Table 5.
Author, Year | Study Design (sample size) | Patient Description | ASA Regimen Evaluated | Hearing Evaluation | Follow-up Time | ASA Exposure Results | No ASA Exposure Results | Time from Exposure to Outcome | Additional Comments |
---|---|---|---|---|---|---|---|---|---|
Jardini, 197837 | Randomized placebo-controlled study (n = 30) |
All diagnosed with RA ASA: 13 women, 2 men Age 19–69 years (mean S3) Placebo: 14 women, 1 man Age 29–76 (mean 51) |
ASA 325 mg (5 grain (1 grain = 65 mg) capsules) × 7 d (dosing frequency not specified) Lactose placebo × 7d |
PT air/bone conduction thresholds at 250–8000 Hz SRT;SDS in quiet (recorded CID W-22) and in noise (−4 dB competing SNR) |
Days 0, 3, and 7 | ASA group had significantly increased PT threshold shifts at 250–8000 Hz except at 2000 Hz as compared to control (P < .05). ASA group had significantly poorer SRTs (P < .05). ASA group had significantly worse discrimination in background noise (P < .05). |
Effect present at day 3 | Moderate BSL (35 mg/100 mL) may adversely affect auditory sensitivity. Thresholds recovered over the course of 1 week. |
Abbreviations: ASA, aspirin (acetylsalicylic acid); BSL blood serum level; CID W-22, word recognition list W-22 created by Central Institute for the Deaf; PT, pure tone; RA: rheumatoid arthritis; SDS, speech discrimination scores; SNR, signal to noise ratio; SRT, speech reception threshold.