Journals / Turkish Journal of Pediatrics / 2019 / Cilt: 61 - Sayı: 3

The effects of enteral artificial amniotic fluid-containing erythropoietin on short term outcomes of preterm infants

Pages
392–398
DOI
—
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

Use of EPO insynthetic amniotic fluid did not affect the frequency of NEC.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Necrotizing Enterocolitis (NEC) is a common devastating gastrointestinaldisease, which usually develops in premature infants.
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Key Findings & Data:In this study, 150 preterm infantswith gestational age 28 weeks or less and birth weight 1250 grams or lesswere enrolled.
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Conclusion & Impact:Use of EPO insynthetic amniotic fluid did not affect the frequency of NEC.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Özet

Necrotizing Enterocolitis (NEC) is a common devastating gastrointestinaldisease, which usually develops in premature infants. Erythropoietin (EPO) asa hematopoietic hormone produced by the kidney can also be naturally foundin amniotic fluid and breast milk. There is some evidence that supports thecontribution of EPO in the prevention of inflammation and intestinal tissuerepair. This study was aimed to determine if oral administration of artificialamniotic fluid with or without EPO would protect preterm infants against NECand improve the certain neonatal outcomes. In this study, 150 preterm infantswith gestational age 28 weeks or less and birth weight 1250 grams or lesswere enrolled. The infants were divided randomly into 3 groups: 1) Controlgroup (n=50) with routine feeding protocol without any administration; 2)Amniotic fluid group (n=50) with 5mL/kg synthetic amniotic fluid; 3) EPOgroup (n=50) with RhuEPO dissolved in the synthetic amniotic fluid. Theadministrations of the study solution were started 3 days after the birth andwere continued for 3 weeks (21 days). The infants in the study groups werefollowed up until discharge and the frequency of NEC, mortality, and othercomplications of the disease among the groups were compared. The mortalityrate in preterm infants of the amniotic fluid and EPO groups were significantlylower than in the control group (p=0.027). We couldn’t find any significantdifferences in the frequency of NEC and other complications among the threestudy groups. The administration of synthetic amniotic fluid (with or withoutEPO) in preterm infants may decrease the mortality rate. Use of EPO insynthetic amniotic fluid did not affect the frequency of NEC.

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Cite This Article

HOSSEİNİ, M., AZAMPOUR, H., RAEİSİ, S., BEHTARİ, M., VALIZADEH, H., SABOOHİ, R. (2019). The effects of enteral artificial amniotic fluid-containing erythropoietin on short term outcomes of preterm infants. Turkish Journal of Pediatrics, Cilt: 61 - Sayı: 3, 392–398. https://ajindex.com/articles/411994

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References (15)

  1. Sugiura T, Kouwaki M, Goto K, et al. Effects of exchange transfusion on cytokine profiles in necrotizing enterocolitis. Pediatr Int 2012; 54: 931- 933
  2. Atici A, Karaman A, Zenciroglu A, et al. Factors affecting mortality in stage 3b necrotizing enterocolitis. Turk J Pediatr 2014; 56: 133-137
  3. Yurdakök M. What next in necrotizing enterocolitis? Turk J Pediatr 2008; 50: 1-11
  4. Garg PM, Ravisankar S, Bian H, Macgilvray S, Shekhawat PS. Relationship between packed red blood cell transfusion and severe form of necrotizing enterocolitis: Acase control study. Indian Pediatr 2015; 52: 1041-1045
  5. Thompson AM, Bizzarro MJ. Necrotizing enterocolitis in newborns: Pathogenesis, prevention and management. Drugs 2008; 68: 1227-1238
  6. Morgan J, Young L, McGuire W. Slow advancement of enteral feed volumes to prevent necrotising enterocolitis in very low birth weight infants. Cochrane Database Syst Rev 2015:CD001241
  7. Dördelmann M, Rau G, Bartels D, et al. Evaluation of portal venous gas detected by ultrasound examination for diagnosis of necrotising enterocolitis. Arch Dis Child Fetal Neonatal Ed 2009; 94: F183-F187
  8. Heida FH, Stolwijk L, Loos MLHJ, et al. Increased incidence of necrotizing enterocolitis in the Netherlands after implementation of the new Dutch guideline for active treatment in extremely preterm infants: Results from three academic referral centers. J Pediatr Surg 2017; 52: 273-276
  9. Ahle M, Drott P, Andersson RE. Epidemiology and trends of necrotizing enterocolitis in Sweden: 1987- 2009. Pediatrics 2013; 132: e443-e451
  10. Holman RC, Stehr-Green JK, Zelasky MT. Necrotizing enterocolitis mortality in the United States, 1979-85. Am J Public Health 1989; 79: 987-989
  11. Narayanan M, Schlueter M, Clyman RI. Incidence and outcome of a 10-fold indomethacin overdose in premature infants. J Pediatr 1999; 135: 105-107
  12. Peter C, Feuerhahn M, Bohnhorst B, et al. Necrotising enterocolitis: Is there a relationship to specific pathogens? Eur J Pediatr 1999; 158: 67-70
  13. Boo NY, Cheah IGS. Risk factors associated with necrotising enterocolitis in very low birth weight infants in Malaysian neonatal intensive care units. Singapore Med J 2012; 53: 826-831
  14. Caplan M. Neonatal necrotizing enterocolitis: clinical observations, pathophysiology, and prevention. In: Martin RJ, Fanaroff AA, Walsh MC (eds). Fanaroff and Martin ‘s Neonatal Perinatal Medicine (10th ed) St Lois: Mosby 2014: 1423-1432
  15. Kumral A, Baskın H, Duman N, et al. Erythrop