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ÖZOFAGUS ATREZİLİ YENİDOĞANLARDA ANESTEZİK RİSKLER, MORBİDİTE VE MORTALİTE

Year 2020, Volume: 27 Issue: 3, 359 - 366, 01.09.2020
https://doi.org/10.17343/sdutfd.638056

Abstract

Giriş:
Özofagus atrezisi (ÖA), özofagusun proksimal ve distal bölümlerinin  bağlantısının olmamasıdır ve 3000-4500 canlı
doğumda bir görülür. Özofagus atrezisi ve trakeoözofageal fistül (TÖF),
beslenme ve solunum sorunlarından dolayı ilk birkaç saatin içinde acilen tanı
konulması gereken konjenital bir anomalidir. Bu defekt, oral sekresyon artışı
ve beslenme anında aspirasyon ve regürjitasyona yol açar. TÖF’lü bebekte,
ağlama ve öksürme anında, hava fistül yolu ile mideye geçer, sonuç olarak mide
ve ince barsak genişler. ÖA’ da onarım ve postoperatif komplikasyonlarla
mücadele etmek genellikle zordur.



Amaç:
Amacımız, özofagus atrezisinde perioperatif yaklaşım, ÖA onarımı sonrası erken
gelişen sonuçlar, komplikasyonlarla ilişkili olabilecek faktörler ve mortaite
oranlarını tanımlamayı amaçladık.



          Gereç ve Yöntemler: Ocak 2010 - Ocak
2018 tarihleri arasında Zekai Tahir Burak Eğitim ve Araştırma Hastanesi’nde
cerrahi onarım geçirmiş olan özofagus atrezili hastaları retrospektif olarak
inceledik. Her grupta yüksek prematürite oranı (% 30), majör kardiyak (% 15) ve
diğer cerrahi malformasyonlar (% 10) bulundu. Özefagus anastomoz cerrahisi
uygulamada ortanca süre en fazla 70 günlük, en kısa 1  günlük bebekler şeklindeydi  (ortalama fark 59 gün,% 95 CI 48.1-70 gün, P
= 0.01).



          Bulgular: Uzun dönem özofagus
atrezisi ameliyatı acil primer anastomoz (n = 10), gecikmiş primer anastomoz (n
= 11), özofagus uzatma teknikleri (n = 12) ve primer özofageal replasman (n =
0) idi. Uzun süreli özofagus atrezisi, zor entübasyon insidansını artırmıyordu
(OR 2.8,% 95 CI 0.6-22.1, P = 0.15), intraoperatif hipoksemi (OR 1.6,% 95 CI
0.6-4.5, P =0 .45) veya hipotansiyon (OR 0.9,% 95 CI 0.5-1.8, P = 0.98) tespit
edildi. Cerrahi süre (180.2- 210.3 dakika, ortalama fark ([% 95 CI], 30
dk [5.5-50.4 dakika], P = 0.03) ve ameliyat sonrası mekanik
ventilasyonda kalma süresi ortalama (180-250.8 saat, ortalama fark [95% CI]
91.8 [34.5-149.1 saat], P <0.01) uzun olmayan özefagus grubu için (tek
seans) daha kısaydı. Genel hastane içi mortalite % 8'idi (ortalama % 7.2, uzun
aşamalı operasyon için % 14 uzun veya 
kısa süreli özefagus atrezisi için % 2.2, % 95 CI 0.4-14, P = 0.85).



             Sonuç: Aşamalı cerrahi gerektiren uzatmalı özofagus atrezi olan
bebeklerde ve normal özofagus atrezisi olan bebeklerde perioperatif
komplikasyon insidansı benzerdir. Bununla birlikte, uzun süreli onarım için
mevcut cerrahi yaklaşımlar daha uzun anestezik maruziyet, özofagus
devamlılığını korumak için çoklu prosedürler gerektirir. Bu durum mortalite ve
morbidite oranını artırır.



ABSTRACT:



Introduction:
Esophageal atresia (OA) is the absence of connection between the proximal and
distal parts of the esophagus and occurs every 3000-4500 live births.
Esophageal atresia and tracheoesophageal fistula (TOF) is a congenital anomaly
which should be diagnosed promptly within the first few hours due to feeding
and respiratory problems. This defect leads to increased oral secretion and
aspiration and regurgitation during feeding. In TOF infants, when crying and
coughing, air passes through the fistula into the stomach, resulting in
enlarged stomach and small intestine. It is often difficult to combat repair
and postoperative complications in OA. The aim of this study was to define the
perioperative approach in esophageal atresia, early outcomes after OA repair,
factors that may be associated with complications and mortality rates.



