Abstract
Background:
The economic impact of intra-articular hyaluronic acid (IAHA) for the treatment of knee pain associated with osteoarthritis (OA) has been evaluated in the United States, but not systematically summarized.
Objective:
We reviewed the literature to determine the economic impact of IAHA for pain associated with knee OA in the United States.
Methods:
A literature review was performed in PubMed (including MEDLINE and MEDLINE In-Process), Embase, the Cochrane Database of Systematic Reviews, and National Health Service Economic Evaluation Database and was limited to English language human studies published from January 2000 to October 2020.
Results:
The literature search identified 215 unique abstracts; of these, 47 were selected for full-text review and 21 studies met the inclusion criteria. Intra-articular hyaluronic acid injections delayed progression to total knee arthroplasty (TKA), and repeated courses of treatment successfully delayed TKA by more than 5 years. Intra-articular hyaluronic acid was found to reduce the use of pain medications overall and reduce the number of patients receiving opioid prescriptions by 6% (P < .001). Several studies showed that IAHA is more cost-effective in treating pain associated with knee OA compared with conventional care with nonsteroidal anti-inflammatory drugs (NSAIDs), analgesics, and corticosteroids, and several authors concluded that IAHA should be the dominant treatment strategy.
Conclusions:
Current studies suggest that IAHA may reduce the use of pain medications, such as NSAIDs and opioids, and impact time to TKA procedures, thus potentially decreasing overall treatment costs of knee OA over time. Furthermore, IAHA was determined to be cost-effective against NSAIDs, corticosteroids, analgesics, and conservative treatment. As the safety and efficacy of IAHA for knee OA have been well established, the findings from our literature review may be used to inform future economic evaluations.
Introduction
Osteoarthritis (OA) is a degenerative joint disease characterized by joint pain and dysfunction that culminates in progressive articular cartilage loss. 1 No curative treatment exists for OA; therefore, the goals for treating OA of the knee are largely palliative and include approaches to relieve pain, slow progression, improve joint biomechanics, increase muscle strength and conditioning, delay total knee arthroplasty (TKA), and preserve functional independence, mobility, and quality of life. 2 Current treatments to alleviate pain and improve daily functioning and disability for patients with OA include physical therapy, weight loss, lifestyle changes, pharmacologic therapies, steroid injections, intra-articular hyaluronic acid (IAHA [also referred to as viscosupplementation]) injections, and surgery.3,4
Viscosupplementation with hyaluronic acid (HA) for OA treatment was approved by the US Food and Drug Administration (FDA) as a class III device for the treatment of knee pain associated with OA in 1997.5,6 Endogenous HA, also referred to as hyaluronate or hyaluronan, is a high-molecular-weight (HMW) biopolymer that is produced by type B synoviocytes and synovial fibroblasts within the joint. The viscoelastic (rheological) properties of HA impart the ability of normal synovial fluid to act as a boundary lubricant and shock absorber to protect cartilage in the joint and permit near frictionless motion in the healthy state. 7 These properties of HA are essentially determined by 2 parameters: molecular weight (the average length of the HA polymer chains) and concentration in the fluid. 8 Patients with knee OA generally display a reduction in both parameters in the synovial fluid of the affected joint, and this loss in viscoelastic synovial fluid function is believed to represent a primary driver in the OA disease process. 8 Accordingly, the premise of viscosupplementation (the supplementation of synovial fluid with exogenous HA to improve the viscoelastic function of the synovial fluid) is to provide HMW-HA at a concentration that is sufficient to generate a therapeutic effect. Since its initial approval in 1997, various HA formulations have been approved in the US market, including those that were avian and bacteriologically derived and those that were cross-linked. 9 The safety of IAHA is well established, 10 and several meta-analyses of the clinical effectiveness of IAHA have been published.11-19
Despite the preponderance of evidence for safety and efficacy, clinical practice guidelines are evolving away from recommendations for IAHA20-22 in a manner that appears to be unfounded on current evidence. This evolution away from HA without clear alternative therapies has begun to limit patient access to IAHA, which may have significant economic impacts downstream. Many economic evaluations of IAHA for the treatment of knee pain in OA have been conducted, but not systematically summarized. The aim of this study was to systematically review economic evidence regarding the impact of IAHA as a treatment of pain associated with knee OA in the United States.
