Loading

JSM Arthritis

Injections of Leukocyte-Reduced Platelet-Rich Plasma in Partial Tears of the Achilles Tendinopathy: A Report of Six Cases

Case Report | Open Access | Volume 2 | Issue 1

  • 1. Department of Orthopaedic Surgery, The Jikei University School of Medicine, Japan
+ Show More - Show Less
Corresponding Authors
Mamoru Yoshida, Department of Orthopaedic Surgery, The Jikei University School of Medicine,3-25-8, Nishi-Shinbashi, Minato-ku, Tokyo, 105-8461 Japan, Tel: 81334331111; Fax: 81334599114
Abstract

A conservative repair for a partial tear conformed in the tendinopathy-affected tendon is difficult, however, in 6 patients with Achilles tendinopathy the partial tears could be repaired by injections of an autologous leukocyte-reduced platelet-rich plasma (PRP). There were 4 men and 2 women with mean age of 64 years and mean disease duration of 7.3 months. High intensity areas in the Achilles tendons were observed in both short tau inversion recovery (STIR) images and T2* images of a magnetic resonance (MR) analysis. The PRP injections were performed for 1 to 3 times during 3 weeks depending on clinical recovery. All cases returned to sport activities at a previous level as without symptoms and the high intensity areas in MR images disappeared at 3 or 4 months after the PRP therapy. The outcomes indicated that PRP injections led to successful repair of partial tears conformed in the Achilles tendinopathy

Keywords

•    Platelet-rich plasma (PRP)
•    Tendinopathy
•    Partial tear
•    Achilles tendon

Citation

Yoshida M, Marumo K (2017) Injections of Leukocyte-Reduced Platelet-Rich Plasma in Partial Tears of the Achilles Tendinopathy: A Report of Six Cases. JSM Arthritis 2(1): 1021.

INTRODUCTION

Partial tears are sometimes observed in tendons affected with tendinopathy, in which complicating tendon tissue degeneration interferes with conservative repair, successful otherwise after acute fresh injuries. Micro-degenerative damages developed due to tendinopathy might produce a pathologic condition that impedes with the normal reparative reaction within the tendon tissue [1].

In the current decade, a therapy of autologous platelet-rich plasma (PRP) injections has been clinically applied in treatment of Achilles tendinopathy and significant therapeutic effects were showed compared to the conventional therapies [2-6]. We attempted to use PRP injections to conservatively repair partial tears observed as high intensity areas (HIA) in magnetic resonance (MR) images in 6 cases for the Achilles tendinopathy [7,8].

PATIENTS AND METHODS

All 6 patients were diagnosed with Achilles tendinopathy by the criteria applied to the previous study [1-6]. They had not recently had any acute injuries. There were 4 men and 2 women with a mean age of 64 years (43 – 95 years). The mean period from the diagnosis to the commencement of PRP therapy was 7.3 (4 - 12) months (Table 1).

Table 1: Profiles and clinical data of 6 cases.

Case(Years Old)

Gender
(months)

Age
(grade)(mm)

PeriodaSports

Vascularity Tear Size

(width × depth × length)         

Number of injections

1

M

43

12marathon

  III4.5 × 2.1×17.8        

2

 

2

M

53

5 football

III5.1 × 2.8 × 10.2        

2

 

3

M

63

7 tennis

IV4.6× 8.8× 25.1

2

 

4

M

63

4 marathon

IV3.5× 2.3 × 9.2         

3

 

5

F

67

12 dance

  III3.8× 4.7 × 16.7  

1

 

6

F

95

5 bowling

III8.0× 2.1 ×27.4        

1

 

a Period from the diagnosis to the first injection of PRP

All patients resisted against any conventional therapies including an eccentric stretching or the injection of a corticosteroid for more than 4 months before decision to receive the PRP treatment.

