Potential Efficacy of High-Dose Inhaled Salbutamol for the Treatment of Abdominal Pain During Oral Food Challenge

BACKGROUND: Abdominal pain is a frequent symptom of IgE-mediated food allergy with limited therapeutic options. Visceral smooth muscle cell relaxation can be induced through beta-adrenergic stimulation. OBJECTIVE: To evaluate the efficacy of inhaled salbutamol empirically used to relieve abdominal pain caused by IgEmediated allergic reactions at 1 center. METHODS: All double-blind placebo-controlled food challenges to peanut performed at 1 center between 2016 and 2021 were reviewed to identify patients who presented abdominal pain as part of their reaction. The primary outcome measure was the delay between the initiation of therapy and improvement of abdominal pain. It was compared between patients who had received inhaled salbutamol as part of their treatment and those who did not. Cox regression was performed to control for potential confounders. RESULTS: During the study period, 186 positive double-blind placebo-controlled food challenges were performed, including 126 for peanut allergy. Of these, 77 were treated for abdominal pain and 57 met the criteria for inclusion in the study. Patients who received salbutamol improved significantly faster (median, 12.5 minutes) than those who did not (median, 65 minutes) (chi(2) 45; P < .0001). In Cox regression, the administration of salbutamol and emesis were found to increase the rate of improvement by a hazard ratio of 11.35 (95% CI, 5.40-23.9; P < .0005) and 4.00-fold (95% CI, 1.90-8.42; P < .0005), respectively. CONCLUSIONS: This retrospective study provides hypothesis generating evidence for the use of salbutamol in the treatment of IgE-mediated abdominal pain. Further investigation in a doubleblind randomized controlled trial is warranted. (C) 2021 American Academy of Allergy, Asthma & Immunology

Automated summary

Inhaled salbutamol has shown significant efficacy in relieving abdominal pain caused by IgE-mediated allergic reactions, leading to faster symptom improvement in patients. This retrospective study provides hypothesis generating evidence for further investigation in a double-blind randomized controlled trial.