Abstract
Knee osteoarthritis is among the leading causes of disability worldwide, imposing a substantial physical, psychological, and economic burden. Nonoperative management remains the cornerstone of initial care for patients before surgical considerations. This narrative review aims to synthesize current international guidelines and supporting evidence for both traditional and emerging nonoperative therapies, providing a pragmatic framework for clinical practice. Evidence consistently supports core interventions, such as patient education, self-management, weight reduction, and structured exercise. Pharmacologic adjuncts, including topical and oral nonsteroidal anti-inflammatory drugs (NSAIDs), may provide symptomatic relief, while intra-articular corticosteroids are appropriate in selected cases. More recent approaches, such as platelet-rich plasma, genicular nerve radiofrequency ablation, and genicular artery embolization, demonstrate early promise, though long-term comparative data remain limited. Optimal outcomes are achieved through patient-centered, multidisciplinary care models that address barriers, like poor adherence to exercise and limited access to weight-loss programs. This review was conducted via targeted PubMed searches using terms related to “knee osteoarthritis,” “non-operative treatment,” “guidelines,” “exercise,” “weight loss,” “NSAIDs,” “intra-articular corticosteroids,” “emerging therapies,” “hyaluronic acid,” “platelet-rich plasma,” “radiofrequency ablation,” and “genicular artery embolization.” Our synthesis followed the Scale for the Assessment of Narrative Review Articles (SANRA) recommendations for narrative reviews to ensure methodological rigor. Effective nonoperative care depends on implementing guideline-concordant strategies, recognizing emerging modalities, and tailoring therapy to patient phenotype. Future priorities include scalable models of care, high-quality comparative effectiveness trials, and closing the gap between guideline recommendations and real-world practice to improve pain, function, and quality of life.
Keywords: exercise, injections, knee osteoarthritis/koa, orthobiologics, osteoarthritis, pharmacologic therapy, weight loss
Introduction and background
Knee osteoarthritis (OA) is one of the most common causes of chronic pain and disability worldwide, creating substantial physical, psychological, and economic burden for both patients and healthcare systems [1-3]. The clinical impact is considerable: up to 80% of affected individuals experience mobility limitations, and approximately one quarter struggle with basic activities of daily living [1,2]. The reported chronic pain is often accompanied by deconditioning, mood disturbance, and increased healthcare utilization, further compounding its societal costs [2,3].
Because definitive management relies on operative intervention, nonoperative alternatives remain focused on symptom control and functional improvement [1,3]. Current clinical practice guidelines from the American Academy of Orthopaedic Surgeons (AAOS) recommend a multimodal approach, with particular emphasis on exercise and weight loss, especially in individuals with obesity [4]. Exercise has consistently shown modest but sustained improvements in pain and function, while weight reduction may provide additive benefit when combined with exercise [2].
Adjunctive options include self-management strategies and education programs, which demonstrate measurable improvements in pain and physical function [1]. Pharmacologic treatments, particularly topical and oral nonsteroidal anti-inflammatory drugs (NSAIDs), offer symptom relief when lifestyle measures are insufficient [2]. And in cases with limited benefit from lifestyle modifications and oral medications, intra-articular corticosteroid injections may be considered for short-term management of refractory pain, although their overall benefit remains limited [1,3].
Taken together, nonoperative strategies represent the cornerstone of care in knee OA, with the ultimate goals of reducing pain, improving function, and maintaining quality of life. This review summarizes current guideline-based recommendations and recent evidence supporting both traditional and emerging approaches to nonoperative management.
Review
Methodology
This narrative review was conducted in accordance with the Scale for the Assessment of Narrative Review Articles (SANRA) [5] recommendations to ensure methodological rigor and transparency in narrative synthesis. While we incorporated elements of structured searching, this work was not designed as a systematic review and did not include a preregistered protocol, formal risk of bias assessment, or meta-analysis.
A literature search was performed in PubMed/MEDLINE up to August 2025 using combinations of key terms including “knee osteoarthritis,” “non-operative treatment,” “guidelines,” “exercise,” “weight loss,” “NSAIDs,” “intra-articular corticosteroids,” “emerging therapies,” “hyaluronic acid,” “platelet-rich plasma,” “radiofrequency ablation,” and “genicular artery embolization.” Selection emphasized international guidelines, randomized controlled trials, meta-analyses, and high-quality observational studies that inform contemporary practice.
Studies addressing non-operative management of knee OA, including non-pharmacologic, pharmacologic, and procedural interventions were included. Exclusion criteria included case reports, single-patient series, in vitro studies, and abstracts without full publication. This methodology was designed to balance breadth and clinical relevance, highlighting evidence most pertinent to clinicians while following SANRA principles for high-quality narrative reviews.
Guideline foundations and core principles
Major international guidelines recommend a patient-focused, multidisciplinary approach with exercise, weight reduction, and education of the patient as the basis for management.
Osteoarthritis Research Society International (OARSI)
Emphasizes a general "core set" of non-pharmacologic management in all patients that includes formal exercise (aerobic, strengthening, neuromuscular, aquatic, or mind-body), weight reduction in obese or overweight patients, and continuing education. Interventions should be based on patient preference, need, and comorbidities, and tailored where feasible. The use of assistive devices such as bracing and walkers is recommended only in select cases. Pharmacologic therapy is considered adjunctive; oral and topical NSAIDs are initial management for relief of symptoms, with intra-articular corticosteroids considered an adjunct to therapy for a short period if prior therapy fails to relieve patient symptoms [4,6].
American College of Rheumatology (ACR) and Arthritis Foundation (AF)
Supports daily, prolonged exercise of any kind, weight loss in overweight or obese patients, self-efficacy or self-management interventions, and patient education. Supervised behavior assistance and intervention are reported to be advantageous by the guideline; Tai Chi, cane use, tibiofemoral bracing, and topical NSAIDs are also endorsed. Oral NSAIDs and intra-articular corticosteroids are likewise indicated for symptom management. Acetaminophen, duloxetine, and tramadol are conditionally endorsed for modest efficacy or safety concerns [1,7].
European League Against Rheumatism (EULAR)
Consistent with the rest of the societies in supporting education, exercise, and weight reduction. Bracing and walking aids are to be utilized as necessary. Pharmacologic therapy, primarily topical and oral NSAIDs, is reserved for chronic pain [4].
National Institute for Health and Care Excellence (NICE)
Recommends exercise as the initial treatment with subsequent weight loss if obese/overweight and self-management/education. Walking sticks and bracing are recommended as needed. Pharmacological treatment, including topical and oral NSAIDs, is recommended only after failure of non-pharmacologic intervention. Finally, intra-articular corticosteroid injections may be used for short-lasting relapses [1].
