Egg allergy preventionThe mistaken belief that you could prevent peanut allergy by withholding peanuts from infants was turned on its head when studies showed the opposite. Now a Japanese group has shown that early introduction of egg is associated with far less egg allergy.1 Children aged 4-5 months with eczema, and consequent high risk of food allergy, who had never been given egg, were randomised to be given heated egg powder or placebo. The egg was started at age 6 months at a low dose (50 mg daily), increased to 250 mg daily from 9 to 12 months. At age 12 months, the incidence of egg allergy was assessed clinically through oral food challenge. The calculated sample size was 150, but the researchers stopped the study after 100 children had been challenged, because 9% of the eggs exposed but 38% of the placebo children had developed diagnosed egg allergy (risk ratio = 0.22, 95% confidence interval 0.08-0.60, P = 0.001). The only difference in adverse events between groups was that 6 of 60 children in the egg group but none of the placebo group were admitted to hospital; P = 0Á022). The novel aspects of this study are the use of heated egg in powder form and the gradual increase in dose. The proportion of all babies who survived without neurodevelopmental impairment increased from 16 to 20%. While these differences were statistically significant, for a parent deciding about resuscitation or intensive care, the message is that just over a third will survive and half the survivors will have major neuro-developmental impairment. The study could not examine lesser degrees of impairment in the 'normal' survivors. The mortality for 22-week gestation infants did not change across the three-time periods (98, 95 and 97%), and only 9 (1.2%) of 749 22-weekers survived without neuro-developmental impairment. Kaiser et al. also examined the use of ICS in pre-school children with EVW. Intermittent ICS -that is, high-dose ICS given at onset of viral upper respiratory tract infection symptoms for 7-10 days -is beneficial when compared to placebo (number needed to treat = 6), with one severe exacerbation (as defined by need for oral corticosteroids) prevented for every six children treated (Fig. 1), 1 and is equivalent to regular ICS in this subgroup. This approach is an attractive therapeutic option as it has the potential to reduce systemic steroid exposure as well as hospital presentations. At present, the optimal dose of intermittent ICS is unknown as the dose varied across the studies included in the meta-analysis and in most cases was greater than the licensed dose for this age group, if licensed at all. 4 We believe that this study has highlighted intermittent ICS as a potential therapeutic option in pre-school children with EVW, and anticipate that further studies will inform translation to clinical practice if a safe and effective dose can be identified.
Reference
Reference
References