Clinical evaluation of intra-articular injection of Tin-117m | VMRR – Dove Medical Press

Introduction

Canine elbow osteoarthritis (OA) is a common sequela from elbow dysplasia.1 Elbow OA is a progressive joint disease characterized by decreased joint range of motion, pain, cartilage destruction, and osteophyte formation.1,2 Treatment is mainly palliative and current strategies often consist of medical management including NSAIDs, analgesics, nutraceuticals, weight control, physical rehabilitation, and changes in activity level.13 Although daily use of NSAIDs may reduce OA pain, these agents have the potential to cause or exacerbate renal, gastrointestinal, and hepatobiliary disorders.4 In addition, it may not be practical for some owners to administer daily medications. Surgery often fails to prevent progression of OA and may not provide superior outcomes to medical management.5,6 Salvage procedures such as elbow replacement have inconsistent outcomes and a high complication rate.1,7,8

Nonsurgical management will likely remain a viable treatment option for dogs with elbow OA; therefore, optimization of current nonsurgical options and development of new innovative nonsurgical treatments are important. The use of intra-articular (IA) injections including platelet-rich plasma, dextrose prolotherapy, autologous protein solution, or stem cells has been reported for OA treatment with mixed results.912 Larger clinical studies are needed to fully understand the effects of these therapies on dogs with OA.

Synovitis precedes development of radiographic OA changes in humans and dogs.2,13,14 It is characterized by marked hyperplasia and permeability of the synovial lining, overexpression of proinflammatory cytokines, infiltration of inflammatory cells, production of degradative enzymes, and synovial neovascularization and proliferation.15 Inflammation sensitizes peripheral neurons in synovial tissue, resulting in joint pain.16 Marked synovitis precedes structural changes in the progression of OA and early intervention targeting joint inflammation, prior to radiographic changes, can delay or prevent chronic arthritic changes.15 Low-dose radiation therapy has direct anti-inflammatory effects on the synovium.17 A small study of 5 dogs with elbow OA concluded that use of single-low-dose radiotherapy may have short-term clinical benefits.18

As synovitis is strongly implicated in OA pathogenesis, surgical and nonsurgical synovectomy (synoviorthesis) have been used to alleviate human synovitis symptoms.19 Another reported method to relieve synovitis is via radiosynoviorthesis (RSO), which involves IA injection of low-energy ionizing radiation to induce apoptosis and ablate inflamed synovial cells.20 Use of this therapy has been reported in humans to treat synovitis in an effort to prevent, delay, or limit arthritic changes.20 Radiosynoviorthesis, primarily involving yttrium-90 (90Y), erbium-169 (169Er), and rhenium-186 (186Re), is an accepted outpatient therapy for treatment of early-stage chronic synovitis in humans with rheumatoid arthritis, psoriatic arthritis, hemophilic arthritis or OA.20,21 The success rate of RSO reported by Zuderman et al was 89% for rheumatoid arthritis and 79% for OA in humans.22 Tin 117m (117mSn) homogeneous colloid was specifically developed to avoid the serious outcomes following treatment with high-energy beta emitters.23 Tin 117m colloid is a non-beta emitter with lower energy from which the conversion electrons have a therapeutic distance of activity of only 300 microns (0.3 mm).

Despite its many advantages, RSO is seldom performed in veterinary medicine, with limited reports including use of 177lutetium-labeled zirconia in dogs and 117mSn homogeneous colloid in rats.2426 In a recent prospective safety study of 5 dogs, blood, urine, feces, and organ scintigraphy counts showed that >99% of 117mSn activity was retained in the elbow joint for approximately 67 weeks.23 There were no adverse effects, and post-mortem evaluation revealed no joint damage. These findings, combined with the potential for protracted clinical improvement after a single IA injection, justify further evaluation of 117mSn for the management of canine OA. The authors designed the current study to assess the value of IA 117mSn for pain management in dogs with naturally occurring elbow OA. Specifically, the authors aimed to quantify changes in peak vertical force (PVF) from force plate gait analysis as the primary outcome measure and canine brief pain inventory (CBPI) scores and elbow goniometry as secondary outcome measures, at multiple time-points for one year after a single unilateral IA injection of 117mSn in dogs with grade 1 or 2 elbow OA. By limiting the study to unilateral elbow injection, the opposite leg is a source of comparison data. The hypothesis was that IA 117mSn-colloid treatment is associated with clinically relevant beneficial effects in dogs with elbow OA.

