Andrew M. Peterson
University of the Sciences
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Featured researches published by Andrew M. Peterson.
Pharmacotherapy | 2004
Simon de Denus; Sarah A. Spinler; Kristin Miller; Andrew M. Peterson
Study Objective. To assess the risk of liver function test (LFT) abnormalities with the use of 3‐hydroxy‐3‐methylglutaryl coenzyme A reductase inhibitors (statins) for the treatment of hyperlipidemia.
Annals of Pharmacotherapy | 2004
Liza Takiya; Andrew M. Peterson; Rebecca S. Finley
OBJECTIVE To identify methods targeted at improving adherence to antihypertensives and determine their effect on adherence using meta-analytic techniques. METHODS A literature search from 1970 to December 2000 using MEDLINE, International Pharmaceutical Abstracts, PsychLit, ERIC, and EMBASE was performed using the terms compliance, adherence, and medication. Randomized articles with an intervention directed at a patient/caregiver, a comparator group, and a minimum of 10 subjects in each intervention group were identified by 3 independent reviewers. Articles that did not report sample size data or adequate results of the intervention were excluded. Sixteen citations focusing on antihypertensive adherence were identified. Of the 16 citations, 6 studied either more than one intervention in the same population or different interventions in different patient populations, yielding 24 cohorts with 2446 patients. RESULTS Fifty-eight percent of the methods focused on behavioral interventions (BIs), 29% studied the effect of a combination of behavioral and educational interventions (BEIs), and 13% utilized educational interventions (EIs) alone. Overall, the study groups were nonhomogenous (Q = 183.92; p < 0.001). However, when the groups were separated by the intervention type, the BIs were homogenous (Q = 1.19; p = 1.00) with an overall effect size (ES) of 0.04 (95% CI −0.01 to −0.09), indicating a trend toward improved adherence. Fifty percent of the BIs were performed in the physicians office; however, setting did not influence the interventions impact (p = 0.13). Within the BIs, no single intervention improved adherence over others. CONCLUSIONS Based on the interventions included in this meta-analysis, there is no single intervention that improves adherence to antihypertensives over others; therefore, a patient-specific approach should be modeled.
Value in Health | 2013
John E. Zeber; Elizabeth Manias; Allison Williams; David S. Hutchins; Waka Anthony Udezi; C.S. Roberts; Andrew M. Peterson
OBJECTIVES Numerous factors influencing medication adherence in chronically ill patients are well documented, but the paucity of studies concerning initial treatment course experiences represents a significant knowledge gap. As interventions targeting this crucial first phase can affect long-term adherence and outcomes, an international panel conducted a systematic literature review targeting behavioral or psychosocial risk factors. METHODS Eligible published articles presenting primary data from 1966 to 2011 were abstracted by independent reviewers through a validated quality instrument, documenting terminology, methodological approaches, and factors associated with initial adherence problems. RESULTS We identified 865 potentially relevant publications; on full review, 24 met eligibility criteria. The mean Nichol quality score was 47.2 (range 19-74), with excellent reviewer concordance (0.966, P < 0.01). The most prevalent pharmacotherapy terminology was initial, primary, or first-fill adherence. Articles described the following factors commonly associated with initial nonadherence: patient characteristics (n = 16), medication class (n = 12), physical comorbidities (n = 12), pharmacy co-payments or medication costs (n = 12), health beliefs and provider communication (n = 5), and other issues. Few studies reported health system factors, such as pharmacy information, prescribing provider licensure, or nonpatient dynamics. CONCLUSIONS Several methodological challenges synthesizing the findings were observed. Despite implications for continued medication adherence and clinical outcomes, relatively few articles directly examined issues associated with initial adherence. Notwithstanding this lack of information, many observed factors associated with nonadherence are amenable to potential interventions, establishing a solid foundation for appropriate ongoing behaviors. Besides clarifying definitions and methodology, future research should continue investigating initial prescriptions, treatment barriers, and organizational efforts to promote better long-term adherence.
PharmacoEconomics | 2005
Andrew M. Peterson; William F. McGhan
There are numerous studies examining the pharmacoeconomic impact of HMG-CoA reductase inhibitor (statin) therapy on healthcare costs and outcomes. A recently published review demonstrated that the cost-benefit of these agents depends primarily on the risk of developing a coronary event. That is, as the risk of a coronary event increases, the cost-effectiveness ratio decreases. The typical cost per life-year saved (LYS) ranged from
Annals of Pharmacotherapy | 2012
Hildegarde J. Berdine; Tanya Dougherty; Jonathan Ference; Kelly Karpa; Jacqueline Klootwyk; Melinda Kozminski; Nicholas Leon; Maria Osborne; Adam C. Welch; Vj Willey; Andrew M. Peterson; Lauren A. Stanchak; Allen G. Whisler
US1800 to
Pharmacotherapy | 2003
Andrew M. Peterson; Liza Takiya; Rebecca S. Finley
US40 000 in patients with pre-existing coronary artery disease (CAD) and from
Value in Health | 2015
David S. Hutchins; John E. Zeber; C.S. Roberts; Allison Williams; Elizabeth Manias; Andrew M. Peterson
US15 000 to >
Pharmacotherapy | 1998
Jennifer Trofe; Andrew M. Peterson
US1 million per LYS in patients without pre-existing CAD.The literature is sparse on the pharmacoeconomics of medication non-compliance in patients taking statin medications. Data from two studies suggest that >75% compliance results in decreased coronary events such as myocardial infarction. However, retrospective database analyses indicate that the average compliance rate hovers around the 65% mark. Many of the studies discuss medication non-compliance as a factor, but do not independently analyse compliance pharmacoeconomically.We examined the pharmacoeconomic impact of non-compliance using published studies that contained pharmacoeconomic data and/or compliance data. In general, we used the placebo arm of these published studies as the surrogate marker for complete non-compliance. The results suggest that for almost 100% compliance versus initial non-compliance, the cost effectiveness of statin medications ranges from
Annals of Pharmacotherapy | 1991
Andrew M. Peterson; Stephen D. Conrad; Jeffrey M. Bell
US4500 to over
PharmacoEconomics | 1994
David B. Nash; Paul E. Windt; Andrew M. Peterson
US250 000 per LYS depending on patient age, presence or absence of risk factors and whether the statin is being used for primary or secondary prevention.Alternate-day or weekly dosing studies were also used to examine the impact of compliance on cost and health outcomes. Alternate-day dosing represented 50% compliance and weekly dosing 29% compliance. Less than full compliance had the expected effect of worse health outcomes and lower drug costs. However, the studies were small and not designed as true pharmacoeconomic studies looking at the relationship between medication compliance and cost.The results of this review suggest that there needs to be further examination of the relationship between compliance with statins and cost effectiveness, and studies need to include compliance in their data collection and analysis.