Submitted Successfully!
To reward your contribution, here is a gift for you: A free trial for our video production service.
Thank you for your contribution! You can also upload a video entry or images related to this topic.
Version Summary Created by Modification Content Size Created at Operation
1 + 2933 word(s) 2933 2021-06-11 06:21:59 |
2 format change Meta information modification 2933 2021-06-23 02:58:07 | |
3 format change Meta information modification 2933 2021-06-23 03:07:51 |

Video Upload Options

Do you have a full video?


Are you sure to Delete?
If you have any further questions, please contact Encyclopedia Editorial Office.
Rodriguez-Arias, J.J. Alcohol Septal Ablation and HCM. Encyclopedia. Available online: (accessed on 25 June 2024).
Rodriguez-Arias JJ. Alcohol Septal Ablation and HCM. Encyclopedia. Available at: Accessed June 25, 2024.
Rodriguez-Arias, Juan Jose. "Alcohol Septal Ablation and HCM" Encyclopedia, (accessed June 25, 2024).
Rodriguez-Arias, J.J. (2021, June 22). Alcohol Septal Ablation and HCM. In Encyclopedia.
Rodriguez-Arias, Juan Jose. "Alcohol Septal Ablation and HCM." Encyclopedia. Web. 22 June, 2021.
Alcohol Septal Ablation and HCM

Hypertrophic cardiomyopathy (HCM) is defined by an unexplained left ventricular hypertrophy, not solely secondary to abnormal loading conditions.

hypertrophic obstructive cardiomyopathy

1. Introduction

Hypertrophic cardiomyopathy (HCM) is defined by an unexplained left ventricular hypertrophy, not solely secondary to abnormal loading conditions. It is a common disease with a reported prevalence of 1:500 individuals. The etiology is usually genetic, with up to 60% of cases being associated with an autosomal dominant trait caused by mutations in cardiac sarcomere protein genes [1][2].
Among patients with HCM, left ventricle outflow tract obstruction (LVOTO) is present in one third of patients at rest and in another third during exertion, strain due to the Valsalva maneuver or after pharmacological stress, giving rise to the term hypertrophic obstructive cardiomyopathy (HOCM). LVOTO is conventionally defined as an instantaneous LV Doppler peak outflow tract gradient of ≥30 mm Hg, but the threshold for invasive treatment is ≥50 mm Hg. Despite many patients being asymptomatic, a variable proportion of them may develop symptoms related to LVOTO or arrhythmic events [1][2][3].
The obstruction mechanism is usually the combination of basal septal hypertrophy and systolic anterior motion (SAM) of the mitral valve. LVOTO is one of the main factors related to morbidity and mortality [4]. When the patient presents symptoms, such as dyspnea, angina, or syncope, which can be attributed to this anatomical feature, the initial approach is pharmacological treatment.
Medical therapy aims to reduce the obstruction gradient and arrhythmia. Reduction of the LVOTO is mainly achieved by means of cardio-selective beta blockers due to their negative inotropic effect, which, in turn, also have antiarrhythmic properties [5]. Other possibilities are verapamil or disopyramide in combination with beta blockers; however, this combination is usually not tolerated due to the anticholinergic side effects [6]
In patients with HOCM who remain severely symptomatic despite guideline-directed medical treatment, invasive treatment or septal reduction therapy (SRT) must be performed.