European Society for Clinical and Economic Aspects of Osteoporosis, Osteoarthritis, and Musculoskeletal Diseases (ESCEO)
Also recommends exercise, weight loss, and education as first-line treatment within a multidisciplinary approach. Pharmacologic therapy is adjunctive with a preference for topical or oral NSAIDs and short courses of oral corticosteroids [6].
Non-pharmacologic interventions such as exercise, weight loss, and patient education are the cornerstone of management for all presented guidelines. Pharmacologic and procedural treatments are adjuncts for refractory symptoms, with therapy being individualized and based on shared decision-making. The guideline recommendations are summarized in Table 1 [1-3,6,7].
Table 1. Summary of recommendations from major international guidelines for nonoperative knee osteoarthritis management.
OARSI: Osteoarthritis Research Society International; ACR: American College of Rheumatology; AF: Arthritis Foundation; EULAR: European League Against Rheumatism; NICE: National Institute for Health and Care Excellence; ESCEO: European Society for Clinical and Economic Aspects of Osteoporosis, Osteoarthritis, and Musculoskeletal Diseases; NSAIDs: Non-steroidal antiinflammatory drugs.
| Intervention | OARSI | ACR/AF | EULAR | NICE | ESCEO |
| Education & self-management | Core | Strong | Core | Core | Core |
| Exercise | Core | Strong | Core | First-line | First-line |
| Weight loss | Core | Strong | Core | First-line | First-line |
| Bracing / cane | Select cases | Strong | Recommended | As needed | As needed |
| Topical NSAIDs | Recommended | Strong | Not addressed | Prefer over oral | Preferred |
| Oral NSAIDs | Recommended | Recommended | Not addressed | After non-pharm | Preferred pharmacologic |
| Intra-articular corticosteroid | Conditional | Strong | Not addressed | For short-term flares | Short course |
| Hyaluronic acid | Against | Conditional against | Not addressed | Do not offer | Selected patients |
| Platelet-rich plasma | Strongly against | Strongly against | Not addressed | Do not offer | Not addressed |
Non-pharmacological interventions
Patient Education & Self-Management
Patient education and self-management are central components of nonoperative care for knee OA, enhancing adherence, coping ability, and informed decision-making. All major international guidelines identify education initiatives as core management strategies. Education provides patients with a clear understanding of OA etiology, prognosis, and treatment options, fostering realistic expectations and enabling active participation in care decisions.
Self-management programs, often multidisciplinary and group-based, combine skill development such as goal setting or problem-solving, guidance on medication and joint protection, and strategies to maintain physical activity. These programs reliably improve self-efficacy, encourage sustained engagement in exercise and weight control, and reduce pain and functional impairment, even when effect sizes are modest. The referenced guidelines strongly endorse self-efficacy and self-management programs for knee OA based on consistent benefit and minimal risk [7].
Education and self-management also address pain-related fear, stress, and depression while providing tools for self-monitoring and modifying patient behavior. These approaches support long-term adherence to exercise and lifestyle modifications, which are essential for symptom control and preserving function [3,6,7]. Incorporating them into standard clinical practice is widely recommended for achieving optimal outcomes [6,7].
Exercise & Physical Activity
Strength training, aerobic exercise, and balance program interventions enhance pathophysiological and functional impairments of primary knee OA and lead to less pain and improved function. As discussed, they are recommended as first-line therapies by the presented international guidelines [1-3,7-9].
Strength training aids periarticular and quadriceps muscle function, joint stability, lowers mechanical load, and alleviates pain. Quadriceps-specific exercise, particularly supervised a minimum of three times per week, is noted as optimal. Moderate intensity aerobic exercise such as walking or cycling improves cardiovascular fitness, preserves weight, and may lower systemic inflammation. Balance and neuromuscular training addresses proprioceptive deficits and functional instability, thereby lowering the risk of falls and improving confidence [3,4,7,8-11].
Beyond guideline recommendations, broader studies indicate strength training, quadriceps-specific exercises, and aerobic exercise have modest benefits on function and pain, without one being superior than another. Thus, recommendations should be patient-specific and based on preference and resources [7-10]. The literature supports that patient‑specific, supervised exercise programs improve compliance and clinical outcomes, with benefits that persist for several months after the formal program concludes [2-4,7-9].
Weight Management
High-quality evidence from randomized controlled trials and meta-analyses establishes that weight loss among obese or overweight individuals with knee OA decreases joint load, relieves pain, and enhances function. Biomechanically, one pound of weight loss is equivalent to decreasing roughly four pounds of compressive load transmitted through the knee during activities of daily living [12].
Clinically, weight loss equivalent to five percent or greater of baseline weight significantly enhances function and pain, and further improvement is noted beyond a 10 percent reduction in weight [7,12]. The literature supports that interventions with diet in addition to exercise show optimal outcomes with weight loss equivalent to seven percent of baseline or greater [13].
Successful weight control interventions are the result of pairing diet counseling and behavioral interventions with exercise, as multicomponent interventions that can include group and individual counseling, follow-up, and social cognitive theory for maximal compliance [12,13]. Education and self-management components allow for skill development and problem-solving to create long-term changes in lifestyle [7,12].
Biomechanical Aids
Orthotics, canes, and braces are beneficial adjuncts in select patients. Patients with reduced stability may benefit from assistive devices such as canes or tibiofemoral bracing, when device‑tolerant and experiencing significant symptomatic instability. Other types of bracing such as patellofemoral devices have mixed support in the literature and international guidelines given their heterogeneity of benefit and patient comfort [7].
For medial compartment OA, valgus or “unloader” braces reduce medial joint load and create short-term functional and pain reduction but are likely to be hindered by pain [14,15]. For these patients, contralateral canes have also been shown to reduce load, enhance stability, and reduce pain [7]. Orthotics such as laterally-wedged insoles have shown variable benefit and are not as widely recommended [14,16].
Physical Modalities
Unlike other musculoskeletal conditions, the literature highlights the limited role of interventions such as transcutaneous electrical nerve stimulation (TENS) and therapeutic ultrasound in the management of knee OA. TENS is related to short-term pain relief but has a less consistent and less remarkable effect on function compared to exercise, bracing, or weight loss [17,18].
Therapeutic ultrasound was shown to yield small-to-moderate functional and pain benefits over placebo, particularly at higher intensities, over 24 treatments in a four to eight week period. Although the data is limited, therapeutic ultrasound and TENS can be used as adjunct treatments, but should not replace first-line recommendations such as exercise and weight loss [19-21].
