| ||||||||||||||
|
|
|||||||||||||
Department of Anaesthesiology and Intensive care; All India Institute of Medical Sciences; Ansari nagar; New Delhi, India; mkarora442{at}hotmail.com
To the Editor:
FreemanSheldon Syndrome (FSS) is an uncommon congenital anomaly associated with a difficult airway (1,2) and a predisposition toward malignant hyperthermia (3). We used a regional technique for the anesthetic management and postoperative analgesia in a child with FSS.
A 1.5-year-old male child, weighing 9.5 kg, with the diagnosis of FSS, was scheduled for correction of bilateral Congenital Talipes Equinovarus. Examination of the childs airway revealed microstomia with mouth opening of 1 cm, micrognathia, small external nares, depressed nasal bridge, limited neck extension, normal dentition, and a relatively large head. We sedated the child with ketamine, followed by a propofol infusion. Surgical anesthesia was provided with a single intrathecal injection of 5 mg 0.5% bupivacaine in dextrose, followed by placing an epidural catheter into the caudal space, which was used to provide an additional 5 mL of 0.5% bupivacaine 50 min into the operation. The operation lasted 95 min. The catheter was maintained until the third postoperative day, and was used to provide analgesia by injections of 0.125% bupivacaine every 6 h.
REFERENCES
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|