Safety, tolerability, and effectiveness of repetitive intravenous dihydroergotamine for refractory chronic migraine with cardiovascular risk factors: A retrospective study

Author:

Wang Victor S.1ORCID,Kosman Justin2,Yuan Hsiangkuo3,Lauritsen Clinton3ORCID,Shrewsbury Stephen4,Aurora Sheena K.4ORCID,Hopkins Mary3,Silberstein Stephen3

Affiliation:

1. Department of Neurology Thomas Jefferson University Philadelphia Pennsylvania USA

2. Thomas Jefferson University College of Population Health Philadelphia Pennsylvania USA

3. Jefferson Headache Center, Department of Neurology Thomas Jefferson University Philadelphia Pennsylvania USA

4. Impel Pharmaceuticals Inc. Seattle Washington USA

Abstract

AbstractBackgroundDihydroergotamine (DHE), like triptans, is contraindicated in patients with ischemic heart disease or coronary vasospasm. Its true safety, tolerability, and efficacy in patients with cardiovascular risk without ischemic heart disease or coronary vasospasm remain unclear.ObjectivesTo assess the safety, tolerability, and effectiveness of repetitive intravenous DHE in patients with cardiovascular risk factors.MethodsA single‐center, retrospective cohort study was conducted at the Jefferson Headache Center inpatient unit for refractory chronic migraine patients treated with our intravenous DHE protocol between January 1, 2019, and October 15, 2019. We evaluated tolerability and effectiveness outcomes based on atherosclerotic cardiovascular disease 10‐year calculated risk scores, stratified into low (<5.0%) and elevated (≥5.0%) risk. Data were presented in mean ± standard deviation or median (25th percentile, 75th percentile) if non‐normally distributed.ResultsAmong 347 patients (median age of 46 [36, 57], femalen = 278 [80.1%]), who received inpatient intravenous DHE, 227 patients (age 53 [45, 60], female 81.1%) had calculable risk scores, 64 (28.2%) had elevated risk, and 38 (16.7%) had cardiology consultations. There were no clinically significant electrocardiogram abnormalities or cardiovascular adverse events. The median hospital length of stay was 6 (5, 7) days. Compared to the low‐risk group, those with elevated risk had higher nausea (31.3% vs. 14.1%,p = 0.008), but similar initial DHE dose (0.5 [0.25, 0.5] vs. 0.5 [0.25, 0.5],p = 0.009), lower final DHE dose (0.75 [0.5, 1] vs. 1 [0.75, 1]p < 0.001), and lower pain reduction after admission (−3.8 [2.1, 6] vs. −5 [3, 7]p = 0.037).ConclusionPatients receiving intravenous DHE by the Jefferson Headache Center inpatient headache protocol had significantly reduced pain severity at discharge. No clinically significant cardiac or electrocardiogram abnormalities were detected in patients with elevated (or low) atherosclerotic cardiovascular disease risk. Repetitive intravenous DHE used by our protocol was safe in refractory chronic migraine patients.

Publisher

Wiley

Subject

Neurology (clinical),Neurology

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