2015 - Texas Children`s Hospital
Transcription
2015 - Texas Children`s Hospital
2015 Texas Children’s Heart Center 6621 Fannin Street Houston, Texas 77030 texaschildrens.org/heartoutcomes texaschildrens.org/refer ©2016 Texas Children’s Hospital. All Rights Reserved. Heart233 060916 H E A RT C E N T E R 2 0 1 5 1 H E A R T C E N T E R O U T C O M E S 2 015 Table of Contents Welcome. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Texas Children’s Hospital and Baylor College of Medicine . . . . . . . . . . . . . . . . . Texas Children’s Heart Center . . . . . . . . . . . . . . Congenital Heart Surgery Service . . . . . . . . . . . . Heart Failure and Transplant Program . 8 . . . . . . . . . . . . . . . . . 26 . . . . . . . . . . . . . . . . . . . . . . . 29 . . . . . . 33 . . . . . . . . . . . . 36 . . . . . . . . . . . . . . . . 37 Preventive Cardiology Program . Cardiovascular Anesthesia . 31 . . . . Adult Congenital Heart Disease Program Cardiovascular Intensive Care Unit. . . . . . . . . . Cardiac Developmental Outcomes Program 41 . . 43 . . . . . . . . . . . . . 44 . . . . . . . . . . . . . . . . . . . . . . . . 46 Outcomes and Impact Service. . . . . . . . . . . . . . . . . . . . 48 . . . . . . . . . . . . . . . . . . . . . . . . . . . . 50 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 58 Medical Staff Directory Publications . Referrals 4 19 Diagnostic Testing and Cardiac Imaging . Leadership Team . 3 . . . . . . . Interventional Cardiology Electrophysiology . 2 For access to Texas Children’s Heart Center outcomes information, visit texaschildrens.org/heartoutcomes. 2 H E A RT C E N T E R 2 0 1 5 Dear colleagues, parents and friends, We are pleased to share with you the 2015 Texas Children’s Heart Center Outcomes Book. With more than 900 operating room cases and over 25,600 patient encounters, this year has been full of activity and growth. This report covers highlights from our Heart Center programs, including incredible patient stories and important programmatic developments. We continue to develop all of our Heart Center teams to better meet the needs of our patients and families. In 2015, we welcomed several new physicians to our center, bringing the combined Heart Center staff to over 125 providers. Our facilities also continue to grow. We opened our first-of-its-kind Pediatric Heart Failure Intensive Care Unit in 2015, aimed at providing highly specialized care for children with heart failure, as well as those requiring intensive care before and after heart transplant, and those on mechanical cardiac support. Texas Children’s Hospital The Woodlands is in its final construction stages and remains on target to open in 2017. We are actively recruiting a team to meet the specific needs of this community. This will be Texas Children’s second community hospital and third pediatric hospital. The main campus of Texas Children’s Hospital is also undergoing a $575 million expansion to improve care and the patient/family experience in high-acuity areas such as surgery and intensive care. In 2015, construction began on a pediatric tower that will be the new home to Texas Children’s Heart Center, including the outpatient clinic, cardiovascular operating rooms and catheterization labs. Slated for completion in 2018, the 25-floor tower will feature state-of-the-art technology and 130 beds for pediatric and cardiovascular intensive care. Texas Children’s Heart Center strives to provide every appropriate procedure available for patients with pediatric and congenital heart disease. Through our innovations in research and commitment to improving all aspects of patient care, our goal is to provide the very best possible treatment for every patient. We hope you enjoy reading about our outstanding team and their activities. Thank you for your interest in our center. Sincerely, Charles D. Fraser, Jr., M.D. Surgeon-in-Chief, Texas Children’s Hospital Chief of Congenital Heart Surgery,Texas Children’s Hospital Susan V. Clayton Chair in Surgery,Texas Children’s Hospital Donovan Chair in Congenital Heart Surgery,Texas Children’s Hospital Professor of Surgery and Pediatrics, Baylor College of Medicine Daniel J. Penny, M.D., Ph.D., M.H.A. Chief of Cardiology,Texas Children’s Hospital Professor of Pediatrics, Baylor College of Medicine Emad B. Mossad, M.D. Director of Pediatric Cardiovascular Anesthesiology,Texas Children’s Hospital Professor of Anesthesiology and Pediatrics, Baylor College of Medicine Lara S. Shekerdemian, M.D., F.R.A.C.P., M.H.A. Chief of Critical Care,Texas Children’s Hospital Professor of Pediatrics, Baylor College of Medicine H E A RT C E N T E R 2 0 1 5 ® Texas Children’s Hospital and Baylor College of Medicine Texas Children’s Hospital is one of the nation’s largest and most comprehensive specialty pediatric hospitals, with more than 3.5 million patient encounters in 2015. Texas Children’s also operates Texas Children’s Health Plan, the nation’s first health maintenance organization (HMO) created just for children, and Texas Children’s Pediatrics, the nation’s largest primary pediatric care network with more than 50 practices throughout the greater Houston community. The main campus of Texas Children’s Hospital is located near downtown Houston in the Texas Medical Center, the largest medical center in the world. The main campus includes nearly 500 licensed inpatient beds; the Clinical Care Center for outpatient visits; the Feigin Center for pediatric research; and Texas Children’s Pavilion for Women, a comprehensive OB/GYN facility with a focus on high-risk births. Located nearby is the Texas Children’s Hospital Jan and Dan Duncan Neurological Research Institute, a basic research institute dedicated to solving childhood neurological diseases. To serve the rapidly growing population in West Houston, Texas Children’s Hospital West Campus opened in 2011 with acute care and critical care beds, an emergency center, surgical suites and more than 20 subspecialty clinics. In 2017, a second community hospital, Texas Children’s Hospital The Woodlands, will open. The mission of Texas Children’s is to create a healthier future for children and women throughout our global community by leading in patient care, education and research. Renowned worldwide for our expertise and breakthrough developments in clinical care and research, Texas Children’s Hospital ranked #4 among top children’s hospitals in the nation and ranked in all 10 pediatric subspecialties in U.S. News & World Report’s list of America’s Best Children’s Hospitals. Texas Children’s Hospital is affiliated with Baylor College of Medicine in the areas of pediatrics, pediatric surgery, and obstetrics and gynecology. Baylor is ranked by U.S. News & World Report as one of the nation’s top 10 medical schools for pediatrics. Currently and throughout our 61-year partnership, Texas Children’s Hospital serves as Baylor’s primary pediatric training site. The collaboration between Texas Children’s Hospital and Baylor is one of the top five such partnerships for pediatric research funding from the National Institutes of Health. With a staff of more than 11,000 employees and more than 2,000 board-certified physicians, pediatric subspecialists, pediatric surgical subspecialists and dentists, Texas Children’s offers more than 40 subspecialties, programs and services. Physicians are employees of Baylor College of Medicine, not Texas Children’s Hospital. Because they practice at Texas Children’s Hospital, they may be referred to as “our team” or “Texas Children’s physicians” throughout this report. 3 4 H E A RT C E N T E R 2 0 1 5 20 19 18 17 Texas Children’s Heart Center is located in the hospital’s main inpatient building, the West Tower, on floors 15 and 17 through 20. The close proximity of the Heart Center’s treatment and administrative areas, perhaps unique in pediatric cardiac care, enables team members to respond quickly to patient and family needs or emergencies and promotes collaboration among the multidisciplinary team. 2 0 t h F LO O R – Heart Center clinics and diagnostic facilities, including the echocardiography lab and cardiovascular clinical research core 19 t h F LO O R – Heart Center administrative offices and conference rooms 15 18 t h F LO O R – 21-bed Cardiovascular Intensive Care Unit; dedicated Heart Center pharmacy; three state-of-the-art cardiovascular operating rooms; three state-of-the-art cardiac catheterization labs; eight-bed holding/catheterization recovery unit 17t h F LO O R – Cardiovascular Anesthesiology administrative offices; Ronald McDonald ® Family Waiting Room with additional private rooms for families to consult with their child’s physicians or to wait during procedures; support services, including social work and child life staff 15t h F LO O R – 22-bed inpatient unit including six “step-down” beds for patients who are healthy enough to leave intensive care but still need close monitoring; 12-bed dedicated Heart Failure Intensive Care Unit H E A RT C E N T E R 2 0 1 5 Pioneers in Pediatric Cardiac Care Texas Children’s Hospital has been a leader in pediatric heart care for 60 years. Led by Denton Cooley, M.D., and Dan McNamara, M.D., the hospital started performing heart surgery in children in 1956. Dr. McNamara, a patriarch of pediatric cardiology, and Dr. Cooley, a pioneer heart surgeon, were among the first to demonstrate that small children could safely undergo heart surgery. Today, Texas Children’s Heart Center is one of the nation’s leading providers of pediatric cardiac care. In 2015, U.S. News & World Report ranked Texas Children’s Heart Center #2 in the nation for pediatric cardiology and heart surgery. Comprising several multidisciplinary teams working in conjunction with pediatric subspecialists throughout the hospital, the Heart Center strives to provide unparalleled care at every point from diagnosis through treatment and follow-up. Nº2 Texas Children’s Heart Center is part of the OptumHealth Pediatric Transplant Centers of Excellence Network and is recognized by Aetna as a Pediatric Congenital Heart Surgery Institute of Excellence. 5 6 H E A RT C E N T E R 2 0 1 5 National and International Reach Texas Children’s commitment to caring for children reaches around the globe. In 2015, our Heart Center cared for patients from more than 30 states and over 15 countries (shown below). We are dedicated to creating a healthier future for children throughout the global community. KUWAIT QATAR CAYMAN ISLANDS H E A RT C E N T E R 2 0 1 5 2015 2015 Texas Children’s Heart Center Overview Surgical procedures Cardiac operations Heart transplants Lung transplants Adult congenital heart disease operations 822 21 TOTA L 8 914 63 Cardiac catheterizations Diagnostic cardiac catheterizations 544 Interventions 454 TOTA L Electrophysiology studies and ablations 132 1,189 Pacemaker and defibrillator implants 59 Diagnostic testing and cardiac imaging Echocardiograms Fetal echocardiograms Electrocardiograms 25,915 1,831 37,138 TOTA L Cardiac MRIs Stress MRIs Holter ® monitors Stress tests 509 71,483 41 5,118 931 Cardiovascular anesthesia Catheterizations and electrophysiology patients 1,129 Cardiovascular operating room patients 982 TOTA L Interventional radiology patients 252 2,791 MRI patients 428 The outpatient clinic at Texas Children’s Heart Center had more than 25,600 patient encounters in 2015. 7 H E A RT C E N T E R 2 0 1 5 Congenital Heart Surgery Service The Congenital Heart Surgery Division provides individualized and comprehensive surgical care for all aspects of pediatric and adult congenital heart disease. We are experienced in the rarest of cases, such as ectopia cordis and other infrequently seen conditions. Texas Children’s Heart Center performs more than 900 surgical procedures annually with outcomes among the best in the country. We treat children of all ages, including preterm and low-birth-weight newborns, and we personalize treatments and procedures to best suit the situation of each child and family. This tailored approach includes cardiopulmonary bypass and neuroprotection strategies focused on the patient’s condition and needs, helping to achieve optimal functional outcomes. The center’s Heart, Lung and Heart-Lung Transplant Programs, among the largest and most successful in the United States, are also part of the Congenital Heart Surgery Division. 2 012 889 2 011 767 2 010 2 013 914 2009 836 2008 836 2 0 07 911 2006 816 769 Volume by year 928 Cardiovascular and thoracic surgery cases 781 8 2 014 2015 According to the Society of Thoracic Surgeons National Database Program, congenital heart surgery programs are considered high-volume programs if they perform more than 250 index operations per year on average. Since 1995, Charles D. Fraser, Jr., M.D., and the Congenital Heart Surgery team have performed more than 14,500 operations on children and adults with congenital heart disease. H E A RT C E N T E R 2 0 1 5 Total cardiopulmonary bypass operations CPB 914 928 305 331 889 340 2 012 2 013 609 549 284 2 011 483 2 010 597 2009 767 836 300 836 297 582 2008 536 2 0 07 539 2006 329 816 293 523 480 508 289 273 769 781 911 Volume by year 2 014 2015 NON-CPB More than 64 percent of operations performed require the use of cardiopulmonary bypass (CPB). Our incidence of mechanical circulatory support postcardiotomy is less than 1 percent. Cardiovascular and thoracic surgery cases 2011 2012 N E O N AT E 31.4% 6.9% 17.1% 4.0% 2013 I N FA N T 44 .6% 4 4. 5% 32 .9% 18.6% 5.1% 5.1% 7. 5% 16. 5% 18. 3% 19.9% 27.7% 30.4% 30.6% 45. 3% 46. 3% 47.4% Percent by age 2015 2 014 CHILD A D U LT Our patients include children of all ages as well as adults who have been treated since infancy or who have been diagnosed with a congenital heart defect later in life. 9 10 H E A RT C E N T E R 2 0 1 5 2015 Mortalities by RACHS -1 classification in 2015 Number of procedures Number of discharge mortalities Percent mortality STS national benchmark Total for Risk Category 1 78 0 0.0% 0.4% Total for Risk Category 2 240 1 0.4% 1.0% Total for Risk Category 3 241 7 2.9% 3.2% Total for Risk Category 4 60 0 0.0% 5.2% Total for Risk Category 5-6 13 2 15.4% 13.4% 632 10 1.6% 2.9% Primary procedure Grand total The Risk Adjustment in Congenital Heart Surgery (RACHS-1)1 categorization is a widely used risk stratification model that analyzes outcomes in congenital heart surgery. The most common surgeries for congenital heart defects are stratified into six risk categories. Surgeries with higher risk are placed in higher categories with Category 6 representing congenital heart surgeries associated with the greatest risk. 1.6% Overall risk-adjusted hospital mortality rate for our program in 2015 was 1.6%2. Data collected by the Society of Thoracic Surgeons (STS) shows the national hospital discharge mortality rate at 2.9%3. 