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Philips SMART Biphasic therapy Application note
Philips SMART Biphasic therapy 
Since Philips introduced the first biphasic waveform for an external defibrillator in 1996, biphasic therapy has gained acceptance and is now recognized as the standard of care. However, the various defibrillator manufacturers recommend a wide range of energy (joules) dosages. This is because defibrillator manufacturers have created distinct biphasic waveform "formulations." So each manufacturer recommends energy doses appropriate for their shock formulation. While energy (joules) remains entrenched in defibrillator vocabulary as a descriptor of shock strength, current (amperes) has been shown to be a better predictor. For meaningful shock strength comparisons of biphasic waveforms, it's necessary to look beyond energy levels and compare the current delivered to the patient.
All presently available Philips HeartStart defibrillators incorporate a proprietary biphasic truncated exponential (BTE) waveform formulation employing high current delivered in a low energy dosage. Further, Philips uses real-time impedance compensation to automatical y adjust the waveform to deliver shock strength personalized to the needs of each patient, starting with the first shock. 
Philips therapy has been rigorously studied and is backed by a substantial body of peer-reviewed, published data demonstrating effectiveness across the full spectrum of patients, including those considered "difficult-to-treat."
While biphasic waveforms effectively terminate arrhythmias, meaningful clinical differences between defibrillators may lie in the amount of energy needed for successful defibrillation and its negative impact on post-resuscitation myocardial function. While high current defibrillates, high energy is associated with negative side effects. So the optimal waveform formulation delivers high current at lower energy doses to help reduce the total energy delivered. Meaningful clinical differences may also lie in how quickly a shock is delivered fol owing the CPR pause, as this may substantial y influence shock success. Only Philips AEDs and the Philips MRx Monitor/Defibrillator in AED mode offer Quick Shock technology, which helps shorten time-to-shock after CPR and increase the chance a shock will successful y return circulation, which may improve survival. 
Philips SMART Biphasic therapy 
Biphasic waveforms use distinct formulations 
Not all biphasic waveforms are the same. Manufacturers 
American Heart Association and European Resuscitation Council 
use distinct shock formulations, making their individual 
positions on current
energy dosages an invalid comparison tool for evaluating their relative shock strength. This can be likened to 
" Because it is accepted that defibril ation is 
accomplished by the passage of sufficient 
Although different drugs within a class may all be 
current through the heart, the concept of 
considered safe and effective, each requires its own 
current-based defibril ation is appealing. 
dosage due to its distinctive molecular structure. For example, statins are proven to lower LDL cholesterol.
Energy is a non-physiologic descriptor of 
Yet, the maximum 80mg dose of Lipitor® (atorvastatin 
defibril ation despite its entrenchment in 
calcium) is not necessarily more therapeutic than 
traditional jargon…Transition to current-
the 40mg maximum dose of Crestor® (rosuvastatin calcium)
based description is timely and should be 
3 simply because it is twice the dose. Because 
each drug in a class has a unique formulation, the 
number of mil igrams of one drug in a class is not 
 – American Heart Association2
necessarily indicative of therapeutic strength relative to another, and does not lend itself to "apples to apples" comparisons.
" Although energy levels are selected for 
defibril ation, it is the transmyocardial current 
Biphasic waveforms as a class have been proven to 
flow that achieves defibril ation. Current 
effectively terminate arrhythmias. They deliver "electric medicine" and, similar to pharmaceutical medications, 
correlates well with successful defibril ation 
use distinctive waveform formulations. For biphasic 
and cardioversion…Future technology may 
waveforms, the formulation is driven by different device 
enable defibril ators to discharge according 
components, waveform shape, and duration, which produce current. According to the American Heart 
to transthoracic current: a strategy that 
Association and European Resuscitation Council, it's 
may lead to greater consistency in shock 
current that defibril ates, not the amount of energy 
success…manufacturers are encouraged to 
(joules).2,3 Due to varying waveform formulations, it is possible for the recommended first shock dosage of 150J 
explore further this move from energy-based 
from one defibril ator manufacturer to deliver higher 
to current-based defibril ation." 
current levels than a 200J first shock from another 
 – European Resuscitation Council3
defibril ator manufacturer, even though the latter delivers a larger energy dosage. 


