The implantable cardioverter-defibrillator: From Mirowski to its current use

Sudden cardiac death is the initial presentation for many patients with cardiac disease. Dr Michel Mirowski was a pioneering cardiologist who recognized the public health importance of this fact. In the 1970s his efforts led to the development of the implantable cardioverter-defibrillator that has revolutionized the ability to prevent and treat sudden cardiac arrest. However, in the first decade of the 2000s these devices remain underutilized in British Columbia and Canada. Increased physician awareness is needed regarding which patients are at high risk of sudden cardiac death and would benefit from this potentially lifesaving therapy.


Sudden cardiac death can be prevented in two broad categories of patients—those who have survived a life-threatening ventricular arrhythmia or who have sustained ventricular tachycardia, and those who have not experienced sudden cardiac arrest but are known to be at increased risk.


By the mid-20th century it was well known that ventricular arrhythmias were the mechanism of death in a large proportion of patients with cardiac disease. The 1960s brought with them the advent of electronic monitoring, cardiopulmonary resuscitation, and synchronized cardioversion.[1-3

Once clinicians had tools at their disposal for the treatment of ventricular arrhythmias, it was not surprising to see the first coronary care units opened in 1962.[2]

While considerable attention was being paid to the treatment of arrhythmias among hospitalized patients, little attention was being paid to the major public health problem of sudden cardiac death (SCD) outside the coronary care unit.[4

SCD is the initial presentation of cardiac disease in 15% of patients[5] and more than 50% of all such deaths occur out of hospital.[6

Michel Mirowski was one of the few clinicians in the 1960s to recognize the scope of the problem of SCD. It was his perseverance that ultimately led to the development of the first successful therapy for out-of-hospital cardiac arrest—the implantable cardioverter-defibrillator (ICD).

Michel Mirowski
Mieczyslaw (Michel) Mirowski was born 14 October 1924 in Warsaw, Poland.[4] The story of his early life is nothing short of incredible. He grew up in a middle-class family among the large Jewish population of Warsaw at that time, but his relatively comfortable life changed dramatically with the outbreak of the Second World War.

With the invasion of Poland by the Nazis in 1939, Michel knew he could not stay in Poland, but he was determined to continue his education. Therefore, at the age of 15, he made the decision to leave his family and flee to Russia along with a friend. He would be the only member of his family to survive the Second World War.

Mirowski spent the following 5 years of the war in the Soviet Union, fleeing the advancing Germans. Des­pite long odds, he continually evaded Russian authorities who were intent on sending refugees to labor camps in Siberia. Somehow, he always managed to find enough work to feed himself and to stave off the malnutrition and disease that was rampant in the Soviet Union at that time. 

After the war ended, Mirowski briefly returned to Poland and began medical school in Gdansk before leaving to pursue his medical education in Western Europe. He eventually enter­ed medical school in Lyon, France, in 1947, despite knowing almost no French or English. It was in Lyon where Mirowski was first attracted to cardiology and also where he met and fell in love with his wife, Anna. 

Upon graduation from medical school in 1954, he worked initially in Tel Aviv, Israel, as a registrar and then pursued further training in Mexico City, Baltimore, and Staten Island. He return­ed to Israel in 1963 to set up a private practice in a small community hospital. 

His new boss, Professor Harry Heller, unwittingly became the inspiration for Mirowski’s research. In 1966 Heller began having episodes of ventricular tachycardia and died soon after. It was with Heller’s death that Mirowski first conceived the idea of an implantable defibrillator.

Development of the ICD
In 1968 Mirowski was recruited to the Sinai Hospital in Baltimore, where he became the director of the hospital’s new coronary care unit and was given protected time for research. Fortunately for this research, the hospital had a division of biomedical engineering and an animal laboratory.[7

At the Sinai, Mirowski joined with Morton Mower, a junior cardiologist on staff with extensive animal research experience, to begin work on an ICD in July 1969.[8] Only a month later they successfully tested their first crude prototype, made from a broken external defibrillator paddle, on a dog.[9

The paper describing their work was eventually published after initial rejections,[10] but there remained considerable antagonism in the cardiology community toward the concept of the ICD. The antagonism also meant that they faced significant difficulty in securing funding for their research.

