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Zarkadis2017 PDF
Zarkadis2017 PDF
ABSTRACT Background: Cervical radiculopathy is a common disorder that portends significant morbidity.
The presence of radiculopathy can have a debilitating effect on patients as well as a significant economic impact.
Active duty military patients with increased physical occupational demands can be significantly impacted by cervical
disease. The resulting disability can have a strong negative impact on operational readiness. Several studies have dem-
onstrated comparably good functional outcomes between cervical disc arthroplasty (CDA) and anterior cervical
discectomy and fusion for single-level disease. To date, no study has specifically evaluated the functional and occupa-
tional outcomes following adjacent 2-level CDA in a young, active patient population as represented by the active duty
military population. Purpose: To evaluate functional and occupational outcomes following adjacent 2-level CDA for
cervical radiculopathy in the U.S. military population. We hypothesized that this population would have excellent
symptomatic relief at the cost of a low return to duty rate. Methods: We performed a case series with prospective
follow-up of all patients who underwent adjacent two-level CDA at a single institution from 2011 to 2014. Each
patient completed the Neck Disability Index questionnaire to assess functional outcome. Primary outcomes of interest
were return to active military duty and complications. Results: Follow-up was available for 18 of 21 (85.7%) patients.
At an average follow-up of 21.4 ± 11.1 months, 12 patients (66.7%) reported complete symptomatic relief and were able
to return to preoperative levels of function. Average self-reported pain score improved from 8.3 preoperatively to 1.1 post-
operatively, and average postoperative Neck Disability Index score was 15.5 compared to 37.0 for those who medically
retired. Radiographic analysis did not show any evidence of subsidence, migration of hardware, or heterotopic ossifica-
tion. The average return to duty time was 9.6 weeks. Discussion: We demonstrate that adjacent two-level CDA is
capable of providing predictable symptomatic relief and maintenance of a high-demand preoperative level of function
for cervical radiculopathy among a population of young and highly active individuals. Adjacent two-level CDA offers
significant relief of symptoms with low risk of complication in a young, active, and high-demand cohort such as the
U.S. military. Adjacent two-level CDA can be performed with the expectation of improving function, relieving symp-
toms, returning to preoperative levels of activity, and maintaining operational readiness.
FIGURE 1. Postoperative anteroposterior and lateral cervical spine radiograph of an adjacent-level C5/C6 and C6/C7 cervical disc arthroplasty.
active duty military patients who have undergone adjacent sure of neck pain and disability associated activities of
2-level CDA at our institution between May 2011 and July daily living.25
2014 (Fig. 1). Surgical logs of the two primary surgeons Occupational outcome was determined by an individual’s
who performed adjacent two-level CDA procedures during ability to (1) maintain their preoperative military occupa-
this period were reviewed. All arthroplasty procedures were tional specialty (MOS), classified according to the individ-
performed using either the ProDisc-C (DePuySynthes, West ual role in the army force structure,26 and (2) remain active
Chester, Pennsylvania ) or the Mobi-C (LDR, Austin, Texas), within the military. All U.S. military active duty personnel
with the exception of 1 patient who received the Secure-C are strictly required to adhere to regularly evaluated fitness
(Globus Medical, Audubon, Pennsylvania). standards. Routine rigorous physical training is required in
The general indications for adjacent-level CDA included the form of organized aerobic exercise, weight training,
the following: (1) clinical examination and history consis- and the performance of a multitude of core military tasks,
tent with cervical radiculopathy, (2) age <50 years old, including the ability to march at least 2 miles while carry-
(3) evidence of cervical spondylosis on diagnostic imag- ing at least 40 pounds of military gear. Physical fitness
ing, (4) absence of facet arthropathy, (5) nonexistence of is formally evaluated semiannually with timed runs as
posterior instability, and (6) preservation of cervical lordosis.
Patients who underwent adjacent two-level CDA procedure,
were active duty and older than 18 years at time of surgery, TABLE I. Telephone Survey
were reachable by phone for follow-up, and were a mini- 1. What Were Your Primary Symptoms Before Surgery?
mum of 12 months from surgery at the time of follow-up 2. What Was Your Preoperative Pain Score on a Scale of 0
were included in this study. Once a patient list was gener- (None) to 10 (Worst Pain I Ever Had)?
ated, demographic data (age at time of surgery, rank at time 3. What Was Your Postoperative Pain Score on a Scale of 0
(None) to 10 (Worst Pain I Ever Had)?
of surgery, race, tobacco use, body mass index, and level of 4. Did the Surgery Provide You With Relief of Those Symptoms?
disease) and patient-centered variables (preoperative symp- 5. How Long Until You Were Back to Full Active Duty After
toms, level of discomfort, postoperative symptoms) were the Surgery (Quantified in Months)?
extracted from the electronic medical record. Respective 6. What Was Your MOS Before Surgery?
contact information was obtained and all patients were then 7. What Was Your MOS After Surgery?