Power-Doppler analyses were performed for all Achilles tendons. In each tendon, a grade of vascularization was evaluated according to the vascularization grading system determined by Del Buono (Table 1) [9]. Magnetic resonance examinations were performed with short tau inversion recovery (STIR) or T2* images and sagittal or transverse sections were constructed for all Achilles tendons. In all cases, the HIAs were observed in both STIR images and T2* images. A HIA in a STIR image indicated a fluid accumulation or inflammation, and a HIA in T2* image indicated a tendon degeneration or fluid accumulation. The borders of HIAs were easily determined in all cases. In our previous studies we have confirmed that HIAs in both STIR images and T2* images reflect partial tears associated with degeneration by comparison of those MR findings with directly inspected tendons during surgery for tendon repairs (Figure 1).

 MR images and a photo of the Achilles tendon in a case, in which  partial tear was surgically repaired. A. A sagittal section, STIR image; B. A  transverse section, STIR image; C. A sagittal section, T2* image; D. A transverse  section, T2* image; E. A photo of the Achilles tendon at surgery. A partial tear  associated with degenerative tissue was observed at the posterior side of the  tendon

Figure 1 MR images and a photo of the Achilles tendon in a case, in which partial tear was surgically repaired. A. A sagittal section, STIR image; B. A transverse section, STIR image; C. A sagittal section, T2* image; D. A transverse section, T2* image; E. A photo of the Achilles tendon at surgery. A partial tear associated with degenerative tissue was observed at the posterior side of the tendon

Therefore, the HIAs in 6 patients from the present study were considered partial tears associated with tendon degeneration. However, detection of partial tears by ultrasonography was rather difficult. Each tear sizes (width, depth or length) were measured in sagittal or transverse sections on STIR images. The mean volume of tears was calculated as 360.5 (74.1 - 1016.1) mm³ .

A 3.0 mL of an autologous leukocyte-reduced PRP was obtained from 20 mL of the whole blood by using the preparation kit (MyCells, Kaylight, Tel Aviv, Israel), accordingly with the manufacturer’s instructions. We obtained an autologous PRP at the mean platelets concentration of 8.8×105 / μL containing leukocytes at the mean concentration of 3.1×103 cells / μL and no erythrocytes. An obtained PRP sample was classified as type 3 according to the Mishra’s classification and as pure PRP in PAW classification since we did not activate PRP before injection.

A point of tenderness at the Achilles tendon was determined and marked. Then, the surface of the skin at the marked region was sterilized with a 10 % povidone-iodine solution and a PRP was slowly and gently injected into or around the tendon by using a 30 G needle via the peppering technique with the patient in prone position without previous anesthesia. An ankle was immobilized with the cast under non-weight bearing conditions for one week. After the cast was removed, ROM exercises were started and a weight bearing was gradually introduced. At 3 weeks after the injections, a total weight bearing was permitted and an efficacy of the PRP therapy was evaluated by clinical examinations. A grade of a pain was recorded with using the visual analog scale (VAS). When the observed effect was not satisfactory, second PRP injections was carried out in the same manner followed by bandaging or brace treatment under total weight bearing conditions. After three weeks, a clinical examination was carried out and the treatment efficacy was evaluated. If the progress in pain reduction stopped and plateaued, an another injection of PRP was administered in the same manner. The mean number of the injections was 1.8. Following the last injection, clinical follow-up was carried out for 12 - 24 months in all cases.

RESULTS

A pain was almost disappeared in all six cases and the final mean value of the VAS was 0.25 (0.0~0.5). All six patients returned to their sport activities as during previous levels with no symptoms. The vascularity grade declined to grade I or grade II. Magnetic resonance images showed that the initially observed HIAs disappeared on STIR images in all cases. The MR images of cases 3 - 5 are shown in (Figures 2- 4).

 MR images of Case 3. A. A sagittal section, STIR image; B. A transverse  section, STIR image; C. A sagittal section, T2* image; D. A transverse section,  T2* image. The high intensity area observed in the Achilles tendon; E. A sagittal  section, STIR image after PRP therapy; F. A transverse section, STIR image after  PRP therapy. The high intensity area on STIR images disappeared after PRP  therapy.

