|Year : 2010 | Volume
| Issue : 5 | Page : 464-466
A late presenting congenital diaphragmatic hernia misdiagnosed as spontaneous pneumothorax
Chitra Sanjeev Juwarkar1, Deependra Suresh Kamble1, Vishal Sawant2
1 Department of Anaesthesia, Goa Medical College, Goa, India
2 Department of Paediatric Surgery, Goa Medical College, Goa, India
|Date of Web Publication||9-Oct-2010|
Chitra Sanjeev Juwarkar
18/UG-2, Kamat Kinara, Post Caranzalem, Goa - 403 002
Source of Support: None, Conflict of Interest: None
Congenital diaphragmatic hernia (CDH) is described as (1) failure of diaphragmatic closure at development, (2) presence of herniated abdominal contents into chest and (3) pulmonary hypoplasia. Usually, pleural space is drained urgently when there is respiratory distress and radiological appearance of mediastinal shift. We present a case of a 5-month-old baby, diagnosed as tension pneumothorax and treated with chest drain insertion. CDH was the intraoperative diagnosis.
Keywords: Chest tube, congenital diaphragmatic hernia, pneumothorax
|How to cite this article:|
Juwarkar CS, Kamble DS, Sawant V. A late presenting congenital diaphragmatic hernia misdiagnosed as spontaneous pneumothorax. Indian J Anaesth 2010;54:464-6
|How to cite this URL:|
Juwarkar CS, Kamble DS, Sawant V. A late presenting congenital diaphragmatic hernia misdiagnosed as spontaneous pneumothorax. Indian J Anaesth [serial online] 2010 [cited 2019 Dec 15];54:464-6. Available from: http://www.ijaweb.org/text.asp?2010/54/5/464/71034
| Introduction|| |
Congenital diaphragmatic hernia (CDH) is herniation of bowels and abdominal solid organs in thoracic cavity, causing pulmonary hypoplasia with decreased pulmonary vasculature and dysfunction of the surfactant system. In severe cases, left ventricular hypoplasia is also observed.
Infants have scaphoid abdomen, barrel-shaped chest and respiratory distress (retractions, cyanosis, grunting respirations). In 1848, Bochdalek first described a CDH case which resulted from developmental failure of posterolateral foramina to fuse properly.  Incidence of CDH is 1:2000 to 1:5000 with equal gender preference.  Incidence of herniation is 78-90% posterolaterally through foramen of Bochdalek, 1.5-6% retrosternally via foramen of Morgagni and 14-24% via oesophageal hiatus. Left-sided herniation is common, as right hemidiaphragm develops earlier and the liver prevents hollow viscus from herniation.  On the affected side, there is right to left shunting of blood. Also, 70-95% cases are diagnosed in the neonatal period; later diagnosis becomes difficult due to vague cardiorespiratory and gastrointestinal symptoms.  Emergency correction is required in most cases.
Usually, plain chest radiograph done after passing a nasogastric tube gives the diagnosis of CDH. However, it may be misinterpreted and diagnosed as pleural effusion/pneumothorax (as in our case), and hence, there is a possible risk of chest tube perforating herniated viscus.  The anaesthetic management of our case was no different from that of an early diagnosed neonatal diaphragmatic hernia.
| Case Report|| |
A 7-kg, 5-month-old, cyanotic male baby was referred to us as a case of spontaneous pneumothorax with respiratory distress unresponsive to medical management.
On examination, the baby was afebrile, irritable, cyanosed, with a heart rate of 146/minute, tachypnoeic with a respiratory rate of 78/minute, with nasal flaring, subcostal and intercostal retraction and grunting. The chest expansion on the left side was decreased and there was a hyper-resonant note with absent air entry. The right lung had decreased air entry with rales and conducted sounds and trachea was deviated to the right. SpO 2 on room air varied between 70 and 80%. Cardiovascular and gastrointestinal system showed no gross anomaly.
Investigations revealed the following: haemoglobin 8.3 g%, Random Blood Sugar level (RBSL) 193 mg%; Arterial Blood Gas (ABG) (FiO 2 34% approx.) revealed pH 7.468, PCO 2 25.5, PO 2 81.1, SaO 2 96.9, HCO 3 18.6, Base Excess (BE) -2.7.
Chest X-ray showed massive, left-sided pneumothorax with mediastinal shift to the right side [Figure 1]. Earlier attempts to drain pneumothorax had failed, and repeat chest X-ray was suggestive of haemopneumothorax, with three Intercostal Chest Tubes (ICTs) introduced on the left side [Figure 2]. A computed tomography (CT) scan revealed a localised area of air pocket, which was reported as encysted pneumothorax or possibly congenital lobar emphysema.
|Figure 1: Plain chest X-ray masquerading as a tension pneumothorax on the left side with mediastinal shift on the right side|
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Paediatric surgeon posted the baby for emergency thoracotomy.
