RESUMEN
We present the fifth "Jatene Lecture on Surgical Innovation" on Innovation in Congenital Heart Surgery, given at the Eighth Scientific Meeting of the World Society for Pediatric and Congenital Heart Surgery and Eighth World Congress of Pediatric Cardiology and Cardiac Surgery in Washington DC in 2023. We highlight what surgical innovation is and how innovation was accomplished in cardiac surgery and particularly in congenital heart surgery. A brief history of the development of congenital heart surgery across the world is summarized and we finally illustrate the South American contributions to congenital heart surgery, acknowledging the great innovations of Adib Jatene and Guillermo Kreutzer to our field.
Asunto(s)
Procedimientos Quirúrgicos Cardíacos , Cardiopatías Congénitas , Humanos , Cardiopatías Congénitas/cirugía , Cardiopatías Congénitas/historia , Procedimientos Quirúrgicos Cardíacos/historia , América del Sur , Historia del Siglo XX , Historia del Siglo XXIRESUMEN
BACKGROUND: Historically, Dr William Glenn performed the first classic superior cavopulmonary anastomosis in a seven-year-old child at Yale in 1958. By 1990, this operation was performed consecutively in over 90 patients. With over 60 years of follow-up, this is the longest survival record of early Glenn patients from the first 30 years. METHODS: We performed a single center, retrospective evaluation of patients undergoing a Glenn operation. A collected list of surviving patients, previously updated in 1988, included demographics, age at procedure, and underlying diagnosis. Follow-up data were obtained in May 2022 using electronic medical records to determine survival, age of survivors, and age of deceased. RESULTS: Ninety-five patients underwent the Glenn operation from 1958 to 1990: 58.9% (n = 56) were male and 41.1% (n = 39) female. Fifteen patients were lost to follow-up, but 12 were alive in 1988. Sixty patients were deceased (68.1%), with an average age of 33.5 ± 18.3(range, 2-78, excluding seven early deaths) years. The oldest patient who passed away was a 78-year-old male with tetralogy of Fallot. Twenty patients remain alive, with an average age of 47.5 (range, 32-66) years. Four patients who are still alive today (20% survivors) are older than 60 years. CONCLUSIONS: Since Dr Glenn's original operation, the technique, timing, and indications have been modified (ie, bidirectional Glenn) to adapt to the current era. By following this initial group of patients, we can approach completion of the survival rates for adult congenital patients who were some of the first pediatric patients to receive this ground-breaking palliative procedure.
Asunto(s)
Procedimiento de Fontan , Cardiopatías Congénitas , Humanos , Masculino , Estudios Retrospectivos , Femenino , Niño , Estudios de Seguimiento , Procedimiento de Fontan/historia , Procedimiento de Fontan/métodos , Preescolar , Adulto , Cardiopatías Congénitas/cirugía , Cardiopatías Congénitas/historia , Cardiopatías Congénitas/mortalidad , Adolescente , Persona de Mediana Edad , Anciano , Adulto Joven , Tasa de Supervivencia , Factores de Tiempo , Puente Cardíaco Derecho/historia , Historia del Siglo XXAsunto(s)
Ingeniería Biomédica/historia , Cardiopatías Congénitas/historia , Implantación de Prótesis de Válvulas Cardíacas/historia , Prótesis Valvulares Cardíacas/historia , Cirugía Torácica/historia , Becas , Cardiopatías Congénitas/cirugía , Implantación de Prótesis de Válvulas Cardíacas/instrumentación , Historia del Siglo XX , Historia del Siglo XXI , Humanos , Diseño de Prótesis/historiaRESUMEN
The etiology of congenital heart diseases is not fully understood yet, however, endocrine disrupting chemicals may have a causative role in their development. The purpose of our study was to examine the association between congenital heart diseases and periconceptional parental occupational exposure to endocrine disrupting chemicals. In our Hungarian population-based case-control study, we examined 2263 live born cases with any congenital heart disease and 6789 matched controls selected between years 1997 to 2002. Occupational exposure was assessed with a job-exposure matrix developed for endocrine disrupting chemicals. Conditional multiple logistic regression analyses were performed to test associations between parental occupational exposure to endocrine disrupting chemicals and congenital heart diseases of the offspring as a whole and by congenital heart disease subtypes. The prevalence of exposure to endocrine disrupting chemicals was 4.5% for both case and control mothers and 19.1% and 19.4% for case and control fathers, respectively. We found a positive association between paternal pesticide (adjusted odds ratio = 1.66, 95% confidence interval: 1.03-2.69) and alkylphenolic compound exposure (adjusted odds ratio = 1.95, 95% confidence interval: 1.30-2.93) and the development of patent ductus arteriosus in the offspring. Alkylphenolic compound exposure occurred among painters, famers, and those working in the food service industry, while pesticide exposure occurred predominantly among farm workers. We identified that certain occupations may increase the occurrence of certain congenital heart disease phenotypes in the offspring. By paying closer attention to those working in these areas, antenatal detection rates of congenital heart diseases may be improved.
