Skip to main content
Journal of Clinical Medicine logoLink to Journal of Clinical Medicine
. 2023 Dec 25;13(1):114. doi: 10.3390/jcm13010114

Impact of Preoperative Frailty on Outcomes in Patients with Cervical Spondylotic Myelopathy Undergoing Anterior vs. Posterior Cervical Surgery

Aladine A Elsamadicy 1,*, Sumaiya Sayeed 1, Josiah J Z Sherman 1, Samuel Craft 1, Benjamin C Reeves 1, Sheng-Fu Larry Lo 2, John H Shin 3, Daniel M Sciubba 2
Editor: Hiroaki Nakashima
PMCID: PMC10779741  PMID: 38202121

Abstract

Introduction: Frailty has been shown to negatively influence patient outcomes across many disease processes, including in the cervical spondylotic myelopathy (CSM) population. The aim of this study was to assess the impact that frailty has on patients with CSM who undergo anterior cervical discectomy and fusion (ACDF) or posterior cervical decompression and fusion (PCDF). Materials and Methods: A retrospective cohort study was performed using the 2016–2019 national inpatient sample. Adult patients (≥18 years old) undergoing ACDF only or PCDF only for CSM were identified using ICD codes. The patients were categorized based on receipt of ACDF or PCDF and pre-operative frailty status using the 11-item modified frailty index (mFI-11): pre-Frail (mFI = 1), frail (mFI = 2), or severely frail (mFI ≥ 3). Patient demographics, comorbidities, operative characteristics, perioperative adverse events (AEs), and healthcare resource utilization were assessed. Multivariate logistic regression analyses were used to identify independent predictors of extended length of stay (LOS) and non-routine discharge (NRD). Results: A total of 37,990 patients were identified, of which 16,665 (43.9%) were in the pre-frail cohort, 12,985 (34.2%) were in the frail cohort, and 8340 (22.0%) were in the severely frail cohort. The prevalence of many comorbidities varied significantly between frailty cohorts. Across all three frailty cohorts, the incidence of AEs was greater in patients who underwent PCDF, with dysphagia being significantly more common in patients who underwent ACDF. Additionally, the rate of adverse events significantly increased between ACDF and PCDF with respect to increasing frailty (p < 0.001). Regarding healthcare resource utilization, LOS and rate of NRD were significantly greater in patients who underwent PCDF in all three frailty cohorts, with these metrics increasing with frailty in both ACDF and PCDF cohorts (LOS: p < 0.001); NRD: p < 0.001). On a multivariate analysis of patients who underwent ACDF, frailty and severe frailty were found to be independent predictors of extended LOS [(frail) OR: 1.39, p < 0.001; (severely frail) OR: 2.25, p < 0.001] and NRD [(frail) OR: 1.49, p < 0.001; (severely frail) OR: 2.22, p < 0.001]. Similarly, in patients who underwent PCDF, frailty and severe frailty were found to be independent predictors of extended LOS [(frail) OR: 1.58, p < 0.001; (severely frail) OR: 2.45, p < 0.001] and NRD [(frail) OR: 1.55, p < 0.001; (severely frail) OR: 1.63, p < 0.001]. Conclusions: Our study suggests that preoperative frailty may impact outcomes after surgical treatment for CSM, with more frail patients having greater health care utilization and a higher rate of adverse events. The patients undergoing PCDF ensued increased health care utilization, compared to ACDF, whereas severely frail patients undergoing PCDF tended to have the longest length of stay and highest rate of non-routine discharge. Additional prospective studies are necessary to directly compare ACDF and PCDF in frail patients with CSM.

Keywords: frailty, cervical spondylotic myelopathy, ACDF, PCDF, length of stay

1. Introduction

Degenerative cervical spondylosis is a common cause of disability in the elderly, with existing studies suggesting a prevalence of radiographic disc herniation in up to 90% of people over 50 years old [1]. Herniated discs, osteophytes, ossified ligaments, and other degenerative changes implicated in cervical spondylosis may cause neck pain and impinge on the spinal cord, producing neurologic dysfunction [2,3,4]. Cervical spondylotic myelopathy (CSM) frequently requires surgical intervention, with both anterior cervical discectomy and interbody fusion (ACDF) and posterior cervical decompression and fusion (PCDF) being commonly performed approaches, though debate remains as to which approach may be superior [5,6]. Given the recent increase in surgical intervention for CSM and the expected aging of the United States’ population [7,8,9], additional studies are necessary to better understand how patient risk-factors impact outcomes within these different surgical approaches.

Frailty, characterized by a reduced physiological reserve, encompasses a wide range of systemic and physiological health outcomes related to the loss of skeletal muscle mass (sarcopenia), reduced bone quality, cognitive dysfunction, and immune system impairment [10,11,12]. Given the physiological complexity and clinical relevance, frailty decision-making tools have been developed to efficiently identify frailty and predict patient outcomes; the modified frailty index (mFI) is such a tool developed using the American College of Surgeons National Surgical Quality Improvement Program (ACS-NSQIP) that has gained widespread use across medical specialties [13,14]. In spine surgery, both the mFI-5 and mFI-11 have been assessed for their ability to identify frailty and predict poor outcomes in patients undergoing surgery for degenerative spine disease [15,16], adult spinal deformity [17], spinal metastases [18], and other disorders [19]. Given the risk of perioperative complications and high healthcare resource utilization in this population [6,20,21,22], studies assessing how frailty impacts patients with degenerative CSM undergoing ACDF or PCDF is necessary for better risk assessment and surgical decision making [23].

The aim of this study was to investigate the impact of preoperative frailty on patients with CSM who undergo ACDF vs. PCDF.

2. Materials and Methods

2.1. Data Source and Patient Population

The national inpatient sample (NIS) database is a stratified discharge database from the Healthcare Cost and Utilization Project (HCUP). The NIS represents 20% of all inpatient admissions from community hospitals in the United States. It is the largest all-payer healthcare database in the US, containing over 7 million hospital admissions (approximately 35 million hospitalizations, weighted) per year. A retrospective study was performed using years 2016, 2017, 2018, and 2019 of the NIS for all adult (≥18 years old) ACDF or PCDF for CSM. The Institutional Review Board was deemed exempted due to the deidentification of patients in the NIS database. As all inpatient admissions were deidentified by HCUP, informed consent was deemed exempt as well.

The International Classification of Diseases, Tenth Revision, Clinical Modification (ICD-10-CM) diagnosis and procedural coding system (PCS) was used to identify patients and their respective comorbidities and surgical interventions. Adult patients with a primary diagnosis code of CSM (ICD-10-CM M47.12) were identified. ICD-10-CM procedural codes were then cross-matched to identify patients in the cohort undergoing ACDF (0RG10A0, 0RG20A0) or PCDF (00NW0ZZ, 0RH104Z) (Appendix A Table A1). The patients who underwent procedures with a posterior approach to the anterior column, as well as those who underwent percutaneous or endoscopic procedures, were excluded, along with patients with a history of traumatic spine fracture or spinal neoplasm (Appendix A Table A1). Additionally, patients undergoing both anterior and posterior approaches in the same indexed procedure or hospitalization were excluded.

2.2. Modified Frailty Index (mFI)

The mFI is a frailty scoring system that was developed utilizing the NSQIP [24], and a validated 11-point scoring system was created that adds 1 point each for impaired functional status, hypertension, history of chronic obstructive pulmonary disease (COPD) or pneumonia, impaired sensorium, diabetes, myocardial infarction, congestive heart failure (CHF), stroke, transient ischemic attack (TIA), percutaneous coronary intervention (PCI), and peripheral vascular disease (PVD) [13]. While originally developed for NSQIP, Subramanian et al. identified ICD-10 codes for the mFI-11 scoring system that we used for our study (Appendix A) [25]. The patients in our cohort were then identified as pre-frail (mFI = 1), frail (mFI = 2), and severely frail (mFI = 3 or more) [26].

2.3. Data Collection

Patient demographics such as age, sex, race, median household income, and insurance provider were all collected from the NIS database. Hospital characteristics such as size by bed volume, region (Northeast, South, Midwest, and West), and type (rural, urban teaching, and urban non-teaching) were also collected. The comorbidities assessed included the 11 comorbidities constituting the mFI and Elixhauser comorbidities, such as deficiency anemias, alcohol use, and paralysis. Other patient characteristics assessed were affective disorder, smoking history, cervicalgia, headache, and dorsalgia (Appendix C Table A3). The data on intraoperative variables such as the number of levels fused and the incidence of cerebrospinal fluid leak or dural tear were also collected (Appendix C Table A3).

The data regarding post-operative complications for each patient were collected by indexing additional diagnoses from the NIS database (Appendix C Table A3). The complications included in the analysis included acute kidney injury, acute post-hemorrhagic anemia, post-operative pain, acute respiratory failure, circulatory complications, mechanical ventilation, nervous system complications, urinary tract infection (UTI), sepsis, dysphagia, mechanical device complication, and displacement of internal fixation device of vertebrae (Appendix C Table A3). In addition, postoperative outcome measures such as hospital length of stay (LOS) and discharge disposition were also assessed. Discharge disposition was classified as routine (patient went home, home with healthcare services), non-routine (patient sent to short-term hospital, skilled nursing facility, intermediate care facility), and other (leaving against medical advice, died in hospital, unknown destination).

