Early or delayed cord clamping during transition of term newborns: does it make any difference in cerebral tissue oxygenation?


Journal

Italian journal of pediatrics
ISSN: 1824-7288
Titre abrégé: Ital J Pediatr
Pays: England
ID NLM: 101510759

Informations de publication

Date de publication:
29 Jul 2024
Historique:
received: 07 12 2023
accepted: 16 07 2024
medline: 30 7 2024
pubmed: 30 7 2024
entrez: 29 7 2024
Statut: epublish

Résumé

According to the World Health Organization's recommendation, delayed cord clamping in term newborns can have various benefits. Cochrane metaanalyses reported no differences for mortality and early neonatal morbidity although a limited number of studies investigated long-term neurodevelopmental outcomes. The aim of our study is to compare the postnatal cerebral tissue oxygenation values in babies with early versus delayed cord clamping born after elective cesarean section. In this study, a total of 80 term newborns delivered by elective cesarean section were included. Infants were randomly grouped as early (clamped within 15 s, n:40) and delayed cord clamping (at the 60th second, n:40) groups. Peripheral arterial oxygen saturation (SpO2) and heart rate were measured by pulse oximetry while regional oxygen saturation of the brain (rSO2) was measured with near-infrared spectrometer. Fractional tissue oxygen extraction (FTOE) was calculated for every minute between the 3rd and 15th minute after birth. (FTOE = pulse oximetry value-rSO2/pulse oximetry value). The measurements were compared for both groups. The demographical characteristics, SpO2 levels (except postnatal 6th, 8th, and 14th minutes favoring DCC p < 0.05), heart rates and umbilical cord blood gas values were not significantly different between the groups (p > 0.05). rSO2 values were significantly higher while FTOE values were significantly lower for every minute between the 3rd and 15th minutes after birth in the delayed cord clamping group (p < 0.05). Our study revealed a significant increase in cerebral rsO2 values and a decrease in FTOE values in the delayed cord clamping (DCC) group, indicating a positive impact on cerebral oxygenation and hemodynamics. Furthermore, the DCC group exhibited a higher proportion of infants with cerebral rSO2 levels above the 90th percentile. This higher proportion, along with a lower of those with such parameter below the 10th percentile, suggest that DCC may lead to the targeted/optimal cerebral oxygenetaion of these babies. As a result, we recommend measuring cerebral oxygenation, in addition to peripheral SpO2, for infants experiencing perinatal hypoxia and receiving supplemental oxygen.

Sections du résumé

BACKGROUND BACKGROUND
According to the World Health Organization's recommendation, delayed cord clamping in term newborns can have various benefits. Cochrane metaanalyses reported no differences for mortality and early neonatal morbidity although a limited number of studies investigated long-term neurodevelopmental outcomes. The aim of our study is to compare the postnatal cerebral tissue oxygenation values in babies with early versus delayed cord clamping born after elective cesarean section.
METHODS METHODS
In this study, a total of 80 term newborns delivered by elective cesarean section were included. Infants were randomly grouped as early (clamped within 15 s, n:40) and delayed cord clamping (at the 60th second, n:40) groups. Peripheral arterial oxygen saturation (SpO2) and heart rate were measured by pulse oximetry while regional oxygen saturation of the brain (rSO2) was measured with near-infrared spectrometer. Fractional tissue oxygen extraction (FTOE) was calculated for every minute between the 3rd and 15th minute after birth. (FTOE = pulse oximetry value-rSO2/pulse oximetry value). The measurements were compared for both groups.
RESULTS RESULTS
The demographical characteristics, SpO2 levels (except postnatal 6th, 8th, and 14th minutes favoring DCC p < 0.05), heart rates and umbilical cord blood gas values were not significantly different between the groups (p > 0.05). rSO2 values were significantly higher while FTOE values were significantly lower for every minute between the 3rd and 15th minutes after birth in the delayed cord clamping group (p < 0.05).
CONCLUSION CONCLUSIONS
Our study revealed a significant increase in cerebral rsO2 values and a decrease in FTOE values in the delayed cord clamping (DCC) group, indicating a positive impact on cerebral oxygenation and hemodynamics. Furthermore, the DCC group exhibited a higher proportion of infants with cerebral rSO2 levels above the 90th percentile. This higher proportion, along with a lower of those with such parameter below the 10th percentile, suggest that DCC may lead to the targeted/optimal cerebral oxygenetaion of these babies. As a result, we recommend measuring cerebral oxygenation, in addition to peripheral SpO2, for infants experiencing perinatal hypoxia and receiving supplemental oxygen.

