66 results on '"Narli N"'
Search Results
2. Incidence and severity of retinopathy of prematurity in Turkey
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Bas, A.Y., Koc, E., Dilmen, U., Oguz, S.S., Ovali, F., Demirel, N., Zenciroglu, A., Tekin, N., Caner, I., Arslanoglu, S., Celik, Y., Öztürk, A., Cömert, S., Bulbul, A., Kultursay, N., Koklu, E., Duman, N., Koksal, N., Salihoglu, O., Coban, A., Demirel, G., Bolat, F., Gökalp, A., Satar, M., Ipek, M.S., Bas, E.K., Narli, N., Mutlu, M., Cetinkaya, M., Akman, I., Yigit, S., Narter, F., Sivasli, E., Ahrabi, A.F., Atalay, Y., Tanyeri, B., Arsan, S., Perk, Y., Ors, R., Tuncer, O., Ecevit, A., Oygur, N., Özdemir, Özmert Muhammet Ali, Hakan, N., Aliefendioglu, D., Acunas, B., Cetin, H., Ozek, E., Tunc, T., Turkmen, M., Aydemir, C., Takci, S., and Bas, A.Y., Department of Neonatology, Etlik Zubeyde Hanim Women's Health Teaching and Research Hospital, Etlik, Keciören, Ankara, 06010, Turkey -- Koc, E., Department of Neonatology, Gazi University, Faculty of Medicine, Ankara, Turkey -- Dilmen, U., Department of Neonatology, Dr. Zekai Tahir Burak Women's Health Education and Research Hospital, Ankara, Turkey -- Oguz, S.S., Department of Neonatology, Dr. Zekai Tahir Burak Women's Health Education and Research Hospital, Ankara, Turkey -- Ovali, F., Zeynep Kamil Maternity and Children's Education and Training Hospital, Istanbul, Turkey -- Demirel, N., Department of Neonatology, Etlik Zubeyde Hanim Women's Health Teaching and Research Hospital, Etlik, Keciören, Ankara, 06010, Turkey -- Zenciroglu, A., Dr Sami Ulus Maternity and Children's Hospital, Ankara, Turkey -- Tekin, N., Osmangazi University Faculty of Medicine, Eskisehir, Turkey -- Caner, I., Ataturk University Faculty of Medicine, Erzurum, Turkey -- Arslanoglu, S., Dr Behcet Uz Children's Hospital, Izmir, Turkey -- Celik, Y., Mersin University Faculty of Medicine, Mersin, Turkey -- Öztürk, A., Erciyes University Faculty of Medicine, Kayseri, Turkey -- Cömert, S., Suleymaniye Maternity, Research and Training Hospital, Istanbul, Turkey -- Bulbul, A., Sisli Hamidiye Etfal Education and Research Hospital, Istanbul, Turkey -- Kultursay, N., Ege University Faculty of Medicine, Izmir, Turkey -- Koklu, E., Megapark Hospital, Kahramanmaras, Turkey -- Duman, N., Dokuz Eylul University Faculty of Medicine, Izmir, Turkey -- Koksal, N., Uludag University Faculty of Medicine, Bursa, Turkey -- Salihoglu, O., Bakirkoy Dr Sadi Konuk Training and Research Hospital, Istanbul, Turkey -- Coban, A., Istanbul University, Istanbul Faculty of Medicine, Istanbul, Turkey -- Demirel, G., Samsun Maternal and Child Health Hospital, Samsun, Turkey -- Bolat, F., Cumhuriyet University Faculty of Medicine, Sivas, Turkey -- Gökalp, A., Kocaeli University Faculty of Medicine, Kocaeli, Turkey -- Satar, M., Cukurova University Faculty of Medicine, Adana, Turkey -- Ipek, M.S., Diyarbakir Maternal and Child Health Hospital, Diyarbakir, Turkey -- Bas, E.K., Gaziantep Children's Hospital, Gaziantep, Turkey -- Narli, N., Metro Hospital, Adana, Turkey -- Mutlu, M., Karadeniz Technical University Faculty of Medicine, Trabzon, Turkey -- Cetinkaya, M., Kanuni Sultan Suleyman Training and Research Hospital, Istanbul, Turkey -- Akman, I., Bahcesehir University Faculty of Medicine, Goztepe Medical Park Hospital, Istanbul, Turkey -- Yigit, S., Hacettepe University Faculty of Medicine, Ankara, Turkey -- Narter, F., Lutfi Kirdar Kartal Education and Research Hospital, Istanbul, Turkey -- Sivasli, E., Gaziantep University Faculty of Medicine, Gaziantep, Turkey -- Ahrabi, A.F., Eskisehir State Hospital, Eskisehir, Turkey -- Atalay, Y., Department of Neonatology, Gazi University, Faculty of Medicine, Ankara, Turkey -- Tanyeri, B., Bezmialem University Faculty of Medicine, Istanbul, Turkey -- Arsan, S., Ankara University Faculty of Medicine, Ankara, Turkey -- Perk, Y., Istanbul University, Cerrahpasa Faculty of Medicine, Istanbul, Turkey -- Ors, R., Necmettin Erbakan University, Meram Faculty of Medicine, Konya, Turkey -- Tuncer, O., Yuzuncu Yil University Faculty of Medicine, Van, Turkey -- Ecevit, A., Baskent University Faculty of Medicine, Ankara, Turkey -- Oygur, N., Akdeniz University Faculty of Medicine, Antalya, Turkey -- Ozdemir, O.M., Pamukkale University Faculty of Medicine, Denizli, Turkey -- Hakan, N., Erzurum Training and Research Hospital, Erzurum, Turkey -- Aliefendioglu, D., Kirikkale University Faculty of Medicine, Kirikkale, Turkey -- Acunas, B., Trakya University Faculty of Medicine, Edirne, Turkey -- Cetin, H., Suleyman Demirel University Faculty of Medicine, Isparta, Turkey -- Ozek, E., Marmara University Faculty of Medicine, Istanbul, Turkey -- Tunc, T., Gulhane Military Medical Academy, Ankara, Turkey -- Turkmen, M., Adnan Menderes University Faculty of Medicine, Aydin, Turkey -- Aydemir, C., Bulent Ecevit University Faculty of Medicine, Zonguldak, Turkey -- Takci, S., Gaziosmanpasa University Faculty of Medicine, Tokat, Turkey
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Male ,congenital, hereditary, and neonatal diseases and abnormalities ,genetic structures ,Turkey ,retrospective study ,prevalence ,Gestational Age ,Review ,Infant, Premature, Diseases ,Severity of Illness Index ,Turkey (republic) ,Neonatal Screening ,newborn ,Risk Factors ,Humans ,controlled study ,Retinopathy of Prematurity ,human ,procedures ,Retrospective Studies ,newborn screening ,Incidence ,prematurity ,Infant, Newborn ,birth weight ,clinical trial ,low level laser therapy ,infant ,major clinical study ,eye diseases ,female ,multicenter study ,priority journal ,risk factor ,retrolental fibroplasia ,disease severity ,sense organs ,newborn intensive care ,Infant, Premature - Abstract
BMJ Publishing Group, Background: The purpose of this study was to estimate the current incidence of retinopathy of prematurity (ROP) and the need for treatment in preterm infants in Turkey. Methods: The study included preterm infants who had been screened for ROP between 2011 and 2013 in 49 neonatal intensive care units. Infants with birth weight (BW) ?1500 g or ?32 weeks' gestational age and those with BW >1500 g or >32 weeks' GA with an unstable clinical course were included. The incidence of any ROP or severe ROP and treatment modalities were determined. Results: The study population included 15 745 preterm infants: 11 803 (75%) with GA ?32 weeks, and 3942 (25%) with GA >32 weeks. Overall, 30% were found to have any stage of ROP, and 5% had severe ROP. Severe ROP was diagnosed in 8.2% of infants with BW ?1500 g and 0.6% of infants with BW >1500 g. Of all infants diagnosed with ROP, 16.5% needed laser photocoagulation, and 20 patients born at >32 weeks' GA required this treatment modality. Vitroretinal surgery was performed in 28 infants with severe ROP: 23 with GA ?28 weeks and 5 with GA 29-32 weeks. Conclusions: The findings of our study have the important implication that more mature babies are at risk of severe ROP requiring treatment. An effective programme for detecting and treating ROP should be established in Turkey., Bas, A.Y.; Department of Neonatology, Etlik Zubeyde Hanim Women's Health Teaching and Research HospitalTurkey
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- 2015
3. #kotumubilirdik. La memoria politica del golpe de Estado del 12 de Septiembre
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Narli, N., Akyildiz, K., Tuba Bircan, and Sociology
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golpe de estado, Turquia, 1980, 12 de septiembre, Kenan Evren ,lcsh:History (General) and history of Europe ,Turquia ,1789 ,D299-475 ,12 de septiembre ,12 september 1980, Turkey, political memory, social media, coup ,golpe de estado ,lcsh:D ,Kenan Evren ,History (General) and history of Europe ,lcsh:D299-475 ,lcsh:1789 ,HIVA-Migration - (Civic) Integr - Abstract
Los autores reflexionan sobre la memoria histórica a partir del recuerdo que ha dejado en la sociedad turca el golpe del 12 de septiembre de 1980, conocido en turco como 12 Eylül Darbesi. Dentro de este ejercicio, cobra especial relieve la figura de su ejecutor, el general Kenan Evren, presidente de Turquía entre 1980 y 1989, fallecido en 2015. El artículo incluye los resultados de sondeos de opinión realizados entre la población turca para establecer el alcance del impacto de ese golpe que marcó la política y la sociedad turcas. El artículo fue escrito y entregado antes del fracasado golpe del 15 de julio de 2016
- Published
- 2016
4. Retrospective analysis of congenital heart disease in the Neonatal Intensive Care Unit at Çukurova University during a 5-year period [Çukurova Üniversitesi Tip Fakültesi Hastanesi Yenidogan Yogun Bakim Ünitelerinde son beş yilda izlenen konjenital kalp hastalarinin retrospektif incelenmesi]
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Zan S., Yapicioglu H., Erdem S., Özlü F., Satar M., Özbarlas N., Narli N., and Çukurova Üniversitesi
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Neonate ,Congenital heart defects - Abstract
In this study, newborns with congenital heart disease in the Cukurova University Neonatal Intensive Care Unit during 2007-2011 have been retrospectively evaluated. The incidence of congenital heart disease in newborn babies admitted to the NICU in the 5 years studied was 6.6% (217/3287 patients). 133 (61.3%) of the patients were cyanotic; 76 (35.1%) were acyanotic. Phenotypic malformations were diagnosed in 18 patients, and genetic syndromes in 12 patients. Catheterization-based interventions or cardiac surgery (61 catheter angiographies and 70 surgical procedures) were performed on 112 (51.6%) patients at mean 5.8 ± 7.4 days of admission by pediatric cardiologists or surgeons. 67 (30.8%) of patients with cardiac malformations died during the neonatal period.