2.4. Statistical Analysis

The national estimates were calculated using discharge-level weights provided by HCUP. The parametric data were expressed as mean ± standard deviation (SD) and compared via one-way Student’s t-test. The nonparametric data were expressed as median (interquartile range) and compared via the Mann–Whitney U test. The nominal data were compared with the χ2 test. For our primary hypothesis, weighted univariate and multivariate logistic regressions were fitted with extended postoperative hospital LOS (as defined by LOS greater than the 75th percentile for the entire cohort) and non-routine discharge (NRD) disposition as the dependent variable. The patients with “other” discharge were excluded from this portion of the analysis to dichotomize routine vs. NRD. A backward stepwise multivariate logistic regression analysis was used to select variables in the final model, using 0.1 as entry and stay criteria. We forced mFI into the model in view of our primary aim. Age and female sex were also forced into the model due to the biological plausibility for confounding. A p-value of less than 0.05 was determined to be statistically significant. The statistical analysis was performed using R Studio, Version 2022.02.4+500 “Prairie Trillium” Release, RStudio Inc., Boston, MA, USA.

3. Results

3.1. Patient Demographics and Hospital Characteristics

A total of 37,990 patients were identified, of which 16,665 (43.9%) were in the pre-frail cohort, 12,985 (34.2%) were in the frail cohort, and 8340 (22.0%) were in the severely frail cohort, Table 1. Of the pre-frail cohort, 11,655 (70.0%) underwent ACDF and 5010 (30.0%) underwent PCDF, Table 1. Of the frail cohort, 8470 (65.2%) underwent ACDF and 4515 (34.8%) underwent PCDF, Table 1. The patients who underwent PCDF were significantly older than the patients who underwent ACDF across frailty cohorts (p < 0.001), and the mean patient age increased with frailty status (p < 0.001), Table 1. Race varied significantly with frailty status, with severely frail cohorts containing greater proportions of non-white patients compared to pre-frail and frail cohorts (p < 0.001), Table 1. A greater proportion of frail and severely frail patients were in the bottom income quartile compared to pre-frail patients (p < 0.001), Table 1. A significantly greater proportion of frail (p < 0.001) and severely frail (p < 0.019) patients held government insurance, Table 1.

Table 1.

Patient Demographics and Hospital Characteristics Among Pre-Frail, Frail, and Severely Frail Patients Undergoing ACDF and PCDF.

Pre-Frail
(n = 16,665)
Frail
(n = 12,985)
Severely Frail
(n = 8340)
p-Value (Totals)
ACDF
(n = 11,655)
PCDF
(n = 5010)
p-Value ACDF
(n = 8470)
PCDF
(n = 4515)
p-Value ACDF
(n = 5170)
PCDF (n = 3170) p-Value
Age (Years)
 Mean ± SD 61.06 ± 11.11 64.67 ± 10.96 <0.001 63.07 ± 10.00 66.21 ± 10.25 <0.001 64.44 ± 9.46 67.74 ± 9.29 <0.001 <0.001
Female (%) 50.4 43.2 <0.001 45.3 38.0 <0.001 37.8 33.1 0.057 <0.001
Race (%) <0.001 0.007 0.182 0.042
 White 76.0 69.1 73.4 67.2 <0.001 73.6 69.6
 Black 13.8 17.7 15.9 21.0 16.8 19.4
 Hispanic 5.8 6.5 6.3 7.4 5.2 7.1
 Other 4.3 6.6 4.3 4.4 4.5 3.9
Income Quartile (%) 0.002 0.007 0.547 <0.001
 0–25th 26.7 23.1 31.8 29.4 33.2 30.7
 26–50th 27.3 24.2 26.5 22.0 27.4 27.5
 51–75th 25.7 27.1 24.8 27.0 24.8 24.8
 76–100th 20.3 25.6 16.9 20.7 14.6 17.0
Healthcare Coverage (%) <0.001 <0.001 0.019 <0.001
 Medicare 44.8 55.7 51.4 60.9 60.8 67.5
 Medicaid 9.8 8.3 10.8 9.4 11.4 11.2
 Private
 Insurance
38.9 30.2 30.6 23.5 21.6 15.6
 Other 6.5 5.8 7.2 6.2 6.2 5.7
Hospital Bed Size (%) 0.014 <0.001 0.079 <0.001
 Small 21.3 18.1 21.1 17.1 16.0 14.7
 Medium 26.2 22.8 29.1 22.1 27.0 22.6
 Large 52.5 59.2 49.8 60.8 57.1 62.8
Hospital Region (%) <0.001 <0.001 <0.001 <0.001
 Northeast 11.7 19.1 11.8 17.1 9.3 17.4
 Midwest 17.3 22.5 17.8 25.2 23.4 28.9
 South 48.5 35.9 52.1 38.1 50.5 36.8
 West 22.5 22.6 18.3 19.6 16.8 17.0
Hospital Type (%) <0.001 <0.001 <0.001 <0.001
 Rural 2.3 2.1 2.8 2.1 3.3 5.5
 Urban Non-Teaching 23.6 11.9 20.8 9.9 22.4 11.4
 Urban
 Teaching
74.1 86.0 76.3 88.0 74.3 83.1

Bold signifies statistical significance of p-value < 0.05.

3.2. Admission and Patient Comorbidities

The comorbidity burden varied notably between cohorts. In comparing frailty cohorts, the prevalence of a number of comorbidities increased with frailty, Table 2. Within the pre-frail cohort, diabetes (ACDF: 11.2% vs. PCDF: 13.9%, p = 0.032), paralysis (ACDF: 1.8% vs. PCDF: 6.8%, p < 0.001), and cervicalgia (ACDF: 0.9% vs. PCDF: 1.8%, p = 0.042) were significantly more prevalent in patients who underwent PCDF compared to patients who underwent ACDF, Table 2. Conversely, impaired sensorium (ACDF: 18.1% vs. PCDF: 14.3%, p = 0.007) and smoking history (ACDF: 12.3% vs. PCDF: 9.3%, p = 0.015) were significantly more prevalent in patients who underwent ACDF, Table 2. The prevalence of other comorbidities was similar between pre-frail patients who underwent ACDF or PCDF, Table 2. The comorbidities that were significantly more prevalent among patients who underwent ACDF included hypertension (ACDF: 86.9% vs. PCDF: 83.3%, p = 0.039), diabetes (ACDF: 63.2% vs. PCDF: 58.4%, p = 0.046), and headache (ACDF: 3.4% vs. PCDF: 1.4%, p = 0.013), Table 2. The prevalence of other comorbidities was similar between severely frail patients who underwent ACDF or PCDF, Table 2.

Table 2.

Admission and Patient Comorbidities Among Pre-Frail, Frail, and Severely Frail Patients Undergoing ACDF and PCDF.

Pre-Frail
(n = 16,665)
Frail
(n = 12,985)
Severely Frail
(n = 8340)
p-Value (Totals)
ACDF
(n = 11,655)
PCDF
(n = 5010)
p-Value ACDF
(n = 8470)
PCDF
(n = 4515)
p-Value ACDF
(n = 5170)
PCDF
(n = 3170)
p-Value
Functional status 2.2 4.2 0.001 5.5 10.9 <0.001 16.0 22.1 0.002 <0.001
Hypertension 60.5 59.6 0.610 80.5 79.4 0.519 86.9 83.3 0.039 <0.001
History of COPD or pneumonia 4.1 3.4 0.368 14.7 12.3 0.094 41.9 39.1 0.264 <0.001
Impaired sensorium 18.1 14.3 0.007 30.4 29.0 0.456 50.7 49.5 0.647 <0.001
Diabetes 11.2 13.9 0.032 46.9 44.6 0.255 63.2 58.4 0.046 <0.001
History of MI 2.4 2.8 0.438 15.3 17.2 0.224 46.4 47.9 0.540 <0.001
History of CHF 0.4 0.7 0.315 3.1 2.3 0.245 14.9 17.5 0.173 <0.001
History of stroke 0.2 0.5 0.168 1.2 1.8 0.274 5.1 6.3 0.313 <0.001
History of TIA 0.1 0.0 0.257 0.1 0.0 0.466 0.1 0.5 0.128 0.135
History of PCI 0.0 0.1 0.127 0.1 0.0 0.465 0.3 0.5 0.544 0.001
PVD 0.7 0.6 0.674 2.2 2.5 0.614 6.8 8.0 0.327 <0.001
Deficiency anemias 0.9 1.5 0.098 1.3 2.1 0.115 1.8 3.8 0.015 <0.001
Alcohol use 1.0 1.4 0.362 2.4 4.3 0.008 3.8 6.3 0.014 <0.001
Paralysis 1.8 6.8 <0.001 3.2 6.6 <0.001 4.1 8.0 0.001 0.001
Affective disorder 26.9 25.5 0.407 29.5 25.0 0.015 34.6 33.1 0.534 <0.001
Smoking history 12.3 9.3 0.015 19.5 18.1 0.379 30.7 31.4 0.758 <0.001
Cervicalgia 0.9 1.8 0.042 0.7 0.7 0.898 0.6 0.3 0.446 0.027
Headache 3.9 3.5 0.527 3.4 2.7 0.291 3.4 1.4 0.013 0.077
Dorsalgia 11.6 11.4 0.871 12.0 12.3 0.852 12.2 11.4 0.619 0.766

Bold signifies statistical significance of p-value < 0.05.

