RESUMEN
Right atrial aneurysm is a rare congenital heart condition defined as a dilation of the right atrium in the absence of an underlying cause [1]. The clinical presentation varies; most patients are asymptomatic, while others may experience arrhythmias or intracavitary thrombi [1, 2]. We report a case.
Asunto(s)
Apéndice Atrial , Aneurisma Cardíaco , Cardiopatías Congénitas , Humanos , Valor Predictivo de las Pruebas , Atrios Cardíacos/diagnóstico por imagen , Atrios Cardíacos/cirugía , Aneurisma Cardíaco/diagnóstico por imagen , Aneurisma Cardíaco/cirugía , Cardiopatías Congénitas/complicaciones , Cardiopatías Congénitas/diagnóstico por imagen , Cardiopatías Congénitas/cirugíaRESUMEN
BACKGROUND: Congenitally corrected transposition of the great arteries is a complex pathology characterised by atrioventricular and ventriculo-arterial discordance. Optimal surgical approaches are still a matter of debate. OBJECTIVE: To evaluate the outcomes of different surgical treatments in a single centre. METHODS: Between 1998 and 2020, 89 patients were studied. The cohort was divided into three groups: physiologic, anatomic, and univentricular repair. RESULT: Physiologic correction (56.18%) was associated with significant tricuspid valve regurgitation progress (42%) and complete AV block (30%) compared to anatomic repair. Right ventricular systolic dysfunction was developed in 14%. Instead, anatomic correction (30.34%) (double switch 59% and Rastelli type 40.7%) presented moderate to severe aortic regurgitation (4%) and left ventricular systolic dysfunction (11%). Complete AV block was developed in 14.8%. Rate of reintervention was 34% for physiologic and 26% for anatomic. Univentricular palliation (13.8%) presented no complications or late mortality during the follow-up. The overall survival at 5 and 10 years, respectively, was 80% (95% CI 69, 87) and 75% (95% CI 62, 84). There was no statistically significant difference in mortality between the groups (p log-rank = 0.5752). CONCLUSION: Management of congenitally corrected transposition of the great arteries remains a challenge. In this cohort, outcomes after physiologic repair were satisfactory in spite of the progression of tricuspid regurgitation and the high incidence of AV block. Anatomic repair improved tricuspid regurgitation but increased the risk of aortic regurgitation and left ventricular systolic dysfunction. The Fontan group showed the lowest incidence of complications.
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Objetivo. Describir el impacto de la pandemia por COVID-19 en el programa de cirugía cardiovascular pediátrica y estimar el tiempo para reducir la lista de espera quirúrgica. Métodos. Estudio descriptivo y retrospectivo. Se compararon resultados quirúrgicos del período preCOVID versus el período COVID. Se utilizó un modelo matemático para estimar el tiempo para reducir la lista de espera. Resultados. Entre el 23 de marzo y el 31 de agosto de 2020 se operaron 83 pacientes, que representan una reducción del 60 %, respecto al período preCOVID. La mediana de edad fue de 6 meses (rango intercuartílico [RIC]: 25-75, 1,8 meses a 2,9 años; p = 0,0023. El tiempo para eliminar la lista de espera varía entre 10 y 19 meses. Conclusiones. El programa tuvo una reducción del 60 %. El tiempo de resolución de la lista de espera puede ser al menos 10 a 19 meses
Objective. To describe the impact of the COVID-19 pandemic on a pediatric cardiovascular surgery program and estimate the necessary time to reduce the surgery waiting list. Methods. Retrospective, descriptive study. Surgical outcomes from the pre-COVID-19 period and COVID-19 period were compared. A mathematical model was used to estimate the time necessary to reduce the waiting list. Results. Between March 23rd and August 31st, 2020, 83 patients underwent surgery, accounting for a 60 % reduction compared to the pre-COVID-19 period. Their median age was 6 months (interquartile range [IQR]: 25-75, 1.8 months to 2.9 years; p = 0.0023). The time necessary to eliminate the waiting list ranges from 10 to 19 months. Conclusions. There was a 60 % reduction in the program. The time required to clear the backlog of cases may range from, at least, 10 to 19 month
Asunto(s)
Humanos , Lactante , Preescolar , Niño , Procedimientos Quirúrgicos Cardiovasculares/tendencias , Listas de Espera , Tiempo de Tratamiento/tendencias , Accesibilidad a los Servicios de Salud/tendencias , Hospitales Públicos/tendencias , Argentina/epidemiología , Estudios Retrospectivos , Pandemias , COVID-19/prevención & control , COVID-19/epidemiología , Modelos TeóricosRESUMEN
OBJECTIVE: To describe the impact of the COVID-19 pandemic on a pediatric cardiovascular surgery program and estimate the necessary time to reduce the surgery waiting list. METHODS: Retrospective, descriptive study. Surgical outcomes from the pre-COVID-19 period and COVID-19 period were compared. A mathematical model was used to estimate the time necessary to reduce the waiting list. RESULTS: Between March 23rd and August 31st, 2020, 83 patients underwent surgery, accounting for a 60 % reduction compared to the pre-COVID-19 period. Their median age was 6 months (interquartile range [IQR]: 25-75, 1.8 months to 2.9 years; p = 0.0023). The time necessary to eliminate the waiting list ranges from 10 to 19 months. CONCLUSIONS: There was a 60 % reduction in the program. The time required to clear the backlog of cases may range from, at least, 10 to 19 months.
