Online ISSN: 3007-0244,
Print ISSN:  2410-4280
QUALITY LIFE OF CHILDREN WITH CONGENITAL MALFORMATIONS OF THE EAR
Introduction. Congenital ear anomalies are congenital changes in the size, shape, or position of various elements of the outer, middle and inner ear, which can lead to conditions ranging from mild hearing loss to absolute deafness, speech impairment, limited social activity and personality disability. Although microtia is not life threatening, it significantly affects the emotional and psychological well-being of the affected child and their parents. These definitions, in turn, are fundamental in the formation of the quality of life of children with congenital malformations of the ear. Aim. To show the importance of the correct assessment of the quality of life of children aged from 2 to 7 with congenital malformations of the ear. Materials and methods. The cross-sectional study. From the compiled general list of children with microtia in the Republic of Kazakhstan, by random sampling by using the random number generator of the Excel program, the sample of children aged from 2 to 7 with a confirmed diagnosis was formed, according to the ICD code X: Q16.0 Congenital absence of the auricle, Q16.1 Congenital absence, atresia and stricture of the auditory passage (external), Q17.2 Microtia. For collecting personal data it was used an on-line service for creating surveys (Google Forms). After preliminary creation of a Google account, the web page was developed with a questionnaire posted on it.For the sociological survey of children, the Russian and validated Kazakh versions of the International questionnaire PedsQL ™ 4.0 GenericCoreScales for parents / guardians of children 2-4 and 5-7 years old were used.Exclusion criteria from the survey: disagreement or lack of consent of the informed parents and / or child; unfilled questionnaires (return of empty formats); when by assessing the quality of life, patients who had acute illnesses within a month before the study or mental disorders.Statistical processing of the research data was carried out using the SPSS 23 package. Comparative analysis between variables was carried out using non-parametric methods: the χ2 test, the method of normalized residuals, the risk odds ratio and the Kruskal-Wallis H-test, the Kendall-Spearman-rank correlation, pairwise comparison of samples using the Kolmogorov-Smirnov-two-sample-z-test. Results and conclusions: The used research method made it possible to define the quantitative assessment of the quality of life of children with microtia and atresia of the external auditory canal in the age of 2-7 years. It was found that in general, in both groups, high indicators were noted on the scale of physical functioning. Parents of previously operated children showed the lowest scores on all four scales of the quality of life indicator. Patients with average and high material well-being gave significantly more often low scores in all parameters. Children with bilateral pathology noted significantly more often low scores on the scales of social and role functioning. Low scores were revealed in parameters of emotional, social and role functioning in the group of 5-7 year old children in comparison with 2-4 year old children. Conclusions. According to the obtained data we came to the conclusion that this research methodology could be acceptable for Kazakhstan, which gives also new opportunities for a comprehensive assessment of the state of health and targeted selection of children for treatment.
Assel Imangaliyeva¹, https://orcid.org/0000-0001-9865-3189 Rimma Sautbayeva¹, https://orcid.org/0000-0002-0935-9840 Тatyana Slazhnеva², https://orcid.org/0000-0003-3632-486X Аigul Medeulova¹, https://orcid.org/0000-0001-6941-4525 Zhanetta Mukanova¹, https://orcid.org/0000-0001-5272-1190 Amangeldy Kulimbetov¹, https://orcid.org/0000-0003-2994-6935 Islam Kamalov¹, https://orcid.org/0000-0001-6047-2411 1 Kazakh National Medical University named after S.D.Asfendizarov, Almaty c., Republic of Kazakhstan; 2 RSE with REM "National Center for Public Health" of the Ministry of Health Republic Kazakhstan, Almaty c., Republic of Kazakhstan.
