Clinical StudyThe safety of instrumented outpatient anterior cervical discectomy and fusion
Introduction
Anterior cervical discectomy and fusion (ACDF) has proven to be a safe and effective procedure for the treatment of a multitude of spinal disorders [1], [2], [3], [4], [5], [6], [7], [8], [9]. A considerable controversy exists regarding the necessity of fusion [10], [11], [12], [13], [14] and instrumentation [4], [15], [16]. However, complication rates are low with instrumented ACDF [17], [18], [19], and there are substantial benefits that have been reported in adding instrumentation, such as beneficial effects on long-term stabilization [1], increased fusion rates for one- and two-level procedures [18], [20], and decreased kyphotic deformity associated with pseudoarthroses [19], [20], [21]. Additionally, the use of plating has been demonstrated to significantly reduce convalescent time, thus decreasing the economic impact of undergoing ACDF [6].
One way to potentially reduce the total cost of surgery is to perform procedures on an outpatient basis. There are substantial benefits to outpatient surgeries besides overall reduced costs, including decreased exposure to nosocomial infections [22], [23]. In a series of 103 patients, Silvers et al. [22] reported that converting single and two-level noninstrumented ACDF from an admitted to an ambulatory procedure is safe, effective, and can substantially reduce the economic impact of the surgery. However, currently there is only one study which assesses outpatient instrumented ACDF, the investigation by Stieber et al. [24].
The purpose of our study was to evaluate the safety and feasibility of performing single, two- and three-level ACDF with instrumentation on an outpatient basis (including patients who would not have met the outpatient inclusion criteria from the Stieber [24] study), in order to potentially diminish the additional cost of hardware, without compromising the purported benefits of instrumentation.
Section snippets
Study design
Over a 2-year period from April 2003 to April 2005, 103 patients were enrolled in our study in order to evaluate the feasibility and safety of performing ACDF with instrumentation procedures on an outpatient basis. This study was a retrospective chart review evaluating the safety of outpatient ACDF with plating. The safety and feasibility of performing ACDF as an outpatient procedure were assessed comparing intraoperative and perioperative complications, which were reported for a 6-month
Complications
Incidences of complications in the patient population are presented as major and minor (Table 3) according to the criteria described in the Methods section. The overall complication rate was 3.8% (n=4), including 1.9% (n=2) major and 1.9% (n=2) minor complications. Six patients (5.8%) in the study had dysphagia, and four (3.9%) had hoarseness of voice. These complications were transient, did not require any treatment, and were not included in the analysis of complication rates. One adverse
Discussion
Anterior cervical discectomy and fusion has long been the treatment of choice for many different spinal disorders. Since originally described by Smith and Robinson [25] and Cloward [26], the ACDF procedure has evolved to include plating. The addition of instrumentation has been shown to be safe, with a low hardware-related complication rate that varies from 0 to 5% [3], [5], [6], [18], [19], [20], [21] for a wide range of clinical indications. There are substantial clinical and financial
Conclusion
Performing ACDF with instrumentation on an outpatient basis is feasible, and it is not associated with higher overall or hardware-related complication rates as compared with a meta-analysis comparison group, suggesting that this procedure is safe to perform on an outpatient basis.
Acknowledgment
This work was supported by the Justin Parker Neurosurgical Research Foundation.
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