2. Septal Reduction Therapy

SRT is mainly indicated by both the American and European guidelines in cases of persistence of symptoms, despite optimized drug therapy (NYHA class III–IV), and a LVOTO gradient ≥ 50 mmHg. There are two main options: surgical and percutaneous treatment [1][2].
Treatment must be individualized, taking into account the anatomic structure, the functional conditions and the patient’s wishes, via a multidisciplinary approach [7]. When making decisions, not only the advantages, but also the disadvantages of each technique must be considered (Figure 1). At present, both invasive options, i.e., septal myectomy (SM) and alcohol septal ablation (ASA), have a recommendation class I in the European and American guidelines [1]. It is worth mentioning that personal preferences currently play a crucial role in the decision-making process. The results of both techniques are largely dependent on the center’s experience. A cardiomyopathy team, comprising a cardiologist expert in HOCM, an interventional cardiologist and a surgeon specialized in ASA and SM respectively, is recommended for evaluations of each patient in the decision-making process [2].
Figure 1. Balance between SM and ASA in the decision-making process.
The best results are achieved in centers with a high volume of procedures, both in SM and ASA. Mortality in SM can be as high as 4–16% compared with that of high volume centers (1%), and in the case of ASA, a lower rate of complications and better survival rates are also observed [8]. American guidelines recommend performing these procedures in reference centers with a very low mortality rate and infrequent major complications [2]. If this is not possible, a reasonable number of at least 10 procedures per year for both SM and ASA is recommended [9].

2.1. Surgical Approach

Even though HCM was initially described in 1958 by D. Teare, the first surgical procedure for its treatment was performed via the aortic root in 1961 [10]. Surgical treatment is based on SM in order to reduce the LVOTO gradient. This procedure is accompanied by surgical treatment of the mitral valve in 10 to 11% of patients, but realignment of papillary muscles and valve plication may also be necessary [11][12].
Morrow’s modified SM is the preferred technique, mostly in young patients or in the presence of other pathologies requiring concomitant treatment, such as mitral valve anomalies or coronary disease.
The worst complication in the surgical treatment of HOCM is ventricular septal defects, and the main risk factors are multiple concurrent surgical treatments (e.g., myectomy and coronary bypass grafting) and septum thickness < 20 mm [13]. In addition, aortic valve regurgitation due to lack of septal support or septal coronary arteries dissection could also occur [14]. New regurgitation jets after surgical treatment should be carefully evaluated to rule-out these complications.
The surgical approach affords great success in restoring quality of life, with reduction of LVOTO in 90% of the cases and low mortality rates [15]. SM mortality rates range from 1 to 2% [16][17][18]. Long-term survival of patients treated surgically is comparable to that of the general population and, in addition, a secondary benefit of reduced risk of sudden cardiac death has been observed [18][19].

2.2. Percutaneous Approach

Furthermore, ASA has the same level of indication of SM according to European and American guidelines. However, the ACC/AHA guidelines establish surgical treatment as the first option, reserving ASA for patients for whom surgery is contraindicated or the risk is considered unacceptable due to severe comorbidities or advanced age. (Table 1) [1][2]
Table 1. Factors in decision-making for the invasive treatment of HOCM.
Favors SM Favors ASA
Clinical factors
Young age +  
Advanced age   +
High surgical risk/severe comorbidity   +
Frailty   +
Cardiac conditions
Previous cardiac surgery   +
Previous pacemaker or defibrillator   +
Right bundle branch block   +
Left bundle branch block +  
Mid-ventricular obstruction +  
Operator related factors
Local operator experience in SM +  
Local operator experience in ASA   +
Patient’s preference ± ±
ASA consists of a selective infusion of high-grade alcohol into a septal branch supplying the basal interventricular septum to create an iatrogenic infarction with the aim of reducing the LVOT gradient. This procedure is less invasive than surgical myectomy, and requires a shorter hospital stay [20]. However, a higher rate of arrhythmic episodes could be related to this technique after the procedure, and in the long term, due to the creation of scar tissue [21]. Also, the results are visible three to six months after the procedure, as this is the time it takes the myocardium to reduce after cell necrosis.
The success of this technique, similar to the surgical approach and other percutaneous procedures, is operator dependent and, in high volume centers, mortality is as low as 1% [22]. There is a steep learning curve for the optimal performance of ASA. Despite there being less difference in the outcome of ASA between low- and high-volume centers, the optimal results of ASA are from highly experienced operators. [23][24]
As main findings, Bytyçi et al. observed a higher rate of pacemaker implantation, higher rates of reintervention and less improvement of clinical symptoms in ASA compared with SM, but in exchange, ASA patients presented lower periprocedural complications [25].

