48 results on '"Uysal, Fahrettin"'
Search Results
2. Effect of Magnesium on Ventricular Extrasystoles in Children.
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Uysal, Fahrettin, Turkmen, Hasan, Genc, Abdusselam, and Bostan, Ozlem M.
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MAGNESIUM , *TREATMENT effectiveness , *AMBULATORY electrocardiography , *DESCRIPTIVE statistics , *ARRHYTHMIA , *DIETARY supplements , *SYMPTOMS , *CHILDREN - Abstract
Magnesium (Mg) is a crucial element for cardiovascular system and its deficiency results in a variety of cardiac arrhythmias. The aim of this study is to determine the effect of oral Mg supplementation on the frequency of ventricular extrasystoles (VES) in children. Magnesium supplementation was given to 42 children who had VES without structural heart disease. Clinical, electrocardiographic, and Holter monitoring studies were reviewed. The mean baseline 24 h VES burden on Holter monitoring was 10.26% ± 4.13% and it was decreased to 6.62% ± 3.88% after. There was no significant difference between the pre-treatment serum Mg levels and the decrease in the frequency of VES. In conclusion, oral Mg therapy was found to be effective at suppressing VES in children regardless of serum Mg levels. Large and randomized studies are needed to demonstrate the effect of magnesium on VES suppression. [ABSTRACT FROM AUTHOR]
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- 2024
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3. Evaluation of Children with Aortic Coarctation: A Single-Center Experience.
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Türkmen, Hasan, Uysal, Fahrettin, Genç, Abdüsselam, Bostan, Özlem M., and Siğnak, Işık Şenkaya
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TRANSLUMINAL angioplasty , *CONGENITAL heart disease , *RISK assessment , *PEARSON correlation (Statistics) , *ACADEMIC medical centers , *T-test (Statistics) , *AORTIC coarctation , *QUESTIONNAIRES , *FISHER exact test , *RETROSPECTIVE studies , *MANN Whitney U Test , *DESCRIPTIVE statistics , *TREATMENT effectiveness , *EARLY intervention (Education) , *LONGITUDINAL method , *KAPLAN-Meier estimator , *MEDICAL records , *ACQUISITION of data , *DISEASE relapse , *COMPARATIVE studies , *DATA analysis software , *ECHOCARDIOGRAPHY , *PROPORTIONAL hazards models , *DISEASE risk factors - Abstract
Objective: Coarctation of the aorta (CoA) accounts for 3.5% of all congenital heart diseases in children. The clinical manifestations range from heart failure to asymptomatic hypertension. Treatment options include surgical repair, balloon angioplasty, and stenting. We aimed to investigate the long-term results of surgery and balloon angioplasty to identify the possible risk factors for recoarctation and predictors associated with early success in treatment modalities. Materials and Methods: The data of 138 children who underwent examinations at a tertiary center between 2015 and 2020 with the diagnosis of CoA were evaluated. The basic demographic characteristics, clinical and echocardiographic findings, results, and treatment methods of the patients were evaluated retrospectively. Results: The mean follow-up period was 75.1 months (range of 1-223). As initial treatment, 75 patients (60.5%) underwent balloon angioplasty, 44 (35.5%) underwent surgery, and 5 (4%) underwent stenting. The early success rate of balloon angioplasty and surgery was 72.5% and 79.5%, respectively. Recoarctation occurred in 47.6% of patients following the first therapy. The median reintervention-free survival time was 138 months for all patients and was significantly higher in the surgery group (P = .025). The recoarctation rate was slightly lower in the surgery group than in those who underwent balloon angioplasty, but it was not statistically significant. None of the clinical and echocardiographic findings were found to be associated with recoarctation or early success. Conclusion: The rate of recoarctation is still high in long-term follow-up after aortic coarctation treatment, and clinical and echocardiographic findings are insufficient to predict the chance of early success and the risk of recoarctation. [ABSTRACT FROM AUTHOR]
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- 2024
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4. Arterial tortuosity syndrome: 40 new families and literature review
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Beyens, Aude, Albuisson, Juliette, Boel, Annekatrien, Al-Essa, Mazen, Al-Manea, Waheed, Bonnet, Damien, Bostan, Ozlem, Boute, Odile, Busa, Tiffany, Canham, Nathalie, Cil, Ergun, Coucke, Paul J., Cousin, Margot A., Dasouki, Majed, De Backer, Julie, De Paepe, Anne, De Schepper, Sofie, De Silva, Deepthi, Devriendt, Koenraad, De Wandele, Inge, Deyle, David R., Dietz, Harry, Dupuis-Girod, Sophie, Fontenot, Eudice, Fischer-Zirnsak, Björn, Gezdirici, Alper, Ghoumid, Jamal, Giuliano, Fabienne, Diéz, Neus Baena, Haider, Mohammed Z., Hardin, Joshua S., Jeunemaitre, Xavier, Klee, Eric W., Kornak, Uwe, Landecho, Manuel F., Legrand, Anne, Loeys, Bart, Lyonnet, Stanislas, Michael, Helen, Moceri, Pamela, Mohammed, Shehla, Muiño-Mosquera, Laura, Nampoothiri, Sheela, Pichler, Karin, Prescott, Katrina, Rajeb, Anna, Ramos-Arroyo, Maria, Rossi, Massimiliano, Salih, Mustafa, Seidahmed, Mohammed Z., Schaefer, Elise, Steichen-Gersdorf, Elisabeth, Temel, Sehime, Uysal, Fahrettin, Vanhomwegen, Marine, Van Laer, Lut, Van Maldergem, Lionel, Warner, David, Willaert, Andy, Collins, Tom R., Taylor, Andrea, Davis, Elaine C., Zarate, Yuri, and Callewaert, Bert
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- 2018
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5. Catheter Ablation of Supraventricular Tachycardia in Children Using Three-Dimensional Electroanatomic Mapping Systems; A Single Center Experience
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UYSAL, Fahrettin, primary, Genc, Abdusselam, additional, Turkmen, Hasan, additional, Kucuker, Hakan, additional, and Bostan, Ozlem M., additional
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- 2023
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6. Evaluation of Clinical Features and Prognosis in Children with Supraventricular Tachycardia
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Uysal, Fahrettin, primary, Özbek, Alper Tunga, additional, Genç, Abdüsselam, additional, and Çil, Ergün, additional
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- 2023
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7. Does Post-COVID-19 Erectile Dysfunction Improve over Time?
