Subject: A multicentre, retrospective, observational survey study to analyse the role of Propranolol in adult female patients with migraine
Headache disorders are among the most prevalent neurologic disorders worldwide. Approximately 30% of adults in the age group 18–65 suffer from
headache disorders and about 30% of these individuals have migraine.1 Female-to-male ratio of 3:1 and an estimated 1-year prevalence of approximately
15% in the general population. The prevalence peaks between the ages of 35 and 39 years, and about 75% of affected persons report the onset of migraine
before the age of 35 years.2 The crude 1 year prevalence of any headache (n = 1,488) in the study population was 63.9 %, with female preponderance
(73.0 % versus 54.4 % in males; OR = 2.3 [1.9-2.7]) and rural preponderance (71.2 % versus 57.3 % urban; OR = 1.8 [1.6-2.1].3
In the Global Burden of Disease study 2016, migraine was reported to be the second highest cause of years lived with disability in the world.4
Management includes lifestyle modifications, acute pharmacological treatment like NSAIDs, triptans and gepants, and, lastly, prophylactic treatment. Preventive medications form the basis of headache management and should be considered in the following cases
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Frequent headaches (four or more attacks per month or eight or more headache days per month)
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Failure, contraindications, side effects or abuse of acute medications
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Patient preference
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Presence of prolonged auras such as hemiplegic migraine, brainstem aura because they do not usually respond to acute treatment
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Impact on the patient’s quality of life and interference in their daily life despite correct treatment with lifestyle modification strategies and acute treatment of migraine
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Menstrual migraine
Oral drugs for migraine prophylaxis include the following therapeutic groups:
Anti- convulsants: topiramate, valproic acid, and gabapentin
Blood pressure medications: Beta/blockers (propranolol)
Anti-depressants: (amitriptyline)5
Propranolol is a nonselective beta-adrenergic receptor blocking agent possessing no other autonomic nervous system activity. It specifically competes with beta-adrenergic receptor agonist agents for available receptor sites. When access to beta-receptor sites is blocked by propranolol,
the chronotropic, inotropic, and vasodilator responses to beta-adrenergic stimulation are decreased proportionately
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