AED Medical OverSight; AED Program, Medical Authorization for AED, Automated External Defibrillator; Medical Prescription, Medical Oversight

Implementing an Automated External Defibrillator (AED) Program may seem like a challenging task, but it definitely doesn't have to be. With our 7 step guide to implementing an AED Program, any organization can successfully complete this task. Today, we will take a look at the fourth step in this process, “Obtain Medical Oversight”.

In today’s technologically advanced world, there are numerous items which we purchase with little or no knowledge of how to operate. So, in order to effectively utilize and/or navigate our new gadget, we must invest in a technical support plan.

Therefore, since most AED Program Coordinators do not have an extensive knowledge of automated external defibrillators (AEDs) or deploying an AED Program, having a technical support plan is a necessity. In our Industry, this technical support plan is referred to as “Medical Oversight”. Medical Oversight can either be obtained through a local Physician or a National Company who specializes in providing Medical Direction. In either case, your chosen Medical Director should provide the following:

• Signed Medical Prescription (FDA Requirement to purchase an AED)
• Site Analysis and AED Placement Recommendation
• Assistance with EMS Registration
• Review of Policy & Procedure Manual
• Review of Training Program
• Post Event Review & Feedback

Furthermore, your Medical Director should also be a sounding board and a mentor to the Program Coordinator.

HOW SHOULD YOU OBTAIN MEDICAL OVERSIGHT?

First and foremost, if you can find a local physician who has AED Program knowledge, this is your best option as you will have the ability to interface with him/her in person. Furthermore, a local Physician will have a tie to the community and a vested interest in the success of the program.

If you are unable to find a local Physician, contracting with a National Medical Oversight Company is the next best thing. Since their primary business is providing Medical Oversight, their physicians and support staff will have the latest information on laws, regulations and trends in the AED industry.

DO LAWS REQUIRE MEDICAL OVERSIGHT?

At the Federal Level, currently, there are no laws requiring Medical Oversight. However, there are certain states that do require it. To find out more about your state’s requirement, contact your local state legislature to obtain details about the requirements in regards to medical oversight.

WHAT IF I OPT NOT TO OBTAIN MEDICAL OVERSIGHT?

If your State does not require Medical Oversight, you are still obligated by the Food & Drug Administration’s Code of Federal Regulations Title 21 Section 801.109 to provide a signed medical authorization. A medical authorization is a physician prescription authorizing you to purchase an AED. If you do not have a physician to provide this form, there are numerous National Medical Direction Companies who can produce on your behalf. As you know, there is always an exception to every rule. In 2005, Philips Medical received clearance from the FDA to sell the Philips Onsite over the counter without a medical authorization. Currently, this is the AED on the market which can be obtained without a medical authorization.

ARE THERE LIABILITY ISSUES ASSOCIATED WITH NOT HAVING MEDICAL OVERSIGHT?

Federal & State Good Samaritan Laws protect individuals and organizations from liability if they do the following:

1. Notify local emergency response personnel or other appropriate entities of the most recent placement of the device within a reasonable period of time after the device was placed.
2. Properly maintain & test the device according to manufacturer’s recommendations.
3. Provide appropriate training to any employee who may be reasonably expected to use device.

As you can see, Good Samaritan Laws do not mention Medical Oversight as a requirement. However, having Medical Oversight will help to insure that the Good Samaritan Laws are accomplished!

Having deployed over 2000 AED Programs across the US, we have found that our most success programs have Medical Oversight. Why have they been more successful than those who have not? The answer is simple…knowledge is power and those who have employed Medical Directors have empowered themselves with the technical knowledge to be successful.

Contact HeartSafe America today to find out more about medical oversite and how to implement an AED Program for your organization. Heart Safe America’s goal is to educate the public about Sudden Cardiac Arrest (SCA) and how AEDs can increase the survival rate.

AED State Laws & Regulations; Automated External Defbrillator, CASA Act, AED Laws, AED Program

Implementing an Automated External Defibrillator (AED) Program may seem like a challenging task, but it definitely doesn't have to be. With our 7 step guide to implementing an AED Program, any organization can successfully complete this task. Today, we will take a look at the third step in this process, “Review State & Federal Laws”.

To have a successful AED Program, it is important for your organization, as well as your AED Program Coordinator, to understand the federal and state laws associated with owning an Automated External Defibrillator (AED).

In 2000, the Federal Government passed the Cardiac Arrest Survival Act (CASA) in an effort to bring awareness to Sudden Cardiac Arrest (SCA) and improve the SCA survival rate of 5%. This Act required all federal buildings to install AEDs and extended Good Samaritan protection to anyone who renders aid (in good faith) to a victim during an emergency.

Click here to view more about the Cardiac Arrest Survival Act (CASA) of 2000.

Each state has its own law(s) that protect organizations who own AEDs. These laws typically mirror the Cardiac Arrest Survival Act of 2000 by extending liability protection to Good Samaritans.

Click here to view the AED laws for each state.
Click here to view the Good Samaritan laws for each state.

Furthermore, with an increase in SCA awareness and numerous studies validating public access defibrillation, many states have instituted laws requiring certain organizations/facilities to place AEDs on site. Lawmakers believe that Fitness Clubs, Athletic Complexes, Schools and Dental Offices are the most likely places for SCA to occur. Therefore, equipping these facilities has been made a top priority.

Click here to view AED requirements for your state.

Contact HeartSafe America today to find out more about the AED laws and how it can affect your organization. Heart Safe America’s goal is to educate the public about Sudden Cardiac Arrest (SCA) and how AEDs can increase the survival rate.

AED Program Decision Makers; Purchasing AED, Automated External Defibrillator, AED Program

Implementing an AED Program may seem like a challenging task, but it definitely doesn't have to be. With the 7 step guide process of implementing an AED Program, any organization can successfully complete this task. The second step in this process is to gain decision maker's support.

When implementing an AED Program, gaining decision maker support is essential because without it, your program will go nowhere!

Therefore, before attempting to get Senior Management’s buy-in, you must do your homework and answer the questions that they will inevitably ask:

• What are the liability implications with an AED program?
• What is the upfront cost and long term cost of ownership of this program?
• What kind of ongoing training, maintenance and man power is involved with this type of program?

If you are able to provide clear answers supported by facts, gaining support for your AED Program will be easy. In an attempt to help you prepare, we have offered some resources below:

First, to address the liability concern for management you will need to educate them on the facts. This can be accomplished by researching OSHA (Occupational Safety and Health Association) and their recommendations on their website. The OSHA website where you can find five supporting articles of information and recommendations on AED programs: http://www.osha.gov/SLTC/aed/index.html - These five supporting articles will allow you to pull specific data and statics on how an AED program, with the proper CPR/AED training can save lives.

These articles and the information they cover are below:

1. Automated External Defibrillators Can Save Lives During Cardiac Emergencies [1 MB PDF*, 2 pages]. OSHA Publication 3174, (2001). Stresses the need for AEDs in the workplace to save lives. States that AEDs are effective, easy to use, and relatively inexpensive.
2. Saving Sudden Cardiac Arrest Victims in the Workplace: Automated External Defibrillators. OSHA Publication 3185-09N, (2003). Also available as a 376 KB PDF, 4 pages. Provides information on the importance of readily-available AEDs, and encourages the installation of the devices in workplaces. Also includes a list of resources for more detailed guidance on the use of AEDs as well as how to obtain qualified training.
3. Cardiac Arrest and Automated External Defibrillators. OSHA Technical Information Bulletin (TIB), (2001, December 17). Also available as an 18 KB PDF, 4 pages. Provides an information resource to aid in decision-making about these devices at individual worksites. Informs employers about the use of automated external defibrillators (AEDs), a life-saving technology, in the treatment of cardiac arrest at work.
4. Automated External Defibrillation in the Occupational Setting. American College of Occupational and Environmental Medicine (ACOEM), (2006, May). Provides position statement of ACOEM urging placement of AEDs in selected workplaces, and guidelines for employer programs.
5. Saving a Life is As Easy as A-E-D. American Red Cross. Includes information on how AEDs work, training programs, and establishing an AED program at your facility.