3. ASA Technique and Considerations

3.1. Anatomical Considerations

A careful structural evaluation should be carried out in patients considered candidates for SRT. It is mandatory to perform a systematic assessment of the LVOT, the septum and mitral valve to exclude other LVOT obstruction mechanisms, and mitral valve abnormalities requiring surgical treatment. [1][2] The contraindications for ASA are anatomical or structural conditions that limit the safety and efficacy of the technique, which cannot be resolved appropriately via a percutaneous approach or which make surgical treatment preferable (Table 2).
Table 2. ASA: indications and contraindications.
Indications Contraindications
Severe symptoms (NYHA III-IV, CCS III-IV angina, presyncope, or recurrent syncope) despite GDMT. Presence of a supra or subvalvular aortic membrane
LVOT gradient ≥ 50 mm Hg at rest or with provocation despite maximum-tolerated medical treatment Severe coronary artery disease requiring coronary artery bypass graft surgery
At least one septal artery supplying the target septal area (left ventricular outflow tract obstruction zone) Severe aortic stenosis requiring surgical valve replacement
Life expectancy > 1 year, absence of comorbidities that would compromise clinical improvement (i.e., severe dementia) Severe valvular or mitral valve abnormality requiring surgical treatment
  Septal thickness > 30 mm or ≤16 mm
Septum morphology must be known in order to predict the feasibility of ASA. The technique may be less effective in cases with extensive septal scarring via cardiac magnetic resonance (CMR), and in patients with very severe hypertrophy (≥30 mm), but there is a lack of data confirming this. Whereas, patients with mild hypertrophy (≤16 mm) are at high risk of septal defects with any SRT [1][26].
The coronary anatomy and concomitant atherosclerotic coronary disease should be assessed before the ASA procedure (even without angina or ischemic symptoms) by invasive coronary angiography [27]. However, in some centers, coronary angiography is performed during the same ASA procedure. Identifying the most suitable septal branch for ablation is essential for the viability of the procedure. In most cases, the suitable artery is the first septal, which commonly arises from the left anterior descending (LAD). However, the first septal sometimes arises from the diagonal, ramus intermedius, left main (LM) or even from the right coronary artery (RCA) [28].

3.2. Role of Echocardiography in ASA

One of the most important advances towards a greater safety and efficacy for this technique was the addition of periprocedural echocardiographic monitoring [29]. Transthoracic echocardiography (TTE) during the intervention avoids the use of double arterial access or transseptal route for gradient measurement, and increases the likelihood of success by selecting the septal branch (or branches) most suitable for treatment.
TTE is performed with the use of intra-coronary injection of echocardiographic contrast, helping to visualize the myocardial area perfused from the septal vessel. Different echocardiographic contrasts can be used. Also, Gelafundin®, a volume expander has been shown to be good for generating myocardial enhancement. The echo-bright contrast should enhance the proximal hypertrophied septum at the point of maximal systolic anterior motion of the anterior mitral valve leaflet with associated septal contact. Also, this tool has played an essential role in ASA, minimizing periprocedural complications [1][30]. Due to the anatomical variations of the territory perfused by the first septal, the area supplied by this vessel may include a variable quantity of myocardial tissue, which could involve apart the hypertrophied basal septum, also the right ventricular septum, free wall and even the apex of the LV. Patients with a large area of myocardium at risk, or who have a significant involvement of the right ventricle, have a higher complication rate, including complete AV block [31]. Knowledge regarding the specific myocardial area perfused by the septal allows us to avoid ablation, which can affect unwanted or potentially dangerous territories [32][33]. The use of TTE was improved in recent years via the three-dimensional assessment of the myocardial distribution of the contrast, this technique can be used in some challenging cases to achieve a better visualization of the enhanced septum [34].

