Cervical Disc Replacement: Trends, Costs, and Complications

Article information

Asian Spine J. 2020;14(5):647-654
Publication date (electronic) : 2020 March 30
doi : https://doi.org/10.31616/asj.2019.0246
Department of Orthopaedic Surgery, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA
Corresponding author: Zorica Buser Department of Orthopaedic Surgery, Keck School of Medicine, University of Southern California, 1450 San Pablo St, HC4 - #5400A, Los Angeles, CA, 90033, USA Tel: +1-323-442-0206, Fax: +1-323-442-6990, E-mail: zbuser@usc.edu
*These authors contributed equally to this work.
Received 2019 August 3; Revised 2019 September 23; Accepted 2019 November 12.

Abstract

Study Design

Retrospective review of insurance database.

Purpose

To investigate national trends, complications, and costs after cervical disc replacement (CDR) using an administrative insurance database representative of the United States population.

Overview of Literature

As CDR continues to be used to treat patients with cervical stenosis, it is important to gain a better understanding of its use on a national level, potential complications, and cost. This information will allow for optimal patient counseling, risk stratification, and healthcare cost assessments. Several prior studies have investigated complications associated with CDR, but they have been limited by small sample size, single institution experiences, limited follow-up, and potential conflicts of interest.

Methods

Patients who underwent single or multilevel CDR between 2007 and 2015 were identified using an insurance database. We collected data on annual trends, reimbursement costs, patient demographic information, hospital information, and information on complications from the time of operation to 1 year postoperative.

Results

Total of 293 patients underwent either single or multilevel CDR. The number of procedures increased nonlinearly over time at an average of 17% per year, with a greater increase seen in the outpatient setting. Less than 3.7% of patients had new onset pain within 1 year after CDR. Within 1 year, 12.3% of patients reported a mechanical and/or bone-related complication. There were no patients who indicated a new nerve injury within 6 months of follow-up. Less than 3.7% of patients presented with dysphagia or dysphonia within 6 months, infection within 3 months, or a revision or reoperation within 1 year. Average reimbursement for single-level inpatient versus outpatient CDR was US $33,696.28 and US $34,675.12, respectively (p=0.29).

Conclusions

This study demonstrated that the use of CDR continued to increase. The most common complication was mechanical and/or bone-related, and cost analysis demonstrated no significant difference between inpatient and outpatient CDR.

Introduction

Cervical spondylosis is a highly variable, progressive disease that may result in stenosis secondary to disc herniation, disc degeneration, osteophyte formation, or hypertrophy of ligamentous structures. Patients with symptomatic cervical spondylosis may present with any combination of axial neck pain, radiculopathy, or myelopathy. Initial conservative management may include lifestyle modification, anti-inflammatory medications, physical therapy, epidural steroid injections, or possible temporary immobilization. Operative intervention may be indicated for patients with persistent symptoms that are refractory to conservative management.

A myriad of surgical techniques is available to decompress cervical stenosis. These range from anterior to posterior approaches with or without fusion. The optimal surgical intervention is still a matter of debate, and the choice of intervention is largely dependent on the anatomic structures causing the resultant stenosis, the number of cervical levels involved, patient-related factors, and surgeon preference. Historically, anterior cervical discectomy and fusion (ACDF) has resulted in excellent outcomes and is the most common surgical treatment for cervical radiculopathy and/or myelopathy [1]. Although the success of ACDF is well documented, it relies on fusion of the involved cervical levels. This leads to increased load transmission and hypermobility at adjacent levels, which predisposes these levels to adjacent segment degeneration (ASD) [2]. Resultant symptomatic ASD may be present in up to 25% of patients at 10 years, and the additional pathology cephalad or caudad to the index fused cervical segment may negate initially good outcomes and necessitate revision decompression and possible further extension of the fused segment(s) [3-5].

Cervical disc replacement (CDR) is a technique developed to maintain disc space height and motion after discectomy to prevent abnormal load transmission at adjacent segments, which would hypothetically decrease the risk for ASD. In vitro results have demonstrated that adjacent segment motion, intradiscal pressure, and joint loading are unchanged after CDR [6]. CDR was initially approved by the Food and Drug Administration in 2007 when initial and subsequent studies demonstrated overall noninferiority to ACDF [7-13]. Over the past decade, CDR has gained popularity among some spine surgeons and has become a viable alternative to ACDF, with some newer data supporting midterm reduction in adjacent segment pathology [14].

Because CDR continues to be used by spine surgeons when treating patients with cervical stenosis, it is important to gain a better understanding of its use on a national level, potential complications, and cost. This will allow for optimal patient counseling, risk stratification, and healthcare cost assessments.

