Literature DB >> 23380251

Disease-modifying drugs for knee osteoarthritis: can they be cost-effective?

E Losina1, M E Daigle, L G Suter, D J Hunter, D H Solomon, R P Walensky, J M Jordan, S A Burbine, A D Paltiel, J N Katz.   

Abstract

OBJECTIVE: Disease-modifying osteoarthritis drugs (DMOADs) are under development. Our goal was to determine efficacy, toxicity, and cost thresholds under which DMOADs would be a cost-effective knee OA treatment.
DESIGN: We used the Osteoarthritis Policy Model, a validated computer simulation of knee OA, to compare guideline-concordant care to strategies that insert DMOADs into the care sequence. The guideline-concordant care sequence included conservative pain management, corticosteroid injections, total knee replacement (TKR), and revision TKR. Base case DMOAD characteristics included: 50% chance of suspending progression in the first year (resumption rate of 10% thereafter) and 30% pain relief among those with suspended progression; 0.5%/year risk of major toxicity; and costs of $1,000/year. In sensitivity analyses, we varied suspended progression (20-100%), pain relief (10-100%), major toxicity (0.1-2%), and cost ($1,000-$7,000). Outcomes included costs, quality-adjusted life expectancy, incremental cost-effectiveness ratios (ICERs), and TKR utilization.
RESULTS: Base case DMOADs added 4.00 quality-adjusted life years (QALYs) and $230,000 per 100 persons, with an ICER of $57,500/QALY. DMOADs reduced need for TKR by 15%. Cost-effectiveness was most sensitive to likelihoods of suspended progression and pain relief. DMOADs costing $3,000/year achieved ICERs below $100,000/QALY if the likelihoods of suspended progression and pain relief were 20% and 70%. At a cost of $5,000, these ICERs were attained if the likelihoods of suspended progression and pain relief were both 60%.
CONCLUSIONS: Cost, suspended progression, and pain relief are key drivers of value for DMOADs. Plausible combinations of these factors could reduce need for TKR and satisfy commonly cited cost-effectiveness criteria.
Copyright © 2013 Osteoarthritis Research Society International. Published by Elsevier Ltd. All rights reserved.

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Year:  2013        PMID: 23380251      PMCID: PMC3670115          DOI: 10.1016/j.joca.2013.01.016

Source DB:  PubMed          Journal:  Osteoarthritis Cartilage        ISSN: 1063-4584            Impact factor:   6.576


  49 in total

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8.  Pharmacologic regimens for knee osteoarthritis prevention: can they be cost-effective?

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10.  Cost-Effectiveness of Tramadol and Oxycodone in the Treatment of Knee Osteoarthritis.

Authors:  Savannah R Smith; Jeffrey N Katz; Jamie E Collins; Daniel H Solomon; Joanne M Jordan; Lisa G Suter; Edward H Yelin; A David Paltiel; Elena Losina
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