The study was designed as a long-term longitudinal and prospective study using serial measurements in dogs. The study protocol was approved by the Institutional Animal Care and Use Committee and informed client consent was obtained prior to study enrollment.

A convenience sample of 23 dogs was used in this study. No sample size calculation was performed. Dogs were eligible if they were, 8kg, at least 1 year of age, had a visible forelimb lameness or pain localizable to one or both elbows, had radiographic evidence of grade 1 or 2 OA in one or both elbows based on international elbow working group (IEWG) classification,27 had no clinically detectable abnormalities including pain in any other joint in the forelimbs, had no comorbid condition likely to preclude a 1-year survival, and had no surgical procedure on any leg in the past 4 months or received any joint injections previously. Elbow OA grading was performed by a single board-certified radiologist. All images were calibrated, and osteophyte size was prioritized over trabecular pattern. Dogs with orthopedic disease affecting either hind limb were considered eligible as long as there was no visible lameness present in any of the hind limbs. Dogs being treated with nutraceuticals and/or medications such as NSAIDs were eligible provided they still had lameness or pain localizable to one or both elbow/s.

Initially, information was collected from dog owners including signalment, duration of OA, and type and duration of current medications/supplements. Owners also completed the CBPI.28,29 After meeting initial evaluation requirements, all dogs received a baseline assessment within 30 days of treatment prior to study participation. Dogs had a physical examination, and the following variables were obtained: CBC, serum biochemistry, urinalysis (UA), bilateral elbow radiographs, bilateral elbow goniometry and PVF using force plate gait analysis. These parameters were also collected post-treatment at 1, 3, 6, 9, and 12 months. Bilateral elbow radiographs were performed at the 12-month follow-up exam. Treatment included a unilateral IA injection of 117mSn in the elbow that was determined to be the source of observable lameness or was more painful when observable lameness was not noted. Dogs were randomly assigned to one of the three 117mSn dose groups (normalized based on body surface area, Supplementary Table 1): low dose (LD): 1.0 mCi (millicuries) or 37 MBq (MegaBequerel), medium dose (MD): 1.75mCi or 64.75 MBq and high dose (HD): 2.5mCi or 92.5 MBq, using a computer-generated randomized table. Observers and owners were masked to the dose group except the radiologist who injected the colloid.

Both sites used the same model force-plate (OR6-WP-1000, Advanced Medical Technology Inc, Newton, MA) and commercially available force-plate analysis software. Data logging (100Hz, Acquire version 7.3, Sharon Software Inc, Dewitt, MI) was triggered by a force of 5N on the force plate. Five successful trials at a velocity of 1.52.5m/sec and acceleration of 0.9 to 0.9m/sec2 were recorded for each leg. Dogs were acclimated and trained to walk across the force plate during the pretreatment gait trial. Trained handlers walked the dogs for all testing. PVF (N/kg) was recorded and normalized to body weight and the mean value of five trials was used for statistical analyses. Body weight distribution % (BW-D%) between the forelimbs was calculated according to the formula: BW-D% = PVFT/(PVFUT + PVFT) 100%, where PVFT = mean PVF of the treated leg, and PVFUT = mean PVF of the contralateral untreated leg.

A positive response was defined as 5% increase in mean PVF at a single time point in the treated leg2934 at months 1, 3, 6, 9, and/or 12 compared with baseline (0 month) for each individual dog evaluated on the force plate.

Owners completed the CBPI28,35 scores at initial evaluation and then monthly from 1 through 12 months except for the 2nd month post treatment. The same individual was required to complete the survey each time. Owners did not have access to their previous scores at each follow-up visit.

A single boarded surgeon from each site performed a physical/orthopedic examination. Elbow goniometry was performed using a standard two-arm plastic goniometer as previously described.36

Dogs were anesthetized, positioned in dorsal recumbency, and the medial aspect of the elbow to be injected was aseptically prepped. The homogeneous 117mSn-colloid (Synovetin OA, Exubrion Therapeutics, Buford, GA) was injected into the joint as previously described.23 After completion of the injection, dogs were recovered from anesthesia and discharged the following morning. Instructions for care and handling with regards to the radioisotope were provided to the owners. All disposables coming in contact with 117Sn were disposed of following all State Regulatory Commission guidelines. Tin 117m is a non-beta emitter in which radiation burns do not occur. The low-energy characteristics of the therapeutic conversion electrons are very different from the higher energy beta emitters (90Y, 169Er, 186Re) commonly used in human RSO.20 As mentioned, elbow injection doses of Tin 117m were based on a chart based on body surface area (Supplementary Table 1) to allow clinicians to adhere to the ALARA (as low as reasonably achievable) principle. Previous studies in both laboratory rats and dogs in which histologic sections were obtained have shown that even with higher doses of homogeneous Tin 117m colloid, beta burns did not occur.23,25 Standard industry precautions were taken when handling homogeneous tin colloid as with any unsealed radiation source as prescribed by the Nuclear Regulatory Commission.