Objetivo. Describir el impacto de la pandemia por COVID-19 en el programa de cirugía cardiovascular pediátrica y estimar el tiempo para reducir la lista de espera quirúrgica. Métodos. Estudio descriptivo y retrospectivo. Se compararon resultados quirúrgicos del período preCOVID versus el período COVID. Se utilizó un modelo matemático para estimar el tiempo para reducir la lista de espera. Resultados. Entre el 23 de marzo y el 31 de agosto de 2020 se operaron 83 pacientes, que representan una reducción del 60 %, respecto al período preCOVID. La mediana de edad fue de 6 meses (rango intercuartílico [RIC]: 25-75, 1,8 meses a 2,9 años; p = 0,0023. El tiempo para eliminar la lista de espera varía entre 10 y 19 meses. Conclusiones. El programa tuvo una reducción del 60 %. El tiempo de resolución de la lista de espera puede ser al menos 10 a 19 meses.
Asunto(s)
COVID-19 , Procedimientos Quirúrgicos Cardiovasculares/tendencias , Accesibilidad a los Servicios de Salud/tendencias , Hospitales Públicos/tendencias , Tiempo de Tratamiento/tendencias , Listas de Espera , Argentina/epidemiología , COVID-19/epidemiología , COVID-19/prevención & control , Niño , Preescolar , Humanos , Lactante , Modelos Teóricos , Pandemias , Estudios RetrospectivosRESUMEN
RESUMEN Objetivo: Analizar los factores de riesgo de evolución desfavorable (ED) en niños con insuficiencia mitral (IM) sometidos a plástica mitral (PM). Métodos: Se analizaron pacientes con IM sometidos a PM entre los años 2004 y 2014. Se definió ED como la reoperación o la IM significativa (3+, moderada a grave, o 4+, grave) durante el seguimiento. Las variables se expresaron como mediana. Se realizó el análisis univariado y el de regresión logística multivariado de los factores predictores de ED. Resultados: Se sometieron a PM 65 pacientes con IM 3+ e IM 4+. La etiología incluyó displasia (44,6%), endocarditis infecciosa (13,8%), fiebre reumática (18,4%), anomalía coronaria (7,7%) y otras (13,8%). La mediana del tiempo de seguimiento fue 26,5 meses (52 pacientes se encuentran aún en seguimiento). El 44,6% presentó disfunción ventricular y el 46,1% hipertensión pulmonar. La cantidad de pacientes con ED fue de 15: 9 fueron reoperados (7 reemplazos valvulares y 2 replástica). El análisis univariado demostró asociación significativa entre ED y las siguientes condiciones: fiebre reumática (p = 0,005), anillo mitral preoperatorio ≥+5 DS (p = 0,002), diámetro sistólico del ventrículo izquierdo (DSVI) ≥ +4 DS (p = 0,022), hipertensión pulmonar (p = 0,024) e IM residual posoperatoria inmediata ≥ moderada (p = 0,021). El análisis multivariado demostró como variables independientes de ED el diámetro del anillo mitral (p = 0,012), la fiebre reumática (p = 0,026) y la IM residual temprana (p = 0,042). No se produjo mortalidad. Conclusiones: La plástica mitral en niños con IM grave demostró resultados favorables a mediano plazo. La fiebre reumática, el diámetro del anillo mitral ≥ +5 DS y la IM residual ≥ 2+ fueron factores predictores de ED. No se hallaron diferencias estadísticamente significativas durante el seguimiento en relación con la edad ni con la presencia de disfunción ventricular.