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Gök, Alper, Altan, Mehmet, Doğan, Ahmet Emin, Eraslan, Aşır, Uysal, Fahrettin Şamil, Öztürk, Ufuk, Saguner, Ardan Muammer; https://orcid.org/0000-0003-1896-0803, İmamoğlu, Muhammet Abdurrahim, Gök, Alper, Altan, Mehmet, Doğan, Ahmet Emin, Eraslan, Aşır, Uysal, Fahrettin Şamil, Öztürk, Ufuk, Saguner, Ardan Muammer; https://orcid.org/0000-0003-1896-0803, and İmamoğlu, Muhammet Abdurrahim
- Abstract
BACKGROUND Some studies have shown that there may be an increase in the frequency of erectile dysfunction after COVID-19. However, no long-term study has investigated whether this is permanent or temporary. In this study, we aimed to examine whether there was an increase in the frequency of erectile dysfunction among individuals with a history of COVID-19, and, if there was, whether their condition improved over time. MATERIALS AND METHODS In this study, a total of 125 healthy male healthcare workers, 95 with and 30 without a history of COVID-19, were evaluated in terms of erectile function. Four study groups were formed. The first three groups consisted of individuals with a history of COVID-19 confirmed by the polymerase chain reaction (PCR) test at different times, who recovered from the disease (time elapsed since COVID-19 positivity: <6 months for Group 1, 6 to 12 months for Group 2, and >12 months for Group 3). The individuals in Group 4 did not have a history of COVID-19 diagnosis. In order to evaluate the erectile function of the participants, they were asked to complete the five-item International Index of Erectile Function questionnaire (IIEF-5). Then, statistical analyses were performed to evaluate whether there was a difference between the groups in terms of the IIEF-5 scores. RESULTS There was a statistically significant difference between the groups in terms of the IIEF-5 scores (p < 0.001), and this difference was determined to be caused by the significantly higher IIEF-5 scores of Groups 3 and 4 compared to Group 1 (p = 0.004 and p < 0.001, respectively). In addition, the IIEF-5 score of Group 4 was statistically significantly higher than that of Group 2 (p < 0.001). However, the IIEF-5 scores did not statistically significantly differ between Groups 1 and 2, Groups 2 and 3, and Groups 3 and 4 (p > 0.999, p = 0.204, and p = 0.592, respectively). CONCLUSION There may be deterioration in erectile function after COVID-19; however, this tends to improve
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- 2023
8. Rare Primary Signet Ring Cell Carcinoma of the Bladder Cancer
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Sarı, Hilmi, primary, Uysal, Fahrettin Şamil, additional, Ekenci, Berk Yasin, additional, Bozpınar, Simay, additional, Çimen, Sertaç, additional, and İmamoğlu, Muhammet Abdurrahim, additional
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- 2023
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9. Does Post-COVID-19 Erectile Dysfunction Improve over Time?
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Gök, Alper, primary, Altan, Mehmet, additional, Doğan, Ahmet Emin, additional, Eraslan, Aşır, additional, Uysal, Fahrettin Şamil, additional, Öztürk, Ufuk, additional, Saguner, Ardan Muammer, additional, and İmamoğlu, Muhammet Abdurrahim, additional
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- 2023
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10. A rare and fatal cause of hypertrophic cardiomyopathy: Danon disease
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Türkmen, Hasan, primary, Uysal, Fahrettin, additional, and Bostan, Özlem Mehtap, additional
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- 2023
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11. Non-transecting urethroplasty in patients with bulbar urethral strictures shorter than three centimeters
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Yılmaz, Muhammet Şahin, primary, Kokurcan, Alihan, additional, Uysal, Fahrettin Şamil, additional, Özenç, Görkem, additional, and Yalçınkaya, Fatih, additional
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- 2022
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12. Correction: Arterial tortuosity syndrome: 40 new families and literature review
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Beyens, Aude, Albuisson, Juliette, Boel, Annekatrien, Al-Essa, Mazen, Al-Manea, Waheed, Bonnet, Damien, Bostan, Ozlem, Boute, Odile, Busa, Tiffany, Canham, Nathalie, Cil, Ergun, Coucke, Paul J., Cousin, Margot A., Dasouki, Majed, De Backer, Julie, De Paepe, Anne, De Schepper, Sofie, De Silva, Deepthi, Devriendt, Koenraad, De Wandele, Inge, Deyle, David R., Dietz, Harry, Dupuis-Girod, Sophie, Fontenot, Eudice, Fischer-Zirnsak, Björn, Gezdirici, Alper, Ghoumid, Jamal, Giuliano, Fabienne, Baena, Neus, Haider, Mohammed Z., Hardin, Joshua S., Jeunemaitre, Xavier, Klee, Eric W., Kornak, Uwe, Landecho, Manuel F., Legrand, Anne, Loeys, Bart, Lyonnet, Stanislas, Michael, Helen, Moceri, Pamela, Mohammed, Shehla, Muiño-Mosquera, Laura, Nampoothiri, Sheela, Pichler, Karin, Prescott, Katrina, Rajeb, Anna, Ramos-Arroyo, Maria, Rossi, Massimiliano, Salih, Mustafa, Seidahmed, Mohammed Z., Schaefer, Elise, Steichen-Gersdorf, Elisabeth, Temel, Sehime, Uysal, Fahrettin, Vanhomwegen, Marine, Van Laer, Lut, Van Maldergem, Lionel, Warner, David, Willaert, Andy, Collins II, Tom R., Taylor, Andrea, Davis, Elaine C., Zarate, Yuri, and Callewaert, Bert
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- 2019
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13. Ventricular Extrasystole in Children: Single-Center Experience.
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Uysal, Fahrettin, Özalp, Şule, Genç, Abdüsselam, Akça, Tuğberk, Türkmen, Hasan, and Bostan, Özlem M.
