26 results on '"Gökmen, Zeynel"'
Search Results
2. Is it Accurate to Separate Glucose-6-Phosphate Dehydrogenase Activity in Neonatal Hyperbilirubinemia as Deficient and Normal?
- Author
-
Kilicdag, Hasan, Gökmen, Zeynel, Ozkiraz, Servet, Gulcan, Hande, and Tarcan, Aylin
- Published
- 2014
- Full Text
- View/download PDF
3. Breast milk as a topical eye drop reduces the severity of ROP: A randomized placebo-controlled trial.
- Author
-
Silahli, Musa, primary, Tekin, Mehmet, additional, Kal, Ali, additional, Gökmen, Zeynel, additional, Büyükeren, Melek, additional, Ozcan, Beyza, additional, Yılmaz, Fatma, additional, Yümlü, Kadir, additional, Torer, Birgin, additional, and Çetinkaya, Bilin, additional
- Published
- 2022
- Full Text
- View/download PDF
4. A Novel Mutation (c.705C>A (p.C235*) (p.Cys235Ter)) in the SFTPB Gene That Causes Severe Respiratory Failure in A Term Newborn
- Author
-
Silahli, Musa, primary and Gökmen, Zeynel, additional
- Published
- 2021
- Full Text
- View/download PDF
5. Pseudohyponatraemia and hyperviscosity due to IVIG therapy in a term newborn
- Author
-
TARCAN, AYLIN, GÖKMEN, ZEYNEL, DIKMENOĞLU, NESLIHAN, and GÜRAKAN, BERKAN
- Published
- 2005
6. Early neonatal outcomes of very-low-birth-weight infants in Turkey: a prospective multicenter study of the Turkish Neonatal Society
- Author
-
Gürsoy, Tuğba (ORCID 0000-0002-6084-4067 & YÖK ID 214691), Koç, Esin; Demirel, Nihal; Baş, Ahmet Yağmur; Işık, Dilek Ulubaş; Hirfanoğlu, İbrahim Murat; Tunc, Turan; Sarı, Fatma Nur; Karatekin, Güner; Özdemir, Ramazan; Altunhan, Hüseyin; Çetinkaya, Merih; Özcan, Beyza; Özkiraz, Servet; Çalkavur, Sebnem; Tekgündüz, Kadir Şerafettin; Taştekin, Ayhan; Özlü, Ferda; Özyurt, Banu Mutlu; Özdemir, Ahmet; Çetinkaya, Bilin; Demirelli, Yaşar; Köklü, Esad; Çelik, Ülker; Tarakçı, Nuriye; Armangil, Didem; Okulu, Emel; Narter, Fatma; Mutlu, Birgul; Mert, Mustafa Kurthan; Bülbül, Ali; Asker, Hüseyin Selim; Uygur, ÖzgÜn; Uslu, İlker Sait; Ertuğrul, Sabahattin; Aydemir, Cumhur; Çelik, Hasan Tolga; Küçüktaşçı, Kazım; Arslan, Selda; Ergin, Hacer; Zenciroğlu, Aysegül; Yurttutan, Sadık; Orman, Ayşen; Tuncer, Oğuz; Yaşa, Beril; Acunas, Betül; Takci, Şahin; Gökmen, Zeynel; Özkan, Hilal; Cömert, Serdar; Üstün, Nuran; Mutlu, Mehmet; Bayraktar, Bilge Tanyeri; Bilgin, Leyla; Tuzun, Funda; Aydemir, Özge; Akdağ, Arzu; Memisoğlu, Aslı; Can, Emrah; Terek, Demet; Beken, Serdar; Turan, Özden; Güzoğlu, Nilüfer; Örs, Rahmi; Kale, Yusuf; Hekimoğlu, Berna; Aylanc, Hakan; Eroğlu, Funda; Şahin, Suzan; Konak, Murat; Sarıcı, Dilek; Kılıç, İlknur; Hakan, Nilay, School of Medicine, Gürsoy, Tuğba (ORCID 0000-0002-6084-4067 & YÖK ID 214691), Koç, Esin; Demirel, Nihal; Baş, Ahmet Yağmur; Işık, Dilek Ulubaş; Hirfanoğlu, İbrahim Murat; Tunc, Turan; Sarı, Fatma Nur; Karatekin, Güner; Özdemir, Ramazan; Altunhan, Hüseyin; Çetinkaya, Merih; Özcan, Beyza; Özkiraz, Servet; Çalkavur, Sebnem; Tekgündüz, Kadir Şerafettin; Taştekin, Ayhan; Özlü, Ferda; Özyurt, Banu Mutlu; Özdemir, Ahmet; Çetinkaya, Bilin; Demirelli, Yaşar; Köklü, Esad; Çelik, Ülker; Tarakçı, Nuriye; Armangil, Didem; Okulu, Emel; Narter, Fatma; Mutlu, Birgul; Mert, Mustafa Kurthan; Bülbül, Ali; Asker, Hüseyin Selim; Uygur, ÖzgÜn; Uslu, İlker Sait; Ertuğrul, Sabahattin; Aydemir, Cumhur; Çelik, Hasan Tolga; Küçüktaşçı, Kazım; Arslan, Selda; Ergin, Hacer; Zenciroğlu, Aysegül; Yurttutan, Sadık; Orman, Ayşen; Tuncer, Oğuz; Yaşa, Beril; Acunas, Betül; Takci, Şahin; Gökmen, Zeynel; Özkan, Hilal; Cömert, Serdar; Üstün, Nuran; Mutlu, Mehmet; Bayraktar, Bilge Tanyeri; Bilgin, Leyla; Tuzun, Funda; Aydemir, Özge; Akdağ, Arzu; Memisoğlu, Aslı; Can, Emrah; Terek, Demet; Beken, Serdar; Turan, Özden; Güzoğlu, Nilüfer; Örs, Rahmi; Kale, Yusuf; Hekimoğlu, Berna; Aylanc, Hakan; Eroğlu, Funda; Şahin, Suzan; Konak, Murat; Sarıcı, Dilek; Kılıç, İlknur; Hakan, Nilay, and School of Medicine
- Abstract
Objective: to investigate the early neonatal outcomes of very-low-birth-weight (VLBW) infants discharged home from neonatal intensive care units (NICUs) in Turkey. Material and methods: a prospective cohort study was performed between April 1, 2016 and April 30, 2017. The study included VLBW infants admitted to level III NICUs. Perinatal and neonatal data of all infants born with a birth weight of.1500 g were collected for infants who survived. Results: data from 69 NICUs were obtained. The mean birth weight and gestational age were 1137 +/- 245 g and 29 +/- 2.4 weeks, respectively. During the study period, 78% of VLBW infants survived to discharge and 48% of survived infants had no major neonatal morbidity. VLBW infants who survived were evaluated in terms of major morbidities: bronchopulmonary dysplasia was detected in 23.7% of infants, necrotizing enterocolitis in 9.1%, blood culture proven late-onset sepsis (LOS) in 21.1%, blood culture negative LOS in 21.3%, severe intraventricular hemorrhage in 5.4% and severe retinopathy of prematurity in 11.1%. Hemodynamically significant patent ductus arteriosus was diagnosed in 24.8% of infants. Antenatal steroids were administered to 42.9% of mothers. Conclusion: the present investigation is the first multicenter study to include epidemiological information on VLBW infants in Turkey. Morbidity rate in VLBW infants is a serious concern and higher than those in developed countries. Implementation of oxygen therapy with appropriate monitoring, better antenatal and neonatal care and control of sepsis may reduce the prevalence of neonatal morbidities. Therefore, monitoring standards of neonatal care and implementing quality improvement projects across the country are essential for improving neonatal outcomes in Turkish NICUs., Turkish Neonatal Society
- Published
- 2019
7. Incidence, risk factors and severity of retinopathy of prematurity in Turkey (TR-ROP study): a prospective, multicentre study in 69 neonatal intensive care units
- Author
-
