EDITOR:

Marfan’s syndrome is a relatively uncommon familial disorder with an incidence of about 1 : 10 000 in most racial and ethnic groups [Reference Prockop, Kuivaniemi, Tromp, Fauci, Martin, Braunwald, Kasper, Isselbacher, Hauser, Wilson, Longo and Randolph1]. It is characterized by widespread abnormalities of the skeletal, cardiovascular and ocular symptoms. Although cervical spine abnormalities including atlantoaxial dislocation are common in these patients, clinical problems associated with them are rare [Reference Hobbs, Sponseller, Weiss and Pyeritz2]. Clinically symptomatic cases of atlantoaxial dislocation in Marfan’s syndrome are rarely reported in literature [Reference Herzka, Sponseller and Pyeritz3,Reference Place and Enzenauer4]. We describe a patient with Marfan’s syndrome undergoing corrective surgery for atlantoaxial dislocation under general anaesthesia.

A 21-yr-old 174 cm male weighing 44 kg presented with a 4-yr history of progressive weakness of all four limbs following the fall of an object on his neck. Gradually, he developed difficulty in getting up from a squatting position without support. His past medical history was unremarkable. On examination, this tall patient revealed typical features of Marfan’s syndrome: arachnodactyly, high arched palate, winging of scapula, ulnar deviation of metacarpophalangeal joints and bilateral congenital talipes equinavarus. There were no significant abnormalities on examination of the cardiovascular system. However, routine transthoracic echocardiography showed aortic root dilatation (42 mm) with normal left ventricular function. The patient had diminished motor power in all four limbs (4/5). His gag reflex was impaired indicating involvement of lower cranial nerves. A magnetic resonance imaging of the cervical spine showed atlantoaxial dislocation with basilar invagination by an abnormally curved odontoid peg with significant cervical cord compression at the level of the atlas. The patient was diagnosed to have a craniovertebral junction anomaly associated with Marfan’s syndrome. Surgical correction was planned, which included trans-oral odontoidectomy and posterior fixation. Two days before surgery, Gardner–Wells tong traction was attached under local anaesthesia to reduce the dislocation. The plan of awake fibreoptic intubation was discussed with the patient. On the day of surgery, he was premedicated with glycopyrrolate 0.2 mg intramuscularly, 1 h before induction. Awake intubation was performed after anaesthetizing the upper airway with lidocaine 4% viscous, bilateral superior laryngeal nerve blocks and a trans-tracheal injection of lidocaine 4%. Standard anaesthetic induction was followed using fentanyl, thiopental and rocuronium. Anaesthesia was maintained with O₂, N₂O (1 : 2) and isoflurane with intermittent bolus of rocuronium and fentanyl. Mean blood pressure (BP) was maintained at about 70–80 mmHg by titrating the inspired concentration of isoflurane along with boluses of fentanyl. Care was taken to prevent hypertensive episodes during various steps of anaesthesia and surgery with the use of an intravenous nitroglycerin infusion. Monitoring parameters included ECG, S_PO₂, etCO₂ and continuous arterial BP. The surgical procedure involved two stages. Transoral odontoidectomy was performed in the supine position followed by posterior fixation in the prone position on a Wilson frame. The intraoperative course was uneventful. At the end of surgery, the patient was turned supine and residual neuromuscular blockade was reversed. The trachea was not extubated but after observing movement in all four limbs, the patient was sedated with midazolam and fentanyl. He was taken to the neurosurgical ICU for overnight pressure-support ventilation, as routine [Reference Rath, Bithal and Guleria6]. The tracheal tube was removed on the first postoperative day, after ensuring satisfactory cough reflex and respiration. There was no change in echocardiography findings on the second postoperative day. At the 3-month follow up, the patient is doing well with improved motor power in all four limbs.