Figure 2 MR images of Case 3. A. A sagittal section, STIR image; B. A transverse section, STIR image; C. A sagittal section, T2* image; D. A transverse section, T2* image. The high intensity area observed in the Achilles tendon; E. A sagittal section, STIR image after PRP therapy; F. A transverse section, STIR image after PRP therapy. The high intensity area on STIR images disappeared after PRP therapy.

MR images of Case 4. A. A sagittal section, STIR image; B. A transverse  section, STIR image; C. A sagittal section, T2* image; D. A transverse section,  T2* image. The high intensity area observed in the Achilles tendon; E. A sagittal  section, STIR image after PRP therapy; F. A transverse section, STIR image after  PRP therapy. The high intensity area on STIR images disappeared after PRP  therapy. A

Figure 3 MR images of Case 4. A. A sagittal section, STIR image; B. A transverse section, STIR image; C. A sagittal section, T2* image; D. A transverse section, T2* image. The high intensity area observed in the Achilles tendon; E. A sagittal section, STIR image after PRP therapy; F. A transverse section, STIR image after PRP therapy. The high intensity area on STIR images disappeared after PRP therapy. A

 MR images of Case 5. A. A sagittal section, STIR image; B. A transverse  section, STIR image; C. A sagittal section, T2* image; D. A transverse section,  T2* image. The high intensity area observed in the Achilles tendon; E. A sagittal  section, STIR image after PRP therapy; F. A transverse section, STIR image after  PRP therapy. The high intensity area on STIR images disappeared after PRP  therapy

Figure 4 MR images of Case 5. A. A sagittal section, STIR image; B. A transverse section, STIR image; C. A sagittal section, T2* image; D. A transverse section, T2* image. The high intensity area observed in the Achilles tendon; E. A sagittal section, STIR image after PRP therapy; F. A transverse section, STIR image after PRP therapy. The high intensity area on STIR images disappeared after PRP therapy

 

DISCUSSION

It has been challenging to conservatively repair partial tears in tendinopathy-affected tendons comparing to those following acute fresh injuries. Hence, partial tears have generally been repaired surgically: the degenerative tissue was resected and the partial tear sutured [1]. There were few reports that partial tears caused by tendinopathy might be conservatively repaired with PRP therapy, although most orthopedic surgeons have considered the PRP therapy efficient in treatment of tendinopathy [2-6]. In the present study, we report that high intensity areas observed in STIR MR images disappeared after application of the PRP therapy, indicating that PRP injections facilitated conservative repair of partial tears conformed in tendinopathy-affected Achilles tendons. However, we still do not know how large a partial tear could be to allow for successful repair with the PRP therapy. In our series, we demonstrated that the repair was possible with a tear having maximum volume of approximately 1000 mm3 . When the width of the tear was 5 mm and the depth 4 mm (approximate mean sizes of the tears in the present study), the length would be 50 mm with the volume of 1000 mm3 . Further investigations are necessary to elucidate the effects of partial tear volume or size on limitations of the PRP therapy.

REFERENCES

1. Kaux JF, Forthomme B, Le Goff C, Crielaard JM, Croisier JL. Current Opinions on Tendinopathy. J Sports Sci Med. 2011; 10: 238-253.

2. Murawski CD, Smyth NA, Newman H, Kennedy JG. A single platelet-rich plasma injection for chronic midsubstance achilles tendinopathy: a retrospective preliminary analysis. Foot Ankle Spec. 2014; 7: 372- 376.

3. Filardo G, Kon E, Di Matteo B, Alessandro Di Martino, Giulia Tesei, Patrizia Pelotti, et al. Platelet-rich plasma injections for the treatment of refractory Achilles tendinopathy: results at 4 years. Blood Transfus. 2014; 12: 533-540.

4. Dallaudière B, Pesquer L, Meyer P, Silvestre A, Perozziello A, Peuchant A, et al. Intratendinous injection of platelet-rich plasma under US guidance to treat tendinopathy: a long-term pilot study. J Vasc Interv Radiol. 2014; 25: 717-723.

5. Guelfi M, Pantalone A, Vanni D, Abate M, Guelfi MG, Salini V. Long-term beneficial effects of platelet-rich plasma for non-insertional Achilles tendinopathy. Foot Ankle Surg. 2015; 21: 178-181.

