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Статті в журналах з теми "Oesophageal atresia"

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Автор: Grafiati

Опубліковано: 4 червня 2022

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1

Hosie, Gareth P., and Melissa Short. "Oesophageal atresia." Surgery (Oxford) 28, no. 1 (January 2010): 38–42. http://dx.doi.org/10.1016/j.mpsur.2009.10.008.

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2

Hosie, Gareth P., and Elizabeth Gavens. "Oesophageal atresia." Surgery (Oxford) 31, no. 12 (December 2013): 618–21. http://dx.doi.org/10.1016/j.mpsur.2013.10.004.

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3

Spitz, L. "Oesophageal atresia." Current Paediatrics 11, no. 4 (August 2001): 281–85. http://dx.doi.org/10.1054/cupe.2001.0187.

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4

Sparey, Colette, and Stephen C. Robson. "Oesophageal atresia." Prenatal Diagnosis 20, no. 3 (March 2000): 251–53. http://dx.doi.org/10.1002/(sici)1097-0223(200003)20:3<251::aid-pd773>3.0.co;2-w.

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5

Myers, N. A. "Oesophageal atresia." Pediatric Surgery International 7, no. 2 (March 1992): 83–85. http://dx.doi.org/10.1007/bf00183907.

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6

Santos, Liliana Pimenta, Diana Coimbra, Catarina Cunha, and Maria Francelina Lopes. "Oesophageal atresia with tracheo-oesophageal fistula, ileal atresia and Hirschsprung’s disease: outcome of a rare phenotype." BMJ Case Reports 12, no. 2 (February 2019): e226675. http://dx.doi.org/10.1136/bcr-2018-226675.

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Анотація:

Oesophageal atresia with or without tracheo-oesophageal fistula, ileal atresia and Hirschsprung’s disease are surgical malformations of the gastrointestinal tract typically diagnosed early in the neonatal period and varying in severity and prognosis. This report describes a full-term male newborn presenting simultaneous oesophageal atresia with distal tracheo-oesophageal fistula, ileal atresia and Hirschsprung’s disease. In addition to the complex types of gastrointestinal malformations involved, the combination of ileal atresia and Hirschsprung’s disease, as well as ganglion cells distal to intestinal atresia, resulted in a challenging diagnosis. Despite a successful outcome, the patient presented increased morbidity and prolonged hospitalisation. We highlight some important findings that may aid the early diagnosis of Hirschsprung’s disease in this clinical setting. To our knowledge, the association of oesophageal atresia/tracheo-oesophageal fistula, ileal atresia and Hirschsprung’s disease has not been previously reported.

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7

El-Nabulsi, B., and R. Carachi. "Familial Esophageal Atresia." Scottish Medical Journal 54, no. 3 (August 2009): 1–4. http://dx.doi.org/10.1258/rsmsmj.54.3.58e.

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Summary The population incidence of oesophageal atresia is 1 in 3000 live birth. Most cases are sporadic but familial cases have been reported. The etiology of oesophageal atresia is multifactorial pathogenic mechanism, in which environmental and polygenic factors contribute to the development of the anomaly. Only 6–7% of cases have abnormal karyotype on chromosomal analysis. When a family history of oesophageal atresia exist, the parents should be offered genetic counseling. Antenatal screening by detailed ultrasound scans which should be done at expert centers. After birth the pediatrician should role out an oesophageal atresia by the passage of a nasogastric tube.

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8

Motshabi, Palesa. "Anaesthesia for oesophageal atresia with or without tracheo-oesophageal atresia." Southern African Journal of Anaesthesia and Analgesia 20, no. 5 (September 3, 2014): 202–8. http://dx.doi.org/10.1080/22201181.2014.979632.

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9

Robb, Andrew, and Anthony Lander. "Oesophageal atresia and tracheo-oesophageal fistula." Surgery (Oxford) 25, no. 7 (July 2007): 283–86. http://dx.doi.org/10.1016/j.mpsur.2007.05.019.

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10

Beasley, Spencer W. "Oesophageal atresia and tracheo-oesophageal fistula." Surgery (Oxford) 34, no. 12 (December 2016): 612–16. http://dx.doi.org/10.1016/j.mpsur.2016.10.004.