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- 2015
5. Is retinopathy of prematurity decreasing? - Comparison of two different periods in the same NICU
- Author
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Satar M., Özlü F., Çekinmez E.K., Yapicioglu-Yildizdaş H., Narli N., Erdem E., Soylu M., and Çukurova Üniversitesi
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Neonate ,Risk factors ,Retinopathy of prematurity - Abstract
PubMedID: 24911851 Retinopathy of prematurity is a retinal vascular disorder seen frequently in very premature infants, and is associated with poor clinical outcomes. The aim of the present study was to assess the association between the incidence of retinopathy of prematurity and mechanical ventilation, oxygen therapy, gestational age, and antenatal steroids in extremely low birth weight infants as well as to retrospectively analyze changes in the incidence and risk factors of retinopathy of prematurity over two study periods.
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- 2014
6. Evaluation and Management of Neonates with Meconium Stained Amniotic Fluid
- Author
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NARLI, N., KIRIMİ, E., SATAR, M., TÜRKMEN, M., HALAZA, M., and YAPICIOĞLU, H.
- Abstract
Objective: The purpose of this study was to evaluateneonates with meconium stained amniotic fluid and toinvestigate whether pulmonary disease and mortalitywere significantly greater in infants with thickmeconium.Method: We evaluated 278 meconium stained neonatesbetween January 1993 ñ February 1999. Amniotic fluidwas defined as thin (221 neonates) or thick (57neonates) by a pediatrician.Results: Compared to neonates with thin meconium,those with thick meconium appeared to havesignificantly greater rates of acidemia, low APGARscores at the 1th and 5th minutes, more need forresuscitation and higher mortality rate. Meconiumaspiration syndrome and hypoxic ischemicencephalopathy were also significantly higher ininfants with thick meconium.Conclusion: Amniotic fluid with thick meconium maycause more respiratory and other complications inneonates than amniotic fluid with thin meconium.Therefore, tracheal suction is recommended for infantsborn depressed and with thick meconium stainedamniotic fluid.Key words: Meconium stained amniotic fluid, neonate
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- 2013
7. Two newborns of heroin-addicted mothers suffering neonatal withdrawal syndrome
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Kale-Çekinmez E., Mutlu B., Yapicioglu H., Özlü F., Asker H., Mert K., Narli N., and Çukurova Üniversitesi
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Heroin ,Withdrawal syndrome ,Opioid ,Newborn - Abstract
PubMedID: 23692726 Neonatal withdrawal syndrome is characterized by non-specific signs and symptoms that occur in infants following in-utero drug exposure. The incidence of neonatal withdrawal syndrome is 16-90% in infants of mothers abusing heroin. Clinical signs of withdrawal syndrome usually occur within the first 48-72 hours after birth. Central nervous system and gastrointestinal system symptoms are the main symptoms. In this case report, two newborns born to the mothers addicted to heroin who suffered neonatal withdrawal syndrome are presented. They were successfully treated with phenobarbital and morphine infusion.
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- 2012
8. A newborn with klinefelter and trisomy 18 syndrome: Case report
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Özlü F., Yapicioglu H., Satar M., Narli N., Özcan K., Tanriverdi N., Erdem S., and Çukurova Üniversitesi
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Trisomy ,Klinefelter syndrome - Abstract
Double trisomy may occur as autosomal with sex chromosome trisomy or double autosomal trisomy. This coincidence is very rare. Trisomy 18, that is first recognized as a specific entity in 1960 by discovery of the extra 18 chromosome, is characterized by intrauterine growth retardation, prominent occiput, micrognathia, rocker-bottom feet. Klinefelter's syndrome, that is described in 1942, is the most common single cause of hypogonadism and infertility. Paternal meiosis errors account for about one half of Klinefelter syndrome while remainder are mostly due to maternal meiosis errors. Here, we present a newborn with trisomy 18 with Klinefelter syndrome (48 XXY, 18+), showing the clinical features of trisomy 18. Copyright © 2012 by Türkiye Klinikleri.
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- 2012
9. A 6-year prospective surveillance of healthcare-associated infections in a neonatal intensive care unit from southern part of Turkey
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Yapicioglu H., Satar M., Ozcan K., Narli N., Ozlu F., Sertdemir Y., Tasova Y., and Çukurova Üniversitesi
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animal structures ,surveillance ,virus diseases ,Healthcare-associated infections ,neonatal intensive care unit ,predominant microorganisms - Abstract
PubMedID: 20412409 Aim: To report the incidence of healthcare-associated infections (HAIs), site of infection and bacterial epidemiology in the Neonatal Intensive Care Unit in a university hospital in Adana, Turkey, between 2001 and 2006. Methods: During these years, HAIs were collected by an active surveillance system. Results: Five hundred one of 2832 infants hospitalised more than 72 h had 1124 HAI. The HAI incidence and incidence density ranged between 14.1 and 29.7 infections/100 patients, and 10.9-17.3 infections/1000 patient days within the study period; 61.5% of HAIs were ventilator-associated infections; 26.2% were bloodstream infections; 3.5% were urinary tract infections; 3.5% were necrotising enterocolitis (Stages II and III) and 1.4% was meningitis. The most frequent pathogens were gram-negative pathogens (75.6% of all infections) followed by gram-positive micro-organisms (21.4%) and Candida species (3.0%). Birthweight, gestational age and Apgar scores were lower and overall mortality rate (32.9% vs. 19.7%) and number of inpatient days were higher in patients with HAIs (for all P < 0.001) when compared with those who did not have HAIs. Furthermore, HAI rate was inversely related to birthweight (P < 0.001). Conclusion: In this study, the overall infection rate is high compared with developed countries and predominant micro-organisms are gram-negative enteric rods. These results strongly suggest the need for improving measures for prevention and control of HAIs in this hospital. © 2010 Paediatrics and Child Health Division (Royal Australasian College of Physicians).
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- 2010
10. A TURKISH NEWBORN INFANT WITH CEREBELLAR AGENESIS/NEONATAL DIABETES MELLITUS AND PTF1A MUTATION
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Ercan Tutak, Satar, M., Yapicioglu, H., Altintas, A., Narli, N., Herguener, Oe, Bayram, Y., and Çukurova Üniversitesi
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PTF1A mutation ,Cerebellar agenesis ,Neonatal diabetes mellitus - Abstract
WOS: 000267880800004 PubMed ID: 19650412 A Turkish newborn infant with cerebellar agenesis/neonatal diabetes mellitus and PTF1A mutation: Classical neonatal diabetes mellitus is defined as hyperglycemia that occurs within the first month of life in term infants. It can be either permanent or transient. Cerebellar agenesis and permanent neonatal diabetes has been previously reported as a new autosomal recessive disorder. Pancreas Transcription Factor 1 Alpha (PTF1A) mutations have been related with this constellation of abnormalities. Here we report a new case of cerebellar agenesis and neonatal diabetes mellitus whose parents are PTF1A mutation carriers.