Mirowski and Mower eventually obtained support from a major pacemaker company in 1970 to further develop the ICD, but after 2 years the company decided there was no market for the device. 

In 1972 Mirowski was introduced to Stephen Heilman, a physician and engineer who had formed a small medical equipment company called Medrad. Heilman was excited by the concept of the ICD and immediately put the company’s engineers at Mirowski and Mower’s disposal. 

The partnership was fruitful and resulted in the production of the first ICD prototype small enough to be completely implanted in a dog in 1975. A film of the first successful defibrillation of a dog implanted with the prototype ICD was released and the now-famous footage catapulted the ICD from relative obscurity to the forefront of cardiac research overnight.

Mirowski and the group at Medrad further refined the prototype to make it suitable for human implantation and eventually received approval for such an implant from the FDA. 

After Mirow­ski and Mower enlisted the aid of colleagues at Johns Hopkins Hospital, cardiac surgeon Myron Weisfeldt and electrophysiologist Philip Reed, the first successful human implant of an ICD was performed in February 1980.[11

Though the first ICD model was a success, it weighed 225 g, required a thoracotomy for implantation of the electrode patches, and was only capable of defibrillation. 

In the years that followed, numerous advances in ICD design have been made. Mirowski and Mower were involved in many of the early refinements, including the development of the capacity of synchronized cardioversion for ventricular tachycardia.[9

True to Mirowski’s original vision, a catheter-electrode-based model developed in the late 1980s could be implanted without a thoracotomy, in a similar manner to the standard pacemaker. 

In the late 1980s Mirowski was diagnosed with multiple myeloma and he succumbed to the disease in 1990. While his invention of the ICD was an enormous advance for cardiac medicine, perhaps his greatest legacy was the attention he drew to the problem of SCD as a whole.

ICDs in 2010
Unlike the early prototypes, modern devices are much smaller, with the newest models weighing as little as 90 g and measuring less than a centimetre thick. In addition to having full pacemaker capabilities, all modern ICDs are capable of overdrive pacing (antitachycardia pacing), which can often terminate ventricular tachycardia without resorting to shock therapy. 

ICDs are also available with biventri­cular pacing (cardiac resynchronization therapy) to improve symptoms in selected patients with ad­vanced heart failure. 

The use of ICDs in Canada and around the world has grown considerably since 1980. In 2008, 593 ICDs were implanted in British Columbia and 5811 were implanted across Canada. 

Although these numbers are ex­pected to rise in the years to come, ICDs currently remain underutilized in Canada, even among survivors of cardiac arrest.[12]

Patient selection
Whether to implant an ICD in a particular patient is a complex decision and involves careful discussion among the health care providers and the pa­tient. 

The ultimate decision to implant an ICD rests with the cardiac electrophysiologist, who will be responsible for appropriate programming and long-term follow-up of the device. It is important for the other treating physicians to know which patients should be referred to a cardiologist or electrophysiologist and considered for an ICD. 

There are two broad categories of patients who can benefit from an ICD. First are patients who have survived a life-threatening ventricular arrhythmia or who have sustained ventricular tachycardia (VT). In this instance, the ICD would be implanted for the secondary prevention of sudden cardiac arrest (SCA). 

The definition of “sustained” VT differs greatly in the literature, but is usually defined as VT resulting in hemodynamic symptoms (syncope, pre-syncope, chest pain) or lasting greater than 30 seconds. 

Second are patients who have not yet experienced SCA but are at increased risk. Here an ICD would be implanted for primary prevention of SCA.