1 Jenkins KJ, Gauvreau K, Newburger JW, et al., Consensus-based method for risk adjustment for surgery for congenital heart disease. J Thorac Cardiovasc Surg. 2002; 123:110-8. 2 007-RACHS-1 Index Surg CHD Volume. 3 Society of Thoracic Surgeons Data Harvest Report, published June 2015. H E A RT C E N T E R 2 0 1 5 2015 Mortalities by age and operation type in 2015 Age CPB cases CPB Non-CPB Non-CPB discharge discharge Discharge cases mortalities mortalities mortality STS Percent national mortality benchmark Neonate (0d - 30d) 68 39 2 3 5/107 4.7% 7.9% Infant (31d - 1y) 175 30 2 0 2/205 1.0% 2 .8% Child (>1y - <18y) 262 20 3 0 3/282 1.1% 1.1% Adult (18y+) 38 0 0 0 0/38 0.0% 1.6% Grand total 543 89 7 3 10/632 1.6% 2 .9% Age-appropriate surgical planning and management allows for outcomes in patients of all ages to be better than the national benchmarks. Patient total combines CPB and non-CPB cases (N=632). 11 42 Atrial septal defect repair 27 22 2008 O V E R A L L H O S P I TA L D I SC H A RG E M O RTA L I T Y R AT E 4 2010 2011 2012 2013 2014 <1% Ventricular septal defect repair 2008 O V E R A L L H O S P I TA L D I SC H A RG E M O RTA L I T Y R AT E 4 0% S T S N AT I O N A L BENCHMARK5 <1% 2 011 57 2 010 56 2009 60 54 2 0 07 53 53 59 70 Volume by year 2006 2015 The Congenital Heart Surgery Division performs an average of 27 atrial septal defect (ASD) closures annually. This includes patients with secundum, coronary, sinus and sinus venosus ASDs. Our hospital survival rate is 100 percent. Our service also offers a minimally invasive approach to ASD closure. 0% S T S N AT I O N A L BENCHMARK5 2009 82 2007 14 24 2006 14 23 32 35 Volume by year 39 H E A RT C E N T E R 2 0 1 5 47 12 2 012 2 013 2 014 2015 Ventricular septal defects (VSD) are the most commonly diagnosed congenital heart defects, and surgical treatment remains the standard of care for children with this condition. This data includes patients with perimembranous, supracristal, inlet or muscular VSDs, and patients with double-chambered right ventricle. The Congenital Heart Surgery Division performs an average of 59 VSD closures each year and in 2015 had a survival rate of 100 percent. 4 Hospital mortality is calculated over the last four years from 2012-2015. 5 STS benchmark data is from 2011-2014. H E A RT C E N T E R 2 0 1 5 Atrioventricular canal repair O V E R A L L H O S P I TA L D I SC H A RG E M O RTA L I T Y R AT E 6 2.0% S T S N AT I O N A L BENCHMARK7 2009 2 010 2 011 2 012 2 013 32 2008 33 2 0 07 20 2006 20 19 31 30 32 38 40 Volume by year 2 014 2015 The Congenital Heart Surgery Division performs an average of 30 operations each year for partial, intermediate and complete atrioventricular (AV) canal defects. 2.4% Tetralogy of Fallot repair 21 2006 2 0 07 2008 O V E R A L L H O S P I TA L D I SC H A RG E M O RTA L I T Y R AT E 6 1.0% S T S N AT I O N A L BENCHMARK7 1.6% 2009 2 012 31 2 013 24 2 011 22 30 2 010 27 31 27 35 42 Volume by year 2 014 Our surgical approach to the repair of tetralogy of Fallot (TOF) is individualized for each patient based on age, anatomy and symptoms. This allows us to attempt repair of the defect while preserving critical parts of the cardiac anatomy, thereby optimizing the patient’s cardiac function over the long term. The Congenital Heart Surgery Division performs an average of 29 TOF repairs each year. 6 Hospital mortality is calculated over the last four years from 2012-2015. 7 STS benchmark data is from 2011-2014. 2015 13 H E A RT C E N T E R 2 0 1 5 Arterial switch operation 2009 16 2 010 2 011 2 012 2 014 2015 The arterial switch operation (ASO) is offered to patients with simple transposition of the great arteries, complex transposition of the great arteries and Taussig-Bing anomaly. Historically, this operation has not been viewed as a viable treatment option for some children due to their size, complex coronary anatomy and associated cardiac malformations. Our outcomes have demonstrated that these characteristics are not associated with increased operative risk. Our hospital survival rate is 100 percent. 0% S T S N AT I O N A L BENCHMARK9 2 013 10 2008 O V E R A L L H O S P I TA L D I SC H A RG E M O RTA L I T Y R AT E 8 18 2 0 07 19 2006 14 12 15 16 29 29 Volume by year 4.1% Norwood operation 2 013 2 014 10 17 21 17 2 0 07 17 2006 15 18 24 28 Volume by year 18 14 2008 O V E R A L L H O S P I TA L D I SC H A RG E M O RTA L I T Y R AT E 8 16.9% S T S N AT I O N A L BENCHMARK9 2009 2 010 2 011 2 012 2015 The Congenital Heart Surgery Service performs an average of 19 Norwood operations per year for hypoplastic left heart syndrome and other single ventricle anomalies. 14.8% 8 Hospital mortality is calculated over the last four years from 2012-2015. 9 STS benchmark data is from 2011-2014. H E A RT C E N T E R 2 0 1 5 Single Ventricle Program The Single Ventricle Home Monitoring Program and Outpatient Clinic at Texas Children’s Heart Center is focused on the care of infants with single ventricle congenital heart defects, which include hypoplastic left heart syndrome (HLHS) and variants, unbalanced atrioventricular septal defects, complex single ventricle and heterotaxy syndrome, among others. Most of these infants will require at least two or three operations within the first few years of life. The goals of these operations are to: (1) allow free flow of blood from the heart out to the body; (2) protect the lungs from high pressure and too much blood flow; and (3) create separate paths for blood to flow to the lungs and out to the body. Infants will typically undergo placement of a shunt or conduit to provide blood flow to the lungs within the first few days of life. For infants with HLHS, reconstruction of the vessel that allows blood to flow to the body (the Norwood operation) is typically performed within the first week of life. The second stage (bidirectional Glenn shunt) is performed at around 3-6 months of age. The period between these operations is called interstage period. The importance of a home monitoring program The interstage period is an important phase in the infant’s well-being and outcome. It is common for infants with single ventricle congenital heart defects to have poor oral intake and weight gain, which may affect their well-being. They may require multiple daily medications, modified feeding and interstage interventions. Common childhood illnesses, such as a cold or diarrhea, can be life-threatening. Early recognition of signs and symptoms is thus necessary to be able to obtain immediate evaluation and intervention. The home monitoring program allows parents and caregivers to actively participate in the care of their babies outside of the hospital by watching for and addressing many of the problems that can be seen in the interstage period. Our program provides support, resources and clinical care to help transition successfully to the second surgery. A team approach to treatment Texas Children’s Congenital Heart Surgery team performs an average of 19 Norwood operations a year for patients with HLHS and other single ventricle heart defects. We take a collaborative approach to the post-surgical care of these infants drawing on the expertise of a multidisciplinary team including Pediatric Cardiology, Congenital Heart Surgery, Interventional Cardiology, Electrophysiology, Cardiac Imaging, Cardiovascular Anesthesia, Genetics and Nutrition Services. Research and quality improvement We are leaders in research involving the many aspects of care of infants with single ventricle heart disease, encompassing genetics, critical care, nutrition and epidemiology. We are part of several studies with the Pediatric Heart Network aiming to further understand and address clinical questions. Our program is also an active member of the National Pediatric Cardiology Quality Improvement Collaborative, a multicenter group focused on improving quality and outcomes for children with single ventricle heart defects who have undergone a Norwood operation. 15 16 H E A RT C E N T E R 2 0 1 5 Patient thrives after complex surgeries for congenital condition Three surgeries and four years after a lifesaving open heart surgery, Stockton Watson is a tenacious and energetic preschooler who recharges at naptime and takes only one medication – a baby aspirin. When his mother, Brittany, had a routine ultrasound at 14 weeks gestation, she learned Stockton’s heart was abnormally shaped. An echocardiogram provided a diagnosis: hypoplastic left heart syndrome (HLHS), a dangerous defect that stunts development of the left ventricle, mitral valve and aortic valve, causing the left ventricle to be too small to function. “The doctors told us HLHS was very serious and life-threatening for our baby,” she said. “It was frightening, but we knew he would have to have surgery to correct the problem.” Immediately, Brittany and her husband, Seth, began to research hospitals and surgical success rates. To their surprise, that wasn’t as easy as they thought it would be. “Most hospitals don’t give out figures, but Texas Children’s shared all the statistics,” she said. “It confirmed that’s where we needed to be.” HLHS typically requires a series of surgeries over the first several years of life. Between surgeries, patients are monitored closely by the Single Ventricle Program. Stockton weighed almost 8 pounds when he was born, and his first surgery was four days later. He spent 11 days in the Cardiovascular Intensive Care Unit and 40 days as an inpatient. “Those first few months were difficult, I have to admit,” Brittany said. “We would get over one hurdle and another would pop up. But he was growing, and everything was progressing toward his second surgery.” Five months later, Stockton had the second procedure. “This surgery gave us a whole new outlook,” Brittany said. “It really changed him, and he started growing more quickly, crawling and talking.” In 2015, when Stockton was 4, his doctors said he was ready for the next surgery. It too was a success, and now the family returns for follow-ups only once a year. Brittany says Stockton brings a great deal of love and happiness to their family, which includes an older sister and younger brother and sister. He enjoys learning and is hitting – often exceeding – developmental milestones. Although it is likely Stockton will need a heart transplant as a young adult, he starts kindergarten next fall with no restrictions except to avoid contact sports. Brittany has become an advocate for people who are affected by HLHS as a member of the National Pediatric Cardiology Quality Improvement Collaboration. “We’re so grateful, and we know Texas Children’s was the right choice,” she said. “They have so much experience and knew exactly what they were doing every step of the way.” H E A RT C E N T E R 2 0 1 5 17 18 H E A RT C E N T E R 2 0 1 5 Coronary Anomalies Program In December 2012, Texas Children’s Hospital created the Coronary Anomalies Program, a multidisciplinary team to care for patients with rare congenital heart defects associated with coronary ischemia, myocardial infarction and sudden death. Coronary artery anomalies are the second-leading cause of sudden cardiac death in children and young adults. Diagnosing these anomalies can be challenging because many individuals with the conditions have no symptoms, and their first manifestations can be sudden cardiac arrest or death. Those who do have symptoms complain most often of chest pain, palpitations, dizziness or fainting during or just after exercise. How to best treat children or young adults with coronary artery anomalies is a subject of debate in the medical community. Most physicians agree that surgery is necessary for patients who show evidence of decreased blood flow to the heart tissue, but how to treat patients who have no physical complaints and show no evidence of reduced blood flow to the heart is unclear. Texas Children’s Hospital has hosted two conferences focused on this topic and is partnering with the Children’s Hospital of Philadelphia to host the 3rd Symposium on Coronary Artery Anomalies, which will be held in Philadelphia in 2016. During the conferences, speakers from leading heart institutions across the country provide a dedicated forum to discuss the diagnosis and management of patients with coronary artery anomalies. Outcomes of patients with anomalous aortic origin of a coronary artery Texas Children’s Coronary Anomalies Program began tracking outcomes in December 2012 and as of April 2016 has recorded: Total patients 134 Surgery treatment 38 Surgical mortality 0 Complications 3 H E A RT C E N T E R 2 0 1 5 Heart Failure and Transplant Program Since its inception in 1984, Texas Children’s Heart Center has performed more than 335 heart transplants, making it one of the largest and most successful programs in the nation. As the number of diagnoses for pediatric heart failure has increased, so has our depth and breadth of experience in treating patients, as has our ability to offer the right mechanical circulatory device to support each child in heart failure. For more information on the Heart Transplant Program, please visit texaschildrens.org/transplant. Since 2011, Texas Children’s Heart Center has been an active member of the Pediatric Heart Transplant Study, which is dedicated to the advancement of the science and treatment of children during listing for and following heart transplantation. The purpose of the group is to establish and maintain an international, prospective, event-driven database for heart transplantation, to use the database to encourage and stimulate basic and clinical research in the field of pediatric heart transplantation, and to promote new therapeutic strategies. Mechanical circulatory support is often used as a bridge to transplantation in children. At Texas Children’s Heart Center, we select a ventricular assist device (VAD) from a variety of options to meet the needs of the individual patient. VAD implantations10 By device Thoratec P-VAD ® 11 Micromed ® Impella ® 7 TOTAL CASES 3 153 HeartWare ® 17 Berlin Heart EXCOR ® Pediatric TandemHeart ® 3 46 ® SynCardia Total Artificial Heart 1 HeartMate II ® 17 Rotaflow® 10 VADs placed from 1995-2015. 