R. Asero, Risk factors for acetaminophen and nimesulide intolerance in patients withNSAID-induced skin disorders, ANN ALLER A, 82(6), 1999, pp. 554-558
Background: Previous studies show skin reactions after exposure to acetamin
ophen and/or nimesulide to occur in about 10% of patients with a history of
urticaria induced by aspirin or other nonsteroidal anti-inflammatory drugs
(NSAIDs). This fact is surprising since cross-reactivity among different N
SAIDs should not occur among subjects without a history of chronic urticari
a.
Objective: To detect risk factors for intolerance to alternative drugs such
as acetaminophen and nimesulide in different groups of patients with a his
tory of adverse skin reactions (urticaria/angioedema, or anaphylaxis) after
the ingestion of aspirin and other NSAIDs.
Methods: Two hundred fifty-six patients with a history of recent pseudoalle
rgic skin reactions caused by NSAIDs underwent elective oral challenges wit
h increasing doses of both acetaminophen and nimesulide. Patients were divi
ded into three groups: A = 69 subjects with chronic urticaria, B = 163 othe
rwise normal subjects with a history of urticaria after the ingestion of as
pirin, and C = 24 otherwise normal subjects with a history of urticaria aft
er the ingestion of pyrazolones but aspirin-tolerant.
Results: Forty-eight (19%) patients reacted to acetaminophen and/or nimesul
ide. Similar numbers of patients with chronic urticaria (23%) and of normal
subjects with a history of aspirin-induced urticaria (19%) did not tolerat
e one of the alternative drugs challenged. Pyrazolones-intolerant patients
showed the lowest number of reactors (4%). Aspirin intolerance represented
a risk factor for acetaminophen- and/or nimesulide-induced urticaria (RR =
5.4). A history of anaphylactoid reactions induced by NSAID represented a r
isk factor for urticaria after the ingestion of the alternative study drugs
(RR = 5.7). Atopic status was associated with a higher risk of reactivity
to nimesulide: this drug induced urticaria in 11/47 (23%) atopics versus 18
/209 (9%) non-atopics (P <.005; RR = 3.2). A history of intolerance to anti
bacterial drugs was not associated with a higher prevalence of reactivity a
gainst acetaminophen and/or nimesulide.
Conclusions: In at least 20% of patients with a history of urticaria/angioe
dema or anaphylaxis induced by aspirin or other NSAIDs, but without a histo
ry of chronic urticaria, cross-reactivity with other NSAIDs occurs. Atopy a
s well as a history of aspirin-induced anapylactoid reactions seem to repre
sent relevant risk factors for intolerance to alternative NSAIDs. In view o
f these findings,aspirin-intolerant patients with such clinical features sh
ould be submitted to peroral tolerance tests with at least two alternative
substances in order to avoid potentially severe reactions.