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DRUG efficacy , *SYNCOPE , *ECHOCARDIOGRAPHY , *AMBULATORY electrocardiography , *EXERCISE tests , *CONVALESCENCE , *CARDIOPULMONARY system , *RETROSPECTIVE studies , *ACQUISITION of data , *MAGNETIC resonance imaging , *MANN Whitney U Test , *ADRENERGIC beta blockers , *DISEASE relapse , *T-test (Statistics) , *SYMPTOMS , *MEDICAL records , *ELECTROCARDIOGRAPHY , *DESCRIPTIVE statistics , *CHI-squared test , *ARRHYTHMIA , *DATA analysis software , *DATA analysis , *LONGITUDINAL method , *CHILDREN - Abstract
Objective: Ventricular extrasystole is one of the most common rhythm disorders in children, and almost all of them are characterized by normal cardiac functions without structural cardiac abnormalities. The aim of this study was to assess the clinical course of ventricular extrasystole in children who did not have cardiac structural abnormalities. Materials and Methods: This retrospective study analyzed 24-hour rhythm Holter recordings performed in our clinic in children. Patients diagnosed with isolated ventricular extrasystole in Holter records and without structural heart disease on echocardiography were included in the evaluation. Results: A total of 20 160 Holter results were evaluated in the study, and 226 patients (male; 66%) met the criteria. The mean follow-up time was 8.7 ± 3.2 years. While 81.8% of the patients were asymptomatic, the most common symptom was palpitation and 5 patients had syncope. Of the patients, 72 (31.8%) received medical therapy. Beta-blockers were the most often prescribed medication. Cardiomyopathy did not develop in any of the patients during the followup period. A partial reduction in the frequency of ventricular extrasystole was observed in 42% of the patients, while complete recovery was observed in 22%. Conclusion: Ventricular extrasystole in children generally has a good prognosis; most of them are asymptomatic, and the rates of spontaneous regression over time are quite high, regardless of the origin. [ABSTRACT FROM AUTHOR]
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- 2023
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14. A novel technique of pulmonary artery banding by means of radiofrequency ablation: An experimental study in rabbits
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Uysal, Fahrettin, primary, Akça, Tuğberk, additional, Genç, Abdüsselam, additional, Avcı Küpeli, Zehra, additional, Özfırat, Erencan, additional, Canatan, Uygur, additional, Uysal, Berfin, additional, and Şenkaya Sığnak, Işık, additional
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- 2022
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15. Utilization of Internet Resources by Surgeons for Continuous Professional Development in the Era of Prevailing COVID-19 Pandemic: Trends and Obstacles
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Cimen, Sanem Guler, primary, Eraslan, Asir, additional, Uysal, Fahrettin Samil, additional, Dogan, Ahmet Emin, additional, Kokurcan, Alihan, additional, Yilmaz, Muhammet Sahin, additional, Baylan, Burhan, additional, and Cimen, Sertac, additional
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- 2022
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16. The Prevalence of Post-COVID-19 Hypertension in Children
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Uysal, Berfin, primary, Akça, Tuğberk, additional, Akacı, Okan, additional, and Uysal, Fahrettin, additional
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- 2022
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17. Complete Atrioventricular Block as a Complication of Varicella Infection in a Child: Recovery With a Single Dose of Intravenous Immunoglobulin Therapy
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Uysal, Fahrettin, Bostan, Ozlem Mehtap, Cetin, Benhur, Uysal, Berfin, Guney, Begum, and Cil, Ergun
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- 2016
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18. Rare Primary Signet Ring Cell Carcinoma of the Bladder Cancer.
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Sarı, Hilmi, Uysal, Fahrettin Şamil, Ekenci, Berk Yasin, Bozpınar, Simay, Çimen, Sertaç, and İmamoğlu, Muhammet Abdurrahim
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ANTIBIOTICS ,ADENOCARCINOMA ,BLADDER tumors ,URINARY organs ,DYSURIA ,RARE diseases - Abstract
Primary signet ring cell carcinoma of the bladder is a rare tumor and it has a poor prognosis and is more mortal than the urothelial cell carnioma. However, most patients apply with painless macroscopic hematuria; rarely do they could apply with urinary tract infection or lower urinary tract symptoms. In this study; a 47-yearold male was referred to our clinic with dysuria, which was antibiotic therapy and symptomatic treatment. In ultrasonography, bladder wall thickening has been seen then patient underwent with cystoscopy. After atypical lesions were seen on the bladder mucosa, random punch biopsies were taken. A pathological examination revealed infiltrative urothelial carcinoma with a poorly differentiated signet ring cell component. As in this case report, patients with signet ring cell bladder cancer, which is rare and has an aggressive course, might only present with non-specific complaints such as dysuria. If atypical lesions are observed during the diagnostic cystoscopy procedure, the threshold should be kept low to decide on biopsy. [ABSTRACT FROM AUTHOR]
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- 2023
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19. Non-transecting urethroplasty in patients with bulbar urethral strictures shorter than three centimeters.
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Yılmaz, Muhammet Şahin, Kokurcan, Alihan, Uysal, Fahrettin Şamil, Özenç, Görkem, and Yalçınkaya, Fatih
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URETHRA stricture ,URETHROPLASTY ,SURGICAL complications ,SURGICAL clinics ,AGE groups ,HEALTH facilities - Abstract
This study aimed to compare the success and postoperative complication rates of the novel non-transecting urethroplasty (NTU) technique and conventional excision-primary anastomosis (EPA) in the surgical treatment of short bulbar urethral strictures. Data of the patients who underwent excision-primary anastomosis or NTU procedures at our center for the surgical treatment of bulbar urethral strictures shorter than 3 cm between January 2010 and December 2018 were retrospectively reviewed. Forty-seven patients fulfilled the eligibility criteria for this study. Among these patients, 22 underwent NTU procedure while 25 underwent EPA. There was no difference between the two groups regarding age, stricture length, etiology, past surgical history, and duration of follow-up. The surgical success rates were 88% and 87,2% in the NTU and EPA groups, respectively (p = 0,603). The complication rates were 12% and 13,6% in NTU and EPA groups, respectively. Two groups were similar concerning complication rates (p = 0,603). The novel NTU and conventional EPA techniques are similar regarding surgical success and complication rates in the surgical treatment of bulbar urethral strictures shorter than three centimeters. [ABSTRACT FROM AUTHOR]
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- 2023
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20. A Rare Anomaly: Recurrent Congenital Aorto-Azygos Fistula After Two Procedure of Transcatheter Occlusion
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Uysal, Fahrettin, Bostan, Ozlem Mehtap, and Cil, Ergun
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- 2015
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21. Outcomes of Kawasaki Disease: A Single-Center Experience
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Uysal, Fahrettin, Bostan, Ozlem Mehtap, Celebi, Solmaz, Uysal, Berfin, Hamitoglu, Serif, and Cil, Ergun
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- 2015
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22. Congenital nephrotic syndrome of NPHS1 associated with cardiac malformation
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Uysal, Berfin, Dönmez, Osman, Uysal, Fahrettin, Akac, Okan, Vuruşkan, Berna Aytaç, and Berdeli, Afig
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- 2015
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23. Effects of levetiracetam treatment on autonomic nervous system functions in pediatric epilepsy patients.
