[Effectiveness and safety of biological therapy in patients with severe asthma in a real clinical practice].
Humans
Asthma
/ drug therapy
Male
Female
Middle Aged
Adult
Antibodies, Monoclonal, Humanized
/ administration & dosage
Anti-Asthmatic Agents
/ administration & dosage
Severity of Illness Index
Quality of Life
Respiratory Function Tests
/ methods
Treatment Outcome
Aged
Biological Therapy
/ methods
Young Adult
Adolescent
biological therapy
real clinical practice
severe asthma
Journal
Terapevticheskii arkhiv
ISSN: 0040-3660
Titre abrégé: Ter Arkh
Pays: Russia (Federation)
ID NLM: 2984818R
Informations de publication
Date de publication:
16 Apr 2024
16 Apr 2024
Historique:
received:
01
08
2022
accepted:
30
03
2024
medline:
7
5
2024
pubmed:
7
5
2024
entrez:
7
5
2024
Statut:
epublish
Résumé
To assess effectiveness and safety of biological therapy in patients with severe asthma during 5 yr follow-up. We recruited 129 adult outpatients (29% males) aged 18-81 yrs with severe asthma were followed up during 5 yrs and were examined for every 3-6 months. Eighty five patients were treated by conventional therapy (ICS/LABA ± tiotropium, montelukast, OCS) only and 44 pts additionally received biologicals (оmalizumab - 9 pts, мepolizumab - 8 pts, benralizumab - 11 pts, dupilumab - 16 pts). Pulmonary function tests were measured by dry spirometer (2120, Vitalograph Ltd., UK). Eosinophil count in blood was assessed by automatic haemoanalyser. Fraction of exhaled nitric oxide was measured by a chemiluminescence analyzer (LR4100; Logan Research, UK). Asthma control and quality of life were assessed by using Russian versions of ACQ-5 and SGRQ. The use of biologicals led to a more significant reduction of exacerbations and OCS use, improvement of lung function, asthma control and quality of life, decrease of eosinophil and fraction of exhaled nitric oxide than conventional therapy of severe asthma ( Long-term use of biologicals added to conventional therapy in patients with severe asthma is characterized by high effectiveness and favorable safety profile. Цель. Провести оценку эффективности и безопасности препаратов моноклональных антител у пациентов с тяжелой бронхиальной астмой (ТБА) в пятилетнем проспективном наблюдении. Материалы и методы. Всего 129 взрослых амбулаторных пациентов (мужчин 29%) с ТБА в возрасте от 18 до 81 года обследованы в течение 5 лет с интервалами 3–6 мес. Стандартную терапию (ингаляционные глюкокортикостероиды / длительно действующие b
Autres résumés
Type: Publisher
(rus)
Цель. Провести оценку эффективности и безопасности препаратов моноклональных антител у пациентов с тяжелой бронхиальной астмой (ТБА) в пятилетнем проспективном наблюдении. Материалы и методы. Всего 129 взрослых амбулаторных пациентов (мужчин 29%) с ТБА в возрасте от 18 до 81 года обследованы в течение 5 лет с интервалами 3–6 мес. Стандартную терапию (ингаляционные глюкокортикостероиды / длительно действующие b
Identifiants
pubmed: 38713038
doi: 10.26442/00403660.2024.03.202626
doi:
Substances chimiques
Antibodies, Monoclonal, Humanized
0
Anti-Asthmatic Agents
0
dupilumab
420K487FSG
benralizumab
71492GE1FX
mepolizumab
90Z2UF0E52
Types de publication
English Abstract
Journal Article
Langues
rus
Sous-ensembles de citation
IM