Data analyses were performed using JMP Pro 15.0 (SAS Institute Inc., Cary, NC). All continuous parameters were presented as mean SD and assessed with a repeated measure ANOVA with a mixed effect model was used with time as the fixed effect and each dog as the random effects with the variance compounds covariance structure within each dose group and within treated or untreated elbow. Kenward-Roger approximation was used to determine the degrees of freedom in the model. A contrast hypothesis was performed at each time point against baseline. Assumptions of these models (linearity, normality of residuals, and homoscedasticity of residuals) and influential data points were assessed by examining standardized residual and quantile plots, and the normality of residual was confirmed with the ShapiroWilk test. Ordinal subjective variables at each time point were presented as median (range). Due to small sample size, the data was combined and compared with baseline and untreated elbow using a Wilcoxon signed-rank test. The outcomes of positive response among 3 groups were evaluated with Fishers exact test. Significance was set at P <0.05.

Demographic characteristics of the study population are shown in Table 1. One dog in the LD-group received a much lower dose, about 40% lower than the prescribed dose of 117mSn-colloid, so that dog was excluded from the study. Another dog (female intact) from the HD-group was excluded because the owner reported the dog had rough play with two other large housemate dogs and was very sore in the front limbs especially on the treated limb at the one-month recheck and the same dog was bred later during the three-month recheck. The exclusion of these 2 dogs resulted in a total of 21 dogs in our study population. Duration of arthritis and type of medical management are shown in Supplementary Table 2. All dogs had visible unilateral lameness except 3 dogs (2 had bilateral grade 1 OA and 3rd one had bilateral grade 2 OA). No adverse effects were observed on physical/orthopedic examination or reported by owners, and no clinically significant laboratory findings were noted related to the IA injection of 117mSn at regularly scheduled re-evaluations.

Table 1 Demographic Characteristics for 21 Dogs with Naturally Occurring Elbow OA Based on 117mSn Dose Group

Both PSS and PIS significantly improved at all time-points except for the 10-month (PSS) and the 10- and 11-month (PIS) (Table 2) scores compared to baseline. No significant differences were noted in QoL scores.

Table 2 Canine Brief Pain Inventory (CBPI) Scores for 21 Dogs with Elbow OA at Pretreatment and at Each Time-Point Post Treatment. Values are Presented as Median (Range)

In the HD group for elbow extension there was a trend in improvement (approaching significance) in the treated leg at 6, and 9 months, respectively, compared to baseline (Table 3). Elbow extension also increased in the untreated leg at 9-month in the HD group and at 6-month in the MD group. In 1 dog from the MD-group, baseline force-plate data for the treated leg was missing and this dog died secondary to GDV after its 3-month evaluation. In 1 dog from the LD-group, five successful repeatable trials during force-plate data collection could not be obtained at the baseline evaluation. These 2 dogs were not included in the force plate data analysis. This resulted in a total of 19 dogs for force plate data analysis. The mean peak vertical force improved in the treated leg in the HD group by 5.4%, 12.0%, 10.1% and 12.3% at 1, 3, 6, and 9 months, respectively, compared to baseline. This increase was statistically significant at the 3- and 9-month time points. The mean PVF was significantly lower (by 9%) in the untreated leg at the12-month time point compared to baseline (Table 4). In the HD group, the mean BW-D% for the treated leg improved compared to baseline and this improvement approached significance at 3- and 9-month time points (Table 4).

Table 3 Evolution of Elbow Extension, Flexion and Range of Motion from Baseline to Month-12 in Treated and Untreated Elbows in 21 Dogs with Elbow OA for All Three 117mSn Dose Groups. The Means of Three Values for Elbow Extension and Flexion Were Recorded Bilaterally. The Data is Summarized as Mean Standard Deviation (SD)

Table 4 Evolution of PVF and BW-D% from Baseline to Month-12 in Nineteen Dogs with Elbow OA for All Three 117Sn Dose Groups. The Data is Summarized as Mean Standard Deviation (SD)

Based on the criteria mentioned above for a positive response, 17 of 19 dogs (89.5%) had a positive response (Table 5). There was no significant difference between the three dose groups for positive responses.