3.3. Adverse Events

In comparing frailty cohorts, the incidence of some AEs increased with frailty, including acute kidney injury (p < 0.001), acute post-hemorrhagic anemia (p = 0.005), post-operative pain (p = 0.005), acute respiratory failure (p < 0.001), circulatory complications (p < 0.001), mechanical ventilation (p < 0.001), urinary tract infection (p < 0.001), sepsis (p < 0.001), and dysphagia (p < 0.001), Table 3. Similarly, the incidence of any complication (p < 0.001) and the number of complications increased with frailty (p < 0.001), Table 3. Within the pre-frail cohort, incidence of any complication (ACDF: 15.4% vs. PCDF: 19.3%, p = 0.008) and the number of complications (p = 0.021) was greater in patients who underwent PCDF. Dysphagia affected a greater proportion of patients who underwent ACDF (ACDF: 8.3% vs. PCDF: 2.3%, p < 0.001), Table 3. Within the frail cohort, the incidence of dysphagia was greatest among patients who underwent ACDF (ACDF: 9.9% vs. PCDF: 3.1%, p < 0.001), Table 3. There were no significant differences in incidence of any complication (ACDF: 18.8% vs. PCDF: 20.6%, p = 0.289) or the number of complications (p = 0.182) between procedure types, Table 3. Within the severely frail cohort, the incidence of any complication (ACDF: 25.3% vs. PCDF: 31.2%, p = 0.011) and the number of complications (p = 0.020) was greater among patients undergoing PCDF, Table 3. The incidence of dysphagia was greatest in patients undergoing ACDF (ACDF: 13.1% vs. PCDF: 3.9%, p < 0.001), Table 3.

Table 3.

Adverse Events Among Pre-Frail, Frail, and Severely Frail Patients Undergoing ACDF and PCDF.

Pre-Frail (n = 16,665) Frail (n = 12,985) Severely Frail
(n = 8340)
p-Value (Totals)
ACDF
(n = 11,655)
PCDF
(n = 5010)
p-Value ACDF
(n = 8470)
PCDF
(n = 4515)
p-Value ACDF
(n = 5170)
PCDF
(n = 3170)
p-Value
Acute kidney injury 1.4 3.6 <0.001 1.7 3.4 0.005 4.7 6.8 0.088 <0.001
Acute post-hemorrhagic anemia 2.4 5.1 <0.001 3.1 7.4 <0.001 3.1 7.4 <0.001 0.005
Post-operative pain 1.7 3.5 0.002 1.4 2.8 0.009 2.2 5.4 0.001 0.005
Acute respiratory failure 1.4 1.8 0.403 2.3 2.4 0.834 6.2 6.2 0.975 <0.001
Circulatory complications 0.3 0.9 0.023 0.4 0.3 0.751 1.3 1.7 0.424 <0.001
Mechanical ventilation 0.7 0.9 0.518 1.5 1.1 0.375 3.3 2.8 0.612 <0.001
Nervous system complications 1.2 2.6 0.003 0.9 2.1 0.009 0.9 2.1 0.040 0.597
UTI 1.5 2.8 0.017 2.1 5.0 <0.001 3.4 6.0 0.010 <0.001
Sepsis 0.1 0.7 0.002 0.4 0.3 0.928 1.3 1.1 0.780 <0.001
Dysphagia 8.3 2.3 <0.001 9.9 3.1 <0.001 13.1 3.9 <0.001 <0.001
Any complication 15.4 19.3 0.008 18.8 20.6 0.289 25.3 31.2 0.011 <0.001
Number of complications 0.021 0.182 0.020 <0.001
 0 84.4 80.7 81.2 78.8 75.2 69.1
 1 12.7 14.7 14.9 15.4 16.8 21.8
 2 2.0 3.6 3.0 4.1 4.5 6.3
 ≥3 0.9 1.0 1.0 1.7 3.5 2.8

Bold signifies statistical significance of p-value < 0.05.

3.4. Postoperative Inpatient Outcomes

Comparing the frailty cohorts, healthcare resource utilization varied significantly between cohorts. The mean LOS (p < 0.001) and NRD rate (p < 0.001) increased significantly with increasing frailty, Table 4. Within the pre-frail cohort, mean LOS (ACDF: 2.3 ± 2.7 days vs. PCDF: 4.1 ± 4.1 days, p < 0.001) and NRD rate (ACDF: 9.0% vs. PCDF: 28.7%, p < 0.001) were significantly greater among patients who underwent PCDF compared to patients who underwent ACDF, Table 4. Within the frail cohort, mean LOS (ACDF: 2.7 ± 3.3 days vs. PCDF: 5.0 ± 7.8 days, p < 0.001) and NRD rate (ACDF: 14.7% vs. PCDF: 39.6%, p < 0.001) were significantly greater among patients who underwent PCDF compared to patients who underwent ACDF, Table 4. Within the severely frail cohort, mean LOS (ACDF: 4.0 ± 5.6 days vs. PCDF: 6.2 ± 6.1 days, p < 0.001) and NRD rate (ACDF: 22.6% vs. PCDF: 46.4%, p < 0.001) were significantly greater among patients who underwent PCDF compared to patients who underwent ACDF, Table 4.

Table 4.

Postoperative Inpatient Outcomes Among Pre-Frail, Frail, and Severely Frail Patients Undergoing ACDF and PCDF.

Pre-Frail
(n = 16,665)
Frail
(n = 12,985)
Severely Frail
(n = 8340)
p-Value (Totals)
ACDF
(n = 11,655)
PCDF
(n = 5010)
p-Value ACDF
(n = 8470)
PCDF
(n = 4515)
p-Value ACDF
(n = 5170)
PCDF
(n = 3170)
p-Value
Length of stay (days)
 Mean ± SD 2.3 ± 2.7 4.1 ± 4.1 <0.001 2.7 ± 3.3 5.0 ± 7.8 <0.001 4.0 ± 5.6 6.2 ± 6.1 <0.001 <0.001
 Median
 [IQR]
1 [1, 2] 3 [2, 5] <0.001 2 [1, 3] 3 [2, 6] <0.001 2 [1, 5] 4 [3, 8] <0.001 <0.001
Disposition (%) <0.001 <0.001 <0.001 <0.001
 Routine 90.8 71.1 85.2 59.9 76.2 53.0
 Non-Routine 9.0 28.7 14.7 39.6 22.6 46.4
 Other 0.2 0.2 0.2 0.4 1.2 0.6

Bold signifies statistical significance of p-value < 0.05.

3.5. Multivariate Regression for Healthcare Utilization for ACDF

On multivariate analysis for extended LOS in patients who underwent ACDF, extended LOS increased with frailty status compared to pre-frail, frailty [OR (CI): 1.39 (1.15, 1.68), p < 0.001], and severe frailty [OR (CI): 2.25 (1.83, 2.76), p < 0.001], Table 5. On multivariate analysis for NRD in patients who underwent ACDF, NRD increased with frailty status compared to pre-frail, frailty [OR (CI): 1.49 (1.21, 1.84), p < 0.001], and severe frailty [OR (CI): 2.22 (1.77, 2.79), p < 0.001], Table 5.

Table 5.

Multivariate Regression for Healthcare Utilization for ACDF.