Mind-Body & Complementary Therapies
Mind-body approaches such as Tai Chi, yoga, and acupuncture can provide moderate relief in pain, function, mobility, and psychological status. Tai Chi has the most evidence, with most randomized trials showing significant pain reduction and decrease in stiffness, balance, and quality of life. The outcomes are reported as effective as those of standard physical therapy [22,23].
Mind-body practices, like Tai Chi or Qigong and yoga also have positive effects, but the evidence is less comprehensive [24,25]. Both improve depression and mental health more than that seen with resistance or aerobic exercise [26].
Acupuncture also has potential benefits in pain and disability, but variable quality evidence has provided tentative suggestions. Mind‑body treatments are safe and potentially useful adjuncts, particularly for patients seeking holistic benefits or concomitant improvement in mood [22,23,26,27].
Pharmacologic treatment
NSAIDs & Analgesics
Oral and topical NSAIDs are strongly recommended as the first-line pharmacologic therapy. Some guidelines recommend topical NSAIDs over oral formulations given their equal effectiveness and lower gastrointestinal, cardiovascular, and renal risk [2,7]. Oral NSAIDs are still appropriate for more widespread or more severe symptoms but at lowest dose and for shorter duration [7,28].
However, many guidelines are in agreement that NSAIDs need to be supplemented by fundamental non-pharmacologic treatments, and augmented by biomechanical devices, physical modalities, and mind-body interventions [1,7].
Intra-articular Injections
Corticosteroids: Cause immediate relief of pain, within four to six weeks and for up to three months. Multiple injections (>three to four per year) indicate virulent cartilage loss and thus are reserved for short-term relief of an acute flare [2,29,30].
Hyaluronic acid (HA): Produces small-to-moderate functional/pain improvements with peak effect at three to six months. Longer duration of relief can be achieved with higher molecular weight preparations, and it provides the greatest benefit for mild-to-moderate OA and for patients with NSAID intolerance [29-31].
Platelet-rich plasma (PRP): The evidence for PRP is polarized. Some studies provide evidence for efficacy in pain relief and function that compares to HA and corticosteroids. PRP may be considered primarily for younger patients with mild‑to‑moderate osteoarthritis; leukocyte‑poor PRP formulations are generally better tolerated than leukocyte‑rich preparations [30-33]. However, some guidelines like AAOS have no recommendations for its routine use for knee OA.
Adjunctive Agents
Serotonin-norepinephrine reuptake inhibitors (SNRIs) like duloxetine can also be recommended in the event of ongoing pain despite optimal non-pharmacologic therapy and NSAIDs, or in the presence of coexisting depression or widespread pain syndromes. Duloxetine provides modest improvements in pain and function for some patients, though its use may be limited by adverse effects such as nausea and sedation [1,7,34].
Opioid agonists like tramadol are conditionally utilized for intractable pain when NSAIDs and other therapy are ineffective or contraindicated, though their use should be limited by virtue of diminished benefit and potential for dependence [1,3,7,34]. Acetaminophen is of poor analgesic efficacy and carries the risk of hepatotoxicity. It is used intermittently in NSAID-intolerant patients. Topical capsaicin is also recommended but in isolated circumstances [34-36].
Not Recommended
Botulinum toxin, fish oil, glucosamine, chondroitin, and disease-modifying agents without proven benefit are not recommended given their lack of supportive evidence [7,37,38]. Other disease-modifying agents like hydroxychloroquine, methotrexate, bisphosphonates, and biologics have shown to provide no improvement [7,39].
A practical summary of treatment alternatives, along with their expected benefits, typical candidates, and key cautions, is provided in Table 2, and is intended to complement the narrative above and to facilitate quick clinical reference. [2,7,28-36,40-51].
Table 2. Pharmacologic and injection options for knee osteoarthritis: typical benefit, candidates, and major cautions.
NSAIDs: Non-steroidal antiinflammatory drugs; GI: Gastrointestinal; CV: Cardiovascular; CNS: Central nervous system; RCT: Randomized controlled trials.
| Intervention | Typical benefit & durability | Optimal candidates/when to consider | Major cautions |
| Topical NSAIDs | Analgesia while used; best for localized knee pain | First-line analgesic option, especially in older adults or those with GI/CV risks | Local skin reactions; avoid over large/broken skin |
| Oral NSAIDs | Short-term analgesia and function gains while on therapy | Flares or persistent pain unresponsive to topical agents | GI bleed/ulcer, kidney injury, CV risk—use lowest effective dose, shortest duration |
| Acetaminophen | Mild analgesia, often modest/temporary | Rescue or when NSAIDs contraindicated | Hepatotoxicity at high doses or with alcohol |
| Duloxetine | Pain reduction in some patients within weeks; benefit persists while on therapy | Co-existing widespread pain and/or depression | Nausea, somnolence; serotonin syndrome risk with other serotonergic drugs |
| Tramadol (weak opioid) | Short-term analgesia; use sparingly | Last-line if other options fail/contraindicated | Dizziness, dependence, GI/CNS adverse effects |
| Intra-articular corticosteroid | Short-term relief ~2–10 weeks (peaks early) | Acute flares, significant synovitis; bridge to rehab | Transient hyperglycemia; potential cartilage effects with frequent/repeated use |
| Hyaluronic acid | Onset weeks; benefit often seen ≥12 weeks; can last ~3–6 months | Patients preferring to avoid/limit NSAIDs or after corticosteroids; shared decision-making | Post-injection flare; cost; variable products |
| Platelet-rich plasma | Several RCT/meta-analyses show pain/function gains that may persist 6–12 months in some protocols | Select patients willing to pay, aiming to delay surgery; heterogeneity requires informed consent | Product heterogeneity; cost; coverage gaps |
| Genicular nerve radiofrequency ablation | Pain relief commonly 3–6 months, sometimes up to 6–12 months | Refractory pain, poor surgical candidates or deferring arthroplasty; after failure of core care/injections | Procedure risks (neuritis, numbness); technique-dependent outcomes |
| Genicular artery embolization | Early studies/pooled analyses show symptom improvement; durability 12–24 months in some cohorts | Refractory moderate–severe pain in specialized centers; when surgery is contraindicated or deferred | Access/site pain; non-target embolization (rare); limited long-term RCTs |
Emerging and innovative therapies
Genicular Artery Embolization (GAE)
GAE is a vigorous treatment, which, according to reports, has produced great pain relief and quality of life improvement in mild-to-moderate OA that has not responded to conservative care. Current literature reports studies with 78-92% of patients experiencing ≥50% relief of typical pain at six to 12 months [40-43]. Side effects for GAE are usually classified as harmless and self-limiting [41,42,44]. GAE remains outside of standard OA practice guidelines but is endorsed by the Society of Interventional Radiology in properly selected candidates who are not eligible for operation [45,46].