          Material
and Methods: We retrospectively reviewed patients with esophageal atresia who
underwent surgical repair in Zekai Tahir Burak Training and Research Hospital
between January 2010 and January 2018. High prematurity rate (30%), major
cardiac (15%) and other surgical malformations (10%) were found in each group.
The median duration of esophageal anastomosis surgery was 70 days and shortest
1 day (mean difference 59 days, 95% CI 48.1-70 days, P = 0.01).



          Results:
Long-term esophageal atresia surgery was emergency primary anastomosis (n =
10), delayed primary anastomosis (n = 11), esophageal lengthening techniques (n
= 12), and primary esophageal replacement (n = 0). Long-term esophageal atresia
did not increase the incidence of difficult intubation (OR 2.8, 95% CI
0.6-22.1, P = 0.15), intraoperative hypoxemia (OR 1.6, 95% CI 0.6-4.5, P =
0.45) or hypotension (OR 0.9, 95% CI 0.5-1.8, P = 0.98). Surgical time (180.2 -
210.3 minutes, mean difference ([95% CI], 30 min [5.5-50.4 minutes], P = 0.03))
and the mean duration of postoperative mechanical ventilation (180-250.8 hours,
mean difference [95% CI) 91.8 [34.5-149.1 h], P <0.01) was shorter for the
non-long esophageal group (single session) Overall in-hospital mortality was 8%
(average 7.2%, 14% for long-term operation, long or short-term esophageal
atresia) 2.2%, 95% CI 0.4-14, P = 0.85).



             Conclusion:
The incidence of perioperative complications is similar in infants with
prolonged esophageal atresia requiring gradual surgery and in infants with
normal esophageal atresia. However, longer surgical approaches for long-term
repair require multiple procedures to maintain esophageal continuity, with
longer anesthetic exposure. This increases the mortality and morbidity rates.

Supporting Institution

YOK

Project Number

YOK

Thanks

.............................