1. Имангалиева А.А., Медеулова А.Р., Муканова Ж.Т., Слажнева Т.И., Бахытова Н.Б. Распространенность врожденных пороков развития уха в Республике Казахстан // Вестник КазНМУ, 2020. №1. С. 285-287. ISSN 2524-0692 2. Alexis J.L., Daniel Im D., Sheryl L.L. Early Familial Experiences With Microtia: Psychosocial Implications for Pediatric Providers // Clinical Pediatrics. Jun 2018, Vol. 57 Issue 7, p775-782. 8p. 3. Akter F; Mennie JC; Stewart K; Bulstrode N. Patient reported outcome measures in microtia surgery. Journal of plastic, reconstructive & aesthetic surgery // J Plast Reconstr Aesthet Surg] 2017 Mar; Vol. 70 (3), pp. 416-424. 4. Bukowski W.M., Sandberg D. Peer relationships and quality of life // Acta Paediatr Suppl. 1999. 88: 108-9 5. Christakis D.A., Johnston B.D., Council F.A. Methodologic issues in pediatric outcomes research // Ambul Pediatr. 2001. 1: 59-62 6. Cox M.J., Paley B. Families as systems // Annu Rev Psychol. 1997. 48: 243-67. 7. Du J.M., Zhuang H.X., Chai J.K., Liu G.F., Wang Y. Guo W.H. Psychological status of congenital microtia patients and relative influential factors: analysis of 410 cases // Zhonghua Yi Xue Za Zhi. 2007, Feb 06. Vol. 87 (6), pp. 383-7 8. Genc S., Kahraman E., Ozel H.E., Arslan I.B., Demir A., Selcuk A. Microtia and congenital aural atresia // The Journal of craniofacial surgery. 2012 Nov; Vol. 23 (6), pp. 1733-5 9. Hamlet C., Harcourt D. Exploring the Experiences of Adults With Microtia: A Qualitative Study // Cleft Palate Craniofac J. 2020. 57(10), 1230-12. 10. Okajima H, Takeichi Y, Umeda K, Baba S. Clinical analysis of 592 patients with microtia. Acta Oto-Laryngologica. 1996;525:18-24 11. Johns A.L., Lewin S.L., Im D.D. Teasing in younger and older children with microtia before and after ear reconstruction // Journal of plastic surgery and hand surgery. 2017, Jun. Vol. 51 (3), pp. 205-209. 12. Klockars T., Rautio J. Embryology and epidemiology of microtia. Department of Otorhinolaryngology, Helsinki University Central Hospital, Helsinki, Finland // Facial plastic surgery. 2009 Aug; Vol. 25 (3), pp. 145-8. 13. Luquetti D.V., Heike C.L., Hing A.V., Cunningham M.L., Cox T.C. Microtia: epidemiology and genetics // Am J Med Genet A. 2012, Jan, Vol. 158A (1), pp. 124-39. 14. Ross M.T., Hutchinson C., Courtney R., Arnott W.L., Woodruff M.A., Powell S.K. Aesthetic reconstruction of microtia: a review of current techniques and new 3D printing approaches // Virtual & Physical Prototyping. Jun 2018, Vol. 13 Issue 2, p.117-130 15. Stallings E.B., Isenburg J.L., Mai C.T., Liberman R.F., Moore C.A., Canfield M.A., Salemi J.L., Kirby R.S., Short T.D., Nembhard W.N., Forestieri N.E., Heinke D. Alverson C.J., Romitti P.A., Huynh M.P., Denson L.E., Judson E.M., Lupo P.J. Population-based birth defects data in the United States, 2011-2015: A focus on eye and ear defects // Birth defects research. 2018, Nov 15. Vol. 110 (19), pp. 1478-1486. 16. Suutarla S., Rautio J., Ritvanen A., Ala-Mello S., Jero J., Klockars T. Microtia in Finland: comparison of characteristics in different populations // International journal of pediatric otorhinolaryngology. 2007, Aug Vol. 71 (8), pp. 1211-7. 17. Sánchez O., Méndez J.R., Gómez E. Guerra D. Clinico-epidemiologic study of microtia // Investigacion clinica. 1997. Dec. Vol. 38 (4), pp. 203-17. 18. Tian-yu Zhang , Neil Bulstrode , Kay W. Chang and etc. International Consensus Recommendations on Microtia, Aural Atresia and Functional Ear Reconstruction // J Int Adv Otol 2019; 15(2): 204-8 DOI: 10.5152/iao.2019.7383, pp. 204-208. 19. Tsang W, Tong M, Ku P, Bhatia K, Yu J, Wong T, van Hasselt C. Contemporary solutions for patients with microtia and congenital aural atresia — Hong Kong experience // Journal of Otology. 2016;11(4):157-164. 20. Varni J., Seid M., Rode C. The Peds QL: measurement model for the pediatric quality of life inventory // Med Care. 1999. 37:126–139 21. Varni J., Seid M., Kurtin P. Peds QL 4.0: reliability and validity of the Pediatric Quality of Life Inventory version 4.0 generic core scales in healthy and patient populations. Med Care. 2001. 39:800–812 References: [1] 1. Imangaliyeva A.A., Medeulova A.R., Mukanova Zh.T., Slazhneva T.I., Bakhytova N.B. Rasprostranennost' vrozhdennykh porokov razvitiya ukha v Respublike Kazakhstan [Prevalence of congenitial malformations of the ear in the Republic of Kazakhstan]. Vestnik KazNMU [Herald KAZNMU], 2020. №1. pp. 285-287. ISSN 2524-0692
Number of Views: 166

Key words:

Category of articles: Original articles

Bibliography link

Imangaliyeva A., Sautbayeva R., Slazhnеva Т., Medeulova А., Mukanova Zh., Kulimbetov A., Kamalov I. Quality life of children with congenital malformations of the ear // Nauka i Zdravookhranenie [Science & Healthcare]. 2021, (Vol.23) 6, pp. 88-96. doi 10.34689/SH.2021.23.6.010

Авторизируйтесь для отправки комментариев