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1.
J Ultrasound ; 26(2): 435-448, 2023 Jun.
Article in English | MEDLINE | ID: mdl-36301438

ABSTRACT

PURPOSE: Respiratory distress syndrome (RDS), also known as hyaline membrane disease, is the most common clinical syndrome encountered among preterm infants, and the complications of the disease account for substantial mortality. Diagnosis of RDS is based on the clinical status of patients in correlation with laboratory parameters and chest X-ray. Lung ultrasound despite its wide use still is not incorporated into diagnostic algorithms. The aim of the study was to evaluate the diagnostic ability of lung ultrasound in diagnosing respiratory distress syndrome as well as in the monitoring of the response to treatment. A secondary aim was to propose a modified ultrasound grading scale. METHODS: The prospective study included 150 neonates with clinical and radiographic signs of neonatal respiratory distress syndrome within the first 24 h of life, with different gestational age (≤ 35 weeks). Lung ultrasound was performed by two radiologists and correlated with a chest X-ray. Two gradation scales (ultrasound and X-ray) were compared and each scale was correlated with the patient's clinical data. RESULTS: In comparison between ultrasound findings and X-ray results showed a statistically significant difference in a favor of ultrasound. Based on the presence of subpleural consolidations, further differentiation of ultrasound profiles were made into subgroups and new ultrasound classification have been proposed. CONCLUSION: Our study showed that lung ultrasound enables the diagnosing of respiratory distress syndrome in premature neonates and also shows a significant correlation with chest X-ray, which is considered as a radiological method of choice for the diagnosis of RDS.


Subject(s)
Infant, Premature , Respiratory Distress Syndrome, Newborn , Humans , Infant, Newborn , Infant , X-Rays , Prospective Studies , Respiratory Distress Syndrome, Newborn/diagnostic imaging , Respiratory Distress Syndrome, Newborn/complications , Respiratory Distress Syndrome, Newborn/therapy , Lung/diagnostic imaging , Ultrasonography
2.
An. pediatr. (2003. Ed. impr.) ; 83(5): 354.e1-354.e6, nov. 2015. tab
Article in Spanish | IBECS | ID: ibc-145412

ABSTRACT

Las recomendaciones incluidas en este documento forman parte de una revisión actualizada de la asistencia respiratoria en el recién nacido. Están estructuradas en 12 módulos y en este trabajo se presenta el módulo 7. El contenido de cada módulo es el resultado del consenso de los miembros del Grupo Respiratorio y Surfactante de la Sociedad Española de Neonatología. Representan una síntesis de los trabajos publicados y de la experiencia clínica de cada uno de los miembros del grupo (AU)


The recommendations included in this document will be part a series of updated reviews of the literature on respiratory support in the newborn infant. These recommendations are structured into twelve modules, and in this work module 7 is presented. Each module is the result of a consensus process including all members of the Surfactant and Respiratory Group of the Spanish Society of Neonatology. They represent a summary of the published papers on each specific topic, and of the clinical experience of each one of the members of the group (AU)


Subject(s)
Female , Humans , Infant, Newborn , Male , Respiration/genetics , Surface-Active Agents/administration & dosage , Surface-Active Agents/pharmacology , Nitric Oxide/deficiency , Nitric Oxide , Pulmonary Atelectasis/enzymology , Pulmonary Atelectasis/metabolism , Hyaline Membrane Disease/metabolism , Hyaline Membrane Disease/pathology , Respiration/immunology , Surface-Active Agents , Surface-Active Agents/metabolism , Nitric Oxide/standards , Nitric Oxide/therapeutic use , Pulmonary Atelectasis/complications , Pulmonary Atelectasis/diagnosis , Hyaline Membrane Disease/complications , Hyaline Membrane Disease/diagnosis
3.
An Pediatr (Barc) ; 83(5): 354.e1-6, 2015 Nov.
Article in Spanish | MEDLINE | ID: mdl-25840706

ABSTRACT

The recommendations included in this document will be part a series of updated reviews of the literature on respiratory support in the newborn infant. These recommendations are structured into twelve modules, and in this work module 7 is presented. Each module is the result of a consensus process including all members of the Surfactant and Respiratory Group of the Spanish Society of Neonatology. They represent a summary of the published papers on each specific topic, and of the clinical experience of each one of the members of the group.