Several studies have investigated complications associated with CDR, but they have been limited by small sample size, single institution experiences, limited follow-up, and potential conflicts of interest [15,16]. The purpose of this study was to investigate national trends, complications, and costs after CDR using an administrative insurance database that allows for longitudinal tracking of patients and captures a demographic that is generally representative of the population of the United States.

Materials and Methods

1. Patients

We performed a retrospective review of the Humana subset of the PearlDiver Patient Record Database (PearlDiver Inc., Warsaw, IN, USA). This commercially available database consists of 20 million patient records from the Humana national health insurance provider from 2007 to 2016. It spans all age groups and represents geographic areas throughout the entire United States. The database allows for the sorting of clinical diagnoses by International Classification of Diseases (ICD) and Current Procedural Terminology (CPT) codes.

Patients undergoing CDR between January 1, 2007 and September 30, 2015 were identified using CPT codes. We collected data on annual trends, reimbursement costs, and patient demographic information, including sex, age, and inpatient or outpatient status. Patients’ data were collected from the time of operation to 1-year postoperation. Common complications were identified and queried in the database using CPT, ICD-9, and ICD-10 codes (Table 1). Patients were followed for 3 months to 1 year following the index procedure to determine if first-instance complications arose. We grouped common complications into seven categories (Table 1). Due to privacy limitations, PearlDiver does not release the exact number of patients if there are fewer than 11 patients in any category.

Procedural and diagnostic codes used to identify patients in the PearlDiver database

The seven complications were pain, those that were mechanical and bone-related, nerve injury, dysphagia and dysphonia, infections, adverse reactions, and revision and reoperations.

The pain category included myelopathy, radiculopathy, arm, neck, and pain due to the implant. Follow-up related to pain lasted for 1-year postprocedure. Pain was separated as either the first instance coded after surgery or as continued pain that had been coded prior to surgery and continued postoperatively. Mechanical and bone-related complications included malpositioning of the implant, pseudarthrosis, heterotrophic ossification, and adjacent disc degeneration for up to 1 year postoperatively. The nerve injury category included nerve root injury, cervical cord injury, dural tear, and C5 palsy for up to 6 months postoperatively. Overall and cervical spine-specific dysphagia and dysphonia were grouped together into one category and followed for 6 months. The infection category included superficial, deep, wound, surgical site, and device-related infections within 3 months postoperatively. Adverse reactions included hemorrhage, embolism, fibrosis, stenosis, and thrombosis within 3 months of surgery. Revision and reoperation procedures were followed for 1 year and included removal of CDR, conversion to ACDF, osteotomy, revision, and cervical discectomy with decompression.

Patient data were completely deidentified and therefore our study did not require institutional review board approval.

2. Statistical analysis

Patients were grouped by age into 5-year increments from 10 to ≥90 years. Incidence was calculated as procedures per 100,000 members. The charge information we used was calculated as amount billed by the institution for each patient for care surrounding the index procedure. T-tests were used to calculate p-values to compare rates, and statistically significant p-values were defined as p<0.05.

Results

1. Demographic trends

We studied 293 patients who received an index CDR between 2009 and 2015. The number of procedures increased nonlinearly over time at an average of 17% per year (Fig. 1, Table 2). Eleven multilevel CDR procedures were performed, all of them in 2015. The number of outpatient procedures increased over time, with 68% of CDR procedures performed in the outpatient setting in 2015 (Table 3). CDR was most commonly performed in patients aged 40 to 54 years old, and 50.1% of patients were female (Table 2). The database reflected information on patients from much of the United States, with 71% of the CDR procedures performed in the South, 16.4% in the Midwest, 11.3% in the West, and <3.7% in the Northeast (Table 2).

Fig. 1.

Breakdown of cervical disc replacement procedures by number of contiguous levels treated. A question mark indicates fewer than 11 patients, where an exact number could not be obtained due to PearlDiver limitations on privacy.

Demographics of patients undergoing cervical disc replacement within the Humana database

Inpatient and outpatient status for patients undergoing cervical disc replacement by year

2. Complications

Fewer than 3.7% of patients (<11) reported new pain within 1 year after CDR, and 74.4% of patients (218) had continued pain within 1 year after CDR. Within 1 year, 12.3% (36) of patients reported a mechanical and/or bone-related complication. No patients had nerve injury within 6 months after CDR. Fewer than 11 patients (<3.7%) presented with dysphagia or dysphonia within 6 months, an infection within 3 months, an adverse reaction within 3 months, or a revision or reoperation within 1 year (Table 4). Due to PearlDiver limitations on privacy, exact numbers could not be obtained.

