Araştırma Makalesi
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Factors Affecting Survival in Patients with Small Bowel Atresia and Stenosis

Yıl 2022, Cilt: 17 Sayı: 2, 59 - 66, 15.07.2022
https://doi.org/10.17517/ksutfd.938290

Öz

Objective: In this study we aimed to investigate the causes of morbidity and mortality and the factors that influence survival in life and growth in patients followed up with small bowel atresia/stenosis.
Material and Methods: Eighty five patients included to this study that admitted to our clinic with duodenal, proximal jejunoileal, distal jejunoileal atresia/stenosis between 2002-2012. Data on patient’s gender, prenatal diagnosis, time of diagnosis, time of birth, birth weight, maternal age, clinical features, associated anomalies, peroperative findings, postoperative hospitalisation, recorded and factors affecting morbidity, mortality and growth parameters analysed.
Results: Eighty five patients were included in this study, 44 female and 41 were male. Thirty five of these patients were duodenal, 29 proximal jejunoileal, 21 distal jejunoileal atresia/stenosis. 58% of the patients was premature. Additional congenital anomaly have seen at 74% of patients with duodenal atresia/
stenosis and 42% of jejunoileal atresia/stenosis. Mortality rate was 18%. Overall complication rate was 20% in all groups and the most common complication was sepsis. It was observed that the presence of congenital anomalies (100%), low birth weight (93%) and the prevalence of prematurity (80%) were increased in patients with mortality. Patients were examined in terms of growth and developement, in duodenal atresia/stenosis group body weight and persantiles were normal, in jejunoileal atresia group persantiles of length was lower.
Conclusion: In patients with small bowel atresia/stenosis prematurity, low birth weight and additional congenital anomalies were higher in patients who died. Appearance of very low rates of late-term complication should be related to the patient’s irregular long term follow up. In patients with jejunoileal atresia/stenosis, persantiles of length were lower and were commend close follow-up of patients for diet and growth in postoperative period.