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11

Beasley, Spencer W. "Oesophageal atresia and tracheo-oesophageal fistula." Surgery (Oxford) 37, no. 11 (November 2019): 623–27. http://dx.doi.org/10.1016/j.mpsur.2019.09.001.

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12

Al-Rawi, O., and PD Booker. "Oesophageal Atresia And Tracheo-Oesophageal Fistula." Continuing Education in Anaesthesia Critical Care & Pain 7, no. 1 (February 2007): 15–19. http://dx.doi.org/10.1093/bjaceaccp/mkl062.

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13

Goyal, A. "Oesophageal atresia and tracheo-oesophageal fistula." Archives of Disease in Childhood - Fetal and Neonatal Edition 91, no. 5 (September 1, 2006): F381—F384. http://dx.doi.org/10.1136/adc.2005.086157.

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14

Sheridan, J., and I. Hyde. "Oesophageal stenosis distal to oesophageal atresia." Clinical Radiology 42, no. 4 (October 1990): 274–76. http://dx.doi.org/10.1016/s0009-9260(05)82117-8.

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15

Smith, Nicola. "Oesophageal atresia and tracheo-oesophageal fistula." Early Human Development 90, no. 12 (December 2014): 947–50. http://dx.doi.org/10.1016/j.earlhumdev.2014.09.012.

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16

Azmy, Amir. "Oesophageal stenosis distal to oesophageal atresia." Journal of Pediatric Surgery 26, no. 7 (July 1991): 868. http://dx.doi.org/10.1016/0022-3468(91)90189-z.

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17

Dash, Swetamayee, Aditya Prasad Padhy, and Abdul Rehman Siddiqi. "A rare variant of tracheoesophageal fistula type -3 with opening at left bronchus." IP Journal of Surgery and Allied Sciences 4, no. 1 (March 15, 2022): 25–28. http://dx.doi.org/10.18231/j.jsas.2022.005.

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Анотація:

Esophageal atresia is an anomaly which is usually congenital but can be acquired in which there is disruption in the continuity of the oesophageal lumen resulting in an upper & lower segment. We present the case of a rare sub-type of Oesophageal atresia Type 3 with distal opening at left bronchus. This is the first case reported in literature in the Kalinga hospital Of Medical Sciences, Bhubaneswar. A 3 day old term male baby who presented as an emergency with difficulty breathing, fever and refusal to feed. Initially managed as early onset neonatal sepsis with aspiration pneumonia in which a diagnosis of oesophageal atresia was finally made.A high index of suspicion for Oesophageal atresia/trachea-oesophageal fistula should prevail when faced with a neonate with the triad: respiratory distress during feeds, regurgitation and persistent frothy salivation. The case discusses about a rare variant of Type 3 oesophageal fistula where the opening is present at the left bronchus.

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18

Escobar, M. A., M. K. Pickens, R. M. Holland, and M. G. Caty. "Oesophageal atresia associated with congenital oesophageal stenosis." Case Reports 2013, may20 1 (May 20, 2013): bcr2013009620. http://dx.doi.org/10.1136/bcr-2013-009620.

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19

Puri, Prem. "Oesophageal atresia with proximal tracheo-oesophageal fistula." Journal of Pediatric Surgery 23, no. 5 (May 1988): 493–94. http://dx.doi.org/10.1016/s0022-3468(88)80469-x.

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20

Puri, P. "Prophylactic oesophageal calibration in oesophageal atresia surgery." Journal of Pediatric Surgery 29, no. 7 (July 1994): 943. http://dx.doi.org/10.1016/0022-3468(94)90030-2.

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21

Ioannides, Adonis S., and Andrew J. Copp. "Embryology of oesophageal atresia." Seminars in Pediatric Surgery 18, no. 1 (February 2009): 2–11. http://dx.doi.org/10.1053/j.sempedsurg.2008.10.002.

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22

Walker, W. S. "Management of oesophageal atresia." Thorax 52, no. 5 (May 1, 1997): 486. http://dx.doi.org/10.1136/thx.52.5.486.

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23

Spitz, L., E. M. Kiely, D. P. Drake, and A. Pierro. "Long-gap oesophageal atresia." Pediatric Surgery International 11, no. 7 (August 1996): 462–65. http://dx.doi.org/10.1007/bf00180083.