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Direk, Meltem Çobanoğulları, Epcacan, Serdar, Özdemir, Asena Ayca, Uysal, Fahrettin, and Okuyaz, Çetin
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AUTONOMIC nervous system physiology ,INTRAVENOUS therapy ,HETEROCYCLIC compounds ,EPILEPSY ,PEDIATRICS ,HEART beat ,DESCRIPTIVE statistics ,ELECTROCARDIOGRAPHY ,ARRHYTHMIA - Abstract
Background: This study investigated the effects of levetiracetam (LEV) treatment on cardiac rhythm and heart rate variability. Methods: The study included two groups of patients diagnosed with non‐lesional epilepsy who had not yet been treated and who presented to the outpatient pediatric neurology clinic at Van Training and Research Hospital, Van, Turkey, between 2019 and 2020. The heart rate variability (HRV) of 47 patients in the first group, before and at the 3rd month of treatment, and intravenous (IV) LEV loading in 13 patients in the second group was evaluated by Holter electrocardiography (ECG). Results: It was determined that the values of triangular index, standard deviation of the RR intervals over a 24‐hour period (SDNN), standard deviation of all 5‐minute mean RR intervals (SDANN), mean of standard deviations of all normal RR intervals (SDNNI), the percentage of RR intervals with >50‐millisecond variation (PNN50), and the square root of mean squared differences of successive RR intervals (RMSSD). HRV of 47 patients under LEV treatment significantly increased in the 3rd month of treatment compared to baseline (p < 0.05). No difference was found in HRV between the intravenous loading and the control group (p > 0.05). Conclusions: Our study suggests that the sympathovagal balance before treatment in the patient group is in favor of the sympathetic nervous system and that the sympathovagal imbalance improves after treatment. Our results show that LEV monotherapy and loading have no negative effect on HRV and potential cardiac arrhythmia risk in children with epilepsy. [ABSTRACT FROM AUTHOR]
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- 2023
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24. ALGORITHMS FROM SYMPTOMS TO DIAGNOSIS IN CHILDREN, EXTENDED AND UPDATED 2nd EDITION
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ÇİL, Ergün, BOSTAN, Özlem Mehtap, EREN, Erdal, and UYSAL, Fahrettin
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Ophthalmology ,Göz Hastalıkları ,book,children,algorithms,diagnosis - Abstract
The first edition of the book "ALGORITHMS FROM SYMPTOMS TO DIAGNOSIS IN CHILDREN" attracted great interest despite all adverse conditions such as the pandemic, and the "EXTENDED AND UPDATED 2nd EDITION" was published immediately
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- 2021
25. The Role of External Loop Recorders in Arrhythmia-Related Symptoms in Children: A Single Center Experience
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Akca, Tugberk, primary, Uysal, Fahrettin, additional, Bostan, Ozlem Mehtap, additional, Genc, Abdusselam, additional, and Turkmen, Hasan, additional
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- 2021
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26. Accelerated idioventricular rhythm resulting in torsades de pointes and cardiac arrest in a child: successfully cryoablated in left’coronary cusp
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Ergul, Yakup, primary, Kafali, Hasan C., additional, and Uysal, Fahrettin, additional
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- 2019
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27. The frequency of asymptomatic urinary system abnormalities in children detected with cineurography imaging during angiocardiography
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Oral, Orcun, primary, Toprak, Muhammet Hamza Halil, additional, Uysal, Fahrettin, additional, Bostan, Ozlem Mehtap, additional, and Cil, Ergun, additional
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- 2019
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28. Accelerated idioventricular rhythm resulting in torsades de pointes and cardiac arrest in a child: successfully cryoablated in left'coronary cusp.
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Ergul, Yakup, Kafali, Hasan C., and Uysal, Fahrettin
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- 2020
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29. Correction: Arterial tortuosity syndrome: 40 new families and literature review
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Beyens, Aude, primary, Albuisson, Juliette, additional, Boel, Annekatrien, additional, Al-Essa, Mazen, additional, Al-Manea, Waheed, additional, Bonnet, Damien, additional, Bostan, Ozlem, additional, Boute, Odile, additional, Busa, Tiffany, additional, Canham, Nathalie, additional, Cil, Ergun, additional, Coucke, Paul J., additional, Cousin, Margot A., additional, Dasouki, Majed, additional, De Backer, Julie, additional, De Paepe, Anne, additional, De Schepper, Sofie, additional, De Silva, Deepthi, additional, Devriendt, Koenraad, additional, De Wandele, Inge, additional, Deyle, David R., additional, Dietz, Harry, additional, Dupuis-Girod, Sophie, additional, Fontenot, Eudice, additional, Fischer-Zirnsak, Björn, additional, Gezdirici, Alper, additional, Ghoumid, Jamal, additional, Giuliano, Fabienne, additional, Baena, Neus, additional, Haider, Mohammed Z., additional, Hardin, Joshua S., additional, Jeunemaitre, Xavier, additional, Klee, Eric W., additional, Kornak, Uwe, additional, Landecho, Manuel F., additional, Legrand, Anne, additional, Loeys, Bart, additional, Lyonnet, Stanislas, additional, Michael, Helen, additional, Moceri, Pamela, additional, Mohammed, Shehla, additional, Muiño-Mosquera, Laura, additional, Nampoothiri, Sheela, additional, Pichler, Karin, additional, Prescott, Katrina, additional, Rajeb, Anna, additional, Ramos-Arroyo, Maria, additional, Rossi, Massimiliano, additional, Salih, Mustafa, additional, Seidahmed, Mohammed Z., additional, Schaefer, Elise, additional, Steichen-Gersdorf, Elisabeth, additional, Temel, Sehime, additional, Uysal, Fahrettin, additional, Vanhomwegen, Marine, additional, Van Laer, Lut, additional, Van Maldergem, Lionel, additional, Warner, David, additional, Willaert, Andy, additional, Collins II, Tom R., additional, Taylor, Andrea, additional, Davis, Elaine C., additional, Zarate, Yuri, additional, and Callewaert, Bert, additional
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- 2018
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30. Surgical excision of a giant cardiac fibroma in an asymptomatic child
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Seçici, Serkan, primary, Uysal, Fahrettin, additional, Yazıcıoğlu, Volkan, additional, Bostan, Özlem Mehtap, additional, and Şenkaya Sığnak, Işık, additional
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- 2017
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31. “Homozygous, and compound heterozygous mutation in 3 Turkish family with Jervell and Lange-Nielsen syndrome: case reports”
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Uysal, Fahrettin, primary, Turkgenc, Burcu, additional, Toksoy, Guven, additional, Bostan, Ozlem M., additional, Evke, Elif, additional, Uyguner, Oya, additional, Yakicier, Cengiz, additional, Kayserili, Hulya, additional, Cil, Ergun, additional, and Temel, Sehime G., additional
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- 2017
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32. Syncope in Children: Is Rhythm Holter Monitoring Necessary?
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Uysal, Fahrettin, primary, Bostan, Özlem Mehtap, additional, Çetinkaya, Fatma, additional, Deniz, Tuba, additional, and Çil, Ergün, additional
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- 2016
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33. Huge thrombus formation 1 year after percutaneous closure of an atrial septal defect with an Amplatzer septal occluder
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Uysal, Fahrettin, primary
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- 2016
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34. Isolated congenital cardiac diverticulum originating from the left ventricular apex: Report of a pediatric case
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Uysal, Fahrettin, primary, Bostan, OzlemMehtap, additional, Toprak, MuhammedHamza Halil, additional, Signak, IsikSenkaya, additional, and Cil, Ergun, additional
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- 2016
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35. Congenital Heart Diseases Followed in Our Neonatal Intensive Care Unit: Frequency, Risk Factors and Prognosis
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Güney Varal, İpek, primary, Köksal, Nilgün, additional, Özkan, Hilal, additional, Bostan, Özlem, additional, Şenkaya Sığınak, Işık, additional, Bağcı, Onur, additional, Doğan, Pelin, additional, and Uysal, Fahrettin, additional
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- 2015
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36. Determination of reference values for tricuspid annular plane systolic excursion in healthy Turkish children
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Uysal, Fahrettin, primary, Bostan, Ozlem Mehtap, additional, and Cil, Ergun, additional
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- 2015
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37. Determination of reference values for tricuspid annular plane systolic excursion in healthy Turkish children.
