Ebstein's anomaly

The annulus of the valve is still in the normal position. The valve leaflets, however, are to a varying degree, attached to the walls and septum of the right ventricle. A subsequent "atrialization" of a portion of the morphologic right ventricle (which is then contiguous with the right atrium) is seen. This causes the right atrium to be large and the anatomic right ventricle to be small in size.{{cn|date=February 2021}}

• S3 heart sound
• S4 heart sound
• Triple or quadruple gallop due to widely split S1 and S2 sounds plus a loud S3 and/or S4
• Systolic murmur of tricuspid regurgitation = Holosystolic or early systolic murmur along the lower left sternal border depending on the severity of the regurgitation
• Right atrial hypertrophy
• Right ventricular conduction defects
• Wolff-Parkinson-White syndrome often accompanies

Image:EbsteinAnomaly.svg down into the right ventricle.]]

While Ebstein's anomaly is defined as the congenital displacement of the tricuspid valve towards the apex of the right ventricle, it is often associated with other abnormalities.{{cn|date=February 2021}}

Typically, anatomic abnormalities of the tricuspid valve exist, with enlargement of the anterior leaflet of the valve. The other leaflets are described as being plastered to the endocardium.{{cn|date=February 2021}}

Tethering the underlying ventricular wall is the most common for the posterior and septal leaflets, and sail-like anterior leaflets may be tethered to the RV free wall also.{{cn|date=October 2021}}

File:ECGs in Ebstein's anomoly with Mahaim accessory pathway.png

About 50% of individuals with Ebstein's anomaly have an associated shunt between the right and left atria, either an atrial septal defect or a patent foramen ovale.{{cite book|last1=Mohan|first1=Jagdish C.|title=A Practical Approach to Clinical Echocardiography.|date=2014|publisher=Jaypee Brothers Medical Pub|isbn=978-93-5152-140-2|page=119}}

About 50% of individuals with Ebstein's anomaly have an accessory pathway with evidence of Wolff-Parkinson-White syndrome, secondary to the atrialized right ventricular tissue. This can lead to abnormal heart rhythms including atrioventricular re-entrant tachycardia.{{cn|date=February 2021}}

Image:Ebstein's anomaly ECG.png

Other abnormalities that can be seen on the ECG include:

1. signs of right atrial enlargement or tall and broad 'Himalayan' P waves
2. first degree atrioventricular block manifesting as a prolonged PR-interval{{cite web |url= https://www.lecturio.com/concepts/atrioventricular-block | title=Atrioventricular Block | website= The Lecturio Medical Concept Library |access-date= 3 July 2021}}
3. low amplitude QRS complexes in the right precordial leads
4. atypical right bundle branch block
5. T wave inversion in V1-V4 and Q waves in V1-V4 and II, III and aVF.{{cite journal |vauthors=Khairy P, Marelli AJ |title=Clinical use of electrocardiography in adults with congenital heart disease |journal=Circulation |volume=116 |issue=23 |pages=2734–46 |date=December 2007 |pmid=18056539 |doi=10.1161/CIRCULATIONAHA.107.691568 |doi-access=free }}

An enlargement of the aorta may occur; an increased risk of abnormality is seen in babies of women taking lithium during the first trimester of pregnancy{{cite journal |vauthors=Attenhofer Jost CH, Connolly HM, Dearani JA, Edwards WD, Danielson GK |title=Ebstein's anomaly |journal=Circulation |volume=115 |issue=2 |pages=277–85 |year=2007 |pmid=17228014 |doi=10.1161/CIRCULATIONAHA.106.619338 |doi-access=free }} (though some have questioned this){{cite journal |vauthors=Yacobi S, Ornoy A |title=Is lithium a real teratogen? What can we conclude from the prospective versus retrospective studies? A review |journal=Isr J Psychiatry Relat Sci |volume=45 |issue=2 |pages=95–106 |year=2008 |pmid=18982835 |url=http://www.psychiatry.org.il/presentation_sender.asp?info_id=53760 |archive-url=https://web.archive.org/web/20200930214149/http://www.psychiatry.org.il/presentation_sender.asp?info_id=53760 |url-status=dead |archive-date=September 30, 2020 }} and in those with Wolff-Parkinson-White syndrome.

