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  <channel rdf:about="http://localhost:8080/xmlui/handle/123456789/11775">
    <title>DSpace Collection: 159-250</title>
    <link>http://localhost:8080/xmlui/handle/123456789/11775</link>
    <description>159-250</description>
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      <rdf:Seq>
        <rdf:li rdf:resource="http://localhost:8080/xmlui/handle/123456789/11907" />
        <rdf:li rdf:resource="http://localhost:8080/xmlui/handle/123456789/11905" />
        <rdf:li rdf:resource="http://localhost:8080/xmlui/handle/123456789/11902" />
        <rdf:li rdf:resource="http://localhost:8080/xmlui/handle/123456789/11900" />
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    <dc:date>2026-04-08T23:14:10Z</dc:date>
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  <item rdf:about="http://localhost:8080/xmlui/handle/123456789/11907">
    <title>Pre- and post-centrifugation stability of total and free prostate specific antigen samples at room temperature storage conditions</title>
    <link>http://localhost:8080/xmlui/handle/123456789/11907</link>
    <description>Title: Pre- and post-centrifugation stability of total and free prostate specific antigen samples at room temperature storage conditions
Authors: Ilardo, Claudio; Hammer-Dedet, Florence
Abstract: Objectives: Considering the recommendations of literature, it was important to note the potential for differences in&#xD;
pre- and post-analytical storage conditions at room temperature between total and free prostate-specific antigen. The&#xD;
aim of our study was to establish whether it would be appropriate to align the pre- and post-analytical times for the&#xD;
determination of free prostate-specific antigen (fPSA) with those for total prostate-specific antigen (tPSA).&#xD;
Methods: Two blood samples were taken from 48 male patients aged 60 to 84. One specimen was centrifuged within&#xD;
one hour of collection. Each sample was tested immediately for total and free PSA. The second blood sample was kept&#xD;
at room temperature for 12 hours before being tested and then reanalyzed 24 hours after blood sampling. Serum specimens&#xD;
were analyzed on the Roche Cobas E801.&#xD;
Results: There were no notable alterations in any PSA forms (p=0.866 and 0.971) or calculated ratios (Kappa=1) for&#xD;
the blood sample that was stored at room temperature for 12 hours prior to processing. Furthermore, all forms of PSA&#xD;
demonstrated stability (p=0.956 and 0.901), and fPSA/tPSA ratios showed good agreement in serum for up to 24 hours&#xD;
at room temperature (Kappa=1).&#xD;
Conclusion: It would be beneficial to extend the pre- and post-analysis times of fPSA to align them with those of tPSA.&#xD;
Following the elevated tPSA discovery, investigating fPSA could be more streamlined, offering an improved patient&#xD;
management solution.&#xD;
Keywords: fPSA/tPSA ratios, free prostate-specific antigen, in vitro stability, total prostate specific antigenstorage</description>
    <dc:date>2025-01-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://localhost:8080/xmlui/handle/123456789/11905">
    <title>Pre- and post-centrifugation stability of total and free prostate specific antigen samples at room temperature storage conditions</title>
    <link>http://localhost:8080/xmlui/handle/123456789/11905</link>
    <description>Title: Pre- and post-centrifugation stability of total and free prostate specific antigen samples at room temperature storage conditions
Authors: Ilardo, Claudio
Abstract: Objectives: Considering the recommendations of literature, it was important to note the potential for differences in&#xD;
pre- and post-analytical storage conditions at room temperature between total and free prostate-specific antigen. The&#xD;
aim of our study was to establish whether it would be appropriate to align the pre- and post-analytical times for the&#xD;
determination of free prostate-specific antigen (fPSA) with those for total prostate-specific antigen (tPSA).&#xD;
Methods: Two blood samples were taken from 48 male patients aged 60 to 84. One specimen was centrifuged within&#xD;
one hour of collection. Each sample was tested immediately for total and free PSA. The second blood sample was kept&#xD;
at room temperature for 12 hours before being tested and then reanalyzed 24 hours after blood sampling. Serum specimens&#xD;
were analyzed on the Roche Cobas E801.&#xD;
Results: There were no notable alterations in any PSA forms (p=0.866 and 0.971) or calculated ratios (Kappa=1) for&#xD;
the blood sample that was stored at room temperature for 12 hours prior to processing. Furthermore, all forms of PSA&#xD;
