Derya nazlı Bugdaycı

Prof. Dr. Derya nazlı Bugdaycı

orcid

Research Focus & Metrics

Academic Career Length

18Years (2009-Present)

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

Representative Publications

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7 December 2010 in Archives of Gerontology and Geriatrics
Verified
Journal Article
Closed access
DBDerya nazlı Bugdaycı
Derya nazlı Bugdaycı
NPNurdan Paker
Nurdan Paker
DDDidem Dere
Didem Dere
EÖEmel Özdemir
Emel Özdemir
NINurhan Ince
Nurhan Ince

30 April 2009 in Journal of Stroke and Cerebrovascular Diseases
Verified
Journal Article
Closed access
NPNURDAN PAKER
NURDAN PAKER
DBDerya nazlı Bugdaycı
Derya nazlı Bugdaycı
DTDemet Tekdos
Demet Tekdos
CDCaglayan Dere
Caglayan Dere
BKBetul Kaya
Betul Kaya

Verified
Journal Article
Open access
PDF file
MOMediha Gonenc Ortakoylu
Mediha Gonenc Ortakoylu
ABAyse Bahadir
Ayse Bahadir
SISinem Iliaz
Sinem Iliaz
DBDerya nazlı Bugdaycı
Derya nazlı Bugdaycı
MUMehmet Atilla Uysal
Mehmet Atilla Uysal
SOSeda Tural Onur
Seda Tural Onur
It is important to identify cases of latent tuberculosis infection (LTBI) who are at risk for tuberculosis (TB) reactivation. We aimed to evaluate the performance of interferon (IFN)-gamma-inducible protein 10 (IP-10) as a marker to detect LTBI in patients with inflammatory rheumatic diseases (IRD). This study comprised 76 consecutive subjects with IRD. Patients with a history of TB or having active TB were excluded. In all patients, IP-10 level was measured and tuberculin skin test (TST) and QuantiFERON-TB Gold In-Tube test (QFT-GIT) were performed. Seventy patients with complete test results were analyzed. Twenty-one (30%) QFT-GIT-positive patients were defined as having LTBI. IP-10 yielded 2197 pg/mL cut-off point. At this cut-off point, IP-10 showed 89% specificity with a sensitivity of 91% (AUC: 0.950, 95% CI 0.906–0.994). TST, QFT-GIT, and IP-10 were positive in 77.1%, 30%, and 44.3% of the patients, respectively. Concordance among the results of TST, QFT-GIT, and IP-10 tests was evaluated. Agreement was poor between IP-10 and TST (58.6%, κ = 0.19), whereas it was good between QFT-GIT and IP-10 (84.3%, κ = 0.65). The results of the present study demonstrated that sensitivity and specificity of released IP-10 were as high as those of QFT-GIT in indicating LTBI in IRD patient group.

18 November 2020 in Neurourology and Urodynamics
Verified
Journal Article
Closed access
PDF file
BÖBülent Önal
Bülent Önal
EKElif A. Kırlı
Elif A. Kırlı
BSBerin Selçuk
Berin Selçuk
DBDerya Buğdaycı
Derya Buğdaycı
GCGünay Can
Günay Can
BÇBülent Çetinel
Bülent Çetinel

19 November 2024 in Disability and Rehabilitation
Verified
Journal Article
Closed access
NPNURDAN PAKER
NURDAN PAKER
BABüşra Şirin Ahısha
Büşra Şirin Ahısha
FKFatma Nur Kesiktas
Fatma Nur Kesiktas
DBDerya nazlı Bugdaycı
Derya nazlı Bugdaycı
YÖYelda Soluk Özdemir
Yelda Soluk Özdemir
This study aimed to investigate the validity and reliability of the 2-Minute Step Test (2MST) in patients with lumbar spinal stenosis (LSS). This cross-sectional study involved 55 volunteers, aged 18-80, diagnosed with lumbar spinal stenosis. The participants were assessed using the 2MST, the 2-Minute Walk Test (2MWT), the 6-Minute Walk Test (6MWT), the Visual Analogue Scale (VAS), and the Oswestry Disability Index (ODI). To evaluate the reliability of the 2MST, test-retest reliability was determined by administering the 2MST again after a 7-day interval. The reliability analysis included the intraclass correlation coefficient (ICC) with a 95% confidence interval (CI), standard error of measurement (SEM), and minimum detectable change at the 95% confidence level (MDC95). For concurrent validity, the correlations of the 2MST with the 2MWT, 6MWT, and ODI were assessed. The 2MST exhibited excellent test-retest reliability (ICC = 0.94, SEM = 5.56, MDC95=15.41) in LSS patients. Additionally, the 2MST showed significant correlations with the 2MWT (r = 0.842, p < 0.001), 6MWT (r = 0.819, p < 0.001), and ODI score (r = -0.722, p < 0.001). This study demonstrated that the 2MST is a valid and reliable tool for assessing exercise capacity in individuals with LSS. NCT06060821.