Eisenmenger’s syndrome overview: Difference between revisions
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{{CMG}} | {{CMG}};'''Associate Editor-In-Chief:''' [[Priyamvada Singh|Priyamavada Singh, MBBS]] [[mailto:psingh13579@gmail.com]] '''''' [[Kristin Feeney|Kristin Feeney, B.S.]] [[mailto:kfeeney@elon.edu]]; {{AIA}} | ||
'''Associate Editor-In-Chief:''' [[Priyamvada Singh|Priyamavada Singh, MBBS]] [[mailto:psingh13579@gmail.com]] ''' | |||
==Overview== | ==Overview== |
Revision as of 13:29, 19 January 2020
Eisenmenger’s syndrome Microchapters |
Diagnosis |
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Eisenmenger’s syndrome ACC/AHA Guidelines for Evaluation of Patients |
Treatment |
Eisenmenger’s syndrome overview On the Web |
American Roentgen Ray Society Images of Eisenmenger’s syndrome overview |
Risk calculators and risk factors for Eisenmenger’s syndrome overview |
'Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1];Associate Editor-In-Chief: Priyamavada Singh, MBBS [[2]] ' Kristin Feeney, B.S. [[3]]; Abdelrahman Ibrahim Abushouk, MD[4]
Overview
Eisenmenger's syndrome or Eisenmenger's reaction is defined as the process in which a left-to-right shunt in the heart causes increased flow through the pulmonary vasculature, which leads to pulmonary hypertension, which finally causes increased pressures in the right side of the heart and reversal of the shunt into a right-to-left shunt. This right to left shunt causes the patient to become cyanotic. Thus, Eisenmenger's syndrome is said to develop when there is a pulmonary artery disease, right-to-left heart shunting and cyanosis