Overall complication rates for cervical disc replacement

3. Cost analysis

For all 293 CDR procedures and complications, the mean reimbursement cost was US $35,711.94. The mean cost was US $34,675.12 for single-level procedures and US $62,292 for multiple-level procedures (Table 5). CDR with a first instance of pain after surgery averaged a higher cost at US $50,768.80 compared with the mean cost of US $38,180.42 for patients who had continued pain. This was a nonsignificant difference (p>0.05) (Table 5). There was also no significant difference between the overall mean cost for all CDR procedures compared to the mean cost for first instance of pain (p>0.05). However, there was a significantly higher cost for patients with continued pain when compared to the overall mean (p<0.05). Mechanical and/or bone-related complication reimbursements had a mean cost of US $47,712.42. The dysphagia and dysphonia reimbursement mean cost was US $31,594.44, while wound infections had a mean cost of US $18,503.67. Adverse reactions had a mean reimbursement cost of US $52,698, and revisions and reoperations incurred a total mean cost of US $90,774.75. Total reimbursements, means, and standard deviations can be found in Table 5.

Total reimbursements for patients undergoing cervical disc replacement

Discussion

CDR is a relatively new treatment option that allows for effective discectomy, restoration of disc space height, and decompression of spinal stenosis while preserving range of motion for the patient. Well-designed studies have demonstrated no inferiority to ACDF, and even superior outcomes in patients with select indications, which has led to increased acceptance and popularity of the procedure [7-13]. Prior studies demonstrated significant increases in CDR utilization from 2006 to 2009, followed by a plateau and slight decrease in use relative to ACDF procedures in more recent years [14-17]. The results of this study differ from prior studies in that the use of CDR continued to increase nonlinearly at a rate of 17% per year from 2009 to 2015 without evidence of a plateau effect in the 7 years assessed. This may be due to the differing nature of the databases being used. The highest percentage of patients who underwent CDR were between ages 40 to 54 years old and approximately 50% were female, similar to other large database studies [18-20].

The most common complication (found in 12.3% of patients) in the first postoperative year after CDR was mechanical and/or bone-related, which included malpositioning of the implant, heterotrophic ossification, and adjacent disc degeneration. However, due to the limitations of the database data, we could not calculate the exact incidence of component malpositioning or migration, as these complications are often grouped together with other similar complications due to the overall low incidence. Another limitation was that we did not have information on the extent of ASD and whether it was symptomatic or asymptomatic.

In our study, less than 3.7% of patients had a revision or reoperation within 1 year. Zhong et al. [21], in a meta-analysis, calculated a similar reoperation rate of 4% due to device malposition, migration, subsidence, or recurring pain after CDR. In a second meta-analysis, a 7.4% incidence of neck pain, implant migration, or radiculopathy was described at 4 years postoperatively [22].

The incidence of heterotopic ossification (HO) was less than 12.3% in the current study. HO is thought to be a dynamic, progressive phenomenon, and therefore its incidence is likely affected by the length of follow-up. Two prior studies that have assessed HO at 1-year follow-up after CDR have described much higher rates of HO, ranging from 17.8% to 44.6% [23,24]. The high rate (74.4%) of continued pain after CDR noted in our study is unlikely to be continued postoperative pain but rather a result of providers continuing to code preoperative radiculopathy or cervicalgia during postoperative follow-up. The constraints of the database study limit us from fully elucidating this point, but when we go by this assumption, we can conclude that costs were higher for patients who had a new incidence of pain within 1 year after CDR.

Dysphagia was present in <3.7% of patients at 6 months after CDR. In previous studies, the incidence of dysphagia has tended to decrease with time. One study noted a 37% incidence at 1 week, 7% incidence at 6 months, and 6% incidence at 12 months postoperatively [25]. Other studies have demonstrated an approximate 11% incidence of dysphagia at 24 to 84 months after CDR [10,26]. It is unclear why an increasing rate of dysphagia was noted with longer follow-up in our current study. No nerve injuries (0%) were noted at 6 months in the current study. Previous studies have demonstrated a 0.9% to 4.1% neurologic complication rate anywhere from 2 to 7 years after CDR [8,26-28]. Infection was also present in <3.7% of patients within 3 months after CDR. This result is consistent with prior studies in the literature that documented infection rates ranging from 0% to 2.9% [8,26,28-30]. Lastly, reoperation or revision within 1 year after CDR occurred in <3.7% of patients. Other large database studies have demonstrated similarly low reoperation rates of <1%, though these studies only assessed revisions within 30 days [30].

