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1.
Pacing Clin Electrophysiol ; 39(5): 471-7, 2016 May.
Artículo en Inglés | MEDLINE | ID: mdl-26920816

RESUMEN

BACKGROUND: To compare the pacing parameters of unipolar versus bipolar temporary ventricular epicardial pacing leads. DESIGN: Prospective Randomized Unblinded Controlled Study. PATIENTS AND METHODS: Fifty patients undergoing surgery for congenital heart disease who were anticipated to require temporary ventricular pacing leads were recruited preoperatively: 25 patients were randomized to receive unipolar temporary ventricular epicardial pacing leads; the remaining 25 were randomized to receive bipolar temporary ventricular epicardial leads. The baseline characteristics of the groups were similar. The pacing parameters were measured daily for up to first seven postoperative days (PODs) with the day of surgery recorded as POD 0. RESULTS: On the day of insertion, the mean pacing and sensing thresholds were similar for both unipolar and bipolar leads. Thresholds progressively deteriorated with each subsequent POD. By POD 4, the mean ± standard deviation pacing threshold of ventricular bipolar lead was 2.87 ± 0.37 mA compared with 5.6 ± 0.85 mA for the unipolar leads (P = 0.005). The decrease in sensing threshold of the unipolar ventricular pacing leads was significantly more than that of bipolar leads (by POD 5, 5.7 ± 2.64 vs 10.33 ± 2.8, P = 0.01). CONCLUSIONS: Our study shows that the bipolar leads (Medtronic 6495, Medtronic Inc., Minneapolis, MN, USA) have superior sensing and pacing thresholds in the ventricular position in patients undergoing surgery for congenital heart disease when compared to the unipolar leads (Medical Concepts Europe VF608ABB, Medical Concepts Europe Inc., Buffalo, NY, USA).


Asunto(s)
Estimulación Cardíaca Artificial/métodos , Cardiopatías Congénitas/terapia , Pericardio , Electrodos , Femenino , Humanos , Masculino , Estudios Prospectivos , Factores de Tiempo
3.
ASAIO J ; 69(1): 122-126, 2023 01 01.
Artículo en Inglés | MEDLINE | ID: mdl-35471245

RESUMEN

Both overfeeding and underfeeding critically ill children are problematic. This prospective pilot study evaluated the resting energy expenditure in infants and children requiring extracorporeal membrane oxygenation (ECMO) support. An indirect calorimeter was used to measure oxygen consumption (VO 2 ) and carbon dioxide production (VCO 2 ) from the mechanical ventilator. Blood gases were used to determine VO 2 and VCO 2 from the ECMO circuit. Values from the mechanical ventilator and ECMO circuit were added, and the resting energy expenditure (REE) (Kcal/kg/day) was calculated. Measurements were obtained > 24 hours after ECMO support was initiated (day 2 of ECMO), 1 day before ECMO discontinuation or transfer, and 1 day after decannulation. Data were compared with the predicted energy expenditure. Seven patients aged 3 months to 13 years were included. The REE varied greatly both above and below predicted values, from 26 to 154 KCal/kg/day on day 2 of ECMO support. In patients with septic shock, the REE was > 300% above the predicted value on day 2 of ECMO. Before ECMO discontinuation, two of six (33%) children continued to have a REE > 110% of predicted. Three patients had measurements after decannulation, all with a REE < 90% of predicted. REE measurements can be obtained by indirect calorimetry in children receiving ECMO support. ECMO may not provide metabolic rest for all children as a wide variation in REE was observed. For optimal care, individual testing should be considered to match calories provided with the metabolic demand.