26 Bio-Medicus ® 22 19 20 H E A RT C E N T E R 2 0 1 5 Advancing the field of pediatric ventricular assist devices In 2012, the United States Food and Drug Administration (FDA) granted humanitarian device exemption for the Berlin Heart EXCOR® Pediatric Ventricular Assist Device (VAD). This approval was the successful result of a multi-year, multi-institution study led by Texas Children’s Hospital. This landmark event has opened the era of pediatric VAD support in North America. The Berlin Heart EXCOR® is the only FDA-approved pediatric VAD. Today, Texas Children’s Hospital continues to advance the field of pediatric ventricular assist devices. Because there are significantly more adult patients with heart failure than pediatric patients, device development is far more advanced in the adult world. Texas Children’s VAD program strives to achieve improved outcomes by finding ways to utilize adult VADs in children. These VADs include the HeartWare HVAD® and Impella catheter VAD®. Since HeartWare is implantable, children on this device can live at home and even attend school. This has significantly improved quality of life of patients compared to the Berlin Heart, which requires inpatient management. Since 2012, Texas Children’s Heart Center has implanted 20 HeartWare and 11 Impella devices – more than any other pediatric center in North America. Our positive results are widely recognized nationally and internationally, resulting in multiple publications.11,12,13 Jarvik Infant VAD Texas Children’s Hospital is also working on the development of a new-generation miniaturized implantable VAD specifically designed for small children, known as the Jarvik Infant VAD. With the support of the federal government through the National Heart, Lung and Blood Institute, this AA-battery-size device is undergoing pre-clinical testing in a chronic animal model, with the anticipation of FDA approval for a human trial within 2016. This will further expand the use of implantable VADs in small children, including babies. Extracorporeal life support Extracorporeal life support (ECLS) is a treatment that helps support children when their heart and/or lungs are unable to supply enough blood flow or oxygen to the body. This support may be necessary after heart surgery or in some children with heart or lung disease. ECLS is provided in the Pediatric Intensive Care Unit, Cardiovascular Intensive Care Unit or Neonatal Intensive Care Unit based on each child’s underlying problem. A specially trained team of cardiac intensivists, surgeons, critical care nurses and ECLS specialists carefully monitors each child’s condition. To provide ECLS, we use extracorporeal membrane oxygenation (ECMO). With ECMO, blood is pumped through the cannulae and into the machine oxygenating the patient’s blood. The oxygenated blood is then returned through the circuit to the body, creating a continuous flow and doing the work of the heart and/or lungs so the patient’s body can heal. 11 Adachi I, Guzmán-Pruneda FA, Jeewa A, Fraser CD Jr, Dean McKenzie E. A modified implantation technique of the HeartWare ventricular assist device for pediatric patients. J Heart Lung Transplant. 2015 Jan; 34(1):134-6. 12 Asaki SY, Dean McKenzie E, Elias B, Adachi I. Rectus-sparing technique for driveline insertion of ventricular assist device. Ann Thorac Surg. 2015 Nov; 100(5):1920-2. 13 Goldman J, Tume S, Jeewa A, Parekh D, Justino H, Adachi I. Impella use for left ventricle decompression in a 6-year-old on ECMO Support: The youngest pediatric patient reported. ASAIO J. 2015; S90. H E A RT C E N T E R 2 0 1 5 Heart transplants14 15 14 11 13 15 16 18 21 32 Volume by year 2007 2008 2009 2010 2011 2012 2013 2014 Heart transplant patient survival rates15 1 YEAR AFTER TRANSPLANT 7/1/12 TO 12 / 31/14 N = 4 7 T E X A S C H I L D R E N ’ S H E A RT C E N T E R 87. 50% 87. 51% 93.10% 92 .77% 95. 58% 96.88% Pediatric age <18 3 YEARS AFTER TRANSPLANT 1/1/10 TO 6 / 3 0 /12 N = 2 9 S RT R E X P E C T E D N AT I O N A L 14 Data includes patients who received heart-and-lung transplants simultaneously. 15 Scientific Registry of Transplant Recipients (SRTR). Program Specific Reports. Table 11 – srtr.org. 2015 21 H E A RT C E N T E R 2 0 1 5 Heart transplant survival curves The following graphs show the survival rates for patients by the number of years after heart transplantation. The lines show the expected survival rates for our patients a number of years after their transplant. Because these are estimates, the shaded areas show the 95 percent confidence limits of the expected survival rates. Survival curves16 By era 100% 80% ERA III: 2005-2015 60% Survival probability 22 40% ERA II: 1999-2004 20% ERA I: 1984-1998 0% ERA I ERA II ERA III 82 62 172 50 41 65 36 28 7 29 8 0 16 0 3 0 5 10 15 20 25 30 Years post transplant 16 Wilcoxen test 1984-1998 vs. 1999-2004: p < 0.9975, 1984-1998 vs 2005-2015: p < 0.04, 1994-2004 vs. 2005-2015: p < 0.0048. Texas Children’s data: 1984-2015, 318 Txs on 318 patients, Age between 0 and 22 years. UNOS data: 1987-2013, 7437 Txs on 6487 patients (3 observations missing data), Age between 0 and 17 years. H E A RT C E N T E R 2 0 1 5 Survival curve vs. UNOS17 Era III (2005-2015) 100% Texas Children’s Survival probability 80% UNOS 60% 40% 20% 0% Texas Children’s UNOS 151 2,909 90 1,690 64 1,011 38 475 14 75 0 0 0 2 4 6 8 10 Years post transplant 17 Wilcoxen test 1984-1998 vs. 1999-2004: p < 0.9975, 1984-1998 vs 2005-2015: p < 0.04, 1994-2004 vs. 2005-2015: p < 0.0048. Texas Children’s data: 1984-2015, 318 Txs on 318 patients, Age between 0 and 22 years. UNOS data: 1987-2013, 7437 Txs on 6487 patients (3 observations missing data), Age between 0 and 17 years. 23 24 H E A RT C E N T E R 2 0 1 5 One family fights breast cancer and heart failure To say Riki Graves’ pregnancy was full of ups and downs would be a vast understatement. On her 38th birthday, just a few weeks after finding out that she and her husband, Chris, were expecting their second child, Riki was diagnosed with breast cancer. After consulting with doctors at MD Anderson Cancer Center, Riki made the deeply personal decision to forego cancer treatments until after her baby was born. “I wanted to provide my daughter with the strongest pregnancy and healthiest beginning to life possible,” she said. Soon after that, during her 20-week ultrasound, the Graves family was dealt a second blow. They found out that their unborn baby, a little girl whom they would name Juliana, had a serious heart condition. Juliana was diagnosed with an unbalanced atrioventricular septal defect with severe biventricular dysfunction, a small aortic arch and severe atrioventricular valve regurgitation. Although the terminology meant little to her, Riki understood Juliana would likely need several heart surgeries, and even then she might not survive. “Hearing those words sent a panic through me that, even now, is hard to describe.” Riki was referred to Texas Children’s Fetal Center.™ Nancy Ayres, M.D., director of Noninvasive Imaging and Fetal Cardiology, and a multidisciplinary team provided care for mother and baby during the pregnancy. On April 9, 2014, Juliana was born weighing 6 pounds, 14 ounces. Charles D. Fraser, Jr., M.D., Texas Children’s surgeon-in-chief and chief of Congenital Heart Surgery, determined that Juliana’s heart was too structurally abnormal and not strong enough for surgery. Juliana was placed on the transplant list on April 21. On April 26, at just 17 days old, she received a new heart. “It is rare to find an organ for her size and age,” said Diana Orosco, R.N., a nurse coordinator assigned to the Graves. “Historically, our center has not performed transplants on babies this young.” Jeffrey Heinle, M.D., surgical director of Texas Children’s Heart and Lung Transplant Program, led the successful transplant surgery on Texas Children’s youngest heart transplant patient to date. “We feel so fortunate that Juliana was cared for by Texas Children’s Hospital,” Riki said. “All the doctors, fellows and nurses who provided extraordinary care and helped us get through – we can’t thank them enough.” Since her heart transplant, Juliana is doing fantastic. She recently celebrated her second birthday and is developing typically. After Juliana was born, Riki received radiation treatment at MD Anderson for her breast cancer and has been in remission since July 2014. H E A RT C E N T E R 2 0 1 5 25 26 H E A RT C E N T E R 2 0 1 5 Interventional Cardiology Thanks to advances in the field, an increasing number of heart conditions can be treated with minimally-invasive catheter-based interventions. Texas Children’s Heart Center, the largest program in the region to offer interventional cardiac catheterization for infants, children and adolescents, performed 1,189 cardiac catheterization procedures in 2015. The full-service cardiac catheterization laboratory performs interventions including: • Balloon valvuloplasty • Balloon angioplasty (using standard as well as “cutting” balloons) • Stent placement (e.g. for pulmonary artery stenosis, coarctation of the aorta, etc.) • Device closure of atrial septal defects, arterial and venous collaterals, coronary fistulae, etc. • Device closure of patent ductus arteriosus, including in low-birth-weight and premature babies • Transcatheter pulmonary valve replacement using the Melody® valve In addition to these relatively common procedures, the Interventional Cardiology team at Texas Children’s Hospital has developed cutting-edge treatment strategies for rare and debilitating conditions such as: • Pulmonary vein stenosis • Venous thrombosis • Multiple muscular ventricular septal defects (“Swiss cheese” septum) • Congenital portosystemic shunts (Abernethy malformation) • Pulmonary arteriovenous malformations (congenital and acquired) • Pulmonary hypertension • Renal artery stenosis • Mid-aortic syndrome • Critical aortic stenosis and hypoplastic left heart syndrome In addition, we provide percutaneous ventricular assist device placement for heart failure (using the Impella® device). Despite being a regional and national referral center for the most complex forms of acquired and congenital heart disease, our team has an extraordinarily low complication rate from cardiac catheterizations (see chart on the following page). In addition, we have a strong culture of attention to radiation safety and continuous quality improvement, and we strive to promote these concepts locally and nationally. Our interventional team is actively involved in research into new treatment strategies for congenital heart disease and is invited to lecture on these topics nationally and internationally. H E A RT C E N T E R 2 0 1 5 Cardiac catheterization laboratory complications By rate Cases without complications 96.20% 0.55% Cases with major complications 3.25% Cases with minor complications 27 28 H E A RT C E N T E R 2 0 1 5 H E A RT C E N T E R 2 0 1 5 Electrophysiology The Arrhythmia and Pacing Service at Texas Children’s Heart Center offers a broad complement of diagnostic and therapeutic options to evaluate and manage heart rhythm abnormalities. We have one of the highest volume pediatric centers in the country for invasive electrophysiology studies and pacemaker/defibrillator implantations, and we maintain success rates for ablations that exceed the national average. Innovation, research and experience have made Texas Children’s Heart Center one of the leading centers in the world for the diagnosis and treatment of arrhythmias in children and adults with congenital heart disease. The Electrophysiology team runs a robust Genetic Arrhythmia Clinic. In 2015, there were more than 500 patient visits for assessment of inherited arrhythmia syndromes, and the team is actively involved in research to improve the management and outcomes of these patients. In collaboration with the Cardiovascular Research Institute, work is underway to identify novel genes and the molecular mechanisms that underlie arrhythmias and sudden death syndromes. Over the past year, our group has discovered new insights into Wolff-Parkinson-White syndrome, catecholaminergic polymorphic ventricular tachycardia, SCN5A overlap syndromes, Long QT syndrome and the muscular dystrophies. Our research spans both the clinical and basic sciences, encompassing a “bed to benchside” approach that strives to improve the overall care of our patients. Supraventricular tachycardia ablation outcomes 2015 Texas Children’s Hospital National benchmark18 A C U T E S U C C E S S R AT E 99% 95.2% Stereotaxis Texas Children’s Hospital is one of only a few hospitals in the U.S. with a remote magnetic navigation (MN) system called Stereotaxis for catheter manipulation. Stereotaxis has been utilized for over 150 ablation cases at Texas Children’s Hospital over the past several years. MN offers theoretic advantages in the treatment of children. The catheter is more flexible and atraumatic than standard catheters, potentially eliminating the risk of heart perforation. It can also be navigated with more precision, allowing for movements as small as one millimeter or deflections as small as one degree. This may result in enhanced accuracy and safety during mapping and ablation of certain arrhythmias in this patient population. Additionally, in order to decrease morbidity associated with radiation exposure during ablation cases, the Arrhythmia and Pacing Service has established protocols utilizing non-fluoroscopic mapping techniques to minimize radiation. This has resulted in a three-fold reduction in fluoroscopy times, with over 100 procedures being performed with minimal radiation (<1 minute) over the past two years (see graphs on the following page). 