Abstract
Study Design:
Retrospective cohort study.
Objectives:
Unplanned reoperation following lumbar spinal fusion is detrimental to patients, providers, and health systems. The aim of this study was to identify risk factors associated with unplanned reoperation following elective posterior lumbar spinal fusion and assess the reasons for reoperation.
Methods:
A retrospective analysis of 22 151 patients from the American College of Surgeons National Surgical Quality Improvement Program data set between 2012 and 2015 was completed. The primary outcome measure was unplanned reoperation within 30 days. Secondary outcome measures were specific diagnoses and procedures associated with unplanned reoperation, as well as time to reoperation from initial procedure. Multiple stepwise logistic regression was employed to determine preoperative variables predictive of unplanned 30-day reoperation.
Results:
Patients with disseminated cancer (OR = 3.44,
Conclusions:
Predictors and causes of unplanned reoperation within 30 days following elective posterior lumbar spinal fusion are identifiable. In this study cohort, obesity, American Society of Anesthesiologists score, disseminated cancer, weight loss, bleeding disorders, and multilevel fusion were identified as significant risk factors for reoperation. Further research investigating risk factor modification on reoperation in elective posterior lumbar spinal fusion is warranted.
Introduction
Each year, more than 200 000 patients undergo lumbar spinal fusion in the United States. 1 Unplanned return to the operating room is a highly undesirable outcome from both clinical and health resource utilization perspectives. Unplanned reoperation within 30 days has been associated with markedly increased mortality rates and charges; Birkmeyer et al reported a 6.9-fold increased risk of mortality and 4.6-fold higher charges associated with unplanned 30-day reoperation in general surgery. 2 Accordingly, efforts to reduce the rate of reoperation in posterior lumbar fusion are warranted, and reduction of adverse events through risk factor modulation and proper patient selection for elective procedures is becoming increasingly important.
Previous studies have focused on either isolated contributors to reoperation 3,4 or reoperation risk in broad, heterogeneous spine surgery cohorts. 5 –7 These investigations have demonstrated the importance of differentiating risk factors by anatomical location, procedure, and approach. 5,7 Additionally, the cause of unplanned reoperation has been shown to be highly specific to the procedure studied. 2 The aim of this study was to evaluate risk factors for unplanned 30-day reoperation after posterior lumbar spinal fusion. This study also examined the specific causes, types of procedures, and timing of reoperations.
Methods
Study Design and Setting
A retrospective analysis was performed using data from the American College of Surgeons National Surgical Quality Improvement Program (ACS NSQIP) data set for the years 2012 to 2015. The ACS NSQIP collects data on preoperative and intraoperative risk factors, as well as morbidity and mortality outcomes for 30 days following major surgical procedures. 8 The data is collected by certified and trained staff and assessed for quality using an interrater reliability audit. Notably, the ACS NSQIP does not contain data for minor cases, patients <18 years old, patients with American Society of Anesthesiologists (ASA) score of 6 (brain-stem-dead organ donor), 9 trauma cases, and solid organ transplant cases. This investigation was deemed exempt from institutional review board approval, given the publicly available and de-identified nature of the NSQIP data set.
Patients
Primary inclusion criterion for this study was the presence of a primary Common Procedural Terminology (CPT) code corresponding to posterior lumbar fusion (22612, 22630, or 22633). Patients were excluded if the procedure was nonelective, deemed emergent, conducted in an outpatient setting, involved any cervical or thoracic levels, or employed anterior, anterolateral, anterior interbody, or lateral excavitary techniques—all of which were evaluated based on presence of other listed CPT codes.
Outcome Measures
Primary outcome, classified as a binary variable, was unplanned return to the operating room within 30 days of the original procedure. The specific reoperation procedure and associated diagnosis were assessed using CPT and International Classification of Disease, Ninth Revision, Clinical Modification (ICD-9-CM) codes, respectively. Days from index procedure to unplanned reoperation were plotted, and the distribution was smoothed with a 3-day trailing average to facilitate trend visualization.