The last aim of our study was to assess the cost associated with CDR in an administrative insurance database. The mean reimbursement cost was US $34,675.12 for single-level procedures and US $62,292 for multiple-level procedures. When including the cost of associated complications, the mean reimbursed cost increased to US $35,711.94. Cost in the PearlDiver database is determined based on the amount billed by an institution for care surrounding or related to the CDR. A study by Saifi et al. [14] determined the mean cost of CDR to be US $13,197, which was calculated as the amount billed by the hospital for the procedure, excluding physician fees. The study of Saifi et al. [14] used the National Inpatient Sample, which only allows the assessment of inpatient data. This partially explains the lower cost documented in their study compared to the present study, which captures both inpatient and outpatient cost data. A study by Radcliff et al. [19] utilized the Blue Health Intelligence database and demonstrated a cost nearly identical to the cost we determined to be associated with CDR, US $34,979.

The results of this study must be interpreted within the limitations of its design. First, a large-scale administrative database was utilized and the accuracy of the results is subject to coding error, particularly when assessing complications. Second, we only assessed postoperative complications from 3 to 12 months after CDR and thereby may be underestimating the true incidence of complications related to CDR. Additionally, PearlDiver does not release the exact number of patients if there are fewer than 11 patients in any category, and we thus had to combine similar complications into groups of related complications and we could not do further subanalysis. Lastly, the PearlDiver database is an insurance database and is not designed to be a true representative sample of the US population. Therefore, the results of this study may not be generalizable to the US population at large.

Although there are limitations to our study, there are significant strengths. First is our use of a large national database that broadly represents the US population. Second, the database allows for the longitudinal tracking of patients across the inpatient and outpatient settings, and so complications and cost are captured in both settings. Lastly, the PearlDiver database is 1 of only a few databases that allows for identification of patients using both CPT and ICD codes, allowing for more accurate identification of a particular cohort.

Conclusions

This study demonstrates that the use of CDR continues to increase in a nonlinear fashion, which contrasts with prior studies demonstrating a plateau or recent relative decrease in CDR. The most common complication, found in 12.3% of patients, was mechanical and/or bone-related, which is slightly higher than what was previously documented in other studies. Complications related to dysphagia had a lower incidence in this study compared to previously reported data. Nerve injury, infection, and reoperation occurred at a rate similar to that seen in other large database studies. Lastly, the cost of CDR calculated in this study was nearly identical to a prior study using an insurance database, further validating those results and lending evidence as to why these numbers should be used in future studies comparing the cost of CDR with the cost of ACDF.

Notes

No potential conflict of interest relevant to this article was reported.

References

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Article information Continued

Fig. 1.

Breakdown of cervical disc replacement procedures by number of contiguous levels treated. A question mark indicates fewer than 11 patients, where an exact number could not be obtained due to PearlDiver limitations on privacy.

Table 1.

Procedural and diagnostic codes used to identify patients in the PearlDiver database

