EXPERIENCE WITH LONG BONES DEFECTS REPLACEMENT ON THE BASIS OF COMBINED USE OF TRANSOSSEOUS OSTEOSYNTHESIS AND OSTEOCONDUCTIVE MATERIALS IN CLINICAL PRACTICE
Reznik L.B.1, Borzunov D.Yu.2, Mokhovikov D.S.2,
Stasenko I.V.1
1Omsk State Medical University, Omsk, Russia,
2Russian Ilizarov Scientific
Center of Restorative Traumatology and Orthopaedics, Kurgan, Russia
Infectious purulent inflammatory
lesions of the bones present the actual problem of the modern medicine [1].
According to the foreign literature, the process of treatment and
rehabilitation is associated with high financial and psychosocial costs, as
well as with high rate of disability. Therefore, understanding the course of
infectious processes and improvement in treatment outcomes are the first priority
tasks for many studies [2, 3, 4]. In 12-61 % of cases, purulent complications
lead to development of chronic osteomyelitis, which is one of the obstinate
complications that cause long term working incapacity and disability [5].
Surgical activity for treating
chronic osteomyelitis is up to 70 % [6]. At that one performs radical necrosequestrectomy
with subsequent bone plastic surgery with use of Ilizarov’s technique and
various artificial or biological implants [6, 7, 8].
Currently, the carbonic composite materials
are widely used [9, 10, 11]. They have the little pore structure and function
as the efficient osteoconductive matrix [12]. At the present time, the carbonic
composite materials are used for craniofacial surgery, surgical treatment of
degenerative and dystrophic disease, spinal disease, for replacement of bone
defects in spine and extremities injuries, as well as for osteomyelitic, tuberculous
and malignant lesions of the bones [13, 14].
The
objective of the study –
to improve the treatment results in patients with
post-resection defects of the diaphyseal portion of the long bones on the basis
of application of transosseous osteosynthesis in combination with
osteoconductive materials.
The tasks of the study:
1) to develop the algorithm for use
of the carbonic implants for replacement of various types of postresection
defects of the long bones in clinical practice;
2) to investigate the treatment
results in the patients with various types of the implants.
MATERIALS AND METHODS
The materials included 25 clinical
cases of the patients who had received the inhospital treatment in the purulent
surgery unit in Omsk Clinical Medicosurgical Center on the basis of the
traumatology and orthopedics unit No.4 of Russian Ilizarov Scientific Center of Restorative
Traumatology and Orthopaedics.
The inclusion criteria were the age from 18 to 70, presence of long bone
defects, the written consent from the patient. The exclusion criteria were pregnancy,
breast feeding, presence of severe decompensated concurrent pathology, inordinate
drinking, previous or present use of drugs, presence of abnormal development of
bone tissue, irreversible changes in soft tissues as result of damage of the
magistral vessels.
All patients were informed about the conditions of the study, the offered
and alternative treatment techniques and the conclusion from the ethical
committee, Omsk State Medical University.
The patients were distributed into two groups with similar age and
gender: the main group (15 patients) and the comparison group (10 patients).
The first group (the comparison group) was used for the retrospective
analysis of the medical records of 10 patients treated in the purulent surgery
unit in Omsk Clinical Medicosurgical Center in 2014-2016. The main surgical
technique was radical necrosequestrectomy with opening of the spinal channel
and resection of ends of fragments. After that, the plastic surgery for a
formed defect was conducted with use of bone cement and subsequent draining of
the postsurgical wound with silicone non-flowing drains.
In the second (main) group 15 patients received the carbonic
nanostructural implant (Fig. 1). The implant was used according to the following
protocol. The region of a bone defect was opened from a skin and soft tissue
incision (recurrent approach during primary surgery). A defect of the long bone
diaphysis was replaced with the carbonic nanostructural implant. The implant
sizes corresponded to the sizes of a resected part of a bone that was provided
by means of intrasurgical preparation with the burrs. Additional stabilization
was realized with the external device with fixing the injured and adjacent (if
it was necessary) segments of the extremity. Considering the necessity of
distraction in the region of a lesion, the first stage included the mounting of
the external fixing device. Then the implant (prepared in concordance with the
sizes of a defect) was placed.
Figure 1. The appearance of the nanostructured carbon implant
The implants were used at the stage of persistent remission of the
infectious process after carrying out the control analyses: general blood
analysis, erythrocyte sedimentation reaction, C-reactive protein.
During mounting the device, first of all, the basic supports were mounted
with maximal distance from an injured region of the segment with consideration
of topography of vascular and neural stems and anatomy of muscles and a bone.
The reducing supports were placed at the level of proximal and distal ends of
fragments (at least 10 mm from a defect). Positioning of the supports was
associated with the geometry of the implant and necessity for its placement
into the proximal and distal marrowy canal for the distance of 5 mm. Aseptic
dressings were placed onto the regions of input and output of the pins. Then
the wound was sutured in layer by layer manner, and the postsurgical wound was
drained with the silicone non-flowing drains.
The analysis of the data was based on the results of the clinical and
X-ray examinations, estimation of life quality with SF-36.
The main criteria for estimation of the short term outcomes of the
treatment were the timeframes and a type of a postsurgical wound healing.
Also during the process of dynamic observation we estimated the absence
of recurrent diseases (fistula opening, development of pathological fractures,
X-ray picture), and correction of orthopedic problems.
The X-ray examinations were conducted before surgical intervention for
verifying the diagnosis and location of the process, as well as after the
surgical treatment on the days 1, 30, 60 and 90 for estimation the time course
of reparative processes in the bone wound.