Uludağ, Günay (ORCID & YÖK ID 175586); Gürsoy, Tuğba (ORCID 0000-0002-6084-4067 & YÖK ID 214691), Baş, Ahmet Yağmur; Demirel, Nihal; Koç, Esin; Işık, Dilek Ulubaş; Hirfanoğlu, İbrahim Murat; Tunç, Turan; Sarı, Fatma Nur; Karatekin, Güner; Köklü, Esad; Altunhan, Hüseyin; Turgut, Hatice; Narter, Fatma; Tarakçı, Nuriye; Tekgündüz, Kadir Şerafettin; Özkiraz, Servet; Aydemir, Cumhur; Özdemir, Ahmet; Çetinkaya, Bilin; Kazancı, Ebru; Taştekin, Ayhan; Calkavur, Şebnem; Özyurt, Banu Mutlu; Demirelli, Yaşar; Asker, Hüseyin Selim; Mutlu, Birgul; Uygur, Özgün; Özkan, Hilal; Armangil, Didem; Özlü, Ferda; Mert, Mustafa Kurthan; Ergin, Hacer; Özcan, Beyza; Baş, Evrim Kıray; Okulu, Emel; Acunas, Betül; Çelik, Ülker; Uslu, Sait İlker; Mutlu, Mehmet; Demir, Nihat; Eroğlu, Funda; Gökmen, Zeynel; Beken, Serdar; Bayraktar, Bilge Tanyeri; Hakan, Nilay; Küçüktaşçı, Kazım; Orman, Ayşen; Cömert, Serdar; Ertuğrul, Sabahattin; Üstün, Nuran; Şahin, Özlem; Terek, Demet; Kale, Yusuf; Konak, Murat; Yurttutan, Sadık; Aydemir, Özge; Zenciroğlu, Aysegül; Sarıcı, Dilek; Güzoğlu, Nilüfer; Hamilçıkan, Şahin; Tüzün, Funda; Örs, Rahmi; Arslan, Selda; Akdağ, Arzu; Memişoğlu, Aslı; Yasa, Beril; Hekimoğlu, Berna; Turan, Özden; Aylanc, Hakan; Takçı, Şahin; Çelik, Tolga; Şahin, Suzan; Kılıç, İlknur; Kara, Caner; Tunay, Zuhal Özen; Çelik, Gökhan; Gözen, İbrahim; Satırtav, Günhal; Polat, Nihat; Oral, Ayşe Yeşim; Tokgöz, Mine; Keleş, Sadullah; Bilgin, Burak; Uğurbaş, Silay Cantürk; Karaca, Çağatay; Keşkek, Nedime Şahinoğlu; Ekinci, Dilbade Yıldız; Balcı, Özlem; Altan, Emir Volkan; Bakbak, Sevda; Ceylan, Nihan Aksu; Kimyon, Sabit; Alyamaç, Günay; Türe, Gamze; Yıldız, Meral; Çalış, Feyza; Sızmaz, Selçuk; Sukgen, Emine; Çetin, Ebru Nevin; Özçimen, Muammer; Demir, Semra Tiryaki; Atila, Huban; Özal, Altan; Tufaner, Gökhan; Yücel, Özlem Eski; Kola, Mehmet; Seven, Erbil; Özdek, Şengül; Durukan, Ali Hakan; Kal, Ali; Çelebi, Ali Riza Cenk; Koytak, İbrahim Arif; Alaçamlı, Göksu; Esme, Arif; Çatak, Onur; Perente, İrfan; Şahin, Alparslan; Akçakaya, Aylin Ardagil; Kıray, Gülünay; Nalçacı, Serhat; Aksoy, Ümit; Bakbak, Ber, School of Medicine, Department of Internal Medicine, Uludağ, Günay (ORCID & YÖK ID 175586); Gürsoy, Tuğba (ORCID 0000-0002-6084-4067 & YÖK ID 214691), Baş, Ahmet Yağmur; Demirel, Nihal; Koç, Esin; Işık, Dilek Ulubaş; Hirfanoğlu, İbrahim Murat; Tunç, Turan; Sarı, Fatma Nur; Karatekin, Güner; Köklü, Esad; Altunhan, Hüseyin; Turgut, Hatice; Narter, Fatma; Tarakçı, Nuriye; Tekgündüz, Kadir Şerafettin; Özkiraz, Servet; Aydemir, Cumhur; Özdemir, Ahmet; Çetinkaya, Bilin; Kazancı, Ebru; Taştekin, Ayhan; Calkavur, Şebnem; Özyurt, Banu Mutlu; Demirelli, Yaşar; Asker, Hüseyin Selim; Mutlu, Birgul; Uygur, Özgün; Özkan, Hilal; Armangil, Didem; Özlü, Ferda; Mert, Mustafa Kurthan; Ergin, Hacer; Özcan, Beyza; Baş, Evrim Kıray; Okulu, Emel; Acunas, Betül; Çelik, Ülker; Uslu, Sait İlker; Mutlu, Mehmet; Demir, Nihat; Eroğlu, Funda; Gökmen, Zeynel; Beken, Serdar; Bayraktar, Bilge Tanyeri; Hakan, Nilay; Küçüktaşçı, Kazım; Orman, Ayşen; Cömert, Serdar; Ertuğrul, Sabahattin; Üstün, Nuran; Şahin, Özlem; Terek, Demet; Kale, Yusuf; Konak, Murat; Yurttutan, Sadık; Aydemir, Özge; Zenciroğlu, Aysegül; Sarıcı, Dilek; Güzoğlu, Nilüfer; Hamilçıkan, Şahin; Tüzün, Funda; Örs, Rahmi; Arslan, Selda; Akdağ, Arzu; Memişoğlu, Aslı; Yasa, Beril; Hekimoğlu, Berna; Turan, Özden; Aylanc, Hakan; Takçı, Şahin; Çelik, Tolga; Şahin, Suzan; Kılıç, İlknur; Kara, Caner; Tunay, Zuhal Özen; Çelik, Gökhan; Gözen, İbrahim; Satırtav, Günhal; Polat, Nihat; Oral, Ayşe Yeşim; Tokgöz, Mine; Keleş, Sadullah; Bilgin, Burak; Uğurbaş, Silay Cantürk; Karaca, Çağatay; Keşkek, Nedime Şahinoğlu; Ekinci, Dilbade Yıldız; Balcı, Özlem; Altan, Emir Volkan; Bakbak, Sevda; Ceylan, Nihan Aksu; Kimyon, Sabit; Alyamaç, Günay; Türe, Gamze; Yıldız, Meral; Çalış, Feyza; Sızmaz, Selçuk; Sukgen, Emine; Çetin, Ebru Nevin; Özçimen, Muammer; Demir, Semra Tiryaki; Atila, Huban; Özal, Altan; Tufaner, Gökhan; Yücel, Özlem Eski; Kola, Mehmet; Seven, Erbil; Özdek, Şengül; Durukan, Ali Hakan; Kal, Ali; Çelebi, Ali Riza Cenk; Koytak, İbrahim Arif; Alaçamlı, Göksu; Esme, Arif; Çatak, Onur; Perente, İrfan; Şahin, Alparslan; Akçakaya, Aylin Ardagil; Kıray, Gülünay; Nalçacı, Serhat; Aksoy, Ümit; Bakbak, Ber, School of Medicine, and Department of Internal Medicine
- Abstract
Background to evaluate the prevalence, risk factors and treatment of retinopathy of prematurity (ROP) in Turkey and to establish screening criteria for this condition. Methods: a prospective cohort study (TR-ROP) was performed between 1 April 2016 and 30 April 2017 in 69 neonatal intensive care units (NICUs). Infants with a birth weight (BW)=1500 g or gestational age (GA)<= 32 weeks and those with a BW> 1500 g or GA> 32 weeks with an unstable clinical course were included in the study. Predictors for the development of ROP were determined by logistic regression analyses. Results: the TR-ROP study included 6115 infants: 4964 (81%) with a GA <= 32 weeks and 1151 (19%) with a GA>32 weeks. Overall, 27% had any stage of ROP and 6.7% had severe ROP. A lower BW, smaller GA, total days on oxygen, late-onset sepsis, frequency of red blood cell transfusions and relative weight gain were identified as independent risk factors for severe ROP in infants with a BW=1500 g. Of all infants, 414 needed treatment and 395 (95.4%) of the treated infants had a BW <= 1500 g. Sixty-six (16%) of the treated infants did not fulfil the Early Treatment for Retinopathy of Prematurity requirements for treatment. Conclusions: screening of infants with a GA <= 34 weeks or a BW<1700 g appears to be appropriate in Turkey. Monitoring standards of neonatal care and conducting quality improvement projects across the country are recommended to improve neonatal outcomes in Turkish NICUs., NA
- Published
- 2018
8. Türkiye sarılık veri tabanı ön inceleme raporu
- Author
-
Çalkavur, Şebnem, ATASAY, FATMA BEGÜM, ARSAN, SAADET, GÜLTEKİN, NAZLI, AKIN, YASEMİN, TANRIVERDİ, SEMA, HANTA, DENİZ, KILIÇ, İLKNUR, ULUBAŞ IŞIK, DİLEK, GÖKMEN, ZEYNEL, ALYAMAÇ DİZDAR, EVRİM, BAŞ, AHMET YAĞMUR, NARTER, FATMA, DEMİREL, NİHAL, HIRFANOĞLU, İBRAHİM MURAT, ERDEVE, ÖMER, TUNÇ, GAFFARİ, ALAN, SERDAR, POLAT, ADEM, ÇETİNKAYA, MERİH, BÜYÜKKALE, GÖKHAN, AKDUMAN, HASAN, OKULU, EMEL, TUNÇ, TURAN, and OLUKMAN, ÖZGÜR
- Published
- 2016
9. Yenidoğanda Diskordan Atriyoventriküler Bağlantılı Çift ÇıkışlıSağ Ventrikül: Olgu Sunumu Ve Literatüre Kısa Bir Bakış
- Author
-
Sert, Ahmet, Aypar, Ebru, Gökmen, Zeynel, Öç, Mehmet, Odabaş, Dursun, and Selçuk Üniversitesi
- Subjects
Genel ve Dahili Tıp - Abstract
