Context: Barriers to the use of cochlear implants in children with profound deafness include device costs, difficulty assessing benefit, and lack of data to compare the implant with other medical interventions. Objective: To determine the quality of life and cost consequences for deaf children who receive a cochlear implant. Design: Cost-utility analysis using preintervention, postintervention, and cross-sectional surveys conducted from July 1998 to May 2000. Setting: Hearing clinic at a US academic medical center. Participants: Parents of 78 profoundly deaf children (average age, 7.5 years) who received cochlear implants. Main Outcome Measures: Direct and total cost to society per quality-adjusted life-year (QALY) using the time-trade-off (TTO), visual analog scale (VAS), and Health Utilities Index - Mark III (HUI), discounting costs and benefits 3% annually. Parents rated their child's health state at the time of the survey and immediately before and 1 year before implantation. Results: Recipients had an average of 1.9 years of implant use. Mean VAS scores increased by 0.27, from 0.59 before implantation to 0.86 at survey. In a subset of participants, TTO scores increased by 0.22, from 0.75 to 0.97 (n=40) and HUI scores increased by 0.39, from 0.25 to 0.64 (n=22). Quality-of-life scores were no different 1 year before and immediately before implantation. Discounted direct costs were $60228, yielding $9029 per QALY using the TTO, $7500 per QALY using the VAS, and $5197 per QALY using the HUI. Including indirect costs such as reduced educational expenses, the cochlear implant provided a savings of $53198 per child. Conclusions: Cochlear implants in profoundly deaf children have a positive effect on quality of life at reasonable direct costs and appear to result in a net savings to society.
|Original language||English (US)|
|Number of pages||7|
|Journal||Journal of the American Medical Association|
|Publication status||Published - Aug 16 2000|
ASJC Scopus subject areas