ICDs for secondary prevention
Not surprisingly, patients who have survived SCA due to ventricular fibrillation (VF) or hemodynamically unstable VT have the highest rate of recurrence and would therefore stand to benefit most from an ICD. 

Similarly, patients who have sustained VT and are highly symptomatic or have underlying structural heart disease are also at high risk of recurrence. 

It was precisely these groups that were studied in the earliest randomized trials of ICD use.[13-15] The largest of these trials was the AVID trial, where the ICD was compared with amioda­rone or sotalol. There was a significant reduction in mortality over 18 months of follow-up favoring the device (24% vs 16% for ICD vs placebo). 

The number needed to treat to prevent one death over 2 years was 12 patients and the cost per life-year saved by an ICD was estimated at US$66 677 in 2002.[16

Based on these trials, the 2005 Canadian Cardiovascular Society/Canadian Heart Rhythm Society guidelines[17] and the more recent 2008 American College of Cardiology/American Heart Association/Heart Rhythm Society guidelines[18] give their strongest level of support for ICD use in these groups. It is important to note that patients with potentially reversible causes of their VT or VF were excluded from these trials.

A less clear-cut situation arises when a patient who is at high risk for ventricular arrhythmias, usually be­cause of an impaired left ventricular ejection fraction (EF), presents with syncope of unknown cause. Here, an electrophysiology study can be of value in deciding which patients might benefit from an ICD. If sustained VT or VF is induced during the study, implantation of an ICD should be considered.[15

Less commonly, patients present with sustained VT but have no evidence of structural heart disease on evaluation. An ICD should be strongly considered in this population, particularly if the VT is associated with severe symptoms (pre-syncope, angina, or heart failure). 

However, some individuals with better-tolerated VT may be amenable to antiarrhythmic therapy or to ablation without the need for an ICD.[19

The recommendations for ICD use for secondary prevention are presented in Table 1.

ICDs for primary prevention
The issue of which patients should receive an ICD for the primary prevention of SCD is considerably more complex. Implantation is not without risk, including inappropriate shocks, device recall or malfunction, and in­creased hospitalization. 

Devices also remain expensive and require long-term follow-up at specialized centres experienced in their management. Considerable research has therefore centred on attempting to identify patients at highest risk for SCD and cases where the potential benefits of ICD use outweigh the risks and the cost.

The most important risk factor for SCD in the primary prevention population is an impaired left ventricular EF, with the risk of VT and VF increasing markedly as the EF drops below 30% to 35%.[20

The risk of SCD is also dependent on the cause of the reduced ejection fraction. Patients with ische­mic heart disease due to a previous MI or severe coronary artery disease are at greater risk than those with non­ischemic cardiomyopathies.

The major clinical trials of ICDs for primary prevention in patients with ischemic heart disease and low EF were almost uniformly positive, with relative reductions of overall mortality of 30% to 50% at over 2 years of follow-up.[21-23

The majority of benefit was seen in patients with ejection fractions less than 30%. In the SCD-HeFT trial of patients with EF less than 30%, the number needed to treat to save one life over almost 4 years of follow-up was 14 patients,[24] and the cost per quality-adjusted life-year saved by an ICD has ranged between US$34000 and US$70200.[25

Certain patients with ejection fractions between 30% and 35% also appeared to benefit in some trials, but only if they had other high-risk markers of either nonsustained VT on monitoring or inducible VT or VF.[21,23] These findings form the basis of the recommendations for ICD implantation in the ischemic heart disease population.

Importantly, most of these trials enrolled patients at least 1 month after MI in an effort to exclude any patient whose ejection fraction was likely to improve with recovery of stunned myocardium. In fact, implantation of an ICD immediately after MI in those with depressed ejection fractions conferred no benefit in two recent trials.[26,27

Similarly, EF can improve significantly after coronary artery bypass grafting (CABG), thereby reducing the risk of SCD. Routine implantation of ICDs at the time of surgery conferred no benefit to patients with EF less than 35% in the CABG-PATCH trial.[28] Therefore, any consideration for an ICD should be delayed until 1 to 3 months after surgery.