Identifiants

pubmed: 39075594
doi: 10.1186/s13052-024-01707-9
pii: 10.1186/s13052-024-01707-9
doi:

Substances chimiques

Oxygen S88TT14065

Types de publication

Journal Article Randomized Controlled Trial Comparative Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

133

Informations de copyright

© 2024. The Author(s).

Références

Hutton EK, Hassan ES. Late vs early clamping of the umbilical cord in full-term neonates: systematic review and meta-analysis of controlled trials. JAMA. 2007;297(11):1241–52. https://doi.org/10.1001/jama.297.11.1241 .
doi: 10.1001/jama.297.11.1241 pubmed: 17374818
Raju TN, Singhal N. Optimal timing for clamping the umbilical cord after birth. Clin Perinatol. 2012;39(4):889–900. https://doi.org/10.1016/j.clp.2012.09.006 .
doi: 10.1016/j.clp.2012.09.006 pubmed: 23164185
Serra G, Giuffrè M, Piro E, Corsello G. The social role of pediatrics in the past and present times. Ital J Pediatr. 2021;47(1):239. https://doi.org/10.1186/s13052-021-01190-6 .
doi: 10.1186/s13052-021-01190-6 pubmed: 34922600 pmcid: 8684095
Mercer JS, Erickson-Owens DA, Deoni SCL, et al. Effects of delayed cord clamping on 4-month ferritin levels, brain myelin content, and neurodevelopment: a Randomized Controlled Trial. J Pediatr. 2018;203:266–e722. https://doi.org/10.1016/j.jpeds.2018.06.006 .
doi: 10.1016/j.jpeds.2018.06.006 pubmed: 30473033 pmcid: 6259583
Delayed Umbilical Cord Clamping After Birth. ACOG Committee Opinion Summary, Number 814. Obstet Gynecol. 2020;136(6):1238–9. https://doi.org/10.1097/AOG.0000000000004168 .
doi: 10.1097/AOG.0000000000004168
Cavallin F, Galeazzo B, Loretelli V, et al. Delayed cord clamping versus early cord clamping in elective cesarean section: a randomized controlled trial. Neonatology. 2019;116(3):252–9. https://doi.org/10.1159/000500325 .
doi: 10.1159/000500325 pubmed: 31266035
Aziz K, Lee HC, Escobedo MB, Hoover AV, Kamath-Rayne BD, Kapadia VS, et al. Part 5: Neonatal Resuscitation 2020 American Heart Association Guidelines for Cardiopulmonary Resuscitation and Emergency Cardiovascular Care. Circulation. 2020;142:524–50. https://doi.org/10.1161/CIR.0000000000000902 .
doi: 10.1161/CIR.0000000000000902
Saugtsad OD, Robertson NJ, Vento M. A critical review of the 2020 International Liaison Committee on Resuscitation treatment recommendations for resuscitating the newly born infant. Acta Paediatr. 2021;110(4):1107–12. https://doi.org/10.1111/apa.15754 .
doi: 10.1111/apa.15754
Wyckoff MH, Wyllie J, Aziz K, de Almeida MF, Fabres J, Fawke J, et al. Neonatal life support: 2020 International Consensus on Cardiopulmonary Resuscitation and Emergency Cardiovascular CareScience with Treatment recommendations.(CoSTR. Circulation. 2020;142:140–84. https://doi.org/10.1161/CIR.0000000000000895 .
doi: 10.1161/CIR.0000000000000895
Piro E, Serra G, Schierz IAM, Giuffrè M, Corsello G. Fetal growth restriction: a growth pattern with fetal, neonatal and long-term consequences. Euromediterranean Biomedical J. 2019;14(09):038–44.
Vural I, Ozdemir H, Teker G, Yoldemir T, Bilgen H, Ozek E. Delayed cord clamping in term large-for-gestational age infants: a prospective randomised study. J Paediatr Child Health. 2019;55(5):555–60. https://doi.org/10.1111/jpc.14242 .
doi: 10.1111/jpc.14242 pubmed: 30288843
Yao AC, Moinian M, Lind J. Distribution of blood between infant and placenta after birth. Lancet. 1969;2(7626):871–3. https://doi.org/10.1016/s0140-6736(69)92328-9 .
doi: 10.1016/s0140-6736(69)92328-9 pubmed: 4186454
