Increased inflammatory response is associated with less favorable functional results 5 years after total knee arthroplasty

Publikation: Beitrag in FachzeitschriftForschungsartikelBeigetragenBegutachtung

Abstract

PURPOSE: Allergy against implant materials is discussed controversially and still not fully understood. Despite these controversies, a relevant number of patients receive hypoallergenic knee implants. The aim of this study was to compare a new coating system with the standard implant in total knee arthroplasty (TKA). Additionally, the influence of proinflammatory cytokines on patient-reported outcome measures (PROMs) was investigated.

METHODS: 120 patients without known metal allergy and without previous metal implants were included. The patients were randomized to receive a coated or standard TKA of the same knee system. 105 patients completed the 5 year follow-up. Patient-reported outcome measures (PROMs) including knee function (Oxford Knee Score, OKS), quality of life (SF36) and UCLA activity scale were assessed. Additionally, several cytokines with a possible role in implant allergy were measured in patient`s serum (IL-1beta, IL-5, IL-6, IL-8, IL-10, IP-10, IFN γ, TNF α). Group comparison was performed using Mann-Whitney U test for continuous values and chi-square test for categorical values.

RESULTS: There were no differences in PROMs between both groups at any follow-up. The majority of patients demonstrated no elevation of the measured blood cytokines. The blood cytokine pattern after 5 years demonstrated no differences between study groups. There was a significant association between elevated IL-8 values and worse results in the overall OKS (p = 0.041), the OKS function component (p = 0.004), the UCLA activity scale (p = 0.007) and the physical component of SF36 (p = 0.001).

CONCLUSION: There were no problems with the new coating during mid-term follow-up and no differences in PROMs between coated and standard TKA. Patients with an increased inflammatory response demonstrated worse functional results, regardless of the implant.

LEVEL OF EVIDENCE: I.

CLINICAL TRIAL REGISTRATION: The study protocol was registered in the US National Institutes of Health's database ( http://www.

CLINICALTRIALS: gov ) registry under NCT00862511.

Details

OriginalspracheEnglisch
Seiten (von - bis)1316-1322
Seitenumfang7
FachzeitschriftKnee Surgery, Sports Traumatology, Arthroscopy
Jahrgang31
Ausgabenummer4
PublikationsstatusVeröffentlicht - Apr. 2023
Peer-Review-StatusJa

Externe IDs

PubMedCentral PMC10049948
Scopus 85124760560
ORCID /0000-0002-1942-9056/work/149798058

Schlagworte

Schlagwörter

  • Humans, Arthroplasty, Replacement, Knee/adverse effects, Quality of Life, Interleukin-8, Knee Prosthesis/adverse effects, Knee Joint/surgery, Osteoarthritis, Knee, Hypersensitivity/etiology, Cytokines, Treatment Outcome, Patient Reported Outcome Measures