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- 2009
11. A Turkish newborn infant with cerebelur agenesis/neonatal diabetes mellitus and PTF1A mutation
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Tutak E., Satar M., Yapicioglu H., Altintaş A., Narli N., Hergüner Ö., Bayram Y., and Çukurova Üniversitesi
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PTF1A mutation ,Cerebellar agenesis ,Neonatal diabetes mellitus - Abstract
PubMedID: 19650412 Classical neonatal diabetes mellitus is defined as hyperglycemia that occurs within the first month of life in term infants. It can be either permanent or transient. Cerebellar agenesis and permanent neonatal diabetes has been previously reported as a new autosomal recessive disorder. Pancreas Transcription Factor 1 Alpha (PTF1A) mutations have been related with this constellation of abnormalities. Here we report a new case of cerebellar agenesis and neonatal diabetes mellitus whose parents are PTF1A mutation carriers.
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- 2009
12. Cord blood cytokine levels in neonates born to mothers with prolonged premature rupture of membranes and its relationship with morbidity and mortality
- Author
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Satar M., Turhan E., Yapicioglu H., Narli N., Ozgunen F.T., Çetiner S., and Çukurova Üniversitesi
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Chorioamnionitis ,Prolonged premature rupture of membranes ,Cytokine - Abstract
PubMedID: 18299272 The purpose of this study was to determine cord blood cytokine levels and their relationship with morbidity and mortality in neonates with prolonged, premature rupture of membranes(PPROM). Forty two premature neonates of 29-35 weeks gestational age with PPROM exceeding 24 hours were considered as the PPROM group and simultaneously, 41 premature neonates without PPROM were considered as the control group. All the neonates were admitted to the Neonatology Unit for further evaluation of subsequent complications such as early neonatal sepsis, pneumonia, intraventicular haemorrhage(IVH), respiratory distress syndrome(RDS), necrotizing enterocolitis(NEC) and chronic lung disease(CLD). Cord blood and mothers' blood samples were obtained during delivery in both groups and tested for IL-6, IL-8 and TNF-? levels. Twenty one percent of patients with PPROM had histological chorioamnionitis. The risk for developing early neonatal sepsis increased significantly in neonates whose mothers had histological chorioamnionitis(p < 0.05). There was a statistically significant relationship between PPROM and risk of developing NEC(p < 0.05); no significant increase was seen as regards early neonatal sepsis, IVH, RDS, pneumonia, or BPD. The mean IL-8 levels in cord blood and mothers' serum were significantly higher in the PPROM group(p < 0.001, p< 0.005). In addition, IL-6 levels found in mothers' serum were significantly higher than those found in the control group(p < 0.01). However, levels in cord blood were similar(p > 0.05). TNF-? levels were similar in both groups(p > 0.05). Neonates who developed NEC had higher IL-8 levels in their cord blood when compared to those without NEC(p < 0.05). In conclusion, the presence of PPROM increases the risk of chorioamnionitis. In addition, PPROM increases the risk of NEC, and patients who developed NEC had significantly higher cord blood IL-8 values. We may conclude that patients with PPROM and higher IL-8 levels in cord blood might be considered as at possible risk of NEC.
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- 2008
13. A newborn infant with intrapericardial rhabdomyosarcoma: A case report
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Tutak E., Satar M., Özbarlas N., Uguz A., Yapicioglu H., Narli N., Bayram I., and Çukurova Üniversitesi
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musculoskeletal diseases ,genetic structures ,Rhabdomyosarcoma ,Newborn ,human activities ,Pericardium ,eye diseases - Abstract
PubMedID: 18664085 Cardiac tumors are uncommon in neonates and most of them are histologically benign. The most common cardiac tumor in neonates and infants is rhabdomyoma. Malignant cardiac tumors are considerably rarer, and rhabdomyosarcoma (RMS) is the leading malignancy. To our knowledge, only one case of intrapericardial RMS was reported in the literature, in a seven-month-old baby. Here we present another newborn baby with intrapericardial RMS.
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- 2008
14. Chromosome and p63 gene analysis of an infant with ectrodactyly-split hand and foot malformation
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Demirhan O., Taştemir D., Narli N., Soyupak S., Özcan K., and Çukurova Üniversitesi
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Split-syndactyly hand ,Cytogenetics ,Flat-syndactyly foot ,Bilateral syndactyly ,Ectrodactyly ,p63 gene - Abstract
Aim: Split hand-split foot malformation (SHFM) results from central ray reduction and presents as median clefts of the hands and feet, syndactyly, aplasia or hypoplasia of the phalanges, metacarpals and metatarsals, which are frequently associated with other phenotypic abnormalities. We aimed to investigate the genetic pathway of SHFM in a child. Materials and methods: Cytogenetic and molecular genetic analysis was performed in a 10-day-old boy with split-syndactyly hand and flat-syndactyly foot. Results: We found a complex chromosomal rearrangement including breaks in 4q12, fragility in the 9q11-13 band region and 9qh+. Cytogenetic results agree with the literature findings. The mutation analysis of the p63 gene revealed no mutation. Conclusion: The phenotype of our patient may be due to variable expressivity and penetrance of the p63 gene and to other genetic factors, or the mutation can be located in the other 4 loci for SHFM. Additional minor modifying genes, which predispose to non-syndromic cleft palate, could also contribute to the expression of the cleft palate component of the EEC syndrome. © TÜBİTAK.
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- 2007
15. Resuscitation of the newborn at birth [Dogumda yenidogan bebegin resüsitasyonu]
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Narli N. and Çukurova Üniversitesi
- Abstract
Approximately 10% of newborns require some degree of active resuscitation at birth. All the equipment should be maintained before delivery as if the baby will be delivered in its worst condition. The person caring the baby should be present in every delivery and should be educated about newborn resuscitation. After delivery, determination of the need for resuscitative efforts should begin immediately and proceed throughout the A, B, C and D resuscitation blocks. With the developing perinatal care, the very extremely preterm babies live more and these babies need different resuscitation management. Resuscitation of these babies begin inutero. Neonatal T-piece resuscitator should be used to prevent valotrauma and barotauma and time for surfactant installation should be managed properly.
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- 2007
16. Evaluation of 21 infants with arrythmia in the neonatal period [Yenidogan döneminde aritmi gelişen 21 vakanin degerlendirilmesi]
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Satar M., Narli N., Özbarlas N., Yapicioglu Yildizdaş H., Küçükosmanoglu O., Özlü F., Özcan K., and Çukurova Üniversitesi
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Neonate ,cardiovascular system ,cardiovascular diseases ,Prenatal ecocardiogram ,Cardiac arrythmia - Abstract
Perinatal arrythmia is described as abnormal heart rates or existence of extrasystoles in the fetal or neonatal period. In this study, neonates admitted to the Çukurova University Neonatal Intensive Care Unit between 1 January 1998-30 June 2003 for arrythmia or who were diagnosed as arrythmia after hospitalization were evaluated retrospectively. In this period, 21 of 4465 patients (0.4% of all patients) was diagnosed as arrythmia. Supraventricular tachycardia were determined in 12 (57.1%), ventricular tachycardia in two (9.5%), and ventricular fibrillation in two (9.5%), atrioventricular block in five (23.8%) patients. When infants in the neonatal intensive care units are classfied according to diagnosis, frequency of arrythmia is low. Although arrythmia in the neonatal period is rare, treatment must be urgent.
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- 2006
17. Barttin mutations in antenatal Bartter syndrome with sensorineural deafness [5]
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Ozlu F., Yapicioglu H., Satar M., Narli N., Ozcan K., Buyukcelik M., Konrad M., and Çukurova Üniversitesi
- Abstract
PubMedID: 16773427 [No abstract available]
- Published
- 2006
18. A neonate with malignant ectomesenchymoma
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Bayram I., Leblebisatan G., Yildizdaş H., Tuncer Ü., Ergin M., Narli N., Tanyeli A., and Çukurova Üniversitesi
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Neonate ,Malignant ectomesenchymoma - Abstract
PubMedID: 16363352 Malignant ectomesenchymoma is a rare tumor reported in head-neck, abdomen and perineal regions. It consists of mesenchymal and neuroectodermal elements. In this tumor group, neoplastic cells are differentiated into neuronal cells. It also has at least one malignant mesenchymal element, generally rhabdomyosarcoma. In this report we present a neonate with ectomesenchymoma.