Katheria AC, Lakshminrusimha S, Rabe H, McAdams R, Mercer JS. Placental transfusion: a review. J Perinatol. 2017;37(2):105–11. https://doi.org/10.1038/jp.2016.151 .
doi: 10.1038/jp.2016.151 pubmed: 27654493
Raju TN. Timing of umbilical cord clamping after birth for optimizing placental transfusion. Curr Opin Pediatr. 2013;25(2):180–7. https://doi.org/10.1097/MOP.0b013e32835d2a9e .
doi: 10.1097/MOP.0b013e32835d2a9e pubmed: 23407180
Rabe H, Gyte GM, Díaz-Rossello JL, Duley L. Effect of timing of umbilical cord clamping and other strategies to influence placental transfusion at preterm birth on maternal and infant outcomes. Cochrane Database Syst Rev. 2019;9(9):CD003248. https://doi.org/10.1002/14651858.CD003248.pub4 .
doi: 10.1002/14651858.CD003248.pub4 pubmed: 31529790
Serra G, Miceli V, Albano S, Corsello G. Perinatal and newborn care in a two years retrospective study in a first level peripheral hospital in Sicily (Italy). Ital J Pediatr. 2019;45(1):152. https://doi.org/10.1186/s13052-019-0751-6 .
doi: 10.1186/s13052-019-0751-6 pubmed: 31783883 pmcid: 6884854
Kc A, Rana N, Målqvist M, Jarawka Ranneberg L, Subedi K, Andersson O. Effects of delayed umbilical cord clamping vs early clamping on anemia in infants at 8 and 12 months: a Randomized Clinical Trial. JAMA Pediatr. 2017;171(3):264–70. https://doi.org/10.1001/jamapediatrics.2016.3971 .
doi: 10.1001/jamapediatrics.2016.3971 pubmed: 28114607
Gomersall J, Berber S, Middleton P, et al. Umbilical cord management at term and late preterm birth: a meta-analysis. Pediatrics. 2021;147(3):e2020015404. https://doi.org/10.1542/peds.2020-015404 .
doi: 10.1542/peds.2020-015404 pubmed: 33632933
Kc A, Malqvist M, Rana N, Ranneberg LJ, Andersson O. Effect of timing of umbilical cord clamping on anaemia at 8 and 12 months and later neurodevelopment in late pre-term and term infants; a facility-based, randomized-controlled trial in Nepal. BMC Pediatr. 2016;16:35. https://doi.org/10.1186/s12887-016-0576-z .
doi: 10.1186/s12887-016-0576-z pubmed: 26965317 pmcid: 4787033
Andersson O, Hellström-Westas L, Andersson D, Domellöf M. Effect of delayed versus early umbilical cord clamping on neonatal outcomes and iron status at 4 months: a randomised controlled trial. BMJ. 2011;343:d7157. https://doi.org/10.1136/bmj.d7157 .
doi: 10.1136/bmj.d7157 pubmed: 22089242 pmcid: 3217058
Chopra A, Thakur A, Garg P, Kler N, Gujral K. Early versus delayed cord clamping in small for gestational age infants and iron stores at 3 months of age - a randomized controlled trial. BMC Pediatr. 2018;18(1):234. https://doi.org/10.1186/s12887-018-1214-8 .
doi: 10.1186/s12887-018-1214-8 pubmed: 30021580 pmcid: 6052555
Radlowski EC, Johnson RW. Perinatal iron deficiency and neurocognitive development. Front Hum Neurosci. 2013;7:585. https://doi.org/10.3389/fnhum.2013.00585 .
doi: 10.3389/fnhum.2013.00585 pubmed: 24065908 pmcid: 3779843
Wolf M, Greisen G. Advances in near-infrared spectroscopy to study the brain of the preterm and term neonate. Clin Perinatol. 2009;36(4):807–34. https://doi.org/10.1016/j.clp.2009.07.007 .
doi: 10.1016/j.clp.2009.07.007 pubmed: 19944837
Almaazmi M, Schmid MB, Havers S, et al. Cerebral near-infrared spectroscopy during transition of healthy term newborns. Neonatology. 2013;103(4):246–51. https://doi.org/10.1159/000345926 .
doi: 10.1159/000345926 pubmed: 23428614
Isobe K, Kusaka T, Fujikawa Y, et al. Measurement of cerebral oxygenation in neonates after vaginal delivery and cesarean section using full-spectrum near infrared spectroscopy. Comp Biochem Physiol Mol Integr Physiol. 2002;132(1):133–8. https://doi.org/10.1016/s1095-6433(01)00539-6 .
