IP Indian Journal of Clinical and Experimental Dermatology 5 (2019) 261–263
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IP Indian Journal of Clinical and Experimental Dermatology
Journal homepage: www.innovativepublication.com
Short Communication
Bilastine in higher doses in chronic spontaneous urticaria
Kiran Godse
1,
*, Gauri Godse
1
1
Dept. of Skin, Shree Skin Centre Nerul, Navi Mumbai, Maharashtra, India
ARTICLE INFO
Article history:
Received 31-05-2019
Accepted 04-09-2019
Available online 14-09-2019
Keywords:
Bilastine
Chronic spontaneous urticaria
Efficacy
ABSTRACT
Objective: To evaluate efficacy and safety of bilastine in higher than usual doses in patients with chronic
spontaneous urticaria (CSU).
Material and Methods: Adult patients with CSU with pruritus and wheal score of more than two
were investigated for complete blood count, urine examination, blood sugar level and thyroid-stimulating
hormone level and treated with bilastine 20 mg (one tablet) before breakfast. In patients who did not show
satisfactory response, dose was increased to 40 mg (two tablets) before breakfast at the end of one week
and 80 mg (two divided doses) at the end of two weeks, if no response seen after the end of one week.
Symptoms were evaluated using urticaria activity score (UAS) and sedation score.
Results: A total of 30 patients (mean age 30.5 years; 56.67% females; baseline mean UAS 5.2) with mean
duration of CSU of 18.9 months were enrolled. Fourteen (51.85%), 10(37.04%) and 2(7.41%) patients
became symptom-free with 20,40, and 80 mg dose of bilastine respectively whereas 1(3.70%) patient not
responding to 80 mg bilastine required cyclosporine. After 1 week of treatment, 3 patients were lost to
follow up. Bilastine was well tolerated without any serious adverse events.
Conclusion: Bilastine is effective and well tolerated in higher (up to 4 times) than normal doses in the
management of chronic spontaneous urticaria.
© 2019 Published by Innovative Publication.
1. Introduction
Chronic spontaneous urticaria is a common dermatological
condition. Although it is not a life threatening condition,
patients suffering from this condition report significant
impairment in the quality of life.
1
Several mediators
are involved in the pathogenesis of allergic conditions.
Out of these, histamine is an important mediator in
pathophysiological course of allergic reactions including
allergic rhinitis and urticaria. Because of the central role
of histamine, antihistamines are considered as the mainstay
of treatment in patients with chronic urticaria. Among the
available antihistamines, first generation agents because of
their potential to cross blood brain barrier are associated
with adverse events related to central nervous system
especially sedation. Second-generation H-1 antihistamines
score over their first generation counterparts in this regards.
Considering the advantages, current clinical guidelines
* Corresponding author.
E-mail address: kvg402@gmail.com (K. Godse).
recommend second-generation H1- antihistamines as initial
treatment of chronic urticaria.
2
Although many second
generation antihistamines are available in the market, each
has its own advantages and limitations. Bilastine is a
new addition to the list of available agents with promising
profile.
Bilastine is a potent and specific H1-antihistamine with
quick onset and long duration of action with good response
in the treatment of chronic spontaneous urticaria (CSU).
3
Moreover, it has several clinical advantages because of its
pharmacological profile which make it suitable for use in
CSU. Bilastine is not associated with risk of cardiotoxicity.
Similarly, it does not interact with cytochrome P450
resulting in very less risk of drug to drug interactions.
Dosage modification is not required in patients with renal
impairment. In a double blind clinical trial, bilastine 20
mg administered for 28 days has been shown to provide
significant reduction in clinical features and improved
patient quality of life in patients with chronic idiopathic
https://doi.org/10.18231/j.ijced.2019.056
2581-4710/© 2019 Published by Innovative Publication. 261