Extended LOS (>3 Days) p-Value Non-Routine Discharge p-Value
mFI-11
 Pre-Frail Reference
 Frail 1.39 (1.15, 1.68) <0.001 1.49 (1.21, 1.84) <0.001
 Severely
 Frail
2.25 (1.83, 2.76) <0.001 2.22 (1.77, 2.79) <0.001
Age 1.00 (0.99, 1.01) 0.382 1.04 (1.03, 1.06) <0.001
Female sex 0.99 (0.84, 1.16) 0.888 0.96 (0.81, 1.15) 0.691
Race
 White Reference
 Black 2.08 (1.67, 2.58) <0.001 2.29 (1.80, 2.91) <0.001
 Hispanic 1.72 (1.27, 2.34) <0.001 1.62 (1.13, 2.31) 0.008
 Other 1.75 (1.19, 2.56) 0.004 1.48 (1.00, 2.19) 0.049
Income Quartile
 0–25th Reference
 26–50th 0.93 (0.76, 1.15) 0.510 1.05 (0.82, 1.33) 0.673
 51–75th 0.84 (0.68, 1.04) 0.117 1.02 (0.79, 1.32) 0.867
 76–100th 0.68 (0.52, 0.89) 0.005 0.73 (0.54, 0.99) 0.040
Healthcare Coverage
 Medicare Reference
 Medicaid 1.20 (0.89, 1.61) 0.225 1.05 (0.71, 1.53) 0.821
 Private
 Insurance
0.71 (0.58, 0.88) 0.002 0.58 (0.45, 0.76) <0.001
 Other 1.05 (0.75, 1.46) 0.792 0.57 (0.37, 0.86) 0.007
Hospital Bed Size
 Small Reference
 Medium 1.39 (1.05, 1.83) 0.020 Removed -
 Large 2.00 (1.56, 2.57) <0.001 Removed -
Hospital Region
 Northeast
 Midwest Removed - Removed -
 South Removed - Removed -
 West Removed - Removed -
Hospital Type
 Rural Reference
 Urban Non-Teaching Removed - 0.91 (0.51, 1.63) 0.747
 Urban
 Teaching
Removed - 1.08 (0.62, 1.89) 0.783
Fusion Levels
 One level Reference
 Two or more Removed - Removed -
Number of Complications
 0 Reference
 1 4.79 (3.98, 5.78) <0.001 2.82 (2.27, 3.51) <0.001
 2 15.16 (10.19, 22.57) <0.001 5.49 (3.75, 8.02) <0.001
 >2 50.14 (23.33, 107.78) <0.001 13.74 (8.02, 23.54) <0.001
Length of Stay - - - -

Removed refers to variables that were included in the univariate regression analysis but did not meet entry criteria (p < 0.1) for the multivariate. Bold signifies statistical significance of p-value < 0.05.

3.6. Multivariate Regression for Healthcare Utilization for PCDF

On multivariate analysis for extended LOS in patients who underwent PCDF, extended LOS increased with frailty status compared to pre-frail, frailty [OR (CI): 1.58 (1.23, 2.03), p < 0.001], and severe frailty [OR (CI): 2.45 (1.88, 3.20), p < 0.001], Table 6. On multivariate analysis for NRD in patients who underwent PCDF, NRD increased with frailty status compared to pre-frail, frailty [OR (CI): 1.55 (1.26, 1.90), p < 0.001], and severe frailty [OR (CI): 1.63 (1.28, 2.07), p < 0.001], Table 6.

Table 6.

Multivariate Regression for Healthcare Utilization for PCDF.

Extended LOS (>6 Days) p-Value Non-Routine Discharge p-Value
mFI-11
 Pre-Frail Reference
 Frail 1.58 (1.23, 2.03) <0.001 1.55 (1.26, 1.90) <0.001
 Severely
 Frail
2.45 (1.88, 3.20) <0.001 1.63 (1.28, 2.07) <0.001
Age 1.02 (1.01, 1.04) 0.002 1.06 (1.05, 1.07) <0.001
Female sex 0.96 (0.77, 1.20) 0.719 1.26 (1.04, 1.52) 0.016
Race
 White Reference
 Black 1.89 (1.45, 2.45) <0.001 1.71 (1.35, 2.17) <0.001
 Hispanic 1.35 (0.92, 1.98) 0.122 1.37 (0.96, 1.96) 0.079
 Other 1.19 (0.72, 1.96) 0.498 1.06 (0.71, 1.59) 0.766
Income Quartile
 0–25th Reference
 26–50th Removed - Removed -
 51–75th Removed - Removed -
 76–100th Removed - Removed -
Healthcare Coverage
 Medicare Reference
 Medicaid 1.75 (1.15, 2.68) 0.010 0.95 (0.65, 1.38) 0.786
 Private
 Insurance
1.14 (0.82, 1.57) 0.441 0.59 (0.45, 0.77) <0.001
 Other 1.47 (0.91, 2.35) 0.113 0.60 (0.39, 0.92) 0.020
Hospital Bed Size
 Small Reference
 Medium 1.47 (1.01, 2.16) 0.047 1.44 (1.04, 1.99) 0.026
 Large 1.58 (1.13, 2.23) 0.008 1.40 (1.05, 1.87) 0.021
Hospital Region
 Northeast Reference
 Midwest Removed - 0.76 (0.57, 1.02) 0.071
 South Removed - 0.67 (0.52, 0.87) 0.003
 West Removed - 0.65 (0.49, 0.87) 0.004
Hospital Type
 Rural Reference
 Urban Non-Teaching Removed - Removed -
 Urban
 Teaching
Removed - Removed -
Fusion Levels
 One level Reference
 Two or more Removed - Removed -
Number of Complications
  0 Reference
 1 3.51 (2.75, 4.51) <0.001 2.63 (2.08, 3.33) <0.001
 2 7.13 (4.69, 10.82) <0.001 4.09 (2.66, 6.30) <0.001
 >2 39.60 (14.85, 105.56) <0.001 8.29 (3.96, 17.35) <0.001
Length of Stay Removed - Removed -

Bold signifies statistical significance of p-value < 0.05.

4. Discussion

In this retrospective national database study of 37,990 patients who underwent ACDF or PCDF for CSM, we found that patient frailty independently impacts ACDF and PCDF patients similarly, with an overall increase in healthcare resource utilization within the PCDF patients.

The decision to pursue anterior vs. posterior approaches for CSM is multifactorial and has been discussed previously, as delineated in Table 7. In a retrospective study of 140 patients who underwent anterior or posterior decompression for CSM, Audat et al. found that neck disability index (NDI) score and radiographic outcomes were similar between approach cohorts at five year follow-up [27]. Similarly, in a systematic review of eight level III retrospective cohort studies of patients who underwent decompression for CSM, Lawrence et al. demonstrated that while incidence of infection and dysphagia varied between approaches, there was no clear generalizable advantage to either an anterior approach (discectomy or corpectomy) or a posterior approach (laminectomy only, laminectomy with fusion, or laminoplasty) for multilevel CSM with respect to treatment effectiveness or safety and suggested that an individualized decision-making strategy is necessary to select the preferred treatment for each patient [28]. Furthermore, in a meta-analysis of ten non-randomized controlled trials evaluating the clinical efficacy of anterior and posterior approaches for multilevel CSM, Luo et al. determined that no clear conclusion could be reached regarding which approach is more efficacious for multilevel CSM [29]. A review comparing the anterior and posterior approaches for degenerative cervical myelopathy by Kato et al. suggests selecting an approach based on radiographic features contributing to spinal cord compression [30]. For example, in cases of CSM due to disc herniation, an anterior approach may be preferred, though a posterior approach may be ideal in CSM related to ligamentum flavum ossification due to the relative ease of accessing these structures with the respective approaches [30,31,32].

Table 7.

Review of Anterior and Posterior Surgical Approaches to Treatment of CSM.

Authors Study Type Key Findings
Wilson JRF et al., 2020 [23] Retrospective study MFI-defined frailty was a more effective predictor of poor outcomes than age alone, with increasing frailty being associated with increased incidence of perioperative complications, increased hospital LOS, and NRD.
Audat ZA et al., 2018 [27] Retrospective study NDI score and radiographic outcomes were similar between anterior and posterior approach cohorts at five year follow-up.
Lawrence BD et al., 2013 [28] Systematic review There was no clear generalizable advantage to either an anterior or posterior approach for multilevel CSM with respect to treatment effectiveness or safety.
Luo J et al., 2015 [29] Meta-analysis No clear conclusion could be reached regarding which approach is more efficacious for multilevel CSM.
Kato S et al., 2018 [30] Review Authors suggest choosing a surgical approach based on radiographic features contributing to spinal cord compression.
Zhu B et al., 2013 [31] Systematic review and meta-analysis In cases of CSM due to disc herniation, an anterior approach may be preferred.
Feng F et al., 2016 [32] Systematic review and meta-analysis A posterior approach may be ideal in CSM related to ligamentum flavum ossification due to the relative ease of accessing these structures, although the anterior approach had better overall postoperative neural function.
Hitchon PW et al., 2019 [33] Retrospective cohort study The anterior approach saw benefits in hospital LOS and restoration of physiologic cervical lordosis compared to the posterior approach, despite similar outcomes in complications, quality of life, and sagittal balance.
Wilkerson CF et al., 2022 [34] Retrospective study The anterior approach was associated with greater improvements in NDI score at both the 3-month and 12-month follow-ups.
Chen Z et al., 2017 [35] Meta-analysis The anterior approach was associated with better postoperative neurologic function.
El-Ghandour NMF et al., 2020 [36] RCT The anterior approach was superior with respect to postoperative pain, NDI score, and hospital LOS, though the posterior approach was associated with reduced incidence of postoperative dysphagia and shorter operative time.
Ghogawala Z et al., 2021 [37] RCT While postoperative complications were significantly more common in the anterior surgery group (including dysphagia, new neurological deficit, 30-day readmission, and reoperation), there were no significant differences in patient-reported outcomes at one year follow-up.
Badhiwala JH et al., 2020 [38] Post hoc analysis Frailty and comorbidities negatively impact functional outcomes in CSM patients undergoing decompression.
Momtaz D et al., 2022 [39] Retrospective study Patient frailty was associated with postoperative AEs, readmission, and reoperation following ACDF.
Elsamadicy AA et al., 2023 [40] Retrospective cohort study Patient frailty was associated with greater AE risk, prolonged hospital LOS, increased rate of NRD, and higher admission costs.
Shin JI et al., 2017 [41] Retrospective cohort study MFI-11-defined frailty was an independent predictor of life-threatening single/multiorgan dysfunction in both the ACDF and posterior cervical fusion cohorts.
Lambrechts MJ et al., 2017 [42] Retrospective cohort study While mFI-11-defined frailty did not significantly impact complication rates, 90-day readmission rates, reoperation rates, or patient-reported outcome measures, patients with severe frailty were significantly more likely to experience longer LOS and NRD.
Medvedev G et al., 2016 [43] Retrospective study In patients who underwent posterior cervical fusion, frailty was predictive of blood transfusion, prolonged extubation greater than 48 h, reintubation, readmission, and reoperation.
Young R et al., 2020 [44] Observational Patients undergoing elective cervical or lumbar surgeries had lower postoperative opioid use and LOS after ERAS implementation.
Bansal T et al., 2022 [45] Narrative review Across many spine surgeries, ERAS protocols reduce health care utilization and involve multimodal pain management and early mobilization.
Elsarrag M et al., 2019 [46] Systematic review ERAS protocols may decrease LOS, costs, and pain in spine surgery.
Debono B et al., 2019 [47] Retrospective study Use of ERAS protocols in patients with ACDF, anterior lumbar interbody fusion, and posterior lumbar fusion led to decreased LOS and improved patient satisfaction.
Soffin EM et al., 2019 [48] Retrospective study Implementation of a multidisciplinary ERAS protocol was feasible and safe, with no 90-day readmissions, among patients who underwent ACDF or cervical arthroplasty.
Debono B et al., 2021 [49] Retrospective study ERAS protocol implementation was associated with a significant reduction in hospital LOS, without increasing risk of postoperative complications.