All of these articles are great to help you illustrate how deploying an AED Program can potentially save a colleague’s life.

One final resource that may be of assistance in gaining the support and funds needed to implement an AED program is the “National Center for Early Defibrillation” - http://www.early-defib.org/ - Early defibrillation can increase the survival rate from less than 5% without and AED, up to 60% with an AED on site. Statistical data like this illustrates the enormous benefit of having an AED program.

The final component necessary to gain the support of Senior Management is finding a reputable company willing to offer your organization the proper AED equipment, training and maintenance at a reasonable cost. At HeartSafe America, Inc., we do just this. With access to 6 AED Manufacturers, a National Training Network and propriety Data Management Program,

HeartSafe America has successfully helped numerous Fortune 500 and Government Agencies gain top level support by offering a turn-key AED Solution at a very aggressive price point.

Contact HeartSafe America today to find out more about implementing an AED Program for your organization. HeartSafe America's goal is to educate the public about Sudden Cardiac Arrest (SCA) and how AEDs can increase the survival rate.

AED Program Coordinator, AED Program, Implement AED Program, Purchase AED, Automated External Defibrillator

Implementing an AED Program may seem like a challenging task, but it definitely doesn't have to be. With the 7 step guide process of implementing an AED Program, any organization can successfully complete this task. The first step in this process is to select an AED Program Coordinator.

When implementing an AED Program, selecting a Program Coordinator is essential to its success. Therefore, it is imperative that your organization choose the best person for the job and clearly outlines his/her responsibilities.

Who chooses the Program Coordinator?

The person and/or persons assigned to starting the AED Program. This person should have some experience with deploying Automated External Defibrillator (AED) or comparable safety programs.

Example: Human Resources, Executive Management, Risk Management, etc.

Who is the ideal person to be Program Coordinator?

From organization to organization, the background and job responsibilities of the Program Coordinator may vary greatly. However, the ideal person should have some medical or safety experience and their job function should include maintaining the well being of the organization.

Example: Nurse, Risk Manager, Safety Director.

What are the responsibilities of the Program Coordinator?

• To make organization aware of Automated External Defibrillator (AED) and its location.
• Select Emergency Response Team and develop Response Plan.
• Review program with organization’s Medical Director.
• Register AED with local fire department.
• Be familiar with Local, State and National AED Laws/Regulations.
• Organize CPR/AED training for personnel, track renewal dates and schedule re-certifications.
• Perform monthly AED inspections and document results.
• Replace AED pads and batteries prior to their expiration or after use.
• Download post event data, review with Medical Director and debrief the individuals involved.

As you can see, the Program Coordinator has a large number of responsibilities and his/her success is directly related to the success of your AED Program. Therefore, selecting a Program Coordinator may be the single most important task in developing your program.

Contact HeartSafe America to find out more about implementing an AED Program and how we can help you implement your program. HeartSafe America's goal is to educate the public about Sudden Cardiac Arrest (SCA) and how AEDs can increase the survival rate.

Zoll AED Plus AED; automated external defibrillator, purchase an AED, CPR

Purchasing an Automated External Defibrillator (AED) can be a difficult decision with numerous manufacturers to choose from and numerous different features. Therefore, understanding the differences and capabilities of each AED is key to selecting the proper AED for your organization. Therefore, today, we will take a look at the Zoll AED Plus.

The most technologically advanced Automated External Defibrillator (AED) on the market today is the Zoll AED Plus. With “Real CPR Help”, the AED Plus provides feedback on compression rate and depth. This feedback helps responders to perform effective CPR at a rate of 100 compressions per minute with a depth of 1 ½ to 2 inches. As the American Heart Association (AHA) promotes “Compression Only” CPR, Zoll’s “Real CPR Help” is a great tool that no other AED on the market has!

Furthermore, the Zoll AED Plus strongly supports the American Heart Association’s Chain of Survival.

• Early Access (Call 9-1-1)
• Early CPR
• Early Defibrillation
• Early Advanced Care

With clear pictures to act as road map for resuscitation, the AED Plus prompts the responder to check responsiveness, call 9-1-1, perform CPR, defibrillate (if needed) and continue to treat a Sudden Cardiac Arrest (SCA) victim until Advanced Care arrives.

In addition to “Real CPR Help” and “Clear Pictures”, the Zoll AED Plus has many other highly effective features which make it ideal for any organization to deploy:

• One Piece Pad: Zoll’s CPR-D Padz is a one piece, pre-connected pair of electrodes which is much easier and quicker to use than two sets of pads. Furthermore, the CPR-D Padz has the longest life of any pad on the market with a 4.5 year expiration.
• Rectilinear Biphasic Waveform: Only biphasic waveform cleared by the FDA to be labeled as clinically superior to monophasic waveforms for the conversion of ventricular fibrillation in high-impedance patients.
• Escalating Energy: If Shock #1 one does not convert the heart at 120 Joules, the device will escalate to 150 Joules for Shock #2. If 3rd Shock is needed, the Zoll AED Plus will increase once again to 200 Joules and deliver its highest energy shock.
• High Durability Rating: With an ingress protection rating of IP55, the Zoll AED Plus has a high resistance to dust & water. Therefore, the AED Plus can be taken virtually anywhere and is ideal for Athletic, Marine and Manufacturing Settings.
• Consumer Batteries: The Zoll AED Plus is the only AED to use consumer batteries which can be purchased from most retailers. Using lithium camera batteries to power itself, Zoll has made replacing batteries convenient and cost effective.
• Useful Cover: Zoll has designed the AED Plus’s cover to be used as a wedge to open the airway. By placing the cover under the victim’s shoulder blades, the body is elevated slightly causing the head to tilt back and the victim’s airway to open.

It is Zoll’s belief that when a victim falls unconscious that a shock will only be needed 50% of the time. However, high quality CPR will be needed 100%. Therefore, Zoll has designed the AED Plus to do what no the AED does, provide CPR coaching and feedback to responders in order to increase effectiveness and maximize positive outcomes.

In designing a simple device which anyone can use, the Zoll AED Plus can be deployed in almost any organization/facility. However, below is a list of industries which we have found it to be the most beneficial in:

• Athletic Facilities
• Government Agencies
• Law Enforcement
• Manufacturing Plants

Contact HeartSafe America today to find out more about the Zoll AED Plus AED and how to implement an AED Program for your organization. HeartSafe America's goal is to educate the public about Sudden Cardiac Arrest and how AEDs can increase the survival rate.

Philips HeartStart OnSite AED, Automated External Defibrillator, Purchase an AED

Purchasing an Automated External Defibrillator (AED) can be a difficult decision with numerous manufacturers to choose from and numerous different features. Therefore, understanding the differences and capabilities of each AED is key to selecting the proper AED for your organization.

The Philips HeartStart OnSite is the first automated external defibrillator (AED) to be cleared by the Food & Drug Administration (FDA) to be sold without a Physician’s Prescription. This clearance was received due to its ease of use which makes it applicable for business or home placement.

In addition to being easy to use, Philips has also made the Heartstart OnSite very affordable to increase wide spread access to Automated External Defibrillators (AEDs).

The Philips HeartStart OnSite has a long-life battery which will last 4 year s installed and 5 years on the shelf. The adult pads are pre-connected and ready for use at any time. The OnSite AED offers an infant/child pad that is to be used on any child 8 years or younger and 55lbs or less. The infant/child pads reduce the amount of energy delivered from the AED.

Furthermore, the Philips HeartStart OnSite has low-energy biphasic therapy which delivers an energy at a protocol of 150 Joules, 150 Joules, 150 Joules. In multiple peer-reviewed studies, this low-energy biphasic therapy has proven to be effective in treating Sudden Cardiac Arrest (SCA) while minimizing post resuscitation heart damage.

