Aulakh Karanvir S, Lopez Mandi J, Hudson Caleb, Gaschen Lorrie, Fabiani Michelle, Beale Brian, Andrews Frank M, Liu Chin-Chi, Lattimer Jimmy
School of Veterinary Medicine, Louisiana State University, Baton Rouge, LA, USA.
Gulf Coast Veterinary Specialists, Houston, TX, USA.
Vet Med (Auckl). 2021 Jun 4;12:117-128. doi: 10.2147/VMRR.S295309. eCollection 2021.
To evaluate the clinical effects of an intra-articular injection of Sn-colloid for management of canine grade 1 or 2 elbow osteoarthritis (OA).
This was a prospective study in 23 dogs with grade 1 or 2 elbow OA. An orthopedic examination and elbow radiographs were performed to confirm the presence of OA. Dogs were randomly assigned to receive unilateral intra-articular (IA) injection of low-dose (LD: 1.0mCi, n =8), medium-dose (MD: 1.75mCi, n =6), or high-dose (HD: 2.5mCi, n =9) of Sn-colloid. The primary outcome measure was peak vertical force (PVF) from force-plate gait analysis and secondary outcome measures included the Canine Brief Pain Inventory score (CBPI) and elbow goniometry. The CBPI was evaluated at pretreatment and then monthly post treatment for 1 year, and goniometry and PVF were evaluated at pretreatment, and at 1, 3, 6, 9 and 12 months post treatment.
PVF improved at 3, and 9 months compared to pretreatment values in the HD group. CBPI scores improved at most of the time points in all dose groups. There was no significant difference in elbow goniometry between treated and untreated elbows. There were no self-reports of any adverse effects of the injection by the owners and none were noted by the examining veterinarian at the time of regularly scheduled re-evaluations.
Sn IA injection was free of any obvious adverse effects, improved CBPI scores, and increased weight bearing in limbs with elbow OA providing preliminary evidence that Sn may be beneficial in the management of elbow OA in dogs. Although Sn appeared to be effective for management of elbow OA in these dogs, this pilot study has inherent limitations; therefore, future studies with larger numbers and with placebo group are needed.
评估关节内注射锡胶体治疗犬1级或2级肘关节骨关节炎(OA)的临床效果。
这是一项针对23只患有1级或2级肘关节OA犬的前瞻性研究。进行骨科检查和肘关节X光片检查以确认OA的存在。将犬随机分配接受低剂量(LD:1.0毫居里,n = 8)、中剂量(MD:1.75毫居里,n = 6)或高剂量(HD:2.5毫居里,n = 9)的锡胶体单侧关节内(IA)注射。主要结局指标是测力板步态分析中的峰值垂直力(PVF),次要结局指标包括犬简短疼痛量表评分(CBPI)和肘关节测角法。在治疗前以及治疗后每月评估1年的CBPI,在治疗前以及治疗后1、3、6、9和12个月评估测角法和PVF。
与HD组的治疗前值相比,PVF在治疗后3个月和9个月有所改善。所有剂量组在大多数时间点的CBPI评分均有所改善。治疗侧与未治疗侧肘关节的测角法无显著差异。主人没有关于注射任何不良反应的自我报告,在定期重新评估时检查兽医也未发现任何不良反应。
关节内注射锡胶体没有任何明显的不良反应,改善了CBPI评分,并增加了患有肘关节OA肢体的负重,这提供了初步证据表明锡可能对治疗犬肘关节OA有益。尽管锡在这些犬中似乎对治疗肘关节OA有效,但这项初步研究有其固有的局限性;因此,需要进行更多数量且设有安慰剂组的未来研究。