Heart to Heart
Vol 1 Issue 4
May 2006
Inside this issue

Cryoablation: A Safer Method for Treating Rhythm Disturbances

New Infrared Spectroscopy (NIRS) and its application in the Heart Center
Early Detection of Heart Transplant Rejection: Room to Improve

Ventricular Assist Device (VAD) for Children

Is there a perfect recipe?

Social Work in the Heart Center

Spotlight on Kris McCullough, R.N.
Spotlight on Wes McKamie, C.C.P.

Cryoablation: A Safer Method for Treating Rhythm Disturbances

Volkan Tuzcu, M.D.; Director of Electrophsiology and Pacing, Arkansas Children's Hospital; Associate Professor of Pediatrics, University of Arkansas for Medical Sciences College of Medicine

Electrophysiology and catheter ablation procedures lead to permanent cure in the majority of patients with tachyarrhythmias. Until recently, RF catheter ablation has been the conventional technique of elimination of abnormal cells responsible for these problems. Using this approach, successful treatment can be achieved in more than 90 percent of patients. Because long-term medication management does not lead to cure and also due to the concerns with medication side effects, most patients and physicians prefer catheter ablation procedure as their treatment approach.

Lately, cryoablation has been used throughout the world for the ablation of tachyarrhythmias originating from the high-risk areas in the heart. Since cryoablation allows us to freeze at different temperatures and therefore reversible effect can be tested, the chance of adverse effects with the ablation in these risky spots has been virtually eliminated. This benefit is even more significant in young children.

We have been utilizing cryoablation as the primary choice of catheter ablation in children for the majority of problems, unlike other centers where it is used only in high-risk areas in the heart. Despite its safety profile, the freezing effect of cryoablation required modification of the technique in order to increase the success rates. Most of the recent studies have reported lower success rates with cryoablation compared to RF ablation, however due to the safety factor it is still utilized commonly. Using our three-dimensional mapping system to guide us in reaching the precise treatment spots, we have achieved similar acute success rates with cryoablation compared to RF ablation. Recent experience with the accessory pathways has revealed acute success rates of about 94 percent. So far, no complications have occurred with the procedure. Besides, no significant complications have been reported thus far in the world.

The future of the tachyarrhythmia management likely will be impacted significantly with the introduction of cryoablation. Catheter ablation is likely to be the primary choice of treatment for most patients and physicians. This is even more significant in children because adverse effects are more likely with the RF ablation in small hearts. Arkansas Children’s Hospital will continue to contribute to the medical and scientific community in the advancement of this new technique’s application in children.

Back to Top

Near Infrared Spectroscopy (NIRS) and its application in the Heart Center

Adfnan T. Bhutta, MBBS, FAAP; Co-Medical Director, Cardiovascular Intensive Care Unit, Arkansas Children’s Hospital; Instructor, Pediatric Critical Care Medicine and Cardiology, University of Arkansas for Medical Sciences College of Medicine


In December 2005, the Heart Center started using a new monitor called the INVOS® cerebral oximeter. Cerebral oximetery is a new patient safety monitor and management tool that has been shown to significantly reduce adverse neurological outcomes. The cerebral oximeters use near-infrared spectroscopy (NIRS) to non-invasively and continuously monitor changes in blood oxygen saturation. It directly monitors changes in the regional oxygen saturation (rSO2) of the predominately venous blood in the brain, which is influenced by oxygen delivery and consumption. When changes in oxygen delivery or consumption occur, the physician can respond with simple interventions to minimize or prevent brain injury.

The use of NIRS technology was first described in humans in the 1970s.  Since then, the  NIRS based technology has found diverse applications in  monitoring of deltoid muscle oxygen supply to guide resuscitation, monitoring of splanchnic circulation in neonates with acute abdomen, and in measurement of regional blood supply in skeletal muscles to assess effects of exercise.

