TY - JOUR
T1 - Development and validation of BLOOMY prediction scores for 14-day and 6-month mortality in hospitalised adults with bloodstream infections
T2 - a multicentre, prospective, cohort study
AU - DZIF BLOOMY study group
AU - Tacconelli, Evelina
AU - Göpel, Siri
AU - Gladstone, Beryl P.
AU - Eisenbeis, Simone
AU - Hölzl, Florian
AU - Buhl, Michael
AU - Górska, Anna
AU - Cattaneo, Chiara
AU - Mischnik, Alexander
AU - Rieg, Siegbert
AU - Rohde, Anna M.
AU - Kohlmorgen, Britta
AU - Falgenhauer, Jane
AU - Trauth, Janina
AU - Käding, Nadja
AU - Kramme, Evelyn
AU - Biehl, Lena M.
AU - Walker, Sarah V.
AU - Peter, Silke
AU - Gastmeier, Petra
AU - Chakraborty, Trinad
AU - Vehreschild, Maria JGT
AU - Seifert, Harald
AU - Rupp, Jan
AU - Kern, Winfried V.
AU - Lemke, Elke
AU - Thoma, Norbert
AU - Wolke, Solvy
AU - Imirzalioglu, Can
AU - Herold, Susanne
AU - Tewes, Nicole
AU - Fritzenwanker, Moritz
AU - Vehreschild, Jörg Janne
AU - Classen, Annika Yanina
AU - Tobys, David
AU - Higgins, Paul
AU - Blum, Yannic
AU - Kleipaß, Matthias
AU - Höltig, Lisa
AU - Nagel, Katharina
AU - Schmauder, Kristina
AU - Künstle, Larissa
AU - Stoll, Elisabeth
AU - Dinkelacker, Ariane Gertraud
AU - Peyerl-Hoffmann, Gabriele
AU - Häcker, Georg
AU - Spitznagel, Heike
AU - Olawumi-Hurter, Sara Christina
N1 - Publisher Copyright:
© 2022 Elsevier Ltd
PY - 2022/5
Y1 - 2022/5
N2 - Background: The burden of bloodstream infections remains high worldwide and cannot be confined to short-term in-hospital mortality. We aimed to develop scores to predict short-term and long-term mortality in patients with bloodstream infections. Methods: The Bloodstream Infection due to Multidrug-resistant Organisms: Multicenter Study on Risk Factors and Clinical Outcomes (BLOOMY) study is a prospective, multicentre cohort study at six German tertiary care university hospitals to develop and validate two scores assessing 14-day and 6-month mortality in patients with bloodstream infections. We excluded patients younger than 18 years or who were admitted to an ophthalmology or psychiatry ward. Microbiological, clinical, laboratory, treatment, and survival data were prospectively collected on day 0 and day 3 and then from day 7 onwards, weekly. Participants were followed up for 6 months. All patients in the derivation cohort who were alive on day 3 were included in the analysis. Predictive scores were developed using logistic regression and Cox proportional hazards models with a machine-learning approach. Validation was completed using the C statistic and predictive accuracy was assessed using sensitivity, specificity, and predictive values. Findings: Between Feb 1, 2017, and Jan 31, 2019, 2568 (61·5%) of 4179 eligible patients were recruited into the derivation cohort. The in-hospital mortality rate was 23·75% (95% CI 22·15–25·44; 610 of 2568 patients) and the 6-month mortality rate was 41·55% (39·54–43·59; 949 of 2284). The model predictors for 14-day mortality (C statistic 0·873, 95% CI 0·849–0·896) and 6-month mortality (0·807, 0·784–0·831) included age, body-mass index, platelet and leukocyte counts, C-reactive protein concentrations, malignancy (ie, comorbidity), in-hospital acquisition, and pathogen. Additional predictors were, for 14-day mortality, mental status, hypotension, and the need for mechanical ventilation on day 3 and, for 6-month mortality, focus of infection, in-hospital complications, and glomerular filtration rate at the end of treatment. The scores were validated in a cohort of 1023 patients with bloodstream infections, recruited between Oct 9, 2019, and Dec 31, 2020. The BLOOMY 14-day score showed a sensitivity of 61·32% (95% CI 51·81–70·04), a specificity of 86·36% (83·80–88·58), a positive predictive value (PPV) of 37·57% (30·70–44·99), and a negative predictive value (NPV) of 94·35% (92·42–95·80). The BLOOMY 6-month score showed a sensitivity of 69·93% (61·97–76·84), a specificity of 66·44% (61·86–70·73), a PPV of 40·82% (34·85–47·07), and a NPV of 86·97% (82·91–90·18). Interpretation: The BLOOMY scores showed good discrimination and predictive values and could support the development of protocols to manage bloodstream infections and also help to estimate the short-term and long-term burdens of bloodstream infections. Funding: DZIF German Center for Infection Research. Translation: For the German translation of the abstract see Supplementary Materials section.
