RESUMO
OBJECTIVE: To determine associations between home oxygen use and 1-year readmissions for preterm infants with bronchopulmonary dysplasia (BPD) discharged from regional neonatal intensive care units. STUDY DESIGN: We performed a secondary analysis of the Children's Hospitals Neonatal Database, with readmission data via the Pediatric Hospital Information System and demographics using ZIP-code-linked census data. We included infants born <32 weeks of gestation with BPD, excluding those with anomalies and tracheostomies. Our primary outcome was readmission by 1 year corrected age; secondary outcomes included readmission duration, mortality, and readmission diagnosis-related group codes. A staged multivariable logistic regression was adjusted for center, clinical, and social risk factors; at each stage we included variables associated at P < .1 in bivariable analysis with home oxygen use or readmission. RESULTS: Home oxygen was used in 1906 of 3574 infants (53%) in 22 neonatal intensive care units. Readmission occurred in 34%. Earlier gestational age, male sex, gastrostomy tube, surgical necrotizing enterocolitis, lower median income, nonprivate insurance, and shorter hospital-to-home distance were associated with readmission. Home oxygen was not associated with odds of readmission (OR, 1.2; 95% CI, 0.98-1.56), readmission duration, or mortality. Readmissions for infants with home oxygen were more often coded as BPD (16% vs 4%); readmissions for infants on room air were more often gastrointestinal (29% vs 22%; P < .001). Clinical risk factors explained 72% of center variance in readmission. CONCLUSIONS: Home oxygen use is not associated with readmission for infants with BPD in regional neonatal intensive care units. Center variation in home oxygen use does not impact readmission risk. Nonrespiratory problems are important contributors to readmission risk for infants with BPD.
Assuntos
Displasia Broncopulmonar/epidemiologia , Displasia Broncopulmonar/terapia , Serviços Hospitalares de Assistência Domiciliar/estatística & dados numéricos , Recém-Nascido Prematuro , Oxigenoterapia/estatística & dados numéricos , Readmissão do Paciente/estatística & dados numéricos , Enterocolite Necrosante/epidemiologia , Feminino , Gastrostomia , Idade Gestacional , Humanos , Renda , Recém-Nascido , Seguro Saúde , Unidades de Terapia Intensiva Neonatal , Masculino , Fatores de Risco , Fatores Sexuais , Estados Unidos/epidemiologiaRESUMO
OBJECTIVES: To identify predictors of home oxygen use in preterm infants with bronchopulmonary dysplasia (BPD) in a statewide cohort, identify hospital variation in home oxygen use, and determine the relationship between home oxygen use and neonatal intensive care unit discharge timing. STUDY DESIGN: This was a secondary analysis of California Perinatal Quality Care Collaborative data. Infants were born <32 weeks of gestation, diagnosed with BPD based on respiratory support at 36 weeks postmenstrual age (PMA), and discharged home. Risk factors for home oxygen use were identified using a logistic mixed model with center as random effect. Estimates were used to calculate each center's observed to expected ratio of home oxygen use, and a Spearman coefficient between center median PMA at discharge and observed and expected proportions of home oxygen use. RESULTS: Of 7846, 3672 infants (47%) with BPD were discharged with home oxygen. Higher odds of home oxygen use were seen with antenatal steroids, maternal hypertension, earlier gestational age, male sex, ductus arteriosus ligation, more ventilator days, nitric oxide, discharge from regional hospitals, and PMA at discharge (receiver operating characteristic area under the curve 0.85). Of 92 hospitals, home oxygen use ranged from 7% to 95%; 42% of observed home oxygen use was significantly higher or lower than expected given patient characteristics. The 67 community hospitals with higher observed rates of home oxygen had earlier median PMA at discharge (correlation -0.27, P = .024). CONCLUSIONS: Clinical and hospital factors predict home oxygen use. Home oxygen use varies across California, with community centers using more home oxygen having a shorter length of stay.
Assuntos
Displasia Broncopulmonar/terapia , Utilização de Instalações e Serviços/estatística & dados numéricos , Serviços Hospitalares de Assistência Domiciliar/estatística & dados numéricos , Oxigenoterapia/estatística & dados numéricos , Utilização de Procedimentos e Técnicas/estatística & dados numéricos , California , Estudos de Coortes , Feminino , Humanos , Recém-Nascido , Recém-Nascido Prematuro , MasculinoRESUMO
Objetivo: Analizar la comprensión de las enfermeras acerca de la atención prestada a los recién nacidos en la terapia de oxígeno en la unidad neonatal de cuidados intermedios e intensivos. Método: Se realizó un estudio descriptivo de enfoque cualitativo, realizado con 16 enfermeros de la unidad neonatal de un hospital público de Petrolina / PE, de diciembre 2015 a enero 2016 a través de entrevistas semiestructuradas. Los datos se analizaron utilizando el análisis de contenido temático. Resultados: Las enfermeras entienden lo que se configura como la terapia de oxígeno, sus indicaciones, efectos y posibles complicaciones asociadas, así como los principales cuidados de enfermería cuales deben estar orientados a los recién nacidos en la terapia con oxígeno suplementario. Conclusión: La calificación y la capacidad de la enfermera que atiende al recién nacido en el uso de la terapia de oxígeno en la unidad neonatal, es esencial para garantizar una atención segura, la identificación precoz de los signos de la adversidad y la prevención de posibles complicaciones
Objective: To analyze nurses' understanding of the care given to newborns in oxygen therapy in the Intermediate and Intensive Neonatal Care Unit. Method: This is a descriptive, qualitative study conducted with 16 nurses from the Neonatal Unit of a public hospital in Petrolina/PE, from December 2015 to January 2016, through a semi-structured interview. Data were analyzed through thematic content analysis. Results: Nurses understand what constitutes oxygen therapy, its indications, purposes and possible associated complications, as well as the main nursing care that should be directed to the newborns in therapy with supplemental oxygen. Conclusion: The qualification and the ability of the nurse to assist the newborn in the use of oxygen therapy, within the Neonatal Unit, is essential in guaranteeing a safe care, in the early identification of signs of adversity and in the prevention of possible complications
Objetivo: Analisar a compreensão do enfermeiro sobre a assistência prestada ao recém-nascido em oxigenoterapia na Unidade de Cuidados Neonatais Intermediários e Intensivos. Método: Trata-se de estudo descritivo, de abordagem qualitativa, realizado com 16 enfermeiros da Unidade Neonatal de um hospital público de Petrolina/PE, de dezembro de 2015 a janeiro de 2016, por meio de entrevista semiestruturada. Os dados foram analisados mediante análise de conteúdo temática. Resultados: Os enfermeiros compreendem o que se configura como oxigenoterapia, suas indicações, finalidades e possíveis complicações associadas, bem como os principais cuidados de enfermagem que devem ser direcionados aos recém-nascidos em terapia com oxigênio suplementar. Conclusão: A qualificação e a habilidade do enfermeiro que assiste ao recém-nascido em uso de oxigenoterapia, dentro da Unidade Neonatal, é imprescindível na garantia de uma assistência segura, na identificação precoce dos sinais de adversidade e na prevenção de possíveis complicações
Assuntos
Humanos , Masculino , Feminino , Recém-Nascido , Adulto , Pessoa de Meia-Idade , Oxigenoterapia/enfermagem , Unidades de Terapia Intensiva Neonatal , Enfermagem Neonatal , Oxigenoterapia/estatística & dados numéricos , Enfermeiras e EnfermeirosRESUMO
CONTEXT: Down syndrome (DS) is the most common chromosomal condition in live-born infants worldwide, and lower respiratory infection caused by respiratory syncytial virus (RSV) is a leading cause of hospital admissions. OBJECTIVE: To evaluate RSV-associated morbidity among children with DS compared with a population without DS. DATA SOURCES: Four electronic databases were searched. STUDY SELECTION: All cohorts or case-control studies of DS with an assessment of RSV infection and the associated morbidity or mortality were included without language restriction. DATA EXTRACTION: Two reviewers independently reviewed all studies. The primary outcomes were hospital admission and mortality. Secondary outcomes included length of hospital stay, oxygen requirement, ICU admission, need for respiratory support, and additional medication use. RESULTS: Twelve studies (n = 1 149 171) from 10 different countries met the inclusion criteria; 10 studies were cohort studies, 1 study was retrospective, and 1 study had both designs. DS was associated with a higher risk of hospitalization (odds ratio [OR]: 8.69; 95% confidence interval [CI]: 7.33-10.30; I2 = 11%) and mortality (OR: 9.4; 95% CI: 2.26-39.15; I2 = 38%) compared with what was seen in controls. Children with DS had an increased length of hospital stay (mean difference: 4.73 days; 95% CI: 2.12-7.33; I2 = 0%), oxygen requirement (OR: 6.53; 95% CI: 2.22-19.19; I2 = 0%), ICU admission (OR: 2.56; 95% CI: 1.17-5.59; I2 = 0%), need for mechanical ventilation (OR: 2.56; 95% CI: 1.17-5.59; I2 = 0%), and additional medication use (OR: 2.65 [95% CI: 1.38-5.08; I2 = 0%] for systemic corticosteroids and OR: 5.82 [95% CI: 2.66-12.69; I2 = 0%] for antibiotics) than controls. LIMITATIONS: DS subgroups with and without other additional risk factors were not reported in all of the included studies. CONCLUSIONS: Children with DS had a significantly higher risk of severe RSV infection than children without DS.