demonstrated stability (p=0.956 and 0.901), and fPSA/tPSA ratios showed good agreement in serum for up to 24 hours&#xD;
at room temperature (Kappa=1).&#xD;
Conclusion: It would be beneficial to extend the pre- and post-analysis times of fPSA to align them with those of tPSA.&#xD;
Following the elevated tPSA discovery, investigating fPSA could be more streamlined, offering an improved patient&#xD;
management solution.&#xD;
Keywords: fPSA/tPSA ratios, free prostate-specific antigen, in vitro stability, total prostate specific antigenstorage</description>
    <dc:date>2025-01-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://localhost:8080/xmlui/handle/123456789/11902">
    <title>The serum NF-κB and adiponectin levels in patients with acute pancreatitis</title>
    <link>http://localhost:8080/xmlui/handle/123456789/11902</link>
    <description>Title: The serum NF-κB and adiponectin levels in patients with acute pancreatitis
Authors: Fevziye Mısırlıoglu, Naile
Abstract: Objectives: This study aimed to evaluate whether serum nuclear factor-kappa B (NF-κB) and adiponectin levels can&#xD;
provide insight into disease progression and serve as potential biomarkers for predicting disease severity in patients&#xD;
with acute pancreatitis (AP).&#xD;
Methods: A total of 49 patients diagnosed with AP and admitted to the Emergency Department of Gaziosmanpaşa&#xD;
Training and Research Hospital were enrolled. An age-matched control group of 49 healthy individuals without AP was&#xD;
also included. Serum levels of NF-κB and adiponectin were measured and compared between groups.&#xD;
Results: Patients with AP exhibited significantly elevated serum NF-κB levels and reduced adiponectin levels compared&#xD;
to the control group (both p&lt;0.001). A strong negative correlation was observed between adiponectin and NF-&#xD;
κB levels in the AP group (r=–0.865, p&lt;0.05). Receiver operating characteristic (ROC) analysis determined the optimal&#xD;
cut-off value for adiponectin as 3.4, with a sensitivity and specificity of 1.000. The optimal cut-off for NF-κB was 1.8, with&#xD;
a sensitivity of 1.000 and specificity of 0.96.&#xD;
Conclusion: The findings suggest that serum NF-κB and adiponectin levels may be valuable biomarkers for assessing&#xD;
disease severity in AP. Their combined use or integration with existing scoring systems could enhance prognostic accuracy.&#xD;
Further experimental and clinical studies are necessary to evaluate the therapeutic potential of adiponectin and&#xD;
to validate these biomarkers for routine clinical use.&#xD;
Keywords: Acute pancreatitis, adiponectin, disease severity, inflammation, nuclear factor kappa B</description>
    <dc:date>2025-01-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://localhost:8080/xmlui/handle/123456789/11900">
    <title>Machine learning-assisted prediction of positive urine cultures using urinalysis and hemogram data: A retrospective cohort study</title>
    <link>http://localhost:8080/xmlui/handle/123456789/11900</link>
    <description>Title: Machine learning-assisted prediction of positive urine cultures using urinalysis and hemogram data: A retrospective cohort study
Authors: Demirci, Ferhat; Arikan, Yusuf
Abstract: Objectives: Urinary tract infections (UTIs) are common and often lead to unnecessary urine culture testing, increasing&#xD;
costs and delaying treatment. This study aims to develop a machine learning (ML) model using urinalysis and hemogram&#xD;
data to predict urine culture positivity and reduce unnecessary testing.&#xD;
Methods: We retrospectively analyzed data from 12,433 patients who underwent urinalysis, urine culture, complete&#xD;
blood count, and CRP testing. After preprocessing and exclusion criteria, data were split into training, test, and validation&#xD;
sets. H2O AutoML was employed to develop and evaluate various ML algorithms.&#xD;
Results: The gradient boosting model demonstrated an AUC-ROC of 0.822 with high sensitivity (73.8%) and negative&#xD;
predictive value (90.4%), making it reliable in ruling out negative cases. Urinary leukocytes, nitrite, and bacterial count&#xD;
were identified as top predictors.&#xD;
Conclusion: ML-based models can improve diagnostic accuracy and reduce unnecessary urine cultures. These models&#xD;
have the potential to be integrated into clinical workflows to enhance cost-effectiveness and minimize empirical antibiotic&#xD;
use.&#xD;
Keywords: Artificial intelligence, diagnostic model, machine learning, predictive analytics, urinalysis, urinary tract infection,&#xD;
urine culture</description>
    <dc:date>2025-01-01T00:00:00Z</dc:date>
  </item>
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