Bangladesh Medical Research Council Bulletin


Home / Archives / Vol 47 No 1 (2021) / Research Articles

Intra-articular Injection of Hyaluronic Acid (HA) and Platelet- rich Plasma (PRP) in the Treatment of Mild and Moderate Osteoarthritis of Knee


Farzana Khan Shoma
Department of Physical Medicine and Rehabilitation, Bangabandhu Sheikh Mujib Medical University, Dhaka, Bangladesh.

Ziaur Rahman Chowdhury
Department of Physical Medicine and Rehabilitation, Bangabandhu Sheikh Mujib Medical University, Dhaka, Bangladesh.

Farzana Hossain
Freelance Researcher, MPH.

Abul Khair Mohammad Salek
Department of Physical Medicine and Rehabilitation, Bangabandhu Sheikh Mujib Medical University, Dhaka, Bangladesh.

Moshiur Rahman Khasru
Department of Physical Medicine and Rehabilitation, Bangabandhu Sheikh Mujib Medical University, Dhaka, Bangladesh.

Md. Nuruzzaman Khandaker
Department of Physical Medicine and Rehabilitation, Bangabandhu Sheikh Mujib Medical University, Dhaka, Bangladesh.

Keywords: Platelet-rich plasma, Hyaluronic acid, Osteoarthritis of knee, Visual analogue scale.

DOI: 10.3329/bmrcb.v47i1.55800

Abstract

Background: Osteoarthritis (OA) is the most prevalent chronic joint disorder worldwide and is associated with significant pain and disability. Introduction of platelet-rich plasma (PRP) injection has been viewed as an advance in the management of OA knee.

Objective: To compare the effectiveness of PRP and Hyaluronic Acid (HA) in the treatment of mild and moderate OA knee

Methods: The present randomized clinical trial had been conducted in the Department of Physical Medicine and Rehabilitation, Bangabandhu Sheikh Mujib Medical University (BSMMU), Dhaka from 2018 to 2019. A total of 154 patients with mild and moderate OA knee were randomly allocated into two groups: group A (received PRP injection) and group B (received HA injection) where 133 patients completed the follow-up schedule. Outcomes were measured by OA specific translated and validated Bengali instrument- Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) questionnaire and visual analogue scale (VAS 0-10). They were followed-up for 6 months.

Results: There was no significant statistical difference at the baseline between the groups regarding age, sex, grading of OA knee, side involvement, mean duration of the disease, VAS scores and WOMAC scores. After one month, VAS score significantly decreased in PRP group compared to HA group (p<0.001). However, there was no statistical difference regarding total WOMAC scores between two groups (p=0.063). In third and sixth month, VAS score significantly decreased in PRP group compared to HA group (p<0.001). Though the stiffness and physical activity scores of WOMAC did not reduce significantly, the pain score reduced significantly in PRP group compared to HA group. In both groups, significant reduction of VAS and WOMAC total scores was observed after six months follow-up compared to baseline values (p<0.001).

Conclusion: Intra-articular platelet-rich plasma improves pain and function of the knee in patients with osteoarthritis. Though intra-articular hyaluronic acid also improves pain and function in the foot, PRP is more effective than hyaluronic acid. Multi-centered clinical trial with long term follow-up should be conducted to see the effects of PRP and HA.

Keywords: Platelet-rich plasma, Hyaluronic acid, Osteoarthritis of knee, Visual analogue scale.

