Literature DB >> 31032913

Episodic and Chronic Migraine in Primary Care.

Nathan P Young1, Lindsey M Philpot2, Robert A Vierkant3, Jordan K Rosedahl3, Sudhindra G Upadhyaya3, Ann Harris4, Jon O Ebbert2,5.   

Abstract

OBJECTIVE: To inform migraine care model development by assessing differences between patients with chronic migraine (CM) and episodic migraine (EM) in the current state of treatment, disability, patient satisfaction, and quality improvement opportunities.
BACKGROUND: Efficient and focused use of scarce resources will be needed to address challenges within large populations of migraine patients.
METHODS: We deployed a cross-sectional survey study of randomly selected migraine patients within a community primary care practice.
RESULTS: There were 516 survey respondents (516/1804 [30%] response rate). CM patients were more likely than EM patients to report care from a neurologist (76/110 [69%] vs 229/406 [56%]; P = .0026), and higher disability according to the Migraine Disability Assessment and Headache Impact Test - 6 questionnaires (P < .0001). CM patients were less likely than EM patients to report overall satisfaction with care (16/110 [38%] vs 156/406 [66%], P = .0002), satisfaction with access to care (17/110 [33%] vs 176/406 [68%], P < .0001), and advice they needed (16/110 [31%] vs 160/406 [62%], P < .0001). Most patients with migraine had been offered triptan medications 377/516 (78%). Overall, 156/516 (31%) of individuals were currently taking any medication for migraine prevention, and 208/516 (40%) including botulinum toxin injections. CM patients were more likely to be taking preventive medication (39/110 [36%] vs 117/406 [29%], P = .0191) and report familiarity with the diagnosis of medication-overuse headache than patients with EM (80/110 [81%] vs 256/406 [69%], P = .0178).
CONCLUSIONS: We observed differences between patients with chronic and EM and expected care delivery improvement opportunities for migraine patients in primary care. CM patients report higher levels of disability and less satisfaction with access to perceived needed medical advice and care. These findings support the need to further develop and study novel care models to efficiently and effectively deliver high-quality care and expertise in limited supply to a diverse migraine population.
© 2019 American Headache Society.

Entities:  

Keywords:  care model; population health; primary care; quality measures; survey; utilization

Year:  2019        PMID: 31032913      PMCID: PMC6625910          DOI: 10.1111/head.13543

Source DB:  PubMed          Journal:  Headache        ISSN: 0017-8748            Impact factor:   5.887


  37 in total

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6.  Central Sensitization Symptom Severity and Patient-Provider Relationships in a Community Setting.

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7.  Loneliness and Migraine Self-Management: A Cross-Sectional Assessment.

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