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- 2005
19. Maternal and neonatal effects of remifentanil used for endotracheal intubation in caesarean section [Sezaryenlerde endotrakeal entübasyon i·çin kullanilan remifentanilin anne ve yenidogandaki etkileri]
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Özalevli M., Gündüz M., Ünlügenç H., Agar S., Narli N., Işik G., and Çukurova Üniversitesi
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Remifentanil ,Caesarean ,Neuroadaptive capacity score ,APGAR score - Abstract
Aim: This prospective, randomised, double-blinded study was performed to compare intubating conditions, maternal and neonatal effects of remifentanil used for endotracheal intubation in caesarean section with succinylcholine. Materials and Methods: Following Faculty ethic committee approval and written informed consent of parturients, ninety-six parturient were assigned randomly to one of three groups. After intravenous administration of atropine 0.5 mg, anaesthesia was induced with thiopental sodium (5 mg kg-1) followed by remifentanil 2,5 µg kg-1 (Group R2) (n=32), remifentanil 3 µg kg-1 (Group R3) (n=32) over 60 seconds or succinylcholine 1.5 mg kg -1 (Group S) (n=32). Intubating conditions and haemodynamic parameters were recorded. Preoperatively and after umbilical cord clamping, maternal blood samples were taken to evaluate plasma renin, glucose, and cortisol, and neonatal umbilical cord blood samples were taken to evaluate blood gas values. New-borns' performance were assessed using APGAR and neuro adaptive capacity scores (NACS). Results: Intubation conditions were significantly better in group R3 and S than in group R2 (p
- Published
- 2005
20. Seckel syndrome: Case report [Seckel sendromu]
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Özcan K., Yildizdaş H.Y., Özlü F., Satar M., Narli N., and Çukurova Üniversitesi
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congenital, hereditary, and neonatal diseases and abnormalities ,otorhinolaryngologic diseases - Abstract
Seckel syndrome, an autosomal recessive syndrome is characterised by microcephaly, dwarfism-prenatal onset growth deficiency, prominent nose, bird- like narrow face, micrognathia, severe mental retardation, chromosomal instability, pancytopenia. Incidence is 1:10000. Here an uncommon case with Seckel Syndrome was reported.
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- 2005
21. A newborn infant with generalized glutathione synthetase deficiency
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Yapicioglu, H., Satar, M., Ercan Tutak, Narli, N., Topaloglu, Ak, and Çukurova Üniversitesi
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Glutathione synthetase deficiency ,Newborn - Abstract
PubMedID: 15074378 Pyroglutamic aciduria (5-oxoprolinuria) is a rare autosomal recessive disorder caused by either glutathione synthetase deficiency (GSSD) or 5-oxoprolinase deficiency. The severe form of the disease, generalized GSSD, is characterized by acute metabolic acidosis, usually present in the neonatal period with hemolytic anemia and progressive encephalopathy. We report a female infant who had a severe metabolic acidosis with high anion gap, hemolytic anemia, and hyperbilirubinemia. High level of 5-oxoproline was detected in her urine and a diagnosis of generalized GSSD was made. She died of severe metabolic acidosis and sepsis at the age of six weeks.
- Published
- 2004
22. Schwartz-Jampel syndrome: Three pediatric case reports
- Author
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Yapicioğlu H, Satar M, dincer yildizdas, Narli N, Suleymanova D, Tutak E, and Çukurova Üniversitesi
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Male ,Child, Preschool ,Schwartz-Jampel syndrome ,Infant, Newborn ,Humans ,Abnormalities, Multiple ,Female ,Osteochondrodysplasias ,Autosomal recessive inheritance ,Myotonia - Abstract
PubMedID: 14577682 Schwartz-Jampel syndrome: three pediatric case reports: Schwartz-Jampel syndrome is a heterogeneous autosomal recessive syndrome defined by myotonia, short stature, bone dysplasia and growth retardation. Three types have been described: type 1A, usually recognized in childhood, with moderate bone dysplasia; type 1B similar to type 1A but recognizable at birth, with more prominent bone dysplasia and type 2, a rare, more severe form with increased mortality in the neonatal period. In this paper we report three pediatric cases, one with neonatal manifestation.
- Published
- 2003
23. A newborn infant with sternal malformation/vascular dysplasia association
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Yapicioglu H., Narli N., Satar M., Soyupak S., Küçükosmanoglu O., and Çukurova Üniversitesi
- Subjects
Sternum ,Supraumbilical raphe ,Umbilicus ,Hemangiomas ,Cleft Lip ,Infant, Newborn ,Sternal malformation ,musculoskeletal system ,Newborn ,body regions ,Cleft Palate ,Humans ,Abnormalities, Multiple ,Female ,cardiovascular diseases ,Facial Neoplasms ,Hemangioma - Abstract
PubMedID: 12017236 Sternal malformation/vascular dysplasia complex was described by Hersch et al. in 1985. The principle findings include cleft of the sternum covered by an atrophic skin, a midline abdominal raphe and hemangiomatosis. The inheritance pattern seems to be sporadic. We report a newborn baby with sternal defect, cleft lip and palate, supraumbilical raphe and hemangiomas.
- Published
- 2002
24. Surfactant replacement therapy in respiratory distress syndrome: Two years of experience [RESPIRATUAR DISTRES SENDROMUNDA SURFAKTAN REPLASMAN TEDAVISI: IKI YILLIK DENEYIM SONUCLARI]
- Author
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Atici A., Satar M., Turkmen M., Narli N., and Çukurova Üniversitesi
- Subjects
Surfactant therapy ,Respiratory distress syndrome ,Preterm infant - Abstract
We present the results of 20 premature infants with respiratory distress syndrome (RDS) treated with exogenous surfactant (Survanta). The mean gestational age of the infants was 29.1 ± 2.8 (23-24) weeks with a mean birth weight of 1248 ± 301 (755-1750) g. Infants with perinatal hypoxic-ischemic encephalopathy, intrauterine infections and congenital malformations were not included in the study. Surfactant (100 mg/kg, 4 ml/kg) was administered intratracheally to neonates within six hours after birth under the rescue strategy. Four infants received a second dose of surfactant after 6-8 hours. A significant decrease was observed in the fraction of inspired oxygen and partial pressure of carbondioxide, and a significant increase was observed in blood pH and partial pressure of oxygen following surfactant therapy. The survival rate was 50% in infants weighing 1501-150 g, and 41.6% in those weighing 1000-1500 g. Four patients weighing less than 1000 g did not survive. Sixteen (80%) patients had some complications, the main complication being systemic infection (40%). These results show that RDS-related mortality can be reduced in our neonatal intensive care unit by administering surfactant to premature infants suffering from RDS.
- Published
- 1996
25. 1130 Evaluation of the Neonates with Cyanotic Congenital Heart Defects Hospitalized in a NICU at Six Years Period
- Author
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Ozlu, F., primary, Satar, M., additional, Ozbarlas, N., additional, Yapicioglu, H., additional, Narli, N., additional, Cekinmez, E. K., additional, and Mert, K., additional
- Published
- 2012
- Full Text
- View/download PDF
26. HealthCare-associated Infections in a Neonatal Intensive Care Unit in Turkey in 2008: Incidence and Risk Factors, A Prospective Study
- Author
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Yapicioglu, H., primary, Ozcan, K., additional, Sertdemir, Y., additional, Mutlu, B., additional, Satar, M., additional, Narli, N., additional, and Tasova, Y., additional
- Published
- 2010
- Full Text
- View/download PDF
27. Increased Serum Malondialdehyde Level in Neonates with Hypoxic-Ischaemic Encephalopathy: Prediction of Disease Severity
- Author
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Kirimi, E, primary, Peker, E, additional, Tuncer, O, additional, Yapicioglu, H, additional, Narli, N, additional, and Satar, M, additional
- Published
- 2010
- Full Text
- View/download PDF
28. Bruck syndrome: osteogenesis imperfecta and arthrogryposis multiplex congenita
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Yapicioğlu, H., primary, Özcan, K., additional, Arikan, Ö, additional, Satar, M., additional, Narli, N., additional, and Özbek, M. H., additional
- Published
- 2009
- Full Text
- View/download PDF
29. May the best friend be an enemy if not recognized early: hypernatremic dehydration due to breastfeeding.
- Author
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Yildizdus HY, Satar M, Tutak E, Narli N, Büyükçelik M, Özlü F, Yldzdaş, Hacer Yapcoğlu, Satar, Mehmet, Tutak, Ercan, Narl, Nejat, Büyükçelik, Mithat, and Ozlü, Ferda