3.3. Step-by-Step and Technical Considerations

The technique for performing ASA differs between centers in the minor details, but the main steps have remained similar since the first description of the procedure (Figure 2). The procedure is carried out with conscious sedation to preserve accurate hemodynamics, vital for the correct estimation of the changes in the gradients during ablation [28].
Figure 2. Main steps of the ASA technique performed in a patient at our center. (a) An extra back-up (EBU) catheter was placed on the ostium of the left main (black arrow); a pig-tail catheter was placed in the left ventricle (LV) for gradient monitoring (red arrow); temporary pacemaker (PM) electro-catheter was placed on the right ventricle (RV) (white arrow). (b) Coronary angiogram showing absence of atheroscletic lesions and the origin of the first septal branch (black arrow). LAD: left anterior descending. (c) The first septal branch is wired and an over-the-wire (OTW) balloon is advanced to this artery (black arrow). (d) Transthoracic echocardiography (TTE) showing hypertrophy of the basal septum (white arrow), which makes contact during systole with the anterior leaflet of mitral valve (red arrow). (e) TTE performed after Gelafundin® (B. Braun, Melsungen, Germany) injection in the septal branch; enhancement of the basal septum can be seen (white arrows), this indicates that the first septal is suitable for ablation. (f) Coronary angiogram showing final result with occlusion of the first septal branch after alcohol injection.
The first step is to obtain an arterial access with a 6 or 7 F sheath, radial or femoral. At the beginning, femoral was the most common access, with a change in the approach in recent years. Radial access was proposed to achieve less patient discomfort, early ambulation, and less vascular complications [35]. Depending on the preferences of the center, two accesses could be performed, one for the catheter used for ablation, and the other for an invasive monitoring of the gradient during the procedure.
The common femoral vein (or internal jugular vein) is punctured and a temporary pacemaker (PM) is placed on the right ventricle. This step is important to ensure a fast response in case of complete atrio-ventricular (AV) block [36].
After vascular accesses are obtained, 100 units per 1 kg of weight of unfractionated heparin should be administrated.
LM ostium should be engaged with standard guide catheters 6–7 F (Judkins left, Amplatz left or Extra Back-Up). If invasive monitoring is performed during the procedure, a pigtail catheter is placed into the left ventricle (LV) via a second arterial access.
The gradient present through the LVOT must be measured using TTE and/or the catheters placed in the aorta and LV.
Coronary angiography is performed to identify a suitable septal branch. The trajectory of the septal arteries can be visualized through right anterior oblique or postero-anterior cranial projections, while the left anterior oblique view allows differentiating whether the septal branches run on the right or left side of the septum.
A 0.014-inch coronary guidewire is advanced to the first septal artery and, through this, an over-the-wire (OTW) balloon is placed in this vessel. In some cases, the takeoff of the septal vessel is extremely angulated, making it difficult to advance the balloon; when this situation occurs, an extra support wire can be used. The size of the balloon should generally be short (1.5–2.5 mm in diameter, 6–10 mm in length, and with a balloon-artery ratio of 1.3:1 approximately or usually 0.25 mm greater than the vessel diameter). Short balloons are recommended to avoid hyperselectivity in the presence of a septal branch with early bifurcation [26][37]. After placing the balloon, the guidewire is removed.
The balloon is inflated at low pressure (5 or 10 atm), and then slow injection of 1–2 mL of angiographic contrast should be performed to test the correct occlusion of the septal, absence of contrast reflux into the LAD, and to rule out the presence of collateral flow from the septal branch toward another branch of the left or right coronary system [26][29]. During balloon inflation, continuous monitoring of the gradient could show a significant reduction, indicating a favorable target vessel and generally predicts a good response to ASA [27].
Echocardiographic contrast is injected through the OTW balloon lumen. The possible area affected by the ablation is evaluated. If the contrast medium enhances an inadequate territory for ASA, the balloon must be deflated and repositioned in another branch. In some cases, it is not possible to identify a suitable vessel that perfuses the base of the hypertrophied septum at the point where maximal systolic anterior motion occurs, in which case the procedure should be discontinued [27]. Inability to identify a satisfactory septal branch occurs in approximately 10% of the candidates.
Having selected the septal target vessel via the prior angiographic and echocardiographic assessment, ˃94° ethanol is injected through the OTW balloon lumen into the branch. The amount of ethanol should be of 1 to 3 mL [1]. Some authors describe an efficient and safe way to measure the quantity of ethanol as 0.1 mL per 1 mm of septal thickness. Higher doses were associated with higher rates of complications and postprocedural mortality [38]. Potential explanations could lie in the more extended infarct scar due to the higher alcohol dose. Ethanol must be injected slowly, usually 1 min per ml. A slow injection, rather than a bolus administration was demonstrated to be safer [27][39].
Analgesics (i.e., morphine) can be administrated to avoid the pain caused by the iatrogenic myocardial infarction.
After instillation, balloon occlusion should be maintained for at least 3 to 5 min. The catheter is flushed with saline before the balloon is deflated and removed from the septal branch to prevent spillage of alcohol into the LAD circulation [27].
The balloon is removed, and a coronary angiogram is performed to ensure septal branch no-reflow and to rule out any unexpected complication.
Continual monitoring is used to measure the effects of ASA in gradient values. A gradient reduction ≥ 50% from baseline is considered successful (by echocardiography or invasive hemodynamics). If the ablation fails to achieve this improvement, a second septal or subseptal branch should be explored [28].
Once the objective of gradient reduction has been achieved, or there are no additional septal branches perfusing the area that need ablation, the procedure is terminated. The arterial accesses are removed and subjected to hemostasis, and the temporary PM is secured.

