Journals / Journal of the Turkish-German Gynecological Association / 2010 / Cilt: 11 - Sayı: 1

Neonatal mortalite ve morbidite üzerine tek doz ve çift doz antenatal kortikosteroid uygulamasının etkisi

Comparison of single and double courses of ntenatal corticosteroid administration on neonatal mortality and morbidity

Pages
38–43
Publication Date
2022-10-18
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

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

Conclusion: When single and two courses of antenatal steroid therapy were compared, there was no statistically significant difference between groups regarding the incidence of RDS and mechanical ventilator treatment.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Objective: We aimed to evaluate the effects of single and double courses of antenatal corticosteroid administration on neonatal mortality and morbidity.
📊
Key Findings & Data:Material and Methods: 232 preterm babies delivered between 01.April 2007 and 31.
💡
Conclusion & Impact:Conclusion: When single and two courses of antenatal steroid therapy were compared, there was no statistically significant difference between groups regarding the incidence of RDS and mechanical ventilator treatment.
🔬Design:Research Article
📍Scope:2007 Verileri
⚙️Variables:Domain Parameters

Abstract

Objective: We aimed to evaluate the effects of single and double courses of antenatal corticosteroid administration on neonatal mortality and morbidity. Material and Methods: 232 preterm babies delivered between 01.April 2007 and 31. March 2008 with gestational ages of 26- 34 weeks were evaluated prospectively. Infants were divided into three groups. The first group did not receive any antenatal betamethasone therapy. The second group received single (two doses of 12 mg betamethasone administered at 24 hour intervals) and the third group received double (repeated course after one week) courses of betamethasone therapy. Results: 156 (67.2%) infants received at least one dose of corticosteroid treatment where 76 (37.8%) did not. Of 156 infants who had received antenatal betamethasone, 36 (23.1%) developed respiratory distress syndrome (RDS), while the incidence of RDS was 35.5% in 76 preterms who didn’t receive antenatal betamethasone (27/76) (p0.05). Conclusion: When single and two courses of antenatal steroid therapy were compared, there was no statistically significant difference between groups regarding the incidence of RDS and mechanical ventilator treatment.

Özet

Amaç: Tek ve çift doz antenatal kortikosteroid uygulamasının neonatal mortalite ve morbiditesi üzerine olan etkisini incelemeyi amaçladık. Materyal ve Metod: 1 Nisan 2007 ve 31 Mart 2008 tarihleri arasında gestasyonel yaşları 26 – 34 hafta arasında olup doğurtulan 232 preterm bebek prospektif olarak değerlendirildi. İnfantlar üç gruba ayrıldı. Birinci grup antenatal betametazon tedavisi almadı. İkinci grup yirmidört saat arayla iki doz 12 mg betametazon alırken üçüncü grup bir hafta arayla ikinci betametazon tedavisi aldı. Bulgular: 156 (%67.2) infant en az tek doz kortikosteroid tedavisi alırken 76’sı (%37.8) kortikosteroid almadı. Antenatal betametazon alan 156 infanttan 36’sında (%23.1) respiaratuar distres sendromu (RDS) gelişirken antenatal betametazon almayan 76 pretermden 27’sinde (%35.5) RDS gelişti (p0.05) Sonuç: Tek kür ve iki kür betametazon uygulaması karşılaştırıldığında, RDS insidansı ve mekanik ventilasyon ihtiyacı yönünden iki grup arasında istatistiksel olarak anlamlı bir fark saptanmadı (p>0.05).

🔖

Cite This Article

ÇELİK, H., AYGÜN, C., TOSUN, M., MALATYALIOĞLU, E., ÇETİNKAYA, M. B., AY, H., BILDIRCIN, F. D. (2022). Neonatal mortalite ve morbidite üzerine tek doz ve çift doz antenatal kortikosteroid uygulamasının etkisi. Journal of the Turkish-German Gynecological Association, Cilt: 11 - Sayı: 1, 38–43. https://ajindex.com/articles/567800

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (16)

  1. Ramsey PS, Goldenberg RL. Obstetric management of prematurity. In: Fanaroff AA, Martin RJ (eds). Neonatal-Perinatal Medicine (7th ed). St Louis: Mosby: 2002; 287-319
  2. Cosmi EV. Prenatal prevention of respiratory distress syndrome: new pharmacologic approaches. Early Hum Dev 1992; 29: 283-6
  3. Crowther CA, Haslam RR, Hiller JE, Doyle LW, Robinson JS. Australasian Colloborative Trial of Repeat Doses of Steroids (ACTORDS) Study Group. Lancet 2006; 367: 1913-9
  4. Wapner RJ, Sorokin Y, Mele L, et al. Long term outcomes after repeated doses of antenatal corticosteroids. NEJM 2007; 357: 1248- 50
  5. Töllner U. Early diagnosis of septicemia in the newborn. Clinical studies and sepsis score. Eur J Pediatr 1982; 138: 331-7
  6. Walsch MC, Klegman RM. Necrotizing enterocolitis: treatment based on staging criteria. Pediatr Clin North Am 1986; 33: 179-201
  7. Creasy RK, Lams JD. Preterm Labor and Delivery. In: Creasy RK, Resnik R (eds). Maternal Fetal Medicine (4th ed). W. B Saunders. 2000: 498-509
  8. NIH Consensus Development Conference Statement. Effect of corticosteroids for fetal maturation on perinatal outcomes. JAMA 1995; 273: 413-8
  9. Crowley P. Prophylactic corticosteroids for preterm birth.Cochrane Database Syst Rev 2000; 2: CD000065
  10. Crowley P, Chalmers I, Keirse MJ. The effects of corticosteroid administration before preterm delivery: an overview of the evidence from controlled trials. Br J Obstet Gynecol. 1990; 97: 11-25
  11. Kari MA, Hallman M, Eronen M, et al: Prenatal dexamethasone treatment in conjunction with rescue therapy of human surfactant: a randomized placebo- controlled multicenter study. Pediatrics 1994; 93: 730-6
  12. Brazilian Neonatal Research Network. Antenatal corticosteroid use and clinical evolution of preterm newborn infants. J Pediatr (Rio J). 2004; 80: 277-84
  13. Gardner MO, Goldenberg RL, Gaudier FL, et al: Predicting low Apgar scores of infants weighing less than 1000 grams: the effect of corticosteroids. Obstet Gynecol 1995; 85: 170-4
  14. Liggins GC, Howie RN. A controlled trial of antepartum glucocorticoid treatment for prevention of the respiratory distress syndrome in premature infants. Pediatrics 1972; 50: 515-25
  15. Ballard RA, Ballard PL. Prevention of neonatal respiratory distress syndrome by pharmacological methods. In: Robinson B, VanGolde LMG (eds). Pulmonary surfactant: From Moleculer Biology to Clinical Practice. New York Elsevier Science Publishers. 1992; 156: 539-60
  16. Madarek EO, Najati N. The effec