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No difference in PROMs between robotic-assisted CR versus PS total knee arthroplasty: a preliminary study

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Abstract

The purpose of this study was to determine if significant clinical differences exist in patient-reported outcome measures (PROMs) between PS and CR TKAs implanted using robotic-assisted technology. This was an IRB-approved retrospective study from an institutional database evaluating 214 knees in 190 patients. Inclusion criteria included: primary RA-TKA, age 22–89 at the time of surgery, preoperative coronal limb deformity within 15º of neutral alignment, and minimum 1-year follow-up. The PS cohort consisted of 103 patients with 107 RA-TKAs, whereas the CR cohort consisted of 87 patients with 107 RA-TKAs. Cohorts were compared on the basis of demographics and PROMs (KSS knee, KSS function, FJS-12, KOOS-JR, WOMAC, and 5-point satisfaction Likert scale) collected preoperatively and at 1-year follow-up. Statistical analyses comparing measures were conducted via Student’s t tests for continuous data and Chi-squared analyses for categorical data. There were no significant differences identified in short-term PROMs at 1-year follow-up between cohorts (all p values > 0.05). 93.1% of patients with CR knees and 94.7% of patients with PS knees reported a satisfaction level of “very satisfied” or “satisfied”. Revision arthroplasty occurred in six knees (2.8%, 3 knees in CR cohort, 3 knees in PS cohort) with no differences in overall complications between groups. The use of RA-TKA technology promoted high patient satisfaction scores within this study, independent of CR or PS implant type with no significant differences in PROMs, satisfaction, revisions, or complications between the two groups.

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Acknowledgements

Harry M. King, Jr.—assistance with data collection and analysis.

Funding

The authors did not receive support from any organization for the submitted work. No funding was received to assist with the preparation of this manuscript. No funding was received for conducting this study. No funds, grants, or other support was received.

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Authors and Affiliations

Authors

Contributions

All authors contributed to the study conception and design. Material preparation, data collection and analysis were performed by JAR, MW, NG, LS and JK. The first draft of the manuscript was written by JAR and all authors commented on previous versions of the manuscript. All authors read and approved the final manuscript. Please note that Dr. JW was added to the list of co-authors during the manuscript revision stage. Dr. Whitaker’s contribution included statistical analysis of the data.

Corresponding author

Correspondence to Arthur L. Malkani.

Ethics declarations

Conflict of interest

Author Jarod A. Richards declares that he has no conflict of interest. Author Mark D. Williams declares that he has no conflict of interest. Author Neil A. Gupta declares that he has no conflict of interest. Author Joseph M. Kitchen declares that he has no conflict of interest. Author John E. Whitaker declares that he has no conflict of interest. Author Langan S. Smith declares that he has no conflict of interest. Author Arthur L. Malkani declares he has received IP royalties, speaker and consultant honoraria, and research support from Stryker Orthopedics. He serves as a reviewer for Journal of Arthroplasty, Bone and Joint Journal, Journal of Knee Surgery and Journal of Hip Surgery.

Ethical approval

This research study was conducted retrospectively from data obtained for clinical purposes. We consulted extensively with the IRB of University of Louisville who determined that our study did not need ethical approval. No human subjects were enrolled or consented. No animals were involved. An IRB official waiver of ethical approval was granted from the IRB of University of Louisville (IRB# 20.0848).

Research involving human and animal participants

This article does not contain any studies with human or animal subjects performed by any of the authors.

Informed consent

This research study was conducted retrospectively from data obtained for clinical purposes. No identifying information about the patients are included. We consulted extensively with the IRB of University of Louisville who determined that our study did not need require informed consent from the subjects. This study was reviewed by the University of Louisville Institutional Review Board (IRB# 20.0848) and determined by the Chair/Vice-Chair of the IRB that the study is exempt according to 45 CFR 46.101(b) under Category 4: Secondary research for which consent is not required.

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Richards, J.A., Williams, M.D., Gupta, N.A. et al. No difference in PROMs between robotic-assisted CR versus PS total knee arthroplasty: a preliminary study. J Robotic Surg 16, 1209–1217 (2022). https://doi.org/10.1007/s11701-021-01352-y

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  • DOI: https://doi.org/10.1007/s11701-021-01352-y

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