Risk Factors for Viridans Group Streptococcal Bacteremia in Neutropenic and Non-neutropenic Patients: A Single Center Case-Case-Control Study

被引:7
|
作者
Chiang, Augusto Dulanto [1 ]
Sinaii, Ninet [2 ]
Palmore, Tara N. [1 ,2 ]
机构
[1] NIAID, 9000 Rockville Pike, Bethesda, MD 20892 USA
[2] NIH, Ctr Clin, 10 Ctr Dr,Room 12C103A,MSC 1899, Bethesda, MD 20892 USA
来源
OPEN FORUM INFECTIOUS DISEASES | 2018年 / 5卷 / 01期
基金
美国国家卫生研究院;
关键词
bacteremia; neutropenia; Streptococcus mitis; viridans; SHOCK SYNDROME; CANCER; SPECTRUM; INFECTIONS; RESISTANCE; VANCOMYCIN; CHILDREN; IMPACT; RATES;
D O I
10.1093/ofid/ofx260
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. Viridans group streptococcal (VGS) bacteremia is common among neutropenic patients. Although VGS bacteremia occurs in non-neutropenic patients, risk factors are not well established. We conducted a case-case-control study to identify risk factors for VGS among neutropenic and non-neutropenic patients. Methods. Patients with VGS bacteremia between January 2009 and December 2014 in our 200-bed clinical research hospital were identified using microbiology records. Neutropenic and non-neutropenic patients at the time of positive culture were matched 1:1 to controls on the basis of neutrophil count (ANC), ward, and length of stay. We extracted demographic, laboratory, medication, and other clinical data from chart reviews. Data were analyzed using McNemar's test, Wilcoxon signed-rank test, and conditional logistic regression modeling. Results. Among 101 patients, 63 were neutropenic and 38 non-neutropenic at the time of VGS bacteremia. In multivariable analysis of neutropenic patients, only lower ANC predicted VGS bacteremia (odds ratio [OR], 0.16; 95% confidence interval [CI], 0.05-0.59; P = 0.006). Recent use of vancomycin was protective (OR, 0.23; 95% CI, 0.07-0.73; P = 0.013). No clinical factors were associated with VGS in the non-neutropenic cases. Conclusions. Only lower ANC nadir increased the risk for VGS bacteremia in the neutropenic group, and vancomycin was protective. Other previously described factors (chemotherapy, radiation, oral conditions) related to neutropenia were not independently associated with VGS bacteremia. No tested clinical factors predicted infection in the non-neutropenic group. Our results suggest that VGS bacteremia should be anticipated when making antimicrobial choices in profoundly neutropenic patients, and merit further exploration in non-neutropenic patients.
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页数:6
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