Научная статья на тему 'PLATELET-RICH PLASMA ADMINISTERING IN OSTEOARTHROSIS TREATMENT'

PLATELET-RICH PLASMA ADMINISTERING IN OSTEOARTHROSIS TREATMENT Текст научной статьи по специальности «Клиническая медицина»

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OSTEOARTHROSIS / PLASMA / PLATELETS / TREATMENT

Аннотация научной статьи по клинической медицине, автор научной работы — Basnaev U.I., Karakursakov N.E., Mykhaylichenko V.Yu., Kriventsov M.A.

Background - According to the data from the published sources worldwide, about 10% of the world population suffers from osteoarthrosis. While searching for novel methods of osteoarthrosis treatment, we proposed administering intra-articular injections of autologous platelet-rich plasma. The goal of this clinical study was to evaluate the effectiveness of autologous platelet-rich plasma injections in osteoarthrosis patient treatment. Methods - This open-label parallel-group study was a pilot randomized controlled trial. An analysis of the treatment outcomes for 128 patients with knee joint arthrosis was performed. All patients were split among three groups, and subjects in two of those were receiving conventional treatment. Clinical efficacy was calculated from pain intensity, determined using Visual Analog Scale, Lequesne index and Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC). Inflammatory response intensity was assessed by superoxide dismutase content and erythrocyte catalase activity. Results - It was demonstrated that administering platelet-rich plasma allowed achieving tangible clinical and laboratory results without any side effects and with very few contraindications. The latter included, for instance, blocking inflammatory process in the joints, thereby inhibiting the oxidative stress, which is the most pathogenetically substantiated treatment of osteoarthrosis. Conclusion - Thus, we have discovered that platelet-rich plasma injections had apparent anti-inflammatory and pain-relieving effects, along with inhibiting action of destructive processes in the cartilaginous tissue, hence improving life quality of the patients with osteoarthrosis.

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Текст научной работы на тему «PLATELET-RICH PLASMA ADMINISTERING IN OSTEOARTHROSIS TREATMENT»

2021. Volume 10. Issue 1 (March). Article CID e0111 DOI: 10.15275/rusomj.2021.0111_

Traumatology and Orthopedics

Original article

Platelet-rich plasma administering in osteoarthrosis treatment

Usein I. Basnaev, Nariman E. Karakursakov, Vyacheslav Yu. Mykhaylichenko, Maxim A. Kriventsov S.I. Georgievsky Medical Academy, V.I. Vernadsky Crimean Federal University, Simferopol, Russia

Received 4 August 2020, Revised 9 December 2020, Accepted 12 February 2021

© 2020, Basnaev U.I., Karakursakov N.E., Mykhaylichenko V.Yu., Kriventsov M.A. © 2020, Russian Open Medical Journal

Abstract: Background — According to the data from the published sources worldwide, about 10% of the world population suffers from osteoarthrosis. While searching for novel methods of osteoarthrosis treatment, we proposed administering intra-articular injections of autologous platelet-rich plasma.

The goal of this clinical study was to evaluate the effectiveness of autologous platelet-rich plasma injections in osteoarthrosis patient treatment.

Methods — This open-label parallel-group study was a pilot randomized controlled trial. An analysis of the treatment outcomes for 128 patients with knee joint arthrosis was performed. All patients were split among three groups, and subjects in two of those were receiving conventional treatment. Clinical efficacy was calculated from pain intensity, determined using Visual Analog Scale, Lequesne index and Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC). Inflammatory response intensity was assessed by superoxide dismutase content and erythrocyte catalase activity.

Results — It was demonstrated that administering platelet-rich plasma allowed achieving tangible clinical and laboratory results without any side effects and with very few contraindications. The latter included, for instance, blocking inflammatory process in the joints, thereby inhibiting the oxidative stress, which is the most pathogenetically substantiated treatment of osteoarthrosis.

Conclusion — Thus, we have discovered that platelet-rich plasma injections had apparent anti-inflammatory and pain-relieving effects, along with inhibiting action of destructive processes in the cartilaginous tissue, hence improving life quality of the patients with osteoarthrosis.

Keywords: osteoarthrosis, plasma, platelets, treatment.

Cite as Basnaev UI, Karakursakov NE, Mykhaylichenko VYu, Kriventsov MA. Platelet-rich plasma administering in osteoarthrosis treatment. Russian Open Medical Journal 2021; 10: e0111.

