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Medicinas Complementares
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1.
Pediatr Int ; 63(7): 813-817, 2021 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-33045763

RESUMO

BACKGROUND: Hemorrhoids are an extremely rare condition in children, and data on its incidence and treatment in the pediatric population remains scarce. We retrospectively reviewed children who underwent sclerotherapy for internal hemorrhoids, and analyzed patients' characteristics and outcomes. METHODS: A total of 14 pediatric patients who underwent sclerotherapy were included. Patients' ages and the required amount of polidocanol, depending on the grade of hemorrhoids, and the correlation between age and volume of sclerosant, were statistically analyzed. RESULTS: Patients had a male predominance with a ratio of 2.5:1 (grade 2:6 patients, grade 3:8 patients). Four children had underlying conditions including portal hypertension and Klippel-Trenaunay syndrome. Of the 14 patients, 43% had constipation requiring medication or enema. Only one minor complication, a perianal ulceration, was found to be associated with sclerotherapy. Patients with grade 3 hemorrhoids required a significantly larger amount of polidocanol than those with grade 2 hemorrhoids. Two patients with grade 3 hemorrhoids required a second session of treatment for recurrence. The success rate of sclerotherapy with polidocanol was 86%. CONCLUSIONS: Sclerotherapy with polidocanol is a safe, effective, and less invasive treatment option for internal hemorrhoids in children. Further studies are needed to investigate this treatment approach.


Assuntos
Hemorroidas , Escleroterapia , Criança , Hemorroidas/tratamento farmacológico , Humanos , Masculino , Polidocanol , Polietilenoglicóis/efeitos adversos , Estudos Retrospectivos , Soluções Esclerosantes/uso terapêutico , Escleroterapia/efeitos adversos , Resultado do Tratamento
2.
Pediatr Int ; 59(4): 515-518, 2017 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-28401746

RESUMO

Neonates with Down syndrome are at risk of developing transient abnormal myelopoiesis (TAM), which is characterized by transient clonal myeloproliferation of the blast cells. TAM can resolve spontaneously, but some patients die at an early age due to organ failure. Liver fibrosis in TAM is a life-threatening condition, but treatment options have not yet been established. Here, we report on the case of an infant with TAM complicated by liver disease, whose hyperbilirubinemia was successfully ameliorated with omega-3 fatty acid (ω3FA) lipid emulsion. Timely ω3FA lipid emulsion may be a feasible treatment for liver disease in TAM before serious liver damage develops.


Assuntos
Síndrome de Down/complicações , Emulsões Gordurosas Intravenosas/uso terapêutico , Ácidos Graxos Ômega-3/uso terapêutico , Reação Leucemoide/complicações , Cirrose Hepática/terapia , Síndrome de Down/diagnóstico , Feminino , Humanos , Recém-Nascido , Reação Leucemoide/diagnóstico , Cirrose Hepática/diagnóstico , Cirrose Hepática/etiologia
3.
J Vet Med Sci ; 78(6): 951-6, 2016 Jul 01.
Artigo em Inglês | MEDLINE | ID: mdl-26902544

RESUMO

Currently, from the viewpoint of animal welfare, anesthesia or analgesia is required during experimental procedures in animals that are likely to cause pain. A part of these anesthetics have been reported to influence a blood biochemical level. It is important for us to understand the effect of the anesthetic on blood biochemistry when we choose the anesthetic agent to be used in experiments. In this study, we examined the blood biochemical changes in mice after administration of a new mixture of three anesthetic agents -medetomidine / midazolam / butorphanol (MMB). We subcutaneously administered two dose combinations of MMB (0.45 / 6 / 7.5 and 0.9 / 12 / 15 mg/kg) in mice, followed by administration of atipamezole, for reversal of anesthetic effects, after 1 hr. Thereafter, blood biochemistry was assessed at 1, 4 and 24 hr after MMB administration. We observed that MMB administration caused a transient increase in blood sugar, inorganic phosphorus, potassium and creatine kinase levels. These, however, returned to the reference range 24 hr after MMB administration. In conclusion, MMB changes the levels of some blood biochemical parameters, but not to an extent that would threaten health. However, when using laboratory animals, this effect of MMB may influence the experimental results, depending on the experimental content. Hence, the choice of anesthetic agents used in laboratory animals should be based on detailed knowledge of their pharmacological effects.


