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H1-antihistamines

H1 antihistaminico Rinitis Alergica

Leukotriene Receptor Antagonist Addition to H1-Antihistamine Is Effective for Treating Allergic Rhinitis: A Systematic Review and Meta-analysis

By Selected articles

Seresirikachorn K, Chitsuthipakorn W, Kanjanawasee D, Khattiyawittayakun L, Snidvongs K.

Histamine and leukotriene are released after being triggered by allergen exposure. The combination of leukotriene receptor antagonist (LTRA) and H1-antihistamine (AH) is utilized to control the allergic rhinitis (AR) symptoms after the failure of either AH or LTRA.

For controlling rhinoconjunctivitis symptoms in patients with AR, AH-LTRA provided greater beneficial effects on composite nasal symptoms, rhinorrhea, and sneezing compared to AH alone. These effects were shown in patients with perennial AR.

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Rinitis Alérgica

Is Quantitative sIgE Serology Suitable for Distinguishing Between Silent Sensitization and Allergic Rhinitis to Dermatophagoides pteronyssinus?

By Selected articles

Gellrich D, Högerle C, Becker S, Gröger M.

Objective: Our study aimed to analyze the concordance between a nasal provocation test with Dermatophagoides pteronyssinus and specific IgE measurements based on real-life data.

Despite the high correlation between sIgE levels and symptoms, no serologic parameter is sufficiently accurate to distinguish between silent sensitization and clinically relevant allergy. Therefore, nasal provocation tests remain the gold standard for assessing clinical relevance in sensitization to D pteronyssinus.

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H1 antihistaminico Rinitis Alergica

Leukotriene Receptor Antagonist Addition to H1-Antihistamine Is Effective for Treating Allergic Rhinitis: A Systematic Review and Meta-analysis

By Selected articles

Seresirikachorn K, Chitsuthipakorn W, Kanjanawasee D, Khattiyawittayakun L, Snidvongs K.

Histamine and leukotriene are released after being triggered by allergen exposure. The combination of leukotriene receptor antagonist (LTRA) and H1-antihistamine (AH) is utilized to control the allergic rhinitis (AR) symptoms after the failure of either AH or LTRA.

For controlling rhinoconjunctivitis symptoms in patients with AR, AH-LTRA provided greater beneficial effects on composite nasal symptoms, rhinorrhea, and sneezing compared to AH alone. These effects were shown in patients with perennial AR.

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Efficacy and safety of bilastine in reducing pruritus in patients with chronic spontaneous urticaria and other skin diseases: an exploratory study

By Articles about Bilastine

Esther Serra, Cristina Campo, Zoltan Novák, Bernardetta Majorek-Olechowska, G Pulka, Aintzane García-Bea & Luis Labeaga (2019)

Journal of Dermatological Treatment

An exploratory, international and multicenter study to evaluate the efficacy of bilastine in the relief of pruritus associated with urticaria and other skin diseases was performed in patients diagnosed of Chronic Spontaneous Urticaria (CSU), eczema/dermatitis, prurigo or cutaneous pruritus.

The first 2 weeks, they were treated with bilastine 20 mg daily. The daily pruritus severity score was assessed. Responders patients stayed on this treatment for the remaining 6 weeks while non-responders were updosed to 40 mg.

The mean change in weekly pruritus severity score from baseline to week 8 was -1.63 ± 0.77 for all patients (p<0.001). The mean change per group was: CSU (-2.1 ± 0.44), cutaneous pruritus (-1.66 ± 0.63), eczema/dermatitis (-1.36 ± 0.79) and prurigo (-1.30 ± 0.92) (all p-values <0.001).

Bilastine at 20 mg and 40 mg showed an excellent profile for both efficacy and safety in reducing pruritus in patients with CSU and other skin disorders.

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The Efficacy of a Two-Fold Increase of H1-Antihistamine in the Treatment of Chronic Urticaria – the Vietnamese Experience

By Selected articles

Thi HT, Thi LP, Van TN, et al..

Vietnamese investigators evaluated the efficacy of increased H1-antihistamine doses in people with chronic urticaria.

Chronic urticaria is a common, debilitating and hard to treat condition. H1-antihistamines are the first line treatment but frequently patients do not get satisfactory relief with the recommended dose. Antihistamine doses may be increased up to four-fold as recommended by European guidelines.

This experience included 102 participants with chronic urticaria who were divided in two groups and treated with 5 mg of levocetirizine or 180 mg of fexofenadine for two weeks, and then increased to 10 mg of levocetirizine or 360 mg of fexofenadine for two more weeks. Wheal, pruritus, size of the wheal, total symptom scores and associated side-effects were measured at beginning, week 2 and week 4.

With the conventional dose, total symptom scores decreased significantly at week 2 and 4 in both groups. However, 26 participants who did not improve at week 2, experienced a two-fold increase in dose, with 11,5% and 38,5% becoming symptom-free at week 4 in levocetirizine and fexofenadine group, respectively. None of the treatments had negative side effects between the conventional dose and the double one.

In conclusion, this study showed that increasing H1-antihistamines dosage by two-fold does not increase the rate of side effects while improving chronic urticaria symptoms.

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