Risk Factors
All NSQIP preoperative patient characteristics (excluding laboratory values) available from 2012 to 2015 were assessed as covariates in the analysis, including patient age, sex, body mass index (BMI) that was calculated from available data on height and weight, and race. Comorbidities were also included as covariates, including diabetes, smoking, dyspnea, ventilator dependency, history of severe chronic obstructive pulmonary disease (COPD), ascites, congestive heart failure in 30 days before surgery, hypertension, acute renal failure, dialysis, disseminated cancer, open/infected wound, steroid use for chronic condition, >10% weight loss in prior 6 months, bleeding disorders, preoperative transfusion in 72 hours prior to surgery, systemic sepsis, and ASA classification. Notably, BMI was categorized as underweight (<18.5), normal weight (18.5-24.9), overweight (25.0-29.9), obesity class I (30.0-34.9), obesity class II (35.0-39.9), and obesity class III (≥40). Comorbidities were analyzed as unique risk factors—rather than as contributors to a comorbidity index (eg, Charlson Comorbidity Index)—as we sought to identify specific characteristics independently associated with unplanned reoperation. Procedural characteristics derived from patient-specific CPT codes were also included as covariates. Surgical approach was included as a covariate and was defined as posterior/posterolateral, posterior interbody, or combined posterior/posterolateral and interbody, based on the primary listed CPT code (22612, 22630, and 22633, respectively). The number of levels fused was assessed based on presence of CPT codes indicating additional fusion levels (22634, 22632, and 22614) and classified as single-level or multilevel (≥2 levels). NSQIP data set year was also included as a covariate.
Statistical Analysis
All statistical analysis was performed utilizing SAS 9.4 (SAS Institute, Cary, NC). Missing data was reported in descriptive statistics, and patients with missing data were excluded from further analyses. Two-tailed χ2 or Fisher’s exact test was performed for categorical variables, as appropriate. Bivariate risk factor analyses examined association of covariates with odds of unplanned 30-day reoperation. Multiple logistic regression was performed to assess independent risk factors associated with reoperation. Stepwise model building was employed, with a threshold α for variable entrance and retention of 0.2 and 0.1, respectively. Odds ratios (ORs) and 95% confidence intervals (CIs) were evaluated for risk factors deemed significantly predictive of unplanned reoperation. No collinearity, as assessed by variable tolerance in a generalized linear model, was observed between potential risk factors. Model goodness-of-fit was assessed using the Hosmer-Lemeshow goodness-of-fit test. Correlations between bleeding disorders, weight loss, and other comorbidities were analyzed. Statistical significance was maintained as
Source of Funding
No funding was received in support of this study.
Results
In total, 22 151 patients undergoing elective posterior lumbar fusion were identified and included in the analysis. The majority of patients were overweight (BMI 25.0-29.9) or obese (BMI > 30; n = 18 259, 82.6%), white (n = 18 666, 84.3%), nondiabetic (n = 18 252, 82.4%), and undergoing single-level procedures (n = 13 056, 58.9%). Overall, 3.4% (n = 745) patients underwent an unplanned reoperation within 30 days of the original procedure (Tables 1 and 2).
Patient and Procedure Characteristics With Bivariate Analyses Examining Relationship to 30-Day Reoperation Rate.
Abbreviations: BMI, body mass index; ASA, American Society of Anesthesiologists.
Patient Comorbidities With Bivariate Analyses Examining Relationship to 30-Day Reoperation Rate.
Abbreviations: COPD, chronic obstructive pulmonary disease; SIRS, systemic inflammatory response syndrome.
Bivariate Analysis
Bivariate analysis was performed to determine the frequency of unplanned return to the operating room by preoperative characteristics. Patient BMI (
Multivariate Analysis
Significant predictors of unplanned reoperation included disseminated cancer (OR = 3.44, 95% CI = 1.46-8.15;
Independent Risk Factors for 30-Day Unplanned Reoperation.
Abbreviations: OR, odds ratio; CI, confidence interval; ASA, American Society of Anesthesiologists; BMI, body mass index.
