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Dive into the research topics where Jessica Ailani is active.

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Featured researches published by Jessica Ailani.


Headache | 2013

Expert consensus recommendations for the performance of peripheral nerve blocks for headaches - A narrative review

Andrew Blumenfeld; Avi Ashkenazi; Uri Napchan; Steven D. Bender; Brad C. Klein; Randall Berliner; Jessica Ailani; Jack Schim; Deborah I. Friedman; Larry Charleston; William B. Young; Carrie E. Robertson; David W. Dodick; Stephen D. Silberstein; Matthew S. Robbins

To describe a standardized methodology for the performance of peripheral nerve blocks (PNBs) in the treatment of headache disorders.


Cephalalgia | 2016

OnabotulinumtoxinA improves quality of life and reduces impact of chronic migraine over one year of treatment: Pooled results from the PREEMPT randomized clinical trial program

Richard B. Lipton; Noah Rosen; Jessica Ailani; Ronald DeGryse; Patrick Gillard; Sepideh F. Varon

Background Chronic migraine (CM) is associated with high impact and reduced health-related quality of life (HRQoL). Methods Patients with CM from PREEMPT (Phase 3 REsearch Evaluating Migraine Prophylaxis Therapy) were randomized (1:1) to receive onabotulinumtoxinA or placebo for two 12-week cycles in the double-blind (DB) phase, followed by three 12-week cycles of open-label (OL) onabotulinumtoxinA (onabotulinumtoxinA/onabotulinumtoxinA (O/O) and placebo/onabotulinumtoxinA (P/O) groups, respectively). HRQoL endpoints were assessed over 56 weeks using the Headache Impact Test (HIT-6) and the Migraine-Specific Quality of Life Questionnaire (MSQ). HIT-6 score reductions ≥2.3 and ≥5 denoted between-group minimally important difference and within-patient clinically meaningful response, respectively. Results A total of 1236 participants (O/O, n = 607; P/O, n = 629) participated in both phases. The DB phase showed significantly reduced HIT-6 and MSQ for onabotulinumtoxinA versus placebo (all p < 0.001). The OL phase showed significantly reduced HIT-6 for O/O versus P/O at weeks 28, 36, and 48, but not 56. All three MSQ domains showed improved HRQoL relative to baseline, but only the role restrictive domain showed a significant difference between O/O and P/O at week 56. Conclusions Benefits of onabotulinumtoxinA on HRQoL versus baseline persisted throughout the OL phase. Statistical superiority in favor of O/O was demonstrated for HIT-6 through 48 weeks and for MSQ (role restrictive) at 56 weeks.


Headache | 2016

The Sphenopalatine Ganglion: Anatomy, Pathophysiology, and Therapeutic Targeting in Headache

Matthew S. Robbins; Carrie E. Robertson; Eugene Kaplan; Jessica Ailani; Larry Charleston; Deena Kuruvilla; Andrew Blumenfeld; Randall Berliner; Noah Rosen; Robert Duarte; Jaskiran Vidwan; Rashmi Halker; Nicole Gill; Avi Ashkenazi

The sphenopalatine ganglion (SPG) has attracted the interest of practitioners treating head and face pain for over a century because of its anatomical connections and role in the trigemino‐autonomic reflex. In this review, we discuss the anatomy of the SPG, as well as what is known about its role in the pathophysiology of headache disorders, including cluster headache and migraine. We then address various therapies that target the SPG, including intranasal medication delivery, new SPG blocking catheter devices, neurostimulation, chemical neurolysis, and ablation procedures.


Headache | 2016

Procedural Headache Medicine in Neurology Residency Training: A Survey of US Program Directors

Matthew S. Robbins; Carrie E. Robertson; Jessica Ailani; Morris Levin; Deborah I. Friedman; David W. Dodick

To survey neurology residency program directors (PDs) on trainee exposure, supervision, and credentialing in procedures widely utilized in headache medicine.


JAMA Neurology | 2018

Evaluation of Galcanezumab for the Prevention of Episodic Migraine: The EVOLVE-1 Randomized Clinical Trial

Virginia L. Stauffer; David W. Dodick; Qi Zhang; Jeffrey Carter; Jessica Ailani; Robert R. Conley

