Random forest modeling can predict infectious complications following trauma laparotomy.


Journal

The journal of trauma and acute care surgery
ISSN: 2163-0763
Titre abrégé: J Trauma Acute Care Surg
Pays: United States
ID NLM: 101570622

Informations de publication

Date de publication:
11 2019
Historique:
pubmed: 20 8 2019
medline: 26 5 2020
entrez: 20 8 2019
Statut: ppublish

Résumé

Identifying clinical and biomarker profiles of trauma patients may facilitate the creation of models that predict postoperative complications. We sought to determine the utility of modeling for predicting severe sepsis (SS) and organ space infections (OSI) following laparotomy for abdominal trauma. Clinical and molecular biomarker data were collected prospectively from patients undergoing exploratory laparotomy for abdominal trauma at a Level I trauma center between 2014 and 2017. Machine learning algorithms were used to develop models predicting SS and OSI. Random forest (RF) was performed, and features were selected using backward elimination. The SS model was trained on 117 records and validated using the leave-one-out method on the remaining 15 records. The OSI model was trained on 113 records and validated on the remaining 19. Models were assessed using areas under the curve. One hundred thirty-two patients were included (median age, 30 years [23-42 years], 68.9% penetrating injury, median Injury Severity Score of 18 [10-27]). Of these, 10.6% (14 of 132) developed SS and 13.6% (18 of 132) developed OSI. The final RF model resulted in five variables for SS (Penetrating Abdominal Trauma Index, serum epidermal growth factor, monocyte chemoattractant protein-1, interleukin-6, and eotaxin) and four variables for OSI (Penetrating Abdominal Trauma Index, serum epidermal growth factor, monocyte chemoattractant protein-1, and interleukin-8). The RF models predicted SS and OSI with areas under the curve of 0.798 and 0.774, respectively. Random forests with RFE can help identify clinical and biomarker profiles predictive of SS and OSI after trauma laparotomy. Once validated, these models could be used as clinical decision support tools for earlier detection and treatment of infectious complications following injury. Prognostic, level III.

Sections du résumé

BACKGROUND
Identifying clinical and biomarker profiles of trauma patients may facilitate the creation of models that predict postoperative complications. We sought to determine the utility of modeling for predicting severe sepsis (SS) and organ space infections (OSI) following laparotomy for abdominal trauma.
METHODS
Clinical and molecular biomarker data were collected prospectively from patients undergoing exploratory laparotomy for abdominal trauma at a Level I trauma center between 2014 and 2017. Machine learning algorithms were used to develop models predicting SS and OSI. Random forest (RF) was performed, and features were selected using backward elimination. The SS model was trained on 117 records and validated using the leave-one-out method on the remaining 15 records. The OSI model was trained on 113 records and validated on the remaining 19. Models were assessed using areas under the curve.
RESULTS
One hundred thirty-two patients were included (median age, 30 years [23-42 years], 68.9% penetrating injury, median Injury Severity Score of 18 [10-27]). Of these, 10.6% (14 of 132) developed SS and 13.6% (18 of 132) developed OSI. The final RF model resulted in five variables for SS (Penetrating Abdominal Trauma Index, serum epidermal growth factor, monocyte chemoattractant protein-1, interleukin-6, and eotaxin) and four variables for OSI (Penetrating Abdominal Trauma Index, serum epidermal growth factor, monocyte chemoattractant protein-1, and interleukin-8). The RF models predicted SS and OSI with areas under the curve of 0.798 and 0.774, respectively.
CONCLUSION
Random forests with RFE can help identify clinical and biomarker profiles predictive of SS and OSI after trauma laparotomy. Once validated, these models could be used as clinical decision support tools for earlier detection and treatment of infectious complications following injury.
LEVEL OF EVIDENCE
Prognostic, level III.

Identifiants

pubmed: 31425495
doi: 10.1097/TA.0000000000002486
doi:

Types de publication

Evaluation Study Journal Article Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

1125-1132

Auteurs

Rondi B Gelbard (RB)

From the Department of Surgery, Emory University School of Medicine (R.B.G., B.M.T., C.J.D., T.B., A.K.), Atlanta, Georgia; Department of Trauma & Surgical Critical Care, Grady Memorial Hospital (R.B.G., B.M.T., C.J.D.), Atlanta, Georgia; Department of Surgery, Uniformed Services University of the Health Sciences (S.S., V.K., E.E.) and Walter Reed National Military Medical Center (S.S., V.K., E.E.), Bethesda, Maryland; Surgical Critical Care Initiative (SC2i) (R.B.G., H.H., S.S., V.K., C.J.D., T.B., A.K., E.E.), Bethesda, Maryland; DecisionQ Corporation (H.H.), Arlington, Virginia; Department of Surgery, Duke University (A.K.), Durham, North Carolina; and Henry M. Jackson Foundation for the Advancement of Military Medicine (S.S., V.K.), Bethesda, Maryland.

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