Assuntos
Síndrome de Down/complicações , Infecções por Vírus Respiratório Sincicial/epidemiologia , Adolescente , Criança , Pré-Escolar , Hospitalização/estatística & dados numéricos , Humanos , Lactente , Unidades de Terapia Intensiva/estatística & dados numéricos , Tempo de Internação/estatística & dados numéricos , Oxigenoterapia/estatística & dados numéricos , Respiração Artificial/estatística & dados numéricos , Infecções por Vírus Respiratório Sincicial/etiologia , Infecções por Vírus Respiratório Sincicial/mortalidade , Fatores de RiscoRESUMO
OBJECTIVE: To compare the neuropsychomotor development in the first year of life of premature infants with and without bronchopulmonary dysplasia. METHODS: A cross-sectional retrospective study was conducted between January 1, 2014, and December 30, 2015, with premature infants weighing < 1,500g at birth and diagnosed with bronchopulmonary dysplasia at the corrected ages of 6 and 9 months, assessed using the DENVER II Developmental Screening Test. Quantitative variables were described as the means, medians and standard deviations. Variables with normal distribution were tested using Student's t test; otherwise, the Mann-Whitney test was used, considering significance at p-value < 0.05. Qualitative variables were expressed as frequencies and percentages. Logistic regression was used with odds ratio analysis to evaluate the effects of other variables as risk factors for changes in neuropsychomotor development. RESULTS: Infants with bronchopulmonary dysplasia showed greater developmental delay compared with those without bronchopulmonary dysplasia (p-value = 0.001). The factors associated with a higher incidence of changes in neuropsychomotor development, in addition to bronchopulmonary dysplasia, were antenatal steroid, gender, birth weight, 5-minute Apgar score, Score for Neonatal Acute Physiology-Perinatal Extension, duration of oxygen therapy, duration of mechanical ventilation and length of hospital stay. Other variables may also have influenced the result, such as drug use by mothers of infants with bronchopulmonary dysplasia. CONCLUSION: Bronchopulmonary dysplasia associated with other pre- and postnatal factors may be considered a risk factor for delayed neuropsychomotor development in the first year of life in premature infants born weighing less than 1,500g.
OBJETIVO: Comparar o desenvolvimento neuropsicomotor de lactentes nascidos prematuramente, com e sem displasia broncopulmonar, no primeiro ano de vida. MÉTODOS: Estudo retrospectivo, do tipo transversal, realizado no período de 1º de janeiro de 2014 a 30 de dezembro de 2015, com lactentes prematuros, com peso < 1.500g ao nascer e diagnóstico de displasia broncopulmonar, na idade corrigida de 6 e 9 meses, avaliados pelo Teste de Triagem do Desenvolvimento DENVER II. As variáveis quantitativas foram descritas em médias, medianas e desvio padrão. Para as variáveis que apresentaram distribuição normal, aplicou-se o teste t de Student; do contrário, foi aplicado o teste de Mann-Whitney, considerando significância o valor de p < 0,05. As variáveis qualitativas foram descritas em frequências e porcentagens. Utilizou-se a regressão logística com análise da razão de chances para avaliar os efeitos das outras variáveis, como fatores de risco para alterações no desenvolvimento neuropsicomotor. RESULTADOS: Os lactentes com displasia broncopulmonar apresentaram maior atraso no desenvolvimento neuropsicomotor quando comparados àqueles sem displasia broncopulmonar (p = 0,001). Os fatores associados com maior incidência para alterações no desenvolvimento neuropsicomotor, além da displasia broncopulmonar, foram: esteroide antenatal, sexo, peso ao nascimento, escore de Apgar no quinto minuto, Score for Neonatal Acute Physiology with Perinatal Extension, tempo de oxigenoterapia, ventilação mecânica e internação. Outras variáveis também podem ter influenciado o resultado, como uso de drogas pelas mães dos lactentes com displasia broncopulmonar. CONCLUSÃO: A displasia broncopulmonar associada a outros fatores pré e pós-natais pode ser considerada fator de risco para o atraso do desenvolvimento neuropsicomotor em lactentes nascidos prematuramente e com peso inferior a 1.500g, no primeiro ano de vida.
Assuntos
Displasia Broncopulmonar/complicações , Deficiências do Desenvolvimento/epidemiologia , Recém-Nascido Prematuro , Desempenho Psicomotor/fisiologia , Adulto , Displasia Broncopulmonar/fisiopatologia , Estudos de Casos e Controles , Estudos Transversais , Deficiências do Desenvolvimento/etiologia , Feminino , Humanos , Incidência , Lactente , Recém-Nascido , Recém-Nascido de muito Baixo Peso , Tempo de Internação , Modelos Logísticos , Masculino , Oxigenoterapia/estatística & dados numéricos , Gravidez , Respiração Artificial/estatística & dados numéricos , Estudos Retrospectivos , Fatores de Risco , Adulto JovemRESUMO
OBJECTIVE: To compare respiratory compliance in late preterm infants (340/7-346/7 weeks) who received antenatal steroids vs matched late preterm infants who did not receive antenatal steroids. STUDY DESIGN: This was a single-center prospective cohort study. Patients were matched for birth weight, gestational age, race, and sex. Respiratory compliance was the primary outcome measured with the single breath occlusion technique. RESULTS: We studied 25 late preterm infants treated with antenatal steroids and 25 matched infants who did not receive antenatal steroids. The treated infants had a significantly increased respiratory compliance/kg (adjusted 95% CI 0.05, 0.49; P = .016) and fewer required continuous positive airway pressure (P = .007) or >24 hours of supplemental oxygen (P = .046). There was no difference in surfactant therapy. CONCLUSIONS: Respiratory compliance was significantly increased in this cohort of late preterm infants born at 340/7-346/7 weeks who received antenatal steroids compared with matched infants who did not receive antenatal steroids. Although not randomized, these data provide physiologic support for the possible beneficial effects of antenatal steroids in late preterm infants.