Asunto(s)
Cardiopatías Congénitas/epidemiología , Cardiopatías Congénitas/etiología , Exposición Materna/efectos adversos , Exposición Profesional/efectos adversos , Estudios de Casos y Controles , Femenino , Cardiopatías Congénitas/historia , Historia del Siglo XX , Historia del Siglo XXI , Humanos , Hungría/epidemiología , Masculino , Oportunidad Relativa , Embarazo , Vigilancia en Salud Pública , Sistema de RegistrosAsunto(s)
Cardiología/historia , Cardiopatías Congénitas/historia , Pediatría/historia , Cardiología/educación , Educación Médica/historia , Cardiopatías Congénitas/diagnóstico por imagen , Cardiopatías Congénitas/patología , Historia del Siglo XX , Historia del Siglo XXI , Humanos , Pediatría/educaciónAsunto(s)
Procedimientos Quirúrgicos Cardíacos/historia , Procedimientos Quirúrgicos Cardíacos/métodos , Cardiopatías Congénitas/historia , Cardiopatías Congénitas/cirugía , Procedimientos Quirúrgicos Cardíacos/mortalidad , Niño , Toma de Decisiones , Predicción , Cardiopatías Congénitas/mortalidad , Historia del Siglo XX , Historia del Siglo XXI , HumanosRESUMEN
The development of the superior cavopulmonary connection is a rich illustration of international influences in congenital cardiac surgery. The bidirectional Glenn and hemi-Fontan procedures have improved survival as both definitive and staged functional single ventricle palliation. The optimal timing of the second-stage superior cavopulmonary procedures varies by center but for low- and intermediate-risk patients, this may be within three to six months after the Norwood procedure. The list of risk factors continues to grow but the most frequently cited factors include atrioventricular valve regurgitation, decreased ventricular function, need for reintervention, and failure to attain nutritional and growth goals. Ongoing prospective, multi-institutional studies, particularly those fostered internationally by the World Society for Pediatric and Congenital Heart Surgery and other associations, will hopefully provide further clarification of the complex management issues related to patients with functional single ventricle physiology.
Asunto(s)
Puente Cardíaco Derecho/métodos , Cardiopatías Congénitas/cirugía , Ventrículos Cardíacos/anomalías , Niño , Femenino , Procedimiento de Fontan/historia , Puente Cardíaco Derecho/historia , Cardiopatías Congénitas/historia , Ventrículos Cardíacos/cirugía , Historia del Siglo XX , Humanos , Lactante , Masculino , Cuidados Paliativos/historia , Arteria Pulmonar/cirugía , Factores de Riesgo , Resultado del Tratamiento , Vena Cava Superior/cirugía , Obstrucción del Flujo Ventricular Externo/historia , Obstrucción del Flujo Ventricular Externo/cirugíaRESUMEN
A life of professional caring, research, teaching, and inspiration-this is the legacy of Dr Stella Zacharioudaki Van Praagh, MD. Among her many outstanding contributions, only a few are recorded here: (1) a new surgical operation for closing apical muscular ventricular septal defects, (2) a newly discovered form of anomalous pulmonary venous drainage and its surgical repair, (3) a new understanding of sinus venosus defects and their surgical repair, (4) the realization that the concept of atrial-level isomerism (mirror-imagery) in the heterotaxy syndromes of asplenia, polysplenia, and single right-sided spleen is erroneous, (5) the understanding that it is possible to diagnose the atrial situs in the majority of cases of the heterotaxy syndromes, and (6) the fact that the concepts of evolution, natural selection, and survival of the fittest were described by Empedocles, an ancient Greek philosopher, in the fifth century bc, and that these concepts were not discovered and published for the first time by Charles Darwin and Alfred Russell Wallace in the 19th century (1858 ad). Dr Stella was conversant with ancient Greek and read it frequently in an ancient Greek study group that she headed. Dr Stella translated from ancient Greek into English a portion of Aristotle's The Physics in which Empedocles' understanding is cited at length. There is no doubt about what Empedocles thought.
