Why the study?
Does intravenous immunoglobulin (IVIg) improve outcomes in children with severe hand, foot and mouth disease?
Does intravenous immunoglobulin (IVIg) improve outcomes in children with severe hand, foot and mouth disease?
A workshop convened to design a randomized, placebo-controlled trial to evaluate the efficacy and safety of IVIg in severe hand, foot and mouth disease, given the current lack of clinical evidence.
The South East Asia Infectious Disease Clinical Research Network convened subject matter experts at a workshop to make consensus recommendations for study design of a clinical trial for use of intravenous immunoglobulin (IVIg) in severe hand, foot and mouth disease (HFMD). HFMD is a highly contagious emerging infection among children in the region, a small proportion of whom develop neurologic and cardiopulmonary complications with high case-fatality rates. The use of IVIg for treatment of severe disease is widespread and a part of local, national, and international guidelines, but no clinical evidence warrants the use of this drug, which is expensive and has potentially serious side effects. During a 2-day workshop in March 2014, a group of HFMD experts reviewed the current evidence related to use of IVIg in HFMD and discussed potential study design, feasibility, inclusion and exclusion criteria, sample size, primary and secondary endpoints, and subsidiary studies for a randomized, placebo-controlled trial.
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Chea et al. (2014) studied this question.
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