Targeted use of prednisolone with the second IVIG dose for refractory K awasaki disease
Abstract Background Prednisolone ( PSL ) has been suggested to be useful for the treatment of Kawasaki disease ( KD ) resistant to i.v. immunoglobulin ( IVIG ), but much remains to be elucidated regarding its use. Methods A total of 1087 subjects were involved in a two‐study multicenter prospective...
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Published in | Pediatrics international Vol. 59; no. 4; pp. 397 - 403 |
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Main Authors | , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
01.04.2017
|
Online Access | Get full text |
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Summary: | Abstract
Background
Prednisolone (
PSL
) has been suggested to be useful for the treatment of Kawasaki disease (
KD
) resistant to i.v. immunoglobulin (
IVIG
), but much remains to be elucidated regarding its use.
Methods
A total of 1087 subjects were involved in a two‐study multicenter prospective investigation of the effects of acute phase therapy on
IVIG
‐resistant
KD
. Subjects resistant to the first dose of
IVIG
were classified into high (≥10 mg/dL) and low (<10 mg/dL) serum C‐reactive protein (
CRP
) groups after the first dose of IVIG.
Results
In the first study, the efficacy of the second dose of
IVIG
in the high
CRP
group was significantly lower than in the low
CRP
group (47.8% vs 76.8%,
P
< 0.005). In the second study,
PSL
was co‐administered with the second dose of
IVIG
to the high
CRP
patients (intensified regimen). The efficacy of the intensified regimen was similar to that of the second dose of
IVIG
in the low
CRP
group (79.4% vs 83.3%). Although the difference in the incidence of persistent coronary artery lesions (
CAL
) between the high and low
CRP
groups was significant in the first study (19.6% vs 3.0%,
P
< 0.005), it was not significant in the second study (8.8% vs 2.4%).
Conclusions
The targeted use of
PSL
with the second dose of
IVIG
in
KD
patients resistant to the first dose of
IVIG
and who are predicted to be resistant to the second dose of
IVIG
, appears to be effective. |
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ISSN: | 1328-8067 1442-200X |
DOI: | 10.1111/ped.13190 |