Table 4.
Study | Study design | Number of patients | Diagnostic discography | Injection method | PRP preparation method | Characteristics of PRP | Volume of whole blood | Injection volume of PRP | Follow-up period | Outcome measure | Maximum improvement time point | Comment |
---|---|---|---|---|---|---|---|---|---|---|---|---|
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Intradiscal injection | ||||||||||||
| ||||||||||||
Akeda et al (2011)72 | Prospective preliminary trial | 6 | Yes | Intradiscal | Buffy coat method | P-PRP releasate ACT: CaCl + 2 autoserum | 200 mL | 2 mL | 6 M | VAS (7.1→1.8**) and RDQ (11→3.2**) | 6 M | |
Bodor et al (2014)73 | Case series | 35 | Yes | Intradiscal | Cascade Autologous Platelet System (ConMed Linvatec) | P-PRP ACT: no | 9 mL | 2 mL | 2–10 M | NRS and ODI (positive response of 2/3 patients) | 1 W–2 M | |
Navani and Hames (2015)74 | Case series | 6 | Yes | Intradiscal | P-PRP system (EmCyte) | L-PRP ACT: no | 60 mL | 1.5–3 mL | 24 W | VPS (50% decrease in 6 patients) | 24 W | |
Levi et al (2016)75 | Prospective trial | 22 | Partial | Intradiscal | Smartprep (Harvest) | L-PRP ACT: no | 30 or 60 mL | 1.5 mL | 6 M | 47% patients (both VAS 50% and ODI 30% improvement) | 6 M | PRP injection just after 0.6 mL of contrast, 0.4 mL of gentamicin, and 0.5 mL of lidocaine |
Tuakli-Wosornu et al (2016)77 Monfett et al (2016)78 | Double-blind randomized controlled trial | 36 treatments and 22 controls | Yes | Intradiscal | Smartprep (Harvest) | L-PRP ACT: no | 30 mL | 1–2 mL | 8 W (RCT) | FRI (control 44–PRP 38*), NRS, SF-36, and modified NASS Outcome Questionnaire | 1–2 years | PRP injection just after 1–2 mL injection of contrast |
Akeda et al (2017)61 | Prospective trial | 14 | Yes | Intradiscal | Buffy coat method | P-PRP releasate ACT: CaCl + auto 2 serum | 200 mL | 2 mL | 10 M | VAS (7.5→3.1**) and RDQ (12.6→5.1**) T2-value: no change | 1 M | Discography on different days from PRP injection |
Lutz (2017)90 | Single case report | 1 | Yes | Intradiscal | Arteriocyte (Magellan) | L-PRP ACT: N/D | N/D | 1.5 mL | 12 M | Improvement T2 nuclear signal intensity↑, type I Modic changes↓ | N/A | PRP injection just after injection of contrast |
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Non-intradiscal injections (facet, epidural, and intramuscular) | ||||||||||||
| ||||||||||||
Aufiero et al (2015)79 | Case report | 5 | N/A | Intraarticular (facet) | N/D | P-PRP ACT: no | N/D | Multiple injection | 6–12 M | VAS | N/A | |
Kirchner and Anitua (2016)80,81 | Observational retrospective pilot study | 86 | Yes | Intradiscal and intraarticular | PRGF system IV (BTI-Biotechnology Institute, Vitoria, Álava, Spain) | PRGF ACT: CaC 2 l | 9 mL | 4 mL (disc) and 2 mL (facet) | 6 M | VAS (8.4→0.8**) 91% excellent 8.1% moderate |
6 M | |
Wu et al (2016)82 | Prospective study | 19 | N/A | Intraarticular (facet) | Centrifuge 2 times soft spin | N/D | 5–10 mL | 0.5 mL | 3 M | VAS (7.05→2.63, P<0.05) RDQ (P<0.05) ODI (54.3→26.3, P<0.05) |
3 M | |
Bhatia and Chopra (2016)84 | Pilot study | 10 | N/A | Epidural | Blood bank No detail | N/D | 100 mL | 5 mL | 3 M | VAS, MODQ index, and SLRT (most of the patients improved in all evaluations) | 3 M | |
Hussein and Hussein (2016)85 | Prospective trial | 104 | N/A | Intramuscular (weekly injection for 6 weeks) | PRP method | L-PRP ACT: CaC 2 l | 50 mL | 2.5 mL | 2 years | NRS (8.81→3.5**) and ODI (36.7→14.7**) | 12–18 M | |
Wu et al (2017)83 | Randomized controlled study | 21 (PRP) 23 (betamethasone) | N/A | Intraarticular (facet) | Centrifuge 2 times soft spin | N/D | 5–10 mL | 0.5 mL | 6 M | PRP> betamethasone (VAS, RDQ, and ODI) | 6 M | |
Cameron and Thielen (2017)86 | Prospective trial | 50 | N/A | Circumferential manner into posterior spine area | N/D | N/D | N/D | N/D | 5 years | VAS (–77% improvement) and ODI | No description | LBP caused by spinal disc herniation |
Comella et al (2017)87 | Prospective trial | 15 | No | Intradiscal | N/D | PRP mixed with stromal vascular fraction | N/D | 1 mL | 6 M (safety 12 M) | VAS (5.6→3.6**), PPI (2.6→1.8*), BDI, ODI, SM-MPQ, SF-12, and DPQ | 6 M |
Note:
P<0.05 and
P<0.01.
Abbreviations: ACT, activation; BDI, Beck Depression Inventory; DPQ, Dallas Pain Questionnaire; FRI, Functional Rating Index; LBP, low back pain; L-PRP, leukocyte- and platelet-rich plasma; M, months; MODQ, Modified Oswestry Disability Questionnaire; N/A, not applicable; N/D, no description; NRS, Numeric Rating Scale; ODI, Oswestry Disability Index; PPI, present pain intensity; P-PRP, Leukocyte-poor PRP; PRP, platelet-rich plasma; RDQ, Roland-Morris Disability Questionnaire; SF, Short Form; SF-MPQ, Short-form McGill Pain Questionnaire; SLRT, Straight Leg Raising Test; VPS, verbal pain scale; W, weeks.