| Literature DB >> 36089637 |
Takao Takeshima1, Kaname Ueda2, Mika Komori3, Anthony J Zagar4, Yongin Kim4, Dena H Jaffe5, Yasuhiko Matsumori6, Koichi Hirata7.
Abstract
INTRODUCTION: Using data from the ObserVational survey of the Epidemiology, tReatment, and Care Of MigrainE study in Japan (OVERCOME [Japan]), we describe the current status of the acute treatment of migraine in Japan.Entities:
Keywords: Acute treatment; Cardiovascular risk factors; Contraindications; Drug therapy; Headache; Japan; Migraine with aura; Migraine without aura; Triptans
Mesh:
Substances:
Year: 2022 PMID: 36089637 PMCID: PMC9525323 DOI: 10.1007/s12325-022-02289-w
Source DB: PubMed Journal: Adv Ther ISSN: 0741-238X Impact factor: 4.070
Demographic and baseline clinical characteristics of survey respondents
| Demographic and clinical characteristics | Totala | Monthly headache days categoryb | ||
|---|---|---|---|---|
| 0–3 | ≥ 4 | |||
| Age, years, mean (SD) | 40.7 (13.0) | 40.3 (13.0) | 41.7 (12.9) | < 0.001d |
| Female | 11,354 (66.5) | 7325 (63.7) | 4029 (72.3) | < 0.001e |
| At least some college education | 11,891 (69.7) | 8119 (70.6) | 3772 (67.7) | < 0.001f |
| Employment status | < 0.001f | |||
| Employed full time | 9557 (56.0) | 6614 (57.5) | 2943 (52.8) | |
| Employed part time | 2826 (16.6) | 1848 (16.1) | 978 (17.6) | |
| Household income ≥ ¥5M | 8131 (47.6) | 5573 (48.5) | 2558 (45.9) | 0.0023f |
| Current smoking habit | 3783 (22.2) | 2435 (21.2) | 1348 (24.2) | < 0.001g |
| BMI (kg/m2), mean (SD) | 21.86 (3.87) | 21.85 (3.76) | 21.88 (4.08) | 0.7006d |
| Pain severity score (min–max: 0–10), mean (SD) | 5.1 (2.2) | 4.8 (2.2) | 5.8 (1.9) | < 0.001d |
| ASC-12, mean (SD) | 3.4 (3.6) | 3.2 (3.6) | 3.8 (3.8) | < 0.001d |
| ASC-12 category | < 0.001f | |||
| None (0–2) | 9011 (52.8) | 6362 (55.3) | 2649 (47.5) | |
| Mild (3–5) | 4288 (25.1) | 2787 (24.2) | 1501 (26.9) | |
| Moderate (6–8) | 2113 (12.4) | 1326 (11.5) | 787 (14.1) | |
| Severe (≥ 9) | 1659 (9.7) | 1023 (8.9) | 636 (11.4) | |
Data are n (%), unless otherwise indicated
ASC-12 Allodynia Symptom Checklist, BMI body mass index, M million, max maximum, min minimum, SD standard deviation
aData in the total column previously reported [3] are age, sex, employment status, and pain severity
bData in the 0–3 monthly headache days column previously reported [4] are age, sex, total employed, pain severity, and total current use of acute treatment. Data for ≥ 4 monthly headache days as a single category have not been previously reported
cPairwise comparisons between migraine headache days categories (0–3 vs. ≥ 4); note that the large sample size may result in statistically significant differences of minimal clinical importance
dt test (continuous variable)
eChi-square test, female versus male
fChi-square test across all categories (education categories: less than high school, high school graduate, college or technical school, university graduate, post-graduate qualification, not sure, or prefer not to answer; employment categories: employed full time, employed part time, homemaker, retired, student, disability payment, not employed and looking for work, not employed and not looking for work, or prefer not to answer; household income categories: < ¥1,000,000, ¥1,000,000–¥2,999,999, ¥3,000,000–¥7,999,999, ¥8,000,000–¥9,999,999, > ¥10,000,000, or prefer not to answer)
gChi-square test, current smoker versus current non-smoker
Fig. 1Level of disability caused by the respondents’ most severe type of headache, stratified by monthly headache days categories. Survey participants responded to the question “Which best describes how your most severe type of headache usually affects you?”