Asunto(s)
Procedimientos Quirúrgicos Cardíacos/historia , Cardiología/historia , Cardiopatías Congénitas/historia , Femenino , Cardiopatías Congénitas/cirugía , Historia del Siglo XX , Historia del Siglo XXI , Humanos , Estados UnidosAsunto(s)
Procedimientos Quirúrgicos Cardíacos/historia , Circulación Extracorporea/historia , Cardiopatías Congénitas/historia , Procedimientos Quirúrgicos Cardíacos/métodos , Preescolar , Circulación Extracorporea/métodos , Femenino , Cardiopatías Congénitas/cirugía , Historia del Siglo XX , Humanos , Lactante , Masculino , MinnesotaRESUMEN
OBJECTIVE: The number of adults with congenital heart disease (CHD) has increased substantially because of medical advances that are extending life expectancy beyond childhood. A historical investigation is timely not only because of this significant demographic shift, but also because stakeholder engagement is increasingly important in shaping research directions. The study questions were: From the perspective of stakeholders, what is known about the medical treatment for the adult CHD cohort in Canada and how has it changed over time? DESIGN/METHODS: We harnessed the use of historical research methods and conducted interviews with 21 key informants in order to articulate a contextualized understanding of the evolution of adult CHD treatment in Canada. The informants recruited were currently or previously located in and/or involved in treatment in seven provinces and two territories across Canada including patients, families, advocates, researchers, and practitioners located in disciplines that included cardiology, cardiovascular surgery, nursing, psychology, dietetics, and kinesiology. RESULTS: Alongside findings that highlighted the significant demographic shift, the findings highlight key themes related to temporal shifts in treatment, emergence of organizational structures and use of evidence, comprehensive approaches to care, and future directions. A critical finding that requires immediate attention is the significantly disproportionate resources to the number of adults living with CHD, and as a result, the real risk of premature death for this population. CONCLUSIONS: The insights provided behoove the community of stakeholders to think creatively on how to draw attention to the inadequacy of resources and the unique and diverse needs of this population.
Asunto(s)
Cardiología/historia , Manejo de la Enfermedad , Cardiopatías Congénitas/historia , Sociedades Médicas/historia , Adulto , Canadá , Cardiopatías Congénitas/terapia , Historia del Siglo XX , Historia del Siglo XXI , HumanosAsunto(s)
Cardiopatías Congénitas , Cirugía Torácica , Adulto , Cardiopatías Congénitas/historia , Cardiopatías Congénitas/cirugía , Historia del Siglo XIX , Historia del Siglo XX , Historia del Siglo XXI , Humanos , Londres , Cirugía Torácica/historia , Cirugía Torácica/organización & administraciónRESUMEN
The history of the first 41 years of the Congenital Heart Surgeons Society (CHSS) was recorded in 2015 which chronicled the metamorphosis of a small informal meeting into a mature organization with bylaws, officers, committees, funded research, the Kirklin-Ashburn Fellowship, and a vision to become the premier organization of congenital heart surgery in North America. Chief among these transformations was the implementation and development of the CHSS Data Center. Member participation, fellowship education, and significant outcomes research have been the hallmark of the CHSS. This incremental historical review highlights continued CHSS sentinel advances. Fifty-three CHSS Data Center manuscripts have been published. Citation scores (number of literature citations that each manuscript has accrued) have been collated and analyzed by cohort study. The average citation score for all manuscripts was 75.4 ± 76.3 (range: 1-333). The Kirklin/Ashburn Fellowship continues to thrive with academic achievements and generous contributions to the endowment. The World Journal of Pediatric and Congenital Heart Surgery has been adopted as the official organ of the CHSS. A Past President's Dinner has been inaugurated serving as a senior advisory committee to the Executive Council. Toronto Work Weekends continue. Congenital Heart Surgeons Society growth has accrued to 159 active members and 82 institutional members. Future considerations include the size, content, and duration of the annual meeting; the potential for increased membership; and political penetrance into national cardiothoracic governing organizations regarding committee appointments, executive council representation, and education initiatives. Congenital Heart Surgeons Society has achieved numerous advances during this incremental period.
Asunto(s)
Procedimientos Quirúrgicos Cardíacos/historia , Cardiología/historia , Cardiopatías Congénitas/historia , Sociedades Médicas/historia , Cardiopatías Congénitas/cirugía , Historia del Siglo XX , Historia del Siglo XXI , Humanos , América del NorteRESUMEN
On September 4th, 2017 it will be 60 years since Dr. Helmut Jeager performed the first successful open-heart surgery in Chile and South America on a patient with a congenital heart defect. He performed the closure of an ostium secundum type inter atrial septal defect, using The Wall - Lillehei extracor-poreal circuit. Although in most cases this type of surgery has been replaced by closure through inter-ventional catheterism, at that time the operation had big medical and news media impact. For children born with a congenital heart defect, cardiac surgery meant a before and after. Before, children less than one-year old had a limited survival rate, about 30% at one year. Now, thanks to cardiac surgery the survival is close to 95% and in most cases life expectancy is normal or with only few limitations.