Subject(s)
Neonatology , Nitric Oxide/administration & dosage , Respiration, Artificial/methods , Surface-Active Agents/administration & dosage , Consensus , Humans , Infant, Newborn
4.
J Perinatol ; 33(5): 401-3, 2013 May.
Article in English | MEDLINE | ID: mdl-23624968

ABSTRACT

We report the case of a newborn with alveolar capillary dysplasia with misalignment of pulmonary veins (ACD/MPV), a rare condition of unknown etiology presenting in the neonatal period with significant persistent pulmonary hypertension. The diagnosis was made by lung biopsy and confirmed at autopsy. Specific genetic analysis demonstrated defects in the FOXF1 gene. The diagnosis of ACD/MPV requires a high level of suspicion and is made by lung biopsy or necropsy examination by a pediatric pathologist with experience in this condition. The availability of genetic testing has led to increasing diagnosis of patients with this lethal disorder and can influence their management, specifically by indicating the need for lung biopsy in a critically ill newborn.


Subject(s)
Forkhead Transcription Factors/genetics , Lung/pathology , Persistent Fetal Circulation Syndrome/pathology , Fatal Outcome , Female , Humans , Infant, Newborn , Mutation , Persistent Fetal Circulation Syndrome/genetics
6.
An Pediatr (Barc) ; 70(2): 137-42, 2009 Feb.
Article in Spanish | MEDLINE | ID: mdl-19217569

ABSTRACT

AIM: To learn the characteristic of the neonatal intensive care units (NICUs) that offer neonatal respiratory assistance in Spain. MATERIAL AND METHOD: A structured survey was developed and sent to all Spanish neonatal units to learn about the respiratory care offered in 2005. RESULTS: A total of 96 Units answered the survey, with an estimated representatively of 63%, with a range from 3 to 92%, depending on the geographical area. Level IIIc Units were in the upper range. Answer the survey 26 units type IIb (27%), 16 IIIa (17%), 40 IIIb (42%) and 14 IIIc (14%). The total number of level III NICU beds was 541 (1.2 beds per 1000 livebirths; range, 0.7-1.7). The mean number of beds per NICU was 4.1 in level IIIa Units, 2.8 in those IIIb and 14.6 in type IIIc NICUs. In level III NICUs, the bed per physician ratio was 2.4 and that of beds per registered nurse was 2.8 (2.2 in level IIIc NICUs). There were a total 13,219 admissions, 54% of those needed mechanical ventilation (36% in IIIa and 65% in level IIIc NICUs). Oxygen blenders for resuscitation at birth were available in 42% of level IIIb and IIIc NICUs. NICUs had one neonatal ventilator per bed, and 63% of units had high frequency ventilation available. All units had nasal-CPAP systems, 25% of level IIIa Units, 58% IIIb and 64% of those type IIIc had systems for nasal ventilation. All level IIIc and 93% of level IIIb NICUs were able to provide inhaled nitric oxygen therapy. Four NICUS offered ECMO. CONCLUSIONS: The mean number of NICU beds per 1000 livebirths is within the lower limits of those been recommended, and there were wide variations among different geographical areas. A 54% of those babies admitted to NICUs required mechanical ventilation. The mean number of NICU beds per registered nurse was 2.8. There was an adequate number of neonatal ventilators (one per bed) and 63% were able to provide HFV. All NICUs hand n-CPAP systems.