Correspondence to Usein I. Basnaev. E-mail: [email protected].

Introduction

As an ailment, osteoarthrosis is an important social and biological issue. According to the data from the published sources worldwide, about 10% of the world population suffers from osteoarthrosis (OA) [1-3]. Federal Statistics Service reported OA among the leading causes of disability in Russia [4], with a steadily increasing morbidity trend over the past two decades, virtually doubling the number of such patients over time [5, 6]. Epidemiological survey data stated that 13% of Russian Federation population has already been ill with OA of the knee and/or hip joint [7, 8].

Inflammation is considered traditionally the cause of OA [9, 10], while activation of free-radical oxidation processes initiates and promotes degenerative changes in the hyaline cartilage. As a result, metabolic impairment of the connective tissue takes place [10, 11]. The latter, in turn, results in articular cartilage degeneration, lipping, inflammation, synovial compaction, as well as damaged ligaments and articular capsule, all of which lead to chronic pain, stiffness, deformation, and movement disorders [12].

There are multiple treatment approaches to OA. Previously, administering cartilage protectors, glucocorticoids, and nonsteroidal anti-inflammatory agents was considered to be the most efficient tactic [13, 14]. However, these medication groups have a number of disadvantages, as well as some adverse side effects [15].

The intra-articular injections of autologous platelet-rich plasma (PRP) were chosen in the process of searching for novel methods of pathogenetic OA therapy [16-19]. The aforementioned methodology had been first applied in 1965 at California University of Science and Medicine to stimulate osteogenesis in patients with maxillary injury [20].

PRP is a highly active agent containing, among others, high concentrations of the platelet-derived growth factor (PDGF), platelet insulin-like growth factor (IGF), vascular endothelial growth factor (VEGF) and transforming growth factor beta (TGF-P). These substances, acting locally on pathological lesion, induce an intensive anti-inflammatory effect stimulating tissue regeneration [23-25]. It was also proved that there are substances with both chondrogenic and osteogenic properties in the platelet alpha-granules, which are also present in PRP [21, 22].

2021. Volume 10. Issue 1 (March). Article CID e0111 DOI: 10.15275/rusomj.2021.0111_

Traumatology and Orthopedics

Figure 1. Study design.

Considering the discussed prerequisites, the urgency of searching for novel highly effective and safe methods of osteoarthritis treatment, and significant therapeutic potential of using autologous platelet-rich plasma, the goal of this clinical study was to evaluate the effectiveness of autologous platelet-rich plasma injections in osteoarthrosis patient treatment.

Material and Methods

Study design

This open-label parallel-group study was a pilot randomized controlled trial aimed to evaluate the effectiveness of autologous PRP injections in OA patient treatment. The study design was based on the analysis of the treatment outcomes for 128 patients with knee joint arthrosis. The clinical diagnosis was identified sensu the Congress of Russian Rheumatologists (1993) [26]. Our research design is presented schematically in the Figure 1. The study inclusion and exclusion criteria were as follows:

Inclusion criteria:

- Signed and dated written informed consent form (WICF) for the study;

- Clinically and radiologically confirmed primary osteoarthritis of the knee joint - grade 3, according to Kellgren and Lawrence classification criteria [29].

Exclusion criteria:

- Secondary gonarthrosis;

- Intra-articular pharmaceutical drug injections during six months prior to the study enrollment;

- HIV infection;

- Patient's disagreement to participate in the study.

All eligible patients were randomly allocated to three groups of comparable baseline traits: age and gender composition, illness duration, and severity of functional and morphological disorders.

2021. Volume 10. Issue 1 (March). Article CID e0111 DOI: 10.15275/rusomj.2021.0111_

Traumatology and Orthopedics

Group 1 (experimental treatment) included 47 patients. Treatment plan in this group included intra-articular PRP injections once a week for 1 month (i.e., a total of 4 PRP injections 7 days apart). We used the conventional preparation technique for autologous plasma with platelet concentration approximately 800x109 per liter [27].

Group 2 (active control) comprised of 38 study subjects. The provided treatment included hyaluronic acid injections into the joint cavity once a week for 1 month.

Group 3 (active control) encompassed 43 patients receiving conventional treatment: cartilage protectors (chondroitin sulfate [Alflutop ®] was administered via 1 mL intramuscular injections once a day for 20 days), non-steroidal anti-inflammatory agents (Meloxicam 15 mg in intramuscular injections twice a day for 5 days, followed by Celecoxib 200 mg orally twice daily for 14 days), proton-pump inhibitors (Omeprazole 20 mg twice a day orally for the entire period of the non-steroidal anti-inflammatory agents dosing), and physical therapy [28].

