(104Kb)Boehm W, Emmel M, Sreeram
N. Balloon Atrial Septostomy: History and Technique. Images Paediatr Cardiol
2006;26:8-14
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(104Kb) |
Boehm W, Emmel M, Sreeram
N. Balloon Atrial Septostomy: History and Technique. Images Paediatr Cardiol
2006;26:8-14
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University Hospital of Cologne, Germany. |
| Transposition of the great arteries | Heart defects, congenital | Catheter, invervention |
| Balloon atrial septostomy |
"...The initial response to this report varied between admiration and horror but, in either case, the procedure stirred the imagination of the "invasive" cardiologists throughout the entire cardiology world and set the stage for all future intracardiac interventional procedures – the true beginning of pediatric and adult interventional cardiology." (Charles E. Mullins, 1998)2
The natural history of untreated transposition of the great vessels in the neonate is poor. Complete correction has been possible since 1959 with the atrial switch procedure, first described by Senning.3 Mustard simplified this method, reducing mortality rates to a reasonable level.4 Best results with both operations were achieved in children beyond six months of age. Therefore an early palliation by creation of an intraatrial communication was imperative. A surgical technique widely practised was described by Blalock and Hanlon in 1950.5 In 1966 Rashkind and Miller described a nonsurgical procedure to create an atrial septal defect, using a balloon catheter.1 Since then it has remained an integral part of cardiac catheterisation in neonates, even after the introduction of the arterial switch procedure by Jatene and associates in 1976.6 Balloon atrial septostomy could be of potential benefit in patients with other severe congenital heart defects, such as tricuspid or mitral atresia, or total anomalous pulmonary venous drainage, with a restrictive foramen ovale. The use of two-dimensional transthoracic echocardiography to monitor the procedure,7-9 and the possibility of using the umbilical vein as an access site10 have simplified this procedure dramatically, so that it can be performed at the bedside in the neonatal intensive care unit.11,12 Used primarily in newborn children under six weeks of age, balloon atrial septostomy has limitations in older infants, due to the increased thickness of the atrial septum. In these cases blade septostomy and static balloon dilation of the atrial septum are prefered to enlarge the interatrial communication. These techniques are however outside the scope of this paper.
Catheter description
A variety of catheters are in use for balloon atrial septostomy. The
most commonly used catheter at the present time, the 5F Miller balloon
atrial septostomy catheter (Edwards Lifesciences, Irvine, CA, USA), needs
an 7F to 8F introducer. The low profile, dual lumen Z-5 atrioseptostomy
catheter13 (Numed, Cornwall, ON, Canada), comes in 4F or 5F
sizes, depending on the balloon diameter, and requires a 5 or 6F introducer,
respectively. The Z-5 catheter is advanced over a guidewire, as opposed
to the Miller catheter.
Technique
The procedure can be performed under sedation or general anaesthesia.
The access can be achieved via the femoral or the umbilical vein. The femoral
vein is punctured in the typical way, an 4 or 5F introducer is placed in
the vessel, and then exchanged for a 7F or 8F introducer, when the Miller
catheter is used. The balloon catheter is advanced into the right atrium.
Then the foramen ovale is crossed and the catheter is positioned in the
left atrium. Correct position is documented via biplane fluoroscopy or
two-dimensional echocardiography. In the anteroposterior fluroscopic projection,
it is sometimes advantageous to position the catheter tip in the orifice
of the left upper pulmonary vein (outside the cardiac silhouette), to confirm
its left atrial location (figures 1 and 2).
The balloon is quickly inflated with 3-4 ml of dilute
radiopaque solution, locked, and then sharply withdrawn into the right
atrium down to the junction of the inferior caval vein. The catheter is
then advanced into the body of the right atrium, so as not to obstruct
inferior caval return, and then deflated rapidly. This maneuver may be
repeated two to three times. The size of the interatrial communication
can be measured directly by echocardiography at the table. The efficacy
is usually immediately obvious, from the rise in systemic arterial saturation
(figures 3-5).
Using the umbilical venous approach, the umbilical cord is cut transversely, flush with the skin, the vein is identified, and the catheter directly inserted into the vessel with the aid of a forceps. The progress of the catheter through the ductus venosus can be monitored either by fluroscopy (in which case the catheter passes from the right of the midline superiorly towards the right atrium in the anteroposterior projection, and from front to back in the lateral projection), or by cross sectional echocardiography. After reaching the right atrium, the procedure is done as described above. Sometimes it may be difficult to pass the catheter into the inferior vena cava due to stenosis or closure the ductus venosus. In this case an 0.018" guidewire and 4F endhole catheter combination can be introduced into the umbilical vein, and then manipulated into the right atrium. Thereafter, a standard 7F or 8F sheath can be used to introduce the septostomy catheter. When using a sheath in the umbilical vein, it must be borne in mind that the tip of the sheath is often inside the right atrium, and may impede withdrawal of the inflated balloon across the septum. It is therefore important to remember to withdraw the sheth well into the ducuts venosus prior to performing the septostomy. With the Z-5 atrioseptostomy catheter, it is easiest to position the guidewire (0.014" or 0.021") in the left upper pulmonary vein. The ballon catheter is advanced over the wire into the left atrium, and the septostomy carried out in a standard fashion.
Although it is a safe procedure, various complications have been reported, in upto 11% of procedures in some series.14-25 These consist of rhythm disturbances (premature ectopic beats, supraventricular tachycardia, atrial flutter and fibrillation, partial or complete heart block, ventricular arrhythmias), perforation of the heart, balloon fragment embolization, laceration of atrioventricular valves, systemic or pulmonary veins and failure of balloon deflation. In practice, it is unusual to have a complication associated with the procedure at the present day.
Discussion
Generally agreed indications for balloon atrial septostomy are: transposition
of the great arteries with or without associated cardiac defects (its role
in patients with a large duct may be questionable, if the systemic saturation
can be adequately maintained with prostaglandin E infusion alone, although
in our experience the combination of a large atrial communication and a
small duct [prostaglandin E infusion maintained at 5 nanograms/kg/min]
appears to produce the most stable hemodynamics), tricuspid atresia with
restrictive ASD, pulmonary atresia with intact ventricular septum and total
anomalous pulmonary venous connection with restrictive ASD. It may be indicated
in patients with hypoplastic left heart syndrome for emergency relief of
the transseptal atrial gradient in neonates with a severely restrictive
interatrial defect. Balloon atrial septostomy is an effective treatment
in infants less than six weeks.26-30 It is inappropriate in
children older than 1-2 months.
Summary
Although the arterial switch operation for transposition of the great
vessels is typically performed within days after birth, and a left to right
shunt through an open ductus arteriosus can be maintained with prostaglandine
E, creation of an additional shunt at the atrial level is easy to achieve,
provides stable arterial oxygen saturations and can therefore be routinely
recommended.
References
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