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24

Auldist, A. W., S. W. Beasley, and N. A. Myers. "Long-gap oesophageal atresia." Pediatric Surgery International 12, no. 8 (August 1997): 620. http://dx.doi.org/10.1007/bf01371915.

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25

Orford, J., M. Glasson, S. Beasley, E. Shi, N. Myers, and D. Cass. "Oesophageal atresia in twins." Pediatric Surgery International 16, no. 8 (November 24, 2000): 541–45. http://dx.doi.org/10.1007/s003830000435.

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26

Legat, Camille, Maissa Rayyan, Herbert Decaluwe, and Katherine Carkeek. "An interesting case of ‘strange lines’ a neonate with oesophageal atresia, tracheo-oesophageal fistula, situs inversus abdominalis and azygos continuation." BMJ Case Reports 12, no. 11 (November 2019): e229929. http://dx.doi.org/10.1136/bcr-2019-229929.

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Анотація:

We describe the case of a term baby boy born via vaginal delivery at 39 weeks gestation with oesophageal atresia, tracheaoesophageal fistula, situs inversus abdominalis and azygos continuation. The azygos continuation was diagnosed after cardiac echo and confirmed on cardiac catherisation after an unexpected umbilical line position on thoracoabdominal X-ray. The baby underwent a right-sided thoracotomy on day 1 of life for repair of the oesophageal atresia. A double fistula, of both the proximal and distal segments, of the oesophagus with short segment stenosis was confirmed. The tracheo-oesophageal fistulae were ligated and divided and the oesophageal atresia repaired by primary anastomosis without complications. The azygos vein was not ligated.

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27

Knottenbelt, Graham, Adam Skinner, and Christian Seefelder. "Tracheo-oesophageal fistula (TOF) and oesophageal atresia (OA)." Best Practice & Research Clinical Anaesthesiology 24, no. 3 (September 2010): 387–401. http://dx.doi.org/10.1016/j.bpa.2010.02.010.

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28

Kumar, Neetu, Jessica Ng, Ankit Chawla, and Simon Clarke. "Oesophageal atresia/tracheo-oesophageal fistula: renal anomaly screening." International Journal of Surgery 12 (November 2014): S67. http://dx.doi.org/10.1016/j.ijsu.2014.08.073.

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29

Traini, Isabelle, Jessica Menzies, Jennifer Hughes, Steven Thomas Leach, and Usha Krishnan. "Oesophageal atresia: The growth gap." World Journal of Gastroenterology 26, no. 12 (March 28, 2020): 1262–72. http://dx.doi.org/10.3748/wjg.v26.i12.1262.

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30

Teague, Warwick J., and Jonathan Karpelowsky. "Surgical management of oesophageal atresia." Paediatric Respiratory Reviews 19 (June 2016): 10–15. http://dx.doi.org/10.1016/j.prrv.2016.04.003.

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31

Bianca, Sebastiano, Marco Bianca, and Giuseppe Ettore. "Oesophageal atresia and Down syndrome." Down Syndrome Research and Practice 8, no. 1 (2002): 29–30. http://dx.doi.org/10.3104/reports.127.

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32

Ioannides, AS, D. Henderson, L. Spitz, and AJ Copp. "Molecular Mechanisms in Oesophageal Atresia." Clinical Science 103, s47 (July 1, 2002): 43P—44P. http://dx.doi.org/10.1042/cs103043pb.

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33

Puri, Prem. "Oesophageal atresia and vertebral anomalies." Journal of Pediatric Surgery 23, no. 5 (May 1988): 494. http://dx.doi.org/10.1016/s0022-3468(88)80472-x.

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34

Burge, D. M. "Oesophageal atresia and associated anomalies." Journal of Pediatric Surgery 24, no. 11 (November 1989): 1204. http://dx.doi.org/10.1016/s0022-3468(89)80134-4.

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35

Chodirker, B. N., A. E. Chudley, K. M. Macdonald, C. R. Harman, and J. A. Evans. "MSAFP levels and oesophageal atresia." Prenatal Diagnosis 14, no. 11 (November 1994): 1086–89. http://dx.doi.org/10.1002/pd.1970141114.