AB - Background: The burden of bloodstream infections remains high worldwide and cannot be confined to short-term in-hospital mortality. We aimed to develop scores to predict short-term and long-term mortality in patients with bloodstream infections. Methods: The Bloodstream Infection due to Multidrug-resistant Organisms: Multicenter Study on Risk Factors and Clinical Outcomes (BLOOMY) study is a prospective, multicentre cohort study at six German tertiary care university hospitals to develop and validate two scores assessing 14-day and 6-month mortality in patients with bloodstream infections. We excluded patients younger than 18 years or who were admitted to an ophthalmology or psychiatry ward. Microbiological, clinical, laboratory, treatment, and survival data were prospectively collected on day 0 and day 3 and then from day 7 onwards, weekly. Participants were followed up for 6 months. All patients in the derivation cohort who were alive on day 3 were included in the analysis. Predictive scores were developed using logistic regression and Cox proportional hazards models with a machine-learning approach. Validation was completed using the C statistic and predictive accuracy was assessed using sensitivity, specificity, and predictive values. Findings: Between Feb 1, 2017, and Jan 31, 2019, 2568 (61·5%) of 4179 eligible patients were recruited into the derivation cohort. The in-hospital mortality rate was 23·75% (95% CI 22·15–25·44; 610 of 2568 patients) and the 6-month mortality rate was 41·55% (39·54–43·59; 949 of 2284). The model predictors for 14-day mortality (C statistic 0·873, 95% CI 0·849–0·896) and 6-month mortality (0·807, 0·784–0·831) included age, body-mass index, platelet and leukocyte counts, C-reactive protein concentrations, malignancy (ie, comorbidity), in-hospital acquisition, and pathogen. Additional predictors were, for 14-day mortality, mental status, hypotension, and the need for mechanical ventilation on day 3 and, for 6-month mortality, focus of infection, in-hospital complications, and glomerular filtration rate at the end of treatment. The scores were validated in a cohort of 1023 patients with bloodstream infections, recruited between Oct 9, 2019, and Dec 31, 2020. The BLOOMY 14-day score showed a sensitivity of 61·32% (95% CI 51·81–70·04), a specificity of 86·36% (83·80–88·58), a positive predictive value (PPV) of 37·57% (30·70–44·99), and a negative predictive value (NPV) of 94·35% (92·42–95·80). The BLOOMY 6-month score showed a sensitivity of 69·93% (61·97–76·84), a specificity of 66·44% (61·86–70·73), a PPV of 40·82% (34·85–47·07), and a NPV of 86·97% (82·91–90·18). Interpretation: The BLOOMY scores showed good discrimination and predictive values and could support the development of protocols to manage bloodstream infections and also help to estimate the short-term and long-term burdens of bloodstream infections. Funding: DZIF German Center for Infection Research. Translation: For the German translation of the abstract see Supplementary Materials section.
UR - http://www.scopus.com/inward/record.url?scp=85123105300&partnerID=8YFLogxK
U2 - 10.1016/S1473-3099(21)00587-9
DO - 10.1016/S1473-3099(21)00587-9
M3 - Journal articles
AN - SCOPUS:85123105300
SN - 1473-3099
VL - 22
SP - 731
EP - 741
JO - The Lancet Infectious Diseases
JF - The Lancet Infectious Diseases
IS - 5
ER -