Çift çıkışlı sağ ventrikül bütün doğumsal kalp defektlerinin nadir bir kardiyak malformasyondur. Anormal ventriküloarteryal bağlantıların heterojen bir grubudur. Her iki büyük arter (pulmoner arter ve aorta) esas olarak morfolojik sağ ventrikülden çıkmaktadır. Diskordan atriyoventriküler bağlantılı çift çıkışlı sağ ventrikül ve hipoplazik pulmoner arterleri olan bir yenidoğanı sunmaktayız. Ekokardiyografi ile tanı konulan nadir karmaşık bir kardiyak malformasyonu bildirdik. Ekokardiyografi ile segmental yaklaşım ve kardiyak segmentlerin ardışık analizi karmaşık kardiyak malformasyonların tanısında ipucudur., Double outlet right ventricle is a rare cardiac malformation of all congenital cardiac defects. It is a heterogeneous group of abnormal ventriculoarterial connections. Both great arteries (pulmonary artery and aorta) arise primarily from the morphological right ventricle. Double outlet right ventricle with discordant atrioventricular connections have been reported rarely in the literature. We report a newborn with double outlet right ventricle with discordant atrioventricular connections and hypoplastic pulmonary arteries. We reported a rare complex cardiac malformation diagnosed by echocardiography. Segmental approach and sequential analysis of cardiac segments by echocardiography are the clue for diagnosis of complex cardiac malformations.
- Published
- 2016
10. Fetal rhabdomyoma with maternal tuberous sclerosis that almost completely filled the left ventricle at an early gestational week.
- Author
-
Çolak, Eser, Özçimen, Emel Ebru, Gökmen, Zeynel, and Gökdemir, Mahmut
- Subjects
ANTICONVULSANTS ,ECHOCARDIOGRAPHY ,FETAL heart ,GESTATIONAL age ,LEFT heart ventricle ,MUSCLE tumors ,MYOCARDIUM ,TUBEROUS sclerosis ,ULTRASONIC imaging ,TREATMENT effectiveness ,CONTINUOUS positive airway pressure ,PREGNANCY outcomes ,FETUS - Published
- 2021
- Full Text
- View/download PDF
11. Poliartrit ile Seyreden Parvovirus B 19 Enfeksiyonu: Olgu Sunumu
- Author
-
GÜNER, Şükrü Nail, GÖKTÜRK, Bahar, GÖKDEMİR, Mahmut, SAKALLI, Hale, GÖKMEN, Zeynel, BASKIN, Esra, and SAATÇİ, Ümit
- Subjects
Artrit,Parvovirus B19,çocuk ,skin and connective tissue diseases - Abstract
Parvovirus B19 is the cause of several distinct clinical syndromes. The most common is erythema infectiosum, a febrile exanthem occurring primarily in children. Recent studies have shown that PV can cause acute arthritis and occasionally a chronic arthropathy. PV is also suspected of playing a role in the pathogenesis of various chronic inflammatory and autoimmune diseases, such as systemic lupus erythematosus and rheumatoid arthritis. In this report, we present a case with acute polyarthricular arthropaty associated with PV and spontaneously resolved within 2 months. ©2006, Fırat Üniversitesi, Tıp Fakültesi, Parvovirus B19 (PV) enfeksiyonu çok farklı klinik sendromlara sebep olur. Çocuklarda ateşli döküntüyle ortaya çıkan eritema infeksiyozum en sık görülen formudur. Son çalışmalar PV'un akut artrite, bazen de kronik artropatiye neden olabildiğini göstermiştir. PV'un aynı zamanda sistemik lupus eritematozus ve romatoid artrit gibi kronik inflamatuar ve otoimmün hastalıkların patogenezinde rol oynadığından şüphe edilmektedir. Bu yazıda, PV ile ilişkili akut poliartiküler artropati ile seyreden ve iki ay içinde kendiliğinden düzelen bir vaka sunulmuştur. ©2006, Fırat Üniversitesi, Tıp Fakültesi
- Published
- 2014
12. Severe hypernatremia associated catheter malposition in an intensive care patient
- Author
-
Silahli, Musa, primary, Gökdemir, Mahmut, additional, Duman, Enes, additional, and Gökmen, Zeynel, additional
- Published
- 2016
- Full Text
- View/download PDF
13. Yenidoğan üfürümlerinin değerlendirilmesi ve izleminde klinik ve ekokardiyografik tanıların karşılaştırılması
- Author
-
Gökmen, Zeynel, Tunaoğlu, Sedef, and Çocuk Sağlığı ve Hastalıkları Anabilim Dalı
- Subjects
Çocuk Sağlığı ve Hastalıkları ,Child Health and Diseases - Abstract
59 ÖZET Çalışmamız 23.08.1999 ile 23.02.2000 tarihleri arasında Gazi Üniversitesi Tıp Fakültesi Kadın Hastalıkları ve Doğum Anabilim Dalı Obstetrik servisinde doğan 618 term ve sağlıklı yenidoğan bebekte yapıldı. Bebekler doğumdan sonraki ilk 48-72 saatte, 2.ay (431 bebek) ve 6. ayda (372 bebek) pediatrist tarafından muayene edilip, üfîirüm duyulanlar Pediatrik Kardiyoloji B.D'ye danışıldı ve EKO incelemeleri yapıldı. Kontrol gurubu olarak örnekleme yöntemi ile seçilen üfîirüm duyulmayan 59 bebek yenidoğan döneminde pediatrik kardiyolog tarafından muayene edilip EKO uygulandı. Üfîirüm duyulma oranlan yenidoğan döneminde %9.4, 2.ayda %13.7 ve ö.ayda %11.3 olarak saptandı. Bebeklerin EKO ile değerlendirilmeleri sonucunda KKH prevalansı; yenidoğan döneminde % 3.9, altı aylık izlem sonrasında ise %4.0 olarak bulundu. Yenidoğan döneminde KKH saptamada pediatrist ve pediatrik kardiyologun klinik değerlendirmesinin sensitivitesi düşük (sırasıyla %33.3 ve %40), spesifîtesi ise yüksek (sırasıyla %95.5 ve %98.9) olarak bulunurken; pediatrist ve pediatrik kardiyolog muayene sonuçlan ile EKO sonuçlan arasında da uyum saptanamadı (Kappa < 0,10). Düşük sensitivite ve uyumsuzluğun EKO ile saptanan ancak klinik bulgu vermeyen ASD, PFO, TY gibi bulgulardan kaynaklandığı bulundu. Pediatrist ve pediatrik kardiyologun tam koyamayıp EKO ile saptanan KKH (ASD, VSD, MY gibi) bu dönem için gerek izlem gerekse tedavi açısından sorun yaratmadığı kanısına vanldı. KKH klinik bulgulannm ortaya çıkması sonucunda, bebekliğin ilerleyen dönemlerinde pediatrist ve pediatrik kardiyolog klinik değerlendirmeleri ile EKO sonuçları arasında uyumun arttığı saptandı (Kappa değerleri pediatristin 2.ay 0.30, 6.ay 0.29; pediatrik kardiyologun 2.ay 0.29, 6.ay 0.45). Sonuç olarak yenidoğan döneminde; pediatristin klinik olarak semptomatik olabilecek KKH saptamada güvenilir olduğu, ancak lezyon spesifik tamda ehil ellerde yapılan EKO incelemesinin en güvenilir yöntem olduğu düşünüldü. 648
- Published
- 2001
14. Kendiliğinden düzelen doğumsal retikülohistiyositoz (Hashimoto-Pritzker Hastalığı): olgu sunumu
- Author
-
Gökmen, Zeynel, primary, Özkiraz, Servet, additional, Kıyıcı, Halil, additional, Ecevit, Ayşe, additional, and Tarcan, Aylin, additional
- Published
- 2011
- Full Text
- View/download PDF
15. Lack of Association BetweenFXIII-Val34Leu,FVII-323 del/ins, and Transforming Growth Factor β1 (915G/T) Gene Polymorphisms and Bronchopulmonary Dysplasia: A Single-Center Study
- Author
-
Ataç, Fatma Belgin, primary, İnce, Deniz Anuk, additional, Verdi, Hasibe, additional, Gökmen, Zeynel, additional, Yazici, Ayse Canan, additional, Gülcan, Hande, additional, Tarcan, Aylin, additional, Taneri, Ayse, additional, Sezgin, Ezgi, additional, and Özbek, Namık, additional
- Published
- 2010
- Full Text
- View/download PDF
16. Erythrocyte Transfusions and Serum Prohepcidin Levels in Premature Newborns With Anemia of Prematurity
- Author
-
Yapakç, Ece, primary, Ecevit, Ayşe, additional, Gökmen, Zeynel, additional, Tarcan, Aylin, additional, and Özbek, Namk, additional
