Hereditary angioedema. Clinical guidelines. (D84.1)

E. A. Bliznetz, Близнец Елена Александровна, E. A. Viktorova, Викторова Екатерина Андреевна,Elena Vishneva,Вишнева Елена Александровна,Eliso M. Dzhobava, Джобава Элисо Мурмановна, N I Ilina, Ильина Наталья Ивановна,N.B. Kuzmenko, Кузьменко Наталья Борисовна,Elena A. Latysheva,Латышева Елена Александровна,Tatiana V. Latysheva,Латышева Татьяна Васильевна,Irina A. Manto,Манто Ирина Александровна,Leyla Namazova-Baranova,Намазова-Баранова Лейла Сеймуровна, Natalia M. Nenasheva,Ненашева Наталья Михайловна, A.N. Pampura, Пампура Александр Николаевич,Aleksander V. Polyakov,Поляков Александр Владимирович, L Selimzianova, Селимзянова Лилия Робертовна,Anna Shcherbina, Щербина Анна Юрьевна

Rossijskij allergologičeskij žurnal(2021)

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摘要
Hereditary angioedema is a rare, potentially life-threatening genetic disease that manifests with skin and mucous/submucosal swelling that occurs under the influence of bradykinin. The clinical guidelines for hereditary angioedema (code for the International Statistical Classification of Diseases and Related Health Problems D84.1) were developed in December 2020 by the Russian Association of Allergology and Clinical Immunology, Association of Medical Geneticists, National Association of Experts in the Field of Primary Immunodeficiencies, Union of Pediatricians of Russia. In December 2020, the project was approved at a meeting of the Scientific and Practical Council of the Ministry of Health of the Russian Federation (December 10, 2020 No. 743/12). The clinical guidelines are devoted to optimizing the clinical care of patients with hereditary angioedema. The topic is relevant owing to the under-diagnosis of hereditary angioedema and insufficient awareness of doctors of various specialties about this problem, as well as the difficulties in managing this category of patients. The clinical guidelines contain information about the epidemiology, etiology, classification, pathogenesis, and common clinical manifestations of hereditary angioedema. Thus, the paper described actual diagnostic approaches and differential diagnosis of hereditary angioedema and established its diagnostic criteria. Medical care algorithms to patients with hereditary angioedema at the prehospital and hospital stages are also described. The principles of pharmacotherapy, including long-term prophylaxis, short-term prophylaxis, and acute therapy, for hereditary angioedema are also presented. Treatment regimens are stratified according to patients’ age and gender. Non-drug measures for the prevention hereditary angioedema attacks are considered. Sections were also added in the edition of the new clinical guidelines of hereditary angioedema. Clinical guidelines for hereditary angioedema are intended for practicing doctors of all specialties, students and teachers of medical universities, residents, graduate students of medical universities.
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