Ekslusi Indications and Evaluation For ASD Closure
Ekslusi Indications and Evaluation For ASD Closure
Ekslusi Indications and Evaluation For ASD Closure
Indications and
Evaluation for
ASD Closure
Performing detailed hemodynamic evaluation of secundum atrial septal defects
using current imaging modalities and closure devices.
BY YOLANDEE BELL-CHEDDAR, MD, AND ZAHID AMIN, MD, FAAP, FSCAI, FACC
Figure 2. Classification of atrial septal rims. Reprinted with Although criteria for closure are met on one level, there may
permission from Amin Z. Catheter Cardiovasc Interv be concurrent data that preclude closure of such defects.
2006;68:778–787.1 Naturally, if the defect is larger than 40 mm, it cannot be
closed with a device because there is no device available
tum; rather, it is a defect in the roof of the coronary sinus that can close defects of such size. Similarly, if a patient has a
that leads to communication between left and right atrium concomitant cardiac lesion that requires surgery, the ASD
through the coronary sinus. Again, ideally this defect is not defect can best be closed at the time of surgery. ASD closure
suited for device closure because of the risk of occluding the is contraindicated in patients with irreversible pulmonary
coronary sinus. hypertension. ASD in such patients acts as a “pop-off”
The subsequent discussion will focus on secundum ASD mechanism, and closure can be detrimental when the right
closure, as these are the only defects (barring PFO) that are heart cannot be decompressed during times of pulmonary
amenable to device closure. hypertensive crisis. We recommend that these patients
undergo cardiac catheterization for calculation of pul-
INDICATIONS FOR ASD CLOSURE monary vascular resistance.
The indications for closure of secundum ASD have been If the pulmonary vascular resistance (PVR) is < 7 Woods
clearly outlined in the 2008 American College of units, then the defect can be closed in the same setting.
Cardiology/American Heart Association guidelines that Pulmonary vascular obstructive disease is rare before 30
were published in the Journal of the American College of years of age and is more common in women. One may con-
Cardiology (Table 1).2 sider using a fenestrated device if there are concerns for ele-
The indications for closure in the pediatric and the adult vated pulmonary artery pressures because the fenestration
population are essentially the same. In pediatric patients, can act as a pop-off when right ventricular pressures are
however, primary attention is directed to symptomatology high.3 There are some data showing that this may be effica-
of recurrent respiratory tract infection and failure to thrive. cious in the short term.4 Some patients may require antipul-
In adults, respiratory symptoms such as shortness of breath monary hypertensive therapy and oxygen at night for a few
tend to occur after the age of 40 years. months after closure. If the PVR is > 7 Woods units, it is best
The indications for ASD closure are based on the type of not to close the ASD. There are data available that suggest
defect and the devices available to treat the defect. At the that closure may be performed in patients with PVR as high
current time, there are two devices that have been as 10 Woods units because symptoms of pulmonary hyper-
approved for device closure by the US Food and Drug tension regress after closure.5
Administration. The Amplatzer septal occluder (St. Jude We believe that ASD closure should be withheld if PVR is
Medical, Inc., St. Paul, MN) can close defects up to 40 mm, > 10 Woods units. We recommend that the patient be
and the Helex septal occluder (Gore & Associates, Flagstaff, started on antipulmonary hypertensive medical therapy,
AZ) can close defects up to 17 mm in diameter. with the help of a pulmonologist, for at least 6 months.
It should be noted that having knowledge of the indica- After this time, the patient should undergo recatheteriza-
tions for device closure is not sufficient to close an ASD. tion to assess PVR and the degree of left-to-right shunt. If
· Right atrial and right ventricular enlargement by echocardiography with or without symptoms. Class I
· ASD minimum diameter should be > 5 mm and < 40 mm on echocardiography.
· Adequate rims of tissue (> 5 mm) from the defect to surrounding structures such as the coronary sinus,
SVC, IVC, and AV valves, as well as the pulmonary veins.
· Presence of an ASD with documented or verified paradoxical embolization and/or documented Class IIa
orthodeoxia-platypnea.
