TY - JOUR
T1 - Development and validation of a parsimonious and pragmatic CHARM score to predict mortality in patients with suspected sepsis
AU - Chen, Kuan Fu
AU - Liu, Su Hsun
AU - Li, Chih Huang
AU - Wu, Chin Chieh
AU - Chaou, Chung Hsien
AU - Tzeng, I. Shiang
AU - Hsieh, Yu Hsiang
AU - Blaney, Gerald N.
AU - Liu, Zhen Ying
AU - Han, Shih Tsung
AU - Chan, Yi Lin
N1 - Publisher Copyright:
© 2016 Elsevier Inc.
PY - 2017/4/1
Y1 - 2017/4/1
N2 - Background We aimed to derive and validate a parsimonious and pragmatic clinical prediction rule using the concepts of Predisposition, Infection, Response, and Organ Dysfunction to predict in-hospital mortality; and to compare it with other prediction rules, as well as with conventional biomarkers for evaluating the mortality risk of patients with suspected sepsis in the emergency department (ED). Methods We conducted a pragmatic cohort study with consecutive ED patients aged 18 or older with documented diagnostic codes of infection and two sets of blood culture ordered by physicians between 2010 and 2012 in a tertiary teaching hospital. Results 7011 and 12,110 patients were included in the derivation cohort and the validation cohort for the final analysis. There were 479 deaths (7%) in the derivation cohort and 1145 deaths (9%) in the validation cohort. Independent predictors of death were absence of Chills (odds ratio: 2.28, 95% confidence interval: 1.75–2.97), Hypothermia (2.12, 1.57–2.85), Anemia (2.45, 1.97–3.04), wide Red cell Distribution Width (RDW) (3.27, 2.63–4.05) and history of Malignancy (2.00, 1.63–2.46). This novel clinical prediction rule (CHARM) performed well for stratifying patients into mortality risk groups (sensitivity: 99.4%, negative predictive value 99.7%, receiver operating characteristic area 0.77). The CHARM score also outperformed the other scores or biomarkers such as PIRO, SIRS, MEDS, CURB-65, C-reactive protein, procalcitonin and lactate (all p < .05). Conclusions In patients with suspected sepsis, this parsimonious and pragmatic model could be utilized to stratify the mortality risk of patients in the early stage of sepsis.
AB - Background We aimed to derive and validate a parsimonious and pragmatic clinical prediction rule using the concepts of Predisposition, Infection, Response, and Organ Dysfunction to predict in-hospital mortality; and to compare it with other prediction rules, as well as with conventional biomarkers for evaluating the mortality risk of patients with suspected sepsis in the emergency department (ED). Methods We conducted a pragmatic cohort study with consecutive ED patients aged 18 or older with documented diagnostic codes of infection and two sets of blood culture ordered by physicians between 2010 and 2012 in a tertiary teaching hospital. Results 7011 and 12,110 patients were included in the derivation cohort and the validation cohort for the final analysis. There were 479 deaths (7%) in the derivation cohort and 1145 deaths (9%) in the validation cohort. Independent predictors of death were absence of Chills (odds ratio: 2.28, 95% confidence interval: 1.75–2.97), Hypothermia (2.12, 1.57–2.85), Anemia (2.45, 1.97–3.04), wide Red cell Distribution Width (RDW) (3.27, 2.63–4.05) and history of Malignancy (2.00, 1.63–2.46). This novel clinical prediction rule (CHARM) performed well for stratifying patients into mortality risk groups (sensitivity: 99.4%, negative predictive value 99.7%, receiver operating characteristic area 0.77). The CHARM score also outperformed the other scores or biomarkers such as PIRO, SIRS, MEDS, CURB-65, C-reactive protein, procalcitonin and lactate (all p < .05). Conclusions In patients with suspected sepsis, this parsimonious and pragmatic model could be utilized to stratify the mortality risk of patients in the early stage of sepsis.
KW - Clinical prediction rule
KW - Mortality
KW - Outcome
KW - Sepsis
KW - Severity of illness index
UR - http://www.scopus.com/inward/record.url?scp=85006274831&partnerID=8YFLogxK
U2 - 10.1016/j.ajem.2016.10.075
DO - 10.1016/j.ajem.2016.10.075
M3 - 文章
C2 - 27832977
AN - SCOPUS:85006274831
SN - 0735-6757
VL - 35
SP - 640
EP - 646
JO - American Journal of Emergency Medicine
JF - American Journal of Emergency Medicine
IS - 4
ER -