Proje Numarası

08.11.2012 13/7

Kaynakça

  • Millar AJW, Rode H, Cywes S. Intestinal atresia and stenosis. Pediatric Surgery. 2005;30:416-434.
  • Kate B, Peter T, Marie A, Fabrizio B, Patricia B, Elisa C. Epidemiology of small intestinal atresia in Europe: a register- based study. Arch Di Child Neonatal. 2012;97:353-358.
  • Kulkarni M. Duodenal and small intestinal atresia. Pediatric Surgery. 2010;28:33-37.
  • Dalla Vechia LK, Grosfel L, Karen W. Intestinal atresia and stenosis: a 25 year experience with 277 cases. Arch Surg. 1998;133:490- 497.
  • Magnuson DK, Schwartz MZ. Stomach and duodenum. Principles and practices of pediatric surgery. Edt Oldham KT, Colombani PN. Lippincot Williams and Wilkins. 2005;72:1149-1179.
  • Kulkarni M. Duodenal and small intestinal atresia. Pediatric Surgery. 2010;28:33-37.
  • Grosfeld JL, Clathworthy HW: The nature of ileal atresia due to intrauterine intussesception. Arch Surg. 1970;100:714.
  • Hannah GP, Julia A, Stephen DW, David Z, Tom J. Intestinal atresias: factors affecting clinical outcomes. Journal of Pediatric Surgery. 2008;43:1244–1248.
  • Rachel ME, Elise R, Koenraad NJA, Van B, Jan BFH, Arend FB. Motor and cognitive outcome at school age of children with surgically treated intestinal obstructions in the neonatal period. Early Human Development. 2013;89:181–185.
  • Grosfeld JL. Jejunoileal atresia and stenosis. In: O’Neill AJ,Rowe MI, Grosfeld JL, Fonkalsrud EW, Coran AG. Pediatric Surgery. 2006 Vol 2, 6th ed, Philadelphia: Mosby.
  • Hemming V, Rankin J. Small intestinal atresia in a defined population: occurence, prenatal diagnosis and survival. Prenat Diagn. 2007;27:1205-1211.
  • Lorimier AA, Fonkalsrud EW, Hays DM. Congenital atresia and stenosis of the jejunum and ileum. Surgery. 1969;65:819-827.
  • Stollman TH, Blaauw I, Wijnen MHWA, van der Staak FHJM, Rieu PNMA, Draaisma JMT et al. Decreased mortality but increased morbidity in neonates with jejunoileal atresia; a study of 114 cases over a 34-year period. Journal of Pediatric Surgery. 2009;44:217–221.
  • Best KE, Tennant PWG, Addor MC, Bianchi F, Boyd P, Calzolari E et al. Epidemiology of small intestinal atresia in Europe: a register- based study. Arch Dis Child Neonatal. 2012;97:353-358.
  • Walker K, Badawi N, Hamid CH, Vora A, Halliday R, Taylor C et al. A population- based study of the outcome after small bowel atresia/stenosis in New South Wales and the Australian Capital Territory, Australia, 1992-2003. Journal of Ped Surg. 2008;43:484-488.
  • Burjonrappa S, Crete E, Bouchard S. Comparative outcomes in intestinal atresia: a clinical outcome and pathophysiology analysis. Pediatr Surg Int. 2011;27(4):437-442.
  • Hayden CK, Schwartz MZ, Davis M, Swischuk LE. Combined esophageal and duodenal atresia: sonographic findings. Am Radiol. 1983;140:225.
  • Veyrac C, Couture A, Saguintaah M, Baud C. MRI of fetal GI tract abnormalities. Abdom Imagıng. 2004;29:411-420.
  • Basu R, Burge DM. The effect of antenatal diagnosis on the management of small bowel atresia. Ped Surg Int. 2004;20:177-179.
  • Tam PKH, Nicholls G. Implications of antenatal diagnosis of small-intestinal atresia in the 1990s. Ped Surg Int. 1999;15:486- 487.
  • Gross RE. Congenital atresia of the intestine and colon. In: Gross RE, editor. The surgery of infancy and childhood: its principles and techniques. Philadelphia (PA): WB Saunders. 1953;150-166.
  • Keckler SJ, Peter SDS, Spilde TL, Ostlie DJ, Snyder CL. The influence of trisomy 21 on the incidence and severity of congenital heart defects in patients with Duodenal atresia. Pediatr Surg Int. 2008;24:921-923.
  • Şencan A, Mir E, Karaca I, Günşar C, Şencan A, Topçu K. Pyloric atresia associated multiple intestinal atresias and pylorocholedochal fistula. Journal of Ped Surg. 2002;42:1362-1364.
  • Kumaran N, Shankar KR, Lloyd DA, Losty PD. Trends in the management and outcome of jejunoileal atresia. Eur J Pediatr Surg. 2002;12:163-167.
  • Cragan JD, Martin ML, Moore CA, Khoury MJ. Descriptive epidemiology of small intestinal atresia. Teratology. 1993;48:441- 450.
  • Sholadoye TT, Mshelbwala PM, Ameh EA. Presentation and outcome of treatment of jejunoileal atresia in Nigeria. Afr J Paediatr Surg. 2018;15(2):84–87.
  • Güler AG, Tuncer R, İskit HS, Alkan M, Zorludemir Ü, Parlakgümüş C ve ark. Çocuk cerrahisi yenidoğan yoğun bakım ünitesinde sağlık bakımı ilişkili enfeksiyonlar ve risk faktörleri. Cukurova Medical Journal 2019;44:455-468.

İnce Barsak Atrezi ve Stenozu Olgularında Sağ Kalımı Etkileyen Faktörler

Yıl 2022, Cilt: 17 Sayı: 2, 59 - 66, 15.07.2022
https://doi.org/10.17517/ksutfd.938290

