Nese Saltoglu

Prof. Dr. Nese Saltoglu


Research Focus & Metrics

Academic Career Length

30Years (1997-Present)

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

Representative Publications

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9 June 2021 in Rheumatology International
Verified
Journal Article
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ESEmire Seyahi
Emire Seyahi
GBGuldaran Bakhdiyarli
Guldaran Bakhdiyarli
MOMert Oztas
Mert Oztas
MKMert Ahmet Kuskucu
Mert Ahmet Kuskucu
YTYeşim Tuyji Tok
Yeşim Tuyji Tok
VHVedat Hamuryudan
Vedat Hamuryudan

1 August 2010 in Clinical Microbiology and Infection
Verified
Journal Article
Closed access
NSNese Saltoglu
Nese Saltoglu
ADA. Dalkiran
A. Dalkiran
TTT. Tetiker
T. Tetiker
HBH. Bayram
H. Bayram
YTY. Tasova
Y. Tasova
MSM. Sert
M. Sert

30 January 2018 in International Journal Of Clinical Practice
Verified
Journal Article
Closed access
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AVAslı Vatan
Aslı Vatan
NSNese Saltoglu
Nese Saltoglu
MYMucahit Yemisen
Mucahit Yemisen
IBIlker Inanc Balkan
Ilker Inanc Balkan
SSSerkan Surme
Serkan Surme
SFStudy Group, Cerrahpasa Diabetic Foot
Study Group, Cerrahpasa Diabetic Foot

1 July 2015 in Clinical Microbiology and Infection
Verified
Journal Article
Closed access
NSNese Saltoglu
Nese Saltoglu
MYM. Yemisen
M. Yemisen
Onder ErgonulOnder Ergonul
Onder Ergonul
AKA. Kadanali
A. Kadanali
GKG. Karagoz
G. Karagoz
MOM. Ozyazar
M. Ozyazar

16 February 2015 in International Journal Of Clinical Practice
Verified
Journal Article
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PDF file
NSNese Saltoglu
Nese Saltoglu
RKR. Karali
R. Karali
MYM. Yemisen
M. Yemisen
ROR. Ozaras
R. Ozaras
IBI. I. Balkan
I. I. Balkan
ROR. Ozturk
R. Ozturk
We aimed to compare community-onset healthcare-associated (CO-HCA) and hospital-acquired (HA) urinary tract infections (UTIs) caused by extended-spectrum beta-lactamase (ESBL)-producing Escherichia coli in terms of epidemiology, clinical outcomes and antimicrobial activities.Patients from both groups with ESBL-producing E. coli detected by urine culture between January 2009 and January 2011 were included in this retrospective study. Relevant demographical, microbiologic and clinical data were obtained from case records.A total of 173 patients (mean age of 58 years, 74% female) were included, of whom 75 (43.4%) had a CO-HCA UTI and 98 (56.6%) had an HA UTI. Eighty (46.2%) patients had more than one comorbid disease, of whom 57 (32.5%) had urological problems. The most common clinical manifestations were pyelonephritis (43.9%) and urosepsis (16.2%). An age of > 65 years (p = 0.005) in addition to urinary catheterisation (p = 0.001), urosepsis (p = 0.001) and mortality (p = 0.001) were significantly more common in the HA UTI group. Acute cystitis (p = 0.027), complicated cystitis (p = 0.001) and non-urologic neoplasm (p = 0.032) were significantly more common in the CO-HCA UTI group. No isolate was resistant to carbapenems or fosfomycin. Sensitivities to nitrofurantoin, amikacin, trimethoprim sulfamethoxazole-trimoxazole and quinolones were 97.6%, 89%, 29.4% and 17.9% respectively. Both groups showed similar rates of antibiotic resistance.ESBL-producing E. coli should be taken into consideration in patients with a CO HCA UTI, not only in hospital settings but also in outpatient settings. We suggest ertapenem as a first-line empirical treatment for patients with an upper UTI and fosfomycin and nitrofurantoin for those with a lower UTI when ESBL-producing E. coli is suspected.

15 April 2021 in The International Journal of Lower Extremity Wounds
Verified
Journal Article
Closed access
PDF file
NSNese Saltoglu
Nese Saltoglu
SSSerkan Surme
Serkan Surme
EEElif Ezirmik
Elif Ezirmik
AKAyten Kadanali
Ayten Kadanali
AKAhmet Furkan Furkan Kurt
Ahmet Furkan Furkan Kurt
KGKLİMİK Society, Diabetic Foot Study Group
KLİMİK Society, Diabetic Foot Study Group
We aimed to determine pathogen microorganisms, their antimicrobial resistance patterns, and the effect of initial treatment on clinical outcomes in patients with diabetic foot infection (DFI). Patients with DFI from 5 centers were included in this multicenter observational prospective study between June 2018 and June 2019. Multivariate analysis was performed for the predictors of reinfection/death and major amputation. A total of 284 patients were recorded. Of whom, 193 (68%) were male and the median age was 59.9 ± 11.3 years. One hundred nineteen (41.9%) patients had amputations, as the minor (n = 83, 29.2%) or major (n = 36, 12.7%). The mortality rate was 1.7% with 4 deaths. A total of 247 microorganisms were isolated from 200 patients. The most common microorganisms were Staphylococcus aureus (n = 36, 14.6%) and Escherichia coli (n = 32, 13.0%). Methicillin resistance rates were 19.4% and 69.6% in S aureus and coagulase-negative Staphylococcus spp., respectively. Multidrug-resistant Pseudomonas aeruginosa was detected in 4 of 22 (18.2%) isolates. Extended-spectrum beta-lactamase-producing Gram-negative bacteria were detected in 20 (38.5%) isolates of E coli (14 of 32) and Klebsiella spp. (6 of 20). When the initial treatment was inappropriate, Klebsiella spp. related reinfection within 1 to 3 months was observed more frequently. Polymicrobial infection (p = .043) and vancomycin treatment (p = .007) were independent predictors of reinfection/death. Multivariate analysis revealed vascular insufficiency (p = .004), hospital readmission (p = .009), C-reactive protein > 130 mg/dL (p = .007), and receiving carbapenems (p = .005) as independent predictors of major amputation. Our results justify the importance of using appropriate narrow-spectrum empirical antimicrobials because higher rates of reinfection and major amputation were found even in the use of broad-spectrum antimicrobials.