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1.
J Paediatr Child Health ; 57(7): 1003-1008, 2021 07.
Artigo em Inglês | MEDLINE | ID: mdl-33565678

RESUMO

AIM: The functional constipation (FC) is a source of an expressive suffering in children, negatively affecting their emotional, social, and physical well-being. The objective of this study is to describe the clinical and behavioural characteristics of children/adolescents with FC. METHODS: A cross-sectional, observational, analytical study was conducted in public places by interviewing parents of children/adolescents about their child's bowel habits and psychological profile. Bowel symptoms were investigated using the Rome IV criteria. The Strengths and Difficulties Questionnaire (SDQ) was used to evaluate the emotional and behavioural problems. RESULTS: Of 799 children/adolescents included, 424 (53.1%) were female. Mean age was 9.1 ± 2.7 years. FC prevalence was 20.4%. The most common symptoms in Rome IV criteria were 'painful or hard bowel movements' (n = 110; 67.5%; 95% confidence interval: 60.0-74.3) and 'retentive posturing or excessive volitional stool retention' (n = 89; 54.6%; 95% confidence interval: 46.9-62.1). Median scores for internalising symptoms (7; interquartile range (IQR): 4-9 vs. 5; IQR: 2-7; P < 0.001) and externalising symptoms (7; IQR 4-11 vs. 6; IQR 3-9; P < 0.001) were higher in constipated children compared to non-constipated participants, respectively. The SDQ domains that were associated with FC were emotional symptoms (median 4, P < 0.001) and conduct problems (median 3, P < 0.001). No association was found between faecal incontinence and median scores for the internalising/externalising symptoms. All Rome IV criteria were associated with abnormal overall SDQ scores. CONCLUSION: Children and adolescents with FC had more emotional and behavioural problems irrespective of whether faecal incontinence was present or not, with higher scores for internalising and externalising symptoms compared to non-constipated children.


Assuntos
Incontinência Fecal , Comportamento Problema , Adolescente , Criança , Constipação Intestinal/epidemiologia , Constipação Intestinal/etiologia , Estudos Transversais , Defecação , Feminino , Humanos , Masculino , Inquéritos e Questionários
2.
Maputo; S. n; 2021. 7 p. Tab., Fig..
Não convencional em Inglês | RDSM | ID: biblio-1344446

RESUMO

Already a major cause of death and disability in high-income countries, the burden of stroke in sub-Saharan Africa is also expected to be high. However, specific stroke data are scarce from resource-poor countries. We studied the incidence, characteristics, and short-term consequences of hospitalizations for stroke in Maputo, Mozambique. Methods­Over 12 months, comprehensive data from all local patients admitted to any hospital in Maputo with a new stroke event were prospectively captured according to the World Health Organization's STEPwise approach to stroke surveillance program. Disability levels (pre- and posthospital discharge) and short-term case-fatality (in-hospital and 28 days) were also studied. Results­Overall, 651 new stroke events (mean age 59.113.2 years and 53% men) were captured by the registry with 601 confirmed by CT scan (83.4%) or necropsy (8.9%). Crude and adjusted (world reference population) annual incidence rates of stroke were 148.7 per 100 000 and 260.1 per 100 000 aged 25 years, respectively. Of these, 531 (81.6%) represented a first-ever stroke event comprising 254 ischemic (42.0%) and 217 (36.1%) an intracerebral hemorrhage. Before admission, 561 patients (86.2%) had hypertension and 271 (41.6%) had symptoms for 24 hours. In-hospital and 28-day case-fatality were 33.3% and 49.6% (72.3% for hemorrhagic stroke), respectively. From almost no preadmission disability, 64.4% of 370 survivors at 28 days had moderate-to-severe disability. Conclusions­The burden of disease associated with stroke is high in Maputo, emphasizing the importance of primary prevention and improvement of the standards of care in a developing country under epidemiological transition


Assuntos
Pacientes , Países em Desenvolvimento , Acidente Vascular Cerebral Hemorrágico , Hipertensão , População , Organização Mundial da Saúde , Estudos Epidemiológicos , Incidência , Causas de Morte , Efeitos Psicossociais da Doença , Acidente Vascular Cerebral , Hospitais
3.
Arq. gastroenterol ; 57(2): 126-130, Apr.-June 2020. tab
Artigo em Inglês | LILACS | ID: biblio-1131650

