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Orthopedics & Rheumatology

Review Article Volume 5 Issue 6

Radiosynovectomy in Rheumatic Diseases

Margaret Wislowska

Central Clinical Hospital MSW, Poland

Correspondence: Margaret Wislowska, Central Clinical Hospital MSW, ul Wolowska, 137 02-507, Warszawa, Poland, Tel 48-609-458-447

Received: July 20, 2016 | Published: October 4, 2016

Citation: Wislowska M (2016) Radiosynovectomy in Rheumatic Diseases. MOJ Orthop Rheumatol 5(6): 00203. DOI: 10.15406/mojor.2016.05.00203

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Abstract

Radiosynovectomy (RS) is a method of local treatment of chronic inflammatory joint diseases, alternative to surgical synovectomy. This method is based on an anti-proliferative and anti-inflammatory character of ionizing radiation. RS is very successful method in case of inefficiency of standard therapies of chronic inflammatory joint diseases and intra-articular injection of glucocorticoids (GCS). RS for chronic inflammatory joint diseases is an effective treatment. RS causes on synovium function reduction of pain, swelling and improves joint mobility-this effect was confirmed in ultrasonography examinations after procedure.

Keywords: Radiosynovectomy, Chronic inflammatory joint diseases, Rheumatoid arthritis, Pigmented villonodular synovitis, Hemophilic arthropathy, Synovium, Ionizing radiation

Introduction

Radiosynovectomy (RS) is a method of topical treatment of chronic arthritis, using the antiproliferative and anti-inflammatory effects of ionizing radiation. Colloidal particles of the radionuclide are phagocytosed by macrophages of inflamed synovium. Beta radiation emitted by the radiopharmaceutical causes to coagulative necrosis of synoviocytes, which absorbed the drug. After treatment there is a significant reduction of the number and size of the villi of the synovium, and also the reduction of the infiltration of synovial mononuclear cells which caused progressive, persisting fibrosis. RS admits to restore the physiological structure and properties of the synovium. If the therapy was applied early in the disease, it restrains the destruction of joint structures, and allows returning full-function of joints.

The response to treatment is obtained with a delay-usually one month to six months after the procedure and may be preceded by a transient severity of inflammation of the synovium and pain. The reduction of pain usually occurs 1 - 3 weeks after RS, and the possible lack of response to treatment can be determined after 6 weeks. Another unsuccessful application of radioisotope after 6 months indicates the ineffectiveness of this therapy. The beneficial effects of treatment can be long-lasting.

RS has been used in the treatment of patients with chronic inflammatory diseases of the musculoskeletal system such as rheumatoid arthritis, ankylosing spondylitis, psoriatic arthritis, reactive arthritis and arthritis associated with chronic non-specific inflammatory bowel disease, gout, chondrocalcinosis, Lyme disease, Behcet's disease, hemophilic arthropathy, pigmented villonodular synovitis, undifferentiated arthritis, recurrent effusions after total knee replacement and osteoarthritis - mainly knee osteoarthritis and crystal synovitis.1 It is an alternative method to surgical synovectomy and intraarticular injection of GCS. Compared with surgery, RS is a minimally invasive procedure without anesthesia, prolonged immobilization and long rehabilitation. It also requires less financial costs. This is a repeatable procedure and gives long-lasting beneficial effects.2 RS is a promising method for the treatment of rheumatic diseases.

The numerous papers show significant improvement of efficacy of RS.3-10 This method was first used in 1952 in patients with rheumatoid arthritis.11 RS is radionuclide therapy of joint synovitis by intra-articular injection of 90Y silicate / citrate or 186Re sulphide or 169Er citrate1 The indication to the therapy are the findings an increase uptake in the blood pool phase (which is the main sign of arthritis) by two-phase bone scintigraphy using technetium -99m-methylene diphosphonate (99mTc-MDP). The success rate of RS is 65-80%.1

The radiopharmaceuticals used in this method1

90Y emits a beta particle with a maximum energy of 2.27 MeV, with the mean energy of 0.935 MeV and an average soft-tissue range of 3.6 mm. The physical half-life is 2.7 days. 186Re emits a beta particle with a maximum energy of 1.07 MeV, with the mean energy of 0.349 MeV, an average soft-tissue range of 1.1 mm and a 9% abundant gamma emission with a photo peak of 0.137 MeV. The physical half-life is 3.7 days. - 169Er emits a beta particle with a maximum energy of 0.34 MeV, with the mean energy of 0.099 MeV and an average soft-tissue range of 0.3 mm. The physical half-life is 9.4 days.

Contraindications for radiosynovectomy are pregnancy and breastfeeding period, local infection, massive hemarthroses and ruptured Baker's cyst.

Potential complications/side effects after radiosynovectomy are listed below12

  1. Local, acute inflammation of the synovium in the treated joint, induced by the administration of radiocolloid, overlaying the present chronic/subacute inflammation (occurring frequently - in approximately 40-50% of patients - with varying degrees of severity).
  2. Intraarticular bleeding (hemarthrosis, most often in patients with severe hemophilia and inhibitors present).
  3. Contamination of the skin with radiocolloid during removal of the needle puncture (rare).
  4. Radiocolloid leakage outside the joint puncture through a hole in the joint capsule or a ruptured bursa, occurring mostly in case of the rupture of Baker's cysts and potential causing irritation or necrosis of the tissue surrounding.
  5. Skin / joint infection following RS.

The therapy is well-tolerated with a low rate of side effects. In respect of the specific uptake of particles in the synovium and short range of beta radiation, the radiation exposure outside the joint is very low. RS with 90Y and 186Re have been shown to reduce the number of bleeding episodes, relieve articular pain, improve the range of joint flexion and extension, muscle strength in flexion and extension, and normalize the thickness of the synovium in patients with chronic hemophilic synovitis.13 Matryba et al.3 evaluated the effect of RS of RA patients and observed the reduction of swelling and joint pain, which occurred in 43.5% of patients. These therapeutic effects of RS were similar to earlier observations14,15 and the best effects were observed after RS of PIP joints of the fingers - the reduction of swelling occurred in all patients. After RS of knee joints- an improvement was observed in 68.7% of patients.3 This effectiveness is best documented for rheumatoid arthritis and hemophilic arthritis. In another group of patients treated with osteoarthritis, hemophilic arthropathy, undifferentiated arthritis, psoriatic arthritis, the reduction of swelling was observed in 50% of patients, and the reduction of pain in 43.3% of cases3 these results are comparable with the results of the paper of Kroger et al.,4 and other studies in which RS achieved good results in about 40% to 80% of patients.5,6 Jahangier et al.7 Confirmed significant improvement in patients who underwent RS due to psoriatic arthritis and in patients with ankylosing spondylitis Gazda et al.8 Demonstrated significant clinical, biochemical and ultrasound improvement in 66% of children who had undergone RS due to juvenile idiopathic arthritis. In pigmented villonodular synovitis RS is particularly useful as an adjuvant therapy after the surgical/arthroscopic removal of the synovium.9 In the treatment of arthritis resulting from Lyme disease and crystal-induced arthritis RS was also efficient.10

The assessment of a significant efficacy of RS, based on the result of the ultrasound examinations, that determines the severity of synovitis before and after treatment, was confirmed by the existing reports.16-19

Acknowledgment

None.

Conflicts of interest

None.

References

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