Assuntos
Anestésicos Combinados/farmacologia , Butorfanol/farmacologia , Medetomidina/farmacologia , Midazolam/farmacologia , Anestesia/veterinária , Anestésicos Combinados/administração & dosagem , Animais , Glicemia/análise , Butorfanol/administração & dosagem , Creatina Quinase/sangue , Masculino , Medetomidina/administração & dosagem , Camundongos , Camundongos Endogâmicos C57BL , Midazolam/administração & dosagem , Fósforo/sangue , Potássio/sangue
4.
Pediatr Int ; 55(4): e93-5, 2013 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-23910816

RESUMO

Milk curd syndrome was first reported in the 1960s, but was gradually forgotten because of its low incidence thereafter. This condition in pre-term infants has been reported over the last decade and has again attracted neonatologists' attention. The present report describes a pre-term infant with milk curd syndrome. Abdominal distension was evident 14 days after the start of feeding with fortified expressed milk. Abdominal X-ray showed multiple intraluminal masses surrounded by a halo of air, and ultrasound indicated hyperechoic masses. Along with that history and the appearance of fecal impaction, the diagnosis of milk curd syndrome was confirmed. This baby was treated with olive oil enemas and successive colonic lavage for 3 days, and the symptoms were relieved. Olive oil enema, which softens hard stools and induces smooth movement of these stools, may be an effective and safe first-line treatment in pre-term infants with milk curd syndrome.


Assuntos
Doenças do Colo/terapia , Enema/métodos , Doenças do Prematuro/terapia , Obstrução Intestinal/terapia , Óleos de Plantas/administração & dosagem , Doenças do Colo/diagnóstico , Diagnóstico Diferencial , Humanos , Recém-Nascido , Recém-Nascido Prematuro , Doenças do Prematuro/diagnóstico , Obstrução Intestinal/diagnóstico , Masculino , Azeite de Oliva , Radiografia Abdominal , Síndrome
5.
J Diabetes Complications ; 22(5): 339-47, 2008.
Artigo em Inglês | MEDLINE | ID: mdl-18413164

RESUMO

AIMS: This study was conducted to evaluate the suitability of a new minipig model for investigating aspects of diabetes such as delayed gastric emptying and glucose metabolism abnormalities, and to test the effects of mitemcinal (GM-611), an orally active erythromycin-derived motilin receptor agonist, on gastric emptying and postprandial glucose in normal and diabetic minipigs. METHODS AND RESULTS: Intravenous injection of 300 mg/kg streptozotocin (STZ) to 5-week-old minipigs induced moderate hyperglycemia (about 200 mg/dl) for >80 weeks without insulin treatment. Decreased insulin production (P<.05), increased area under the glucose curve (P<.05), and slower glucose disappearance (P<.05) were demonstrated, and there was no severe inhibition of body weight gain, liver failure, or renal failure. Gastric emptying was significantly delayed in diabetic minipigs (P<.05) at 80 weeks, but not at 40 weeks, post-STZ. Oral administration of mitemcinal (5 mg/kg) at 80 weeks accelerated gastric emptying and induced a similar postprandial glucose profile in normal and diabetic minipigs with delayed gastric emptying. CONCLUSIONS: The new diabetic minipig model showed suitability for investigating diabetes, gastric emptying, and plasma glucose excursions. Since delayed gastric emptying and irregular plasma glucose excursions are characteristic of diabetic gastroparesis, the accelerating and regulating effects of mitemcinal on this model add to the existing evidence that mitemcinal is likely to be useful for treating diabetic gastroparesis.


Assuntos
Glicemia/efeitos dos fármacos , Diabetes Mellitus Experimental/complicações , Eritromicina/análogos & derivados , Esvaziamento Gástrico/efeitos dos fármacos , Gastroparesia/tratamento farmacológico , Período Pós-Prandial/efeitos dos fármacos , Administração Oral , Animais , Diabetes Mellitus Experimental/induzido quimicamente , Diabetes Mellitus Experimental/tratamento farmacológico , Diabetes Mellitus Experimental/fisiopatologia , Avaliação Pré-Clínica de Medicamentos , Eritromicina/administração & dosagem , Eritromicina/farmacologia , Eritromicina/uso terapêutico , Esvaziamento Gástrico/fisiologia , Fármacos Gastrointestinais/administração & dosagem , Fármacos Gastrointestinais/farmacologia , Fármacos Gastrointestinais/uso terapêutico , Gastroparesia/induzido quimicamente , Gastroparesia/fisiopatologia , Ilhotas Pancreáticas/efeitos dos fármacos , Ilhotas Pancreáticas/fisiopatologia , Rim/efeitos dos fármacos , Rim/fisiopatologia , Fígado/efeitos dos fármacos , Fígado/fisiopatologia , Masculino , Período Pós-Prandial/fisiologia , Estreptozocina , Suínos , Porco Miniatura
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