Advertisement for orthosearch.org.uk
Results 1 - 2 of 2
Results per page:
Applied filters
Include Proceedings
Dates
Year From

Year To
Orthopaedic Proceedings
Vol. 94-B, Issue SUPP_X | Pages 146 - 146
1 Apr 2012
Kanwar A Anderton M Peet H Wigfield C
Full Access

To assess concordance between hospital coding and clinician coding for patients undergoing spinal instrumentation procedures and determine if our coding systems result in accurate financial reimbursement from the primary care trust (PCT).

We conducted a one year retrospective review of 41 patients who underwent spinal instrumentation procedures. Data collected from IT systems included: operation description, clinician procedure code, hospital procedure code, Hospital Health Resource grouping (HRG), clinician HRG, instrumentation costs and PCT reimbursement fees. From this data we compared coding based re-imbursement fees and actual surgical costs, taking into account exact instrumentation prices.

In all cases the primary hospital and clinician coding values differed. Using the clinician code would have altered the HRG group in 16 patients. Using solely clinician coding would have generated less financial reimbursement than using hospital coding.

In 23 patients undergoing complex spinal procedures, instrumentation costs represented a significant proportion of the final fee obtained from the PCT, thus leaving a small proportion for the associated hospital stay costs. This suggests instrumentation costs are inadequately reimbursed from the PCT.

Hospital coding appears more accurate than clinician coding and results in greater financial reimbursement. On the whole, we found there to be insufficient reimbursement from the PCT. The variable and sometimes substantial cost of spinal instrumentation procedures results in inadequate reimbursement for many procedures. We feel the payment by results (PBR) scheme is suboptimal for such procedures and adequate reimbursement can only be achieved by direct billing on an individual case basis.


Orthopaedic Proceedings
Vol. 84-B, Issue SUPP_III | Pages 335 - 335
1 Nov 2002
Wigfield C Gill S Nelson R Metcalf N Robertson J
Full Access

Objective: To assess the safety, clinical stability and capacity to preserve motion in the cervical spine of a newly designed cervical intervertebral disc replacement for patients with degenerative disc disease.

Design: A prospective cohort pilot study.

Subjects: Fifteen patients considered to be at risk of developing adjacent level degenerative changes received the artificial joint. Patients had either radiculopathy and/or myelopathy with radiological evidence of compression.

Outcome Measures: Radiological evidence of stability of the device and preservation of motion at the operated level and adverse events associated with the procedure. Secondary outcome measures were changes in scores on SF-36, Neck Disability Index, European Myelopathy Score and Visual Analogue Pain Scale assessments.

Results: The artificial joint maintained motion at the operated in all patients. The procedure was considered safe to be performed by experienced spine surgeons. The device was stable with no dislocation of components or backing out of screws. Improvements were noted in all of the assessment scores though statistical significance was not achieved.

Conclusions: Cervical intervertebral motion can be maintained with this device which at two years is clinically stable. The long-term influence of this device remains unknown.