Risk factors for mortality in patients with acute leukemia and bloodstream infections in the era of multiresistance

被引:86
作者
Garcia-Vidal, Carolina [1 ]
Cardozo-Espinola, Celia [1 ]
Puerta-Alcalde, Pedro [1 ]
Marco, Francesc [2 ,3 ]
Tellez, Adrian [1 ]
Aguero, Daiana [1 ]
Romero-Santana, Francisco [1 ,4 ]
Diaz-Beya, Marina [5 ]
Gine, Eva [5 ]
Morata, Laura [1 ]
Rodriguez-Nunez, Olga [1 ]
Antonio Martinez, Jose [1 ]
Mensa, Josep [1 ]
Esteve, Jordi [5 ]
Soriano, Alex [1 ]
机构
[1] Hosp Clin IDIBAPS, Infect Dis Dept, Barcelona, Spain
[2] Hosp Clin Barcelona, Ctr Diagnost Biomed, Microbiol Dept, Barcelona, Spain
[3] Univ Barcelona, Hosp Clin, ISGlobal, Barcelona Ctr Int Hlth Res CRESIB, Barcelona, Spain
[4] Hosp Insular Univ Gran Canaria, Internal Med Dept, Las Palmas Gran Canaria, Spain
[5] Hosp Clin DIBAPS, Hematol Dept, Barcelona, Spain
关键词
ACUTE MYELOID-LEUKEMIA; GRAM-NEGATIVE BACILLI; PSEUDOMONAS-AERUGINOSA; HEMATOLOGICAL MALIGNANCIES; ANTIMICROBIAL RESISTANCE; NEUTROPENIC PATIENTS; CANCER-PATIENTS; BACTEREMIA; EPIDEMIOLOGY; BACTERIAL;
D O I
10.1371/journal.pone.0199531
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
Objectives We assess the epidemiology and risk factors for mortality of bloodstream infection (BSI) in patients with acute leukemia (AL). Methods Prospectively collected data of a cohort study from July 2004 to February 2016. Multivariate analyses were performed. Results 589 episodes of BSI were documented in 357 AL patients, 55% caused by gram-positive bacteria (coagulase-negative staphylococci 35.7%, Enterococcus spp 10.8%) and 43.5% by gram-negative bacteria (E. coli 21%, PA 12%). We identified 110 (18.7%) multidrug-resistant (MDR) microorganisms, especially MDR-Pseudomonas aeruginosa (7%) and extended-spectrum beta-lactamase producing Enterobacteriaceae (7%). The 30-day mortality was 14.8%. Age (OR 3.1; 95% CI 1.7-5.7); chronic lung disease (4.8; 1.1-21.8); fatal prognosis according to McCabe index (13.9; 6.4-30.3); shock (3.8; 1.9-7.7); pulmonary infection (3.6; 1.3-9.9); and MDR-PA infections with inappropriate treatment (12.8; 4.1-40.5) were related to mortality. MDR-PA BSI was associated to prior antipseudomonal cephalosporin use (9.31; 4.38-19.79); current use of betalactams (2.01; 1.01-4.3); shock (2.63; 1.03-6.7) and pulmonary source of infection (9.6; 3.4-27.21). Conclusions MDR organisms were commonly isolated in BSI in AL. Inappropriate empiric antibiotic treatment for MDR-PA is the primary factor related to mortality that can be changed. New treatment strategies to improve the coverage of MDR-PA BSI should be considered in those patients with risk factors for this infection.
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页数:12
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