ABSTRACT Objective: The aim of this study was to analyze risk factors of unfavorable outcome (UO) in patients with mitral regurgitation (MR) undergoing mitral valve repair (MVR). Methods: Patients with MR who had undergone MVR from 2004 to 2014 were retrospectively analyzed. Unfavorable outcome was defined as reoperation or significant MR [moderate to severe (3+) or severe MR (4+)] during follow-up. Variables were expressed as median. Univariate and multivariate logistic regression analyses were performed to identify predictive factors of UO. Results: Sixty five patients with MR3+ and MR4+ underwent MVR. Etiology was dysplasia in 44.6% of cases, infective endocarditis in 13.8%, rheumatic fever in 18.4%, abnormal coronary origin in 7.7% and other disorders in 13.8%. Median follow-up time was 26.5 months (52 patients are still being followed-up).Ventricular dysfunction was documented in 44.6% of cases and 46.1% had pulmonary hypertension. Fifteen patients presented UO and 9 were reoperated (7 valve replacements and 2 re-repairs). Univariate analysis demonstrated a significant association between UO and the following conditions: rheumatic fever (p=0.005), preoperative mitral annulus ≥+5 SD (p=0.002), left ventricular end-systolic diameter ≥+4 SD (p=0.022), pulmonary hypertension (p=0.024) and immediate postoperative residual MR ≥ moderate (p=0.021). Multivariate analysis demonstrated mitral annulus diameter (p=0.012), rheumatic fever (p=0.026) and early residual MR (p=0.042) as independent variables of UO. No deaths occurred in this series. Conclusions: Mitral valve repair in children with severe MR demonstrated mid-term favourable results. Rheumatic fever, mitral annulus diameter ≥+5 SD and immediate postoperative residual MR ≥2+ were predictive factors of UO. Neither age at surgery nor ventricular dysfunction showed statistically significant differences during follow-up.
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Objetivo: Describir resultados de membrana de oxigenación extracorpórea en pacientes con cirugía cardíaca y analizar los factores de riesgos de morbimortalidad. Métodos: Estudio retrospectivo, de pacientes cardíacos con asistencia circulatoria. Se registraron variables, diagnóstico, cirugía, puntaje Risk Adjustment for Congenital Heart Surgery (RACHS), momento de colocación, canulación, días de asistencia en internación, complicaciones, sobrevida y seguimiento. Se analizaron los riesgos edad, peso, RACHS, patología uni- o biventricular, momento de colocación, días de asistencia e internación, y complicaciones. Análisis estadístico descriptivo y de regresión logística para factores de riesgo. Resultados: En 5295 admisiones, 72 pacientes requirieron membrana de oxigenación extracorpórea (1,37 %). Edad mediana: 6,5 meses (rango intercuartilo -RIQ-: 20 días-2 años); peso: 5,5 kg (RIQ: 3,25-9,5); tiempo de bomba: 188 min (RIQ: 134-246,5); de clampeo: 92 min (65-117). La canulación fue en quirófano en 34 casos (47 %). La mediana de asistencia fue 3 días (RIQ: 2-5), y de internación, 20 (RIQ: 11-32). La sobrevida al alta fue 49 %; 8 pacientes fallecieron durante el seguimiento. La complicación más frecuente fue hemorragia ( 57 %). El peso <5 kg (p = 0,01) y vasopresores en asistencia (p = 0,012) tuvieron riesgo de mortalidad. La sobrevida a 10 años fue del 77 %, con 84 % en clase funcional 1-2 y el 37 % presentaba algún grado de retardo madurativo. Conclusiones: La complicación más frecuente fue la hemorragia; peso y vasopresores se asociaron con mortalidad.
Objective: To describe the results of extracorporeal membrane oxygenation in patients undergoing heart surgery and analyze the risk factors for morbidity and mortality. Methods: Retrospective study conducted in cardiac patients under circulatory support. Outcome measures, diagnosis, surgery, Risk Adjustment for Congenital Heart Surgery (RACHS) score, implantation time, cannulation, length of support during stay, complications, survival, and follow-up were recorded. Risks were analyzed in relation to age, weight, RACHS score, single-ventricle or biventricular disease, implantation time, length of support and stay, and complications. Descriptive statistical and logistic regression analyses for risk factors were done. Results: Among 5295 hospitalizations, 72patients required extracorporeal membrane oxygenation (1.37 %). Median age: 6.5 months (interquartile range [IQR]: 20 days-2 years); weight: 5.5 kg (IQR: 3.25-9.5); pump time: 188 min (IQR: 134- 246.5); clamp time: 92 min (65-117). Cannulation was done in the operating room in 34 cases (47 %). The median length of support was 3 days (IQR: 2-5), and of stay, 20 days (IQR: 11-32). Survival at discharge was 49 %; 8 patients died during follow-up. The most common complication was bleeding (57 %). Weight<5 kg (p = 0.01) and vasopressor use during support (p = 0.012) were associated with a risk for mortality. The survival rate at 10 years was 77 %; 84% of patients corresponded to functional class 1-2, and 37% had some degree of developmental delay.
