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. 2023 Sep 1;24(1):120.
doi: 10.1186/s10194-023-01652-8.

Who cares about migraine? Pathways and hurdles in the European region - access to care III

Gloria Vaghi  1   2 , Roberto De Icco  3   4 , Cristina Tassorelli  3   4 , Peter J Goadsby  5 , Teófila Vicente-Herrero  6 , Elena Ruiz de la Torre  7
Affiliations

Who cares about migraine? Pathways and hurdles in the European region - access to care III

Gloria Vaghi et al. J Headache Pain. .

Abstract

Background: Migraine is a highly prevalent primary headache disorder and a leading cause of disability. Difficulties in access to care during diagnostic and therapeutic journey contribute to the disease burden. Several target-specific drugs have reached the market in the past four years and have modified the treatment paradigm in migraine. The aim of this study is to provide an updated snapshot of the pathways and hurdles to care for migraine in different European countries by directly asking patients.

Methods: In 2021 the European Migraine and Headache Alliance proposed a 39-item questionnaire that was administered online to an adult migraine population in European countries. Questions were focused on socio-demographic and migraine data, access to diagnosis and treatment, disease-related burden and the main channel for disease information.

Results: A total of 3169 questionnaires were returned from 10 European countries. Responders were predominantly females, age range 25-59 years, with a migraine history longer than 10 years in 82% of cases, and with at least 8 headache days per month in 57% of cases. Respondents reported limitations in social, working and personal life during both the ictal and interictal phase. The activities mostly impaired during the attacks were driving (55%), cooking or eating (42%), taking care of family/childcare (40%) and getting medicines at the pharmacy (40%). The most frequently reported unmet need was the long delay between the first visit and migraine diagnosis: 34% of respondents had to see ≥ 4 specialists before being correctly diagnosed, and between the diagnosis and treatment prescription: > 5 years in 40% of cases. The most relevant needs in terms of quality of life were the desire for a lower migraine frequency, an effective treatment and a greater involvement in society.

Conclusions: Data from the present survey point to the existence and persistence of multiple hurdles that result in significant limitations to access to care and to the patients' social life. A close cooperation between decision makers, healthcare workers and patients is needed to overcome these barriers.

Keywords: Access to care; Burden; Chronic migraine; Disability; Headache; Migraine; Pain; Quality of life.

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Conflict of interest statement

The authors declare no competing interests.

Figures

Fig. 1
Fig. 1
Number of specialists visited to get the final diagnosis. Total respondents N. 2519 (Question 3.1.2) (Percentages are approximated to the nearest unit)
Fig. 2
Fig. 2
Follow-up of migraine patients. Total respondents N. 2509 (Question 3.1.4) (Percentages are approximated to the nearest unit)
Fig. 3
Fig. 3
Percentage of patients who underwent follow-up in a specialized center according to country of origin. Total respondents N. 2514 (Questions 3.1.7)
See this image and copyright information in PMC

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