C-reactive protein-guided antibiotic treatment strategy for neonates with suspected early-onset sepsis
HE Yun-Yan, CHEN Feng, ZHANG Yu, XIANG Ling-Ling, LIU Yi-Xi, HUA Zi-Yu
Department of Neonatology, Children's Hospital of Chongqing Medical University/Ministry of Education Key Laboratory of Child Development and Disorders/National Clinical Research Center for Child Health and Disorders/China International Science and Technology Cooperation Base of Child Development and Critical Disorders//Chongqing Key Laboratory of Pediatrics, Chongqing 400014, China
Abstract Objective To evaluate the efficacy and safety of C-reactive protein (CRP)-guided antibiotic treatment strategy for neonates with suspected early-onset sepsis (EOS). Methods A total of 428 neonates, with a gestational age of > 35 weeks, who were admitted to the Children's Hospital of Chongqing Medical University from February to July, 2019 and were suspected of EOS were enrolled as the observation group. The effect of antibiotic treatment was prospectively observed, and if clinical symptoms were improved and CRP was < 10 mg/L in two consecutive tests, discontinuation of antibiotics was considered. A total of 328 neonates (gestational age of > 35 weeks) who were admitted to this hospital from February to July, 2018 and were suspected of EOS were enrolled as the control group, and the use of antibiotics was analyzed retrospectively. The two groups were compared in terms of duration of antibiotic treatment, length of hospital stay, incidence rate of repeated infection and clinical outcome. Results Compared with the control group, the observation group had significantly shorter duration of antibiotic treatment and length of hospital stay (P < 0.05). There were no significant differences in the incidence rate of repeated infection and clinical outcome between the two groups (P > 0.05). Conclusions For neonates with a gestational age of > 35 weeks and a suspected diagnosis of EOS, CRP-guided antibiotic treatment strategy can shorten duration of antibiotic treatment and length of hospital stay and does not increase the incidence rate of repeated infection. Therefore, it holds promise for clinical application.
Ting JY, Roberts A, Sherlock R, et al. Duration of initial empirical antibiotic therapy and outcomes in very low birth weight infants[J]. Pediatrics, 2019, 143(3). pii:e20182286.
[2]
Bakhuizen SE, de Haan TR, Teune MJ, et al. Meta-analysis shows that infants who have suffered neonatal sepsis face an increased risk of mortality and severe complications[J]. Acta Paediatr, 2014, 103(12):1211-1218.
[3]
Oliver EA, Reagan PB, Slaughter JL, et al. Patterns of empiric antibiotic administration for presumed early-onset neonatal sepsis in neonatal intensive care units in the United States[J]. Am J Perinatol, 2017, 34(7):640-647.
[4]
Cordero L, Ayers LW. Duration of empiric antibiotics for suspected early-onset sepsis in extremely low birth weight infants[J]. Infect Control Hosp Epidemiol, 2003, 24(9):662-666.
[5]
van Herk W, el Helou S, Janota J, et al. Variation in current management of term and late-preterm neonates at risk for early-onset sepsis:an international survey and review of guidelines[J]. Pediatr Infect Dis J, 2016, 35(5):494-500.
[6]
Fjalstad JW, Stensvold HJ, Bergseng H, et al. Early-onset sepsis and antibiotic exposure in term infants:a nationwide population-based study in Norway[J]. Pediatr Infect Dis J, 2016, 35(1):1-6.
[7]
Klingenberg C, Kornelisse RF, Buonocore G, et al. Culture-negative early-onset neonatal sepsis-at the crossroad between efficient sepsis care and antimicrobial stewardship[J]. Front Pediatr, 2018, 6:285.
[8]
Goksör E, Alm B, Thengilsdottir H, et al. Preschool wheeze-impact of early fish introduction and neonatal antibiotics[J]. Acta Paediatr, 2011, 100(12):1561-1566.
[9]
Cotten CM, Taylor S, Stoll B, et al. Prolonged duration of initial empirical antibiotic treatment is associated with increased rates of necrotizing enterocolitis and death for extremely low birth weight infants[J]. Pediatrics, 2009, 123(1):58-66.
[10]
Saini SS, Dutta S, Ray P, et al. Short course versus 7-day course of intravenous antibiotics for probable neonatal septicemia:a pilot, open-label, randomized controlled trial[J]. Indian Pediatr, 2011, 48(1):19-24.
[11]
Pasha YZ, Ahmadpour-Kacho M, Behmadi R, et al. 3-Day versus 5-day course of intravenous antibiotics for suspected early onset neonatal sepsis:a randomized controlled trial[J]. Iran J Pediatr, 2014, 24(6):673-678.
[12]
Stocker M, van Herk W, EI Helou S, et al. Procalcitonin-guided decision making for duration of antibiotic therapy in neonates with suspected early-onset sepsis:a multicentre, randomised controlled trial (NeoPIns)[J]. Lancet, 2017, 390(10097):871-881.
[13]
Benitz WE, Han MY, Madan A, et al. Serial serum C-reactive protein levels in the diagnosis of neonatal infection[J]. Pediatrics, 1998, 102(4):E41.
NICE. Antibiotics for early-onset neonatal infection:antibiotics for the prevention and treatment of early-onset neonatal infection[M]. London:RCOG Press, 2012:1-40.
[17]
Polin RA; Committee on Fetus and Newborn. Management of neonates with suspected or proven early-onset bacterial sepsis[J]. Pediatrics, 2012, 129(5):1006-1015.
[18]
Yu Z, Liu J, Sun Q, et al. The accuracy of the procalcitonin test for the diagnosis of neonatal sepsis:a meta-analysis[J]. Scand J Infect Dis, 2010, 42(10):723-733.
[19]
Ruan L, Chen GY, Liu Z, et al. The combination of procalcitonin and C-reactive protein or presepsin alone improves the accuracy of diagnosis of neonatal sepsis:a meta-analysis and systematic review[J]. Crit Care, 2018, 22(1):316.
[20]
Kawamura M, Nishida H. The usefulness of serial C-reactive protein measurement in managing neonatal infection[J]. Acta Paediatr, 1995, 84(1):10-13.
[21]
Coggins SA, Wynn JL, Hill ML, et al. Use of a computerized C-reactive protein (CRP) based sepsis evaluation in very low birth weight (VLBW) infants:a five-year experience[J]. PLoS One, 2013, 8(11):e78602.
[22]
Hofer N, Zacharias E, Müller W, et al. An update on the use of C-reactive protein in early-onset neonatal sepsis:current insights and new tasks[J]. Neonatology, 2012, 102(1):25-36.
Tsai MH, Chu SM, Hsu JF, et al. Risk factors and outcomes for multidrug-resistant Gram-negative bacteremia in the NICU[J]. Pediatrics, 2014, 133(2):e322-e329.