8. Were You on Flight Status Before Surgery?
interviewed via standardized telephone survey (Table I). a. If Yes, Were You Able to Stay on Flight Status?
All patients were read a disclosure of risks associated with 9. Were You on Airborne Status Before Surgery?
release of their medical information and consent for par- a. If Yes, Were You Able to Stay on Airborne Status?
ticipation in the survey was obtained. Each patient com- 10. Have You Deployed Since the Surgery?
pleted the Neck Disability Index (NDI) questionnaire as a 11. Were There Any Adverse Outcomes Associated
With the Surgery?
metric of functional outcome, which is a validated mea-
TABLE III. Return to Duty Patients nificant improvement in their average pain scores postopera-
tively. Furthermore, surgery had no impact on MOS, as all
Returned to Duty 12/18 (66.7%)
Age (Year), Mean ± SD 39.5 ± 4.8
personnel who returned to active duty were able to go back
Relief After Surgery 12 (100.0%) to their previous roles.
Reported Adverse Outcomes The demographic captured in our series is consistent with
Chronic Pain 1 that of those typically affected by cervical radiculopathy.1,2,6
Paresthesia 1 Our cohort is unique in that the mean age (40 years old)
Preoperative Pain Score 8.3 ± 1.7
Postoperative Pain Score 1.08 ± 1.4
and activity level have not previously been investigated.
p < 0.0001 CDA has been shown to be effective for pain relief while
Neck Disability Index 15.5 ± 12.1 preserving cervical motion and decreasing the incidence
Military Occupational Specialty of adjacent-level disease.8–11,13,23,24,27 Single-level CDA
Combat Arms 5 (41.7%) has furthermore been described as a good option for treating
Combat Support 3 (25.0%)
Combat Service Support 4 (33.3%)
active duty military patients.19,23,24,26 There have been
Time to RTD (Week), Mean ± SD 9.6 ± 11.7 several studies comparing multilevel CDA to multilevel
Maintained Flight Status 1/1 (100%) fusions.15 In a comparison of two-level CDA to two-level
Maintained Airborne Status n/a ACDF, the authors found similar outcomes at 3-month
Postop Combat Deployment 0 follow-up.15,17,18 At 24 months, however, CDA demon-
n/a, not applicable. strated improved subjective functional outcomes. In the
largest comparative study to date, Davis et al17 compared
standardized outcome measures following two-level CDA to
There were not any device-related or approach-related two-level fusion in a multicenter prospective randomized
complications encountered for any of the patients. Cervical trial at 2 and later 4-year18 follow-up. The CDA cohort dem-
spine radiographs were available for 17 of 21 (80.9%) onstrated a statistically significant improvement in the NDI
subjects, for which radiographic analysis did not show scores, SF-12 physical component scores, patient satisfaction
any evidence of subsidence, migration of hardware, or as well as decreased reoperation rates when compared to
heterotopic ossification at final follow-up. Three patients two-level fusion.17,18 Neither study evaluated the occupa-
reported chronic pain (16.7%) and 1 reported unilateral tional outcomes following surgery or controlled for activity
upper extremity paresthesia postoperatively (6%). No patient level of the cohort. The patient population in our study
went on to require revision surgery or reoperation within the could be considered a closed more homogeneous population
study period. of young athletic individuals.