Acute treatment for migraine among OVERCOME (Japan) survey respondents
| Acute treatment characteristics | Totala | Monthly headache days categoryb | ||
|---|---|---|---|---|
| 0–3 | ≥ 4 | |||
| Current use of acute treatment (prescription and/or OTC) | 14,869 (87.1) | 9802 (85.3) | 5067 (90.9) | < 0.001d |
| OTC | 12,835 (75.2) | 8643 (75.2) | 4192 (75.2) | 0.9432d |
| Acute prescription | 9078 (53.2) | 5674 (49.4) | 3404 (61.1) | < 0.001d |
| NSAIDs | 6262 (36.7) | 3802 (33.1) | 2460 (44.1) | < 0.001d |
| Triptan | 2533 (14.8) | 1416 (12.3) | 1117 (20.0) | < 0.001d |
| Ergotamine | 466 (2.7) | 286 (2.5) | 180 (3.2) | 0.0052d |
| Current use of preventive medication | 1567 (9.2) | 854 (7.4) | 713 (12.8) | < 0.001d |
| Timing of taking triptans among current triptan userse | ||||
| At the first sign of an attack | 677 (30.7) | 370 (30.6) | 307 (30.8) | 0.9239d |
| When the pain is mild | 812 (36.8) | 437 (36.2) | 375 (37.6) | 0.4770d |
| When the pain is moderate or severe | 643 (29.2) | 346 (28.6) | 297 (29.8) | 0.5471d |
| After I’ve tried another medication | 130 (5.9) | 65 (5.4) | 65 (6.5) | 0.2565d |
| Don’t remember | 156 (7.1) | 98 (8.1) | 58 (5.8) | 0.0369d |
| Among those who delay taking triptans, reason(s) for delayf | ||||
| I wait to see whether the attack will go away on its own | 273 (36.0) | 143 (35.3) | 130 (36.7) | 0.6854d |
| I try to save it for really bad attacks | 250 (32.9) | 118 (29.1) | 132 (37.3) | 0.0171d |
| I may not realize that it is going to be a migraine or severe headache | 229 (30.2) | 118 (29.1) | 111 (31.4) | 0.5062d |
| Ever use triptan(s) | 3433 (20.1) | 1994 (17.3) | 1439 (25.8) | < 0.001d |
| Effectiveness of triptansg | 0.0076h | |||
| They all worked well | 334 (20.5) | 214 (23.2) | 120 (16.9) | |
| Some worked well, others worked poorly | 1016 (62.2) | 544 (59.1) | 472 (66.3) | |
| They all worked poorly | 136 (8.3) | 81 (8.8) | 55 (7.7) | |
| Don’t remember | 147 (9.0) | 82 (8.9) | 65 (9.1) | |
Data are n (%)
NSAIDs nonsteroidal anti-inflammatory drugs, OTC over the counter
aCurrent acute treatment use (any OTC, NSAIDs, triptans, and ergotamine) for the total migraine group have been previously reported [3]
bThe overall current use of acute treatment in the 0–3 monthly headache days column has been previously reported [4]. Data for ≥ 4 monthly headache days as a single category have not been previously reported
cPairwise comparisons between migraine headache days categories (0–3 vs. ≥ 4); note that the large sample size may result in statistically significant differences of minimal clinical importance
dChi-square test, “yes” versus “no”
eResponses were missing from n = 327 current triptan users
fThis question was asked if respondents took triptans when their pain was moderate or severe or after trying another medication. Top three reasons shown; additional reasons for delaying taking triptans are listed in Supplementary Table S1. Respondents could select more than one option
gThis question was asked of respondents who had ever used triptans (both current and former users) and who reported using/having used two or more triptans
hChi-square test across all categories
