Tracheo esophageal fistula Dr. S. Parthasarathy MD., DA., DNB, MD (Acu), Dip. Diab. DCA, Dip. Software statistics, PhD(physiology) Mahatma Gandhi Medical.

Slides:



Advertisements
Similar presentations
Principles of neonatal Surgery
Advertisements

Pneumothorax & pneumopericardium
ENDOTRACHEAL INTUBATION. NEONATAL FLOW ALGORITHM BIRTHBIRTH Term gestation? Amnlotic fluid clear? Breathing or crying? Good muscle tone?u Provide warmth.
In the name of god Case presentation Dr.Mohammad Nemati.
Surgical Neonatal Vomiting
University of Tennessee College of Veterinary Medicine Department of Large Animal Clinical Sciences Esophageal Choke Horse Owners Seminar March 17, 2007.
Prepared by : Maha Hmeidan RN,MsN
General Principles of Postoperative Care The mortality of elective surgery of pulmonary and esophageal resection remains 2 to 4 times than that of elective.
Dr. S. Parthasarathy MD., DA., DNB, MD (Acu), Dip. Diab. DCA, Dip. Software statistics PhD (physio) Mahatma Gandhi medical college and research institute,
Tracheoesophageal Fistula
بسم الله الرحمن الرحيم.
Congenital Anomalies Fred Hill, MA, RRT. Abdominal Wall Defects Omphalocele - central defect in umbilicus, covered by a membrane Gastroschisis - cleft.
Development of respiratory system
Endotracheal Tube By Dr. Hanan Said Ali
Lines and Tubes.
Single-lung Ventilation for Pulmonary Lobe Resection in a Newborn Tariq Alzahrani Demonstrator College of Medicine King Saud University.
Tracheal Agenesis Rita Fakhoury CRNA Laura Wetzel CRNA.
Congenital Anomalies of G.I.T
TUBES, CATHETERS and DEVICES …and when they go BAD.
MECONIUM ASPIRATION SYNDROME
Neonatal Surgical Issues (Part 1) Sue Ann Smith, MD Neonatologist.
Post operative complications
Bowel Obstruction: Infants and Children
Prepared by Dr. Mahmoud Abdel-Khalek Pediatric Anesthesia.
Dr. S. Parthasarathy MD., DA., DNB, MD (Acu), Dip. Diab. DCA, Dip. Software statistics PhD(physiology) Mahatma gandhi medical college and research institute,
Of Rings, Slings and many other things Diego Gonzalez M.D. Gregory Gordon M.D. Metrohealth Medical Center November 26, 2002.
Dr. Sam Chippington Martin Churchill-Coleman
Dr. S. Parthasarathy MD., DA., DNB, MD (Acu), Dip. Diab. DCA, Dip. Software statistics Ph D (physiology) Mahatma Gandhi medical college and research institute,
Obstructive Sleep Apnea of Obese Adults Obstructive Sleep Apnea of Obese Adults Pathophysiology and Perioperative Airway Management Anesthesiology, 2009,
TRACHEOESOPHAGEAL FISTULA: Tracheoesophageal fistula (TEF) is a common congenital anomaly of the respiratory tract, with an incidence of approximately.
Basic Life Support (BLS) Advanced Life Support (ALS) Dr. Yasser Mostafa Prof. of Chest Diseases Ain Shams University.
Trigeminal (Gasserian) Ganglion Block
Alyssa Brzenski MD May 2, Overview Background Pre-repair bronchoscopy Thorascopic repair To extubate or not? Esophageal atresia – treatment of long-gap.
University of California, San Francisco
Procedures. Chapter 15 page 448 Objectives Spell and define key terms State the purpose of endotracheal intubation and describe how to assist with this.
Nadeen mohamed mamdouh Habib