Other studies have suggested that the anterior approach is the preferred approach in most cases of CSM [33,34,35,36]. In a retrospective cohort study of 89 patients who underwent anterior or posterior decompression surgery for CSM at a single institution, Hitchon et al. recommended the anterior approach due to the benefits in hospital LOS and restoration of physiological cervical lordosis compared to the posterior approach, despite similar outcomes in complications, quality of life, and sagittal balance [33]. Similarly, in a multi-institutional database study of 1151 patients who underwent decompression surgery for CSM, Wilkerson et al. observed that after controlling for baseline differences between patients who underwent anterior or posterior surgery, the anterior approach was associated with greater improvements in NDI score at both the 3 month and 12 month follow-ups [34]. A similar conclusion was made in a meta-analysis of 25 studies including 1843 patients who underwent decompression for CSM [35]. However, no large, prospective randomized clinical trials (RCT) have been published in the literature. In a small, single institutional RCT of 68 patients who underwent surgery for multilevel degenerative cervical myelopathy, El-Ghandour et al. found that the anterior approach was superior with respect to postoperative pain, NDI score, and hospital LOS, though the posterior approach was associated with reduced incidence of postoperative dysphagia and shorter operative time [36]. In a more recently published RCT of 163 patients randomized to anterior surgery (ACDF) or posterior surgery (laminectomy with fusion or laminoplasty) at fifteen large hospitals in the U.S. and Canada, Ghogawala et al. found that while postoperative complications were significantly more common in the anterior surgery group (including dysphagia, new neurological deficit, 30-day readmission, and reoperation), there were no significant differences in patient-reported outcomes at one year follow-up [37]. Our study demonstrated similar findings with regards to rates of dysphagia for the ACDF cohort; however, the length of hospitalizations and total number of complications were increased in the PCDF cohort in comparison. Additional studies may be warranted to better elucidate the clinical and radiographical criteria for the varying approaches.

Frailty has been suggested to contribute to the progression of CSM and suboptimal improvement in patient outcomes following both anterior and posterior decompressive approaches [38]. In a retrospective NSQIP database study of 17,662 patients who underwent ACDF for a number of indications, Momtaz et al. found that patient frailty was associated with postoperative AEs, readmission, and reoperation following ACDF [39]. Additionally, in a multi-institutional NSQIP database study of 41,369 patients who underwent surgery for CSM from 2010 to 2018, Wilson et al. found that mFI-defined frailty was a more effective predictor of poor outcomes than age alone, with increasing frailty being associated with increased incidence of perioperative complications, increased hospital LOS, and NRD [23]. Similarly, in a retrospective NIS database cohort study of 29,305 patients who underwent ACDF for CSM, Elsamadicy et al. found that patient frailty, was associated with greater AE risk, prolonged hospital LOS and increased rate of NRD [40]. Similar findings have been shown with posterior approach as well. In a retrospective cohort study of 6965 patients who underwent ACDF or posterior cervical fusion, Shin et al. demonstrated that mFI-11-defined frailty was an independent predictor of Clavien-Dindo grade IV complications (life-threatening single/multiorgan dysfunction requiring intermediate care or intensive care unit management) in both the ACDF and posterior cervical fusion cohorts [41]. Similarly, in a retrospective cohort study of 165 patients who underwent PCDF at an academic medical center from 2014 to 2020, Lambrechts et al. found that while mFI-11-defined frailty did not significantly impact complication rates, 90-day readmission rates, reoperation rates, or patient-reported outcome measures, patients with severe frailty were significantly more likely to experience longer LOS and NRD [42]. Additionally, in a retrospective NSQIP study of 5627 patients who underwent posterior cervical fusion, Medvedev et al. found that frailty was predictive of blood transfusion, prolonged extubation greater than 48 h, reintubation, readmission, and reoperation [43]. In the present study utilizing the mFI-11 to identify frailty, we found that increasing frailty influenced increasing postoperative AEs and experiencing greater hospital LOS and rates of NRD. Given the increased risk of suboptimal outcomes in frail patients who undergo decompression for CSM, preoperative identification of frailty and patient preoptimization are necessary.

As increased frailty has a negative impact on clinical outcomes, these outcomes may then disproportionately affect patients who are socioeconomically disadvantaged. Our study found that the frail and severely frail cohorts contained a significantly higher proportion of non-white patients, patients in the lowest income quartile, and those covered by government insurance. Moreover, on multivariate analysis, non-white race was independently associated with greater odds of increased LOS and NRD, while being in the highest income quartile or having private insurance was associated with lower odds of increased LOS and NRD among patients undergoing ACDF. Among patients undergoing PCDF, black race and having Medicaid insurance were associated with higher odds of increased LOS. Thus, our present study indicates that not only do socioeconomically disadvantaged groups have greater frailty scores but also that they are associated with poorer hospital outcomes. Because of the impact on clinical outcomes, it is crucial that healthcare delivery continues to be equitable and target patients’ individual needs.

With the increased identification of risk factors associated with poor outcomes following spine surgery, many have sought to develop methods to improve perioperative patient optimization to reduce complications and improve efficiency of healthcare delivery while maintaining patient safety [44]. These methods, commonly referred to as enhance recovery after surgery (ERAS) protocols, include optimizing nutrition, incorporating multimodal pain control, encouraging early ambulation, and limiting urinary catheterization, with the goal of improving patient outcomes [45]. In spine surgery, implementation of ERAS protocols has been shown to reduce opioid consumption, hospital LOS, and accelerate time to ambulation following surgery [44,45,46,47]. More specifically, some have sought to determine how implementation of ERAS protocols may affect outcomes following cervical spine surgery [48,49]. In a retrospective study of 33 patients who underwent ACDF or cervical arthroplasty for numerous indications, Soffin et al. found that implementation of a multidisciplinary ERAS protocol was feasible and safe, with no 90-day readmissions [48]. In a retrospective study of 404 propensity score-matched patients who underwent ACDF for degenerative cervical radiculopathy at a single institution, Debono et al. observed that ERAS protocol implementation was associated with a significant reduction in hospital LOS, without increasing risk of postoperative complications [49]. To our knowledge, no studies have assessed the effectiveness of an ERAS protocol for North American patients with high frailty scores who undergo cervical spine surgery specifically for CSM. Given that in our study, we found that severely frail patients had longer hospital stays and greater rates of non-routine discharge, utilizing protocols that would encourage early ambulation, effective pain management, and shorter length of stay may prove especially useful for this population. Thus, additional studies are necessary to determine whether an ERAS protocol similar to those utilized in other populations would be effective in the CSM population and how patient frailty may affect ERAS protocol effectiveness.

