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. 2019 Nov;8(11):1149-1156.
doi: 10.1002/sctm.18-0285. Epub 2019 Jul 21.

Functional Outcomes Following Microfragmented Adipose Tissue Versus Bone Marrow Aspirate Concentrate Injections for Symptomatic Knee Osteoarthritis

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Functional Outcomes Following Microfragmented Adipose Tissue Versus Bone Marrow Aspirate Concentrate Injections for Symptomatic Knee Osteoarthritis

Kenneth Mautner et al. Stem Cells Transl Med. 2019 Nov.

Abstract

This study aimed to determine whether autologous orthobiologic tissue source affects pain and functional outcomes in patients with symptomatic knee osteoarthritis (OA) who received microfragmented adipose tissue (MFAT) or bone marrow aspirate concentrate (BMAC) injection. We retrospectively reviewed prospectively collected data from patients who received BMAC or MFAT injection for symptomatic knee OA. Patients completed baseline and follow-up surveys. Each survey included the Knee Injury and Osteoarthritis Outcome Score (KOOS) questionnaire, Emory Quality of Life (EQOL) questionnaire, and Visual Analog Scale (VAS) for pain. The follow-up responses were compared with baseline for all patients and between BMAC and MFAT groups. A total of 110 patients met inclusion criteria, with 76 patients (BMAC 41, MFAT 35) and 106 knees (BMAC 58, MFAT 48) having appropriate follow-up data. The BMAC group included 17 females and 24 males, with a mean age of 59 ± 11 years. The MFAT group included 23 females and 12 males, with a mean age of 63 ± 11 years. Minimum follow-up time was 0.5 years. Mean follow-up time was 1.80 ± 0.88 years for BMAC and 1.09 ± 0.49 years for MFAT. Both groups had significant improvement in EQOL, VAS, and all KOOS parameters preprocedure versus postprocedure (p < .001). There was not a significant difference when comparing postprocedure scores between groups (p = .09, .38, .63, .94, .17, .15, .70, respectively). These data demonstrate significant improvement in pain and function with both MFAT and BMAC injections in patients with symptomatic knee OA without a significant difference in improvement when comparing the two autologous tissue sources. Stem Cells Translational Medicine 2019;8:1149-1156.

Keywords: Adipose; Adipose stem cells; Adult stem cells; Arthritis; Bone marrow; Mesenchymal stem cells; Stem cells.

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Conflict of interest statement

K.M. currently receives book royalties from Elsevier and McGraw‐Hill, and is a minor investor in Tenex Health. The other authors indicated no potential conflicts of interest.

Figures

Figure 1
Figure 1
Responder rate by Kellgren–Lawrence grade.
Figure 2
Figure 2
Knee Injury and Osteoarthritis Outcome Score at baseline and follow‐up.

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References

    1. Osteoarthritis (OA; CDC website). Available at https://www.cdc.gov/arthritis/basics/osteoarthritis.htm. Accessed April 3, 2018.
    1. Kotlarz H, Gunnarsson CL, Fang H, et al. Insurer and out‐of‐pocket costs of osteoarthritis in the US: Evidence from national survey data. Arthritis Rheum 2009;60:3546–3553. - PubMed
    1. Nguyen US, Zhang Y, Zhu Y, et al. Increasing prevalence of knee pain and symptomatic knee osteoarthritis: Survey and cohort data. Ann Intern Med 2011;155:725–732. - PMC - PubMed
    1. Vos T, Flaxman AD, Naghavi M, et al. Years lived with disability (YLDs) for 1160 sequelae of 289 diseases and injuries 1990–2010: A systematic analysis for the Global Burden of Disease Study 2010. Lancet 2012;380:2163–2196. - PMC - PubMed
    1. Lawrence RC, Felson DT, Helmick CG, et al. Estimates of the prevalence of arthritis and other rheumatic conditions in the United States. Part II. Arthritis Rheum 2008;58:26–35. - PMC - PubMed