OESOPHAGEAL ATRESIA Anne Aspin Types of oesophageal atresia and fistula 86%7% 4%
Lecture 21Development of respiratory system
Respiratory Distress in Neonates
MOHANNAD IBN HOMAID Esophageal Atresia and Trachesophageal Fistulas.
Inguinal Hernia of Premature Infants
Intercostal drainage Dr. S. Parthasarathy MD., DA., DNB, MD (Acu), Dip. Diab. DCA, Dip. Software statistics PhD(physiology) Mahatma Gandhi medical college.
Dr. S. Parthasarathy MD., DA., DNB, MD (Acu), Dip. Diab. DCA, Dip. Software statistics PhD (physio) Mahatma Gandhi medical college and research institute.
TRACHEA. What is Trachea bony tube that connects the nose and mouth to the lungs.
Dr. Sama ul Haque.   Discuss the formation of the lung buds.  Describe the development of larynx.  Explain the mechanism of formation of trachea,
Esophageal atresia.
1- For supporting ventilation in patient with some pathologic disease as:- : Upper airway obstruction : Respiratory failure : Loss of conciousness.
M & M Conference October 15, 2008 Stephen F. Dierdorf, M.D.
Post-Operative Care Adenocarcinoma. Post-Operative Care After esophagectomy, patients go to an intensive care unit for 24 to 48 hours. They are usually.
Anaesthesia risk Dr. S. Parthasarathy MD., DA., DNB, MD (Acu), Dip. Diab. DCA, Dip. Software statistics PhD (physio) Mahatma Gandhi medical college and.
TrachoEsophagial fistula (TEF)
Term female neonate born via emergent C- section due to non-reassuring fetal heart tracing is unstable at birth and required emergent ETT, NGT, and central.
Upper Airway management
5 wk old IVF twin born at 34 1/2 wks gestation weighing 2 pounds, 2 ounces. Pt not gaining weight and is only 5 pounds. Pt also has stridor since birth.
Thoracic Trauma Chapter 4.
Pain facts 5 Dr. S. Parthasarathy MD., DA., DNB, MD (Acu), Dip. Diab. DCA, Dip. Software statistics PhD (physio) Mahatma Gandhi medical college and research.
Congenital atresia of esophagus : Incidence : Is a relatively common congenital Mal formation occurring in about one in ( 2500 – 3000 ) life births and.
Oesphegeal Atresia Dr. Abdul Rahman A. Sulaiman. Oesphegeal Atresia incidence : 1 in 4000 live birth classification : 1- proximal atresia with distal.
Dr. S. Parthasarathy MD., DA., DNB, MD (Acu), Dip. Diab. DCA, Dip. Software statistics,Ph D(physiology) Mahatma Gandhi medical college and research institute,
Prepared by : Dr. Irene Roco
Dr S Spijkerman. Anaesthesia for adenotonsillectomy Airway is shared with the surgeon Risk of complications with Boyle-Davis mouth gag Day case surgery.
Case 5- Hypoxia after anesthesia Group A. Case scenario A 37 years of age male who arrives in the post anesthetic care unit following surgical removal.
Mediastinal Masses 2010 WOFAPS Meeting George W. Holcomb, III, M.D., MBA Surgeon-in-Chief Children’s Mercy Hospital Kansas City, Missouri.
EMERGENCY ANAESTHESIA Dr. Bassam Al-Barzangi Jordan University Hospital.
University of California, San Francisco
Rerespiratory distress in neonate Dr. Bassam kh.Aalabbasi
Congenital Anomalies Ralph Vogel, RN, PhD, CPNP.
Chapter 25 Respiratory Care Modalities
Anesthesia for Tracheoesophageal Fistula Repair
Presentation transcript:

