Prevalence of Cobalturia Among Adults With Joint Replacements

This cohort study examines the association of cobalt-chrome arthroprosthetic components with adverse reactions to metallic debris, such as cobaltism.


Introduction
Twenty million North Americans have cobalt-chrome arthroprosthetic components, and 1 million have metal-on-metal hip replacements. 1Cobalt is a mitochondrial toxin-encephalopathy and cardiomyopathy (cobaltism) may occur from iatrogenic, industrial, dietary, or arthroprosthetic cobalt exposure. 2,3In unexposed populations, the 95th percentile of cobalt levels in urine and blood are 1 part per billion (ppb) and 0.4 ppb, respectively. 3ar and corrosion of cobalt-chrome joint implantations can result in periprosthetic tissue inflammation or necrosis, also known clinically as adverse reactions to metallic debris. 1,4riprosthetic cobalt-chrome metallosis is disseminated systemically and may result in arthroprosthetic cobaltism. 1,3,4Systemic cobalt dissemination can result in brain hypometabolism and atrophy; patients with levels of cobalt in blood as low as 1.1 ppb and in urine as low as 4.1 ppb are reported as having cobalt encephalopathy. 5,6

Methods
This cohort study analyzed redacted data from 1 orthopedic clinic.The institutional review board at the University of Alaska Anchorage designated the study to be exempt, and patients provided written informed consent for this study.Patients with a suspected hip, knee, or shoulder replacement containing cobalt-chrome were screened with a spot screening of cobalt in urine.Levels of cobalt in blood were then determined for patients with cobalt levels in urine 1 ppb or higher.Patients were designated as cobalt-positive if cobalt levels in urine were 1 ppb or higher or if levels in blood were 0.4 ppb or higher.The reference laboratory test results threshold for reporting cobalt in urine and blood are generally 1 ppb and 0.5 ppb, respectively.Patients with cobalt levels below the reporting threshold in either were assigned half the threshold value.All P values were from 2-sided tests and results were deemed statistically significant at P < .05. Analysis was conducted using Prism version 9.1.1(GraphPad).This study followed the Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) reporting guideline.
Paired cobalt levels in urine and blood (144 patients) correlated significantly (cobalt in blood = 0.25 × cobalt in urine; P < .001).Paired joint-fluid and urine cobalt (57 patients) correlated significantly (joint fluid = 20 × cobalt in urine; P < .001).Patients were classified by type, location, number, and brand of their implantation (Table ).These classes were risk-grouped based on mean cobalt levels in urine (ie, extreme, greater than 20 ppb; high, between 1 and 21 ppb; low, less than 1 ppb).Abbreviation: IQR, interquartile range.
a Threshold for cobalt positivity was 1 ppb or higher of cobalt in urine.
b Ceramic heads containing Zirconia are indistinguishable from cobalt-chrome femoral heads radiographically, these 11 patients had no cobalt-chrome implantation.Extreme-risk implantations (37 patients; mean cobalt in urine, 54.1 ppb; median, 9.7 ppb) were exclusively metal-on-metal hip prosthetics.High-risk implantations (167 patients; mean cobalt in urine, 6.1 ppb; median, 1.2 ppb) consisted of hip constructs with a cobalt-chrome acetabular part (Dual-Mobility) or a modular cobalt-chrome neck, 2 brands of metal-on-plastic hips prone to headneck taper corrosion, cobalt-chrome-containing joint replacements at different locations, bilateral or revision knee arthroplasties, and shoulder implantations.Low-risk implantations (36 patients; mean cobalt in urine, 0.4 ppb; median, 0.5 ppb) consisted of ceramic-on-plastic hips (with no cobaltchrome part), several brands and models of metal-on-plastic hips (with cobalt-chrome femoral head) with head-neck tapers not prone to corrosion, and unilateral primary-knee replacements (with 1 to 2 cobalt-chrome parts, no taper junctions, and metal-on-plastic articulation).

Discussion
Most patients presenting to our clinic with cobalt-chrome hip, knee, or shoulder implantations were cobalturic (ie, cobalt levels in urine of 1 ppb or above) and had cobalt levels in urine or blood in excess of levels associated with encephalopathy.Patients were rarely aware of type, brand, or materials of their replaced joint(s).However, the radiographic appearances of extreme-risk metal-on-metal hips and high-risk modular-neck hips are distinctive (Figure ).Only 2 models of joint replacements have been recalled in the US for cobalt-chrome metallosis complications: 1 extreme-risk hip with a metalon-metal articulation (Johnson & Johnson) and 1 high-risk hip with a modular cobalt-chrome neck (Stryker).Patients with recalled implantations are likely monitored, and many have required revision surgery for cobalt-chrome metallosis complications.Millions of residents of North America implanted with nonrecalled extreme-risk or high-risk implantations are likely not monitored and are likely experiencing cobalturia.[3][4][5][6] This study has several limitations.The study was conducted with patients from a single-surgeon clinic.The author-surgeon (S.S.T.) has published the index case report of arthroprosthetic cobaltism from contemporary metal-on-metal hip replacements and is case 1 in that report.The author's position as patient, surgeon, physician, and researcher introduces the possibility for observer basis.
Therefore, it is critical the findings of this report be replicated by other investigators without a personal or financial conflict of interest.Observer basis is unlikely to be a significant factor in this study because reference laboratory determined urine, blood, and joint fluid cobalt concentrations and the type, location, and brand of cobalt-chrome arthroprosthetic implantations studied are not open in interpretation.Multiple coauthors insured the veracity of the data.

Figure . B 4 Downloaded
Figure.Images of Metal-on-Metal and Modular-Neck Hip Implantations

Table .
Risk of Cobalt-Chrome Implantation by Cobalt Levels in Urine and Blood