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Humanos , Recién Nacido , Lactante , Preescolar , Niño , Adolescente , Oxigenación por Membrana Extracorpórea , Factores de Riesgo , Cardiopatías CongénitasRESUMEN
Objective: To describe the results of extracorporeal membrane oxygenation in patients undergoing heart surgery and analyze the risk factors for morbidity and mortality. Methods: Retrospective study conducted in cardiac patients under circulatory support. Outcome measures, diagnosis, surgery, Risk Adjustment for Congenital Heart Surgery (RACHS) score, implantation time, cannulation, length of support during stay, complications, survival, and follow-up were recorded. Risks were analyzed in relation to age, weight, RACHS score, single-ventricle or biventricular disease, implantation time, length of support and stay, and complications. Descriptive statistical and logistic regression analyses for risk factors were done. Results: Among 5295hospitalizations, 72 patients required extracorporeal membrane oxygenation (1.37 %). Median age: 6.5 months (interquartile range [IQR]: 20 days-2 years); weight: 5.5 kg (IQR: 3.25-9.5); pump time: 188 min (IQR: 134246.5); clamp time: 92 min (65-117). Cannulation was done in the operating room in 34 cases (47 %). The median length of support was 3 days (IQR: 2-5), and of stay, 20 days (IQR: 1132). Survival at discharge was 49 %; 8 patients died during follow-up. The most common complication was bleeding (57 %). Weight < 5 kg (p = 0.01) and vasopressor use during support (p = 0.012) were associated with a risk for mortality. The survival rate at 10 years was 77 %; 84 % of patients corresponded to functional class 1-2, and 37 % had some degree of developmental delay. Conclusions: The most common complication was bleeding; weight and vasopressor use were associated with mortality.
Objetivo: Describir resultados de membrana de oxigenación extracorpórea en pacientes con cirugía cardíaca y analizar los factores de riesgos de morbimortalidad. Métodos: Estudio retrospectivo, de pacientes cardíacos con asistencia circulatoria. Se registraron variables, diagnóstico, cirugía, puntaje Risk Adjustment for Congenital Heart Surgery (RACHS), momento de colocación, canulación, días de asistencia en internación, complicaciones, sobrevida y seguimiento. Se analizaron los riesgos edad, peso, RACHS, patología uni- o biventricular, momento de colocación, días de asistencia e internación, y complicaciones. Análisis estadístico descriptivo y de regresión logística para factores de riesgo. Resultados: En 5295 admisiones, 72 pacientes requirieron membrana de oxigenación extracorpórea (1,37 %). Edad mediana: 6,5 meses (rango intercuartilo -RIQ-: 20 días-2 años); peso: 5,5 kg (RIQ: 3,25-9,5); tiempo de bomba: 188 min (RIQ: 134-246,5); de clampeo: 92 min (65-117). La canulación fue en quirófano en 34 casos (47 %). La mediana de asistencia fue 3 días (RIQ: 2-5), y de internación, 20 (RIQ: 11-32). La sobrevida al alta fue 49 %; 8 pacientes fallecieron durante el seguimiento. La complicación más frecuente fue hemorragia ( 57 %). El peso <5 kg (p = 0,01) y vasopresores en asistencia (p = 0,012) tuvieron riesgo de mortalidad. La sobrevida a 10 años fue del 77 %, con 84 % en clase funcional 1-2 y el 37 % presentaba algún grado de retardo madurativo. Conclusiones: La complicación más frecuente fue la hemorragia; peso y vasopresores se asociaron con mortalidad.
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Procedimientos Quirúrgicos Cardíacos/métodos , Oxigenación por Membrana Extracorpórea/métodos , Cardiopatías Congénitas/terapia , Vasoconstrictores/administración & dosificación , Argentina , Preescolar , Estudios de Seguimiento , Cardiopatías Congénitas/mortalidad , Hemorragia/epidemiología , Humanos , Lactante , Recién Nacido , Tiempo de Internación , Estudios Retrospectivos , Factores de Riesgo , Tasa de Supervivencia , Factores de Tiempo , Resultado del TratamientoRESUMEN
Introducción. La comunicación interventricular (CIV) es la cardiopatía congénita más frecuente y el cierre quirúrgico primario es la estrategia de elección para corregirla. El objetivo es describir los resultados de la reparación quirúrgica en menores de 1 año y analizar factores de riesgo de morbilidad y mortalidad. Pacientes y métodos. Estudio retrospectivo; se incluyeron todos los pacientes con CIV operados entre 2004 y 2011. Se registraron variables demográficas, de la cirugía y del posoperatorio: edad, peso, síndrome genético, tipo de CIV, días de internación, complicaciones y evolución. Como factores de riesgo de mortalidad y morbilidad, se analizaron edad < 6 m, peso < 3 kg, síndrome de Down, desnutrición e infección respiratoria previa. Resultados. Se operaron 256 pacientes, con edad de 5,3 meses (21 d-1 a), peso de 4,75 kg (2,2-13), 32% con síndrome de Down y 17,5% con ventilación mecánica preoperatoria. La CIV tipo perimembranosa fue la más frecuente (62%). El 28% presentó alguna complicación y el 7% requirió reoperación por sangrado, infección o defecto. La mediana de internación fue de 6 días (1-185). Se registró una mortalidad posoperatoria de 3%. La desnutrición, edad < 6 m, peso < 3 kg y la infección respiratoria previa se asociaron a una internación prolongada. No se identificaron factores de riesgo para la mortalidad. Conclusión. En nuestra institución, el cierre quirúrgico primario de la CIV es un procedimiento con resultados satisfactorios.