Genicular Nerve Radiofrequency Ablation (RFA)
RFA suppresses pain transmission by destroying the genicular nerve branches. Recent studies from the literature have shown greater short-term relief of pain and function compared with corticosteroids, HA, NSAIDs, acetaminophen, and placebos [15,47-51]. Improvement is documented as greatest at six months, when 74% of patients experienced ≥50% pain relief, which can persist for as long as 12 months in some patients [48,49].
Intravascular Laser Irradiation of Blood (ILIB)
ILIB is not established in OA guidelines and has poor-quality evidence. Early evidence elsewhere provides promising anti-inflammatory effects, but evidence is lacking for OA [52].
Gene Therapy
Experimental, disease‑modifying approaches targeting inflammatory pathways (e.g., IL‑1β inhibition) and anabolic pathways (e.g., intra‑articular tumor growth factor (TGF)‑β1 or fibroblast growth factor (FGF)‑18 delivery) have shown promising results in preclinical studies and early‑phase clinical trials. Transgene expression over many years alleviated inflammation and cartilage loss in animal models [53-56]. However, regulatory approval of any OA gene therapy has not been clearly established.
Bone Marrow Aspirate Concentrate
Bone marrow aspirate concentrate (BMAC) is derived from bone marrow harvested through aspiration, then processed to yield a concentrate of mesenchymal stem cells and cytokines which is then administered via an intra-articular injection. Some studies report significant short- to mid-term pain and functional value, but without perceived superiority to adipose-derived stem cell therapy (ADSC) or other orthobiologics such as PRP [57-60]. In the literature, both BMAC and adipose-derived stromal vascular fraction (SVF) have shown symptomatic benefit, with SVF offering superior pain relief, but functional outcome was equal for both modalities [58,61-63]. Long-term outcomes demonstrate sustained benefit up to four years in some cohorts, but cumulative evidence is inconsistent due to heterogeneity of preparation and patient recruitment [59,64].
Adipose-Derived Stem Cells (ADSC)
ADSCs are harvested from fat tissue, usually through liposuction, and concentrated for use as an injectable orthobiologic. Some studies have showed that the infrapatellar fat pad (IFP) can be harvested arthroscopically as a viable and consistent source of ADSCs. In these studies, cells attached and grew in culture, had clonogenic potential, and exhibited multilineage differentiation, including robust chondrogenic capacity. Notably, IFP-derived stromal vascular fraction cells had greater CD105 expression than the other adipose sources, consistent with greater regenerative potential [65].
Umbilical Cord Stem Cells
Umbilical cord-derived mesenchymal stem cells (UC-MSCs) are isolated from postnatal umbilical tissue and processed as an injectable biologic with potential anti-inflammatory and regenerative effects. Some studies have shown moderate improvement in function and pain at short to intermediate term follow-up, with a safety profile equivalent to BMAC and ADSC therapy, with no concerning adverse events reported in the available literature [66-70]. The available comparison studies reveal that both UC-MSCs and ADSC provide symptomatic relief, with the greatest improvement in pain for the ADSCs and the best functional result for the UC-MSCs on the Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) measure [61,71].
Hematopoietic Stem Cells
Hematopoietic stem cells (HSC) do not play a role in the management of knee OA due to the focus on mesenchymal stem cell (MSC) therapies, such as BMAC, adipose tissue, or UC-MSC [66-72]. HSC, the progenitors of blood lineages, have limited research for their applications in OA management and thus are not recommended for intra-articular injection in knee OA.
Corticosteroid formulations
Methylprednisolone acetate, triamcinolone acetonide, and betamethasone all induce short-term pain relief when administered as intra-articular corticosteroid injections for knee O, with maximal effect at one to six weeks and fading at 12-24 weeks. Their side effect profiles are similarly comparable, with most being self-limiting local reactions like pain, swelling, and infrequently infection or post-injection flare. Clinical comparative trials prove that methylprednisolone acetate has possibly more intense analgesic effect up to six weeks than triamcinolone acetonide and betamethasone but there is no difference in their effect by 12 weeks, with comparable functional benefit or duration of action after that point [73-78]. Betamethasone and triamcinolone acetonide are equivalent to methylprednisolone acetate in terms of overall pain and function outcomes, although triamcinolone hexacetonide has shown more intense and immediate pain relief in some series [74-78]. Given that no differences in systemic adverse effects or cartilage toxicity have been observed among the different corticosteroids in the setting of single or infrequent doses, major guidelines have not established a preference between corticosteroid alternatives for intra-articular injection.
Integrated multidisciplinary care and implementation barriers
Optimal care is achieved through collaboration among physical therapists, physicians, dietitians, and allied health professionals. This leads to concerted, tailored, and evidence-based care. Obstacles to optimal OA care include disparities in weight-management resources, variable availability of supervised exercise, and lack of compliance with long-term activity regimens [79].
Conclusions
Nonoperative care remains the foundation of knee OA management. Lifestyle adaptation, structured education, formal exercise programs, and weight loss are consistently recommended as first-line treatments, with pharmacotherapy, biomechanical aids, and selected intra-articular injections serving as adjuncts when symptoms persist. At the same time, newer therapeutic alternatives are generating growing interest. While early results are promising, evidence is still limited by the heterogeneity of protocols, short follow-up, and modest sample sizes.
Future research priorities include high-quality comparative efficacy studies of emerging interventions against established care; extended follow-up to clarify the durability of benefits; phenotype-directed treatment strategies; and scalable models of multidisciplinary care to improve access, adherence, and real-world implementation. Patient-targeted, team-based approaches remain the most promising pathway to sustainable improvements in pain, function, and quality of life for individuals living with knee OA.
Disclosures
Conflicts of interest: In compliance with the ICMJE uniform disclosure form, all authors declare the following:
Payment/services info: All authors have declared that no financial support was received from any organization for the submitted work.
Financial relationships: All authors have declared that they have no financial relationships at present or within the previous three years with any organizations that might have an interest in the submitted work.
Other relationships: All authors have declared that there are no other relationships or activities that could appear to have influenced the submitted work.