Methods
Data sources and selection
A flow chart of Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) is presented in Figure 1. A literature review was performed in PubMed (including MEDLINE and MEDLINE In-Process), Embase, the Cochrane Database of Systematic Reviews, and the National Health Service Economic Evaluation Database (NHSEED). The database searches were limited to English language human studies published from January 2000 to October 2020. The review was limited to January 2000, as this date represents the timepoint shortly after IAHA was FDA-approved. The search terms included combinations of MeSH (Medical Subject Headings) terms and free text (Table 1).

Preferred Reporting Items for Systematic Reviews and Meta-Analyses diagram. NHSEED indicates National Health Service Economic Evaluation Database.
Study search terms.
Abbreviations: MeSH, Medical Subject Headings; OA, osteoarthritis.
The titles and abstracts (level 1) and full-text articles (level 2) were screened by 2 researchers using predetermined inclusion and exclusion criteria. Included studies were limited to those providing information on economic evaluations (ie, cost-effectiveness, cost utility, cost minimization, or other comparative economic analysis, and studies related to cost drivers or cost implications for IAHA in adults in the United States). Publications fulfilling the exclusion criteria (ie, those that did not report economic results or outcomes, were not conducted in the United States, were nonsystematic review or opinion articles, and did not report results or outcomes [eg, study design only]) were excluded. Bibliographies of review articles and included papers were reviewed to identify any additional economic publications. Relevant data (eg, study design, patient population, interventions, costs, and efficacy results) were extracted into a table from the selected full-text articles.
Results
The literature search identified 215 unique abstracts; of these, 47 were selected for full-text review and 21 studies met the selection criteria and were extracted (Figure 1). The included economic evaluations comprise 13 retrospective reviews of claims or electronic health records data, 1 cost-of-illness model, 6 cost-effectiveness analyses, and 2 cost-utility analyses.
Impact of IAHA on TKA
Several studies evaluated the impact of knee OA treatment with IAHA on time to TKA.23-27 Each of these studies concluded that the use of IAHA is associated with longer time to TKA (Table 2). A retrospective analysis of data from 2006 to 2016 in the Optum Clinformatics database by Ong et al 25 reported a longer median time to TKA of ~7 months for those who received IAHA versus those who did not. Another retrospective analysis using data from 2007 through 2013 in the IMS Health PharMetrics Plus database found that the median time to TKA for those receiving IAHA was more than 4 times longer than it was for those who did not receive IAHA (median: 484 days vs 114 days; P < .0001). 23
Impact of IAHA on time to TKA.
Abbreviations: HCRU, health care resource utilization; HER, electronic health records; HA, hyaluronic acid; HMW, high molecular weight; IAHA, intra-articular hyaluronic acid; NSAID, nonsteroidal anti-inflammatory drug; OA, osteoarthritis; PT, physical therapy; Q2, quarter 2; TKA, total knee arthroplasty.
Furthermore, these studies also demonstrated that repeated courses of IAHA were associated with longer delays to TKA. Using data from 2007 to 2010 in the IMS Health PharMetrics Plus database, Dasa et al 24 determined that repeated courses of IAHA can delay TKA for up to 3 years. Specifically, the mean times to TKA for those receiving 1, 2, 3, 4, and ⩾5 courses of IAHA were 375.6, 617.6, 777.0, 855.6, and 971.5 days, respectively. 24 Ong et al 25 reported that the median time to TKA after 1 course of an avian-derived, cross-linked IAHA was 21 months (1.8 years); after ⩾5 courses, it was 59 months (4.9 years). The median time to TKA after 1 course of all other IAHA products reported in the data set was 20 months (1.7 years); after ⩾5 courses, it was 61 months (5.1 years). This finding was confirmed in a second retrospective analysis of the Optum Clinformatics database (data from 2006 to 2016) in which the median time from first IAHA treatment to TKA was ~6 months with 1 treatment and approximately 4 years with ⩾5 treatments. 27 Altman et al 23 found that IAHA injections are associated with dose-dependent increase in time to TKA: the mean time to TKA for patients receiving no IAHA was 0.7 years and was 3.6 years for patients who received ⩾5 courses.