Table 5 Dog Number, 117mSn Dose Group, and Treatment Outcome in 19 Dogs Undergoing Force-Plate Analysis

The radiographic OA scores significantly increased both in treated elbows and untreated elbows at 12-month recheck compared to pretreatment scores (Table 6). There was no significant difference in OA score change from baseline between treated and untreated elbows at the time of the 12-month evaluation for all dose groups (Table 6).

Table 6 Radiographic OA Scores for Treated and Untreated Elbows for Study Dogs with Elbow OA at Pretreatment and at 12-Month Recheck. The 12-Month Radiographs Were Available for 18 Dogs

The ability to use RSO as a localized treatment with lasting results and no systemic adverse effects could make it a valuable therapeutic option for veterinary patients with OA. In our study, the use of IA 117mSn in dogs with elbow OA resulted in clinically relevant beneficial effects lasting for up to 9 months-based on force plate data with statistically significant improvement at 3 and 9 months post-injection and trending towards improvement (approaching significance) at 6 months post injection. The beneficial effects lasted for 1-year post injection based on CBPI data. This duration of RSO response is similar to what has been reported in humans where the response can last for a few months to several years.17

Radiosynoviorthesis (RSO) has been successfully used in human medicine for more than 60 years in many countries, particularly in Europe where it was first described and where its use conforms to guidelines published by the European Association of Nuclear Medicine.22,3739 RSO has been an accepted outpatient therapy for treatment of early stage chronic synovitis in rheumatoid arthritis, psoriatic arthritis, hemophilic arthritis and OA patients for decades.3941 Current standards in human clinical practice generally take a conservative approach by recommending initial treatment with front-line therapies including systemic NSAIDs, glucocorticoids, and local joint therapies such as corticosteroid and hyaluronic acid injections prior to RSO.37 However, in patients that either respond poorly or have adverse side effects following these traditional therapies, RSO is a useful option that should now be considered in veterinary medicine. Traditional veterinary arthritis therapies when successful are oftentimes less costly than RSO using homogeneous tin colloid (117mSn). It can become costly when these initial traditional therapies cannot successfully manage elbow osteoarthritis and alternatives such as stem cell or platelet-rich plasma therapies are considered. The treatment in our study was evaluated specifically to manage canine arthritic elbows because oftentimes traditional veterinary arthritis therapies are not successful in dogs with elbow OA.1,2,4,912

The patients in this study were treated with homogeneous tin colloid (117mSn) containing microparticles (diameter 1.5 to 20.0 microns) of the radioisotope tin 117m (117mSn). These microparticles when injected into a joint are engulfed by intra-articular macrophages, which are killed by apoptosis due to the tin 117m conversion electron (CE) radiation.41 Admittedly, we had limited short-term evaluation for any adverse effects related to 117mSn injection. The absence of any adverse effects in the present study and in a previous experimental study, is most likely due to unique characteristics of 117mSn.23,25,26 Tin 117m emits abundant conversion electrons, low-energy particles with a short, non-diminishing penetration range of approximately 300m in tissue. Other radionuclides that emit beta particles result in variable tissue penetration and can result in damaging irradiation of adjacent non-target tissues.20 117mSn has a life of nearly 14 days, providing an ideal duration of effect spanning several lives to achieve therapeutic results and to enable short-term stability during storage and handling. Studies in rats and colony bred dogs have confirmed the safety of structures within the joint (cartilage, bone) and adnexal structures following IA injection with homogeneous tin colloid (117mSn).23,26 In addition to conversion electrons, 117mSn emits radiation, which is non-therapeutic but readily detectable by scintigraphy. In humans, the risk of infection after IA RSO is very small (1:35,000) and septic arthritis is uncommon.20 Similarly, none of the dogs in our study developed any infection related to 117mSn IA injection. Overall, in humans RSO has very low rate of adverse effects.41 Joint flare ie more pain and joint effusion due to intensification of inflammation (radiosynovitis) within 24 weeks after RSO is the most common adverse effect.20 This may be considered a natural course of the treatment due to rapid and extensive synovial necrosis when using higher energy beta-emitters. In humans, the joint flare from radiosynovitis is the main reason to consider co-injection of steroids. Routinely steroids are co-injected into large joints (shoulder, knee, and hip) because radiosynovitis is common in these joints.20 Even though canine joints are much smaller than human joint but this should be taken into consideration in dogs also in future studies involving RSO of these large joints.

