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Published on: August 8, 2022
Anaesthesia and perioperative transoesophageal echocardiography in obstructive hypertrophic cardiomyopathy
Don Jose Palamattam1, Nagarjuna Panidapu1, Balaji Srimurugan2
1Department of Cardiac Anaesthesia, Amrita Institute of Medical Sciences, Kochi, Kerala 682041 India.
Insights
Hypertrophic cardiomyopathy (HCM) involves myocardial thickening and remodelling. This review covers anesthetic, intraoperative, and postoperative management for obstructive HCM patients.
Area of Science:
- Cardiology
- Cardiovascular Medicine
Background:
- Hypertrophic cardiomyopathy (HCM) is a myocardial disease characterized by thickening, remodeling, and reduced chamber size.
- Disarrayed myocardial fibers cause asymmetric thickening, with diagnosis often based on left ventricle wall thickness >15 mm and specific septal-to-posterior ratios.
- Common features include left ventricle outflow tract obstruction (LVOTO), systolic anterior motion (SAM) of the mitral valve, and mitral regurgitation (MR).
Purpose of the Study:
- To review anesthetic considerations for patients with obstructive hypertrophic cardiomyopathy.
- To highlight intraoperative transesophageal echocardiography (TEE) applications in managing obstructive HCM.
- To discuss postoperative management strategies for patients with obstructive HCM.
Main Methods:
- This is a review article, synthesizing existing knowledge on anesthetic and perioperative management of obstructive HCM.
- Key diagnostic criteria and common clinical features of HCM are discussed.
- Focus is placed on anesthetic implications, TEE use, and postoperative care.
Main Results:
- Obstructive HCM presents with potential for dynamic LVOTO, SAM, and MR, leading to symptoms like dyspnea, syncope, heart failure, or sudden cardiac death (SCD).
- Anesthetic management requires careful consideration of hemodynamics to avoid exacerbating LVOTO.
- Intraoperative TEE is crucial for assessing cardiac function and guiding management.
Conclusions:
- Effective perioperative management is vital for patients with obstructive HCM to mitigate risks associated with anesthesia and surgery.
- Understanding HCM pathophysiology and potential complications is essential for anesthesiologists and cardiac care teams.
- This review provides a framework for optimizing care in this patient population.
Abstract:
Hypertrophic cardiomyopathy (HCM) is a primary disease of the myocardium, characterised by increased myocardial thickening, myocardial remodelling and reduced chamber size. Disarrayed arrangement of myocardial fibres leads to asymmetric or localised thickening of myocardial segments. When the left ventricle (LV) wall thickness exceeds 15 mm or more, with the septal to posterior wall thickness ratio above 1.3 either by echocardiography or cardiac magnetic resonance imaging (CMRI) without any identifiable causes, it is considered as HCM. Features common to HCM include dynamic left ventricle outflow tract obstruction (LVOTO), systolic anterior motion (SAM) of anterior mitral leaflet (AML) and mitral regurgitation (MR) with a posteriorly directed jet. Patients may be asymptomatic or present with dyspnoea, syncope, heart failure or sudden cardiac death (SCD) due to sustained ventricular tachycardia (VT). This review article highlights upon the anaesthetic considerations, intraoperative transoesophageal echocardiography (TEE) and postoperative management of obstructive HCM patient.
Supplementary Information:
The online version contains supplementary material available at 10.1007/s12055-025-02083-7.
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