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Effective Date: 07/01/2007 |
Title: Percutaneous Transluminal Septal Myocardial Ablation (PTSMA)
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Revision Date: 10/01/2015
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Document: BI201:00
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CPT Code(s): C1886
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Public Statement
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Effective Date:
a)
This policy
will apply to all services performed on or after the above revision date which
will become the new effective date.
b)
For all
services referred to in this policy that were performed before the revision
date, contact customer service for the rules that would apply.
1)
For all
services referred to in this policy that were performed before the revision
date, contact customer service for the rules that would apply. Percutaneous
Transluminal Septal Myocardial Ablation (PTSMA) is a minimally invasive
treatment of an unusual form of cardiomyopathy.
2)
PTSMA is done
to improve the heart`s ability to pump blood when the septum has become enlarged
and thickened from Hypertrophic Obstructive Cardiomyopathy (HOCM). The septum is
the heart muscle that separates the right and left ventricles of the heart. The
septal enlargement and thickening blocks the heart from being able to pump blood
out efficiently. HOCM may cause symptoms such as chest pain, shortness of
breath, and dizziness, especially with exertion. HOCM may even cause sudden
death.
3)
PTSMA
requires pre-authorization.
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Medical Statement
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1)
Percutaneous
Transluminal Septal myocardial ablation (PTSMA) by alcohol-induced septal branch
occlusion is considered medically necessary for hypertrophic obstructive
cardiomyopathy (HOCM) (I42.1) in adults when all of the following
criteria are met:
a)
Member has
severe symptoms (e.g., dyspnea (R06.00 – R06.09), angina pectoris
(I20.0 – I20.9), [pre]syncope (R55), palpitations (R00.2) or
heart failure (I50.1 – I50.9)) despite optimal drug therapy (e.g.,
beta-blockers, calcium-antagonists), dual chamber pacing (DDD) therapy and/or
ineffective previous surgical myotomy/myectomy; and
b)
Member is
classified as New York Heart Association class III or IV ; and
c)
Member has a
classical, asymmetric subaortic HOCM identified by echocardiography (ECHO), and
no other forms of cardiomyopathy; and
d)
ECHO shows
left ventricular wall thickness of greater than 13 mm in adults in the absence
of another cause for left ventricular hypertrophy (LVH); and
e)
Member has
systolic anterior motion of the mitral valve on ECHO; and
f)
Member has a
resting left ventricular outflow tract (LVOT) gradient of greater than 30 mm Hg
or a stressed gradient of greater than 60 mm Hg, or member has less severe
symptoms and LVOT of greater than 50 mm Hg at rest or greater than 100 mm Hg
under stress; and
g)
Member does
not have coronary artery disease (CAD) that would preclude performance of the
procedure. HAYES B
The
Stages of Heart Failure – NYHA Classification
In order to determine the best course of therapy, physicians often
assess the stage of heart failure according to the New York Heart Association (NYHA)
functional classification system. This system relates symptoms to everyday
activities and the patient`s quality of life.
Class Patient Symptoms
Class I (Mild) No limitation of physical activity. Ordinary physical activity
does not cause undue fatigue, palpitation, or dyspnea (shortness of breath).
Class II (Mild) Slight limitation of physical activity. Comfortable at rest, but
ordinary physical activity results in fatigue, palpitation, or dyspnea.
Class III (Moderate) Marked limitation of physical activity. Comfortable at
rest, but less than ordinary activity causes fatigue, palpitation, or dyspnea.
Class IV (Severe) Unable to carry out any physical activity without discomfort.
Symptoms of cardiac insufficiency at rest. If any physical activity is
undertaken, discomfort is increased.
Codes Used In This BI:
C1886 Catheter, extravascular tissue ablation, any
modality (insertable)
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Limits
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Percutaneous
transluminal septal myocardial ablation is considered experimental and
investigational for all other indications.
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Background
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1)
Hypertrophic
obstructive cardiomyopathy (HOCM), also known as idiopathic hypertrophic
subaortic stenosis (IHSS), is a primary, sometimes familial and genetically
determined myocardial hypertrophy with an incidence of about 0.2%. About 25% of
the patients have dynamic left ventricular outflow tract (LVOT) obstruction,
which usually develops during puberty and increases in severity until the age of
18 to 20 years. Not infrequently, HOCM is diagnosed for the first time in the
elderly.
2)
This
condition is characterized by a super-normally contracting left ventricle,
asymmetric septal hypertrophy, which affects mainly the interventricular septum,
increased ventricular wall thickness (left ventricular wall thickness of > 13 mm
in adults in the absence of another cause for left ventricular hypertrophy (LVH);
15 mm in an athlete), and systolic anterior motion of the mitral valve.
3)
Asymptomatic
adult patients probably do not require therapy or risk stratification studies,
unless there is a malignant family history of sudden death or occupational need
(airline pilot). Management decisions are dominated by the need to address
sometimes disabling symptoms of dyspnea, angina pectoris, stress-induced
syncope, palpitations or heart failure, and risk of sudden death. Treatment of
symptomatic patients with HOCM aims at reduction of the left ventricular outflow
tract gradient and improvement of diastolic filling either by pharmacological
therapy with negative inotropic drugs (beta-blockers, calcium-antagonists),
permanent DDD pacemaker therapy (i.e., dual chamber, dual pacing, dual sensing),
or surgical myotomy/myectomy.
