Duburcq Anne, Molins Manon, Debremaeker Sabine, Joie Julie, Lopes Luna, Nevoret Camille, Begasse de Dhaem Olivia
CEmka - Healthcare Consulting and Research, 43, Boulevard du Maréchal Joffre, Bourg-La-Reine, 92340, France.
MoiPatient - Participatory Research Platform, 29 Bis, Rue Buffon, Paris, 75005, France.
J Headache Pain. 2025 Apr 14;26(1):76. doi: 10.1186/s10194-025-02018-y.
This study aims to improve the understanding of the patient journey via the perspectives of patients with migraine.
The questionnaire was created by patients. It was based on the experiences of 24 patients with migraine and 4 members of the patient advocacy organization La Voix des Migraineux. Two focus groups were held to assess the various dimensions of the patient journey. This survey was accessible on the MoiPatient online platform between March 19th and May 17th, 2022.
Out of the 683 participants (average age: 41.8 years; female: 92.4%; average age at first migraine attack: 16.2 years), 95.9% had received a formal migraine diagnosis from a physician. Migraine had a significant impact on most participants (96.0% had a severe HIT-6 score and 70.7% had severe disability on the MIDAS). Unmet patients' needs highlighted in this study included diagnosis delay (mean 7.5 years), treatment delay, limited access to neurologists and/or headache specialists, long trial-and-error process of different medications (participants had tried an average of 5.6 acute treatments and 5.0 preventive treatments), numerous (7.2 side effects per participants on average) and often inadequately addressed side effects, suboptimal patient education, and the need for a therapeutic, empathic, and supportive relationship between patients and healthcare professionals. Participants had a negative perception of the care journey and experience with healthcare professionals: 36.2% described their care journey as an uphill battle ("parcours du combatant"). More than half of patients did not feel heard nor supported by healthcare professionals.
Patients with migraine have to face a multitude of complex obstacles trying to get the care they deserve. The burden of disease is amplified by the complexity of the migraine patient's journey, both in terms of diagnosis and treatment. This study highlights specific areas in need for improvement.
本研究旨在通过偏头痛患者的视角,增进对患者就医过程的理解。
问卷由患者创建。它基于24名偏头痛患者和患者权益倡导组织“偏头痛之声”的4名成员的经历。举办了两个焦点小组来评估患者就医过程的各个方面。该调查于2022年3月19日至5月17日在MoiPatient在线平台上开放。
在683名参与者中(平均年龄:41.8岁;女性:92.4%;首次偏头痛发作的平均年龄:16.2岁),95.9%的人已从医生处获得正式的偏头痛诊断。偏头痛对大多数参与者有重大影响(96.0%的人HIT - 6评分严重,70.7%的人在MIDAS上有严重残疾)。本研究中突出的未满足的患者需求包括诊断延迟(平均7.5年)、治疗延迟、看神经科医生和/或头痛专科医生的机会有限、不同药物漫长的试错过程(参与者平均尝试了5.6种急性治疗和5.0种预防性治疗)、众多的(平均每位参与者有7.2种副作用)且往往未得到充分处理的副作用、不理想的患者教育,以及患者与医护人员之间需要建立治疗性、共情性和支持性的关系。参与者对就医过程和与医护人员的经历有负面看法:36.2%的人将他们的就医过程描述为一场艰苦的战斗(“战士之路”)。超过一半的患者感觉未被医护人员倾听和支持。
偏头痛患者在试图获得应有的治疗时必须面对众多复杂的障碍。偏头痛患者就医过程在诊断和治疗方面的复杂性加剧了疾病负担。本研究突出了需要改进的具体领域。