Table 1. Pain intensity dynamics sensu VAS in OA patients

Pain scale

Baseline values 1 month 3 months 6 months

Group 1 (n=47) 5.8±0.3 4.6±0.4 3 2±0 1* ** *** 2.1±0.2*,**,***

At rest Group 2 (n=38) 5.4±0.5 4.1±0.3* 3.8±0.2* 3.3±0.3*

Group 3 (n=43) 5.7±0.3 5.0±0.4 4.3±0.3 3.7±0.2*

Group 1 (n=47) 6.8±0.1 5.8±0.3 4 5±o 1* ** *** 4.3±0.2*,**

During walking Group 2 (n=38) 6.7±0.3 5.4±0.3 5.0±0.2* 4.8±0.1*

Group 3 (n=43) 6.8±0.2 6.1±0.4 5.1±0.2* 4.2±0.1*

* - p<0.05 compared with the appropriate baseline value; ** - p<0.05 compared with Group 2 within the same follow-up period; *** - p<0.05 compared

with Group 3 within the same follow-up period.

Table 2. WOMAC dynamics in OA patients

Patient groups Symptoms Baseline values 1 month 3 months 6 months

Pain severity 161.2±34.1 105.2±24.1 61.17±19.5* 39.24±15.1*

Group 1 (n=47) Motion stiffness 63.2±25.1 30.7±19.1 18.5±14.3* 11.4±12.1*

Functional impairment 224.7±36.2 149.4±23.2 103.4±18.9* 55.4±14.1*

Pain severity 158.8±38.5 88.8±18.2* 75.7±17.1* 42.5±11.9*

Group 2 (n=38) Motion stiffness 65.7±24.7 40.4±19.9 24±14.1 15.8±14.5*

Functional impairment 226.8±40.1 151±26.1 121.1±15.6* 60.4±16.8*

Pain severity 155.±39.1 121.5±21.4 88.4±15.1 55.4±11.4*

Group 3 (n=43) Motion stiffness 66.7±28.1 49.1±20.4 32.8±16.4 19.8±16.1*

Functional impairment 226.8±31.9 168.1±19.3 95.3±18.1* 71.2±15.1*

* - p<0.05 compared with the appropriate baseline value; ** - p<0.05 compared with Group 2 within the same follow-up period; *** - p<0.05 compared

with Group 3 within the same follow-up period.

Table 3. Lequesne index dynamics in OA patients

Patient groups Baseline values 1 month 3 months 6 months

Group 1 (n=47) 12.1±0.3 8 1±0 2* ** *** 6.4±0.3*,*** 4.1±0.6*,***

Group 2 (n=38) 11.9±0.5 9.4±0.3* 6.8±0.2* 5.5±0.1*

Group 3 (n=43) 11.9±0.2 10.1±0.3 9.5±0.3* 6.8±0.4*

* - p<0.05 compared with the appropriate baseline value; ** - p<0.05 compared with Group 2 within the same follow-up period; *** - p<0.05 compared

with Group 3 within the same follow-up period.

Table 4. Dynamics of biochemical parameters in OA patients

Patient groups Parameters Baseline values 1 month 3 months 6 months

Group 1 (n=47) Superoxide dismutase Erythrocyte catalase 757.8±194.1 54.9±11.1 877.2±124.2 35.2±13.4 1241.1±115.7*,**,*** 27.4±9.8* 1378.4±175.1*,**,*** 22.4±8.1*

Group 2 (n=38) Superoxide dismutase Erythrocyte catalase 704.1±207.1 58.1±12.8 760.2±115.3 50.7±11.5 807.8±107.1 40.4±5.1 850.4±112.8 35.4±3.1*

Group 3 (n=43) Superoxide dismutase Erythrocyte catalase 728.4±197.4 56.2±13.4 770.2±104.2 51.5±14.3 801.1±105.2 42.1±6.8 842.7±114.3 36.8±3.8

* - p<0.05 compared with the appropriate baseline value; ** - p<0.05 compared with Group 2 within the same follow-up period; *** - p<0.05 compared

with Group 3 within the same follow-up period.