The baby [American Society of Anaesthesiologists (ASA) grade III E] was shifted to Operation Theatre, wrapped in cotton wool gamgees in a radiant warmer, receiving O 2 by hood and a vein secured with 24-g i.v. cannula. Resuscitative drugs/airway cart were kept ready. ECG, pulse oximeter and neonatal BP cuff were attached. The baby was premedicated with i.v. atropine 0.14 mg, dexamethasone 2.5 mg and ondansetron 1 mg.
After preoxygenating the baby with 100% oxygen by mask using Jackson Rees' (JR) circuit for 5 minutes, ketamine 14 mg was administered i.v. and halothane in 100% oxygen delivered in increments from 0.5 to 3% maintaining spontaneous ventilation. During induction, SpO 2 gradually started dropping; hence, tracheal intubation was immediately done with size 4 uncuffed oral endotracheal tube. After confirming optimum air entry on both the sides, the tube was fixed and the neonate was allowed to breathe spontaneously. Ventilation was then assisted as saturation started improving. Anaesthesia was now maintained with 100% oxygen and 1% halothane with assisted ventilation using JR circuit.
The baby was placed in a right lateral position for a left thoracotomy incision. Surprisingly, bowel loops popped out of left thoracotomy incision, pointing to a diagnosis of CDH. The baby was immediately made supine to proceed for laparotomy [Figure 3]. Neuromuscular blockade was then achieved with i.v. pancuronium 0.7 mg and the ventilation controlled. On withdrawing the bowel loops from thoracic cavity, both oxygen saturation and air entry improved remarkably. Analgesia was provided with i.v. pethidine 3.5 mg.
ECG, BP and SpO 2 were monitored intraoperatively. Also, i.v. fluids were given as per Holliday Segar formula using Isolyte-P (50 ml/hour; maintenance fluid + operative loss), and blood loss (approx. 50 ml) was replaced with fresh whole blood. At the end of operation, i.v. ondansetron 1 mg and dexamethasone 2.5 mg was repeated. Residual muscle blockade was reversed with i.v. neostigmine 0.35 mg and i.v. atropine 0.14 mg. Once respiratory efforts were adequate, the baby was extubated after thorough oral and tracheal suctioning.
Postoperatively, there was improved air entry and SpO 2 was maintained at 96% on room air. The baby was shifted to intensive care unit on a mobile warmer with O 2 administered via polymask. Postoperative chest X-ray showed good bilateral lung expansion, and chest drains were then removed after 72 hours. Rest of the postoperative period was uneventful. The baby was discharged after 7 days.
| Discussion|| |
Bush et al.  as well as a recent publication in Hong Kong Journal of Paediatrics described a case of CDH misdiagnosed as pneumothorax, resulting in ICT insertion. Hence, investigations like chest X-ray (with or without nasogastric tube insertion), contrast studies, CT scan and laparoscopy are to be done to exclude diaphragmatic herniation. 
Our case was similar to this with the only difference being presentation at 5 months after birth which probably led to the mistaken diagnosis. The initial fall in SpO 2 and the subsequent improvement following reduction of contents of hernia sac are self-explanatory.
Initially, reduction of herniated viscera and diaphragmatic defect closure were emergently performed following birth. With the recent understanding that pulmonary hypoplasia and hypertension determine the outcome of CDH,  surgical intervention has been delayed enabling preoperative stabilisation of the patient's clinical condition. Failure to thrive requires gastrostomy tube placement to improve the caloric intake. The goal of CDH management is lung expansion avoiding over distension; therefore, inspiratory pressures should be lowest. High frequency ventilation lowers the ventilator pressures and normalises PaCO 2 . Frequent radiography helps in assessment of lung expansion. Extra Corporeal Membrane Oxygenation (ECMO) is used for very sick infants, but is available at fewer centres.
Face mask ventilation and nitrous oxide cause gastric insufflation, further impairing circulation/respiration, and hence, they are avoided. We used only 100% O 2 as SpO 2 dropped below 90% and we avoided N 2 O (facility to provide air lacked in our anaesthesia machines). In theory, positive pressure ventilation preferentially ventilates normal lung. At the same time any re-expansion of collapsed lung will exacerbate the mass effect, thereby worsening the circulation. Collapsed lung should therefore be isolated and normal lung ventilated with small tidal volumes/pressures using a double lumen tube, until decompression of affected hemithorax is achieved. At least single lumen tube with bronchial blocker should be considered.  We have no experience of one lung ventilation technique with double lumen tubes in our institute.
Caudal epidural anaesthesia is good, but is rarely opted in case of emergencies. Introduction of epidural nerve stimulation and ultrasound guidance for inserting epidural catheter up to mid-thoracic segments have been described. 
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[Figure 1], [Figure 2], [Figure 3]