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| __NOTOC__
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| {{Thoracic aortic aneurysm}}
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| {{CMG}}
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| ==2010 ACC/ AHA Guidelines - Recommendations for counseling and management of Chronic aortic disease in pregnancy <ref name="pmid20233780">{{cite journal |author=Hiratzka LF, Bakris GL, Beckman JA, ''et al.'' |title=2010 ACCF/AHA/AATS/ACR/ASA/SCA/SCAI/SIR/STS/SVM guidelines for the diagnosis and management of patients with Thoracic Aortic Disease: a report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines, American Association for Thoracic Surgery, American College of Radiology, American Stroke Association, Society of Cardiovascular Anesthesiologists, Society for Cardiovascular Angiography and Interventions, Society of Interventional Radiology, Society of Thoracic Surgeons, and Society for Vascular Medicine |journal=[[Circulation]] |volume=121 |issue=13 |pages=e266–369 |year=2010 |month=April |pmid=20233780 |doi=10.1161/CIR.0b013e3181d4739e |url=}}</ref>(DO NOT EDIT)==
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| {|class="wikitable"
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| | colspan="1" style="text-align:center; background:LightGreen"|[[ACC AHA guidelines classification scheme#Classification of Recommendations|Class I]]
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| |bgcolor="LightGreen" | '''1.''' Women with Marfan syndrome and aortic dilatation, as well as patients without Marfan syndrome who have known aortic disease, should be counseled about the risk of aortic dissection as well as the heritable nature of the disease prior to pregnancy''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: C]])''
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| |bgcolor="LightGreen" |'''2.'''For pregnant women with known thoracic aortic dilatation or a familial or genetic predisposition for aortic dissection, strict blood pressure control, specifically to prevent Stage II hypertension, is recommended. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: C]])''
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| |bgcolor="LightGreen" |'''3.''' For all pregnant women with known aortic root or ascending aortic dilatation, monthly or bimonthly echocardiographic measurements of the ascending aortic dimensions are recommended to detect aortic expansion until birth. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: C]])''
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| |bgcolor="LightGreen" |'''4.'''For imaging of pregnant women with aortic arch, descending, or abdominal aortic dilatation, magnetic resonance imaging (without gadolinium) is recommended over computed tomographic imaging to avoid exposing both the mother and fetus to ionizing radiation. Transesophageal echocardiogram is an option for imaging of the thoracic aorta. '' ([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence:C]])''
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| |bgcolor="LightGreen" |'''5.'''Pregnant women with aortic aneurysms should be delivered where cardiothoracic surgery is available. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence:C]])''
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| {|class="wikitable"
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| | colspan="1" style="text-align:center; background:LemonChiffon"|[[ACC AHA guidelines classification scheme#Classification of Recommendations|Class IIa]]
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| |bgcolor="LemonChiffon"|'''1.''' Fetal delivery via cesarean section is reasonable for patients with significant aortic enlargement, dissection, or severe aortic valve regurgitation ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence:C]])''
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| {|class="wikitable"
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| | colspan="1" style="text-align:center; background:LemonChiffon"|[[ACC AHA guidelines classification scheme#Classification of Recommendations|Class IIb]]
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| |bgcolor="LemonChiffon"|'''1.''' If progressive aortic dilatation and/or advancing aortic valve regurgitation are documented, prophylactic surgery may be considered ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence:A]])''
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| ==References==
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| {{Reflist|2}}
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| [[Category:Cardiology]]
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| [[Category:Obstetrics]]
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