A 5-second jolt from 
Theoretical y, when 
the typical 1200V 
taser used by law 
enforcement would 
incapacitate a person, 
conductive surface, 
but the person would 
such as a person's 
only absorb a 1/4J 
tongue, the person 
would eventual y absorb 360J.
Current, not energy, determines shock strength
Waveform formulation key terms
If the connectors of a common 9V battery were placed on a person's tongue, the person would eventual y 
Capacitor – A key component of the defibril ator design that stores electrons. 
absorb 360J. Of course, no one would consider using a 
Manufacturers have created distinct waveform formulations that use various 
9V battery to defibril ate a patient as it lacks sufficient 
size capacitors to generate voltage and current for defibril ation. The size 
voltage and current. 
of the capacitor impacts the amount of energy (joules) needed to produce voltage and current. Smal er capacitors typical y use fewer joules to pack the 
On the other hand, a person incapacitated by the typical 
necessary voltage and current punch for effective defibril ation. Whereas, 
1200V taser used by law enforcement for 5 seconds would larger capacitors usual y use more joules to achieve comparable levels.
only absorb a ¼J shock. After one excruciating minute, 
Voltage – The force that pushes the electrons through the patient. The 
just 3J would be absorbed. With sufficient voltage and 
amount of voltage stored on the capacitor drives the amount of current 
current, a ¼J shock can be quite strong indeed.
available for defibril ation. The higher the voltage level, the greater the force and amount of current that can be delivered for defibril ation.
The point of these examples is that while energy (joules) 
Current – The movement of electrons, measured in amperes, which achieves 
remains entrenched in defibril ator vocabulary as a 
defibril ation. For biphasic waveforms, distinctive formulations driven by 
descriptor of shock strength, published studies have 
different device components, waveform shape, and duration produce current.
shown that current (amperes) is a better predictor.4,5 The American Heart Association and the European 
Impedance – The resistance of the body to the flow of current, which is 
Resuscitation Council are both advocating a shift to 
measured in ohms. Human impedance levels typical y range from 25 ohms to 
current-based defibril ation.
180 ohms.
Voltage gradient – Reflects the actual intensity of a defibril ation shock in 
For effective defibril ation, a defibril ator must generate 
terms of the electric field it generates within the myocardium itself. Accurate 
high voltage in order to drive a sufficiently high current 
measurement of intracardiac voltage gradients requires instrumenting the 
over the duration when the heart cel s are physiological y 
heart with electrodes to capture the data.
most receptive to defibril ation (See Table 1 for 
Duration – The period over which the current is delivered to the heart. The 
Waveform formulation key terms). Therefore, for 
goal is to deliver therapy over an optimal time period to increase the chance 
meaningful shock strength comparisons of biphasic 
of defibril ation.
waveforms, it is necessary to look beyond energy and compare the current delivered to the patient.
Philips SMART Biphasic therapy 
The Philips SMART Biphasic waveform formulation to the heart – when comparing each manufacturer's 
When Philips set out to design the first biphasic 
recommended first shock energy setting. The authors 
waveform for an external defibril ator, the engineers concluded that energy descriptors correlate poorly chose a smal er 100 microfarad (μF) capacitor that 
to actual shock intensities and provide an inaccurate 
used fewer joules to pack the necessary voltage and 
measure of relative shock strength among different 
current punch for effective defibril ation. Philips 
external defibril ators. The authors also concluded that 
patented the use of a smal er capacitor for external 
peak current is a better measure of shock strength.
defibril ation, which led other manufacturers to select larger (200 μF) capacitors for their 
The Philips SMART Biphasic waveform formulation 
formulations. Larger capacitors typical y use more 
delivers high voltage to drive high current and generate 
joules to achieve voltage and current, meaning shock high voltage gradients at the heart with fewer joules.
strength, comparable to Philips. Using standard protocols, this means that Philips delivers higher 
Voltage levels by recommended first shock energy setting
shock strength starting with the first shock than other typical biphasic waveforms that escalate their 
energy levels to reach equivalent shock strength. 