Assuntos
Betametasona/uso terapêutico , Terapias Fetais , Glucocorticoides/uso terapêutico , Recém-Nascido Prematuro , Complacência Pulmonar , Adulto , Estudos de Casos e Controles , Estudos de Coortes , Pressão Positiva Contínua nas Vias Aéreas/estatística & dados numéricos , Feminino , Idade Gestacional , Humanos , Recém-Nascido , Masculino , Oxigenoterapia/estatística & dados numéricos , Gravidez , Cuidado Pré-Natal , Surfactantes Pulmonares/uso terapêutico , Síndrome do Desconforto Respiratório do Recém-Nascido/prevenção & controle , Testes de Função RespiratóriaRESUMO
Durante el invierno las infecciones respiratorias agudas bajas (IRAB) determinan un incremento en la demanda asistencial, afectando sobre todo a los niños más pequeños. El objetivo de la investigación fue describir las características clínicas, modalidades de tratamiento y evolución de los menores de 2 años hospitalizados en el Hospital Pediátrico-Centro Hospitalario Pereira Rossell por IRAB de etiología viral durante el invierno de 2014. Se realizó un estudio descriptivo, retrospectivo, describiendo las características de los menores de 2 años hospitalizados del 9/6 al 21/9/2014 por IRAB de probable etiología viral. Se describieron las características epidemiológicas y clínicas, el tratamiento realizado y la evolución de los pacientes. En el período evaluado egresaron 742 niños (34% de los egresos de la institución). Tenían una mediana de edad de 4 meses; 18% presentaba al menos un factor de riesgo de IRAB grave. Se identificó al virus respiratorio sincicial en 59,6%. La estadía hospitalaria tuvo una mediana de 4 días. En las salas de cuidados moderados se aplicó ventilación no invasiva a 46 niños, y oxigenación de alto flujo a 129 niños, logrando una mejoría clínica en el 87,0% y el 87,6% respectivamente. Ingresaron a unidades de cuidados intensivos 217 niños, 54% requirió asistencia ventilatoria mecánica. Dos pacientes fallecieron. En el período evaluado los niños pequeños con IRAB representaron una importante proporción de los egresos, con importante carga asistencial. La mayoría eran niños sin factores de riesgo. La aplicación de las técnicas de tratamiento en cuidados moderados fue efectiva, permitiendo disminuir la demanda de camas de cuidados intensivos.
During the winter, low acute respiratory infections (LARI) determine an increase in care demand, especially affecting younger children. The objective of the research was to describe the clinical characteristics, treatment modalities and evolution of children under 2 years of age hospitalized at the Hospital Pediátrico-Centro Hospitalario Pereira Rossell for viral etiology LARI during the 2014 winter. A descriptive, retrospective study was conducted, describing the characteristics of children under 2 years hospitalized between 9/6 and 9/21/2014 for LARI of probable viral etiology. The following features were described: epidemiological and clinical characteristics, treatment performed and patient's evolution. During the period evaluated, 742 children were discharged (34% of the institution's admissions). They had a median age of 4 months; 18% had at least one risk factor for severe LARI. Respiratory syncytial virus was identified in 59.6%. The hospital stay had a median of 4 days. In moderate care rooms noninvasive ventilation was applied to 46 children, and high flow oxygenation to 129 children, achieving clinical improvement in 87.0% and 87.6%, respectively. Two hundred and seventeen children were admitted 54% required mechanical ventilation. Two patients died. In the evaluated period small children with LARI represented a significant proportion of the discharges, with an important burden of care. The majority were children without risk factors. The application of treatment techniques in moderate care was effective, allowed a decrease in the demand for intensive care beds.
Durante o inverno, as infecções respiratórias agudas baixas (IRAB) determinam o aumento da demanda de cuidados, afetando especialmente as crianças menores. O objetivo da pesquisa foi descrever as características clínicas, as modalidades de tratamento e a evolução de crianças menores de dois anos hospitalizados no Hospital Pediátrico-Centro Hospitalario Pereira Rossell devido a IRAB de etiologia viral, durante o inverno de 2014. Foi realizado um estudo descritivo e retrospectivo, descrevendo as características das crianças menores de 2 anos hospitalizadas entre 9/6 e 21/9/2014 devido a IRAB de provável etiologia viral. Descreveram-se: características epidemiológicas e clínicas, tratamento realizado e evolução dos pacientes. Durante o período avaliado, 742 crianças foram hospitalizadas (34% dos ingressos da instituição). Tinham uma idade média de 4 meses; 18% tinham pelo menos um fator de risco para IRAB severa. O vírus sincicial respiratório foi identificado em 59,6%. A estadia hospitalaria teve uma mediana de 4 dias. Em salas de cuidados moderados, a ventilação não invasiva foi aplicada a 46 crianças e a oxigenação de alto fluxo a 129 crianças, atingindo melhora clínica em 87,0% e 87,6%, respectivamente. Foram internadas em unidades de terapia intensiva 217 crianças, 54% necessitaram de ventilação mecânica. Dois pacientes faleceram. No período avaliado, as crianças pequenas com IRAB representaram uma proporção significativa das despesas, com um carga importante de atendimento. A maioria carecia de fatores de risco. A aplicação de técnicas de tratamento em cuidados moderados foi eficaz, permitindo uma diminuição da demanda por leitos de terapia intensiva.
Assuntos
Humanos , Masculino , Feminino , Recém-Nascido , Lactente , Pré-Escolar , Oxigenoterapia/estatística & dados numéricos , Infecções Respiratórias/diagnóstico , Infecções Respiratórias/terapia , Ventilação de Alta Frequência/estatística & dados numéricos , Infecções por Vírus Respiratório Sincicial/diagnóstico , Ventilação não Invasiva/estatística & dados numéricos , Infecções Respiratórias/etiologia , Infecções Respiratórias/mortalidade , Criança Hospitalizada/estatística & dados numéricos , Doença Aguda , Epidemiologia Descritiva , Estudos Retrospectivos , Fatores de Risco , Infecções por Vírus Respiratório Sincicial/complicações , Clima Frio/efeitos adversos , Distribuição por IdadeRESUMO
RESUMO Objetivo: Comparar o desenvolvimento neuropsicomotor de lactentes nascidos prematuramente, com e sem displasia broncopulmonar, no primeiro ano de vida. Métodos: Estudo retrospectivo, do tipo transversal, realizado no período de 1º de janeiro de 2014 a 30 de dezembro de 2015, com lactentes prematuros, com peso < 1.500g ao nascer e diagnóstico de displasia broncopulmonar, na idade corrigida de 6 e 9 meses, avaliados pelo Teste de Triagem do Desenvolvimento DENVER II. As variáveis quantitativas foram descritas em médias, medianas e desvio padrão. Para as variáveis que apresentaram distribuição normal, aplicou-se o teste t de Student; do contrário, foi aplicado o teste de Mann-Whitney, considerando significância o valor de p < 0,05. As variáveis qualitativas foram descritas em frequências e porcentagens. Utilizou-se a regressão logística com análise da razão de chances para avaliar os efeitos das outras variáveis, como fatores de risco para alterações no desenvolvimento neuropsicomotor. Resultados: Os lactentes com displasia broncopulmonar apresentaram maior atraso no desenvolvimento neuropsicomotor quando comparados àqueles sem displasia broncopulmonar (p = 0,001). Os fatores associados com maior incidência para alterações no desenvolvimento neuropsicomotor, além da displasia broncopulmonar, foram: esteroide antenatal, sexo, peso ao nascimento, escore de Apgar no quinto minuto, Score for Neonatal Acute Physiology with Perinatal Extension, tempo de oxigenoterapia, ventilação mecânica e internação. Outras variáveis também podem ter influenciado o resultado, como uso de drogas pelas mães dos lactentes com displasia broncopulmonar. Conclusão: A displasia broncopulmonar associada a outros fatores pré e pós-natais pode ser considerada fator de risco para o atraso do desenvolvimento neuropsicomotor em lactentes nascidos prematuramente e com peso inferior a 1.500g, no primeiro ano de vida.