In addition, the Philips Heartstart OnSite has countless features which make it one of the best AEDS on the market. However, below are a few key ones:

• “Pull” Tab – The “Pull” tab can be pulled to activate the AED. It is the only AED on the market that has the “Pull” tab feature. Many AED require the responder to push an on/off button to activate the AED.
• CPR Coaching – The OnSite has CPR Coaching. The CPR Coaching feature assists the responder on the frequency and the depth of the compressions.
• “I” Button – The “I” Button serves two purposes on the OnSite AED. The first purpose is to inform the owner of the AED that there is an issue with the AED. If your Philips OnSite AED is beeping, you can push the “I” button, and the AED will inform you as to what the issue is with the AED. The second purpose is to inform the EMS responders of the events of the emergency. The AED will give a recount of the event details that have occurred.
• Self Tests – The Onsite does daily, weekly and monthly self-tests to ensure its functionality. If it passes each, a “green light flashing” will appear signifying that it is “ready for use”.

Finally, due to its ease of use & economical price point, the Philips Heartstart Onsite has become the most widely distributed AED in the world and has proven to be ideal for deployment in the following organizations:

• Schools
• Churches
• Small Businesses
• Gyms

Contact HeartSafe America today to find out more about the Philips HeartStart OnSite AED and how to implement an AED Program. HeartSafe America's goal is to educate the public about Sudden Cardiac Arrest (SCA) and how AEDs increase the survival rate.

Medtronic/Physio Control LifePak CR+ AED; Automated External Defibrillator, Purchase an AED, AED Program, LifePak, Defibrillator

Purchasing an Automated External Defibrillator (AED) can be a difficult decision with numerous manufacturers to choose from and numerous different features. Therefore, understanding the differences and capabilities of each AED is key to selecting the proper AED for your organization.

As individuals, businesses, churches and other organizations pursue the possibility of obtaining an Automated External Defibrillator (AED), determining which device to purchase can be a little over whelming and confusing. Therefore, our goal is to help you understand the differences & capabilities of each AED. With that being said, today’s blog will take an in depth look at Physio-Control’s LIFEPAK CR Plus.

The LIFEPAK CR Plus Automated External Defibrillator (AED) is a device with professional grade functionality, designed specifically for the “lay person” environment. The simple to use CR PLUS AED employs one of the most advanced technologies in defibrillation available on the consumer market. This technology is called “Adaptive Biphasic” and is the same technology used by EMS and hospitals nationwide.

In simple terms, Adaptive means the internal brain of the AED will “adapt” the amount of energy and length of the current based on the victim’s heart rhythm. Biphasic indicates how the current will travel. “Bi” (meaning two) signifies that the current will cross the heart twice, making the shock more effective.

The CR PLUS is available in two configurations, “Semi-Automatic” or “Automatic.” In the semi-automatic configuration, once the pads have been applied to the victim’s chest, the AED will analyze the heart rhythm to determine if a shock is needed. If a shockable rhythm is detected, the CR Plus will advise the rescuer to “push the red flashing button” to deliver a shock.

In the fully-automatic configuration, once the pads have been applied to the victim’s chest, the AED will analyze the heart rhythm to determine if a shock is needed. If a shockable rhythm is detected, the CR Plus will begin charging, instruct the rescuer to “stand back”, and deliver a shock without rescuer assistance. Both versions of the CR Plus are programmed to shock only if one of two rhythms is detected, Ventricular Fibrillation (VFIB) or Ventricular Tachycardia (VTAC).

Both CR Plus configurations employ an escalating energy protocol of:

Shock #1: 200 joules
Shock #2: 300 joules
Shock #3: 360 joules

This protocol is used by a large number of Medical Professionals and has shown to be more effective in defibrillating patients with higher impedance Furthermore, the CR Plus is equipped with pediatric capability which will automatically reduce the amount of energy by 1/3 when the pediatric pads are connected. Pediatric pads are designed to be used on children under the age of 8 years old or 55lbs and under.

Another safety feature of the CR Plus is its motion detection sensor. This safety mechanism determines if the victim is inadvertently being moved or touched by a live person when a shock is about to be delivered. This will prevent the other person from being shocked as well and avoid another potential risk of a problem.

Finally, The LIFEPAK CR Plus is virtually maintenance free and has one date to monitor to replace both the pads and the batteries. If the display window at the top of the device shows “OK”, it is “Rescue Ready”. To avoid power failure and maintain its “Rescue Ready” status, the device has two power sources, a small trickle charge battery and a larger internal battery. The internal battery has the ability to retain a charge for up to another 12 months after the expiration of the trickle charge battery. However, this is NOT recommended by Physio-Control.

The CR Plus has many great features that make it applicable for any public access setting. However, what sets it apart from other AEDs is its ability to adapt to the patient and deliver a highly effective shock. This is why so many of the following organizations have chosen Physio-Control.

• Medical & Healthcare Professionals
• Fortune 1000 Corporations
• Federal & State Agencies
• Law Enforcement Agencies
• School Districts

Contact HeartSafe America today to find out more about the Medtronic/Physio Control LifePak CR+ and how to implement your AED Program. HeartSafe America's goal is to educate the public about Sudden Cardiac Arrest and how AEDs can increase the survival rate.

HeartSine Samaritan PAD AED, Automated External Defibrillator, AED Program, Purchasing an AED

Purchasing an Automated External Defibrillator (AED) can be a difficult decision with numerous manufacturers to choose from and numerous different features. Therefore, understanding the differences and capabilities of each AED is key to selecting the proper AED for your organization.

The HeartSine Samaritan PAD Automated External Defibrillator (AED) is a device that’s ideal for any organization. Not only is it the lightest (2.4 lbs) of all the AEDs on the market, but also the most durable. With an IP rating of 56 against dust and water, the HeartSine Samaritan can be exposed to various weather conditions which allows it to be taken virtually anywhere.

Unlike its competitors, the HeartSine Samaritan utilizes PAD-PAKs (adult & pediatric). These PAD-PAKs consist of one set of pad and a battery sealed together with one expiration date. Each PAD-PAK has a lifespan of 3.5 years , keeping the cost of replacement pads/batteries to a minimum. The PAD-PAKs also aviation ready, meaning the HeartSine Samaritan can be used during flight in the event someone experience sudden cardiac arrest (SCA).

The HeartSine Samaritan performs self tests daily, weekly, and monthly to ensure the AED is fully functional. The status indicator light will flash to let the responder know that this AED is rescue ready at any time. With clear voice prompts, the HeartSine Samaritan assists responders during an emergency and allowing the responder to bridge the gap until local EMS arrives. Not only does its lighted visual and audio display help guide the responder step by step, but this feature helps the responder understand what the next step should be. If a shock is needed, the “shock button” illuminates and should be pushed.

A key factor when deciding purchasing any electronic device is the manufacturer’s warranty. The HeartSine offers one of the longest warranties on the market, 7 years. The PAD-PAK itself has a 3 year warranty. The long warranty demonstrates the manufacturer’s extraordinary commitment to quality.

The HeartSine Samarian has the ability to record any event that occurs during its use. It will record the ECG trace and duration, shock delivery information, and the CPR intervals. This information can be downloaded to your computer using the HeartSine Data Cable. Furthermore, the USB data cable can also be used to update the Samaritan to the latest AHA Guidelines.

As you can see, there are many advantages to owning the Heartsine Samaritan. Below is a list of major business sectors that have found to Samaritan to be an ideal fit.

• Electric Companies
• Construction Companies
• School Districts
• Fortune 500 Companies
• Government Entities
• Churches

Contact HeartSafe America today to find out more about the HeartSine Samaritan PAD AED and how to implement your AED Program. HeartSafe America’s goal is to educate the public about Sudden Cardiac Arrest and how AEDs can increase the survival rate.

Philips HeartStart FRx AED; Automated External Defibrillator; AED Program, AED for your organization

Purchasing an Automated External Defibrillator (AED) can be a difficult decision with numerous manufacturers to choose from and numerous different features. Therefore, understanding the differences and capabilities of each AED is key to selecting the proper AED for your organization.

In an effort to help Automated External Defibrillators (AEDs) buyers understand the differences and capabilities between defibrillators, HeartSafe America is reviewing the top public access defibrillators on the market. Last week, we began our six part series with the Defibtech Lifeline, whose advantages were ease of use, functional design, CPR Coaching and durability. Today, we will take a look at the Philips Heartstart FRx, the newest member to the Philips Family.