2021. Volume 10. Issue 1 (March). Article CID e0111 DOI: 10.15275/rusomj.2021.0111_

Traumatology and Orthopedics

Study assessments

The effectiveness of treatment was assessed from clinical and laboratory data. Among all other clinical parameters, pain intensity in the joint (at rest or while walking) was rated using the Visual Analog Scale (VAS). We used standard VAS, presented as a 10 cm line with descriptive anchors along it (0 = no pain; 1-3 = mild pain; 4-6 = moderate to severe pain; 7-9 = very severe pain; 10 = worst possible pain). Functional state of affected joints was scored sensu Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) and Lequesne algofunctional index [30, 31]. Patient monitoring was carried out at the beginning of the treatment period (baseline value), as well as 1, 3 and 6 months after the completion of the treatment course.

The laboratory data included assessment of the dynamic pattern for superoxide dismutase (SOD) content and erythrocyte catalase activity. Similar to clinical evaluation, laboratory tests were performed at the beginning of the treatment period (baseline value), as well as 1, 3 and 6 months after the treatment completion.

To evaluate and compare the effectiveness of intra-articular PRP injections versus standard treatment, the statistical analyses of collected data were performed, using Statistica software, version 10.0 (StatSoft, USA). Prior to statistical comparisons, we tested our data for normality - both graphically and via Shapiro-Wilk test. The descriptive statistics were presented as mean values (M), standard deviations and standard errors (m). To compare the parameters between the study groups, the ANOVA test was conducted. The patterns were considered statistically significant at p-values<0.05.

Results

The dynamics of parameters characterizing the clinical effectiveness is presented in Tables 1-3.

In the course of our study, we demonstrated that the differences in pain intensity among the patients from the study groups 1, 2 and 3 were already quite obvious after just a month in the post-treatment period, even though the differences from the baseline values were not statistically significant on most occasions (Table 1). Patients in Group 2 exhibited the best response to the treatment after 1 month: their pain intensities, according to VAS, were 4.1±0.3 (p=0.02) at rest and 5.4±0.3 (p=0.003) during walking. Reduction in pain intensity was observed in this group, compared both with the baseline value within this group and with other treatment groups. However, 3 months after the treatment completion, the situation has changed. The lowest pain intensities sensu VAS were registered in Group 1 with PRP administering: 3.2±0.1 (p<0.001) at rest and 4.5±0.1 (p<0.001) during walking. These results were significantly lower, compared with other groups and the baseline values of this group. Such dynamics remained in place even 6 months after the treatment course completion. The analysis of collected data suggested that administering hyaluronic acid has inhibited the pain syndrome in the fastest way. However, long-term results demonstrated the superiority of PRP injections for pain relief.

The analysis of WOMAC values showed similar results (Table 2), although no statistically significant differences were found between the study groups. A month after treatment, the most effective technique of pain relief involved intra-articular injections of hyaluronic acid. In Group 2, the pain intensity sensu WOMAC

was 88.8±18.2, which was lower than in other treatment groups at the same period. However, as for joint stiffness and functional impairment, patients in Group 1 had the best outcomes: 30.7±19.1 and 149.4±23.2, respectively. In this case, similar tendency was observed throughout the whole follow-up period of the study. Also, pain intensity after 3 months in the group with PRP administering (61.71±19.5) was lower than in other groups, and compared with the previous assessment points within the group. These findings may suggest that PRP injections effectively relieved the pain, as well as reduced motion stiffness and functional lesions in OA patients. Thus, WOMAC values have demonstrated the superiority, or at least noninferiority, of PRP administering, compared with conventional treatment via anti-inflammatory medications and hyaluronic acid.

The dynamics of disability changes exhibited the following trend (Table 3): in a month after therapy completion, for patients from all study groups, the Lequesne index showed the significant degree of disability and varied from 8.1±0.2 to 10.1±0.3. However, the smallest value of the disability index was observed in Group 1 (8.1±0.2), which was significantly lower than in other study groups at the same period of time (p<0.001, compared with both Group 2 and Group 3). Three months after the treatment completion, Lequesne index values in patients of Groups 1 and 2 have decreased moderately (6.4±0.3 and 6.8±0.2, respectively), while in Group 3, receiving standard treatment, its value was still high (9.5±0.3). After 6 post-treatment months, the following outcomes were obtained: the patients in Group 1 had the minimum Lequesne index value of 4.1±0.6 (p<0.001, compared with Group 3), which matched the mild degree of joint dysfunction; subjects in Group 2 had its mean value of 5.5±0.6 (also considered mild dysfunction; and in Group 3, the index value was 6.8±0.4, implying a moderate to severe degree of disability. Based on provided data, it could be noted that PRP injections have significantly improved Lequesne index scores in OA patients, whereas the patients with standard treatment scheme (Group 3) exhibited the poorest improvement of disability. Based on this finding, we propose that PRP injections improve the quality of life in OA patients. However, further studies are needed to assess the PRP effect on long-term quality of life.

