Araştırma Makalesi
BibTex RIS Kaynak Göster

İndirekt Hiperbilirubinemide Exchange Transfüzyon Uygulanması: Tek Merkez Deneyimi

Yıl 2022, Cilt: 19 Sayı: 2, 388 - 393, 28.08.2022
https://doi.org/10.35440/hutfd.1085670

Öz

Amaç: Hiperbilirubinemi yenidoğan bebeklerde sık görülen bir klinik durum ve bilirubin ensefalopatisi günümüzde hala önemli bir sağlık sorunu olmaya devam etmektedir. Bilirubin endişesinin azalması ve etyolojik değerlendirmelerin yeterince yapılamaması kernikterus gibi ciddi sorunlara yol açmaktadır. Bu çalışmada, bir yıllık sürede indirekt hiperbilirubinemi nedeni ile exchange transfüzyon yapılan hastalarda, bilirubin ensefalopatisi gelişimi ve etiyolojik nedenleri değerlendirilmiştir.
Yöntem: Eylül 2020-Ağustos 2021 tarihleri arasında Neonatoloji kliniğine indirek hiperbilirubinemi nedeni ile yatan ve kan değişimi uygulanan yenidoğanlar retrospektif olarak incelendi. Demografik veriler, laboratuvar parametreleri, kan değişimine bağlı komplikasyonların gelişme sıklığı araştırıldı.
Bulgular: Çalışmaya %61.3(38)’ü erkek, %38.7(24)’ü kız olmak üzere 62 bebek alındı. Hastaların %53.2(33)’ü sezaryen ile doğurtulmuştu. Ortalama gebelik yaşı median 38(36-41) hafta olup, doğum ağırlığı ortalama 3063±478 gram bulundu. Hastaların ortalama başvuru yaşı median 5 (1-22) gün olarak bulundu. Olguların etyolojik değerlendirilmesinde %27.4(44)’ünde Rh uyuşmazlığı, %50(31)’inde ABO uyuşmazlığı, %46.8(29)’unda Subgrup uyuşmazlıklarının olduğu görüldü. Hastaların %33.8(21)’inde birden fazla uyuşmazlık tespit edildi. Olguların %21(13)’ünde Glukoz 6 fosfat dehidrogenaz enzim eksikliği saptandı. Hastaların %4.8(3)’ünde etyolojik bir neden bulunamadı.
Sonuç: İndirek hiperbilirubinemi ve buna bağlı bilirubin ensefalopatisi halen ciddi bir sorun olmaya devam etmekte ve bu nedenle de exchange transfüzyon uygulanması gerekebilmektedir. İndirek hiperbilirubinemiye bağlı ciddi morbidite ve hatta mortalitelerin azaltılması açısından bilirubin izlemi yakından yapılmalı ve etyolojik değerlendirmeler ile riskli bebekler önceden tespit edilmelidir.