ABSTRACT Objective: To compare the neuropsychomotor development in the first year of life of premature infants with and without bronchopulmonary dysplasia. Methods: A cross-sectional retrospective study was conducted between January 1, 2014, and December 30, 2015, with premature infants weighing < 1,500g at birth and diagnosed with bronchopulmonary dysplasia at the corrected ages of 6 and 9 months, assessed using the DENVER II Developmental Screening Test. Quantitative variables were described as the means, medians and standard deviations. Variables with normal distribution were tested using Student's t test; otherwise, the Mann-Whitney test was used, considering significance at p-value < 0.05. Qualitative variables were expressed as frequencies and percentages. Logistic regression was used with odds ratio analysis to evaluate the effects of other variables as risk factors for changes in neuropsychomotor development. Results: Infants with bronchopulmonary dysplasia showed greater developmental delay compared with those without bronchopulmonary dysplasia (p-value = 0.001). The factors associated with a higher incidence of changes in neuropsychomotor development, in addition to bronchopulmonary dysplasia, were antenatal steroid, gender, birth weight, 5-minute Apgar score, Score for Neonatal Acute Physiology-Perinatal Extension, duration of oxygen therapy, duration of mechanical ventilation and length of hospital stay. Other variables may also have influenced the result, such as drug use by mothers of infants with bronchopulmonary dysplasia. Conclusion: Bronchopulmonary dysplasia associated with other pre- and postnatal factors may be considered a risk factor for delayed neuropsychomotor development in the first year of life in premature infants born weighing less than 1,500g.
Assuntos
Humanos , Masculino , Feminino , Gravidez , Recém-Nascido , Lactente , Adulto , Adulto Jovem , Desempenho Psicomotor/fisiologia , Displasia Broncopulmonar/complicações , Recém-Nascido Prematuro , Deficiências do Desenvolvimento/epidemiologia , Oxigenoterapia/estatística & dados numéricos , Respiração Artificial/estatística & dados numéricos , Displasia Broncopulmonar/fisiopatologia , Estudos de Casos e Controles , Modelos Logísticos , Deficiências do Desenvolvimento/etiologia , Incidência , Estudos Transversais , Estudos Retrospectivos , Fatores de Risco , Recém-Nascido de muito Baixo Peso , Tempo de InternaçãoRESUMO
Resumen: Introducción: las infecciones respiratorias agudas bajas (IRAB) constituyen un importante problema de salud en invierno. El centro de referencia nacional en Uruguay ofrece a niños con IRAB ventilación no invasiva (VNI) y cánula nasal de alto flujo (CNAF) en cuidados moderados. Objetivo: describir las características clínicas, tratamiento y evolución de los niños asistidos en la Unidad de Cuidados Respiratorios Especiales Agudos (CREA) del Hospital Pediátrico de referencia nacional. Material y método: estudio retrospectivo, descriptivo. Se incluyeron todos los niños hospitalizados por IRAB asistidos en CREA que recibieron VNI y/o CNAF entre 1/1/13 y 31/12/16. Se revisaron historias clínicas. Variables: características clínicas, tratamientos, complicaciones, evolución y destino. Resultados: se asistieron 650 niños (348 con CNAF; 302 con VNI); sexo masculino 63% (407). Bronquiolitis 63% (406), se detectó virus respiratorio sincicial (VRS) en 60% (388). Media de edad en niños que recibieron CNAF 11 meses (9 días-108 meses); promedio duración de la técnica: 3 días. Requirieron ingreso a unidades de cuidados intensivos (UCI): 12% (43); asistencia ventilatoria mecánica (AVM): 6% (22). Media de edad en niños que recibieron VNI :12 meses (1-132 meses); media de duración de la técnica: 3 días. Requirieron ingreso a UCI 16% (49); AVM: 9,6% (29). No se registraron fallecimientos ni complicaciones graves. Conclusiones: el 85% de los niños completó su tratamiento en la Unidad CREA. El porcentaje de niños que requirió AVM fue bajo. La implementación de estas técnicas en cuidados moderados redujo la necesidad de ingreso a UCI y probablemente la necesidad de AVM.
Summary: Introduction: acute lower respiratory tract infections (LRTI) are a major health problem in winter. The National Reference Center in Uruguay offers children with LRTI, non-invasive ventilation (NIV) and high-flow nasal cannula (CNAF) in moderate care. Objective: to describe the clinical characteristics, treatment and evolution of the children assisted in Special Respiratory Care Acute (CREA unit), in a national pediatric reference hospital. Patients and methods: retrospective, descriptive study. All children hospitalized for LRTI assisted in CREA who received NIV and / or CNAF between 1/1/13 and 12/31/16 were included in the study. Clinical records were reviewed. Variables: clinical characteristics, treatment, complications, evolution and destination. Results: a total of 650 children were assisted (348 with CNAF, 302 with NIV); male sex 63% (407). Bronchiolitis 63% (406), Respiratory Syncytial Virus (RSV) was detected in 60% (388). Mean age in children receiving CNAF was 11 months (9 days - 108 months); mean duration of technique was 3 days. Required admission to intensive care unit (ICU): 12% (43); invasive ventilation (IV) 6% (22). Mean age in children receiving NIV 12 months (1-132 months); mean duration of technique 3 days. Required admission to the ICU 49 (16%); IV 29 (9.6%). There were no deaths or serious complications. Conclusions: 85% of this group of children completed their treatment in the CREA unit. The percentage of children who required IV was low. The implementation of these techniques in moderate care reduced the need to enter an ICU and the need for IV.