3.4. Postprocedural Care

After the procedure is completed, the patient is transferred to the coronary unit for monitoring. The length of stay in this unit is usually three days, one to two days if the patient already had a permanent PM or defibrillator. Subsequently, the patient must remain admitted to the general cardiology ward for 24 to 48 h [28]. Before, Creatine kinase (CK) was measured during this period as a way to predict the efficacy of the ablation. Although a correlation between the ethanol dose and the myocardial necrosis area measured by cardiac biomarkers is recognized, CK levels have not been proven to predict procedural success or LVOT gradient reduction at follow-up [40].
There is no general agreement as to how long the patient should keep the temporary PM. However, it could be removed before transfer from the coronary unit if there is no high-grade or complete AV block.
In the absence of significant bradyarrhythmia, the preprocedural negative inotropic and chronotropic medications could be restarted at a lower dose, especially beta blockers [28].


  1. Elliott, P.M.; Uk, C.; Anastasakis, A.; Germany, M.A.B.; Germany, M.B.; Cecchi, F.; France, P.C.; Alain, A.; France, H.; Lafont, A.; et al. 2014 ESC guidelines on diagnosis and management of hypertrophic cardiomyopathy the task force for the diagnosis and management of hypertrophic cardiomyopathy of the european society of cardiology (ESC). European 2014, 35, 2733–2779.
  2. Burke, M.A.; Day, S.M.; Deswal, A.; Elliott, P.; Evanovich, L.L.; Hung, J.; Kimmelstiel, C.; Kittleson, M.; Link, M.S.; Maron, M.S.; et al. Circulation AHA/ACC CLINICAL PRACTICE GUIDELINE 2020 AHA/ACC guideline for the diagnosis and treatment of patients with hypertrophic cardiomyopathy association joint committee on clinical practice guidelines. Circulation 2020, 142, 558–631.
  3. Veselka, J.; Faber, L.; Liebregts, M.; Cooper, R.; Januska, J.; Kashtanov, M.; Dabrowski, M.; Hansen, P.R.; Seggewiss, H.; Hansvenclova, E.; et al. Short- And long-term outcomes of alcohol septal ablation for hypertrophic obstructive cardiomyopathy in patients with mild left ventricular hypertrophy: A propensity score matching analysis. Eur. Heart J. 2019, 40, 1681–1687.
  4. Richard, P.; Charron, P.; Carrier, L.; Ledeuil, C.; Cheav, T.; Pichereau, C.; Benaiche, A.; Isnard, R.; Dubourg, O.; Burban, M.; et al. Hypertrophic cardiomyopathy: Distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategy. Circulation 2003, 107, 2227–2232.
  5. Corrado, D.; Basso, C.; Schiavon, M.; Thiene, G. Does sports activity enhance the risk of sudden cardiac death? J. Cardiovasc. Med. 2006, 7, 228–233.
  6. Sherrid, M.V.; Barac, I.; McKenna, W.J.; Elliott, P.M.; Dickie, S.; Chojnowska, L.; Casey, S.; Maron, B.J. Multicenter Study of the Efficacy and Safety of Disopyramide in Obstructive Hypertrophic Cardiomyopathy. J. Am. Coll. Cardiol. 2005, 45, 1251–1258.
