Abstract
BACKGROUND AND PURPOSE: Cauda equina syndrome typically requires emergent MR imaging to detect compressive lesions on the cauda equina, which may require surgical decompression. While CT is sometimes performed as a complementary imaging technique to evaluate osseous integrity in patients with cauda equina syndrome, the accuracy of CT in detecting significant spinal stenosis and cauda equina impingement is not well-defined in the literature. We hypothesized that percentage thecal sac effacement on CT of the lumbar spine would have high sensitivity and high negative predictive value in evaluating significant spinal stenosis and cauda equina impingement.
MATERIALS AND METHODS: We analyzed imaging studies for 151 consecutive patients with clinically suspected cauda equina syndrome. The percentage thecal sac effacement (<50%, ≥50%) was determined on CT and MR imaging. The presence or absence of cauda equina impingement was determined on MR imaging. Using MR imaging as the reference standard, we performed statistical analysis to determine the accuracy of CT in predicting significant spinal stenosis (percentage thecal sac effacement, ≥50%) and cauda equina impingement.
RESULTS: Forty of 151 patients had a percentage thecal sac effacement of ≥50% on MR imaging. Nineteen of 40 had cauda equina impingement. Readers determined that there was a CT percentage thecal sac effacement of <50% in 97/151 cases, and CT percentage thecal sac effacement of ≥50% in 54/151 cases. Reader sensitivity for the detection of significant spinal stenosis (MR percentage thecal sac effacement of ≥50%) was 0.98; specificity, 0.86; positive predictive value, 0.72; and negative predictive value, 0.99. No cases read as CT percentage thecal sac effacement of <50% were found to have cauda equina impingement.
CONCLUSIONS: CT percentage thecal sac effacement of ≥50% predicts significant spinal stenosis on MR imaging in patients with clinically suspected cauda equina syndrome. CT percentage thecal sac effacement of <50% appears to reliably rule out cauda equina impingement. This imaging marker may serve as an additional tool for the clinician in deciding whether MR imaging can be deferred.
ABBREVIATIONS:
- CEI
- cauda equina impingement
- CES
- cauda equina syndrome
- PTSE
- percentage thecal sac effacement
Cauda equina syndrome (CES) requires emergent imaging to rule out compressive lesions on the cauda equina, which could necessitate emergent surgical decompression. Failure of the timely recognition and treatment of CES can result in debilitating long-term neurologic complications such loss of bowel, bladder, and sexual function. MR imaging is the established imaging criterion standard to screen for the various etiologies accounting for CES, including degenerative disc disease, trauma, neoplasm, infection, and hematoma.1⇓⇓⇓–5
The clinical presentation of CES is defined by a broad range of symptoms and physical examination findings including severe low back pain, bilateral sciatica, lower extremity weakness, bladder/bowel dysfunction, saddle numbness, or reduced rectal tone. Some of these symptoms are common and nonspecific to CES, presenting the clinician with the diagnostic challenge of deciding which patients warrant further evaluation with MR imaging.4,6⇓⇓–9
The prevalence of cauda equina syndrome among the general population is estimated between 1 in 33,000 to 1 in 100,000 and is diagnosed in approximately 0.04% of patients presenting to the emergency department with low back pain.10⇓⇓–13 Friedman et al13 reviewed data for the 2.63 million annual emergency department visits in the United States for low back pain and found imaging performed in 45% of cases, with 2.8% of all patients scanned with MR imaging and 5.5% scanned with CT, resulting in an overall cost of >$819 million to US payers.11,13 Studies have demonstrated that most MR images obtained to evaluate CES do not demonstrate concordant pathology; however, these scans are nonetheless frequently ordered, given the impact of missing or delaying a diagnosis of CES.1,4⇓–6,9,11,14
While CT is sometimes performed as a complementary imaging technique to evaluate osseous integrity in patients with CES, the diagnostic accuracy of CT in detecting significant spinal stenosis and cauda equina impingement (CEI) compared with MR imaging is not well-defined in the literature.
The purpose of this study was to evaluate whether CT could reliably identify significant spinal stenosis and rule out cauda equina impingement in patients presenting with clinically suspected cauda equina syndrome.
Materials and Methods
Patient Selection
This study was Health Insurance Portability and Accountability Act–compliant and was approved by our institutional review board. During a 12-month period, we reviewed the clinical and imaging data of 4691 consecutive lumbar spine MR imaging examinations performed at our institution. One hundred fifty-one patients met the following inclusion criteria: 1) acute neurologic symptoms (new onset or worsening of symptoms within the past 48 hours) with clinical suspicion of cauda equina syndrome (symptoms include severe low back pain, bilateral sciatica, lower extremity weakness, bladder/bowel dysfunction, saddle numbness, or reduced rectal tone); 2) CT of the lumbar spine performed within 48 hours of MR imaging; and 3) no interval operation or change in symptoms between CT or MR imaging.