Tracheo esophageal fistula Dr. S. Parthasarathy MD., DA., DNB, MD (Acu), Dip. Diab. DCA, Dip. Software statistics, PhD(physiology) Mahatma Gandhi Medical College and Research Institute, Puducherry, India

What is it ?? There is a connection between trachea and esophagus Congenital Sometimes plain esophageal atresia is talked with fistula

GROSS classification

Why does it happen ?? The embryogenesis - not completely defined. The trachea and esophagus develop from a common site, the foregut, in the first 4 to 5 weeks of gestation. Both the esophagus and the trachea originate from the median ventral diverticulum of the primitive foregut. The TEF lesion results from failure of the two structures to separate during division of the endoderm.

1 in C A E C A E

Diagnosis antenatal polyhydramnios Excessive salivation choking, coughing,aspiration pneumonia, cyanosis. Attempts at feeding - met with explosive vomiting passing an oral (nasal) gastric tube is impossible. A chest radiograph of a coiled oral gastric tube in the cervical esophageal pouch is diagnostic. No contrast please

VACTERL A common association is the VACTERL complex, consisting of vertebral, anorectal, cardiac, tracheoesophageal, renal, and limb defects VATER, VACTER and VACTERL 30 % may have !! But the ligation of a TEF is urgent.

Preoperative management --FUSA F eedings – NO U pright positioning S uctioning intermittent A ntibiotic administration Dehydration and acid base to be corrected Should we intubate preop ?? Does this prevent aspiration

Two ways of aspiration If significant aspiration pneumonia definitive corrective surgery ?? decompressing gastrostomy local or caudal anesthesia

Waterson prognostic criteria Weight - > 2.5, 1.8 – 2.5, <1.8 Associated anomalies Pneumonia A, B or C

Preoperative work up Echocardiography ( routine + right sided aortic arch) X ray chest Blood gases Lumbar ultrasound – Xray spines – caudal ?? USG abdomen Rigid bronchoscopy (airway + fogarty) Tracheoscopy flexible (Zurisch et al) 1 unit of packed red blood cells should be type and crossed matched

Surgery Repair primary repair involves isolation and ligation of the fistula followed by primary anastamosis of the esophagus. A staged repair is possible in sick neonates Posterior thoracotomy Thoracoscopic Bronchoscopic clipping of H Sometimes stabilizing and do it in 7 – 10 days FUSA remains

Gastrostomy

Sometimes During gastrostomy, they may clamp the fistula with esophagostomy and do the surgery after a few months also. Esophagostomy done from the neck to remove the secretions Described

Routine monitors Precordial steth in the left axilla Adequate IV access Radial artery cannulation (Lt) or umbilical 0.15 mg atropine IV Temperature, IV fluids Urine output – 1 ml/kg /hour

Anaesthetic management

Awake intubation Inhalation Induction Intubation in sitting posture Proper suctioning Circuits, scopes, cuffed ETT, Neonatal ventilators

Fish mouth fixation

Principle Intubate purposely Rt main bronchus Withdraw slightly to get bilateral air entry Reverse the curve of the tube Reverse the side of murphy eye Gas leak Ventilate lungs and not the fistula

Ventilation - adequate ?? Gastric distension Gastrostomy to water – to ETCO2 Tube kink Anomaly – different Even OLV

Ventilate to the stomach – fistula – no ventilation Tight bag with occlusion of the fistula

To prevent leak

Its easier to describe spontaneous – but open chest with surgeon pushing the right lung its difficult to maintain with spontaneous appropriate positioning of ETT is mandatory.

Spontaneous or controlled Are we sure – we are ventilating the lungs and not the fistula ?? Allow spontaneous & Give caudal 0.5–1 mL/ kg of 0.25% bupivacaine with epinephrine (5 μg/mL) Try threading far up.. But guarantee ?? USG Fentanyl Relaxants after clamping the fistula

No caudal ?? Avoidance of regional anesthesia with its corresponding decrease in systemic vascular resistance is warranted in patients with coexisting congenital heart disease such as hypoplastic left heart syndrome (HLHS). Cautious caudal in CVS diseases

Intra op problems left lateral decubitus position. During the surgical repair, the right lung is compressed and packed away, which may result in hypoxia. the trachea and/or endotracheal tube is compressed and occluded by the surgeon. Alternatively, the endotracheal tube can become obstructed by blood clots or may migrate into the fistula tract.

Intra op problems During localisation of the fistula, an anaesthesiologist can help the surgeon by applying traction to the wire loop. Some routinely use 100% oxygen during these anesthetics, even in premature infants who are at risk for developing the ROP. Class C -- bad lungs HFO used - reports !! Extubate in healthy infants -- class A Otherwise ??

Intra op problems The surgeon will get hold of the fistula and pull it. It will dislodge the position of ETT. The rt. Lung is collapsed by the surgeon. The tube becomes RT. endobronchial. ?? No ventilation – that’s why keep the steth Left axilla and watch for breath sounds..

Prognosis

Post op problems Surgical postoperative complications include anastomotic leak, stricture, gastro esophageal reflux, tracheomalacia, recurrent TEF. flush ligation is a must. Otherwise - Diverticulum –stasis, infection and giving way

Thoracoscopic approach The advantages Reduction of musculoskeletal sequelae that often develop following open thoracotomy in the newborn period. These have been well described as “winged” scapula, asymmetry of thoracic wall and thoracic scoliosis. superior visualization of fistula and surrounding structures including vagus nerve with the thoracoscopic approach.

Post op giving way Don’t extend Neck of neonate anastomosis will stretch and give way as there is always a gap between the two ends of oesophagus, which surgeon has mobilised to bring together

Post operative problems Need for ventilation arises secondary to  Compression of lung for several hours  Pre-existing aspiration pneumonia  Is always preferred in the backdrop of other coexistent congenital anomalies

Summary Incidence Types Commonest Clinical features FUSA Intubation and positioning, techniques Intra op hypoxemia Waterson, spitz, post op ventilation

Thank you all