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1.
Rev Med Chir Soc Med Nat Iasi ; 117(2): 483-7, 2013.
Artigo em Inglês | MEDLINE | ID: mdl-24340534

RESUMO

UNLABELLED: Diabetes mellitus (DM) represents an important problem of public health according to the worldwide statistical data. In Romania, the national program is facing the same situation: increasing incidence (both for children and adults) and prevalence of this disease. AIM: To evaluate the results of the national program for DM through some indirect indicators. MATERIAL AND METHODS: This study represents a descriptive analysis of hospitalized DM cases between 1.01.2009 and 31.03.2013, in Romania. The lack of statistical data available from the Ministry of Public Health (the latest update on the web page for DM is from 2007) makes the evaluation of the outcomes of this program quite difficult. An indirect evaluation is possible using the national hospital registrations for DM complications, recorded by the National School of Management and Public Health. For diagnostic registration was used the classification for Diagnostic Related Group (DRG), version HCFA DRG v. 18. RESULTS: Despite the facilities offered to diabetic patients through the program, the burden of DM over the health system is quite large due to the large number of patients having complications. CONCLUSIONS: Even the objectives of the program appear to be accomplished; the indirect outcomes of the evaluation suggest that could be a gap between the hospital specialist and family doctors and a lack of health education for patients with DM.


Assuntos
Diabetes Mellitus/epidemiologia , Tempo de Internação/estatística & dados numéricos , Adulto , Criança , Diabetes Mellitus/diagnóstico , Diabetes Mellitus Tipo 1/epidemiologia , Diabetes Mellitus Tipo 2/epidemiologia , Inquéritos Epidemiológicos/métodos , Humanos , Incidência , Prevalência , Romênia/epidemiologia
2.
Rev Med Chir Soc Med Nat Iasi ; 117(1): 88-94, 2013.
Artigo em Inglês | MEDLINE | ID: mdl-24505898

RESUMO

UNLABELLED: Celiac disease (CD) is an immune-mediated enteropathy triggered by the ingestion of gluten in genetically susceptible individuals and neurologic manifestations may be one of the presentations form. The aim of this study was to report the incidence of neurologic manifestations in children with CD. MATERIAL AND METHODS: Between 2000-2010, 48 children aged 2-18 years diagnosed with CD have been monitored. The diagnosis of CD was made by serological tests and intestinal biopsy. The study protocol included: measurement of weight and height, biological and immunological tests, histological examination, questionnaires filled out by parents about their child motor development and some neurologic signs, psychological exam, electroencephalogram, and brain CT-scan. RESULTS: 16 of the 48 children presented one or more neurologic symptoms as the onset manifestation of CD. The neurologic signs in order of frequency were: headache/migraine, attention-deficit/hyperactivity disorder, epileptic seizures, mental retardation, cerebellar ataxia and behavior disorders. Brain CT-scan showed cerebral calcifications in 3 patients with epilepsy, and atrophy in 2 cases with cerebellar ataxia. All children received gluten free diet, but a favorable course was noticed only in the children with migraine and epilepsy, in the other patients this diet having no influence on neurologic symptoms. CONCLUSIONS: This study proved the variety of neurologic symptoms that can be included in the clinical signs of celiac disease in pediatric patients. That is why in the presence of different neurologic symptoms of unknown etiology and resistant to treatment, celiac disease must be taken into account and laboratory investigations have to include intestinal biopsy and immunological test.


Assuntos
Encefalopatias/etiologia , Doença Celíaca/complicações , Adolescente , Transtorno do Deficit de Atenção com Hiperatividade/etiologia , Estatura , Índice de Massa Corporal , Peso Corporal , Encefalopatias/diagnóstico , Encefalopatias/imunologia , Doença Celíaca/diagnóstico , Doença Celíaca/dietoterapia , Doença Celíaca/imunologia , Ataxia Cerebelar/etiologia , Criança , Pré-Escolar , Eletroencefalografia , Epilepsia/etiologia , Feminino , Humanos , Incidência , Deficiência Intelectual/etiologia , Masculino , Transtornos Mentais/etiologia , Estudos Prospectivos , Romênia/epidemiologia , Inquéritos e Questionários
3.
Rev Med Chir Soc Med Nat Iasi ; 116(2): 580-7, 2012.
Artigo em Romano | MEDLINE | ID: mdl-23077957

RESUMO

Cystic fibrosis (CF) is a disease that degrades the local defense mechanisms of the lower respiratory tract. As a result, patients develop recurrent infections that progressively deteriorates antiinfection defenses and represent the major cause of mortality. A hallmark of those infections is the diversity of microorganisms isolated from broncho-alveolar lavage or sputum. The clinical significance of isolates is different, the recognition of the role in altering of respiratory function being important in guiding antibiotic therapy. Current data support pathogenicity in CF of S. aureus, P. aeruginosa and B. cepacia complex, the latter two being considered "preterminal bacteria". S. aureus was the most common cause of mortality and morbidity in preantibiotic era. Today, life expectancy was improved with the introduction of antistaphylococcal antibiotics. Hypermutation of P. aeruginosa--the most common species isolated from patients with CF, is the essential factor in the development of multi-resistance to antibiotics. As P. aeruginosa, B. cenocepacia is a virulent species that cause infections with poor prognosis. Microorganisms with secondary role (H. influenzae, S. maltophilia, atypical Mycobacteria, Aspergillus spp) whose clinical significance has not been clarified yet, require further studies.