However, the most common application of this technology has been in assessing regional cerebral saturation. This application stems from the multiple studies which have shown a positive correlation between cerebral oxygenation as measured by NIRS and jugular venous saturation. One of theses studies was conducted by members of our heart team at Arkansas Children’s Hospital. Clinical studies in adults have suggested that a decline in rSO2 values of >20 percent from baseline or absolute values of less than 50 are associated with decreased cognitive function and prolonged ICU stay . Such a sharp decline from a baseline measurement or a low absolute value may affect long-term neurological outcome.
           
As many as 50 percent of neonatal patients undergoing cardiac surgery on cardiopulmonary bypass (CPB) are at risk for developing mild ischemic lesions, primarily in the form of PVL, postoperatively. Therefore, a monitor that allows clinicians to follow trends in cerebral oxygenation could identify critical periods associated with inadequate oxygenation, which in turn could lead to early interventions to minimize such periods.

After initially being utilized in the operating rooms, it is now increasingly being used as a non-invasive method to monitor regional oxygen saturations during post-operative period after cardiac surgery; and some experts have suggested that rSO2 should be routinely used to guide therapy to minimize periods of low oxygen delivery.

In November 2005, Somanetics Corporation (the makers of the only commercially available NIRS monitors in the United States) received clearance from the FDA to expand monitoring with the INVOS® system in regions of the body other than the brain.  This allows monitoring of oxygen in skeletal muscle tissues and abdominal organs in addition to the brain (commonly referred to as regional somatic saturation) .  When combined with brain oxygenation monitoring, additional information is available for clinical decision-making in infants and children in the operating room and critical care areas.

The non-invasive measurement is made with two sensors, called SomaSensors. Harmless near-infrared light passes through the skin into deeper tissue. With two detectors at different distances from the light source, two depths of penetration are measured. The difference in these measurements eliminates signals common to both, minimizing changes occurring in superficial tissue such as the skin.

Continuous visibility of cerebral and somatic oxygen saturation levels allows individualized patient care in real time and alerts the team members of a potential problem much earlier. This has been not as easily possible in the past, as it required placement of invasive catheters and lines inside the heart, veins or pulmonary arteries. We hope that the availability of this device at each bed in the CVICU and for selected patients on CV East will further enhance the ability of our team to provide the best possible care for our patients.

Back to Top

Early Detection of Heart Transplant Rejection: Room to Improve

R. Erik Edens, M.D., Ph.D.; Assistant Professor of Pediatric Cardiology, University of Arkansas for Medical Sciences College of Medicine; Arkansas Children’s Hospital Research Institute

Every year more than 25,000 organs are transplanted into patients in the United States, according to data from the United Network for Organ Sharing. This includes nearly 300 pediatric heart transplants. Organs transplanted from one person to another are continually at risk of being recognized by the recipient’s immune system and rejected. In patients who have received heart transplants, rejection may result in severe illnesses and even death.  

Heart transplant rejection is challenging to diagnose.  Essentially, two primary techniques are used to detect rejection: heart biopsy and echocardiogram. Heart biopsy is a procedure conducted in the catheterization laboratory during which tiny pieces of the heart are removed for examination under a microscope.  When rejection occurs, we see a type of white blood cell called a lymphocyte amongst the heart muscle cells where normally no lymphocytes would be present (see pictures).  Heart biopsies are procedures that children uniformly dislike. They also are somewhat invasive and carry some procedural risk.  The development of new testing that could decrease or even eliminate the need for heart biopsies would be welcomed by patients, families and doctors alike. 

The second method commonly used to detect rejection is echocardiography. An echo is an ultrasonic picture of the heart used in transplant patients to examine how well the heart is functioning and to determine the thickness of the heart muscle.  Echo images can provide important clues about the possibility of rejection.  Unfortunately, echo is not capable of detecting rejection at early stages and sometimes significant damage can occur to the transplanted heart before rejection can be detected by echo. Clearly, better methods to detect rejection early and easily are needed to improve the survival and health of these special patients.