Resumo: Introdução: as infecções respiratórias agudas baixas (IRAB) são um importante problema de saúde no inverno. O centro de referência nacional no Uruguai oferece ventilação não invasiva (NIV) e cânula nasal de alto fluxo (CNAF) em cuidados moderados às crianças com IRAB. Objetivo: descrever as características clínicas, tratamento e evolução das crianças atendidas na Unidade Especial de Tratamento Respiratório Agudo (CREA) do Hospital de Referência Nacional de Pediatria. Pacientes e métodos: estudo retrospectivo, descritivo. No estudo foram incluídas todas as crianças hospitalizadas por causa da IRAB atendidas no CREA que receberam VNI e / ou CNAF entre 1/1/13 e 31/12/16. Foram revisadas as histórias clínicas. Variáveis: características clínicas, tratamentos, complicações, evolução e destino. Resultados: 650 crianças foram atendidas (348 com CNAF, 302 com NIV); sexo masculino 63% (407). Bronquiolite 63% (406), o Vírus Respiratório Sincicial (VRS) foi detectado em 60% (388). Idade média em crianças que receberam CNAF: 11 meses (9 dias-108 meses); Duração média da técnica: 3 dias. Necessidade para admissão nas unidades de terapia intensiva (UTI): 12% (43); assistência ventilatória mecânica (MAV) 6% (22). Idade média em crianças que receberam VNI: 12 meses (1-132 meses); duração média da técnica: 3 dias. Deveram ser admitidos na UTI: 16% (49); AVM 9,6% (29). Nenhuma morte ou complicações sérias foram registradas. Conclusões: 85% das crianças completaram o tratamento na unidade CREA. A porcentagem de crianças que necessitaram de AVM foi baixa. A implementação dessas técnicas em cuidados moderados reduziu a necessidade de internação na UTI e, provavelmente, a necessidade de MAV.
Assuntos
Humanos , Masculino , Oxigenoterapia/estatística & dados numéricos , Infecções Respiratórias/terapia , Ventilação de Alta Frequência/estatística & dados numéricos , Ventilação não Invasiva/estatística & dados numéricos , Infecções Respiratórias/diagnóstico , Infecções Respiratórias/etiologia , Uruguai , Unidades de Terapia Intensiva Pediátrica , Criança Hospitalizada , Epidemiologia Descritiva , Estudos RetrospectivosRESUMO
OBJECTIVES: To describe the frequency and extent of delivery room resuscitation and evaluate the association of delivery room resuscitation with neonatal outcomes in moderately preterm (MPT) infants. STUDY DESIGN: This was an observational cohort study of MPT infants delivered at 290/7 to 336/7 weeks' gestational age (GA) enrolled in the Neonatal Research Network MPT registry. Infants were categorized into 5 groups based on the highest level of delivery room intervention: routine care, oxygen and/or continuous positive airway pressure, bag and mask ventilation, endotracheal intubation, and cardiopulmonary resuscitation including chest compressions and/or epinephrine use. The association of antepartum and intrapartum risk factors and discharge outcomes with the intensity of resuscitation was evaluated. RESULTS: Of 7014 included infants, 1684 (24.0%) received routine care and no additional resuscitation, 2279 (32.5%) received oxygen or continuous positive airway pressure, 1831 (26.1%) received bag and mask ventilation, 1034 (14.7%) underwent endotracheal intubation, and 186 (2.7%) received cardiopulmonary resuscitation. Among the antepartum and intrapartum factors, increasing GA, any exposure to antenatal steroids and prolonged rupture of membranes decreased the likelihood of receipt of all levels of resuscitation. Infants who were small for GA (SGA) had increased risk of delivery room resuscitation. Among the neonatal outcomes, respiratory support at 28 days, days to full oral feeds and length of stay were significantly associated with the intensity of delivery room resuscitation. Higher intensity of resuscitation was associated with increased risk of mortality. CONCLUSIONS: The majority of MPT infants receive some level of delivery room resuscitation. Increased intensity of delivery room interventions was associated with prolonged respiratory and nutritional support, increased mortality, and a longer length of stay.
Assuntos
Reanimação Cardiopulmonar/estatística & dados numéricos , Pressão Positiva Contínua nas Vias Aéreas/estatística & dados numéricos , Intubação Intratraqueal/estatística & dados numéricos , Oxigenoterapia/estatística & dados numéricos , Salas de Parto , Feminino , Humanos , Recém-Nascido , Recém-Nascido Prematuro , Recém-Nascido Pequeno para a Idade Gestacional , Masculino , Avaliação de Resultados em Cuidados de Saúde , Estudos Prospectivos , Sistema de Registros , Fatores de RiscoRESUMO
BACKGROUND: Noninvasive ventilation (NIV) has proven to be useful in the management of children with acute respiratory failure as a result of acute lower respiratory infection. Despite this, evidence addressing the initiation and/or discontinuation criteria of NIV in children remains limited. The objective of this study was to evaluate the usefulness and clinical impact of an NIV protocol in hospitalized children with acute respiratory failure because of acute lower respiratory infection. METHODS: A randomized controlled clinical trial was carried out among subjects admitted during the winter season at Hospital Josefina Martinez between May and October of 2013. Inclusion criteria were age 3 months to 2 y, diagnosis of acute lower respiratory infection and requiring NIV according to a Modified Wood Scale score of ≥ 4 points. Subjects were randomized to NIV management according to medical criteria (control group) or to protocolized management of NIV (protocol group). Hours of NIV, hospital stay, and supplemental oxygen use after discontinuation of NIV, severity changes after NIV initiation, respiratory symptoms, and proportion of intubations were considered as events of interest. RESULTS: A total of 23 subjects were analyzed in the control group and 24 were analyzed in the protocol group. Hours of hospital stay, NIV, and supplemental oxygen post-NIV were not significantly different between groups (P = .70, .69, and .68, respectively). There were also no differences in intubation rate (3 of 29 for the control group and 2 of 31 for the protocol group). For the total sample there was a statistically significant decrease in the Modified Wood Scale score after 1 h of NIV (P < .001). A similar result was observed when performing a stratified intragroup analysis. CONCLUSIONS: We observed that the implementation of an NIV management protocol that integrates initiation and discontinuation criteria for NIV is feasible. However, its use showed no advantages over a non-protocolized strategy.
Assuntos
Protocolos Clínicos , Ventilação não Invasiva/métodos , Insuficiência Respiratória/terapia , Infecções Respiratórias/complicações , Doença Aguda , Criança , Feminino , Humanos , Intubação/estatística & dados numéricos , Tempo de Internação/estatística & dados numéricos , Masculino , Oxigenoterapia/estatística & dados numéricos , Insuficiência Respiratória/microbiologia , Resultado do TratamentoRESUMO
Importance: Perioperative lung-protective ventilation has been recommended to reduce pulmonary complications after cardiac surgery. The protective role of a small tidal volume (VT) has been established, whereas the added protection afforded by alveolar recruiting strategies remains controversial. Objective: To determine whether an intensive alveolar recruitment strategy could reduce postoperative pulmonary complications, when added to a protective ventilation with small VT. Design, Setting, and Participants: Randomized clinical trial of patients with hypoxemia after cardiac surgery at a single ICU in Brazil (December 2011-2014). Interventions: Intensive recruitment strategy (n=157) or moderate recruitment strategy (n=163) plus protective ventilation with small VT. Main Outcomes and Measures: Severity of postoperative pulmonary complications computed until hospital discharge, analyzed with a common odds ratio (OR) to detect ordinal shift in distribution of pulmonary complication severity score (0-to-5 scale, 0, no complications; 5, death). Prespecified secondary outcomes were length of stay in the ICU and hospital, incidence of barotrauma, and hospital mortality. Results: All 320 patients (median age, 62 years; IQR, 56-69 years; 125 women [39%]) completed the trial. The intensive recruitment strategy group had a mean 1.8 (95% CI, 1.7 to 2.0) and a median 1.7 (IQR, 1.0-2.0) pulmonary complications score vs 2.1 (95% CI, 2.0-2.3) and 2.0 (IQR, 1.5-3.0) for the moderate strategy group. Overall, the distribution of primary outcome scores shifted consistently in favor of the intensive strategy, with a common OR for lower scores of 1.86 (95% CI, 1.22 to 2.83; P = .003). The mean hospital stay for the moderate group was 12.4 days vs 10.9 days in the intensive group (absolute difference, -1.5 days; 95% CI, -3.1 to -0.3; P = .04). The mean ICU stay for the moderate group was 4.8 days vs 3.8 days for the intensive group (absolute difference, -1.0 days; 95% CI, -1.6 to -0.2; P = .01). Hospital mortality (2.5% in the intensive group vs 4.9% in the moderate group; absolute difference, -2.4%, 95% CI, -7.1% to 2.2%) and barotrauma incidence (0% in the intensive group vs 0.6% in the moderate group; absolute difference, -0.6%; 95% CI, -1.8% to 0.6%; P = .51) did not differ significantly between groups. Conclusions and Relevance: Among patients with hypoxemia after cardiac surgery, the use of an intensive vs a moderate alveolar recruitment strategy resulted in less severe pulmonary complications while in the hospital. Trial Registration: clinicaltrials.gov Identifier: NCT01502332.