Introduction

Osteoarthritis (OA) is the most common form of joint disease and among the top 10 causes of disability worldwide.1 This degenerative joint disease is characterised by erosion of the articular cartilage, hypertrophy of bone at the margins (osteophytes), subchondral sclerosis, and a range of biochemical and morphologic alterations of the synovial membrane and joint capsule.2 With aging of the population and increasing obesity, OA arises as a major public health problem and an important financial burden for the global economy.3 It is more common in women than men.4 OA of the knee, the principal large joint to be affected, results in disabling knee symptoms in an estimated 10% of people older than 55 years, a quarter of whom are severely disabled.5 The primary objectives in OA treatment focus on pain reduction, joint mobility improvement, and functional impairment limitation. Furthermore, secondary goals are centred on the reduction of disease progression and improvement of muscular strength, in order to preserve patients’ independence and quality of life.6

Current treatments aim at alleviating these symptoms by several different methods: Non-pharmacological treatments like education, exercise, lifestyle changes), Pharmacological treatments like paracetamol, NSAIDs, topical treatments and invasive interventions like intra-articular injections, lavage, arthroplasty.7 However, most of the treatments have limited tolerability and their efficacy is limited to relieving pain.8

Viscosupplementation (such as HA), prolotherapy (such as dextrose), platelet-rich plasma (PRP) therapy, and stem cell therapy have been considered for the treatment of knee OA to increase tissue healing and to slow down the progression of degeneration.9

High-molecular-weight HA is a natural disaccharide polymer that can mimic the synovial fluid. In addition to supporting joint lubrication, HA can inhibit the inflammatory process and stimulate cartilage regeneration.10-13

Hyaluronic acid is important in maintaining articular cartilage integrity, being one of the major glycosaminoglycans in the extracellular matrix. By binding proteoglycans, it provides and maintains intra- articular lubrication, optimizing the viscoelastic properties of synovial fluid.14 Synovial fluid with normal HA concentration acts as a viscous lubricant during slow joint movements and as an elastic shock absorber during rapid joint movements.15 HA functions through anti-inflammatory, anabolic, analgesic, and chondroprotective mechanisms.16

Platelet-rich plasma could be defined as autologous blood with platelets concentration of 94% while normal platelets concentration is only 6%.17 PRP injections intend to trigger the inflammatory response, which promotes the healing process by renovating injured tissue structure and simultaneously preventing further tissue degeneration.18 Infiltration with autologous blood, buffered platelet rich plasma or autologous growth factors seems promising, but requires further investigation.19

PRP has shown promise in the treatment of various musculoskeletal conditions including chronic lateral epicondylitis, osteoarthritis, plantar fasciitis, muscle strain, ligament sprain, cartilage damage, fractures, tendon injury and has been approved by the International Olympic Committee in the treatment of soft tissue injuries and tendon disorders.20 The key components of PRP are the platelets which store and release a wide range of bioactive factors including growth factors that can modify the biological environment at injury sites, thus enhancing tissue healing. PRP is not known to have any adverse effects unlike the commonly used nonsteroid anti- inflammatory drugs (NSAIDS) that are known to affect the gastrointestinal, cardiovascular and renal systems.21 There is scarcity of published data about the effectiveness in the management of knee OA with PRP and HA in Bangladesh. Hence this study had been conducted with the objective of comparing the effectiveness of Platelet-rich plasma (PRP) and Hyaluronic Acid (HA) in the treatment of mild and moderate osteoarthritis of the knee.

Materials and Methods

The study was a randomized clinical trial conducted in the Department of Physical Medicine and Rehabilitation, Bangabandhu Sheikh Mujib Medical University (BSMMU), Shahbagh, Dhaka from 2018 to 2019. With an alpha error of 0.05, 90% power, a standard deviation of 16.36 and a minimal clinically significant difference of 9.02,11 the minimum sample size was 69 for each group. Considering a possible drop out of 10%, a total of 154 patients were required.

Inclusion criteria: Adult patients of both sex, diagnosed according to the criteria developed by the American College of Rheumatology Radiologic and Clinical Criteria for Osteoarthritis (ACR) were included in the study.

Exclusion criteria: Patients having history/ evidence of acute swollen joint (septic arthritis), recent trauma, fracture, unstable knee joint, malignancy, tubercular arthritis, Inflammatory disease (e.g. rheumatoid arthritis, psoriatic arthritis, SpA) etc. and patients on therapy with anticoagulant, severe anemia, receiving aspirin or nonsteroidal anti-inflammatory drugs (NSAIDs) within a week ago, bleeding disorder were excluded from the study.