Immunologists have recognized for decades that immune cells communicate with one another in our bodies by sending small proteins through the bloodstream to other cells.  These protein messages are different depending on what the cell wants to communicate to the other cells. For example, there likely are different proteins released when infection occurs than when rejection occurs.  It likely would be tremendously helpful to doctors and nurses caring for transplant patients to be able to detect and decode these protein messages and thus understand what the immune system is doing at any given time. 

Until recent years we have had only very limited ability to test the blood of transplant patients for these protein messages.  Most previous testing methods required several teaspoons of blood for each protein to be tested. A recent technological advance called Luminex Bead Array uses a dual laser detection system and is so sensitive that up to 100 proteins can be detected on as little as two drops of blood.  The ACH Research Institute purchased one of these instruments in 2004, and it has been used in a variety of research projects conducted at ACHRI.

We have received grant funding to pay for testing of transplant patient serum using the Luminex instrument.  A team of researchers from Cardiology, Microbiology & Immunology, Pathology and Biostatistics are assisting us in this endeavor. Our hope is that the Luminex technology will allow us to develop a safe and rapid blood test for transplant patients that will allow us to detect rejection at earlier stages, and thus to change treatment plans before any damage occurs to the transplanted heart.

Back to Top

Ventricular Assist Device (VAD) for Children

Michiaki Imamura, M.D., Ph.D .; Pediatric Cardiac Surgeon, Arkansas Children’s Hospital; Assistant Professor, Department of Surgery, University of Arkansas for Medical Sciences College of Medicine.

Management of Severe Heart Failure
The heart is the organ pumping blood in two directions: to the whole body and to the lungs. The heart has two pumping chambers of the left and right ventricles.  The left ventricle is pumping blood to the whole body. The right ventricle is pumping blood to the lungs.
When the people suffer severe heart failure (decrease in pumping ability of the heart), medical treatment is instituted at first.  After the medical treatment is maximized or is expected not to be enough to control heart failure, surgical treatment is considered.  Occasionally, the mechanisms of this heart failure are anatomical problems of holes inside the heart, narrow pathways of the blood or malfunctioning valves. In these situations conventional operations of closing holes, opening pathways or repairing valves are performed. In other instances, the mechanism of heart failure is the heart muscle itself.  This problem may be temporary or  permanent. If the patient is suffering severe heart failure temporarily, the patient is treated with mechanical circulatory support of ECMO or VAD.  The use of this machine is called “bridge to recovery”.  If a child is suffering heart failure permanently, the patient needs cardiac transplantation. While waiting for cardiac transplantation, some patients experience further deterioration and need ECMO or VAD. This type of usage is named “bridge to transplantation”.   
Additionally, in some cases only the left or right ventricle gets severe heart failure, in the other cases both right and left ventricles get severe heart failure. 

What is ECMO?
The ECMO is extracorporeal membrane oxygenation, and consists of tubes, artificial heart (pump) and lung (oxygenator).  This modality has been used at our center for more than 15 years.  Our center has among the most experience in the world in this modality.   This system works great for relatively short periods of up to two weeks.  Occasionally, we need to continue this usage more than two weeks. The benefits of this system are that it is a simple procedure and it provides support for the lungs. ECMO is the only mechanism able to provide support to both the heart and lungs. The deficits of this support are high tendency of cerebrovascular event (stroke and cerebral bleeding), necessity of periodical circuit change and inability of free mobilization. With this system, children usually need mechanical ventilatory support with an endotracheal tube and cannot eat by themselves. 