Description Code
Cervical disc replacement
Single-level CPT-22856
Multi-level CPT-22858
Pain ICD-9-D-7231, ICD-9-D-7234, ICD-9-D-3369, ICD-9-D-72271, ICD-9-D-99675, ICD-9-D-99679, ICD-9-D-7295, ICD-10-D-M542, ICD-10-D-M5412, ICD-10-D-M5413, ICD-10-D-G959, ICD-10-D-M5000, ICD-10-D-T8584, ICD-10-D-M79601:M79603, ICD-10-D-M79621, ICD-10-D-M79622, ICD-10-D-M79629, ICD-10-D-M79631, ICD-10-D-M79632, ICD-10-D-M79639
Dysphagia & dysphonia ICD-9-D-78720, ICD-9-D-78729, ICD-9-D-78442, ICD-10-D-R1310, ICD-10-D-R1319, ICD-10-D-R490
Nerve injury ICD-9-D-9517, ICD-9-D-9530, ICD-9-D-9073, ICD-9-D-99812, ICD-9-D-8068, ICD-9-D-8069, ICD-9-D-9529, ICD-9-D-9072, ICD-9-D-34931, ICD-9-D-34939, ICD-9-D-34440:34442, ICD-9-D-3442, ICD-10-D-S0489, ICD-10-D-S142, ICD-10-D-M96840, ICD-10-D-M96841, ICD-10-D-S14101:S14109, ICD-10-D-G9741, ICD-10-D-G9611, ICD-10-D-G8320:G8322, ICD-10-D-G8623, ICD-10-D-G8624, ICD-10-D-G830
Mechanical & bone-related ICD-9-D-99659, ICD-9-D-V454, ICD-9-D-72810, ICD-9-D-72819, ICD-9-D-72813, ICD-9-D-99799, ICD-9-D-99640:99646, ICD-9-D-99649, ICD-10-D-T85625, ICD-10-D-T85628, ICD-10-D-M960, ICD-10-D-M679, ICD-10-D-M6150, ICD-10-D-M6158, ICD-10-D-M5030, ICD-10-D-M9689, ICD-10-D-T84498, ICD-10-D-T84039, ICD-10-D-T84029, ICD-10-D-T84019, ICD-10-D-T84049, ICD-10-D-T84059, ICD-10-D-T84069, ICD-10-D-T84119, ICD-10-D-T84129, ICD-10-D-T84199, ICD-10-D-T84498
Infection ICD-9-D-99851, ICD-9-D-99859, ICD-9-D-99660, ICD-9-D-99663, ICD-9-D-99666, ICD-9-D-99669, ICD-9-D-99667, ICD-9-D-99677, ICD-9-D-99678, ICD-10-D-T81.40:T81.43, ICD-10-D-T84.48, ICD-10-D-T84.50, ICD-10-D-T85.79, ICD-10-D-T84.7, ICD-10-D-T84.9, ICD-10-D-T84.60, ICD-10-D-T84.63
Adverse reaction ICD-9-D-99811, ICD-9-D-99812, ICD-10-D-M96830, ICD-10-D-M96831, ICD-10-D-T8481:T8483, ICD-10-D-T8485, ICD-10-D-T8586
Revisions & reoperations CPT-22864, CPT-22554, CPT-22220, CPT-22861, CPT-63075, ICD-9-P-8009, ICD-9-P-8102, ICD-9-P-8101, ICD-9-P-7739, ICD-9-P-8466, ICD-9-P-8051

CPT, Current Procedural Terminology; ICD, International Classification of Diseases.

Table 2.

Demographics of patients undergoing cervical disc replacement within the Humana database

Characteristic No. of patients (%)
Sex
 Female 147 (50.1)
 Male 146 (49.9)
Age (yr)
 25–29 <11 (<3.7)
 30–34 15 (5.1)
 35–39 34 (11.6)
 40–44 57 (19.4)
 45–49 60 (20.5)
 50–54 54 (18.4)
 55–59 28 (9.6)
 60–64 23 (7.8)
 65–69 11 (3.7)
 70–74 <11 (<3.7)
Year of procedure
 2009 15 (5.1)
 2010 16 (5.5)
 2011 11 (3.7)
 2012 <11 (<3.7)
 2013 40 (36.2)
 2014 67 (22.8)
 2015 139 (47.4)
Region
 Midwest 48 (16.4)
 Northeast <11 (<3.7)
 South 208 (71.0)
 West 33 (11.3)
Total surgeries 293

Table 3.

Inpatient and outpatient status for patients undergoing cervical disc replacement by year

Procedure type Year
2013 2014 2015
Inpatient 23 26 47
Outpatient 21 44 99
Total 44 70 146

Table 4.

Overall complication rates for cervical disc replacement

Complications No. of patients (%)
Pain
 First instance <11 (<3.7)
 Continued 218 (74.4)
Mechanical and bone-related 36 (12.3)
Dysphagia/dysphonia <11 (<3.7)
Infection <11 (<3.7)
Adverse reaction <11 (<3.7)
Revision or reoperations <11 (<3.7)
Nerve injury 0
Total surgeries 293

Table 5.

Total reimbursements for patients undergoing cervical disc replacement

Variable Total (US $) Mean±standard deviation (US $) No. of patients
Levels
 Single 9,778,385.00 34,675.12±30,341.35 282
 Multiple 685,213.00 62,292.09±28,527.74 11
Complications
 Pain
  First instance 253,844.00 50,768.80±33,396.68 <11
  Continued 8,323,331.00 38,180.42±32,268.60 218
 Mechanical and bone-related 1,717,647.00 47,712.42±49,494.71 36
 Dysphagia/dysphonia 284,350.00 31,594.44±29,366.38 <11
 Infection 55,511.00 18,503.67±8,131.62 <11
 Adverse reaction 52,698.00 52,698.00 <11
 Revision or reoperation 363,099.00 90,774.75±104,107.41 <11
 Nerve injury 0 0 0
Overall 10,463,598.00 35,711.94±30,682.92 293