18 Based on data from the Pediatric Radiofrequency Catheter Ablation Registry. Kugler JD, Danford DA, Houston KA, et al. Pediatric radiofrequency catheter ablation registry success, fluoroscopy time, and complication rate for supraventricular tachycardia: comparison of early and recent eras. J Cardiovasc Electrophysiol. 2002 Apr; 13(4):336-41. 29 H E A RT C E N T E R 2 0 1 5 Changes in fluoroscopy time for ablation procedures Fluoro time in minutes By month 100 75 50 25 20 Ap 12 ril 20 Ju 12 n 20 1 Ju 2 l2 01 2 Se p 20 1 N ov 2 2 D 012 ec 20 Fe 12 b 20 M 13 ar 20 M 13 ay 20 Ju 13 n 20 Au 13 g2 01 N ov 3 20 Jan 13 20 Fe 14 b 20 M 14 ar 20 Ju 14 n 20 Au 14 g2 0 O 14 ct 20 1 D ec 4 20 Jan 14 20 Fe 15 b 20 Ju 15 n 20 1 Ju 5 l2 01 5 Au g2 01 5 D ec 20 15 0 Jan 30 Date of procedure Mean and median of fluoroscopy time By year 32 .89 (22 .87 ) 25.17 (4.15,10 4.4) 2012 17.99 (19.85) 9.45 (0.0 0, 90.42) 2013 2014 2015 4.4 4 (6. 38) 1.91 (0.0 0, 32 .15) 3.62 (4 .77 ) 1. 54 (0.0 0, 24 .68) MEAN (SD) MEDIAN (RANGE) H E A RT C E N T E R 2 0 1 5 Diagnostic Testing and Cardiac Imaging Each year, our noninvasive imaging lab performs more than 25,000 echocardiograms for fetuses, infants, children and adults with congenital or acquired heart disease. The imaging lab provides transesophageal, epicardial, intracardiac and transthoracic echocardiogram support in the catheterization labs and operating rooms on a daily basis. The main echocardiography lab consists of 10 rooms with a four-bed sedation bay and a state-of-the-art physician work area that houses five reading stations. Fetal echocardiograms 1,800 600 607 538 2015 946 899 1,000 767 1,200 953 1,400 800 2014 1,253 1,600 1,831 1,592 2,000 1,781 Volume by year 400 200 2006 2007 2008 2009 2010 2011 2012 2013 Fetal cardiac interventions For some fetuses with cardiovascular conditions, fetal cardiac intervention is available at Texas Children’s Hospital to try to improve the physiology of the heart before birth. Texas Children’s Fetal Center™ at Texas Children’s Pavilion for Women is one of only a few centers in the world capable of providing the full array of fetal cardiac interventions, which involves a coordinated effort among a large, multidisciplinary team of fetal cardiologists, obstetricians and gynecologists, interventional cardiologists, congenital heart surgeons, fetal imaging experts, maternal and fetal anesthesiologists, and other clinical specialists. We offer the following fetal cardiac interventions: • Fetal arrhythmia evaluation and treatment – While some abnormal fetal rhythm problems are benign, others may result in fetal heart failure and can pose a risk to the fetus and mother. We offer a variety of therapies that are customized for both the fetus and mother. We collaborate closely with adult cardiologists to protect the safety of both fetus and mother during treatment. • Fetal hypoplastic left heart syndrome (HLHS) and related conditions – We offer three fetal cardiac interventions for babies with small left heart structures, with the type of therapy depending on the fetal heart anatomy. 31 32 H E A RT C E N T E R 2 0 1 5 - For fetal aortic stenosis, which progresses to HLHS, we offer aortic valvuloplasty. This procedure is performed by a multidisciplinary team and consists of placing a small balloon across the fetal aortic valve to enlarge it and to promote blood flow through the left side of the heart. - For fetuses with HLHS or mitral valve dysplasia and a restrictive or intact atrial septum, we offer fetal atrial septal intervention. For this procedure, either a balloon or stent is placed across the atrial septum of the heart to decrease the pressure in the left atrium and to help the fetal lungs recover before birth. - For fetuses with small left-sided structures who may need neonatal heart surgery but do not meet the criteria for the above procedures, we are conducting an experimental study protocol in which we provide daily home oxygen to mothers, also known as maternal hyperoxygenation, to promote fetal left heart growth. Stress MRI There is a growing need within pediatrics for the accurate assessment of myocardial perfusion due to both acquired and congenital heart defects. At Texas Children’s Hospital, we are one of the few pediatric centers in the country to offer stress MRI by multiple pharmacologic stress agents. This technology has been shown to be superior to many other noninvasive modalities in the adult population, and Texas Children’s Hospital is adopting many of these same principles and applying them to the pediatric population. These examinations involve the dedicated and coordinated efforts of a pediatric cardiologist, pediatric radiologist, cardiac pharmacologist, cardiac MRI technician and MRI physicist. H E A RT C E N T E R 2 0 1 5 Adult Congenital Heart Disease Program The Adult Congenital Heart Disease (ACHD) Program at Texas Children’s Hospital offers a single point of care for patients with congenital heart disease from birth to adulthood. Our program offers the full range of ACHD services and specialties including surgery, diagnostic and interventional cardiac catheterization, noninvasive imaging (including cardiac MRIs and coronary CT angiography), arrhythmia services and more. ACHD clinic encounters19 Volume by year 1, 556 2012 1,217 1,793 2013 1, 373 2 ,054 2014 1, 529 2 ,423 2015 1,782 CLINIC VISITS PAT I E N T S Congenital heart disease diagnoses of ACHD patients In 2015 Other 11% Atrioventricular septal defect 20% Tetralogy of Fallot 12% 6% Ventricular septal defect 18% 9% Coarctation of the aorta 9% Atrial septal defect 19 Volumes reflect patients age 18 years or older. 15% Single ventricle Transposition of the great arteries 33 34 H E A RT C E N T E R 2 0 1 5 Living life to the fullest, despite congenital heart condition Falon Wiesner-Jones has spent 33 years defying the odds, including giving birth to two healthy babies after she was told her chances to get pregnant were slim to none. Diagnosed at 6 weeks old with transposition of the great arteries, a life-threatening heart defect, Falon has had more than 15 procedures, including three open-chest surgeries at Texas Children’s. At age 4, Falon had her first open heart surgery, performed by Denton Cooley, M.D., at Texas Children’s. At 5, she received a pacemaker. Although she couldn’t participate in contact sports, she did everything else – band, 4-H, ballet, gymnastics, skiing – even cheerleading. “My parents never babied me; they only encouraged me,” she said. “My mom always told me I should go and live my life rather than watch it pass me by.” When she was 16, Falon learned she had Stage II heart failure. Although she feels healthy most of the time, it is a condition that requires a lifetime of careful maintenance. During college at Texas A&M University, Falon fell in love with her husband, Chad. Following graduation, they moved to New York and then Dallas. Falon has had two major complications and surgeries in adulthood. At 28 years old, Falon transitioned to Texas Children’s Adult Congenital Heart Disease (ACHD) Program for specialized follow-up care for her condition. “I’ve been at Texas Children’s since day one, and they really know me and my entire history,” Falon said. “It is so reassuring to be able to continue my care here, and to have all the resources I need in one spot.” When Falon became pregnant with her first child, the ACHD team and Texas Children’s Pavilion for Women maternal-fetal medicine specialists worked hand-in-hand and closely monitored the condition of both mother and child. “In the past, we used to tell women who had grown up with congenital heart disease not to get pregnant,” said Wayne Franklin, M.D., director of Texas Children’s Adult Congenital Heart Disease Program. “But we have since found that with excellent cardiology care and maternal-fetal medicine, these patients can have good outcomes with their pregnancies.” After delivering a healthy baby girl in 2011, Falon went on to have a healthy son in late 2015. “I have been very fortunate, and there isn’t a day that goes by I don’t thank God for my blessings,” she said. “I may still have many obstacles to face in the future, but with the help of Texas Children’s I am looking forward to seeing my children grow up and accomplish their dreams.” H E A RT C E N T E R 2 0 1 5 35 36 H E A RT C E N T E R 2 0 1 5 Preventive Cardiology Program The Preventive Cardiology Program at Texas Children’s Heart Center is part of our mission to provide the best possible care and outcomes for our patients. Focused on medically managing the risk factors of acquired heart disease in children, the Preventive Cardiology Program cares for patients with a strong personal or family history of cardiac disease, elevated cholesterol, high blood pressure or Kawasaki disease. Our goal is to prevent future cardiac disease and events such as heart attack and stroke through early detection and intervention and by educating children and families on how to better care for themselves. Abnormal cholesterol and high blood pressure are well recognized conditions in adults. It surprises many people that these conditions can also arise in childhood, and that they lay the foundation for heart disease in adulthood. Research shows that normalizing cholesterol values and reducing high blood pressure in children may help prevent or slow the development of heart disease as they reach adulthood. The goal of the Preventive Cardiology Program is to prevent heart attack, stroke and other acute cardiac events later in life, to decrease mortality and to increase a child’s future quality of life. Typically, our patients have abnormal cholesterol levels or high blood pressure or have been diagnosed with Kawasaki Disease, which can increase the risk of cardiac disease in adulthood. Our patients may have other conditions such as liver disease, obesity, diabetes or metabolic syndrome that directly cause cholesterol or blood pressure abnormalities. Others, perhaps through a poor diet, lack of physical activity or other lifestyle factors, may be at a higher risk for cardiac disease and on an early pathway to acquired heart disease in adulthood. With more than half a century of leadership in the care of patients with congenital heart disease, Texas Children’s has pioneered many of the now-standard procedures and therapies in pediatric cardiovascular care. The Preventive Cardiology Program uses a collaborative approach to treating patients, drawing on the expertise of a multidisciplinary team of specialists, including experts in pediatric cardiology, heart disease prevention, physical activity, nephrology, endocrinology and nutrition. H E A RT C E N T E R 2 0 1 5 Cardiovascular Anesthesia Pediatric Cardiovascular Anesthesia at Texas Children’s Hospital provides sedation and anesthesia services for all congenital cardiac operations and for children with congenital heart disease undergoing various non-cardiac procedures. Services are also provided for catheterization and electrophysiology procedures as well as imaging studies in MRI, CT and interventional radiology. Cardiovascular anesthesia cases 2011 2012 2 013 982 1,129 1,002 1,094 2 014 252 428 152 184 430 462 910 880 839 924 109 125 347 375 855 955 By location 2015 MRI I N T E RV E N T I O N A L R A D I O L O G Y C O N G E N I TA L H E A RT S U R G E RY O P E R AT I N G RO O M S C AT H E T E R I Z AT I O N A N D E L E C T RO P H Y S I O L O G Y The Pediatric Cardiovascular Anesthesia Division treated more than 2,700 patients in 2015. Beyond anesthetic care, the division actively participates in the daily care of patients in the Cardiovascular Intensive Care Unit. 37 H E A RT C E N T E R 2 0 1 5 Reduction in cryoprecipitate waste in the pediatric cardiovascular operating room: A goal-directed transfusion pathway In the United States, although the volume of blood and blood products needed for surgeries continues to increase annually, the amount of blood donated annually remains the same. Thus, it is important for health care organizations to responsibly manage blood/blood products and reduce the amount wasted in the OR due to over-ordering or over-estimating need. Texas Children’s Pediatric Cardiovascular Anesthesia Division recently embarked on a quality improvement project led by Erin Gottlieb, M.D., to introduce a goal-directed transfusion pathway based on results from rotational thromboelastometry (ROTEM®) and to limit the waste of cryoprecipitate, a blood product used to treat coagulation abnormalities in congenital heart surgery that was identified as highly vulnerable to waste. The graphs below show a sustained decrease in cryoprecipitate waste after education and implementation of the transfusion pathway, along with a corresponding increase in the use of ROTEM® and fibrinogen concentrate (substitute for cryoprecipitate). The results were recently presented at the Congenital Cardiac Anesthesia Society and Society for Pediatric Anesthesia meetings and since then, multiple peer institutions have implemented similar measures in their CVORs. Texas Children’s Heart Center has found this pathway to be effective at reducing wasted blood as well as cryoprecipitate and is using it in cardiovascular surgeries. Cryoprecipitate waste in the CVOR By month 80 Units wasted 70 60 UCL 50 40 30 LCL 20 10 December November October September August July June May April March February January 2015 December November October September 2014 0 In 2015 45 8 40 7 35 6 30 5 25 4 20 3 15 10 2 5 1 0 0 March April May June July August September October November December NUMBER OF ROTEM® ORDERED NUMBER OF PATIENTS WHO RECEIVED FIBRINOGEN CONCENTRATE Number of patients who received fibrinogen concentrate ROTEM ® and fibrinogen concentrate trends Number of tests ordered 38 H E A RT C E N T E R 2 0 1 5 Early extubation in the pediatric cardiac operating rooms Early extubation in the cardiac operating rooms can have a positive impact on patient outcomes, including reducing the risk of pneumonia, infections and other complications and improving patient comfort. Texas Children’s Hospital participated in a multicenter quality improvement