  7. Rigopoulos, A.G.; Seggewiss, H. A Decade of percutaneous septal ablation in hypertrophic cardiomyopathy. Circ. J. 2011, 75, 28–37.
  8. Kim, L.K.; Swaminathan, R.V.; Looser, P.; Minutello, R.M.; Wong, S.C.; Bergman, G.; Naidu, S.S.; Gade, C.L.F.; Charitakis, K.; Singh, H.S.; et al. Hospital volume outcomes after septal myectomy and alcohol septal ablation for treatment of obstructive hypertrophic cardiomyopathy: US nationwide inpatient database, 2003–2011. JAMA Cardiol. 2016, 1, 324–332.
  9. Elliott, P.; Andersson, B.; Arbustini, E.; Bilinska, Z.; Cecchi, F.; Charron, P.; Dubourg, O.; Kühl, U.; Maisch, B.; McKenna, W.J.; et al. Classification of the cardiomyopathies: A position statement from the european society of cardiology working group on myocardial and pericardial diseases. Eur. Heart J. 2008, 29, 270–276.
  10. Morrow, A.G.; Brockengbrough, E.C. Surgical treatment of idiopathic hypertrophic subaortic stenosis: Technic and hemodynamic results of subaortic ventriculomyotomy. Ann. Surg. 1961, 154, 181–189.
  11. Kotkar, K.D.; Said, S.M.; Dearani, J.A.; Schaff, H.V. Hypertrophic obstructive cardiomyopathy: The mayo clinic experience. Ann. Cardiothorac. Surg. 2017, 6, 329–336.
  12. Ferrazzi, P.; Spirito, P.; Iacovoni, A.; Calabrese, A.; Migliorati, K.; Simon, C.; Pentiricci, S.; Poggio, D.; Grillo, M.; Amigoni, P.; et al. Transaortic chordal cutting mitral valve repair for obstructive hypertrophic cardiomyopathy with mild septal hypertrophy. J. Am. Coll. Cardiol. 2015, 66, 1687–1696.
  13. Sherrid, M.V.; Chaudhry, F.A.; Swistel, D.G. Obstructive hypertrophic cardiomyopathy: Echocardiography, pathophysiology, and the continuing evolution of surgery for obstruction. Ann. Thorac. Surg. 2003, 75, 1684.
  14. Swaminathan, M.; DeBruijn, N.P.; Glower, D.D.; Mathew, J.P. Unexpected transesophageal echocardiographic finding after septal myectomy. J. Cardiothorac. Vasc. Anesth. 2002, 16, 384–385.
  15. Maron, B.J.; Dearani, J.A.; Ommen, S.R.; Maron, M.S.; Schaff, H.V.; Nishimura, R.A.; Ralph-Edwards, A.; Rakowski, H.; Sherrid, M.V.; Swistel, D.G.; et al. Low operative mortality achieved with surgical septal myectomy role of dedicated hypertrophic cardiomyopathy centers in the management of dynamic subaortic obstruction. J. Am. Coll. Cardiol. 2015, 66, 1307–1308.
  16. Woo, A.; Rakowski, H. Does myectomy convey survival benefit in hypertrophic cardiomyopathy? Heart Fail. Clin. 2007, 3, 275–288.
  17. Panaich, S.S.; Badheka, A.O.; Chothani, A.; Mehta, K.; Patel, N.J.; Deshmukh, A.; Singh, V.; Savani, G.T.; Arora, S.; Patel, N.; et al. Results of ventricular septal myectomy and hypertrophic cardiomyopathy (from nationwide inpatient sample [1998–2010]). Am. J. Cardiol. 2014, 114, 1390–1395.
  18. Ommen, S.R.; Maron, B.J.; Olivotto, I.; Maron, M.S.; Cecchi, F.; Betocchi, S.; Gersh, B.J.; Ackerman, M.J.; McCully, R.B.; Dearani, J.A.; et al. Long-term effects of surgical septal myectomy on survival in patients with obstructive hypertrophic cardiomyopathy. J. Am. Coll. Cardiol. 2005, 46, 470–476.