One of the complex pathogenesis elements of cartilaginous degenerative changes in OA is an activation of the free-radical oxidation and lipid peroxidation [32]. Hence, reliable indicators reflecting the inflammatory response intensity in OA are superoxide dismutase (SOD) content and erythrocyte catalase activity level (Table 4). The baseline concentrations of SOD and scavenger enzymes in all study groups were far from their normal ranges (1092-1817 U/g Hb and 18.4-25.0 mU/g Hb, respectively [33]), which confirmed the ailment duration and severity of inflammatory process. In a month after the treatment course, an increase in SOD content of 877.2±124.2 was observed in patients of Group 1, compared both with the baseline value and with the parameter values in Groups 2 and 3 during the same period (760.2±115.3 and 770.2±104.2, respectively), although these changes were not statistically significant. The same dynamics was observed during the further follow-up period. In 3 months after the treatment completion, SOD content was normalized in Group 1 (1241.1±115.7, p<0.001, compared with both Group 2 and Group 3), while in Groups 2 and 3, this parameter values were still far from their normal range (807.8±107.1 and 801.1±105.2, correspondingly).

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Traumatology and Orthopedics

Similar trend was observed during the assessment of changes in erythrocyte catalase activity level. The reduction of scavenger enzyme content to 35.2±13.4 in patients of Group 1, albeit not statistically significant, was noted already in a month after the treatment completion. However, this trend continued, and already in 3 months, the parameter has reached its normal values; whereas in Groups 2 and 3, decrease of catalase activity level was less prominent. A month after treatment, it was 50.7±11.5 and 51.5±14.3 in Group 2 and Group 3, respectively, which did not differ significantly from the baseline values. Over the entire post-treatment follow-up study period, we did not observe this parameter approaching normal values. Analysis of the laboratory data suggested that intra-articular PRP injections had the most apparent anti-inflammatory effect in OA patients, while the hyaluronic acid and chondroitin sulfate did not affect the dynamics of the inflammatory process noticeably.

Discussion

Choosing an effective management and treatment plan for OA is still controversial and debatable. Quite often, in this disease, administering hyaluronic acid injections is preferred, due to relatively rapid pain relief. However, habitually, the remission period lasts no more than 6-8 months, after which the second therapy course is required [13, 34]. The available published data indicated a large number of side effects caused by hyaluronic acid injections, both local and systemic, which can be reasonable explained by an abundant blood supply and lymph flow in the area of the synovial membrane [35]. Among oral medications, a group of cartilage protectors stands out. Their mechanism of action is aimed directly at the regeneration of cartilage tissue. However, this technique has several disadvantages, such as limited bioavailability of cartilage protectors, their low effectiveness in terms of pain relief, and a long period from the start of their administering to some substantial clinical effect [36, 37].

Based on the outcomes of this pilot study, we could recommend to administer the autologous human PRP as a treatment for OA. During the study, we discovered that PRP injections had a more evident effect, compared with hyaluronic acid and a standard therapy plan that included cartilage protectors for pain relief. Already in a month, the pain intensity in Group 1, according to the VAS score, was significantly lower than Groups 2 and 3, both at rest and during walking. A similar pattern was observed when evaluating the WOMAC and Lequesne index values.

We established a similar trend when analyzing biochemical changes. PRP exhibited superiority and greater effectiveness, probably, due to its mechanism of action. It is obvious that autologous PRP blocks the inflammatory process in the joints, thereby inhibiting the development of oxidative stress, which is the most pathogenetically substantiated treatment for OA. On the other hand, the action of hyaluronic acid is directed at the synovial fluid, blocking the inflammatory mediators and stimulating the cartilage synthesis. In turn, cartilage protectors usually affect the destruction process of macromolecular structures, while stimulating recovery in interstitial tissue and articular cartilage tissue, along with normalization of hyaluronic acid biosynthesis.

