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1.
Arch. argent. pediatr ; 119(3): 162-169, Junio 2021. tab, ilus
Artigo em Inglês, Espanhol | LILACS, BINACIS | ID: biblio-1222431

RESUMO

Introducción. Existe poca evidencia de la influencia de variables emocionales en la lactancia de madres de recién nacidos de muy bajo peso al nacer (RNMBPN). El objetivo de este estudio fue medir la producción de leche materna (PLM) en dos momentos de la internación neonatal y su asociación con los niveles de ansiedad, depresión y autoeficacia en lactancia en madres de RNMBPN.Población y métodos. Estudio prospectivo, observacional, multicéntrico en madres de RNMBPN (500-1500 g), en 9 centros de la Red NEOCOSUR. La PLM se obtuvo midiendo lo extraído por cada madre. Se utilizaron las escalas STAI para ansiedad, BDI para depresión, y, la escala piloto ALMA para autoeficacia. Estas fueron aplicadas a los 14 días de vida y a las 36 semanas posmenstruales. Se registraron, además, las características biosociales de madres y neonatos. Resultados. Participaron 118 madres. La PLM media a los 14 días fue de 169 ml (desvío estándar ­DE­ ± 132,4) y de 285 ml (DE ± 266,9) a las 36 semanas, y se asoció significativamente con percepción de autoeficacia en lactancia (p < 0,001), que se mantuvo durante la hospitalización. Existió una tendencia a menor producción en madres con mayores índices de depresión a los 14 días de vida de su hijo, pero no a las 36 semanas. No se encontró asociación entre PLM y ansiedad. No se encontraron asociaciones consistentemente significativas con variables biosociales. Conclusión. La PLM se asoció positivamente con autoeficacia en lactancia; no se encontró asociación con ansiedad y depresión en madres de RNMBPN


Introduction. There is little evidence regarding the influence of emotional variables on breastfeeding among mothers of very low birth weight infants (VLBWIs). The objective of this study was to measure breast milk production (BMP) at two points in time during neonatal hospitalization and its association with anxiety, depression, and breastfeeding self-efficacy levels among mothers of VLBWIs.Population and methods. Prospective, observational, and multicenter study in mothers of VLBWIs (500-1500 g) from 9 NEOCOSUR Network centers. BMP was obtained by measuring the amount extracted by each mother. The STAI scale was used for anxiety, the BDI scale for depression, and the ALMA pilot scale for self-efficacy. They were administered at 14 days of life and at 36 weeks of postmenstrual age. The biosocial characteristics of mothers and neonates were also recorded.Results. A total of 118 mothers participated. Mean BMP was 169 mL (standard deviation [SD]: ± 132.4) at 14 days and 285 mL (SD: ± 266.9) at 36 weeks, and it was significantly associated with the perception of breastfeeding self-efficacy (p < 0.001), which was maintained during hospitalization. There was a lower production trend among mothers with higher depression indices at 14 days of life, but not at 36 weeks. No association was observed between BMP and anxiety. No consistently significant associations were observed with biosocial variables.Conclusion. BMP was positively associated with breastfeeding self-efficacy; no association was observed with anxiety and depression among mothers of VLBWIs


Assuntos
Humanos , Feminino , Recém-Nascido , Adulto , Aleitamento Materno , Ansiedade , Estudos Prospectivos , Recém-Nascido de muito Baixo Peso , Autoeficácia , Depressão , Mães
2.
Rev. méd. Chile ; 147(5): 612-617, mayo 2019. tab, graf
Artigo em Inglês | LILACS | ID: biblio-1043156

