverse effects during the subsequent IVIg courses. Copyright (C) 2001 S. Karger AG, Basel.
引用
收藏
页码:133 / 137
页数:5
相关论文
共 15 条
[1]  
[Anonymous], 1999, MMWR MORB MORTAL WKL, V48, P518
[2]   IVIG adverse reaction: Potential role of cytokines and vasoactive substances [J].
Bagdasarian, A ;
Tonetta, S ;
Harel, W ;
Mamidi, R ;
Uemura, Y .
VOX SANGUINIS, 1998, 74 (02) :74-82
[3]   Complications of intravenous immune globulin treatment in neurologic disease [J].
Brannagan, TH ;
Nagle, KJ ;
Lange, DJ ;
Rowland, LP .
NEUROLOGY, 1996, 47 (03) :674-677
[4]   A CONTROLLED TRIAL OF INTRAVENOUS IMMUNE GLOBULIN TO REDUCE NOSOCOMIAL INFECTIONS IN VERY-LOW-BIRTH-WEIGHT INFANTS [J].
FANAROFF, AA ;
KORONES, SB ;
WRIGHT, LL ;
WRIGHT, EC ;
POLAND, RL ;
BAUER, CB ;
TYSON, JE ;
PHILIPS, JB ;
EDWARDS, W ;
LUCEY, JF ;
CATZ, CS ;
SHANKARAN, S ;
OH, W ;
CASSADY, G ;
BRAUNE, K ;
HACK, M ;
NEWMAN, NS ;
LITTLE, G ;
NATTIE, C ;
BAIN, RP ;
VERTER, J ;
YOUNES, N ;
HAWES, S ;
MURAN, G ;
BANDSTRA, ES ;
MARTINEZ, S ;
YAFFE, SJ ;
MALLOY, M ;
COOKE, R ;
MOORE, J ;
BURCHFIELD, J ;
HORBAR, JD ;
LEAHY, K .
NEW ENGLAND JOURNAL OF MEDICINE, 1994, 330 (16) :1107-1113
[5]  
Fisman DN, 1997, CAN J CARDIOL, V13, P775
[6]   In vivo administration of intravenous immunoglobulin (IVIg) can lead to enhanced erythrocyte sequestration [J].
Kessary-Shoham, H ;
Levy, Y ;
Shoenfeld, Y ;
Lorber, M ;
Gershon, H .
JOURNAL OF AUTOIMMUNITY, 1999, 13 (01) :129-135
[7]   A study of 20 SLE patients with intravenous immunoglobulin - clinical and serologic response [J].
Levy, Y ;
Sherer, Y ;
Ahmed, A ;
Langevitz, P ;
George, J ;
Fabbrizzi, F ;
Terryberry, J ;
Meissner, M ;
Lorber, M ;
Peter, JB ;
Shoenfeld, Y .
LUPUS, 1999, 8 (09) :705-712
[8]   Serologic and clinical response to treatment of systemic vasculitis and associated autoimmune disease with intravenous immunoglobulin [J].
Levy, Y ;
Sherer, Y ;
George, J ;
Langevitz, P ;
Ahmed, A ;
Bar-Dayan, Y ;
Fabbrizzi, F ;
Terryberry, J ;
Peter, J ;
Shoenfeld, Y .
INTERNATIONAL ARCHIVES OF ALLERGY AND IMMUNOLOGY, 1999, 119 (03) :231-238
[9]   Adverse effects of intravenous immunoglobulin therapy [J].
Nydegger, UE ;
Sturzenegger, M .
DRUG SAFETY, 1999, 21 (03) :171-185
[10]   A CONTROLLED TRIAL OF INTRAVENOUS IMMUNOGLOBULIN-G IN CHRONIC FATIGUE SYNDROME [J].
PETERSON, PK ;
SHEPARD, J ;
MACRES, M ;
SCHENCK, C ;
CROSSON, J ;
RECHTMAN, D ;
LURIE, N .
AMERICAN JOURNAL OF MEDICINE, 1990, 89 (05) :554-560