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Uysal, Fahrettin, Bostan, Özlem Mehtap, and Çil, Ergun
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CARDIAC contraction , *ECHOCARDIOGRAPH research , *CHILDREN'S health , *CHILDREN , *HEART failure - Abstract
Objective: Tricuspid annular plane systolic excursion (TAPSE) is an echocardiographic measurement used for evaluating right ventricular systolic function. While established reference values of TAPSE exist for the adult population, only a limited number of studies have attempted to evaluate reference values for the pediatric population. The aim of the present study was to determine the reference values for TAPSE in healthy children in Turkey. Methods: A total of 765 healthy children aged between 0 and 18 years, all of whom were referred to our clinic with cardiac murmurs, were evaluated prospectively. Patients with no cardiac pathologies or other disorders were excluded from the study. The measurement of TAPSE was obtained using a 2D-guided M-mode technique with echocardiography, and the relationship between age and surface area with TAPSE was investigated. The statistical analysis was carried out using the SPSS 20.0 software package (SPSS Inc., Chicago, IL, USA, 2012). Results: The mean TAPSE value was found to be 19.56±5.54mm, and no significant difference was identified between male and female children. TAPSE values showed a positive correlation with increasing age and surface area. The mean TAPSE value was 9.09±1.36 mm in newborns and 25.91±3.60 mm in the 13-18 years age group. A negative correlation was seen between TAPSE and heart rate. Conclusion: In the present study, the reference values for TAPSE in healthy Turkish children were presented in percentile tables and the corresponding z-scores were determined. These reference values may be useful in daily practice for the evaluation of right ventricular systolic function in children. [ABSTRACT FROM AUTHOR]
- Published
- 2016
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38. Yenidoğan Yoğun Bakım Ünitemizde İzlenen Konjenital Kalp Hastalıkları: Sıklığı, Risk Faktörleri ve Prognoz.
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Varal, İpek Güney, Köksal, Nilgün, Özkan, Hilal, Bostan, Özlem, Sığınak, Işık Şenkaya, Bağcı, Onur, Doğan, Pelin, and Uysal, Fahrettin
- Abstract
Copyright of Journal of Current Pediatrics / Guncel Pediatri is the property of Galenos Yayinevi Tic. LTD. STI and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
- Published
- 2015
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39. Atypical presentation of moyamoya disease with pulmonary hypertension: A case report.
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Kızılkaya, Mete Han, Uysal, Fahrettin, Gürbüz, Emre, Taşkapılıoğlu, Mevlüt Özgür, and Bostan, Özlem Mehtap
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- *
SYNCOPE , *RIGHT ventricular hypertrophy , *ELECTROCARDIOGRAPHY , *PULMONARY function tests , *MOYAMOYA disease , *PULMONARY hypertension - Abstract
The article presents a cases study of a 15-year-old male presented with recurrent syncope while climbing stairs. Topics discussed include right ventricular hypertrophy revealed in electrocardiography; performing thorax high-resolution computed tomography, pulmonary function test, serologic tests for connective tissue disorders and coagulation studies; and diagnosis of moyamoya disease with pulmonary hypertension.
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- 2018
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40. An unusual cause of aortic regurgitation: accessory mitral valve.
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Kızılkaya, Mete Han, Uysal, Fahrettin, Bostan, Özlem Mehtap, and Yazıcıoğlu, Volkan
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- *
CARDIOVASCULAR disease diagnosis , *ECHOCARDIOGRAPHY - Abstract
The article presents a case study of a 17-year-old boy was diagnosed with suspected accessory mitral valve (AMV) during the evaluation of a cardiac murmur with no other associated anomalies, aortic regurgitation (AR), and followed up for 8 years by serial transthoracic echocardiography.
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- 2018
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41. Author's Reply.
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Uysal, Fahrettin
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THROMBOSIS , *PLATELET aggregation inhibitors , *INFLAMMATION - Abstract
A response from the author of the article "Huge thrombus formation 1 year after percutaneous closure of an atrial septal defect with an Amplatzer septal occluder" in the previous issue is presented.
- Published
- 2016
42. Arterial tortuosity syndrome: 40 new families and literature review
- Author
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Uludağ Üniversitesi/Tıp Fakültesi/Pediatrik Kardiyoloji Anabilim Dalı., Uludağ Üniversitesi/Tıp Fakültesi/Histoloji ve Embriyoloji Anabilim Dalı., Uludağ Üniversitesi/Tıp Fakültesi/Tıbbi Genetik Anabilim Dalı., Bostan, Özlem Mehtap, Temel, Şehime Gülsün, Uysal, Fahrettin, AAG-8558-2021, AAG-8385-2021, and AAH-4421-2021
- Subjects
System ,Male ,Diaphragm hernia ,SLC2A10 protein, human ,Biopsy ,CTGF protein, human ,Review ,Pulmonary artery stenosis ,Skin disease ,Gene ,Pathology ,Pylorus stenosis ,Molecular genetics ,Child ,Aorta ,Connective tissue growth factor ,Skin ,Fibril ,SLC2A10 ,Smad2 protein ,Aortic aneurysm ,Genetics & heredity ,Recessive cutis laxa ,Pulmonary ,Arteries ,Neonatal respiratory distress syndrome ,Brain hemorrhage ,Artery ,Arterial tortuosity syndrome ,Pedigree ,Collagen synthesis ,Phenotype ,Vascular tissue ,Diagnostic imaging ,Female ,Abnormalities ,Mutations ,Human ,Adult ,Histology ,Adolescent ,Child, preschool ,Vascular malformations ,Clinical article ,SLC2A10 gene ,TGF beta signaling ,Pathophysiology ,SMAD2 protein, human ,Brain ischemia ,Glucose transport proteins, facilitative ,Stomach perforation ,Skin diseases, genetic ,Cutis Laxa ,Arterial Tortuosity Syndrome ,Mutation ,Blood vessel biopsy ,Electron microscopy ,Respiratory distress syndrome, newborn ,Skin biopsy ,Genetics ,Humans ,Gene mutation ,Human tissue ,Neonatal hemorrhage ,Connective tissue disease ,Glucose transporter ,Hernia, diaphragmatic ,Autosomal recessive disorder ,Mesenteric artery occlusion ,Aortic stenosis ,Infant ,Aneurysm ,Elastic fiber ,Clinical feature ,Human cell ,Congenital blood vessel malformation ,Preschool child ,Vessels ,Transforming growth factor beta ,GLUT10 ,Marfan-syndrome ,Controlled study ,Nucleotide sequence ,Joint instability - Abstract