RESUMO

ABSTRACT Background: The Health Assessment Questionnaire Disability Index (HAQDI) is one of the main instruments used to evaluate functional status in rheumatoid arthritis (RA). Aim: To assess the reliability and validity of the Spanish version of HAQDI in Chilean RA population. Materials and Methods: The questionnaire was applied to 98 patients with RA aged 44 ± 12 years (90% women). Reliability was assessed using Cronbach's alpha statistic for internal consistency. Construct validity was assessed by comparing total HAQDI value and eight HAQDI domains with multiple parameters of disease activity. Discriminant validity was evaluated by classifying disease activity in low, medium or high and evaluating HAQDI value in each category. Floor and ceiling effects were evaluated. To assess construct validity, principal components analysis was performed using varimax rotation. Results: There were no issues in the comprehensibility of the questionnaire. Mean HAQDI score was 1.57 ± 0.66. Standardized Cronbach's Alpha was 0.883. Correlations between Chilean HAQ domains had a p value less than 0.001, and values ranged from 0.317 to 0.597. Activity parameters, DAS 28 and CDAI were significantly correlated with HAQDI domains. Mean HAQDI values were 0.98 ± 0.59,1.45 ± 0.57, and 1.90 ± 0.56 for mild, moderate and severe disease activity. A principal components analysis identified two factors that accounted for 70.0% of total variability. Conclusions: This study shows that the Spanish version of HAQDI is reliable and valid and can be used in Chilean patients with RA.


Antecedentes: El Health Assessment Questionnaire Disability Index es uno de los principales instrumentos utilizados para evaluar incapacidad funcional en la artritis reumatoide (AR). Objetivo: Evaluar la fiabilidad y validez del HAQDI en la población chilena con AR. Material y Método: El cuestionario fue respondido por 98 pacientes con AR de 44 ± 12 años de edad (90% mujeres). La confiabilidad se evaluó usando la estadística alfa de Cronbach. La validez de constructo se evaluó comparando el valor total de HAQDI y de cada uno de sus dominios con múltiples parámetros de actividad de la enfermedad. La validez discriminante se evaluó clasificando la actividad de la enfermedad en bajo, medio o alto y evaluando el valor de HAQDI en cada categoría. Se determinaron efectos de piso y techo. Se realizó un análisis factorial utilizando rotación de varimax. Resultados: El valor promedio del HAQDI fue de 1,57 ± 0.66. El alfa estandarizado de Cronbach fue 0,883. Las correlaciones entre dominios de HAQDI tuvieron un valor p < 0,001 con valores entre 0,317 y 0,597. Los parámetros de actividad se correlacionaron significativamente con los dominios HAQDI. Se encontraron diferencias significativas entre el puntaje de HAQDI en relación con los grados de actividad de la enfermedad. Los valores medios de HAQDI fueron 0,98 ± 0,59, 1,45 ± 0,57 y 1,90 ± 0,56 para actividad leve, moderada y severa, respectivamente. El análisis de componentes principales identificó dos factores que representaron el 70.0% de la variabilidad total. Conclusiones: La versión española de HAQDI es confiable y válida en pacientes chilenos con AR.


Assuntos
Humanos , Masculino , Feminino , Adulto , Pessoa de Meia-Idade , Artrite Reumatoide/fisiopatologia , Inquéritos e Questionários/normas , Avaliação da Deficiência , Valores de Referência , Índice de Gravidade de Doença , Chile , Reprodutibilidade dos Testes , Estatísticas não Paramétricas , Idioma
3.
Rev. chil. pediatr ; 90(1): 36-43, 2019. tab
Artigo em Espanhol | LILACS | ID: biblio-990884

