Product Differences in Intra-articular Hyaluronic Acids for Osteoarthritis of the Knee

被引:135
作者
Altman, Roy D. [1 ,2 ]
Bedi, Asheesh [1 ,3 ]
Karlsson, Jon [1 ,4 ]
Sancheti, Parag [1 ,5 ]
Schemitsch, Emil [1 ,6 ]
机构
[1] Univ Calif Los Angeles, David Geffen Sch Med, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, David Geffen Sch Med, Div Rheumatol & Immunol, Rehabil Bldg,1000 Vet Ave, Los Angeles, CA 90024 USA
[3] Univ Michigan, Dept Orthopaed Surg, Ann Arbor, MI 48109 USA
[4] Sahlgrens Univ Hosp, Sahlgrenska Acad, Dept Orthoped, Gothenburg, Sweden
[5] Sancheti Inst Orthopaed & Rehabil, Pune, Maharashtra, India
[6] Univ Toronto, Dept Orthopaed Surg, Toronto, ON, Canada
关键词
knee; hyaluronic acid; osteoarthritis; viscosupplementation; RANDOMIZED CONTROLLED-TRIAL; MOLECULAR-WEIGHT HYALURONAN; G-F; 20; CONTROLLED CLINICAL-TRIAL; NON-INFERIORITY TRIAL; PLATELET-RICH PLASMA; FACTORS PRGF-ENDORET; TERM-FOLLOW-UP; DOUBLE-BLIND; SODIUM HYALURONATE;
D O I
10.1177/0363546515609599
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
100224 [整形外科学];
摘要
Background: Knee osteoarthritis (OA) is a common and often disabling joint disorder among adults that may result in impaired activity and daily function. A variety of treatment options are currently available and prescribed for knee OA depending on the severity of the disorder and physician preference. Intra-articular hyaluronic acid (IA-HA) injection is a treatment for knee OA that reportedly provides numerous biochemical and biological benefits, including shock absorption, chondroprotection, and anti-inflammatory effects within the knee. Clarity is needed as to whether the available IA-HA products should be considered for therapy as a group or whether there are significant differences in the products that need to be considered in treatment of OA of the knee. Purpose: To determine whether there are differences in efficacy and safety with respect to intrinsic properties of available IA-HA injections for knee OA. Study Design: Meta-analysis. Methods: A comprehensive literature search of the Medline, EMBASE, and PubMed databases was conducted for all existing randomized trials of IA-HA. The primary outcome measure analyzed was the mean pain score at the reported follow-up nearest to 26 weeks after injection. Pooled efficacy and safety results were recorded for subgroupings of HA product characteristics. Results: A total of 68 studies were included for analysis. Products with an average molecular weight 3000 kDa provided favorable efficacy results when compared with products of an average molecular weight <3000 kDa. Products with a molecular weight 3000 kDa demonstrated significantly fewer discontinuations due to treatment-related adverse events than did 1500 kDa counterparts, while trial discontinuation rates were similar between biological fermentation-derived HA products and avian-derived HA. The results did not demonstrate a significant difference in the occurrence of effusion across molecular weight subgroups. Additionally, biological fermentation-derived HA had a significantly smaller incidence of effusion than did avian-derived HA. Biological fermentation-derived HA demonstrated fewer acute flare-ups at the injection site than did avian-derived HA products, while high-molecular-weight products demonstrated the highest rate of injection site flare-up. Conclusion: Despite similarities, IA-HA products should not be treated as a group, as there are differences in IA-HA products that influence both efficacy and safety. In the available literature, IA-HA products with a molecular weight 3000 kDa and those derived from biological fermentation relate to superior efficacy and safetyfactors that may influence selection an IA-HA product for OA of the knee.
引用
收藏
页码:2158 / 2165
页数:8
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