Original article
Presumed “sulfa allergy” in patients with intracranial hypertension treated with acetazolamide or furosemide: cross-reactivity, myth or reality?

https://doi.org/10.1016/j.ajo.2004.02.019Get rights and content

Abstract

Purpose

To determine whether acetazolamide or furosemide produce allergic cross-reactions in patients with self-reported “sulfa allergy.”

Design

Retrospective case series.

Methods

A retrospective review included patients with intracranial hypertension and a self-reported sulfa allergy treated with either acetazolamide or furosemide seen at the University of Iowa Hospitals and Clinics from 1972 to 2003. All presumed medication-related side effects were collected, including both predictable adverse effects (for example, paresthesias, fatigue) and unpredictable adverse reactions (for example, cutaneous fixed eruptions, urticaria, Stevens-Johnson syndrome, toxic epidermal necrolysis, angioedema, anaphylaxis).

Results

We reviewed 363 charts. Of these, 329 patients (91%) were excluded. Of the remaining 34 cases that did report a so-called sulfa allergy, 13 (38%) received acetazolamide alone, 7 (21%) received furosemide alone, and 14 (41%) received both acetazolamide and furosemide. Of the 27 patients who received acetazolamide, 10 (37%) had no documented allergic cross-reaction to sulfa, and 2 (7%) cases had urticaria. The remaining 15 (56%) of acetazolamide-treated patients experienced predictable adverse reactions for this drug (for example, paresthesias). No patient experienced a severe allergic cross-reaction to sulfa. Of 21 patients who received furosemide, no unpredictable adverse reactions or allergic cross-reactions to sulfa were noted.

Conclusions

We find little clinical or pharmacological evidence to suggest that a self-reported sulfa allergy is likely to produce a life-threatening cross-reaction with acetazolamide or furosemide. These medications should be considered for intracranial hypertension if the risk-to-benefit ratio warrants their use.

Section snippets

Methods

A retrospective chart review was performed of all patients with the diagnosis of presumed idiopathic intracranial hypertension from 1972 to 2003 at the University of Iowa Hospitals and Clinics, Department of Ophthalmology, Division of Neuro-Ophthalmology. This study was performed with appropriate institutional review board approval and in compliance with applicable Health Insurance Portability and Accountability Act regulations. Inclusion criteria were as follows: 1) a clinical diagnosis of

Results

We reviewed 363 charts. All patients had been seen between 1972 and 2003 at the Department of Ophthalmology at the University of Iowa Hospitals and Clinics, Iowa City, Iowa. Patient follow-up ranged from 7 weeks to 21 years, with a median of 2.5 years, and a mean of 4.13 years. Of these 363 patients, 322 (89%) were excluded because of absence of self-reported sulfa allergy. Of the remaining 41 (11%) charts of patients with self-reported sulfa allergy, 5 additional charts were excluded because

Discussion

Although the literature on the treatment of idiopathic intracranial hypertension suggests that patients with sulfa allergy should not take acetazolamide or furosemide, the evidence supporting this recommendation is weak. The same product warnings appear for other sulfonamide nonantimicrobial agents used in ophthalmology, including brinzolamide, dorzolamide, and methazolamide.1

The majority of patients who report a sulfa allergy have actually had an adverse reaction to a sulfonamide antimicrobial

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