Subject(s)
Intensive Care Units, Neonatal , Respiration, Artificial/statistics & numerical data , Humans , Infant, Newborn
8.
An. pediatr. (2003, Ed. impr.) ; 70(2): 137-142, feb. 2009. tab
Article in Spanish | IBECS | ID: ibc-59234

ABSTRACT

Objetivo: conocer el tipo de unidades de cuidados intensivos neonatales (UCIN) que proporcionan asistencia respiratoria neonatal en España y sus características. Material y método: encuesta multicéntrica estructurada para conocer la actividad asistencial respiratoria prestada por las UCIN en 2005. Resultados: contestaron 96 unidades neonatales con una representatividad estimada en un 63%, con un intervalo entre el 3 y el 92%, según las áreas geográficas; las unidades IIIc se encuentran en el rango superior. Contestaron la encuesta 26 unidades tipo IIb (27%), 16 IIIa (17%), 40 IIIb (42%) y 14 IIIc (14%). Las camas totales de intensivos de nivel III fue de 541 (1,2 camas cada 1.000 recién nacidos vivos; intervalo, 0,7-1,7). La media de camas por unidad fue de 4,1 para las IIIa, 2,8 para las IIIb y 14,6 para las IIIc. En las unidades de nivel III, la relación camas/médicos fue de 2,4 camas/medico y la de camas/enfermeras 2,8 camas/enfermera (2,2 en nivel IIIc). Hubo un total de 13.219 ingresos, de los que el 54% precisó ventilación (el 36% en las IIIa y el 65% en las IIIc). La posibilidad de reanimación en el paritorio con mezcla de gases (aire y oxígeno) sólo la tiene el 42% de las IIIb y IIIc. La relación respirador/cama fue de 1/1; el 63% puede proporcionar ventilación de alta frecuencia (VAF). Todas disponen de sistemas de presión positiva continua nasal (CPAP-n). Sistemas para aplicar ventilación nasal intermitente están disponibles en el 25% de las IIIa, el 58% de las IIIb y el 64% de las IIIc. Todas las IIIc y el 93% de las IIIb pueden proporcionar oxido nítrico inhalado. Cuatro unidades disponían de ECMO. Conclusiones: la media de camas de UCIN de nivel III cada mil nacidos está en el límite bajo de lo recomendable, con notables diferencias regionales. La necesidad de ventilación mecánica fue del 54%. La relación de camas por enfermera fue de 2,8. Existe una buena dotación de respiradores (1 por cama) con alta disponibilidad de VAF (63%). Todas las unidades disponen de CPAP-n (AU)


Aim: To learn the characteristic of the neonatal intensive care units (NICUs) that offer neonatal respiratory assistance in Spain. Material and method: A structured survey was developed and sent to all Spanish neonatal units to learn about the respiratory care offered in 2005. Results: A total of 96 Units answered the survey, with an estimated representatively of 63%, with a range from 3 to 92%, depending on the geographical area. Level IIIc Units were in the upper range. Answer the survey 26 units type IIb (27%), 16 IIIa (17%), 40 IIIb (42%) and 14 IIIc (14%). The total number of level III NICU beds was 541 (1.2 beds per 1000 livebirths; range, 0.7–1.7). The mean number of beds per NICU was 4.1 in level IIIa Units, 2.8 in those IIIb and 14.6 in type IIIc NICUs. In level III NICUs, the bed per physician ratio was 2.4 and that of beds per registered nurse was 2.8 (2.2 in level IIIc NICUs). There were a total 13,219 admissions, 54% of those needed mechanical ventilation (36% in IIIa and 65% in level IIIc NICUs). Oxygen blenders for resuscitation at birth were available in 42% of level IIIb and IIIc NICUs. NICUs had one neonatal ventilator per bed, and 63% of units had high frequency ventilation available. All units had nasal-CPAP systems, 25% of level IIIa Units, 58% IIIb and 64% of those type IIIc had systems for nasal ventilation. All level IIIc and 93% of level IIIb NICUs were able to provide inhaled nitric oxygen therapy. Four NICUS offered ECMO. Conclusions: The mean number of NICU beds per 1000 livebirths is within the lower limits of those been recommended, and there were wide variations among different geographical areas. A 54% of those babies admitted to NICUs required mechanical ventilation. The mean number of NICU beds per registered nurse was 2.8. There was an adequate number of neonatal ventilators (one per bed) and 63% were able to provide HFV. All NICUs hand n-CPAP systems (AU)