- Published
- 2009
- Full Text
- View/download PDF
17. Atypical Fryns syndrome: clinical, radiological and pathological findings.
- Author
-
Serhat Aygün, Murat, Sekmenli, Tamer, Çiftçi, İlhan, Gökmen, Zeynel, Tolu, İsmet, and Mutlu-Aygün, Fuldem
- Abstract
Fryns syndrome is an autosomal recessive hereditary disease, including abnormal facies, small thorax with widely spaced hypoplastic nipples, distal limb and nail hypoplasia, and diaphragmatic hernia with pulmonary hypoplasia. The aim of the present report is to increase awareness of Fryns syndrome and its association with rare abnormalities such as cecal duplication cyst, horseshoe kidney and butterfly vertebra. We report a male 20-day-old baby with congenital diaphragmatic hernia (CDH), horseshoe kidney, butterfly vertebra, cleft palate, distal finger hypoplasia, left inguinal hernia, typical facial appearance for Fryns syndrome, and cecal duplication cyst. Fryns syndrome is the one of the most common syndromes associated with congenital diaphragmatic defect (CDH), reported in up to 10% of patients with CDH. Although no eye abnormality was seen in our patient, other findings were similar to the other typical diagnostic findings, with the exception of cecal duplication cyst and some other defects not defined before. [ABSTRACT FROM AUTHOR]
- Published
- 2014
18. Lack of Association Between FXIII-Val34Leu, FVII-323 del/ins, and Transforming Growth Factor β1 (915G/T) Gene Polymorphisms and Bronchopulmonary Dysplasia: A Single-Center Study.
- Author
-
Ataç, Fatma Belgin, İnce, Deniz Anuk, Verdi, Hasibe, Gökmen, Zeynel, Yazici, Ayse Canan, Gülcan, Hande, Tarcan, Aylin, Taneri, Ayse, Sezgin, Ezgi, and Özbek, Namık
- Subjects
BRONCHOPULMONARY dysplasia ,ARTIFICIAL respiration complications ,TRANSFORMING growth factors ,GENETIC research ,GENOTYPE-environment interaction - Abstract
Bronchopulmonary dysplasia (BPD) is a multifactorial disease of preterm infants that is characterized by airway injury, inflammation, and parenchymal remodeling. Extravascular fibrin deposits in septae and alveoli due to the altered fibrin turnover are the pathological hallmarks of BPD that strongly indicates the importance of the imbalance in the competing activities of coagulation and fibrinolysis. Activation of the coagulation cascade leads to intraalveolar fibrin deposition in many inflammatory pulmonary disorders. Increased fibrin formation or decreased fibrinolysis may cause extravascular fibrin deposition. We evaluated the association between FXIII-Val34Leu, FVII-323 del/ins, and transforming growth factor β1 ( TGF-β
1 ) (915G/T) gene polymorphisms in patients with BPD. The study group consisted of 98 preterm infants with BPD. Ninety-four of the 192 preterm neonates were without BPD and sampled for the control group. Restriction fragment size analyses were performed by examining digested PCR products for FXIII-Val34Leu, FVII-323 del/ins, and TGF-β1 (915G/C) genotypes. No significant associations were found between FXIII-Val34Leu, FVII-323 del/ins, TGF-β1 (915G/C) gene polymorphisms and BPD phenotype in our population. Further studies with other genes are required for the identification of molecular predisposing factors for BPD that may help in the development of new treatments and hence might allow for targeting of this treatment to a “high-risk” subgroup, reducing unnecessary exposure to potentially harmful therapies. [ABSTRACT FROM AUTHOR]- Published
- 2010
- Full Text
- View/download PDF
19. A Rare Case of Ectopia Cordis with Double Outlet Right Ventricle.
- Author
-
Silahlı, Musa, Gökmen, Zeynel, and Gökdemir, Mahmut
- Subjects
- *
NEONATAL intensive care , *CONGENITAL heart disease , *CHEST (Anatomy) - Abstract
Ectopiacordis is a rare anomaly. It is described that hearth is placed as partially or totally outside of thoracic cavity. Sometimes this can be accompanied liver and other organs such as intestine. Congenital heart defects are also likely to accompany to this situation. So, we present an ectopiacordis with double outlet right ventricule case who has lived for 121 days in neonatal intensive care unit. [ABSTRACT FROM AUTHOR]