Health care resource utilization
Pain management modalities commonly used in patients with knee OA include nonnarcotic analgesics (ie, acetaminophen), nonsteroidal anti-inflammatory drugs (NSAIDs), glucosamine and/or chondroitin sulfate, intra-articular corticosteroids (ICSs), and opioids (ie, tramadol). Inappropriate use of these modalities may be associated with side effects and may pose an economic burden to the health care system.28-32
Table 3 presents details on the health care resource utilization studies identified.3,33-39 Intra-articular HA injection may reduce the use of pain medications (Table 3).3,33 In a retrospective claims analysis of patients who received their first IAHA injection between 2004 and 2011, McIntyre et al 3 found a 10% reduction in the average number of NSAID prescriptions filled and a 15% reduction in the number of patients receiving any NSAID prescription (P < .001). Furthermore, there was a 55% reduction in the average number of steroid injection prescriptions filled and a 57% reduction in the number of patients receiving any steroid prescription (P < .001). While the number of opioid prescriptions filled increased by 12%, the number of patients getting any opioid prescription fell by 6% (P < .001).
Health care resource utilization studies.
Abbreviations: CPT, Current Procedural Terminology; HA, hyaluronic acid; HMW, high molecular weight; IAHA, intra-articular hyaluronic acid; ICS, intra-articular corticosteroids; NSAID, nonsteroidal anti-inflammatory drugs; OA, osteoarthritis; PT, physical therapy; Q2, quarter 2; TKA, total knee arthroplasty.
Another retrospective claims analysis of patients who received high-concentration non-avian HMW-HA injections between 2008 and 2015 found that NSAID and steroid prescription use was reduced significantly in the 6-month post-injection period among the study cohort. 33 The proportion of patients filling these prescriptions following non-avian HMW-HA injections was also reduced (P < .001). In addition, the number of patients getting any opioid prescription was reduced significantly following non-avian HMW-HA injections (P < .001). 33
Studies suggest that IAHA may reduce the use of pain medications, such as NSAIDs, and delay TKA procedures,3,23-26 thus potentially decreasing overall treatment costs over time. Two studies reported that IAHA accounts for 16% 34 to 29% 35 of OA treatment–related expenditures in the 12 months leading up to TKA. A large, retrospective analysis of the Blue Cross Blue Shield claims database found that for patients with knee OA, those treated with IAHA had lower 4-year total medical care costs than those treated with ICSs or those who received TKA. 36 Specifically, the 4-year per member per month costs for the IAHA, ICS, and TKA cohorts were $733, $1230, and $1548, respectively. 36 This study also reported lower use and costs of opioids in the IAHA cohort. 36
Another large claims database analysis determined the contribution of IAHA and TKA to overall knee OA–related direct costs using the Optum Clinformatics data set (2006-2016). 37 The cost of treating patients over a 2-year period following knee OA diagnosis was nearly $5 billion. For the IAHA patients who subsequently underwent TKA within 2 years of diagnosis, the cost of IAHA contributed to only 1.7% of the overall cost of treating those patients. However, a large proportion (84.1%) of IAHA patients did not undergo TKA within 2 years of their diagnosis. The authors reported that if these patients had instead been treated immediately with TKA, it would have cost an estimated $1.84 billion. By not undergoing TKA within 2 years of diagnosis of knee OA, these IAHA patients had potential savings of $1.54 billion, after accounting for other therapies that were used. 37
A large, retrospective claims analysis of the IMS Health PharMetrics Plus database comparing disease-specific costs and risks of TKA among patients receiving different IAHA treatments reported that meaningful differences in unadjusted mean (median) disease-specific costs exist among IAHA products, ranging from $13 160 ($4804) to $14 959 ($6388). 38 This study also reported that some IAHA products had both a higher proportion of patients who received TKA and a shorter delay to TKA than others. 38 The authors concluded that the analysis of administrative claims data provides real-world evidence that meaningful differences exist among some HA products in disease-specific cost and time to knee replacement surgery.
