Literature DB >> 14524731

Newer formulations of the triptans: advances in migraine management.

Jonathan Paul Gladstone1, Marek Gawel.   

Abstract

Migraine is a common, frequently incapacitating, headache disorder that imposes a substantial burden on both the individual patient and society. The last two decades have witnessed an explosion in our understanding of the pathophysiology of migraine, and in our development of an efficacious and diverse therapeutic armamentarium. There are several routes of drug administration available to patients with migraine. All the serotonin 5-HT(1B/1D) receptor agonists (triptans) are available as oral tablets (sumatriptan, rizatriptan, zolmitriptan, naratriptan, almotriptan, frovatriptan and eletriptan). Only sumatriptan is available as a subcutaneous injection. Some triptans are also available via newer routes of administration, including orally disintegrating tablets (rizatriptan and zolmitriptan), rectal suppositories (sumatriptan) and intranasal sprays (sumatriptan and zolmitriptan). Oral disintegrating tablets and other non-oral triptan routes (subcutaneous, intranasal, rectal) are a useful alternative to conventional oral tablets for patients who have difficulty swallowing pills or prefer not to do so, and for patients whose nausea and/or vomiting precludes swallowing tablets and/or makes the likelihood of complete absorption unpredictable. This is important because epidemiological studies in migraine reveal that the vast majority of patients (>90%) have experienced nausea during a migraine attack and more than 50% have nausea with the majority of attacks. Similarly, most (almost 70%) have vomited at some time during an attack and of these patients, almost one-third vomit in the majority of attacks. The newer formulations, rapidly dissolving tablets and intranasal sprays, afford patients the opportunity to use abortive therapy without the need for liquids, at anytime and anywhere, at the onset of a migraine attack. Furthermore, the intranasal sprays are absorbed rapidly and have a prompt onset of action allowing for significant pain free rates versus placebo as early as 15 minutes post administration. The ability to administer treatment early in a migraine attack and have a rapid onset of action is particularly important in acute migraine treatment in order to prevent the development of central sensitisation. While many patients and physicians choose conventional oral tablets because of familiarity and ease of administration, the newer formulations, oral disintegrating tablets and intranasal sprays, should be given consideration as first-line agents in selected patients.

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Year:  2003        PMID: 14524731     DOI: 10.2165/00003495-200363210-00002

Source DB:  PubMed          Journal:  Drugs        ISSN: 0012-6667            Impact factor:   9.546


  77 in total

Review 1.  Fast-dissolve drug delivery systems.

Authors:  W Habib; R Khankari; J Hontz
Journal:  Crit Rev Ther Drug Carrier Syst       Date:  2000       Impact factor: 4.889

2.  Practice parameter: evidence-based guidelines for migraine headache (an evidence-based review): report of the Quality Standards Subcommittee of the American Academy of Neurology.

Authors:  S D Silberstein
Journal:  Neurology       Date:  2000-09-26       Impact factor: 9.910

Review 3.  The nasal delivery of drugs.

Authors:  M S Quraishi; N S Jones; J D Mason
Journal:  Clin Otolaryngol Allied Sci       Date:  1997-08

Review 4.  Newer intranasal migraine medications.

Authors:  C D Logemann; L M Rankin
Journal:  Am Fam Physician       Date:  2000-01-01       Impact factor: 3.292

5.  The development of cutaneous allodynia during a migraine attack clinical evidence for the sequential recruitment of spinal and supraspinal nociceptive neurons in migraine.

Authors:  R Burstein; M F Cutrer; D Yarnitsky
Journal:  Brain       Date:  2000-08       Impact factor: 13.501

6.  Prevalence and burden of migraine in the United States: data from the American Migraine Study II.

Authors:  R B Lipton; W F Stewart; S Diamond; M L Diamond; M Reed
Journal:  Headache       Date:  2001 Jul-Aug       Impact factor: 5.887

7.  When should triptans be taken during a migraine attack?

Authors:  J Schoenen
Journal:  CNS Drugs       Date:  2001       Impact factor: 5.749

8.  Rizatriptan tablet versus wafer: patient preference.

Authors:  J U Adelman; L K Mannix; R L Von Seggern
Journal:  Headache       Date:  2000-05       Impact factor: 5.887

9.  Symptomatic and nonsymptomatic headaches in a general population.

Authors:  B K Rasmussen; J Olesen
Journal:  Neurology       Date:  1992-06       Impact factor: 9.910

10.  Safety and efficacy of rectal prochlorperazine for the treatment of migraine in the emergency department.

Authors:  E B Jones; E R Gonzalez; J G Boggs; J A Grillo; R K Elswick
Journal:  Ann Emerg Med       Date:  1994-08       Impact factor: 5.721

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  4 in total

1.  Effectiveness and satisfaction with zolmitriptan 5 mg nasal spray for treatment of migraine in real-life practice: results of a postmarketing surveillance study.

Authors:  Hans-Christoph Diener; Stefan Evers
Journal:  Clin Drug Investig       Date:  2007       Impact factor: 2.859

2.  Preliminary brain-targeting studies on intranasal mucoadhesive microemulsions of sumatriptan.

Authors:  Tushar K Vyas; A K Babbar; R K Sharma; Shashi Singh; Ambikanandan Misra
Journal:  AAPS PharmSciTech       Date:  2017-03-08       Impact factor: 3.246

Review 3.  Translational pain research: achievements and challenges.

Authors:  Jianren Mao
Journal:  J Pain       Date:  2009-07-22       Impact factor: 5.820

Review 4.  Optimal management of severe nausea and vomiting in migraine: improving patient outcomes.

Authors:  Miguel Ja Láinez; Ana García-Casado; Francisco Gascón
Journal:  Patient Relat Outcome Meas       Date:  2013-10-11
  4 in total

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