Table 2.
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 |
---|---|---|---|---|---|---|---|---|---|
Abdala, 200523 | Prospective cohort (n = 41, 10 of which were ASA exposed) | Adult ASA recipients: age 22–37 years (n = 10) Children with mild SNHL (n = 8) Healthy term–born neonates (n = 23) |
ASA 975 mg (3 tablets of 325 mg) Q6h for 4 d | Air and bone conduction audiogram Immittance testing DP-gram DPOAE |
Baseline, then 72 h and 96 h afterward | Mean audiometric threshold increase at 96 h: 12.7 dB at 1500 Hz, 14.3 dB at 6000 Hz. Significant correlation between serum level and audiometry (r = 0.75, P = .19) |
Subjects were compared to their own baseline | 72,96 h | Audiometric results were not directly correlated with DPOAE results |
Day, 198925 | Prospective cohort, double-blinded (n = 8) |
Age 22–46 years with normal hearing at the outset Male healthy volunteers |
ASA in 4 serial scheduled doses: (1) 1.95 g/d (2) 3.25 g/d (3) 4.55 g/d (4) 5.85 g/d for 7 d each |
Pure-tone thresholds measured at 250–8000 Hz | On the seventh day of each treatment period | Mean HL per frequency (dB HL) 1.95g/d = 4.38 3.25g/d = 11.56 4.55g/d = 40.56 5.85g/d= 112.5 Mean Tinnitus intensity (dB HL) 1.95g/d = 25.50 3.25 g/d= 36.38 4.55 g/d= 51.00 5.85 g/d= 62.13 |
Subjects were compared to their own baseline. HL expressed as mean decrease from pretreatment thresholds in both ears | Effect present at 1 week | Hearing and tinnitus had a dose-dependent response to ASA level (P < .05). |
Abbreviations: ASA, aspirin (acetylsalicylic acid); DPOAE, distortion product otoacoustic emissions; HL, hearing loss; SNHL, sensorineural hearing loss.