A validated preoperative score for predicting 30-day readmission after 1-2 level elective posterior lumbar fusion

A validated preoperative score for predicting 30-day readmission after 1-2 level elective posterior lumbar fusion

Deeptee Jain, Paramjit Singh, Mayur Kardile, Sigurd H. Berven

March 2019, pp 1 - 7
DOI
10.1007/s00586-019-05937-y
First Online: 09 March 2019
Abstract

Purpose

To develop a model to predict 30-day readmission rates in elective 1–2 level posterior lumbar spine fusion (PSF) patients.

Methods

In this retrospective case control study, patients were identified in the State Inpatient Database using ICD-9 codes. Data were queried for 30-day readmission, as well as demographic and surgical data. Patients were randomly assigned to either the derivation or the validation cohort. Stepwise multivariate analysis was conducted on the derivation cohort to predict 30-day readmission. Readmission after posterior spinal fusion (RAPSF) score was created by including variables with odds ratio (OR) > 1.1 and p 

Results

There were 92,262 and 90,257 patients in the derivation and validation cohorts. Thirty-day readmission rates were 10.9% and 11.1%, respectively. Variables in RAPSF included: age, female gender, race, insurance, anterior approach, cerebrovascular disease, chronic pulmonary disease, congestive heart failure, diabetes, hemiplegia/paraplegia, rheumatic disease, drug abuse, electrolyte disorder, osteoporosis, depression, obesity, and morbid obesity. Linear regression between readmission rate and RAPSF fits the derivation cohort and validation cohort with an adjusted r 2 of 0.92 and 0.94, respectively, and a coefficient of 0.011 (p 

Conclusion

The RAPSF can accurately predict readmission rates in PSF patients and may be used to guide an evidence-based approach to preoperative optimization and risk adjustment within alternative payment models for elective spine surgery.

Level of evidence

3.

Graphical abstract

These slides can be retrieved under Electronic Supplementary Material.[Figure not available: see fulltext.]