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Table 7. Secondary Clinical Outcomes for the Early Stage and Late Stage Groups.
OA grade (n)

Mean ± SD (95% CI)

JSSF
Group, P = .04; time, P < .001 in repeated measures ANOVA
Early-stage (7)
Baseline
56.9 ± 8.8 (53.1-66.1)
4 weeks
72.3 ± 7.6 (66.7-77.9)
12 weeks
76.9 ± 6.9 (71.7-82.0)
24weeks
66.2 ± 19.7 (51.7-80.9)
Late-stage (13)
Baseline
48.5 ± 14.0 (40.9-56.2)
4 weeks
69.8 ± 10.4 (64.1-75.4)
12 weeks
65.1 ± 12.3 (58.4-71.8)
24 weeks
65.0 ± 15.0 (56.9-73.1)
SAFE-Q Pain and pain related
Group, P < .001; time, P = .03 in repeated measures ANOVA
Early-stage (7)
Baseline
56.9 ± 14.4 (46.2-67.5)
4 weeks
70.0 ± 13.2 (60.3-79.8)
12 weeks
75.3 ± 11.6 (66.7-83.9)
24 weeks
66.2 ± 18.8 (48.2-76.2)
Late-stage (13)
Baseline
41.2 ± 14.3 (40.9-56.2)
4 weeks
51.4 ± 14.8 (64.1-75.4)
12 weeks
54.3 ± 14.2 (46.6-62.0)
24 weeks
52.8 ± 18.4 (42.8-62.8)

P value

Baseline vs 4 weeks:
Baseline vs 12 weeks:
Baseline vs 24 weeks:

.009a
.09
.009
.11

Baseline vs 4 weeks:
Baseline vs 12 weeks:
Baseline vs 24 weeks:

.005a
.005
.04
.07

.16a

.22a

Abbreviations: JSSF scale, Japanese Society for Surgery of the Foot ankle/hindfoot scale; SAFE-Q, Self-Administered Foot Evaluation Questionnaire.
a
Kruskul-Wallis test. Other P values are for the post-hoc tests.

the last injection, and the effect was diminished at 24
weeks. This trend is consistent with previous reports that
showed that the effect of an intra-articular injection of
PRP on knee and hip cartilage degeneration and OA
peaked at 2 to 3 months after the treatment and then gradually decreased.15,22,23 In addition, the results of this study
might change depending on the number of injections,
treatment dose and intervals, patient selection and education, and postprocedural rehabilitation, which are essential
to maximize the therapeutic effect of PRP.42
We used the ultrasonography-guided technique for
intra-articular injections to minimize the risk of extra-articular injections because the purpose of this study was to
assess the efficacy of PRP. However, injections without
ultrasonography guidance may be more common in clinical practice because of the cost and time with the use of
ultrasonography.43 In these cases, the risk of extra-articular
injections may be higher, resulting in a diminished treatment effect.39
Our study has several limitations. First, the number of
patients was small, and no control group was included. The
main purpose of this study was to confirm the safety of intraarticular injections of PRP in patients with primary varus

ankle OA.29 Thus, we conducted a single-arm study with a
small number of patients that the institutional review board
of our institute permitted. The results of this study could provide important information for which the number of patients
can be estimated for future studies to confirm the efficacy of
PRP. Second, we evaluated the patients for 6 months. We
determined the period on the basis of previous reports.23,26
However, considering that the efficacy lasted for at least 6
months in this study, a longer follow-up may be required for
future studies. Third, the frequency and number of injections, the volume and concentration of PRP, and the activation method were determined based on previous reports.12,22,26
However, the results might change if different treatment protocols are used. For example, the number and dose of hyaluronic acid injections for ankle OA have an impact on the
clinical outcome,41 and the same may be true for PRP injections. In addition, the concentration of platelets in PRP is
largely dependent on the extraction method (Table 1).24
Although the mean concentration, 5.1 times higher than that
in whole blood, was comparable to that in previous studies,
which ranged from 2- to 6-fold,15 future research should
focus on the optimal platelet concentration to obtain maximal efficacy. Fourth, the patients in this study had various



Table of Contents for the Digital Edition of Foot & Ankle International - June 2017

Contents
Foot & Ankle International - June 2017 - Intro
Foot & Ankle International - June 2017 - Cover1
Foot & Ankle International - June 2017 - Cover2
Foot & Ankle International - June 2017 - i
Foot & Ankle International - June 2017 - ii
Foot & Ankle International - June 2017 - Contents
Foot & Ankle International - June 2017 - iv
Foot & Ankle International - June 2017 - v
Foot & Ankle International - June 2017 - vi
Foot & Ankle International - June 2017 - vii
Foot & Ankle International - June 2017 - viii
Foot & Ankle International - June 2017 - 1A
Foot & Ankle International - June 2017 - 1B
Foot & Ankle International - June 2017 - ix
Foot & Ankle International - June 2017 - x
Foot & Ankle International - June 2017 - xi
Foot & Ankle International - June 2017 - xii
Foot & Ankle International - June 2017 - 2A
Foot & Ankle International - June 2017 - 2B
Foot & Ankle International - June 2017 - xiii
Foot & Ankle International - June 2017 - xiv
Foot & Ankle International - June 2017 - xv
Foot & Ankle International - June 2017 - xvi
Foot & Ankle International - June 2017 - 3A
Foot & Ankle International - June 2017 - 3B
Foot & Ankle International - June 2017 - xvii
Foot & Ankle International - June 2017 - xviii
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Foot & Ankle International - June 2017 - CT1
Foot & Ankle International - June 2017 - CT2
Foot & Ankle International - June 2017 - 4A
Foot & Ankle International - June 2017 - 4B
Foot & Ankle International - June 2017 - Cover3
Foot & Ankle International - June 2017 - Cover4
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