Using 2012 Medicare Part B claims, Schmajuk et al 39 evaluated patterns of IAHA use across the United States and calculated total payments by Medicare. They reported that Medicare reimbursed for 1 161 924 administrations of IAHA and, on average per administration, paid $179 for the drug and $69 for the injection. 39 The authors suggested that payers and providers should be judicious in their utilization of IAHA within the Medicare population due to the high utilization and cost burden.
Cost-effectiveness
All cost-effectiveness studies identified40-47 are included in Table 4. Waddell et al 40 developed a cost-of-illness model to demonstrate potential savings associated with IAHA treatment in a managed care setting (Table 4). A hypothetical cohort of patients categorized as having mild, moderate, or severe OA of the knee was followed over a 3-year time period. The 3-year savings associated with adding ⩾1 course of IAHA therapy to the standard treatment pathway for OA of the knee was $8 810 771. 40 The savings per patient with OA receiving IAHA across 3 years was $4706. 40
Cost-effectiveness studies.
Abbreviations: HMW, high molecular weight; IAHA, intra-articular hyaluronic acid; ICER, incremental cost-effectiveness ratio; LMW, low molecular weight; NSAID, nonsteroidal anti-inflammatory drug; OA, osteoarthritis; PRP, platelet-rich plasma; PT, physical therapy; QALY, quality-adjusted life-year; TKA, total knee arthroplasty; WTP, willingness to pay.
Several studies have shown that IAHA is more cost-effective in knee OA compared with conventional care with NSAIDs, analgesic, and corticosteroids.41-43,47 Several authors conclude that IAHA should therefore be the dominant treatment strategy.
The cost-effectiveness of IAHA in adults with moderate-to-severe knee pain due to OA who either failed to respond or responded poorly to conventional therapy was evaluated in the US marketplace. Two decision analytic models were developed that compared IAHA treatment with either continuation of patients’ baseline conventional care (NSAIDs, acetaminophen, physical therapy, and assistive devices) with an assumption of no disease progression (model 1) or escalating conventional care (NSAIDs and analgesics, corticosteroid injections, and surgery), which included escalating costs because of disease progression (model 2). 41 In model 1, the average utility gain among patients treated with IAHA (n = 214) was 0.163 quality-adjusted life-years (QALYs) (95% confidence interval [CI], –0.162 to 0.488) over 52 weeks. For the conventional care group, patients in this simulation were maintained on their prescribed OA care and did not gain any QALYs. Total treatment costs were $3469 for the IAHA group and $4562 for the conventional care group treated with NSAIDs and analgesics. Because IAHA treatment was effective and less costly than conventional care, IAHA was the dominant strategy and no incremental cost-effectiveness ratio (ICER) was calculated. Furthermore, sensitivity analyses showed that IAHA remained the dominant treatment strategy except when QALYs were set at the lowest end of the 95% CI. In model 2, among patients achieving a response after 2 courses of IAHA, an average of 0.23 QALYs were gained over the 1-year period. Among nonresponders (those who failed to achieve a ⩾20% improvement from baseline on Western Ontario and McMaster Universities Osteoarthritis Index [WOMAC] pain score), the average QALYs gained was 0.08. Total treatment cost over 1 year was $1446 for the IAHA group and $516 for the conventional care group. The number of QALYs gained was 0.16 for the IAHA group and 0.14 for the conventional care group. The average cost-effectiveness ratio was $8816/QALY for IAHA and $3686/QALY for escalating conventional care. The ICER for IAHA, with conventional treatment as the baseline strategy, was $38 741/QALY gained. 41 Results from 1-way sensitivity analyses showed that the ICER calculated for IAHA was most sensitive to response rates in both the IAHA and the conventional care groups. Furthermore, in a probabilistic sensitivity analysis with Monte Carlo simulation, when the willingness-to-pay level was set at $50 000/QALY, IAHA was shown to be a cost-effective strategy for OA treatment in ~70% of simulations. 41
Another economic study evaluated a single, 8-week multimodal knee OA treatment program, which included weekly IAHA injections for 3 to 5 weeks along with physical therapy, rehabilitation, and education. 42 Findings suggest that IAHA was cost-effective and lowered knee arthroplasty use through 2 years of follow-up; however, it is unclear whether the cost-effectiveness was driven by IAHA, physical therapy, or both.
