Effects of the intradiscal implantation of stromal vascular fraction plus platelet rich plasma in patients with degenerative disc disease

Journal of Translational Medicine

Research

Robert Silbert¹  Kristin Comella²  Michelle Parlo² 

[1] PM&R Associates, 6640 Parkdale Place, 46254, Indianapolis, IN, USA;US Stem Cell Inc, 13794 NW 4th Street, Suite 212, 33325, Sunrise, FL, USA;

关键词: Stromal vascular fraction (SVF);    Platelet rich plasma (PRP);    Adipose derived stromal/stem cells (ADSCs);    Stem cells;    Adipose tissue;    Degenerative disc disease;    Back pain;    Cell therapy;   

DOI  :  10.1186/s12967-016-1109-0

 received in 2016-10-12, accepted in 2016-12-08,  发布年份 2017

来源: Springer

【 摘 要 】

BackgroundStromal vascular fraction (SVF) can easily be obtained from a mini-lipoaspirate procedure of fat tissue and platelet rich plasma (PRP) can be obtained from peripheral blood. The SVF contains a mixture of cells including ADSCs and growth factors and has been depleted of the adipocyte (fat cell) population. We evaluated the safety and efficacy of administering SVF and PRP intra-discally into patients with degenerative disc disease.MethodsA total of 15 patients underwent a local tumescent liposuction procedure to remove approximately 60 ml of fat tissue. The fat was separated to isolate the SVF and the cells were delivered into the disc nucleus of patients with degenerative disc disease. The subjects were then monitored for adverse events, range of motion, visual analog scale (VAS), present pain intensity (PPI), Oswestry Disability Index (ODI), Beck Depression Inventory (BDI), Dallas Pain Questionnaire and Short Form (SF)-12 scores over a period of 6 months. Safety events were followed for 12 months.ResultsNo severe adverse events (SAEs) were reported during a 12 month follow up period with no incidences of infection. Patients demonstrated statistically significant improvements in several parameters including flexion, pain ratings, VAS, PPI, and short form questionnaires. In addition, both ODI and BDI data was trending positive and a majority of patients reported improvements in their Dallas Pain Questionnaire scores.ConclusionsOverall, patients were pleased with the treatment results. More importantly, the procedure demonstrated a strong safety profile with no severe adverse events or complications linked to the therapy.Trial registration NCT02097862. Name of registry: www.clinicaltrials.gov. https://clinicaltrials.gov/ct2/show/NCT02097862?term=bioheart&rank=6. Date of registration: March 25, 2014; Date of enrollment: March 2014

【 授权许可】

CC BY   
© The Author(s) 2017