Randomization: To keep the study blinded, all patients underwent blood harvesting to obtain autologous PRP, which was then used only in the PRP group. Before the injection, the syringe was appropriately covered to prevent patients from discovering the substance they were receiving. Group selection was done randomly by the way of lottery. Patients were divided into two groups: group A and group B. In each group, 77 patients were allocated. In group A, patients were allocated with single dose intra-articular injection PRP (10 ml) and in group B, patients were allocated with single dose intra-articular HA (Sylocet) (4 ml) injection.

Before injection patient was prohibited to take NSAID at least 7 days. The injection was administered through a direct parapatellar approach using 10 cc disposable syringe. If effusion was present in the knee would be aspirated and send to laboratory for synovial fluid analysis. Aspiration was performed by using a separate sterile syringe before injection. The patient was then observed for 15-20 min and then discharged.

Post-injection protocol: The use of NSAID was prohibited. Because there might be discomfort experienced by the patient at the site of the injection for up to 48 hours, patients were encouraged to ice the injection site, elevate the limb and modify activities. Patients were discharged to home with instruction to limit their activities for 48 hours.

Paracetamol was allowed for break-thru pain < 2000mg/day. Quadriceps strengthening exercise was advised in the form of extension of knees10 repetition 2 times daily. Instruction for activity of daily living (ADLs) was prescribed for all patients. Respondents of both groups were assessed to see the effects of treatment at 4th week, 12th week, and 24th week.

Outcome measures: Outcome were measured by OA specific translated and validated Bengali instrument- Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) questionnaire. The WOMAC evaluates 3 dimensions: pain, stiffness, and physical function with 5, 2, and 17 questions, respectively. The Likert version of the WOMAC is rated on an ordinal scale of 0 to 4, with lower scores indicating lower levels of symptoms or physical disability. Each subscale is summated to a maximum score of 20, 8, and 68, respectively.22

Pain score was collected on visual analogue scale (VAS 0-10). A VAS is usually a horizontal line, 100 mm in length, anchored by word descriptors at each end. The patient marks on the line the point that they felt represents their perception of their current state. The VAS score was determined by measuring in millimeters from the left hand end of the line to the point that the patient marked.

Data processing and analysis: Data were collected by the investigator who was involved in administering the injection. The statistical analysis was conducted using SPSS (statistical package for social science) version 25 statistical software. Associations of categorical data were assessed using Chi-square test and continuous data were assessed using Independent Sample t-test and paired t test. Here, p<0.05 was considered significant. Here, all p-values were two sided.

Ethical implication: The protocol of the study was approved by the Ministry of Science and Technology Government of People’s Republic of Bangladesh Secretariat, Dhaka. The G.O. no. was 39.00.0000.09.02.90.18-19. Informed written consent was taken from every patient after adequate explanation of the purpose and procedure of the study. Privacy, anonymity and confidentiality of data were maintained strictly. They were assured of protection of their safety. Each patient enjoyed every right to participate or refuse or even withdraw from the study at any point of time.

Results

A total 150 patients were included in the study. They were followed up for 6 months. Among the patients, 65 patients in group A and 68 patients in group B completed the study. Hence, this section presented the results of 133 patients. The mean ages of the patients were 51.3 (±6.5) (range: 37.0-67.0) and 52.7 (±5.4) (range: 40.0-

65.0) years in group A and group B respectively. Out of 133 patients, 38 (58.5%) patients in group A and 39 (57.4%) patients in group B were female. The mean duration of disease of the patients were 14.5 (±6.6) and 16.6 (±6.4) months in group A and group B respectively. The mean VAS score of the patients were 7.6 (±0.6) and 7.4 (±0.5) in group A and group B respectively. The mean WOMAC total score of the patients were 1966.6 (±78.7) and 1974.1 (±91.2) in group A and group B respectively. There was no significant statistical difference at the baseline between the groups regarding age, grading of OA knee, side involvement, mean duration of disease, Visual Analogue Scale (VAS) scores and WOMAC scores.