What is VAD?
VADs consist of tubes, pumps and power sources and controllers.  Blood is sucked from the heart and returned to the circulation, and this can assist the heart in pumping blood.  There are several kinds of classification of VADs.  One is intracorporeal (pump is staying inside the body) or  extracorporeal (outside the body).  The other is pulsatile and non-pulsatile. The last is LVAD, RVAD and BiVAD. LVAD is the abbreviation of left ventricular assist device: helps the left ventricle. RVAD is that of right ventricular assist device: helps the right ventricle. BiVAD is that of biventricular assist device: helps both the left and right ventricles. BiVAD is the support of two ventricles.  Some systems have the ability to be used as BiVAD.  Others are only used as LVAD. 
In adults, several types of VADs such as HeartMate, Novacor, Abiomed, Thoratec and DeBakey have been used for more than decade. 
The advantages of VAD are that it is easy to mobilize the patient after implantation and the durability of longer period support.  The disadvantages of VAD are bleeding, infection, thromboembolism (stroke), hemolysis (red blood cell damage), and necessity of median sternotomyoperation (heart surgery).  Previously, several adolescent patients required these types of support in our hospital. They were transferred to another adult hospital in town and had implantation there.  In our heart center, we have used two kinds of VAD in the last two years. One is DeBakey VAD Child, and another is Berlin Heart. 

What is DeBakey VAD Child?
DeBakey VAD Child is a miniaturized heart pump.  This pump works by electromagnetic energy, which creates a magnetic field.  The pump consists of an external part and an internal part.  The internal part with propels is rotating and blood flows between these two parts.  This heart pump is named after its designer and renowned heart surgeon Michael DeBakey.   This pump creates flow continuously and does not create pulsation. 
This machine was first manufactured for the adult. Recently, tubing parts of this machine were modified to fit to children.  DeBakey VAD Child has the same actual pump part as the regular DeBakey VAD.  In September 2004, we performed the second implantation of this type of device in a 14-year-old boy.  Subsequently, this patient had successful cardiac transplantation.   

What is Berlin Heart?
Berlin Heart is a paracorporeal (outside the body) pneumatic pump VAD.  Blood is sucked into the pump and ejected into the artery.  This pump produces pulsation. This VAD has awide range of different sizes of pumps and cannulae.  This pump has been used in patients ranging from neonates to adults.  This device currently is not allowed by the FDA for use.  For this system, usage permission from the FDA is required each time.  Since April 2005, we have used this device four times. Two patients had BiVAD and others had LVAD.  The second patient had successful bridge to transplantation.  The last two patients were on support on April 14, 2006.  A total of 41 pediatric patients inthe United States had this device from 2000 through April 14, 2006. 

What is the difference between DeBakey VAD Child and Berlin Heart?
DeBakey does not create pulsation, but Berlin Heart does.  The pump of the device is outside the body in Berlin Heart and is inside the body in DeBakey VAD Child.  DeBakey VAD Child has better ambulation after implantation.  Berlin Heart has an ability to be used as RVAD or BiVAD as well as LVAD.  DeBakey VAD Child is only used for LVAD. 

What is the future direction of ACH Heart Center for Heart Failure Management?   
Because we have been taking care of a large number of heart failure patients with ECMO, VAD and cardiac transplantation, we are one of theleading centers for managing pediatric heart failure. 

We have to keep up with new medical and surgical advancements in this field. We have to keep improving and evolving our team. Since 2004,  six children’s hospitals in the United States, including our hospital, were chosen to use DeBakey VAD Child. 

Back to Top

Is there a perfect recipe?

Luis M. Zabala, M.D.; Assistant Professor of Anesthesiology, section of Pediatric Cardiac Anesthesiology, University of Arkansas for Medical Sciences College of Medicine; Arkansas Children’s Hospital

Lynn Harness, C.C.P.; Department of Pediatric Perfusion, Arkansas Children’s Hospital


The repair of congenital heart defects in the pediatric population requires, in many instances, extracorporeal circulation by means of cardiopulmonary bypass (CPB). The CPB circuit must be primed with either blood or crystalloid solution to provide an air-free circuit to be integrated with the patient’s own circulation. Once on bypass, hemodilution takes place. Consequently, the concentrations of all cellular and protein components in the intravascular compartment decrease, thus decreasing plasma oncotic pressure. A decrease in intravascular oncotic pressure causes fluid to move towards the extra vascular space to tissues with higher oncotic pressure, producing edema. This affects all organs, including kidneys, brain, liver, heart and lungs.