4)
Left
ventricular myotomy and myectomy (Morrow`s procedure) has been the standard
therapy for patients with severe symptoms (New York Heart Association functional
class III-IV) that persist despite adequate pharmacotherapy and DDD pacing.
5)
In 1994, as
an alternative to surgery, non-surgical Percutaneous Transluminal Septal
Myocardial Ablation (PTSMA) by alcohol-induced septal branch occlusion was
introduced to decrease left ventricular outflow tract (LVOT) gradient and
improve symptoms in patients with HOCM. This method was substantially improved
by the introduction of echocardiographic guidance in 1996.
6)
PTSMA
involves transcatheter selection of one or two small septal branches of the left
anterior descending artery, threading a small, short, low-pressure angioplasty
balloon into position to occlude the artery, and the instillation of absolute
alcohol into the myocardium. The resultant localized myocardial infarction
reduces the amount of septal myocardium, opening up the left ventricular outflow
tract. Compared with surgical myectomy, the literature shows that PTSMA has the
advantage of being minimally invasive, easily repeated, and with relatively low
major morbidity/mortality risk for patients with co-morbid conditions.
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Reference
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Hayes Inc., Medical Technology
Directory; Alcohol ablation for obstructive cardiomyopathy, Jan 2001.
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Spirito P. Alcohol septal
ablation in the management of obstructive hypertrophic cardiomyopathy. Ital
Heart J. 2000; 1(11):721-725.
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Maron BJ. Role of alcohol septal
ablation in treatment of obstructive hypertrophic cardiomyopathy. Lancet.
2000; 355(9202):425-426.
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Seggewiss H. Current status of
alcohol septal ablation for patients with hypertrophic cardiomyopathy. Curr
Cardiol Rep. 2001; 3(2):160-166.
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Kim JJ. Improvement in exercise
capacity and exercise blood pressure response after transcoronary alcohol
ablation therapy of septal hypertrophy in hypertrophic cardiomyopathy. Am J
Cardiol. 1999; 83(8):1220-1223.
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Kuhn H. Transcoronary ablation of
septal hypertrophy (TASH): A new treatment option for hypertrophic
obstructive cardiomyopathy. Z Kardiol. 2000; 89(Suppl 4):IV41-IV54.
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Faber L. Percutaneous
transluminal septal myocardial ablation for hypertrophic obstructive
cardiomyopathy: Long term follow up of the first series of 25 patients.
Heart. 2000; 83(3):326-331.
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Seggewiss H. Current status of
alcohol septal ablation for patients with hypertrophic cardiomyopathy. Curr
Cardiol Rep. 2001; 3(2):160-166.
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Qin JX, Shiota T, Lever HM, et
al. Outcome of patients with hypertrophic obstructive cardiomyopathy after
percutaneous transluminal septal myocardial ablation and septal myectomy
surgery. J Am Coll Cardiol. 2001; 38(7):1994-2000.
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Mutlak D, Gruberg L, Reisner S,
et al. Non-surgical myocardial reduction in hypertrophic obstructive
cardiomyopathy. Isr Med Assoc J. 2002; 4(2):86-90.
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Jiang T, Wu X, Jia C, et al.
Percutaneous transluminal septal myocardial ablation in patients with
hypertrophic obstructive cardiomyopathy. Chin Med J (Engl). 2002;
115(1):26-30.
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Kovacic JC, Muller D.
Hypertrophic cardiomyopathy: State-of-the-art review, with focus on the
management of outflow obstruction. Intern Med J. 2003; 33(11):521-529.
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National Institute for Clinical
Excellence (NICE). Interventional procedure overview of non-surgical
reduction of myocardial septum. London, UK: NICE; November 2003. Available
at:
http://www.nice.org.uk/page.aspx?o=90963
. Accessed September 13, 2005.
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Li ZQ, Cheng TO, Zhang WW, et al.
Percutaneous transluminal septal myocardial ablation for hypertrophic
obstructive cardiomyopathy: The Chinese experience in 119 patients from a
single center. Int J Cardiol. 2004;93(2-3):197-202.
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Veselka J, Prochazkova S,
Duchonova R, et al. 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;63(2):231-235.
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National Institute for Clinical
Excellence (NICE). Non-surgical reduction of myocardial septum.
Interventional Procedure Guidance 40. London, UK: NICE; February 2004.
Available at:
http://www.nice.org.uk/page.aspx?o=104270.
Accessed September 13, 2005.
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van der Lee C, ten Cate FJ,
Geleijnse ML, et al. Percutaneous versus surgical treatment for patients
with hypertrophic obstructive cardiomyopathy and enlarged anterior mitral
valve leaflets. Circulation. 2005;112(4):482-488.
- Alam M,
Dokainish H, Lakkis N. Alcohol septal ablation for hypertrophic obstructive
cardiomyopathy: a systematic review of published studies. J Inter Cardiol.
2006 Aug.; 19(4); 319-327.
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Application to Products
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This policy applies to all health plans administered by QualChoice, both those insured by QualChoice and those that are self-funded by the sponsoring employer, unless there is indication in this policy otherwise or a stated exclusion in your medical plan booklet. Consult the individual plan sponsor Summary Plan Description (SPD) for self-insured plans or the specific Evidence of Coverage (EOC) for those plans insured by QualChoice. In the event of a discrepancy between this policy and a self-insured customer’s SPD or the specific QualChoice EOC, the SPD or EOC, as applicable, will prevail. State and federal mandates will be followed as they apply.
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Changes: QualChoice reserves the right to alter, amend, change or supplement benefit interpretations as needed.
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