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36

Bhaskar Rao, Chanda, Jayapal K, Subbarao P, Narasimharao K, and Mohd Zakir Mohiddin Owois. "OESOPHAGEAL ATRESIA: 10 YEARS STUDY." Journal of Evolution of Medical and Dental Sciences 4, no. 102 (June 1, 2016): 16743–46. http://dx.doi.org/10.14260/jemds/2015/2507.

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37

Zhou, Jia-liang, Wu-ping Ge, Xiao-chun Zhu, Yuan-long Fang, Tao Song, and Song Tian. "Case of membranous oesophageal atresia." Archives of Disease in Childhood - Fetal and Neonatal Edition 103, no. 5 (April 11, 2018): F492. http://dx.doi.org/10.1136/archdischild-2018-314919.

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38

Chittmittrapap, S., L. Spitz, E. M. Kiely, and R. J. Brereton. "Oesophageal atresia and associated anomalies." Archives of Disease in Childhood 64, no. 3 (March 1, 1989): 364–68. http://dx.doi.org/10.1136/adc.64.3.364.

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39

Ninan, George. "Renal ultrasonography in oesophageal atresia." Journal of Pediatric Surgery 28, no. 3 (March 1993): 501. http://dx.doi.org/10.1016/0022-3468(93)90276-q.

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40

Patel, R. V., B. More, C. K. Sinha, and S. Singh. "Situs inversus totalis, oesophageal atresia and tracheo-oesophageal fistula." Case Reports 2013, jun03 1 (June 3, 2013): bcr2013009955. http://dx.doi.org/10.1136/bcr-2013-009955.

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41

Choudhry, M., P. A. Boyd, P. F. Chamberlain, and K. Lakhoo. "Prenatal diagnosis of tracheo-oesophageal fistula and oesophageal atresia." Prenatal Diagnosis 27, no. 7 (2007): 608–10. http://dx.doi.org/10.1002/pd.1745.

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42

Roberts, Kiera, Jonathan Karpelowsky, Dominic A. Fitzgerald, and Soundappan SV Soundappan. "Outcomes of oesophageal atresia and tracheo-oesophageal fistula repair." Journal of Paediatrics and Child Health 52, no. 7 (May 20, 2016): 694–98. http://dx.doi.org/10.1111/jpc.13211.

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43

Ga�ner, Ingmar, and Theresa E. Geley. "Sonographic evaluation of oesophageal atresia and tracheo-oesophageal fistula." Pediatric Radiology 35, no. 2 (October 7, 2004): 159–64. http://dx.doi.org/10.1007/s00247-004-1329-y.

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44

Baggaley, A., T. Reid, J. Davidson, P. de Coppi, and A. Botha. "Late life revision surgery for dilated colonic conduit in long gap oesophageal atresia." Annals of The Royal College of Surgeons of England 100, no. 7 (September 2018): e185-e187. http://dx.doi.org/10.1308/rcsann.2018.0120.

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Анотація:

Long gap oesophageal atresia presents a surgical challenge as there is insufficient length of the oesophagus to restore continuity. Oesophageal replacement is generally achieved using a conduit, taken from the stomach, jejunum or colon. Preferences of approach vary between and within surgical centres. Specific to colonic interposition, the continued growth and dilation of the interposed segment may lead to redundancy. Revision surgery in these cases is challenging and has been sparsely described in adult patients. We present two patients who had colonic interposition for long gap oesophageal atresia in infancy and who then underwent successful revision surgery in their fifth decade.

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45

Dastamani, Antonia, Neha Malhorta, Maria Güemes, Kate Morgan, Clare M. Rees, Mehul Dattani, and Pratik Shah. "Post-Prandial Hyperinsulinaemic Hypoglycaemia after Oesophageal Surgery in Children." Hormone Research in Paediatrics 91, no. 3 (August 9, 2018): 216–20. http://dx.doi.org/10.1159/000491647.

