Postoperative CT-analysis of pedicle screw insertion with 3D-printed guides in spinal deformity surgery showed a 100% accuracy of screw placement within the “safe zone” without any violation of the pedicle wall or other structures. Most inserted screws (80%) were placed in the high-thoracic and thoracic spine, and all analyzed thoracic and lumbar screws were positioned precisely within the pedicle. Superimpose CT-analysis demonstrated minimal deviations between planned and achieved pedicle screw positioning, at < 0.92 mm and < 2.91°, respectively, for linear and angular deviation. The achieved accuracy of pedicle screw entry point and intrapedicular screw trajectory fell well within the defined tolerances set for acceptance (< 1.5 mm for linear deviation and < 5° for angular deviation). Most of the deviations were seen both at the insertion point and final positioning of the screw head and at the distal tip of the screw; not within the pedicle itself. The screw positions were possibly slightly altered during maneuvers associated with deformity correction [21]. Nevertheless, the absence of any pedicle wall violations or perforation of any vertebral body cortices, clearly demonstrates the high level of accuracy obtained while adopting this technique in our clinical practice.
The use of intraoperative patient specific 3D-printed guides for each instrumented vertebra in spinal deformity surgery renders the use of intraoperative 2D fluoroscopy for pedicle screw insertion superfluous. However, we still advise to intraoperatively check and identify the 12th thoracic vertebral body by a single PA and lateral 2D fluoroscopy image and to subsequently count toward and determine the most cranial vertebra to be instrumented, prior to starting pedicle screw preparation and insertion. The use of intraoperative patient specific 3D-printed guides prevents the C-arm from physically interfering with the surgical team during screw insertion. In addition, intraoperative radiation loads for both the patient and surgical team are minimized and in doing so the ALARA (as low as reasonably achievable) concept of radiation dosage is realized. On the other hand, a preoperative CT-scan is necessary in all cases for planning purposes. The radiation load of this preoperative low-dose CT-scan, however, is generally very modest, depending on the number of vertebrae selected for instrumentation, overall scanning length, the age of the patient, body mass index and gender. In our series, the dose-length-product (DLP) for the low-dose CT-scan according to the MySpine® protocol measured for the first case amounted to 123 mGycm. The mean DLP for the low-dose CT-scan according to the local ULD MySpine® protocol with an additional SPS filter (Sn), amounted to 39,25 mGycm (range 18–54) in the next 4 patients (Table 1). The effective dose, calculated by using the conversion factor for DLP to effective dose, adapted for age and body part and according to the new International Commission on Radiological Protection (ICRP) recommendations [22], was 2.21 mSv in the first patient. The mean effective dose for the next 4 patients amounted to 0.56 mSv (range 0.26–0.74) (Table 1). In comparison, the mean effective dose of a standard standing full spine PA and lateral radiograph is 0.7 mSv [14].
Of the planned 124 screws, a total of 8 screws could not be inserted because of the flat anatomy of the pedicles, as revealed on the low-dose CT-scan (Fig. 3). In our experience, we found that the 3D digital preoperative planning helps the surgeon to recognize these occasionally flat pedicles, often located at the concave side of the thoracic curvature, and thereby helps preventing accidental neurological complications potentially caused by screw insertion attempts into these altered pedicles. In a total number of 17 instances, the surgeon intraoperatively decided not to insert a contralateral screw so as to both avoid a 100% screw density as well as facilitate posterior spinal fusion.
Correct docking of the 3D guide requires meticulous preparation of the bony anatomy including the spinous process. However, removing the interspinous ligament at the most proximal instrumented thoracic vertebra possibly increases the risk of postoperative proximal junctional kyphosis. In order to prevent future proximal junctional kyphosis in thoracolumbar spinal deformity surgery, we advise adding proximal ‘topping-off’ laminar hooks into the instrumentation.
Before introducing this new patient matching technique for pedicle screw insertion in spinal deformity surgery with intraoperative patient specific 3D-printed guides into our clinical practice, a prospective risk analysis was performed, according to the Bow-Tie model [23]. This was done in order to identify existing and missing barriers for potential critical events. The analysis was carried out by a multidisciplinary team, consisting of two orthopedic surgeons, the unit head of the OR department, a scrub nurse, a representative of the central sterilization department, a representative of the radiology department, an independent neurosurgeon and a representative of the company providing us with the technology and hardware. The analysis was supervised by 2 senior advisors of the Hospital Quality and Risk & Safety department. The analyzing team defined the potential critical events in a brainstorming session on how to avoid the patients suffering from any potential adverse event associated with the clinical adoption of a new surgical technique. Subsequently, the risk factors and the current and required barriers in the pre, per- and postoperative process were identified. Based on the reported outcome of this meeting, an implementation plan with defined responsibilities and associated timelines was developed. In total, 18 potential adverse events were identified, analyzed and addressed in this plan. In addition, some critical features regarding the intended use of 3D-printed patient specific guides in spinal deformity cases were recognized. First of all, at the time of preforming this prospective risk analysis, it routinely took the supplying company two to three weeks to have all components of the technology available for elective surgery. This technique, therefore, is not suitable for use in acute procedures such as trauma or oncology cases. Spinal deformity surgeries however, are planned well in advance, which makes the use of 3D-printed patient specific guides a viable option for this type of surgery. Secondly, since confidential patient information is, albeit encrypted, shared digitally with the team from MySpine®, provisions and requirements related to processing and saving of patient’s data according to the General Data Protection Regulation (GDPR) should be taken into account. Finally, screw misplacement was considered to constitute a significant potential adverse event to be measured and evaluated. It was therefore recommended to include a postoperative assessment of screw insertion accuracy in the first 5 patients as part of the implementation plan. This recommendation served as the basis for the current report.
We acknowledge several limitations to this study. Firstly, this was a single-center study involving five consecutive patients. For a more reliable superimpose CT-analysis of pedicle screw insertion accuracy using 3D-printed patient specific guides for spinal deformity surgeries, a larger number of evaluated patients and pedicle screws would be needed. We did, however, demonstrate a high accuracy of pedicle screw insertion in the first 5 patients we treated with the help of this technology, while routinely planned postoperative CT-scan imaging for such an assessment would significantly increase the cumulative radiation loads of these patients. Secondly, these five consecutive patients were all operated on by a single surgical team. This might have had an effect on the results based on the nature of its learning curve. Thirdly, we did not report on clinical patient outcomes such as fixation failure, quality of life assessments or fusion rates, which would have emanated from a long-term follow-up. These should also be evaluated in future studies.