Both PSS and PIS significantly improved at all time points except for PSS at 10 months and for PIS at 10 and 11 months which were not statistically significant compared to baseline, but these scores were still improved compared with baseline. A caregiver placebo effect may have played a role in improvement of CBPI as this effect has been shown to occur approximately 57% of the time for pet owners evaluating their dogs with lameness from osteoarthritis.34 In addition to this a lack to control group makes this measure less ideal compared to force plate gait analysis to determine outcome. However, it would be implausible to expect a placebo effect to persist for the 1-year duration of the study. In addition, the CBPI has been shown to allow reliable quantification of the owners assessment of the severity and impact of clinically relevant chronic pain-related behaviors with the dog in its normal environment.28,29 The QoL item (poor, fair, good, very good, excellent) is a stand-alone item and is used initially as a criterion validity assessment in the validation of the severity and interference scores.35 It takes very large changes in pain scores to elicit a change in the QoL category, which could be a potential reason why we did not see any significant improvement in this category.35 In future studies, QoL as an outcome measure should be better approached with a global assessment of change over time (ie, much worse, worse, same, better, much better).

Goniometry is an economic and simple measurement of joint angles used to objectively assess joint function.42 Mean elbow extension improved by 7 degrees at 6-month and by 10 degrees at 9-month follow-up time point in the treated elbow in the HD-group. However, mean elbow extension also increased in the untreated leg by 7 degrees at 9 months in the HD group and by 8 degrees at 6 months in the MD group. Therefore, our results indicate that there was no significant difference in this outcome measure between treated and untreated elbows.

The force-plate gait analysis is an established objective gold standard for quantification of leg function and pain in dogs with appendicular joint OA.29 It is considered to provide an accurate and unbiased assessment. However, without a placebo treatment group, we are unable to know if other external factors influenced the dogs in a way that may have resulted in improved leg function. A caregiver placebo effect as mentioned above does not exist for appropriately acquired force plate gait analysis. In addition, in a randomized, blinded, placebo-controlled crossover study where every dog received tramadol or carprofen or placebo during the study period, the authors found no change in PVF over a 10-day period in the placebo group.33 Additionally, in our study the untreated opposite leg served as a source of comparison data. The improvement noted in PVF in our study is larger than what has been previously reported.29,32,33

One of the limitations of this pilot study was a small sample size. Another limitation was the lack of a placebo or control group; however, OA is a progressive disease. The lack of any therapy for osteoarthritis would not have been acceptable for an ethical committee for running a control group for up to 1 year. While using client-owned dogs is a strength of the study, it is also a limitation. Studies of naturally occurring OA in dogs are associated with potential confounding factors, such as the potential for owner errors in study compliance and variations in the home environment. However, this is the environment in which the agent will be used and assessed by veterinarians and owners. Dogs were allowed to continue previous medical management (NSAIDs or other analgesics) during the study. It is possible that use of these medications could have biased our results. Ideally, dogs would have all been taken off of medical management and undergone a washout period before enrollment. The authors elected to allow dogs to be continued on any previous medications for multiple reasons: to avoid increasing pain should the IA injection fail to control pain, to provide pain control in the untreated leg, to allow the study to be clinically relevant, and for the study to be reflective of the general canine population with OA. Future studies might include more stringent exclusion criteria. We focused on the elbow joint for consistency; it would be interesting to know the effects of this treatment on other arthritic joints.

The safe use of any radioisotope requires documented training by veterinarians and support staff. There is a recommended licensing, treatment and post-treatment caretaker instruction process published by the US Nuclear Regulatory Commission for the safe use of 117mSn in the US.43 Unlike I-131 and Tc 99m radiation quarantine is not indicated for 117mSn as it is not excreted in any appreciable amount. Instead, 117mSn is retained within the joint and is eventually cleared by the lymphatics to the liver as microparticles of inert (nonradioactive) tin.23,25,26 However, there are gamma emissions that must be measured at 1 meter post treatment to determine the amount of interaction with a patient by household members. All household members are to monitor and follow their interactions within 3 feet (from treated joint(s) to center of torso) prescribed by written instructions for 2 weeks. For dogs in which there is an extended close association (sleeping in the same bed, sitting beneath an occupied office chair or in ones lap > 4 hrs daily) there could be a longer period of abstaining from these behaviors for up to 46 weeks following 117mSn radiosynoviorthesis.43,44 All patients can return to normal activities and interactions with anyone beyond 3 feet immediately post treatment.43,44