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Introduction: Post-prandial hyperinsulinaemic hypoglycaemia (PPHH) is a recognized complication of various gastric surgeries in children, but rarely reported after oesophageal atresia repair. We report 2 children diagnosed with PPHH after oesophageal surgery and the challenges of their management. Case 1: A 2-year-old boy diagnosed with oesophageal atresia at birth was surgically repaired requiring 6 oesophageal dilatations in the first year of life. At 11 months of age, he manifested hypoglycaemic seizures and investigations confirmed PPHH. Acarbose and diazoxide trials failed. He was managed with 17-h continuous gastrostomy feeds. Currently, he is 28 months old with euglycaemia on daytime bolus gastrostomy feeds and overnight 12-h continuous gastrostomy feeds. Case 2: A 6-month-old girl diagnosed with Wolf-Hirschhorn syndrome and tracheo-oesophageal fistula was surgically repaired, requiring monthly oesophageal dilatations. At 5 months of age, she was reported to have hypoglycaemia and PPHH was confirmed. She responded to diazoxide and continuous nasogastric tube feeds, but developed pulmonary hypertension possibly diazoxide-induced. Subsequently, diazoxide was stopped and normoglycaemia was secured via 20-h continuous gastrostomy feeds. Conclusion: PPHH may be an underdiagnosed complication in children undergoing surgery for oesophageal atresia. These children must be monitored closely for symptoms of hypoglycaemia and if there are concerns must be screened for possible PPHH. Our cases demonstrate that continuous feeding regimens might be the only therapeutic option, until PPHH gradually lessens in intensity over time.

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46

Aworanti, Olugbenga, Ezio Giulio Landi, and Alan Mortell. "Predictors of recurrent strictures after oesophageal atresia repair." Journal of Neonatal Surgery 10 (January 20, 2021): 8. http://dx.doi.org/10.47338/jns.v10.919.

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Анотація:

Background: Anastomotic strictures continue to complicate the outcome after oesophageal atresia (OA) repair. Multiple variables contribute to the development of strictures, and oesophageal dilatations are the mainstay of treatment. We aim to analyse the factors that impact the timing for initiation of oesophageal dilatations, the duration, frequency, and success of the dilatation regimen for OA. Methods: It was a retrospective review of data (13-year) of children who underwent repair for Gross type C OA (OA with distal tracheo-oesophageal fistula). The delayed anastomosis was performed for long gap OA. Leaks were clinically obvious or identified on contrast swallow. Strictures that were symptomatic underwent oesophageal dilatations. Results: The data of 72 children were analysed. The stricture rate was 37.5%. Ten had delayed repair, out of which 50% developed strictures compared to 35.5% who had a primary repair (P=0.48). There was no statistical difference in the mean birth weight (BW) and gestational age (GA) of children who developed strictures compared to those with no strictures (2.74kg vs 2.63Kg; P =0.548; 37.4 weeks vs 37.3 weeks; P=0.9). Children that underwent a delayed repair required significantly more dilatation sessions (12 vs 2 median sessions; P =0.001) and had a significantly prolonged duration of treatment (610 vs 63 median days; P = 0.013). There was a significant negative correlation between the GA and BW and the number of dilatation sessions required (P=0.03 and P=0.02, respectively). Linear regression revealed that delayed repair was the most important factor related to the number of dilatation sessions required (p <0.001); this was followed by lower GA or BW (p = 0.0265) and early onset of dilatations (p=0.0471). Conclusions: The early onset of oesophageal dilatation for oesophageal strictures or when they occur in premature babies or those that have had a delayed repair, it should be anticipated that they would be refractory or recurrent.

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47

Kabiri, M., A. Barkat, and Lamdouar N. Bouazzaoui. "974 Oesophageal Atresia: About 62 Cases." Pediatric Research 68 (November 2010): 485. http://dx.doi.org/10.1203/00006450-201011001-00974.

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48

Rintala, Risto J., Saara Sistonen, and Mikko P. Pakarinen. "Outcome of Oesophageal Atresia Beyond Childhood." Journal of Pediatric Gastroenterology and Nutrition 52 (May 2011): S35—S36. http://dx.doi.org/10.1097/mpg.0b013e318212808e.

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49

de Lagausie, P. "GER in Oesophageal Atresia: Surgical Options." Journal of Pediatric Gastroenterology and Nutrition 52 (May 2011): S27—S28. http://dx.doi.org/10.1097/mpg.0b013e3182133155.

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50

Desai, P., J. Morris, and L. Segal. "611 Oesophageal Atresia and Associated Anomalies." Archives of Disease in Childhood 97, Suppl 2 (October 1, 2012): A177. http://dx.doi.org/10.1136/archdischild-2012-302724.0611.

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