After one month, the VAS score was 5.3 ±0.4 in group A while in group B it was 5.6 ±0.5. Student t test showed that VAS score was significantly lower in PRP group compared to HA group as p&lt;0.001. The WOMAC total score was 1830.8 ±77.3 in group A and in group B it was 1855.1 ±72.8. There was no statistical difference regarding total WOMAC scores between two groups as the p value was 0.063 (obtained by Student-t test) (table I).

Criteria Group A (n=65)
Mean±SD (Range)
Group B (n=68)
Mean±SD (Range)
p value
VAS 5.3 ±0.4 (5.0-6.0) 5.6 ±0.5 (5.0-6.0) <0.001
Pain WOMAC 362.3 ±5.5 (350.0-370.0) 365.1 ±4.3 (360.0-375.0) 0.002
Stiffness WOMAC 126.1 ±11.6 (110.0-160.0) 128.1 ±10.3 (115.0-145.0) 0.311
Physical activity WOMAC 1342.3 ±73.5 (1200.0-1450.0) 1361.9 ±75.9 (1230.0-1455.0) 0.132
WOMAC total 1830.8 ±77.3 (1665.0-1945.0) 1855.1 ±72.8 (1745.0-1950.0) 0.063
Foot notes: bold value indicates the level of significance p≤0.05
Abbreviations: SD: Standard Deviation, VAS: Visual Analogue Scale, WOMAC: Western Ontario and McMaster Universities Osteoarthritis Index

After three months, the VAS score was 4.2 ±0.4 in group A while in group B it was 4.7 ±0.5. Student t test showed that VAS score was significantly lower in PRP group compared to HA group (p&lt;0.001). The pain WOMAC and stiffness WOMAC were significantly lower in group A compared to group B (p&lt;0.001 and p=0.010). However, there was no statistical difference regarding WOMAC physical activity scores between two groups as the p value was 0.275. The WOMAC total score was 1687.5 ±76.8 in group A and in group B it was 1711.9 ±63.9. There was significant statistical difference regarding total WOMAC scores between two groups as the p value was 0.048 (obtained by Student-t test) (table II).

Criteria Group A (n=65)
Mean± SD
Group B (n=68)
Mean± SD
p value
VAS 4.2±0.4 (4.0-5.0) 4.7 ±0.5 (4.0-5.0) <0.001
Pain WOMAC 349.8 ±3.8 (340.0-355.0) 354.1±4.0 (350.0-365.0) <0.001
Stiffness WOMAC 117.6 ±11.8 (100.0-150.0) 121.8±4.5 (115.0-135.0) 0.010
Physical activity WOMAC 1240.3 ±78.9 (1100.0-1350.0) 1254.1 ±66.1 (1150.0-1355.0) 0.275
WOMAC total 1687.5 ±76.8 (1535.0-1805.0) 1711.9 ±63.9 (1605.0-1820.0) 0.048
Foot notes: bold value indicates the level of significance p≤0.05
Abbreviations: SD: Standard Deviation, VAS: Visual Analogue Scale, WOMAC: Western Ontario and McMaster Universities Osteoarthritis Index

At six month, the VAS score was 3.3 ±0.4 in group A while in group B it was 3.6 ±0.5. VAS score was significantly lower in PRP group compared to HA group (p&lt;0.001). The pain WOMAC was significantly lower in group A compared to group B p&lt;0.001). However, there was no statistical difference regarding WOMAC stiffness and physical activity scores between two groups as the p value was 0.651 and 0.058. The WOMAC total score was 1541.1 ±70.6 in group A and in group B it was 1571.2 ±66.5. There was significant statistical difference regarding total WOMAC scores between two groups as the p value was 0.012 (obtained by Student-t test) (table III).

