Journals / Akdeniz Tıp Dergisi / 2021 / Cilt: 7 - Sayı: 1

The Incidence and Etiology of Neonatal Cholestasis in Newborn Infants

Yenidoğan Bebeklerde Neonatal Kolestaz İnsidansı ve Etiyolojisi

Pages
143–154
Publication Date
2022-10-11
DOI
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AI Summary & Key Takeaways

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⚡ TL;DR(Too Long; Didn't Read)

Infants in theparenteral-nutrition group demonstrated earlier gestation p

📌 3 Key Takeaways

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Objective & Hypothesis:Objective: To evaluate the incidence, characteristic features, etiologies, and the clinical and laboratory outcome of neonatal cholestasis at the neonatal intensive care unit.Material and Methods: All newborns with direct bilirubin levels >2 mg/dl or 20% of total bilirubin when total bilirubin was >5 mg/dl were enrolled in this retrospective, single-center, cohort study.
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Key Findings & Data:Statistical analyses were performed on three main group categories metabolic-genetic conditions, parenteral-nutritionassociated, and others .Results: The cholestasis incidence was 8.5/1000 live births.
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Conclusion & Impact:Infants in theparenteral-nutrition group demonstrated earlier gestation p
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Yenidoğan · Kolestaz · Bilirubin

Abstract

Objective: To evaluate the incidence, characteristic features, etiologies, and the clinical and laboratory outcome of neonatal cholestasis at the neonatal intensive care unit.Material and Methods: All newborns with direct bilirubin levels >2 mg/dl or 20% of total bilirubin when total bilirubin was >5 mg/dl were enrolled in this retrospective, single-center, cohort study. The perinatal characteristics, initial complaints, clinical and laboratory features were extracted. The etiology of cholestasis was recorded as metabolic-genetic conditions, syndromic, biliary, nutritional, cardiovascular, infectious, endocrine conditions and unknown origin. Statistical analyses were performed on three main group categories metabolic-genetic conditions, parenteral-nutritionassociated, and others .Results: The cholestasis incidence was 8.5/1000 live births. Parenteral-nutrition 36.4% and metabolic-genetic conditions 32.7% constituted the most common etiologies. The study population had a 76.4% rate of preterm delivery. Infants in theparenteral-nutrition group demonstrated earlier gestation p

Özet

Amaç: Yenidoğan yoğun bakım ünitesinde yatan bebeklerde kolestaz sıklığının, karakteristik özelliklerinin, etiyolojilerinin, klinik ve laboratuvar verileri eşliğinde değerlendirilmesi amaçlandı.Gereç ve Yöntemler: Tek merkezli, retrospektif, 2016-2020 yıllarını kapsayan kohort çalışmaya direkt bilirubin değeri >2 mg/dl ya da total bilirubin seviyesi >5 mg/dl iken direkt bilirubin değerinin total bilirubinin >%20 olan yenidoğanlar alındı. Hastaların perinatal özellikleri, başvuru şikayetleri, klinik, laboratuvar verileri kaydedildi. Kolestaz nedenleri metabolik-genetik, sendromik, bilier, nutrisyonel, kardiyovasküler, enfeksiyon, endokrin ve sebebi açıklanamayan nedenler olarak gruplandırıldı. İstatistiksel değerlendirme üç temel grupta metabolik-genetik, parenteral-nutrisyonilişkili, diğerleri yapıldı. Bulgular: Neonatal kolestaz sıklığı 8,5/1000 yenidoğan olarak saptandı. En sık nedenleri parenteral nutrisyon %36,4 ile metabolik-genetik hastalıklar %32,7 oluşturdu. Çalışmaya alınan hastaların %76,4’ünü preterm-yenidoğanlar oluştururken, parenteral-nutrisyon grubundaki pretermler, gestasyon yaşı açısından en düşük hafta, doğum kilosu açısından ise en düşük doğum ağırlığına sahipti üç grup arasında sırasıyla p

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Cite This Article

KIHTIR, Z., ÇELİK, K., ONGUN, H., ACARBULUT, İ., SAĞLAM, C., OYGÜR, N. (2022). The Incidence and Etiology of Neonatal Cholestasis in Newborn Infants. Akdeniz Tıp Dergisi, Cilt: 7 - Sayı: 1, 143–154. https://ajindex.com/articles/434249

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References (12)

  1. Magyar MA, Metropulos D, Antoon JW. Direct Hyperbi- lirubinemia in an Infant. Clin Pediatr 2017; 56:696-9.
  2. Cairo SB, Osak AH, Berkelhamer SK, McLaughlin C, Rothstein DH. Direct hyperbilirubinemia in newborns with gastroschisis. Pediatr Surg Int 2019; 35:293-301.
  3. Fawaz R, Baumann U, Ekong U, Fischler B, Hadzic N, Mack CL, Karpen SJ. Guideline for the evaluation of cholestatic jaundice in infants: Joint recommendations of the North American Society for pediatric gastroentero- logy, hepatology, and nutrition and the european society for pediatric gastroenterology, hepatology, and nutrition. J Pediatr Gastroenterol Nutr 2017; 64:154-68.
  4. Bıçakcıoğlu I, Özdemir R, Turgut H, Gökçe İK, Seli- moğlu MA. Neonatal kolestaz: 94 olgunun geriye dönük incelenmesi. Çocuk Sağlığı ve Hastalıkları Dergisi 2017; 60:129-38.
  5. DaniC, PratesiS, RaimondiF, RomagnoliC. Task Force for Hyperbilirubinemia of the Italian Society of Neonato- logy. Italian guidelines for the management and treatment of neonatal cholestasis. Ital J Pediatr 2015; 41:69. Lauriti G, Zani A, Aufieri R, Cananzi M, Chiesa PL, Eaton S, Pierro A. Incidence, prevention, and treatment of parenteral nutrition-associated cholestasis and intesti- nal failure-associated liver disease in infants and children: a systematic review. JPEN J Parenter Enteral Nutr 2014; 38:70-85.
  6. İpek M, Aydın M, Zenciroğlu A, Gökçe S, Okumuş N, Gülaldı NC. Conjugated hyperbilirubinemia in the neonatal intensive care unit. Turk J Gastroenterol 2013; 24:406-14.
  7. Satrom K, Gourley G. Cholestasis in preterm infants. Clin Perinatol 2016; 43:355-73.
  8. Lane E, Murray KF. Neonatal Cholestasis. Pediatr Clin North Am 2017; 64:621-39.
  9. Sarı S, Eğritaş Ö, Barış Z, Ünlüsoy A, Bükülmez A, Dalgıç B. Bebeklik çağı kolestatik karaciğer hastalıkları: 190 olgu- nun geriye dönük değerlendirilmesi. Türk Pediatri Arşivi 2012; 47:167-73.
  10. TufanoM, Nicastro E, Giliberti P, Vegnente A, Raimondi F, Lorio R. Cholestasis in neonatal intensive care unit: Incidence, aetiology and management. Acta Paediatr 2009; 98:1756-61.
  11. Çoban A, Türkmen M, Gürsoy T. Türk Neonatoloji Derneği yenidoğan sarılıklarında yaklaşım, izlem ve tedavi rehberi 2014, (https://www.neonatology.org.tr/ storage/2020/04/Sarilik.pdf). Lee WS, Sokol RJ. Intestinal microbiota, lipids, and the pathogenesis of intestinal failure-associated liver disease. J Pediatr 2015; 167:519-26.
  12. Bove KE, Heubi JE, Balistreri WF, Setchell KD. Bile acid synthetic defects and liver disease: A comprehensive review. Pediatr Dev Path