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1.
Tuberk Toraks ; 56(3): 310-4, 2008.
Artículo en Turco | MEDLINE | ID: mdl-18932033

RESUMEN

Mycoplasma pneumoniae infection is usually mild course and self-limited. Parapneumonic effusion is not a common feature of M. pneumoniae. The treatment of parapneumonic effusion is macrolides and chest tube with adequate pleural drainage. We report here on a child with M. pneumoniae infection complicated by massive parapneumonic effusion. Protracted course of fever and respiratory distress was noted in patient. Pneumothorax was occurred subsequent to chest tube drainage.


Asunto(s)
Macrólidos/uso terapéutico , Mycoplasma pneumoniae/aislamiento & purificación , Derrame Pleural/etiología , Neumonía por Mycoplasma/complicaciones , Neumotórax/etiología , Tubos Torácicos , Niño , Drenaje , Femenino , Humanos , Derrame Pleural/epidemiología , Derrame Pleural/terapia , Neumonía por Mycoplasma/diagnóstico , Neumonía por Mycoplasma/terapia , Neumotórax/epidemiología
2.
Can J Gastroenterol Hepatol ; 2017: 8130596, 2017.
Artículo en Inglés | MEDLINE | ID: mdl-28656129

RESUMEN

AIM: The aim of this study is to evaluate the effects of the synbiotic Bifidobacterium lactis B94 plus inulin addition to the standard triple therapy on Helicobacter pylori (H. pylori) infection eradication rates. METHODS: Children aged 6-16 years who had biopsy proven H. pylori infection were randomly classified into two groups. The first group received the standard triple therapy consisting of amoxicillin + clarithromycin + omeprazole. The second group was treated with the standard triple therapy and Bifidobacterium lactis B94 (5 × 109 CFU/dose) plus inulin (900 mg) for 14 days, concurrently. Eradication was determined by 14C-urea breath test 4-6 weeks after therapy discontinuation. RESULTS: From a total of 69 H. pylori infected children (F/M = 36/33; mean ± SD = 11.2 ± 3.0 years), eradication was achieved in 20/34 participants in the standard therapy group and 27/35 participants in the synbiotic group. The eradication rates were not significantly different between the standard therapy and the synbiotic groups [intent-to-treat, 58.8% and 77.1%, resp., p = 0.16; per-protocol, 64.5% and 81.8%, resp., p = 0.19]. There was no difference between the groups in terms of symptom relief (p = 0.193). The reported side effects were ignorable. CONCLUSION: Considering the eradication rates, synbiotic addition to therapy showed no superiority over the standard triple therapy conducted alone. This trial is registered with NCT03165253.


Asunto(s)
Antibacterianos/administración & dosificación , Infecciones por Helicobacter/tratamiento farmacológico , Helicobacter pylori/efectos de los fármacos , Inulina/administración & dosificación , Simbióticos/administración & dosificación , Adolescente , Amoxicilina/administración & dosificación , Bifidobacterium animalis , Pruebas Respiratorias , Niño , Claritromicina/administración & dosificación , Método Doble Ciego , Quimioterapia Combinada , Femenino , Infecciones por Helicobacter/microbiología , Humanos , Análisis de Intención de Tratar , Masculino , Omeprazol/administración & dosificación , Resultado del Tratamiento
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