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1.
J Soc Cardiovasc Angiogr Interv ; 3(6): 101933, 2024 Jun.
Article in English | MEDLINE | ID: mdl-39132597

ABSTRACT

Background: The CardioMEMS is an implantable device for hemodynamic monitoring approved by the US Food and Drug Administration for adult patients with heart failure. It has been used in the adult population without structural heart disease and with congenital heart diseases, but we do not have data in the pediatric population. Methods: We report the initial single-center experience of the CardioMEMS implantation in children. Feasibility of device implantation, procedural outcomes, and clinical utility in the pediatric population were evaluated. Results: The CardioMEMS device was implanted without technical complications in 8 pediatric patients (mean age 7 years and mean weight 27.9 kg) with pulmonary hypertension (6/8, 75%) and heart failure (2/8, 25%). The device was delivered via femoral access in 7 (85%) patients and implanted in the left pulmonary artery in 7 (85%). The noninvasive recording of pulmonary pressures in patients with pulmonary hypertension allowed the monitoring of the evolution of mean pulmonary artery pressure, intensifying vasodilator treatment, and avoiding control cardiac catheterizations. In patients with heart failure, pulmonary hemodynamic monitoring guided the decongestive treatment prior to heart transplantation. Conclusions: The implantation of CardioMEMS in the pediatric population is a feasible procedure that allows the noninvasive hemodynamic monitoring of patients with heart failure and pulmonary hypertension. Its implementation in selected patients aids in outpatient follow-up and therapeutic management of patients with complex cardiac conditions, avoiding invasive procedures that require hospitalization. Further large-scale studies in the pediatric population are recommended.

2.
Int J Mol Sci ; 23(18)2022 Sep 09.
Article in English | MEDLINE | ID: mdl-36142358

ABSTRACT

BACKGROUND: Pulmonary arterial hypertension (PAH) is a severe and rare disease with an important genetic background. The influence of genetic testing in the clinical classification of pediatric PAH is not well known and genetics could influence management and prognosis. OBJECTIVES: The aim of this work was to identify the molecular fingerprint of PH children in the REgistro de pacientes con HIpertensión Pulmonar PEDiátrica (REHIPED), and to investigate if genetics could have an impact in clinical reclassification and prognosis. METHODS: We included pediatric patients with a genetic analysis from REHIPED. From 2011 onward, successive genetic techniques have been carried out. Before genetic diagnosis, patients were classified according to their clinical and hemodynamic data in five groups. After genetic analysis, the patients were reclassified. The impact of genetics in survival free of lung transplantation was estimated by Kaplan-Meier curves. RESULTS: Ninety-eight patients were included for the analysis. Before the genetic diagnoses, there were idiopathic PAH forms in 53.1%, PAH associated with congenital heart disease in 30.6%, pulmonary veno-occlusive disease-PVOD-in 6.1%, familial PAH in 5.1%, and associated forms with multisystemic disorders-MSD-in 5.1% of the patients. Pathogenic or likely pathogenic variants were found in 44 patients (44.9%). After a genetic analysis, 28.6% of the cohort was "reclassified", with the groups of heritable PAH, heritable PVOD, TBX4, and MSD increasing up to 18.4%, 8.2%, 4.1%, and 12.2%, respectively. The MSD forms had the worst survival rates, followed by PVOD. CONCLUSIONS: Genetic testing changed the clinical classification of a significant proportion of patients. This reclassification showed relevant prognostic implications.