TECHNOLOGY
In designing the FRx, Philips started with the following proven technology used in their Onsite and FR2 AEDs:

• Smart Biphasic Waveform: Philips biphasic waveform delivers a highly effective defibrillation shock that is also gentle to the heart. Its SMART Analysis ensures that the FRx only shocks when it should. After the pads are placed on the body, Smart Analysis automatically assesses the victim’s heart rhythm and if a shockable rhythm is detected, it will advise the responder to press the “flashing orange” shock button. However, if a shockable rhythm is not present, the FRx will prompt the responder to begin CPR and will not deliver a shock even if the orange shock button is pressed.
• Quickshock: If Smart Analysis determines that a shock is needed, Philips Quickshock feature allows the FRx to deliver a shock in approximately 8 seconds. Its ability to charge and deliver a shock so quickly, minimizes the interruption of CPR Chest Compressions, thereby increasing the chance in a successful return to spontaneous circulation.
• CPR Coaching: Whether a shock is delivered or not, effective CPR is vital to saving the victim. However, since CPR is rarely practiced outside of yearly/ bi-yearly renewal courses, having a reminder can be helpful. The FRx’s CPR Coaching proves this reminder with clear voice instructions to assist the responder with CPR basics and a metronome to keep chest compression cadence.

INFANT CHILD CAPABILITY
Every AED on the market today has the ability to reduce the energy level to shock children under the age of 8 years old. Normally, this is achieved using a 2nd set of pads. However, the Philips FRx employs an Infant Child Key which is easier to use, quicker to activate and a cost of ownership savings. The FRx’s Infant Child Key is a major technological advancement and a huge advantage over competitors.

EASE OF USE
Designed for the lay-person, the Philips FRx uses voice prompts, a lighted visual display and CPR Coaching to guide minimally trained responders through the save process. These are the same features which have earned the FRx’s sister device, the Philips Onsite, numerous accolades as the “easiest device for a lay-responders to use”.

DURABILITY
In order to make the Philips FRx applicable for any setting, Philips designed it to be very rugged and durable. With a high rating against water & dust, the Philips FRx can be deployed in environments where rain & solid particles are a factor.

TRAINER OPTION
When purchasing an AED, training your organization with a “like” device is very important. However, most AEDs on the market require that you spend another $300-400 to purchase a separate trainer. Fortunately, the Philips FRx allows you to convert the “live” device into a trainer with the acquisition of training pads. By simply plugging the training pads into the Philips FRx, these pads activate the FRx’s training mode and suspend the defibrillator’s ability to deliver a shock. The training mode allows the user to run eight different training scenarios.

MANUFACTURER STABILITY
When purchasing any product, manufacturer reputation and stability is a huge consideration. Reputation is an indication of how reliable the product is and stability tells you if the company will be around to service the product. With over 100 years in the medical field and over 500,000 AEDs deployed worldwide, Philips is the industry leader and the most stable company in an industry. Therefore, when purchasing Philips AED, consumers will have great confidence that their Philips will work now and in the future.

As you can see, the Philips FRx has been designed to meet the needs of any organization. With innovative technology, clear narration, high durability, trainer option and a very stable manufacturer, the Philips FRx can be considered the best device on the market to deploy in a public access setting. However, we have found that the FRx to ideal for the following organizations:

• Athletic Departments/Teams
• Chemical Plants
• Law Enforcement Agencies
• Electric Companies
• Manufacturing Plants

Contact HeartSafe America today to find out more about the Philips HeartStart FRx AED and how to implement your AED Program. HeartSafe America’s goal is to educate the public about sudden cardiac arrest and how AEDs increase the survival rate.

Defibtech LifeLine AED; Automated External Defibrillator, SCA, Purchasing AED, Sudden Cardiac Arrest, CPR

Purchasing an Automated External Defibrillator (AED) can be a difficult decision with numerous manufacturers to choose from and numerous different features. Therefore, understanding the differences and capabilities of each AED is key to selecting the proper AED for your organization. Over the course of six weeks, we will review the top six AEDs on the market today.

One of the most user friendly devices on the market today is Defibtech Lifeline AED. With its bright yellow color, built in handle, large buttons and clear voice prompts, the Lifeline has been designed to be clearly visible, easy to transport and very easy to use.

The Defibtech LifeLine has text, lights, and voice prompts to assist the responder through the rescue. This feature makes it easy for any responder, trained or not, to feel confident during a rescue that he or she will be able to help save a life.

The Defibtech LifeLine has pre-connected adult pads. The pads sit in a pocket in the back of the AED so that they are ready for use at any time. The Defibtech LifeLine offers a 5 year battery or a 7 year battery for its AED.

The newest feature on the Defibtech LifeLine is the CPR Coaching Metronome. The metronome feature helps the responder know the rhythm of the CPR compressions and how often to give them.

The Defibtech LifeLine has an IP rating of 55. This IP rating is one of the highest IP ratings for an AED. The IP ratings vary from AED to AED. When an AED receives its IP rating it means that, that particular AED has been put through the solid (dust) and water particle test.

The Defibtech LifeLine performs self tests daily, weekly, and monthly to ensure the AED is fully functional. The status indicator light will flash to let the responder know that this AED is rescue ready at any time.

Some of the major business sectors that have equipped themselves with the Defibtech LifeLine include the following:

• School Districts
• Construction Companies
• Government Entities
• Churches

HeartSafe America assists organizations all over the United States with implementing their AED Programs. One of the organizations that HeartSafe America has worked with is Pearland ISD, a school district in Texas. Pearland ISD owns the Defibtech LifeLine AEDs, and this school district has recently had to use the Defibtech LifeLine AED to receive a student who was at practice for his sport and collapsed. The student went into Sudden Cardiac Arrest and because Pearland ISD had the Defibtech LifeLine on site, this student had a fighting chance. This student survived Sudden Cardiac Arrest due to the fact that there was an AED present.

To view more about this story, CLICK HERE.

Contact HeartSafe America today to find out more about the Defibtech LifeLine AED and how to implement your AED Program. HeartSafe America’s goal is to educate the public about sudden cardiac arrest and how AEDs increase the survival rate.

AEDs in the workplace; automated external defibrillators, sudden cardiac arrest, SCA, CPR Training, OSHA

Many organizations struggle with the thought of purchasing an automated external defibrillator (AED) for the workplace due to the fact that many organizations are unaware of what the AED’s purpose is and how it can save lives. Understanding the benefit of an AED in the workplace could save a life.

Is there a benefit of having AEDs in the work place?

The answer to this question is absolutely!

In our continuous effort to educate the public about the benefits of automated external defibrillators (AEDs), HeartSafe recently blogged about the American Heart Association’s three minute from “drop to shock” rule. This clearly illustrates the benefit of having AEDs in the work place for several reasons.

It is a common misconception that local EMS are able to respond to the scene of an accident immediately. It is important to realize that the national average response time for local EMS ranges anywhere from 6 to 12 minutes. Being aware of this information is key to survival. With every minute that passes, a victim in sudden cardiac arrest (SCA) loses a 7%-10% chance of survival if not defibrillated. Unfortunately, a victim is facing only a 40% chance of survival if EMS arrives at the six-minute mark.

Envision a normal office setting and your colleague or business partner is sitting in a cubicle next to you and all of the sudden he starts having chest pains and loss of breath. He then falls out of his chair on to the floor unconscious. It appears he has had a heart attack which has lead to cardiac arrest. You immediately call 911 and the clock starts ticking. You quickly retrieve the AED onsite, begin CPR, then apply the pads of the AED on the chest and follow the guidance the AED verbally gives you to begin treatment. The device begins analyzation and tells you to push the shock button to deliver the first shock. Your colleague comes to and appears to wake up. You continue to care for him until EMS has arrived, but he is now conscious and can answer you when you speak to him. EMS finally arrives after 8 minutes and begins to care for him.

