PMID- 32047830 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20231113 IS - 2325-9671 (Print) IS - 2325-9671 (Electronic) IS - 2325-9671 (Linking) VI - 8 IP - 1 DP - 2020 Jan TI - Hyaluronic Acid Injections or Oral Nonsteroidal Anti-inflammatory Drugs for Knee Osteoarthritis: Systematic Review and Meta-analysis of Randomized Trials. PG - 2325967119897909 LID - 10.1177/2325967119897909 [doi] LID - 2325967119897909 AB - BACKGROUND: Intra-articular hyaluronic acid (HA) injections and oral nonsteroidal anti-inflammatory drugs (NSAIDs) are common treatments for symptomatic knee osteoarthritis (OA). However, the comparative effects of these treatments are unclear. PURPOSE: To compare the efficacy and safety of intra-articular HA injections compared with oral NSAIDs for the treatment of knee OA. STUDY DESIGN: Systematic review; Level of evidence, 1. METHODS: We systematically searched Medline, Embase, and the Cochrane Central Register of Controlled Trials for randomized trials of knee OA treatment with HA injections compared with oral NSAIDs. The main outcomes were knee pain, knee function, adverse events (AEs), serious AEs, study withdrawals, and study withdrawals because of AEs. Pooled effect sizes were reported at the final follow-up with standardized mean difference (SMD) for efficacy outcomes and risk ratio (RR) for safety outcomes. RESULTS: In 6 randomized trials of 831 patients (414 HA, 417 NSAIDs), with follow-up ranging from 5 to 26 weeks, HA injections were associated with small, statistically significant improvements in knee pain (SMD, 0.15; P = .04) and knee function (SMD, 0.23; P = .01) compared with oral NSAIDs. The risk of AEs was lower with HA compared with NSAIDs (19.8% vs 29.0%; RR, 0.74; P = .01). The risk of a serious AE (RR, 1.37; P = .71), study withdrawal (RR, 1.05; P = .68), or study withdrawal because of an AE (RR, 0.65; P = .22) was comparable between groups. Gastrointestinal concerns were the most frequent AE reported, occurring more often with NSAIDs (23.4% vs 14.1%; P = .001). AEs reported more frequently with HA injections were injection site pain (11.7% vs 4.7%; P < .001), headache (8.4% vs 4.4%; P = .03), and arthralgia (8.1% vs 2.9%; P = .001). Significant heterogeneity or publication bias was not observed for any outcome. CONCLUSION: Comparing short-term outcomes of HA injections with oral NSAIDs for treatment of knee OA, HA injections provided statistically significant but not clinically important improvements in knee pain and function, along with a lower overall risk of AEs. CI - (c) The Author(s) 2020. FAU - Miller, Larry E AU - Miller LE AD - Miller Scientific Consulting, Inc, Asheville, North Carolina, USA. FAU - Fredericson, Michael AU - Fredericson M AD - Department of Orthopaedic Surgery, Division of Physical Medicine and Rehabilitation, Stanford University Medical School, Stanford, California, USA. FAU - Altman, Roy D AU - Altman RD AD - Division of Rheumatology and Immunology, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, California, USA. LA - eng PT - Journal Article PT - Review DEP - 20200127 PL - United States TA - Orthop J Sports Med JT - Orthopaedic journal of sports medicine JID - 101620522 PMC - PMC6985976 OTO - NOTNLM OT - knee function OT - knee pain OT - nonsteroidal anti-inflammatory drug OT - safety OT - viscosupplementation COIS- One or more of the authors has declared the following potential conflict of interest or source of funding: L.E.M. has consulting affiliations with DePuy Synthes and OsteoArthritis Centers of America. M.F. has received honoraria from Fidia Pharma and hospitality payments from DePuy and Ipsen Innovation. R.D.A. has received speaking fees from Genzyme and Iroko Pharmaceuticals; hospitality payments from Bioventus; honoraria from Teva Pharmaceuticals; and consulting fees from Meda Pharmaceuticals, Insys Therapeutics, Ferring Pharmaceuticals, Pfizer, Genzyme, Iroko Pharmaceuticals, Novartis, Merck Sharp & Dohme, and Sanofi-Aventis. He also reports affiliations with GlaxoSmithKline, Sorrento, and Theralogix. AOSSM checks author disclosures against the Open Payments Database (OPD). AOSSM has not conducted an independent investigation on the OPD and disclaims any liability or responsibility relating thereto. EDAT- 2020/02/13 06:00 MHDA- 2020/02/13 06:01 PMCR- 2020/01/27 CRDT- 2020/02/13 06:00 PHST- 2019/09/25 00:00 [received] PHST- 2019/10/10 00:00 [accepted] PHST- 2020/02/13 06:00 [entrez] PHST- 2020/02/13 06:00 [pubmed] PHST- 2020/02/13 06:01 [medline] PHST- 2020/01/27 00:00 [pmc-release] AID - 10.1177_2325967119897909 [pii] AID - 10.1177/2325967119897909 [doi] PST - epublish SO - Orthop J Sports Med. 2020 Jan 27;8(1):2325967119897909. doi: 10.1177/2325967119897909. eCollection 2020 Jan.