Assuntos
Infecções Bacterianas/microbiologia , Fibrose Cística/microbiologia , Infecções Respiratórias/microbiologia , Escarro/microbiologia , Antibacterianos/uso terapêutico , Infecções Bacterianas/tratamento farmacológico , Infecções Bacterianas/mortalidade , Lavagem Broncoalveolar , Infecções por Burkholderia/complicações , Burkholderia cenocepacia/isolamento & purificação , Fibrose Cística/complicações , Fibrose Cística/tratamento farmacológico , Fibrose Cística/mortalidade , Humanos , Prognóstico , Infecções por Pseudomonas/complicações , Pseudomonas aeruginosa/isolamento & purificação , Infecções Respiratórias/complicações , Infecções Respiratórias/tratamento farmacológico , Infecções Respiratórias/mortalidade , Infecções Estafilocócicas/complicações , Staphylococcus aureus/isolamento & purificação , Análise de Sobrevida
4.
Rev Med Chir Soc Med Nat Iasi ; 116(3): 898-901, 2012.
Artigo em Inglês | MEDLINE | ID: mdl-23272549

RESUMO

Current standards of sputum examination in respiratory infections with opportunistic bacteria cannot be applied to patients with cystic fibrosis due to their particularities. In 2010, a working group from Great Britain established standards for microbiological processing of samples from patients with cystic fibrosis. Recommendations on sample collection, transportation, storage, and processing, identification of bacterial isolates and in vitro antibiotic susceptibility are made. Also recommended is that the multidisciplinary team monitoring patients with cystic fibrosis to include a microbiologist.


Assuntos
Bactérias/isolamento & purificação , Fibrose Cística/microbiologia , Infecções Respiratórias/microbiologia , Antibacterianos/uso terapêutico , Fibrose Cística/tratamento farmacológico , Humanos , Comunicação Interdisciplinar , Testes de Sensibilidade Microbiana/métodos , Monitorização Fisiológica , Guias de Prática Clínica como Assunto , Infecções Respiratórias/tratamento farmacológico , Romênia , Manejo de Espécimes , Escarro/microbiologia
5.
Rev Med Chir Soc Med Nat Iasi ; 114(1): 34-8, 2010.
Artigo em Romano | MEDLINE | ID: mdl-20509273

RESUMO

Children with cystic fibrosis (CF) are at risk for poor growth. A major goal in the management of CF patients is to maintain a good nutritional status as it improves long-term survival. A balanced diet, which includes adequate calories and the right vitamin and mineral supplements, is key to good nutrition and health. The authors present the improvements in management of nutrition that have occurred, particularly over the past 20 years. They also present the dietetic reccomandations for each group of age.


Assuntos
Fibrose Cística/dietoterapia , Suplementos Nutricionais , Apoio Nutricional/métodos , Adolescente , Criança , Pré-Escolar , Fibrose Cística/complicações , Fibrose Cística/fisiopatologia , Progressão da Doença , Humanos , Lactente , Recém-Nascido , Avaliação Nutricional , Estado Nutricional , Guias de Prática Clínica como Assunto , Resultado do Tratamento
6.
Rev Med Chir Soc Med Nat Iasi ; 110(1): 38-43, 2006.
Artigo em Romano | MEDLINE | ID: mdl-19292076

RESUMO

Obesity is currently the most prevalent nutritional disease of children and adolescents and a common health problem. Besides the bio-ecologic and socio-economic factors (genetical, professional, cultural, educational), the exogenous factors (nutritional) have a pro-obesity action by increasing the caloric intake determining energy imbalance. The authors present the role of nutrition in the occurrence of obesity in children and adolescents and its role in the treatment of the disease.


Assuntos
Dieta , Ingestão de Energia , Obesidade/dietoterapia , Obesidade/prevenção & controle , Adolescente , Índice de Massa Corporal , Restrição Calórica/métodos , Criança , Carboidratos da Dieta/administração & dosagem , Gorduras na Dieta/administração & dosagem , Proteínas Alimentares/administração & dosagem , Comportamento Alimentar , Saúde Global , Promoção da Saúde , Humanos , Estilo de Vida , Micronutrientes , Obesidade/epidemiologia , Prevalência , Fatores de Risco , Romênia/epidemiologia
7.
Rev Med Chir Soc Med Nat Iasi ; 110(4): 801-6, 2006.
Artigo em Romano | MEDLINE | ID: mdl-17438879

RESUMO

Good nutrition is essential for normal growth and development. Cystic fibrosis (CF) is commonly associated with energy deficiency in children. Malnutrition is a very frequent complication and contributes significantly toward morbidity in CF. Although malnutrition due to pancreatic enzyme insufficiency is correctable, the majority of CF patients are underweight and have short stature. During the last few decades, improved treatment measures and nutritional support in CF have increased survival and quality of life in these patients. Patients with CF must receive a hypercaloric and hyper-proteic diet, with a high fat content, a normal quantity of carbohydrates and with pancreatic and liposoluble vitamin supplements in case of pancreatic insufficiency.


Assuntos
Fibrose Cística/complicações , Fibrose Cística/dietoterapia , Gorduras na Dieta/administração & dosagem , Proteínas Alimentares/administração & dosagem , Ingestão de Energia , Desnutrição Proteico-Calórica/dietoterapia , Desnutrição Proteico-Calórica/etiologia , Criança , Pré-Escolar , Fibrose Cística/mortalidade , Nutrição Enteral/métodos , Humanos , Nutrição Parenteral/métodos , Desnutrição Proteico-Calórica/mortalidade , Qualidade de Vida , Análise de Sobrevida
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