
极低/超低出生体重儿迟发型败血症发生情况及其危险因素分析
赵小朋, 周伟, 李旭芳, 宋燕燕, 张庭艳, 梁红
中国当代儿科杂志 ›› 2017, Vol. 19 ›› Issue (11) : 1129-1133.
极低/超低出生体重儿迟发型败血症发生情况及其危险因素分析
Incidence of late-onset sepsis in very low birth weight and extremely low birth weight infants and risk factors for late-onset sepsis
目的 探讨新生儿重症监护病房(NICU)极低/超低出生体重儿迟发型败血症(LOS)的发生情况及危险因素。方法 收集2011年1月至2013年12月入住NICU的极低或超低出生体重儿的临床资料,根据是否合并LOS分为两组:LOS组和无LOS组。回顾性分析LOS的发生率、病死率、常见病原菌及危险因素。结果 纳入的226例极低/超低出生体重儿中,117例(51.8%)发生了LOS,其中45例为确诊LOS,72例为临床诊断LOS。LOS组患儿病死率为13.7%(16/117),明显高于无LOS组(5/109,4.6%),差异有统计学意义(P < 0.05)。共培养出51株病原菌,其中32株(63%)为革兰阴性细菌,16株(31%)为革兰阳性细菌,3株(6%)为真菌。多因素logistic回归分析显示,胎龄、小于胎龄儿、肠外营养持续时间、经外周静脉穿刺中心静脉置管(PICC)、机械通气是极低/超低出生体重儿LOS发生的独立影响因素(OR分别为:0.84、1.59、1.34、3.11、4.55,均P < 0.05)。结论 极低/超低出生体重儿LOS的发生率及病死率较高。LOS常见病原菌为革兰阴性细菌。胎龄低、肠外营养持续时间长、小于胎龄儿、PICC或机械通气的极低/超低出生体重儿LOS的发生危险可能增加。
Objective To investigate the incidence of late-onset sepsis (LOS) in very low birth weight (VLBW) and extremely low birth weight (ELBW) infants in the neonatal intensive care unit (NICU) and the risk factors for LOS. Methods A retrospective analysis was performed for the clinical data of all VLBW and ELBW infants who were hospitalized in the NICU between January 2011 and December 2013. According to the presence or absence of LOS, these infants were divided into LOS group and non-LOS group. The incidence and mortality rates of LOS, common pathogenic bacteria, and risk factors for LOS were analyzed. Results Of the 226 VLBW and ELBW infants, 117 (51.8%) developed LOS, among whom 45 had a confirmed diagnosis of LOS and 72 had a clinical diagnosis of LOS. The LOS group had a significantly higher mortality rate than the non-LOS group[13.7% (16/117) vs 4.6% (5/109); P < 0.05]. Bacterial culture found 51 strains of pathogenic bacteria, among which 32 (63%) were Gram-negative bacteria, 16 (31%) were Gram-positive bacteria, and 3 (6%) were fungi. The multivariate logistic regression analysis showed that gestational age, small for gestational age (SGA), duration of parenteral nutrition, peripherally inserted central catheter (PICC) placement, and mechanical ventilation were independent risk factors for LOS in VLBW and ELBW infants (OR=0.84, 1.59, 1.34, 3.11, and 4.55 respectively; P < 0.05). Conclusions LOS has high incidence and mortality rates in VLBW and ELBW infants. Common pathogenic bacteria of LOS are Gram-negative bacteria. Low gestational age, long duration of parenteral nutrition, SGA, PICC placement, and mechanical ventilation may increase the risk of LOS in VLBW and ELBW infants.
迟发型败血症 / 危险因素 / 极低出生体重儿 / 超低出生体重儿
Late-onset sepsis / Risk factor / Very low birth weight infant / Extremely low birth weight infant
[1] Shim GH, Kim SD, Kim HS, et al. Trends in epidemiology of neonatal sepsis in a tertiary center in Korea:a 26-year longitudinal analysis, 1980-2005[J]. J Korean Med Sci, 2011, 26(2):284-289.
[2] Qazi SA, Stoll BJ. Neonatal sepsis:a major global public health challenge[J]. Pediatr Infect Dis J, 2009, 28(1 Suppl):S1-S2.
