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Intradiscal administration of autologous platelet-rich plasma in patients with Modic type 1 associated low back pain: A prospective pilot study.
Kawabata, Soya; Nagai, Sota; Ito, Kei; Takeda, Hiroki; Ikeda, Daiki; Kawano, Yusuke; Kaneko, Shinjiro; Shiraishi, Yukako; Sano, Yuichiro; Ohno, Yoshiharu; Fujita, Nobuyuki.
Afiliação
  • Kawabata S; Department of Orthopaedic Surgery, School of Medicine Fujita Health University Toyoake Aichi Japan.
  • Nagai S; Department of Orthopaedic Surgery, School of Medicine Fujita Health University Toyoake Aichi Japan.
  • Ito K; Department of Orthopaedic Surgery, School of Medicine Fujita Health University Toyoake Aichi Japan.
  • Takeda H; Department of Spine and Spinal Cord Surgery, School of Medicine Fujita Health University Toyoake Aichi Japan.
  • Ikeda D; Department of Orthopaedic Surgery, School of Medicine Fujita Health University Toyoake Aichi Japan.
  • Kawano Y; Department of Orthopaedic Surgery, School of Medicine Fujita Health University Toyoake Aichi Japan.
  • Kaneko S; Department of Spine and Spinal Cord Surgery, School of Medicine Fujita Health University Toyoake Aichi Japan.
  • Shiraishi Y; Department of Clinical Affairs Zimmer Biomet G.K. Tokyo Japan.
  • Sano Y; Canon Medical Systems Corporation Otawara Tochigi Japan.
  • Ohno Y; Department of Diagnostic Radiology, School of Medicine Fujita Health University Toyoake Aichi Japan.
  • Fujita N; Joint Research Laboratory of Advanced Medical Imaging, School of Medicine Fujita Health University Toyoake Aichi Japan.
JOR Spine ; 7(1): e1320, 2024 Mar.
Article em En | MEDLINE | ID: mdl-38500785
ABSTRACT

Background:

Various treatments for chronic low back pain (LBP) have been reported; among them, platelet-rich plasma (PRP) as a regenerative medicine has attracted much attention. Although Modic type 1 change (MC1) is associated with LBP, no treatment has been established so far. In addition, no studies have administered PRP to intervertebral discs (IVDs) in patients with LBP, targeting MC1 only. Thus, the purpose of this study was to determine the safety and efficacy of PRP administration to the IVDs in patients with MC1 experiencing LBP.

Methods:

PRP was injected intradiscally to 10 patients with MC1 experiencing LBP. Patients were followed prospectively for up to 24 weeks after primary administration. Physical condition, laboratory data, and lumbar x-ray images were evaluated for safety assessment. Furthermore, to evaluate the effectiveness of PRP, patient-reported outcomes were considered. In addition, changes in MC1 were assessed using magnetic resonance imaging (MRI).

Results:

There were no adverse events in the laboratory data or lumbar X-ray images after administration. The mean visual analog scale, which was 70.0 ± 13.3 before the treatment, significantly decreased 1 week after PRP administration and was 39.0 ± 28.8 at the last observation. Oswestry disability index and Roland Morris disability questionnaire scores promptly improved after treatment, and both improved significantly 24 weeks after PRP administration. Follow-up MRI 24 weeks after treatment showed a significant decrease in the mean high-signal intensity of fat-suppressed T2-weighted imaging from 10.1 to 7.90 mm2 compared with that before PRP administration.

Conclusions:

The safety and efficacy of PRP administration to the IVDs of patients with MC1 experiencing LBP were identified. Post-treatment MRI suggested improvement in inflammation, speculating that PRP suppressed inflammation and consequently relieved the patient's symptoms. Despite the small number of patients, this treatment is promising for patients with MC1 experiencing LBP. The study protocol has been reviewed and approved by the Certified Committee for Regenerative Medicine and the Japanese Ministry of Health, Labor and Welfare (Japan Registry of Clinical Trials [jRCT] No. jRCTb042210159).
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: JOR Spine Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: JOR Spine Ano de publicação: 2024 Tipo de documento: Article