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1.
Minerva Pediatr ; 66(2): 141-6, 2014 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-24835447

RESUMO

AIM: The aim of the present study was to determine the prevalence of vitamin D supplementation and risk factors for non-supplemented infants in Izmir, Turkey. METHODS: This cross-sectional study was carried out in Well-Child Care Clinics in Izmir, Turkey. Parents filled a questionnaire about socio-demographic characteristics and the use of vitamin D. SPSS version 16.0 was used for statistical analysis. RESULTS: A total of 1002 children (aged 1 to 24 months) were enrolled in the study. The supplementation rates of vitamin D were 77% in the first 3 months of life, 57% at 10 to 12 months. Economic status of family, education of parents, occupational status of mothers and parity were associated factors with the use of vitamin D supplements in infants (P<0.05). However, when the data were analyzed using logistic regression analysis, only education of mother seems to be statistically significant independent variable in decreasing non-supplementation/ irregular supplementation. CONCLUSION: Vitamin D supplementation rates seem to be not satisfactory in Izmir. Therefore, the importance of vitamin D supplementation in infants should be emphasized in every well-child care visit to prevent vitamin D deficiency.


Assuntos
Conservadores da Densidade Óssea/uso terapêutico , Colecalciferol/uso terapêutico , Deficiência de Vitamina D/prevenção & controle , Conservadores da Densidade Óssea/administração & dosagem , Aleitamento Materno , Pré-Escolar , Colecalciferol/administração & dosagem , Estudos Transversais , Feminino , Humanos , Lactente , Masculino , Prevalência , Fatores de Risco , Fatores Socioeconômicos , Resultado do Tratamento , Turquia
2.
Clin Exp Rheumatol ; 23(5): 689-92, 2005.
Artigo em Inglês | MEDLINE | ID: mdl-16173248

RESUMO

OBJECTIVE: There is not enough evidence about the relationship between free radicals and male osteoporosis. In this study we investigated the role of free oxygen radicals and antioxidants on male osteoporosis in 31 male patients with primary osteoporosis and 21 subjects as controls. METHODS: Bone mineral densities (BMD) of the lumbar and femoral neck region were evaluated using dual energy X-ray absorbsiometry. Serum malondialdehyde (MDA) and nitric oxide (NO) levels and superoxide dismutase (SOD) and glutathione peroxidase (GPx) activities were measured by analytical methods. In addition, serum osteocalcine and C telopeptide levels were determined to evaluate bone turnover MDA and NO levels and SOD activity were significantly increased (p < 0.05) in osteoporotic males. RESULTS: There was a negative correlation between SOD and lumbar BMD levels (r= -0.328; p = 0.021). The same trend was observed between NO and lumbar BMD (r = -0.473; p = 0.001) and femoral neck BMD values (r = -0.540; p = 0.000). There was no significant correlation between free radical levels and bone turnover markers. CONCLUSION: The data indicate an increase in free oxygen radical levels. As a result, antioxidant defenses would compromise in primary male osteoporotic patients. Therefore, it may be suggested that oxidative stress plays an important role in the pathophysiology of primary male osteoporosis.


Assuntos
Osteoporose/metabolismo , Estresse Oxidativo/fisiologia , Espécies Reativas de Oxigênio/metabolismo , Densidade Óssea/fisiologia , Remodelação Óssea/fisiologia , Humanos , Masculino , Pessoa de Meia-Idade , Osteoporose/fisiopatologia
4.
Pediatr Int ; 43(4): 379-84, 2001 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-11472583