To date, numerous studies described the positive effect of the autologous plasma use in the treatment of degenerative disorders of the musculoskeletal system. However, the mechanism of PRP action has not yet been fully understood. Sampson S. et al. has

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proved that autologous plasma, injected into the ears of rabbits as an injectable scaffold, stimulated chondrogenesis. These results were confirmed by the data of the biopsy histological examination and magnetic resonance imaging [38, 39]. According to Anitua E. et al., use of PRP in patients with osteoarthritis of the knee joints resulted in increase of the hyaluronic acid content and angiogenesis [40].

The results of the study by Chahla J. et al. demonstrated a statistically significant superiority of PRP, compared with hyaluronic acid injections, in the treatment of OA patients. The use of autologous plasma made it possible to achieve a more prolonged effect: after six months, the pain intensity was significantly lower than in patients treated with hyaluronic acid [41]. There is also reliable data on the successful use of PRP in lateral epicondylitis. The obtained results indicated a significant improvement of the joint function in patients treated with autologous plasma [42].

Therefore, the results of many studies implied the effectiveness of the autologous plasma use in the treatment of inflammatory and degenerative diseases of the musculoskeletal system. However, the mechanism of PRP action has not yet been fully understood, and possible adverse side effects and contraindications have not been yet studied. Hence, PRP administering in OA patients is a promising research area that requires further careful analysis.

Conclusion

The use of autologous PRP in the treatment of OA patients allowed us obtaining the superior, or at least noninferior, outcome according to both clinical (relieving pain syndrome, and reducing both functional impairment and motion stiffness) and laboratory (increasing SOD content and decreasing erythrocyte catalase activity level) parameters, compared with active comparator treatment schemes. Based on the results of this pilot study, with the certain limitations, PRP therapy could be considered an optimal method for treating OA patients.

Limitations

Although this clinical pilot study has demonstrated the effectiveness of intra-articular PRP injections for patients with osteoarthritis on a fairly large sample of patients, the obtained results should be interpreted with some limitations. In particular, the presented study was not a blinded and sufficiently controlled trial. Also, the goal of this pilot study did not involve a comprehensive assessment of the safety and tolerability of various treatment schemes, as well as evaluation of the impact on the quality of life in patients. These and other parameters require more detailed studies. Finally, for some of studied parameters, only hypothetical trends rather than confirmed statistically significant differences were shown. Partially, this was due to a fairly large variability of the studied parameters. As a consequence, a further study, completed on a much larger sample of patients, as well as their additional standardization by the baseline values of parameters, would likely lead to an increase in the statistical power and greater reliability of prospective results.

Ethical approval

All patients, willing to be included in clinical study, provided written informed consent prior to the study and any study-related procedures. All

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procedures involving human participants, performed during the study, were in accordance with the ethical standards of the institutional and national research committee and with the 1964 Declaration of Helsinki and its later amendments. Study protocol and WICF for study participants were approved by the Institutional Review Board (IRB) (No. 6 of June 4, 2020).

Acknowledgments

This study was partly supported by the V.I. Vernadsky Crimean Federal University Development Program for 2015-2024 (Research and Technological Development Topic No. VG07/2020).

Conflict of interest

The authors declare no conflicts of interest pertaining to this project. References

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2021. Volume 10. Issue 1 (March). Article CID e0111 DOI: 10.15275/rusomj.2021.0111_

Traumatology and Orthopedics

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Authors:

Usein I. Basnaev - PhD, Assistant Professor, Department of Traumatology and Orthopedics, S.I. Georgievsky Medical Academy, V.I. Vernadsky Crimean Federal University, Simferopol, Russia. http://orcid.org/0000-0002-1757-9595.

Nariman E. Karakursakov - PhD, Assistant Professor, Department of General Surgery, S.I. Georgievsky Medical Academy, V.I. Vernadsky Crimean Federal University, Simferopol, Russia. http://orcid.org/0000-

0002-6691-9349.

Vyacheslav Yu. Mykhaylichenko - MD, Professor, Chair of the Department of General Surgery, S.I. Georgievsky Medical Academy, V.I. Vernadsky Crimean Federal University, Simferopol, Russia. http://orcid.org/0000-

0003-4204-5912.

Maxim A. Kriventsov - MD, Professor, Chair of the Department of Anatomic Pathology, S.I. Georgievsky Medical Academy, V.I. Vernadsky Crimean Federal University, Simferopol, Russia. https://orcid.org/0000-0001-5193-4311.

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