TY - JOUR
T1 - Intravenous immunoglobulin therapy in systemic onset juvenile rheumatoid arthritis
T2 - A followup study
AU - Uziel, Yosef
AU - Laxer, Ronald M.
AU - Schneider, Rayfel
AU - Silverman, Earl D.
PY - 1996/5
Y1 - 1996/5
N2 - Objective. To report the short and longterm effect of intravenous immunoglobulin (IVIG) in patients with systemic onset juvenile rheumatoid arthritis (SOJRA). Methods. A retrospective chart review of 27 patients with SOJRA treated with IVIG and followed for 37.1 ± 18.2 months was undertaken. Indications for treatment were fever, arthritis, or steroid dependency. Results. We treated 27 patients with SOJRA with IVIG monthly for 3-54 months. Six months after IVIG therapy, 20 patients had at least a 50% decrease in at least one of the following: the number of days of fever; prednisone dose; or the number of active joints. Five patients failed to respond to IVIG, and 2 dropped out after 3 and 4 months. At last followup visit (mean 37.6 ± 18 months), 11 of the initial 20 responder group patients were in remission, while 3 had significantly improved but still had active arthritis, and 6 were now unresponsive. Of the initial 5 patients in the nonresponder group, 4 had nonresponsive arthritis and 1 had improved at last followup. Three patients in the responder group subsequently developed other diseases. Conclusion. The main benefit of IVIG therapy to most of our patients was a significant improvement in the systemic features, with resolution of fever and a significant reduction in the steroid dose. The efficacy of IVIG in altering the course of arthritis was less predictable. We suggest that IVIG has a role in the management of SOJRA, but it should be limited to patients with severe SOJRA in whom prolonged unresponsiveness to standard therapy is present.
AB - Objective. To report the short and longterm effect of intravenous immunoglobulin (IVIG) in patients with systemic onset juvenile rheumatoid arthritis (SOJRA). Methods. A retrospective chart review of 27 patients with SOJRA treated with IVIG and followed for 37.1 ± 18.2 months was undertaken. Indications for treatment were fever, arthritis, or steroid dependency. Results. We treated 27 patients with SOJRA with IVIG monthly for 3-54 months. Six months after IVIG therapy, 20 patients had at least a 50% decrease in at least one of the following: the number of days of fever; prednisone dose; or the number of active joints. Five patients failed to respond to IVIG, and 2 dropped out after 3 and 4 months. At last followup visit (mean 37.6 ± 18 months), 11 of the initial 20 responder group patients were in remission, while 3 had significantly improved but still had active arthritis, and 6 were now unresponsive. Of the initial 5 patients in the nonresponder group, 4 had nonresponsive arthritis and 1 had improved at last followup. Three patients in the responder group subsequently developed other diseases. Conclusion. The main benefit of IVIG therapy to most of our patients was a significant improvement in the systemic features, with resolution of fever and a significant reduction in the steroid dose. The efficacy of IVIG in altering the course of arthritis was less predictable. We suggest that IVIG has a role in the management of SOJRA, but it should be limited to patients with severe SOJRA in whom prolonged unresponsiveness to standard therapy is present.
KW - Intravenous immunoglobulins
KW - Juvenile rheumatoid arthritis
KW - Systemic onset
UR - http://www.scopus.com/inward/record.url?scp=0029951884&partnerID=8YFLogxK
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C2 - 8724308
AN - SCOPUS:0029951884
SN - 0315-162X
VL - 23
SP - 910
EP - 918
JO - Journal of Rheumatology
JF - Journal of Rheumatology
IS - 5
ER -