· Net left-to-right shunting, pulmonary artery pressures less than two-thirds systemic levels, pulmonary vas- Class IIb
cular resistance less than two-thirds systemic vascular resistance, when either is responsive to pulmonary
vasodilators, or test occlusion of the defect is successful.
criteria are met, then the defect can be closed in the same EVALUATION FOR ASD CLOSURE
setting. In general, ASD closure is recommended in all symp- The first ASD closure via transcatheter approach was per-
tomatic and asymptomatic patients with PVR < 10 Woods formed in 1976.6 After a hiatus of several years, the closure
units. However, it is absolutely contraindicated in patients process restarted in the late 1980s and has significantly pro-
with PVR of 15 Woods unit or more. Patients with PVR gressed during the last 12 years.
between 10 and 15 should have aggressive antipulmonary A physical examination of a patient with ASD usually
hypertensive treatment and evaluation before exploring reveals subtle findings, and hence the diagnosis may be
ASD closure. missed. Echocardiographic evaluation can confirm the diag-
Patients with evidence of left ventricular dysfunction, nosis. Echocardiography is not only important for the diag-
whether diastolic or systolic, represent a group that is at nosis but is crucial in determining suitability for device clo-
increased risk. These patients with ASD are generally older sure. In addition, it is the primary modality on which the
than 60 years and have a history of congestive cardiac fail- interventionist depends during the closure procedure. The
ure. The left ventricle is less compliant than the right ventri- determination can be made whether a particular ASD is
cle in these patients. The ASD tends to act as a pop-off for suitable for transcatheter closure—not just from a typologi-
the left ventricle (as opposed to the right ventricle in cal perspective but also for size determination and the ade-
patients with pulmonary hypertension), leading to compen- quacy of rims for device placement. For the Amplatzer
satory fluid retention. Closure of the ASD may therefore device, the rims should be 5 mm or larger (excluding the
result in acute left heart failure and pulmonary congestion. aortic rim), as suggested by the manufacturer in the instruc-
During the cardiac catheterization procedure, evaluation of tions-for-use pamphlet. If 5 mm is considered to be an ade-
left atrial pressures or pulmonary capillary wedge pressures quate rim size, then aortic rim deficiency will be common
after temporarily occluding the defect is very helpful. because more than 40% of patients with ASD have an aortic
A significant increase in left atrial pressure and a drop rim that is < 5 mm.7 Therefore, aortic rim deficiency is not a
in cardiac output is a clear indication that the patient will generalized contraindication to device closure. The aortic
require aggressive diuresis and anti-heart failure medica- rim, however, is the most important rim when it comes to
tions. After ASD closure, it is also recommended to leave device-related complications such as erosion.8 Aortic rim
a catheter in the pulmonary artery to measure pul- deficiency in multiple transesophageal echocardiography
monary artery pressures overnight in these patients for (TEE) views should be considered a contraindication to
optimal pressure measurement. Sometimes, it is best to device closure.
optimize these patients with anti-heart failure medica- The Amplatzer septal occluder is a self-centering device,
tions and diuretics before device closure. These patients and its size is determined by its waist. The left disc is 6 mm
have been found to do very well at subsequent device larger than the waist for devices up to 10 mm, 7 mm larger
closure. The Contraindications to ASD Closure sidebar sum- for devices up to 32 mm, and 8 mm larger for devices up to
marizes what we believe to be the major contraindications 40 mm. The right atrial disc is 4 mm larger than the waist for
to device placement in secundum ASD. devices up to 10 mm and 5 mm larger for all other sizes.
Figure 4. Use of TEE for defect evaluation and device closure. ASD in short-axis aortic view (A). ASD in four-chamber view (B).
ASD with color flow in bicaval view (C). Short-axis aortic view after Amplatzer device placement (D). Bicaval view after
Amplatzer device placement (E).
A B C
Figure 5. TEE standard views for evaluation of atrial septum. This patient has a PFO. Four-chamber view (A). Short-axis aortic
view (B). Bicaval view (C). The white arrow points toward the PFO type opening.