RESUMO

BACKGROUND: Measles outbreaks seem to occur every 2- to 3-year intervals in Turkey. However, sero-epidemiological studies are limited. Knowing the prevalence of measles susceptibility as measured either by serologic markers of immunity or surveys of vaccination coverage is an important tool to assess the risk for measles outbreaks. METHODS: In order to determine the seroprevalence of measles antibodies among a 1 to 29-year-old population in Izmir (Turkey) and to develop the best vaccination policy for measles, a total of 600 people aged from 1 to 29 were selected for the study with cluster sampling. The information on sociodemographic characteristics, vaccination status and measles history was gathered for each participant. Measles-specific IgG antibodies were screened qualitatively by using microenzyme immune assay for 595 subjects. RESULTS: Of the 595 participants screened for the measles antibodies, 56 (9.4%) were seronegative. The proportion of the susceptible individuals in the age groups of 1-4, 5-9, 10-14, 15-19 and 20-29 was 20.0, 10.4, 6.0, 10.3 and 3.0%, respectively. The logistic regression analysis showed that none of the independent characteristics (sex, socioeconomic status, past measles history, vaccination status) with the exception of age group, was significantly associated with measles seronegativity. CONCLUSION: The optimal measles vaccination policy for Turkey may be to increase vaccination coverage above 90%, to conduct a catch-up campaign covering persons aged 1-19, regardless of previous vaccination status. Another factor to consider is to adopt a routine two-dose vaccination, giving the first dose at 12-15 months of age and the second dose at school entry.


Assuntos
Política de Saúde , Sarampo/epidemiologia , Vacinação , Adolescente , Adulto , Criança , Pré-Escolar , Análise por Conglomerados , Feminino , Humanos , Lactente , Masculino , Sarampo/prevenção & controle , Estudos Soroepidemiológicos , Fatores Socioeconômicos , Turquia/epidemiologia
5.
Vaccine ; 19(28-29): 3936-9, 2001 Jul 16.
Artigo em Inglês | MEDLINE | ID: mdl-11427268

RESUMO

Several studies have documented the efficacy of low-dose intradermal administration of hepatitis B vaccine. However, little is known about the duration of protection provided by low-dose intradermal administration of hepatitis B vaccine. This study reports results from a 5-year follow up period of 200 healthy children (100 infants and 100 preschool children) immunized intradermally with 2 microg doses of recombinant hepatitis B vaccine (GenHevac B) at months 0,1, and 6. In the 8th week after the third vaccine dose, 97% of the children developed anti-HBs antibodies higher than or equal to 10 mlU ml(-1), and the antiHBs geometric mean titre (GMT) was 676 mlU ml(-1). In month 18 and year 5, the anti-HBs GMT decreased to approximately one-third (220 mlU ml(-1)) and one-tenth (68 mlU ml(-1)) of the initial levels, respectively. However, 87% of the children had protective levels of anti-HBs (> or =10 mlU ml(-1)) after 5 years. Among 156 children followed for 5 years, none became positive for anti-HBc and/or HbsAg. Seven children who were seronegative after 5 years developed anti-HBs antibodies higher than 1000 mlU ml(-1) after an additional 10 microg intramuscular hepatitis B vaccine. Persistent immunologic memory over periods of 5 years or more is evident, the anamnestic antibody response to a booster dose of vaccine, even in these children who have lost antibody. We conclude that intradermal administration of 2 microg recombinant hepatitis B vaccine provides long-term protection against hepatitis B virus in infants and preschool children.


Assuntos
Vacinas contra Hepatite B/administração & dosagem , Criança , Pré-Escolar , Feminino , Seguimentos , Anticorpos Anti-Hepatite B/sangue , Humanos , Esquemas de Imunização , Imunização Secundária , Memória Imunológica , Lactente , Injeções Intradérmicas , Masculino , Fatores de Tempo , Turquia , Vacinas Sintéticas/administração & dosagem
6.
Eur J Haematol ; 64(6): 411-5, 2000 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-10901595

RESUMO

The objectives of this study were to investigate the effectiveness of oral megadose methylprednisolone (OMMP) therapy in children with chronic immune thrombocytopenic purpura (ITP). Twenty-two patients were given oral methylprednisolone daily for 7 d (30 mg/kg for 3 d and then 20 mg/kg for 4 d). OMMP therapy was repeated once per month if the platelet count was less than 20,000/mm3 at the 30th day of therapy, for up to six courses. The number of platelets of all patients increased gradually during the OMMP therapy, with a peak number at the 7th day, then decreased until the 14th day, and remained relatively stable until 12 months. During the study no patient had a platelet count less than 20,000/mm3 at the 3rd day and 50,000/mm3 at the 7th day. Although the number of platelets was gradually decreased between the 7th and 14th days, it remained above 100,000/mm3 for at least 12 months in the nine patients, and above 20,000/mm3 in the four patients. None of these 13 patients required hospitalization or therapy during the follow-up period. All of the patients tolerated the medication well. None of them reported side-effects that were severe enough to discontinue therapy. We conclude that OMMP therapy is a safe, easy and effective therapy in children with refractory chronic ITP, and it may provide long-term remission in about two thirds of the patients.