RESUMO

INTRODUCCIÓN: Múltiples factores influyen en el riesgo de morbimortalidad del prematuro con restricción del crecimiento intrauterino (RCIU). La comparación de gemelos con crecimiento intrauterino discordante permite evaluar su efecto, excluyendo factores maternos y manejo prenatal. Nuestro objetivo fue evaluar el efecto de la RCIU sobre la morbilidad aguda, crónica y mortalidad, en parejas de recién nacidos gemelares prematuros extremos. PACIENTES Y MÉTODO: Gemelos menores de 1500 g y 30 semanas de gestación, de la Red Neocosur. Se realizaron análisis separados de pares de gemelos concordantes, discordantes leves y severos, evaluando el efecto de la RCIU sobre morbi-mortalidad. Se realizó análisis multivariado para establecer magnitud del efecto. RESULTADOS: 459 pares de gemelos, 227 concordantes, 110 discordantes leves y 122 severos. Entre los concordantes solo hubo diferencia en uso de oxígeno a las 36 semanas. En discordantes leves, el menor tuvo menos enfermedad de membrana hialina y requirió menos dosis de surfactante, pero tuvo un mayor riesgo de Displasia broncopulmonar (DBP) o muerte. En discordantes severos, el menor presentó mayor mortalidad, sepsis, utilización y permanencia en ventilación mecánica, pese a menor frecuencia de enfermedad de membrana hialina. En regresión múltiple, el riesgo combinado de DBP o muerte fue mayor en gemelo menor y discordante severo. CONCLUSIÓN: En gemelos discordantes, la patología respiratoria aguda fue más frecuente en el gemelo mayor, aunque el riesgo de DBP o muerte fue mayor en el gemelo con RCIU.


INTRODUCTION: Multiple factors influence the risk of morbidity and mortality of premature infants with intrauterine growth restriction (IUGR). The comparison of twins with different intrauterine growth allows evaluating the effect of the restriction, excluding maternal factors and prenatal mana gement. Our objective was to assess the effect of IUGR on acute and chronic morbidity, and mortality of extreme preterm twins. PATIENTS AND METHOD: Twins weighing less than 1500 grams and gesta tion equal to or less than 30 weeks, of the Neocosur Network. Separate analyses were performed on concordant twin pairs, and on mild and severe discordant twins, evaluating the effect of IUGR on morbidity and mortality. A multivariate analysis was performed in order to establish the impact of this effect. RESULTS: 459 twin pairs, 227 concordant twins, 110 of mild discordance, and 122 of severe discordance. Among the concordant ones, there was only a difference in oxygen uptake at 36 weeks. In those of mild discordance, the smaller twin presented a lower frequency of hyaline membrane disease and required fewer doses of surfactant, but had a higher risk of bronchopulmonary dysplasia (BPD) or death. In severe discordant twins, the smaller one presented higher mortality, sepsis, use and permanence in mechanical ventilation, despite the lower frequency of hyaline membrane disease. In multiple regression analysis, the combined risk of BPD or death was higher in the smaller twin and of severe discordance. CONCLUSION: In discordant twins, the acute respiratory pathology was more frequent in the larger one, although the risk of BPD or death was higher in the one with IUGR.


Assuntos
Humanos , Masculino , Feminino , Recém-Nascido , Displasia Broncopulmonar/etiologia , Doenças em Gêmeos/etiologia , Retardo do Crescimento Fetal/fisiopatologia , Sepse Neonatal/etiologia , Prognóstico , Displasia Broncopulmonar/diagnóstico , Displasia Broncopulmonar/mortalidade , Recém-Nascido Prematuro , Estudos de Casos e Controles , Modelos Logísticos , Estudos Retrospectivos , Fatores de Risco , Recém-Nascido de muito Baixo Peso , Doenças em Gêmeos/diagnóstico , Doenças em Gêmeos/mortalidade , Sepse Neonatal/diagnóstico , Sepse Neonatal/mortalidade
4.
Arch. argent. pediatr ; 113(4): 303-309, ago. 2015. graf, tab
Artigo em Inglês, Espanhol | LILACS, BINACIS | ID: lil-757041

