Why the study?
Evidence regarding the effects of different doses of intravenous immunoglobulin in children with severe hand, foot and mouth disease was synthesized to provide a scientific basis for clinical practice.
Does intravenous immunoglobulin combined with conventional therapy improve recovery times in children with severe hand, foot and mouth disease?
Does intravenous immunoglobulin combined with conventional therapy improve recovery times in children with severe hand, foot and mouth disease?
IVIG combined with conventional therapy, particularly at a high dose of 1 g/kg/day, accelerates fever clearance and rash regression in children with severe hand, foot and mouth disease.
OBJECTIVE: To conduct a meta-analysis of evidence from randomized controlled trails (RCTs) of different doses of intravenous immunoglobulin (IVIG) in children with severe hand, foot and mouth disease (HFMD) to provide the scientific basis for clinical practice. METHODS: A search of PubMed-Medline, CNKI, Wanfang, and VIP database (until June 30, 2017) was performed and Software RevMan5.3 was used to evaluate the effect of different doses of IVIG on HFMD in RCTs. We used random-effects models (or fixed-effects models) and generic inverse variance methods to process quantitative data, followed by a leave-one-out method for sensitivity analysis. RESULTS: From a total of 420 entries identified via searches, 8 RCTs involving 1,450 patients were included in the final analysis. The results of the meta-analysis showed that compared with conventional therapy alone, conventional therapy combined with IVIG had shorter fever clearance time, shorter rash regression time, and shorter clinical cure time. Subgroup analyses showed that the high-dose group (1 g/kg/day) had shorter fever clearance time (p < 0.05), shorter rash regression (p< 0.05), shorter remission time of neurological symptoms (p < 0.05), but longer clinical cure time (p > 0.05). CONCLUSION: The high-dose group has a better prognosis; however, the advantages and disadvantages should be carefully considered when deciding the doses in the treatment of severe HFMD.
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Wei et al. (2019) studied this question.
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