Fig. 2Respondent-reported effectiveness of their current acute medication (mTOQ-4 categories). Results are shown as percentages of respondents currently using acute medication (n = 14,869). There was a significant difference between monthly headache days categories (0–3 [n = 9802] vs. ≥ 4 [n = 5067]) across all mTOQ-4 categories (chi-square test; p < 0.001). mTOQ-4 4-Item Migraine Treatment Optimization Questionnaire
CV comorbidities, procedures, and risk factors
| Total | |
|---|---|
| Any CV event or procedure | 1759 (10.3) |
| Any CV event | 1708 (10.0) |
| Aneurysm | 860 (5.0) |
| Angina | 609 (3.6) |
| Stroke | 360 (2.1) |
| Claudication | 334 (2.0) |
| Cerebral hemorrhage | 323 (1.9) |
| Myocardial infarction | 306 (1.8) |
| DVT | 237 (1.4) |
| TIA | 218 (1.3) |
| Any CV procedure | 512 (3.0) |
| tPA injection | 205 (1.2) |
| Cerebral artery stent | 200 (1.2) |
| Coronary artery stent | 199 (1.2) |
| Carotid artery stent | 198 (1.2) |
| Carotid artery surgery | 196 (1.2) |
| Coronary angioplasty | 184 (1.1) |
| Coronary bypass surgery | 177 (1.0) |
| Peripheral artery bypass surgery | 173 (1.0) |
| CVRFs | |
| Any CVRF | 9026 (52.9) |
| Current smokers | 3783 (22.2) |
| Postmenopausal women | 2321 (20.4) |
| BMI ≥ 25 kg/m2 | 2414 (16.4) |
| Hypertension | 2167 (12.7) |
| Male aged ≥ 45 years | 2006 (11.8) |
| Hyperlipidemia | 1823 (10.7) |
| Female aged ≥ 55 years | 1720 (10.1) |
| Diabetes | 774 (4.5) |
Data are n (%)
BMI body mass index, CV cardiovascular, CVRF cardiovascular risk factor, DVT deep vein thrombosis, TIA transient ischemic attack, tPA tissue plasminogen activator
Fig. 3Percentage of patients with potential unmet needs for acute treatment, stratified across monthly headache days categories. The patient groups were defined as Group A, insufficient effect of current acute treatments; Group B, history of oral triptan use; Group C, potential contraindications to triptans; Group D, CVRFs. Respondents could be categorized into multiple groups (see text for further details). Respondents in any of Groups A–D were considered to have ≥ 1 potential unmet need; those in Groups A, B, or C but not D were considered likely candidates for novel acute treatments. Asterisks indicate pairwise comparisons between monthly headache days categories (0–3 vs. ≥ 4): *p < 0.05, **p < 0.01, ***p < 0.001. CVRF cardiovascular risk factor
| Unmet needs for acute treatment of migraine in Japan, particularly for people with cardiovascular disease (CVD) or cardiovascular risk factors (CVRFs), are not currently well understood. |
| The OVERCOME (Japan) observational study assessed diagnosis, symptomatology, treatment, and impact of migraine in a representative sample of the Japanese population. |
| Survey results reported here include the types of acute medications used, patient-reported medication effectiveness, and CVD and/or CVRFs in people with migraine in Japan. |
| Potential unmet needs, such as insufficient effectiveness of current treatments, former triptan use, contraindications to triptans, and/or CVRFs, were reported by nearly three-quarters (74.1%) of people with migraine in Japan. |
| The impacts of these potential unmet needs may include substantial disability related to migraine and reduced options for acute treatment. |
| There are substantial opportunities for improving the care of people with migraine in Japan, including prescription of novel acute medications. |