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Dive into the research topics where Andrew Nelsen is active.

Publication


Featured researches published by Andrew Nelsen.


Annals of Neurology | 2009

Medullary pain facilitating neurons mediate allodynia in headache-related pain†

Rebecca M. Edelmayer; Todd W. Vanderah; Lisa A. Majuta; En‐Tan Zhang; Beatriz Fioravanti; Milena De Felice; Juliana G. Chichorro; Michael H. Ossipov; Tamara King; Josephine Lai; Shashi H. Kori; Andrew Nelsen; Keri E. Cannon; Mary M. Heinricher; Frank Porreca

To develop and validate a model of cutaneous allodynia triggered by dural inflammation for pain associated with headaches. To explore neural mechanisms underlying cephalic and extracephalic allodynia.


Headache | 2007

Gastric Stasis Occurs in Spontaneous, Visually Induced, and Interictal Migraine

Sheena K. Aurora; Shashidhar Kori; Patricia M. Barrodale; Andrew Nelsen; Susan A. McDonald

Objective.— To evaluate and compare gastric motility and emptying during spontaneous migraine to previous observations from induced migraine.


Cardiovascular Therapeutics | 2013

Rapid Transition from Inhaled Iloprost to Inhaled Treprostinil in Patients with Pulmonary Arterial Hypertension

Robert C. Bourge; Victor F. Tapson; Zeenat Safdar; Raymond L. Benza; Richard N. Channick; Erika B. Rosenzweig; Shelley Shapiro; Richard James White; Christopher Shane McSwain; Stephen Karl Gotzkowsky; Andrew Nelsen; Lewis J. Rubin

Background Inhaled treprostinil is a prostacyclin analog approved for the treatment of pulmonary arterial hypertension (PAH) that may provide a more convenient treatment option for patients receiving inhaled iloprost while maintaining the clinical benefit of inhaled prostacyclin therapy. Aims In this open-label safety study, 73 PAH patients were enrolled with primarily World Health Organization Class II (56%) or III (42%) symptoms. At baseline, most patients (93%) were receiving 5 μg of iloprost per dose but 38% of patients reported a dosing frequency below the labeled rate of 6–9 times daily. Patients initiated inhaled treprostinil at 3 breaths four times daily (qid) at the immediate next scheduled iloprost dose. The primary objective was to assess the safety of rapid transition from iloprost to inhaled treprostinil; clinical status and quality of life were also assessed. Results Most patients (84%) achieved the target treprostinil dose of 9 breaths qid and remained on study until transition to commercial therapy (89%). The most frequent adverse events (AEs) were cough (74%), headache (44%), and nausea (30%), and five patients prematurely discontinued study drug due to AE (n = 3), disease progression (n = 1), or death (n = 1). At week 12, the time spent on daily treatment activities was reduced compared to baseline, with a mean total savings of 1.4 h per day. Improvements were also observed at week 12 for 6-min walk distance (+16.0; P < 0.001), N-terminal pro-B-type natriuretic peptide (−74 pg/mL; P = 0.001), and the Cambridge Pulmonary Hypertension Outcome Review (all domains P < 0.001). Conclusions Pulmonary arterial hypertension patients can be safely transitioned from inhaled iloprost to inhaled treprostinil while maintaining clinical status.


Headache | 2014

Consistency of return to normal function, productivity, and satisfaction following migraine attacks treated with sumatriptan/naproxen sodium combination.

Stephen H. Landy; Roger K. Cady; Andrew Nelsen; Jonathan White; M. Chris Runken

To assess the consistency of improved functioning, productivity, and medication satisfaction in migraines treated with a single tablet of sumatriptan 85 mg/naproxen sodium 500 mg (S/NS) using an early intervention approach.


Pulmonary circulation | 2018

Dosing characteristics of oral treprostinil in real-world clinical practice

Vijay Balasubramanian; Chad R. Messick; Meredith Broderick; Andrew Nelsen

Pharmacokinetic studies with oral treprostinil demonstrate that three times daily (TID) dosing reduces peak-to-trough plasma trepostinil fluctuations compared with twice daily (BID) dosing. TID dosing may allow for faster titration, higher total daily doses, and potentially improve the tolerability of oral trepostinil. This analysis, which looks at the real-world dosing of oral treprostinil, supports the utility of TID dosing.


Health and Quality of Life Outcomes | 2013

Treatment satisfaction is associated with improved quality of life in patients treated with inhaled treprostinil for pulmonary arterial hypertension

Hubert Chen; Erika B. Rosenzweig; S. Karl Gotzkowsky; Andrew Nelsen; Robert C. Bourge


Journal of Heart and Lung Transplantation | 2011

195 Safely Transitioning from Inhaled Iloprost to Inhaled Treprostinil Sodium – Results from a Multicenter Open-Label Study in Patients with Pulmonary Arterial Hypertension

Robert C. Bourge; Victor F. Tapson; Zeenat Safdar; Raymond L. Benza; Richard N. Channick; Erika B. Rosenzweig; Shelley M. Shapiro; C.S. McSwain; A. Gotzkowsky; Andrew Nelsen; Lewis J. Rubin


american thoracic society international conference | 2010

Transitioning Patients From Inhaled Iloprost To Inhaled Treprostinil Sodium: An Interim Analysis

Robert C. Bourge; Victor F. Tapson; Zeenat Safdar; Raymond L. Benza; Richard N. Channick; Erika B. Rosenzweig; Shelley M. Shapiro; Lewis J. Rubin; C.S. McSwain; S K. Gotzkowsky; Andrew Nelsen


International Journal of Cardiology | 2017

The impact of delayed treatment on 6-minute walk distance test in patients with pulmonary arterial hypertension: A meta-analysis

Carmine Dario Vizza; Roberto Badagliacca; Chad R. Messick; Youlan Rao; Andrew Nelsen; Raymond L. Benza


Chest | 2018

THE EFFECT OF TREPROSTINIL DOSE ON TIME TO ALL CAUSE AND PULMONARY ARTERIAL HYPERTENSION-RELATED HOSPITALIZATIONS

Meredith Broderick; Gautam V. Ramani; Erick Borg; Amanda Vaughn Saunders; Andrew Nelsen

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Robert C. Bourge

University of Alabama at Birmingham

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Raymond L. Benza

Allegheny General Hospital

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Lewis J. Rubin

University of California

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Victor F. Tapson

Cedars-Sinai Medical Center

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Zeenat Safdar

Baylor College of Medicine

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Hubert Chen

Research Triangle Park

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