Criteria Group A (n=65)
Mean± SD
Group B (n=68)
Mean± SD
p value
VAS 3.3 ±0.4 (3.0-4.0) 3.6 ±0.5 (3.0-4.0) <0.001
Pain WOMAC 329.5 ±10.1(315.0-345.0) 336.0 ±7.0(325.0-345.0) <0.001
Stiffness WOMAC 97.2 ±10.0 (85.0-120.0) 97.9 ±5.4 (90.0-110.0) 0.651
Physical activity WOMAC 1114.3 ±71.1 (1000.0-1050.0) 1137.3 ±67.9 (1250.0-1250.0) 0.058
WOMAC total 1541.1 ±70.6 (1400.0-1675.0) 1571.2 ±66.5 (1445.0-1690.0) 0.012
Foot notes: bold value indicates the level of significance p≤0.05
Abbreviations: SD: Standard Deviation, VAS: Visual Analogue Scale, WOMAC: Western Ontario and McMaster Universities Osteoarthritis Index

The VAS score significantly decreased in group A from 7.6 ±0.6 to 3.3 ±0.4 after six months follow up (p<0.001, obtained by paired t test). The WOMAC total scores significantly decreased in group A from 1966.6 ±78.7 to 1541.1 ±70.6 after six months follow up (p <0.001, obtained by paired t test). In group B, the VAS score significantly decreased in group A from 7.41 ±0.5 to 3.6 ±0.5 after six months follow up (p <0.001, obtained by paired t test). The WOMAC total scores also significantly decreased in group A from 1974.1 ±91.2 to 1571.2 ±66.5 after six months follow up (p<0.001, obtained by paired t test) (table IV).

Criteria Before treatment
Mean± SD
After treatment
Mean± SD
p value
Group A
VAS 7.57±0.56 3.28±0.45 <0.001
WOMAC total 1966.63±78.69 1541.08±70.61 <0.001
Group B
VAS 7.41 ±0.55 3.57 ±0.49 <0.001
WOMAC total 1974.12 ±91.22 1571.25 ±66.54 <0.001
Foot notes: bold value indicates the level of significance p≤0.05
Abbreviations: SD: Standard Deviation, VAS: Visual Analogue Scale, WOMAC: Western Ontario and McMaster Universities Osteoarthritis Index

Consort Flow Diagram

Discussion

The present randomized clinical trial study had been conducted to compare the effects of intra-articular PRP and HA injection in the management of mild to moderate knee OA. The mean age of the patients was more than 50 years which matched other studies.11,23,24 In the study, conducted in Iran, the mean age of patients was shown 56.0 years and 61.0 years in PRP and HA group respectively while the Italian study found the mean age of patients was 55.0 years and 58.0 years in PRP and HA group respectively.11,23 Spakova et al. showed the mean age of patients was 52.0 and 53.0 years in PRP and HA group respectively.24 More than half of the patients in both groups were found female. Women are about twice as likely as men to develop OA. Although women have a lower prevalence of OA than men before age 50 years, there is a marked increase in prevalence among women after 50.2

At the initial stage of treatment, the VAS scores of the patients was 7.6 (±0.5) in group A which significantly decreased to 3.3 (±0.4) after six months of intervention with PRP (p>0.001). The platelet concentrate is activated by addition of calcium chloride, which results in the formation of platelet gel and this stimulate the release of growth factors and bioactive molecules.26 In group B, the VAS scores also significantly decreased from 7.4 (±0.5) to 3.6 (±0.5) after six months of intervention with HA (p<0.001). The analgesic properties of HA could be attributed to a specific activity on opioid receptors.27

After one month of intervention, there was highly significant statistical difference between the two groups regarding the VAS scores (p<0.001) which was consistent at the end of six months (p<0.001) which supported other study (p=0.0034 and p<0.001 respectively).28

After one month of treatment, significant statistical difference was observed in the pain subscale between the two groups. However, other subscales and WOMAC total scores did not show any significant statistical difference. After three months of treatment, highly significant statistical difference was observed in the pain subscale and significant statistical difference was observed in the stiffness subscale. However, physical activity subscales did not show any significant statistical difference. At the end of six month, highly significant statistical difference was observed in the pain subscale only. Though, stiffness and physical activity subscales did not show any significant statistical difference, the WOMAC total scores reduced significantly in PRP group than HA group.