Assuntos
Metilprednisolona/administração & dosagem , Púrpura Trombocitopênica Idiopática/tratamento farmacológico , Administração Oral , Adolescente , Criança , Pré-Escolar , Feminino , Humanos , Masculino , Metilprednisolona/uso terapêutico , Contagem de Plaquetas , Resultado do Tratamento
8.
Vaccine ; 18(26): 2979-84, 2000 Jul 01.
Artigo em Inglês | MEDLINE | ID: mdl-10825599

RESUMO

The effects of vitamin A and vitamin E supplementation on the IgG response to tetanus toxoid after primary immunization were evaluated in a prospective, randomized controlled clinical trial involving 89 healthy infants with normal serum vitamin A and E levels at 2 months of age. Before the first dose of DPT vaccine, the infants were randomly enrolled into four different study groups [Group I (n=24): 30,000 IU vitamin A for 3 days just after each three doses of primary vaccination, Group II (n=21): 150 mg oral vitamin E for only 1 day after the injections for primary immunization, Group III (n=21): vitamins A and E together in the same order, Group IV (n=23) no vitamin after DPT vaccines]. Serum tetanus antitoxin (IgG) titres were measured three times; initially at 2 months of age before the first dose of DPT, secondly at 5 months of age 1 month after primary immunization and thirdly at 16-18 months of age before the booster dose of DPT. Before the first dose of the DPT vaccine, 1 month after the third DPT injection and at 16-18 months before the booster dose of DPT, there was no significant difference in serum tetanus antitoxin levels between these four groups. A significant increase was observed in all the groups when serum tetanus antitoxin levels before (2 months) and after (5 months) primary immunization were compared. In addition, serum antibody levels against tetanus significantly decreased in the four groups before booster vaccination. Before the beginning of primary immunization, 15 infants (16.8%) had serum tetanus antitoxins (IgG) below protective level. After three doses of DPT, all the infants had protective antitoxin levels. At 16-18 months of age before booster dose, four infants (10%) also had serum tetanus antitoxins (IgG) below the protective level. No side-effects were observed except bulging fontanelle in two infants in Group I.


Assuntos
Antitoxina Tetânica/sangue , Toxoide Tetânico/imunologia , Vitamina A/farmacologia , Vitamina E/farmacologia , Formação de Anticorpos/efeitos dos fármacos , Vacina contra Difteria, Tétano e Coqueluche/imunologia , Humanos , Imunização , Imunoglobulina G/sangue , Recém-Nascido , Estudos Prospectivos
10.
Paediatr Perinat Epidemiol ; 14(1): 64-9, 2000 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-10703036

RESUMO

Vitamin A deficiency even at subclinical levels is associated with increased childhood mortality. There have been few studies related to vitamin A status of children in Turkey. The aim of this study was to assess vitamin A status of children aged 6-59 months in Izmir, Turkey, and to evaluate the relationship of these levels with nutritional status. One hundred and sixty children were selected for the study using the cluster sampling method. Serum retinol levels were measured by high-performance liquid chromatography (HPLC) and ranged from 9.8 to 59.2 micrograms/dL (mean 29.3 +/- 9.5 micrograms/dL). Levels were below the lower limit of the normal range in 15.6% of the children. Deficient and marginal serum retinol among stunted children were observed in 16% and 42% respectively. There was a statistically significant relationship between low serum retinol and stunting (P < 0.05). Although xerophthalmia and other clinical signs of vitamin A deficiency are rarely seen, subclinical vitamin A deficiency is a public health problem in Izmir, Turkey.


