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. 2012 Feb;3(Suppl 1):19–30. doi: 10.1055/s-0031-1298605

Table 5. Complications and adverse events following single-level and multilevel C-ADR.*.

Single level, % (n/N) Multilevel, % (n/N) P Follow-up, y
Reoperation
Coric et al 7 (2010) 5.0 (2/40) 16.7 (2/12) NR 2
Huppert et al 5 (2011) 2.3 (4/175) 3.6 (2/56) NS 2
Pimenta et al 4 (2007) 4.2 (3/71) 2.9 (2/69) NS NR
Revision
Huppert et al 5 (2011) 0.6 (1/175) 0 (0/56) NS 2
Heterotopic ossification
Any
Huppert et al 5 (2011) 66.7 (110/165) 55.0 (61/111) .02 2
Tu et al 8 (2011) 30.0 (6/20) 75.0 (12/16) .007 1
Grade IV
Coric et al 7 (2010) 0 (40) 8.3 (1/12) NR 2
Huppert et al 5 (2011) 10.3 (17/165) 7.2 (8/111) NS 2
Pimenta et al 4 (2007) 1.4 (1/71) 0 (0/69) NR NR
Dysphagia
Huppert et al 5 (2011) 4.0 (7/175) 16.1 (9/56) .002 2
Device subsidence
Huppert et al 5 (2011) 1.1 (2/175) 0 (5/56) NS 2
Device migration
Huppert et al 5 (2011) 0.6 (1/175) 1.8 (1/56) NS 2
Infection
Pimenta et al 4 (2007) 0 (0/71) 0 (0/69) NR
Mortality
Pimenta et al 4 (2007) 0 (0/71) 0 (0/69) NR
Any event
Goffin et al 3 (2010) 66.3 (61/92) 40.0 (4/10) NR 6
*

Incidences reflect the number of patients with one or more adverse event/complication. C-ADR indicates cervical artificial disc replacement; NR, not reported; and NS, not significant.

Approximately 60% of all reported adverse events occurred 2 years after index surgery and about 15% of these events were continuations of earlier reports.