This study revealed negative correlation between NLR and Stroop interference scores. We need further prospective studies with larger sample size to investigate role of inflammation on cognitive functions.
BackgroundNeeds based biopsychosocial distress instrument for cancer patients (CANDI) is a scale based on needs arising due to the effects of cancer.ObjectivesThe aim of this research was to determine the reliability and validity of the CANDI scale in the Turkish language.Patients and MethodsThe study was performed with the participation of 172 cancer patients aged 18 and over. Factor analysis (principal components analysis) was used to assess construct validity. Criterion validities were tested by computing Spearman correlation between CANDI and hospital anxiety depression scale (HADS), and brief symptom inventory (BSI) (convergent validity) and quality of life scales (FACT-G) (divergent validity). Test-retest reliabilities and internal consistencies were measured with intraclass correlation (ICC) and Cronbach-α.ResultsA three-factor solution (emotional, physical and social) was found with factor analysis. Internal reliability (α = 0.94) and test-retest reliability (ICC = 0.87) were significantly high. Correlations between CANDI and HADS (rs = 0.67), and BSI (rs = 0.69) and FACT-G (rs = -0.76) were moderate and significant in the expected direction.ConclusionsCANDI is a valid and reliable scale in cancer patients with a three-factor structure (emotional, physical and social) in the Turkish language.
INTRODUCTION: Breast-cancer is a common-cause of death in women.(1) We investigated the effects of before/after-NACT on hemoglobin-albumin-lymphocyte-platelet (HALP) scores and of changes therein on clinical/pathological-responses. MATERIALS AND METHODS: One-hundred-twenty-seven breast-cancer-patients receiving-NACT between December 2009 -January 2019 were investigated retrospectively. RESULTS: The mean -age was 50.3±12.3 (min 27 -max 79), and 125 patients (98.4 %) were women. Fiftyfour (42.5 %) were premenopausal and 71 (55.9 %) postmenopausal. Invasive-ductal-carcinoma was present in 111 patients (92.5 %). Eighty patients (70.2 %) were ≤ T2 and 34 (29.8 %) > T2. Lymph-node-status was positive in 99 patients (83.2 %) and negative in 20 (16.8 %). Ki-67 was ≤ 10 % in 22 (28.9 %), 11-20 % in 23 (30.3 %), and > 20 % in 31 (40.8 %). Complete clinical response was observed in 27 (21.3 %), partialresponse in 76 (59.8 %), stable-disease in 21 (16.5 %), and progressive-disease in 3 patients (2.4 %). The objective-response-rate (ORR) was 103 (81.1 %). Pathological-complete-response (pCR) was observed in 24 patients (18.9 %). ORR was higher in Ki-67 > 20 % compared to ≤ 10 % and 10-20 % (90.3 % vs 59.0 % / 78.3 %, respectively, p: 0.027), but no difference occurred in pCR. Neutrophil-lymphocyte-ratio (NLR), platelet-lymphocyte-ratio (PLR), prognostic-nutritional-index (PNI), and HALP were measured before/after NACT. Associations with ORR and pCR were investigated via changes in these with NACT (excepting-PNI), but no-signifi cant results emerged. CONCLUSIONS: Higher ORR occurred post-NACT in patients with Ki-67 >20 %, while NLR, PLR, PNI, and HALP before/after-NACT and post-NACT-changes (excepting-PNI) had no-effect on ORR/pCR (Tab. 5, Ref. 21).
Aims
Insulin degludec/aspart (IDegAsp) and insulin glargine U300 (IGlarU300) have recently emerged as popular new‐generation insulin analogues. The aim of this real‐life study was to investigate the patient profiles in which IGlarU300 and IDegAsp were preferred and the insulin combinations after which each of them were mostly used and also to analyse the effect of these two insulin analogues on blood glucose regulation and hypoglycaemia.
Materials and Methods
The retrospective study included 174 patients that were switched from basal insulin, basal‐bolus insulin, or premixed insulin to IGlarU300 or IDegAsp due to uncontrolled blood glucose levels or history of hypoglycaemia. Hypoglycaemia, body weight, body mass index (BMI), fasting plasma glucose (FPG) and HbA1c levels over 3‐month periods were evaluated for each patient.
Results
There were 84 and 90 patients in the IGlarU300 and IDegAsp groups, respectively. Body weight was similar in both groups. Baseline FPG and HbA1c levels in the IGlarU300 and IDegAsp groups were 9.0%, 175.5 mg/dL and 9.4%, 193.5 mg/dL, respectively. A significant decrease was found in FPG and HbA1c levels in both groups (138.5, 7.8 vs 141.5, 8.2; P < .001 for all). Moreover, a significant weight gain was observed in both groups (P < .05 for both). The prevalence of hypoglycaemia in both groups decreased significantly and consistently between months 1 and 9 (P < .001). At month 12, although this decrease continued in the IGlarU300 group (P = .013), no significant decrease was observed in the IDegAsp group (P = .057).
Conclusion
Both twice‐daily IDegAsp ± bolus insulin and IGlarU300 basal bolus insulin therapies are effective and safe treatment modalities.
Aims/Introduction: Insulin Degludec/Aspart (IDegAsp) and Insulin
Glargine U300 (IGlarU300) have recently emerged as popular
new-generation insulin analogs. The aim of this real-life study was to
investigate the patient profiles in which IGlarU300 and IDegAsp were
preferred and the insulin combinations after which each of them were
mostly used, and also to analyze the effect of these two insulin analogs
on blood glucose regulation and hypoglycemia. Materials and Methods: The
retrospective study included 174 patients that were switched from basal
insulin, basal+bolus insulin, or premixed insulin to IGlarU300 or
IDegAsp due to uncontrolled blood glucose levels or history of
hypoglycemia. Hypoglycemia, body weight, body mass index (BMI), fasting
blood glucose (FBG), and HbA1c levels over three-month periods were
evaluated for each patient. Results: There were 84 and 90 patients in
the IGlarU300 and IDegAsp groups, respectively. Body weight was similar
in both groups. Baseline FBG and HbA1c levels in the IGlarU300 and
IDegAsp groups were 9.0%, 175.5 mg/dl and 9.4%, 193.5 mg/dl,
respectively. A significant decrease was found in FBG and HbA1c levels
in both groups (138.5, 7.8 vs. 141.5, 8.2; p<0.001 for all).
Moreover, a significant weight gain was observed in both groups
(p<0.05 for both). The prevalence of hypoglycemia in both
groups decreased significantly and consistently between month 1 and 9
(p<0.001). At month 12, although this decrease continued in
the IGlarU300 group (p=0.013), no significant decrease was observed in
the IDegAsp group(p=0.057). Conclusion: Both twice-daily IDegAsp±bolus
insulin and IGlarU300+bolus insulin therapies are effective and safe
treatment modalities.
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