project to create clinical practice guidelines (CPG) to try to shorten the length of time patients spend on a ventilator following two types of surgeries: tetralogy of Fallot and coarctation repair. Teams from five leading pediatric heart centers looked into the factors that contribute to longer ventilation periods and created guidelines to help address these issues. The centers then adopted standardized guidelines and evaluated the changes in outcomes in the OR and the ICU. At Texas Children’s, the anesthesia portion of the project was led by David F. Vener, M.D., and included teams from Cardiovascular Anesthesia, the Cardiovascular Intensive Care Unit, Cardiovascular Surgery and Nursing, among others. The guidelines resulted in a significant reduction in time to extubation and ICU length of stay at all participating centers. At Texas Children’s, the mean hours of ventilation went from 66 hours to 5.5 hours following adoption of the CPG for patients with tetralogy of Fallot, and the mean length of stay in the CVICU went from 6.2 to 4.2 days. For coarctation, the mean hours of ventilation went from 21.2 hours to 12 hours following adoption of the CPG, and the mean length of stay in the CVICU went from 5 days to 4.8 days. Tetralogy of Fallot ICU length of stay (days) Post-op ventilation (hours) 250 35 30 Pre CPG 200 25 150 20 15 100 10 50 5 0 0 ICU length of stay (days) Post CPG Post-op ventilation (hours) 250 40 200 30 150 20 100 10 50 0 0 39 40 H E A RT C E N T E R 2 0 1 5 Leaders in cardiovascular anesthesia education Transesophageal Echocardiography for Congenital Heart Disease, edited by Texas Children’s physicians Pierre C. Wong, M.D., and Wanda C. Miller-Hance, M.D., focuses on the application of imaging modality in patients with congenital heart disease. Published in early 2014, this book provides practical and instructive information, supplemented with figures/illustrations and highquality videos. It is a resource for clinicians and trainees who wish to obtain basic knowledge or advance their understanding of the field. Gregory’s Textbook of Pediatric Anesthesia introduces the basics of the field and explains how they are applied to contemporary practice both in and out of the operating room. Co-edited by Dean B. Andropoulos, M.D., chief of Anesthesiology at Texas Children’s Hospital, the book uses an evidencebased approach and is supplemented by in-depth case studies that spotlight best practices in action across all the major subspecialties. It also contains extensive information on anesthesia care for patients with congenital heart disease. Anesthesia for Congenital Heart Disease, edited by Dean B. Andropoulos, M.D., Stephen A. Stayer, M.D., Emad B. Mossad, M.D., and Wanda C. Miller-Hance, M.D., is the leading textbook in the field of pediatric cardiac anesthesia. Now in its 3rd edition, this textbook contains information on the rapid advances in surgery and anesthesia for congenital heart disease that have occurred in recent years, including neonatal cardiac surgery and anesthesia, treatment of single ventricle patients, new diagnostic modalities and developments in the catheterization laboratory. It also addresses mechanical support of circulation, embryology and quality/outcomes management. Following the inaugural American Board of Anesthesiology Pediatric Anesthesiology subspecialty board exam, Texas Children’s Hospital is now home to more than 60 subspecialty board-certified pediatric anesthesiologists. H E A RT C E N T E R 2 0 1 5 Cardiovascular Intensive Care Unit The Cardiovascular Intensive Care Unit (CVICU) includes cardiac intensivists, advanced practice providers, nurses, respiratory therapists, social workers, dietitians and support staff who provide intensive care to newborns, infants, children and young adults with congenital and acquired heart disease. With a total of 33 beds, the CVICU cares for patients undergoing surgery for congenital and acquired heart disease, as well as those with end-stage heart failure before and after heart transplantation. This year, in partnership with Cardiovascular Surgery, Heart Failure and Interventional Cardiology, we expanded our mechanical support program to include the largest pediatric utilization of a novel device, the Impella.® New Heart Failure Intensive Care Unit In July 2015, the CVICU launched the Heart Failure Intensive Care Unit, the first of its kind in the nation. This highly specialized 12-bed unit focuses on the treatment of children with heart failure, as well as those requiring intensive care before and after heart transplant, and those on mechanical cardiac support. Renowned faculty and training programs CVICU faculty includes leaders in pediatric cardiac intensive care, with certification in pediatric critical care, pediatric cardiology and pediatric anesthesiology. Texas Children’s also has the largest dedicated CVICU advanced training program in the country. The Pediatric Cardiac Critical Care Instructorship is a 12-month didactic and clinical training program for individuals who have completed fellowships in pediatric critical care medicine or pediatric cardiology and wish to pursue an additional year of training in pediatric cardiac intensive care. This training program provides a unique interface among critical care medicine, cardiology, cardiothoracic surgery and cardiac anesthesia. Texas Children’s also offers a fourth year of specialized training in neonatal cardiac critical care. The first of its kind in the nation, this program provides one position each year to neonatologists who desire additional training in newborn critical heart disease. The opening of the Heart Failure Intensive Care Unit. 41 42 H E A RT C E N T E R 2 0 1 5 Nursing care in the Cardiovascular Intensive Care Unit The CVICU at Texas Children’s Hospital has 106 specialized pediatric intensive care registered nurses on staff. The hours per patient day equivalent in the CVICU are 22.52 compared to the national benchmark of 26.16. Benchmark data is pulled from Children’s Hospital Association of like units. All newly admitted surgical cases receive a minimum ratio of 1:1 nursing care. More than 95 percent of the CVICU registered nurses have a bachelor’s degree in nursing with a 22 percent rate of attainment of certification in critical care nursing. Cardiology Patient Care Unit The Cardiology Patient Care Unit is a 22-bed mixed intermediate and acute care unit caring for newborns, infants, children and young adults with heart disease. The unit is staffed by pediatric cardiologists, as well as a team of cardiology fellows, cardiac advanced practice providers, medical residents and cardiac trained registered nurses. In 2015, there were 1,222 patient encounters in this unit. Nursing care in the Cardiology Patient Care Unit The Cardiology Patient Care Unit at Texas Children’s Hospital has 54 registered nurses on staff. The hours per patient day equivalent in the acute care unit are 13.7, compared to the national benchmark of 15.9. The unit has a 65 percent rate of attainment for certification in pediatric nursing. Almost 90 percent of the cardiology acute care registered nurses have a bachelor’s degree in nursing, with the remaining 11 percent currently pursuing their bachelor’s degree in nursing. Cardiovascular Simulation Program Texas Children’s Heart Center developed an in-situ simulation program in 2012 to ensure nurses are prepared for patient emergencies and other high-risk clinical scenarios. The goals of the program are to improve patient safety through early identification of patient issues and to improve crisis resource management and teamwork skills. Program leaders established a curriculum and learning matrix in order to track objectives and progress. In 2015, the in-situ simulation room provided over 300 learning opportunities on the cardiology floor. H E A RT C E N T E R 2 0 1 5 Cardiac Developmental Outcomes Program Until recently, most neurodevelopmental follow-up of congenital heart disease patients has been in the context of research studies. Texas Children’s Heart Center’s Cardiac Developmental Outcomes Program focuses on medical, social and developmental health in order to help children reach their maximum potential. Launched in April 2013, the program was created to provide routine neurodevelopmental assessments and referrals for babies and children with congenital heart disease who have undergone early surgery. Since the program’s creation, the team has assessed 375 babies and children and provided referrals to a variety of specialists including speech and language, hearing, neurology and behavioral experts. The team includes developmental pediatricians and psychologists who work with the Heart Center to identify any problems at the earliest possible stage. This provides an opportunity for early intervention in order to minimize the impact of issues during childhood. The program provides family-centered care, in which the child’s parents or caregivers are directly consulted and involved in their child’s assessment and interventions for developmental progress. We also help families find resources in their communities that support their child’s development. 43 44 H E A RT C E N T E R 2 0 1 5 Outcomes & Impact Service The Outcomes & Impact Service at Texas Children’s Hospital measures important clinical outcomes and the impact of care on the quality of life and functional status of our patients over time. The team’s goal is to deliver the highest value of health care to the patient. By tracking outcomes, we learn about what happens to our patients, and we also learn about our performance as a health care delivery organization. We know we must continue to strive toward excellence in care delivery. In addition to providing statistics, we strive to engage patients and families in a conversation about the choices they face that will impact their health. Our team includes outcomes nurses dedicated to different clinical specialties, computer programmers, data architects and specialists, and a statistician who works closely with clinical and administrative teams to measure, improve and share our outcomes. The goals of our service are to: • Track and improve our clinical outcomes • Understand the impact of those outcomes on the lives of our patients and families over time • Make our outcomes data available in a form accessible by the general public • Partner with patients and families in understanding outcomes data • Help patients and families know what questions to ask when seeking medical treatment For more information, please visit texaschildrens.org/outcomes-and-impact-service. H E A RT C E N T E R 2 0 1 5 45 46 H E A RT C E N T E R 2 0 1 5 Meet Our Leaders Charles D. Fraser, Jr., M.D., is surgeonin-chief, co-director of Texas Children’s Heart Center and chief of the Congenital Heart Surgery Division at Texas Children’s Hospital. His academic appointments include professor of Surgery in the Michael E. DeBakey Department of Surgery (tenured) at Baylor College of Medicine, professor of Pediatrics at Baylor College of Medicine and adjunct professor of Bioengineering at Rice University. Dr. Fraser holds the Clayton Chair in Surgery and the Donovan Chair in Congenital Heart Surgery at Texas Children’s Hospital. Dr. Fraser has a clinical appointment at the Texas Heart Institute, where he serves as director of the Adult Congenital Heart Surgery Program. Dr. Fraser’s education began as an undergraduate at the University of Texas at Austin, where he graduated with honors in mathematics. He received his medical degree with honors from the University of Texas Medical Branch at Galveston. His residency and fellowship training took place at The John Hopkins Hospital. He completed additional fellowship training in congenital heart surgery at the Royal Children’s Hospital in Melbourne, Australia. After joining the faculty at Cleveland Clinic, Dr. Fraser was recruited to Texas Children’s Hospital in July 1995 to establish a dedicated pediatric congenital heart surgery program. Daniel J. Penny, M.D., Ph.D., M.H.A., is chief of Cardiology at Texas Children’s Hospital, co-director of Texas Children’s Heart Center and professor of Pediatrics at Baylor College of Medicine. Dr. Penny obtained his medical degree from the National University of Ireland and received a doctoral degree for his thesis, “Functional Analysis of Fontan Circulation,” from the University of London. He completed fellowship training in pediatric cardiology at the Royal Children’s Hospital in Melbourne and received a second doctoral degree at Monash University, Australia, for his studies on neonatal circulation. Dr. Penny worked as a pediatric cardiologist at the Royal Brompton Hospital and Great Ormond Street Hospital in London. Before coming to Texas Children’s Hospital, he was the chief of Cardiology at the Royal Children’s Hospital of Melbourne and a professor in the Department of Pediatrics within the University of Melbourne. H E A RT C E N T E R 2 0 1 5 Emad B. Mossad, M.D., is director of Pediatric Cardiovascular Anesthesiology at Texas Children’s Hospital and co-director of Texas Children’s Heart Center. He is also a professor of Anesthesiology at Baylor College of Medicine. Dr. Mossad’s training began as an undergraduate at Cairo University, Egypt. His medical degree is from University of Cairo Medical School, and his residency and fellowship training in cardiac anesthesia took place at the Cleveland Clinic Foundation. He completed a pediatric anesthesia fellowship at Children’s National Medical Center of George Washington University and an echocardiography fellowship at the Cleveland Clinic. Prior to joining Texas Children’s Hospital in 2008, Dr. Mossad served as section head for Congenital Cardiac Anesthesia at the Cleveland Clinic from 1997-2008. Dr. Mossad is actively involved in several professional societies, including service on committees for the Society of Cardiovascular Anesthesiologists and Society for Pediatric Anesthesia. He is also a founding board member and currently serves as president of the Congenital Cardiac Anesthesia Society. Additionally, Dr. Mossad has 38 peer-reviewed publications and eight book chapters, mostly in his field of interest of coagulation management and perioperative care of children and adults with congenital heart disease. He also has a strong interest in the training and education of fellows and residents in the disciplines of pediatric and cardiac anesthesia. Lara S. Shekerdemian, M.D., F.R.A.C.P., M.H.A., is chief of Critical Care at Texas Children’s Hospital and co-director of Texas Children’s Heart Center. She also serves as the vice chair of Clinical Affairs for the Department of Pediatrics and professor of Pediatrics at Baylor College of Medicine. She graduated from Birmingham University Medical School and was awarded a postgraduate doctoral degree for her thesis, “Cardiopulmonary Interactions in Congenital Heart Disease,” from the University of Birmingham. Dr. Shekerdemian trained in pediatrics and pediatric cardiology and undertook postgraduate research in London. She trained in critical care in London and Toronto. She was previously on faculty at the Great Ormond Street Hospital in London and was most recently the chief of Critical Care at The Royal Children’s Hospital in Melbourne. Her research and clinical interests include extracorporeal life support, brain injury in infants and children with heart disease, and outcomes in children after admission to the intensive care unit. 47 48 H E A RT C E N T E R 2 0 1 5 Texas Children’s Heart Center Medical Staff To view online profiles for each of our physicians, visit texaschildrens.org/heart. Congenital Heart Surgery Charles D. Fraser, Jr., M.D., Chief Iki Adachi, M.D. Jeffrey S. Heinle, M.D. Lauren Kane, M.D. E. Dean McKenzie, M.D. Carlos Mery, M.D. Pediatric Cardiology Daniel J. Penny, M.D., Ph.D., M.H.A., Chief Hugh Allen, M.D., Ph.D. Carolyn A. Altman, M.D., F.A.C.C., F.A.S.E. Rachel Arnold, P.A.