The trials of ICD for primary prevention in patients with nonischemic cardiomyopathies were less conclusive. The two earliest trials showed no benefit with ICD use, but they were small and likely underpowered.[29,30

Two larger subsequent trials showed a reduction in SCD and overall mortality, albeit a smaller reduction than that seen in the ischemic heart disease population.[24,31] Again, those with ejection fractions less than 30% were most likely to benefit. 

Some patients with recently diagnos­ed nonischemic cardiomyopathy will be expected to have significant recovery of their EF with medical therapy. Therefore, it is recommended that these patients be on maximal medical therapy for at least 9 months before assessing their candidacy for an ICD.

There is also a role for ICDs in the primary prevention of SCD in patients who have preserved ejection fractions but conditions that predispose them to ventricular arrhythmias (such as hypertrophic cardiomyopathy, long QT syndrome, arrhythmogenic right ventricular cardiomyopathy, or Brugada syndrome). An evaluation by an electrophysiologist is essential for identifying high-risk patients who would benefit from an ICD.

The recommendations for ICD use for primary prevention of SCD are summarized in Table 2. The Canadian and American guidelines differ somewhat in their recommendations and we have emphasized the Canadian recommendations where conflicts arise.[17,18]

When not to implant
As well as knowing who might benefit from ICD therapy, it is important for treating physicians to know who is not an appropriate candidate (see Table 3). 

Patients with VT or VF due to reversible causes should not receive an ICD. This includes patients with VT or VF within the first 48 hours of an acute MI due to electrolyte abnormalities or due to the effects of drug use or intoxication. 

Patients with incessant VT or VF are also not candidates for an ICD until their arrhythmia is brought under control with antiarrhythmic or ablation therapies. 

Severe psychiatric conditions are also relative contraindications for an ICD, especially if follow-up will be dif­ficult or if ICD discharges would exacerbate the psychiatric condition. 

Patients with severe symptomatic heart failure (NYHA class IV) or with frequent hospitalizations are more likely to die from cardiac pump failure than VT or VF and should not have an ICD implanted unless their clinical status improves.[32

Similarly, patients whose life expectancy is less than 1 year due to cardiac or noncardiac disease are not likely to survive to benefit from an ICD.

Summary
Sudden cardiac death remains an im­portant public health problem today. Thanks to the pioneering work of Michel Mirowski and colleagues, patients at high risk for SCD can be treated effectively with an ICD. 

Increasing physician awareness in British Columbia regarding the ap­propriate indications for device im­plantation will enhance the delivery of this potentially lifesaving therapy to those patients who need it most.

Abbreviations
ARVC: arrhythmogenic right ventricular cardiomyopathy
CABG: coronary artery bypass grafting
CHF: congestive heart failure
EF: ejection fraction
EPS: electrophysiology study
HCM: hypertrophic cardiomyopathy
ICD: implantable cardioverter-defibrillator
MI: myocardial infarction
NYHA: New York Heart Association
PCI: percutaneous coronary intervention
VF: ventricular fibrillation
VT: ventricular tachycardia

Competing interests
Dr Tung has received research funding from Medtronic Canada. He has also received speaking fees from Boston Scientific Canada and St. Jude Medical Canada.


