Literature DB >> 18652105

Anesthetic considerations for cesarean section in the parturient with familial cardiomyopathy.

W L Wood1, K M Kuczkowski, B R Beal.   

Abstract

Dilated cardiomyopathy (DCM) is a heart muscle disease characterized by ventricular dilatation and impaired systolic cardiac function. DCM is defined by the presence of: a) fractional myocardial shortening less then 25% (> 2 SD) and/or ejection fraction less than 45% (> 2 SD); and b) left ventricular end diastolic diameter (LVEDD) greater than 117% excluding any known cause of myocardial disease. Familial dilated cardiomyopathy (FDC) accounts for 20-48% of all DCM cases, and is defined by the presence of two or more affected relatives with DCM meeting the above diagnostic criteria or a relative of a DCM patient with unexplained sudden death before the age of 35 years. We herein present the first reported case in the literature of a parturient with FDC undergoing urgent Cesarean section (secondary to worsening cardiac function) and briefly highlight anesthetic considerations for parturients with this heart condition.

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Year:  2008        PMID: 18652105

Source DB:  PubMed          Journal:  Acta Anaesthesiol Belg        ISSN: 0001-5164


  3 in total

1.  Anaesthetic management of a case of dilated cardiomyopathy for emergency appendectomy.

Authors:  Ravi Raj; Mritunjay Kumar; Meenu Batra
Journal:  Anesth Essays Res       Date:  2014 Jan-Apr

2.  Dilated cardiomyopathy in acromegaly: Case report and anesthesia management.

Authors:  Abhijit S Nair; Anand M Nirale; K Sriprakash; T V S Gopal
Journal:  Anesth Essays Res       Date:  2013 Sep-Dec

3.  Anesthetic Management of a Patient with Dilated Cardiomyopathy and End-stage Renal Disease for Emergency Strangulated Hernia Repair Surgery.

Authors:  Gaurav Sindwani; Aditi Suri; Amit Rastogi
Journal:  Anesth Essays Res       Date:  2017 Oct-Dec
  3 in total

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