RESUMO

Introducción. El nacimiento de un hijo prematuro es un evento estresante para sus padres. El objetivo de este estudio fue determinar el estrés inicial de padres de recién nacidos de muy bajo peso de nacimiento (RNMBPN) hospitalizados en 12 unidades de cuidados intensivos neonatales en una red neonatal sudamericana, identificar los factores asociados y comparar el nivel de estrés parental en centros públicos vs. privados. Población y métodos. Estudio transversal en madres/padres de RNMBPN (de 500 a 1500 g). El estrés parental inicial se midió utilizando la Escala de Estrés Parental en una escala de 1 (bajo estrés) a 5 (alto estrés). Las características sociodemográficas de las madres/padres y de los neonatos fueron recolectadas y asociadas a los niveles de estrés parental. Resultados. Participaron del estudio 273 padres / madres de un total de 218 RNMBPN. La encuesta fue aplicada en el 5,9 ± 2,0 días de vida del recién nacido. El estrés parental total promedio fue de 3,1 ± 0,8, y la subescala rol parental fue aquella que puntuó más alto (3,6). Tener un menor nivel educacional, estar desempleado, no haber tomado al recién nacido en brazos y el requerimiento de apoyo ventilatorio se asociaron a mayor estrés parental. El estrés fue mayor en madres que en padres y en centros públicos que en privados. Conclusiones. En padres de RNMBPN, se encontró un estrés inicial moderado. El factor más relevante fue la alteración en su rol parental. El estrés parental fue mayor en las madres y en los centros públicos. Se requiere una mayor sensibilización, investigación e intervención en esta área.


Introduction. The birth of a premature baby is a stressful event for parents. The objective of this study was to determine early stress in parents of very low birth weight infants (VLBWIs) hospitalized in 12 neonatal intensive care units from a South American Neonatal Network, to identify associated factors, and to compare the level of parental stress in public versus private healthcare facilities. Population and Methods. Cross-sectional study in mothers/fathers of VLBWIs (500 to 1500 g). Early parental stress was measured using the Parental Stressor Scale, with a score from 1 (low stress) to 5 (high stress). The sociodemographic characteristics of parents and newborn infants were collected and associated with levels of parental stress. Results. The study included273 fathers/mothers of a total of218 VLBW preterm infants. The survey was administered at 5.9 ± 2.0 days of life. The average total parental stress was 3.1 ± 0.8, and the highest score was obtained for the parental role subscale (3.6). A lower education level, unemployment, not having held the newborn infant, and respiratory support requirement were associated with higher parental stress levels. Stress was higher among mothers than fathers, and at public facilities versus private ones. Conclusions. Among parents of VLBWIs, a moderate early parental stress was observed. Parental role alteration was the most relevant factor. Parental stress was higher among mothers and at public healthcare facilities. A greater sensitization, further research and interventions in this area are required.


Assuntos
Humanos , Recém-Nascido , Adulto , Pais/psicologia , Estresse Psicológico , Estudos Transversais , Recém-Nascido de muito Baixo Peso , Hospitalização , Unidades de Terapia Intensiva
5.
Arch. argent. pediatr ; 112(5): 405-412, oct. 2014. tab, ilus
Artigo em Inglês, Espanhol | LILACS, BINACIS | ID: biblio-1159638

RESUMO

Objetivo. Analizar la supervivencia y morbilidad relevante según edad gestacional (EG) en recién nacidos de muy bajo peso de nacimiento (RNMBPN) o < 1500 g y, con estos resultados, confeccionar una cartilla para proporcionar información a profesionales de la salud perinatal y padres de prematuros de muy bajo peso. Diseño del estudio. Se utilizaron los datos recogidos prospectivamente de los recién nacidos con peso al nacer de 500 a 1500 g ingresados a 45 centros participantes de la Red Neonatal Neocosur entre enero de 2001 y diciembre de 2011. Resultados. Se analizaron los datos de 8234 RNMBPN con EG entre 24 +0 y 31 +6 semanas. La mortalidad global fue 26% (IC 95% 25,0-26,9), que incluye 2,6% que falleció en sala de partos. Las cartillas de supervivencia y morbilidad para cada semana de gestación se construyeron a partir de los datos obtenidos. La supervivencia al momento del alta aumentó de 29% a las 24 semanas de EG a 91% a las 31 semanas (p < 0,001). La incidencia de morbilidad neonatal relevante se relacionó inversamente con la EG (p < 0,001). Globalmente, 30,8% presentó retinopatía del prematuro; 25%, displasia broncopulmonar; 10,9%, enterocolitis necrotizante; 7,2%, hemorragia intraventricular grave; y 4,6%, leucomalacia periventricular. De los sobrevivientes, 47,3% no presentó ninguna de estas 5 patologías. Conclusiones. Se desarrolló un instrumento de utilidad clínica, con datos regionales actualizados, que determina semana a semana la supervivencia y morbilidad de los RN que nacen entre las 24 +0 y las 31 +6 semanas de EG. Esta información puede emplearse en la toma de decisiones perinatales y en la información parental.