6. de Jones S, de Vos RJ, Weir A, Hans T M van Schie , Sita M A , et al. One-year follow-up of platelet-rich plasma treatment in chronic Achilles tendinopathy: A double-blind randomized placebo-controlled trial. Am J Sports Med. 2011; 39: 1623-1629.

7. Yoshida M, Marumo K. An autologous platelet-rich plasma therapy against 4 cases for tendinopathy accompanied with partial tendon tears. Japanese Journal of Orthopaedic Sports Medicine. 2016; 36: 91- 95.

8. Yoshida M, Marumo K. Clinical outcomes of an autologous platelet-rich plasma therapy for Achilles tendinopathy. Japanese Journal of Orthopaedic Sports Medicine. 2016(in press). 9. Del Buono A, Chan O, Maffulli N. Achilles tendon: functional anatomy and novel emerging models of imaging classification. Int Orthop. 2013; 37: 715-721

Yoshida M, Marumo K (2017) Injections of Leukocyte-Reduced Platelet-Rich Plasma in Partial Tears of the Achilles Tendinopathy: A Report of Six Cases. JSM Arthritis 2(1): 1021.

Received : 22 Mar 2017
Accepted : 08 Apr 2017
Published : 11 Apr 2017
Journals
Annals of Otolaryngology and Rhinology
ISSN : 2379-948X
Launched : 2014
JSM Schizophrenia
Launched : 2016
Journal of Nausea
Launched : 2020
JSM Internal Medicine
Launched : 2016
JSM Hepatitis
Launched : 2016
JSM Oro Facial Surgeries
ISSN : 2578-3211
Launched : 2016
Journal of Human Nutrition and Food Science
ISSN : 2333-6706
Launched : 2013
JSM Regenerative Medicine and Bioengineering
ISSN : 2379-0490
Launched : 2013
JSM Spine
ISSN : 2578-3181
Launched : 2016
Archives of Palliative Care
ISSN : 2573-1165
Launched : 2016
JSM Nutritional Disorders
ISSN : 2578-3203
Launched : 2017
Annals of Neurodegenerative Disorders
ISSN : 2476-2032
Launched : 2016
Journal of Fever
ISSN : 2641-7782
Launched : 2017
JSM Bone Marrow Research
ISSN : 2578-3351
Launched : 2016
JSM Mathematics and Statistics
ISSN : 2578-3173
Launched : 2014
Journal of Autoimmunity and Research
ISSN : 2573-1173
Launched : 2014
JSM Head and Neck Cancer-Cases and Reviews
ISSN : 2573-1610
Launched : 2016
JSM General Surgery Cases and Images
ISSN : 2573-1564
Launched : 2016
JSM Anatomy and Physiology
ISSN : 2573-1262
Launched : 2016
JSM Dental Surgery
ISSN : 2573-1548
Launched : 2016
Annals of Emergency Surgery
ISSN : 2573-1017
Launched : 2016
Annals of Mens Health and Wellness
ISSN : 2641-7707
Launched : 2017
Journal of Preventive Medicine and Health Care
ISSN : 2576-0084
Launched : 2018
Journal of Chronic Diseases and Management
ISSN : 2573-1300
Launched : 2016
Annals of Vaccines and Immunization
ISSN : 2378-9379
Launched : 2014
JSM Heart Surgery Cases and Images
ISSN : 2578-3157
Launched : 2016
Annals of Reproductive Medicine and Treatment
ISSN : 2573-1092
Launched : 2016
JSM Brain Science
ISSN : 2573-1289
Launched : 2016
JSM Biomarkers
ISSN : 2578-3815
Launched : 2014
JSM Biology
ISSN : 2475-9392
Launched : 2016
Archives of Stem Cell and Research
ISSN : 2578-3580
Launched : 2014
Annals of Clinical and Medical Microbiology
ISSN : 2578-3629
Launched : 2014
JSM Pediatric Surgery
ISSN : 2578-3149
Launched : 2017
Journal of Memory Disorder and Rehabilitation