doi: 10.1016/s1095-6433(01)00539-6
Schierz IAM, Serra G, Antona V, Persico I, Corsello G, Piro E. Infant developmental profile of Crisponi syndrome due to compound heterozygosity for CRLF1 deletion. Clin Dysmorphol. 2020;29(3):141–3. https://doi.org/10.1097/MCD.0000000000000325 .
doi: 10.1097/MCD.0000000000000325 pubmed: 32433043
Serra G, Antona V, Giuffrè M, et al. Interstitial deletions of chromosome 1p: novel 1p31.3p22.2 microdeletion in a newborn with craniosynostosis, coloboma and cleft palate, and review of the genomic and phenotypic profiles. Ital J Pediatr. 2022;48(1):38. https://doi.org/10.1186/s13052-022-01232-7 .
doi: 10.1186/s13052-022-01232-7 pubmed: 35246213 pmcid: 8896361
Baenziger O, Stolkin F, Keel M, et al. The influence of the timing of cord clamping on postnatal cerebral oxygenation in preterm neonates: a randomized, controlled trial. Pediatrics. 2007;119(3):455–59. https://doi.org/10.1542/peds.2006-2725 .
doi: 10.1542/peds.2006-2725 pubmed: 17332197
Piro E, Serra G, Schierz IAM, Giuffrè M, Corsello G. Neonatal ten-year retrospective study on neural tube defects in a second level University Hospital. Ital J Pediatr. 2020;46(1):72. https://doi.org/10.1186/s13052-020-00836-1 .
doi: 10.1186/s13052-020-00836-1 pubmed: 32448340 pmcid: 7247239
Serra G, Felice S, Antona V, et al. Cardio-facio-cutaneous syndrome and gastrointestinal defects: report on a newborn with 19p13.3 deletion including the MAP 2 K2 gene. Ital J Pediatr. 2022;48(1):65. https://doi.org/10.1186/s13052-022-01241-6 .
doi: 10.1186/s13052-022-01241-6 pubmed: 35509048 pmcid: 9069788
Valero J, Desantes D, Perales-Puchalt A, Rubio J, Diago Almela VJ, Perales A. Effect of delayed umbilical cord clamping on blood gas analysis. Eur J Obstet Gynecol Reprod Biol. 2012;162(1):21–3. https://doi.org/10.1016/j.ejogrb.2012.01.020 .
doi: 10.1016/j.ejogrb.2012.01.020 pubmed: 22405491
De Paco C, Florido J, Garrido MC, Prados S, Navarrete L. Umbilical cord blood acid-base and gas analysis after early versus delayed cord clamping in neonates at term. Arch Gynecol Obstet. 2011;283(5):1011–4. https://doi.org/10.1007/s00404-010-1516-z .
doi: 10.1007/s00404-010-1516-z pubmed: 20499075
Andersson O, Hellström-Westas L, Andersson D, Clausen J, Domellöf M. Effects of delayed compared with early umbilical cord clamping on maternal postpartum hemorrhage and cord blood gas sampling: a randomized trial. Acta Obstet Gynecol Scand. 2013;92(5):567–74. https://doi.org/10.1111/j.1600-0412.2012.01530.x .
doi: 10.1111/j.1600-0412.2012.01530.x pubmed: 22913332
Wiberg N, Källén K, Olofsson P. Delayed umbilical cord clamping at birth has effects on arterial and venous blood gases and lactate concentrations. BJOG. 2008;115(6):697–703. https://doi.org/10.1111/j.1471-0528.2008.01708.x .
doi: 10.1111/j.1471-0528.2008.01708.x pubmed: 18410652
Tanriverdi S, Pelit B, Tekinli I. The effect of cord clamping time on cord blood gas in term newborn babies born by cesarean section. Perinat J. 2023;31(0). https://doi.org/10.2399/prn.23.0311001 .
Yang S, Duffy JY, Johnston R, Fall C, Fitzmaurice LE. Association of a delayed cord-clamping protocol with hyperbilirubinemia in term neonates. Obstet Gynecol. 2019;133(4):754–61. https://doi.org/10.1097/AOG.0000000000003172 .
doi: 10.1097/AOG.0000000000003172 pubmed: 30870273
Qian Y, Ying X, Wang P, Lu Z, Hua Y. Early versus delayed umbilical cord clamping on maternal and neonatal outcomes. Arch Gynecol Obstet. 2019;300(3):531–43. https://doi.org/10.1007/s00404-019-05215-8 .