Objective. To analyze survival and relevant morbidity by gestational age (GA) in very low birth weight (VLBW) infants (<1500 g) and, based on these data, develop a fact sheet to provide information to perinatal healthcare providers and very low birth weight preterm infants ́parents. Study Design. Data were prospectively collected in relation to newborn infants with a birth weight between 500 g and 1500 g admitted to 45 sites of the Neocosur Neonatal Network (Red Neonatal Neocosur) between January 2001 and December 2011. Results. Data on 8234 VLBW with a GA between 24 +0 and 31 +6 weeks were analyzed. Overall mortality was 26% (95% CI: 25.0-26.9), including 2.6% of deaths in the delivery room. Fact sheets for survival and morbidity for each week of gestation were developed based on collected data. Survival at discharge increased from 29% at 24 weeks of GA to 91% at 31 weeks of GA (p < 0.001). The incidence of relevant neonatal morbidity was inversely related to GA (p < 0.001). Overall, 30.8% had retinopathy of prematurity, 25% bronchopulmonary dysplasia, 10.9% necrotizing enterocolitis, 7.2% severe intraventricular hemorrhage, and 4.6% periventricular leukomalacia. Among survivors, 47.3% had none of these five conditions. Conclusions. A tool for use in a clinical setting was developed based on updated regional data for establishing week-to-week survival and morbidity of newborn infants born between 24 +0 and 31 +6 weeks of GA. This information could be used to make decisions related to perinatal care and for counseling parents.


Assuntos
Humanos , Masculino , Feminino , Recém-Nascido , Doenças do Recém-Nascido/mortalidade , América do Sul , Taxa de Sobrevida , Estudos Retrospectivos , Estudos de Coortes , Idade Gestacional , Recém-Nascido de muito Baixo Peso
6.
Rev. méd. Chile ; 142(5): 574-578, mayo 2014. ilus, tab
Artigo em Espanhol | LILACS | ID: lil-720665

RESUMO

Background: Waist-to-height ratio (WHtR) is a cardiometabolic risk indicator in children. A value greater than or equal to 0.55 is an effective screening tool for identifying obese children with metabolic syndrome. However, it is unclear whether this cutoff can be applied equally to any age or gender. Aim: To analyze the variability of WHtR by age, gender and pubertal stage in elementary school children. Patients and Methods: Cross-sectional study in 2,980 school children (6-14 years old, 51% male) of Santiago, Chile. We measured weight, height and waist circumference and calculated body mass index and WHtR. Pubertal stage was assessed and classified as peripubertal (Tanner I and II) and pubertal (Tanner III, IV and V). Results: The mean age was 9.9 ± 2.3 years, with no gender difference (p = 0.5). Eighty one percent of boys and 59.4% of girls were peripubertal (p < 0.001). The association between age-adjusted WHtR by gender and pubertal stage was not significant (p = 0.409). Therefore mean, standard deviation and percentiles of WHtR were calculated without sex and pubertal stage segmentations. Conclusions: Since WHtR does not vary with age, gender and pubertal status in elementary school children, it is possible to use a single cutoff value, previously defined in this population, to identify children with cardiometabolic risk.


