Download Oesophageal Atresia by N. A. Myers (auth.), S. W. Beasley, N. A. Myers, A. W. PDF

By N. A. Myers (auth.), S. W. Beasley, N. A. Myers, A. W. Auldist (eds.)

This publication on oesophageal atresia and tracheo-oesophageal fistula units out to explain all points of a congenital anomaly which has been defined as 'the epitome of contemporary surgical procedure' and 'the raison d' etre of paediatric surgery'. even if the literature comprises references to the survival of 1 child with oesophageal atresia (without fistula) who was once born in 1935, the main part of the oesophageal atresia tale issues the main widespread anomaly, specifically oesophageal atresia with a distal tracheo-oesophageal fistula. the 1st long term survivals of infants born with this anomaly have been in 1939; it truly is acceptable accordingly that this publication might be compiled 50 years later. surgical procedure and neonatal care have made notable advances in this part century, and nowhere is that this extra noticeable than within the box of neonatal surgical procedure. however the care of the child with oesophageal atresia calls for greater than a health practitioner and a neonatologist, and our adventure has proven the necessity for a multidisci­ plinary technique concerning anaesthetists, extensive care therapists, thor­ acic physicians, basic paediatricians, cardiologists and cardiac surgeons, orthopaedic surgeons, radiologists, nephrologists and geneti­ cists. The involvement of representatives of all of those disciplines is clear within the pages that keep on with and within the checklist of participants; despite the fact that, a principal topic within the care of sufferers with oesophageal atresia is they, and their households, may be able to establish with one surgeon who has the last word accountability for sufferer care and the counselling of the family.

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Oesophageal Atresia

This e-book on oesophageal atresia and tracheo-oesophageal fistula units out to explain all features of a congenital anomaly which has been defined as 'the epitome of contemporary surgical procedure' and 'the raison d' etre of paediatric surgery'. even supposing the literature comprises references to the survival of 1 child with oesophageal atresia (without fistula) who was once born in 1935, the most important element of the oesophageal atresia tale matters the main widespread anomaly, particularly oesophageal atresia with a distal tracheo-oesophageal fistula.

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9 (eds P. P. Rickham, W. C. Hecker and J. Prevot), Baltimore, University Park Press, pp. 63-76. Pringle, K. C. (1983) Pathology of esophageal atresia with tracheoesophageal fistula. Presented at 16th Annual Meeting of Pacific Association of Pediatric Surgeons, Fukuoka, Japan. Rosenthal, A. H. (1931) Congenital atresia of the esophagus with tracheoesophageal fistula: report of eight cases. Arch. , 12, 756-72. Schmitz, J. A. (1923) Ueber die formale Genese der Oesophagusmissbildungen. Virchow's Arch.

Surg. Gynecol. , 76, 672-88. Howard, R. (1950) Oesophageal atresia with tracheo-oesophageal fistula: report of six cases with two successful oesophageal anastomoses. Med. J. , i, 401-4. Kluth, D. (1976) Atlas of esophageal atresia. J. Pediatr. , 11, 901-19. Myers, N. A. (1986) The history of oesophageal atresia and tracheooesophageal fistula - 1670-1984. Progr. Pediatr. , 20, 106-57. PART TWO Basic Sciences 2 Epidemiology and genetics A. 1 J. BRADY and N. A. MYERS Introduction Although oesophageal atresia and tracheo-oesophageal fistula are relatively common birth defects, little is known of their genetics and epidemiology.

10 Geographic clustering Ozimek et al. (1982), in a study from the state of North Carolina, found no evidence for regional clustering of oesophageal atresia. Little other information is available regarding the demographic distribution. In the 10-year group, 69% were from the metropolitan area and the remainder from country districts, comparable to the overall population distribution in Victoria. However, these data do not take into account geographical factors relating to place of conception and address of the mother during pregnancy, and therefore have little epidemiological significance.

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