References

1. Kouwenhoven WB, Jude JR, Knickerbocker GG. Closed-chest cardiac massage. JAMA 1960;173:1064-1067. PubMed abstract
2. Lee TH, Goldman L. The coronary care unit turns 25: Historical trends and future directions. Ann Intern Med 1988;108:887-894. PubMed abstract
3. Lown B, Fakhro AM, Hood WB Jr, et al. The coronary care unit. New perspectives and directions. JAMA 1967;199:188-198. PubMed abstract
4. Kastor JA. Michel Mirowski and the automatic implantable defibrillator. Am J Cardiol 1989;63:977-982 contd. PubMed abstract
5. Kannel WB, Doyle JT, McNamara PM, et al. Precursors of sudden coronary death. Factors related to the incidence of sudden death. Circulation 1975;51:606 - 613. PubMed abstract
6. Gillum RF. Sudden coronary death in the United States: 1980–1985. Circulation 1989;79:756-765. PubMed abstract
7. Mendeloff AI. Michel Mirowski and the Department of Medicine at the Sinai Hospital of Baltimore. Pacing Clin Electrophysiol 1991;14(5 Pt 2):873-874. PubMed abstract
8. Mower MM. Building the AICD with Michel Mirowski. Pacing Clin Electrophysiol 1991;14(5 Pt 2):928-934. PubMed abstract
9. Kastor JA. Michel Mirowski and the automatic implantable defibrillator. Am J Cardiol 1989;63:1121-1126. PubMed abstract
10. Mirowski M, Mower MM, Staewen WS, et al. Standby automatic defibrillator. An approach to prevention of sudden coronary death. Arch Intern Med 1970;126:158-161. PubMed abstract
11. Mirowski M, Reid PR, Mower MM, et al. Termination of malignant ventricular arrhythmias with an implanted automatic defibrillator in human beings. N Engl J Med 1980;303:322-324. PubMed abstract
12. Birnie DH, Sambell C, Johansen H, et al. Use of implantable cardioverter defibrillators in Canadian and US survivors of out-of-hospital cardiac arrest. CMAJ 2007;177:41-46. PubMed abstract
13. Kuck KH, Cappato R, Siebels J, et al. Randomized comparison of antiarrhythmic drug therapy with implantable defibrillators in patients resuscitated from cardiac arrest: The Cardiac Arrest Study Hamburg (CASH). Circulation 2000;102:748-754. PubMed abstract
14. The Antiarrhythmics Versus Implantable Defibrillators (AVID) Investigators. A comparison of antiarrhythmic-drug therapy with implantable defibrillators in patients resuscitated from near-fatal ventricular arrhythmias. N Engl J Med 1997;337:1576-1583. PubMed abstract
15. Connolly SJ, Gent M, Roberts RS, et al. Canadian implantable defibrillator study (CIDS): A randomized trial of the implantable cardioverter defibrillator against amiodarone. Circulation 2000;101:1297-1302. PubMed abstract
16. Larsen G, Hallstrom A, McAnulty J, et al. Cost-effectiveness of the implantable cardioverter-defibrillator versus antiarrhythmic drugs in survivors of serious ventricular tachyarrhythmias: Results of the Antiarrhythmics Versus Implantable Defibrillators (AVID) economic analysis substudy. Circulation 2002;105:2049-2057. PubMed abstract
17. Tang AS, Ross H, Simpson CS, et al. Canadian Cardiovascular Society/Canadian Heart Rhythm Society position paper on implantable cardioverter defibrillator use in Canada. Can J Cardiol 2005;21(suppl A):11A-18A. PubMed abstract
18. Epstein AE, DiMarco JP, Ellenbogen KA, et al. ACC/AHA/HRS 2008 Guidelines for Device-Based Therapy of Cardiac Rhythm Abnormalities: A report of the American College of Cardiology/Ameri­can Heart Association Task Force on Practice Guidelines (Writing Committee to Revise the ACC/AHA/NASPE 2002 Guideline Update for Implantation of Cardiac Pacemakers and Antiarrhythmia Devices) developed in collaboration with the American Association for Thoracic Surgery and Society of Thoracic Surgeons. J Am Coll Cardiol 2008;51:e1-62. PubMed abstract