References

  • 1. Spitz L. Oesophageal atresia. Orphanet J Rare Dis. 2007;2:24.
  • 2. Leoncini E, Bower C, Nassar N. Oesophageal atresia and tracheooesophageal fistula in Western Australia: prevalence and trends. J Paediatr Child Health. 2015;51:1023-1029.
  • 3. Van der Zee DC, Bagolan P, Faure C, et al. Position paper of INoEA working group on long-gap esophageal atresia: for better care. Front Pediatr. 2017;5:63.
  • 4. Pedersen RN, Calzolari E, Husby S, et al. Oesophageal atresia: prevalence, prenatal diagnosis and associated anomalies in 23 European regions. Arch Dis Child. 2012;97:227-232.
  • 5. Spitz L. Esophageal atresia. Lessons I have learned in a 40-year experience. J Pediatr Surg. 2006;41:1635-1640.
  • 6. Lee HQ, Hawley A, Doak J, et al. Long-gap oesophageal atresia: comparison of delayed primary anastomosis and oesophageal replacement with gastric tube. J Pediatr Surg. 2014;49:1762-1766.
  • 7. Sroka M, Wachowiak R, Losin M, et al. The Foker technique (FT) and Kimura advancement (KA) for the treatment of children with long-gap esophageal atresia (LGEA): lessons learned at two European centers. Eur J Pediatr Surg. 2013;23:3-7.
  • 8. Foker JE, Kendall TC, Catton K, et al. A flexible approach to achieve a true primary repair for all infants with esophageal atresia. Semin Pediatr Surg. 2005;14:8-15.
  • 9. Bairdain S, Foker JE, Smithers CJ, et al. Jejunal interposition after failed esophageal atresia repair. J Am Coll Surg. 2016;222:1001- 1008.
  • 10. Maheshwari R, Trivedi A, Walker K, et al. Retrospective cohort study of long-gap oesophageal atresia. J Paediatr Child Health. 2013;49:845-849.
  • 11. Al-Shanafey S, Harvey J. Long gap esophageal atresia: an Australian experience. J Pediatr Surg. 2008;43:597-601.
  • 12. Bairdain S, Zurakowski D, Vargas SO, et al. Long-gap esophageal atresia is a unique entity within the esophageal atresia defect spectrum. Neonatology. 2017;111:140-144.
  • 13. Knottenbelt G, Costi D, Stephens P, et al. An audit of anesthetic management and complications of tracheo-esophageal fistula and esophageal atresia repair. Pediatr Anesth. 2012;22:268-274.
  • 14. Andropoulos DB, Rowe RW, Betts JM. Anaesthetic and surgical airway management during tracheo-oesophageal fistula repair. Paediatr Anaesth. 1998;8:313-319.
  • 15. Spitz L. Esophageal atresia: past, present, and future. J Pediatr Surg. 1996;31:19-25.
  • 16. Spitz L. Esophageal atresia and tracheoesophageal fistula in children. Curr Opin Pediatr. 1993;5:347-352.
  • 17. Gross RE. The Surgery of Infancy and Childhood. Philadelphia: W.B.Saunders; 1953.
  • 18. Morini F, Bagolan P. Gap measurement in patients with esophageal atresia: not a trivial matter. J Pediatr Surg. 2015;50:218.
  • 19. Spitz L, Kiely EM, Morecroft JA, et al. Oesophageal atresia: at-risk groups for the 1990s. J Pediatr Surg. 1994;29:723-725.
  • 20. Rittler M, Paz JE, Castilla EE. VACTERL association, epidemiologic definition and delineation. Am J Med Genet. 1996;63:529-536.
  • 21. Foker JE, Kendall Krosch TC, Catton K, et al. Long-gap esophageal atresia treated by growth induction: the biological potential and early follow-up results. Semin Pediatr Surg. 2009;18:23-29.
  • 22. Van der Zee DC, Gallo G, Tytgat SH. Thoracoscopic traction technique in long gap esophageal atresia: entering a new era. Surg Endosc. 2015;29:3324-3330.
  • 23. Aite L, Bevilacqua F, Zaccara A, et al. Short-term neurodevelopmental outcome of babies operated on for low-risk esophageal atresia: a pilot study. Dis Esophagus. 2014;27:330-334.
  • 24. Tytgat SH, van Herwaarden MY, Stolwijk LJ, et al. Neonatal brain oxygenation during thoracoscopic correction of esophageal atresia. Surg Endosc. 2016;30:2811-2817.
  • 25. Conforti A, Giliberti P, Mondi V, et al. Near infrared spectroscopy: experience on esophageal atresia infants. J Pediatr Surg. 2014;49:1064-1068.
  • 26. Holland AJ, Ron O, Pierro A, et al. Surgical outcomes of esophageal atresia without fistula for 24 years at a single institution. J Pediatr Surg. 2009;44:1928-1932.
  • 27. Foker JE, Linden BC, Boyle EM, Jr., et al. Development of a true primary repair for the full spectrum of esophageal atresia. Ann Surg. 1997; 226: 533-541; discussion 541-533.
Year 2020, Volume: 27 Issue: 3, 359 - 366, 01.09.2020
https://doi.org/10.17343/sdutfd.638056

