Evidence map›Paper›PMID 33594686›Full record

Observational studyHeadache2021

Understanding the migraine treatment landscape prior to the introduction of calcitonin gene-related peptide inhibitors: Results from the Assessment of TolerabiliTy and Effectiveness in MigrAINe Patients using Preventive Treatment (ATTAIN) study.

Ariane K Kawata, Neel Shah, Jiat-Ling Poon, Shannon Shaffer, Sandhya Sapra, Teresa K Wilcox, Shweta Shah, Stewart J Tepper, David W Dodick, Richard B Lipton

Registry-linked trialOpen access · hybridAbstract readObservational Study
In one paragraph

Observational study in Headache, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05598723 (A Randomized, Double-Blind Study on the Effect of OnabotulinumtoxinA), which is not on this map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
5.5field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT05598723 phase3recruitingnot on this mapstarted 2023, after this paper: background citation

A Randomized, Double-Blind Study on the Effect of OnabotulinumtoxinA (BOTOX®) vs. IncobotulinumtoxinA (XEOMIN®) Botulinum Toxin in Adults With Chronic Migraine

TypeinterventionalSponsorNaval Medical Center Camp LejeuneRan2023 to 2027Enrolled128ConditionsChronic MigraineArmsIncobotulinumtoxinA (XEOMIN®), OnabotulinumtoxinA (BOTOX®)
3 · Its place in the literature

Who cites it

23 citing papers in PubMed, 48 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 5 institutions in 1 country.

Ariane K KawataEvidera, Bethesda, MD, USA.
Neel ShahAmgen Inc., Thousand Oaks, CA, USA.
Jiat-Ling PoonEvidera, Bethesda, MD, USA.
Shannon ShafferEvidera, Bethesda, MD, USA.
Sandhya SapraAmgen Inc., Thousand Oaks, CA, USA.
Teresa K WilcoxEvidera, Bethesda, MD, USA.
Shweta ShahAmgen Inc., Thousand Oaks, CA, USA.
Stewart J TepperGeisel School of Medicine at Dartmouth, Hanover, NH, USA.
David W DodickMayo Clinic, Phoenix, AZ, USA.
Richard B LiptonAlbert Einstein College of Medicine and Montefiore Headache Center, Bronx, NY, USA.
Ithaka Harbors · USAmgen (United States) · USAlbert Einstein College of Medicine · USDartmouth College · USMayo Clinic Hospital · US

Funding

Amgen Inc.
6 · The paper itself

Abstract

backgroundCalcitonin gene-related peptide (CGRP) inhibitors were introduced in the United States (US) in 2018. To understand the changing patterns of preventive treatment following the introduction of these new agents, we must first characterize the patterns which preceded their introduction.

objectiveTo characterize the burden, unmet need, and treatment patterns in patients with migraine initiating preventive migraine medications before the introduction of CGRP inhibitors in the US.

methodsBetween March 2016 and October 2017, we enrolled episodic (EM) and chronic migraine (CM) patients initiating or changing preventive treatment at primary care or neurology clinic visits in the US, in a real-world observational study using a prospective cohort design. At baseline and monthly thereafter for 6 months, we collected data from study sites and patients on migraine frequency, treatment modifications, migraine impact on functioning, and work productivity for a descriptive analysis of migraine patient experience and treatment patterns.

resultsFrom the sample of 234 completers, 118 had EM (50.4%) and 116 had CM (49.6%). Mean age at enrollment was 41 years (SD = 12) and mean age at first migraine diagnosis was 22 years (SD = 11). Most participants were females (n = 204/234; 87.2%) and white (n = 178/234; 76.1%). The majority (n = 164/234; 70.1%) had not used preventive migraine treatment in the 5 years prior to enrollment (treatment naïve). At baseline, mean monthly migraine days were 9.6 days (SD = 5.0) for the preventive treatment naïve group and 12.4 days (SD = 7.0) for treatment experienced patients. The majority had severe Migraine Disability Assessment (Grade IV, total score ≥21), including 67.1% (n = 110/164) of the preventive treatment naïve and 77.1% (n = 54/70) of the preventive treatment experienced patients. Headache Impact Test total scores indicating severe impairment (score >59) occurred in 88.4% (n = 145/164) of the treatment naïve and 88.6% (n = 62/70) of treatment experienced patients. Mean work productivity loss as measured by the Work Productivity and Activity Impairment questionnaire in the subsample of employed patients was 53.3% loss. The most used acute medications at baseline were nonsteroidal anti-inflammatory agents (n = 124/234; 53.0%), acetaminophen-based products (n = 112/234; 47.9%), and triptans (n = 105/234; 44.9%). The most commonly initiated preventive treatments were topiramate (n = 100/234; 42.7%), tricyclic antidepressants (n = 39/234; 16.7%), beta-blockers (n = 26/234; 11.1%), and onabotulinumtoxinA (n = 24/234; 10.3%). Over the 6-month follow-up period, almost half of patients (n = 116/234, 49.6%) modified their preventive treatment and discontinued treatment (n = 88/312 total modifications; 28.2%) or modified their pattern of use by increasing, decreasing, or skipping doses (n = 224/312 total modifications; 71.8%), often without seeking medical advice. Avoiding side effects was the main reason reported among patients who discontinued (n = 52/88; 59.1%), decreased frequency or dose (n = 37/89; 41.6%), and skipped doses (n = 29/86; 33.7%). Perceived lack of efficacy was another frequent reason reported among those who discontinued (n = 20/88; 22.7%), decreased frequency or dose (n = 15/89; 16.9%), and skipped doses (n = 18/86; 20.9%). Despite initiation of preventive treatment and improvements observed in number of headache and migraine days, migraine patients continued to experience substantial disability, headache impact, and reduced productivity throughout the 6-month follow-up period.

conclusionsPrior to 2018, the burden of migraine was high for patients initiating preventive treatments. Despite having more than 9 days of migraine per month on average, the majority (70.1%) of patients initiating prevention had been treatment naïve, indicating underuse of preventive treatments. The preventive treatments used in this study were poorly tolerated and were reported by patients to lack efficacy, resulting in suboptimal adherence. The high discontinuation rates suggest that the preventive medications being offered during the period of the study did not meet the treatment needs of patients. In addition, the decisions by about half of patients to alter their prescribed treatment plan without consulting their provider can pose substantial health risks. These findings pertain to the broad set of preventive treatments initiated in this study and do not support inferences about individual preventive treatments, due to limitations in sample size. These findings suggest the need for more effective and better tolerated preventive treatment options.

Indexed as

AcetaminophenAdrenergic beta-AntagonistsAdultAnalgesics, Non-NarcoticAnticonvulsantsAntidepressive Agents, TricyclicAnti-Inflammatory Agents, Non-SteroidalBotulinum Toxins, Type AChronic DiseaseFemaleFollow-Up StudiesHumansMaleMiddle AgedMigraine DisordersNeuromuscular AgentsAcetaminophenAdrenergic beta-AntagonistsAnalgesics, Non-NarcoticAnticonvulsantsAntidepressive Agents, TricyclicAnti-Inflammatory Agents, Non-SteroidalBotulinum Toxins, Type ANeuromuscular Agentsonabotulinum toxin ASerotonin 5-HT1 Receptor AgonistsTopiramateburdendiscontinuationmigraineobservationalpreventiontreatment adherence

Identifiers

PMID33594686
PMCPMC8048891
OpenAlexW3131502707

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.