19. Simpson CS, O’Neill BJ, Sholdice MM, et al. Canadian Cardiovascular Society commentary on implantable cardioverter defibrillators in Canada: Waiting times and access to care issues. Can J Cardiol 2005;21(suppl A):19A-24A. PubMed abstract
20. Burns RJ, Gibbons RJ, Yi Q, et al. The relationships of left ventricular ejection fraction, end-systolic volume index and infarct size to six-month mortality after hospital discharge following myocardial infarction treated by thrombolysis. J Am Coll Cardiol 2002;39:30-36. PubMed abstract
21. Buxton AE, Lee KL, Fisher JD, et al. A randomized study of the prevention of sudden death in patients with coronary artery disease. Multicenter Unsustained Tachycardia Trial Investigators. N Engl J Med 1999;341:1882-1890. PubMed abstract
22. Moss AJ, Zareba W, Hall WJ, et al. Prophylactic implantation of a defibrillator in patients with myocardial infarction and reduced ejection fraction. N Engl J Med 2002;346:877-883. PubMed abstract
23. Moss AJ, Hall WJ, Cannom DS, et al. Improved survival with an implanted defibrillator in patients with coronary disease at high risk for ventricular arrhythmia. Multicenter Automatic Defibrillator Implantation Trial Investigators. N Engl J Med 1996;335:1933-1940. PubMed abstract
24. Bardy GH, Lee KL, Mark DB, et al. Amiodarone or an implantable cardioverter-defibrillator for congestive heart failure. N Engl J Med 2005;352:225-237. PubMed abstract
25. Sanders GD, Hlatky MA, Owens DK. Cost-effectiveness of implantable cardioverter-defibrillators. N Engl J Med 2005;353:1471-1480. PubMed abstract
26. Hohnloser SH, Kuck KH, Dorian P, et al. Prophylactic use of an implantable cardioverter-defibrillator after acute myocardial infarction. N Engl J Med 2004;351:2481-2488. PubMed abstract
27. Steinbeck G, Andresen D, Seidl K, et al. Defibrillator implantation early after myo­cardial infarction. N Engl J Med 2009;361:1427-1436. PubMed abstract
28. Bigger JT Jr. Prophylactic use of implanted cardiac defibrillators in patients at high risk for ventricular arrhythmias after coronary-artery bypass graft surgery. Coronary Artery Bypass Graft (CABG) Patch Trial Investigators. N Engl J Med 1997;337:1569-1575. PubMed abstract
29. Strickberger SA, Hummel JD, Bartlett TG, et al. Amiodarone versus implantable cardioverter-defibrillator: Randomized trial in patients with nonischemic dilated cardiomyopathy and asymptomatic nonsustained ventricular tachycardia—AMIOVIRT. J Am Coll Cardiol 2003;41:1707-1712. PubMed abstract
30. Bansch D, Antz M, Boczor S, et al. Primary prevention of sudden cardiac death in idiopathic dilated cardiomyopathy: The Cardiomyopathy Trial (CAT). Circulation 2002;105:1453-1458. PubMed abstract
31. Kadish A, Dyer A, Daubert JP, et al. Prophylactic defibrillator implantation in patients with nonischemic dilated cardiomyopathy. N Engl J Med 2004;350:2151-2158. PubMed abstract
32. Setoguchi S, Nohria A, Rassen JA, et al. Maximum potential benefit of im­plantable defibrillators in preventing sudden death after hospital admission because of heart failure. CMAJ 2009;180:611-616. PubMed abstract


Dr Deyell is an electrophysiology fellow at the University of British Columbia and is based at St. Paul’s Hospital. Dr Tung is an electrophysiologist at St. Paul’s Hospital and a clinical assistant professor at UBC. Dr Ignaszewski is a clinical professor of medicine and head of the UBC Division of Cardiology.

Marc W. Deyell, MD, FRCPC,, Stanley Tung, MD, FRCPC,, Andrew Ignaszewski, MD, FRCPC. The implantable cardioverter-defibrillator: From Mirowski to its current use. BCMJ, Vol. 52, No. 5, June, 2010, Page(s) 248 - Clinical Articles.



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