doi: 10.1007/s00404-019-05215-8 pubmed: 31203386 pmcid: 6694086
Katheria AC, Brown MK, Faksh A, et al. Delayed cord clamping in newborns born at term at risk for resuscitation: a feasibility Randomized Clinical Trial. J Pediatr. 2017;187:313–7. https://doi.org/10.1016/j.jpeds.2017.04.033 .
doi: 10.1016/j.jpeds.2017.04.033 pubmed: 28526223
Mohammad K, Tailakh S, Fram K, Creedy D. Effects of early umbilical cord clamping versus delayed clamping on maternal and neonatal outcomes: a Jordanian study. J Matern Fetal Neonatal Med. 2021;34(2):231–7. https://doi.org/10.1080/14767058.2019.1602603 .
doi: 10.1080/14767058.2019.1602603 pubmed: 30931665
Shinohara E, Kataoka Y. Prevalence and risk factors for hyperbilirubinemia among newborns from a low-risk birth setting using delayed cord clamping in Japan. Jpn J Nurs Sci. 2021;18(1):e12372. https://doi.org/10.1111/jjns.12372 .
doi: 10.1111/jjns.12372 pubmed: 32803859
Backes CH, Rivera BK, Haque U, et al. Placental transfusion strategies in very preterm neonates: a systematic review and meta-analysis. Obstet Gynecol. 2014;124(1):47–56. https://doi.org/10.1097/AOG.0000000000000324 .
doi: 10.1097/AOG.0000000000000324 pubmed: 24901269
Fogarty M, Osborn DA, Askie L, et al. Delayed vs early umbilical cord clamping for preterm infants: a systematic review and meta-analysis. Am J Obstet Gynecol. 2018;218(1):1–18. https://doi.org/10.1016/j.ajog.2017.10.231 .
doi: 10.1016/j.ajog.2017.10.231 pubmed: 29097178
Nesheli HM, Esmailzadeh S, Haghshenas M, Bijani A, Moghaddams TG. Effect of late vs early clamping of the umbilical cord (on haemoglobin level) in full-term neonates. J Pak Med Assoc. 2014;64(11):1303–5.
pubmed: 25831651
Consonni S, Vaglio Tessitore I, Conti C, et al. Umbilical cord management strategies at cesarean section. J Obstet Gynaecol Res. 2020. https://doi.org/10.1111/jog.14501 .
doi: 10.1111/jog.14501 pubmed: 32961613
McDonald SJ, Middleton P, Dowswell T, Morris PS. Effect of timing of umbilical cord clamping of term infants on maternal and neonatal outcomes. Evid Based Child Health. 2014;9(2):303–97. https://doi.org/10.1002/ebch.1971 .
doi: 10.1002/ebch.1971 pubmed: 25404605
Smit M, Dawson JA, Ganzeboom A, Hooper SB, van Roosmalen J, te, Pas AB. Pulse oximetry in newborns with delayed cord clamping and immediate skin-to-skin contact. Arch Dis Child Fetal Neonatal Ed. 2014;99(4):309 – 14. https://doi.org/10.1136/archdischild-2013-305484 .
Dawson JA, Kamlin CO, Wong C, et al. Changes in heart rate in the first minutes after birth. Arch Dis Child Fetal Neonatal Ed. 2010;95(3):177–81. https://doi.org/10.1136/adc.2009.169102 .
doi: 10.1136/adc.2009.169102
De Bernardo G, Giordano M, De Santis R, et al. A randomized controlled study of immediate versus delayed umbilical cord clamping in infants born by elective caesarean section. Ital J Pediatr. 2020;46(1):71. https://doi.org/10.1186/s13052-020-00835-2 .
doi: 10.1186/s13052-020-00835-2 pubmed: 32448358 pmcid: 7247269
Bozzetti V, Paterlini G, Bel, Fv, et al. Cerebral and somatic NIRS-determined oxygenation in IUGR preterm infants during transition. J Matern Fetal Neonatal Med. 2016;29(3):443–6. https://doi.org/10.3109/14767058.2014.1003539 .
doi: 10.3109/14767058.2014.1003539 pubmed: 25604088
Bruckner M, Pichler G, Urlesberger B. NIRS in the fetal to neonatal transition and immediate postnatal period. Semin Fetal Neonatal Med. 2020;25(2):101079. https://doi.org/10.1016/j.siny.2020.101079 .
doi: 10.1016/j.siny.2020.101079 pubmed: 32007425