Abstract

Project Number

YOK

References

  • 1. Spitz L. Oesophageal atresia. Orphanet J Rare Dis. 2007;2:24.
  • 2. Leoncini E, Bower C, Nassar N. Oesophageal atresia and tracheooesophageal fistula in Western Australia: prevalence and trends. J Paediatr Child Health. 2015;51:1023-1029.
  • 3. Van der Zee DC, Bagolan P, Faure C, et al. Position paper of INoEA working group on long-gap esophageal atresia: for better care. Front Pediatr. 2017;5:63.
  • 4. Pedersen RN, Calzolari E, Husby S, et al. Oesophageal atresia: prevalence, prenatal diagnosis and associated anomalies in 23 European regions. Arch Dis Child. 2012;97:227-232.
  • 5. Spitz L. Esophageal atresia. Lessons I have learned in a 40-year experience. J Pediatr Surg. 2006;41:1635-1640.
  • 6. Lee HQ, Hawley A, Doak J, et al. Long-gap oesophageal atresia: comparison of delayed primary anastomosis and oesophageal replacement with gastric tube. J Pediatr Surg. 2014;49:1762-1766.
  • 7. Sroka M, Wachowiak R, Losin M, et al. The Foker technique (FT) and Kimura advancement (KA) for the treatment of children with long-gap esophageal atresia (LGEA): lessons learned at two European centers. Eur J Pediatr Surg. 2013;23:3-7.
  • 8. Foker JE, Kendall TC, Catton K, et al. A flexible approach to achieve a true primary repair for all infants with esophageal atresia. Semin Pediatr Surg. 2005;14:8-15.
  • 9. Bairdain S, Foker JE, Smithers CJ, et al. Jejunal interposition after failed esophageal atresia repair. J Am Coll Surg. 2016;222:1001- 1008.
  • 10. Maheshwari R, Trivedi A, Walker K, et al. Retrospective cohort study of long-gap oesophageal atresia. J Paediatr Child Health. 2013;49:845-849.
  • 11. Al-Shanafey S, Harvey J. Long gap esophageal atresia: an Australian experience. J Pediatr Surg. 2008;43:597-601.
  • 12. Bairdain S, Zurakowski D, Vargas SO, et al. Long-gap esophageal atresia is a unique entity within the esophageal atresia defect spectrum. Neonatology. 2017;111:140-144.
  • 13. Knottenbelt G, Costi D, Stephens P, et al. An audit of anesthetic management and complications of tracheo-esophageal fistula and esophageal atresia repair. Pediatr Anesth. 2012;22:268-274.
  • 14. Andropoulos DB, Rowe RW, Betts JM. Anaesthetic and surgical airway management during tracheo-oesophageal fistula repair. Paediatr Anaesth. 1998;8:313-319.
  • 15. Spitz L. Esophageal atresia: past, present, and future. J Pediatr Surg. 1996;31:19-25.
  • 16. Spitz L. Esophageal atresia and tracheoesophageal fistula in children. Curr Opin Pediatr. 1993;5:347-352.
  • 17. Gross RE. The Surgery of Infancy and Childhood. Philadelphia: W.B.Saunders; 1953.
  • 18. Morini F, Bagolan P. Gap measurement in patients with esophageal atresia: not a trivial matter. J Pediatr Surg. 2015;50:218.
  • 19. Spitz L, Kiely EM, Morecroft JA, et al. Oesophageal atresia: at-risk groups for the 1990s. J Pediatr Surg. 1994;29:723-725.
  • 20. Rittler M, Paz JE, Castilla EE. VACTERL association, epidemiologic definition and delineation. Am J Med Genet. 1996;63:529-536.
  • 21. Foker JE, Kendall Krosch TC, Catton K, et al. Long-gap esophageal atresia treated by growth induction: the biological potential and early follow-up results. Semin Pediatr Surg. 2009;18:23-29.
  • 22. Van der Zee DC, Gallo G, Tytgat SH. Thoracoscopic traction technique in long gap esophageal atresia: entering a new era. Surg Endosc. 2015;29:3324-3330.
  • 23. Aite L, Bevilacqua F, Zaccara A, et al. Short-term neurodevelopmental outcome of babies operated on for low-risk esophageal atresia: a pilot study. Dis Esophagus. 2014;27:330-334.
  • 24. Tytgat SH, van Herwaarden MY, Stolwijk LJ, et al. Neonatal brain oxygenation during thoracoscopic correction of esophageal atresia. Surg Endosc. 2016;30:2811-2817.
  • 25. Conforti A, Giliberti P, Mondi V, et al. Near infrared spectroscopy: experience on esophageal atresia infants. J Pediatr Surg. 2014;49:1064-1068.
  • 26. Holland AJ, Ron O, Pierro A, et al. Surgical outcomes of esophageal atresia without fistula for 24 years at a single institution. J Pediatr Surg. 2009;44:1928-1932.
  • 27. Foker JE, Linden BC, Boyle EM, Jr., et al. Development of a true primary repair for the full spectrum of esophageal atresia. Ann Surg. 1997; 226: 533-541; discussion 541-533.
There are 27 citations in total.

Details

Primary Language Turkish
Subjects Surgery
Journal Section Araştırma Makaleleri
Authors

Bilge Aslan

Feray Aydın This is me

Project Number YOK
Publication Date September 1, 2020
Submission Date October 25, 2019
Acceptance Date February 14, 2020
Published in Issue Year 2020 Volume: 27 Issue: 3

Cite

Vancouver Aslan B, Aydın F. ÖZOFAGUS ATREZİLİ YENİDOĞANLARDA ANESTEZİK RİSKLER, MORBİDİTE VE MORTALİTE. Med J SDU. 2020;27(3):359-66.

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