Clinical Biomechanics 18 (2003) S33–S39
www.elsevier.com/locate/clinbiomech
Enhancing mechanical strength during early fracture healing
via shockwave treatment: an animal study
Robert Wen-Wei Hsu
a
a,*
, Ching-Lung Tai b, Chris Yu-Chih Chen a, Wei-Hsiu Hsu a,
Swei Hsueh c
Department of Orthopaedics, Chang Gung Memorial Hospital, Chang Gung Medical College, Chang Gung University, No. 6, West Section,
Chia-Pu Road, Putz, Chia-yi, Taiwan, ROC
b
Biomechanical Laboratory, Chang Gung Memorial Hospital, Chang Gung Medical College, Chang Gung University, No. 6, West Section,
Chia-Pu Road, Putz, Chia-yi, Taiwan, ROC
c
Department of Pathology, Chang Gung Memorial Hospital, Chang Gung Medical College, Chang Gung University, No. 6, West Section,
Chia-Pu Road, Putz, Chia-yi, Taiwan, ROC
Abstract
Objective. This investigation aims to determine (1) whether shockwave treatment helps fracture healing and (2) whether the effect
of shockwave treatment on fracture healing is dose dependent.
Design. Shockwave was applied over tibial osteotomy in an animal model to assess its effect on the healing of the fracture.
Methodology. Bilateral tibial diaphyseal transverse osteotomy was conducted on 42 rabbits, dividing into experimental and
control group, immobilized using an external skeletal fixator, with one leg tested with shockwave therapy and the contralateral leg
acting as the control without therapy. Serial radiography and measurement of bone mineral density via dual-energy X-ray absorptiometry were performed to assess the fracture healing. The experimental animals had two or three sessions of shockwave
therapy (5000 impulses, 0.32 mJ/mm2 , Orthopedice) over the osteotomy sites on day 7, 21 and 35; while the control group did not
receive any treatment. The animals were sacrificed on day 42 or 56. Then, bilateral tibias were harvested and sent for mechanical
tests as well as the histological examination. The pertinent statistic methods were applied to analyze the results.
Background. Shockwave therapy has become a useful alternative approach in treating various orthopedic conditions, but the
mechanism which it works remains unclear. Thus far, shockwave therapy has been found effective in treating long bone pseudoarthrosis, but whether it can benefit fresh fracture healing continues to be debated.
Results. Higher union rates occurred during the early but not the late stages in the experimental group, while mechanical strength
was higher in the experimental group than in the control group. No significant dose-dependent response occurred between the
second and third applications of shockwave treatment. No significant difference in mechanical strength occurred between the experimental groups at 4 weeks and the control group at 6 weeks, or between the experimental groups at 6 and 8 weeks. Furthermore,
no significant correlation occurred between the absolute values of maximum torque and bone mineral density.
Conclusion. Based on this investigation, shockwave treatment has a positive effect on early fracture healing while its long term
effects require further investigation.
Relevance
Shockwave therapy can be a useful alternative adjunct modality in the treatment of fresh long bone fracture.
2003 Elsevier Science Ltd. All rights reserved.
Keywords: Shockwave therapy; Dual-energy X-ray absorptiometry; Biomechanical tests
1. Introduction
For the past decade, shockwave has been employed
for the fragmentation of stone in the kidney and lower
*
Corresponding author.
E-mail address: orthboss@cgmh.org.tw (R.W.-W. Hsu).
urinary tract in the interest of avoiding surgical intervention (Chaussy et al., 1980). In the field of orthopedics,
shockwave has been used for the therapy of delayed or
non-union of fracture of the long bones (Valchanou and
Michailov, 1991). There are three shockwave generator
systems: electrohydraulic, piezoelectric and electromagnetic systems. The high energy shock can be produced by
a 1-ls spark discharge from a bipolar electrode on a high
0268-0033/03/$ - see front matter 2003 Elsevier Science Ltd. All rights reserved.
doi:10.1016/S0268-0033(03)00082-2
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R.W.-W. Hsu et al. / Clinical Biomechanics 18 (2003) S33–S39
voltage condenser. The electrode is placed in the geometric focus of an ellipsoid reflector. The high voltage
discharge in a water medium gives rise to an explosive
evaporation of water and generates the shockwaves.
