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Journal of the National Medical Association logoLink to Journal of the National Medical Association
. 2005 Aug;97(8):1135–1142.

Hearing thresholds in sickle cell anemia patients: emerging new trends?

Ademola Aderibigbe 1, Foluwasayo E Ologe 1, Benjamin A Oyejola 1
PMCID: PMC2575988  PMID: 16173329

Abstract

PURPOSE OF STUDY: Advances in medicine resulting in better understanding of sickle cell disease and general improvement of the well-being of the sufferers even in the developing countries have positively affected the dreadful outlook of this disease with resultant increase in the population of sickle cell disease patients reaching adulthood, and less severe complications. We therefore set out to evaluate the presence and severity of sensorineural hearing loss in sickle cell anemia (SCA) patients in the light of the overall improvement in the morbidity and mortality. METHODS: A prospective case control study of SCA patients attending our adult SCA clinic and control subjects from homozygous hemoglobin AA patients attending the staff clinic of the hospital for routine medical tests. Tympanometry and diagnostic audiometry were performed on each patient. MAIN FINDINGS: Forty-six SCA patients (21 males, 45.7%) aged 16-48 years with a mean age of 22.9 years +/- 6.45 and 42 controls (24 males, 57.1%) aged 15-39 years with a mean age of 23.7 years +/- 5.69 were included in this study. The average hearing thresholds of SCA patients were consistently higher than controls in all frequencies tested in both right and left ears. Of the 92 ears of SCA patients tested, 95.7% exhibited hearing thresholds within normal limits, and 4.3% had mild hearing loss. The controls had thresholds within normal limits. CONCLUSION: The incidence of significant sensorineural hearing loss in SCA seems to have reduced in line with the general improvement and survival of SCA patients. The hearing loss is worse in the right ear and has a female preponderance. We hope that more aggressive primary and secondary prevention and adequate treatment of sickle cell crisis would reduce if not eliminate the hearing loss found in SCA.