Assuntos
Deficiência de Vitamina A/epidemiologia , Pré-Escolar , Feminino , Transtornos do Crescimento/etiologia , Humanos , Lactente , Masculino , Turquia/epidemiologia , Vitamina A/sangue
11.
Eur J Epidemiol ; 16(11): 1039-42, 2000.
Artigo em Inglês | MEDLINE | ID: mdl-11421473

RESUMO

In order to assess immunity to diphtheria in Izmir, Turkey, a total of 743 persons 1-70 years of age were selected with cluster sampling. The information on socio-demographic characteristics, vaccination status and diphtheria history was gathered for each participant. Diphtheria antitoxin levels were measured qualitatively by using micro-enzyme immune assay. Of studied population, 79.1% had fully protective antitoxin levels (> or = 0.1 IU/ml). Diphtheria protection rates showed a gradual age-related decrease, reaching minimum in the 30-44 age group, in which 40.2% of these subjects had antibody titre below the full protective level. The diphtheria antitoxin geometric mean titer was highest in the 5-9 year age group (1.05 IU/ml). Then, geometric mean titer decreased with increasing age, and reached the minimum level in the 30-44 age group (0.19 IU/ml). These results suggest that in Izmir, Turkey, full serological protection against diphtheria is only detectable in 60% of the adult population. The enhancement of diphtheria immunity by booster vaccinations in adolescents and adults should be considered in Turkey.


Assuntos
Antitoxina Diftérica/análise , Difteria/epidemiologia , Difteria/imunologia , Adolescente , Adulto , Idoso , Análise de Variância , Anticorpos Antibacterianos/análise , Distribuição de Qui-Quadrado , Criança , Pré-Escolar , Feminino , Humanos , Lactente , Masculino , Pessoa de Meia-Idade , Turquia/epidemiologia , População Urbana
12.
Pediatr Infect Dis J ; 18(7): 577-80, 1999 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-10440431

RESUMO

BACKGROUND: The European Advisory Group on the Expanded Program on Immunization of WHO has recommended that by 2010 or earlier congenital rubella should be well-controlled or eliminated in all countries in Europe. Debate on the introduction of rubella vaccine into national immunization schedules continues to occur, and data on rubella and congenital rubella syndrome in Turkey are insufficient. OBJECTIVE: To determine age-specific rubella seroprevalence in the 1- to 29-year-old unvaccinated population in Izmir, Turkey. METHODS: A total of 600 unvaccinated persons 1 to 29 years old were selected for the study with cluster sampling in Izmir, Turkey. The information on sociodemographic characteristics and disease history was gathered for each participant, and in 580 of them rubella-specific IgG antibodies were assayed quantitatively by the micro-enzyme immunoassay. RESULTS: Of the 580 participants tested for rubella antibodies, 135 (23.3%) were seronegative. The proportions of susceptible individuals were 61.7, 29.5, 12.4, 10.3 and 8.4% in the age groups of 1 to 4, 5 to 9, 10 to 14, 15 to 19 and 20 to 29 years, respectively. Of the young women 15 to 19 years of age, 13.5% were susceptible to rubella infection. CONCLUSIONS: Because a substantial proportion of women in their childbearing years are susceptible to rubella, immunization efforts should be directed at infants or prepubertal children.


Assuntos
Anticorpos Antivirais/sangue , Síndrome da Rubéola Congênita/epidemiologia , Vacina contra Rubéola , Vírus da Rubéola/imunologia , Rubéola (Sarampo Alemão)/epidemiologia , Adolescente , Adulto , Distribuição por Idade , Criança , Pré-Escolar , Suscetibilidade a Doenças , Feminino , Humanos , Técnicas Imunoenzimáticas , Imunoglobulina G/sangue , Lactente , Masculino , Estudos Soroepidemiológicos , Distribuição por Sexo , Turquia/epidemiologia , Vacinação
14.
Acta Paediatr Jpn ; 40(3): 256-8, 1998 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-9695301