-C. Nancy A. Ayres, M.D., F.A.C.C., F.A.S.E. Manish Bansal, M.D. Judith A. Becker, M.D. Tasha Bryant, M.S.N., R.N., F.N.P.-C., C.P.N.P.-A.C. Antonio G. Cabrera, M.D. Allison Callender, P.A.-C. Leigh Carreon, M.S.N., R.N., C.P.N.P.-A.C. Constance Cephus, Ph.D., R.N., C.P.N.P.-A.C./P.C. Kwonsoo Chun, M.D. Cristina Clawson, M.S.N., R.N., C.P.N.P.-A.C. Lisa D’Alessandro, M.D. Caridad De La Uz, M.D. Susan W. Denfield, M.D. Heather A. Dickerson, M.D. William J. Dreyer, M.D., F.A.C.C., F.A.A.P. Peter Ermis, M.D. Yuxin Fan, M.D. Wayne J. Franklin, M.D. Angela Gooden, M.S.N., R.N., C.P.N.P.-A.C./P.C. Mary Hoang, M.S.N., R.N., C.P.N.P.-A.C./P.C. Ben Jacob, P.A.-C. Aamir Jeewa, M.D. Henri Justino, M.D., C.M., F.R.C.P.C., F.A.C.C., F.S.C.A.I. Josh A. Kailin, M.D. Asra Khan, M.D. Jeffrey J. Kim, M.D. Michele Krenek, M.S.N., R.N., F.N.P.-C. Julie K. Kuzin, M.S.N., R.N., C.P.N.P.-A.C./P.C. William Buck Kyle, M.D. Wilson Lam, M.D. Renna Lange, M.S.N., R.N., C.P.N.P.-A.C. M. Regina Lantin-Hermoso, M.D. Emily J. Lawrence, D.O. Katherine Lindle, M.D. Aimee Liou, M.D. Keila N. Lopez, M.D., M.P.H. Shiraz A. Maskatia, M.D. Wanda C. Miller-Hance, M.D. Christina Miyake, M.D. Silvana M. Molossi, M.D., Ph.D. Douglas S. Moodie, M.D., M.S. Shaine A. Morris, M.D., M.P.H. Taylor Morse, M.S.N., R.N., C.P.N.P.-A.C. Antonio R. Mott, M.D. Michael R. Nihill, M.D. Cory V. Noel, M.D. Richard E. O’Brien, P.A.-C. Elena C. Ocampo, M.D., F.A.A.P., F.A.C.C. Dhaval R. Parekh, M.D. Ricardo H. Pignatelli, M.D. Jack Price, M.D. Athar M. Qureshi, M.D. Priscila P. Reid, M.S.N., R.N., F.N.P.-C., C.P.N.P.-A.C. Alan F. Riley, M.D. Shannon M. Rivenes, M.D. Craig Rusin, M.D. Alexia B. Santos, M.D. Amy Sanyahumbi, M.D. Tobias Schlingmann, M.D. David W. Sapire, M.D. Andrea Sawyer-Gray, M.S.N., R.N., C.P.N.P.-A.C. Thomas J. Seery, M.D. S. Kristen Sexson Tejtel, M.D., Ph.D. America Suh, M.S.N., A.P.R.N., F.N.P.-C. Santiago O.Valdes, M.D. Thomas A.Vargo, M.D. Giles W.Vick III, M.D., Ph.D. Steven B. Wolfe, M.D. Betul Yilmaz, M.D. Justin Zachariah, M.D., M.P.H. Cardiovascular Anesthesia Emad B. Mossad, M.D., Director Dean B. Andropoulos, M.D. Tamra Baker, C.R.N.A. Beth Barraza, R.N., C.P.N.P. Kenneth M. Brady, M.D. Lisa A. Caplan, M.D. Barbi DeMoss, R.N., C.P.N.P. R. Blaine Easley, M.D. Jennifer Esplana, C.R.N.A. H E A RT C E N T E R 2 0 1 5 Erin A. Gottlieb, M.D. Stuart R. Hall, M.D. Rhonda Martone, C.R.N.A. Wanda C. Miller-Hance, M.D. Princy Mohan, R.N., C.P.N.P. Pablo Motta, M.D. Laura Oates, C.R.N.A. Elyse Parchmont, C.R.N.A. Zoel Quinonez, M.D. Ashraf Resheidat, M.D. Premal Trivedi, M.D. David F.Vener, M.D. Lauren Weaver, C.R.N.A. Saeed Yacouby, C.R.N.A. Jennifer Yborra, R.N., P.N.P.-A.C. Jordana Goldman, M.D. Parag Jain, M.D. Javier Lasa, M.D. Jack F. Price, M.D. Ashraf Resheidat, M.D. Dantin J. Roddy, M.D. Sebastian Tume, M.D. Eric A. Williams, M.D., M.S., M.M.M., F.A.A.P. Instructors in Pediatric Cardiac Critical Care Charlie Bergstrom, M.D. Mohammad Ebraheem, M.D. Rhiannon Hickok, M.D. Mary K. Olive, M.D. Developmental Outcomes Cardiac Critical Care Lara S. Shekerdemian, M.D., F.R.A.C.P., M.H.A., Chief Paul A. Checchia, M.D., F.A.A.P., F.C.C.M., F.A.C.C., Medical Director Barbara-Jo Achuff, M.D. Natasha Afonso, M.D. Marc Anders, M.D. Patricia Bastero, M.D. Aarti Bavare, M.D., M.P.H. Kenneth Brady, M.D. Ronald A. Bronicki, M.D. Antonio G. Cabrera, M.D. Heather Chandler, M.D. Heather A. Dickerson, M.D. Ronald B. Easley, M.D. Lara S. Shekerdemian, M.D., F.R.A.C.P., M.H.A., Medical Director Eboni Smith, M.D., Clinic Lead Sonia Monteiro, M.D. Lisa Noll, Ph.D. Daniel J. Penny, M.D., Ph.D., M.H.A. Estrella Mazarico de Thomas, R.N., Outcomes Clinic Coordinator Margaret Whitehead, R.N., Outcomes Research Coordinator Quality Eric A. Williams, M.D., M.S., M.M.M., F.A.A.P., Medical Director Kathleen E. Carberry, R.N., M.P.H., Director, Outcomes & Impact Service 49 50 H E A RT C E N T E R 2 0 1 5 Texas Children’s Heart Center Publications Abd Ellah N, Taylor L, Troja W, Owens K, Ayres N, Pauletti G, Jones H. Development of non-viral, trophoblast-specific gene delivery for placental therapy. PloS one. 2015;10:e0140879. Achuff BJ, Nicolson SC, Elci OU, Zuppa AF. Intraoperative dexmedetomidine reduces postoperative mechanical ventilation in infants after open heart surgery. Pediatr Crit Care Med. 2015 Jun;16(5):440-7. Acosta S, Penny DJ, Rusin CG. An effective model of blood flow in capillary beds. Microvasc Res. 2015;100:40-47. Acosta S, Puelz C, Riviere B, Penny DJ, Rusin CG. Numerical method of characteristics for one-dimensional blood flow. J Comput Phys. 2015;294:96-109. Adachi I, Burki S, Zafar F, Morales DL. Pediatric ventricular assist devices. J Thorac Dis. 2015;7(12): 2194-2202. Adachi I, Guzman-Pruneda FA, Jeewa A, Fraser CD Jr., McKenzie DE. A modified implantation technique of the Heartware ventricular assist device for pediatric patients. J Heart Lung Transplant. 2015;34:134-136. Adachi I, Guzman-Pruneda FA, Khan MS, McKenzie ED, Fraser CD Jr. Ventricular assist device in children with cardiac graft failure. ASAIO J. 2015;61:729-730. Adachi I, Khan MS, Guzman-Pruneda FA, Fraser CD 3rd, Mery CM, Denfield SW, Dreyer WJ, Morales DL, McKenzie ED, Heinle JS, Fraser CD Jr. Evolution and impact of ventricular assist device program on children awaiting heart transplantation. Ann Thorac Surg. 2015;99:635-640. Adachi I, Shekerdemian L, Checchia PA, Fraser CD Jr. Treatment of Heart Failure: Mechanical Support. In: Rogers’ Textbook of Pediatric Intensive Care. Nichols D, Shaffner H, 5th edition. Lippincott Williams & Wilkins, Philadelphia, PA. 2015. Akcan Arikan A, Williams EA, Graf JM, Kennedy CE, Patel B, Cruz AT. Resuscitation bundle in pediatric shock decreases acute kidney injury and improves outcomes. J Pediatr. 2015;167:1301-5. Akinkuotu AC, Sheikh F, Olutoye OO, Lee TC, Fernandes CJ, Welty SE, Ayres NA, Cass DL. Giant omphaloceles: Surgical management and perinatal outcomes. J Surg Res. 2015;198:388-392. Altman CA. Appropriate use criteria: Vital new link in the chain of quality in pediatric echocardiography. J Am Coll Cardiol. 2015;66:1141-1143. Altman CA, Barker P. Highlights of the 26(th) scientific sessions’ pediatric congenital track. J Am Soc Echocardiogr. 2015;28:25A. Anderson R, Moodie DS, McLaughlin ES. Interview with Roberts Anderson. Congenit Heart Dis. 2015;10:96-104. Asaki SY, McKenzie ED, Elias B, Adachi I. Rectus-sparing technique for driveline insertion of ventricular assist device. Ann Thorac Surg. 2015;100:1920-1922. Axelrod DM, Alten JA, Berger JT, Hall MW, Thiagarajan R, Bronicki RA. Immunologic and infectious diseases in pediatric cardiac critical care: Proceedings of the 10th International Pediatric Cardiac Intensive Care Society Conference. World J Pediatr Congenit Heart Surg. 2015 Oct;6(4):575-87. Bainbridge MN, Davis EE, Choi WY, Dickson A, Martinez HR, Wang M, Dinh H, Muzny DM, Pignatelli R, Katsanis N, Boerwinkle E, Gibbs RA, Jefferies JL. Loss of function mutations in NNT are associated with left ventricular noncompaction. Circ Cardiovasc Genet. 2015;8:544-552. Baker EH, Altman CE. Maternal ratings of child health and child obesity, variations by mother’s race/ ethnicity and nativity. Matern Child Health J. 2015;19:1000-1009. Banka P, Robinson JD, Uppu SC, Harris MA, Hasbani K, Lai WW, Richmond ME, Fratz S, Jain S, Johnson TR, Maskatia SA, Lu JC, Samyn MM, Patton D, Powell AJ. Cardiovascular magnetic resonance techniques and findings in children with myocarditis: A multicenter retrospective study. J Cardiovasc Magn Reson. 2015;17:96. Barton AL, Moffett BS, Valdes SO, Miyake C, Kim JJ. Efficacy and safety of high-dose propranolol for the management of infant supraventricular tachyarrhythmias. J Pediatr. 2015;166:115-118. H E A RT C E N T E R 2 0 1 5 Bastero P, DiNardo JA, Pratap JN, Schwartz JM, Sivarajan VB. Early perioperative management after pediatric cardiac surgery: Review at PCICS 2014. World J Pediatr Congenit Heart Surg. 2015 Oct;6(4):565-74. Beaty RS, Moffett BS, Hall S, Kim J. Evaluating the safety of intraoperative antiarrhythmics in pediatric cardiac surgery patients. Pediatr Cardiol. 2015;36(7):1465-1469. Beg K, Latson LA, Pettersson G, Wallace L, Qureshi AM. Aorta-to-left atrial fistula developing after surgical removal of an atrial septal occlusion device eight years after original implantation. World J Pediatr Congenit Heart Surg. 2015;6:320-323. Bolin EH, Maskatia SA, Tate AL, Petit CJ. Older age at completion of fontan procedure is associated with improved percentage of predicted maximum oxygen uptake. Tex Heart Inst J. 2015;42:333-340. Brady K, Andropoulos DB, Kibler K, Easley RB. A new monitor of pressure autoregulation: What does it add? Anesth Analg. 2015;121(5):1121-3. Bronicki RA. Cardiopulmonary interactions in children with heart failure. Curr Cardiol Rev. 2015 Nov 19. Bronicki RA, Anas NG. The right therapy at the right time in the right patient. Pediatr Crit Care Med. 2015 May;16(4):389-90. Bronicki RA, Fortenberry J, Schreiber M, Potenziano J, Stauffer J, Young J, Checchia PA, Anas NG. Multicenter randomized controlled trial of inhaled nitric oxide for pediatric acute respiratory distress syndrome. J Pediatr. 2015 Feb;166(2):365-369. Cabrera AG, Chen DW, Pignatelli RH, Khan MS, Jeewa A, Mery CM, McKenzie ED, Fraser CD Jr. Outcomes of anomalous left coronary artery from pulmonary artery repair: Beyond normal function. Ann Thorac Surg. 2015 Apr;99(4):1342-7. doi: 10.1016/j.athoracsur.2014.12.035. Epub 2015 Feb 26. Caplan L. S11. Pain is in the eye of the beholder. J Anesth Hist. 2015;1(3):91-2. Cephus CE, Qureshi AM, Sexson-Tejtel SK, Goss JA, Moodie DS. Liver transplantation for HoFH in children: Single center experience. Congenit Heart Dis. 2015;10:520-528. Chan-Dominy AC, Rahiman SN, Anders M, Butt W. Extracorporeal membrane oxygenation and severe portopulmonary hypertension following liver transplantation: Brief report. Int J Artif Organs. 2015 Aug 4;38(6):337-42. Chan-Dominy AC, Anders M, Millar J, Horton S, Best D, Brizard C, D’Udekem Y, Hilton A, Butt W. Extracorporeal membrane modality conversions. Perfusion. 2015 May;30(4):291-4. Chiang DY, Kim JJ, Valdes SO, de la Uz C, Fan Y, Orcutt J, Domino M, Smith M, Wehrens XH, Miyake CY. Loss-of-function scn5a mutations associated with sinus node dysfunction, atrial arrhythmias, and poor pacemaker capture. Circ Arrhythm Electrophysiol. 2015;8:1105-1112. Chyu M, Austin T, Calisir F, Chanjaplammootil S, Davis MJ, Favela J, Gan H, Gefen A, Haddas R, HahnGoldberg S, Hornero R, Yu-Li Huang, Jensen O, Jiang Z, Katsanis JS, Lee JA, Lewis G, Lovell NH, Luebbers HT, Morales GG, Matis T, Matthews JT, Mazur L, Ng EYK, Oommen KJ, Ormand K, Rohde T, SánchezMorillo D, Sanz-Calcedo JG, Sawan M, Shen CL, Shieh JS, Su CT, Sun L, Sun M, Tewolde SN, Williams EA, Yan C, Zhang J, Zhang YT. Healthcare engineering defined: A white paper. J Healthc Eng. 2015;6(4):635-48. Cocoros NM, Kleinman K, Priebe GP, Gray JE, Logan L, Larsen G, Sammons J, Toltzis P, Miroshnik I, Horan K, Burton M, Sims S, Harper M, Coffin S, Sandora T, Hocevar SN, Checchia PA, Klompas M, Lee GM. Ventilator-associated events in neonates and children: A new paradigm. Crit Care Med. 2015 Oct 30. [Epub ahead of print] Coleman RD, Checchia PA. “Extracorporeal Support In High-Risk Patients: Extracorporeal Membrane Oxygenation and Extracorporeal Lung Assist.” In Current Concepts in Pediatric Critical Care 2015. Graciano AL, ed., Society of Critical Care Medicine, 2015. Cruz SM, Akinkuotu AC, Rusin CG, Cass DL, Lee TC, Welty SE, Olutoye OO. A novel multimodal computational system using near-infrared spectroscopy to monitor cerebral oxygenation during assisted ventilation in CDH patients. J Pediatr Surg. 2015. D’Alto M, Romeo E, Argiento P, Di Salvo G, Badagliacca R, Cirillo AP, Kaemmerer H, Bossone E, Naeije R. Pulmonary arterial hypertension: The key role of echocardiography. Echocardiography. 2015;32 Suppl 1:S23-37. 51 52 H E A RT C E N T E R 2 0 1 5 Desai MS, Eblimit Z, Thevananther S, Kosters A, Moore DD, Penny DJ, Karpen SJ. Cardiomyopathy reverses with recovery of liver injury, cholestasis and cholanemia in mouse model of biliary fibrosis. Liver Int. 2015;35:1464-1477. Desai SK, Sayama C, Vener D, Brayton A, Briceño V, Luerssen TG, Jea A. The feasibility and safety of using sublaminar polyester bands in hybrid spinal constructs in children and transitional adults for neuromuscular scoliosis. J Neurosurg Pediatr. 