Miller et al 47 constructed a cost-effectiveness model from long-term clinical outcomes and cost utility in a subgroup of patients treated with an avian-derived, non–cross-linked HA from a previous study. 42 The cost-effectiveness of a single, 8-week multimodal knee OA treatment program (1 cycle of 5 intra-articular knee injections of sodium hyaluronate given at weekly intervals along with physical therapy, rehabilitation, and education) was compared with usual care in a hypothetical control group that did not participate in the program. 47 The multimodal knee OA treatment program was highly cost-effective compared with usual care, with a base-case ICER of $6000/QALY. The percentage of simulations with an ICER below a $50 000 willingness-to-pay limit was 97.2%.
Rosen et al 43 evaluated the cost-effectiveness of treating patients with knee OA with HMW IAHA compared with low-molecular-weight (LMW) HA and conservative treatment while considering the disease stage. Decision-analytic models were created for early/moderate OA, as well as late-stage knee OA. Models for late-stage knee OA assumed a range of response rates to IAHA treatments (10%-50%) and included conservative treatment (physical therapy/exercise, braces/orthosis) and medications (NSAIDs and analgesics). The models compared the cost/QALY gained for these treatments with the use of either LMW or HMW IAHA. Incremental cost-effectiveness ratios were calculated for each treatment in relation to HMW IAHA. For early to moderate knee OA, HMW IAHA was dominant over LMW IAHA and physical therapy/exercise, as it was less expensive and provided greater benefit. Only HMW IAHA was cost-effective versus braces/orthosis and NSAID/analgesic medications based on a willingness-to-pay threshold of $50 000. In the model of 50% response rate to IAHA for late-stage OA, HMW IAHA remained cost-effective compared with physical therapy/exercise and braces/orthosis, but not with NSAID/analgesic medications, at a willingness-to-pay threshold of $50 000. In the worst-case scenario (10% responder rate to IAHA), HMW IAHA was no longer cost-effective in any circumstance. 43
Samuelson et al 44 examined the cost-effectiveness of a series of intra-articular platelet-rich plasma injections (total of 3 injections) compared with IAHA for the treatment of symptomatic knee OA. In the model, the base case assumes an otherwise healthy individual presenting to an orthopedist’s office as a new patient for the evaluation and treatment of symptomatic knee OA. The authors concluded that both treatment options would be considered cost-effective, and platelet-rich plasma injections were not more cost-effective than IAHA injections. 44
Rosen et al 45 examined and compared the cost utility of different IAHA products relative to one another and to conventional care. A single US payer economic evaluation was conducted comparing multiple IAHA products. Across all IAHA products, a bacteriologically derived, non–cross-linked IAHA preparation had the most favorable cost-utility ratio ($US 2015: $5785.52/QALY). When compared with conventional care, all IAHA products were cost-effective based on the assumption of a willingness-to-pay threshold of $50 000/QALY.