Objective. Ventricular septal defect (VSD) is the most common congenital heart disease; primary surgical closure is the usual strategy for repairing it. Our objective is to describe results of surgical repair in children under 1 year of age and analyze risk factors for morbidity and mortality. Patients and Methods. Retrospective study; all patients with VSD repaired between 2004 and 2011 were included. Demographic, surgical procedure and postoperative variables were recorded: age, weight, genetic syndrome, type of VSD, length of stay, complications and outcome. Risk factors of mortality and morbidity: age < 6 m, weight < 3 kg, Down, malnutrition and respiratory infection prior syndrome were analyzed. Results. 256 patients, age 5.3 months (21d-1y), weight 4.75 kg (2.2 to 13), 32% with Down syndrome and 17.5% with preoperative mechanical ventilation were operated. Perimembranous VSD was the most frequent type (62%). 28% experienced complications and 7% required reoperation for bleeding, infection or defect. The median hospital stay was 6 days (1-185). Postoperative 30 days mortality was 3%. Age < 6 m, weight < 3 kg, malnutrition and prior respiratory viral infection were associated with prolonged hospitalization, but no risk factors for mortality were identified. Conclusion. The primary surgical closure of the VSD is a procedure with satisfactory results at our institution.
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Humanos , Masculino , Femenino , Recién Nacido , Lactante , Defectos del Tabique Interventricular/cirugía , Complicaciones Posoperatorias/epidemiología , Estudios Retrospectivos , Factores de Riesgo , Hospitales PúblicosRESUMEN
OBJECTIVE: Ventricular septal defect (VSD) is the most common congenital heart disease; primary surgical closure is the usual strategy for repairing it. Our objective is to describe results of surgical repair in children under 1 year of age and analyze risk factors for morbidity and mortality. PATIENTS AND METHODS: Retrospective study; all patients with VSD repaired between 2004 and 2011 were included. Demographic, surgical procedure and postoperative variables were recorded: age, weight, genetic syndrome, type of VSD, length of stay, complications and outcome. Risk factors of mortality and morbidity: age < 6 m, weight < 3 kg, Down, malnutrition and respiratory infection prior syndrome were analyzed. RESULTS: 256 patients, age 5.3 months (21d-1y), weight 4.75 kg (2.2 to 13), 32% with Down syndrome and 17.5% with preoperative mechanical ventilation were operated. Perimembranous VSD was the most frequent type (62%). 28% experienced complications and 7% required reoperation for bleeding, infection or defect. The median hospital stay was 6 days (1-185). Postoperative 30 days mortality was 3%. Age < 6 m, weight < 3 kg, malnutrition and prior respiratory viral infection were associated with prolonged hospitalization, but no risk factors for mortality were identified. CONCLUSION: The primary surgical closure of the VSD is a procedure with satisfactory results at our institution.
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Defectos del Tabique Interventricular/cirugía , Femenino , Hospitales Públicos , Humanos , Lactante , Recién Nacido , Masculino , Complicaciones Posoperatorias/epidemiología , Estudios Retrospectivos , Factores de RiesgoRESUMEN
OBJECTIVE: Ventricular septal defect (VSD) is the most common congenital heart disease; primary surgical closure is the usual strategy for repairing it. Our objective is to describe results of surgical repair in children under 1 year of age and analyze risk factors for morbidity and mortality. PATIENTS AND METHODS: Retrospective study; all patients with VSD repaired between 2004 and 2011 were included. Demographic, surgical procedure and postoperative variables were recorded: age, weight, genetic syndrome, type of VSD, length of stay, complications and outcome. Risk factors of mortality and morbidity: age < 6 m, weight < 3 kg, Down, malnutrition and respiratory infection prior syndrome were analyzed. RESULTS: 256 patients, age 5.3 months (21d-1y), weight 4.75 kg (2.2 to 13), 32
with Down syndrome and 17.5
with preoperative mechanical ventilation were operated. Perimembranous VSD was the most frequent type (62
). 28
experienced complications and 7
required reoperation for bleeding, infection or defect. The median hospital stay was 6 days (1-185). Postoperative 30 days mortality was 3
. Age < 6 m, weight < 3 kg, malnutrition and prior respiratory viral infection were associated with prolonged hospitalization, but no risk factors for mortality were identified. CONCLUSION: The primary surgical closure of the VSD is a procedure with satisfactory results at our institution.