Author Contributions
Acquisition, analysis, or interpretation of data: Gabriel Gonzalez-Diaz, Derick Rodríguez-Reyes, Ricardo Vargas-Figueroa, Amanda S. Vázquez-Lloret, Hiram E. Luigi Martinez
Critical review of the manuscript for important intellectual content: Gabriel Gonzalez-Diaz, Derick Rodríguez-Reyes, Amanda S. Vázquez-Lloret, Hiram E. Luigi Martinez, Rafael Señeriz Ortiz
Supervision: Gabriel Gonzalez-Diaz, Hiram E. Luigi Martinez
Concept and design: Derick Rodríguez-Reyes, Ricardo Vargas-Figueroa, Rafael Señeriz Ortiz
Drafting of the manuscript: Ricardo Vargas-Figueroa
References
- 1.Evaluation and treatment of knee pain: a review. Duong V, Oo WM, Ding C, Culvenor AG, Hunter DJ. JAMA. 2023;330:1568–1580. doi: 10.1001/jama.2023.19675. [DOI] [PubMed] [Google Scholar]
- 2.Osteoarthritis of the knee. Sharma L. N Engl J Med. 2021;384:51–59. doi: 10.1056/NEJMcp1903768. [DOI] [PubMed] [Google Scholar]
- 3.Diagnosis and treatment of hip and knee osteoarthritis: a review. Katz JN, Arant KR, Loeser RF. JAMA. 2021;325:568–578. doi: 10.1001/jama.2020.22171. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 4.AAOS clinical practice guideline summary: management of osteoarthritis of the knee (nonarthroplasty), third edition. Brophy RH, Fillingham YA. J Am Acad Orthop Surg. 2022;30:0–9. doi: 10.5435/JAAOS-D-21-01233. [DOI] [PubMed] [Google Scholar]
- 5.SANRA-a scale for the quality assessment of narrative review articles. Baethge C, Goldbeck-Wood S, Mertens S. Res Integr Peer Rev. 2019;4:5. doi: 10.1186/s41073-019-0064-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 6.Nonpharmacological and nonsurgical approaches in OA. Bierma-Zeinstra S, van Middelkoop M, Runhaar J, Schiphof D. Best Pract Res Clin Rheumatol. 2020;34:101564. doi: 10.1016/j.berh.2020.101564. [DOI] [PubMed] [Google Scholar]
- 7.2019 American College of Rheumatology/Arthritis Foundation guideline for the management of osteoarthritis of the hand, hip, and knee. Kolasinski SL, Neogi T, Hochberg MC, et al. Arthritis Rheumatol. 2020;72:220–233. doi: 10.1002/art.41142. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8.Exercise for osteoarthritis of the knee. Lawford BJ, Hall M, Hinman RS, et al. Cochrane Database Syst Rev. 2024;12:0. doi: 10.1002/14651858.CD004376.pub4. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Effects of physical activity in knee and hip osteoarthritis: a systematic umbrella review. Kraus VB, Sprow K, Powell KE, et al. Med Sci Sports Exerc. 2019;51:1324–1339. doi: 10.1249/MSS.0000000000001944. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10.Impact of exercise type and dose on pain and disability in knee osteoarthritis: a systematic review and meta-regression analysis of randomized controlled trials. Juhl C, Christensen R, Roos EM, Zhang W, Lund H. Arthritis Rheumatol. 2014;66:622–636. doi: 10.1002/art.38290. [DOI] [PubMed] [Google Scholar]
- 11.Effects of three types of resistance training on knee osteoarthritis: a systematic review and network meta-analysis. Jiang Y, Tan Y, Cheng L, Wang J. PLoS One. 2024;19:0. doi: 10.1371/journal.pone.0309950. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 12.Effect of diet and exercise on knee pain in patients with osteoarthritis and overweight or obesity: a randomized clinical trial. Messier SP, Beavers DP, Queen K, et al. JAMA. 2022;328:2242–2251. doi: 10.1001/jama.2022.21893. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13.Comparison of weight loss interventions in overweight and obese adults with knee osteoarthritis: a systematic review and network meta-analysis of randomized trials. Shahid A, Thirumaran AJ, Christensen R, Venkatesha V, Henriksen M, Bowden JL, Hunter DJ. Osteoarthritis Cartilage. 2025;33:518–529. doi: 10.1016/j.joca.2024.08.012. [DOI] [PubMed] [Google Scholar]
- 14.Braces and orthoses for treating osteoarthritis of the knee. Duivenvoorden T, Brouwer RW, van Raaij TM, Verhagen AP, Verhaar JA, Bierma-Zeinstra SM. Cochrane Database Syst Rev. 2015;2015:0. doi: 10.1002/14651858.CD004020.pub3. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 15.Consensus guidelines on interventional therapies for knee pain (STEP guidelines) from the American Society of Pain and Neuroscience. Hunter CW, Deer TR, Jones MR, et al. J Pain Res. 2022;15:2683–2745. doi: 10.2147/JPR.S370469. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16.Physical therapy and orthopaedic equipment-induced reduction in the biomechanical risk factors related to knee osteoarthritis: a systematic review and Bayesian network meta-analysis of randomised controlled trials. Huang XM, Yuan FZ, Chen YR, Huang Y, Yang ZX, Lin L, Yu JK. BMJ Open. 2022;12:0. doi: 10.1136/bmjopen-2021-051608. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 17.Effects of transcutaneous electrical nerve stimulation (TENS) in people with knee osteoarthritis: a systematic review and meta-analysis. Wu Y, Zhu F, Chen W, Zhang M. Clin Rehabil. 2022;36:472–485. doi: 10.1177/02692155211065636. [DOI] [PubMed] [Google Scholar]
- 18.Transcutaneous electrical nerve stimulation in patients with knee osteoarthritis: evidence from randomized-controlled trials. Chen LX, Zhou ZR, Li YL, Ning GZ, Li Y, Wang XB, Feng SQ. Clin J Pain. 2016;32:146–154. doi: 10.1097/AJP.0000000000000233. [DOI] [PubMed] [Google Scholar]
- 19.A meta-analysis of analgesic effect of ultrasound therapy for patients with knee osteoarthritis. Liu Y, Wang Y, Wang Y, Jia X. J Ultrasound Med. 2022;41:1861–1872. doi: 10.1002/jum.15866. [DOI] [PubMed] [Google Scholar]