Literature on multilevel CDA in a military population is
DISCUSSION limited. The two existing studies16,19 reported >95% reso-
We demonstrate that adjacent two-level CDA is capable lution of symptoms and return to active duty following
of providing predictable symptomatic relief and maintenance multilevel CDA. However, patients with multilevel CDA
of a high-demand preoperative level of function for cervi- were evaluated only in a limited subgroup analysis. As a
cal radiculopathy among a population of young and highly result, little prognostic information could be extrapolated
active individuals. We found that the majority of subjects from the findings in either study and neither functional nor
(66.67%) were able to return to full activities at their previ- occupational outcomes of the multilevel CDA subgroup
ous level of functionality by 12 weeks and that both the were evaluated. In this study, this cohort of interest was spe-
RTD and medical evaluation board (MEB) groups had sig- cifically isolated. Our results were more dramatic than those
of the previous studies in that 83% of patients reported com-
plete symptomatic resolution and 2 of 3 patients were able
TABLE IV. Medical Evaluation Board Patients to continue on active duty. Although the results of those
Medical Evaluation Board 6/18 (33.3%) patients who were able to remain active were exceptional,
Age (Year), Mean ± SD 41.2 ± 7.7
this study highlights shortcomings of multilevel CDA in
Relief After Surgery 3 (50%) the high-demand patients. The rate of complications in our
Reported Adverse Outcomes series was similarly low (6%).
Chronic Pain 2 There are several limitations to this study. First, this is a
Preoperative Pain Score 5.8 ± 1.6 relatively small case series with retrospective reviewed data.
Postoperative Pain Score 3.5 ± 1.6
p < 0.01
As a result, this study lacks adequate power for greater statis-
Neck Disability Index 37.0 ± 8.9 tical analysis. It is further limited by the lack of a control
Military Occupational Specialty group. However, given the unique nature of this patient popu-
Combat Arms 2 (33.3%) lation, our findings contribute to the growing but still limited
Combat Support 0 (0%) body of literature evaluating functional outcomes following
Combat Service Support 4 (66.7%)
multilevel CDA. Our average follow-up additionally allows
us to prognosticate primarily short- and midterm outcomes. 11. Murrey D, Janssen M, Delamarter R, et al: Results of the prospective,
Finally, as we did not control for other patient comorbidities, randomized, controlled multicenter Food and Drug Administration inves-
tigational device exemption study of the ProDisc-C total disc replacement
it is possible that patients who went on to MEB for separation
versus anterior discectomy and fusion for the treatment of 1-level symp-
had other issues beyond the surgery that influenced their abil- tomatic cervical disc disease. Spine J 2009; 9(4): 275–86.
ity to return to active duty. Future studies with greater patient 12. McAfee PC, Reah C, Gilder K, Eisermann L, Cunnignham B: A meta-
numbers and longer follow-up will provide for increased analysis of comparative outcomes following cervical arthroplasty or
external validity so as to guide spine surgeons in the manage- anterior cervical fusion: results from four prospective multi-center ran-
ment of multilevel cervical radiculopathy in the young, active, domized clinical trials and up to 1226 patients. Spine (Phila Pa 1976)
2012; 37(11): 943–52.
and high-demand cohort.
13. Sasso RC, Anderson PA, Riew KD, Heller JG: Results of cervical
The impact of our findings support the current literature arthroplasty compared with anterior discectomy and fusion: four-year
that adjacent 2-level CDA offers significant relief of symp- clinical outcomes in a prospective, randomized controlled trial. J Bone
toms with low risk of complication in a young, active, and Joint Surg Am 2011; 93(18): 1684–92.
high-demand cohort such as the U.S. military. We have 14. Zigler JE, Delamarter R, Murrey D, Spivak J, Janssen M: ProDisc-C
further demonstrated that the majority of individuals will and anterior cervical discectomy and fusion as surgical treatment for
single-level cervical symptomatic degenerative disc disease: five-year
be able to return to high-demand activity in the short term within results of a Food and Drug Administration study. Spine (Phila Pa 1976)
a relatively short period following multilevel spinal surgery. 2013; 38(3): 203–9.
As a result of the present findings, we would recommend 15. Cheng L, Nie L, Hou Y: Fusion versus Bryan cervical disc in two-level
that an adjacent two-level CDA be used to treat multilevel cervical disc disease: a prospective, randomised study. Int Orthop 2009;
cervical disease in active high-demand patients. In doing so, the 33(5): 1347–51.
16. Cody JP, Kang DG, Tracey RW, Wagner SC, Rosner MK, Lehman RA
spine surgeon can perform this operation with the expectation
Jr: Outcomes following cervical disc arthroplasty: a retrospective
of improving function, relieving symptoms, returning to pre- review. J Clin Neurosci 2014; 21(11): 1901–4.
operative levels of activity, and maintaining operational readiness. 17. Davis RJ, Kim KD, Hisey MS, et al: Cervical total disc replacement
with anterior discectomy and fusion for treatment of 2-level symptom-
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