This supports the findings of other studies that showed PRP having superior results versus HA in the treatment of knee OA. Sanchez et al.29 showed that PRP is better in pain, physical activity and overall WOMAC scores in 5 weeks compared to HA (p=0.010). Spakova et al.24 showed statistically significant better results in the PRP group compared to HA at 3 month follow up periods in WOMAC scores (p<0.01). Kon et al.30 showed that the PRP group showed better results than the HA group at 6 months follow up (p<0.005). Raeissadat et al. reported that at the 12-month follow- up, WOMAC pain score and bodily pain significantly improved in both groups; however, better results were determined in the PRP group compared to the HA group (p<0.001).11

No adverse effect was observed in any group. PRP is prepared from autologous blood, so any concerns of allergic reactions or disease transfer are eliminated. PRP does not promote hyperplasia, carcinogenesis, or tumor growth.31

Conclusion

Findings of the study suggest that the use of autologous PRP and HA are safe and effective methods for treatment of mild to moderate osteoarthritis of the knee. The PRP group had significantly greater reduction in VAS scores at one, three and six months and significantly greater WOMAC physical activity improvement at three and six months compared to the HA group. Multi-centered clinical trial with larger numbers of patients are needed to confirm these findings and to investigate the persistence of the beneficial effects observed.

Acknowledgments

Transfusion medicine department of BSMMU for technical support.