Image Acquisition
All imaging was performed in accordance with standard institutional spine imaging protocols. Noncontrast lumbar spine CT was acquired in the helical mode (5-mm thickness, 100 kV, auto-mAs) and reformatted at 2-mm intervals. Lumbar spine CTs obtained in conjunction with CT abdomen/pelvic examinations were reconstructed from the CT abdomen/pelvis source data and had the same scanning parameters following administration of 80–90 mL of nonionic contrast (iopamidol, Isovue Multipack-370; Bracco, Princeton, New Jersey). All axial CT acquisitions were reconstructed in the sagittal and coronal planes, in both soft-tissue and bone algorithms.
MR imaging was performed on multiple different 1.5T and 3T scanners across our institution. Sagittal T2WI parameters were the following: TR/TE = 3600/100 ms, matrix = 290 × 230, NEX = 2, section thickness = 3 mm, gap = 0 mm. Axial T2WI parameters were the following: TR/TE = 5500/100 ms, matrix = 290 × 230, NEX = 1.5, section thickness = 3 mm, gap = 0 mm.
Image Analysis
We analyzed by visual inspection the percentage thecal sac effacement (≥50%, <50%) on lumbar spine CT and the percentage thecal sac effacement (≥50%, <50%) on lumbar spine MR imaging. The percentage thecal sac effacement was determined by visually inspecting the area of the thecal sac at the most stenotic level by using the axial and sagittal planes and comparing it with a normal level above or below the stenosis (Fig 1). A threshold of 50% thecal sac effacement was used because this was easily reproducible and, on the basis of preliminary analysis, was a threshold below which the cauda equina and conus medullaris would not be impinged.
Images were reviewed independently by 2 radiologists: a Certificate of Added Qualification–certified neuroradiologist with 9 years of radiology experience and a radiology resident with 1 year of radiology experience. The presence or absence of cauda equina impingement on MR imaging was also recorded. Cauda equina impingement was defined as complete effacement of CSF within the thecal sac secondary to an extrinsically compressing lesion. The underlying dominant cause of spinal stenosis on MR imaging was recorded (traumatic osseous retropulsion, degenerative changes, tumor, hematoma, infection). Levels analyzed spanned T12/L1 through L5/S1. Early tapering of the thecal sac secondary to prominent epidural fat was not considered positive for cauda equina impingement unless associated with a superimposed compressive lesion. Interpreting radiologists were blinded to all clinical and imaging report information. MR images were reviewed 2 weeks following review of CT images with readers blinded to the CT interpretation. Any disagreements were resolved by consensus.
Statistical Analysis
Using lumbar spine MR imaging as the reference standard, we performed statistical analysis to determine the sensitivity, specificity, positive predictive value, and negative predictive value of lumbar spine CT in detecting percentage thecal sac effacement of ≥50% and cauda equina impingement on MR imaging. MedCalc 11.5.1.0 software (MedCalc Software, Mariakerke, Belgium) was used to perform statistical analysis. Statistical significance was P < .05. Interrater agreement for imaging markers was determined by using the κ statistic.
Results
Patient demographics and clinical characteristics of the study population are listed in the Table. Of 151 patients, 40 had MR imaging percentage thecal sac effacement (MR-PTSE) of ≥50% (23 degenerative, 12 traumatic, 3 neoplastic, 1 hematoma, 1 infection). Of 40 patients with MR-PTSE of ≥50%, 19 had cauda equina impingement (10 degenerative, 6 traumatic, 2 neoplastic, 1 hematoma). One hundred eleven patients had MR-PTSE of <50%. No patients with MR-PTSE of <50% had cauda equina impingement.
On the basis of the evaluation of lumbar spine CT, the readers determined that there was CT-PTSE of <50% in 97/151 cases and CT-PTSE of ≥50% in 54/151 cases. Reader sensitivity for the detection of significant spinal stenosis (MR-PTSE of ≥50%) was 98% (95% CI, 87%–100%), specificity was 86% (95% CI, 79%–92%), positive predictive value was 72% (95% CI, 58%–84%), and negative predictive value was 99% (95% CI, 94%–100%).
No cases read as CT-PTSE of <50% were found to have cauda equina impingement. One false-negative case of CT-PTSE of <50% underestimated the stenosis in a patient with MR-PTSE of ≥50% without cauda equina impingement. All cases of CT-PTSE of ≥50% corresponded to the concordant level of maximum lumbar spinal stenosis on MR imaging.
Of 151 cases, 86 CTs were performed with contrast and 65 CTs were performed without contrast. There was no significant difference in sensitivity (P = .37) or specificity (P = .06) for predicting MR-PTSE of ≥50% between the 2 groups. Interreader agreement for determination of CT-PTSE was good (κ = 0.62).
Soft-tissue resolution of lumbar spine CT with the application of the CT-PTSE marker to rule out degenerative CEI (Fig 1), identify patients at risk for degenerative CEI (Fig 2) and neoplastic CEI (Fig 3) is demonstrated. Figure 4 shows how, in the setting of trauma, CT can readily identify a patient at risk for traumatic CEI by delineating osseous effacement of the thecal sac. In certain cases, streak artifacts from hardware or surrounding bone limited the diagnostic accuracy of the CT-PTSE marker (Fig 5).