Another effect of CPB is the initiation of a complex sequence of humoral and cellular interactions responsible for a generalized inflammatory reaction which leads to increased vascular permeability and postoperative tissue edema. Such events occur during exposure of the patient’s blood to the surfaces of the CPB circuit. In addition to hemodilution, this inflammatory reaction is associated with increased bleeding, generalized edema, myocardial depression, low cardiac output, prolonged respiratory impairment and prolonged ICU stay.

Strategies intended to improve outcomes in pediatric patients following cardiopulmonary bypass (CPB) have been aimed primarily at improving surgical techniques, controlling the inflammatory response through anesthesia and perfusion interventions, and at limiting the degree of hemodilution during extracorporeal circulation.

Overwhelming improvements have unfolded in the field of pediatric congenital heart disease over the past two decades. A better understanding of the patient’s response to extracorporeal circulation has prompted the search for a “magic recipe” in an attempt to improve clinical outcomes. At our institution, the combination of superior surgical skills, patient-specific anesthesia techniques and innovative perfusion strategies has set us apart from other pediatric institutions. This brings us closer to our goal: the best outcome possible.

The addition of modified ultrafiltration (MUF) to the management strategy of our patients represents a step forward in achieving better clinical outcomes. MUF is a technique that removes excess fluid from the patient’s vascular system, thus increasing colloid oncotic pressure. By restoring intravascular colloid oncotic pressure, the fluid gradient generated by hemodilution reverses, creating a net movement of fluid back into the intravascular space, decreasing tissue edema.

MUF is performed after weaning the patient from CPB but before protamine administration and arterial decannulation. The mechanics of our circuit involve withdrawing blood from the aortic cannula, pumping the blood through a filtration unit and re-infusing warm hemoconcentrated blood into the patient through a venous cannula. The result is blood with a high oncotic pressure. This hemoconcentrated blood is then reinfused directly into the patient’s right heart/lungs before entering the systemic circulation. This helps reduce pulmonary edema.

MUF is usually instituted at a rate of 10-30 ml/kg with a target volume of ultrafiltrate of 15-30/ml/kg/min over an interval of 10 to 15 minutes. Also, blood from the venous reservoir of the CPB circuit is pumped to the MUF circuit; this allows processing of the extracorporeal circuit volume and re-infusion of this hemoconcentrated circuit volume along with the patient’s hemoconcentrated blood through the venous cannula. End points of MUF vary among pediatric institutions and can be defined by time, total volume removed, or goal hematocrit. At our institution, we utilize MUF for a period of at least 10 minutes with great success.

The use of this technique has provided consistent evidence of reduced postoperative blood loss, decreased blood product transfusion and significant reduction in the accumulation of total body water following CPB. The reduction in total body water is associated with improved respiratory mechanics, improved myocardial function, increased blood pressure and increased hematocrit following MUF. In addition, some authors suggest that MUF attenuates the CPB induced coagulopathy and significantly decreases certain pro and anti-inflammatory mediators responsible for acute renal failure, prolonged mechanical ventilation, and capillary leak syndrome, among others.   

This novel perfusion strategy, in addition to intravenous steroids, advances in anesthetic myocardial preconditioning, limited cardiopulmonary bypass and cross clamp times. Post-operative cardiac intensive care by specialized physicians may pave the road for a “perfect recipe” in the future.