- Published
- 2005
30. Is oral indomethacin effective in treatment of preterm infants with patent ductus arteriosus?
- Author
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Satar, M., Yapicioglu, H., Narli, N., Ozbarlas, N., Kucukosmanoglu, O., Ercan Tutak, and Çukurova Üniversitesi
- Subjects
Patent ductus arteriosus ,Oral indomethacin - Abstract
PubMedID: 15214742 Twenty-one preterm infants (with a mean gestational age and birth weight of 29.3 weeks and 1288.6 g) and nine pretem infants (with a mean gestational age and birth weight of 29.6 weeks and 1153.1 g) were treated with an enteral preparation of indomethacin and with intravenous indomethacin, respectively, for the closure of hemodynamically significant ductus arteriosus. The patients received three doses of either oral indomethacin capsule (Endol, Deva, Turkey) or intravenous indomethacin (Confortid, Dumex GmBH, Germany) in a dose of 0.2 mg/kg at 12-hour intervals. The ductus was closed in 17 (81%) and 7 (77%) of the babies in the orally and intravenously treated groups, respectively (p>0.05). There was no significant difference in blood urea nitrogen, creatinine levels or thrombocyte counts in either group before and after treatment with indomethacin (p>0.05). No side effect was reported in the oral indomethacin group. Oral indomethacin may be an alternative to the intravenous preparation in developing countries if the intravenous form is not available or not affordable.
31. Lung ultrasound score in the decision of patent ductus arteriosus closure in neonates.
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Ozdemir M, Tepe T, Ozlu F, Yapicioglu H, Atmıs A, Demir F, Unal I, and Narli N
- Subjects
- Humans, Infant, Newborn, Female, Male, Infant, Premature, Echocardiography methods, Ultrasonography methods, Treatment Outcome, Ductus Arteriosus, Patent diagnostic imaging, Ductus Arteriosus, Patent physiopathology, Lung diagnostic imaging, Lung physiopathology
- Abstract
Purpose: We aimed to investigate the role of lung ultrasound (LUS) score in the closure of hemodynamically insignificant patent ductus arteriosus (PDA) and the clinical findings of the patients before and after closure., Methods: The study groups (107 preterm neonates under 34 gestational weeks) were classified as hemodynamically significant PDA (group 1), hemodynamically insignificant PDA with closure therapy (group 2), hemodynamically insignificant PDA without closure therapy (group 3), and no PDA group (group 4) based on the echocardiography. 6- and 10-region LUS scores were compared for each group., Results: There was a significant difference between groups 1 and 3 on first, third, and seventh days. In contrast, groups 1 and 2 had similar LUS scores on the first, third, and seventh days. There was a negative correlation between LUS scores on the first and third days and gestational age, birth weight, the first- and fifth-minute APGAR scores, and there was a positive correlation between aortic root to left atrium ratio, and PDA diameter/weight ratio., Conclusion: We observed that LUS scores in patients with hemodynamically insignificant PDA treated with closure therapy were similar to in patients with hemodynamically significant PDA. Thus, LUS score can have role in PDA closure in preterm neonates. However, more comprehensive studies are needed., (© 2024 Wiley Periodicals LLC.)
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- 2024
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32. Factors predicting kidney replacement therapy in pediatric earthquake victims with crush syndrome in the first week following rescue.
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Atmis B, Bayazit AK, Cagli Piskin C, Saribas E, Piskin FC, Bilen S, Ozgur Horoz O, Ekinci F, Turker I, Telefon HA, Unal I, Yilmaz HL, Narli N, and Yildizdas D
- Subjects
- Humans, Child, Female, Adolescent, Male, Retrospective Studies, Renal Dialysis, Phosphorus, Crush Syndrome complications, Crush Syndrome diagnosis, Crush Syndrome therapy, Earthquakes, Acute Kidney Injury diagnosis, Acute Kidney Injury etiology, Acute Kidney Injury therapy
- Abstract
Crush syndrome due to traumatic rhabdomyolysis is one of the most significant problems to occur following earthquakes. On February 6, 2023, millions of people in Turkey were affected by two consecutive Kahramanmaraş earthquakes. The present study reports the analysis of clinical and laboratory findings of crush syndrome in pediatric earthquake victims admitted to our hospital from our region where the earthquake had a devastating effect. Clinical and laboratory findings concerning earthquake victims with crush syndrome were analyzed within the first week to determine what factors are predictive of kidney replacement therapy (KRT). The data of patients were retrospectively collected from medical records. A total of 310 children were admitted as earthquake victims to the pediatric emergency department. Ninety-seven (31%) of these patients had crush syndrome. Fifty-three (55%) of those with crush syndrome were female. The mean age was 10.9 ± 4.7 years, and the mean time under the rubble was 30.6 ± 23.8 h. Twenty-two patients (23%) required KRT. Hemodialysis was applied to 16 (73%) of them, and hemodiafiltration was applied to the other six (27%) in the pediatric intensive care unit. Regarding creatine kinase (CK) levels, the area under the receiver operating characteristic (ROC) curve (AUC) for predicting KRT was 0.905 (95% confidence interval [CI] 0.848-0.963; p < 0.001). The optimal cut-off value was 40,000 U/L with a sensitivity of 86% and a specificity of 83%. In terms of the percentage of body area crushed, the AUC for predicting KRT was 0.907 (95% CI 0.838-0.976; p < 0.001). The optimal cut-off value was 30% with a sensitivity of 86% and a specificity of 88%. Multiple logistic regression analysis showed that each 10% increase in body area crushed (OR 4.16, 95% CI 1.58-10.93, p = 0.004) and 1 mg/dl increase in the serum phosphorus level (OR 4.19, 95% CI 1.71-10.28, p = 0.002) were significant risk factors for dialysis treatment., Conclusions: Crush syndrome and kidney problems are common following disasters like earthquakes. Clinical and laboratory findings at admission can predict dialysis requirement in earthquake victims. While CK elevation, body area crushed percentage, and increased phosphorus level were predictive of dialysis treatment, time under the rubble was not. Even if the patients were under the rubble for a short time, acute kidney injury (AKI) may develop as a result of severe hypovolemia due to crush injuries, and patients may need KRT., What Is Known: •Crush syndrome after earthquakes needs to be treated carefully in victims and can cause AKI and mortality when not treated timely and appropriately., What Is New: •CK level elevation, body area crushed percentage, and increased phosphorus level are predictive of dialysis treatment. •The time under the rubble may not be predictive of dialysis requirement., (© 2023. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)
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- 2023
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33. Birth weight, head circumference, and length of newborns are unaffected by maternal levels of vitamin B12 and folate.
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Yapicioglu Yildizdas H, Erdogan BG, Tepe T, Goruroglu O, Ozlu F, Satar M, and Narli N
- Subjects
- Birth Weight, Female, Ferritins, Folic Acid, Humans, Infant, Infant, Newborn, Micronutrients, Pregnancy, Vitamin B 12, Vitamin B 12 Deficiency epidemiology
- Abstract
Vitamin B12, folate, and other micronutrients are essential for healthy growth. We hypothesized that there is a high prevalence of vitamin B12 deficiency in mothers and their newborns, and that blood serum vitamin B12 and folate levels may affect anthropometric measurements at birth. A total of 204 newborn babies and their 196 mothers were included. Blood samples of newborns and mothers were obtained for vitamin B12 (<200 pg/mL) and folate (<3 ng/mL) deficiencies. Additionally, iron and ferritin levels were measured. The mean gestational age and birth weight were 37.2 ± 2.6 (22.3-41) weeks and 3045 ± 770 (505-4525) g, respectively. All micronutrient levels in cord blood were higher than maternal levels (P = .001). A total of 96.3% of mothers and 64.5% of babies had vitamin B12 deficiency; 4% of mothers and none of the infants had folate deficiency. In total, 38.2% of mothers and 10.6% of infants had ferritin deficiency and 38.7% of mothers and 41.4% of newborns had iron deficiency. There was a negative correlation between cord vitamin B12 level and birth weight and head circumference (r = -0.21, P = .004 and r = -0.16, P = .036, respectively), whereas no correlation was found between maternal micronutrient status and anthropometric measurements of newborns. In conclusion, anthropometric measurements were unaffected by maternal levels, but vitamin B12 deficiency is very common in pregnant women and newborn babies. Mothers and their infants may benefit from early diagnosis and treatment. Awareness of vitamin B12 deficiency in pregnant women and newborns should be increased in Turkey., Competing Interests: Conflict of interest None declared., (Copyright © 2022. Published by Elsevier Inc.)
- Published
- 2022
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34. Intravenous Immunoglobulin Use in Hemolytic Disease Due to ABO Incompatibility to Prevent Exchange Transfusion.
