%0 Journal Article
%T Understanding immune-mediated cobalt/chromium allergy to orthopaedic implants: a meta-synthetic review.
%A Chen A
%A Kurmis AP
%J Arthroplasty
%V 6
%N 1
%D 2024 Feb 2
%M 38303027
暂无%R 10.1186/s42836-023-00227-x
%X <B>BACKGROUND: </B>The frequency of primary joint replacement surgery continues to increase worldwide. While largely considered biologically inert entities, an increasing body of evidence continues to validate a not insignificant incidence of allergic reactions to such implants. Little previous work has explored genuinely immune-mediated reactivity in this context. In the absence of a contemporary published summary on the topic, this paper explored the current state of understanding of cobalt/chromium allergy and proposes a patient management algorithm whereby such immune reactions are clinically suggested.<BR><B>METHODS: </B>A structured, systematic literature review was performed by following PRISMA search principles to provide an updated review of this area.<BR><B>RESULTS: </B>Thirty-six topic-related articles were identified, the majority reflecting lower tiers of scientific evidence with a lack of homogeneous quantitative data to facilitate valid cohort comparisons. Largely, the available literature represented small case series' or expert opinions.<BR><B>CONCLUSIONS: </B>Despite increasing clinical awareness and acknowledgement of true allergy to joint replacement components, this review highlighted that the evidence base underpinning the diagnosis and management of such patients is limited. Both patient-reported metal allergy or skin patch testing are grossly unreliable methods and show almost no correlation with true immune reactivity. Recent studies suggested a potential role for patient-specific in vitro cellular activation testing and/or targeted genetic testing when cobalt/chromium allergy is clinically suspected. However, while likely representing the contemporary "best available" approaches both can be costly undertakings, are not yet universally available, and still require broader validation in non-research settings before wider uptake can be championed.