Assuntos
Adolescente , Criança , Feminino , Humanos , Masculino , Obesidade/fisiopatologia , Razão Cintura-Estatura , Fatores Etários , Chile , Estudos Transversais , Obesidade/diagnóstico , Puberdade/fisiologia , Valores de Referência , Fatores Sexuais , Fatores Socioeconômicos
7.
Rev. méd. Chile ; 141(1): 95-103, ene. 2013. ilus, tab
Artigo em Espanhol | LILACS | ID: lil-674051

RESUMO

Background: The determination ofthyroid stimulating hormone (TSH) reference values is critical for the diagnosis ofthyroid diseases. Aim: To explore and discuss different definitions to establish TSH reference values using a Chilean national survey sample. Material and Methods: The 2009-2010 Chilean National Health Survey recruited 5,416participants between the ages of 15 and 96years, from all geographic regions of Chile, including urban and rural zones. TSH was measured in a random subsample of 2,785 adults. Median value, 2.5 and 97.5 percentiles were described in three different populations: total survey population, "disease-free population" and the "laboratory kit disease free population". Results: TSH values were higher among women, the elderly and the less educated population. The 97.5 percentile value in the disease-free population was 7.46 uUl/ml. Using this value as a cut-off, hypothyroidism prevalence would be 4.8% in Chile and estimated pharmacological treatment coverage would be 58%. When laboratory kit cut-offs are used, prevalence rises to 22% and treatment coverage drops to 12%. The 2.5 percentile value in the disease-free population was 0.83 uUl/ml, which yields an estimated hyperthyroidism prevalence of3.89%. Conclusions: Median TSH concentration values in the Chilean "disease-free population" are higher than those proposed by laboratory kits and those of developed countries. TSH values in the general population of Chile are also higher in women, the elderly and the less educated population.


Assuntos
Adolescente , Adulto , Idoso , Idoso de 80 Anos ou mais , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Adulto Jovem , Inquéritos Epidemiológicos/estatística & dados numéricos , Doenças da Glândula Tireoide/diagnóstico , Tireotropina/sangue , Chile/epidemiologia , Inquéritos Epidemiológicos/métodos , Valores de Referência , Doenças da Glândula Tireoide/epidemiologia
8.
Rev. méd. Chile ; 140(10): 1268-1275, oct. 2012. graf, tab
Artigo em Espanhol | LILACS | ID: lil-668699

RESUMO

Background: Cardiovascular risk factors must be controlled since childhood. Aim: To assess the association of carotid intima media thickness (CIMT) with the components of the metabolic syndrome in Children. Material and Methods: Cross sectional assessment of 299 children aged 11.5 ± 0.9years (58% women) with and without metabolic syndrome components. Anthropometric parameters and blood pressure were measured and a blood sample was obtained to measure blood glucose and lipids. CIMT was measured using high resolution ultrasound. Results: Ninety three percent of children were post puberal, 64% were overweight and 25% had metabolic syndrome. Mean and maximum CIMT correlated with systolic blood pressure (r = 0.21 and 0.21 respectively p < 0.01). Children with a CIMTover the 75th percentile had higher blood pressure and lower HDL cholesterol. A stepwise logistic regression accepted both variables as predictors of CIMT with odds ratios for mean CIMT of 1.46 (1.19-1-79) and 0.81 (0.7-0.94) perfive units of change, respectively. Conclusions: In this group of children systolic blood pressure and HDL cholesterol are associated to CIMT.


Assuntos
Adolescente , Criança , Feminino , Humanos , Masculino , Pressão Sanguínea , Doenças Cardiovasculares/etiologia , Espessura Intima-Media Carotídea , HDL-Colesterol/sangue , Síndrome Metabólica/complicações , Chile/epidemiologia , Estudos Transversais , Obesidade/complicações , Obesidade/epidemiologia , Razão de Chances , Fatores de Risco , Sístole
9.
Rev. méd. Chile ; 139(11): 1435-1443, nov. 2011. ilus
Artigo em Espanhol | LILACS | ID: lil-627573