Asunto(s)
Oxigenación por Membrana Extracorpórea , Lactante , Humanos , Niño , Proyectos Piloto , Estudios Prospectivos , Dióxido de Carbono/metabolismo , Enfermedad Crítica , Metabolismo Energético
4.
Pediatr Crit Care Med ; 13(1): 16-21, 2012 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-21478791

RESUMEN

OBJECTIVE: To evaluate the relationship between duration of mechanical ventilation before the initiation of extracorporeal life support and the survival rate in children with respiratory failure. Extracorporeal life support has been used as a rescue therapy for >30 yrs in children with severe respiratory failure. Previous studies suggest patients who received >7-10 days of mechanical ventilation were not acceptable extracorporeal life support candidates as a result of irreversible lung damage. DESIGN: A retrospective review encompassing the past 10 yrs of the International Extracorporeal Life Support Organization Registry (January 1, 1999, to December 31, 2008). SETTING: Extracorporeal Life Support Organization Registry database. PATIENTS: A total of 1325 children (≥ 30 days and ≤ 18 yrs) met inclusion criteria. INTERVENTIONS: None. MEASUREMENTS AND MAIN RESULTS: The following pre-extracorporeal life support variables were identified as independently and significantly related to the chance of survival: 1) >14 days of ventilation vs. 0-7 days was adverse (odds ratio, 0.32; p < .001); 2) the presence of a cardiac arrest was adverse (odds ratio, 0.56; p = .001); 3) pH per 0.1-unit increase was protective (odds ratio, 1.15; p < .001); 4) oxygenation index, per 10-unit increase was adverse (odds ratio, 0.95; p = .002); and 5) any diagnosis other than sepsis was related to a more favorable outcome. Patients requiring >7-10 or >10-14 days of pre-extracorporeal life support ventilation did not have a statistically significant decrease in survival as compared with patients who received 0-7 days. CONCLUSIONS: There was a clear relationship between the number of mechanical ventilation days before the initiation of extracorporeal life support and survival. However; there was no statistically significant decrease in survival until >14 days of pre-extracorporeal life support ventilation was reached regardless of underlying diagnosis. We found no evidence to suggest that prolonged mechanical ventilation should be considered as a contraindication to extracorporeal life support in children with respiratory failure before 14 days.


Asunto(s)
Causas de Muerte , Oxigenación por Membrana Extracorpórea/métodos , Sistema de Registros , Respiración Artificial/métodos , Insuficiencia Respiratoria/mortalidad , Insuficiencia Respiratoria/terapia , Niño , Preescolar , Enfermedad Crítica/mortalidad , Enfermedad Crítica/terapia , Bases de Datos Factuales , Progresión de la Enfermedad , Oxigenación por Membrana Extracorpórea/mortalidad , Femenino , Mortalidad Hospitalaria/tendencias , Humanos , Lactante , Unidades de Cuidados Intensivos , Modelos Logísticos , Masculino , Respiración Artificial/efectos adversos , Insuficiencia Respiratoria/diagnóstico , Medición de Riesgo , Análisis de Supervivencia , Factores de Tiempo
5.
Pediatrics ; 118(5): e1580-3, 2006 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-17000784

RESUMEN

A 3-month-old infant presented to the pediatric emergency department with respiratory distress and tetany after ingestion of a phosphate-containing oral laxative. The initial phosphorus level was 38.3 mg/dL. With aggressive fluid resuscitation and intravenous calcium administration, the infant completely recovered. Although the risks of phosphate-containing enemas are well described, life-threatening hyperphosphatemia can also result from administration of phosphate-containing oral laxatives. Aggressive fluid hydration is the mainstay of treatment. Intravenous calcium administration may be necessary to avoid hemodynamic collapse despite the theoretical possibility of metastatic calcifications. Physicians should be alerted to the possibility of phosphate toxicity and hypocalcemic tetany in young children when treated with over-the-counter laxatives. Caregivers should be advised not to administer over-the-counter laxatives to infants without physician supervision.


Asunto(s)
Catárticos/efectos adversos , Hipocalcemia/inducido químicamente , Trastornos del Metabolismo del Fósforo/inducido químicamente , Tetania/inducido químicamente , Administración Oral , Catárticos/administración & dosificación , Humanos , Lactante , Masculino , Índice de Severidad de la Enfermedad
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