Effectiveness and safety of levocetirizine 10 mg versus a combination of levocetirizine 5 mg and montelukast 10 mg in chronic urticaria resistant to levocetirizine 5 mg: A double-blind, randomized, controlled trial

Indian J Dermatol Venereol Leprol. 2017 Sep-Oct;83(5):561-568. doi: 10.4103/ijdvl.IJDVL_551_16.

Abstract

Background: Chronic urticaria is a vexing problem for patients and treating physicians alike. The EAACI/GA[2]LEN/EDF/WAO guidelines advocate an increased antihistamine dosage up to four times the standard, before adding leukotriene receptor antagonists. Patients are frequently intolerant of these higher dosages. We conducted this study to determine whether the addition of leukotriene receptor antagonists to the standard antihistamine dose was comparable to higher dosages of antihistamines alone, in terms of efficacy, safety and quality of life changes. We compared levocetirizine 10 mg (double dose of standard) versus a combination of levocetirizine 5 mg and montelukast 10 mg in cases of chronic urticaria not responding to single daily dose of 5 mg levocetirizine.

Methods: A single-center, double-blind, randomized, active-controlled, parallel group phase IV trial (CTRI/2014/12/005261) was conducted on 120 patients of chronic urticaria of either sex not responding to 5 mg levocetirizine. Patients were randomized into receiving either levocetirizine 10 mg or levocetirizine 5 mg + montelukast 10 mg for 4 weeks. Primary outcome measures were Urticaria Activity Score (UAS) and Urticaria Total Severity Score (TSS). Routine hematological and biochemical tests and treatment-emergent adverse events were monitored for safety.

Results: Fifty-two patients on levocetirizine 10 mg group and 51 patients on levocetirizine 5 mg + montelukast 10 mg group were analyzed. UAS and TSS reduced significantly in both treatment groups and reduction of score were comparable in between the groups (P = 0.628, P = 0.824, respectively). Among adverse effects, sedation was noted significantly more (P = 0.013) in levocetirizine 10 mg group. Quality of life was significantly improved in levocetirizine 5 mg + montelukast 10 mg group (P = 0.031).

Limitations: The limitation of the study was that the follow-up period was 4 weeks.

Conclusion: EAACI/GA[2]LEN/EDF/WAO guidelines need to be more flexible in allowing usage of montelukast before escalation of anti-histamine dosage.

Publication types

  • Comparative Study
  • Randomized Controlled Trial

MeSH terms

  • Acetates / administration & dosage*
  • Acetates / adverse effects
  • Adolescent
  • Adult
  • Aged
  • Cetirizine / administration & dosage*
  • Cetirizine / adverse effects
  • Chronic Disease
  • Cyclopropanes
  • Double-Blind Method
  • Drug Resistance / drug effects
  • Drug Resistance / immunology
  • Drug Therapy, Combination
  • Female
  • Follow-Up Studies
  • Histamine H1 Antagonists, Non-Sedating / administration & dosage
  • Histamine H1 Antagonists, Non-Sedating / adverse effects
  • Humans
  • Hypnotics and Sedatives / administration & dosage
  • Hypnotics and Sedatives / adverse effects
  • Leukotriene Antagonists / administration & dosage
  • Leukotriene Antagonists / adverse effects
  • Male
  • Middle Aged
  • Quinolines / administration & dosage*
  • Quinolines / adverse effects
  • Sulfides
  • Treatment Outcome
  • Urticaria / diagnosis*
  • Urticaria / drug therapy*
  • Urticaria / immunology
  • Young Adult

Substances

  • Acetates
  • Cyclopropanes
  • Histamine H1 Antagonists, Non-Sedating
  • Hypnotics and Sedatives
  • Leukotriene Antagonists
  • Quinolines
  • Sulfides
  • levocetirizine
  • montelukast
  • Cetirizine