Bleeding Disorder and Weight Loss Correlations
Bleeding disorders were positively correlated with diabetes (
Correlation of Bleeding Disorder and Weight Loss >10% With Other Comorbidities.a
aBoldface values indicate
Characteristics of Unplanned Reoperation
The most common procedures included hematoma drainage (n = 66, 9.9% of procedures), drainage of lumbar spine abscess (n = 61, 9.1%), exploration of spinal fusion (n = 59, 8.8%), and drainage of complex, postoperative wound infection (n = 55, 8.2%). The most common diagnoses included postoperative infection (n = 121, 21.1% of procedures), hematoma (n = 57, 9.9%), mechanical complication of internal orthopedic device (n = 51, 8.9%), seroma (n = 42, 7.3%), and accidental dura puncture/laceration (n = 21, 3.7%; Tables 5 and 6). Unplanned reoperation exhibited local maxima on 4, 16, and 23 days postoperatively, as assessed visually (Figure 1).
Diagnoses Associated With 30-Day Unplanned Reoperation.
Abbreviation: ICD-9-CM, International Classification of Disease, Ninth Revision, Clinical Modification.
Procedure Types Associated With 30-Day Unplanned Reoperation.
Abbreviation: CPT, Common Procedural Terminology.
Distribution of days to unplanned reoperation from day of procedure.
Discussion
This analysis identified disseminated cancer, weight loss >10% in the prior 6 months, bleeding disorders, ASA score of 3, BMI ≥35, and multilevel fusion as risk factors for unplanned return to the operating room within 30 days. The most common diagnosis associated with reoperation was postoperative infection. This data provides important information for providers regarding the risk factors and characteristics of unplanned reoperation following posterior lumbar spinal fusion.
In a study of lumbar fusion for degenerative diseases, Martin et al identified higher rates of 90-day reoperation among female patients, patients with higher numbers of comorbidities, procedures with anterior approach, and procedures utilizing bone morphogenetic protein. 10 Our analysis of posterior lumbar fusion patients did not find a significant difference in 30-day unplanned reoperation rates by patient sex, though it is possible (but unlikely) that the increased risk among female patients in Martin et al’s study manifests primarily in the 30- to 90-day postoperative period. Furthermore, our investigation identified ASA score of 3 (vs 1 and 2) to be a risk factor for reoperation; ASA score of 4 and 5 did not exhibit a significant effect. It is possible that patients with particularly high preoperative disease burden receive more intensive pre- and postoperative care, decreasing likelihood of reoperation. However, it is also possible that low sample size in this group (n = 472, 2.1%) may have limited our results. Future studies of lumbar spinal fusion patients with significant preoperative comorbidity burden may further clarify this finding.
Bekelis et al examined NSQIP data from 2005 to 2010 to determine risk factors associated with 30-day return to the operating room in a diverse cohort of patients undergoing discectomy, corpectomy, and lumbar fusion of cervical, thoracic, and lumbar levels, finding corpectomy, non-anterior approach, weight loss, bleeding disorders, dialysis, peripheral vascular disease, COPD, and tobacco use to be significant risk factors. 6 Notably, the NSQIP definition for “return to the operating room” in Bekelis et al’s study included both planned and unplanned reoperations, while our investigation only considers unplanned events. Our investigation aligns reasonably well with this study supporting increased risk borne by patients with weight loss and bleeding disorders. Furthermore, our correlation analysis suggests that iatrogenic bleeding disorders secondary to anticoagulation therapy may play a prominent role in reoperation risk, although detailed analysis of complications is not possible due to limitations in the granularity of NSQIP data. We also observed that patients with preoperative weight loss are frequently those with metastatic cancer. As both cancer and weight loss appeared as independent risk factors in multivariate analysis, it is possible that these 2 comorbidities act synergistically to increase risk of reoperation following lumbar spinal fusion and indicate physiologic frailty of the patient. In both bivariate- and covariate-adjusted analyses, however, we did not observe significant differences in 30-day unplanned reoperation rates by dialysis, COPD, or smoking status. Additionally, peripheral vascular disease is not included in the 2015 NSQIP public use file, and was therefore not included in our analysis. As our cohort was restricted to posterior lumbar arthrodesis, it is possible that these additional factors are not relevant to the posterior lumbar fusion population specifically. It is also possible that careful surgeon patient selection in elective lumbar spinal surgery may have mitigated these risks in more recent years, as compared to the 2005 to 2010 period covered by Bekelis et al’s study. Finally, it is possible that patients with these characteristics may be predisposed to planned, but not unplanned, reoperations.