Öz

Amaç: İnce barsak atrezi/stenozu nedeniyle takip edilen hastaların morbidite ve mortalite nedenlerini ve sağ kalımı etkileyen faktörleri araştırmak, büyüme ve gelişmelerini incelemektir.
Gereç ve Yöntemler: 2002-2012 yılları arasında duodenal, proksimal jejunoileal, distal jejunoileal atrezi/stenoz nedeniyle takip edilen 85 hasta çalışmaya dâhil edildi. Hastaların cinsiyeti, prenatal tanısı olup olmadığı, tanı konulma zamanı, doğum haftası, kilosu, anne yaşı, klinik özellikleri, eşlik eden anomaliler, ameliyattaki bulgular, ameliyat sonrası hastanede kalış süresi ile ilgili veriler kaydedilerek morbidite ve mortaliteyi etkileyen faktörler ve büyüme gelişme parametreleri incelendi.
Bulgular: Çalışmaya dâhil edilen 85 hastanın 44’ü kız, 41’i erkekti. Hastaların 35’inde duodenal, 29’unda proksimal jejunoileal, 21’inde ise distal jejunoileal atrezi/stenoz mevcuttu. Hastaların %58’inde prematürite mevcuttu. Duodenal atrezi/stenozu olan hastalarda eşlik eden konjenital anomali oranı %74,
jejunoileal atrezi/stenozu olan hastalarda %42 idi. Çalışma grubunda mortalite oranı %18, erken ve geç dönem komplikasyon oranı %20 olup, en sık görülen komplikasyon sepsisti. Mortalite ile sonuçlanan hastalarda eşlik eden konjenital anomali varlığı (%100), düşük doğum ağırlığı (%93) ve prematürite sıklığının (%80) artmış olduğu görüldü. Hastalar büyüme gelişme açısından incelendiğinde duodenal atrezi/stenoz grubunda vücut ağırlığı ve kilo persentillerinin normal değerlerde olduğu, jejunoileal atrezilerde ise boy persentillerinin düşük olduğu tespit edildi.
Sonuç: İnce barsak atrezisi/stenozu nedeniyle tedavisi yapılan ve kaybedilen hastalarda prematürite, düşük doğum ağırlığı ve eşlik eden konjenital anomali sıklığının artmış olduğu bulunmuştur. Geç dönem komplikasyon oranının düşük olmasının, hastalardaki takip düzensizliğine bağlı veri eksikliğinden kaynaklandığı düşünülmüştür. Jejunoileal atrezi/stenozu olan hastalarda boy persentilleri düşük olup çalışma grubundaki tüm hastaların ameliyat sonrası dönemde beslenme ve büyüme-gelişme açısından yakın takip edilmesini öneriyoruz.