- Published
- 2019
- Full Text
- View/download PDF
20. Erythrocyte Transfusions and Serum Prohepcidin Levels in Premature Newborns With Anemia of Prematurity.
- Author
-
Yapakçı, Ece, Ecevit, Ayşe, Gökmen, Zeynel, Tarcan, Aylin, and Özbek, Namık
- Published
- 2009
- Full Text
- View/download PDF
21. Early neonatal outcomes of very-low-birthweight infants in Turkey: A prospective multicenter study of the Turkish Neonatal Society
- Author
-
Hüseyin Selim Asker, Emrah Can, Cumhur Aydemir, Betül Acunaş, Ali Bulbul, Turan Tunc, Kadir Şerafettin Tekgündüz, Hasan Tolga Çelik, Şahin Takcı, Ramazan Ozdemir, Ahmet Ozdemir, Mehmet Mutlu, Ferda Özlü, Yasar Demirelli, Beyza Ozcan, Rahmi Ors, Fatma Nur Sari, Ilknur Kilic, Guner Karatekin, Dilek Ulubas Isik, Banu Mutlu Özyurt, Berna Hekimoğlu, Sabahattin Ertuğrul, Murat Konak, Selda Arslan, Nuriye Tarakci, Ozgun Uygur, Serdar Cömert, Sadık Yurttutan, Kazim Kucuktasci, Emel Okulu, Arzu Akdag, Nilay Hakan, Nilüfer Güzoğlu, Tugba Gursoy, Hakan Aylanç, Şebnem Çalkavur, Asli Memisoglu, Ayşegül Zenciroğlu, Bilin Cetinkaya, Serdar Beken, Ozge Aydemir, Hacer Ergin, Ibrahim Murat Hirfanoglu, Yusuf Kale, Didem Armangil, Suzan Sahin, Bilge Tanyeri Bayraktar, Özden Turan, Huseyin Altunhan, Servet Ozkiraz, İlker Uslu, Nihal Demirel, Funda Eroglu, Zeynel Gokmen, Aysen Orman, Leyla Bilgin, Esin Koç, Beril Yasa, Demet Terek, Funda Tuzun, Esad Koklu, Nuran Üstün, Birgul Mutlu, Ahmet Yagmur Bas, Merih Cetinkaya, Hilal Özkan, Fatma Narter, Mustafa Kurthan Mert, Ayhan Tastekin, Ulker Celik, Dilek Sarici, Oğuz Tuncer, KOÇ E., DEMİREL N., BAŞ A. Y., Isik D. U., HIRFANOĞLU İ. M., Tunc T., Sari F. N., Karatekin G., ÖZDEMİR R., Altunhan H., et al., Ege Üniversitesi, MÜ, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, Hakan, Nilay, Dicle Üniversitesi, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, Çocuk Sağlığı ve Hastalıkları Ana Bilim Dalı, Ertuǧrul, Sabahattin, Selçuk Üniversitesi, OMÜ, Gürsoy, Tuğba (ORCID 0000-0002-6084-4067 & YÖK ID 214691), Koç, Esin, Demirel, Nihal, Baş, Ahmet Yağmur, Işık, Dilek Ulubaş, Hirfanoğlu, İbrahim Murat, Tunc, Turan, Sarı, Fatma Nur, Karatekin, Güner, Özdemir, Ramazan, Altunhan, Hüseyin, Çetinkaya, Merih, Özcan, Beyza, Özkiraz, Servet, Çalkavur, Sebnem, Tekgündüz, Kadir Şerafettin, Taştekin, Ayhan, Özlü, Ferda, Özyurt, Banu Mutlu, Özdemir, Ahmet, Çetinkaya, Bilin, Demirelli, Yaşar, Köklü, Esad, Çelik, Ülker, Tarakçı, Nuriye, Armangil, Didem, Okulu, Emel, Narter, Fatma, Mutlu, Birgul, Mert, Mustafa Kurthan, Bülbül, Ali, Asker, Hüseyin Selim, Uygur, ÖzgÜn, Uslu, İlker Sait, Ertuğrul, Sabahattin, Aydemir, Cumhur, Çelik, Hasan Tolga, Küçüktaşçı, Kazım, Arslan, Selda, Ergin, Hacer, Zenciroğlu, Aysegül, Yurttutan, Sadık, Orman, Ayşen, Tuncer, Oğuz, Yaşa, Beril, Acunas, Betül, Takci, Şahin, Gökmen, Zeynel, Özkan, Hilal, Cömert, Serdar, Üstün, Nuran, Mutlu, Mehmet, Bayraktar, Bilge Tanyeri, Bilgin, Leyla, Tuzun, Funda, Aydemir, Özge, Akdağ, Arzu, Memisoğlu, Aslı, Can, Emrah, Terek, Demet, Beken, Serdar, Turan, Özden, Güzoğlu, Nilüfer, Örs, Rahmi, Kale, Yusuf, Hekimoğlu, Berna, Aylanc, Hakan, Eroğlu, Funda, Şahin, Suzan, Konak, Murat, Sarıcı, Dilek, Kılıç, İlknur, School of Medicine, Acibadem University Dspace, KKÜ, and Kırıkkale Üniversitesi
- Subjects
Male ,Turkey ,Temel Bilimler (SCI) ,very low birth weight ,ÇOK DİSİPLİNLİ BİLİMLER ,Pathology and Laboratory Medicine ,blood culture ,Pediatrics ,Infant, Newborn, Diseases ,lung dysplasia ,sepsis ,Families ,0302 clinical medicine ,newborn ,Pregnancy ,Birth Weight ,Medicine ,Prospective Studies ,Children ,[Anahtar Kelime Yok] ,Organic Compounds ,adult ,steroid ,Pregnancy Outcome ,clinical trial ,Retinopathy of prematurity ,cohort analysis ,Bronchopulmonary dysplasia ,Necrotizing enterocolitis ,Morbidity ,Mortality ,Health ,Prematurity ,Infections ,Countries ,Distress ,Sepsis ,Physical Sciences ,disease severity ,prospective study ,survival rate ,medicine.medical_specialty ,Science ,Article ,patent ductus arteriosus ,03 medical and health sciences ,Signs and Symptoms ,turkey (bird) ,Intensive Care Units, Neonatal ,Intensive care ,Humans ,Retinopathy of Prematurity ,human ,Retinopathy ,necrotizing enterocolitis ,MULTIDISCIPLINARY SCIENCES ,Chemical Compounds ,Biology and Life Sciences ,Neonates ,Doğa Bilimleri Genel ,medicine.disease ,major clinical study ,neonatal intensive care unit ,Health Care ,hospital discharge ,Ophthalmology ,Low birth weight ,multicenter study ,NATURAL SCIENCES, GENERAL ,Population Groupings ,Health Statistics ,Neonatology ,Developmental Biology ,genetic structures ,morbidity ,hemodynamics ,Neonatal Care ,Turkey (republic) ,Medicine and Health Sciences ,Infant, Very Low Birth Weight ,030212 general & internal medicine ,gestational age ,Prospective cohort study ,Science and technology ,Multidisciplinary ,Temel Bilimler ,Gestational age ,newborn disease ,Chemistry ,female ,Natural Sciences (SCI) ,brain hemorrhage ,Retinal Disorders ,Steroids ,Female ,Neonatal Sepsis ,newborn morbidity ,medicine.symptom ,Natural Sciences ,Infants ,Research Article ,Adult ,Birth weight ,Gestational Age ,Turkish Neonatal Society ,Diagnostic Medicine ,030225 pediatrics ,retinopathy ,controlled study ,outcome assessment ,perinatal period ,Multidisipliner ,business.industry ,Organic Chemistry ,prematurity ,Infant, Newborn ,infant ,Age Groups ,People and Places ,Study ,business ,Early Neonatal Outcomes - Abstract
Beken, Serdar/0000-0002-8609-2684; BAS, AHMET YAGMUR/0000-0002-1329-2167; Bulbul, Ali/0000-0002-3510-3056; Karatekin, Guner/0000-0001-7112-0323, WOS: 000534242500056, PubMed: 31851725, Objective To investigate the early neonatal outcomes of very-low-birth-weight (VLBW) infants discharged home from neonatal intensive care units (NICUs) in Turkey. Material and methods A prospective cohort study was performed between April 1, 2016 and April 30, 2017. the study included VLBW infants admitted to level III NICUs. Perinatal and neonatal data of all infants born with a birth weight of.1500 g were collected for infants who survived. Results Data from 69 NICUs were obtained. the mean birth weight and gestational age were 1137 +/- 245 g and 29 +/- 2.4 weeks, respectively. During the study period, 78% of VLBW infants survived to discharge and 48% of survived infants had no major neonatal morbidity. VLBW infants who survived were evaluated in terms of major morbidities: bronchopulmonary dysplasia was detected in 23.7% of infants, necrotizing enterocolitis in 9.1%, blood culture proven late-onset sepsis (LOS) in 21.1%, blood culture negative LOS in 21.3%, severe intraventricular hemorrhage in 5.4% and severe retinopathy of prematurity in 11.1%. Hemodynamically significant patent ductus arteriosus was diagnosed in 24.8% of infants. Antenatal steroids were administered to 42.9% of mothers. Conclusion the present investigation is the first multicenter study to include epidemiological information on VLBW infants in Turkey. Morbidity rate in VLBW infants is a serious concern and higher than those in developed countries. Implementation of oxygen therapy with appropriate monitoring, better antenatal and neonatal care and control of sepsis may reduce the prevalence of neonatal morbidities. Therefore, monitoring standards of neonatal care and implementing quality improvement projects across the country are essential for improving neonatal outcomes in Turkish NICUs., Turkish Neonatal Society [2-2016]; Turkish Neonatal Society, This study was supported by the Turkish Neonatal Society, http://www.neonatology.org.tr, number 2-2016, received by AYB. Turkish Neonatal Society funded the study's online registry system. the funder had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
