Edyta Sutkowska

Dr. Edyta Sutkowska

Wroclaw Medical University
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

View All Publications
9 July 2019 in Journal of Diabetes Research
Verified
Journal Article
Open access
PDF file
ESEdyta Sutkowska
Edyta Sutkowska
KSKrzysztof Sutkowski
Krzysztof Sutkowski
MSMichał Sokołowski
Michał Sokołowski
EFEdward Franek
Edward Franek
SDSzymon Dragan
Szymon Dragan
The abnormal plantar pressure distribution and value play a key role in the formation of plantar calluses and diabetic foot ulcer. The prevalence of the highest pressure different distribution and its association with various factors among patients with diabetes is not well known. The study purpose was to evaluate the prevalence of different regions for the highest pressure on the sole and its association with selected factors among patients with diabetes. Medical records of nonulcer patients were retrospectively analysed. The relationship between pressure patterns on the sole obtained during a pedobarographic test as a semiquantitative assessment with colourful print analysis and neuropathy, gender, age, and BMI was searched. The most common location of the highest pressure was the central part of the forefoot. No association was found between the different highest pressure regions and age, sensory neuropathy, calluses, and foot deformities. The highest pressure on the lateral part of the foot and midfoot was observed more often in females and in patients with a BMI≥35. The prevalence of the highest pressure on the forefoot was more common in patients with a BMI<35. Conclusions. The most frequent regions of the highest pressure on the sole in patients with diabetes were the central part of the forefoot (2-3 metatarsal heads) with no simple relationship to the assessed variables other than BMI<35. Female gender and higher BMI seem to be responsible for shifting the place of the highest pressure to other places of the foot.

18 November 2018 in BioMed Research International
Verified
Journal Article
Open access
PDF file
Agata StanekAgata Stanek
Agata Stanek
Bahare FazeliBahare Fazeli
Bahare Fazeli
SBStanisław Bartuś
Stanisław Bartuś
ESEdyta Sutkowska
Edyta Sutkowska

3 April 2012 in Annals of Oncology
Verified
Journal Article
Open access
PDF file
ATA. J. Tafur
A. J. Tafur
WWW. E. Wysokinski
W. E. Wysokinski
RMR. D. McBane
R. D. McBane
EWE. Wolny
E. Wolny
ESEdyta Sutkowska
Edyta Sutkowska
JHJ. A. Heit
J. A. Heit
Patients with active cancer are often on chronic anticoagulation and frequently require interruption of this treatment for invasive procedures. The impact of cancer on periprocedural thromboembolism (TE) and major bleeding is not known. Two thousand one hundred and eighty-two consecutive patients referred for periprocedural anticoagulation (2484 procedures) using a standardized protocol were followed forward in time to estimate the 3-month incidence of TE, major bleeding and survival stratified by anticoagulation indication. For each indication, we tested active cancer and bridging heparin therapy as potential predictors of TE and major bleeding. Compared with patients without cancer, active cancer patients (n = 493) had more venous thromboembolism (VTE) complications (1.2 % versus 0.2 % ; P = 0.001), major bleeding (3.4 % versus 1.7 % ; P = 0.02) and reduced survival (95 % versus 99 % ; P < 0.001). Among active cancer patients, only those chronically anticoagulated for VTE had higher rates of periprocedural VTE (2 % versus 0.16 % ; P = 0.002) and major bleeding (3.7 % versus 0.6 % ; P < 0.001). Bridging with heparin increased the rate of major bleeding in cancer patients (5 % versus 1 % ; P = 0.03) without impacting the VTE rate (0.7 % versus 1.4 % , P = 0.50). Cancer patients anticoagulated for VTE experience higher rates of periprocedural VTE and major bleeding. Periprocedural anticoagulation for these patients requires particular attention to reduce these complications.

1 April 2012 in Gene
Verified
Journal Article
Closed access
ESEdyta Sutkowska
Edyta Sutkowska
JGJustyna Gil
Justyna Gil
ASAgnieszka Stembalska
Agnieszka Stembalska
AHAneta Hill-Bator
Aneta Hill-Bator
ASAndrzej Szuba
Andrzej Szuba

3 June 2021 in Scientific Reports
Verified
Journal Article
Open access
PDF file
ESEdyta Sutkowska
Edyta Sutkowska
PFPaulina Fortuna
Paulina Fortuna
JWJerzy Wiśniewski
Jerzy Wiśniewski
KSKarolina Sutkowska
Karolina Sutkowska
PHPaweł Hodurek
Paweł Hodurek
BKBernadetta Kaluza
Bernadetta Kaluza
This prospective study aimed to analyze whether the patients with pre-diabetes (pre-DM) reach the TC (therapeutic concentration) of the metformin during repeated, low, constant drug dose. The guidelines do not recommend any metformin dose for this group of patients. Based on the previous study after a dose of 1700 mg/day the patients seem to reach the therapeutic drug concentration, which guarantees the glycemic effect. Twenty patients with new-diagnosed pre-DM were treated with a 1500 mg/day regimen of the metformin for 15 weeks. The serum concentration of the drug was assessed by liquid chromatography-mass spectrometry technique at 6 and 15 week of the treatment. The correlation of the serum metformin concentration with BMI (body mass index) and patients’ weight was also performed. The mean metformin concentration was: 4.65 μmol/L (± 2.41) and 5.41 μmol/L (± 3.44) (p = 0.27) after 6 and 15 weeks of the treatment respectively. There was a positive correlation between the serum concentration of the metformin and body weight (but not BMI) in the 15th week of the therapy (p = 0.04)- the higher body weight the higher concentration of the metformin. Patients with pre-diabetes can be successfully treated with a low dose of metformin, to reach the drug’s therapeutic concentration. Body weight can impact the metformin serum concentration during long-term treatment what should be taken into consideration when choosing the dose because of its pleiotropic effect e.g. on the cardiovascular system via reduction of the oxidative stress and would be not connected with the drug’s hypoglycemic effect.ClinicalTrials.gov number: NCT03398356; date of first registration: 01/07/2018.

18 December 2012 in Journal of Gastroenterology
Verified
Journal Article
Closed access
PDF file
ESEdyta Sutkowska
Edyta Sutkowska
RMRobert D. McBane
Robert D. McBane
ATAlfonso J. Tafur
Alfonso J. Tafur
KSKrzysztof Sutkowski
Krzysztof Sutkowski
DGDiane E. Grill
Diane E. Grill
WWWaldemar E. Wysokinski
Waldemar E. Wysokinski