- Author
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Okulu E, Erdeve O, Kilic I, Olukman O, Calkavur S, Buyukkale G, Cetinkaya M, Ulubas D, Demirel N, Hanta D, Ertugrul S, Gultekin ND, Tuncer O, Demir N, Bilgin L, Narli N, Yildiz D, Terek D, Koroglu OA, Seren C, Ozyazici E, Ozdemir R, Turgut H, Narter F, Akin Y, Ozyazici A, Zenciroglu A, Asker HS, Gokmen Z, Salihli M, Bulbul A, Zubarioglu U, Atasay B, and Koc E
- Abstract
Introduction: Intravenous immunoglobulin (IVIG) has been widely used to treat the hemolytic disease of the newborn (HDN). Although it has been shown that IVIG treatment reduces the duration of phototherapy and hospitalization, the use of IVIG in hemolytic disease due to ABO incompatibility has been controversial in recent years. This study aimed to investigate the role of IVIG in the prevention of exchange transfusion in infants with ABO HDN who presented with bilirubin levels at or above the level of exchange transfusion., Materials and Methods: This study evaluated the data of infants with ABO HDN in the Turkish Neonatal Jaundice Online Registry. The infants with ABO HDN who met the total serum bilirubin level inclusion criteria (within 2-3 mg/dL of exchange transfusion or even above exchange transfusion level) were included in the study according to the guidelines from the American Academy of Pediatrics and the Turkish Neonatal Society. All patients were managed according to the unit protocols recommended by these guidelines and received light-emitting diode (LED) phototherapy. Infants who only received LED phototherapy, and who received one dose of IVIG with LED phototherapy were compared., Results: During the study period, 531 term infants were included in the study according to inclusion criteria. There were 408 cases in the phototherapy-only group, and 123 cases in the IVIG group. The demographic findings and the mean bilirubin and reticulocyte levels at admission were similar between the groups ( p > 0.05), whereas the mean hemoglobin level was slightly lower in the IVIG group ( p = 0.037). The mean age at admission was earlier, the need for exchange transfusion was higher, and the duration of phototherapy was longer in the IVIG group ( p < 0.001, p = 0.001, and p < 0.001, respectively). The rate of re-hospitalization and acute bilirubin encephalopathy (ABE) was higher in the IVIG group ( p < 0.001 and p = 0.01, respectively)., Conclusion: In this study, we determined that one dose of IVIG did not prevent an exchange transfusion nor decrease the duration of phototherapy in infants, who had bilirubin levels near or at exchange transfusion level, with hemolytic disease due to ABO incompatibility., Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest., (Copyright © 2022 Okulu, Erdeve, Kilic, Olukman, Calkavur, Buyukkale, Cetinkaya, Ulubas, Demirel, Hanta, Ertugrul, Gultekin, Tuncer, Demir, Bilgin, Narli, Yildiz, Terek, Koroglu, Seren, Ozyazici, Ozdemir, Turgut, Narter, Akin, Ozyazici, Zenciroglu, Asker, Gokmen, Salihli, Bulbul, Zubarioglu, Atasay, Koc and Turkish Neonatal Society IVIG Study Group.)
- Published
- 2022
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35. Effect of Short-Term Morbidities, Risk Factors and Rate of Growth Failure in Very Low Birth Weight Preterms at Discharge.
- Author
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Yapicioglu Yildizdas H, Simsek H, Ece U, Ozlu F, Sertdemir Y, Narli N, and Satar M
- Subjects
- Comorbidity, Energy Intake, Female, Gestational Age, Growth Disorders epidemiology, Humans, Incidence, Infant Nutritional Physiological Phenomena, Infant, Newborn, Infant, Premature, Diseases epidemiology, Infant, Small for Gestational Age growth & development, Male, Parenteral Nutrition, Patient Discharge, Risk Factors, Growth Disorders etiology, Infant, Premature growth & development, Infant, Very Low Birth Weight growth & development
- Abstract
Background: Very low birth weight (VLBW) infants often demonstrate postnatal growth failure (PGF). We aimed to analyze incidence and risk factors for PGF in surviving VLBW infants hospitalized more than 28 days., Materials and Methods: Fenton growth chart (2013) was used for Z-scores for birth weight (BW) and discharge weight. Infants with a decrease in their Z-scores at discharge >1 were considered as 'PGF group' and with a decrease >2 were considered as 'severe PGF group'., Results: One hundred and forty-one of 148 (95.3%) infants had PGF, 88 of 141 (62.4%) had severe PGF. There were significant differences in gestational age, birth and discharge weight, and days to regain BW, age of first and full enteral feeding, duration of parenteral nutrition, lipid emulsions, intubation and hospitalization between groups (p < 0.05). Vasopressor treatment, nosocomial infection, patent ductus arteriosus and bronchopulmonary dysplasia rates were significantly higher in severe PGF group (p < 0.05)., Conclusion: PGF remains a serious problem in our unit. All VLBW preterm infants should be followed for PGF., (© The Author(s) [2019]. Published by Oxford University Press. All rights reserved. For permissions, please email: journals.permissions@oup.com.)
- Published
- 2020
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36. Turkish Neonatal Society guideline on the safe transport of newborn.
- Author
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Narli N, Kırımi E, and Uslu S
- Abstract
The rational presentation form of perinatal care in developed countries is evaluated within the regionalization program. Neonatal transport is the main step for the regionalization of perinatal care. It is a very important factor for reducing neonatal mortality and morbidity, especially in developing countries. Neonatal transport is a system integrity that includes more than one essential matter. Neonatal transport requires special hardware and serious organization because it can be a caused of mortality and morbidity in its own right. This guideline deals with the transport of newborn infants (definitions, personnel, technical equipment, stabilization conditions, special medical conditions, communication), and the current situation in our country and standard approaches. It should not be forgotten that changes in public space will also change the approach and that every baby should be evaluated within himself or special conditions., Competing Interests: Conflict of Interest: No conflict of interest was declared by the authors.
- Published
- 2018
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37. Infantile rhabdoid tumor mimicking hepatic hemangioendothelioma.
- Author
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Kupeli S, Yöntem A, Narli N, Doran F, and Soyupak S
- Subjects
- Hemangioendothelioma diagnostic imaging, Hemangioendothelioma pathology, Humans, Infant, Newborn, Male, Rhabdoid Tumor diagnostic imaging, Rhabdoid Tumor pathology, Tomography Scanners, X-Ray Computed, Diagnosis, Differential, Hemangioendothelioma diagnosis, Rhabdoid Tumor diagnosis
- Published
- 2016
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- View/download PDF
38. Pseudomonas aeruginosa infections due to electronic faucets in a neonatal intensive care unit.
- Author
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Yapicioglu H, Gokmen TG, Yildizdas D, Koksal F, Ozlu F, Kale-Cekinmez E, Mert K, Mutlu B, Satar M, Narli N, and Candevir A
- Subjects
- Bacteremia epidemiology, Bacteremia prevention & control, Cross Infection epidemiology, Cross Infection prevention & control, Disease Outbreaks, Female, Humans, Infant, Newborn, Infection Control, Male, Pseudomonas Infections epidemiology, Pseudomonas Infections prevention & control, Water Supply, Bacteremia transmission, Cross Infection transmission, Equipment Contamination, Fomites microbiology, Intensive Care Units, Neonatal, Pseudomonas Infections transmission, Pseudomonas aeruginosa isolation & purification
- Abstract
Aim: To evaluate the role of electronic faucets in a newborn intensive care unit during a Pseudomonas aeruginosa outbreak., Methods: After three patients had P. aeruginosa bacteremia, environmental cultures including those from patient rooms, incubator, ventilators, total parenteral nutrition solutions, disinfection solutions, electronic and hand-operated faucet filters/water samples after removing filters and staff hands were taken., Results: Only filters of electronic faucets and water samples after removing filters and one liquid hand soap showed P. aeruginosa (3-7 × 106 cfu/mL). We have removed the electronic faucets and new elbow-operated faucets were installed. Pulsed-field gel electrophoresis analysis of outbreak-blood culture isolates from two patients and isolates from electronic water faucets/one liquid hand soap indicated the presence of 90.7% genetically related subtype, probably from the same clone. Water cultures from new faucets were all clean after installation and after 7 months., Conclusion: We suggest that electronic faucets may be considered a potential risk for P. aeruginosa in hospitals, especially in high-risk units., (© 2011 The Authors. Journal of Paediatrics and Child Health © 2011 Paediatrics and Child Health Division (Royal Australasian College of Physicians).)
- Published
- 2012
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39. Healthcare-associated infections in a neonatal intensive care unit in Turkey in 2008: incidence and risk factors, a prospective study.