Assuntos
Procedimentos Cirúrgicos Cardíacos/efeitos adversos , Hipóxia/terapia , Oxigenoterapia/métodos , Complicações Pós-Operatórias/terapia , Alvéolos Pulmonares/fisiologia , Respiração Artificial/métodos , Índice de Gravidade de Doença , Idoso , Barotrauma/epidemiologia , Pressão Sanguínea/fisiologia , Cuidados Críticos/estatística & dados numéricos , Feminino , Frequência Cardíaca/fisiologia , Mortalidade Hospitalar , Humanos , Hipóxia/etiologia , Incidência , Tempo de Internação , Pneumopatias/prevenção & controle , Masculino , Pessoa de Meia-Idade , Razão de Chances , Oxigenoterapia/estatística & dados numéricos , Pressão Parcial , Respiração com Pressão Positiva/métodos , Complicações Pós-Operatórias/prevenção & controle , Volume de Ventilação PulmonarRESUMO
OBJECTIVE: Retrospective studies have shown home oxygen to be a safe alternative to hospitalization for some patients with bronchiolitis living at high altitudes. We aimed to prospectively describe adverse events, follow-up, duration of home oxygen, factors associated with failure, and caregiver preferences. METHODS: This was a prospective observational study of hypoxemic bronchiolitis patients ages 3 to 18 months who were discharged from a tertiary care pediatric emergency department on home oxygen over three winters (2011-2014). Caregivers were contacted on postdischarge days ~3, 7, 14, and 28 while on oxygen. Caregivers not reached by phone were sent a survey and their primary care physicians were contacted. Records of admitted subjects were reviewed. Outcome measures included hospital readmission, positive pressure ventilation (noninvasive or intubation), outpatient follow-up, duration of home oxygen therapy, and caregiver satisfaction. RESULTS: A total of 274 patients were enrolled. Forty-eight (17.5%) were admitted and 225 (82.1%) were discharged on oxygen. The median age was 8 months. Eighteen subjects were lost to follow-up. A total of 196 (87.1%) were successfully treated with outpatient oxygen, and 11 (4.9%) failed outpatient therapy and were hospitalized. Only one hospitalized patient required invasive ventilation. The median duration of home oxygen was 7 days. Child noncompliance was the most common problem (reported by 14%). The median caregiver comfort level with home oxygen was 9 of 10. Eighty-eight percent of caregivers would again choose home oxygen over admission. CONCLUSIONS: This study confirms that outpatient oxygen therapy can reduce hospitalizations due to bronchiolitis in a relatively high-altitude setting, with low failure and complication rates. Caregivers are comfortable with home oxygen and prefer it to hospitalization.
Assuntos
Bronquiolite/terapia , Cuidadores/psicologia , Serviço Hospitalar de Emergência/estatística & dados numéricos , Oxigenoterapia/estatística & dados numéricos , Assistência Ambulatorial/estatística & dados numéricos , Feminino , Seguimentos , Humanos , Lactente , Masculino , Oxigenoterapia/psicologia , Cooperação do Paciente/estatística & dados numéricos , Alta do Paciente/estatística & dados numéricos , Readmissão do Paciente/estatística & dados numéricos , Estudos Prospectivos , Resultado do TratamentoRESUMO
El oxígeno (O2) es una de las drogas más utilizadas en clínica, su uso no está exento de riesgos. Existen guias internacionales para su uso, pero en nuestro medio no sabemos si se aplican. Nuestro objetivo fue describir la forma en que se utiliza y controla la oxígenoterapia en los 3 hospitales de la red del Servicio de Salud Talcahuano. Aplicamos una encuesta un día de agosto de 2016 a los pacientes hospitalizados en las instituciones de la red que recibían O2 en ese momento. Se recolectaron datos sobre la prescripción, administración y seguimiento de la terapia de O2. De los 381 pacientes auditados, un 13,7% recibía oxígenoterapia. Los diagnósticos más frecuentes fueron de causa respiratoria (46,15%) y cardiológica (25%). La indicación la dio un médico en 88,5% de los casos y en un 3,8% no había registro. En un 17,3% de los pacientes no había fundamento para la indicación. Se indicó una dosis fija en el 75% con una meta de SaO2 en el 50%, siendo naricera y máscara de Venturi los métodos de administración más frecuentes monitorizándose con oximetría de pulso en los hospitales menos complejos y gasometría arterial en el hospital terciario. La duración media de la oxígenoterapia fue de 7,8 días. Habiendo un buen fundamento y control de la oxígenoterapia aún no se indican metas a obtener. No hay un buen registro de la indicación ni de los cambios realizados. Creemos útil la realización periódica de este tipo de control para optimizar su uso evitando los potenciales efectos adversos en los pacientes.
Abstract Oxygen is a commonly used drug in clinics and its use must be judicious. There are guidelines for oxygen therapy but we ignore if these are respected in our country. We conducted an audit of oxygen therapy by applying a survey to 381 patients in the three hospitals of Talcahuano Public Health Service. The day of the audit 13.7% of the hospitalized patients were on oxygen, most of them with respiratory (46.15%) or cardiovascular (25%) diseases. Indication of O2 administration was given by a physician in 88.5% and there was not registry in 3.8% of the cases. There was not foundation for supplying O2 in 13.3% of patients. A fixed dose was indicated in 75% of cases and 50% had an oximetry value as a target. Oxygen was administered in most of the cases by nasal prongs and Venturi masks. Monitoring was based on pulse oximetry in the less complex hospitals and on arterial blood gases in the tertiary hospital. 100% of patients at urgency ward were receiving a different dose from that indicated at their admission time and none of them had a registry of the new dose. Mean duration of therapy was 7.8 days. We believe our results might represent what is going on with oxygen therapy in our country; having a good foundation and monitoring, we still don t use targets and there is a bad system of registry. We think that it would be advisably to carry out audits on oxygen therapy at national level on regular basis.