RESUMO

Background: Plasma insulin and HOMA (homeostasis model assessment) index, used to determine insulin resistance, do not have local standard values for children and adolescents in Chile. Aim: To establish the normal reference intervals for insulin and HOMA in children and adolescents aged 10-15 years, according to sex and puberal maturation. Material and Methods: A cross-sectional study of 2,153 children and adolescents from Puente Alto County was performed, during 2009 and 2010. Anthropometry and self-report of puberal maturation were assessed. Fasting glucose (hexoquinase) and insulin blood levels (chemiluminiscence), were determined and HOMA index was calculated. Percentile distributions of these variables were calculated. Results: The reference group included only subjects with normal body mass index and fasting blood glucose (n = 1,192). Girls had higher insulin and HOMA values than boys (12.5 ± 6.0 and 9.1 ± 4.9 μϋ/mL (p < 0.01) and 2.7 ± 1.4 and 2.1 ± 1,1 (p < 0.01), respectively). Subjects with Tanner I and IIpuberal stages had lower insulin and HOMA mean values than subjects with Tanner III and IV (9.0 ± 4.3 and 12.5 ± 6.2μϋ/ml (p < 0.01) and2.0 ± 1 and2.8 ± 1.4 (p < 0.01), respectively). Conclusions: The 90th percentile of insulin and HOMA distributions according to sex and maturation, was selected as the upper cut-off point to identify individuals with insulin resistance. HOMA cutoff point for Tanner I and II boys was 3.2, for Tanner I and II girls was 4.1, for Tanner III and IV boys was 4.2 and for Tanner III and IV girls was 5.0.


Assuntos
Adolescente , Criança , Feminino , Humanos , Masculino , Glicemia/fisiologia , Homeostase/fisiologia , Resistência à Insulina/fisiologia , Insulina/sangue , Puberdade/fisiologia , Índice de Massa Corporal , Chile/epidemiologia , Estudos Transversais , Jejum/sangue , Valores de Referência , Fatores Sexuais , Estatísticas não Paramétricas
10.
Rev. méd. Chile ; 139(6): 710-716, jun. 2011. ilus
Artigo em Espanhol | LILACS | ID: lil-603115

RESUMO

Background: The Chilean Ministry of Health has been using standards for nutritional evaluation and weight gain recommendations during pregnancy in the last 25 years. In the meantime new standards have been developed. Aim: To study the combined infl uence of preconception maternal nutritional status and gestational weight gain, using new standards to classify those parameters, on perinatal outcomes. Material and Meihods: A cohort of 11,465 healthy pregnant women was prospectively followed until term. Their pre-gestational nutritional status was classified using the body mass Índex cut-offs in use in the United States (USA). Their gestational weight gain was classified using categories proposed in a Danish study. Perinatal outcomes included were risky birth weight, i.e. < 3000 g and ≥ 4000 g, and cesarean delivery. Relative risks for those perinatal outcomes were calculated for all combined categories of pre-gestational nutritional status and gestational weight gain. Results: Relative risks of almost all gestational weight gain results were statistically significant for women having a normal pre-gestational nutritional status meanwhile all of them were not significant for underweight women. Overweight and obese women had similar relative risks valúes as normal women. However, many of them were not significant, especially in obese women. Conclusions: There is an independent and combined infl uence of preconception nutritional status and gestational weight gain on perinatal outcomes, when using standards to classify those parameters developed in the USA and Denmark, respectively.