Escalating potential y wastes time and shocks during 
Voltage levels by recommended first shock energy setting
Philips (100 µF capacitor)
Another biphasic waveform (200 µF capacitor)
The amount of voltage stored on the defibril ator's 
capacitor determines the amount of current delivered 
to the patient, which is responsible for defibril ating the 
heart and considered a more accurate measure of shock 
Philips (100 µF capacitor)
Another biphasic waveform (200 µF capacitor)
strength. Figure 1 shows that the Philips waveform 
Measurements based on a resistive load of 80 ohms.
(using a 100 μF capacitor) at its recommended first shock energy setting can produce significantly higher voltage than another common biphasic waveform (using 
Delivered current by recommended first shock energy setting
a 200 μF capacitor) at its recommended first shock setting.6 Philips distinct waveform formulation uses 
fewer joules to achieve higher voltage levels. 
Delivered current by recommended first shock energy setting
Higher voltage drives higher current to the patient. 
Applying basic physics, namely Ohm's Law, Figure 2 shows 
Philips (100 µF capacitor)
Another biphasic waveform (200 µF capacitor)
how the Philips formulation is able to generate higher 
current with fewer joules at its recommended first shock 
Assumes an average patient impeda 30
nce of 80 ohms.
energy setting than that of another common biphasic waveform (using a 200 μF capacitor).
Philips (100 µF capacitor)
Another biphasic waveform (200 µF capacitor)
waveform requires more energy to deliver current 
Measures of shock strength:
equivalent to the Philips waveform.
First shock (simulated human impedance at 75 ohms )
A swine study by Niemann, et al.8 * measured whether 
energy or peak current measured at the body surface is a better predictor of the actual shock electric-
field strength to which the heart is exposed. Porcine 
hearts were instrumented with electrodes to measure 
voltage gradients within the heart achieved by various 
defibril ator brands. Figure 3 demonstrates that Philips 
delivers the highest observed peak current and voltage 
Peak voltage gradient (V/cm)
Peak current (Amps)
gradients – meaning more defibrillation therapy right 
Philips SMART Biphasic therapy 
Evidence-based therapy with consistently 
With no head-to-head comparison data available, two 
peer-reviewed, published clinical trials using different 
As the first biphasic waveform in an external 
biphasic waveforms in out-of-hospital, long-downtime VF 
defibril ator, the performance of Philips therapy has 
patients were of similar size, design, and purpose.25,28* 
been rigorously studied and reported in numerous 
The observed response conditions for these studies 
peer-reviewed, published manuscripts. They reflect 
were largely similar in terms of average patient weight, 
waveform performance in both animals9–12 and humans, 
cal -to-shock time, percent of witnessed arrest, and 
including the chal enging long-duration VF relevant to 
percent of bystander CPR. The first study by Schneider, 
hospital code teams and responders in out-of-hospital 
et al. using Philips biphasic therapy (150J fixed-energy 
settings.13–26 These data demonstrate consistently high 
protocol) showed a 96% first shock efficacy. Seventy-
efficacy, regardless of factors such as: patient size, age, 
six (76) percent of patients experienced return of 
impedance, incidence of refibril ation, or underlying 
spontaneous circulation (ROSC). Of surviving patients, 
cause of cardiac arrest, including myocardial infarction. 
94% showed good/moderate neurological function. Survival to discharge was 28%. The second study by van 
Philips therapy was the first biphasic therapy 
Alem et al. using Physio-Control's high-energy biphasic 
with sufficient evidence to receive a Class IIa 
therapy (200-360J escalating energy protocol) also 
recommendation from the American Heart Association: 
reported a high first shock efficacy of 98%. Sixty-one 
"Standard of care", "Intervention of choice".27 
percent of patients experienced ROSC and 14% survived 
In contrast, some biphasic therapies on the market 
to discharge. (Figure 4) 
today have limited or no published out-of-hospital clinical data. With no published, peer-reviewed 
Another study by Stiel , et al.29 * using Physio-Control's 
studies in humans directly comparing the performance 
high-energy biphasic therapy (200-360J escalating 
of various biphasic waveforms in treating VF, the 
energy protocol) reported first shock efficacy of 89%. 