- Published
- 2019
22. Incidence, risk factors and severity of retinopathy of prematurity in Turkey (TR-ROP study): a prospective, multicentre study in 69 neonatal intensive care units
- Author
-
Bas, Ahmet Yagmur, Demirel, Nihal, Koc, Esin, Isik, Dilek Ulubas, Hirfanoglu, Ibrahim Murat, Tunc, Turan, Sari, Fatma Nur, Karatekin, Guner, Koklu, Esad, Altunhan, Huseyin, Turgut, Hatice, Narter, Fatma, Tarakci, Nuriye, Tekgunduz, Kadir Serafettin, Ozkiraz, Servet, Aydemir, Cumhur, Ozdemir, Ahmet, Cetinkaya, Bilin, Kazanci, Ebru, Tastekin, Ayhan, Calkavur, Sebnem, Ozyurt, Banu Mutlu, Demirelli, Yasar, Asker, Huseyin Selim, Mutlu, Birgul, Uygur, Ozgun, Ozkan, Hilal, Armangil, Didem, Ozlu, Ferda, Mert, Mustafa Kurthan, Ergin, Hacer, Ozcan, Beyza, Bas, Evrim Kiray, Okulu, Emel, Acunas, Betul, Celik, Ulker, Uslu, Sait Ilker, Mutlu, Mehmet, Demir, Nihat, Eroglu, Funda, Gokmen, Zeynel, Beken, Serdar, Bayraktar, Bilge Tanyeri, Hakan, Nilay, Kucuktasci, Kazim, Orman, Aysen, Comert, Serdar, Ertugrul, Sabahattin, Ustun, Nuran, Sahin, Ozlem, Terek, Demet, Kale, Yusuf, Konak, Murat, Yurttutan, Sadik, Aydemir, Ozge, Zenciroglu, Aysegul, Sarici, Dilek, Guzoglu, Nilufer, Hamilcikan, Sahin, Gursoy, Tugba, Tuzun, Funda, Ors, Rahmi, Arslan, Selda, Akdag, Arzu, Memisoglu, Asli, Yasa, Beril, Hekimoglu, Berna, Turan, Ozden, Aylanc, Hakan, Takci, Sahin, Celik, Tolga, Sahin, Suzan, Kilic, Ilknur, Kara, Caner, Tunay, Zuhal Ozen, Celik, Gokhan, Gozen, Ibrahim, Satirtav, Gunhal, Polat, Nihat, Oral, Ayse Yesim, Tokgoz, Mine, Keles, Sadullah, Bilgin, Burak, Ugurbas, Silay Canturk, Karaca, Cagatay, Keskek, Nedime Sahinoglu, Ekinci, Dilbade Yildiz, Balci, Ozlem, Altan, Emir Volkan, Bakbak, Sevda, Ceylan, Nihan Aksu, Kimyon, Sabit, Alyamac, Gunay, Ture, Gamze, Yildiz, Meral, Calis, Feyza, Sizmaz, Selcuk, Sukgen, Emine, Cetin, Ebru Nevin, Ozcimen, Muammer, Demir, Semra Tiryaki, Atila, Huban, Ozal, Altan, Tufaner, Gokhan, Yucel, Ozlem Eski, Kola, Mehmet, Seven, Erbil, Ozdek, Sengul, Durukan, Ali Hakan, Kal, Ali, Celebi, Ali Riza Cenk, Koytak, Ibrahim Arif, Alacamli, Goksu, Esme, Arif, Catak, Onur, Perente, Irfan, Sahin, Alparslan, Akcakaya, Aylin Ardagil, Kiray, Gulunay, Nalcaci, Serhat, Aksoy, Umit, Bakbak, Berker, Comez, Aysegul, Gursoy, Huseyin, Kabatas, Emrah Utku, Petricli, Ikbal Seza, Yumusak, Mehmet Erhan, Kirgiz, Ahmet, Uludag, Gunay, Yaman, Aylin, Dadaci, Zeynep, Karatas, Ali, Celiker, Hande, Cebeci, Zafer, Esenulku, Mahmut Cenap, Akkoyun, Imren, Ersan, Ismail, Demir, Selim, Kadayifcilar, Sibel, Unsal, Ayse Ipek Akyuz, Hocaoglu, Mumin, Grp, T. R.-R.O.P. Study, Ege Üniversitesi, Zonguldak Bülent Ecevit Üniversitesi, Çukurova Üniversitesi, Çocuk Sağlığı ve Hastalıkları, KOYTAK, İBRAHİM ARİF, Uludağ, Günay (ORCID & YÖK ID 175586), Gürsoy, Tuğba (ORCID 0000-0002-6084-4067 & YÖK ID 214691), Baş, Ahmet Yağmur, Demirel, Nihal, Koç, Esin, Işık, Dilek Ulubaş, Hirfanoğlu, İbrahim Murat, Tunç, Turan, Sarı, Fatma Nur, Karatekin, Güner, Köklü, Esad, Altunhan, Hüseyin, Turgut, Hatice, Narter, Fatma, Tarakçı, Nuriye, Tekgündüz, Kadir Şerafettin, Özkiraz, Servet, Aydemir, Cumhur, Özdemir, Ahmet, Çetinkaya, Bilin, Kazancı, Ebru, Taştekin, Ayhan, Calkavur, Şebnem, Özyurt, Banu Mutlu, Demirelli, Yaşar, Asker, Hüseyin Selim, Mutlu, Birgul, Uygur, Özgün, Özkan, Hilal, Armangil, Didem, Özlü, Ferda, Mert, Mustafa Kurthan, Ergin, Hacer, Özcan, Beyza, Baş, Evrim Kıray, Okulu, Emel, Acunas, Betül, Çelik, Ülker, Uslu, Sait İlker, Mutlu, Mehmet, Demir, Nihat, Eroğlu, Funda, Gökmen, Zeynel, Beken, Serdar, Bayraktar, Bilge Tanyeri, Hakan, Nilay, Küçüktaşçı, Kazım, Orman, Ayşen, Cömert, Serdar, Ertuğrul, Sabahattin, Üstün, Nuran, Şahin, Özlem, Terek, Demet, Kale, Yusuf, Konak, Murat, Yurttutan, Sadık, Aydemir, Özge, Zenciroğlu, Aysegül, Sarıcı, Dilek, Güzoğlu, Nilüfer, Hamilçıkan, Şahin, Tüzün, Funda, Örs, Rahmi, Arslan, Selda, Akdağ, Arzu, Memişoğlu, Aslı, Yasa, Beril, Hekimoğlu, Berna, Turan, Özden, Aylanc, Hakan, Takçı, Şahin, Çelik, Tolga, Şahin, Suzan, Kılıç, İlknur, Kara, Caner, Tunay, Zuhal Özen, Çelik, Gökhan, Gözen, İbrahim, Satırtav, Günhal, Polat, Nihat, Oral, Ayşe Yeşim, Tokgöz, Mine, Keleş, Sadullah, Bilgin, Burak, Uğurbaş, Silay Cantürk, Karaca, Çağatay, Keşkek, Nedime Şahinoğlu, Ekinci, Dilbade Yıldız, Balcı, Özlem, Altan, Emir Volkan, Bakbak, Sevda, Ceylan, Nihan Aksu, Kimyon, Sabit, Alyamaç, Günay, Türe, Gamze, Yıldız, Meral, Çalış, Feyza, Sızmaz, Selçuk, Sukgen, Emine, Çetin, Ebru Nevin, Özçimen, Muammer, Demir, Semra Tiryaki, Atila, Huban, Özal, Altan, Tufaner, Gökhan, Yücel, Özlem Eski, Kola, Mehmet, Seven, Erbil, Özdek, Şengül, Durukan, Ali Hakan, Kal, Ali, Çelebi, Ali Riza Cenk, Koytak, İbrahim Arif, Alaçamlı, Göksu, Esme, Arif, Çatak, Onur, Perente, İrfan, Şahin, Alparslan, Akçakaya, Aylin Ardagil, Kıray, Gülünay, Nalçacı, Serhat, Aksoy, Ümit, Bakbak, Berker, Çömez, Ayşegül, Gürsoy, Hüseyin, Kabataş, Emrah Utku, Petricli, İkbal Seza, Yumuşak, Mehmet Erhan, Kırgız, Ahmet, Yaman, Aylin, Dadacı, Zeynep, Karataş, Ali, Çeliker, Hande, Cebeci, Zafer, Esenülkü, Mahmut Cenap, Akkoyun, İmren, Ersan, İsmail, Demir, Selim, Kadayıfçılar, Sibel, Ünsal, Ayşe İpek Akyüz, Hocaoğlu, Mümin, School of Medicine, Department of Internal Medicine, MÜ, Kırıkkale Üniversitesi, Selçuk Üniversitesi, Bas, Ahmet Yagmur, Koc, Esin, Isik, Dilek Ulubas, Hirfanoglu, Ibrahim Murat, Tunc, Turan, Sari, Fatma Nur, Karatekin, Guner, Koklu, Esad, Altunhan, Huseyin, Tarakci, Nuriye, Tekgunduz, Kadir Serafettin, Ozkiraz, Servet, Ozdemir, Ahmet, Cetinkaya, Bilin, Kazanci, Ebru, Tastekin, Ayhan, Calkavur, Sebnem, Ozyurt, Banu Mutlu, Demirelli, Yasar, Asker, Huseyin Selim, Uygur, Ozgun, Ozkan, Hilal, Ozlu, Ferda, Ozcan, Beyza, Bas, Evrim Kiray, Acunas, Betul, Celik, Ulker, Uslu, Sait Ilker, Eroglu, Funda, Gokmen, Zeynel, Kucuktasci, Kazim, Orman, Aysen, Comert, Serdar, Ertugrul, Sabahattin, Ustun, Nuran, Sahin, Ozlem, Yurttutan, Sadik, Aydemir, Ozge, Zenciroglu, Aysegul, Sarici, Dilek, Guzoglu, Nilufer, Hamilcikan, Sahin, Gursoy, Tugba, Tuzun, Funda, Ors, Rahmi, Akdag, Arzu, Memisoglu, Asli, Hekimoglu, Berna, Turan, Ozden, Takci, Sahin, Celik, Tolga, Sahin, Suzan, Kilic, Ilknur, Tunay, Zuhal Ozen, Celik, Gokhan, Gozen, Ibrahim, Satirtav, Gunhal, Oral, Ayse Yesim, Tokgoz, Mine, Keles, Sadullah, Ugurbas, Silay Canturk, Karaca, Cagatay, Keskek, Nedime Sahinoglu, Ekinci, Dilbade Yildiz, Balci, Ozlem, Alyamac, Gunay, Ture, Gamze, Yildiz, Meral, Calis, Feyza, Sizmaz, Selcuk, Cetin, Ebru Nevin, Ozcimen, Muammer, Ozal, Altan, Tufaner, Gokhan, Yucel, Ozlem Eski, Ozdek, Sengul, Celebi, Ali Riza Cenk, Koytak, Ibrahim Arif, Alacamli, Goksu, Catak, Onur, Perente, Irfan, Sahin, Alparslan, Akcakaya, Aylin Ardagil, Kiray, Gulunay, Nalcaci, Serhat, Aksoy, Umit, Comez, Aysegul, Gursoy, Huseyin, Kabatas, Emrah Utku, Petricli, Ikbal Seza, Yumusak, Mehmet Erhan, Kirgiz, Ahmet, Uludag, Gunay, Dadaci, Zeynep, Karatas, Ali, Celiker, Hande, Esenulku, Mahmut Cenap, Akkoyun, Imren, Ersan, Ismail, Kadayifcilar, Sibel, Unsal, Ayse Ipek Akyuz, Hocaoglu, Mumin, OMÜ, Tıp Fakültesi, and Acibadem University Dspace