These wave reflected from the walls of the ellipsoid and
directed to a second focus in the biological tissue
(Chaussy, 1968; Eisenberger and Muller, 1987). The
shockwaves are not hindered by a water medium, yet
the wave acts destructively on bones and calculi in the
human body (Haberman, 1987). Although shockwave
therapy has become a popular method of treating various orthopedic conditions such as pseudoarthrosis
(Plaisier et al., 1994; Rompe et al., 1997), calcifying
tendonitis of the shoulder joint (Dahmen et al., 1992;
Loew et al., 1995, 1999; Rompe et al., 1995), plantar
fasciitis (Rompe et al., 1996a,b; Krischek et al., 1998),
lateral epicondylitis of the elbow joint (Maier et al., 2000;
Rompe et al., 1996c,d, 1998; Krischek et al., 2000),
avascular necrosis of femoral head (Forriol et al., 1994),
its effectiveness remains debatable (Plaisier et al., 1994).
Previous reports reveal that, besides surgical interventions, shockwave treatment is an attractive alternative
approach for treating bony pseudoarthrosis (Valchanou
and Michailov, 1991; Rompe et al., 1997). However, the
precise mechanism through which bone healing is accelerated with this method remains unclear (Delius et al.,
1995). Several investigations demonstrated stimulatory
effects at the cellular and molecular levels (Forriol et al.,
1994; Kusnierczak et al., 2000). However, whether such
effects have any influence on fracture healing is unknown
because the fracture healing process involves biological
changes as well as mechanical properties. The purposes
of this study were to investigate (1) that whether shockwave has a positive effect on the fracture healing, and (2)
that the effect of shockwave treatment on fracture healing is dose dependent.
2. Methods
2.1. Animal experimental design
Forty-two 4-month old male New Zealand rabbits,
each weighing 3.5 kg were enrolled in this study. The
animals were supplied from the animal laboratory of
Chang Gung Memorial Hospital and raised according
to the guidelines of the National Science Council, Taiwan. Under sterile condition and general anesthesia with
ketamine hydrochloride (Ketalar, Parke-Davies, Taiwan) and Rompun (Bayer, Leverkusen, Germany) intravenous injection, the rabbit was put in the supine
position. A 5-cm longitudinal skin incision was made
over the anterior aspect of the middle portion of the
right leg. Exposed the tibia and four stainless-steel
screws were inserted. Then a custom-made external fixator with four screws were applied to immobilize the
tibia. The perisoteum was elevated and the tibia was
osteotomized transversely using a airtome under saline
irrigation. All the animals were intravenously injected
with Keflin prophylactic antibiotics. After surgery, the
animals were allowed to bear partial or full weight as
tolerated. The animals were monitored daily for food
and water intake, pin site infection, and ambulation. All
studied animals were cared in accordance with regulations of the National Institute of Health of Taiwan
under the supervision of a licensed veterinarian
The animals were randomly assigned to the experimental and control groups, labeled groups E and C, respectively. In group IE (n ¼ 6), the rabbits received 5000
impulses, and 0.32 mJ/mm2 shockwave treatment (Haupt
et al., 1992; Johannes et al., 1994; Seemann et al., 1992) at
the osteotomy site using Orthospece (therapy zone:
25 · 95 mm; energy density: up to 0.32 mJ/mm2 , pulse
rate: 1–2.5 Hz (M E D I S P E C Ltd., MD, USA) on Days 7
and 21. Meanwhile, in group IC (n ¼ 6), the osteotomy
site received no treatment. At the bilateral tibias of each
animal, periodical plain radiography and bone mineral
density (BMD) measurement using dual-energy X-ray
absorptiometry (DEXA) were conducted before surgery
and weekly after surgery. On Day 28, the animals were
sacrificed by intra-venous injection of over-dosed sedatives, and the bilateral tibias were harvested and sent for
torsional testing by a Materials Testing System (MTS)
machine. Meanwhile, the rabbits in groups IIE-1 (n ¼ 6),
IIE-2 (n ¼ 6) and IIC (n ¼ 6), received radiographic examination and DEXA study before surgery and weekly
after surgery. The animals were sacrificed on Day 42.
Additionally, the rabbits in group IIE-1 received two
sessions of shockwave treatment with the same dose and
frequency as in group IE, while the rabbits in group IIE-2
received one additional shockwave treatment on Day 35.
The animals in groups IIIE (n ¼ 6) and IIIC (n ¼ 6), received plain radiographic examination and DEXA study
before surgery and weekly after surgery. The animals were
sacrificed on Day 56. Besides the two shockwave treatments on Days 7 and 21, group IIIE received one additional shockwave treatment on Day 35, just as in group
IIE-2. As with group IC, no treatment was applied onto
the osteotomy site of the 12 rabbits in group IIC and IIIC.