- Author
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Yapicioglu H, Ozcan K, Sertdemir Y, Mutlu B, Satar M, Narli N, and Tasova Y
- Subjects
- Catheter-Related Infections epidemiology, Catheter-Related Infections microbiology, Cross Infection microbiology, Female, Humans, Incidence, Infant, Newborn, Male, Pneumonia, Ventilator-Associated epidemiology, Pneumonia, Ventilator-Associated microbiology, Prospective Studies, Risk Factors, Turkey epidemiology, Cross Infection epidemiology, Intensive Care Units, Neonatal statistics & numerical data
- Abstract
In this study, we have prospectively recorded healthcare-associated infections (HAIs) in NICU and found incidence density as 18 infections per 1000 patient days. Of the infections, 51.3% was bacteriemia (BSI), and 45.1% was ventilator-associated pneumonia (VAP). Gram-negative microorganisms were predominant in VAP and Staphylococcus epidermidis was the leading microorganism (53.0% of BSIs) in BSIs. Multivariate logistic regression analysis showed the importance of hood O(2) use in days (RR: 1.3) and total parenteral nutrition use in days (RR: 1.09) for BSIs. Umbilical arterial catheterization in days (RR: 1.94), ventilator use in days (RR: 1.05), chest tube (RR: 12.55), orogastric feeding (RR: 3.32) and total parenteral nutrition in days (RR: 1.05) were found to be significantly associated with VAP. In conclusion, incidence density in our unit is high and Gram-negative rods are predominant similar to developing countries. These results strongly suggest improving measures of prevention and control of HAIs in the unit.
- Published
- 2011
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40. A 6-year prospective surveillance of healthcare-associated infections in a neonatal intensive care unit from southern part of Turkey.
- Author
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Yapicioglu H, Satar M, Ozcan K, Narli N, Ozlu F, Sertdemir Y, and Tasova Y
- Subjects
- Humans, Infant, Newborn, Population Surveillance methods, Prospective Studies, Turkey epidemiology, Cross Infection epidemiology, Intensive Care Units, Neonatal
- Abstract
Aim: To report the incidence of healthcare-associated infections (HAIs), site of infection and bacterial epidemiology in the Neonatal Intensive Care Unit in a university hospital in Adana, Turkey, between 2001 and 2006., Methods: During these years, HAIs were collected by an active surveillance system., Results: Five hundred one of 2832 infants hospitalised more than 72 h had 1124 HAI. The HAI incidence and incidence density ranged between 14.1 and 29.7 infections/100 patients, and 10.9-17.3 infections/1000 patient days within the study period; 61.5% of HAIs were ventilator-associated infections; 26.2% were bloodstream infections; 3.5% were urinary tract infections; 3.5% were necrotising enterocolitis (Stages II and III) and 1.4% was meningitis. The most frequent pathogens were gram-negative pathogens (75.6% of all infections) followed by gram-positive micro-organisms (21.4%) and Candida species (3.0%). Birthweight, gestational age and Apgar scores were lower and overall mortality rate (32.9% vs. 19.7%) and number of inpatient days were higher in patients with HAIs (for all P<0.001) when compared with those who did not have HAIs. Furthermore, HAI rate was inversely related to birthweight (P<0.001)., Conclusion: In this study, the overall infection rate is high compared with developed countries and predominant micro-organisms are gram-negative enteric rods. These results strongly suggest the need for improving measures for prevention and control of HAIs in this hospital.
- Published
- 2010
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41. A Turkish newborn infant with cerebellar agenesis/neonatal diabetes mellitus and PTF1A mutation.
- Author
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Tutak E, Satar M, Yapicioğlu H, Altintaş A, Narli N, Hergüner O, and Bayram Y
- Subjects
- Cerebellum parasitology, Consanguinity, Cordocentesis, Diabetes Mellitus, Type 1 diagnosis, Fetal Growth Retardation genetics, Frameshift Mutation, Genetic Carrier Screening, Humans, Infant, Infant, Newborn, Magnetic Resonance Imaging, Male, Pedigree, Respiratory Distress Syndrome, Newborn diagnosis, Respiratory Distress Syndrome, Newborn genetics, Cerebellum abnormalities, DNA Mutational Analysis, Diabetes Mellitus, Type 1 genetics, Transcription Factors genetics
- Abstract
Classical neonatal diabetes mellitus is defined as hyperglycemia that occurs within the first month of life in term infants. It can be either permanent or transient. Cerebellar agenesis and permanent neonatal diabetes has been previously reported as a new autosomal recessive disorder. Pancreas Transcription Factor 1 Alpha (PTF1A) mutations have been related with this constellation of abnormalities. Here we report a new case of cerebellar agenesis and neonatal diabetes mellitus whose parents are PTF1A mutation carriers.
- Published
- 2009
42. A neonate with homozygous protein C deficiency with a homozygous Arg178Trp mutation.
- Author
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Ozlu F, Kyotani M, Taskin E, Ozcan K, Kojima T, Matsushita T, Yapicioğlu H, Takagi A, Saşmaz I, Satar M, and Narli N
- Subjects
- Base Sequence, Disseminated Intravascular Coagulation etiology, Female, Homozygote, Humans, Infant, Newborn, Molecular Sequence Data, Pedigree, Polymerase Chain Reaction, Protein C Deficiency complications, Protein C Deficiency physiopathology, IgA Vasculitis etiology, Mutation, Protein C Deficiency genetics
- Abstract
Homozygous protein C deficiency affects approximately 1/400,000 to 1/1,000,000 live births. Homozygous protein C deficiency is associated with catastrophic and fatal purpura fulminans-like or thrombotic complications and disseminated intravascular coagulation. In the present patient, genetic study revealed Arg178Trp, a mutation found widely in European population; but this is the first case of homozygous Arg178Trp mutation who suffered from catastrophic purpura fulminans phenotype.
- Published
- 2008
- Full Text
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43. A newborn infant with intrapericardial rhabdomyosarcoma: a case report.
- Author
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Tutak E, Satar M, Ozbarlas N, Uğuz A, Yapicioğlu H, Narli N, and Bayram I
- Subjects
- Female, Humans, Infant, Newborn, Heart Neoplasms pathology, Rhabdomyosarcoma pathology
- Abstract
Cardiac tumors are uncommon in neonates and most of them are histologically benign. The most common cardiac tumor in neonates and infants is rhabdomyoma. Malignant cardiac tumors are considerably rarer, and rhabdomyosarcoma (RMS) is the leading malignancy. To our knowledge, only one case of intrapericardial RMS was reported in the literature, in a seven-month-old baby. Here we present another newborn baby with intrapericardial RMS.
- Published
- 2008
44. Cord blood cytokine levels in neonates born to mothers with prolonged premature rupture of membranes and its relationship with morbidity and mortality.
- Author
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Satar M, Turhan E, Yapicioglu H, Narli N, Ozgunen FT, and Cetiner S
- Subjects
- Adult, Chorioamnionitis blood, Chorioamnionitis mortality, Cytokines metabolism, Enterocolitis, Necrotizing complications, Female, Humans, Infant, Newborn, Infant, Premature, Interleukin-6 blood, Interleukin-8 blood, Neonatology methods, Pregnancy, Risk, Sepsis blood, Cytokines blood, Enterocolitis, Necrotizing blood, Enterocolitis, Necrotizing mortality, Fetal Blood metabolism, Fetal Membranes, Premature Rupture blood, Fetal Membranes, Premature Rupture mortality
- Abstract
The purpose of this study was to determine cord blood cytokine levels and their relationship with morbidity and mortality in neonates with prolonged, premature rupture of membranes (PPROM). Forty two premature neonates of 29-35 weeks gestational age with PPROM exceeding 24 hours were considered as the PPROM group and simultaneously, 41 premature neonates without PPROM were considered as the control group. All the neonates were admitted to the Neonatology Unit for further evaluation of subsequent complications such as early neonatal sepsis, pneumonia, intraventicular haemorrhage (IVH), respiratory distress syndrome (RDS), necrotizing enterocolitis (NEC) and chronic lung disease (CLD). Cord blood and mothers' blood samples were obtained during delivery in both groups and tested for IL-6, IL-8 and TNF-alpha levels. Twenty one percent of patients with PPROM had histological chorioamnionitis. The risk for developing early neonatal sepsis increased significantly in neonates whose mothers had histological chorioamnionitis (p < 0.05). There was a statistically significant relationship between PPROM and risk of developing NEC (p < 0.05); no significant increase was seen as regards early neonatal sepsis, IVH, RDS, pneumonia, or BPD. The mean IL-8 levels in cord blood and mothers' serum were significantly higher in the PPROM group (p < 0.001, p< 0.005). In addition, IL-6 levels found in mothers' serum were significantly higher than those found in the control group (p < 0.01). However, levels in cord blood were similar (p > 0.05). TNF-alpha levels were similar in both groups (p > 0.05). Neonates who developed NEC had higher IL-8 levels in their cord blood when compared to those without NEC (p < 0.05). In conclusion, the presence of PPROM increases the risk of chorioamnionitis. In addition, PPROM increases the risk of NEC, and patients who developed NEC had significantly higher cord blood IL-8 values. We may conclude that patients with PPROM and higher IL-8 levels in cord blood might be considered as at possible risk of NEC.