- Subjects
Male ,BLOOD-TRANSFUSION ,Pediatrics ,Turkey ,INFANTS ,Logistic regression ,0302 clinical medicine ,Risk Factors ,FOR-GESTATIONAL-AGE ,Prevalence ,Birth Weight ,Infant, Very Low Birth Weight ,Prospective Studies ,Prospective cohort study ,[Anahtar Kelime Yok] ,Neovascularisation ,Incidence ,Incidence (epidemiology) ,Gestational age ,Retinopathy of prematurity ,Clinical Science ,Sensory Systems ,Female ,Infant, Premature ,Child health (paediatrics) ,Retina ,Treatment medical ,congenital, hereditary, and neonatal diseases and abnormalities ,medicine.medical_specialty ,Birth weight ,Gestational Age ,Sepsis ,03 medical and health sciences ,Cellular and Molecular Neuroscience ,Neonatal Screening ,Intensive Care Units, Neonatal ,030225 pediatrics ,Intensive care ,medicine ,Humans ,Retinopathy of Prematurity ,business.industry ,Child Health (paediatrics) ,Infant, Newborn ,[No Keywords] ,Infant ,medicine.disease ,eye diseases ,Ophthalmology ,For-Gestational-Age ,TR-ROP Study ,030221 ophthalmology & optometry ,Treatment Medical ,Blood-Transfusion ,WEIGHT ,Weight ,Infants ,Severity of Retinopathy ,business ,Medicine - Abstract
Background To evaluate the prevalence, risk factors and treatment of retinopathy of prematurity (ROP) in Turkey and to establish screening criteria for this condition., Methods A prospective cohort study (TR-ROP) was performed between 1 April 2016 and 30 April 2017 in 69 neonatal intensive care units (NICUs). Infants with a birth weight (BW)=1500 g or gestational age (GA) 1500 g or GA> 32 weeks with an unstable clinical course were included in the study. Predictors for the development of ROP were determined by logistic regression analyses., Results The TR-ROP study included 6115 infants: 4964 (81%) with a GA 32 weeks. Overall, 27% had any stage of ROP and 6.7% had severe ROP. A lower BW, smaller GA, total days on oxygen, late-onset sepsis, frequency of red blood cell transfusions and relative weight gain were identified as independent risk factors for severe ROP in infants with a BW=1500 g. Of all infants, 414 needed treatment and 395 (95.4%) of the treated infants had a BW, Conclusions Screening of infants with a GA
- Published
- 2018
23. Term infantlarda plasental transfüzyonun hemodinamik etkileri
- Author
-
Tekin, Mehmet, Gökmen, Zeynel, and Çocuk Sağlığı ve Hastalıkları Anabilim Dalı
- Subjects
Massage ,Vena cava superior ,Placenta ,Hemodynamics ,Infant ,Umbilical cord ,Çocuk Sağlığı ve Hastalıkları ,Child Health and Diseases ,Infant-newborn - Abstract
Doğum sonrası göbek bağının bağlanmasında en uygun zamanlama ile ilgili öneriler ilk çağlardan itibaren farklılıklar göstermiştir. Erken kord klempleme (EKK) işlemi modern tıpta doğumun üçüncü evresinin yönetiminde bir rutin haline gelmiştir ancak bu durumun fizyolojik bir temelinin olmadığı düşünülmektedir. EKK hızlı resüsitasyona olanak sağlarken plasental transfüzyon yöntemleri de özellikle prematüre bebeklerde morbidite ve mortaliteyi azaltabilecek olumlu hemodinamik katkılar sağlamaktadır. Yenidoğanlarda kardiyak output ve damar akımlarının değerlendirilmesinde Doppler ultrason güvenilir bir yöntemdir. Ancak özellikle doğum sonrası erken adaptasyon döneminde fetal yolaklar açık olduğundan geleneksel yöntemlerle hemodinamik değerlendirme yapabilmek mümkün gözükmemektedir. Üst gövde venöz sisteminin drenajını (%80'i beyin kaynaklı) sağlayan superior vena cava (SVC) akımının ölçümü serebral perfüzyonun iyi bir göstergesi olarak kabul edilmektedir. Fetal şantlardan etkilenmemesi doğum sonrası erken adaptasyon döneminde kullanımını değerli kılmaktadır. Bu çalışmada plasental transfüzyon yöntemlerinden olan umbilikal kord sıvazlamanın (UKS) term bebeklerin hemodinamisi üzerine olan etkilerini değerlendirdik. Çalışma grubumuz 150 term bebekten (74 erkek, 76 kız) oluştu. UKS işlemi göbek bağı klemplenmeden 20 cm'lik kısmın yaklaşık 10 cm/sn hızla en az 3 kez (3-5 kez) anneden bebeğe doğru sıvazlanması şeklinde uygulanırken, UKS uygulanmayacak grupta (EKK) klempleme işlemi doğumdan sonra ilk 10 saniye içerisinde yapıldı. SVC akımı ölçümleri ile ilgili görüntüler doğum sonrası ilk 6 saat içerisinde randomizasyondan bilgisi olmayan deneyimli bir çocuk kardiyoloğu tarafından kayıt altına alındı ve daha sonra yapılan ölçümler de bu görüntüler üzerinden aynı araştırmacı tarafından yapıldı. Çalışmaya alınan hastaların maternal ve neonatal demografik özellikleri benzerdi. SVC akımı UKS grubunda 132,47±37,04 ml/kg/dk iken, EKK grubunda 126,62±34,35 ml/kg/dk idi. Beklentimiz doğrultusunda çalışma grubunda SVC akımı istatiksel olarak anlamlı düzeyde olmasa da daha yüksek çıktı. Çalışmamıza katılan obstetrisyenlerin UKS konusundaki deneyimlerinin benzer düzeyde olmamasının istatiksel anlamlılık açısından olumsuz etkide bulunmuş olabileceğini düşünüyoruz ve daha geniş populasyonlu çalışmaların istatiksel anlamlılık ortaya koyabileceğini öngörmekteyiz. Bununla birlikteprematüre bebeklerin aksine term bebeklerde plasental transfüzyon ile elde edilen kan hacmi artışı kompanze edilmiş olabilir ve serebral kan akımı otoregülasyonu ile birlikte SVC akımında anlamlı bir artış oluşması engellenmiş olabilir. Sonuç olarak bu çalışmamızla sağlıklı term bebeklerde ilk altı saat içerisindeki SVC akım normatif değerlerini ortaya koymuş ve plasental transfüzyon yöntemlerinin bu bebeklerin SVC akımında anlamlı düzeyde olmasa da yükselme sağladığını göstermiş olduk. Recommendations regarding the optimal timing of postnatal umbilical cord attachment have been different from the earliest ages. Immediately cord clamping (ICC) has become a routine in the management of the third phase of birth at modern medicine, but this is thought to be without a physiological basis. While ICC allows rapid resuscitation, placental transfusion methods provide positive hemodynamic contributions, especially in premature infants, which may reduce morbidity and mortality. Doppler ultrasound is a reliable method for evaluating cardiac output and vascular flow in newborns. However, it is not possible to perform haemodynamic evaluation by conventional methods because of open fetal pathways, especially during the early postnatal adaptation. Measurement of superior vena cava flow, which provides drainage of the upper body venous system (80% from the brain) is considered a good indicator of cerebral perfusion. It is not affected by fetal shunts and this characteristic makes it valuable to use during early postnatal adaptation period. In this study, we evaluated the effects of umbilical cord milking (UCM), which is a placental transfusion method, on hemodynamics of term babies. Our study group consisted of 150 term babies (74 males, 76 females). The UCM procedure was performed by milking from the mother to the baby at least 3 times (3-6 times) at a speed of about 10cm/sec at 20cm