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Platelet-Rich Plasma Releasate versus Corticosteroid for the Treatment of Discogenic Low Back Pain: A Double-Blind Randomized Controlled Trial.
Akeda, Koji; Ohishi, Kohshi; Takegami, Norihiko; Sudo, Takao; Yamada, Junichi; Fujiwara, Tatsuhiko; Niimi, Rui; Matsumoto, Takeshi; Nishimura, Yuki; Ogura, Toru; Tamaru, Satoshi; Sudo, Akihiro.
Affiliation
  • Akeda K; Department of Orthopaedic Surgery, Mie University Graduate School of Medicine, Tsu 514-8507, Japan.
  • Ohishi K; Department of Transfusion Medicine and Cell Therapy, Mie University Hospital, Tsu 514-8507, Japan.
  • Takegami N; Department of Orthopaedic Surgery, Mie University Graduate School of Medicine, Tsu 514-8507, Japan.
  • Sudo T; Department of Orthopaedic Surgery, Mie University Graduate School of Medicine, Tsu 514-8507, Japan.
  • Yamada J; Department of Orthopaedic Surgery, Mie University Graduate School of Medicine, Tsu 514-8507, Japan.
  • Fujiwara T; Department of Orthopaedic Surgery, Mie University Graduate School of Medicine, Tsu 514-8507, Japan.
  • Niimi R; Niimi Orthopedics Clinic, Kuwana 511-0934, Japan.
  • Matsumoto T; Department of Transfusion Medicine and Cell Therapy, Mie University Hospital, Tsu 514-8507, Japan.
  • Nishimura Y; Clinical Research Support Center, Mie University Hospital, Tsu 514-8507, Japan.
  • Ogura T; Clinical Research Support Center, Mie University Hospital, Tsu 514-8507, Japan.
  • Tamaru S; Clinical Research Support Center, Mie University Hospital, Tsu 514-8507, Japan.
  • Sudo A; Department of Orthopaedic Surgery, Mie University Graduate School of Medicine, Tsu 514-8507, Japan.
J Clin Med ; 11(2)2022 Jan 07.
Article in En | MEDLINE | ID: mdl-35053999
ABSTRACT
Clinical application of platelet-rich plasma is gaining popularity in treating low back pain (LBP). This study investigated the efficacy and safety of platelet-rich plasma releasate (PRPr) injection into degenerated discs of patients with discogenic LBP. A randomized, double-blind, active-controlled clinical trial was conducted. Sixteen patients with discogenic LBP received an intradiscal injection of either autologous PRPr or corticosteroid (CS). Patients in both groups who wished to have PRPr treatment received an optional injection of PRPr eight weeks later. The primary outcome was change in VAS from baseline at eight weeks. Secondary outcomes were pain, disability, quality of life (QOL), image analyses of disc degeneration, and safety for up to 60 weeks. The VAS change at eight weeks did not significantly differ between the two groups. Fifteen patients received the optional injection. Compared to the CS group, the PRPr group had a significantly improved disability score at 26 weeks and walking ability scores at four and eight weeks. Radiographic disc height and MRI grading score were unchanged from baseline. PRPr caused no clinically important adverse events. PRPr injection showed clinically significant improvements in LBP intensity equal to that of CS. PRPr treatment relieved pain, and improved disability and QOL during 60 weeks of observation.
Key words

Full text: 1 Database: MEDLINE Type of study: Clinical_trials Language: En Journal: J Clin Med Year: 2022 Type: Article Affiliation country: Japan

Full text: 1 Database: MEDLINE Type of study: Clinical_trials Language: En Journal: J Clin Med Year: 2022 Type: Article Affiliation country: Japan