- Published
- 2008
- Full Text
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45. Accentuated varicella exanthems due to cast application.
- Author
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Kara A, Kurtul T, Ilke N, Yildirim I, Devrim I, Cengiz AB, Tezer H, and Seçmeer G
- Subjects
- Adolescent, Forearm virology, Hot Temperature, Humans, Male, Pressure, Casts, Surgical virology, Chickenpox pathology, Chickenpox virology, Herpesvirus 3, Human growth & development, Severity of Illness Index
- Abstract
We report a case of 14-year-old male with local augmentation of varicella zoster exanthems on the forearm on which cast application was performed. After 1 week, the first varicella zoster exanthems began to appear on the left forearm under the cast and trunk, while lesions on the other forearm and extremities were very rare. We postulated that the local pressure and heat increased the number of exanthems.
- Published
- 2007
- Full Text
- View/download PDF
46. Barttin mutations in antenatal Bartter syndrome with sensorineural deafness.
- Author
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Ozlu F, Yapicioğlu H, Satar M, Narli N, Ozcan K, Buyukcelik M, Konrad M, and Demirhan O
- Subjects
- Chloride Channels, Humans, Infant, Newborn, Male, Bartter Syndrome genetics, Hearing Loss, Sensorineural genetics, Membrane Proteins genetics, Mutation genetics
- Published
- 2006
- Full Text
- View/download PDF
47. Ultrasonographic measurement of subarachnoid space in normal term newborns.
- Author
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Narli N, Soyupak S, Yildizdaş HY, Tutak E, Ozcan K, Sertdemir Y, and Satar M
- Subjects
- Body Height, Body Weight, Female, Gestational Age, Head anatomy & histology, Humans, Infant, Newborn, Male, Prospective Studies, Term Birth, Ultrasonography, Subarachnoid Space anatomy & histology, Subarachnoid Space diagnostic imaging
- Abstract
This study was conducted in order to assess the normal range of subarachnoid space width in healthy term newborns. A total of 230 healthy newborns were evaluated within the first 28 days of life. Measurements were correlated with body weight, height and head circumference. Mean measurements for falx-cortex and craniocortical widths and the correlations are given in tables. Subarachnoid space widths increased as weight, height and head circumference increased and the correlation was statistically significant.
- Published
- 2006
- Full Text
- View/download PDF
48. The effect of human growth hormone on superoxide dismutase activity, glutathione and malondialdehyde levels of hypoxic-ischemic newborn rat brain.
- Author
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Yapicioğlu H, Satar M, Canacankatan N, Tutak E, Sertdemir Y, Antmen E, and Narli N
- Subjects
- Animals, Animals, Newborn, Brain enzymology, Brain Chemistry, Brain Stem chemistry, Brain Stem enzymology, Carotid Artery, Common surgery, Cerebellum chemistry, Cerebellum enzymology, Human Growth Hormone adverse effects, Humans, Hypoxia-Ischemia, Brain enzymology, Hypoxia-Ischemia, Brain etiology, Ligation, Lipid Peroxidation drug effects, Rats, Glutathione analysis, Human Growth Hormone pharmacology, Hypoxia-Ischemia, Brain metabolism, Malondialdehyde analysis, Superoxide Dismutase metabolism
- Abstract
Objectives: We investigated the effect of human growth hormone (GH) on newborn rat brain superoxide dismutase, glutathione and malondialdehyde (MDA) levels in hypoxic-ischemic (H-I) newborn rats., Methods: Fourty-eight 7 days old newborn rats were randomized to a healthy (n: 15), H-I (n: 18) and GH administered H-I (GH-H-I, n: 15) group. Permanent, left common carotid ligation was performed in the H-I groups. In the GH-H-I group, 50 mg/kg human GH (Norditropin Simplex, Novo Nordisk A/S) was administered subcutaneously just before carotid artery ligation. Two hours after ligation, rats were subjected to 2 h of hypoxemia and then were decapitated. Right and left cerebral hemispheres (CHs) and cerebellum-brain stem (C-BS) were separated., Results: Glutathione levels of each region were not statistically different from each other in and between the groups. Superoxide dismutase levels were higher in C-BSs compared to CHs (for each comparison p < 0.01). CHs and C-BS MDA levels were similar in the control and H-I groups but MDA levels of both CHs of the GH-H-I group were significantly higher than the levels of the H-I group (p = 0.01; p = 0.024, respectively). Left CH MDA level of GH-H-I group was higher compared to left CH MDA of the control group (p = 0.045) while there was no difference between right CHs. In the GH-H-I group, left CH MDA level was higher than the C-BS (p = 0.03). MDA levels of the C-BSs did not differ between the groups (p > 0.05)., Conclusion: Although we have not evaluated the effect of GH histopathologically, increased lipid peroxidation especially in the H-I (left) hemisphere of the GH treated rats might suggest that GH treatment may be harmful in H-I encephalopathy., (Copyright 2006 S. Karger AG, Basel.)
- Published
- 2006
- Full Text
- View/download PDF
49. A neonate with malignant ectomesenchymoma.
- Author
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Bayram I, Leblebisatan G, Yildizdaş H, Tuncer U, Ergin M, Narli N, and Tanyeli A
- Subjects
- Facial Neoplasms drug therapy, Facial Neoplasms metabolism, Fatal Outcome, Female, Humans, Immunohistochemistry, Infant, Newborn, Mesenchymoma drug therapy, Mesenchymoma metabolism, Facial Neoplasms diagnosis, Mesenchymoma diagnosis
- Abstract
Malignant ectomesenchymoma is a rare tumor reported in head-neck, abdomen and perineal regions. It consists of mesenchymal and neuroectodermal elements. In this tumor group, neoplastic cells are differentiated into neuronal cells. It also has at least one malignant mesenchymal element, generally rhabdomyosarcoma. In this report we present a neonate with ectomesenchymoma.
- Published
- 2005
50. The activity and kinetics of pyruvate kinase in hypoxic newborns.
- Author
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Narli N, Satar M, Kayrin L, Yapicioğlu H, Ozlü F, and Budgayci R
- Subjects
- Adenosine Diphosphate analysis, Adenosine Triphosphate analysis, Female, Humans, Hypoxia blood, Infant, Newborn, Kinetics, Male, Oxygen metabolism, Erythrocytes enzymology, Glycolysis, Hypoxia enzymology, Pyruvate Kinase analysis
- Abstract
Pyruvate kinase (PK) plays a key role in erythrocytes, which obtain most of their energy from glycolysis. This study investigated erythrocyte energy metabolism in hypoxic newborns, measuring pyruvate kinase activity, kinetic, and ATP levels in hypoxia. Forty-nine babies who had cord pH value lower than 7.2 and Apgar scores lower than 7 in the first minute were accepted as the hypoxic group, and 48 babies who had cord pH value higher than 7.2 and an Apgar score higher than 7 in the first minute were taken as controls. The erythrocyte mean PK activity was found to be lower (16.9+/-8.5 [5.8-47.9] EU/gHb) in the hypoxic group than the control group (21.3+/-10.9 [3.9-44.3] EU/gHb) (p<.05). The mean ATP value of hypoxic group was higher (19.2+/-11.3 [3.9-37.6] mM) compared to control group (13.8+/-7.16 [3.9-28.7] mM). In the kinetic study, with different ADP concentrations in the control group, the substrate amount (Km) that is needed to reach the half-maximum of enzyme activity (Vmax=27.7 Eu/gHb) was found to be 2.70 mM, but it was 1.47 mM to reach Vmax (22.7 Eu/gHb) in the hypoxic group. Vmax was 41.67 Eu/gHb and Km was 8.33 mM in the control group at different PEP concentrations, whereas Vmax was 21.7 Eu/gHb and Km was 0.89 mM in the hypoxic group. Increase in the ATP level while ePK activity decreases, suggesting that glycolysis increases in hypoxia. In the kinetic study, the substrate amount needed for reaching the half-maximum of enzyme activity was less in the hypoxic group, probably suggests that pyruvate kinase increases glycolysis by increasing its affinity to the substrates. In this way, erythrocytes may gain the energy required for oxygen delivery to tissues and maintaining ion gradient. This arrangement possibly proceeds from sygmoidal structure of pyruvate kinase.
- Published
- 2005
- Full Text
- View/download PDF
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