Subject(s)
Humans , Infant, Newborn , Intensive Care Units, Neonatal/statistics & numerical data , Respiration, Artificial/statistics & numerical data , Health Services Research , Spain
9.
An Pediatr (Barc) ; 68(3): 224-31, 2008 Mar.
Article in Spanish | MEDLINE | ID: mdl-18358132

ABSTRACT

OBJECTIVES: To investigate the aetiology, clinical course and response to treatment of neonatal chylothorax. PATIENTS AND METHOD: Prospective study over a 2-year period in a neonatal intensive care unit of a tertiary university hospital. All newborns followed a predefined therapeutic protocol that included the sequential administration of total parenteral nutrition (TPN), octreotide and surgery. The influence of aetiology on outcome and response to treatment was investigated. RESULTS: The study included 22 newborns. Surgery for congenital heart disease (CHD) (n = 14) and congenital diaphragmatic hernia (n = 4) were the most common aetiologies. The incidence of chylothorax in these aetiological groups was 11.2 % (95 % CI 5.7-16.8 %) and 26.6 % (95 % CI 4.3-40 %), respectively. Medical treatment was successful in 17 patients. Five of the 10 patients who did not respond to TPN were successfully treated with octreotide; none of the patients in whom octreotide failed responded to the subsequent 3 weeks of TPN. No side-effects were observed during octreotide administration. No significant association between aetiology and response to treatment was found, although all 4 patients who ultimately required surgery were in the CHD group. All patients had complications attributable to chylothorax. Five patients died during the 6 months of follow-up although mortality was never directly attributed to chylothorax. CONCLUSIONS: Most patients can be successfully managed with medical treatment but early surgery should be considered in patients who do not respond to medical treatment. Aetiology is the main determinant of mortality. Randomized controlled studies are needed to demonstrate the efficacy and adequate timing of application of each therapeutic intervention.


Subject(s)
Chylothorax , Gastrointestinal Agents/therapeutic use , Octreotide/therapeutic use , Suction/methods , Algorithms , Chylothorax/etiology , Chylothorax/physiopathology , Chylothorax/therapy , Combined Modality Therapy , Gestational Age , Humans , Infant, Newborn , Injections, Intravenous , Prospective Studies
10.
An. pediatr. (2003, Ed. impr.) ; 68(3): 224-231, mar. 2008. ilus, tab
Article in Es | IBECS | ID: ibc-63608

ABSTRACT

Objetivos: Investigar la etiología, curso clínico y respuesta al tratamiento del quilotórax neonatal. Pacientes y método: Estudio prospectivo en la unidad de cuidados intensivos neonatales de un hospital terciario durante un período de 2 años. Se aplicó un protocolo terapéutico predefinido consistente en la administración secuencial de nutrición parenteral total (NPT), octreótide y cirugía. Se investigó la influencia de la etiología sobre la evolución y respuesta al tratamiento. Resultados: Se incluyeron 22 recién nacidos. Las causas más frecuente fueron la cirugía cardíaca (n = 14) y la hernia diafragmática (n = 4), en las que la incidencia de quilotórax fue del 11,2 % (intervalo de confianza del 95 % [IC 95 %]: 5,7-16,8 %) y del 26,6 % (IC 95 %: 4,3-40 %), respectivamente. Un total de 17 pacientes respondieron al tratamiento médico. El octreótide fue eficaz en 5 de los 10 pacientes en que fracasó la NPT; ninguno de los pacientes en que fracasó el octreótide mejoraron tras 3 semanas de NPT. No se observaron complicaciones atribuibles al octreótide. No observamos una asociación significativa entre la etiología y la respuesta al tratamiento, aunque los 4 pacientes que requirieron cirugía pertenecieron al grupo de recién nacidos postoperados de cardiopatía congénita. Todos presentaron complicaciones atribuibles al quilotórax. Fallecieron 5 pacientes durante los 6 meses de seguimiento pero en ningún caso la muerte fue directamente atribuible al quilotórax. Conclusiones: Debe considerarse una cirugía precoz en la minoría de pacientes que no responden al tratamiento médico. La etiología es el principal determinante de la mortalidad. Son necesarios estudios aleatorizados controlados que establezcan la eficacia y momento de aplicación de las diferentes opciones terapéuticas (AU)