Assuntos
Humanos , Masculino , Feminino , Adulto , Pessoa de Meia-Idade , Idoso , Idoso de 80 Anos ou mais , Adulto Jovem , Oxigenoterapia/métodos , Auditoria Clínica/métodos , Serviços de Saúde , Oxigenoterapia/estatística & dados numéricos , Chile , Inquéritos e Questionários , Monitorização FisiológicaRESUMO
ABSTRACT INTRODUCTION: The currently common musculoskeletal disorders have been increasingly treated surgically, and the pain can be a limiting factor in postoperative rehabilitation. RATIONALE: Patient controlled analgesia (PCA) controls pain, but its adverse effects can interfere with rehabilitation and in the patient discharge process. This study becomes important, since there are few studies evaluating this correlation. OBJECTIVES: To compare the outcomes of patients who used and did not use patient controlled analgesia in postoperative orthopedic surgery with respect to pain, unscheduled need for O2 (oxygen), and time of immobility and in-hospital length of stay. METHODS: This is an observational, prospective study conducted at Hospital Abreu Sodré from May to August 2012. The data was daily obtained through assessments and interviews of patients undergoing total hip arthroplasty (THA) and total knee arthroplasty (TKA), thoracolumbar spine arthrodesis (long PVA), cervical spine arthrodesis (cervical AVA) and lumbar spine arthrodesis (lumbar PVA). RESULTS: The study showed some differences between groups, namely: the painful level was higher in the group undergoing lumbar PVA without PCA compared with the group with PCA (p = 0.03) and in the group of long PVA without PCA in the early postoperative period. This latter group used O2 for a longer time (p = 0.09). CONCLUSION: In this study, PCA was useful for analgesia in patients undergoing lumbar PVA and probably would have influenced the usage time of O2 in the group of long PVA in face of a larger sample. The use of PCA did not influence the time of leaving the bed and the in-hospital length of stay for the patients studied.
RESUMO INTRODUÇÃO: As disfunções musculoesqueléticas, comuns atualmente, têm sido cada vez mais tratadas cirurgicamente e a dor é pode ser um fator limitante na reabilitação pós-operatória. JUSTIFICATIVA: A analgesia controlada pelo paciente (PCA) controla a dor, porém seus efeitos adversos podem interferir no processo de reabilitação e alta dos pacientes. Esta pesquisa torna-se importante, pois poucos estudos avaliam essa correlação. OBJETIVOS: Comparar a evolução dos pacientes que usaram e não usaram PCA no pós-operatório de cirurgias ortopédicas em relação à dor, à necessidade de O2 (oxigênio) não programada e ao tempo de imobilização e internação hospitalar. MÉTODOS: Estudo observacional, prospectivo, feito no Hospital da AACD de maio a agosto de 2012. Obtiveram-se dados diários por meio de avaliação e entrevista dos pacientes submetidos à artroplastia total de quadril (ATQ) e joelho (ATJ), artrodese de coluna toracolombar (AVP longa), coluna cervical (AVA cervical) e coluna lombar (AVP lombar). RESULTADOS: O estudo evidenciou algumas diferenças entre os grupos: o nível álgico foi maior no grupo submetido à AVP lombar sem PCA em relação ao com PCA (p = 0,03) e no grupo de AVP longa sem PCA no primeiro pós-operatório. Nesse último grupo, houve uso de O2 por mais tempo (p = 0,09). CONCLUSÃO: Neste estudo, a PCA mostrou-se útil para analgesia em pacientes submetidos à AVP lombar e provavelmente teria influência no tempo de uso de O2 no grupo de AVP longa caso a amostra fosse maior. O uso da PCA não influenciou no tempo de saída do leito e de internação hospitalar nos pacientes estudados.
Assuntos
Humanos , Masculino , Feminino , Dor Pós-Operatória/tratamento farmacológico , Analgesia Controlada pelo Paciente/estatística & dados numéricos , Procedimentos Ortopédicos , Manejo da Dor/métodos , Oxigenoterapia/estatística & dados numéricos , Fatores de Tempo , Estudos Prospectivos , Recuperação de Função Fisiológica , Tempo de Internação/estatística & dados numéricos , Pessoa de Meia-IdadeRESUMO
INTRODUCTION: The currently common musculoskeletal disorders have been increasingly treated surgically, and the pain can be a limiting factor in postoperative rehabilitation. RATIONALE: Patient controlled analgesia (PCA) controls pain, but its adverse effects can interfere with rehabilitation and in the patient discharge process. This study becomes important, since there are few studies evaluating this correlation. OBJECTIVES: To compare the outcomes of patients who used and did not use patient controlled analgesia in postoperative orthopedic surgery with respect to pain, unscheduled need for O2 (oxygen), and time of immobility and in-hospital length of stay. METHODS: This is an observational, prospective study conducted at Hospital Abreu Sodré from May to August 2012. The data was daily obtained through assessments and interviews of patients undergoing total hip arthroplasty (THA) and total knee arthroplasty (TKA), thoracolumbar spine arthrodesis (long PVA), cervical spine arthrodesis (cervical AVA) and lumbar spine arthrodesis (lumbar PVA). RESULTS: The study showed some differences between groups, namely: the painful level was higher in the group undergoing lumbar PVA without PCA compared with the group with PCA (p=0.03) and in the group of long PVA without PCA in the early postoperative period. This latter group used O2 for a longer time (p=0.09). CONCLUSION: In this study, PCA was useful for analgesia in patients undergoing lumbar PVA and probably would have influenced the usage time of O2 in the group of long PVA in face of a larger sample. The use of PCA did not influence the time of leaving the bed and the in-hospital length of stay for the patients studied.
Assuntos
Analgesia Controlada pelo Paciente/estatística & dados numéricos , Procedimentos Ortopédicos , Manejo da Dor/métodos , Dor Pós-Operatória/tratamento farmacológico , Feminino , Humanos , Tempo de Internação/estatística & dados numéricos , Masculino , Pessoa de Meia-Idade , Oxigenoterapia/estatística & dados numéricos , Estudos Prospectivos , Recuperação de Função Fisiológica , Fatores de TempoRESUMO
INTRODUCTION: The Community-Acquired Pneumonia Organization (CAPO) is an international observational study in 130 hospitals, with a total of 31 countries, to assess the current management of hospitalized patients with community-acquired pneumonia (CAP). 2 Using the centralized database of CAPO was decided to conduct this study with the aim of evaluate the level of adherence with national guidelines in Venezuela, to define in which areas an intervention may be necessary to improve the quality of care of hospitalized patients with CAP. METHODS: In this observational retrospective study quality indicators were used to evaluate the management of hospitalized patients with CAP in 8 Venezuelan's centers. The care of the patients was evaluated in the areas of: hospitalization, oxygen therapy, empiric antibiotic therapy, switch therapy, etiological studies, blood cultures indication, and prevention. The compliance was rated as good (>90%), intermediate (60% to 90%), or low (<60%). RESULTS: A total of 454 patients with CAP were enrolled. The empiric treatment administered within 8 hours of the patient arrival to the hospital was good (96%), but the rest of the indicators showed a low level of adherence (<60%). CONCLUSION: We can say that there are many areas in the management of CAP in Venezuela that are not performed according to the national guidelines of SOVETHORAX.1 In any quality improvement process the first step is to evaluate the difference between what is recommended and what is done in clinical practice. While this study meets this first step, the challenge for the future is to implement the processes necessary to improve the management of CAP in Venezuela.