ISSN : 2578-319X
Launched : 2016
JSM Tropical Medicine and Research
ISSN : 2578-3165
Launched : 2016
JSM Head and Face Medicine
ISSN : 2578-3793
Launched : 2016
JSM Cardiothoracic Surgery
ISSN : 2573-1297
Launched : 2016
JSM Bone and Joint Diseases
ISSN : 2578-3351
Launched : 2017
JSM Bioavailability and Bioequivalence
ISSN : 2641-7812
Launched : 2017
JSM Atherosclerosis
ISSN : 2573-1270
Launched : 2016
Journal of Genitourinary Disorders
ISSN : 2641-7790
Launched : 2017
Journal of Fractures and Sprains
ISSN : 2578-3831
Launched : 2016
Journal of Autism and Epilepsy
ISSN : 2641-7774
Launched : 2016
Annals of Marine Biology and Research
ISSN : 2573-105X
Launched : 2014
JSM Health Education & Primary Health Care
ISSN : 2578-3777
Launched : 2016
JSM Communication Disorders
ISSN : 2578-3807
Launched : 2016
Annals of Musculoskeletal Disorders
ISSN : 2578-3599
Launched : 2016
Annals of Virology and Research
ISSN : 2573-1122
Launched : 2014
JSM Renal Medicine
ISSN : 2573-1637
Launched : 2016
Journal of Muscle Health
ISSN : 2578-3823
Launched : 2016
JSM Genetics and Genomics
ISSN : 2334-1823
Launched : 2013
JSM Anxiety and Depression
ISSN : 2475-9139
Launched : 2016
Clinical Journal of Heart Diseases
ISSN : 2641-7766
Launched : 2016
Annals of Medicinal Chemistry and Research
ISSN : 2378-9336
Launched : 2014
JSM Pain and Management
ISSN : 2578-3378
Launched : 2016
JSM Women's Health
ISSN : 2578-3696
Launched : 2016
Clinical Research in HIV or AIDS
ISSN : 2374-0094
Launched : 2013
Journal of Endocrinology, Diabetes and Obesity
ISSN : 2333-6692
Launched : 2013
Journal of Substance Abuse and Alcoholism
ISSN : 2373-9363
Launched : 2013
JSM Neurosurgery and Spine
ISSN : 2373-9479
Launched : 2013
Journal of Liver and Clinical Research
ISSN : 2379-0830
Launched : 2014
Journal of Drug Design and Research
ISSN : 2379-089X
Launched : 2014
JSM Clinical Oncology and Research
ISSN : 2373-938X
Launched : 2013
JSM Bioinformatics, Genomics and Proteomics
ISSN : 2576-1102
Launched : 2014
JSM Chemistry
ISSN : 2334-1831
Launched : 2013
Journal of Trauma and Care
ISSN : 2573-1246
Launched : 2014
JSM Surgical Oncology and Research
ISSN : 2578-3688
Launched : 2016
Annals of Food Processing and Preservation
ISSN : 2573-1033
Launched : 2016
Journal of Radiology and Radiation Therapy
ISSN : 2333-7095
Launched : 2013
JSM Physical Medicine and Rehabilitation
ISSN : 2578-3572
Launched : 2016
Annals of Clinical Pathology
ISSN : 2373-9282
Launched : 2013
Annals of Cardiovascular Diseases
ISSN : 2641-7731
Launched : 2016
Journal of Behavior
ISSN : 2576-0076
Launched : 2016
Annals of Clinical and Experimental Metabolism
ISSN : 2572-2492
Launched : 2016
Clinical Research in Infectious Diseases
ISSN : 2379-0636
Launched : 2013
JSM Microbiology
ISSN : 2333-6455
Launched : 2013
Journal of Urology and Research
ISSN : 2379-951X
Launched : 2014
Journal of Family Medicine and Community Health
ISSN : 2379-0547
Launched : 2013
Annals of Pregnancy and Care
ISSN : 2578-336X
Launched : 2017
JSM Cell and Developmental Biology
ISSN : 2379-061X
Launched : 2013
Annals of Aquaculture and Research
