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        <title>Congenital Heart Disease and Pediatric Cardiology</title>
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        <description>Clinical Topic Feed: Congenital Heart Disease and Pediatric Cardiology</description>
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                    <title>Clinical Algorithm For the Follow-Up of Aortic Valve Disease</title>
<link>/Latest-in-Cardiology/Articles/2026/10/14/12/36/Clinical-Algorithm-For-the-Follow-Up-of-Aortic-Valve-Disease</link>                    <description>The incidence of valvular aortic stenosis (AS) is estimated to be 0.2-0.4 per 1,000 live births. Bicuspid aortic valve (BAV) is the most common cause of AS and one of the most common types of congenital heart disease, with an incidence estimated by autopsy studies of approximately 1%.</description>
                    <pubdate>1791999900000</pubdate>
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                    <title>Racial and Ethnic Differences Not Associated With Late Presentation, Adverse Outcomes in TCR</title>
<link>/Latest-in-Cardiology/Journal-Scans/2026/10/14/09/58/Racial-and-Ethnic-Differences</link>                    <description>Racial and ethnic differences were not associated with late presentation or adverse outcomes in patients with coarctation of the aorta (CoA) undergoing transcatheter coarctation repair (TCR); however, higher median household income was independently associated with less risk of adverse outcomes, according to a recent study...</description>
                    <pubdate>1791982800000</pubdate>
                    <category>Articles and Stories</category>
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                    <title>SUBLIME: LIRA Method Effective, Safe and Reproducible For TAVR Patients With BAV</title>
<link>/Latest-in-Cardiology/Journal-Scans/2026/10/05/13/56/SUBLIME</link>                    <description>A TAVR sizing method for bicuspid aortic valve (BAV) anatomy using the level of implantation at the raphe (LIRA) approach demonstrated favorable procedural and clinical outcomes and good reproducibility across centers, according to results from the SUBLIME study published Sept. 28 in JACC: Cardiovascular Interventions.</description>
                    <pubdate>1791303120000</pubdate>
                    <category>Articles and Stories</category>
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                    <title>Online Exclusive | Inaugural Fellow Focuses on Rural Gaps in Congenital Heart Care</title>
<link>/Latest-in-Cardiology/Articles/2026/10/01/01/Online-Exclusive-Inaugural-Fellow</link>                    <description>Diagnosing and managing heart disease can be challenging in any setting, but rural communities face distinct barriers, including long travel distances and limited access to specialty care.</description>
                    <pubdate>1790856900000</pubdate>
                    <category>Articles and Stories</category>
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                    <title>The Pulse of ACC | Remembering Robert L. Frye; ACC.27-WCC Registration Countdown, More</title>
<link>/Latest-in-Cardiology/Articles/2026/10/01/01/Pulse-of-ACC</link>                    <description>Quick-read articles of particular interest to ACC members.</description>
                    <pubdate>1790856360000</pubdate>
                    <category>Articles and Stories</category>
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                    <title>ACC Featured Jobs For October 2026</title>
<link>/Latest-in-Cardiology/Articles/2022/01/01/01/01/ACC-Featured-Jobs</link>                    <description>Ready to explore a new professional opportunity? Browse the list below of featured jobs and take the next step in your career!</description>
                    <pubdate>1790848980000</pubdate>
                    <category>Articles and Stories</category>
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                    <title>Right Heart, Wrong Way: A Neonate With Ebstein Anomaly</title>
<link>/Education-and-Meetings/Patient-Case-Quizzes/2026/09/01/17/37/Right-Heart-Wrong-Way</link>                    <description>A full-term male infant develops respiratory distress shortly after birth. An echocardiogram shows Ebstein anomaly with severe tricuspid valve (TV) displacement and severe regurgitation, estimated right ventricular systolic pressure (RVSP) 35 mm Hg above the right atrial (RA) pressure...</description>
                    <pubdate>1788305220000</pubdate>
                    <category>Educational Activities</category>
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                    <title>ESC Releases New Guidelines For Cardiac Rehab, CKD and HF</title>
<link>/Latest-in-Cardiology/Articles/2026/08/29/08/48/mon-guidelines-esc-2026</link>                    <description>The European Society of Cardiology (ESC) released three major guideline updates during ESC Congress 2026 related to cardiac rehabilitation, chronic kidney disease (CKD) and heart failure (HF).</description>
                    <pubdate>1788164580000</pubdate>
                    <category>Articles and Stories</category>
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                    <title>Clinical Practice Algorithm For the Follow-Up of Unrepaired and Repaired Ventricular Septal Defects</title>
<link>/Latest-in-Cardiology/Articles/2023/05/30/10/47/Clinical-Practice-Algorithm-For-the-Follow-Up-of-Unrepaired-and-Repaired-Ventricular-Septal-Defects</link>                    <description>Ventricular septal defects (VSDs) are the most common form of congenital heart disease (CHD) diagnosed in childhood. There is a wide variation in clinical practice for the management of common types of VSDs.</description>
                    <pubdate>1787745480000</pubdate>
                    <category>Articles and Stories</category>
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                    <title>Clinical Practice Algorithm For the Follow-Up of Unrepaired and Repaired Patent Ductus Arteriosus</title>
<link>/Latest-in-Cardiology/Articles/2022/10/31/13/02/Clinical-Practice-Algorithm-For-the-Follow-Up-of-Unrepaired-and-Repaired-PDA</link>                    <description>Isolated patent ductus arteriosus (PDA) is a relatively common defect, accounting for 5-10% of congenital heart defects (excluding premature infants).1 Given the increased use of echocardiography, incidental detection of asymptomatic silent PDAs is on the rise.</description>
                    <pubdate>1787745300000</pubdate>
                    <category>Articles and Stories</category>
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