Proje Numarası

08.11.2012 13/7

Kaynakça

  • Millar AJW, Rode H, Cywes S. Intestinal atresia and stenosis. Pediatric Surgery. 2005;30:416-434.
  • Kate B, Peter T, Marie A, Fabrizio B, Patricia B, Elisa C. Epidemiology of small intestinal atresia in Europe: a register- based study. Arch Di Child Neonatal. 2012;97:353-358.
  • Kulkarni M. Duodenal and small intestinal atresia. Pediatric Surgery. 2010;28:33-37.
  • Dalla Vechia LK, Grosfel L, Karen W. Intestinal atresia and stenosis: a 25 year experience with 277 cases. Arch Surg. 1998;133:490- 497.
  • Magnuson DK, Schwartz MZ. Stomach and duodenum. Principles and practices of pediatric surgery. Edt Oldham KT, Colombani PN. Lippincot Williams and Wilkins. 2005;72:1149-1179.
  • Kulkarni M. Duodenal and small intestinal atresia. Pediatric Surgery. 2010;28:33-37.
  • Grosfeld JL, Clathworthy HW: The nature of ileal atresia due to intrauterine intussesception. Arch Surg. 1970;100:714.
  • Hannah GP, Julia A, Stephen DW, David Z, Tom J. Intestinal atresias: factors affecting clinical outcomes. Journal of Pediatric Surgery. 2008;43:1244–1248.
  • Rachel ME, Elise R, Koenraad NJA, Van B, Jan BFH, Arend FB. Motor and cognitive outcome at school age of children with surgically treated intestinal obstructions in the neonatal period. Early Human Development. 2013;89:181–185.
  • Grosfeld JL. Jejunoileal atresia and stenosis. In: O’Neill AJ,Rowe MI, Grosfeld JL, Fonkalsrud EW, Coran AG. Pediatric Surgery. 2006 Vol 2, 6th ed, Philadelphia: Mosby.
  • Hemming V, Rankin J. Small intestinal atresia in a defined population: occurence, prenatal diagnosis and survival. Prenat Diagn. 2007;27:1205-1211.
  • Lorimier AA, Fonkalsrud EW, Hays DM. Congenital atresia and stenosis of the jejunum and ileum. Surgery. 1969;65:819-827.
  • Stollman TH, Blaauw I, Wijnen MHWA, van der Staak FHJM, Rieu PNMA, Draaisma JMT et al. Decreased mortality but increased morbidity in neonates with jejunoileal atresia; a study of 114 cases over a 34-year period. Journal of Pediatric Surgery. 2009;44:217–221.
  • Best KE, Tennant PWG, Addor MC, Bianchi F, Boyd P, Calzolari E et al. Epidemiology of small intestinal atresia in Europe: a register- based study. Arch Dis Child Neonatal. 2012;97:353-358.
  • Walker K, Badawi N, Hamid CH, Vora A, Halliday R, Taylor C et al. A population- based study of the outcome after small bowel atresia/stenosis in New South Wales and the Australian Capital Territory, Australia, 1992-2003. Journal of Ped Surg. 2008;43:484-488.
  • Burjonrappa S, Crete E, Bouchard S. Comparative outcomes in intestinal atresia: a clinical outcome and pathophysiology analysis. Pediatr Surg Int. 2011;27(4):437-442.
  • Hayden CK, Schwartz MZ, Davis M, Swischuk LE. Combined esophageal and duodenal atresia: sonographic findings. Am Radiol. 1983;140:225.
  • Veyrac C, Couture A, Saguintaah M, Baud C. MRI of fetal GI tract abnormalities. Abdom Imagıng. 2004;29:411-420.
  • Basu R, Burge DM. The effect of antenatal diagnosis on the management of small bowel atresia. Ped Surg Int. 2004;20:177-179.
  • Tam PKH, Nicholls G. Implications of antenatal diagnosis of small-intestinal atresia in the 1990s. Ped Surg Int. 1999;15:486- 487.
  • Gross RE. Congenital atresia of the intestine and colon. In: Gross RE, editor. The surgery of infancy and childhood: its principles and techniques. Philadelphia (PA): WB Saunders. 1953;150-166.
  • Keckler SJ, Peter SDS, Spilde TL, Ostlie DJ, Snyder CL. The influence of trisomy 21 on the incidence and severity of congenital heart defects in patients with Duodenal atresia. Pediatr Surg Int. 2008;24:921-923.
  • Şencan A, Mir E, Karaca I, Günşar C, Şencan A, Topçu K. Pyloric atresia associated multiple intestinal atresias and pylorocholedochal fistula. Journal of Ped Surg. 2002;42:1362-1364.
  • Kumaran N, Shankar KR, Lloyd DA, Losty PD. Trends in the management and outcome of jejunoileal atresia. Eur J Pediatr Surg. 2002;12:163-167.
  • Cragan JD, Martin ML, Moore CA, Khoury MJ. Descriptive epidemiology of small intestinal atresia. Teratology. 1993;48:441- 450.
  • Sholadoye TT, Mshelbwala PM, Ameh EA. Presentation and outcome of treatment of jejunoileal atresia in Nigeria. Afr J Paediatr Surg. 2018;15(2):84–87.
  • Güler AG, Tuncer R, İskit HS, Alkan M, Zorludemir Ü, Parlakgümüş C ve ark. Çocuk cerrahisi yenidoğan yoğun bakım ünitesinde sağlık bakımı ilişkili enfeksiyonlar ve risk faktörleri. Cukurova Medical Journal 2019;44:455-468.
Toplam 27 adet kaynakça vardır.

Ayrıntılar

Birincil Dil Türkçe
Konular Sağlık Kurumları Yönetimi
Bölüm Araştırma Makaleleri
Yazarlar

Selcan Türker Çolak 0000-0003-4481-0163

Murat Alkan 0000-0002-5588-4793

Recep Tuncer 0000-0003-4670-8461

Proje Numarası 08.11.2012 13/7
Erken Görünüm Tarihi 11 Temmuz 2022
Yayımlanma Tarihi 15 Temmuz 2022
Gönderilme Tarihi 18 Mayıs 2021
Kabul Tarihi 30 Ağustos 2021
Yayımlandığı Sayı Yıl 2022 Cilt: 17 Sayı: 2

Kaynak Göster

AMA Türker Çolak S, Alkan M, Tuncer R. İnce Barsak Atrezi ve Stenozu Olgularında Sağ Kalımı Etkileyen Faktörler. KSÜ Tıp Fak Der. Temmuz 2022;17(2):59-66. doi:10.17517/ksutfd.938290