Jordan B. King
Kaiser Permanente
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Publication
Featured researches published by Jordan B. King.
Jacc-Heart Failure | 2016
Jordan B. King; Rashmee U. Shah; Adam P. Bress; Richard E. Nelson; Brandon K. Bellows
OBJECTIVES The objective of this study was to determine the cost-effectiveness and cost per quality-adjusted life year (QALY) gained of sacubitril-valsartan relative to enalapril for treatment of heart failure with reduced ejection fraction (HFrEF). BACKGROUND Compared with enalapril, combination angiotensin receptor-neprilysin inhibition (ARNI), as is found in sacubitril-valsartan, reduces cardiovascular death and heart failure hospitalization rates in patients with HFrEF. METHODS Using a Markov model, costs, effects, and cost-effectiveness were estimated for sacubitril-valsartan and enalapril therapies for the treatment of HFrEF. Patients were 60 years of age at model entry and were modeled over a lifetime (40 years) from a third-party payer perspective. Clinical probabilities were derived predominantly from PARADIGM-HF (Prospective Comparison of ARNI With ACEI to Determine Impact on Global Mortality and Morbidity in Heart Failure). All costs and effects were discounted at a 3% rate annually and are presented in 2015 U.S. dollars. RESULTS In the base case, sacubitril-valsartan, compared with enalapril, was more costly (
Diabetes Care | 2017
Adam P. Bress; Jordan B. King; Kathryn Evans Kreider; Srinivasan Beddhu; Debra L. Simmons; Alfred K. Cheung; Yingying Zhang; Michael Doumas; John Nord; Mary Ellen Sweeney; Addison A. Taylor; Charles Herring; William J. Kostis; James R. Powell; Anjay Rastogi; Christianne L. Roumie; Alan Wiggers; Jonathan S. Williams; Reem Yunis; Athena Zias; Greg W. Evans; Tom Greene; Michael V. Rocco; William C. Cushman; David M. Reboussin; Mark N. Feinglos; Vasilios Papademetriou
60,391 vs.
The New England Journal of Medicine | 2017
Adam P. Bress; Brandon K. Bellows; Jordan B. King; Rachel Hess; Srinivasan Beddhu; Zugui Zhang; Dan R. Berlowitz; Molly B. Conroy; Larry Fine; Suzanne Oparil; Lewis E. Kazis; Natalia Ruiz-Negrón; Jamie Powell; Leonardo Tamariz; Jeff Whittle; Jackson T. Wright; Mark A. Supiano; Alfred K. Cheung; William S. Weintraub; Andrew E. Moran
21,758) and more effective (6.49 vs. 5.74 QALYs) over a lifetime. The cost-effectiveness of sacubitril-valsartan was highly dependent on duration of treatment, ranging from
Pharmacotherapy | 2015
Jordan B. King; Adam P. Bress; Austin D. Reese; Mark A. Munger
249,411 per QALY at 3 years to
Pharmacotherapy | 2016
Adam P. Bress; Jordan B. King; Diana I. Brixner; Adrian Kielhorn; Harshali K. Patel; Juan Maya; Vinson C. Lee; Joseph Biskupiak; Mark A. Munger
50,959 per QALY gained over a lifetime. CONCLUSIONS Sacubitril-valsartan may be a cost-effective treatment option depending on the willingness-to-pay threshold. Future investigations should incorporate real-world evidence with sacubitril-valsartan to further inform decision making.
Journal of Critical Care | 2017
Hamid Shokoohi; Grant W. Berry; Murteza Shahkolahi; Jackson King; Jordan B. King; Mohammad Salimian; Ameneh Poshtmashad; Ali Pourmand
OBJECTIVE To determine whether the effects of intensive (<120 mmHg) compared with standard (<140 mmHg) systolic blood pressure (SBP) treatment are different among those with prediabetes versus those with fasting normoglycemia at baseline in the Systolic Blood Pressure Intervention Trial (SPRINT). RESEARCH DESIGN AND METHODS This was a post hoc analysis of SPRINT. SPRINT participants were categorized by prediabetes status, defined as baseline fasting serum glucose ≥100 mg/dL versus those with normoglycemia (fasting serum glucose <100 mg/dL). The primary outcome was a composite of myocardial infarction, acute coronary syndrome not resulting in myocardial infarction, stroke, acute decompensated heart failure, or death from cardiovascular causes. Cox regression was used to calculate hazard ratios for study outcomes with intensive compared with standard SBP treatment among those with prediabetes and normoglycemia. RESULTS Among 9,361 participants randomized (age 67.9 ± 9.4 years; 35.5% female), 3,898 and 5,425 had baseline prediabetes and normoglycemia, respectively. After a median follow-up of 3.26 years, the hazard ratio for the primary outcome was 0.69 (95% CI 0.53, 0.89) and 0.83 (95% CI 0.66, 1.03) among those with prediabetes and normoglycemia, respectively (P value for interaction 0.30). For all-cause mortality, the hazard ratio with intensive SBP treatment was 0.77 (95% CI 0.55, 1.06) for prediabetes and 0.71 (95% CI 0.54, 0.94) for normoglycemia (P value for interaction 0.74). Effects of intensive versus standard SBP treatment on prespecified renal outcomes and serious adverse events were similar for prediabetes and normoglycemia (all interaction P > 0.05). CONCLUSIONS In SPRINT, the beneficial effects of intensive SBP treatment were similar among those with prediabetes and fasting normoglycemia.
Therapeutics and Clinical Risk Management | 2015
Jordan B. King; Marisa B Schauerhamer; Brandon K. Bellows
BACKGROUND In the Systolic Blood Pressure Intervention Trial (SPRINT), adults at high risk for cardiovascular disease who received intensive systolic blood‐pressure control (target, <120 mm Hg) had significantly lower rates of death and cardiovascular disease events than did those who received standard control (target, <140 mm Hg). On the basis of these data, we wanted to determine the lifetime health benefits and health care costs associated with intensive control versus standard control. METHODS We used a microsimulation model to apply SPRINT treatment effects and health care costs from national sources to a hypothetical cohort of SPRINT‐eligible adults. The model projected lifetime costs of treatment and monitoring in patients with hypertension, cardiovascular disease events and subsequent treatment costs, treatment‐related risks of serious adverse events and subsequent costs, and quality‐adjusted life‐years (QALYs) for intensive control versus standard control of systolic blood pressure. RESULTS We determined that the mean number of QALYs would be 0.27 higher among patients who received intensive control than among those who received standard control and would cost approximately
The Clinical Journal of Pain | 2017
Julie M. Fritz; Jordan B. King; Carrie McAdams-Marx
47,000 more per QALY gained if there were a reduction in adherence and treatment effects after 5 years; the cost would be approximately
Pharmacotherapy | 2017
Jordan B. King; Rashmee U. Shah; Amy M. Sainski-Nguyen; Joseph Biskupiak; Mark A. Munger; Adam P. Bress
28,000 more per QALY gained if the treatment effects persisted for the remaining lifetime of the patient. Most simulation results indicated that intensive treatment would be cost‐effective (51 to 79% below the willingness‐to‐pay threshold of
Journal of Cardiovascular Electrophysiology | 2018
Mihail G. Chelu; Alan K. Morris; Eugene Kholmovski; Jordan B. King; Gagandeep Kaur; Michelle Silver; Joshua Cates; Frederick T. Han; Nassir F. Marrouche
50,000 per QALY and 76 to 93% below the threshold of