Kaynakça

  • 1. Kaplan M, Muraca M, Hammerman C, et al. inbalance between production and conjugation of bilirubin : A fundamental concept in the mechanism of neonatal jaundice. Pediatrics 2002; 110: e47.
  • 2. Kliegman R, Stanton B, Geme JS, ( eds ). Nelson Textbook of Pediatrics , 21rd edition . Philadelphia , PA: Elsevier; 2019.
  • 3. Maisels MJ, Bhutani VK, Bogen D Newman TB, Stark AR, Watchko JF. Hyperbilirubinemia in the newborn infant ≥35 weeks gestation : an update with clarification _ Pediatrics 2009; 124: 1193-1198.
  • 4. Çoban A, Kaynak Türkmen M, Gürsoy T. Turkish neonatology society approach, follow-up and treatment guide in neonatal jaundice. Turkish Pediatrics Ars . 2018;53(1):172-179.
  • 5. American Academy of Pediatrics Subcommittee on Hyperbilirubinemia . Management of hyperbilirubinemia in the newborn infant 35 or more weeks of gestation . Pediatrics 2004;114:297-316.
  • 6. Besli GE, Metin F, Aksit MA, Saltik S. Long-term Effects of Indirect Hyperbilirubinemia on Auditory and Neurological Functions in Term Newborns _ Civil Med J 2020;35:29-39.
  • 7. Kaplan M, Bromiker R, Hammerman C. Severe neonatal hyperbilirubinemua and kernicterus: are still problems in the third millennium ?. Neonatology 2011 ;100 (4):354-362.
  • 8. Diamond , Louis K. , Fred H. Allen Jr , and William O. Thomas Jr . " Erythroblastosis fetalis with exchange transfusion ." New England Journal of Medicine 244.2 (1951): 39-49.
  • 9. Campbell Wagemann S, Mena Nannig P. Severe hyperbilirubinemia in newborns, risk factors and outcomes. Rev Chil Pediatr 2019 ;90 (3):267-274.
  • 10. Tıraş Ü, Yılmaz R, Dallar Y. Neonatal exchange transfusion: A four-year Ankara hospital experience. Journal of ADU Faculty of Medicine 2008; 9(2): 5-10.
  • 11. Narlı N, Satar M, Özlü F, Yapıcıoğlu H, Özcan K. Etiological evaluation of infants with hyperbilirubinemia hospitalized in Çukurova University neonatal intensive care unit . Journal of CU Faculty of Medicine 2004; 29:51-55.
  • 12. Bhutani VK, Johnson LH, Maisels MJ, et al. Kernicterus: epidemiological statesgies for its prevention through systems based approaches. J Perinatol . 2004 ;24 (10):650-662.
  • 13. Moise KJ. Fetal anemia due to non-Rhesus-D red cell allo -immunization. Semin Fetal Neonatal Med. 2008; 13: 207-214.
  • 14. K Çelik , S Aydin Koker , MT Özkul , Ö Olukman , TH Karapinar , RC Vergin , Ş Çalkavur Impact of Minor Blood Group Incompatibility Versus ABO and Rh Blood Group Incompatibility in Newborns with Indirect Hyperbilirubinaemia : A Single-Centre Clinical Experience HK. J Paediatr 2019 ;24:120 -126.
  • 15. Sharad K. Singh, SN Singh, Mala Kumar, Shalini Tripathi , Arpita Bhriguvanshi , Tulika Chandra, Ashutosh Kumar. Etiology and clinical profile of neonates with pathological unconjugated hyperbilirubinemia with special reference to Rhesus (Rh) D, C, and E incompatibilities: A tertiary care center experience. clinical epidemiology and Global Health 4 ( 2016 ) 95–100.
  • 16. Ozkaya H, Bahar A, Ozkan A, Karademir F, Gocmen I, Mete Z. ABO, RH and subgroup ( Kell , c, e) incompatibilities in newborns with indirect hyperbilirubinemia. Turk J Pediatr 2000; 35:30-35.
  • 17. Duguid JKM. Antenatal serological testing and prevention of hemolytic disease of the newborn. J Clin Pathol 1997; 50: 193-196.
  • 18. Erdeve O, Okul E, Olukman O, Ulubas D, Buyukkale G, Narter F, Tunc G, Atasay B, Gultekin ND, Arsan S, Koc E. The Turkish neonatal Jaundice Online Registry : A national root cause analysis . ploS one . 2018 Feb 23;13(2):e0193108.
  • 19. Zahed Pasha , Y. , Alizadeh-Tabari , S., Zahed Pasha , E. et al. etiology and therapeutic management of neonatal jaundice in Iran: a systematic review and meta- analysis. World J Pediatrics (2020).
  • 20. Sgro M, Campbell D, Shah V. Incidence and causes of severe neonatal hyperbilirubinemia in Canada . CMAJ 2006; 175: 587-590.

