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. 2021 Sep 15;12:740517. doi: 10.3389/fimmu.2021.740517

Table 4.

Factor-specific incidences of adverse reactions to high-dose IVIG*.

Patient basis (n=388) Infusion basis (n=2888)
Adverse reaction Adverse reaction
No Yes p value No Yes p value
Gender, n (%)
Male 169 (96.0) 7 (4.0) 961 (98.6) 14 (1.4)
Female 186 (87.7) 26 (12.3) 0.003 1820 (95.6) 83 (4.4) < 0.001
Age, n (%)
< 15 years 196 (99.0) 2 (1.0) 314 (99.4) 2 (0.6)
≥ 15 years 159 (83.7) 31 (16.3) < 0.001 2467 (96.3) 95 (3.7) 0.003
IVIG doses (average, g/kg BW) 3.0 10.9 0.003 0.65 0.48 0.004
Indication, n (%)
Autoimmune 344 (91.2) 33 (8.8) 2759 (96.6) 97 (3.4)
Neuromuscular 52 (73.2) 19 (26.8) 973 (93.7) 65 (6.3)
Dermatologic 51 (87.9) 7 (12.1) 1078 (97.8) 24 (2.2)
ITP 59 (96.7) 2 (3.3) 339 (99.4) 2 (0.6)
EGPA 13 (81.2) 3 (18.8) 149 (97.4) 4 (2.6)
Kawasaki disease 169 (98.8) 2 (1.2) 220 (99.1) 2 (0.9)
Others 11 (100.0) 0 (0.0) 22 (100.0) 0 (0.0)

*The high-dose IVIG is more than 0.7 g/kg body weight per course.

The values indicate the cumulative doses from multiple treatment of IVIG on one patient.

BW, body weight of patient.