This example provides clarity on why having AED’s in the work place is a necessity! An article by the Department of Labor Occupational Health & Safety Administration (OSHA) states that in 1999 – 2000 815 out of 6339 fatalities (13%) in the work place were due to sudden cardiac arrest (SCA). The conclusions of this article determined that “The earlier defibrillation is administered, the better chance at survival for the victim.” The proper placement and implementation of AEDs and CPR/AED Heartsaver training in the work environment helps “bridge” the gap between the time a victim has a cardiac event, to the time when EMS arrives on the scene to take over.

CLICK HERE to view the OSHA article.

Understanding what Sudden Cardiac Arrest is and accepting that it can affect anyone, at any age, at any given moment emphasizes the importance of AEDs in the work place. After all, the life you save may be great friend or colleague.

Contact HeartSafe America today to find out more about the benefits of AEDs in the work place. HeartSafe America's goal is to educate the public about Sudden Cardiac Arrest (SCA) and how AEDs can increase the survival rate.

Defibtech Voluntary Recall; AED, Automated External Defibrillator, Battery Pack

Defibtech, manufacture of the LifeLine and the ReviveR automated external defibrillators (AEDs), has issued a voluntary recall on 5,000+ DBP-2800 Battery Packs.

Defibtech has issued a voluntary recall on 5,000+ DBP-2800 Battery Packs that were manufactured prior to June 2007. The reason for the voluntary recall is due to the fact that the automated external defibrillator (AED) may falsely detect an error condition during the charging for a shock and it could cancel the shock therapy even though it may be needed.

Defibtech has secured the serial numbers for all the affected DBP-2800 Battery Packs manufactured prior to June 2007. To see if your DBP-2800 Battery Pack is affected, CLICK HERE.

If your DBP-2800 Battery Pack is one of the affected battery packs, please contact Defibtech for details about getting the battery pack issue corrected as soon as possible.

To view more details about the Defibtech Voluntary Recall, CLICK HERE.

Contact HeartSafe America today for all your Defibtech AED and AED replacement accessory needs. HeartSafe America’s goal is to educate the public about Sudden Cardiac Arrest (SCA) and how AEDs can increase the survival rate.

AED Replacement Accessories; Expiring AED Parts, Automated External Defibrillator, Good Samaritan

All Automated External Defibrillators (AEDs) have pads and batteries with expiration dates and must be replaced according to the expiration date.

Once an organization or company has equipped themselves with an automated external defibrillator (AED), it is imperative that inspections are performed on a monthly basis. Not only are monthly inspections a prerequisite for the Good Samaritan law, but it also reminds the organization when the pads and batteries expire.

Below are some commonly asked questions regarding replacement parts.

Why do my AED electrode pads expire?

• AED electrode pads are comprised of an adhesive gel and tin. Once they exceed their expiration date, they may not be able to function properly or will lose their ability to “stick” to a victim. Manufacturers cannot guarantee that the pads will function past their expiration date. Just like a band aid, AED electrode pads tend to dry out faster once exposed to air.

When do my pads expire?

• AED pads expire typically every two years. Manufacturers such as HeartSine and Zoll use a different formula which allows the pads to last longer than two years.

How often will I have to replace my batteries?

• Like the electrode pads, each manufacturer has a different expiration date. Battery expiration dates or shelf life can vary anywhere from 2 years to 7 years. The battery shelf life is not a set date and varies manufacturer to manufacturer. The shelf life date can usually be found on the battery.

Does my AED battery have an expiration date listed on it?

• Yes. Most batteries have an expiration date with the exception of Cardiac Science. Cardiac Science lists when the battery was manufactured versus the battery shelf life.

Should I purchase an extra set of pads or battery?

• This is not a legal statue or precedent that requires a spare pad be available. However, it is always a good idea to have an extra battery or set of pads, just in case the primary is not functionality proper. Most manufacturers will include a spare set of pads in their initial AED Ship Set.

Contact HeartSafe America today to find out more about replacement accessories for your AED or to place an order for your replacement accessories. HeartSafe America's goal is to educate the public about Sudden Cardiac Arrest (SCA) and how AEDs can increase the survival rate.

Philips Voluntary Recall; AED, Automated External Defibrillator, Defibrillator

Philips has announced a voluntary recall on the Philips HeartStart OnSite and the Philips HeartStart FRx automated external defibrillators (AEDs).

The Philips voluntary recall that has been issued is for a small amount of affected Philips OnSites and Philips FRx AEDs. The reason for this voluntary recall is due to the fact that a relay in the devices is not up to Philips' performance standards. The affected relays came from one manufacture and were in a single lot. There have been no reports of the device's relay failing, but the potential of failure does not meet Philips' standards.

The Philips AEDs that were affected by the recall were manufactured during March 2010. Philips is contacting the customers directly in regards to this matter.

If you have not been contacted and you are concerned that your AED may be part of the recall, you can input your serial number and it will search their system to verify that your AED is or is not on the recall list. Click here to input your serial number.

It read more about the recall, please CLICK HERE.

Contact HeartSafe America if you have any questions regarding your AED, AED replacement accessories, or general questions about AEDs and Sudden Cardiac Arrest. Our goal is to educate the public about Sudden Cardiac Arrest and how AEDs can increase the survival rate.

CPR & AED Awareness Week; AED, Automated External Defibrillators, Sudden Cardiac Arrest, SCA, CPR, CPR Training

CPR & AED Awareness Week has been created by the American Heart Association to promote the importance of being trained in CPR and how automated external defibrillators (AEDs) can help to increase the survival rate from Sudden Cardiac Arrest (SCA).

CPR & AED Awareness week is from June 1 through June 7, 2010. The goal of the American Heart Association (AHA) is to inform the public about Cardiopulmonary Resuscitation (CPR) and how CPR can help to save a life. Along with CPR, automated external defibrillators (AEDs) are use to revive patients suffering from Sudden Cardiac Arrest (SCA).

HeartSafe America is an official AHA training site for CPR and AED training courses. HeartSafe America’s goal is to educate the public about Sudden Cardiac Arrest and how CPR and AEDs can help to increase the survival rate.

Have you considered CPR Training? Interested in an AED for your organization?

Contact HeartSafe America today to find out more about CPR Training and how your organization can implement an AED Program.

AED Post Event Review, Automated External Defibrillator, Sudden Cardiac Arrest, SCA, Event Review

Not sure what to do after using your AED during an emergency? Every Automated External Defibrillator (AED) has the ability to record the event that takes place during an emergency. All AEDs store event information and it can be downloaded from the AED for review.

Hopefully at this point your organization has purchased an Automated External Defibrillator (AED) to protect your members and staff from Sudden Cardiac Arrest (SCA). The possibility of using the AED, while slim, is definitely real. Therefore, it is very important to know how to use the AED and equally as important to know what to do after a usage.

Once an event has occurred, positive or negative, you must download the event data and forward it to the responding Physician and your Medical Director. Currently, every device on the market will record a minimum of 15 minutes of ECG analysis. Furthermore, some devices can record up to 8 hours of ECG or a short duration of both audible and ECG data. To find out your device's capability, consult your user's manual.

To download the event data, you must first have a computer with the appropriate manufacture's software. Most manufactures offer a basic version which can be downloaded for "Free" from the following sites:

• Cardiac Science Rescuelink
  Download link: Must contact Cardiac Science Tech Support to obtain link
• HeartSine EVO Saver Software
  Download Link: http://www.heartsine.com/index.php?page_id=152
• Defibtech Event Review Software
  Download Link: http://www.defibtech.com/downloads_utilities.html
• Physio Control LIFENET DT Express
  Download Link: CD Only, Field Service Rep can perform download for small fee.
• Philips Review Express
  Download Link
• Welch Allyn Smartlink Event Pro Software
  Download Link: Must send device in
• Zoll Rescue Net Code Review
  Download Link: http://www.zolldata.com/web/codeReview.aspx
  

After the software has been downloaded to your computer, the AED must be connected directly to the computer to review the event data. Currently, there are two methods for connecting and accessing this data:

• IRDA Adapter: Adapater connects through the computer's USB and allows the data to be transferred from the AED to the computer by lining up the infarred windows.
  Definition: http://en.wikipedia.org/wiki/Infrared_Data_Association
  
• Data Cable: Cable connects through the computer's USB port and allows data to be transferred through a direct connection between the AED and the computer.