Objectives: To investigate the aetiology, clinical course and response to treatment of neonatal chylothorax. Patients and method: Prospective study over a 2-year period in a neonatal intensive care unit of a tertiary university hospital. All newborns followed a predefined therapeutic protocol that included the sequential administration of total parenteral nutrition (TPN), octreotide and surgery. The influence of aetiology on outcome and response to treatment was investigated. Results: The study included 22 newborns. Surgery for congenital heart disease (CHD) (n = 14) and congenital diaphragmatic hernia (n = 4) were the most common aetiologies. The incidence of chylothorax in these aetiological groups was 11.2 % (95 % CI 5.7-16.8 %) and 26.6 % (95 % CI 4.3-40 %), respectively. Medical treatment was successful in 17 patients. Five of the 10 patients who did not respond to TPN were successfully treated with octreotide; none of the patients in whom octreotide failed responded to the subsequent 3 weeks of TPN. No side-effects were observed during octreotide administration. No significant association between aetiology and response to treatment was found, although all 4 patients who ultimately required surgery were in the CHD group. All patients had complications attributable to chylothorax. Five patients died during the 6 months of follow-up although mortality was never directly attributed to chylothorax. Conclusions: Most patients can be successfully managed with medical treatment but early surgery should be considered in patients who do not respond to medical treatment. Aetiology is the main determinant of mortality. Randomized controlled studies are needed to demonstrate the efficacy and adequate timing of application of each therapeutic intervention (AU)


Subject(s)
Humans , Male , Female , Infant, Newborn , Chylothorax/diagnosis , Chylothorax/etiology , Chylothorax/therapy , Heart Defects, Congenital/diagnosis , Heart Defects, Congenital/etiology , Pleural Effusion/etiology , Hernia, Diaphragmatic/complications , Hypoalbuminemia/complications , Hypoalbuminemia/diagnosis , Clinical Protocols , Prognosis , Pleural Effusion/complications , Hernia, Diaphragmatic/diagnosis , Pleural Effusion/therapy , Prospective Studies , Hyponatremia/complications , Hyponatremia/diagnosis , Hyperbilirubinemia/complications , Infant Mortality/trends
11.
Farm Hosp ; 31(5): 311-4, 2007.
Article in Spanish | MEDLINE | ID: mdl-18052634

ABSTRACT

OBJECTIVE: Oral administration of hypertonic solutions can contribute to intestinal damage in the initial stages of neonatal necrotizing enterocolitis. The purpose of this study is to determine the osmolality of oral liquid dosage forms used in a division of neonatology and to establish some recommendations for their dilution. METHOD: The osmolality of 26 oral liquid dosage forms has been measured using the freezing-point depression method. RESULTS: Oral liquid dosage forms used in the division of neonatology present an osmolality greater than 350 mOsm/kg H2O. 19.2% of all the analysed forms presented an osmolality lower than 1500 mOsm/kg H2O, 80.7% were over that figure, while 23% presented an extremely high osmolality (> 5,000 mOsm/kg H2O). CONCLUSIONS: Knowledge of osmolality of oral liquid dosage forms in the division of neonatology enables the risk of intestinal aggression caused by enteral administration of the medication to be assessed.