Çalışmada 64 yazar bulunmaktadır. Bu yazarlardan sadece Bursa Uludağ Üniversitesi mensuplarının girişleri yapılmıştır. Purpose: We delineate the clinical spectrum and describe the histology in arterial tortuosity syndrome (ATS), a rare connective tissue disorder characterized by tortuosity of the large and medium-sized arteries, caused by mutations in SLC2A10. Methods: We retrospectively characterized 40 novel ATS families (50 patients) and reviewed the 52 previously reported patients. We performed histology and electron microscopy (EM) on skin and vascular biopsies and evaluated TGF-beta signaling with immunohistochemistry for pSMAD2 and CTGF. Results: Stenoses, tortuosity, and aneurysm formation are widespread occurrences. Severe but rare vascular complications include early and aggressive aortic root aneurysms, neonatal intracranial bleeding, ischemic stroke, and gastric perforation. Thus far, no reports unequivocally document vascular dissections or ruptures. Of note, diaphragmatic hernia and infant respiratory distress syndrome (IRDS) are frequently observed. Skin and vascular biopsies show fragmented elastic fibers (EF) and increased collagen deposition. EM of skin EF shows a fragmented elastin core and a peripheral mantle of microfibrils of random directionality. Skin and end-stage diseased vascular tissue do not indicate increased TGF-beta signaling. Conclusion: Our findings warrant attention for IRDS and diaphragmatic hernia, close monitoring of the aortic root early in life, and extensive vascular imaging afterwards. EM on skin biopsies shows disease-specific abnormalities. Deanship of Scientific Research, King Saud University, Riyadh, Saudi Arabia (RGP-VPP-301) Special Research Fund, Flanders of Ghent University (01N04516) Natural Sciences and Engineering Research Council of Canada (NSERC) CGIAR (NSERC RGPIN 355710) Ghent University (BOF14/01M01108) FWO (FWOOPR2013025301)
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- 2018
43. Extracorporeal membrane oxygenation support after pediatric cardiac surgery: Our single-center experience
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Irem Iris Kan, Mustafa Güneş, Ahmet Yuksel, Işik Şenkaya Siğnak, Mehmet Hadi Çağlayan, Atıf Yolgösteren, Fahrettin Uysal, Uludağ Üniversitesi/Tıp Fakültesi/Kalp ve Damar Cerrahisi Anabilim Dalı., Uludağ Üniversitesi/Tıp Fakültesi/Çocuk Kardiyolojisi Anabilim Dalı., Yüksel, Ahmet, Yolgösteren, Atıf, Kan, İrem İris, Uysal, Fahrettin, Çăglayan, Mehmet Hadi, Sığnak, Şenkaya Işık, AAG-2372-2021, and AAH-4421-2021
- Subjects
Pulmonary and Respiratory Medicine ,Life-support ,medicine.medical_specialty ,medicine.medical_treatment ,Failure ,030204 cardiovascular system & hematology ,Single Center ,03 medical and health sciences ,0302 clinical medicine ,medicine ,Extracorporeal membrane oxygenation ,Venoarterial ,Ecmo ,Mechanical support ,Ventricular Assist Device ,Pediatrics ,Heart Transplantation ,Children ,Pediatric cardiac surgery ,Transplantation ,Congenital heart-disease ,business.industry ,Cardiac surgery ,030228 respiratory system ,Anesthesia ,Postcardiotomy circulatory failure ,Surgery ,Cardiology and Cardiovascular Medicine ,business ,Circulatory support - Abstract
Background: In this study, we present our five-year extracorporeal membrane oxygenation experiences in patients requiring mechanical support after pediatric open heart surgery. Methods: We retrospectively reviewed the medical records of 29 children (16 males, 13 females; mean age 21.6 months; range 5 days to 162 months) who underwent open heart surgery and required extracorporeal membrane oxygenation support due to postcardiotomy circulatory failure between February 2010 and March 2015. Results: The most common diagnosis was tetralogy of Fallot in eight patients (27.5%). The most common extracorporeal membrane oxygenation indication was failure to wean from cardiopulmonary bypass in 12 (41%) patients. The mean duration of extracorporeal membrane oxygenation support was 6.9 days (range 14 hours to 32 days). The most common complication related to extracorporeal membrane oxygenation support was renal insufficiency in 14 patients (48.3%). Fourteen patients (48%) were able to be successfully weaned from extracorporeal membrane oxygenation support, while six patients (20.7%) were discharged without any neurological sequelae. No significant predictor of mortality was found. Failure to wean from cardiopulmonary bypass resulted improved outcomes than other extracorporeal membrane oxygenation indications. Conclusion: Extracorporeal membrane oxygenation provides an effective cardiopulmonary support for cardiopulmonary failure after pediatric open heart surgery. Careful patient selection, and correct timing and appropriate management of extracorporeal membrane oxygenation are crucial for optimal outcomes.
- Published
- 2016
44. Huge thrombus formation 1 year after percutaneous closure of an atrial septal defect with an Amplatzer septal occluder
- Author
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Ergun Cil, Fahrettin Uysal, Güneş M, Şenkaya Sığnak I, Özlem M. Bostan, Uludağ Üniversitesi/Tıp Fakültesi/Çocuk Kardiyolojisi Anabilim Dalı., Uludağ Üniversitesi/Tıp Fakültesi/Kalp Damar Cerrahisi Anabilim Dalı., Uysal, Fahrettin, Bostan, Özlem Mehtap, Sığnak, Işık Şenkaya, Güneş, Mustafa, Çil, Ergün, AAG-8558-2021, AAH-4421-2021, AAH-3865-2021, and AAG-9324-2021
- Subjects
0301 basic medicine ,Male ,Percutaneous ,Cardiac & cardiovascular systems ,Heart diseases ,Heart murmur ,Transthoracic echocardiography ,030204 cardiovascular system & hematology ,Diagnosis, differential ,Septal occluder device ,Device failure ,0302 clinical medicine ,Equipment failure ,Pathological anatomy ,Letter to the Editor ,Heart septal defect ,Blood clotting ,Amplatzer Septal Occluder ,Septal Occluder Device ,Thrombosis ,Heart septal defects, atrial ,Echocardiography ,Cardiology ,Diagnostic imaging ,Differential diagnosis ,Cardiology and Cardiovascular Medicine ,Human ,medicine.medical_specialty ,Atrioventricular septal defect ,Adolescent ,Heart Atrium Septum Defect ,Septal Occluder ,03 medical and health sciences ,Postoperative complications ,Internal medicine ,Case report ,Evaluation and follow up ,medicine ,Device ,Humans ,Transcatheter closure ,Thrombus ,Placement ,Inflammation ,business.industry ,medicine.disease ,Note ,Patent foramen ovale ,Argon plasma coagulation ,030104 developmental biology ,Cardiovascular system & cardiology ,Septal occluder ,Therapy ,Risk factor ,business ,Percutaneous aortic valve - Abstract
The Amplatzer septal occluder (ASO) has become the device of choice for interventional closure of atrial septal defects (ASDs) in many institutions during the last decades. Although excellent results have been reported for the device, concerns have arisen about the long-term complications (1). Of these complications, thrombus formation was rarely seen after 1 year in patients (2–4). This is the first report of a pediatric patient of a huge thrombus developing on an ASO device detected by transthoracic echocardiography on a routine examination after 1 year of implantation without a risk factor.
