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Anesthetic implications of the anomalous origin of coronary artery (AOCA)

Rahul Shabadi

Department of Anesthesia, College of medicine and health sciences, Sultan Qaboos University, Oman

E-mail : drrahoolndrrahool@gmail.com

Nasser Al-Kemyani

Department of Anesthesia, College of medicine and health sciences, Sultan Qaboos University, Oman

Salman Siddiqui

Department of Anesthesia, College of medicine and health sciences, Sultan Qaboos University, Oman

Ramnarayan Rao

Department of Anesthesia, College of medicine and health sciences, Sultan Qaboos University, Oman

Tarek Alameddine

Department of Anesthesia, College of medicine and health sciences, Sultan Qaboos University, Oman

DOI: 10.15761/GAPM.1000153

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Abstract

This Article includes 2 case reports describing Anomalous Origin of the Coronary Artery (AOCA), the potentially fatal condition which warrants modification of anesthesia management. Our aim is to not only to highlight the potentially dangerous coronary anomalous origins, their association with sudden cardiac arrest but also addressing the anesthetic precautions and  management plans for the patients with Abnormal Origin of Coronary Artery (AOCA).

Key words

 Abnormal Origin of Coronary artery (AOCA), sudden cardiac death, Anesthesia management

Case 1

A 62 years female with previous history of bioprosthetic mitral valve replacement done 9 years back, presented with dyspnea on exertion. She had raised JVP and pulsatile hepatomegaly. On transthoracic echocardiography she was found to have severe leaking bioprosthetic valve causing severe mitral regurgitation. It was associated with tricuspid regurgitation and pulmonary hypertension. She had previous few admissions with cardiogenic shock and slow atrial fibrillation for which she was on tablet Warfarin and tablet Digoxin. Coronary angiography showed, Left Main Coronary artery (LMCA) originating aberrantly from the right coronary cusp almost very close to the Right Coronary artery (RCA) origin. LMCA was very long, wide and without any obstructive lesion bifurcating into Left Anterior descending (LAD) and Circumflex (CX). There were no major lesions in the coronaries. The Patient had no other comorbid conditions. The mitral valve replacement and tricuspid annuloplasty was proposed for the patient. The anesthesia Induction was done as per institutional protocol. Intra-operative transesophageal echocardiography revealed bioprosthetic mitral valve with severe mitral regurgitation. The Mean Gradient across Mitral valve was 3.7 mm Hg. The right and left atrium were dilated. Tricuspid valve showed severe regurgitation associated with hepatic venous flow reversal. Tricuspid annulus was 3.87 cms. Pulmonary systolic BP was 43-45 mmHg. Aortic and Pulmonary valves were normal. Rt. Coronary sinus of Valsalva giving rise to RCA and LMCA was seen well (Figure 1). Left ventricular function was 35-40%. Inferior wall hyperkinesia was noted. Right ventricle was Grade II dilated. Mitral valve replacement with bioprosthetic valve size 29 mm was performed through trans-septal approach. Tricuspid valve annuloplasty with Carpenter Edward MC3 ring size 32 mm was done. Separation from CPB was done as per the protocol. Patient needed inotropes, Adrenaline 0.06 mcg/kg/min, Noradrenaline 0.06 mcg/kg/min and Dopamine 5 mcgs/kg/min. Patient was paced venticularlly for slow heart rate. After the completion of Inj. Protamine, the patient developed ventricular fibrillation. It was not responding to defibrillation so it was decided to reinitiate the CPB. Trial of separation from CPB was given after 20-25 min. of the rest. Inj. Amiodarone 300 mg was given on pump before separation. Pt was paced venticularly for slow junctional rhythm. Patient again had recurrent ventricular fibrillation episodes at the chest closure. It responded to the internal defibrillation DC shocks. Pt was again put on CPB due to persistent ventricular arrhythmias. This time supported for 1.5 hr on CPB. Inspite of all this efforts she had malignant arrhythmias after shifting to ICU. She didn’t respond to medical management and patient’s condition deteriorated continuously and on the next day patient expired in the ICU.