2015;15(3):328-37. Dewey FE, Grove ME, Priest JR, Waggott D, Batra P, Miller CL, Wheeler M, Zia A, Pan C, Karzcewski KJ, Miyake C, Whirl-Carrillo M, Klein TE, Datta S, Altman RB, Snyder M, Quertermous T, Ashley EA. Sequence to medical phenotypes: A framework for interpretation of human whole genome DNA sequence data. PLoS Genet. 2015;11:e1005496. Ermis P, Franklin W, Mulukutla V, Parekh D, Ing F. Left ventricular hemodynamic changes and clinical outcomes after transcatheter atrial septal defect closure in adults. Congenit Heart Dis. 2015;10:E48-53. Ezon DS, Maskatia SA, Sexson-Tejtel K, Dreyer WJ, Jeewa A, Denfield SW. Tissue doppler imaging measures correlate poorly with left ventricular filling pressures in pediatric cardiomyopathy. Congenit Heart Dis. 2015;10:E203-209. Feltes TF, Roth SJ, Almodovar MC, Andropoulos DB, Bohn DJ, Costello JM, Gajarski RJ, Mott AR, Koenig P. Task force 5: Pediatric cardiology fellowship training in critical care cardiology. J Am Coll Cardiol. 2015;66:712-722. Frank DB, Crystal MA, Morales DL, Gerald K, Hanna BD, Mallory GB Jr, Rossano JW. Trends in pediatric pulmonary hypertension-related hospitalizations in the United States from 2000-2009. Pulm Circ. 2015;5(2):339-348. Fraser CD Jr. 50th anniversary landmark commentary on Bender HW Jr, Stewart JR, Merrill WH, Hammon JW Jr, Graham TP Jr. Ten years’ experience with the Senning operation for transposition of the great arteries: Physiological results and late follow-up. Ann Thorac Surg. 1989;47:218-23. Ann Thorac Surg. 2015;100(4):1152-1153. Fraser CD Jr. Evolution of the pediatric and congenital heart surgery service at Texas Children’s Hospital: 1954-2015. Semin Thorac Cardiovasc Surg. 2015;27(4):380-387. Fraser CD Jr. The journey toward improved hypoplastic left heart syndrome outcomes continues – another small step. J Thorac Cardiovasc Surg. 2015;149(6):1487. Fraser CD Jr. The ongoing quest for an ideal surgical repair for tetralogy of Fallot: Focus on the pulmonary valve. J Thorac Cardiovasc Surg. 2015;149(5):1364. Freud LR, Escobar-Diaz MC, Kalish BT, Komarlu R, Puchalski MD, Jaeggi ET, Szwast AL, Freire G, Levasseur SM, Kavanaugh-McHugh A, Michelfelder EC, Moon-Grady AJ, Donofrio MT, Howley LW, Tierney ES, Cuneo BF, Morris SA, Pruetz JD, van der Velde ME, Kovalchin JP, Ikemba CM, Vernon MM, Samai C, Satou GM, Gotteiner NL, Phoon CK, Silverman NH, McElhinney DB, Tworetzky W. Outcomes and predictors of perinatal mortality in fetuses with Ebstein anomaly or tricuspid valve dysplasia in the current era: A multicenter study. Circulation. 2015;132:481-489. Frischhertz BP, Shamszad P, Pedroza C, Milewicz DM, Morris SA. Thoracic aortic dissection and rupture in conotruncal cardiac defects: A population-based study. Int J Cardiol. 2015;184:521-527. Gaies M, Cooper DS, Tabbutt S, Schwartz SM, Ghanayem N, Chanani NK, Costello JM, Thiagarajan RR, Laussen PC, Shekerdemian LS, Donohue JE, Willis GM, Gaynor JW, Jacobs JP, Ohye RG, Charpie JR, Pasquali SK, Scheurer MA. Collaborative quality improvement in the cardiac intensive care unit: Development of the Paediatric Cardiac Critical Care Consortium (PC4). Cardiol Young. 2015;25(5):951-7. Gaies M, Tabbutt S, Schwartz SM, Bird GL, Alten JA, Shekerdemian LS, KlugmanD, Thiagarajan RR, Gaynor JW, Jacobs JP, Nicolson SC, Donohue JE, Yu S, Pasquali SK, Cooper DS. Clinical epidemiology of extubation failure in the pediatric cardiac ICU: A report from the pediatric cardiac critical care consortium. Pediatr Crit Care Med. 2015;16(9):837-45. Gao Y, Jacot JG. Stem cells and progenitor cells for tissue-engineered solutions to congenital heart defects. Biomark Insights. 2015;10(Suppl 1):139-146. Gaynor JW, Stopp C, Wypij D, Andropoulos DB, Atallah J, Atz AM, Beca J, Donofrio MT, Duncan K, Ghanayem NS, Goldberg CS, Hövels-Gürich H, Ichida F, Jacobs JP, Justo R, Latal B, Li JS, Mahle WT, McQuillen PS, Menon SC, Pemberton VL, Pike NA, Pizarro C, Shekerdemian LS, Synnes A, Williams I, Bellinger DC, Newburger JW; International Cardiac Collaborative on Neurodevelopment (ICCON) Investigators. Neurodevelopmental outcomes after cardiac surgery in infancy. Pediatr. 2015;135(5):816-25. H E A RT C E N T E R 2 0 1 5 Goldberg JF, Vesel TP, Jeewa A, Adachi I. Pulmonary artery band reduces left atrial pressure in dilated cardiomyopathy. Ann Thorac Surg. 2015;100:e35-36. Goldsworthy M, Franich-Ray C, Kinney S, Shekerdemian L, Beca J, Gunn J. Relationship between socialemotional and neurodevelopment of 2-year-old children with congenital heart disease. Congenit Heart Dis. 2015 Dec. Grunwell JR, Weiss SL, Cvijanovich NZ, Allen GL, Thomas NJ, Freishtat RJ, Anas N, Meyer K, Checchia PA, Shanley TP, Bigham MT, Fitzgerald J, Howard K, Frank E, Harmon K, Wong HR. Differential expression of the Nrf2-linked genes in pediatric septic shock. Critical Care. 2015 Sep 17;19(1):327. Guzman-Pruneda FA, Orr Y, Trost JG, Zhang W, Das S, Melicoff E, Maddox J, Nugent M, Mery CM, Adachi I, Schecter MG, Mallory GB, Morales DL, Heinle JS, McKenzie ED. Bronchial artery revascularization and en bloc lung transplant in children. J Heart Lung Transplant. 2015. Herbert J, Guzman-Pruneda FA, Sumner EE, McKenzie ED. Simultaneous repair of right-sided coarctation and vascular ring. Ann Thorac Surg. 2015;100(1):334-336. Husain S, Rahman S, Baisden C, Forgione D, Kane L, Neish S, Calhoon JH, Jacobs ML. Creating a “value index”: A method to compare regional programs performing congenital heart surgery. J Health Care Finance. 2015;42(2):1-12. Jabbar AA, Franklin WJ, Simpson L, Civitello AB, Delgado RM 3rd, Frazier OH. Improved systemic saturation after ventricular assist device implantation in a patient with decompensated dextrotransposition of the great arteries after the Fontan procedure. Tex Heart Inst J. 2015;42:40-43. Jacobs JP, O’Brien SM, Pasquali SK, Gaynor JW, Mayer, JE Jr, Karamlou T, Welke KF, Filardo G, Han JM, Kim S, Quintessenza JA, Pizarro C, Tchervenkov CI, Lacour-Gayet F, Mavroudis C, Backer CL, Austin EH 3rd, Fraser CD Jr, Tweddell JS, Jonas RA, Edwards FH, Grover FL, Prager RL, Shahian DM, Jacobs ML. The Society of Thoracic Surgeons congenital heart surgery database mortality risk model: Part 2-clinical application. Ann Thorac Surg. 2015;100(3):1063-1070. Jadhav SP, Golriz F, Atweh LA, Zhang W, Krishnamurthy R. CT angiography of neonates and infants: Comparison of radiation dose and image quality of target mode prospectively ECG-gated 320-MDCT and ungated helical 64-MDCT. AJR Am J Roentgenol. 2015;204(2):W184-91. Jeewa A, Chin C, Pahl E, Atz AM, Carboni MP, Pruitt E, Naftel DC, Rodriguez R, Dipchand AI. Pediatric Heart Transplant Study I. Outcomes after percutaneous coronary artery revascularization procedures for cardiac allograft vasculopathy in pediatric heart transplant recipients: A multi-institutional study. J Heart Lung Transplant. 2015;34:1163-1168. Joyce N, Wellenius GA, Dore DD, Newburger JW, Zachariah JP. Patterns of lipid lowering therapy among children ages 8-20 years. J Pediatr. 2015;167:113-119 e111. Kaul B, Sheikh F, Zamora IJ, Mehollin-Ray AR, Cassady CI, Ayres NA, Cass DL, Olutoye OO. 5, 4, 3, 2, 1: Embryologic variants of pentalogy of Cantrell. J Surg Res. 2015;199:141-148. Khan MS, Zhang W, Taylor RA, Dean McKenzie E, Mallory GB, Schecter MG, Morales DL, Heinle JS, Adachi I. Survival in pediatric lung transplantation: The effect of center volume and expertise. J Heart Lung Transplant. 2015;34:1073-1081. Kienstra CM, Hergenroeder AC, Riley AA, Justino H. Hypertension in an adolescent athlete. Clin Pediatr. 2015. Kindel SJ, Law YM, Chin C, Burch M, Kirklin JK, Naftel DC, Pruitt E, Carboni MP, Arens A, Atz AM, Dreyer WJ, Mahle WT, Pahl E. Improved detection of cardiac allograft vasculopathy: A multi-institutional analysis of functional parameters in pediatric heart transplant recipients. J Am Coll Cardiol. 2015;66:547-557. Knudson JD, Cabrera AG. The pathophysiology of heart failure. Curr Cardiol Rev. 2015. Krishnamurthy R, Pednekar A, Atweh LA, Vogelius E, Chu ZD, Zhang W, Maskatia S, Masand P, Morris SA, Krishnamurthy R, Muthupillai R. Clinical validation of free breathing respiratory triggered retrospectively cardiac gated cine balanced steady-state free precession cardiovascular magnetic resonance in sedated children. J Cardiovasc Magn Reson. 2015;17:1. Kudchadkar SR, Yaster M, Punjabi AN, Quan SF, Goodwin JL, Easley RB, Punjabi NM. Temporal characteristics of the sleep EEG power spectrum in critically ill children. J Clin Sleep Med. 2015;11(12):1449-54. 53 54 H E A RT C E N T E R 2 0 1 5 Kulkarni M, Gokulakrishnan G, Price JF, Fernandes C, Leeflang M, Pammi M. Diagnosing significant PDA using natriuretic peptides in preterm neonates: A systematic review. Pediatr. 2015;135:e510-525. Kyle WB, Decker J, Macicek SL, Valdes SO, Morales D, Hong B, Price JF, Dreyer WJ, Denfield SW, Kim JJ. Arrhythmias in children with ventricular assist devices. Cardiol Young. 2015;25:255-260. Kyle UG, Shekerdemian LS, Coss-Bu JA. Growth failure and nutrition considerations in chronic childhood wasting diseases. Nutr Clin Pract. 2015;30(2):227-38. Lara D, Morris SA, Maskatia SA, Challman M, Nguyen M, Feagin DK, Schoppe L, Zhang J, Bhatt A, SexsonTejtel SK, Lopez KN, Lawrence EJ, Andreas S, Wang Y, Belfort M, Ruano R, Ayres NA, Altman C, Aagaard K, Becker J. 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Echocardiographic parameters of right ventricular diastolic function in repaired tetralogy of fallot are associated with important findings on magnetic resonance imaging. Congenit Heart Dis. 2015;10:E113-122. McCluskey Smith B, Guzman-Pruneda F, Mery CM, Justino H, Qureshi AM,Parekh D. Use of large diameter stents with maximal expansion limits re-intervention in treatment of native coarctation of the aorta [Abstract]. J Am Coll Cardiol. 2015;65(10S): A525. McKenzie ED. Are better results from anatomy or surgery? J Thorac Cardiovasc Surg. 2015;149(2):514. McNeal C, Gregory S, Zachariah J, Copeland L, Cassidy A, Tom J, Wright E, VanWormer J. Temporal trends in lipid screening for familial hypercholesterolemia in youth. Clin. Cardiol. 2015;38:1-18. Mery CM, Guzman-Pruneda FA, De Leon LE, Zhang W, Terwelp MD, Bocchini CE, Adachi I, Heinle JS, McKenzie ED, Fraser CD Jr. Risk factors for development of endocarditis and reintervention in patients undergoing right ventricle to pulmonary artery valved conduit placement. J Thorac Cardiovasc Surg. 2015. Mery CM, Guzman-Pruneda FA, Trost JG Jr., McLaughlin E, Smith BM, Parekh DR, Adachi I, Heinle JS, McKenzie ED, Fraser CD Jr. Contemporary results of aortic coarctation repair through left thoracotomy. Ann Thorac Surg. 2015;100:1039-1046. Miyake CY, Kim JJ. Arrhythmias in left ventricular noncompaction. Card Electrophysiol Clin. 2015;7:319-330. Miyake CY, Motonaga KS, Fischer-Colbrie ME, Chen L, Hanisch DG, Balise RR, Kim JJ, Dubin AM. Risk of cardiac disease and observations on lack of potential predictors by clinical history among children presenting for cardiac evaluation of mid-exertional syncope. Cardiol Young. 2015:1-7. Moffett BS, Garner A, Zapata T, Orcutt J, Niu M, Lopez KN. Serum digoxin concentrations and clinical signs and symptoms of digoxin toxicity in the paediatric population. Cardiol Young. 2015:1-6. Moffett BS, Garrison JM, Hang A, Morris SA, Tsang R, Dinh K, Griffiths P, Bronicki R, Checchia PA. Prostaglandin availability and association with outcomes for infants with congenital heart disease. Pediatr Cardiol. 2015. Moffett BS, Hilvers PS, Dinh K, Arikcan A, Checchia PA, Bronicki RA. Vancomycin-associated acute kidney injury in pediatric cardiac intensive care patients. Congenit Heart Dis. 2015;10:E6–E10. Moffett BS, Lupo PJ, delaUz CM, Valdes SO, Miyake CY, Decker JA, Kim JJ. Efficacy of digoxin in comparison with propranolol for treatment of infant supraventricular tachycardia: Analysis of a large, national database. Cardiol Young. 2015;25:1080-1085. Moffett BS, Mossad EB, Tobias JD, Cabrera AG. Dexmedetomidine utilisation and outcomes of children with trisomy 21 undergoing congenital heart disease surgery. 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Congenit Heart Dis. 2015;10:95. Moodie D. An interview with Dr. Robert Anderson. Congenit Heart Dis. 2015;10:1. Moon-Grady AJ, Morris SA, Belfort M, Chmait R, Dangel J, Devlieger R, Emery S, Frommelt M, Galindo A, Gelehrter S, Gembruch U, Grinenco S, Habli M, Herberg U, Jaeggi E, Kilby M, Kontopoulos E, Marantz P, Miller O, Otano L, Pedra C, Pedra S, Pruetz J, Quintero R, Ryan G, Sharland G, Simpson J, Vlastos E, Tworetzky W, Wilkins-Haug L, Oepkes D. International fetal cardiac intervention registry: A worldwide collaborative description and preliminary outcomes. J Am Coll Cardiol. 2015;66:388-399. Morris SA. Arterial tortuosity in genetic arteriopathies. Curr Opin Cardiol. 2015;30:587-593. Mossad E. News from the pediatric anesthesia societies: The Congenital Cardiac Anesthesia Society. Paediatr Anaesth. 2015;25(11):1071. Netto R, Mondini M, Pezzella C, Romani L, Lucignano B, Pansani L, D’Argenio P, Cogo P. Parenteral nutrition is one of the most significant risk factors for nosocomial infections in a pediatric cardiac intensive care unit. JPEN J Parenter Enteral Nutr. 2015. Nusbaum DM, Brady KM, Kibler KK, Blaine Easley R. Acute hypercarbia increases the lower limit of cerebral blood flow autoregulation in a porcine model. Neurol Res. 2015;27. Pignatelli RH, Ghazi P, Chandra-Bose Reddy S, Thompson P, Cui Q, Castro J, Okcu MF, Jefferies JL. Erratum to: Abnormal myocardial strain indices in children receiving anthracycline chemotherapy. Pediatr Cardiol. 2015;36:1617. Pignatelli RH, Ghazi P, Reddy SC, Thompson P, Cui Q, Castro J, Okcu MF, Jefferies JL. Abnormal myocardial strain indices in children receiving anthracycline chemotherapy. Pediatr Cardiol. 2015;36:1610-1616. Prakash A, Adlakha H, Rabideau N, Hass CJ, Morris SA, Geva T, Gauvreau K, Singh MN, Lacro RV. Segmental aortic stiffness in children and young adults with connective tissue disorders: Relationships with age, aortic size, rate of dilation, and surgical root replacement. Circulation. 