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Platelet-Rich Plasma Releasate versus Corticosteroid for the Treatment of Discogenic Low Back Pain: A Double-Blind Randomized Controlled Trial

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...

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Autores principales: Akeda, Koji, Ohishi, Kohshi, Takegami, Norihiko, Sudo, Takao, Yamada, Junichi, Fujiwara, Tatsuhiko, Niimi, Rui, Matsumoto, Takeshi, Nishimura, Yuki, Ogura, Toru, Tamaru, Satoshi, Sudo, Akihiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8777786/
https://www.ncbi.nlm.nih.gov/pubmed/35053999
http://dx.doi.org/10.3390/jcm11020304
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author Akeda, Koji
Ohishi, Kohshi
Takegami, Norihiko
Sudo, Takao
Yamada, Junichi
Fujiwara, Tatsuhiko
Niimi, Rui
Matsumoto, Takeshi
Nishimura, Yuki
Ogura, Toru
Tamaru, Satoshi
Sudo, Akihiro
author_facet Akeda, Koji
Ohishi, Kohshi
Takegami, Norihiko
Sudo, Takao
Yamada, Junichi
Fujiwara, Tatsuhiko
Niimi, Rui
Matsumoto, Takeshi
Nishimura, Yuki
Ogura, Toru
Tamaru, Satoshi
Sudo, Akihiro
author_sort Akeda, Koji
collection PubMed
description 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.
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spelling pubmed-87777862022-01-22 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 J Clin Med Article 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. MDPI 2022-01-07 /pmc/articles/PMC8777786/ /pubmed/35053999 http://dx.doi.org/10.3390/jcm11020304 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Akeda, Koji
Ohishi, Kohshi
Takegami, Norihiko
Sudo, Takao
Yamada, Junichi
Fujiwara, Tatsuhiko
Niimi, Rui
Matsumoto, Takeshi
Nishimura, Yuki
Ogura, Toru
Tamaru, Satoshi
Sudo, Akihiro
Platelet-Rich Plasma Releasate versus Corticosteroid for the Treatment of Discogenic Low Back Pain: A Double-Blind Randomized Controlled Trial
title Platelet-Rich Plasma Releasate versus Corticosteroid for the Treatment of Discogenic Low Back Pain: A Double-Blind Randomized Controlled Trial
title_full Platelet-Rich Plasma Releasate versus Corticosteroid for the Treatment of Discogenic Low Back Pain: A Double-Blind Randomized Controlled Trial
title_fullStr Platelet-Rich Plasma Releasate versus Corticosteroid for the Treatment of Discogenic Low Back Pain: A Double-Blind Randomized Controlled Trial
title_full_unstemmed Platelet-Rich Plasma Releasate versus Corticosteroid for the Treatment of Discogenic Low Back Pain: A Double-Blind Randomized Controlled Trial
title_short Platelet-Rich Plasma Releasate versus Corticosteroid for the Treatment of Discogenic Low Back Pain: A Double-Blind Randomized Controlled Trial
title_sort platelet-rich plasma releasate versus corticosteroid for the treatment of discogenic low back pain: a double-blind randomized controlled trial
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8777786/
https://www.ncbi.nlm.nih.gov/pubmed/35053999
http://dx.doi.org/10.3390/jcm11020304
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