Infection was the most common cause of 30-day reoperation in our analysis, involved in >20% of such events. Previous studies have identified diabetes status, smoking status, ASA classification ≥3, weight loss, dependent functional status, disseminated cancer, obesity, and greater number of levels fused as predictive of increased risk for surgical site infection following spine surgery. 11 –14 As expected, many of these factors overlap with those we identified as predictive of reoperation. It is notable, however, that dependent functional status, diabetes, and smoking status did not emerge as independent risk factors in our cohort.
Comparison of this study to previous investigations highlights the need for longitudinal risk factor modeling in orthopedic spine surgery as the prevalence of (and attention given to) various comorbidities changes over time. Retrospective analysis of large health care data sets will identify risk factors for complications in the context of the dominant standard of care and over the time period of interest. Comorbidities that are widely well-managed may not emerge as predictive of complications in retrospective analyses. The corpus of literature on risk factors thus provides a perspective on areas for potential improvement that is delimited both clinically and temporally. Frequent reexamination of retrospective risk factor analyses is warranted.
The necessity of modulating preoperative risk factors may increase as providers continue to share greater economic responsibility for patient care. This is particularly true within bundled payment windows, such as the 90-day period in Medicare’s Total Joint Replacement program. 15 Iorio et al published a 2016 analysis of an urban, tertiary academic medical center’s experience with the program and demonstrated that decreased length of stay potentially led to downstream cost-savings. It is possible that, with success of this program, Medicare may implement Bundled Payment for Care Improvement programs across additional orthopedic and neurosurgical procedures. Aggressive modulation of preoperative risk factors—where possible—may be instrumental to financial sustainability under the model.
This study was constrained to the information provided in the ACS NSQIP data set. As a result, follow-up beyond 30 days was not obtained, constraining our ability to make inferences regarding long-term outcomes (eg, revision fusion rate, late infection, etc). Missing data occurred at high frequency for reoperation procedure type (10.1%, n = 75) and diagnosis associated with reoperation (23.1%, n = 172). Additionally, the variables contained in the NSQIP are general in nature and do not provide specific information on patient preoperative medications and disease progression, as well as other important clinical characteristics. As with many retrospective data set analyses, our pool of potential risk factors was limited, and it is possible that additional risk factors exist that were not present in the NSQIP data set. However, these limitations are present in most extant data set research, and we believe that the NSQIP data quality and large sample size sufficiently compensate for these factors. Finally, despite this study’s large sample size, select risk factors were present in very few patients. Out of the identified risk factors for 30-day reoperation, disseminated cancer (n = 59, 0.3%), and weight loss >10% in previous 6 months (n = 43, 0.2%) had particularly low incidence. While the likelihood of type 1 error is not affected by sample size (as threshold α was set at
Conclusions
This analysis examined risk factors for unplanned 30-day reoperation in patients undergoing elective, posterior lumbar spinal fusion. Disseminated cancer, weight loss >10% in the prior 6 months, bleeding disorders, ASA score of 3, BMI ≥35, and multilevel fusion were identified as risk factors for reoperation. Furthermore, the increased risk of reoperation in patients with bleeding disorders may be related to anticoagulation therapy. As return to the operating room is clinically adverse and costly to health systems, health care teams may elect to prioritize management of these comorbidities prior to elective surgery, where possible.
Footnotes
Declaration of Conflicting Interests
The author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.
Funding
The author(s) received no financial support for the research, authorship, and/or publication of this article.