BMD measurements were made using a Hologic
QDR 2000 dual-energy X-ray absorptiometry (Hologic
Inc., Boston, MA, USA). To obtain a reproducible
value corrected for individual differences, the preoperative BMD of the middle portion of the tibias was used
as the internal control.
2.2. The biomechanical test
After sacrifice, the bilateral tibias were harvested by
stripping the soft tissues. All specimens were stored at
)20 C until testing. After thawing for 24 h, any soft
tissue was removed from each specimen, and the speci-
R.W.-W. Hsu et al. / Clinical Biomechanics 18 (2003) S33–S39
mens were then fixed by embedding each end of the
segment in a rectangular metal frame with acrylic (AcriliMete) along the longitudinal axis. The length of the
non-embedded portion was maintained at a constant 6.2
cm for all specimens. Screws or pincers, which could
increase stress levels, were not used to fix the construct.
At the stage of embedding, a specially designed external
fixator with axial alignment was used to clamp the
rectangular metal frames. The application of this external fixator provided two surfaces with right angle,
which maintained the alignment of both ends of the
rectangular metal frames. The alignment of the harvested tibiae embedded in the acrylic cement was thus
ensured. The acrylic–tibia–acrylic assembly was then
mounted on a specially designed symmetrical grip with a
rectangular holder, which prevented the specimen from
sliding during torsional testing. After the specimens
were clamped, the torsional test was performed at a
constant rotational rate of 1/s using a MTS machine
(Bionix 858, MTS Company, Minneapolis, MN, USA).
The relationship between torque value and rotational
angle was recorded simultaneously at an increment of
0.2 using MTS Teststar II software. To assess the effect
of shockwaves on the healing rate of fracture tibia at
various healing periods, the torque magnitude at failure
for each individual specimen was selected for comparison by using Student-t (two tailed) statistical analysis. A
significant difference was reported at P < 0:05.
3. Results
3.1. The radiographic evaluation
Two independent radiologists assessed the fracture
healing during the radiographic examinations after
surgery.
S35
Three animals were excluded from the study due to the
postoperative complications. In the plain radiographic
study for assessing the healing of the osteotomy, the rate
of complete healing following shockwave treatment was
significantly higher in the experimental than the control
groups during the early stage (within 28 days, IE vs IC:
P -value ¼ 0:001) but not in the late stage (after 42 days:
IIE-1/IIE-2 vs IIC and IIIE vs IIIC: P > 0:05). The
alignment of the diaphyseal osteotomy of all the rabbits
remained essentially normal (angle of angulation <10;
minimal shortening/lengthening) throughout the course
of the experiment.
3.2. Measurement of bone mineral density
The BMD assessment looked at the change in the
ratio of BMD values between the callus of the osteotomy site of the operated limbs and the middle portion of
the non-operated limbs, which were used as the internal
control, of the same animal. No significant differences
over the BMD changes existed between the experimental
and the control groups (IE vs IC groups from Day 0–28;
IIE-1, IIE-2 vs IIC groups from Day 0–42; IIIE vs IIIC
groups from Day 0–56.
3.3. Mechanical strength of fracture healing
Fig. 1 illustrates the typical diagram of torque vs
angle curve in the biomechanical testing, showing that
the torque magnitude increased linearly with increasing
angle before failure. However, torque magnitude declined significantly once maximal torque was reached.
Following the failure of the tibia, the fluctuation phenomenon of torque value was observed. It was due to
the ‘‘damping’’ effect of the lower segment of the tibia
Fig. 1. Typical torque vs angle curve. The magnitude of the torque increased linearly with increasing angle before failure, but declined significantly
once maximal torque reached. The peak torque was the failure point of the tibia during torsional testing.