Clinical response to RSO is usually expected to have some lag phase that can last from weeks to months.20 In humans, the effect in the knee is seen as soon as 4 weeks.20 In the current study, improvement was noted in dogs at 1-month evaluation, similar to humans. In humans, the full therapeutic impact of RSO can take 46 months and duration of response depends on already existing joint damage.20 Similarly in our study full therapeutic effect as shown by significantly improved objective measurements such as PVF (and improvement in BW-D% approaching significance) was achieved at 3 months post treatment. Advanced-stage OA and pre-existing joint damage are negative outcome predictors of RSO in humans.45 Thus, the best responders would be patients with limited joint damage or the patients with large amounts of inflammation/effusion rather than advanced degenerative changes. Our study population included dogs with mild to moderate (grade 1 to 2) degree of OA and, as in human studies, a good clinical response was noted. Future studies in dogs with advanced OA are indicated to evaluate the effects of IA 117mSn in those cases.

In conclusion, IA injection of 117mSn improved CBPI scores and increased weight-bearing associated with elbow OA, providing preliminary evidence that 17mSn is beneficial in the management of elbow OA in dogs. This localized therapy with protracted results can be considered as an adjunct to other nonsurgical or surgical treatments or as a stand-alone therapy for elbow OA and might be useful for patients that cannot tolerate traditional OA medications such as NSAIDs. Although 17mSn appeared to be effective for the treatment of elbow OA, this pilot study has inherent limitations; therefore, future studies with larger numbers of dogs and with placebo group are needed.

The study protocol was approved by Institutional Animal Care and Use Committee (Protocol #16-008) and the Radiation Safety Office of the Louisiana State University (site A) and Medical Director Board and Radiation Safety Committee of Gulf Coast Veterinary Specialists (site B). All dogs were client-owned and written consent was obtained before study enrollment. This study adhered to veterinary care best practice guidelines.

The authors thank the LSU and GCVS force-plate teams and Sarah Keeton, PhD for her invaluable assistance in managing all data records.

Dr Andrews reports grants from Exubrion Therapeutics, during the conduct of the study. Dr Lattimer reports grants from Exubrion Therapeutics, during the conduct of the study. Dr Lattimer, however, had a career long interest in therapeutics of this type and has participated in privately and publicly funded work that employs radiopharmaceuticals and devices. None of this work has been done in the last several years except that associated with the parent project to this work. The study was funded by Exubrion Therapeutics, Buford, GA, USA. Drs. Aulakh, Hudson, and Fabiani are advisory board members for Exubrion Therapeutics and receive a small honorarium for consultation. All authors declare no other conflicts of interest related to this report.

1. Krotscheck U, Bottcher P. Surgical diseases of the elbow. In: Veterinary Surgery: Small Animal. Vol. 1. 2nd ed. St. Louis, MS: Elsevier; 2018.

2. Coppieters E, Gielen I, Verhoeven G, et al. Erosion of the medial compartment of the canine elbow: occurrence, diagnosis and currently available treatment options. Vet Comp Orthop Traumatol. 2015;28:918. doi:10.3415/VCOT-13-12-0147

3. Sanderson RO, Beata C, Flipo RM, et al. Systematic review of the management of canine osteoarthritis. Vet Rec. 2009;164:418424. doi:10.1136/vr.164.14.418

4. Innes JF, Clayton J, Lascelles BD. Review of the safety and efficacy of long-term NSAID use in the treatment of canine osteoarthritis. Vet Rec. 2010;166:226230. doi:10.1136/vr.c97

5. Burton NJ, Owen MR, Kirk LS, et al. Conservative versus arthroscopic management for medial coronoid process disease in dogs: a prospective gait evaluation. Vet Surg. 2011;40:972980. doi:10.1111/j.1532-950X.2011.00900.x

6. Dempsey LM, Maddox TW, Comerford EJ, et al. A comparison of owner-assessed long-term outcome of arthroscopic intervention versus conservative managemento f dogs with medial coronoid process disease. Vet Comp Orthop Traumatol. 2019;32:19. doi:10.1055/s-0038-1676293

7. Dejardin L, Guillou R. Total elbow replacement in dogs. In: Johnston S, Tobias K, editors. Veterinary Surgery: Small Animal. Vol. 1. 2nd ed. St. Louis, MS: Elsevier;2018:885896

8. Conzemius MG, Aper RL, Corti LB. Short-term outcome after total elbow arthroplasty in dogs with severe, naturally occurring osteoarthritis. Vet Surg. 2003;32:545552. doi:10.1111/j.1532-950X.2003.00545.x

9. Franklin SP, Cook JL. Prospective trial of autologous conditioned plasma versus hyaluronan plus corticosteroid for elbow osteoarthritis in dogs. Can Vet J. 2013;54:881884.