Subject(s)
Hospitals , Administration, Oral , Drug Therapy , Enterocolitis, Necrotizing/drug therapy , Humans , Infant, Newborn , Osmolar Concentration
12.
Farm. hosp ; 31(5): 311-314, sept.-oct. 2007. tab
Article in Es | IBECS | ID: ibc-63238

ABSTRACT

Objetivo: La administración oral de soluciones hipertónicaspuede participar en la lesión intestinal en la fase inicial de la enterocolitisnecrotizante neonatal. El objetivo del estudio es determinarla osmolalidad de las fórmulas farmacéuticas orales líquidasutilizadas en una unidad de neonatología y establecer recomendacionesde dilución.Método: Se ha medido la osmolalidad de 26 fórmulas farmacéuticasorales líquidas por el método de descenso crioscópico.Resultados: Las fórmulas farmacéuticas orales líquidas utilizadasen la unidad de neonatología presentan una osmolalidad superiora 350 mOsm/kg H2O. Del total analizado, el 19,2% de las fórmulaspresentaban una osmolalidad inferior a 1.500 mOsm/kgH2O, el 80,7% superior y el 23% presentaban una osmolalidadextremadamente alta (> 5.000 mOsm/kg H2O).Conclusiones: El conocimiento de la osmolalidad de las fórmulasfarmacéuticas orales líquidas administradas en la unidad deneonatología permite valorar el riesgo de agresividad intestinalque produce la administración enteral de la medicación


Objective: Oral administration of hypertonic solutions can contributeto intestinal damage in the initial stages of neonatal necrotizingenterocolitis. The purpose of this study is to determine the osmolalityof oral liquid dosage forms used in a division of neonatologyand to establish some recommendations for their dilution.Method: The osmolality of 26 oral liquid dosage forms hasbeen measured using the freezing-point depression method.Results: Oral liquid dosage forms used in the division ofneonatology present an osmolality greater than 350 mOsm/kgH2O. 19.2% of all the analysed forms presented an osmolalitylower than 1500 mOsm/kg H2O, 80.7% were over that figure,while 23% presented an extremely high osmolality (> 5,000mOsm/kg H2O).Conclusions: Knowledge of osmolality of oral liquid dosageforms in the division of neonatology enables the risk of intestinalaggression caused by enteral administration of the medication tobe assessed


Subject(s)
Humans , Male , Female , Infant, Newborn , Osmolar Concentration , Hypertonic Solutions/analysis , Enterocolitis, Necrotizing/chemically induced , Enterocolitis, Necrotizing/prevention & control , Pharmaceutical Preparations/analysis , Hypertonic Solutions/administration & dosage , Intensive Care Units, Neonatal
15.
An Pediatr (Barc) ; 64(3): 260-6, 2006 Mar.
Article in Spanish | MEDLINE | ID: mdl-16527094

ABSTRACT

The recommendations in this document describe the current indications for inhaled nitric oxide (iNO) treatment in the newborn and clearly distinguish between those supported by scientific evidence and those for which evidence is still lacking, such as its use in preterm infants. The methodology for iNO administration, its dosage and the main secondary effects are discussed, and the reasons for lack of response to this treatment are analyzed.


Subject(s)
Infant, Newborn, Diseases/therapy , Nitric Oxide/administration & dosage , Administration, Inhalation , Endothelium-Dependent Relaxing Factors/administration & dosage , Heart Defects, Congenital , Hernias, Diaphragmatic, Congenital , Humans , Infant, Newborn , Infant, Premature , Persistent Fetal Circulation Syndrome , Respiratory Distress Syndrome, Newborn
16.
An. pediatr. (2003, Ed. impr.) ; 64(3): 260-265, mar. 2006.
Article in Es | IBECS | ID: ibc-045706

ABSTRACT

Las recomendaciones incluidas en este documento señalan las indicaciones actuales del tratamiento con óxido nítrico inhalado (ONi) en el recién nacido, diferenciando claramente las apoyadas en evidencia científica de las que todavía no lo están, como su uso en prematuros. Tras comentar la metodología, dosificación y efectos secundarios, se insiste en las causas de falta de respuesta al ONi