- Published
- 2015
45. Determination of reference values for tricuspid annular plane systolic excursion in healthy Turkish children
- Author
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Özlem M. Bostan, Fahrettin Uysal, Ergun Cil, Uludağ Üniversitesi/Tıp Fakültesi/Çocuk Kardiyolojisi Anabilim Dalı., Uysal, Fahrettin, Bostan, Özlem Mehtap, Çil, Ergün, AAH-4421-2021, AAH-3865-2021, AAG-9324-2021, and AAG-8558-2021
- Subjects
Male ,Pediatrics ,Percentile ,Survival ,Cardiac & cardiovascular systems ,Turkey ,Physiology ,Heart murmur ,Adult population ,Failure ,Tricuspid valve disease ,Reference Values ,Turkey (bird) ,Medicine ,Body surface ,Child ,Heart palpitation ,Thorax pain ,Original Investigation ,Correlation analysis ,Normal human ,Tricuspid annular plane systolic excursion ,Cardiac Murmurs ,Human experiment ,Echocardiography ,Child, Preschool ,Cardiology ,Female ,Tricuspid Valve ,Anatomy ,Cardiology and Cardiovascular Medicine ,Human ,Adult ,TAPSE ,medicine.medical_specialty ,Adolescent ,Systole ,Heart rate ,Heart right ventricle function ,Right-ventricular-function ,Article ,percentile ,Internal medicine ,Pressure ,Humans ,Prospective study ,Tetralogy ,Congenital heart-disease ,business.industry ,healthy children ,Significant difference ,Excursion ,Infant, Newborn ,Infant ,Heart arrhythmia ,Newborn ,right ventricle systolic function ,Systolic heart murmur ,Cardiovascular system & cardiology ,Young adult ,Preschool child ,Dysfunction ,Reference values ,Ventricular Function, Right ,School child ,business ,Repair ,Reference value ,Pediatric population ,Heart Left Ventricle ,Pulmonary Hypertension - Abstract
Objective: Tricuspid annular plane systolic excursion (TAPSE) is an echocardiographic measurement used for evaluating right ventricular systolic function. While established reference values of TAPSE exist for the adult population, only a limited number of studies have attempted to evaluate reference values for the pediatric population. The aim of the present study was to determine the reference values for TAPSE in healthy children in Turkey. Methods: A total of 765 healthy children aged between 0 and 18 years, all of whom were referred to our clinic with cardiac murmurs, were evaluated prospectively. Patients with no cardiac pathologies or other disorders were excluded from the study. The measurement of TAPSE was obtained using a 2D-guided M-mode technique with echocardiography, and the relationship between age and surface area with TAPSE was investigated. The statistical analysis was carried out using the SPSS 20.0 software package (SPSS Inc., Chicago, IL, USA, 2012). Results: The mean TAPSE value was found to be 19.56 +/- 5.54 mm, and no significant difference was identified between male and female children. TAPSE values showed a positive correlation with increasing age and surface area. The mean TAPSE value was 9.09 +/- 1.36 mm in newborns and 25.91 +/- 3.60 mm in the 13-18 years age group. A negative correlation was seen between TAPSE and heart rate. Conclusion: In the present study, the reference values for TAPSE in healthy Turkish children were presented in percentile tables and the corresponding z-scores were determined. These reference values may be useful in daily practice for the evaluation of right ventricular systolic function in children.
- Published
- 2015
46. Çocuklarda senkop: Ritim holter monitörizasyonu gerekli mi?
- Author
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Uludağ Üniversitesi/Tıp Fakültesi/Çocuk Sağlığı ve Hastalıkları Anabilim Dalı/Çocuk Kardiyoloji Bilim Dalı., Uludağ Üniversitesi/Tıp Fakültesi/Çocuk Sağlığı ve Hastalıkları Anabilim Dalı., Uysal, Fahrettin, Bostan, Özlem Mehtap, Çetinkaya, Fatma, Deniz, Tuba, and Çil, Ergün
- Subjects
Senkop ,Holter monitörizasyonu ,Children ,Gizli uzun QT sendromu ,Syncope ,Holter monitoring ,Concealed long QT syndrome ,Çocuk - Abstract
Introduction: Holter monitoring (HM) is usually used in patients with syncope when etiology cannot be explained with history, physical examination and electrocardiography (ECG). In this study the objective was to evaluate the diagnostic value of HM in children with syncope. Materials and Methods: Databases were collected retrospectively by analyzing the HM results of 3.122 pediatric patients between 2010-2014. Gender, age at diagnosis, detailed clinical history, physical examination, 12-lead electrocardiographic and echocardiographic results were noted using standardized form. Results: The study included 323 patients with syncope with a mean age of 13.21±3.67. There were 199 female and 124 male patients in this study. Among all patients 284 (87.9%) had normal HM results, while 11 (3.4%) patients had abnormal Holter studies that consider to explain as syncope. Three of 11 patients with abnormal Holter results diagnosed through ECG before HM, hence, the diagnostic value of HM was calculated as 2.4%. In contrast, diagnostic value of HM in patients with positive family history was found to be 16.6%. In this study, 7 patients were considered to have long QT syndrome according to their HM findings. Conclusions: Detailed clinical history has a great value in children with syncope. As a result, HM has low diagnostic value if the patients are not in high risk group. However, HM was considered to be important because of concealed long QT syndrome especially if the patient had positive family history and exercise related syncope. Giriş: Senkop geçiren hastalarda anamnez, fizik muayene ve elektrokardiyografi (EKG) ile etiyoloji açıklanamıyorsa genellikle Holter monitörizasyonu (HM) yapılır. Bu çalışmada senkoplu çocuklarda HM’nin tanısal değerinin belirlenmesi amaçlanmıştır. Gereç ve Yöntem: Bu çalışmada 2010-2014 yılları arasında hastalara uygulanan toplam 3,122 HM retrospektif olarak incelendi. Hastaların cinsiyet, tanı yaşı, ayrıntılı anamnez, fizik muayene, 12-derivasyon EKG ve ekokardiyografik sonuçları standart form kullanılarak kayıt edildi. Bulgular: Çalışmaya yaş ortalaması 13,21±3,67 olan 323 hasta dahil edildi. Hastaların 199’u kız, 124’ü erkek idi. Tüm hastaların 284’ünde (%87,9) Holter sonuçları normal saptanırken 11 hastada (%3,4) senkopu açıklayan anormal Holter sonuçları tespit edildi. Anormal Holter sonuçları olan 11 hastanın üçünde HM öncesinde uygulanan EKG ile tanı konduğu için HM’nin tanısal değeri %2,4 olarak hesaplandı. Aile öyküsü pozitif olan çocuklarda ise HM’nin tanısal değeri %16,6 olarak bulundu. Çalışmada EKG’si normal olan yedi hastada ise HM sonucu ile uzun QT sendromu düşünüldü. Sonuç: Senkop geçiren çocuklarda ayrıntılı anamnez çok değerlidir. Sonuç olarak HM’nin, yüksek risk grubu olmayan hastalarda tanısal değeri düşüktür. Ancak özellikle pozitif aile öyküsü olanlarda ve eforla ilişkili senkopu olan çocuklarda gizli uzun QT sendromu açısından HM’nin değerli olabileceği düşünüldü.