RESUMO

ABSTRACT BACKGROUND: Recently it was shown an association between lower urinary tract symptoms in mothers and their children. However, the role of functional constipation in this binomial is unclear. OBJECTIVE: To evaluate bladder and bowel dysfunction between mothers and children. METHODS: A population-based cross-sectional study. Mothers and their children responded a self-administrated questionnaire composed by Rome IV criteria, International Consultation on Incontinence Questionnaire - Overactive Bladder, Dysfunctional Voiding Scoring System and demographic questions. RESULTS: A total of 441 mother-child pairs was obtained. Children's mean age was 9.1±2.7 years, with 249 (56.5%) female. Mothers' mean age was 35.7±6.1 years. Isolated constipation was present at 35 (7.9%) children and 74 (16.8%) mothers. Isolated lower urinary tract symptoms were present in 139 (31.5%) children and 92 (20.9%) mothers and bladder bowel dysfunction occurred in 51 (11.6%) children and 78 (17.7%) mothers. There wasn't any association between isolated lower urinary tract symptoms in children and isolated lower urinary tract symptoms in mothers (P=0.31). In univariate analysis there were an association between bladder bowel dysfunction in children and bladder bowel dysfunction in mothers (OR=4.8 IC 95% 2.6-9.6, P<0.001) and isolated constipation in children and isolated constipation in mothers (OR=3.0 IC 95% 1.4-6.4, P=0.003). In multivariate analysis mothers with bladder bowel dysfunction was the only independent factor associated with bladder bowel dysfunction in children (OR=5.4 IC 95% 2.5-11.6, P<0.001). CONCLUSION: Mothers with bladder bowel dysfunction are more likely to have a child with bladder bowel dysfunction. Association between these two dysfunctions plays an important role in this familiar presentation.


RESUMO CONTEXTO: Recentemente foi demonstrada associação entre sintomas do trato urinário inferior entre mães e filhos. No entanto, o papel da constipação funcional neste binômio não é claro. OBJETIVO: Avaliar a disfunção vésico-intestinal entre mães e filhos. MÉTODOS: Estudo transversal de base populacional. As mães e os filhos responderam a um questionário de autorresposta, composto pelos critérios de Roma IV, International Consultation on Incontinence Questionnaire - Overactive Bladder, Dysfunctional Voiding Scoring System e perguntas sociodemográficas. RESULTADOS: Foram estudados 441 pares mãe-filho. A idade média dos filhos foi de 9,1±2,7 anos, sendo 249 (56,5%) do sexo feminino. A idade média das mães foi de 35,7±6,1 anos. A constipação sem sintomas do trato urinário inferior estava presente em 35 (7,9%) crianças e 74 (16,8%) mães. Sintomas do trato urinário inferior isolados estavam presentes em 139 (31,5%) crianças e 92 (20,9%) mães e a disfunção vésico-intestinal ocorreu em 51 (11,6%) crianças e 78 (17,7%) mães. Não houve associação entre sintomas isolados do trato urinário inferior em crianças e sintomas isolados do trato urinário inferior em mães (P=0,31). Na análise univariada, houve associação entre disfunção vésico-intestinal em crianças e disfunção vésico-intestinal em mães (OR=4,8 IC 95% 2,6-9,6; P<0,001) e constipação isolada em crianças e constipação isolada em mães (OR=3,0 IC 95 % 1,4-6,4; P=0,003). Na análise multivariada, mães com disfunção vésico-intestinal foi o único fator de associação independente para disfunção vésico-intestinal em crianças (OR=5,4 IC 95% 2,5-11,6; P<0,001). CONCLUSÃO: Mães com disfunção vésico-intestinal têm maior probabilidade de ter filhos com disfunção vésico-intestinal. A associação entre constipação e sintomas do trato urinário inferior desempenha um papel importante nesta apresentação familiar.