- 20.Effects of therapeutic ultrasound for knee osteoarthritis: a systematic review and meta-analysis. Wu Y, Zhu S, Lv Z, et al. Clin Rehabil. 2019;33:1863–1875. doi: 10.1177/0269215519866494. [DOI] [PubMed] [Google Scholar]
- 21.Efficacy of non-pharmacological treatments for knee osteoarthritis: a systematic review and network meta-analysis. Cao S, Zan Q, Wang B, Fan X, Chen Z, Yan F. Heliyon. 2024;10:0. doi: 10.1016/j.heliyon.2024.e36682. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 22.The effects of Tai Chi on pain and other health indicators in people with osteoarthritis: an updated systematic review and dose-response meta-analysis. Zhao A, Brown WJ, Coombes JS, Liu X. Osteoarthritis Cartilage. 2025;33:933–950. doi: 10.1016/j.joca.2025.05.013. [DOI] [PubMed] [Google Scholar]
- 23.Impact of Tai Chi on physical and mental well-being in individuals with knee osteoarthritis: a systematic review and meta-analysis. Wu D, Liu Y, Xue Z, Han S, Zhou M. Am J Phys Med Rehabil. 2025;104:998–1006. doi: 10.1097/PHM.0000000000002762. [DOI] [PubMed] [Google Scholar]
- 24.Effects of different mind-body exercises on pain in patients with knee osteoarthritis: a pairwise, network, and dose-response meta-analysis. Wu B, Liu W, Wang S, Li H, Yin M. Complement Ther Med. 2025;92:103188. doi: 10.1016/j.ctim.2025.103188. [DOI] [PubMed] [Google Scholar]
- 25.Mind-body exercises for osteoarthritis: an overview of systematic reviews including 32 meta-analyses. de-la-Casa-Almeida M, Villar-Alises O, Rodríguez Sánchez-Laulhé P, Martinez-Calderon J, Matias-Soto J. Disabil Rehabil. 2024;46:1699–1707. doi: 10.1080/09638288.2023.2203951. [DOI] [PubMed] [Google Scholar]
- 26.Nonpharmacological approaches for pain and symptoms of depression in people with osteoarthritis: systematic review and meta-analyses. Burley CV, Casey AN, Jones MD, Wright KE, Parmenter BJ. Sci Rep. 2023;13:15449. doi: 10.1038/s41598-023-41709-x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 27.Effects of mind-body exercise on knee osteoarthritis: a systematic review and meta-analysis of randomized controlled trials. Qiao H, Hao X, Wang G. BMC Musculoskelet Disord. 2024;25:229. doi: 10.1186/s12891-024-07278-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 28.Effectiveness and safety of non-steroidal anti-inflammatory drugs and opioid treatment for knee and hip osteoarthritis: network meta-analysis. da Costa BR, Pereira TV, Saadat P, et al. BMJ. 2021;375:0. doi: 10.1136/bmj.n2321. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 29.Intra-articular knee injections and progression of knee osteoarthritis: data from the osteoarthritis initiative. Bharadwaj UU, Lynch JA, Joseph GB, et al. Radiology. 2025;315:0. doi: 10.1148/radiol.233081. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 30.Estimated time to maximum medical improvement of intra-articular injections in the treatment of knee osteoarthritis-a systematic review. Mojica ES, Markus DH, Hurley ET, Blaeser AM, Jazrawi LM, Campbell KA, Strauss EJ. Arthroscopy. 2022;38:980–988. doi: 10.1016/j.arthro.2021.08.026. [DOI] [PubMed] [Google Scholar]
- 31.Hyaluronic acid and platelet-rich plasma for the management of knee osteoarthritis. Gilat R, Haunschild ED, Knapik DM, Evuarherhe A Jr, Parvaresh KC, Cole BJ. Int Orthop. 2021;45:345–354. doi: 10.1007/s00264-020-04801-9. [DOI] [PubMed] [Google Scholar]
- 32.Relative efficacy of intra-articular injections in the treatment of knee osteoarthritis: a systematic review and network meta-analysis. Singh H, Knapik DM, Polce EM, et al. Am J Sports Med. 2022;50:3140–3148. doi: 10.1177/03635465211029659. [DOI] [PubMed] [Google Scholar]
- 33.Platelet-rich plasma, bone marrow aspirate concentrate, and hyaluronic acid injections outperform corticosteroids in pain and function scores at a minimum of 6 months as intra-articular injections for knee osteoarthritis: a systematic review and network meta-analysis. Jawanda H, Khan ZA, Warrier AA, et al. Arthroscopy. 2024;40:1623–1636. doi: 10.1016/j.arthro.2024.01.037. [DOI] [PubMed] [Google Scholar]
- 34.CDC clinical practice guideline for prescribing opioids for pain - United States, 2022. Dowell D, Ragan KR, Jones CM, Baldwin GT, Chou R. MMWR Recomm Rep. 2022;71:1–95. doi: 10.15585/mmwr.rr7103a1. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 35.Pharmaceutical treatment of osteoarthritis. Richard MJ, Driban JB, McAlindon TE. Osteoarthritis Cartilage. 2023;31:458–466. doi: 10.1016/j.joca.2022.11.005. [DOI] [PubMed] [Google Scholar]
- 36.Effect of opioid vs nonopioid medications on pain-related function in patients with chronic back pain or hip or knee osteoarthritis pain: the SPACE randomized clinical trial. Krebs EE, Gravely A, Nugent S, et al. JAMA. 2018;319:872–882. doi: 10.1001/jama.2018.0899. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 37.Associations of fish oil supplementation with risks of osteoarthritis and arthroplasty: a large population-based prospective cohort study. Li Z, Chen Y, Gao Y, Xu B, Guo VY, Zhang W, Wu IX. J Nutr. 2025;155:3466–3478. doi: 10.1016/j.tjnut.2025.07.017. [DOI] [PubMed] [Google Scholar]
- 38.Treatment of osteoarthritis of the knee (nonarthroplasty) Richmond J, Hunter D, Irrgang J, et al. J Am Acad Orthop Surg. 2009;17:591–600. doi: 10.5435/00124635-200909000-00006. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 39.Osteoarthritis management: updated guidelines from the American College of Rheumatology and Arthritis Foundation. Buelt A, Narducci DM. https://www.aafp.org/pubs/afp/issues/2021/0115/p120.html. Am Fam Physician. 2021;103:120–121. [PubMed] [Google Scholar]