Back to Top

Social Work in the Heart Center

Janna Vandiver, LMSW; clinical social worker in the CVICU and Cardiology Clinic, Arkansas Children’s Hospital

Many times when families are admitted to the hospital, they do not expect to meet a social worker as part of their care team. However, here at ACH we have 25 master’s level social workers who serve our families. What does a medical social worker do? The goal of social work in the Heart Center is to recognize the impact of illness on patients and their families and to assist families in coping with the unpredictability of illness. Most patients admitted to the Heart Center are scheduled to undergo or have already undergone heart surgery or another procedure. This can be a frightening time for both the patient and his or her family. Depending on the age of the patient, a social worker will work with the patient and family members to assess their understanding of the patient’s diagnosis, condition and treatment. The social worker will complete an assessment to gather information about their social support and life outside the hospital. This information will help to determine what, if any, assistance they may need from social work, the hospital or outside agencies.

  1. Referrals are often made to assist families in accessing community resources such as counseling and early intervention services. This assessment is also an opportunity to identify beliefs, customs and ways of coping that are unique to the family and may impact the care and services we provide. Determining whether a family has had any experiences in a medical setting or being aware of their educational background and capacity to comprehend complex information will assist staff when providing information to a family.

During the hospitalization, a social worker will continue to provide support to families as they experience the emotional ups and downs that often occur while their child is in the hospital. Some examples of interactions that a social worker would have with a family might be problem solving and conflict resolution, advocating for the family’s or patient’s needs or preferences, facilitating communication with other staff and providing encouragement to get involved and be informed about the care of their child.

  1. As significant people in a child’s life, parents will often feel helpless or out of control while their child is hospitalized and members of the staff are caring for their child. Sometimes families are not comfortable asking questions or expressing their opinions and may need to be encouraged to share their thoughts and feelings about their experience or their wishes for the child. For some families, being informed will diminish their anxieties about the hospital, procedures and the care that is provided. For other families, too much information is overwhelming and can intensify their uncertainty and apprehension. It is important to be aware of how a family functions when interacting with it. A psychosocial assessment of the patient and his or her family can offer this and other helpful information.

Social work also performs a variety of other duties in the Heart Center. For example, a social worker is assigned to every heart transplant patient to provide support for the family throughout its journey. An assessment is conducted before a patient is listed for a heart, and emotional support is provided during the transplant process and post transplant during clinic visits. When a death occurs in the Heart Center, a social worker is present at the time of death to provide support and written grief materials, to assist with contacting a funeral home and also to follow up with bereavement support after the family returns home. Families may need concrete services during their hospitalization such as transportation or lodging arrangements, and a Family Services Assistant (who is also part of the Social Work department) can provide assistance and appropriate referrals for those needs.

When families come to ACH they are faced with new sights, new sounds, new people and in the Heart Center they may be learning a new vocabulary about their child’s heart condition. Any information we can obtain about a family to make the care we provide more personal and individualized will help us serve the families with care, love and hope. Our goal is for ACH to meet not only the medical needs of the family, but also the emotional and psychosocial needs, in order to make a potentially overwhelming experience more positive for the patient and his or her family.

Back to Top

Spotlight on Kris McCullough, R.N.

Nurse in the CVICU

What is your role at ACH, and how long have you worked here?
I am an R.N. in CVICU – East.  I have worked at ACH for two and a half years.

Why is your job rewarding?
It is very fulfilling to see patients come in so sick and see them being discharged able to walk without using oxygen or able to eat without working up a sweat and running out of breath. Or when our patients come in for clinic visits and take the time to come upstairs to see us, and they’re smiling and doing so well, it makes everything we do worthwhile.

How did you become interested in pediatric cardiology or cardiovascular surgery?
I was an adult-care cardiac nurse prior to coming to ACH.  The heart has always fascinated me because of all of the problems that can occur; whether congenital or not, and still function. After taking a couple of years off from nursing and getting a B.B.A. in Finance, I decided that I might be able to “handle” pediatrics, and I really wanted to stay in cardiology.  I didn’t realize that adult cardiology and pediatric cardiology have absolutely NOTHING in common!  I haven’t regretted it yet!

