B. Lang et J. Dooley, FAILURE OF PULSE INTRAVENOUS METHYLPREDNISOLONE TREATMENT IN JUVENILEDERMATOMYOSITIS, The Journal of pediatrics, 128(3), 1996, pp. 429-432
Objective. To review the experience with high-dose intravenous pulse m
ethylprednisolone (IVMP) therapy in patients with juvenile dermatomyos
itis (JDM) in our institution. Study design. We reviewed the charts of
seven consecutive patients (four female subjects; three male subjects
; age 3 to 18 years (mean age 8 years)) treated for JDM between 1989 a
nd 1999. Results. All patients met the criteria of Bohan and Peter for
JDM and were treated within 3 months of onset of weakness, All receiv
ed initial treatment with IVMP, 30 mg/kg per day for 3 days, administe
red weekly for between 1 and 4 weeks. Treatment with orally administer
ed prednisone was required because of deteriorating muscle strength an
d persistent elevation of creatine kinase activity despite IVMP in fiv
e patients, increased skin vasculitis in one patient, and elevated cre
atine kinase activity with no improvement in strength in one patient.
Conclusion. We conclude that muscle strength in patients with JDM may
deteriorate during pulse IVMP therapy when this is used alone as initi
al treatment, even early in the course of the illness, We recommend ei
ther conventional high doses of orally administered corticosteroids or
IVMP with oral corticosteroid therapy as initial treatment of JDM.