Exchange Transfusion in Indirect Hyperbilirubinemia: A Single Center Experience

Yıl 2022, Cilt: 19 Sayı: 2, 388 - 393, 28.08.2022
https://doi.org/10.35440/hutfd.1085670

Öz

Objective: Hyperbilirubinemia is a common clinical condition in newborn infants, and bilirubin encephalopathy remains an important health problem today. Decreased bilirubin anxiety and inadequate etiological evaluations lead to serious problems such as kernicterus. In this study, the development of bilirubin encephalopathy and its etiological causes were evaluated in patients who received exchange transfusion due to indirect hyperbilirubinemia for a period of one year.
Methods: Newborns admitted to the Neonatology clinic between September 2020 and August 2021 due to indirect hyperbilirubinemia and undergoing exchange transfusion were analyzed retrospectively. Demographic data, laboratory parameters, and incidence of complications related to exchange transfusion were investigated.
Results: A total of 62 infants, 61.3%(38) boys and 38.7%(24) girls, were included in the study. 53.2%(33) of the patients were delivered by cesarean section. Mean gestational age was 38(36-41) weeks and mean birth weight was 3063±478 grams. The median age at presentation was found to be 5 (1-22) days. In the etiological evaluation of the cases, 27.4%(44) Rh incompatibility, 50%(31) ABO incompatibility, 46.8%(29) Subgroup incompatibility were observed. More than one discrepancy was detected in 33.8%(21) of the patients. Glucose 6 phosphate dehydrogenase enzyme deficiency was detected in 21% (13) of the cases. No etiological cause was found in 4.8%(3) of the patients.
Conclusion: Indirect hyperbilirubinemia and related bilirubin encephalopathy still remain a serious problem and therefore exchange transfusion may be required. In order to reduce serious morbidity and even mortality due to indirect hyperbilirubinemia, bilirubin monitoring should be done closely and risky babies should be determined in advance with etiological evaluations.