RESUMO

BACKGROUND: To assess the efficacy of benzathine penicillin G (BPG) prophylaxis in recurrent streptococcal pharyngitis in children. METHODS: One hundred and sixty children, aged 4-11 years, who experienced at least two episodes of group A beta-hemolytic streptococcal (GABHS) pharyngitis during a 4-month observation period between September and December 1995 were randomly divided into two groups. During the following 4-month period between January and April 1996, 80 children received BPG prophylaxis every 3 weeks as a single intramuscular injection of 1.2 million units for a body weight greater than 27 kg and a half dose for 27 kg or less. Eighty children were accepted as a control group and were not given BPG prophylaxis. RESULTS: The children in the BPG group experienced significantly less GABHS pharyngitis than those in the control group during the second 4-month period (16 vs 244 episodes, respectively, P < 0.001). BPG prophylaxis decreased streptococcal pharyngitis by 92% in the children in the study group, while the frequency of GABHS pharyngitis was unchanged in those in the control group during the second 4-month period compared with the first 4-month period. CONCLUSIONS: The data in the present study demonstrated that intramuscular BPG prophylaxis is very effective in preventing GABHS pharyngitis in children. It is recommended that it is used every 3 weeks in at least the fall-winter seasons in children susceptible to frequent GABHS pharyngitis.


Assuntos
Antibioticoprofilaxia/métodos , Penicilina G Benzatina/uso terapêutico , Penicilinas/uso terapêutico , Faringite/prevenção & controle , Infecções Estreptocócicas/prevenção & controle , Criança , Pré-Escolar , Feminino , Humanos , Injeções Intramusculares , Masculino , Faringite/microbiologia , Infecções Estreptocócicas/microbiologia
15.
Vaccine ; 16(16): 1511-5, 1998 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-9711797

RESUMO

Two hundred infants and two hundred preschool children were randomly assigned to receive either 10 micrograms of recombinant hepatitis B vaccine (GenHevac B) intramuscularly (i.m.) or 2 micrograms intradermally (ID) in the deltoid region at 0, 1 and 6 months. Antibody to hepatitis B surface antigen (anti-HBs) was tested eight weeks after the third vaccine dose. Standard dose i.m. and low-dose ID administration of recombinant hepatitis B vaccine produced comparable rates of anti-HBs equal to or higher than 10 mIU ml-1 in infants (98% and 94%, respectively) and preschool children (98% and 100%, respectively). Although i.m. vaccination produced higher anti-HBs concentrations than ID vaccination both in infants (geometric mean titre-GMT, 935 versus 621 mIU ml-1) and preschool children (GMT, 1393 versus 804 mIU ml-1), the differences were not statistically significant (p > 0.05). The preschool children tended to have higher anti-HBs concentrations than the infants. No clinically serious adverse effects were observed in both vaccine groups; however, induration and hyperpigmentation at the injection site were more often seen in the study population that was vaccinated intradermally. We conclude that intradermal administration of 2 micrograms recombinant hepatitis B vaccine is safe and effective in infants and preschool children, and may be an acceptable, less expensive alternative to full-dose i.m. vaccination for mass immunization, especially in developing countries.


Assuntos
Vacinas contra Hepatite B/administração & dosagem , Vacinas Sintéticas/administração & dosagem , Criança , Pré-Escolar , Relação Dose-Resposta a Droga , Feminino , Antígenos de Superfície da Hepatite B/sangue , Vacinas contra Hepatite B/imunologia , Humanos , Lactente , Injeções Intradérmicas , Injeções Intramusculares , Masculino , Vacinas Sintéticas/imunologia
16.
Turk J Pediatr ; 40(1): 89-95, 1998.
Artigo em Inglês | MEDLINE | ID: mdl-9673534

RESUMO

Removal of white blood cells (WBCs) from blood components before transfusion by filters with at least 3 log10 depletion may prevent or delay leukocyte-associated transfusion reactions such as HLA alloimmunization, non-hemolytic febrile reactions, transmitted infections (e.g., CMV, HTLV-1), and immunomodulation. The aim of this study was to compare the leukocyte removal efficiency (LRE) of six commercial bedside filters that are said to achieve 3 log10 (Bio R-01), Leucostop 4LT-1, Pall RC 50) and 4 log10 (Bio R-01 Plus, Pall RC 400, Pall RC XL-1) WBC depletion. A total of 430 units of whole blood ranging from 32 to 92 for each filter type were analyzed by an automated counter before and after filtration. Postfiltration blood samples were also evaluated for WBCs by Nageotte chamber. All the filters demonstrated leukocyte removal about 1 log10 less than the manufacturer's claim. The fourth generation filters showed a better performance than the third generation filters. Of them, Pall RC XL-1 showed the best efficacy with 99.93 percent leukocyte removal and a median residual WBCs of 1.6 x 10(6) per unit. These results indicate that the fourth generation filters, which are designed for the filtration of packed red cells, in particular Pall RC XL-1, are also able to reduce WBCs from whole blood below the critical antigenic leukocyte load (5 x 10(6)), and can be efficiently used for polytransfused patients to prevent alloimmunization.