- 40.Genicular artery embolization as a treatment for osteoarthritis related knee pain: a systematic review and meta-analysis. Epelboym Y, Mandell JC, Collins JE, et al. Cardiovasc Intervent Radiol. 2023;46:760–769. doi: 10.1007/s00270-023-03422-0. [DOI] [PubMed] [Google Scholar]
- 41.Geniculate artery embolization for the treatment of mild to moderate knee osteoarthritis improves pain and function at short-term follow-up with significant procedural heterogeneity described across the literature: a systematic review. Berreta RS, Rubin J, Manivannan A, et al. Arthroscopy. 2025;41:2117–2133. doi: 10.1016/j.arthro.2024.07.033. [DOI] [PubMed] [Google Scholar]
- 42.Bridging the gap between injections and surgery: meta-analysis of genicular artery embolization in knee osteoarthritis. Abussa R, Jeremic A. Acad Radiol. 2025 doi: 10.1016/j.acra.2025.05.011. [DOI] [PubMed] [Google Scholar]
- 43.Genicular artery embolization in moderate to severe knee osteoarthritis: technique, safety and clinical outcome. Taheri Amin A, Frommhold I, Huebner A, et al. Cardiovasc Intervent Radiol. 2025;48:340–350. doi: 10.1007/s00270-025-03983-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 44.Genicular artery embolization for the treatment of knee pain secondary to osteoarthritis. Bagla S, Piechowiak R, Hartman T, Orlando J, Del Gaizo D, Isaacson A. J Vasc Interv Radiol. 2020;31:1096–1102. doi: 10.1016/j.jvir.2019.09.018. [DOI] [PubMed] [Google Scholar]
- 45.Comparison of minimally invasive procedures to treat knee pain secondary to osteoarthritis: a systematic review and meta-analysis. Sajan A, Mehta T, Griepp DW, Chait AR, Isaacson A, Bagla S. J Vasc Interv Radiol. 2022;33:238–248. doi: 10.1016/j.jvir.2021.11.004. [DOI] [PubMed] [Google Scholar]
- 46.Society of Interventional Radiology Research reporting standards for genicular artery embolization. Ahmed O, Epelboym Y, Haskal ZJ, et al. J Vasc Interv Radiol. 2024;35:1097–1103. doi: 10.1016/j.jvir.2024.04.018. [DOI] [PubMed] [Google Scholar]
- 47.Thermal nerve radiofrequency ablation for the nonsurgical treatment of knee osteoarthritis: a systematic literature review. Chen AF, Mullen K, Casambre F, Visvabharathy V, Brown GA. J Am Acad Orthop Surg. 2021;29:387–396. doi: 10.5435/JAAOS-D-20-00522. [DOI] [PubMed] [Google Scholar]
- 48.Radiofrequency ablation in cooled monopolar or conventional bipolar modality yields more beneficial short-term clinical outcomes versus other treatments for knee osteoarthritis: a systematic review and network meta-analysis of randomized controlled trials. Wu L, Li Y, Si H, Zeng Y, Li M, Liu Y, Shen B. Arthroscopy. 2022;38:2287–2302. doi: 10.1016/j.arthro.2022.01.048. [DOI] [PubMed] [Google Scholar]
- 49.The effectiveness of fluoroscopically guided genicular nerve radiofrequency ablation for the treatment of chronic knee pain due to osteoarthritis: a systematic review. Fogarty AE, Burnham T, Kuo K, et al. Am J Phys Med Rehabil. 2022;101:482–492. doi: 10.1097/PHM.0000000000001813. [DOI] [PubMed] [Google Scholar]
- 50.Genicular nerve radiofrequency ablation for the treatment of painful knee osteoarthritis: current evidence and future directions. Conger A, Gililland J, Anderson L, Pelt CE, Peters C, McCormick ZL. Pain Med. 2021;22:0–3. doi: 10.1093/pm/pnab129. [DOI] [PubMed] [Google Scholar]
- 51.Effectiveness of radiofrequency ablation of the genicular nerves of the knee for the management of intractable pain from knee osteoarthritis. Lee SH, Choi HH, Kwak SG, Chang MC. https://www.painphysicianjournal.com/current/pdf?article=Nzg0OA%3D%3D&journal=161. Pain Physician. 2024;27:0–29. [PubMed] [Google Scholar]
- 52.Influence of intravascular laser irradiation of blood (ILIB) on inflammatory cytokines and nitric oxide in vivo: a systematic review. Vasconcelos MR, Cardoso-Silva L, Barbosa AC, Borsatto MC, Corona SA. Lasers Med Sci. 2024;39:85. doi: 10.1007/s10103-024-04031-0. [DOI] [PubMed] [Google Scholar]
- 53.Gene therapy for the treatment of osteoarthritis: advances and prospective. Rana A, Malviya R, Rajput S, Sridhar SB, Shareef J. Curr Pharm Des. 2025;31:0. doi: 10.2174/0113816128384412250709130211. [DOI] [PubMed] [Google Scholar]
- 54.Gene therapy pipelines for osteoarthritis: current innovations, operational challenges, and future directions. Peitso V, Ng K, Ellis R, Reginster JY, Evans CH, Mobasheri A. Connect Tissue Res. 2025;66:458–465. doi: 10.1080/03008207.2025.2520319. [DOI] [PubMed] [Google Scholar]
- 55.Application of gene therapy in osteoarthritis. Li Y, Li B, Nagy A, Kim C. Connect Tissue Res. 2025;66:450–457. doi: 10.1080/03008207.2025.2533332. [DOI] [PubMed] [Google Scholar]
- 56.Osteoarthritis gene therapy in 2022. Evans CH, Ghivizzani SC, Robbins PD. Curr Opin Rheumatol. 2023;35:37–43. doi: 10.1097/BOR.0000000000000918. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 57.Bone marrow aspirate concentrate for the treatment of knee osteoarthritis: a systematic review. Keeling LE, Belk JW, Kraeutler MJ, Kallner AC, Lindsay A, McCarty EC, Postma WF. Am J Sports Med. 2022;50:2315–2323. doi: 10.1177/03635465211018837. [DOI] [PubMed] [Google Scholar]
- 58.Clinical efficacy of bone marrow aspirate concentrate versus stromal vascular fraction injection in patients with knee osteoarthritis: a systematic review and meta-analysis. Bolia IK, Bougioukli S, Hill WJ, Trasolini NA, Petrigliano FA, Lieberman JR, Weber AE. Am J Sports Med. 2022;50:1451–1461. doi: 10.1177/03635465211014500. [DOI] [PubMed] [Google Scholar]
- 59.Management of knee osteoarthritis using bone marrow aspirate concentrate: a systematic review. Migliorini F, Pilone M, Ascani J, Schäfer L, Jeyaraman M, Maffulli N. Br Med Bull. 2025;153:0. doi: 10.1093/bmb/ldae016. [DOI] [PubMed] [Google Scholar]