Subject(s)
Pulmonary Arterial Hypertension , Pulmonary Veno-Occlusive Disease , Child , Familial Primary Pulmonary Hypertension/genetics , Genetic Background , Humans , Pulmonary Arterial Hypertension/genetics , Pulmonary Veno-Occlusive Disease/pathology , Registries
3.
PLoS One ; 14(3): e0213210, 2019.
Article in English | MEDLINE | ID: mdl-30840669

ABSTRACT

INTRODUCTION: Bronchopulmonary dysplasia (BPD) is the most common chronic lung disease in childhood, related to prematurity, and the most common cause of pulmonary hypertension (PH) secondary to pulmonary disease in children. Moderate and severe BPD have a worse outcome and relate more frequently with PH. The prediction of moderate or severe BPD development in extremely premature newborns is vital to implement preventive strategies. Starting with the hypothesis that molecular biomarkers were better than clinical and echocardiographic factors, this study aims to explore the ability of clinical, echocardiographic and analytical variables to predict moderate or severe BPD in a cohort of extremely preterm infants. PATIENTS AND METHODS: We designed a prospective longitudinal study, in which we followed a cohort of preterm newborns (gestational age <28 weeks and weight ≤ 1250 grams). In these newborns we recorded weekly clinical and echocardiographic variables as well as blood and tracheal aspirate samples, to analyze molecular biomarkers (IL-6, IL-1, IP10, uric acid, HGF, endothelin-1, VEGF, CCL5). Variables and samples were collected since birth up to week 36 (postmenstrual age), time-point at which the diagnosis of BPD is established. RESULTS: We included 50 patients with a median gestational age of 26 weeks (IQR 25-27) and weight of 871 g (SD 161,0) (range 590-1200g). Three patients were excluded due to an early death. Thirty-five patients (74.5%) developed BPD (mild n = 14, moderate n = 15, severe n = 6). We performed a logistic regression in order to identify risk factors for moderate or severe BPD. We compared two predictive models, one with two variables (mechanical ventilation and inter-ventricular septum flattening), and another-one with an additional molecular biomarker (ET-1). CONCLUSIONS: The combination of clinical and echocardiographic variables is a valuable tool for determining the risk of BPD. We find the two variable model (mechanical ventilation and echocardiographic signs of PH) more practical for clinical and research purposes. Future research on BPD prediction should be oriented to explore the potential role of ET-1.


Subject(s)
Biomarkers/blood , Bronchopulmonary Dysplasia/diagnosis , Echocardiography/methods , Infant, Extremely Premature/blood , Infant, Low Birth Weight/blood , Infant, Premature, Diseases/diagnosis , Risk Assessment/methods , Bronchopulmonary Dysplasia/epidemiology , Bronchopulmonary Dysplasia/metabolism , Female , Follow-Up Studies , Gestational Age , Humans , Infant, Newborn , Infant, Premature, Diseases/epidemiology , Infant, Premature, Diseases/metabolism , Longitudinal Studies , Male , Pregnancy , Prognosis , Prospective Studies , Risk Factors , Spain/epidemiology
4.
Cytotherapy ; 20(11): 1337-1344, 2018 11.
Article in English | MEDLINE | ID: mdl-30327248

ABSTRACT

BACKGROUND: Bronchopulmonary dysplasia (BPD) is the most prevalent sequelae of premature birth, for which therapeutic options are currently limited. Mesenchymal stromal cells (MSCs) are a potential therapy for prevention or reversal of BPD. SERIES OF CASES: We report on two infants with severe BPD in whom off-label treatment with repeated intravenous doses of allogeneic bone marrow-derived MSCs were administered. We analyzed the temporal profile of serum and tracheal cytokines and growth factors as well as safety, tolerability and clinical response. The administration of repeated intravenous doses of MSCs in two human babies with severe and advanced BPD was feasible and safe and was associated with a decrease of pro-inflammatory molecules and lung injury biomarkers. Both patients were at very advanced stages of BPD with very severe lung fibrosis and did not survive the disease. CONCLUSIONS: MSCs are a promising therapy for BPD, but they should be administered in early stages of the disease.