After a connection has been established, the manufacture's software program should be run to receive "event data" from the AED. After the data is downloaded, it can be emailed or printed depending on the software's capabilities.Finally, after the data download is complete, it is imperative that the pads and/or battery be replaced so the AED can be placed back into service.

Contact HeartSafe America today to find out more about post even reviews and purchasing replacement AED accessories. Our goal is to educate the public about Sudden Cardiac Arrest and how AEDs can help increase the survival rate of SCA.

Data Management Solutions; AED Tracking, AED Program, Automated External Defibrillator, SCA

Data Management Solution program is a simple way for any organization to keep their AED program on track. The AED Program Coordinator will be able to track each of the AEDs using our Data Management Solution program.

When implementing an Automated External Defibrillator (AED) Program, performing monthly inspections, tracking replacement part expiration dates and monitoring CPR/AED training renewals can be time consuming and difficult to keep up with.

Therefore, in an effort to assist organizations in maintaining a successful and legally compliant AED Program, HeartSafe America has developed a proprietary web-based tracking program with the following features and functionality:

• Stores a master list of all AEDs, locations and contact personnel.
• Provides quick reference to AED serial numbers and all part numbers.
• Monthly inspection log which sends email reminders if inspection is not performed.
• Tracks replacement part expiration dates and sends email notifications.
• Designated section to document incidents and log event data.
• Tracks CPR/AED certified personnel and sends email renewal reminders.
• Numerous comprehensive reports to help AED Coordinator easily manage AED Program.
• Multiple security levels to limit user access based on AED Program responsibilities.

This software program is known as our “Data Management Solution (DMS)” and is currently being used by numerous Fortune 1000 companies.

Many organizations have similar questions as to why our Data Management Solution (DMS) program would be a good fit for their organization. At HeartSafe America, we want to ensure that every one our clients experiences the benefits of our DMS program. Below are some frequently asked questions (FAQs) about our Data Management Solution program.

How will the data management solutions program be beneficial to my organization?

Our Data Management Solution (DMS) program allows an organization to manage their AED Program by organizing device information in a centralized web-based location for quick access. Having this information organized and readily available eliminates confusion, duplication and most importantly, keeps the AEDs “rescue ready”.

If my organization has AED in different locations, will my organization be able to track these AEDS?

Our DMS allows any organization to track an AED regardless of location. Once an AED is entered into the system, it is assigned to a specific location where the location can be viewed by the Site Coordinator and AED Program Coordinator regardless of geographic location.

Will the program notify my organization to perform the monthly inspections?

Monthly inspection reminders are sent out each month on the designated inspection date to the Site Coordinator or assigned inspector. If the inspection is not performed on the designated inspection date, the DMS will continue to email reminders until inspection is performed and entered into the system. These reminders should insure that your monthly inspections are being performed, keeping your organization legally compliant and your devices operational.

Will the DMS Program alert my organization when pads and batteries expire?

When your AED is entered into our DMS Program, the expiration dates for all replacement parts are documented. Then, at 90, 60 and 30 days prior to expiration, the DMS will automatically send an email reminder to Site Coordinator, Backup Site Coordinator and Program Coordinator alerting them to replace this part.

Can my organization track the personnel with CPR/AED training and when their renewals are due?

Our DMS allows your organization to input trained personnel along with their renewal date and certificate type. Then, at 60 and 30 days prior to the renewal, our DMS will automatically send an email reminder to the email address designated in this section.

If an emergency should happen and the AED is used, can my organization log the incident?

Our DMS has an incident log which can be utilized to track any instance when the AED is used. Whether the outcome is successful, unsuccessful or a non event, this information is an important historical reference to be utilized for comparison and training purposes.

Contact HeartSafe America today to find out how our data management solutions program can be an asset to your organization’s AED program. Our goal is to educate the public about Sudden Cardiac Arrest (SCA) and how AEDs can decrease the lives lost to SCA.

AED Liability, Automated External Defibrillator, Sudden Cardiac Arrest, SCA, CPR, Good Samaritan

Liability. This is a “fear” that weighs heavily on everyone’s mind when considering purchasing an Automated External Defibrillator (AED) for their organization. All 50 states have created “Good Samaritan” and AED Laws to protect responders, organizations, and the victim. Understanding these laws is key to implementing a successful AED Program.

Is there a liability factor owning an AED (Automated External Defibrillator)?

This question tends to be the number one factor in determining if a corporate, fitness, church or any other organization considers purchasing an automated external defibrillator (AED) for their facility.

There are several factors supporting why liability should no longer be the number one deterrent when considering implementing an AED program. With the passing of the CASA act (Cardiac Arrest Survival Act) of 2000, passed by Bill Clinton, immunity measures from liability for the entity and/or person utilizing an AED in good faith have been enacted on a federal level.

The Cardiac Arrest Survival Act (CASA)1 now requires the U.S. Secretary of the Health and Human Services Department to establish guidelines for placing AEDs in federal buildings. These guidelines must include the proper placement of the AEDs and the appropriate procedures are followed:

• Implement the appropriate training program of the AED device and CPR (Cardiopulmonary Resuscitation)
• Ensure the proper testing and ongoing maintenance of the AED
• Ensuring the proper licensed medical direction and oversight of the program
• Ensure that local EMS (Emergency Medical Services) have been notified of the devices and incidents and uses of the devices

When these guidelines were published, they lead to community based defibrillation programs leading to more unified state AED laws, regulations and training requirements, otherwise known as “Good Samaritan” laws.

Mr. Richard Lazar, a legal expert on emergency medical services topics and an advisor to the National Center for Early Defibrillation states: “The perceptions and fear of legal liability continue to serve as barriers to large-scale adoption of public access defibrillation (PAD) programs in out-of-hospital settings.”

With the help of the medical community’s experience of implementing multiple PAD programs across the US and the advancement in technology, AEDs have become more accessible and easier to purchase without the fear of liability. The trend and fear of not having an AED available at larger, more populated facilities, such as fitness facilities or sporting event venues, is starting to actually turn the other direction.

In the last several years, the liability factor for not having an AED has come up in multiple law suits across the country. Two of the most notable law suits happened in Florida on two separate occasions.

The first of which occurred at the Busch Gardens Theme Park when a 13 year old child died from Sudden Cardiac Arrest (SCA). The park did NOT have an AED on site and was sued by the family. The Jury awarded a judgment of $500,000.00 in damages to the victim’s family.

A second example of a liability issue for not having an AED on site came to light at the “Q Sports Club” fitness center, in Florida. In this particular case a 42 year old gentleman went into SCA and the facility did not have an AED on sight. They were not able to revive the gentleman and he ended up in a coma with no brain function. This case settled out of court for the sum of 2.25 million dollars.

Cases like these clearly illustrate the liability risks that impact businesses can be greatly reduced by implementing AED programs. Obtaining the proper medical direction, following Good Samaritan laws, and receiving the proper CPR/AED training from an experienced and accredited training center, are all major factors in implementing a successful and compliant program.

Contact HeartSafe America to find out more about implementing your AED program utilizing the direction of your state’s Good Samaritan Laws and the CASA act of 2000 guidelines. HeartSafe America offers AEDs from the top AED manufactures. Our goal is to help educate the public about Sudden Cardiac Arrest and how AEDs can help decrease the number of deaths from Sudden Cardiac Arrest with the proper AED program and training.

1 Lazar R.A. Understanding legal issues: National Center for Early Defibrillation

HeartSafe America; AED Program, AED Implementation, Automated External Defibrillator, Sudden Cardiac Arrest, SCA, AED Laws, CPR Training

An Automated External Defibrillator (AED) Program is key to reducing the number of deaths that occur from Sudden Cardiac Arrest (SCA). Our 7 step process based on the American Heart Association’s recommendations will assist any organization in implementing an AED program.