- 60.Bone marrow aspirate concentrate is equivalent to platelet-rich plasma for the treatment of knee osteoarthritis at 2 years: a prospective randomized trial. Anz AW, Plummer HA, Cohen A, Everts PA, Andrews JR, Hackel JG. Am J Sports Med. 2022;50:618–629. doi: 10.1177/03635465211072554. [DOI] [PubMed] [Google Scholar]
- 61.Effect of mesenchymal stromal cells transplantation on the outcomes of patients with knee osteoarthritis: a systematic review and meta-analysis. Xie RH, Gong SG, Song J, Wu PP, Hu WL. J Orthop Res. 2024;42:753–768. doi: 10.1002/jor.25724. [DOI] [PubMed] [Google Scholar]
- 62.Cell-based versus corticosteroid injections for knee pain in osteoarthritis: a randomized phase 3 trial. Mautner K, Gottschalk M, Boden SD, et al. Nat Med. 2023;29:3120–3126. doi: 10.1038/s41591-023-02632-w. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 63.Autologous stem cell therapy in knee osteoarthritis: a systematic review of randomised controlled trials. Wiggers TG, Winters M, Van den Boom NA, Haisma HJ, Moen MH. Br J Sports Med. 2021;55:1161–1169. doi: 10.1136/bjsports-2020-103671. [DOI] [PubMed] [Google Scholar]
- 64.Intra-articular injection of bone marrow aspirate concentrate (mesenchymal stem cells) in KL grade III and IV knee osteoarthritis: 4 year results of 37 knees. Pabinger C, Lothaller H, Kobinia GS. Sci Rep. 2024;14:2665. doi: 10.1038/s41598-024-51410-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 65.Arthroscopic harvest of adipose-derived mesenchymal stem cells from the infrapatellar fat pad. Dragoo JL, Chang W. Am J Sports Med. 2017;45:3119–3127. doi: 10.1177/0363546517719454. [DOI] [PubMed] [Google Scholar]
- 66.Stem cell injections for osteoarthritis of the knee. Whittle SL, Johnston RV, McDonald S, et al. Cochrane Database Syst Rev. 2025;4:0. doi: 10.1002/14651858.CD013342.pub2. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 67.Effects of the umbilical cord mesenchymal stem cells in the treatment of knee osteoarthritis: a systematic review and meta-analysis. Xiao Z, Wang X, Li C, Luo L, Li W. Medicine (Baltimore) 2024;103:0. doi: 10.1097/MD.0000000000040490. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 68.Efficacy of a single dose of cryopreserved human umbilical cord mesenchymal stromal cells for the treatment of knee osteoarthritis:a randomized, controlled, double-blind pilot study. Pico OA, Espinoza F, Cádiz MI, et al. Cytotherapy. 2025;27:188–200. doi: 10.1016/j.jcyt.2024.09.005. [DOI] [PubMed] [Google Scholar]
- 69.A phase I dose-escalation clinical trial to assess the safety and efficacy of umbilical cord-derived mesenchymal stromal cells in knee osteoarthritis. Matas J, García C, Poblete D, et al. Stem Cells Transl Med. 2024;13:193–203. doi: 10.1093/stcltm/szad088. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 70.Repeated intra-articular injections of umbilical cord-derived mesenchymal stem cells for knee osteoarthritis: a phase I, single-arm study. Ao Y, Duan J, Xiong N, et al. BMC Musculoskelet Disord. 2023;24:488. doi: 10.1186/s12891-023-06555-y. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 71.Decadal analysis of efficacy and safety profiles of mesenchymal stem cells from varied sources in knee osteoarthritis patients: A systematic review and network meta-analysis. Tang X, Huang H, Hao L. Exp Gerontol. 2024;192:112460. doi: 10.1016/j.exger.2024.112460. [DOI] [PubMed] [Google Scholar]
- 72.Intra-articular injections of mesenchymal stem cells without adjuvant therapies for knee osteoarthritis: a systematic review and meta-analysis. Tan SH, Kwan YT, Neo WJ, et al. Am J Sports Med. 2021;49:3113–3124. doi: 10.1177/0363546520981704. [DOI] [PubMed] [Google Scholar]
- 73.Efficacy comparisons of the intraarticular steroidal agents in the patients with knee osteoarthritis. Yavuz U, Sökücü S, Albayrak A, Oztürk K. Rheumatol Int. 2012;32:3391–3396. doi: 10.1007/s00296-011-2188-0. [DOI] [PubMed] [Google Scholar]
- 74.Efficacy of triamcinolone hexacetonide versus methylprednisolone acetate intraarticular injections in knee osteoarthritis: a randomized, double-blinded, 24-week study. Lomonte AB, de Morais MG, de Carvalho LO, Zerbini CA. J Rheumatol. 2015;42:1677–1684. doi: 10.3899/jrheum.150297. [DOI] [PubMed] [Google Scholar]
- 75.Intra-articular and soft tissue injections, a systematic review of relative efficacy of various corticosteroids. Garg N, Perry L, Deodhar A. Clin Rheumatol. 2014;33:1695–1706. doi: 10.1007/s10067-014-2572-8. [DOI] [PubMed] [Google Scholar]
- 76.Intra-articular steroids in knee osteoarthritis: a comparative study of triamcinolone hexacetonide and methylprednisolone acetate. Pyne D, Ioannou Y, Mootoo R, Bhanji A. Clin Rheumatol. 2004;23:116–120. doi: 10.1007/s10067-003-0841-z. [DOI] [PubMed] [Google Scholar]
- 77.Efficacy of methylprednisolone acetate versus triamcinolone acetonide intra-articular knee injection in patients with chronic inflammatory arthritis: a 24-week randomized controlled trial. Kumar A, Dhir V, Sharma S, Sharma A, Singh S. Clin Ther. 2017;39:150–158. doi: 10.1016/j.clinthera.2016.11.023. [DOI] [PubMed] [Google Scholar]
- 78.Intra-articular corticosteroids for osteoarthritis of the knee. da Costa BR, Hari R, Jüni P. JAMA. 2016;316:2671–2672. doi: 10.1001/jama.2016.17565. [DOI] [PubMed] [Google Scholar]
- 79.Primary care-based models of care for osteoarthritis; a scoping review. Cunningham J, Doyle F, Ryan JM, et al. Semin Arthritis Rheum. 2023;61:152221. doi: 10.1016/j.semarthrit.2023.152221. [DOI] [PubMed] [Google Scholar]