The statistical analysis of the results was conducted with consideration
of the observation units, a type of estimated data and the study design. The
median (P50) and the percentiles of the variational series (lower Q1 and upper
Q3 quartile) were used for description of the quantitative variables.
Mann-Whitney U-test was used for comparison of the quantitative data (two
independent populations).
The p value of 0.05 was
considered as the critical level of significance in all procedures of the
statistical analysis. The biometrical analysis was conducted with STATISTICA
6.0.
RESULTS
The
age of the patients was 48 (36-54) in the main group and 49 (37-53) in the
control group (U = 74.00, p = 0.978).
The
patients were distributed according to their gender: the main group – 11 men
(73.3 %) and 4 women (26.7 %), the control group – 7 men (70 %) and 3 women (30
%).
Refusal
from analgetics and, as result, management of pain syndrome were on the day 4
(3-5) in the main group and on the day 3.5 (3-5) in the control group (U =
70.5, p = 0.806).
Dosed
physical load to the operated extremity was on the week 3 (2-4) in the main
group and also on the week 3 (1-6) in the control group (U = 74.0, p = 0.978).
The
developing callus was visualized on the X-ray image from the week 8 (Fig. 2,
3).
Figure 2. X-ray imaging and the developing callus in the main group (8 weeks)
Figure 3. X-ray imaging and the developing callus in the control group (8 weeks)
Full
load to the operated extremity was on the week 3 (2-4) in the main group and
also on the week 3, but with higher variability (1-6) in the control group.
The
analysis of uniformity of development of callus showed the good uniformity
along the whole fracture in the main group, with periosteal pattern at the
initial stages of development and with ingrowth into the implant on all sides.
The
most reliable sign of fracture consolidation was absence of pain and of edema
increase during the clinical testing.
SF-36
was used for analysis of life quality. There were not any statistically
significant differences between the groups in relation to PH and MH before and
after the surgical treatment.
Some
trends were identified during the analysis of the treatment outcomes in
dependence on size of a bone defect. The
defect
size
was
3 cm
(2.8-3.8) in
the
main
group.
This value was 5.25 cm (2-7)
in the control group. Despite the significant variability in the borders of a
defect in the control group, the differences were not statistically significant
(U = 58.5, p = 0.367).
The
positive outcomes of the treatment were observed in 60 % of the cases in the
main group and in 20 % in the control group.
The
further analysis of each group showed that the size defect was 2.8 cm (2.5-3.0)
in the cases with the positive treatment outcomes in the main group. The defect
size was 3.95 cm (3.58-4.4) in the patients of the same group with requirement
for additional surgical intervention (Fig. 4). The
differences
between
these
values
were
statistically
significant
(p
< 0.001).
The
results for the mean defect size with positive and negative outcomes of the
treatment were 10 % and 15 % correspondingly according to the uniform
classification of long bones defects (Barabash Yu.A., Barabash A.P.) [15].
Figure 4. The defect size in the main group with positive and negative treatment outcomes (the median value)
Clinical cases
Clinical case No.1
The patient G, age of 56, was treated during 18 days. The diagnosis was: “Chronic posttraumatic osteomyelitis of the left tibial bone, a fistula type” (Fig. 5).
Figure 5. The two-plane X-ray images of the left leg in the patient G. before surgery
The
patient received the surgery: correcting osteotomy, fixation of the left leg
bones with Ilizarov device, replacement of a defect with the carbonic implant.
The size of the replaced defect was 2.5 cm. The X-ray control examination was
conducted on the first day after the surgery (Fig. 6). The postsurgical period
was without complications. The wound healed with the primary intention. The sutures
were removed on the day 15. Consolidation was after 10 weeks. The clinical
testing showed the insignificant pain syndrome. Ilizarov device was partially
dismounted. It was fully dismounted after 14 weeks. The total time of the
follow-up was 2 years (Fig. 7). There were no complications and recurrent
process of chronic osteomyelitis during that period.
Figure 6. The two-plane X-ray images of the left leg in the patient G. after surgery
Figure 7. The two-plane X-ray images of the left leg in the patient G. two years after surgery
Clinical case No.2
The patient K., age of 36, was treated during 28 days. The diagnosis was “Chronic postsurgical osteomyelitis of the middle one-third of the left humerus diaphysis, a fistula type” (Fig. 8).
Figure 8. The two-plane X-ray images of the left humerus in the patient K. before surgery
The
patient received the surgery: necrosequestrectomy, replacement of a defect with
the carbonic implant, Ilizarov device fixation. The control X-ray examination
was conducted within 24 hours after the surgery (Fig. 9). The postsurgical
period was without complications. The wound healed with primary intention. The sutures
were removed on the day 17. The patient was discharged in satisfactory
condition for outpatient treatment. By the moment of 14th week some
complications appeared: a fracture of the pins, disordered integrity of bone
regenerate as result of instability of bone fragments and recurrent opening of
the fistula (Fig. 10).
Figure 9. The two-plane X-ray images of the left humerus in the patient K. after surgery
Figure 10. The two-plane X-ray images of the left humerus in the patient K. after the fracture
CONCLUSION
1.
The use of the nanostructural carbonic material for replacement of defects
optimizes the formation of bone regenerate and provides the positive osteointegration
on the border between the bone and the implant.
2.
The developed technique improves the treatment outcomes in patients with
defects in combination with extrafocal transosseous fixation for defect
replacement not more than 10-15 % of segment length.
3.
The use of the carbonic nanostructural implant does not increase the duration
of the surgical treatment and has no statistically significant differences from
the technique of bone cement filling.
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