Nurdan Erol

Dr. Nurdan Erol


Research Focus & Metrics

Academic Career Length

22Years (2005-Present)

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

Representative Publications

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19 August 2021 in Cardiology in the Young
Verified
Journal Article
Closed access
PDF file
NENurdan Erol
Nurdan Erol
AAAbdullah Alpinar
Abdullah Alpinar
CECigdem Erol
Cigdem Erol
ESErdal Sari
Erdal Sari
KAKubra Alkan
Kubra Alkan
Objective: This study was conducted to evaluate the persisting Covid-19-related symptoms of the cases included in our study and to assess their cardiac findings to determine the impact of Covid-19 on children’s cardiovascular health.Methods: In this study, 121 children between the ages of 0– and 18 with Covid-19 were evaluated based on their history, blood pressure values, and electrocardiography and echocardiography results. These findings were compared with the findings of the control group which consisted of 95 healthy cases who were in the same age range as the study group and did not have Covid-19. The results were evaluated using the statistics program, SPSS 21.Results: There was no significant difference between the study group and the control group in terms of age, weight, and body mass index. The clinical symptoms (chest and back pain, dizziness, headache, palpitation, fatigue, shortness of breath, loss of balance, coughing) of 37.2% of the cases persisted for at least 1 month after Covid-19 recovery. Statistically significant differences were found in systolic blood pressure, left ventricular ejection fraction, relative wall thickness, and tricuspid annular plane systolic excursion.Conclusion: The continuation of some cases’ clinical symptoms post-recovery indicates that long Covid infection can be observed in children. The fact that statistically significant differences were observed between the echocardiographic parameters of the study and control groups suggests that Covid-19 may have effects on the cardiovascular system. To shed light on the long Covid cases among children and the infection’s cardiac impacts, it would be beneficial to conduct more comprehensive studies on this matter.

11 August 2011 in The International Journal of Cardiovascular Imaging
Verified
Journal Article
Closed access
PDF file
AEAbdullah Erdem
Abdullah Erdem
TSTurkay Sarıtas
Turkay Sarıtas
CZCenap Zeybek
Cenap Zeybek
IYIlker Kemal Yucel
Ilker Kemal Yucel
NENurdan Erol
Nurdan Erol
ACAhmet Celebı
Ahmet Celebı

1 March 2019 in International Journal of Medical Informatics
Verified
Journal Article
Closed access
IEİlKim Ecem Emre
İlKim Ecem Emre
NENurdan Erol
Nurdan Erol
YAYusuf İzZet Ayhan
Yusuf İzZet Ayhan
YÖYalçın Özkan
Yalçın Özkan
ÇEÇiğdem Erol
Çiğdem Erol

13 April 2013 in Catheterization and Cardiovascular Interventions
Verified
Journal Article
Closed access
PDF file
TSTurkay Saritas
Turkay Saritas
MKMehmet Gungor Kaya
Mehmet Gungor Kaya
YLYat Yin Lam
Yat Yin Lam
AEAbdullah Erdem
Abdullah Erdem
CACelal Akdeniz
Celal Akdeniz
ACAhmet Celebi
Ahmet Celebi

1 July 2013 in Balkan Medical Journal
Verified
Journal Article
Closed access
IDIbrahim Halil Demir
Ibrahim Halil Demir
AEAbdullah Erdem
Abdullah Erdem
TSTurkay Saritas
Turkay Saritas
FDFadli Demir
Fadli Demir
NENurdan Erol
Nurdan Erol
ACAhmet Celebi
Ahmet Celebi
Aortopulmonary window (APW) is a communication between the ascending aorta and the pulmonary artery in the presence of two separate semilunar valves and is the rarest of septal defects. To present our experience with the diagnosis and outcome of APW cases. Retrospective cohort study. Between June 2003 and October 2011, thirteen patients were diagnosed with APW. Clinical features of patients, findings of echocardiographic and angiographic examination, results of surgical intervention and follow-up were reviewed retrospectively. Eleven children (10 days to 16 years), underwent surgical correction of APW. In a 12-month-old boy, the defect was repaired by the transcatheter approach. In addition to APW repair, closure of VSD was performed in 2 patients. APW were associated with interruption in two patients; one also had a complex pathology. None of the patients died due to complications of surgical or transcatheter procedures. After a median follow-up period of 40 months, the patients were asymptomatic and none of them required additional medication, except for the patient with complex pathology including an interrupted aortic arch, who underwent balloon angioplasty for recoarctation. In any infant with the findings of congestive heart failure and failure to thrive, APW must be kept in mind as a differential diagnosis. In isolated APW cases before 6 months of age, echocardiography is often sufficient for diagnosis. In complex cases, cardiac catheterisation is performed for the comprehensive evaluation of associated defects. After 6 months, cardiac catheterisation could be utilised to perform vasoreactivity testing and, if possible, to close the defect.

9 June 2005 in Journal of Tropical Pediatrics
Verified
Journal Article
Closed access
NKNihal Karatoprak
Nihal Karatoprak
ZAZeynep Atay
Zeynep Atay
NENurdan Erol
Nurdan Erol
SGSevil Bilir Goksugur
Sevil Bilir Goksugur
OCOmer Ceran
Omer Ceran
To present a rare case of actinomycotic suppurative thyroiditis in an infant with provision of the etiology, pathogenesis, clinical findings and treatment of this rare disease. A report of an 18-month-old female infant who presented with fever, erythema, induration and tenderness of the neck. The patient had the diagnosis of acute suppurative thyroiditis after a series of laboratory evaluation. She was treated successfully with surgical debridement and intravenous penicillin G. Although rare, Actinomyces spp. should be considered in the etiology of acute suppurative thyroiditis. Because of its fastidious nature the probability of positive culture is low, thus, the microbiology laboratory should be called in advance to make preparations before culture and transport.