  19. Maron, B.J.; Rowin, E.J.; Udelson, J.E.; Maron, M.S. Clinical spectrum and management of heart failure in hypertrophic cardiomyopathy. JACC Hear. Fail. 2018, 6, 353–363.
  20. Sorajja, P. Alcohol septal ablation for obstructive hypertrophic cardiomyopathy: A word of balance. J. Am. Coll. Cardiol. 2017, 70, 489–494.
  21. Noseworthy, P.A.; Rosenberg, M.A.; Fifer, M.A.; Palacios, I.F.; Lowry, P.A.; Ruskin, J.N.; Sanborn, D.M.; Picard, M.H.; Vlahakes, G.J.; Mela, T.; et al. Ventricular arrhythmia following alcohol septal ablation for obstructive hypertrophic cardiomyopathy. Am. J. Cardiol. 2009, 104, 128–132.
  22. Veselka, J.; Faber, L.; Liebregts, M.; Cooper, R.; Januska, J.; Krejci, J.; Bartel, T.; Dabrowski, M.; Hansen, P.R.; Almaas, V.M.; et al. Outcome of alcohol septal ablation in mildly symptomatic patients with hypertrophic obstructive cardiomyopathy: A long-term follow-up study based on the euro-alcohol septal ablation registry. J. Am. Heart Assoc. 2017, 6, 1–6.
  23. Sorajja, P.; Valeti, U.; Nishimura, R.A.; Ommen, S.R.; Rihal, C.S.; Gersh, B.J.; Hodge, D.O.; Schaff, H.V.; Holmes, D.R. Outcome of alcohol septal ablation for obstructive. Circulation 2015, 118, 131–139.
  24. Nishimura, R.A.; Seggewiss, H.; Schaff, H.V. Hypertrophic obstructive cardiomyopathy: Surgical myectomy and septal ablation. Circ. Res. 2017, 121, 771–783.
  25. Bytyçi, I.; Nistri, S.; Mörner, S.; Henein, M.Y. Alcohol septal ablation versus septal myectomy treatment of obstructive hypertrophic cardiomyopathy: A systematic review and meta-analysis. J. Clin. Med. 2020, 9, 3062.
  26. Pelliccia, F.; Niccoli, G.; Gragnano, F.; Limongelli, G.; Moscarella, E.; Andò, G.; Esposito, A.; Stabile, E.; Ussia, G.P.; Tarantini, G.; et al. Alcohol septal ablation for hypertrophic obstructive cardiomyopathy: A contemporary reappraisal. EuroIntervention 2019, 15, 411–417.
  27. Holmes, D.R.; Valeti, U.S.; Nishimura, R.A. Featured topics alcohol septal ablation for hypertrophic cardiomyopathy: Indications and technique. Catheter. Cardiovasc. Interv. 2005, 389, 375–389.
  28. Spaziano, M.; Sawaya, F.J.; Lefèvre, T. Alcohol septal ablation for hypertrophic obstructive cardiomyopathy: Indications, technical aspects, and clinical outcomes. J. Invasive Cardiol. 2017, 29, 404–410.
  29. El Masry, H.; Breall, J.A. Alcohol septal ablation for hypertrophic obstructive cardiomyopathy alcohol septal ablation for hypertrophic obstructive cardiomyopathy. Curr. Cardiol. Rev. 2014, 4, 193.
  30. Savarimuthu, S.; Harky, A. Alcohol septal ablation: A useful tool in our arsenal against hypertrophic obstructive cardiomyopathy. J. Cardiac Surg. 2020, 35, 2017–2024.
  31. Monakier, D.; Woo, A.; Puri, T.; Schwartz, L.; Ross, J.; Jamorski, M.; Yang, H.; Liu, Z. Usefulness of myocardial contrast echocardiographic quantification of risk area for predicting postprocedural complications in patients undergoing septal ethanol ablation for obstructive hypertrophic cardiomyopathy. Am. J. Cardiol. 2004, 94, 1515–1522.
