Chenghui Li
University of Arkansas for Medical Sciences
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Publication
Featured researches published by Chenghui Li.
Pharmacoepidemiology and Drug Safety | 2011
Chenghui Li; Bradley C. Martin
With the heightened concern over acetaminophen overdose induced liver toxicity, it is important to track the overdose incidences over time. We estimated the trends in emergency department (ED) visits attributable to acetaminophen overdoses and compared the risk across sociodemographic groups and geographic regions.
Journal of the American Geriatrics Society | 2016
Joshua D. Brown; Lisa C. Hutchison; Chenghui Li; Jacob T. Painter; Bradley C. Martin
To compare the predictive validity of the 2003 Beers, 2012 American Geriatrics Society (AGS) Beers, and Screening Tool of Older Persons’ potentially inappropriate Prescriptions (STOPP) criteria.
Pharmacotherapy | 2012
Sharvari M. Bhurke; Bradley C. Martin; Chenghui Li; Amy M. Franks; Zoran Bursac; Qayyim Said
To examine the effect of the drug interaction between clopidogrel and proton pump inhibitors (PPIs) on the risk of an adverse cardiovascular event.
American Journal of Preventive Medicine | 2012
Chenghui Li; Carolyn M. Dresler
BACKGROUND Although most Medicaid programs have some coverage for tobacco-cessation treatments, little is known about how well the covered treatments are utilized among Medicaid enrollees. PURPOSE To examine the impact of Arkansas Medicaid coverage of tobacco-cessation treatment on utilization of FDA-approved tobacco-cessation pharmacotherapies and counseling services by Medicaid enrollees. METHODS This study used Arkansas Medicaid administrative claims data from October 1, 2003, to June 30, 2008. Trend changes in the following monthly measures were examined: (1) total number of pharmacy claims for each covered pharmacotherapy; (2) total number of medical claims for counseling services; and (3) total number of unique enrollees who received each type of covered tobacco-cessation treatment. Average unit of defined daily dose and days with treatment stratified by tobacco-cessation products within 180 days after the first tobacco-cessation treatment were examined for intensity of treatment. Data collection was finished in 2009 and analysis was completed in 2011. RESULTS By June 30, 2008, a total of 12,673 enrollees received some tobacco-cessation treatments, and 77% of them received pharmacotherapies only. Implementation of the coverage expansion generated an initial increase in utilization of tobacco-cessation medications but quickly declined after 3 months. Utilization increased again when varenicline was added, but also decreased sharply after 6 months. Patterns of monthly claims for counseling services appeared to be inconsistent with the policy change. CONCLUSIONS Medicaid coverage alone may have limited sustained effect on increasing utilization of the covered tobacco-cessation treatments among Medicaid enrollees.
Journal of Managed Care Pharmacy | 2017
Julian Casciano; Jerry A. Krishnan; Zenobia Dotiwala; Chenghui Li; Shawn X. Sun
BACKGROUND The European Respiratory Society and American Thoracic Society (ERS/ATS) published guidelines in 2014 for the evaluation and treatment of asthma. These guidelines draw attention to management of patients with asthma that remains uncontrolled despite therapy. One phenotypic characteristic of therapy-resistant asthma is eosinophil elevation. It is important to better understand the burden of care gaps in this patient subgroup in order to support improved treatment strategies in the future. OBJECTIVE To quantify the economic burden of asthma patients with and without peripheral blood eosinophil elevation. METHODS A retrospective cohort study was conducted using data from patients aged 12 years or older with a diagnosis of asthma using electronic health records of over 2 million patients between 2004-2010. Patients with a diagnosis of chronic obstructive pulmonary disease, Churg Strauss syndrome/Wegeners granulomatosis, eosinophilia, cystic/pulmonary fibrosis, allergic bronchopulmonary aspergillosis, or lung cancer in the 12-month period before the date of asthma diagnosis were excluded. Patients with asthma were followed for 12 months after their initial asthma diagnosis to identify those with controlled versus uncontrolled asthma based on ERS/ATS criteria. Patients with at least 1 peripheral blood eosinophil test result of ≥ 400 cells/µL were classified as those with elevated eosinophils. Total annual paid-claim cost was compared by eosinophil levels within the controlled and uncontrolled asthma subgroups. Costs were adjusted to 2015 U.S. dollars. Patients were stratified by control level, and generalized linear modeling regressions were used to assess the magnitude of increase in cost of the elevated eosinophil group. RESULTS A total of 2,701 patients were included in the study, of which 17% had uncontrolled asthma and 21% had elevated eosinophils. The mean total annual cost of patients with uncontrolled asthma was more than 2 times the cost of those with controlled asthma (
Healthcare | 2015
Anand R. Shewale; Jill T. Johnson; Chenghui Li; David Nelsen; Bradley C. Martin
18,341 vs.
American Journal of Health-system Pharmacy | 2015
Julian Casciano; Zenobia Dotiwala; Robert Kemp; Chenghui Li; Jennifer Cai; Ronald Preblick
8,670, P < 0.001). Patients with uncontrolled asthma in the elevated eosinophil group had almost double the total cost (
Drug and Alcohol Dependence | 2015
Anand R. Shewale; Mrudula S. Borse; Joshua D. Brown; Chenghui Li
28,644 vs.
Sleep Health | 2018
Ellyn E. Matthews; Chenghui Li; Christopher R. Long; Marie-Rachelle Narcisse; Bradley C. Martin; Pearl Anna McElfish
14,188, P = 0.008) compared with those with blood eosinophil levels in a normal range. Similarly, patients classified as those with controlled asthma in the elevated eosinophil group had almost twice the average costs as those without elevated eosinophils (
Journal of Managed Care Pharmacy | 2017
Julian Casciano; Jerry A. Krishnan; Mary Buatti Small; Chenghui Li; Zenobia Dotiwala; Bradley C. Martin
14,754 vs.