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R.W.-W. Hsu et al. / Clinical Biomechanics 18 (2003) S33–S39
Table 1
Results of biomechanical test at 4 weeks
Rabbit
Maximum
torque
(N mm)
IC Group (non-shockwave treatment)
1
Right
256
Left
1312
2
Right
417
Left
1514
3
Right
881
Left
1815
4
Right
781
Left
1952
5
Right
577
Left
1882
6
Right
325
Left
1625
Mean
SD
IE Group (shockwave treatment)
1
Right
1213
Left
2048
2
Right
1716
Left
3025
3
Right
1425
Left
2542
4
Right
1187
Left
2319
5
Right
1131
Left
2096
6
Right
1008
Left
1738
Mean
SD
Table 2
Result of biomechanical test at 6 weeks
Percentage of
maximum torque
(right/left)
19.5
27.6
48.5
40.0
30.7
20.0
31.0
11.4
59.2
56.7
56.1
51.2
54.0
58.0
55.9
3.0
mounted on the MTS load cell. Tables 1–3 list the
maximal torque for each group, emphasizing the ratio
of maximal torque between the bilateral tibial diaphysis
of the same animal. The ratios of the maximal torques of
the experimental groups are significantly higher than the
control groups (IE vs IC: P ¼ 0:0021; IIE-1 and IIE-2 vs
IIC: P ¼ 0:0001; IIIE vs IIIC: P ¼ 0:039). As shown in
Fig. 2, a gradual increase in maximum torques were
demonstrated over the experimental and the control
groups (P < 0:01). A statistical difference thus exists
between the two groups at each healing periods. However, no significant dose-dependent response exists between two times and three times shockwave treatment
(IIE-1 vs IIE-2: P ¼ 0:48). And also no significant differences of the maximal torques were found between the
groups of IE (experimental group with shockwave
therapy at 4 weeks) vs IIC (6 weeks control group
without shockwave therapy); IIE (experimental group at
6 weeks) vs IIIC (control group at 8 weeks). Overall, no
significant correlation exists between the absolute values
of the maximum torque and BMD (correlation coefficient ¼ 0.56, P ¼ 0:055).
Rabbit
Maximum
torque
(N mm)
IIC Group (non-shockwave treatment)
1
Right
734
Left
1397
2
Right
1113
Left
2242
3
Right
965
Left
1789
4
Right
1530
Left
2783
5
Right
1243
Left
1958
Mean
SD
IIE-1 Group (shockwave treatment)
1
Right
1493
Left
2423
2
Right
1516
Left
2045
3
Right
1265
Left
1649
4
Right
1398
Left
1770
5
Right
1839
Left
2292
Mean
SD
IIE-2 Group (shockwave treatment)
1
Right
1993
Left
2549
2
Right
1715
Left
2411
3
Right
1497
Left
2256
4
Right
2157
Left
2627
5
Right
1468
Left
1998
6
Right
1894
Left
2518
Mean
SD
Percentage of
maximum torque
(right/left)
52.5
49.6
53.9
54.9
63.5
54.9
5.2
61.6
74.1
76.7
79.0
80.2
72.8
7.5
78.2
71.1
66.4
82.1
73.5
75.2
75.6
5.5
3.4. The histologic examination
The histology examination was taken from the fracture sites after the torsional test. The specimens of
Groups I and II represented the time point at the fourth
and sixth week, respectively. In the present study, the
osteotomy patterns were identical, and more cartilage
portion implied less mineralization. Callus formation in
Group IC showed cartilaginous nucleus center with osteochondroid new bone formation on both sides, while
callus in Group IE showed similar pattern with a smaller
amount of cartilage and more mature bony trabeculaes
(Fig. 3). Therefore, the Group IE had better healing
status than Group IC. Group IIE with matured bony
R.W.-W. Hsu et al. / Clinical Biomechanics 18 (2003) S33–S39
S37
Table 3
Results of biomechanical test at 8 weeks
Rabbit
Maximum
torque
(N mm)
IIIC Group (non-shockwave treatment)
1
Right
1002
Left
2034
2
Right
1923
Left
2613
3
Right
1648
Left
2461
4
Right
2046
Left
2771
5
Right
1015
Left
1750
6
Right
2196
Left
2807
Mean
SD
IIIE Group (shockwave treatment)
1
Right
1834
Left
2354
2
Right
1883
Left
2075
3
Right
1285
Left
1927
4
Right
1575
Left
1802
5
Right
2351
Left
2751
Mean
SD
Percentage of
maximum torque
(right/left)
49.3
73.6
66.9
73.8
58.0
78.2
66.7
11.1
77.9
90.8
66.7
87.4
85.5
81.7
9.6
Fig. 3. (A) Histology of Group IC showed callus formation with cartilaginous nucleus center and osteochondroid new bone formation on
both sides at 4 weeks (200, H&E stain). (B) Histology of Group IE
showed callus with smaller amount of cartilage and more mature bony
trabeculaes, as compared to Group IC at 4 weeks (200, H&E stain).
4. Discussions
Fig. 2. The mean percentage of the maximum torque vs healing periods. The mean percentage of maximum torque gradually increases
with healing periods in both the experimental and control groups.
bridge existed as compared to the soft callus interposition of Group IIC. Callus in Group IIC showed young
bone with osteoid matrix and active osteoblast and
Group IIE showed new bone with mature bony trabeculaes (Fig. 4). The histological pictures corresponded
well with the biomechanical tests.