  32. Faber, L.; Seggewiss, H.; Ziemssen, P.; Gleichmann, U. Intraprocedural myocardial contrast echocardiography as a routine procedure in percutaneous transluminal septal myocardial ablation: Detection of threatening myocardial necrosis distant from the septal target area. Catheter. Cardiovasc. Interv. 1999, 47, 462–466.
  33. Faber, L.; Seggewiss, H.; Gleichmann, U. Percutaneous transluminal septal myocardial ablation in hypertrophic obstructive cardiomyopathy. results with respect to intraprocedural myocardial. Differences 1998, 98, 2415–2421.
  34. Luis, J.; Mur, M.; Tahoces, L.S.; Luis, J.; Barceló, M.; Muñoz, D.R.; Hernández, R.; Fernández-golfín, C.; Luis, J.; Gómez, Z. Alcohol septal ablation in hypertrophic cardiomyopathy. 3d contrast echocardiography allows localization and quanti fi cation of the extension of intraprocedural vascular recruitment. Int. J. Cardiol. 2014, 174, 761–762.
  35. Sawaya, F.J.; Louvard, Y.; Spaziano, M.; Morice, M.C.; Hage, F.; El-Khoury, C.; Roy, A.; Garot, P.; Hovasse, T.; Benamer, H.; et al. Short and long-term outcomes of alcohol septal ablation with the trans-radial versus the trans-femoral approach a single center-experience. Int. J. Cardiol. 2016, 220, 7–13.
  36. El-Jack, S.S.; Nasif, M.; Blake, J.W.; Dixon, S.R.; Grines, C.L.; O’Neill, W.W. Predictors of complete heart block after alcohol septal ablation for hypertrophic cardiomyopathy and the timing of pacemaker implantation. J. Interv. Cardiol. 2007, 20, 73–76.
  37. Afanasyev, A.V.; Bogachev-prokophiev, A.V.; Kashtanov, M.G.; Astapov, D.A.; Zalesov, A.S.; Budagaev, S.A.; Sharifulin, R.M.; Idov, E.M.; Zheleznev, S.I. Myectomy versus alcohol septal ablation in patients with hypertrophic obstructive cardiomyopathy. Interact. Cardiovasc. Thorac. Surg. 2020, 31, 158–165.
  38. Chang, S.M.; Nagueh, S.F.; Spencer, W.H.; Lakkis, N.M. Complete heart block: Determinants and clinical impact in patients with hypertrophic obstructive cardiomyopathy undergoing nonsurgical septal reduction therapy. J. Am. Coll. Cardiol. 2003, 42, 296–300.
  39. Kuhn, H.; Strunk-mueller, C.; Bartelsmeier, M. Survival after transcoronary ablation of septal hypertrophy in hypertrophic obstructive cardiomyopathy (TASH): A 10 year experience. Clin. Res. Cardiol. 2008, 243, 234–243.
  40. Veselka, J.; Procházková, Š.; Duchoňová, R.; Bolomová-Homolová, I.; Páleníčková, J.; Tesař, D.; Červinka, P.; Honěk, T. Alcohol septal ablation for hypertrophic obstructive cardiomyopathy: Lower alcohol dose reduces size of infarction and has comparable hemodynamic and clinical outcome. Catheter. Cardiovasc. Interv. 2004, 235, 231–235.
Subjects: Others
Contributor MDPI registered users' name will be linked to their SciProfiles pages. To register with us, please refer to :
View Times: 451
Revisions: 3 times (View History)
Update Date: 23 Jun 2021
Video Production Service