Unicompartmental knee arthroplasty vs. high tibial osteotomy for medial knee osteoarthritis (UNIKORN): a study protocol of a randomized controlled trial

被引:2
|
作者
Siren, Juuso [1 ,2 ]
Ramo, Lasse [1 ,2 ]
Rantasalo, Mikko [1 ,2 ]
Komulainen, Olli [1 ,2 ]
Skants, Noora [3 ]
Reito, Aleksi [4 ]
Kosola, Jussi [5 ]
Lindahl, Jan [1 ,2 ]
机构
[1] Univ Helsinki, Dept Orthopaed & Traumatol, Topeliuksenkatu 5, Helsinki 00260, Finland
[2] Helsinki Univ Hosp, Topeliuksenkatu 5, Helsinki 00260, Finland
[3] HUS Helsinki Univ Hosp, Peijas Hosp, Dept Anaesthesiol Intens Care & Pain Med, Sairaalakatu 1, Vantaa 01400, Finland
[4] Tampere Univ Hosp, Dept Orthopaed & Traumatol, Elamanaukio 2, Tampere 33520, Finland
[5] Kanta Hame Cent Hosp, Dept Orthopaed & Traumatol, Ahvenistontie 20, Hameenlinna 13530, Finland
基金
芬兰科学院;
关键词
High tibial osteotomy; Unicompartmental knee arthroplasty; Intention to treat; Superiority trial; Knee osteoarthritis; Activity monitoring; Randomized controlled trial; TIME-DEPENDENT IMPROVEMENT; PATIENT SATISFACTION; HIP; DIFFERENCE; REGISTRY; WEDGE; JOINT; PAIN;
D O I
10.1186/s13063-023-07263-7
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
BackgroundMedial knee osteoarthritis (OA) is a common health problem resulting in knee pain and limiting patients' physical activity. After failed conservative treatment, unicompartmental knee arthroplasty (UKA) and high tibial osteotomy (HTO) are possible surgical treatment options for this condition. There is a paucity of high-quality evidence in the literature comparing objective and subjective outcomes of these procedures. Also, there is no common agreement on whether these procedures provide comparable results in late-stage medial knee OA patients. MethodsWe will perform a prospective randomized controlled trial comparing HTO and UKA in patients with late-stage medial knee OA. 100 patients with isolated medial knee OA (KL III-IV) are assigned to either UKA (n = 50) or HTO (n = 50) procedure in patients 45-65 years of age. Our primary outcome will be KOOS5 at one year postoperatively. Secondary outcomes include OARSI physical assessment, length of stay, wearable activity watch, radiographs (OA progression according to Kellgren-Lawrence classification), patient-reported outcomes (KOOS subscales, pain visual analog scale [VAS], Lysholm, and Oxford knee scores), and adverse events (conversion to total knee arthroplasty, surgery-related complications, need for revision surgery) outcomes. Our hypothesis is that neither of the interventions is superior as measured with KOOS5 at 12 months. Ethics and disseminationThe institutional review board of the Helsinki and Uusimaa Hospital District has approved the protocol. We will disseminate the findings through peer-reviewed publications.
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页数:9
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