Clinical and Laboratory Factors That Predict Death in Very Low Birth Weight Infants Presenting With Late-onset Sepsis

被引:52
作者
Levit, Orly [1 ]
Bhandari, Vineet [1 ]
Li, Fang-Yong [2 ]
Shabanova, Veronika [2 ]
Gallagher, Patrick G. [1 ]
Bizzarro, Matthew J. [1 ]
机构
[1] Yale Univ, Sch Med, Dept Pediat, New Haven, CT 06510 USA
[2] Yale Univ, Sch Med, Dept Epidemiol & Publ Hlth, New Haven, CT 06510 USA
基金
美国国家卫生研究院;
关键词
infection; newborn infant; risk factors for death; gram-negative; fungal; late-onset sepsis; NEONATAL RESEARCH NETWORK; INTENSIVE-CARE-UNIT; RISK-FACTORS; NATIONAL-SURVEY; INFECTIONS; MORTALITY; SURVEILLANCE; DEFINITION; CANDIDEMIA; OUTCOMES;
D O I
10.1097/INF.0000000000000024
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: Late-onset sepsis (LOS) in very low birth weight (VLBW) infants is associated with significant morbidity and mortality. The ability to predict mortality in infants with LOS based on clinical and laboratory factors at presentation of illness remains limited. Objectives: To identify predictors of sepsis-associated mortality from a composite risk profile that includes demographic data, category of infecting organism, clinical and laboratory data at onset of illness. Study Design: Data were collected from VLBW infants with at least 1 episode of LOS admitted to Yale Neonatal Intensive Care Unit from 1989 through 2007. Episodes were categorized as Gram-positive, Gram-negative or fungal. Multivariate logistic regression analysis was used to compare and contrast different types of infections and to assess independent risk factors for death. Results: Four hundred twenty-four cases of LOS were identified in 424 VLBW infants. Of these, 262 (62%) were categorized as Gram-positive, 126 (30%) as Gram-negative and 36 (8%) as fungal. Multivariate analyses revealed that infants with Gram-positive infections had significantly lower odds of death compared to those with Gram-negative (adjusted odds ratio: 0.17; 95% confidence interval: 0.08-0.36) or fungal LOS (adjusted odds ratio: 0.22; 95% confidence interval: 0.07-0.64). Need for intubation, initiation of pressors, hypoglycemia and thrombocytopenia as presenting laboratory signs of infection and necrotizing enterocolitis were independent risk factors for sepsis-related death. Conclusions: We identified presenting clinical and laboratory factors, including category of infecting organism, which predict the increased risk of LOS-related death. This information can be useful in estimating prognosis shortly after the onset of disease.
引用
收藏
页码:143 / 146
页数:4
相关论文
共 22 条
[1]   Mortality following blood culture in premature infants: Increased with Gram-negative bacteremia and candidemia but not Gram-positive bacteremia [J].
Benjamin Jr. D.K. ;
DeLong E. ;
Cotten C.M. ;
Garges H.P. ;
Steinbach W.J. ;
Clark R.H. .
Journal of Perinatology, 2004, 24 (3) :175-180
[2]   Neonatal candidiasis among extremely low birth weight infants: Risk factors, mortality rates, and neurodevelopmental outcomes at 18 to 22 months [J].
Benjamin, DK ;
Stoll, BJ ;
Fanaroff, AA ;
McDonald, SA ;
Oh, W ;
Higgins, RD ;
Duara, S ;
Poole, K ;
Laptook, A ;
Goldberg, R .
PEDIATRICS, 2006, 117 (01) :84-92
[3]   Organism-specific platelet response and factors affecting survival in thrombocytopenic very low birth weight babies with sepsis [J].
Bhat, M. A. ;
Bhat, J. I. ;
Kawoosa, M. S. ;
Ahmad, S. M. ;
Ali, S. W. .
JOURNAL OF PERINATOLOGY, 2009, 29 (10) :702-708
[4]   Late-Onset Sepsis in Very Low Birth Weight Infants from Singleton and Multiple-Gestation Births [J].
Boghossian, Nansi S. ;
Page, Grier P. ;
Bell, Edward F. ;
Stoll, Barbara J. ;
Murray, Jeffrey C. ;
Cotten, C. Michael ;
Shankaran, Seetha ;
Walsh, Michele C. ;
Laptook, Abbot R. ;
Newman, Nancy S. ;
Hale, Ellen C. ;
McDonald, Scott A. ;
Das, Abhik ;
Higgins, Rosemary D. .
JOURNAL OF PEDIATRICS, 2013, 162 (06) :1120-+
[5]   Risk factors and prevention of late-onset sepsis in premature infants [J].
Downey, L. Corbin ;
Smith, P. Brian ;
Benjamin, Daniel K., Jr. .
EARLY HUMAN DEVELOPMENT, 2010, 86 (01) :S7-S12
[6]   Validation of the National Institutes of Health consensus definition of bronchopulmonary dysplasia [J].
Ehrenkranz, RA ;
Walsh, MC ;
Vohr, BR ;
Jobe, AH ;
Wright, LL ;
Fanaroff, AA ;
Wrage, LA ;
Poole, K .
PEDIATRICS, 2005, 116 (06) :1353-1360
[7]   CDC DEFINITIONS FOR NOSOCOMIAL INFECTIONS, 1988 [J].
GARNER, JS ;
JARVIS, WR ;
EMORI, TG ;
HORAN, TC ;
HUGHES, JM .
AMERICAN JOURNAL OF INFECTION CONTROL, 1988, 16 (03) :128-140
[8]   Risk factors for late onset gram-negative sepsis in low birth weight infants hospitalized in the neonatal intensive care unit [J].
Graham, PL ;
Begg, MD ;
Larson, E ;
Della-Latta, P ;
Allen, A ;
Saiman, L .
PEDIATRIC INFECTIOUS DISEASE JOURNAL, 2006, 25 (02) :113-117
[9]   CDC/NHSN surveillance definition of health care-associated infection and criteria for specific types of infections in the acute care setting [J].
Horan, Teresa C. ;
Andrus, Mary ;
Dudeck, Margaret A. .
AMERICAN JOURNAL OF INFECTION CONTROL, 2008, 36 (05) :309-332
[10]   Early and late onset sepsis in very-low-birth-weight infants from a large group of neonatal intensive care units [J].
Hornik, C. P. ;
Fort, P. ;
Clark, R. H. ;
Watt, K. ;
Benjamin, D. K., Jr. ;
Smith, P. B. ;
Manzoni, P. ;
Jacqz-Aigrain, E. ;
Kaguelidou, F. ;
Cohen-Wolkowiez, M. .
EARLY HUMAN DEVELOPMENT, 2012, 88 :S69-S74