In treating pseudoarthrosis of long bone fracture, the
high reported success rate makes shockwave treatment
an attractive non-operative option for patients (Plaisier
et al., 1994; Forriol et al., 1994). However, the precise
mechanism of shockwave-induced tissue healing remains
uncertain (Delius et al., 1995). The effect of shockwaves
on bony structures should be unsophisticated idea that
shockwave treatment causes microfractures and subsequent new bone formation.
In the present study, the fracture healing occurred
through the indirect healing process due to less rigid
external fixation. Proliferation and differentiation of the
mesenchymal cell at the fracture site resulted in the formation of the callus, which consisted of fibrous tissue,
cartilage and woven bone. Cartilage predominated in the
central region with lower oxygen tension. As the vascular
invasion with better oxygenation, the endochondral ossification was carried out (Bassett and Herrmann, 1961;
Bassett, 1962). Herein, shockwave treatment displays a
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R.W.-W. Hsu et al. / Clinical Biomechanics 18 (2003) S33–S39
Fig. 4. (A) Histology of Group IIC showed callus with osteoid matrix
in young bone and active osteoblast at 6 weeks (200, H&E stain). (B)
Histology of Group IIE showed new bone with mature bony trabeculaes at 6 weeks (200, H&E stain).
positive effect on early callus formation and mechanical
strength. A straightforward radiographic evaluation indicated that initial gap healing following shockwave
treatment, especially within 4 weeks of bony union, appears faster than without shockwave treatment, a revelation that agrees with observations of clinical outcomes.
In cases of pseudoarthrosis treated with shockwave, accelerated healing occurs both symptomatically and radiographically (Rompe et al., 1997; Forriol et al., 1994).
However, the positive influence of shockwaves on gap
filling appears to decline after 6 weeks of bony healing.
The reasons for and impact of the differential effect on
osteotomy healing with time are unknown.
The phenomenon that the maximal torque of the
diaphyseal osteotomy in the experimental group is significantly higher than that in the control group is clinically interesting. The mechanical strength of the two
groups begins to differ significantly as early as 4 weeks
and through 6 weeks and 8 weeks of osteotomy healing.
In this animal model, shockwave treatment clearly enhances the mechanical properties of early osteotomy
healing, and may also promote early bone healing in
clinical practice. If so, then the indication of shockwave
treatment can be extended to the cases of fresh fractures.
Mirroring the degree of gap healing with simple radiography, the enhancement of mechanical strength is
accompanied by faster gap filling in most of the experimental animals. This phenomenon might imply that
shockwave treatment encourages structural organization during callus formation. The results of histological
examination clarified, and further strengthened this
phenomenon. From the perspective view, the stronger
mechanical properties of fracture callus are beneficial
for early weight bearing.
This study found little to indicate that dosage influenced the response of shockwave treatment on maximal
torque of the healed diaphyseal osteotomy. The healing
of the osteotomies was not affected, regardless of whether they were treated with two or three applications of
shockwaves for a period of 6 weeks. Shockwaves may
affect osteotomy healing earlier, i.e. before 4 weeks. If
so, the effect of shockwave treatment on early gap filling
before 4 weeks instead of late union after 4 weeks might
be explained. However, extensive further study is required to define the optimal treatment dosage for enhancing new bone formation.
One confusing result is the weak correlation between
the value of BMD and the mechanical strength of the
diaphyseal osteotomy. No significant difference exists
between the BMD of the experimental and control
groups. BMD was supposed to be relevant to the
quantity of bone mass and the degree of mineralization.
However, the BMD value may not represent the degree
of structural organization, which is essential to the mechanical strength. In fact, the validity and reliability of
the DEXA for measuring the actual calcium content of
long bones continues to be debated as well as the correlation between BMD and mechanical properties. To
our knowledge, no agreement presently exists on the
effect of shockwave treatment on BMD.
5. Conclusion
Shockwave treatment positively influences the early
healing of diaphyseal osteotomy by achieving superior
maximal torsion strength and a higher rate of fracture
union, but does not influence BMD values. The longterm effect of shockwave treatment on fracture healing
deserves further study. Finally, the influence of shockwave treatment on callus structure reorganizations is
another issue worth further investigation.
Acknowledgement
The authors would like to thank Chang Gung Memorial Hospital for financially supporting this research
under Contract No. CMRP909.
R.W.-W. Hsu et al. / Clinical Biomechanics 18 (2003) S33–S39
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