An echocardiogram is the most common and specific way to diagnose Ebstein’s anomaly because it effectively shows all 4 chambers of the heart, which displays the distance between the hinge point of the septal leaflet of the tricuspid valve and the anterior leaflet of the mitral valved (displacement index) to determine if the value is greater than 8mm/m².{{cite journal |last1=Alsaied |first1=Tarek |last2=Christopher |first2=Adam B. |last3=Da Silva |first3=Jose |last4=Gupta |first4=Aditi |last5=Morell |first5=Victor O. |last6=Lanford |first6=Lizabeth |last7=Weinberg |first7=Jacqueline G. |last8=Feingold |first8=Brian |last9=Seery |first9=Thomas |last10=Hoskoppal |first10=Arvind |last11=Goldstein |first11=Bryan H. |last12=Johnson |first12=Jennifer A. |last13=Olivieri |first13=Laura J. |last14=De Fonseca Da Silva |first14=Luciana |title=Multimodality Imaging in Ebstein Anomaly |journal=Pediatric Cardiology |date=23 September 2022 |volume=44 |issue=1 |pages=15–23 |doi=10.1007/s00246-022-03011-x|pmid=36151322 |s2cid=252496690 }}

Ebstein's cardio physiology typically presents as an (antidromic) AV reentrant tachycardia with associated pre-excitation. In this setting, the preferred medication treatment agent is procainamide. Since AV-blockade may promote conduction over the accessory pathway, drugs such as beta blockers, calcium channel blockers, and digoxin are contraindicated{{cn|date=February 2021}}.

If atrial fibrillation with pre-excitation occurs, treatment options include procainamide, flecainide, propafenone, dofetilide, and ibutilide, since these medications slow conduction in the accessory pathway causing the tachycardia and should be administered before considering electrical cardioversion. Intravenous amiodarone may also convert atrial fibrillation and/or slow the ventricular response.{{cn|date=February 2021}}

The Canadian Cardiovascular Society (CCS) recommends surgical intervention for these indications:{{Cite journal | doi = 10.1016/S0828-282X(10)70356-1 | last1 = Silversides | first1 = C. K. | last2 = Salehian | first2 = O. | last3 = Oechslin | first3 = E. | last4 = Schwerzmann | first4 = M. | last5 = Vonder Muhll | first5 = I. | last6 = Khairy | first6 = P. | last7 = Horlick | first7 = E. | last8 = Landzberg | first8 = M. | last9 = Meijboom | first9 = F. | last10 = Warnes | first10 = C. | last11 = Therrien | first11 = J. | title = Canadian Cardiovascular Society 2009 Consensus Conference on the management of adults with congenital heart disease: Complex congenital cardiac lesions | journal = The Canadian Journal of Cardiology | volume = 26 | issue = 3 | pages = e98–117 | year = 2010 | pmid = 20352139 | pmc = 2851473}}

• Limited exercise capacity (NYHA III-IV)
• Increasing heart size (cardiothoracic ratio greater than 65%)
• Important cyanosis (resting oxygen saturation less than 90% - level B)
• Severe tricuspid regurgitation with symptoms
• Transient ischemic attack or stroke

The CCS further recommends patients who require operation for Ebstein's anomaly should be operated on by congenital heart surgeons who have substantial specific experience and success with this operation. Every effort should be made to preserve the native tricuspid valve.

Ebstein's anomaly was named after Wilhelm Ebstein,{{WhoNamedIt|synd|435}}W. Ebstein. Über einen sehr seltenen Fall von Insufficienz der Valvula tricuspidalis, bedingt durch eine angeborene hochgradige Missbildung derselben. Archiv für Anatomie, Physiologie und wissenschaftliche Medicin, Leipzig, 1866, 238-254. who in 1866 described the heart of the 19-year-old patient Joseph Prescher. Joseph Prescher was cyanotic with dyspnea, palpitations, jugular venous distension, and cardiomegaly. At autopsy, “Ebstein described an enlarged and fenestrated anterior leaflet of the tricuspid valve.” In addition, “the posterior and septal leaflets were hypoplastic, thickened, and adherent to the right ventricle. There was also a thinned and dilated atrialized portion of the right ventricle, an enlarged right atrium, and a patent foramen ovale.”{{cite journal |last1=Attenhofer Jost |first1=Christine H. |last2=Connolly |first2=Heidi M. |last3=Dearani |first3=Joseph A. |last4=Edwards |first4=William D. |last5=Danielson |first5=Gordon K. |title=Ebstein's Anomaly |journal=Circulation |date=16 January 2007 |volume=115 |issue=2 |pages=277–285 |doi=10.1161/circulationaha.106.619338 |pmid=17228014 }}

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{{Medical resources

| DiseasesDB = 4039

| ICD10 = {{ICD10|Q|22|5|q|20}}

| ICD9 = {{ICD9|746.2}}

| ICDO =

| OMIM = 224700

| MedlinePlus = 007321

| eMedicineSubj = article

| eMedicineTopic = 154447

| MeshID = D004437

}}

{{Commons category|Ebstein's anomaly}}

{{Congenital malformations and deformations of circulatory system}}

Category:Congenital heart defects