Subject(s)
Bronchopulmonary Dysplasia/therapy , Lung/pathology , Mesenchymal Stem Cell Transplantation/methods , Administration, Intravenous , Biomarkers/blood , Bronchopulmonary Dysplasia/diagnostic imaging , Cytokines/blood , Female , Humans , Infant , Infant, Newborn , Infant, Premature , Mesenchymal Stem Cell Transplantation/adverse effects , Mesenchymal Stem Cells , Trachea/metabolism
7.
Pediatr Res ; 73(1): 95-103, 2013 Jan.
Article in English | MEDLINE | ID: mdl-23138399

ABSTRACT

BACKGROUND: Inodilators are routinely used in cardiovascular surgery with cardiopulmonary bypass (CPB). Information regarding safety and tolerability of the novel molecule, levosimendan (LEVO), in newborns is anecdotal; no pharmacokinetic data in this population are available. METHODS: This was a phase I, randomized, and blinded study. Neonates undergoing surgical repair for congenital heart defects received stepwise dose increases of milrinone (MR; 0.5-1 µg/kg/min, n = 9) or LEVO (0.1-0.2 µg/kg/min, n = 11) as an i.v. continuous infusion, starting before CPB. Infants had continuous, time-locked, physiological, and near-infrared spectroscopy (NIRS) (cerebral and peripheral) recordings during the first 24 h, and at 48 and 96 h postsurgery. Serial biochemistry and pharmacokinetic studies were performed. RESULTS: During the first 24 h postsurgery, patients showed time-related, group-independent increased cerebral tissue oxygenation and decreased diastolic blood pressure; in addition, group-dependent differences in heart rate and peripheral perfusion were found. Early postsurgery, MR-treated infants showed lower pH, higher glycemia, and higher inotrope score. The groups differed in cerebral NIRS-derived variables from 24 to 96 h. Study drug withdrawal at 96 h was more frequent with LEVO. LEVO intermediate metabolites were detected in plasma at day 14 after surgery. CONCLUSION: LEVO is well tolerated in critically ill neonates. LEVO may have advantages over MR in terms of the dosing regimen.


Subject(s)
Cardiotonic Agents/pharmacology , Cardiotonic Agents/pharmacokinetics , Cardiovascular Surgical Procedures/methods , Heart Defects, Congenital/surgery , Vasodilator Agents/pharmacology , Vasodilator Agents/pharmacokinetics , Blood Pressure/drug effects , Cardiotonic Agents/administration & dosage , Cerebrum/metabolism , Heart Rate/drug effects , Humans , Hydrazones , Infant, Newborn , Infusions, Intravenous , Oxygen/metabolism , Pyridazines , Simendan , Spectroscopy, Near-Infrared , Time Factors , Vasodilator Agents/administration & dosage
8.
Rev. esp. cardiol. (Ed. impr.) ; 64(8): 674-680, ago. 2011.
Article in Spanish | IBECS | ID: ibc-89899

ABSTRACT

Introducción y objetivos. El desplazamiento sistólico del plano del anillo tricuspídeo (siglas en inglés, TAPSE) es una medida ecocardiográfica que permite evaluar adecuadamente la función sistólica del ventrículo derecho y se emplea habitualmente en adultos. No obstante, hay poca información sobre los valores de referencia de TAPSE en niños. Nuestro objetivo fue determinar valores de referencia de TAPSE en niños españoles y evaluar su relación con la edad y la superficie corporal. Métodos. Incluimos prospectivamente a 405 sujetos (neonatos hasta 18 años, el 53% varones) remitidos para evaluación de soplo cardiaco. Excluimos a los sujetos con cardiopatía o cualquier otra enfermedad. Recogimos la medida por modo M de TAPSE y variables antropométricas. Analizamos la reproducibilidad intraobservador e interobservadores de las mediciones. Resultados. El TAPSE medio fue 17,09±5,09cm, sin diferencias significativas entre sexos. Se demostró adecuado un modelo de regresión curvilínea, con valores incrementales proporcionales a los estratos de edad, talla, peso, índice de masa corporal y superficie corporal. La superficie corporal presentó una importante correlación positiva con los valores de TAPSE (r=0,81), mientras que la frecuencia mantuvo una correlación negativa (r=−0,74). El análisis multivariable confirmó estas correlaciones, así como las interacciones entre variables (edad, talla, peso, superficie corporal). Aportamos gráficas con las estimaciones poblacionales normales para TAPSE ajustadas por edad y superficie corporal. Conclusiones. Presentamos valores de referencia de TAPSE para población pediátrica española. La medida del TAPSE fue reproducible y se relacionó directamente con la edad y la superficie corporal. Estos valores de referencia podrían guiar la toma clínica de decisiones (AU)