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OBJECTIVE: To describe the results of congenital heart surgery at the Hospital de Pediatría J. P.Garrahan. METHODS: Between 2004 and 2009, 2942 patients, median age 2.5 years (1 d to 22.5 y), median weight 11.5 kg (1.6 kg to 96 kg), and 84% with cardiopulmonary bypass, were analyzed. Adjusted mortality risk analysis using RACHS and Aristotle score was performed. Newborn surgery and one stage repair in Fallot and ventricular septal defect with coarctation were analyzed as subgroupes. RESULTS: Mortality was 5.5%. Required mechanical ventilation 45%, 5% peritoneal dialysis, 12% delayed sternal closure and 8.4% reoperation. Twenty five percent with previous surgery, and 10% in poor clinical conditions. RACHS-1 categories morality distribution were 0.4% in one, 2.4% in two, 7.1% in three, 14% in four y 34 % in 5 and 6. One stage repair was performed in 84% of Fallots and 90% of ventricular septal defects with coarctation, with 3.2% and 10% mortality rate respectively. Two hundred and five newborns were operated with cardiopulmonary bypass with a mortality rate of 15% in the last year. CONCLUSIONS: Almost every congenital heart disease can be repaired without previous palliation, with satisfactory results in our institution. Poor clinical conditions significantly increased morbidity and mortality.
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Cardiopatías Congénitas/cirugía , Adolescente , Argentina , Niño , Preescolar , Hospitales Públicos , Humanos , Lactante , Recién Nacido , Resultado del Tratamiento , Adulto JovenRESUMEN
Objetivo: Describir los resultados en cirugía cardiovascular del Hospital de Pediatría J. P. Garrahan. Métodos: Se analizaron 2942 pacientes entre 2004 y 2009; de los cuales, 84% con circulación extracorpórea, mediana de edad 2.5 años, rango de un día a 22.5 años y peso 11.5 kg (1.6 kg a 96 kg); con cirugías previas 25% y 10% malas condiciones preoperatorias. Se analizó la mortalidad por RACHS-1 y Aristóteles, la cirugía neonatal, la cirugía en un tiempo de Fallot y de comunicación interventricular con coartación de aorta. Resultados: La mortalidad fue 5.5%. Requirió ventilación mecánica 45%, 5% diálisis peritoneal, 12% cierre esternal diferido y 8.4% reoperación. De los Fallot 84% y 90% de las comunicaciones interventriculares con coartación se repararon en un tiempo, con 3.2% y 10% de mortalidad respectivamente. Se operaron 205 neonatos con bomba y con 15% de mortalidad en el último año. Las malas condiciones previas aumentaron la morbilidad, (Odds ratio 3.63 IC 95%, 2.27 -4.81) y la mortalidad (Odds ratio 6.47 IC 95%, 4.36 - 9.60). La mortalidad por RACHS fue 0.4% en categoría uno, 2.4% en la dos, 7.1% en la tres, 14% en la cuatro y 34% en la cinco y seis. Conclusiones: En nuestra institución la mayoría de las cardiopatías se resuelven en un tiempo con resultados satisfactorios. Las malas condiciones preoperatorias aumentan significativamente la morbimortalidad.
Objective: To describe the results of congenital heart surgery at the Hospital de Pediatría J. P.Garrahan. Methods: Between 2004 and 2009, 2942 patients, median age 2.5 years (1 d to 22.5 y), median weight 11.5 kg (1.6 kg to 96 kg), and 84% with cardiopulmonary bypass, were analyzed. Adjusted mortality risk analysis using RACHS and Aristotle score was performed. Newborn surgery and one stage repair in Fallot and ventricular septal defect with coarctation were analyzed as subgroupes. Results: Mortality was 5.5%. Required mechanical ventilation 45%, 5% peritoneal dialysis, 12% delayed sternal closure and 8.4% reoperation. Twenty five percent with previous surgery, and 10% in poor clinical conditions. RACHS-1 categories morality distribution were 0.4% in one, 2.4% in two, 7.1% in three, 14% in four y 34 % in 5 and 6. One stage repair was performed in 84% of Fallots and 90% of ventricular septal defects with coarctation, with 3.2% and 10% mortality rate respectively. Two hundred and five newborns were operated with cardiopulmonary bypass with a mortality rate of 15% in the last year. Conclusions: Almost every congenital heart disease can be repaired without previous palliation, with satisfactory results in our institution. Poor clinical conditions significantly increased morbidity and mortality.