This study has some limitations that may have implications on interpretation and generalizability. Although all variables were recorded preoperatively, intraoperatively, and postoperatively, they were reviewed retrospectively and, thus, are subject to the limitations of retrospective analyses. Given that the diagnoses in the NIS database are organized by diagnostic codes, some collected data have been misclassified, incomplete, or incorrectly identified in the database. Additionally, while the NIS database offers a relatively high sample size, some granular patient- and hospital-level details may be missed. Moreover, we are not able to control for the degree of neurological injury and radiographic stenosis, two key aspects of the clinical presentation that may impact surgical decision-making, postoperative recovery, and length of stay, and non-routine discharge. Similarly, the data regarding unplanned hospital readmission and reoperation rates are not available in the NIS. Furthermore, the impact of frailty is assessed after the decision for surgical intervention is made, and we are limited by the NIS database to assess the varying degrees of frailty in all patients considered for surgery. Because we only included patients who underwent surgical procedures, we cannot generalize to all patients with CSM, many of whom may not have received surgery and only received medical management due to their high frailty status. Finally, we are also limited by a potential selection bias that may have occurred, and our sample may not represent the entire population as a whole. Despite these limitations, this study sheds light on the impact that preoperative frailty has on complications and healthcare resource utilization in patients who undergo anterior or posterior decompression and fusion for CSM.

5. Conclusions

Our study suggests that preoperative frailty may impact outcomes after surgical treatment for CSM, with more frail patients having greater health care utilization and a higher rate of adverse events. Patients undergoing PCDF increased health care utilization, compared to ACDF; thus, severely frail patients undergoing PCDF tended to have the longest length of stay and highest rate of non-routine discharge. Additional prospective studies are necessary to identify the optimum surgical approach in frail patients incorporating clinical and radiographic metrics.

Appendix A

Table A1.

Inclusion and Exclusion Criteria.

Diagnosis or Procedure ICD-10 Codes
Inclusion
ACDF 0RG10A0, 0RG20A0
Cervical Laminectomy 00NW0ZZ
Cervical Internal Fixation 0RH104Z
Exclusion
Traumatic spinal fracture S12.0x, S12.1x, S12.2x, S12.4x, S12.5x, S12.6x, S12.8x, S17.x, S22.0x, S32.0x, S32.1x
Neoplasms of vertebral column, spinal cord, meninges of spinal cord C41.2, C41.9, C70.1, C70.9, C72.0, C72.1, C72.9
Percutaneous/Endoscopic Posterior cervical fusion, Posterior approach to Anterior Column 0RG207J, 0RG20AJ, 0RG20JJ, 0RG20KJ, 0RG2371, 0RG237J, 0RG23AJ, 0RG23J1, 0RG23JJ, 0RG23K1, 0RG23KJ, 0RG2471, 0RG247J, 0RG24AJ, 0RG24J1, 0RG24JJ, 0RG24K1, 0RG24KJ, 0RG107J, 0RG10AJ, 0RG10JJ, 0RG10KJ, 0RG1371, 0RG137J, 0RG13AJ, 0RG13J1, 0RG13JJ, 0RG13K1, 0RG13KJ, 0RG1471, 0RG147J, 0RG14AJ, 0RG14J1, 0RG14JJ, 0RG14K1, 0RG14KJ

Appendix B

Table A2.

Modified Frailty Index.

Comorbidities in mFI-11 ICD-10 Codes
Functional status H54, R26.0-R26.9, R27.0-R27.9, R41, R41.81, R54, S72, Z73, Z74.1, Z73.6, Z74
History of hypertension requiring medication I10, I11, I12, I13, I15
History of chronic obstructive pulmonary disease or pneumonia J12, J13, J14, J15, J16, J17, J18, J43, J44
History of impaired sensorium A81.0, F00-F03, F01, F04, F05, F06, F10, F11-F19, G20, G30, H35
History of diabetes mellitus E10, E11, E13, E14
History of myocardial infarction I21, I22, I25
History of congestive heart failure I50, U80.2
History of stroke with neurologic deficit I61, I63, I69
History of TIA or stroke without neurological deficit G45
History of PCI, angina, or stenting I20
History of peripheral vascular disease or ischemic rest pain I70.2, I73, I77.9, I77.1

Appendix C

Table A3.

ICD-10 Codes for Patient Characteristics, Intraoperative Variables, and Adverse Events.

Diagnosis or Procedure ICD-10 Codes
Affective disorder F30.x, F31.x, F32.x, F33.x, F34.x, F41.x
Smoking history F17210, F17213, F17290, F17293
Cervicalgia M542
Headache G441, R51, G43909, G43919, G43901, G43911
Dorsalgia M54, M540, M5400, M5401, M5402, M5403, M5404, M5405, M5406, M5407, M5408, M5409M541, M5410, M5411, M5412, M5413, M5414, M5415, M5416, M5417, M5418, M542, M543, M5430, M5431, M5432, M544, M5440, M5441, M5442, M545, M546, M548, M5481, M5489, M549
Fusion of 1 cervical level 0RG10A0, 0RG1071, 0RG10J1, 0RG10K1
Fusion of 2 or more cervical levels 0RG20A0, 0RG2071, 0RG20J1, 0RG20K1
CSF leak or dural tear G96.0, G96.1, G96.11
Acute kidney injury N170, N171, N172, N178, N179
Acute post-hemorrhagic anemia D62
Post-operative pain G8918
Acute respiratory failure J810, J952, J9582, J95821, J95822, J95831, J960, J9600, J9601, J9602, J962, J9620, J9621, J9622
Circulatory complications I97, I970, I971, I9711, I97110, I97111, I9712, I97120, I97121, I9713, I97130, I97131, I9719, I97190, I97191, I972, I973, I974, I9741, I97410, I97411, I97418, I9742, I975, I9751, I9752, I976, I9761, I97610, I97611, I97618, I9762, I97620, I97621, I97622, I9763, I97630, I97631, I97638, I9764, I97640, I97641, I97648, I977, I9771, I97710, I97711, I9779, I97790, I97791, I978, I9781, I97810, I97811, I9782, I97820, I97821, I9788, I9789
Mechanical ventilation 09HN7BZ, 09HN8BZ, 0BH13EZ, 0BH17EZ, 0BH18EZ, 5A19054, 5A1935Z, 5A1945Z, 5A1955Z
Nervous system complications G97.82
UTI N39.0
Sepsis A41, A410, A4101, A4102, A411, A412, A413, A414, A415, A4150, A4151, A4152, A4153, A4159, A418, A4181, A4189, A419
Dysphagia R13, R130, R131, R1310, R1311, R1312, R1313, R1314, R1319
Mechanical device complication T84216, T84216A, T84218, T84218A, T84226, T84226A, T84228, T84228A, T84296, T84296A, T84298, T84298A, T8431, T84310, T84310A, T84318, T84318A, T8432, T84320, T84320A, T84328, T84328A, T8439, T84390, T84390A, T84398, T84398A
Displacement of internal fixation device of vertebrae T84226A

Author Contributions

Conceptualization, A.A.E.; methodology, A.A.E. and S.S.; software, S.S.; formal analysis, A.A.E. and S.S.; data curation, S.S.; writing—original draft preparation, J.J.Z.S., S.C. and B.C.R.; writing—review and editing, A.A.E., S.S., S.-F.L.L., J.H.S. and D.M.S.; supervision, A.A.E., S.-F.L.L., J.H.S. and D.M.S. All authors have read and agreed to the published version of the manuscript.

Institutional Review Board Statement

The Institutional Review Board was deemed exempted due to the deidentification of patients in the NIS database. As all inpatient admissions were deidentified by HCUP, informed consent was deemed exempt as well.

Informed Consent Statement

As all inpatient admissions were deidentified by HCUP, informed consent was deemed exempt.

Data Availability Statement

Data used for this study is from the National Inpatient Sample, publicly available from the Healthcare Cost and Utilization Project. More information can be found at http://www.hcup-us.ahrq.gov/nisoverview.jsp (accessed on 20 November 2023).

Conflicts of Interest

The authors declare no conflicts of interest.

Funding Statement

The authors received no external funding.