Assuntos
Adulto , Feminino , Humanos , Recém-Nascido , Gravidez , Peso ao Nascer/fisiologia , Índice de Massa Corporal , Resultado da Gravidez/epidemiologia , Aumento de Peso/fisiologia , Chile/epidemiologia , Métodos Epidemiológicos , Cuidado Pré-Concepcional , Valores de Referência , Fatores de Risco
11.
Rev. méd. Chile ; 138(11): 1357-1364, nov. 2010. graf, tab
Artigo em Espanhol | LILACS | ID: lil-572952

RESUMO

Background: Chile has the highest gallbladder cancer (GBC) death rate world-wide, affecting mainly Southern areas of the country. Aim: To compare the survival of GBC patients treated in hospitals located in areas with low and high risk for GBC. Material and Methods: Medical records of all patients with GBC admitted to one public hospital located in southern Chile, a public hospital and a private clinic, both located in Metropolitan Santiago, were reviewed. Cases were analyzed by age, sex, stage at diagnosis, ethnicity, socioeconomic status (SES) and rural residence. Survival was calculated using Kaplan Meier method. Results: A total of 598 cases (469 women), were analyzed. No differences in age or sex among hospitals were detected. At the moment of diagnosis, 75, 50 and 44 percent of cases from the hospital in southern Chile, the public hospital in Santiago and the private clinic in Santiago, were in stage IV, respectively. Five years survival was lower in the public hospital in southern Chile than in the public hospital in Santiago (10.7 and 14.4 percent respectively, p < 0.05) but not statistically different from the figure at the private clinic in Santiago (13.0 percent). However, when adjusting for stage at the moment of diagnosis, no difference in survival between the three hospitals, was found. The median days of survival were 1,559, 188, 70 and 69 for stages I, II, III and IV respectively. Conclusions: GBC mortality is high. The stage at the moment of diagnosis is only significant predictor of survival.


Assuntos
Adulto , Idoso , Idoso de 80 Anos ou mais , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Neoplasias da Vesícula Biliar/mortalidade , Mortalidade Hospitalar , Setor Privado/estatística & dados numéricos , Setor Público/estatística & dados numéricos , Chile/epidemiologia , Neoplasias da Vesícula Biliar/patologia , Estadiamento de Neoplasias , Estudos Retrospectivos , Fatores de Risco , População Rural/estatística & dados numéricos , Fatores Socioeconômicos , Análise de Sobrevida
12.
Rev. méd. Chile ; 137(9): 1145-1152, sep. 2009. ilus, tab
Artigo em Espanhol | LILACS | ID: lil-534015

RESUMO

Background: Diabetic retinopathy is one of the most common causes of blindness among adults. Aim: To report the natural history of diabetic retinopathy among Chilean patients with type 1 diabetes followed for a mean of 18 years. Material and methods: Retrospective review of medical records of 39 patients aged 26 to 70 years, (20 females, 78 eyes) with type 1 diabetes controlled by the same ophthalmologist from 1971 to 2008. A questionnaire was sent to each patient and their treating physician to request information about the evolution of the disease and metabolic control. Results: The questionnaire was answered by 24 patients (62 percent) and 21 attending physicians (54 percent). Small hard drusen were observed in 25 patients (64 percent). In 12 cases the drusen were detected before the development of any type of retinopathy. Eleven women became pregnant and retinopathy progressed in four of them. Twently three patients (59 percent) developed proliferative diabetic retinopathy (PDR). Patients with PDR had a significantly longer duration of diabetes and worse glycemic control. There was a higher frequency of diabetic nephropathy in the PDR group, but only 13 patients out of 23 with PDR had nephropathy. The retinopathy progressed to high risk PDR two years after successful kidney-pancreas transplantation in one patient. Conclusions. In patients with type 1 diabetes mellitus, small hard drusen may be the initial manifestation of diabetic retinopathy. Risk factors for progression to PDR were duration of diabetic and poor glycemic control. Nephropathy was more prevalent in patients with PDR, but a significant group of PDR patients did not have demonstrable nephropathy (RevMéd Chile 2009; 137:1145-52).


Assuntos
Adulto , Idoso , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Gravidez , Diabetes Mellitus Tipo 1/complicações , Retinopatia Diabética/etiologia , Progressão da Doença , Chile , Nefropatias Diabéticas/diagnóstico , Retinopatia Diabética/diagnóstico , Métodos Epidemiológicos , Drusas Retinianas/diagnóstico , Fatores de Risco , Fatores de Tempo
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