What do you want people to know about the Heart Center at Arkansas Children's Hospital?
That everything we do is for the patient. Our staff is knowledgeable and approachable. From the surgeons to housekeeping, we all contribute a part in the patients’ care. We do what we do because we enjoy it. We attempt to make the patient and family as comfortable as we can so they can feel confident in the care their child is getting.

What do you enjoy most about working with children?
The perks! There is nothing better than holding a baby and having them smile up at you or fall asleep on your shoulder. When the family stops by to see us after a clinic visit, you know that somehow, you have touched that family in a positive way, and they are very grateful for that.

What has been your most memorable moment working in the Heart Center at Arkansas Children's Hospital?
I have a bunch of good memories, but the most memorable would be one that happened very recently. One of our patients, who had been through a couple of transplants and had recently been put on comfort-care and then became one of our “miracles”, had asked another nurse to come tell me “not to be afraid to come see” her. It was wonderful to think that she had thought of me (along with many others, but what an honor to be included in this group of people!) when she really needed to be thinking about getting better. This “miracle” is why I tell people that I became a nurse. No matter how bad it gets, the good always outweighs the bad.

What is your greatest professional achievement?
Actually, my greatest professional achievement is non-nursing.  It was being chosen “Outstanding Student in General Finance” and being asked to be a Marshal and walk at the head of the line at graduation.

Back to Top

Spotlight on Wes McKamie, C.C.P.

Perfusionist, Pediatric Cardiothoracic Surgery

What is your role at ACH, and how long have you worked here?
I am a cardiovascular perfusionist, and I will have my one-year anniversary in June of 2006.  This is my second time as an employee of ACH. I worked as a Respiratory Therapist from 2000 to 2003.    

 How is your job rewarding?
I feel my job is rewarding in a number of ways. I not only get to do something that I am fascinated by, but I also get to be a part of giving children second chances at life. 

How did you become interested in pediatric cardiology or cardiovascular surgery?  During my time as a respiratory therapist, I became part of the ECMO team here, and that is what opened my eyes to the world of cardiac surgery and perfusion. I felt that this area of service would keep me consistently motivated and give me a chance to grow professionally. 

What do you want people to know about the Heart Center at Arkansas Children's Hospital?
 It is a place that truly is filled with some of the best individuals I have ever met. The amount of care and compassion that I see given to the children we serve here is amazing.

What do you enjoy most about working with children
Working with children is very rewarding because you know that you are helping someone who has a lot of promise before them. These kids have been faced with some tremendous challenges and to see them overcome those day in and day out is a great feeling.

What has been your most memorable moment working in the Heart Center at Arkansas Children's Hospital? 
So far I would have to say the placement of the Berlin Heart into our hurricane victim and then transplanting him would have to be my most memorable moment.

What is your greatest professional achievement? 
My greatest achievement thus far is being hired to be a part of one of the best heart centers in the country.

Back to Top

 

New Nurses in the Heart Center

During the last few months, the Heart Center at Arkansas Children’s Hospital welcomed 13 new nurses to the team. We are excited to have them on-board to help us better fulfill our mission of providing care, love and hope to the region’s youngest cardiac patients.

 

Back to Top

 

 

 





Arkansas Children's Hospital
Arkansas Children's Hospital, 800 Marshall St., Little Rock, AR 72202-3591, (501) 364-1100 or TDD (501) 364-1184

Web Site Feedback Survey | ACH is a tobacco free campus.

Joint Notice of Privacy Practices | Terms & Conditions of Use | Report Concerns About Patient Care & Safety | Site Index

About ACH | Your Visit to ACH | Community Outreach Programs
Medical Services | Career Opportunities | Volunteer Opportunities
ACH Foundation | Press Room | Resources | Research | Kids Only | Contact Us