Footnotes

Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

References

  • 1.Theodore N. Degenerative Cervical Spondylosis. N. Engl. J. Med. 2020;383:159–168. doi: 10.1056/NEJMra2003558. [DOI] [PubMed] [Google Scholar]
  • 2.Baron E.M., Young W.F. Cervical spondylotic myelopathy: A brief review of its pathophysiology, clinical course, and diagnosis. Neurosurgery. 2007;60:S35–S41. doi: 10.1227/01.NEU.0000215383.64386.82. [DOI] [PubMed] [Google Scholar]
  • 3.Young W.F. Cervical spondylotic myelopathy: A common cause of spinal cord dysfunction in older persons. Am. Fam. Physician. 2000;62:1064–1070, 1073. [PubMed] [Google Scholar]
  • 4.Sobański D., Staszkiewicz R., Stachura M., Gadzieliński M., Grabarek B.O. Presentation, Diagnosis, and Management of Lower Back Pain Associated with Spinal Stenosis: A Narrative Review. Med. Sci. Monit. Int. Med. J. Exp. Clin. Res. 2023;29:e939237-1. doi: 10.12659/MSM.939237. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Rowland L.P. Surgical treatment of cervical spondylotic myelopathy: Time for a controlled trial. Neurology. 1992;42:5–13. doi: 10.1212/WNL.42.1.5. [DOI] [PubMed] [Google Scholar]
  • 6.Wang M.C., Chan L., Maiman D.J., Kreuter W., Deyo R.A. Complications and mortality associated with cervical spine surgery for degenerative disease in the United States. Spine. 2007;32:342–347. doi: 10.1097/01.brs.0000254120.25411.ae. [DOI] [PubMed] [Google Scholar]
  • 7.Patil P.G., Turner D.A., Pietrobon R. National trends in surgical procedures for degenerative cervical spine disease: 1990–2000. Neurosurgery. 2005;57:753–758. doi: 10.1227/01.NEU.0000175729.79119.1d. discussion 753-8. [DOI] [PubMed] [Google Scholar]
  • 8.Marquez-Lara A., Nandyala S.V., Fineberg S.J., Singh K. Current trends in demographics, practice, and in-hospital outcomes in cervical spine surgery: A national database analysis between 2002 and 2011. Spine. 2014;39:476–481. doi: 10.1097/BRS.0000000000000165. [DOI] [PubMed] [Google Scholar]
  • 9.Neifert S.N., Martini M.L., Yuk F., McNeill I.T., Caridi J.M., Steinberger J., Oermann E.K. Predicting Trends in Cervical Spinal Surgery in the United States from 2020 to 2040. World Neurosurg. 2020;141:e175–e181. doi: 10.1016/j.wneu.2020.05.055. [DOI] [PubMed] [Google Scholar]
  • 10.Clegg A., Young J., Iliffe S., Rikkert M.O., Rockwood K. Frailty in elderly people. Lancet. 2013;381:752–762. doi: 10.1016/S0140-6736(12)62167-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Panayi A., Orkaby A., Sakthivel D., Endo Y., Varon D., Roh D., Orgill D., Neppl R., Javedan H., Bhasin S., et al. Impact of frailty on outcomes in surgical patients: A systematic review and meta-analysis. Am. J. Surg. 2019;218:393–400. doi: 10.1016/j.amjsurg.2018.11.020. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Agarwal N., Goldschmidt E., Taylor T., Roy S., Dunn S.C.A., Bilderback A., Friedlander R.M., Kanter A.S., Okonkwo D.O., Gerszten P.C., et al. Impact of Frailty on Outcomes Following Spine Surgery: A Prospective Cohort Analysis of 668 Patients. Neurosurgery. 2021;88:552–557. doi: 10.1093/neuros/nyaa468. [DOI] [PubMed] [Google Scholar]
  • 13.Subramaniam S., Aalberg J.J., Soriano R.P., Divino C.M. New 5-Factor Modified Frailty Index Using American College of Surgeons NSQIP Data. J. Am. Coll. Surg. 2018;226:173–181.e8. doi: 10.1016/j.jamcollsurg.2017.11.005. [DOI] [PubMed] [Google Scholar]
  • 14.Tsiouris A., Hammoud Z.T., Velanovich V., Hodari A., Borgi J., Rubinfeld I. A modified frailty index to assess morbidity and mortality after lobectomy. J. Surg. Res. 2013;183:40–46. doi: 10.1016/j.jss.2012.11.059. [DOI] [PubMed] [Google Scholar]
  • 15.Elsamadicy A.A., Freedman I.G., Koo A.B., David W.B., Reeves B.C., Havlik J., Pennington Z., Kolb L., Shin J.H., Sciubba D.M. Modified-frailty index does not independently predict complications, hospital length of stay or 30-day readmission rates following posterior lumbar decompression and fusion for spondylolisthesis. Spine J. 2021;21:1812–1821. doi: 10.1016/j.spinee.2021.05.011. [DOI] [PubMed] [Google Scholar]
  • 16.Flexman A.M., Charest-Morin R., Stobart L., Street J., Ryerson C.J. Frailty and postoperative outcomes in patients undergoing surgery for degenerative spine disease. Spine J. 2016;16:1315–1323. doi: 10.1016/j.spinee.2016.06.017. [DOI] [PubMed] [Google Scholar]
  • 17.Yagi M., Michikawa T., Hosogane N., Fujita N., Okada E., Suzuki S., Tsuji O., Nagoshi N., Asazuma T., Tsuji T., et al. The 5-Item Modified Frailty Index Is Predictive of Severe Adverse Events in Patients Undergoing Surgery for Adult Spinal Deformity. Spine. 2019;44:E1083–E1091. doi: 10.1097/BRS.0000000000003063. [DOI] [PubMed] [Google Scholar]
  • 18.Elsamadicy A.A., Havlik J.L., Reeves B., Sherman J., Koo A.B., Pennington Z., Hersh A.M., Sandhu M.R.S., Kolb L., Lo S.-F.L., et al. Assessment of Frailty Indices and Charlson Comorbidity Index for Predicting Adverse Outcomes in Patients Undergoing Surgery for Spine Metastases: A National Database Analysis. World Neurosurg. 2022;164:e1058–e1070. doi: 10.1016/j.wneu.2022.05.101. [DOI] [PubMed] [Google Scholar]
  • 19.Pierce K.E.B., Naessig S.B., Kummer N.B., Larsen K.B., Ahmad W., Passfall L.B., Krol O.B., Bortz C.B., Alas H.B., Brown A.B., et al. The Five-item Modified Frailty Index is Predictive of 30-day Postoperative Complications in Patients Undergoing Spine Surgery. Spine. 2021;46:939–943. doi: 10.1097/BRS.0000000000003936. [DOI] [PubMed] [Google Scholar]
  • 20.Passias P.G., Jalai C.M., Worley N., Vira S., Hasan S., Horn S.R., Segreto F.A., Bortz C.A., White A.P., Gerling M., et al. Predictors of Hospital Length of Stay and 30-Day Readmission in Cervical Spondylotic Myelopathy Patients: An Analysis of 3057 Patients Using the ACS-NSQIP Database. World Neurosurg. 2018;110:e450–e458. doi: 10.1016/j.wneu.2017.11.009. [DOI] [PubMed] [Google Scholar]
  • 21.De la Garza-Ramos R., Goodwin C.R., Abu-Bonsrah N., Jain A., Miller E.K., Neuman B.J., Protopsaltis T.S., Passias P.G., Sciubba D.M. Prolonged length of stay after posterior surgery for cervical spondylotic myelopathy in patients over 65years of age. J. Clin. Neurosci. 2016;31:137–141. doi: 10.1016/j.jocn.2016.02.017. [DOI] [PubMed] [Google Scholar]
  • 22.Elsamadicy A.A., Koo A.B., Lee M., David W.B., Kundishora A.J., Robert S.M., Kuzmik G.A., Coutinho P.O., Kolb L., Laurans M., et al. Associated risk factors for extended length of stay following anterior cervical discectomy and fusion for cervical spondylotic myelopathy. Clin. Neurol. Neurosurg. 2020;195:105883. doi: 10.1016/j.clineuro.2020.105883. [DOI] [PubMed] [Google Scholar]
  • 23.Wilson J.R.F., Badhiwala J.H., Moghaddamjou A., Yee A., Wilson J.R., Fehlings M.G. Frailty Is a Better Predictor than Age of Mortality and Perioperative Complications after Surgery for Degenerative Cervical Myelopathy: An Analysis of 41,369 Patients from the NSQIP Database 2010–2018. J. Clin. Med. 2020;9:3491. doi: 10.3390/jcm9113491. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24.Pazniokas J., Gandhi C., Theriault B., Schmidt M., Cole C., Al-Mufti F., Santarelli J., Bowers C.A. The immense heterogeneity of frailty in neurosurgery: A systematic literature review. Neurosurg. Rev. 2021;44:189–201. doi: 10.1007/s10143-020-01241-2. [DOI] [PubMed] [Google Scholar]
  • 25.Subramaniam A.M., Ueno R., Tiruvoipati R.M., Darvall J.F., Srikanth V.M., Bailey M.P., Pilcher D.M.M.F.F., Bellomo R.M. Comparing the Clinical Frailty Scale and an International Classification of Diseases-10 Modified Frailty Index in Predicting Long-Term Survival in Critically Ill Patients. Crit. Care Explor. 2022;4:e0777. doi: 10.1097/CCE.0000000000000777. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26.Naftchi A.F., Vellek J., Stack J., Spirollari E., Vazquez S., Das A., Greisman J.D., Stadlan Z., Tarawneh O.H., Zeller S., et al. Frailty as a Superior Predictor of Dysphagia and Surgically Placed Feeding Tube Requirement After Anterior Cervical Discectomy and Fusion Relative to Age. Dysphagia. 2022;38:837–846. doi: 10.1007/s00455-022-10505-6. [DOI] [PubMed] [Google Scholar]
