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This document discusses factors that influence morbidity and mortality in cases of oesophageal atresia and/or tracheo-oesophageal fistula repair. It outlines the various types of anomalies, clinical presentations, diagnostic methods, aims of studying outcomes, and approach to patient preparation, surgery, and post-operative evaluation. Factors like birth weight, pre-operative pneumonia or sepsis, associated congenital anomalies, surgical complications, and gap length between oesophageal ends are assessed for their impact on outcomes of repairing these conditions.
This document discusses factors that influence morbidity and mortality in cases of oesophageal atresia and/or tracheo-oesophageal fistula repair. It outlines the various types of anomalies, clinical presentations, diagnostic methods, aims of studying outcomes, and approach to patient preparation, surgery, and post-operative evaluation. Factors like birth weight, pre-operative pneumonia or sepsis, associated congenital anomalies, surgical complications, and gap length between oesophageal ends are assessed for their impact on outcomes of repairing these conditions.
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This document discusses factors that influence morbidity and mortality in cases of oesophageal atresia and/or tracheo-oesophageal fistula repair. It outlines the various types of anomalies, clinical presentations, diagnostic methods, aims of studying outcomes, and approach to patient preparation, surgery, and post-operative evaluation. Factors like birth weight, pre-operative pneumonia or sepsis, associated congenital anomalies, surgical complications, and gap length between oesophageal ends are assessed for their impact on outcomes of repairing these conditions.
Copyright:
Attribution Non-Commercial (BY-NC)
Formati disponibili
Scarica in formato PPT, PDF, TXT o leggi online su Scribd
of oesophageal atresia and/or tracheo-oesophageal fistula repair Guide:-Dr A.K.Sharma(MS) Prof. and HOD Deptt. Of surgery Co-guide- Dr A.Memon(Mch) Asstt. Professor (paediatric surgery unit) Pt.J.N.M. MEDICAL COLLEGE & DR. B.R.A.M.HOSPITAL RAIPUR Duration of work- JULY 2006 TO SEPTEMBER 2008 Name of candidate:- Dr Rajan Kumar INTRODUCTION
Tracheo – oesophageal fistula and/or
oesophageal atresia are common life threatening malformations with an incidence of approximately 1 in 3500 birth. OA/TOF are among the most gratifying paediatric surgical conditions to treat In the distant past, nearly all infants born with OA/TOF died Despite the facts that there are several common varieties of this anomaly,and the underlying cause remain obscure,a careful approach consisting of meticulous perioperative care and attention to the technical detail of the operation can result in excellent prognosis in most cases. There are several factors influencing the outcome – Birth weight Sepsis Pneumonia Associated congenital anomaly Others Anatomic varieties Type C (most common) Proximal oesophageal atresia (esophagus continous with mouth ending in a blind loop superior to sternal angle) with a distal esophagus communicating from lower trachea or carina. Type A Proximal and distal oesophageal bud. A normal oesophagus with missing segment. Type D Proximal esophageal termination on lower carina or trachea with distal oesophagus arising from the carina. Type E (H) :- A variant of type D If the two segments of oesophagus communicate, this is termed as H – type fistula due to its resemblance to letter H. Late presentation Prognosis good Most easy to treat, but difficult to diagnose. Type B Proximal esophageal termination on lower trachea with distal esophageal bud Etiology and pathology presentations The esophagus and trachea share a common embryologic origin. They typically divide into separate tubes by approximately the thirty sixth day of gestation. Failure of this occurrence can results in spectrum of anomalies. Recent studies are suggestive of some molecular mechanisms underlying this condition like deficiency in sonic-hedgehog signaling pathway, Expression of thyroid transcription factor1(TTF-1) and fibroblast growth factor(FGF-10) Some reports are suggestive of genetic basis but no definitively results obtained Associated anomalies Cardiovascular 29% (PDA , VSD, ) Anorectal 14% Genitourinary 14% Gastrointestinal 13% Vertebral/skeletal 10% Respiratory 6% Genetic 4% Other 11% - VACTER : Vertebral anomalies, Anorectal malformation, Cardiac anomalies, Tracheo- esophageal fistula, Renal agenesis, Radial limb deformities. - Anopthalmia – oesophageal genital syndrome - Associated with fanconi anaemia - Asso. With Trisomy 18 & 21 - Feingold syndrome (oculodigito esophagoduodenal syndrome) Clinical presentations
Frothing /excessive salivation from mouth
Respiratory distress Cyanosis Regurgitation of feed from mouth and nose Abdominal distension Tracheo – oesophageal fistula can be suspected antenatally by USG of mother if polyhydramnios is present and fetal gastric shadow absent. Diagnosis
If in a new born 10-12 F rigid catheter will not
pass per orally >10cm from the lower alveolar ridge. Plain radiograph of chest abdomen shows the tip of catheter arrested in superior mediastinum suggestive of oesophageal atresia where as , gas in gastrointestinal tract (stomach) S/o distal trachaeo oesophageal fistula. AIMS AND OBJECTIVES To evaluate the factors influencing morbidity and mortality in cases of tracheo oesophageal fistula repair. To know the preoperative causes responsible for poor outcome of operation To know the intraoperative events/findings which can lead to poor outcome. To know the important causes leading to morbidity and mortality of cases of tracheo-oesophageal fistula in post- operative period. This study can help us to improve outcome in oesophageal atresia and/or tracheo-oesophageal fistula cases in future. MATERIAL AND METHODS In our study we are including all cases of oesophageal atresia and/or tracheo- oesophageal fistula which were admitted in Dr.B.R.A.M.Hospital,Raipur from july 2006 to september 2008. Our aim is to evaluate the various factors which are responsible for morbidity and mortality of TOF repair in our setup. Material required
All cases of tracheo – oesophageal fistula
admitted in paediatric surgery unit (gen. surgery) Dr.B.R.A.M.Hospital,Raipur during july 2006 to September 2008 After stabilizing the child, posted for surgery All the clinical data of child , intraoperative findings , post operative result filled in proforma and results will be evaluated. Preparation of patient
Patients should be prepared for surgery with stabilization
of vitals , infection and correction of sugar or electrolyte abnormalities Risk categorization On basis of Birth weight Presence of pneumonia Severity of associated congenital anomaly Baby with low birthweight, pneumonia and associated congenital anomaly are on very high risk . Operative approach -Operation is performed under general endotracheal anaesthesia with dependable vascular access. -Position : left lateral position with right upper limb over the ear -Incision – Curved incision approx 5 to 6cm long is made 1cm below the scapula extending anteriorly towards nipple and to the midline in between vertebrae and medial border of scapula -The chest is opened through the 4th or 5th intercostals space by dividing the intercostal muscle . -Extra pleural approach The following intraoperative findings are noted in proforma : -Length of gap between proximal and distal oesophageal end -If long gap – feeding gastrostomy/oesophagostomy and ligation of fistula -If short gap-end to end oesophago-oesophagostomy done with ligation of fistula. -Intra-operative ABG -Intra operative SPO2 monitoring -Intra operative complication (if any) -Duration of surgery -Immediate post op extubation done or not Complications
Early- sepsis, pneumonia, pleural
effusion, leakage and pneumothorax.
Late- recurrent fistula
formation,stricture,gastro-oesophageal reflux,pneumonitis. Evaluation of case
The all findings recorded and filled in the
proforma.
Observations and results
All the observations will be recorded in proforma and will be evaluated to find out the factors influencing the outcome of cases tracheo-oesophageal fistula repair. Discussion and conclusion It will be done with observation and results of present study and will be compared with observations and results presented by other workers in past.