As a result of the American Heart Association, state legislation and notable deaths such as Tim Russert (Moderator of NBC’s “Meet The Press”), Sudden Cardiac Arrest (SCA) awareness is at an all-time high. Therefore, many churches, schools, and corporations are proactively protecting their members from this deadly disease with Automated External Defibrillators (AED). While buying an AED does not guarantee every victim will be saved, it will substantially increase survival rates from 5% to 65-75%. However, in order to achieve maximum results, a comprehensive program must be implemented. Below is a list of steps to do so:

1. Select a Program Coordinator:
   Accountability is the key to any project. Therefore, a single individual must be selected to implement the program and maintain it after initial deployment is completed.
2. Get Decision Makers Support:
   In any organization, it all starts at the top. Therefore, in order for the program to gain notoriety and thrive financially, support from executive leadership is needed. Since most Decision Makers are subjected to large amounts of stress and long hours, SCA should be a concern for them and gaining support should be easy once the facts are presented.
3. Review State & Federal Laws:
   Laws exist to protect people. Therefore, to implement an effective program, the Coordinator must familiarize himself or herself with the Laws that have been put in place to protect those who purchase AEDs and use them.
4. Obtain Medical Oversight:
   As lay people, we may not understand the full scope of implementing an AED Program. Therefore, employing a Medical Professional to oversee program development, deployment and maintenance will have a profound impact on its success. Think of it as a “Technical Support Plan” for your computer. **In some states, Medical Direction and Oversight is a requirement**
5. AED Selection:
   When selecting an AED, research and compare the features of different devices to find the one that best fits your organizational needs. If possible, work with a multi-line AED Distributor who can help you understand the key differences between the devices and consult on the selection.
6. AED Placement:
   If I had to rank the importance of each step, AED Placement would be at the very top. Since AED and AED Cabinets are not the most attractive pieces of décor, many organizations try to hide them or unknowingly place them in inappropriate spots. However, in order to achieve the American Heart Association’s goal of three minutes from drop to “shock”, AEDs must be placed in high traffic, centrally located areas near other emergency medical equipment. In following this recommendation, the device will be very visible and easily accessible if a Sudden Cardiac Arrest occurs.
7. Training:
   All AEDs on the market today have clear prompts, which guide the responder through the save. However, as the old saying goes: “practice makes perfect”. Therefore, it is highly recommend that your entire organization attend a CPR/AED training course administered by the American Heart Association, American Red Cross or equivalent training organization. If training everyone is cost prohibitive, select an appropriate number of individuals to be designated as an Emergency Response Team and have them trained.

Once these steps have been completed, the real work begins. During the initial deployment, enthusiasm and interest will be extremely high. However, after training is completed and the AEDs are placed in their cabinets, most will forget that they exist. Therefore, the Program Coordinator will be responsible for keeping the program compliant and visible. Below is a list of ongoing AED Program responsibilities:

• Monthly Inspections: Every month, the AED(s) must be inspected to ensure functionality. This inspection consists of checking the status indicator and the pad expiration dates (Adult & Pediatric). If the status indicator is “flashing” and the pads are within the expiration, the device is “Rescue Ready”.
• CPR/AED Training: Depending on the training curriculum which your organization has chosen, training renewals will occur every year or every other year. Therefore, the Program Coordinator must track the renewals and schedule re-certifications.
• Ongoing Awareness: As new members join the organization and old members forget, periodic AED reminders should be published. These reminders should include AED location, list of trained responders and protocol for responding.

Deciding to purchase an AED is a great decision and an excellent benefit for your members and/or employees but this decision cannot be validated without proper deployment. Therefore, it is essential that you follow these steps to ensure that if the time arises, your AED Program is prepared to save a life!

Contact HeartSafe America to find out more about implementing your AED program for your organization. HeartSafe America offers six of the top AED manufacturers. Our goal is to help educate the public about Sudden Cardiac Arrest and how AEDs can help decrease the number of deaths from Sudden Cardiac Arrest.

HeartSafe America: Sudden Cardiac Arrest, SCA, AED, Automated External Defibrillator, Drop to Shock

Sudden Cardiac Arrest (SCA) is the leading cause of death in the United States, accounting for over 300,000 lives per year. Therefore, to lessen the odds of another life being lost, it is critical that every business, school, and church equip themselves with an automated external defibrillator (AED).

Early defibrillation is the essential key to surviving a Sudden Cardiac Arrest and the 3^rd link in the American Heart Association’s Chain of Survival. In order to give a victim an optimal chance to live, the American Heart Association recommends defibrillation within the first 3-5 minutes. A victim's chances of surviving SCA decrease by 7-10% with every minute that passes without defibrillation. Therefore, a cardiac arrest victim who does not receive a shock within 8-10 minutes has less than a 20% chance of survival. Unfortunately, few attempts at resuscitation succeed after 10 minutes.

Once an organization has made a proactive decision to protect its members with an Automated External Defibrillator, placement is key to optimizing response times. When determining the location, it is ideal to use a three-minute time frame or the “drop to shock” principle. Once the victim “drops”, the rescuer has ideally no more than three minutes to retrieve the AED, return to the victim, apply the pads and deliver the first shock. This principle will also help determine the number of AEDs needed to sufficiently cover a facility.

An AED should be placed in high traffic, easily accessible area such as a hallway, lobby, or other area where people congregate. When an area has been identified, the AED should be mounted near other emergency medical equipment (First Aid Kit, Fire Alarm).

In addition to determining the correct number of AEDs and placement, there are several other important elements to deploying a successful AED program such as designating a program director, medical oversight, selecting an AED, notifying local EMS and implementing a training program.

Contact HeartSafe America to find out more about sudden cardiac arrest and how your organization can save lives by using the “drop to shock” principle to equip your organization with AEDs. HeartSafe America’s goal is to educate the public about sudden cardiac arrest and how AEDs can save lives.

HeartSafe America; FDA; Medtronic; Physio Control; AED, AEDs

On February 19, 2010, the FDA has released Medtronic/Physio-Control from any and all shipping and manufacturing restrictions. Physio-Control is free to ship worldwide once again.

On February 19, 2010, Medtronic/Physio-Control received approval from the US Food and Drug Administration to resume unrestricted shipments. This approval comes a little over three years after Physio-Control voluntarily suspended shipments as a result of quality system issues identified in a 2006 FDA Audit. Since Physio-Control’s “Stop Ship” announcement in January 2007, they have been working diligently to identify deficiencies and improve all processes. Therefore, in December 2009, Physio-Control completed all of the stipulations set out in 2008 Consent Decree and extended an audit invitation to FDA. After several months of reviewing and re-reviewing all processes, the FDA confirmed Physio-Control to be in compliance and rendered a decision to lift all restrictions.

CLICK HERE to view the letter by Brian Webster, President of Physio-Control.

Contact HeartSafe America today to order all of your Medtronic/Physio-Control products.

HeartSafe America; CPR Training, CPR, Cardiopulmonary Resuscitation, AHA

Cardiopulmonary Resuscitation (CPR) is one of the most basic forms of training an individual can receive to assist a victim during an emergency. Understanding how CPR can be effective during an emergency is important. Training in CPR can make a big difference in the survival rate of a victim.

Below are some frequently asked questions (FAQs) about CPR.

What is CPR?

Cardiopulmonary Resuscitation (CPR) is the process of using chest compressions along with breaths to restore a victim’s heartbeat and breathing.CPR is performed when a victim has stopped breathing and he or she has no pulse.CPR provides a continuous flow of oxygen and blood throughout the body.Our brains can only survive 5 minutes without oxygen without doing permanent damage.CPR can double the survival rate of a victim that has no pulse and has stopped breathing.

What are the current CPR guidelines?

Currently, the American Heart Association recommends that a responder use mouth-to-mouth resuscitation along with chest compressions to perform proper CPR.The AHA guidelines recommend two breaths to 30 chest compressions. Of course, the AHA guidelines are updated every 5 years to increase the rate of survival from using CPR.

If you are a responder and you are unable or unwilling to provide breaths to the victim, then the AHA recommends doing a chest compressions only method.The chest compressions only method still gives the victim a fighting chance at survival.

What is the purpose of CPR Training?

