Nomogram for predicting 90-day mortality in patients with Acinetobacter baumannii-caused hospital-acquired and ventilator-associated pneumonia in the respiratory intensive care unit

Objective We built a prediction model of mortality risk in patients the with Acinetobacter baumannii (AB)-caused hospital-acquired (HAP) and ventilator-associated pneumonia (VAP). Methods In this retrospective study, 164 patients with AB lower respiratory tract infection were admitted to the respira...

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Veröffentlicht in:Journal of international medical research 2023-03, Vol.51 (3), p.3000605231161481-3000605231161481
Hauptverfasser: Pei, Yongjian, Huang, Yongkang, Pan, Xue, Yao, Zhen, Chen, Chen, Zhong, Anyuan, Xing, Yufei, Qian, Bin, Minhua, Shi, Zhou, Tong
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container_title Journal of international medical research
container_volume 51
creator Pei, Yongjian
Huang, Yongkang
Pan, Xue
Yao, Zhen
Chen, Chen
Zhong, Anyuan
Xing, Yufei
Qian, Bin
Minhua, Shi
Zhou, Tong
description Objective We built a prediction model of mortality risk in patients the with Acinetobacter baumannii (AB)-caused hospital-acquired (HAP) and ventilator-associated pneumonia (VAP). Methods In this retrospective study, 164 patients with AB lower respiratory tract infection were admitted to the respiratory intensive care unit (RICU) from January 2019 to August 2021 (29 with HAP, 135 with VAP) and grouped randomly into a training cohort (n = 115) and a validation cohort (n = 49). Least absolute shrinkage and selection operator regression and multivariate Cox regression were used to identify risk factors of 90-day mortality. We built a nomogram prediction model and evaluated model discrimination and calibration using the area under the receiver operating characteristic curve (AUC) and calibration curves, respectively. Results Four predictors (days in intensive care unit, infection with carbapenem-resistant AB, days of carbapenem use within 90 days of isolating AB, and septic shock) were used to build the nomogram. The AUC of the two groups was 0.922 and 0.823, respectively. The predictive model was well-calibrated; decision curve analysis showed the proposed nomogram would obtain a net benefit with threshold probability between 1% and 100%. Conclusions The nomogram model showed good performance, making it useful in managing patients with AB-caused HAP and VAP.
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Methods In this retrospective study, 164 patients with AB lower respiratory tract infection were admitted to the respiratory intensive care unit (RICU) from January 2019 to August 2021 (29 with HAP, 135 with VAP) and grouped randomly into a training cohort (n = 115) and a validation cohort (n = 49). Least absolute shrinkage and selection operator regression and multivariate Cox regression were used to identify risk factors of 90-day mortality. We built a nomogram prediction model and evaluated model discrimination and calibration using the area under the receiver operating characteristic curve (AUC) and calibration curves, respectively. Results Four predictors (days in intensive care unit, infection with carbapenem-resistant AB, days of carbapenem use within 90 days of isolating AB, and septic shock) were used to build the nomogram. The AUC of the two groups was 0.922 and 0.823, respectively. The predictive model was well-calibrated; decision curve analysis showed the proposed nomogram would obtain a net benefit with threshold probability between 1% and 100%. Conclusions The nomogram model showed good performance, making it useful in managing patients with AB-caused HAP and VAP.</description><identifier>ISSN: 0300-0605</identifier><identifier>EISSN: 1473-2300</identifier><identifier>DOI: 10.1177/03000605231161481</identifier><identifier>PMID: 36935582</identifier><language>eng</language><publisher>London, England: SAGE Publications</publisher><subject>Acinetobacter baumannii ; Carbapenems ; Hospitals ; Humans ; Intensive care ; Intensive Care Units ; Mortality ; Nomograms ; Pneumonia ; Pneumonia, Ventilator-Associated - drug therapy ; Pneumonia, Ventilator-Associated - etiology ; Retrospective Clinical Research Report ; Retrospective Studies ; Ventilators</subject><ispartof>Journal of international medical research, 2023-03, Vol.51 (3), p.3000605231161481-3000605231161481</ispartof><rights>The Author(s) 2023</rights><rights>The Author(s) 2023. 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Methods In this retrospective study, 164 patients with AB lower respiratory tract infection were admitted to the respiratory intensive care unit (RICU) from January 2019 to August 2021 (29 with HAP, 135 with VAP) and grouped randomly into a training cohort (n = 115) and a validation cohort (n = 49). Least absolute shrinkage and selection operator regression and multivariate Cox regression were used to identify risk factors of 90-day mortality. We built a nomogram prediction model and evaluated model discrimination and calibration using the area under the receiver operating characteristic curve (AUC) and calibration curves, respectively. Results Four predictors (days in intensive care unit, infection with carbapenem-resistant AB, days of carbapenem use within 90 days of isolating AB, and septic shock) were used to build the nomogram. The AUC of the two groups was 0.922 and 0.823, respectively. The predictive model was well-calibrated; decision curve analysis showed the proposed nomogram would obtain a net benefit with threshold probability between 1% and 100%. Conclusions The nomogram model showed good performance, making it useful in managing patients with AB-caused HAP and VAP.</abstract><cop>London, England</cop><pub>SAGE Publications</pub><pmid>36935582</pmid><doi>10.1177/03000605231161481</doi><orcidid>https://orcid.org/0000-0002-9853-6596</orcidid><orcidid>https://orcid.org/0000-0003-2806-9192</orcidid><oa>free_for_read</oa></addata></record>
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subjects Acinetobacter baumannii
Carbapenems
Hospitals
Humans
Intensive care
Intensive Care Units
Mortality
Nomograms
Pneumonia
Pneumonia, Ventilator-Associated - drug therapy
Pneumonia, Ventilator-Associated - etiology
Retrospective Clinical Research Report
Retrospective Studies
Ventilators
title Nomogram for predicting 90-day mortality in patients with Acinetobacter baumannii-caused hospital-acquired and ventilator-associated pneumonia in the respiratory intensive care unit
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