Assuntos
Filtração/instrumentação , Leucaférese/instrumentação , Incompatibilidade de Grupos Sanguíneos/etiologia , Incompatibilidade de Grupos Sanguíneos/prevenção & controle , Desenho de Equipamento , Estudos de Avaliação como Assunto , Humanos , Contagem de Leucócitos
17.
Turk J Pediatr ; 40(2): 201-9, 1998.
Artigo em Inglês | MEDLINE | ID: mdl-9677725

RESUMO

Left ventricular filling patterns were assessed by Doppler echocardiography in 63 beta-thalassemia major patients, aged for to 21 years, with no clinical evidence of congestive heart failure and 63 age- and sex-matched normal controls. The patients with beta-thalassemia major were divided into three age groups, namely four to nine years (6.8 +/- 1.5 years), 10-15 years (12.1 +/- 1.6 years) and older than 15 years (17.3 +/- 1.7 years). They were compared with age- and sex-matched normal controls in respects of Doppler diastolic indices. The ratio between the early and late (atrial) peaks of flow velocity was higher and peak flow velocity in late diastole was significantly lower in patients with beta-thalassemia major as compared to controls in all three age groups (p < .001). As compared with the controls, peak early diastolic flow velocity was also significantly higher in the thalassemics aged 10 to 15 years (92 +/- 16 vs 80 +/- 12 cm/s, P < .01) and in those older than 15 years (95 +/- 16 vs 79 +/- 13 cm/s, p < .001). Restrictive left ventricular diastolic abnormalities were detected in a total of 34 (54%) patients with beta-thalassemia major, whereas left ventricular systolic abnormalities were identified only eight (13%) of them. None of the patients without left ventricular diastolic abnormalities showed left ventricular systolic abnormalities. There was not any significant correlation between the hematologic parameters, such as mean serum ferritin, maximum serum ferritin and the number of blood units transfused, and left ventricular Doppler diastolic indices (p > .05). From the data presented here, we therefore conclude that left ventricular diastolic abnormalities develop in patients with beta-thalassemia major in the early phase of the disease and before the appearance of systolic abnormalities, when clinical symptoms of congestive heart failure are absent.


Assuntos
Disfunção Ventricular Esquerda/diagnóstico por imagem , Disfunção Ventricular Esquerda/etiologia , Talassemia beta/complicações , Adolescente , Velocidade do Fluxo Sanguíneo , Transfusão de Sangue , Estudos de Casos e Controles , Criança , Pré-Escolar , Diástole , Ecocardiografia Doppler , Feminino , Ferritinas/sangue , Hemoglobinas/análise , Humanos , Masculino , Disfunção Ventricular Esquerda/fisiopatologia , Talassemia beta/sangue , Talassemia beta/terapia
18.
Paediatr Perinat Epidemiol ; 12(2): 176-81, 1998 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-9620567

RESUMO

In children, the treatment of acute diarrhoea with the World Health Organization (WHO) standard oral rehydration solution (ORS) provides effective rehydration but does not reduce the severity of diarrhoea. In community practice, carob bean has been used to treat diarrhoeal diseases in Anatolia since ancient times. In order to test clinical antidiarrhoeal effects of carob bean juice (CBJ), 80 children, aged 4-48 months, who were admitted to SSK Tepecik Teaching Hospital with acute diarrhoea and mild or moderate dehydration, were randomly assigned to receive treatment with either standard WHO ORS alone or a combination of standard WHO ORS and CBJ. Three patients were excluded from the study because of excessive vomiting. In the children receiving ORS + CBJ the duration of diarrhoea was shortened by 45%, stool output was reduced by 44% and ORS requirement was decreased by 38% compared with children receiving ORS alone. Weight gain was similar in the two groups at 24 h after the initiation of the study. Hypernatraemia was detected in three patients in the ORS group but in none of those in the ORS + CBJ group. The use of CBJ in combination with ORS did not lead to any clinical metabolic problem. We therefore conclude that CBJ may have a role in the treatment of children's diarrhoea after it has been technologically processed, and that further studies would be justified.