American Heart Association (AHA) advises, "The 
Forty nine (49) percent of patients experienced ROSC 
safety and efficacy data related to specific biphasic 
and 82% of surviving patients showed good/moderate 
waveforms must be evaluated on an individual basis."27 
neurological function. Survival to discharge was 16%. 
Accordingly, clinicians are cautioned about generalizing 
This study also included a low-energy (150J non-
conclusions about one manufacturer's biphasic therapy's 
escalating energy protocol) arm that used a low-current 
performance to other manufacturer's therapy. 
design not comparable to the Philips high-current 150J waveform. Rather, the study compared a manufacturer's standard adult high energy/high current protocol with the same manufacturer's non-standard adult low energy/
Two out-of-hospital defibrillation trials
low current protocol. 
(Physio-Control not 
Philips therapy 150J
Physio-Control therapy 200-360J
Philips SMART Biphasic therapy 
Proven across the full spectrum of patients
Philips therapy has been proven highly effective across the full spectrum of patients, even those considered "difficult-to-treat." 23-26,30,31 
The results of some of these published, peer-reviewed studies are summarized in Table 2.
patient group
Overweight and obese 
White RD, et al. Critical Care Medicine. First shock efficacy and subsequent shock success, resuscitation, 
(BMI > 25) patients
and survival were not related to patient body weight. Philips 150J fixed-energy protocol appears effective and appropriate. 
High/low impedance patients White RD, et al. Resuscitation. 2005.* 24 With the Philips 150J fixed-energy protocol, efficacy was high. 
Impedance had no bearing on defibril ation, ROSC, or survival at discharge.
Refibril ating patients
Hess EP, et al. Resuscitation. 2008.* 26
No significant difference in the frequency of shock success between initial and recurrent episodes of VF using a Philips 150J fixed-energy protocol was observed. VF recurrence is common and does not adversely affect shock success, ROSC or survival.
Myocardial infarction patients Schneider T, et al. 
Over half the patients in this study were diagnosed with acute 
Circulation. 2000.* 25
myocardial infarction, but VF was successful y terminated for all patients using a Philips 150J fixed-energy protocol, with a 96% first shock efficacy. 
Atrial fibril ation patients
Santomauro M, et al. Italian Heart 
Only the Philips biphasic waveform demonstrated 100% 
Journal. 2004.* 30
cardioversion success for AF compared with patients treated with a monophasic or the Zoll Rectilinear Biphasic™ waveform. The Philips biphasic waveform required less total energy (statistical y significant) and fewer shocks per patient (not significant). The Philips waveform appears to achieve a higher success rate at lower energy levels. 
Philips real-time impedance compensation delivers 
optimized therapy 
One major contributor to Philips biphasic therapy's 
effectiveness across the full spectrum of patients 
is real-time impedance-compensation technology, 
which optimizes every shock. Philips defibril ators automatical y measure patient impedance and in real-
time dynamical y vary the waveform. Personalized 
therapy is delivered to each patient, including the difficult-to-treat ones, starting with the first shock for 
the best chance of success. Figure 5 shows how the 
Philips waveform is adjusted to compensate for varying 
impedance levels.32
Philips SMART Biphasic therapy 
Meaningful clinical differences among 
Tang, et al.33 *compared the impact of various 
defibril ation waveforms delivered at different energy 
Dysfunction from high energy
settings on post-resuscitation myocardial function using 
When responding to a sudden cardiac arrest emergency, 
an animal model, which effectively isolated the impact of 
terminating VF quickly is the only priority. However, in 
just the defibril ation shocks. The study showed that for 
the calm of the defibril ator selection process, there is 
swine in long-duration VF, higher current/lower energy 
the opportunity to consider the side effects of waveform 
and a higher current/higher energy waveform were 
design, particularly in resuscitation situations that require 
equal y effective at defibril ating. However, the higher 
multiple shocks. Animal studies suggest that electric shocks energy waveform was associated with significantly higher 
can have a negative inotropic influence on cardiac function levels of harmful cardiac dysfunction.