10. Guercio A, Di Marco P, Casella S, et al. Production of canine mesenchymal stem cells from adipose tissue and their application in dogs with chronic osteoarthritis of the humeroradial joints. Cell Biol Int. 2012;36:189194. doi:10.1042/CBI20110304

11. Wanstrath AW, Hettlich BF, Su L, et al. Evaluation of a single intra-articular injection of autologous protein solution for treatment of osteoarthritis in a canine population. Vet Surg. 2016;45:764774. doi:10.1111/vsu.12512

12. Sherwood JM, Roush JK, Armbrust LJ, et al. Prospective evaluation of intra-articular dextrose prolotherapy for treatment of osteoarthritis in dogs. J Am Anim Hosp Assoc. 2017;53:135142. doi:10.5326/JAAHA-MS-6508

13. Quinn R, Preston C. Arthroscopic assessment of osteochondrosis of the medial humeral condyle treated with debridement and sliding humeral osteotomy. Vet Surg. 2014;43:814818. doi:10.1111/j.1532-950X.2014.12260.x

14. Sellam J, Berenbaum F. The role of synovitis in pathophysiology and clinical symptoms of osteoarthritis. Nat Rev Rheumatol. 2010;6:625635. doi:10.1038/nrrheum.2010.159

15. de Lange-brokaar BJ, Ioan-Facsinay A, van Osch GJ, et al. Synovial inflammation, immune cells and their cytokines in osteoarthritis: a review. Osteoarthritis Cartilage. 2012;20:14841499. doi:10.1016/j.joca.2012.08.027

16. McDougall JJ. Arthritis and pain. Neurogenic origin of joint pain. Arthritis Res Ther. 2006;8:220. doi:10.1186/ar2069

17. Kresnik E, Mikosch P, Gallowitsch HJ, et al. Clinical outcome of radiosynoviorthesis: a meta-analysis including 2190 treated joints. Nucl Med Commun. 2002;23:683688. doi:10.1097/00006231-200207000-00013

18. Kapatkin AS, Nordquist B, Garcia TC, et al. Effect of single dose radiation therapy on weight-bearing lameness in dogs with elbow osteoarthritis. Vet Comp Orthop Traumatol. 2016;29:338343. doi:10.3415/VCOT-15-11-0183

19. Ishii K, Inaba Y, Mochida Y, et al. Good long-term outcome of synovectomy in advanced stages of the rheumatoid elbow. Acta Orthop. 2012;83:374378. doi:10.3109/17453674.2012.702391

20. Chojnowski MM, Felis-Giemza A, Kobylecka M. Radionuclide synovectomy - essentials for rheumatologists. Reumatologia. 2016;3:108116. doi:10.5114/reum.2016.61210

21. Szentesi M, Nagy Z, Gher P, et al. A prospective observational study on the long-term results of. Eur J Nucl Med Mol Imaging. 2019;46:16331641. doi:10.1007/s00259-019-04350-3

22. Zuderman L, Liepe K, Zphel K, et al. Radiosynoviorthesis (RSO): influencing factors and therapy monitoring. Ann Nucl Med. 2008;22:735741. doi:10.1007/s12149-008-0167-7

23. Lattimer JC, Selting KA, Lunceford JM, et al. Intraarticular injection of a Tin-117 m radiosynoviorthesis agent in normal canine elbows causes no adverse effects. Vet Radiol Ultrasound. 2019;60:567574. doi:10.1111/vru.12757

24. Polyak A, Nagy LN, Drotar E, et al. Lu-177-labeled zirconia particles for radiation synovectomy. Cancer Biother Radiopharm. 2015;30:433438. doi:10.1089/cbr.2015.1881

25. Doerr C, Stevenson NR, Gonzales G. Homogeneous Sn-117m col- loid radiosynovectomy results in rat models of joint disease [abstract]. J Nucl Med. 2015;1243.

26. Doerr C, Bendele A, Simon J. Validation of the use of homoge- neous Sn-117m colloid radiosynoviorthesis in a GLP osteoarthritis rat model [abstract]. J Nucl Med. 2016;323.