An economic model was developed to estimate the current and potential impact that a bacteriologically derived, non–cross-linked HMW IAHA preparation may have on QALYs in the US population with symptomatic knee OA. 46 The number of US patients with symptomatic knee OA in 2015 and the number of patients with TKA were used to estimate the projected total number of eligible patients who may benefit from the use of HMW IAHA versus conventional care. Results demonstrated that with current use, a bacteriologically derived, non–cross-linked HMW IAHA is estimated to save 36 730 QALY/year among the US population and has the potential to save an additional 369 181 QALY/year if used by all eligible patients.
Discussion
Intra-articular HA injections constitute a mature nonpharmacological therapeutic product market for knee pain in OA. A US retrospective claims database analysis estimated that 3 million patients with knee OA were eligible to receive IAHA treatment; however, only approximately 40% (1 238 353/3 051 968) of patients received treatment. 46 Furthermore, some major insurance carriers still do not pay for IAHA injections or require that patients fail conservative therapies, such as over-the-counter therapies, prior to the use of IAHA. The current continuum of care includes use of over-the-counter therapies followed by prescription pain medicines, corticosteroid injections, IAHA treatments, and, finally, end-stage joint replacement. Delaying the use of IAHA until patients present with advanced OA (grade IV) has been theorized to reduce its effectiveness and is inconsistent with published appropriate use criteria, which state an “uncertain” benefit in patients with advanced OA. 48 In addition, the conservative therapies currently being leveraged are palliative and are intended to alleviate pain through pharmacologic means, which may contribute to adverse events (AEs) associated with polypharmacy and drug interactions that may require acute and emergency intervention. The physiologic state of the knee with OA does not improve or remain static but continues to degrade over time. Thus, palliative therapies, such as corticosteroids, that can cause tissue atrophy and mask pain may alter innate repair and adaptive and protective mechanisms. 40 This may exacerbate and potentially accelerate degeneration of the osteoarthritic knee and the need for TKA. 49
The results of this literature review focusing on the US market demonstrate that using IAHA may delay time to TKA for up to 5 years. This finding is important because not all patients are ready for TKA when it is indicated, and because of comorbidities, many patients are contraindicated for TKA. Although no published research shows that IAHA reduces the direct incidence and corresponding cost of TKA, IAHA provides substantial clinical and economic benefits by delaying TKA. Our review identified evidence that with IAHA use, medical costs were lower (adjusted 4-year per patient per month costs) for patients treated with IAHA than for those treated with ICSs or TKA, 36 use of other pain medications was reduced,3,33,36 and substantial cost savings were feasible.37,40 Furthermore, IAHA was determined to be cost-effective against NSAIDs, corticosteroids, analgesics, 41 and conservative treatment. 43
Nonsteroidal anti-inflammatory drugs are often recommended and prescribed to treat pain in OA; however, if not used appropriately, they can be associated with adverse effects, including gastrointestinal toxicity, cardiovascular toxicity, and risk of acute myocardial infarction and heart failure. 31 This is of particular concern when treating older patients with OA, and these added complications may pose a significant economic burden to the US health care system. 28
Similarly, recent meta-analyses assessing the efficacy and safety of opioids versus placebo in patients with OA showed little evidence that opioids are beneficial for pain or function and reported high rates of AEs. 50 Any reduction in opioid use can have far-reaching economic benefits for society, especially given that current data indicate that narcotics are no more effective than NSAIDs in this population.29,51 Finally, growing evidence shows that multiple-course, intra-articular steroid injections lack long-term efficacy and may actually be detrimental, especially with chronic administration in patients with OA.49,52 Recent studies have demonstrated that AEs after intra-articular steroid injection, which include accelerated OA progression, subchondral insufficiency fracture, complications of osteonecrosis, and rapid joint destruction with bone loss, are becoming more recognized by physicians. 32 These AEs may add additional economic burden to the US health care system. Overall, the utilization of cost-effective, nonpharmacological treatment modalities with improved safety profiles, such as IAHA injections, is important and may provide cost-saving opportunities for the health care system.