Introduction and objectives. Tricuspid annular plane systolic excursion (TAPSE) is an echocardiographic measure that allows us to assess right ventricular systolic function. TAPSE measurement is common in adults but reference values for children are scarce. Our objective was to establish reference values for TAPSE in Spanish children and to determine the relationship of these values with age and body surface. Methods. This prospective study included 405 patients (from newborn to age 18 years, 53% male) referred for assessment of cardiac murmurs. Patients with confirmed cardiac or any other disease were excluded. We collected TAPSE measurements by M-mode echocardiography and recorded anthropometric variables. We analyzed the intra- and interobserver reproducibility of these measurements. Results. Mean TAPSE values were 17.09±5.09cm with nonsignificant differences between sexes. A curvilinear regression model proved appropriate, with values increasing in proportion to age group, height, weight, body mass index, and body surface. Body surface showed a strong positive correlation with TAPSE values (r=0.81), whereas frequency had a negative correlation (r=–0.74). Multivariate analysis confirmed these correlations and the interactions between variables (age, height, weight, body surface). Graphs of estimated normal population-based TAPSE values adjusted by age and body surface are provided. Conclusions. We present reference values for TAPSE in Spanish children and adolescents. The TAPSE measurement was reproducible and associated directly with age and body surface. These reference values could guide decision making in daily clinical practice (AU)


Subject(s)
Humans , Male , Female , Infant, Newborn , Infant , Child, Preschool , Child , Adolescent , Ventricular Function/physiology , /methods , Echocardiography , Anthropometry/methods , Ventricular Function , Prospective Studies , Reference Values , 28599 , Confidence Intervals
9.
Rev Esp Cardiol ; 64(8): 674-80, 2011 Aug.
Article in English, Spanish | MEDLINE | ID: mdl-21684663

ABSTRACT

INTRODUCTION AND OBJECTIVES: Tricuspid annular plane systolic excursion (TAPSE) is an echocardiographic measure that allows us to assess right ventricular systolic function. TAPSE measurement is common in adults but reference values for children are scarce. Our objective was to establish reference values for TAPSE in Spanish children and to determine the relationship of these values with age and body surface. METHODS: This prospective study included 405 patients (from newborn to age 18 years, 53% male) referred for assessment of cardiac murmurs. Patients with confirmed cardiac or any other disease were excluded. We collected TAPSE measurements by M-mode echocardiography and recorded anthropometric variables. We analyzed the intra- and interobserver reproducibility of these measurements. RESULTS: Mean TAPSE values were 17.09 ± 5.09 cm with nonsignificant differences between sexes. A curvilinear regression model proved appropriate, with values increasing in proportion to age group, height, weight, body mass index, and body surface. Body surface showed a strong positive correlation with TAPSE values (r = 0.81), whereas frequency had a negative correlation (r = -0.74). Multivariate analysis confirmed these correlations and the interactions between variables (age, height, weight, body surface). Graphs of estimated normal population-based TAPSE values adjusted by age and body surface are provided. CONCLUSIONS: We present reference values for TAPSE in Spanish children and adolescents. The TAPSE measurement was reproducible and associated directly with age and body surface. These reference values could guide decision making in daily clinical practice.


Subject(s)
Echocardiography, Transesophageal , Systole , Tricuspid Valve/diagnostic imaging , Tricuspid Valve/physiology , Adolescent , Child , Child, Preschool , Female , Humans , Infant , Infant, Newborn , Male , Prospective Studies , Reference Values
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