27. Ondreka N, Tellhelm B. Explanation of grading according to IEWG and discussion of cases, Proceedings, 31th annual meeting of the International Elbow Working Group (IEWG), Verona, Italy; 2017. Available from: http://www.vet-iewg.org/wp-content/uploads/2017/03/IEWG-proceedings2016.pdf. Accessed May 5, 2021.

28. Brown DC, Boston RC, Coyne JC, et al. Ability of the canine brief pain inventory to detect response to treatment in dogs with osteoarthritis. J Am Vet Med Assoc. 2008;233:12781283. doi:10.2460/javma.233.8.1278

29. Brown DC, Boston RC, Farrar JT. Comparison of force plate gait analysis and owner assessment of pain using the Canine Brief Pain Inventory in dogs with osteoarthritis. J Vet Intern Med. 2013;27:2230. doi:10.1111/jvim.12004

30. Roush JK, Cross AR, Renberg WC, et al. Evaluation of the effects of dietary supplementation with fish oil omega-3 fatty acids on weight bearing in dogs with osteoarthritis. J Am Vet Med Assoc. 2010;236:6773. doi:10.2460/javma.236.1.67

31. Mirza MH, Bommala P, Richbourg HA, Rademacher N, Kearney MT, Lopez MJ. Gait changes vary among horses with naturally occurring osteoarthritis following intra-articular administration of autologous platelet-rich plasma. Front Veterin Sci. 2016;3. doi:10.3389/fvets.2016.00029

32. Vijarnsorn M, Kwananocha I, Kashemsant N, et al. The effectiveness of marine based fatty acid compound (PCSO-524) and firocoxib in the treatment of canine osteoarthritis. BMC Vet Res. 2019;15:349. doi:10.1186/s12917-019-2110-7

33. Budsberg SC, Torres BT, Kleine SA, et al. Lack of effectiveness of tramadol hydrochloride for the treatment of pain and joint dysfunction in dogs with chronic osteoarthritis. J Am Vet Med Assoc. 2018;252:427432. doi:10.2460/javma.252.4.427

34. Conzemius MG, Evans RB. Caregiver placebo effect for dogs with lameness from osteoarthritis. J Am Vet Med Assoc. 2012;241:13141319. doi:10.2460/javma.241.10.1314

35. Brown DC. The canine brief pain inventory; 2021. Available from: http://www.caninebpi.com. Accessed May 5, 2021.

36. Jaegger G, Marcellin-Little DJ, Levine D. Reliability of goniometry in labrador retrievers. Am J Vet Res. 2002;63:979986. doi:10.2460/ajvr.2002.63.979

37. Kampen WU, Voth M, Pinkert J, et al. Therapeutic status of radiosynoviorthesis of the knee with yttrium [90Y] colloid in rheumatoid arthritis and related indications. Rheumatology (Oxford). 2007;46:1624. doi:10.1093/rheumatology/kel352

38. Karavida N, Notopoulos A. Radiation Synovectomy: an effective alternative treatment for inflamed small joints. Hippokratia. 2010;14:2227.

39. Klett R, Lange U, Haas H, et al. Radiosynoviorthesis of medium-sized joints with rhenium-186-sulphide colloid: a review of the literature. Rheumatology (Oxford). 2007;46:15311537. doi:10.1093/rheumatology/kem155

40. Schneider P, Farahati J, Reiners C. Radiosynovectomy in rheumatology, orthopedics, and hemophilia. J Nucl Med. 2005;46(Suppl 1):48S54S.

41. Knut L. Radiosynovectomy in the therapeutic management of arthritis. World J Nucl Med. 2015;14:1015. doi:10.4103/1450-1147.150509

42. Lascelles BD, Dong YH, Marcellin-Little DJ, et al. Relationship of orthopedic examination, goniometric measurements, and radiographic signs of degenerative joint disease in cats. BMC Vet Res. 2012;8:10. doi:10.1186/1746-6148-8-10

43. Procedure for use of Synovetin OA [Note: licensee to modify to match specific facility operations]; 2021. Available from: https://www.nrc.gov/docs/ML2028/ML20282A514.pdf. Accessed May 5, 2021.

44. Wendt RE, Selting KA, Lattimer JC, et al. Radiation safety considerations in the treatment of canine skeletal conditions using 153Sm, 90Y, and 117mSn. Health Phys. 2020;118:702710. doi:10.1097/HP.0000000000001222

45. Liepe K. Efficacy of radiosynovectomy in rheumatoid arthritis. Rheumatol Int. 2012;32:32193224. doi:10.1007/s00296-011-2143-0

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