While these findings are focused on the US market, and thus are generalizable only to the US market, studies in other countries have reported similar findings. In Canada, studies have determined that IAHA may be cost-effective.53,54 In the Netherlands, researchers reported that IAHA added to usual care (defined according to guidelines of the Dutch Orthopedic Association) for knee OA is probably cost-effective. 55 In France, HA may provide medical benefits at an acceptable cost. 56 In Spain, IAHA may reduce health system economic burden by delaying the implantation of a prosthetic knee. 57 Similarly, in Italy IAHA use resulted in reduced economic burden by decreasing medication consumption and drug-related AEs and by delaying surgery; the authors note that IAHA was likely cost-effective. 58
Reducing total medical care costs, minimizing opioid and analgesic utilization to an appropriate amount, and improving patient quality of life should be treatment goals of physicians selecting therapies for patients with knee OA. Achieving these goals will be ever more crucial with the movement from traditional fee-for-service payment models to value-based payment models. As IAHA injections have been widely studied in mild to moderate knee OA where they have been proven to benefit patients, these treatments need to come sooner in the continuum of care. Given the emerging evidence for potentially contraindicating steroid injections in the treatment of knee OA, perhaps the time has come to consider a new continuum of care that obviates the need for steroid injections for a patient to become eligible for nonpharmacologic IAHA treatment.
Limitations
Our study is not without limitations. One limitation of this systematic literature review is that we did not assess the quality of these studies on a quality assessment rating scale. Second, the age of certain studies may make them less relevant in the current health care environment, as treatment modalities and costs for knee OA have changed over the last 20 years. Finally, many of these studies (62%) are retrospective reviews of claims or electronic health records. Retrospective database reviews present inherent limitations, including the limited ability to measure disease severity. Furthermore, the results of these database studies are only representative of the patient populations within those databases.
Conclusions
As economic spending on health care continues to rise within the US, it is becoming ever more important to evaluate the economic value of treatment modalities to help support evidence-based decision-making. Our literature review shows that IAHA is cost-effective for the treatment of pain associated with knee OA and suggests that IAHA may reduce the use of pain medications, such as NSAIDs and opioids, and impact time to TKA procedures. As the disease burden is projected to increase for patients with knee OA, it will be important that researchers take a broader methodological approach when evaluating the economic value of IAHA, such as consideration for work-related time off due to OA, effects of QALYs, additional costs related to adverse effects of other treatments, and TKA or need for revision procedures. The findings from our literature review may be used to form future economic evaluations and inform payers regarding potential cost savings associated with IAHA treatments.
Footnotes
Funding:
The author(s) disclosed receipt of the following financial support for the research, authorship, and/or publication of this article: This work was supported by DePuy Synthes (Raynham, Massachusetts). DePuy Synthes oversaw the study concept, research methodology, writing, and review of this article. This research was performed under a research contract between RTI Health Solutions and DePuy Synthes.
Declaration of conflicting interest:
The author(s) declared the following potential conflicts of interest with respect to the research, authorship, and/or publication of this article: BB and WP are employees of DePuy Synthes. DePuy Synthes currently distributes ORTHOVISC and MONOVISC high-molecular-weight HA products. MM, CM, and CC-M are employees of RTI Health Solutions and were paid consultants to DePuy Synthes in connection with the conduct of the study and development of this article. The authors report no other conflicts of interest in this work. MM, CM, and CC-M are employees of RTI Health Solutions. WP and BB are employees of DePuy Synthes.
Author Contributions
WP and BB conceived the study, contributed to the study design, secured funding, and critically reviewed and revised the manuscript. MM designed the study; acquired, analyzed, and interpreted the data; provided study supervision; and drafted the manuscript. CM and KC-M contributed to the study design and study concepts, interpreted the data, and critically reviewed and revised the manuscript.