References

  1. Martel-Pelletier J, Boileau C, Pelletier JP, Roughley PJ. Cartilage in normal and osteoarthritis conditions. Best Pract Res Clin rheumato. 2008;22:351-84.
    DOI: 10.1016/j.berh.2008.02.001
  2. Di cesare P, Haudenschild D, Samuels J, Abramson S. Pathogenesis of Osteoarthritis. In: Firestein GS, Budd R, Gabriel SE, McInnes IB, O’Dell JR, editors. Kelley’s Textbook of Rheumatology. 10th ed. Philadelphia: Elsevier Health Sciences; 2017. p.1865.
  3. Neogi T. The epidemiology and impact of pain in osteoarthritis. Osteoarthritis Cartilage. 2013;21:1145-53.
    DOI: 10.1016/j.joca.2013.03.018
  4. Felson DT, Naimark A, Anderson J, Kazis L, Castelli W, Meenan RF. The prevalence of knee osteoarthritis in the elderly. The Framingham Osteoarthritis Study. Arthritis Rheum. 1987;30:914-8.
    DOI: 10.1002/art.1780300811
  5. Peat G, McCarney R, Croft P. Knee pain and osteoarthritis in older adults: a review of community burden and current use of primary health care. Ann Rheum Dis. 2001;60:91-7.
    DOI: 10.1136/ard.60.2.91
  6. Snibbe JC, Gambardella RA. Treatment options for osteoarthritis. Orthopedics. 2005;28:S215-20.
    DOI: 10.3928/0147-7447-20050202-06
  7. Jordan KM, Arden NK, Doherty M, Bannwarth B, Bijlsma JW, Dieppe P, Gunther K, Hauselmann H, Herrero-Beaumont G, Kaklamanis P, Lohmander S. EULAR Recommendations 2003: an evidence based approach to the management of knee osteoarthritis: Report of a Task Force of the Standing Committee for International Clinical Studies Including Therapeutic Trials (ESCISIT). Ann Rheum Dis. 2003;62:1145- 55.
    DOI: 10.1136/ard.2003.011742
  8. Bjordal JM, Ljunggren AE, Klovning A, Slørdal L. Non-steroidal anti-inflammatory drugs, including cyclo-oxygenase-2 inhibitors, in osteoarthritic knee pain: meta-analysis of randomised placebo controlled trials. Bmj. 2004;329:1317.
    DOI: 10.1136/bmj.38273.626655.63
  9. Brown GA. AAOS clinical practice guideline: treatment of osteoarthritis of the knee: evidence-based guideline, 2nd edition. J Am Acad Orthop Surg. 2013;21:577–9.
    DOI: 10.5435/JAAOS-21-09-577
  10. Vincent K, Percival SS, Conrad BP, Seay AN, Montero C, Vincent KR. Hyaluronic acid (HA) viscosupplementation on synovial fluid inflam•mation in knee osteoarthritis: a pilot study. Open Orthop J. 2013;20:378–84.
    DOI: 10.2174/1874325001307010378
  11. Raeissadat SA, Rayegani SM, Hassanabadi H, Fathi M, Ghorbani E, Babaee M, Azma K. Knee osteoarthritis injection choices: hyaluronic acid versus platelet rich plasma. Clin Med Insights Arthritis Musculoskelet Disord. 2015;7:1-8.
    DOI: 10.4137/CMAMD.S17894
  12. Andia I, Abate M. Knee osteoarthritis: hyaluronic acid, platelet-rich plasma or both in association? Expert Opin Biol Ther. 2014;14:635–49.
    DOI: 10.1517/14712598.2014.889677
  13. Moreland LW. Intra-articular hyaluronan (hyaluronic acid) and hylans for the treatment of osteoarthritis: mechanisms of action. Arthritis Res Ther. 2003;5:54–67.
    DOI: 10.1186/ar623
  14. Fam H, Bryant JT, Kontopoulou M. Rheological properties of synovial fluids. Biorheology. 2007:1;44:59-74. Available From: content.iospress.com/articles/biorheology/bir452
  15. Brockmeier SF, Shaffer BS. Viscosupplementation therapy for osteoarthritis. Sports Med Arthrosc Rev. 2006;14:155-62. Available From: journals.lww.com/sportsmedarthro/Abstract/2006/09000/Viscosupplementation_ Therapy_ for_Osteoarthritis.7.aspx [accessed at January 2020]
  16. Axe JM, Snyder-Mackler L, Axe MJ. The role of visco- supplementation. Sports Med Arthrosc Rev. 2013;21:18-22.
    DOI: 10.1097/JSA.0b013e3182673241
  17. DeLong JM, Russell RP, Mazzocca AD. Platelet-rich plasma: the PAW classification system. Arthroscopy. 2012;28:998- 1009.
    DOI: 10.1016/j.arthro.2012.04.148
  18. Mishra A, Pavelko T. Treatment of chronic elbow tendinosis with buffered platelet-rich plasma. Am J Sports Med. 2006;34:1774-8.
    DOI: 10.1177/0363546506288850
  19. Palacio EP, Schiavetti RR, Kanematsu M, Ikeda TM, Mizobuchi RR, Galbiatti JA. Effects of platelet-rich plasma on lateral epicondylitis of the elbow: prospective randomized controlled trial. Revista Brasileira de Ortopedia (English Edition). 2016;51:90-5.