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Selected References

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  1. Aderibigbe A., Arije A., Akinkugbe O. O. Glomerular function in sickle cell disease patients during crisis. Afr J Med Med Sci. 1994 Jun;23(2):153–160. [PubMed] [Google Scholar]
  2. Ahmed Hafiz O., Dennis John H., Ballal Seifeddin G. The accuracy of self-reported high noise exposure level and hearing loss in a working population in Eastern Saudi Arabia. Int J Hyg Environ Health. 2004 Jul;207(3):227–234. doi: 10.1078/1438-4639-00291. [DOI] [PubMed] [Google Scholar]
  3. Ajulo S. O., Osiname A. I., Myatt H. M. Sensorineural hearing loss in sickle cell anaemia--a United Kingdom study. J Laryngol Otol. 1993 Sep;107(9):790–794. doi: 10.1017/s0022215100124442. [DOI] [PubMed] [Google Scholar]
  4. Akenzua G., Akinyanju O., Kulozik A., Whitehead S., Morris J., Serjeant B. E., Serjeant G. Sickle cell anaemia in Nigeria: a comparison between Benin and Lagos. Afr J Med Med Sci. 1994 Jun;23(2):101–107. [PubMed] [Google Scholar]
  5. Applebaum E. L., Frankel A. Extramedullary hematopoiesis of the middle ear. Am J Otolaryngol. 1989 Jul-Aug;10(4):287–290. doi: 10.1016/0196-0709(89)90010-0. [DOI] [PubMed] [Google Scholar]
  6. Atsina K. K., Ankra-Badu G. Sensorineural hearing loss in Ghanaians with sickle cell anaemia. Trop Geogr Med. 1988 Jul;40(3):205–208. [PubMed] [Google Scholar]
  7. Cruickshanks Karen J., Tweed Ted S., Wiley Terry L., Klein Barbara E. K., Klein Ronald, Chappell Rick, Nondahl David M., Dalton Dayna S. The 5-year incidence and progression of hearing loss: the epidemiology of hearing loss study. Arch Otolaryngol Head Neck Surg. 2003 Oct;129(10):1041–1046. doi: 10.1001/archotol.129.10.1041. [DOI] [PubMed] [Google Scholar]
  8. Gould H. J., Crawford M. R., Smith W. R., Beckford N., Gibson W. R., Pettit L., Bobo L. Hearing disorders in sickle cell disease: cochlear and retrocochlear findings. Ear Hear. 1991 Oct;12(5):352–354. doi: 10.1097/00003446-199110000-00008. [DOI] [PubMed] [Google Scholar]
  9. Jerger J., Chmiel R., Stach B., Spretnjak M. Gender affects audiometric shape in presbyacusis. J Am Acad Audiol. 1993 Jan;4(1):42–49. [PubMed] [Google Scholar]
  10. MacDonald C. B., Bauer P. W., Cox L. C., McMahon L. Otologic findings in a pediatric cohort with sickle cell disease. Int J Pediatr Otorhinolaryngol. 1999 Jan 25;47(1):23–28. doi: 10.1016/s0165-5876(98)90152-5. [DOI] [PubMed] [Google Scholar]
  11. Ogisi F. O., Okafor L. A. Assessment of auditory function in sickle cell anaemia patients in Nigeria. Trop Geogr Med. 1987 Jan;39(1):28–31. [PubMed] [Google Scholar]
  12. Ologe F. E., Okoro E. O. Type 2 diabetes and hearing loss in black Africans. Diabet Med. 2005 May;22(5):664–665. doi: 10.1111/j.1464-5491.2005.01479.x. [DOI] [PubMed] [Google Scholar]
  13. Ologe Foluwasayo E., Okoro Emmanuel O., Oyejola Benjamin A. Hearing function in Nigerian children with a family history of type 2 diabetes. Int J Pediatr Otorhinolaryngol. 2004 Dec 25;69(3):387–391. doi: 10.1016/j.ijporl.2004.11.009. [DOI] [PubMed] [Google Scholar]
  14. Onakoya P. A., Nwaorgu O. G. B., Shokunbi W. A. Sensorineural hearing loss in adults with sickle cell anaemia. Afr J Med Med Sci. 2002 Mar;31(1):21–24. [PubMed] [Google Scholar]
  15. Pearson J. D., Morrell C. H., Gordon-Salant S., Brant L. J., Metter E. J., Klein L. L., Fozard J. L. Gender differences in a longitudinal study of age-associated hearing loss. J Acoust Soc Am. 1995 Feb;97(2):1196–1205. doi: 10.1121/1.412231. [DOI] [PubMed] [Google Scholar]
  16. Piltcher O., Cigana L., Friedriech J., Ribeiro F. A., da Costa S. S. Sensorineural hearing loss among sickle cell disease patients from southern Brazil. Am J Otolaryngol. 2000 Mar-Apr;21(2):75–79. doi: 10.1016/s0196-0709(00)85001-2. [DOI] [PubMed] [Google Scholar]
  17. Rahimy Mohamed Cherif, Gangbo Annick, Ahouignan Gilbert, Adjou Roselyn, Deguenon Chantal, Goussanou Stephanie, Alihonou Eusebe. Effect of a comprehensive clinical care program on disease course in severely ill children with sickle cell anemia in a sub-Saharan African setting. Blood. 2003 Apr 17;102(3):834–838. doi: 10.1182/blood-2002-05-1453. [DOI] [PubMed] [Google Scholar]
  18. Tsibulevskaya G., Oburra H., Aluoch J. R. Sensorineural hearing loss in patients with sickle cell anaemia in Kenya. East Afr Med J. 1996 Jul;73(7):471–473. [PubMed] [Google Scholar]
  19. Yetunde A., Anyaegbu C. C. Profile of the Nigerian sickle cell anaemia patients above 30 years of age. Cent Afr J Med. 2001 Apr;47(4):108–111. [PubMed] [Google Scholar]

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