Importance Migraine is a disabling neurological disease characterized by severe headache attacks. Treatment options reduce migraine frequency for many patients, but adverse effects lead to discontinuation in many patients. Objective To demonstrate that galcanezumab is superior to placebo in the prevention of episodic migraine with or without aura. Design, Setting, and Participants The EVOLVE-1 (Evaluation of LY2951742 in the Prevention of Episodic Migraine 1) trial was a double-blind, randomized, placebo-controlled (January 11, 2016, to March 22, 2017) trial comparing galcanezumab (120 mg and 240 mg) vs placebo. Patients received treatments once monthly for 6 months (subcutaneous injection via prefilled syringe) and were followed up for 5 months after their last injection. It was a multicenter, clinic-based study involving 90 sites in North America. Participants in the study were adults (aged 18 to 65 years) with at least a 1-year history of migraine, 4 to 14 migraine headache days per month and a mean of at least 2 migraine attacks per month within the past 3 months, and were diagnosed prior to age 50 years. During the study, no other preventive medications were allowed. A total of 1671 patients were assessed; 809 did not meet study entry or baseline criteria, and 858 were included in the intent-to-treat population. Interventions Patients were randomized (2:1:1) to monthly placebo, galcanezumab, 120 mg, and galcanezumab, 240 mg. Main Outcomes and Measures The primary outcome was overall mean change from baseline in the number of monthly migraine headache days during the treatment period. Secondary measures included at least 50%, at least 75%, and 100% reduction in monthly migraine headache days, migraine headache days with acute medication use, and scores from the Migraine-Specific Quality of Life questionnaire, Patient Global Impression of Severity, and Migraine Disability Assessment. Treatment-emergent adverse events and serious adverse events were reported. Results Of the 1671 patients assessed, 858 (mean age, 40.7 years; 718 women [83.7%]) met study entry criteria and received at least 1 dose of investigational product. The primary objective was met for both galcanezumab doses; treatment with galcanezumab significantly reduced monthly migraine headache days (both P < .001) by 4.7 days (120 mg) and 4.6 days (240 mg) compared with placebo (2.8 days). All key secondary objectives were also significant after multiplicity adjustment. There were no meaningful differences between 120-mg and 240-mg doses of galcanezumab on measures of efficacy. Completion rate during treatment was high (81.9%; n = 718), and the incidence of discontinuation owing to adverse events was less than 5% across all treatment groups. Conclusions and Relevance Galcanezumab 120-mg and 240-mg monthly injections provided clinical benefits and improved functioning. The incidence rate of adverse events was low, demonstrating the favorable tolerability profile of galcanezumab. Trial Registration ClinicalTrials.gov Identifier: NCT02614183


Current Pain and Headache Reports | 2010

Tension-Type Headache and Women: Do Sex Hormones Influence Tension-Type Headache?

Jessica Ailani

Most of the world’s population has suffered from a tension-type headache (TTH) at some point in their lives. The pathophysiology of this disease is not well understood, but TTH shares many features with migraine, leading to the belief that TTH and migraine may be on different ends of the same disease spectrum. There are many shared triggers between migraine and TTH, menstruation being one of them. Does menses being a trigger for TTH make TTH more like migraine, or does the role of sex hormones in TTH give us insight into the unique pathophysiology of this disease? This article will review TTH, concentrating on the role of sex hormones as a trigger for TTH.


Archive | 2019

Chronic Daily Headache and Comorbid Disorders

Sara Siavoshi; Carrie Dougherty; Jessica Ailani

Chronic daily headache is a group of disorders that are common and seen frequently in the healthcare setting. Along with the disability associated with frequent headaches, chronic daily headache has comorbid conditions that can increase disability and decrease life satisfaction. Understanding and managing these comorbid conditions are important, not only to improve the quality of care we provide to persons with chronic daily headache but to help reduce disability. This chapter will review common comorbidities seen with chronic daily headache such as mood disorders, musculoskeletal disease, head trauma, epilepsy, stroke, sleep disorders, asthma and allergies, thyroid dysfunction, obesity, and cardiovascular disease. We will also highlight potential reasons for the coexistence of these disorders.


Brain Sciences | 2016

An Unusual Case of Post-Traumatic Headache Complicated by Intracranial Hypotension

Sara Siavoshi; Carrie Dougherty; Jessica Ailani; Kaustubh Yadwadkar; Frank Berkowitz

We present a case of post-traumatic headache complicated by intracranial hypotension resulting in an acquired Chiari malformation and myelopathy with syringomyelia. This constellation of findings suggest a possible series of events that started with a traumatic cerebral spinal fluid (CSF) leak, followed by descent of the cerebellar tonsils and disruption of CSF circulation that caused spinal cord swelling and syrinx. This unusual presentation of post-traumatic headache highlights the varying presentations and the potential sequelae of intracranial hypotension. In addition, the delayed onset of upper motor neuron symptoms along with initially normal head computerized tomography scan (CT) findings, beg the question of whether or not a post-traumatic headache warrants earlier magnetic resonance imaging (MRI).


Current Pain and Headache Reports | 2015

Diagnose and Adios: Practical Tips for the Ongoing Evaluation and Care of TAC Patients Taking Indomethacin

Laura B. Xanders; Jessica Ailani

Paroxysmal hemicrania and hemicrania continua are primary headache disorders characterized by unilateral attacks of severe pain around the orbit with associated autonomic features. They are unique in their absolute response to indomethacin. Diagnosis is made when patients with suspected paroxysmal hemicrania or hemicrania continua have the resolution of headache with therapeutic doses of indomethacin. Once diagnosis is made, limited data exists on the ongoing management of these patients. For patients who do not tolerate indomethacin, or wish to come off medication, there remain few options. This article will discuss the diagnosis of paroxysmal hemicrania and hemicrania continua and the ongoing management of patients on indomethacin, as well as options for patients who do not tolerate or need to come off indomethacin.


Current Neurology and Neuroscience Reports | 2014

Migraine and Patent Foramen Ovale

Jessica Ailani

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Matthew S. Robbins

Albert Einstein College of Medicine

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Deborah I. Friedman

University of Texas Southwestern Medical Center

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Sara Siavoshi

MedStar Georgetown University Hospital

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Avi Ashkenazi

Thomas Jefferson University Hospital

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Morris Levin

University of California

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