  • 27.Audat Z.A., Fawareh M.D., Radydeh A.M., Obeidat M.M., Odat M.A., Bashaireh K.M., Barbarawi M.M., Nusairat M.T., Ibraheem A.B., Audat M.Z. Anterior versus posterior approach to treat cervical spondylotic myelopathy, clinical and radiological results with long period of follow-up. SAGE Open Med. 2018;6:2050312118766199. doi: 10.1177/2050312118766199. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28.Lawrence B.D., Jacobs W.B., Norvell D.C., Hermsmeyer J.T., Chapman J.R., Brodke D.S. Anterior versus posterior approach for treatment of cervical spondylotic myelopathy: A systematic review. Spine. 2013;38:S173–S182. doi: 10.1097/BRS.0b013e3182a7eaaf. [DOI] [PubMed] [Google Scholar]
  • 29.Luo J., Cao K., Huang S., Li L., Yu T., Cao C., Zhong R., Gong M., Zhou Z., Zou X. Comparison of anterior approach versus posterior approach for the treatment of multilevel cervical spondylotic myelopathy. Eur. Spine J. 2015;24:1621–1630. doi: 10.1007/s00586-015-3911-4. [DOI] [PubMed] [Google Scholar]
  • 30.Kato S., Ganau M., Fehlings M.G. Surgical decision-making in degenerative cervical myelopathy-Anterior versus posterior approach. J. Clin. Neurosci. 2018;58:7–12. doi: 10.1016/j.jocn.2018.08.046. [DOI] [PubMed] [Google Scholar]
  • 31.Zhu B., Xu Y., Liu X., Liu Z., Dang G. Anterior approach versus posterior approach for the treatment of multilevel cervical spondylotic myelopathy: A systemic review and meta-analysis. Eur. Spine J. 2013;22:1583–1593. doi: 10.1007/s00586-013-2817-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 32.Feng F., Ruan W., Liu Z., Li Y., Cai L. Anterior versus posterior approach for the treatment of cervical compressive myelopathy due to ossification of the posterior longitudinal ligament: A systematic review and meta-analysis. Int. J. Surg. 2016;27:26–33. doi: 10.1016/j.ijsu.2016.01.038. [DOI] [PubMed] [Google Scholar]
  • 33.Hitchon P.W., Woodroffe R.W., Noeller J.A., Helland L., Hramakova N., Nourski K.V. Anterior and posterior approaches for cervical myelopathy: Clinical and radiographic outcomes. Spine. 2019;44:615–623. doi: 10.1097/BRS.0000000000002912. [DOI] [PubMed] [Google Scholar]
  • 34.Wilkerson C.G., Sherrod B.A., Alvi M.A., Asher A.L., Coric D., Virk M.S., Fu K.-M., Foley K.T., Park P., Upadhyaya C.D., et al. Differences in Patient-Reported Outcomes Between Anterior and Posterior Approaches for Treatment of Cervical Spondylotic Myelopathy: A Quality Outcomes Database Analysis. World Neurosurg. 2022;160:e436–e441. doi: 10.1016/j.wneu.2022.01.049. [DOI] [PubMed] [Google Scholar]
  • 35.Chen Z., Liu B., Dong J., Feng F., Chen R., Xie P., Rong L. A Comparison of the Anterior Approach and the Posterior Approach in Treating Multilevel Cervical Myelopathy: A Meta-Analysis. Clin. Spine Surg. 2017;30:65–76. doi: 10.1097/BSD.0000000000000398. [DOI] [PubMed] [Google Scholar]
  • 36.El-Ghandour N.M.F., Soliman M.A.R., Ezzat A.A.M., Mohsen A., Zein-Elabedin M. The safety and efficacy of anterior versus posterior decompression surgery in degenerative cervical myelopathy: A prospective randomized trial. J. Neurosurg. Spine. 2020;33:288–296. doi: 10.3171/2020.2.SPINE191272. [DOI] [PubMed] [Google Scholar]
  • 37.Ghogawala Z., Terrin N., Dunbar M.R., Breeze J.L., Freund K.M., Kanter A.S., Mummaneni P.V., Bisson E.F., Barker F.G., Schwartz J.S., et al. Effect of Ventral vs Dorsal Spinal Surgery on Patient-Reported Physical Functioning in Patients With Cervical Spondylotic Myelopathy: A Randomized Clinical Trial. JAMA. 2021;325:942–951. doi: 10.1001/jama.2021.1233. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 38.Badhiwala J.H., Khan O., Wegner A., Jiang F., Wilson J.R.F., Morgan B.R., Ibrahim G.M., Wilson J.R., Fehlings M.G. A partial least squares analysis of functional status, disability, and quality of life after surgical decompression for degenerative cervical myelopathy. Sci. Rep. 2020;10:16132. doi: 10.1038/s41598-020-72595-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 39.Momtaz D., Prabhakar G., Gonuguntla R., Ahmad F., Ghali A., Kotzur T., Nagel S., Chaput C. The 8-item Modified Frailty Index Is an Effective Risk Assessment Tool in Anterior Cervical Decompression and Fusion. Glob. Spine J. 2022 doi: 10.1177/21925682221127229. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 40.Elsamadicy A.A., Koo A.B., Sarkozy M., David W.B., Reeves B.C., Patel S., Hansen J., Sandhu M.R.S., Hengartner A.C., Hersh A., et al. Leveraging HFRS to assess how frailty affects healthcare resource utilization after elective ACDF for CSM. Spine J. 2023;23:124–135. doi: 10.1016/j.spinee.2022.08.004. [DOI] [PubMed] [Google Scholar]
  • 41.Shin J.I., Kothari P., Phan K., Kim J.S., Leven D., Lee N.J., Cho S.K. Frailty Index as a Predictor of Adverse Postoperative Outcomes in Patients Undergoing Cervical Spinal Fusion. Spine. 2017;42:304–310. doi: 10.1097/BRS.0000000000001755. [DOI] [PubMed] [Google Scholar]
  • 42.Lambrechts M.J., Tran K., Conaway W., Karamian B.A., Goswami K., Li S., O’Connor P., Brush P., Canseco J., Kaye I.D., et al. Modified Frailty Index as a Predictor of Postoperative Complications and Patient-Reported Outcomes after Posterior Cervical Decompression and Fusion. Asian Spine J. 2023;17:313. doi: 10.31616/asj.2022.0262. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 43.Medvedev G., Wang C., Cyriac M., Amdur R., O’Brien J. Complications, Readmissions, and Reoperations in Posterior Cervical Fusion. Spine. 2016;41:1477–1483. doi: 10.1097/BRS.0000000000001564. [DOI] [PubMed] [Google Scholar]
  • 44.Young R., Cottrill E., Pennington Z., Ehresman J., Ahmed A.K., Kim T., Jiang B., Lubelski D., Zhu A.M., Wright K.S., et al. Experience with an Enhanced Recovery After Spine Surgery protocol at an academic community hospital. J. Neurosurg. Spine. 2020;34:680–687. doi: 10.3171/2020.7.SPINE20358. [DOI] [PubMed] [Google Scholar]
  • 45.Bansal T., Sharan A.D., Garg B. Enhanced recovery after surgery (ERAS) protocol in spine surgery. J. Clin. Orthop. Trauma. 2022;31:101944. doi: 10.1016/j.jcot.2022.101944. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 46.Elsarrag M., Soldozy S., Patel P., Norat P., Sokolowski J.D., Park M.S., Tvrdik P., Kalani M.Y.S. Enhanced recovery after spine surgery: A systematic review. Neurosurg. Focus. 2019;46:E3. doi: 10.3171/2019.1.FOCUS18700. [DOI] [PubMed] [Google Scholar]
  • 47.Debono B., Corniola M.V., Pietton R., Sabatier P., Hamel O., Tessitore E. Benefits of Enhanced Recovery After Surgery for fusion in degenerative spine surgery: Impact on outcome, length of stay, and patient satisfaction. Neurosurg. Focus. 2019;46:E6. doi: 10.3171/2019.1.FOCUS18669. [DOI] [PubMed] [Google Scholar]
  • 48.Soffin E.M., Wetmore D.S., Barber L.A., Vaishnav A.S., Beckman J.D., Albert T.J., Gang C.H., Qureshi S.A. An enhanced recovery after surgery pathway: Association with rapid discharge and minimal complications after anterior cervical spine surgery. Neurosurg. Focus. 2019;46:E9. doi: 10.3171/2019.1.FOCUS18643. [DOI] [PubMed] [Google Scholar]
  • 49.Debono B., Sabatier P., Boniface G., Bousquet P., Lescure J.-P., Garnaud V., Hamel O., Lonjon G. Implementation of enhanced recovery after surgery (ERAS) protocol for anterior cervical discectomy and fusion: A propensity score-matched analysis. Eur. Spine J. 2021;30:560–567. doi: 10.1007/s00586-020-06445-0. [DOI] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Data Availability Statement

Data used for this study is from the National Inpatient Sample, publicly available from the Healthcare Cost and Utilization Project. More information can be found at http://www.hcup-us.ahrq.gov/nisoverview.jsp (accessed on 20 November 2023).


Articles from Journal of Clinical Medicine are provided here courtesy of Multidisciplinary Digital Publishing Institute (MDPI)

RESOURCES