Gallardo-Pizarro Antonio, Teijón-Lumbreras Christian, Monzo-Gallo Patricia, Aiello Tommaso Francesco, Chumbita Mariana, Peyrony Olivier, Gras Emmanuelle, Pitart Cristina, Mensa Josep, Esteve Jordi, Soriano Alex, Garcia-Vidal Carolina
Department of Infectious Diseases, Hospital Clinic of Barcelona-IDIBAPS, 08036 Barcelona, Spain.
Facultat de Medicina i Ciències de la Salut, Universitat de Barcelona (UB), c. Casanova, 143, 08036 Barcelona, Spain.
Antibiotics (Basel). 2024 Dec 28;14(1):13. doi: 10.3390/antibiotics14010013.
The rise of multidrug-resistant (MDR) infections demands personalized antibiotic strategies for febrile neutropenia (FN) in hematological malignancies. This study investigates machine learning (ML) for identifying patient profiles with increased susceptibility to bloodstream infections (BSI) during FN onset, aiming to tailor treatment approaches. From January 2020 to June 2022, we used the unsupervised ML algorithm KAMILA to analyze data from hospitalized hematological malignancy patients. Eleven features categorized clinical phenotypes and determined BSI and multidrug-resistant Gram-negative bacilli (MDR-GNB) prevalences at FN onset. Model performance was evaluated with a validation cohort from July 2022 to March 2023. Among 462 FN episodes analyzed in the development cohort, 116 (25.1%) had BSIs. KAMILA's stratification identified three risk clusters: Cluster 1 (low risk), Cluster 2 (intermediate risk), and Cluster 3 (high risk). Cluster 2 (28.4% of episodes) and Cluster 3 (43.7%) exhibited higher BSI rates of 26.7% and 37.6% and GNB BSI rates of 13.4% and 19.3%, respectively. Cluster 3 had a higher incidence of MDR-GNB BSIs, accounting for 75% of all MDR-GNB BSIs. Cluster 1 (27.9% of episodes) showed a lower BSI risk (<1%) with no GNB infections. Validation cohort results were similar: Cluster 3 had a BSI rate of 38.1%, including 78% of all MDR-GNB BSIs, while Cluster 1 had no GNB-related BSIs. Unsupervised ML-based risk stratification enhances evidence-driven decision-making for empiric antibiotic therapies at FN onset, crucial in an era of rising multi-drug resistance.
多重耐药(MDR)感染的增加需要针对血液系统恶性肿瘤患者发热性中性粒细胞减少症(FN)制定个性化的抗生素治疗策略。本研究探讨了机器学习(ML)在识别FN发作期间血流感染(BSI)易感性增加的患者特征方面的应用,旨在调整治疗方法。2020年1月至2022年6月,我们使用无监督ML算法KAMILA分析了住院血液系统恶性肿瘤患者的数据。11个特征对临床表型进行了分类,并确定了FN发作时BSI和多重耐药革兰氏阴性杆菌(MDR-GNB)的患病率。使用2022年7月至2023年3月的验证队列评估模型性能。在开发队列分析的462例FN发作中,116例(25.1%)发生了BSI。KAMILA分层确定了三个风险组:第1组(低风险)、第2组(中风险)和第3组(高风险)。第2组(发作的28.4%)和第3组(43.7%)的BSI发生率较高,分别为26.7%和37.6%,GNB BSI发生率分别为13.4%和19.3%。第3组MDR-GNB BSI的发生率较高,占所有MDR-GNB BSI的75%。第1组(发作的27.9%)的BSI风险较低(<1%),无GNB感染。验证队列的结果相似:第3组的BSI发生率为38.1%,包括所有MDR-GNB BSI的78%,而第1组无GNB相关的BSI。基于无监督ML的风险分层增强了FN发作时经验性抗生素治疗的循证决策,这在多重耐药性不断上升的时代至关重要。