Figure 1. TEE image showing Left Main Coronary Artery (LMCA) originating from Right Sinus of Valsalva. (Patient 1)

Case 2

19 years old male 166 cm tall and weighing 125 kg and his BMI was 45, a morbidly obese. He was known case of IDDM, adult Still's disease, Autoimmune hepatitis and hypertensive retinopathy. He had a previous admission for NSTMI. The patient was complaining of exertional chest pain which was persistent since more than 6 month. It was associated with shortness of breath, palpitation and dizziness. These symptoms were present mainly on exertion. His METs were estimated as 4-5. He was not smoker. He had a strong family history of IHD in mother. The Cardiac CT showed the anomalous right coronary artery arising from the left coronary sinus of Valsalva. RCA was dominant and located anterosuperior to the origin of the LMCA. There was narrowing of the proximal segment and narrowing of the ostium and coursing between the root of the aorta and the main pulmonary artery. LM, LAD, LCX and their branches were normal. Myocardial perfusion study was normal. Tran-thoracic echocardiography was normal with ejection fraction of 60%. The induction of anesthesia was done as per institutional protocol. Intraoperative trans-esophageal echocardiography was performed. It revealed left ventricular hypertrophy and good function. Mitral valve showed mild regurgitation. Aortic valve was tri-leaflet. The LMCA origin seen well and Right Coronary Artery origin seen near to LM origin (Figure 2). Right Ventricular function was good and other valves were normal. On Pump De-roofing of right Coronary Ostia was done. Separation from CPB was done without inotropes. Postsurgical repair transesophageal echocardiography showed the flow through right coronary ostium and the nonturbulent flow through the RCA. There was absence of new regional wall motion abnormality of left ventricle. The patient’s recovery was uneventful in ICU and was discharged home on 7th post-operative day.

Figure 2. TEE showing Right Coronary Artery originating from Left Coronary sinus of Valsalva. (Patient 2)

Figure 3. Cardiac CT SCAN image showing Right Coronary Artery originating from Left Coronary sinus of Valsalva. (Patient 2)

Discussion

Congenital anomalies of the coronary arteries officially reported to occur in 0.6% - 1.3% of the general population [1]. Coronary artery anomalies can occur in association with other congenital heart defects or as an isolated abnormality. The clinical presentation and severity of coronary artery anomalies varies considerably. Certain coronary artery anomalies are found incidentally, and are clinically silent. But at the other end of the disease spectrum are anomalies which may present clinically. They present with angina, dyspnea, and syncope as happened with our second case and in severe cases arrhythmias, myocardial infarction, and sudden death [2,3]. After the Hypertrophic cardiomyopathy, the anomalous origin of coronary arteries (AOCA) is the most common causes of sudden cardiac death in young adults in the USA. It is found in 13% of autopsies in post mortem cases [4,5]. Of many subtypes of this anomaly two most important subtypes are those in which the left main coronary artery originates from the right sinus of Valsalva (ALMCA) or the right coronary artery originates from the left sinus of Valsalva (ARCA). In a majority of cases intramural course of the anomalous coronary artery is found, it traverses within the aortic wall, between the aorta and pulmonary artery, then leaves the aortic wall from the correct sinus. Both of the aforementioned defects (ALMCA and ARCA), particularly those have an intramural course, have been associated with sudden cardiac death [4].

Sudden death occurs in these patients because of a reduction in blood flow in the anomalous vessel, resulting in myocardial ischemia or infarction [6]. The pathophysiology is due to reduced coronary blood flow in these patients. Due to acute take off of the anomalous coronary artery often takes, the ostium of the anomalous artery is slit-like, rather than round as in its normal counterpart. During systole this slit-like orifice gets further compressed, which may occlude further blood flow. Also proposed theory is that kinking or torsion of the anomalous artery may occur as it travels between the great vessels. Another hypothesis is the intramural path within the aortic wall, and can be is a potentially lethal condition due to compression of the coronary artery which might occur during times of increased aortic pressure, like during exercise. Most likely multifactorial effect may precipitates myocardial ischemia, infarction, and sudden cardiac death in cases of AOCA. Amongst them the most important being, the increased in aortic wall tension and the sizes of Aortic and Pulmonary roots, leading to compression or kinking of abnormal course of coronary.  The patients diagnosed with ALMCA or ARCA, should be immediately considered for the treatment. Though medical management is an option, surgery remains the most widely used [6-10]. At present the general agreement among most physicians is, if a patient is symptomatic or shows evidence of ischemia in the presence of an ALMCA or ARCA, surgery should be offered, particularly below of 30 years of the age [4,10]. Most worrying surgery in this patient subtype would be aortic valve replacement. These patients especially with intramural course can have worsening of the condition because of the extrinsic compression by prosthetic ring [11]. AOCA has been linked with genetic association. Family history of sudden cardiac death or history suggestive of angina in absence of risk factors of myocardial infarction especially in young patient should raise the suspicion AOCA [12].           