    DOI: 10.1016/j.rboe.2015.03.014
  20. Chiew SK, Ramasamy TS, Amini F. Effectiveness and relevant factors of platelet-rich plasma treatment in managing plantar fasciitis: A systematic review. J Res Med Sci. 2016;21:38.
    DOI: 10.4103/1735-1995.183988
  21. Zhou Y, Wang JH. PRP treatment efficacy for tendinopathy: a review of basic science studies. BioMed Res Int. 2016;2016.
    DOI: 10.1155/2016/9103792
  22. Rabbani MG, Haq SA, Bellamy N, Islam MN, Choudhury MR, Naheed A, Ahmed S, Shahin A. Development, linguistic and clinimetric validation of the WOMAC® VA3. 01 Bangla for Bangladesh Index. Rheumatol Int. 2015;35:997-1003.
    DOI: 10.1007/s00296-014-3192-y
  23. Filardo G, Kon E, Di Martino A, Di Matteo B, Merli ML, Cenacchi A, Fornasari PM, Marcacci M. Platelet-rich plasma vs hyaluronic acid to treat knee degenerative pathology: study design and preliminary results of a randomized controlled trial. BMC musculoskeletal disorders. 2012;13:229. Available From: www.biomedcentral.com/1471-2474/13/229
  24. Spaková T, Rosocha J, Lacko M, Harvanová D, Gharaibeh A. Treatment of Knee Joint Osteoarthritis with Autologous Platelet-Rich Plasma in Comparison with Hyaluronic Acid. Am J Phys Med Rehabil. 2012; 91: 411-7.
    DOI: 10.1097/PHM.0b013e3182aab72
  25. Cole BJ, Karas V, Hussey K, Merkow DB, Pilz K, Fortier LA. Hyaluronic acid versus platelet-rich plasma: a prospective, double-blind randomized controlled trial comparing clinical outcomes and effects on intra-articular biology for the treatment of knee osteoarthritis. Am J Sports Med. 2017;45:339-46.
    DOI: 10.1177/0363546516665809
  26. Anitua E, Andia I, Ardanza B, Nurden P, Nurden AT. Autologous platelets as a source of proteins for healing and tissue regeneration. Thromb Haemost. 2004;91:4-15.
    DOI: 10.1160/TH03-07-0440
  27. Zavan B, Ferroni L, Giorgi C, Calò G, Brun P, Cortivo R, Abatangelo G, Pinton P. Hyaluronic acid induces activation of the ê-opioid receptor. PloS one. 2013;8:e55510.
    DOI: 10.1371/journal.pone.0055510
  28. Lana JF, Weglein A, Sampson SE, Vicente EF, Huber SC, Souza CV, Ambach MA, Vincent H, Urban-Paffaro A, Onodera CM, Annichino-Bizzacchi JM. Randomized controlled trial comparing hyaluronic acid, platelet-rich plasma and the combination of both in the treatment of mild and moderate osteoarthritis of the knee. J Stem Cells Regen Med. 2016;12:69-78.
    PMID: 28096631
  29. Sánchez M, Anitua E, Azofra J, Aguirre JJ, Andia I. Intra- articular injection of an autologous preparation rich in growth factors for the treatment of knee OA: a retrospective cohort study. Clin Exp Rheumatol. 2008;26:910-3. Available From: www.clinexprheumatol.org/article.asp?a=3505
  30. Kon E, Mandelbaum B, Buda R, Filardo G, Delcogliano M, Timoncini A, Fornasari PM, Giannini S, Marcacci M. Platelet- rich plasma intra-articular injection versus hyaluronic acid viscosupplementation as treatments for cartilage pathology: from early degeneration to osteoarthritis. Arthrosc. J. Arthrosc. Relat. Surg. 2011; 27:1490–1501.
    DOI: 10.1016/ j.arthro.2011.05.011
  31. Sampson S, Gerhardt M, Mandelbaum B. Platelet rich plasma injection grafts for musculoskeletal injuries: a review. Curr Rev Musculoskelet Med 2008;1:165-74.
    DOI: 10.1007/s12178-008-9032-5
Correspondence: Farzana Khan Shoma
Department of Physical Medicine and Rehabilitation, Bangabandhu Sheikh Mujib Medical University, Dhaka, Bangladesh
farzanadmck53@gmail.com
ORCID 0000-0002-5355-490X
Download

None


Submission
2020-06-21

Accepted
2021-03-30

Published
2021-04-01


Apply citation style format of Bangladesh Medical Research Council


Issue
Vol 47 No 1 (2021)

Section
Research Articles


Ethical Clearance
Ministry of Science and Technology, Dhaka, Bangladesh.


Financial Support
Ministry of Science and Technology, Dhaka, Bangladesh.


Conflict of Interest
There is no conflict of Interest.


|| An open access, peer-revewed (single-blind) journal of the Bangladesh Medical Research Council ||

ISSN: 2224-7238 (Online) || ISSN: 0377-9238 (Print)