- Published
- 2015
47. Congenital heart diseases followed in our neonatal ıntensive care unit: Frequency, risk factors and prognosis
- Author
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Uludağ Üniversitesi/Tıp Fakültesi/Çocuk Sağlığı ve Hastalıkları Anabilim Dalı/Neonatoloji Bilim Dalı., Uludağ Üniversitesi/Tıp Fakültesi/Çocuk Sağlığı ve Hastalıkları Anabilim Dalı/Çocuk Kardiyoloji Bilim Dalı., Uludağ Üniversitesi/Tıp Fakültesi/Kalp Damar Cerrahi Anabilim Dalı., Varal, İpek Güney, Köksal, Nilgün, Özkan, Hilal, Bostan, Özlem, Sığınak, Işık Şenkaya, Bağcı, Onur, Doğan, Pelin, and Uysal, Fahrettin
- Subjects
Neonatal ,Yenidoğan ,Konjenital kalp hastalığı ,Intensive care unit ,Yoğun bakım ,Congenital heart disease - Abstract
Giriş: Hastanemiz yenidoğan yoğun bakım ünitesinde izlenen bebekler arasında doğumsal kalp hastalığı tanısı alanları sıklık, risk faktörleri ve prognozları açısından retrospektif olarak incelemek ve bu hastaların mortalitesinin azaltılması için yapılması gerekenleri literatür ışığında değerlendirmek. Gereç ve Yöntem: Ocak 2008-Ocak 2013 tarihleri arasında Uludağ Üniversitesi, yenidoğan yoğun bakım ünitesinde izlenen 1,175 hastadan konjenital kalp hastalığı nedeniyle yatışı yapılan 99 hasta alınmıştır. Bulgular: Çalışmaya alınan 99 olgunun 54’ü erkek (%54,5), 45’i kız (%45,5) idi. Olguların %82,9’u term bebeklerden oluşuyordu ve ortalama doğum kiloları 3,142±592 gr bulundu. Siyanotik konjenital kalp hastalıklarından en sık 14 olgu (%14,1) ile büyük arter transpozisyonu görülürken 8 hastada Fallot tetralojisi saptandı. Asiyanotik konjenital kalp hastalıklarından en sık total atrio ventriküler (AV) kanal defekti saptandı. Antenatal tanı alma oranı 55 hasta ile %55,6 idi. Hastaların 35’i (%35,3) kaybedildi, ortalama ölüm günü 22. gündü. Kaybedilen hastaların çoğunluğunu büyük arter transpozisyonu ve total AV kanal defekti tanılı olgular oluşturuyordu. Sonuç: Konjenital kalp hastalıklarında mortaliteyi düşürmek için yapılması gereken iki önemli unsur vardır. Birincisi gebelikte annelerin takiplerinin düzenli yapılması ve antenatal tanı alma oranlarının daha da arttırılmasıdır. İkincisi ise sadece konjenital kalp hastalıkları ile ilgilenen bir ekip tarafından kısa sürede opere edilerek yine kardiyak cerrahi post operatif bakım tecrübesi olan bir ekiple izlenmesidir. İdeal olan bölgesel kardiyak cerrahi yoğun bakım merkezleri kurarak, tüm doğan konjenital kalp hastalıklarının doğum sonrası bu merkezlere sevk edilmesi ve konusunda tecrübeli ekip tarafından erken zamanda opere edilerek, bakımının sağlanmasıdır. Ülkemizde konjenital kalp hastalıklarının morbiditesi ve mortalitesinin iyileştirilebilmesi için sağlık bakanlığı tarafından konu ivedilikle ele alınmalı ve sorunun çözümüne yönelik organizasyonlar gerçekleştirilmelidir. Introduction: To evaluate babies diagnosed as congenital heart disease in terms of frequency, risk factors and prognosis and to determine the issues to be covered to reduce the mortality in these patients in the scope of the literature. Materials and Methods: Ninety-nine patients diagnosed as congenital heart disease were enrolled among 1.175 patients who were admitted to neonatal intensive care unit in Uludağ University Hospital between January 2008 and January 2013. Results: Fifty-four patients (54.5%) of 99 cases included in the study were male and 45 (45.5%) cases were female. Of cases, 82.9% were term and mean birth weight was 3.142±592 gr. Most common diagnosis was transposition of great arteries seen in 14 cases (14.1%), followed by complete atrioventricular septal defect and aortic hypoplasia, 11 cases for each. Mortality rate was 35.3% (35 of 99 patients) and mean time of death was 22 days. Antenatal diagnosis rate was 55.6% (55 of 99 patients). Conclusions: It appears to be two major issues to address in order to reduce the mortality in congenital heart defects. Firstly, rate of proper follow-up in pregnancies and prenatal diagnosis must be increased. Secondly, these patients must be operated in the exact appropriate time by exclusive congenital heart surgeons, and subsequently managed by experienced post-operative care staff. Therefore, establishment of regional cardiac surgery/intensive care units and referral of all congenital heart defects to these centers would be ideal. In order to reduce the mortality and morbidity of congenital heart defects, these issues must be covered by the Ministry of Health and necessary initiatives must be established as urgently as possible.
- Published
- 2015
48. A novel technique of pulmonary artery banding by means of radiofrequency ablation: An experimental study in rabbits.
- Author
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Uysal F, Akça T, Genç A, Avcı Küpeli Z, Özfırat E, Canatan U, Uysal B, and Şenkaya Sığnak I
- Abstract
Background: The aim of this study was to evaluate the efficacy and feasibility of a novel method of narrowing pulmonary arteries with catheter angiography using radiofrequency energy in rabbits., Methods: A total of nine New Zealand white rabbits weighing 3.0 to 4.2 kg each were utilized in this experimental study. After the location of pulmonary artery was confirmed by echocardiography and angiography, radiofrequency energy was applied by starting with 5 W energy for the first time and increasing by 5 W, if there was no rupture to a maximum of 20 W. Multiple applications of radiofrequency energy with different durations were performed at different levels of the pulmonary artery. Eight weeks later, surviving rabbits were sacrificed. The pulmonary arteries were removed for histological investigation., Results: Five rabbits remained alive after the experiment. There was a significant correlation between radiofrequency power and the degree of vessel thickness change in the pulmonary artery. The endothelial integrity of the tunica intima was impaired in all groups and the diameter of vessel was thickened by an average of 3.5 times., Conclusion: The narrowing of the pulmonary artery using radiofrequency energy was successfully performed in a small sample size of experimental animals in this study., Competing Interests: Conflict of Interest: The authors declared no conflicts of interest with respect to the authorship and/or publication of this article., (Copyright © 2022, Turkish Society of Cardiovascular Surgery.)
- Published
- 2022
- Full Text
- View/download PDF
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