without clamping the umbilical cord, whereas the clamping in the non-UCM group (ICC) was performed within the first 10 seconds after birth. Images of SVC flow measurements were recorded by an experienced child cardiologist without randomization within the first 6 hours postpartum and then measurements were made by the same investigator over these images. Maternal and neonatal demographic characteristics of the patients in the study were similar. The SVC flow was 132,47 ± 37,04 ml/kg/min in the UCM group and 126,62 ± 34,35 ml/kg/min in the ICC group. Unsurprisingly SVC flow volume was higher in study group but not statistically significant. The experiences of the participating obstetricians were not at similar level about the UCM and this may have affected adversely about the statistical significance. We anticipate that studies with wider populations may change this situation.With this, contrary to premature infants, blood volume increase which obtained by placental transfusion may be compensated and a significant increase in SVC flow may be prevented together with the cerebral blood flow autoregulation. In conclusion, we have revealed normative values of SVC flow volume in the first six hours in healthy term babies and we have shown that placental transfusion methods increase these infants SVC flow volume, but not to a significant extent. 53
- Published
- 2017
24. Atypical Fryns syndrome: clinical, radiological and pathological findings.
- Author
-
Aygün MS, Sekmenli T, Çiftçi İ, Gökmen Z, Tolu İ, and Mutlu-Aygün F
- Subjects
- Humans, Infant, Newborn, Male, Radiography, Facies, Hernia, Diaphragmatic diagnostic imaging, Hernia, Diaphragmatic pathology, Limb Deformities, Congenital diagnostic imaging, Limb Deformities, Congenital pathology
- Abstract
Fryns syndrome is an autosomal recessive hereditary disease, including abnormal facies, small thorax with widely spaced hypoplastic nipples, distal limb and nail hypoplasia, and diaphragmatic hernia with pulmonary hypoplasia. The aim of the present report is to increase awareness of Fryns syndrome and its association with rare abnormalities such as cecal duplication cyst, horseshoe kidney and butterfly vertebra. We report a male 20-day-old baby with congenital diaphragmatic hernia (CDH), horseshoe kidney, butterfly vertebra, cleft palate, distal finger hypoplasia, left inguinal hernia, typical facial appearance for Fryns syndrome, and cecal duplication cyst. Fryns syndrome is the one of the most common syndromes associated with congenital diaphragmatic defect (CDH), reported in up to 10% of patients with CDH. Although no eye abnormality was seen in our patient, other findings were similar to the other typical diagnostic findings, with the exception of cecal duplication cyst and some other defects not defined before.
- Published
- 2014
25. Lack of association between FXIII-Val34Leu, FVII-323 del/ins, and transforming growth factor beta1 (915G/T) gene polymorphisms and bronchopulmonary dysplasia: a single-center study.
- Author
-
Ataç FB, Ince DA, Verdi H, Gökmen Z, Yazici AC, Gülcan H, Tarcan A, Taneri A, Sezgin E, and Ozbek N
- Subjects
- Amino Acid Substitution genetics, Female, Humans, INDEL Mutation, Infant, Newborn, Leucine genetics, Male, Polymorphism, Genetic, Turkey, Valine genetics, Bronchopulmonary Dysplasia genetics, Factor VII genetics, Factor VIII genetics, Genetic Predisposition to Disease, Transforming Growth Factor beta1 genetics
- Abstract
Bronchopulmonary dysplasia (BPD) is a multifactorial disease of preterm infants that is characterized by airway injury, inflammation, and parenchymal remodeling. Extravascular fibrin deposits in septae and alveoli due to the altered fibrin turnover are the pathological hallmarks of BPD that strongly indicates the importance of the imbalance in the competing activities of coagulation and fibrinolysis. Activation of the coagulation cascade leads to intraalveolar fibrin deposition in many inflammatory pulmonary disorders. Increased fibrin formation or decreased fibrinolysis may cause extravascular fibrin deposition. We evaluated the association between FXIII-Val34Leu, FVII-323 del/ins, and transforming growth factor beta1 (TGF-beta(1)) (915G/T) gene polymorphisms in patients with BPD. The study group consisted of 98 preterm infants with BPD. Ninety-four of the 192 preterm neonates were without BPD and sampled for the control group. Restriction fragment size analyses were performed by examining digested PCR products for FXIII-Val34Leu, FVII-323 del/ins, and TGF-beta(1) (915G/C) genotypes. No significant associations were found between FXIII-Val34Leu, FVII-323 del/ins, TGF-beta(1) (915G/C) gene polymorphisms and BPD phenotype in our population. Further studies with other genes are required for the identification of molecular predisposing factors for BPD that may help in the development of new treatments and hence might allow for targeting of this treatment to a "high-risk" subgroup, reducing unnecessary exposure to potentially harmful therapies.
- Published
- 2010
- Full Text
- View/download PDF
26. Erythrocyte transfusions and serum prohepcidin levels in premature newborns with anemia of prematurity.
- Author
-
Yapakçi E, Ecevit A, Gökmen Z, Tarcan A, and Ozbek N
- Subjects
- Female, Ferritins blood, Hepcidins, Humans, Infant, Newborn, Iron blood, Iron Overload blood, Iron Overload prevention & control, Male, Anemia, Neonatal blood, Anemia, Neonatal therapy, Antimicrobial Cationic Peptides blood, Erythrocyte Transfusion, Infant, Premature, Infant, Premature, Diseases blood, Infant, Premature, Diseases therapy, Protein Precursors blood
- Abstract
Hepcidin is a regulatory peptide hormone acts by limiting intestinal iron absorption and promoting iron retention. Determining the level of hepcidin in anemia of prematurity might be important in preventing iron overload. This study aimed to determine serum levels of prohepcidin in newborns with anemia of prematurity, to assess the effect of a single erythrocyte transfusion on serum prohepcidin levels, and to determine the possible relationships between prohepcidin levels and serum iron and complete blood count parameters. Nineteen premature newborns with anemia of prematurity who had been treated with erythrocyte transfusions were included in this study. Just before, and 48 hours after, each transfusion, venous blood samples were collected from patients. Serum prohepcidin levels before and after erythrocyte transfusion were 206.5+/-27.3 and 205.7+/-47.1 ng/mL, respectively; no statistically significant differences were found. No significant differences existed before or after transfusion regarding serum total iron and ferritin levels, iron-binding capacity, or mean corpuscular hemoglobin concentration. No significant correlations existed between serum prohepcidin levels and other parameters, either before or after transfusions. Our results showed that there were no statistically significant differences between serum prohepcidin levels before and after a single erythrocyte transfusion in premature newborns.
- Published
- 2009
- Full Text
- View/download PDF
Catalog
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.