Kaynakça

  • 1. Kaplan M, Muraca M, Hammerman C, et al. inbalance between production and conjugation of bilirubin : A fundamental concept in the mechanism of neonatal jaundice. Pediatrics 2002; 110: e47.
  • 2. Kliegman R, Stanton B, Geme JS, ( eds ). Nelson Textbook of Pediatrics , 21rd edition . Philadelphia , PA: Elsevier; 2019.
  • 3. Maisels MJ, Bhutani VK, Bogen D Newman TB, Stark AR, Watchko JF. Hyperbilirubinemia in the newborn infant ≥35 weeks gestation : an update with clarification _ Pediatrics 2009; 124: 1193-1198.
  • 4. Çoban A, Kaynak Türkmen M, Gürsoy T. Turkish neonatology society approach, follow-up and treatment guide in neonatal jaundice. Turkish Pediatrics Ars . 2018;53(1):172-179.
  • 5. American Academy of Pediatrics Subcommittee on Hyperbilirubinemia . Management of hyperbilirubinemia in the newborn infant 35 or more weeks of gestation . Pediatrics 2004;114:297-316.
  • 6. Besli GE, Metin F, Aksit MA, Saltik S. Long-term Effects of Indirect Hyperbilirubinemia on Auditory and Neurological Functions in Term Newborns _ Civil Med J 2020;35:29-39.
  • 7. Kaplan M, Bromiker R, Hammerman C. Severe neonatal hyperbilirubinemua and kernicterus: are still problems in the third millennium ?. Neonatology 2011 ;100 (4):354-362.
  • 8. Diamond , Louis K. , Fred H. Allen Jr , and William O. Thomas Jr . " Erythroblastosis fetalis with exchange transfusion ." New England Journal of Medicine 244.2 (1951): 39-49.
  • 9. Campbell Wagemann S, Mena Nannig P. Severe hyperbilirubinemia in newborns, risk factors and outcomes. Rev Chil Pediatr 2019 ;90 (3):267-274.
  • 10. Tıraş Ü, Yılmaz R, Dallar Y. Neonatal exchange transfusion: A four-year Ankara hospital experience. Journal of ADU Faculty of Medicine 2008; 9(2): 5-10.
  • 11. Narlı N, Satar M, Özlü F, Yapıcıoğlu H, Özcan K. Etiological evaluation of infants with hyperbilirubinemia hospitalized in Çukurova University neonatal intensive care unit . Journal of CU Faculty of Medicine 2004; 29:51-55.
  • 12. Bhutani VK, Johnson LH, Maisels MJ, et al. Kernicterus: epidemiological statesgies for its prevention through systems based approaches. J Perinatol . 2004 ;24 (10):650-662.
  • 13. Moise KJ. Fetal anemia due to non-Rhesus-D red cell allo -immunization. Semin Fetal Neonatal Med. 2008; 13: 207-214.
  • 14. K Çelik , S Aydin Koker , MT Özkul , Ö Olukman , TH Karapinar , RC Vergin , Ş Çalkavur Impact of Minor Blood Group Incompatibility Versus ABO and Rh Blood Group Incompatibility in Newborns with Indirect Hyperbilirubinaemia : A Single-Centre Clinical Experience HK. J Paediatr 2019 ;24:120 -126.
  • 15. Sharad K. Singh, SN Singh, Mala Kumar, Shalini Tripathi , Arpita Bhriguvanshi , Tulika Chandra, Ashutosh Kumar. Etiology and clinical profile of neonates with pathological unconjugated hyperbilirubinemia with special reference to Rhesus (Rh) D, C, and E incompatibilities: A tertiary care center experience. clinical epidemiology and Global Health 4 ( 2016 ) 95–100.
  • 16. Ozkaya H, Bahar A, Ozkan A, Karademir F, Gocmen I, Mete Z. ABO, RH and subgroup ( Kell , c, e) incompatibilities in newborns with indirect hyperbilirubinemia. Turk J Pediatr 2000; 35:30-35.
  • 17. Duguid JKM. Antenatal serological testing and prevention of hemolytic disease of the newborn. J Clin Pathol 1997; 50: 193-196.
  • 18. Erdeve O, Okul E, Olukman O, Ulubas D, Buyukkale G, Narter F, Tunc G, Atasay B, Gultekin ND, Arsan S, Koc E. The Turkish neonatal Jaundice Online Registry : A national root cause analysis . ploS one . 2018 Feb 23;13(2):e0193108.
  • 19. Zahed Pasha , Y. , Alizadeh-Tabari , S., Zahed Pasha , E. et al. etiology and therapeutic management of neonatal jaundice in Iran: a systematic review and meta- analysis. World J Pediatrics (2020).
  • 20. Sgro M, Campbell D, Shah V. Incidence and causes of severe neonatal hyperbilirubinemia in Canada . CMAJ 2006; 175: 587-590.
Toplam 20 adet kaynakça vardır.

Ayrıntılar

Birincil Dil İngilizce
Konular Klinik Tıp Bilimleri
Bölüm Araştırma Makalesi
Yazarlar

İbrahim Deger 0000-0001-8093-5583

Seçkin İlter Bu kişi benim 0000-0002-7354-3925

Yayımlanma Tarihi 28 Ağustos 2022
Gönderilme Tarihi 11 Mart 2022
Kabul Tarihi 18 Temmuz 2022
Yayımlandığı Sayı Yıl 2022 Cilt: 19 Sayı: 2

Kaynak Göster

Vancouver Deger İ, İlter S. Exchange Transfusion in Indirect Hyperbilirubinemia: A Single Center Experience. Harran Üniversitesi Tıp Fakültesi Dergisi. 2022;19(2):388-93.

Harran Üniversitesi Tıp Fakültesi Dergisi  / Journal of Harran University Medical Faculty