Wolfsberger CH, Pichler-Stachl E, Höller N, et al. Cerebral oxygenation immediately after birth and long-term outcome in preterm neonates-a retrospective analysis. BMC Pediatr. 2023;23(1):145. https://doi.org/10.1186/s12887-023-03960-z .
doi: 10.1186/s12887-023-03960-z pubmed: 36997902 pmcid: 10061688
Pfurtscheller D, Wolfsberger CH, Höller N, et al. Cardiac output and regional-cerebral-oxygen-saturation in preterm neonates during immediate postnatal transition: an observational study. Acta Paediatr. 2023;112(7):1404–12. https://doi.org/10.1111/apa.16745 .
doi: 10.1111/apa.16745 pubmed: 36880893
Finn D, Ryan DH, Pavel A, et al. Clamping the umbilical cord in premature deliveries (CUPiD): neuromonitoring in the immediate newborn period in a randomized, controlled trial of preterm infants born at < 32 weeks of gestation. J Pediatr. 2019;208:121–e1262. https://doi.org/10.1016/j.jpeds.2018.12.039 .
doi: 10.1016/j.jpeds.2018.12.039 pubmed: 30879732
Baik N, Urlesberger B, Schwaberger B, et al. Reference ranges for cerebral tissue oxygen saturation index in term neonates during immediate neonatal transition after birth. Neonatology. 2015;108(4):283–6. https://doi.org/10.1159/000438450 .
doi: 10.1159/000438450 pubmed: 26330229
De Carli A, Andresen B, Giovannella M, et al. Cerebral oxygenation and blood flow in term infants during postnatal transition: BabyLux project. Arch Dis Child Fetal Neonatal Ed. 2019;104(6):648–53. https://doi.org/10.1136/archdischild-2018-316400 .
doi: 10.1136/archdischild-2018-316400
Baik-Schneditz N, Schwaberger B, Mileder L, et al. Cardiac output and cerebral oxygenation in term neonates during neonatal transition. Child (Basel). 2021;8(6):439. https://doi.org/10.3390/children8060439 .
doi: 10.3390/children8060439
Okulu E, Haskologlu S, Guloglu D, et al. Effects of umbilical cord management strategies on stem cell transfusion, delivery room adaptation, and cerebral oxygenation in term and late preterm infants. Front Pediatr. 2022;10:838444. https://doi.org/10.3389/fped.2022.838444 .
doi: 10.3389/fped.2022.838444 pubmed: 35444969 pmcid: 9013943
Schwaberger B, Ribitsch M, Pichler G, et al. Does physiological-based cord clamping improve cerebral tissue oxygenation and perfusion in healthy term neonates? - a randomized controlled trial. Front Pediatr. 2023;10:1005947. https://doi.org/10.3389/fped.2022.1005947 .
doi: 10.3389/fped.2022.1005947 pubmed: 36699304 pmcid: 9869382
Binder C, Urlesberger B, Avian A, Pocivalnik M, Müller W, Pichler G. Cerebral and peripheral regional oxygen saturation during postnatal transition in preterm neonates. J Pediatr. 2013;163(2):394–9. https://doi.org/10.1016/j.jpeds.2013.01.026 .
doi: 10.1016/j.jpeds.2013.01.026 pubmed: 23434123

Auteurs

Baran Cengiz Arcagok (BC)

Department of Pediatrics, Division of Neonatology, School of Medicine, Acibadem University, Istanbul, Turkey. baranarcagok@hotmail.com.

Hulya Bilgen (H)

Department of Pediatrics, Division of Neonatology, School of Medicine, Marmara University, Istanbul, Turkey.

Hulya Ozdemir (H)

Department of Pediatrics, Division of Neonatology, School of Medicine, Marmara University, Istanbul, Turkey.

Asli Memisoglu (A)

Department of Pediatrics, Division of Neonatology, School of Medicine, Marmara University, Istanbul, Turkey.

Dilsad Save (D)

Department of Public Health, School of Medicine, Marmara University, Istanbul, Turkey.

Eren Ozek (E)

Department of Pediatrics, Division of Neonatology, School of Medicine, Marmara University, Istanbul, Turkey.

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