Assuntos
Humanos , Feminino , Criança , Adulto , Constipação Intestinal , Sintomas do Trato Urinário Inferior , Mães , Estudos Transversais
4.
Arq Gastroenterol ; 57(2): 126-130, 2020.
Artigo em Inglês | MEDLINE | ID: mdl-32401953

RESUMO

BACKGROUND: Recently it was shown an association between lower urinary tract symptoms in mothers and their children. However, the role of functional constipation in this binomial is unclear. OBJECTIVE: To evaluate bladder and bowel dysfunction between mothers and children. METHODS: A population-based cross-sectional study. Mothers and their children responded a self-administrated questionnaire composed by Rome IV criteria, International Consultation on Incontinence Questionnaire - Overactive Bladder, Dysfunctional Voiding Scoring System and demographic questions. RESULTS: A total of 441 mother-child pairs was obtained. Children's mean age was 9.1±2.7 years, with 249 (56.5%) female. Mothers' mean age was 35.7±6.1 years. Isolated constipation was present at 35 (7.9%) children and 74 (16.8%) mothers. Isolated lower urinary tract symptoms were present in 139 (31.5%) children and 92 (20.9%) mothers and bladder bowel dysfunction occurred in 51 (11.6%) children and 78 (17.7%) mothers. There wasn't any association between isolated lower urinary tract symptoms in children and isolated lower urinary tract symptoms in mothers (P=0.31). In univariate analysis there were an association between bladder bowel dysfunction in children and bladder bowel dysfunction in mothers (OR=4.8 IC 95% 2.6-9.6, P<0.001) and isolated constipation in children and isolated constipation in mothers (OR=3.0 IC 95% 1.4-6.4, P=0.003). In multivariate analysis mothers with bladder bowel dysfunction was the only independent factor associated with bladder bowel dysfunction in children (OR=5.4 IC 95% 2.5-11.6, P<0.001). CONCLUSION: Mothers with bladder bowel dysfunction are more likely to have a child with bladder bowel dysfunction. Association between these two dysfunctions plays an important role in this familiar presentation.


Assuntos
Constipação Intestinal , Sintomas do Trato Urinário Inferior , Mães , Adulto , Criança , Estudos Transversais , Feminino , Humanos
5.
Arch. esp. urol. (Ed. impr.) ; 54(5): 458-463, jun. 2001.
Artigo em Es | IBECS | ID: ibc-1516

RESUMO

OBJETIVOS: Presentación de un caso clínico-patológico de síndrome de Cushing de origen primariamente suprarrenal por hiperplasia cortical nodular masiva, cuadro que da a la glándula un aspecto pseudotumoral susceptible de ser confundido con neoplasia. MÉTODO: En una revisión de patología quirúrgica de la glándula suprarrenal recientemente realizada en nuestro hospital, se encontraron un total de 82 piezas de adrenalectomía correspondientes al período de veinte años 1978-1998. De estas 82 piezas, 44 (53,6 por ciento) fueron casos de patología cortical y 10 de ellas (12,1 por ciento), hiperplasias. Un solo caso correspondía a una hiperplasia cortical macronodular con agrandamiento glandular masivo. RESULTADO: Varón de 53 años, alcohólico crónico con obesidad cushinoide e hipercortisolismo, que en el estudio radiológico (ecografía, TAC) mostró un aumento de tamaño, asimétrico, de ambas glándulas suprarrenales, con presencia de macronódulos. El estudio analítico y la resonancia magnética nuclear de la silla turca pusieron en evidencia el carácter primario del hipercortisolismo. Se realizó adrenalectomía de la glándula dominante (la izquierda, cuya actividad se demostró en la gammagrafía con I 131). Los niveles de cortisol post-operatorio se normalizaron y se han mantenido hasta la fecha, 18 meses después de la intervención quirúrgica. La glándula extirpada pesaba 104 grs. y presentaba una transformación macronodular total. CONCLUSIONES: La hiperplasia macronodular con marcado agrandamiento glandular es una rara causa de hipercortisolismo suprarrenal primario autónomo, hipófiso- independiente. Siempre es bilateral. Las glándulas están significativamente aumentadas de peso (de 60 a 180 grs. de peso conjunto) y muestran nódulos que van desde escasos milímetros hasta 4 cms., amarillos o dorados, no encapsulados. Las células que los constituyen son poco activas, por lo que es necesario un gran aumento de tamaño glandular para que produzca el síndrome de Cushing. Los aspectos clínicos y bioquímicos y la radiología pueden ser fuente de confusión y sugerir una neoplasia córtico-suprarrenal. El tratamiento es la adrenalectomía (AU)


Assuntos
Pessoa de Meia-Idade , Masculino , Humanos , Síndrome de Cushing , Diagnóstico Diferencial , Córtex Suprarrenal , Hiperfunção Adrenocortical , Doenças das Glândulas Suprarrenais , Hiperplasia , Hiperfunção Adrenocortical
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