Assuntos
Antidiarreicos/uso terapêutico , Diarreia/terapia , Fabaceae , Plantas Medicinais , Polissacarídeos/uso terapêutico , Soluções para Reidratação/normas , Doença Aguda , Distribuição de Qui-Quadrado , Pré-Escolar , Desidratação/terapia , Fabaceae/uso terapêutico , Feminino , Galactanos , Humanos , Hipernatremia/etiologia , Hipernatremia/prevenção & controle , Lactente , Masculino , Mananas , Medicina Tradicional , Fitoterapia , Gomas Vegetais , Soluções para Reidratação/efeitos adversos , Resultado do Tratamento , Turquia , Equilíbrio Hidroeletrolítico/efeitos dos fármacos
19.
Acta Paediatr Jpn ; 39(2): 215-7, 1997 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-9141257

RESUMO

Two hundred and twenty-four children aged 6 months to 5 years, with rectal temperatures greater than or equal to 30 degrees (104 degrees F), were randomly treated with sponging alone or with medication including a single oral dose of aspirin 15 mg/kg, or paracetamol 15 mg/kg, or ibuprofen 8 mg/kg. Twenty-three children were excluded from the final analysis because they did not complete the study. Demographic characteristics of the patients were found to be comparable in all groups. Rectal temperatures were recorded every 30 min for a 3 h period. During the first 30 min of intervention, sponging was found to be more effective than all of the three medications. After 60 min, the effects of each medication became superior to sponging with tepid water in reducing body temperature. Twenty-three children were excluded from the final analysis because they did not complete the study. Comparing the effect of the three different medications, it was seen that the antipyretic efficacy of aspirin and ibuprofen were significantly more than paracetamol 3 h after intervention (P < 0.05). For the management of fever over 39 degrees C, it is therefore recommended to give children an antipyretic drug, preferably ibuprofen, and at the same time to begin sponging to provide a rapid and sustained antipyresis


Assuntos
Analgésicos não Narcóticos/uso terapêutico , Banhos , Febre/terapia , Acetaminofen/uso terapêutico , Aspirina/uso terapêutico , Pré-Escolar , Feminino , Humanos , Ibuprofeno/uso terapêutico , Lactente , Masculino , Temperatura , Resultado do Tratamento , Água
20.
Acta Paediatr Jpn ; 39(1): 34-6, 1997 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-9124050

RESUMO

In the present study, the risk of exposure to aflatoxin in infants fed breast milk and formula was investigated. For this purpose, aflatoxin B1 (AFB1) was determined in the serum of both breast-fed and formula-fed infants. Serum AFB1 positivity was significantly higher in the formula-feeding (F) group than the breast-feeding (B) group (42.8 vs 8.5%, P < 0.01). The AFB1 concentration in different commercial formulas was also determined. Aflatoxin B1 was found in seven of the eight newly opened packages of different brands of formula. The concentrations showed a statistically significant increase at the 30th day after opening the packages (P < 0.01). Although AFB1 concentrations in the formulas were found to be within acceptable limits for most countries, still, its existence must be carefully evaluated because future influences of very small amounts of aflatoxin on the growing organism have not been fully elucidated. Therefore, it was again concluded that for infants, human milk is safer than commercial formulas because of the lower contamination risk of aflatoxin. Also, commercial formulas must be regularly examined by authorities for the possible risk of aflatoxin contamination.


Assuntos
Aflatoxina B1/sangue , Aleitamento Materno , Alimentos Infantis/análise , Feminino , Humanos , Lactente , Masculino , Estudos Prospectivos
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