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Predicting outcome following colorectal cancer surgery using a colorectal biochemical and haematological outcome model (Colorectal BHOM)
Author(s) -
Farooq N.,
Patterson A. J.,
Walsh S. R.,
Prytherch D. R.,
Justin T. A.,
Tang T. Y.
Publication year - 2011
Publication title -
colorectal disease
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.029
H-Index - 89
eISSN - 1463-1318
pISSN - 1462-8910
DOI - 10.1111/j.1463-1318.2010.02434.x
Subject(s) - medicine , colorectal cancer , logistic regression , colorectal surgery , discriminative model , hematology , outcome (game theory) , surgery , cancer , abdominal surgery , artificial intelligence , computer science , mathematics , mathematical economics
Aim To present a new biochemistry and haematology outcome model which uses a minimum dataset to model outcome following colorectal cancer surgery, a concept previously shown to be feasible with arterial operations. Method Predictive binary logistic regression models (a mortality and morbidity model) were developed for 704 patients who underwent colorectal cancer surgery over a 6‐year period in one hospital. The variables measured included 30‐day mortality and morbidity. Hosmer–Lemeshow goodness of fit statistics and frequency tables compared the predicted vs the reported number of deaths. Discrimination was quantified using the c‐index. Results There were 573 elective and 131 nonelective interventional cases. The overall mean predicted risk of death was 7.79% (50 patients). The actual number of reported deaths was also 50 patients (χ 2 = 1.331, df = 4, P ‐value = 0.856; no evidence of lack of fit). For the mortality model, the predictive c‐index was = 0.810. The morbidity model had less discriminative power but there was no evidence of lack of fit (χ 2 = 4.198, df = 4, P ‐value = 0.380, c‐index = 0.697). Conclusions The Colorectal Biochemistry and Haematology Outcome mortality model suggests good discrimination (c‐index > 0.8) and uses only a minimal number of variables. However, it needs to be tested on independent datasets in different geographical locations.