Cases reported "Marfan Syndrome"

Filter by keywords:



Filtering documents. Please wait...

1/4. Anaesthetic management of two paediatric patients with Hecht-Beals syndrome.

    We undertook the anaesthetic management of two children with Hecht-Beals syndrome for orthopaedic surgery under general anaesthesia. Both patients had arachnodactyly, kyphoscoliosis, and multiple congenital joint contractures, but limited mandible excursion was not obvious preoperatively in either, although mental retardation made it difficult for them to cooperate with mouth examination. They had no apparent difficulties with their mouths in daily activities. The anaesthesia records of one patient showed that intubation had been difficult in an earlier procedure. The other patient also had a history of difficult intubation, with slight tearing of the corners of her mouth during an intubation procedure. During slow induction of general anaesthesia with sevoflurane, face mask ventilation was easily performed. We attempted to visualize the larynx under anaesthesia with muscle relaxation, but we were unsuccessful because of the limited mouth opening. After several trials, blind oral intubations were fortunately successful in both patients. There were no postoperative problems with the airway.
- - - - - - - - - -
ranking = 1
keywords = anaesthesia
(Clic here for more details about this article)

2/4. Anaesthetic management of a caesarean section in a patient with Marfan's syndrome and aortic dissection.

    This report describes a case of a Stanford Type B aortic dissection (originating distal to the left subclavian artery and extending to the aortic bifurcation and proximal left iliac artery) in a 31-year-old primigravid woman who was at 39 weeks gestation and had Marfan's syndrome. The dissection was managed conservatively. Caesarean section was performed under epidural anaesthesia with aggressive control of hypertension. Postoperatively, there was no extension of the dissection and no aneurysm formation. She was discharged from hospital two weeks after delivery and remained asymptomatic at six months. There are no plans for surgical intervention.
- - - - - - - - - -
ranking = 0.25
keywords = anaesthesia
(Clic here for more details about this article)

3/4. Dural ectasia: a likely cause of inadequate spinal anaesthesia in two parturients with Marfan's syndrome.

    We report two cases of Caesarean section in patients with Marfan's syndrome where continuous subarachnoid anaesthesia failed to provide an adequate surgical block. This was possibly because of dural ectasia, which was confirmed by a computed tomography scan in both cases.
- - - - - - - - - -
ranking = 1.25
keywords = anaesthesia
(Clic here for more details about this article)

4/4. Anaesthesia for caesarean section in a Marfan patient with recurrent aortic dissection.

    PURPOSE: We report the anaesthetic management of a 34-yr-old pregnant woman with recurrent aortic dissection and marfan syndrome for Caesarean section. CLINICAL FEATURES: She presented at 28 wk gestation with recurrent aortic dissection and had undergone aortic valve replacement and coronary ostia reimplantation (Bentall procedure) in the first trimester of pregnancy. She was treated in hospital with labetalol, anticoagulants and steroids and daily echocardiographic examination until 34 wk when caesarean section was planned. After positioning radial artery and CVP catheters and a transoesophageal echocardiographic probe, general anaesthesia was induced with thiopentone and maintained with isoflurane, and endotracheal intubation was facilitated with vecuronium. The site of incision was infiltrated with lidocaine before surgery which was uneventful. The patient was discharged at 10 days. CONCLUSIONS: With appropriate preoperative care and monitoring, uneventful general anaesthesia for caesarean section was achieved in a patient with marfan syndrome in the presence of recurrent aortic dissection.
- - - - - - - - - -
ranking = 0.5
keywords = anaesthesia
(Clic here for more details about this article)


Leave a message about 'Marfan Syndrome'


We do not evaluate or guarantee the accuracy of any content in this site. Click here for the full disclaimer.