Why fexofenadine is considered as a truly non-sedating antihistamine with no brain penetration: a systematic review

被引:0
|
作者
Ansotegui, Ignacio J. [1 ]
Bousquet, Jean [2 ,3 ,4 ,5 ]
Canonica, Giorgio Walter [6 ,7 ]
Demolys, Pascal [8 ,9 ]
Gomez, Rene Maximiliano [10 ,11 ]
Meltzer, Eli O. [12 ]
Murrieta-Aguttes, Margarita [13 ]
Naclerio, Robert M. [14 ]
Rosario Filho, Nelson [15 ]
Scadding, Glenis K. [16 ,17 ]
机构
[1] Hosp Quironsalud Bizkaia, Dept Allergy & Immunol, Bilbao, Spain
[2] Charite Univ Med Berlin, Inst Allergol, Berlin, Germany
[3] Free Univ Berlin, Berlin, Germany
[4] Humboldt Univ, Berlin, Germany
[5] Humboldt Univ, Fraunhofer Inst Translat Med & Pharmacol ITMP, Allergol & Immunol, Berlin, Germany
[6] Human Univ, Personalized Med Asthma & Allergy Clin, Milan, Italy
[7] Human Res Hosp, Milan, Italy
[8] Montpellier Univ Hosp, Div Allergy, Dept Pulmonol, Montpellier, France
[9] Univ Montpellier, IDESP, INSERM, Montpellier, France
[10] Catholic Univ Salta, Sch Hlth Sci, Salta, Argentina
[11] Ayre Fdn, Alas Med Inst, Salta, Argentina
[12] Univ Calif San Diego, Dept Pediat, Div Allergy & Immunol, La Jolla, CA 92093 USA
[13] Sanofi, Neuilly Sur Seine, France
[14] Johns Hopkins Univ, Dept Otolaryngol Head & Neck Surg, Baltimore, MD USA
[15] Univ Fed Parana, Dept Pediat, Parana, PR, Brazil
[16] RNENT Hosp, London, England
[17] UCL, Dept Immun & Infect, London, England
关键词
Fexofenadine; antihistamines; sedation; drowsiness; non-drowsy; clinical trials; allergy; POSITRON-EMISSION-TOMOGRAPHY; HISTAMINE H-1-RECEPTOR OCCUPANCY; H-1 RECEPTOR OCCUPANCY; ORALLY-ADMINISTERED ANTIHISTAMINES; SEASONAL ALLERGIC RHINITIS; DOUBLE-BLIND; PSYCHOMOTOR FUNCTION; DRIVING PERFORMANCE; SEDATION SCALE; 180; MG;
D O I
10.1080/03007995.2024.2378172
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
ObjectiveFexofenadine is a second-generation inverse agonist of H1-receptor of histamine which is highly selective with proven efficacy in relieving symptoms associated with allergic conditions. It has an additional benefit of not penetrating the blood-brain barrier and therefore do not induce sedation and not impair the cognitive function/psychomotor performance. This review aimed at providing evidence based on available controlled studies to reinforce the non-sedative property of fexofenadine for treating patients with allergic rhinitis and urticaria.MethodsWe performed an electronic literature search using keywords such as fexofenadine, drowsiness, somnolence, sedation, fatigue, cognitive, impairment, psychomotor, driving performances, sleep, rapid eye movement, alertness, clinical study, in vitro study, in vivo study, and pharmacodynamics in the Embase search engine. The review included randomized controlled trials, review articles, systematic reviews, and meta-analyses, together with post-marketing analysis conducted in healthy subjects and patients with allergy and were focused on comparing the antihistaminic potential or safety of fexofenadine with other antihistamines or placebo.ResultsPositron emission tomography (PET) and proportional impairment ratio (PIR) data along with other objective tests from various studies confirmed the non-sedative property of fexofenadine. Results of brain H1-receptor occupancy (H1RO) obtained from PET showed no H1RO by fexofenadine, the receptor which is known to cause sedation of H1 antihistamines. Most studies calculating PIR value as 0 showed fexofenadine to be a non-impairing oral antihistamine regardless of dose. Clinical trials in adults and children showed fexofenadine to be well tolerated without sedative effect or impairment of cognitive/psychomotor function even at higher than recommended doses.ConclusionPublished literature based on various parameters and clinical trials conducted for evaluating the effect of fexofenadine on sedation and central nervous system shows fexofenadine is both clinically effective and non-sedating.
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页码:1297 / 1309
页数:13
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