Abstract
In a subset of aspirin-tolerant asthmatics, administration of aspirin improves respiratory symptoms. We present a patient with chronic rhinosinusitis with nasal polyps who exhibited relief of nasal obstruction and nasal discharge and improvement in the sense of smell following oral administration of 150 mg of aspirin daily. Improvement in the patency of the nasal passages was documented by nasal endoscopy and magnetic resonance imaging. Improvement of olfactory function was documented by validated psychophysical olfactory testing and by means of olfactory event-related potentials.
Introduction
In contrast to aspirin-exacerbated respiratory disease, there are some reports about patients in whom asthma improves with aspirin, although those reports provide few data on aspirin's impact on chronic rhinosinusitis or olfaction.1–3
Case Report
We saw a 54-year-old non-smoking male, with a 3-year history of fluctuating sense of smell, profuse rhinorrhea, and nasal obstruction. Since he had started taking 150 mg of aspirin per day to prevent atherosclerosis, he observed an improvement of his sense of smell and a decrease of rhinorrhea and nasal obstruction. After taking aspirin in the morning his sense of smell would improve and be normal around lunchtime and would then gradually deteriorate in the afternoon. He had a history of essential hypertension, for which he was on felodipine 5 mg and ramipril 5 mg daily. He reported bronchial hyper-responsiveness to volatile chemicals, but he did not have asthma. Allergy skin prick testing to common aeroallergens was negative.
We tested for chronic rhinosinusitis and olfactory function on 3 different days. On day 1 he took aspirin in the morning, and the olfaction tests were performed at least 4 hours after aspirin ingestion. The next day (day 2) he did not take aspirin until all the tests were completed. On day 3 and day 4 he took aspirin in the morning. He had been on aspirin for 44 hours when the final test was performed, but at least 7 hours after his last aspirin dose.
Figure 1 shows images from nasal endoscopy on aspirin and off aspirin. Figure 2 shows magnetic resonance images on aspirin, at 29 hours off aspirin, and 44 hours after resuming aspirin.
Nasal cavities on aspirin (upper row) and off aspirin (lower row). In this patient, on aspirin the left side is decongested and dry and the right side, which has a polyp in the olfactory cleft, is fairly decongested and wet. Off aspirin the mucosa showed marked edema and clear nasal discharge on the right, and the left side is congested and wet.
Magnetic resonance images (T2-weighted, coronal slices) on aspirin (upper row) after 29 hours off aspirin (middle row), and 44 hours after resuming aspirin (bottom row). The arrow indicates the right inferior turbinate. On aspirin the turbinate's mucosa is less swollen than it is off aspirin. There are no major morphological changes on either side of the olfactory cleft.
We assessed olfaction with the validated Sniffin' Sticks test kit (Table 1).4 We measured olfactory event-related potentials with an air-dilution olfactometer (OM2S, Burghart, Wedel, Germany) with cinnamon aldehyde (20% v/v) stimuli, with a duration 200 ms and an interstimulus interval 30 s, in a constant stream of humidified air (Fig. 3).5
The TDI Scores While on Aspirin, When 29 Hours Off Aspirin, and 44 Hours After Resumption of Aspirin, and the Corresponding Scores
Olfactory event-related potentials while on aspirin, off aspirin, and 44 hours after resuming aspirin (top). Olfactory event-related potentials could only be obtained from the left nostril while on aspirin. Off aspirin no responses could be obtained from either side. Response peaks are indicated by markers. Stimulus onset starts at 530 ms after onset of recordings.
Discussion
There have been few reports, mainly from the late 1970s and 1980s, of aspirin-tolerant asthmatics who experienced bronchodilatation from aspirin or other cyclooxygenase inhibitors.1–3,6,7 The benefit was reported to occur within 30–60 min after of aspirin ingestion, and to last several hours, and in one case 3 days.3 Symptom improvement was observed only with cyclooxygenase inhibitors, and it was hypothesized that the effect was caused by a diversion of the arachidonic acid metabolism toward cyclooxygenase products.2
Our patient did not have asthma but did report bronchial hyper-responsiveness to volatile chemicals. Lung-function tests on and off aspirin would be desirable, but our patient declined lung function testing, because he did not feel any respiratory impairment or lung-function difference on versus off aspirin. He did accede to nasal endoscopy, magnetic resonance imaging, and olfaction testing. While he was on aspirin he was normosmic, 29 hours off aspirin he was anosmic, and olfactory function had returned to normal 44 hours after restarting aspirin (see Table 1). Olfactory event-related potentials could be obtained while the patient was on aspirin, but could not be obtained when the patient was off aspirin for 29 hours. Polyps in the right olfactory cleft that prevented air from reaching the olfactory receptors might explain why olfactory event-related potentials could be obtained only from the left nostril. Birhinally-obtained olfactory test results by means of the Sniffin' Sticks test represent olfactory function of the better nostril. That is why it is possible that he had irrecoverable loss of olfaction on the right side,8 but the absence of right-side olfaction might have been from nasal congestion that might have been reversed by a higher dose of aspirin.9
There have been no broad-based epidemiological studies on the prevalence of aspirin-relieved respiratory disease. The available data suggest a prevalence of 0.5–2% among asthmatic patients.3,7,10 Upper-respiratory-tract inflammation and chronic rhinosinusitis frequently reduce olfaction and decrease quality of life,11–13 and the available therapies are limited and their effects transitory.14,15 A study is needed on whether aspirin-tolerant patients with chronic rhinosinusitis and/or asthma benefit from ingested or topical aspirin.16 Topical lysine aspirin desensitizes aspirin-exacerbated respiratory disease, and has been reported to be safe and suitable for long-term use.17 Some patients with olfactory loss due to chronic rhinosinusitis, with or without nasal polyps, might benefit from aspirin.
Footnotes
- Correspondence: Volker Gudziol MD, Smell and Taste Clinic, Department of Otorhinolaryngology, University of Dresden Medical School, Fetscherstrasse 74, 01307 Dresden, Germany. E-mail: volker.gudziol{at}uniklinikum.dresden.de.
The authors have disclosed no conflicts of interest.
- Copyright © 2012 by Daedalus Enterprises Inc.
References