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Adolescente , Niño , Preescolar , Humanos , Lactante , Recién Nacido , Adulto Joven , Cardiopatías Congénitas/cirugía , Argentina , Hospitales Públicos , Resultado del TratamientoRESUMEN
INTRODUCTION: Four hundred newborns die every year in our country suffering from congenital heart disease. Definitive surgical repair, whenever possible, is nowadays the optimal therapeutic strategy. Our goal is to describe mortality and morbidity in neonatal surgery with cardiopulmonary bypass in a tertiary public hospital in Argentina. PATIENTS AND METHODS: Descriptive, retrospective study. Every patient, younger than 45 days, with cardiac surgery requiring cardiopulmonary bypass, at the Garrahan Hospital between 2004 and 2008 was included. Demographic, surgical and postoperative data were collected. Adjusted mortality risk analysis, and descriptive statistics from the most frequent diagnosis were performed. Results are expressed as median and rank or percentage. RESULTS: 200 newborns were operated, 62% males. Median age was 21 days (r 1- 45) and median weight 3.1 kg (r 1.6-6.2). Total anomalous pulmonary venous return, transposition of great arteries an hypoplastic left heart syndrome diagnoses accounted for 75% of the procedures. Median length of stay was 12 days (r 0-191), and 6 days of mechanical ventilation (r 0-180). Eighteen percent of the patients required peritoneal dialysis. Whole series mortality was 19% and fell to 14% in 2008. Unstable preoperative condition and postoperative complications increased mortality, OR= 2.23 (1.02-4.89) and OR= 10 (3.6-33.4), respectively. CONCLUSIONS: Our postoperative mortality is similar to those reported in foreign countries databases. Patients with unstable preoperative condition and post-operative complications had higher mortality.
Asunto(s)
Cardiopatías/congénito , Cardiopatías/cirugía , Procedimientos Quirúrgicos Cardíacos , Femenino , Humanos , Lactante , Recién Nacido , Masculino , Estudios Retrospectivos , Factores de TiempoRESUMEN
Introducción. En nuestro país fallecen anualmente 400 niños con cardiopatía congénita, en el 1er mes de vida. La cirugía constituye la estrategia actual para su tratamiento. El objetivo es describir la mortalidad hospitalaria y las complicaciones de la cirugía cardíaca neonatal con circulación extracorpórea en un hospital público de alta complejidad. Pacientes y métodos. Estudio descriptivo retrospectivo. Se registraron datos demográficos, de la cirugía y del postoperatorio de los pacientes con circulación extracorpórea, menores de 45 días, operados en el Hospital Garrahan, entre 2004-2008. Se realizó un análisis por patologías y de mortalidad ajustado por riesgo. Los resultados se expresan en mediana e intervalo, o en porcentaje, según corresponda. Resultados. Se operaron 200 recién nacidos, 62 por ciento varones. La edad fue 21 (1- 45) días y el peso 3,1 (1,6-6,2) kg. Anomalía total de retorno venoso pulmonar, transposición de grandes arterias y síndrome de corazón izquierdo hipoplásico concentraronel 75 por ciento de las cirugías. El tiempo de internación fue 12 (0-191) días, con 6 (0-180) días de ventilación mecánica, y 18 por ciento de los pacientes requirieron diálisis. La mortalidad global fue 19 por ciento y 14 por ciento en el último año analizado. Los pacientes en mala condición preoperatoria, así como los que presentaron complicaciones, exhibieron una mortalidad mayor (OR= 2,23 [1,02-4,89] y OR= 10 [3,6-33,4], respectivamente). Conclusiones. La mortalidad postoperatoria es similar a la comunicada en bases de datos del exterior. Los pacientes con mala condición preoperatoria y aquellos con complicaciones presentaron mayor mortalidad en nuestra serie.(AU)
Introduction. Four hundred newborns die every year in our country suffering from congenital heart disease. Definitive surgical repair, whenever possible, is nowadays the optimal therapeutic strategy. Our goal is to describe mortality and morbidity in neonatal surgery with cardiopulmonary bypass in a tertiary public hospital in Argentina. Patients and methods. Descriptive, retrospective study. Every patient, younger than 45 days, with cardiac surgery requiring cardiopulmonary bypass, at the Garrahan Hospital between 2004 and 2008 was included. Demographic, surgical and postoperative data were collected. Adjusted mortality risk analysis, and descriptive statistics from the most frequent diagnosis were performed. Results are expressed as median and rank or percentage. Results. 