Assuntos
Infecções Comunitárias Adquiridas/terapia , Fidelidade a Diretrizes , Administração Oral , Adulto , Idoso , Antibacterianos/administração & dosagem , Antibacterianos/uso terapêutico , Sangue/microbiologia , Infecções Comunitárias Adquiridas/sangue , Infecções Comunitárias Adquiridas/tratamento farmacológico , Infecções Comunitárias Adquiridas/etiologia , Infecções Comunitárias Adquiridas/prevenção & controle , Substituição de Medicamentos , Uso de Medicamentos , Feminino , Hospitalização/estatística & dados numéricos , Humanos , Infusões Intravenosas , Pacientes Internados , Masculino , Pessoa de Meia-Idade , Oxigenoterapia/estatística & dados numéricos , Educação de Pacientes como Assunto , Indicadores de Qualidade em Assistência à Saúde , Estudos Retrospectivos , Abandono do Hábito de Fumar , VenezuelaRESUMO
BACKGROUND: Surgical burden is a large and neglected global health problem in low- and middle-income countries. With the increasing trauma burden, the goal of this study was to evaluate the trauma capacity of hospitals in the central plateau of Haiti. MATERIALS AND METHODS: The World Health Organization Emergency and Essential Surgical Care survey was adapted with a focus on trauma capacity. Interviewers along with translators administered the survey to key hospital staff. RESULTS: Seven hospitals in the region were surveyed. Of the hospitals surveyed, 3/7 had functioning surgical facilities. None of the hospitals had trauma registries. 71% of the hospitals had no formal trauma guidelines. 2/7 hospitals had a general surgeon available 100% of the time. All surgical facilities had oxygen cylinders available 100% of the time, but three of the primary level hospitals only had it available 51%-90% of the time. Intubation equipment was available at 57% of the facilities. Ventilators were only available in the operating room. Only the largest hospital had a computed tomography scanner. Other hospitals (66%) had a functioning x-ray machine 76%-90% of the time. Hospitals (57%) had an ultrasound machine. The most common reasons for referral were lack of appropriate facilities and supplies at the primary level care centers or lack of trained personnel at higher-level facilities. CONCLUSIONS: Trauma capacity in the central plateau of Haiti is limited. There is a great need for more personnel, trauma training at all staff levels, emergency care guidelines, trauma registries, and imaging equipment and training, specifically in ultrasonography. To accomplish this, coordination is needed between the Haitian government and local and international nongovernmental organizations.
Assuntos
Países em Desenvolvimento/estatística & dados numéricos , Número de Leitos em Hospital/estatística & dados numéricos , Respiração Artificial/estatística & dados numéricos , Centro Cirúrgico Hospitalar/estatística & dados numéricos , Centros de Traumatologia/estatística & dados numéricos , Estudos Transversais , Equipamentos e Provisões Hospitalares/estatística & dados numéricos , Saúde Global/estatística & dados numéricos , Haiti/epidemiologia , Pesquisas sobre Atenção à Saúde , Humanos , Oxigenoterapia/estatística & dados numéricos , Atenção Primária à Saúde/organização & administração , Atenção Primária à Saúde/estatística & dados numéricos , Centros de Cuidados de Saúde Secundários/estatística & dados numéricos , Centro Cirúrgico Hospitalar/organização & administração , Centros de Atenção Terciária/organização & administração , Centros de Atenção Terciária/estatística & dados numéricos , Tomografia Computadorizada por Raios X/estatística & dados numéricos , Centros de Traumatologia/organização & administração , Ultrassonografia/estatística & dados numéricosRESUMO
INTRODUCTION: Respiratory syncytial virus (RSV) is one of the leading causes of acute lower respiratory infection (ALRI) in infants and young children. Although ALRI is a major public health problem in developing countries located in tropical areas, studies about RSV epidemiology in these regions are scarce. METHODS: In a retrospective cohort study, we investigated the epidemiology and predictive variables that reflect disease severity and mortality in young children hospitalized with ALRI due to RSV in Colombia, South-America, during a 2-year period (2009-2011). RESULTS: Of a total of 6,344 children with a diagnosis of ALRI, we selected 2,147 (33.8%) that were positive for RSV. After controlling for pre-existing conditions, we found that independent predictors of severe disease in our population included age <6 months (RR 2.01; CI 95% 1.70-2.38; P < 0.001), prematurity (RR 1.61; CI 95% 1.20-2.17; P = 0.001), congenital heart disease (RR 2.03; CI 95% 1.16-3.54; P = 0.013), and mixed RSV-adenovirus infection (RR 2.09; CI 95% 1.60-2.73; P < 0.001). Multivariate analysis identified that cancer (RR 31.60; CI 95% 5.97-167.13; P < 0.001) is a predictor of mortality in our RSV-infected pediatric population independently of age and other co-morbidities. CONCLUSIONS: RSV is an important cause of ALRI in infants and young children living in tropical regions, especially during the rainy season. The identified predictors of severe disease and mortality should be taken into account when planning interventions to reduce the burden of ALRI in young children living in these regions.
Assuntos
Bronquiolite Viral/mortalidade , Infecções por Vírus Respiratório Sincicial/mortalidade , Infecções por Adenoviridae/epidemiologia , Fatores Etários , Bronquiolite Viral/epidemiologia , Bronquiolite Viral/fisiopatologia , Pré-Escolar , Estudos de Coortes , Coinfecção/epidemiologia , Colômbia/epidemiologia , Cardiopatias Congênitas/epidemiologia , Humanos , Lactente , Recém-Nascido , Recém-Nascido Prematuro , Unidades de Terapia Intensiva Pediátrica/estatística & dados numéricos , Nefropatias/epidemiologia , Análise Multivariada , Neoplasias/epidemiologia , Oxigenoterapia/estatística & dados numéricos , Análise de Regressão , Infecções por Vírus Respiratório Sincicial/epidemiologia , Infecções por Vírus Respiratório Sincicial/fisiopatologia , Estudos Retrospectivos , Fatores de Risco , Estações do Ano , Índice de Gravidade de DoençaRESUMO
OBJECTIVE: To examine the functional outcomes of children who underwent a tracheostomy in the initial hospitalization after birth and to determine their correlates. STUDY DESIGN: We administered the validated 43-item Functional Status-II (FS-II) questionnaire by Stein and Jessop over the telephone to caregivers of surviving children. The FS-II items generated a total score, age-specific: (1) total; (2) general health (GH); and (3) responsiveness, activity, or interpersonal functioning (IPF) scores in specific age group categories. RESULTS: FS-II was administered to 51/62 (82.2%) survivors at a median (range) age of 5 (1-10) years; 27% children were on the ventilator and 43% required devices. About 40% of children had a median of 1 (1-4) hospitalization in the previous 6 months. Scores were >2 SD below means in 55%, 24%, and 55% cases for age-specific T, GH, and R/A/IPF scores respectively. The T and R/A/IPF scales were significantly higher in those with private, rather than public, maternal insurance, as were T and R/A/IPF scores for children ≥ 4 years, compared with younger children. On regression analysis, FS-II T, GH, and R/A/IPF scores were independently associated with maternal private insurance (P = .02). R/A/IPF scores were also significantly associated with corrected age at FS-II administration. CONCLUSIONS: One-third of surviving children who underwent tracheostomy during their initial hospitalization remained technology-dependent. The parental FS-II questionnaires revealed low R/A/IPF scores, especially at younger ages and in those with maternal public insurance. Further research on family-level interventions to improve functional outcomes in this population is warranted.