Ry. Lin et al., Improved outcomes in patients with acute allergic syndromes who are treated with combined H-1 and H-2 antagonists, ANN EMERG M, 36(5), 2000, pp. 462-468
Study objective: Although the addition of H-2 blockers to H-1 antagonists h
as been promoted for use in anaphylaxis, there have been no large studies e
stablishing the advantage of this approach in treating acute allergic syndr
omes. In this study we tested the hypothesis that combined H-1 and H-2 bloc
kage results in improved outcomes in patients treated for acute allergic sy
ndromes compared with treatment with H-1 blockade alone.
Methods: In a randomized, double-blind, placebo-controlled trial, 91 adult
patients with acute allergic syndromes were treated with either 50 mg of di
phenhydramine and saline solution (control group) or with 50 mg of diphenhy
dramine and 50 mg of ranitidine (active group). These patients were treated
with parenteral administration. Patients were recruited from an emergency
department at an urban academic medical center. The primary endpoints were
resolution of urticaria, angioedema, or erythema at 2 hours after protocol
treatment. Areas of cutaneous involvement, heart rates, blood pressures, re
spiratory findings, and symptom scores were also assessed at baseline, 1 ho
ur, and 2 hours.
Results: There were significantly more patients without urticaria at 2 hour
s among the patients in the active group compared with those in the control
group. Both groups had similar proportions of urticaria at baseline. Logis
tic regression models to predict resolution of urticaria, which accounted f
or baseline urticarial involvement, showed odds ratios in favor of the acti
ve group treatment. Similar findings were observed when the absence of boil
1 urticaria and angioedema was considered as the dependent variable. There
was not a significant difference between the 2 groups with regard to the a
bsence of erythema or angioedema (irrespective of the presence of urticaria
) at 2 hours. Blood pressure and symptoms did not show differences between
the 2 groups over time. Lower heart rates were observed 1 hour after treatm
ent in the active treatment group (mean reduction 10 beats/min) compared wi
th those found in the placebo group (mean reduction 6 beats/min).
Conclusion: These data show that adding H-2 blockers to H-1 antagonists res
ults in additional improvement of certain cutaneous outcomes for patients p
resenting with acute allergic syndromes. These findings favor the recommend
ation for using combined H-1 and H-2 antihistamines in acute allergic syndr
omes.