Discussion
The purpose of this study was to determine whether CT could reliably and safely identify patients with significant spinal stenosis and cauda equina impingement. Our results demonstrate that CT-PTSE has a high sensitivity and high negative predictive value for detecting significant spinal stenosis on MR imaging. On the basis of careful analysis of CT alone, the readers missed no cases of cauda equina impingement.
The American College of Radiology Appropriateness Criteria for the evaluation of cauda equina syndrome lists MR imaging of the lumbar spine as a level 9 rating (“usually appropriate”), with CT of the lumbar spine listed as a level 5 rating (“may be appropriate”).2 This determination is based on the superior soft-tissue contrast resolution of MR imaging in evaluating lumbar spine pathology, particularly for visualizing nerve roots within the thecal sac, anatomy not readily visible on CT. We found that with careful adjustment of the CT window-level settings, in addition to bone, CT can distinguish the margins of the thecal sac by identifying various levels of soft-tissue attenuation within and around the spinal canal, including intervertebral discs, epidural fat, and CSF within the thecal sac. This limited soft-tissue resolution of CT allows one to reliably determine the PTSE, a marker that we hypothesized could infer the presence or absence of underlying cauda equina impingement when applied with a threshold of 50%. We found CT-PTSE a useful imaging marker in predicting significant spinal stenosis on MR imaging and one that excluded cauda equina impingement in our patient population.
While CT cannot replicate the superior soft-tissue contrast resolution of MR imaging in evaluating lumbar spine pathology, careful analysis of CT-PTSE can help radiologists communicate to the clinician their suspicion of significant spinal stenosis and cauda equina impingement. This imaging marker may be particularly useful in the community setting where some centers may have limited access to MR imaging in the emergency department. On the basis of our observations, a clinician could potentially decide to defer MR imaging in cases with a low clinical suspicion and CT-PTSE of <50% or to expedite MR imaging in cases of CT-PTSE of ≥50%.
As a screening tool, application of the CT-PTSE imaging marker could potentially lower associated health care costs by decreasing the number of low-diagnostic-yield MR imaging examinations or shifting visits to primary care settings, where costs and the propensity for imaging may be less.15 In our study, we identified 97/151 (64%) patients with CT-PTSE of <50%, none of whom had cauda equina impingement on MR imaging. Provided that there is a corresponding low clinical suspicion for CES, this represents nearly two-thirds of our patient population where MR imaging could have been deferred on the basis of CT results. Using the national average of combined technical and professional component 2016 Medicare payment rates for MRI and CT of the lumbar spine without contrast of $245.26 and $180.81 respectively, we determined that the estimated cost savings per 1000 patients imaged with CT would be approximately $41,248. We recognize that this is likely a low estimate considering the higher costs paid by private commercial insurers and potential additional expenditures associated with hospital admissions or transferring patients to other facilities for MR imaging.13
There were several limitations to our study. We used a retrospective design and included both contrast and noncontrast CT examinations of the lumbar spine; however, there was no significant difference in our results when adjusting for the presence of contrast. Most of our cases were degenerative and traumatic in etiology, and we had few cases of tumor, infection, or hemorrhage. The level of reader experience was also relatively low (9 years and 1 year, respectively); however, neither reader missed any case of cauda equina impingement, and increased reader experience might have improved the specificity and positive predictive value of results obtained in this study. Additionally, there are limitations related to the 50% PTSE threshold. While we did not encounter patients with a low-lying conus medullaris, it is possible that those patients could experience distal thoracic cord or conus impingement at a PTSE of <50%. It is also possible that in patients with congenital spinal stenosis, a PTSE of <50% could result in cauda equina impingement.
Considering the aforementioned limitations of this study, the CT-PTSE marker to exclude cauda equina impingement may be best-suited for those with a low pretest clinical suspicion. Clinicians may choose to lower their threshold for obtaining MR imaging in cases of suspected infection, hemorrhage, tumor, congenital spinal stenosis, when symptoms or findings are localized to the thoracolumbar junction or in cases in which CT is degraded by artifacts.
These results should be validated in a larger prospective study. Areas for additional future investigation may include optimizing CT scanning parameters to reduce artifacts and further improve the accuracy of the CT-PTSE imaging marker.
Conclusions
CT-PTSE of ≥50% predicts significant spinal stenosis on MR imaging in patients with clinically suspected cauda equina syndrome. CT-PTSE <50% appears to reliably rule out cauda equina impingement. This imaging marker may serve as an additional tool for the clinician in helping to decide whether MR imaging can be deferred, and it has the potential to lower associated health care costs.
References
- Received May 28, 2016.
- Accepted after revision August 23, 2016.
- © 2017 by American Journal of Neuroradiology