ISSN : 2379-0881
Launched : 2014
Clinical Research in Pulmonology
ISSN : 2333-6625
Launched : 2013
Journal of Immunology and Clinical Research
ISSN : 2333-6714
Launched : 2013
Annals of Forensic Research and Analysis
ISSN : 2378-9476
Launched : 2014
JSM Biochemistry and Molecular Biology
ISSN : 2333-7109
Launched : 2013
Annals of Breast Cancer Research
ISSN : 2641-7685
Launched : 2016
Annals of Gerontology and Geriatric Research
ISSN : 2378-9409
Launched : 2014
Journal of Sleep Medicine and Disorders
ISSN : 2379-0822
Launched : 2014
JSM Burns and Trauma
ISSN : 2475-9406
Launched : 2016
Chemical Engineering and Process Techniques
ISSN : 2333-6633
Launched : 2013
Annals of Clinical Cytology and Pathology
ISSN : 2475-9430
Launched : 2014
JSM Allergy and Asthma
ISSN : 2573-1254
Launched : 2016
Journal of Neurological Disorders and Stroke
ISSN : 2334-2307
Launched : 2013
Annals of Sports Medicine and Research
ISSN : 2379-0571
Launched : 2014
JSM Sexual Medicine
ISSN : 2578-3718
Launched : 2016
Annals of Vascular Medicine and Research
ISSN : 2378-9344
Launched : 2014
JSM Biotechnology and Biomedical Engineering
ISSN : 2333-7117
Launched : 2013
Journal of Hematology and Transfusion
ISSN : 2333-6684
Launched : 2013
JSM Environmental Science and Ecology
ISSN : 2333-7141
Launched : 2013
Journal of Cardiology and Clinical Research
ISSN : 2333-6676
Launched : 2013
JSM Nanotechnology and Nanomedicine
ISSN : 2334-1815
Launched : 2013
Journal of Ear, Nose and Throat Disorders
ISSN : 2475-9473
Launched : 2016
JSM Ophthalmology
ISSN : 2333-6447
Launched : 2013
Journal of Pharmacology and Clinical Toxicology
ISSN : 2333-7079
Launched : 2013
Annals of Psychiatry and Mental Health
ISSN : 2374-0124
Launched : 2013
Medical Journal of Obstetrics and Gynecology
ISSN : 2333-6439
Launched : 2013
Annals of Pediatrics and Child Health
ISSN : 2373-9312
Launched : 2013
JSM Clinical Pharmaceutics
ISSN : 2379-9498
Launched : 2014
JSM Foot and Ankle
ISSN : 2475-9112
Launched : 2016
JSM Alzheimer's Disease and Related Dementia
ISSN : 2378-9565
Launched : 2014
Journal of Addiction Medicine and Therapy
ISSN : 2333-665X
Launched : 2013
Journal of Veterinary Medicine and Research
ISSN : 2378-931X
Launched : 2013
Annals of Public Health and Research
ISSN : 2378-9328
Launched : 2014
Annals of Orthopedics and Rheumatology
ISSN : 2373-9290
Launched : 2013
Journal of Clinical Nephrology and Research
ISSN : 2379-0652
Launched : 2014
Annals of Community Medicine and Practice
ISSN : 2475-9465
Launched : 2014
Annals of Biometrics and Biostatistics
ISSN : 2374-0116
Launched : 2013
JSM Clinical Case Reports
ISSN : 2373-9819
Launched : 2013
Journal of Cancer Biology and Research
ISSN : 2373-9436
Launched : 2013
Journal of Surgery and Transplantation Science
ISSN : 2379-0911
Launched : 2013
Journal of Dermatology and Clinical Research
ISSN : 2373-9371
Launched : 2013
JSM Gastroenterology and Hepatology
ISSN : 2373-9487
Launched : 2013
Annals of Nursing and Practice
ISSN : 2379-9501
Launched : 2014
JSM Dentistry
ISSN : 2333-7133
Launched : 2013
Author Information X