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. 2019 Jul 23;8:F1000 Faculty Rev-1167. [Version 1] doi: 10.12688/f1000research.19355.1

Table 1. Summary of the literature reviewed in this article investigating the treatment of phantom limb pain.

Authors, year,
and sample
size
Site (and
percentage)
of
amputation
Reason(s) for
amputation and
percentages
Mean time
(range)
since
amputation
Treatment
groups
Treatment
duration
Main outcome
measure(s)
Assessments Findings Risk of bias
Dumanian
et al. 9 (2019)
(n = 28)
UE = 13%
LE = 87%
Trauma = 90%
Infection = 10%
(Less than 1
year to more
than 10
years)
1. Targeted
muscle
reinnervation
2. Standard
neuroma surgery
N/A Change in NRS worst
pain from baseline to 12
months post-operatively
for PLP and residual limb
pain
Baseline
3 months
6 months
9 months
12 months
No significant between-
group differences in
worst PLP or residual
limb pain 1 year post-
surgery
High risk
Malavera
et al. 16 (2016)
(n = 54)
LE = 100% Trauma = 100% 7.8 years 1. Active rTMS
2. Sham rTMS
20 stimuli of
6 seconds
each (54-
second
intervals),
5 days per
week for 2
weeks
PLP intensity measured
via a visual analogue
scale (VAS)
Baseline
15 days post-
rTMS
30 days post-
rTMS
No significant between-
group differences in
PLP scores at either
follow-up time
Low risk
Brunelli
et al. 19 (2015) (n = 40)
AK = 73%
BK = 27%
Dysvascular = 70%
Other = 30%
458
days
1. SAIPAN
protocol
2. Standard
treatment
~1 hour two
times per
week for 4
weeks
1. PLP intensity, rate,
duration, and bother
measured via Prosthesis
Evaluation Questionnaire
(PEQ) and Brief Pain
Inventory (BPI)
2. Phantom limb symptom
(PLS) intensity, rate, and
bother measured via PEQ
Baseline
1 month
2 months
Significant group
differences in PLP rate,
duration, and bother
from PEQ at 2-month
follow-up only. No
significant differences
with BPI. Significant
group differences in
PLS rate, intensity,
and bother at 2-month
follow-up only.
High risk
Finn
et al. 20 (2017)
(n = 15)
AE = 40%
BE = 60%
Trauma = 100% 4.5 months
(0.55–24
months)
1. MT
2. Control
(covered mirror)
3. Control
(mental
visualization)
15 minutes
5 days per
week for 4
weeks
PLP intensity measured
via VAS
Baseline
4 weeks
No between-group
comparisons reported
for main outcome
measure
High risk
Anaforoğlu
Külünkoğlu
et al. 21 (2019) (n = 40)
BK = 100% Trauma = 100% 13.25
months
(3–53
months)
1. MT
2. Phantom
exercise (PE)
15 minutes
of MT daily
at home for 4 weeks

PE group
performed
exercises
daily with 15
repetitions
1. PLP intensity measured
via VAS

2. Quality of life evaluated
via SF-36

3. Psychological status
measured using BDI
Baseline
4 weeks
3 months
6 months
Significant group
difference in VAS PLP
severity, BDI scores,
and PF, SF, MH, and V
subscales of the SF-36
in favour of the MT
group at all follow-up
times
High risk
Ol et al. 22
(2018) (n = 45)
BK = 100% Trauma = 100% (15–32
years)
1. MT
2. Tactile
3. Combination
(mirror and
tactile therapy)
5 minutes
every
morning
and night for
4 weeks
PLP intensity measured
via VAS
Baseline
5 weeks
3 months
after end of
treatment
No significant between-
group differences in
PLP scores at either
follow-up time
High risk
Ramadugu
et al. 23 (2017)
(n = 60)
AE = 8%
BE = 8%
AK = 34%
BK = 50%
NR NR 1. MT
2. Control
(covered mirror)
15 minutes
every day
for 4 weeks
PLP intensity measured
via VAS and the short
form of the McGill Pain
Questionnaire
Baseline
4 weeks
8 weeks
12 weeks
16 weeks
(20 weeks,
control only)
No between-group
comparisons reported
for main outcome
measures
High risk
Tilak et al. 24
(2016) (n = 26)
UE = 26%
LE = 74%
NR 45 days 1. MT
2. Contralateral
transcutaneous
electrical nerve
stimulation
20 minutes
every day
for 4 days
PLP intensity measured
via VAS and Universal
Pain Score (UPS)
Baseline
4 days
No significant between-
group differences in
PLP intensity at the end
of treatment
High risk
Rothgangel
et al. 25 (2018)
(n = 75)
AK = 61%
K = 7%
BK = 32%
Trauma = 32%
Dysvascular = 40%
Tumor = 14%
Other = 14%
~35 months 1. MT followed
by teletreatment
using
augmented
reality
2. MT followed
by self-delivered
MT
3. Sensomotor
exercises to
the intact limb
followed by
self-delivered
exercises
At least 10
30-minute
sessions
across
4 weeks
followed
by 6 weeks
of self-
delivered
treatment
PLP frequency, duration,
and intensity (measured
via NRS)
Baseline
4 weeks
10 weeks
6 months
No significant between-
group differences
at 4- or 10-week
follow-up. At 6-month
follow-up, there were
significant between-
group differences on
PLP duration only, in
favor of MT followed by
self-delivered MT.
High risk
Rostaminejad
et al. 26 (2017)
(n = 60)
AK = 40%
BK = 60%
Diabetes = 45%
Trauma = 50%
Cancer = 5%
(2–38 months) 1. EMDR
2. Routine care
12 one-hour
sessions
over 1
month
PLP intensity measured
via the subjective units of
distress scale and pain
rating scale
Baseline
1 month
24 months
No between-group
comparisons reported
for main outcome
measures
High risk

Results from interventions using targeted muscle reinnervation, repetitive transcranial magnetic stimulation (rTMS), mirror therapy (MT), augmented reality, and eye movement desensitization and repossessing (EMDR) therapy are summarized above. For each study, the site, reason, and mean time since amputation are shown. Treatment groups and duration as well as main outcome measures, times of assessment, and major findings are included. The final column describes the article’s global risk-of-bias rating as assessed by the Cochrane Collaboration’s tool 8. UE and LE refer to upper and lower extremity amputations, respectively. AK, BK, AE, and BE refer to amputations performed above (A) and below (B) the knee (K) and elbow (E) joint. NR denotes information that was not reported by the author. NRS refers to the numeric 0–10 rating scale. BDI, Beck Depression Inventory; MH, mental health; N/A, not applicable; PF, physical functioning; PLP, phantom limb pain; SAIPAN, Santa Lucia Alleviation Intervention for Phantom in Amputees’ Neurorehabilitation; SF, social functioning; SF-36, 36-Item Short Form Survey; V, vitality.