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Anaesthetic management of a patient with hypertrophic obstructive cardiomyopathy posted for emergency lower segment caesarean section
Author(s) -
PradnyaM Bhalerao,
PritamB Adsule,
RadhikaM Marathe
Publication year - 2017
Publication title -
journal of obstetric anaesthesia and critical care
Language(s) - English
Resource type - Journals
eISSN - 2249-9539
pISSN - 2249-4472
DOI - 10.4103/joacc.joacc_19_17
Subject(s) - medicine , ventricular outflow tract obstruction , hypertrophic cardiomyopathy , cardiology , interventricular septum , caesarean section , cardiomyopathy , exacerbation , pregnancy , heart failure , ventricle , biology , genetics
Hypertrophic cardiomyopathy is characterised by asymmetric hypertrophy of the interventricular septum causing intermittent obstruction of the left ventricular outflow tract. This disease may present to the anaesthesiologist in an undiagnosed form during routine pre-operative visit. Surgery and anaesthesia often complicate the peri-operative outcome in this group of patients. A 22-year-old patient was brought in for emergency lower segment caesarean section. She was a diagnosed case of hypertrophic obstructive cardiomyopathy (HOCM) with severe left ventricular outflow tract obstruction and moderate subaortic stenosis. Factors such as tachycardia, hypovolemia, vasodilatation, and increased cardiac contractility leads to exacerbation of this obstruction. We managed this case successfully considering the pathological issues caused by the disease and pregnancy

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