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Infecțiile sistemului bronhopulmonar la copii cu imunodeficiențe primare

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dc.contributor.author Tomacinschii, Cristina
dc.contributor.author Șciuca, Svetlana
dc.date.accessioned 2022-11-14T12:51:42Z
dc.date.available 2022-11-14T12:51:42Z
dc.date.issued 2022
dc.identifier.citation TOMACINSCHII, Cristina, ȘCIUCA, Svetlana. Infecțiile sistemului bronhopulmonar la copii cu imunodeficiențe primare. In: Culegerea de lucrări a Conferinței Internaționale "Imunopedia": ed. 2, 9-10 septembrie/ Svetlana Șciuca, Alexis Cochino [et al]. Chişinău: s.n., 2022 (CEP Medicina), pp. 72-80. ISBN 978-9975-82-300-5. en_US
dc.identifier.isbn 978-9975-82-300-5
dc.identifier.uri http://repository.usmf.md/handle/20.500.12710/22525
dc.description.abstract Primary immunodeficiencies (PIDs) are genetic diseases of the immune system, with quantitative and/or qualitative defects of one or more of its components, being affected: the development, function, and/or morphology of the immune system. Respiratory manifestations in IDP are represented by a varied spectrum, representing the most frequent cause of morbidity (63-88%), but also of mortality (30-65%). Timely diagnosis and appropriate therapy can improve or at least slow down the progression of these complications Aim: Considering the increased frequency of infections among patients with primary immunodeficiencies, it was proposed to evaluate respiratory infections and pathogens involved in pediatric primary immunodeficiencies. Methods: 14 children with primary immunodeficiencies (42.8% with primary immunodeficiencies due to antibody deficiency and 57.2% with combined primary immunodeficiencies) were included in the study. The diagnosis of PID was confirmed by the evaluation of serum IgA, IgM, IgG by the ELISA method in the immunology laboratory of IMC Chisinau, the determination of lymphocytes and lymphocyte subpopulations by lymphocyte immunophenotyping, genetic research. The frequency of infections was determined by analysis of laboratory charts, and oropharyngeal smear 73 and sputum bacteriology and subsequent culture were performed to identify the pathogens involved. Results: In the studied group, pneumonia was present in 49.2% of patients with combined immunodeficiency, in the case of patients with humoral link damage, pneumonia was more common among those with variable common immunodeficiency (84%), hyperIgM (81%) and disease Bruton (62%). In their etiology, following the culture of sputum and oropharyngeal secretions, the following were determined: St. Aureus 38.4% (95%CI 13.8-68.4%); Str beta haemolytic 46.1% (95% CI 19.2-74.8%); Cl. Pneumoniae 30.7% (95%CI 9-61.4%); Str. Pyogenes 53.8% (95%CI 25.1-80.7%); Candida white. 38.4% (95%CI 13.8-68.4%); P. aeruginosa 15.3% (95%CI 1.9-45.4%); H. Influenzae 30.7% (95%CI 9-61.4%); Moraxella cath. 23.8% (95%CI 5-53.8%); P. jirovecii 7.6% (95%CI 0.1-36%); Respiratory infections in immunodeficient patients are usually severe, persistent, caused by unusual, atypical, or opportunistic microorganisms, and recurrent compared to infections in non-IPD patients. Conclusion: Primary immunodeficiencies are predominantly rare diseases with clinical and immunological polymorphism. Severe IDPs in children evolve with pulmonary infections with polyresistant and opportunistic germs, which determine major risks of unfavorable developments. Early diagnosis, preventive measures, and immunoglobulin replacement treatments reduce the risks of acquiring infections with polyresistant germs and improve the prognosis and quality of life of patients. en_US
dc.language.iso ro en_US
dc.publisher Universitatea de Stat de Medicină şi Farmacie "Nicolae Testemiţanu" din Republica Moldova en_US
dc.relation.ispartof Conferința Internațională "Imunopedia": ediția 2, 9-10 septembrie 2022, Chișinău en_US
dc.title Infecțiile sistemului bronhopulmonar la copii cu imunodeficiențe primare en_US
dc.title.alternative Infections of the bronchopulmonary system in children with primary immunodeficiency en_US
dc.type Article en_US


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