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No clinical difference between TiN-coated versus uncoated cementless CoCrMo mobile-bearing total knee arthroplasty; 10-year follow-up of a randomized controlled trial

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Knee Surgery, Sports Traumatology, Arthroscopy Aims and scope

Abstract

Purpose

Improvement of biomechanical properties of cobalt–chromium–molybdenum (CoCrMo) implant surface and reduction of adhesive wear is achieved by titanium–nitride (TiN) coating in vitro. Less pain, higher postoperative outcome scores and a lower revision rate after TKA with a TiN-coated CoCrMo TKA compared with uncoated CoCrMo TKA after 10-year follow-up was hypothesized.

Methods

In a double-blinded RCT, 101 patients received a cementless mobile-bearing CoCrMo TKA, either TiN-coated or uncoated. The primary outcome measure was the visual analogue scale (VAS) score for pain and secondary outcome measures were the Knee Society Score (KSS), Oxford Knee Score (OKS), revision rate and adverse events. Patients were assessed at 6 weeks, 6 months, 1 year, 5 years and 10 years, postoperatively.

Results

68 patients (67%) were available for 10-year follow-up. No difference was found in any of the assessed outcome measures with a mean decrease in VAS score (31.6 ± 22.9) and a mean increase in OKS (10.9 ± 8.4), KSS (29.3 ± 31.4), KSSK (26.4 ± 18.2) and KSSF (4.1 ± 22.9). Overall revision rate was 7% (coated 6% vs uncoated 8%) without additional revision procedures between 5 and 10-year follow-up.

Conclusions

The in vitro potential benefits of TiN coating did not result in better clinical outcome when compared to an uncoated cementless TKA. Pain, functional outcome and revision rates were comparable after 10-year follow-up. TiN-coated cementless TKA provides comparable good long-term results, similar to uncoated cementless CoCrMo TKA.

Level of evidence

Level 1, Therapeutic Study

Netherlands Trial Register

NL2887/NTR3033.

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Funding

R. P. van Hove received funding from the Foundation of Orthopedic Research, Spaarne Hospital Hoofddorp, The Netherlands.

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Correspondence to Jan K. G. Louwerens.

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The remaining authors declare that they have no conflict of interest.

Ethical approval

All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki Declaration and its later amendments or comparable ethical standards. The study was approved by the Bioethics Committee of the VU University Medical Center Amsterdam (No. 2005/194). The trial was registered with the Netherlands National Trial Registry (NTR 3033).

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167_2020_5997_MOESM1_ESM.docx

Supplementary Figure A. Full study flow diagram. Number of patients assessed for eligibility, inclusion, randomization and allocation to either the intervention, TiN group or the control, CoCrMo group, lost to follow-up and analysis. TiN, titanium nitride-coated total knee prosthesis, CoCrMo cobalt–chromium–molybdenum total knee prosthesis, V1 visit 1 at 6 weeks, V2 visit 2 at 6 months, V3 visit 3 at 1 year, V4 visit 4 at 5 years, V5 visit after ten years. (DOCX 23 kb)

Supplementary Table A. Baseline parameters (DOCX 14 kb)

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Louwerens, J.K.G., Hockers, N., Achten, G. et al. No clinical difference between TiN-coated versus uncoated cementless CoCrMo mobile-bearing total knee arthroplasty; 10-year follow-up of a randomized controlled trial. Knee Surg Sports Traumatol Arthrosc 29, 750–756 (2021). https://doi.org/10.1007/s00167-020-05997-4

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