The anesthetic experiences about the AOCA and its management are limited. Most of them are mainly from cardiac surgery and cardiology literatures. An anesthesiologist has to be cautious from preoperative evaluation of the patient till the post- operative period, as these patients are at very high risk of sudden cardiac death during induction of anesthesia [5]. Sudden cardiac death under anesthesia is associated with arrhythmogenic right ventricular cardiomyopathy, myocardial diseases, fibrosis of the Bundle of Hiss, AOCA were the most frequently found diseases. The cases where an anomalous origin or route of the coronary artery was identified, can have circulatory arrest during induction of anesthesia [5]. Preoperative evaluation of heart function with ECG, echocardiography and intraoperative transesophageal echocardiography will play pivotal role in patient management. These patients may present with non ST MIs, as this second case was presented or the patient can still have ongoing ischemia. The factors which will increase rate pressure product and eventually oxygen demand of the heart can lead to untoward event.

The emphasize will be to maintenance of hemodynamic stability (avoiding hypotension, hypertension, and tachycardia) and the optimization of oxygen-carrying capacity (avoiding hypoxia and anemia), to preserve the fine balance between myocardial oxygen supply and demand. So during Induction, the extra caution to be given to maintain the heart rate 60-80 beats/min and blood pressure with 30% of the baseline value. Taking into consideration of the compression effects from aorta and pulmonary trunk, the factors which will cause distension of aorta or pulmonary trunk should be avoided. This includes preoperative strenuous exercise or exertion, rapid transfusion of the fluids, hypoxia, and hypercarbia [12]. Intraoperative 5 lead ECG for monitoring of ST segment, invasive arterial and central venous pressure monitoring will give close idea about the hemodynamics. The fluid overload can be easily avoided by CVP monitoring and transesophageal echocardiography. Intraoperative transesophageal echocardiography helps to find out the course of the coronary artery. It helps us to monitor contractility, new RWMA, left ventricular filling and preload. The Most important is, it is the first tool which will give an idea about surgical repair and its outcome in patients who are undergoing surgical intervention for coronary artery. The nonturbulent flow in the coronaries, absence of new RWMA, presence of good contractility of the heart can give fair idea about the surgical repair. The presence of New RWMA or poor LV function, increasing requirements of the Inotropes, absent laminar flow, presence turbulent flow in the coronary ostia or coronaries should be considered as alarming signs.

Conclusion

The patents diagnosed with Abnormal Origin of Coronary origin should be dealt with extra precautions, as the risk of sudden cardiac arrests are high. The anesthesiologist should explain this risk to the patient and family well. This kind of anomaly warrants modification of anesthesia management plan and more close cardiac monitoring. Transesophageal echocardiography can be very useful tool to monitor these patients, especially who come for surgical intervention for coronary arteries.

References

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Editorial Information

Editor-in-Chief

Article Type

Review Article

Publication history

Received date: June 03, 2016
Accepted date: July 08, 2016
Published date: July 13, 2016

Copyright

©2016 Shabadi R. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Citation

Shabadi R (2016) Anesthetic implications of the anomalous origin of coronary artery (AOCA). Glob Anesth Perioper Med 2: doi: 10.15761/GAPM.1000153

Corresponding author

Rahul Shabadi

Department of Anesthesia, College of medicine and health sciences, Sultan Qaboos University, Oman, Tel: +968-24144778 Extn: 4738

E-mail : drrahoolndrrahool@gmail.com

Figure 1. TEE image showing Left Main Coronary Artery (LMCA) originating from Right Sinus of Valsalva. (Patient 1)

Figure 2. TEE showing Right Coronary Artery originating from Left Coronary sinus of Valsalva. (Patient 2)

Figure 3. Cardiac CT SCAN image showing Right Coronary Artery originating from Left Coronary sinus of Valsalva. (Patient 2)