2015;132:595-602. Puelz C, Canic S, Riviere B, Rusin C. Comparison of reduced models for blood flow using Runge-Kutta discontinuous galerkin methods. Fluid Dyn. 2015. Rhee CJ, Fraser CD 3rd, Kibler K, Easley RB, Andropoulos DB, Czosnyka M, Varsos GV, Smielewski P, Rusin CG, Brady KM, Kaiser JR. Ontogeny of cerebrovascular critical closing pressure. Pediatr Res. 2015;78(1):71-5. Roddy DJ, Spaeder MC, Pastor W, Stockwell DC, Klugman D. Unplanned extubations in children: Impact on hospital cost and length of stay. Pediatr Crit Care Med. 2015;16:572-575. Ross RD, Brook M, Feinstein JA, Koenig P, Lang P, Spicer R, Vincent JA, Lewis AB, Martin GR, Bartz PJ, Fischbach PS, Fulton DR, Matherne GP, Reinking B, Srivastava S, Printz B, Geva T, Shirali GS, Weinberg P, Wong PC, Armsby LB, Vincent RN, Foerster SR, Holzer RJ, Moore JW, Marshall AC, Latson L, Dubin AM, Walsh EP, Franklin W, Kanter RJ, Saul JP, Shah MJ, Van Hare GF, Feltes TF, Roth SJ, Almodovar MC, Andropoulos DB, Bohn DJ, Costello JM, Gajarski RJ, Mott AR, Stout K, Valente AM, Cook S, Gurvitz M, Saidi A, Webber SA, Hsu DT, Ivy DD, Kulik TJ, Pahl E, Rosenthal DN, Morrow R, Mahle WT, Murphy AM, Li JS, Law YM, Newburger JW, Daniels SR, Bernstein D, Marino BS. 2015 SPCTPD/ACC/AAP/AHA training guidelines for pediatric cardiology fellowship programs (revision of the 2005 training guidelines for pediatric cardiology fellowship programs). J Am Coll Cardiol. 2015. Ruano R, Javadian P, Kailin JA, Maskatia SA, Shamshirsaz AA, Cass DL, Zamora IJ, Sangi-Haghpeykar H, Lee TC, Ayres NA, Mehollin-Ray A, Cassady CI, Fernandes C, Welty S, Belfort MA, Olutoye OO. Congenital heart anomaly in newborns with congenital diaphragmatic hernia: A single-center experience. Ultrasound Obstet Gynecol. 2015;45:683-688. 55 56 H E A RT C E N T E R 2 0 1 5 Sami SA, Moffett BS, Karlsten ML, Cabrera AG, Price JF, Dreyer WJ, Denfield SW, Jeewa A. Novel use of tolvaptan in a pediatric patient with congestive heart failure due to Duchenne muscular dystrophy and congenital adrenal hyperplasia. J Pediatr Pharmacol Ther. 2015;20:393-396. Santoro G, Gaio G, Capozzi G, Giugno L, Palladino MT, Capogrosso C, D’Aiello AF, Caianiello G, Russo MG. Fate of hypoplastic pulmonary arteries after arterial duct stenting in congenital heart disease with duct-dependent pulmonary circulation. JACC Cardiovasc Interv. 2015;8:1626-1632. Schweiger M, Vanderpluym C, Jeewa A, Canter CE, Jansz P, Parrino PE, Miera O, Schmitto J, Mehegan M, Adachi I, Hubler M, Zimpfer D. Outpatient management of intra-corporeal left ventricular assist device system in children: A multi-center experience. Am J Transplan. 2015;15:453-460. Scully BB, Fan C, Grigoryan B, Jacot JG, Vick GW, 3rd, Kim JJ, Fraser CD, Jr., Grande-Allen KJ, Morales DL. Remodeling of ECM patch into functional myocardium in an ovine model: A pilot study. J Biomed Mater Res B Appl Biomater. 2015. Seery T, Boswell H, Lara A. Caring for refugee children. Pediatr Rev. 2015;36:323-338, quiz 339-340. Siruguppa K, Tume S. Ventricular Septal Defects. In: The Pediatric Cardiac Intensive Care Handbook. Jones M, Klugman D, Fitzgerald R, Kohr LM, Costello JC, Berger, JT, Bronicki R, 1st edition. Washington, DC; 2015. Snyder C, Moodie D. American Academy of Pediatrics section on cardiology meeting. Congenit Heart Dis. 2015;10:288-290. Stephens EH, Odell D, Stein W, LaPar DJ, DeNino WF, Aftab M, Berfield K, Eilers, AL, Groth S, Lazar JF, Robich MP, Shah AA, Smith DA, Stock C, Tchantchaleishvili V, Mery CM, Turek JW, Salazar J, Nguyen TC. A decade of change: Training and career paths of cardiothoracic surgery residents 2003 to 2014. Ann Thorac Surg. 2015;100(4):1305-13; discussion 1313-4. Tsang R, Checchia P, Bronicki RA. Hemodynamic monitoring in the acute management of pediatric heart failure. Curr Cardiol Rev. 2015 Nov 19. [Epub ahead of print] Tume SC, Goldberg J, Molossi S, Bronicki RA. Pharmacologic approach to heart failure. Curr Cardiol Rev. 2015. Tume S. Heartmate II. In: The Pediatric Cardiac Intensive Care Handbook. Jones M, Klugman D, Fitzgerald R, Kohr LM, Costello JC, Berger JT, Bronicki R, 1st edition. Washington, DC; 2015. Valdes SO. Public access defibrillation programs: Improving outcomes worldwide. J Am Heart Assoc. 2015;4:e002631. Varsos GV, Kolias AG, Smielewski P, Brady KM, Varsos VG, Hutchinson PJ, Pickard JD, Czosnyka M. A noninvasive estimation of cerebral perfusion pressure using critical closing pressure. J Neurosurg. 2015;123(3):638-48. Walden M, Cephus CE, Gordon MD, Hagan J. The great American cookie experiment: Engaging staff nurses in research. J Pediatr Nurs. 2015;30:508-515. Weia BC, Adachi I, Jacot JG. Clinical and molecular comparison of pediatric and adult reverse remodeling with ventricular assist devices. Artif Organs. 2015;39:691-700. Williams EA, Nikolai D, Ladwig L, Miller C, Fredeboelling E. Development of “swarm” as a model for high reliability, rapid problem-solving, and institutional learning. Jt Comm J Qual Patient Saf. 2015;41(11):508-13. Wilmot I, Cephus CE, Cassedy A, Kudel I, Marino BS, Jefferies JL. Health-related quality of life in children with heart failure as perceived by children and parents. Cardiology in the Young. 2015:1-9. Wong HR, Cvijanovich NZ, Anas N, Allen GL, Thomas NJ, Bigham MT, Weiss SL, Checchia PA, Meyer K, Shanley TP, Quasney M, Hall M, Gedeit R, Freishtat RJ, Nowak J, Shekhar RS, Gertz S, Dawson E, Howard K, Harmon K, Beckman E, Frank E, Lindsell CJ. Developing a clinically feasible personalized medicine approach to pediatric septic shock. Am J Respir Crit Care Med. 2015 Feb 1;191(3):309-15. Wong HR, Cvijanovich NZ, Anas N, Allen GL, Thomas NJ, Bigham MT, Weiss SL, Fitzgerald J, Checchia PA, Meyer K, Quasney M, Hall M, Gedeit R, Freishtat RJ, Nowak J, Raj SS, Gertz S, Howard K, Harmon K, Lahni P, Frank E, Hart KW, Lindsell CJ. Prospective testing and redesign of a temporal biomarker based risk model for patients with septic shock: Implications for septic shock biology. EBioMedicine. 2015 Nov 22;2(12):2087-93. H E A RT C E N T E R 2 0 1 5 Wong HR, Cvijanovich NZ, Anas N, Allen GL, Thomas NJ, Bigham MT, Weiss SL, Fitzgerald J, Checchia PA, Meyer K, Shanley TP, Quasney M, Hall M, Gedeit R, Freishtat RJ, Nowak J, Shekhar RS, Gertz S, Dawson E, Howard K, Harmon K, Lahni P, Frank E, Hart KW, Lindsell CJ. A multi-biomarker-based risk model for estimating the risk of septic acute kidney injury. Crit Care Med. 2015 Aug;43(8):1646-53. Yang PC, Moreno JD, Miyake CY, Vaughn-Behrens SB, Jeng MT, Grandi E, Wehrens XH, Noskov S, Clancy CE. In silico prediction of drug therapy in catecholaminergic polymorphic ventricular tachycardia. J Physiol. 2015. Yang X, Wang T, Lin X, Yue X, Wang Q, Wang G, Fu Q, Ai X, Chiang DY, Miyake CY, Wehrens XH, Chang J. Genetic deletion of rnd3/rhoe results in mouse heart calcium leakage through upregulation of protein kinase A signaling. Circ Res. 2015;116:e1-e10. Zachariah JP, Hwang S, Hamburg NM, Benjamin EJ, Larson MG, Levy D, Vita JA, Sullivan LM, Mitchell GF, Vasan RS. Circulating adipokines and vascular function: Cross-sectional associations in a community-based cohort. Hypertension. 2015. Zachariah JP, McNeal CJ, Copeland LA, Fang-Hollingsworth Y, Stock EM, Sun F, Song JJ, Gregory ST, Tom JO, Wright EA, VanWormer JJ, Cassidy-Bushrow AE. Temporal trends in lipid screening and therapy among youth from 2002 to 2012. J Clin Lipidol. 2015;9:S77-87. Zachariah JP, Samnaliev M. Echo-based screening of rheumatic heart disease in children: A cost-effectiveness Markov model. J Med Econ. 2015;18:410-419. Zafar F, Jefferies JL, Tjossem CJ, Bryant R 3rd, Jaquiss RD, Wearden PD, Rosenthal DN, Cabrera AG, Rossano JW, Humpl T, Morales DL. Biventricular Berlin Heart EXCOR pediatric use across the United States. Ann Thorac Surg. 2015;99:1328-1334. 57 56 H E A RT C E N T E R 2 0 1 4 Texas Children’s Heart Center Referrals To refer your pediatric patient to Texas Children’s Heart Center, please call 832-82-HEART (832-824-3278). Congenital Heart Surgery The Congenital Heart Surgery service at Texas Children’s Hospital offers same-day surgical consultation appointments. To make an appointment for a same-day consultation, call 832-TCH-APPT (832-824-2778). For additional appointment information or to speak with a division administrator, please call 832-826-2030. Cardiology, Adult Congenital Heart Disease and the Cardiovascular Intensive Care Unit 832-82-HEART (832-824-3278) Heart Transplant Program 866-683-8032 Cardiovascular Anesthesia 832-826-5831 Referrals Visit texaschildrens.org/refer for more information about referring a patient, or learn more aboutCongenital Texas Children’s Heart Center at texaschildrens.org/heart. Heart Surgery The Congenital Heart Surgery Service at Texas Children’s Hospital offers same-day surgical consultation appointments. To make an appointment for a same-day consultation, call 832-TCH-APPT (832-824-2778). For additional appointment information or to speak with a division administrator, please call 832-826-2030. Heart Transplant Program 866-683-8032 Cardiology, Adult Congenital Heart Disease and Cardiovascular Intensive Care Unit 832-82-HEART (832-824-3278) Cardiovascular Anesthesia 832-826-5831 To refer a patient to Texas Children’s Heart Center, please call 832-82-HEART (832-824-3278). With six decades of experience in caring for children’s hearts, Texas Children’s Heart Center combines leading, world-class technology with a compassionate, family-centered approach to pediatric cardiac care. Our multidisciplinary team of pediatric cardiologists, cardiovascular surgeons, cardiovascular anesthesiologists, perfusionists, adult congenital heart disease specialists, cardiac intensivists, nurses, child life specialists and support staff work together to surround patients with expertise at every point from diagnosis through treatment in order to provide the best possible results. Meet the Texas Children’s Heart Center team. (FLIP OPEN) Visit texaschildrens.org/refer for more information about referring a patient or learn more about Texas Children’s Heart Center at texaschildrens.org/heart. H E A RT C E N T E R 2 0 1 5 Wong HR, Cvijanovich NZ, Anas N, Allen GL, Thomas NJ, Bigham MT, Weiss SL, Fitzgerald J, Checchia PA, Meyer K, Shanley TP, Quasney M, Hall M, Gedeit R, Freishtat RJ, Nowak J, Shekhar RS, Gertz S, Dawson E, Howard K, Harmon K, Lahni P, Frank E, Hart KW, Lindsell CJ. A multi-biomarker-based risk model for estimating the risk of septic acute kidney injury. Crit Care Med. 2015 Aug;43(8):1646-53. Yang PC, Moreno JD, Miyake CY, Vaughn-Behrens SB, Jeng MT, Grandi E, Wehrens XH, Noskov S, Clancy CE. In silico prediction of drug therapy in catecholaminergic polymorphic ventricular tachycardia. J Physiol. 2015. Yang X, Wang T, Lin X, Yue X, Wang Q, Wang G, Fu Q, Ai X, Chiang DY, Miyake CY, Wehrens XH, Chang J. Genetic deletion of rnd3/rhoe results in mouse heart calcium leakage through upregulation of protein kinase A signaling. Circ Res. 2015;116:e1-e10. Zachariah JP, Hwang S, Hamburg NM, Benjamin EJ, Larson MG, Levy D, Vita JA, Sullivan LM, Mitchell GF, Vasan RS. Circulating adipokines and vascular function: Cross-sectional associations in a community-based cohort. Hypertension. 2015. Zachariah JP, McNeal CJ, Copeland LA, Fang-Hollingsworth Y, Stock EM, Sun F, Song JJ, Gregory ST, Tom JO, Wright EA, VanWormer JJ, Cassidy-Bushrow AE. Temporal trends in lipid screening and therapy among youth from 2002 to 2012. J Clin Lipidol. 2015;9:S77-87. Zachariah JP, Samnaliev M. Echo-based screening of rheumatic heart disease in children: A cost-effectiveness Markov model. J Med Econ. 2015;18:410-419. Zafar F, Jefferies JL, Tjossem CJ, Bryant R 3rd, Jaquiss RD, Wearden PD, Rosenthal DN, Cabrera AG, Rossano JW, Humpl T, Morales DL. Biventricular Berlin Heart EXCOR pediatric use across the United States. Ann Thorac Surg. 2015;99:1328-1334. 57 56 H E A RT C E N T E R 2 0 1 4 Texas Children’s Heart Center Referrals To refer your pediatric patient to Texas Children’s Heart Center, please call 832-82-HEART (832-824-3278). Congenital Heart Surgery The Congenital Heart Surgery service at Texas Children’s Hospital offers same-day surgical consultation appointments. To make an appointment for a same-day consultation, call 832-TCH-APPT (832-824-2778). For additional appointment information or to speak with a division administrator, please call 832-826-2030. Cardiology, Adult Congenital Heart Disease and the Cardiovascular Intensive Care Unit 832-82-HEART (832-824-3278) Heart Transplant Program 866-683-8032 Cardiovascular Anesthesia 832-826-5831 Referrals Visit texaschildrens.org/refer for more information about referring a patient, or learn more aboutCongenital Texas Children’s Heart Center at texaschildrens.org/heart. Heart Surgery The Congenital Heart Surgery Service at Texas Children’s Hospital offers same-day surgical consultation appointments. To make an appointment for a same-day consultation, call 832-TCH-APPT (832-824-2778). For additional appointment information or to speak with a division administrator, please call 832-826-2030. Heart Transplant Program 866-683-8032 Cardiology, Adult Congenital Heart Disease and Cardiovascular Intensive Care Unit 832-82-HEART (832-824-3278) Cardiovascular Anesthesia 832-826-5831 To refer a patient to Texas Children’s Heart Center, please call 832-82-HEART (832-824-3278). With six decades of experience in caring for children’s hearts, Texas Children’s Heart Center combines leading, world-class technology with a compassionate, family-centered approach to pediatric cardiac care. Our multidisciplinary team of pediatric cardiologists, cardiovascular surgeons, cardiovascular anesthesiologists, perfusionists, adult congenital heart disease specialists, cardiac intensivists, nurses, child life specialists and support staff work together to surround patients with expertise at every point from diagnosis through treatment in order to provide the best possible results. Meet the Texas Children’s Heart Center team. (FLIP OPEN) Visit texaschildrens.org/refer for more information about referring a patient or learn more about Texas Children’s Heart Center at texaschildrens.org/heart. Texas Children’s Heart Center 2015 Texas Children’s Heart Center 6621 Fannin Street Houston, Texas 77030 texaschildrens.org/heartoutcomes texaschildrens.org/refer ©2016 Texas Children’s Hospital. All Rights Reserved. Heart233 060916