[3] Dong Y, Speer CP. Late-onset neonatal sepsis:recent developments[J]. Arch Dis Child Fetal Neonatal Ed, 2015, 100(3):F257-F263.
[4] 余加林, 吴仕孝. 败血症[M]//邵肖梅, 叶鸿瑁, 丘小汕. 实用新生儿学. 第4版. 北京:人民卫生出版社, 2011:340-342.
[5] Afjeh SA, Sabzehei MK, Fahimzad SA, et al. Antibiotic therapy for very low birth weigh newborns in NICU[J]. Iran J Pediatr, 2016, 26(2):e2612.
[6] de Souza Rugolo LM, Bentlin MR, Mussi-pinhata M, et al. Late-onset sepsis in very low birth weight infants:a Brazilian Neonatal Research Network Study[J]. J Trop Pediatr, 2014, 60(6):415-421.
[7] Alfaleh KM. Incidence of late onset neonatal sepsis in very low birth weight infants in a tertiary hospital:an ongoing challenge[J]. Sultan Qaboos Univ Med J, 2010, 10(2):227-230.
[8] Lim WH, Lien R, Huang YC, et al. Prevalence and pathogen distribution of neonatal sepsis among very-low-birth-weight infants[J]. Pediatr Neonatol, 2012, 53(4):228-234.
[9] Camacho-Gonzalez A, Spearman PW, Stoll BJ. Neonatal infectious diseases:evaluation of neonatal sepsis[J]. Pediatr Clin North Am, 2013, 60(2):367-389.
[10] Leal YA, Álvarez -Nemegyei J, Velázquez JR, et al. Risk factors and prognosis for neonatal sepsis in southeastern Mexico:analysis of a four-year historic cohort follow-up[J]. BMC Pregnancy Childbirth, 2012, 12:48.
[11] 陈历耋, 傅万海, 游楚明, 等. 新生儿重症监护病房患儿医院感染病原菌分布及耐药性[J]. 中华围产医学杂志, 2013, 16(10):611-613.
[12] 姜娜, 汪盈, 王琦, 等. 超早产儿医院感染及其危险因素分析[J]. 中华儿科杂志, 2014, 52(2):137-141.
[13] Grisaru-Soen G, Friedman T, Dollberg S, et al. Late-onset bloodstream infections in preterm infants:a 2-year survey[J]. Pediatr Int, 2012, 54(6):748-753.
[14] Brady MT. Health care-associated infections in the neonatal intensive care unit[J]. Am J Infect Control, 2005, 33(5):268-275.
[15] Hoyos OA, Suarez GM, Massaro CM, et al. Bloodstream infection in a neonatology unit of Medellin-Colombia, 2008-2009[J]. Rev Chilena Infectol, 2010, 27(6):491-498.
[16] Perlman SE, Saiman L, Larson EL. Risk factors for late-onset health care-associated bloodstream infections in patients in neonatal intensive care units[J]. Am J Infect Control, 2007, 35(3):177-182.
[17] Bartels DB, Schwab F, Geffers C, et al. Nosocomial infection in small for gestational age newborns with birth weight < 1500 g:a multicentre analysis[J]. Arch Dis in Child Fetal Neonatal Ed, 2007, 92(6):F449-F453.
[18] Downey LC, Smith PB, Benjamin DK Jr. Risk factors and prevention of late-onset sepsis in premature infants[J]. Early Hum Dev, 2010, 86(Suppl 1):7-12.
[19] Samanta S, Farrer K, Breathnach A, et al. Risk factors for late onset gram-negative infections:a case-control study[J]. Arch Dis Child Fetal Neonatal Ed, 2011, 96(1):F15-F18.
[20] Abdel-Wahab F, Ghoneim M, Khashaba M, et al. Nosocomial infection surveillance in an Egyptian neonatal intensive care unit[J]. J Hosp Infect, 2013, 83(3):196-199.
[21] Yuan TM, Chen LH, Yu HM. Risk factors and outcomes for ventilator-associated pneumonia in neonatal intensive care unit patients[J]. J Perinat Med, 2007, 35(4):334-338.
广东省医学科研项目(A2015494)。