The recommendations in this document describe the current indications for inhaled nitric oxide (iNO) treatment in the newborn and clearly distinguish between those supported by scientific evidence and those for which evidence is still lacking, such as its use in preterm infants. The methodology for iNO administration, its dosage and the main secondary effects are discussed, and the reasons for lack of response to this treatment are analyzed


Subject(s)
Infant, Newborn , Humans , Infant, Newborn, Diseases/therapy , Nitric Oxide/administration & dosage , Administration, Inhalation , Endothelium-Dependent Relaxing Factors/administration & dosage , Heart Defects, Congenital , Hernia, Diaphragmatic/congenital , Infant, Premature , Persistent Fetal Circulation Syndrome , Respiratory Distress Syndrome, Newborn
17.
An Esp Pediatr ; 50(3): 279-84, 1999 Mar.
Article in Spanish | MEDLINE | ID: mdl-10334052

ABSTRACT

OBJECTIVE: We present 12 newborns with acute renal failure (ARF) of different etiologies that were treated with continuous arterio-venous hemofiltration (CAVH). PATIENTS AND METHODS: Gestational age and birth weight ranged from 26-42 weeks and 700-4, 700 grams, respectively. The umbilical artery and vein were most frequently used as vascular accesses. Two types of filters were used: Gambro FH 22 and Amicon Minifilter. RESULTS: Treatment lasted from 8 to 120 hours. We obtained an ultrafiltration median of 25 ml/h ranging from 10.75 mL/h to 82.8 mL/h (4.1-31.8 mL/k/h). The volume balance was negative in all patients. Treatment was well tolerated. Complications included hypotension when the system was started and hypoglycemia. CAVH was stopped because of normalization of renal function in 6 cases and death in the other 6. In the latter, cardiac malformation was the cause of death in 3 cases and multiple organ failure in the other 3. CONCLUSIONS: CAVH is useful is the treatment of ARF in the oligoanuric newborn.


Subject(s)
Acute Kidney Injury/therapy , Hemofiltration , Female , Hemofiltration/instrumentation , Hemofiltration/methods , Humans , Infant, Newborn , Male
18.
An Esp Pediatr ; 49(6): 615-8, 1998 Dec.
Article in Spanish | MEDLINE | ID: mdl-9972625

ABSTRACT

OBJECTIVE: To assess the therapeutic effect of G-CSF in newborns with neutropenia. METHODS: Newborn with evidence of both peripheral neutropenia and decreased granulocytic precursors in tibial bone marrow aspirate were included in the study. G-CSF was perfused intravenously over 2 hours at dose of 10 micrograms/kg/day, during 4-8 days. CBC were obtained immediately before each dose of G-CSF. RESULTS: Neutropenia followed neonatal sepsis in four cases and maternal pre-eclampsia in three. Prior to treatment, peripheral blood granulocyte (PMNL) counts ranged from 420 to 1,073/mm3. Once G-CSF infusion was started, counts returned to normal within 24-48 hours. No adverse effects related to G-CSF administration were noticed. CONCLUSIONS: G-CSF induces a significant increase in peripheral PMNL counts in newborn with neutropenia, in the absence of significant toxic effects. Our date suggest a potential role for G-CSF in the prophylaxis and treatment of sepsis in the neutropenic newborn, although widespread recommendation must await further, controlled studies.


Subject(s)
Granulocyte Colony-Stimulating Factor/administration & dosage , Neutropenia/drug therapy , Combined Modality Therapy , Drug Evaluation , Granulocyte Colony-Stimulating Factor/adverse effects , Humans , Infant, Newborn , Infusions, Intravenous , Leukocyte Count/drug effects , Neutropenia/blood , Neutrophils/cytology , Neutrophils/drug effects , Recombinant Proteins , Time Factors
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