depending on the clinical circumstances, the energy dosage, 
the number of shocks delivered, and the underlying cardiac Table 3 demonstrates that the high energy waveform 
function.10,32,33 Too many shocks can cause transient 
(200 μF capacitor at 360J) required up to nine times the 
cardiac injury, such as decreased contractility and reduced total energy delivered as the low energy waveform (100 cardiac output during the critical period immediately after μF capacitor at 150J) to achieve equivalent results. severe cardiac compromise.10,33,34 While this type of injury is not permanent, clinical data suggest that during a code 
Table 3 also shows the negative impact of the total 
this stunning may be significant, complicating subsequent 
delivered energy on ejection fraction, considered a 
interventions in the emergency department or intensive 
representative measure of dysfunction. Conversely, 
care unit and potential y impacting patient outcomes.10,33,35
high peak current was the only positive predictor of increased survival, which reinforces the importance of 
Higher-energy defibril ation waveforms, whether 
current in the defibril ation equation. 
monophasic or biphasic, are associated with increased post-shock cardiac dysfunction. Experimental33,34 and clinical35 
Tang, et al.33 concluded that maximizing survival while 
studies suggest that in typical out-of-hospital multi-shock 
minimizing myocardial dysfunction may be achieved 
resuscitations, total energy delivered is a negative predictor with a waveform formulation that delivers higher peak of myocardial function. An animal study noted a correlation current while minimizing total energy delivered. between post-resuscitation myocardial dysfunction and early death after initial successful resuscitation.33
Philips distinct biphasic waveform formulation is able to deliver high peak current at low energy levels. This type of lower energy shock has been shown to have fewer 
negative inotropic consequences than higher energy 
shocks. This clinical difference could be particularly meaningful for the long downtime SCA patients, both 
in and out-of-hospital, who typical y require multiple 
Median peak current
shocks and could help make post-resuscitation interventions in the ED or ICU more successful. 
Survival (to 72 hours)
Median number of shocks to 
Philips biphasic therapy delivers its strongest therapy 
from the first shock to maximize effectiveness, 
Median CPR duration (seconds)
yet minimize total energy delivered. In contrast, 
Median total energy required
defibril ators that employ high energy formulations typical y start with weaker shocks (lower current 
Median ejection fraction at 
delivered at lower energy settings) and escalate 
30 minutes (% of baseline)**
to higher energy settings in the event of failure, 
Table 333
** A representative measure of dysfunction. A lower 
 number compared to baseline means more dysfunction. 
presumably to balance the trade off between shock 
Philips SMART Biphasic therapy 
Time-to-shock after CPR and shock success
Shock success 20%
Pre-shock pause (seconds)
Figure 641
strength and potential post-shock dysfunction. 
Philips HeartStart AEDs and the MRx Monitor/
Assuming the Guidelines 2005-recommended 
Defibril ator in AED mode shock as fast as 8-10 seconds 
protocol2, it could take up to 6 minutes (including 
(typical) after CPR pause using a technology cal ed 
CPR intervals) to reach such an escalating, high-
"Quick Shock." This unique feature shortens time-to-
energy biphasic waveform's maximum shock strength. 
shock after CPR, thereby increasing the chance that a 
Philips does not face this trade off.
shock will successful y return circulation and, in turn, improve survival. 
Time-to-shock fol owing CPR pause impacts shock successAnimal and clinical studies show that in longer downtime situations (>4 minutes), CPR immediately prior to defibril ation can help restore normal heartbeats in more patients.36,37 Yet, the beneficial effects of CPR disappear in seconds, making time-to-shock fol owing CPR critical.38,39 Thus, another key therapy attribute is how quickly the defibril ator delivers a shock fol owing a CPR pause. In fact, a formulation that includes shorter time-to-shock fol owing CPR may substantial y influence shock success.40
A clinical study evaluating the impact of pre-shock 
CPR interruptions on shock effectiveness reported 
that, "…a 5 second decrease in pre-shock pause was 
associated with an 86% increase in the odds of shock 
success (p=0.02)." The study concluded that, "…
consideration should be given to the use of newer-
generation AEDs with shorter (<10 seconds) analysis 
times."41 * (Figure 6) 
Philips SMART Biphasic therapy 
Biphasic waveforms have become the standard of care for external defibril ation. Manufacturers have created distinctive formulations and recommend energy (joule) dosages appropriate for their waveforms. While energy remains entrenched in defibril ator vocabulary as a descriptor of shock strength, current has been shown to be a better predictor. For meaningful shock strength comparisons of biphasic waveforms, it's necessary to look beyond energy levels and compare the current delivered to the patient. 
