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Prevalence of hearing loss in adults with sickle cell disease

M R Crawford1, H J Gould, W R Smith

  • 1Memphis State University, Tennessee.

Ear and Hearing
|October 1, 1991
PubMed

Insights

Adults with sickle cell disease (SCD) have a high incidence of hearing loss, particularly those with sickle cell C disease. Routine hearing tests are recommended for all adult SCD patients.

Area of Science:

  • Hematology
  • Audiology
  • Public Health

Background:

  • Sickle cell disease (SCD) is a genetic blood disorder associated with various complications.
  • Hearing impairment is a potential, yet often overlooked, complication in adults with SCD.

Purpose of the Study:

  • To investigate the prevalence of hearing impairment in adult subjects with sickle cell disease.
  • To identify any correlation between hemoglobin type and hearing status in this population.

Main Methods:

  • Audiologic assessment was performed on 75 adult subjects diagnosed with sickle cell disease.
  • Subjects were categorized by hemoglobin type for comparative analysis.

Main Results:

  • 41% of adult subjects with sickle cell disease failed the hearing screening.
  • Individuals with sickle cell C disease demonstrated the highest incidence of hearing loss.
  • All examined sickle cell disease patient groups showed a higher prevalence of hearing loss compared to the general population.

Conclusions:

  • Adults with sickle cell disease are at a significantly increased risk for hearing loss.
  • Routine audiologic screening should be integrated into the standard medical care for adults with sickle cell disease.
  • Early detection and management of hearing loss can improve quality of life for individuals with SCD.

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