CPR is a simple procedure that can be performed by anyone, but with proper training the responder has a better chance of helping the victim to survive. Being prepared for any situation whether it is an emergency or non-emergency is important.

CPR Training is one of the most basic methods of rescue that any individual could be prepared for. Anyone can be a victim of drowning, sudden cardiac arrest, or other medical condition which can cause the heart to stop.With CPR Training, a responder will learn how to perform effective chest compressions to keep blood and oxygen flowing to the brain and to give breaths that keep oxygen in the lungs.

Do you or your organization need CPR Training?

HeartSafe America offers a variety of life saving courses to equip individuals with the knowledge of how to aid a victim during an emergency.HeartSafe America offers the following life saving courses:

• Basic Life Support for Healthcare Provider
• Heartsaver CPR Training & AED Use
• Heartsaver CPR Training with Infant
• Heartsaver CPR Training & AED Use with Infant
• Heartsaver First Aid Only
• Heartsaver First Aid & CPR Training
• Heartsaver Pediatric First Aid with Infant
• Heartsaver Pediatric First Aid without Infant
• Blood Borne Pathogens Training

HeartSafe America is an official American Heart Association Training Site that trains individuals as well as large organizations in life saving courses.

Contact HeartSafe America today to get more information about the life saving courses offered and to register yourself or your organization for the courses.

HeartSafe America; Maryland House Bill 293; AED, AEDs

The State of Maryland has introduced House Bill 293 which required a physical therapy office to have an automated external defibrillator (AED) on site and to have a staff member trained in CPR and how to use the AED.

On January 27, 2010, the State of Maryland introduced House Bill 293. House Bill 293 will require Physical Therapy Office to have an automated external defibrillator (AED) on site. The House Bill 293 does not apply to any licensed physical therapist who works in a setting outside of the physical therapy office or hospital or related institutions stated in Article 19-301 of the Health – GeneralHouse Bill 293 prohibits any licensed physical therapist from performing physical therapy unless there is an automated external defibrillator present and there is a staff member present that has received certification in CPR and the use of the AED.

House Bill 293 will go into effect on October 1, 2010.

CLICK HERE for more details about House Bill 293.

Cardiac Science recalls 12,200 more AEDs

Cardiac Science voluntarily recalls 12,200 more automated external defibrillators (AEDs). These AEDs may fail to deliver therapy to a victim suffering from Sudden Cardiac Arrest.

During February 2010, Cardiac Science has issued another voluntary recall for an additional 12,200 automated external defibrillators (AEDs). The voluntary recall is a separate issue from the November 2009 recall. The AEDs included are the Cardiac Science Powerheart, CardioVive, and CardioLive. The AEDs that have been affected were manufactured during October 19, 2009 through January 15, 2010. The AEDs may fail to deliver therapy, thus leading to a possible death of the victim.

The following Cardiac Science AED models are included in the voluntary recall:

• CardioVive models: 92532
• CardioLive models: 9200G, 9231

Cardiac Science will ship replacement models starting February 15, 2010. If you are concerned that your AED is one of the affected models, please check the serial number of your AED here.

HeartSafe America; Revised State of Oregon Senate Bill 556; Senate Bill 1006; AED, AEDs

The State of Oregon is requiring certain organizations to have an automated external defibrillator on site. Senate Bill 556 went into affect on January 1, 2010. Senate Bill 1006 was released in February 2010 with revisions to Senate Bill 556.

On January 1, 2010, the State of Oregon’s Senate Bill 556 will take effect. The State of Oregon created Senate Bill 556 to ensure the safety of anyone that suffers from sudden cardiac arrest at a place of business by requiring organizations to obtain an automated external defibrillator (AED).

During February 2010, the State of Oregon has released a revision of Senate Bill 556. The State of Oregon’s Senate Bill 1006 has specified in detail which organizations are required to have an automated external defibrillator (AED) on site. The revisions require organizations that a single building, with 50,000 square feet with indoor floor space, where business activities are conducted and has at least 50 or more persons in the building a day to have an AED.

Senate Bill 1006 now includes “health clubs” as a required organization that will need to have an AED if that organization falls under the guidelines of the bill. A health club is described as any organization where exercise or athletic activities take place and the patrons participate by paying a fee.

The only organizations that are excluded from Senate Bill 1006 are facilities associated with the education service district, public charter school, or school district.

To view more details about Senate Bill 1006, please CLICK HERE.

HeartSafe America; State of Oregon Senate Bill 556; AED, AEDs

The State of Oregon has instituted a new AED law that requires certain organizations to obtain an AED for their locations. This new AED law goes into effect on January 1, 2010.

On January 1, 2010, the State of Oregon’s Senate Bill 556 will take effect. The State of Oregon created Senate Bill 556 to ensure the safety of anyone that suffers from sudden cardiac arrest at a place of business by requiring organizations to obtain an automated external defibrillator (AED).

The organizations that are required to purchase an AED are organizations that have a public access building of 50,000 square feet or more and that have 25 or more people in the building at one time. The only organizations that are excluded from this new law are schools and churches.

To view the details about the State of Oregon’s Senate Bill 556, please CLICK HERE.

Of course, it is recommended that an organization should evaluate their building to determine if they need more than one AED. The reason for the evaluation is due to “drop and shock” rule. The “drop and shock” rule states that it should take no more than 2-3 minutes for a responder to retrieve the AED, drop the AED, and shock the victim. This rule gives the victim the largest possibility of surviving sudden cardiac arrest.

HeartSafe America, Inc. would like to assist the organizations in the State of Oregon that are required to obtain an AED. HeartSafe America offers six of the top AED manufactures. HeartSafe America works with each organization on a one on one basis to determine the proper amount of AEDs necessary to stay within the 2-3 minute “drop and shock” rule.

Contact HeartSafe America or shop our online store today to find out how you can make your organization “heart safe”.

Cardiac Science Recall on Powerheart and CardiacVive AEDs

Cardiac Science issued a voluntary recall in November 2009 on Powerheart and Cardiac Vive AEDs. The FDA issued a warning letter about the defective AEDs.

During November 2009, Cardiac Science Corporation issued a voluntary recall on Powerheart and CardioVive automated external defibrillators (AEDs) manufactured during August 2003. The reason for the recall is due to the fact that the AED is failing to deliver an electrical shock. The self-test that the AED performs on itself does not show that there is an error with the machine. If a responder attempts to use the defective AED, then the victim has to potential to not receive an electrical needed to restart his or her heart.

Cardiac Science Corporation is correcting the issues with each of the affected AEDs by performing voluntary field corrections on the AED.The following Cardiac Science AED models are included in the voluntary recall:

• Powerheart models: 9300A, 9300C, 9300D, 9300E, 9390A, 9390E
• CardioVive models: 92531, 92532, 92533

If your organization owns one of either of these AED models, you are encouraged to contact Cardiac Science immediately to ensure your AED is not a defective model. The FDA has released a warning letter since Cardiac Science has issued its voluntary recall. The FDA felt that the voluntary recall that Cardiac Science was not sufficient, and felt that a warning letter needed to be released since the AED had the potential to fail to function properly. The FDA wanted to make sure the public knew of the severity of the defective AEDs. The FDA recommends that if another AED is available on site that it should be used in place of the Cardiac Science AED until Cardiac Science corrects the defective AEDs.

To view the FDA warning letter, please CLICK HERE.

Philips Issues Worldwide Recall of Select HeartStart FR2+ AEDs

On September 28, 2009, Philips announced a worldwide recall on the HeartStart FR2+ AEDS. The recall is a voluntary recall, it was not mandated by the FDA. Philips is recalling the HeartStart FR2+ AEDs that were manufactured during May, 2007 thru Janurary, 2008.

The reason for the recall is due to a faulty memory chip in the Philips HeartStart FR2+ AED. Philips is concerned that the memory chip may fail and cause the AED not to function properly.

If you are concerned that your Philips HeartStart FR2+ AED may be part of the recall, you can click on the link below and check your serial number. If you have any questions in regards to the recall or your HeartStart AED, you can contact Philips at 1-800-263-3342.

www.philips.com/FR2PlusAction

If you are interested in the full story that this blog was based on, please click here.