Marfan’s syndrome is a connective tissue disorder caused by mutation in a gene (FBN1) on chromosome 15, which encodes the glycoprotein fibrillin1, the principal component of extracellular matrix microfibrils [Reference Judge and Dietz5]. It is inherited as an autosomal dominant trait. Common manifestations of this disease include mitral valve prolapse, aortic root dilatation, dissection, lens dislocation and myopia, arachnodactyly, kyphoscoliosis, sternal deformities and dural ectasia. Scoliosis has been reported in 40–70% of patients. Radiological analysis of the cervical spine revealed increased prevalence of atlantoaxial dislocation, basilar invagination and increased odontoid height [Reference Herzka, Sponseller and Pyeritz3]. Such patients may present with features of dysfunction of brainstem, cerebellum, spinal cord and cranial nerves. They may also complain of pain, stiffness and restriction of neck movements, vertigo, confusion, transient attacks of unconsciousness, weakness and parasthesiae of limbs and respiratory abnormalities [Reference Rath, Bithal and Guleria6]. Our patient presented with quadriparesis due to compression of bony structures in the upper cervical spinal cord. Securing of the airway in these patients may be challenging not only because excessive manipulation of the atlanto-occipital joint has to be avoided but also because of the associated airway abnormalities. Excessive traction during laryngoscopy for tracheal intubation should be avoided to prevent jaw dislocation due to associated joint laxity. Hence, it is appropriate to carry out fibreoptic intubation, preferably while being awake, in these patients.

Anaesthetic management in patients with atlantoaxial dislocation has rarely been described [Reference Rath, Bithal and Guleria6]. Its association with Marfan’s syndrome even with a normal cardiovascular system makes these patients at risk for anaesthesia. The cardiovascular manifestations may include mitral valve prolapse, mitral regurgitation, enlargement of the aorta, aortic dissection, aortic rupture or aortic regurgitation. Cardiac arrhythmias may be primary or secondary and are a potential cause of sudden death. Appropriate antibiotic prophylaxis for bacterial endocarditis is required.

As pulsatile flow is more important than steady-state hypertension in producing aortic dissection, it is appropriate to add a beta blocker to decrease myocardial contractility and aortic pressure rise. Prophylactic beta blockers have also been shown to decrease the size of aortic dilatation [Reference Shores, Berger, Murphy and Pyeritz7]. In our patient, as the aortic dilatation was 42 mm (normal 20–38 mm), a beta blocker was not used. Inhalational agents, which reduce the velocity of ventricular contraction, are ideal; however, no single anaesthetic agent or technique has demonstrated superiority. Control of BP alone by vasodilators may increase left ventricular ejection velocity, and, hence, it should be combined with beta blockade to prevent dissection.

Reduction in connective tissue elasticity makes all the joints prone to dislocation especially when the patient is anaesthetized, and careful positioning and handling is required. In our patient, surgery consisted of two steps performed in supine and prone positions, respectively. A mouth gag with tongue retractor is used to access the posterior pharyngeal wall, and here mandibular dislocation remains a possibility. The use of Gardner–Wells tong traction to reduce dislocation is questionable as it may further add to the problems in a cervical spine with lax joints. However, in our patient all these manoeuvres were uneventful.

Anterior chest deformity can contribute to a restrictive pattern of lung disease [Reference Prockop, Kuivaniemi, Tromp, Fauci, Martin, Braunwald, Kasper, Isselbacher, Hauser, Wilson, Longo and Randolph1,Reference Shores, Berger, Murphy and Pyeritz7] and skeletal changes including kyphoscoliosis can lead to decreased pulmonary function [Reference Rath, Bithal and Guleria6]. Widening of distal airspaces with bullae or blebs predisposes to spontaneous pneumothorax, and this must be borne in mind during anaesthesia with positive pressure ventilation.

In conclusion, we successfully managed a patient undergoing corrective surgery for atlantoaxial dislocation with basilar invagination in Marfan’s syndrome, under general anaesthesia. The possibility for acute airway, cardiovascular and respiratory complications in these subgroup of patients necessitates careful preoperative assessment and optimal anaesthetic techniques to avoid potential complications.