Philips distinct waveform formulation is able to generate high voltage and deliver high current, which produces high voltage gradients using fewer joules. It's common for other defibril ator manufacturers to use larger capacitors for their formulations and deliver significantly more energy to achieve voltage and current, meaning shock strength, comparable to Philips. 
Philips evidence-based therapy has been rigorously studied and is supported by a substantial body of peer-reviewed, published data. It has been clinical y proven to deliver high first shock efficacy for long-downtime SCA patients and effectively defibrillate across the full spectrum of patients, including those labeled "difficult-to-treat." In contrast, some biphasic therapies on the market today have limited or no published out-of-hospital clinical data. Philips success across such a broad patient population is due in part to its real-time impedance-compensation technology, which automatical y optimizes every shock to deliver personalized therapy to each patient starting with the first shock. 
Key waveform design attributes may result in meaningful clinical dif erences among waveforms. Total delivered energy is a negative predictor of myocardial function and survival. Philips approach reduces the total energy delivered, which minimizes the risk of post-shock myocardial dysfunction. This means Philips can deliver its strongest shock from the outset, without the need to consider tradeof s with dysfunction. In addition, clinical data demonstrate that the sooner a shock is delivered after CPR, the higher the chances of shock success. Only Philips HeartStart AEDs and the MRx Monitor/Defibril ator in AED mode of er Quick Shock technology, which helps shorten time-to-shock after CPR and increase the chance a shock wil successful y return circulation, which may improve survival.
Philips SMART Biphasic therapy 
1 Physicians' Desk Reference. 2008. 62nd Edition.
23 White RD, Blackwel TH, Russel JK, Jorgenson DB. Body weight does 
2 American Heart Association Guidelines 2005 for Cardiopulmonary 
not af ect defibril ation, resuscitation or survival in patients with out-of-
Resuscitation and Emergency Cardiovascular Care. Circulation. 
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2004; 32(9) Supplement: S387-S392. 
3 European Resuscitation Council Guidelines 2005. Resuscitation. 2005; Vol 
24 White RD, Blackwel TH, Russel JK, Snyder DE, Jorgenson DB. 
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Transthoracic impedance does not af ect defibril ation, resuscitation or 
4 Dorian P, Wang MJ. Defibril ation and impedance are determinants of 
survival in patients with out-of-hospital cardiac arrest treated with 
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5 Kerber RE, Martins JB, Kienzle MG, et al. Energy, current, and 
25 Schneider T, Martens PR, Paschen H, et al. Multicenter, randomized, 
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6 Measurements were made by discharging a standard Philips HeartStart 
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depth and pre-shock pauses predict defibril ation failure during cardiac 
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defibril ators. New England Journal of Medicine. 
* Ask your Philips sales rep for a research summary of this article.
21 Gurnett CA, Atkins DL. Successful use of a biphasic waveform automated 
Lipitor® is a registered trademark of Parke-Davis, A Division of 
external defibril ator in a high-risk child. American Journal 
Warner-Lambert Company LLC, A Pfizer Company.
of Cardiology. 2000;86:1051- 1053.
Crestor® is a registered trademark of AstraZeneca Pharmaceuticals LP.
22 Martens PR, Russel JK, Wolcke B, et al. Optimal response to cardiac 
Physio-Control® is a registered trademark of Physio-Control, Inc., 
arrest study: defibril ation waveform effects. 
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ZOLL® is a registered trademark of ZOLL Medical Corporation.
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