Željka Draušnik

Dr. Željka Draušnik


Research Focus & Metrics

Academic Career Length

11Years (2016-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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8 July 2016 in Hrvatska revija za rehabilitacijska istraživanja
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Journal Article
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ŽDŽeljka Draušnik
Željka Draušnik
VŠVesna Štefančić
Vesna Štefančić
TBTomislav Benjak
Tomislav Benjak
U Republici Hrvatskoj se, u Registru osoba s invaliditetom prati broj osoba s oštećenjem sluha kod kojih je utvrđen invaliditet temeljem tog oštećenja. Podatke u Registar dostavlja Zavod za vještačenje, profesionalnu rehabilitaciju i zapošljavanje osoba s invaliditetom. Prema Registru, u Hrvatskoj živi 13 609 osoba čiji je invaliditet uzrokovan oštećenjem sluha (0,32%), no uspoređujući taj podatak s podacima međunarodnih istraživanja nailazimo na velike razlike. Podaci o prevalenciji oštećenja sluha u svijetu pokazuju 16 puta veću učestalost od one trenutno evidentirane u Registru. Ostale međunarodne procjene također upućuju na veću prevalenciju oštećenja sluha nego što je zabilježena u Hrvatskoj. Jedan od glavnih razloga ovakvih razlika raspon je oštećenja sluha koji se uzima u obzir. U hrvatskom registru prati se broj osoba kod kojih je oštećenje sluha dovelo do invaliditeta, dok međunarodna istraživanja obuhvaćaju i blaža oštećenja koja ne dovode do invaliditeta. Drugi, jednako bitan, razlog jest činjenica da se međunarodna istraživanja temelje na procjenama, dok se za Hrvatsku koriste točni podaci prikupljeni putem rješenja o invaliditetu.

3 April 2020 in Sigurnost
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LPLovela Machala Poplašen
Lovela Machala Poplašen
ŽDŽeljka Draušnik
Željka Draušnik
DVDorja Vočanec
Dorja Vočanec
HBHana Brborović
Hana Brborović
SAŽETAK: Infografika je komunikacijski alat u digitalnom okruženju koji, širokoj zajednici, na lako razumljiv način vizualno predstavlja informaciju, podatke ili znanja. Ovaj rad prikazuje infografiku kao oblik komunikacije te...

28 October 2025 in Medicina
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Journal Article
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TBTomislav Benjak
Tomislav Benjak
AVAna Vuljanić
Ana Vuljanić
ŽDŽeljka Draušnik
Željka Draušnik
IBIrena Barišić
Irena Barišić
ZMZrinka Mach
Zrinka Mach
GVGorka Vuletić
Gorka Vuletić
Background and Objectives: Individuals with Down syndrome (DS) represent a specific and vulnerable population requiring improvements in public health and social policies to ensure equal opportunities, longer life expectancy, and better quality of life. Accurate epidemiological and demographic indicators are essential for planning and evaluating interventions. This study aims to assess the prevalence of DS in Croatia from 2014 to 2024, analyzing demographic characteristics and regional distribution. A comparative analysis with international data and a review of national policies related to persons with disabilities and DS are also included. Materials and Methods: Data on the prevalence of DS were collected from the National Registry of Persons with Disabilities, where reporting individuals with DS is mandatory for the realization of legal rights. This ensures high data quality and representativeness. Prevalence per 1000 live births was calculated based on data from the national birth database and the registry. Results: The overall prevalence of DS in Croatia increased from 3.7 to 5.3 per 10,000 population during the observed period, while prevalence among live-born infants ranged from 1.1 to 1.5 per 1000. Males were slightly more represented (52.5%). The most common comorbidities included congenital heart defects. The mean age of individuals with DS was 28 years, with 12 individuals recorded as being older than 65 years and one individual aged 85. Conclusions: The DS prevalence in Croatia is comparable to data from European Union countries. The observed increase in prevalence and in the total number of individuals with disabilities highlights the need for continuous development and adaptation of national policies. As a signatory of the Convention on the Rights of Persons with Disabilities, Croatia is actively working to improve its legislative framework and support systems to ensure equal rights and enhance quality of life for individuals with DS.