200 newborns were operated, 62 percent males. Median age was 21 days (r 1- 45) and median weight 3.1 kg (r 1.6-6.2). Total anomalous pulmonary venous return, transposition of great arteries and hypoplastic left heart syndrome diagnoses accounted for 75 percent of the procedures. Median length of stay was 12 days (r 0-191), and 6 days of mechanical ventilation (r 0-180). Eighteen percent of the patients required peritoneal dialysis. Whole series mortality was 19 percent and fell to 14 pecent in 2008. Unstable preoperative condition and postoperative complications increased mortality, OR= 2.23 (1.02-4.89) and OR= 10 (3.6-33.4), respectively. Conclusions. Our postoperative mortality is similar to those reported in foreign countries databases. Patients with unstable preoperative condition and post-operative complications had higher mortality.(AU)
Asunto(s)
Humanos , Recién Nacido , Mortalidad Infantil , Circulación Extracorporea/estadística & datos numéricos , Cardiopatías Congénitas/complicaciones , Cardiopatías Congénitas/mortalidad , Cardiopatías Congénitas/cirugía , Cirugía General , Epidemiología Descriptiva , Estudios Retrospectivos , Dados EstadísticosRESUMEN
Introducción. En nuestro país fallecen anualmente 400 niños con cardiopatía congénita, en el 1er mes de vida. La cirugía constituye la estrategia actual para su tratamiento. El objetivo es describir la mortalidad hospitalaria y las complicaciones de la cirugía cardíaca neonatal con circulación extracorpórea en un hospital público de alta complejidad. Pacientes y métodos. Estudio descriptivo retrospectivo. Se registraron datos demográficos, de la cirugía y del postoperatorio de los pacientes con circulación extracorpórea, menores de 45 días, operados en el Hospital Garrahan, entre 2004-2008. Se realizó un análisis por patologías y de mortalidad ajustado por riesgo. Los resultados se expresan en mediana e intervalo, o en porcentaje, según corresponda. Resultados. Se operaron 200 recién nacidos, 62 por ciento varones. La edad fue 21 (1- 45) días y el peso 3,1 (1,6-6,2) kg. Anomalía total de retorno venoso pulmonar, transposición de grandes arterias y síndrome de corazón izquierdo hipoplásico concentraronel 75 por ciento de las cirugías. El tiempo de internación fue 12 (0-191) días, con 6 (0-180) días de ventilación mecánica, y 18 por ciento de los pacientes requirieron diálisis. La mortalidad global fue 19 por ciento y 14 por ciento en el último año analizado. Los pacientes en mala condición preoperatoria, así como los que presentaron complicaciones, exhibieron una mortalidad mayor (OR= 2,23 [1,02-4,89] y OR= 10 [3,6-33,4], respectivamente). Conclusiones. La mortalidad postoperatoria es similar a la comunicada en bases de datos del exterior. Los pacientes con mala condición preoperatoria y aquellos con complicaciones presentaron mayor mortalidad en nuestra serie.
Introduction. Four hundred newborns die every year in our country suffering from congenital heart disease. Definitive surgical repair, whenever possible, is nowadays the optimal therapeutic strategy. Our goal is to describe mortality and morbidity in neonatal surgery with cardiopulmonary bypass in a tertiary public hospital in Argentina. Patients and methods. Descriptive, retrospective study. Every patient, younger than 45 days, with cardiac surgery requiring cardiopulmonary bypass, at the Garrahan Hospital between 2004 and 2008 was included. Demographic, surgical and postoperative data were collected. Adjusted mortality risk analysis, and descriptive statistics from the most frequent diagnosis were performed. Results are expressed as median and rank or percentage. Results. 200 newborns were operated, 62 percent males. Median age was 21 days (r 1- 45) and median weight 3.1 kg (r 1.6-6.2). Total anomalous pulmonary venous return, transposition of great arteries and hypoplastic left heart syndrome diagnoses accounted for 75 percent of the procedures. Median length of stay was 12 days (r 0-191), and 6 days of mechanical ventilation (r 0-180). Eighteen percent of the patients required peritoneal dialysis. Whole series mortality was 19 percent and fell to 14 pecent in 2008. Unstable preoperative condition and postoperative complications increased mortality, OR= 2.23 (1.02-4.89) and OR= 10 (3.6-33.4), respectively. Conclusions. Our postoperative mortality is similar to those reported in foreign countries databases. Patients with unstable preoperative condition and post-operative complications had higher mortality.