C-Reactive Protein, Procalcitonin, and White Blood Count to Rule Out Neonatal Early-onset Sepsis Within 36 Hours: A Secondary Analysis of the Neonatal Procalcitonin Intervention Study

被引:69
|
作者
Stocker, Martin [1 ]
van Herk, Wendy [2 ]
el Helou, Salhab [3 ]
Dutta, Sourabh [3 ]
Schuerman, Frank A. B. A. [4 ]
van den Tooren-de Groot, Rita K. [5 ]
Wieringa, Jantien W. [5 ]
Janota, Jan [6 ,7 ,8 ]
van der Meer-Kappelle, Laura H. [9 ]
Moonen, Rob [10 ]
Sie, Sintha D. [11 ]
de Vries, Esther [12 ]
Donker, Albertine E. [13 ]
Zimmerman, Urs [14 ]
Schlapbach, Luregn J. [15 ,16 ,17 ,18 ]
de Mol, Amerik C. [19 ]
Hoffman-Haringsma, Angelique [20 ]
Roy, Madan [21 ]
Tomaske, Maren [22 ]
Kornelisse, Rene F. [23 ]
van Gijsel, Juliette [24 ]
Visser, Eline G. [2 ]
Plotz, Frans B. [25 ]
Heath, Paul [26 ]
Achten, Niek B. [25 ]
Lehnick, Dirk [27 ]
van Rossum, Annemarie M. C. [2 ]
机构
[1] Childrens Hosp Lucerne, Dept Paediat, Neonatal & Paediat Intens Care Unit, Luzern, Switzerland
[2] Erasmus MC, Sophia Childrens Hosp, Dept Paediat, Div Paediat Infect Dis & Immunol,Univ Med Ctr, Rotterdam, Netherlands
[3] McMaster Univ, Div Neonatol, Hamilton Hlth Sci, Childrens Hosp, Hamilton, ON, Canada
[4] Isala Women & Childrens Hosp, Dept Neonatal Intens Care Unit, Zwolle, Netherlands
[5] Haaglanden Med Ctr, Dept Paediat, The Hague, Netherlands
[6] Motol Univ Hosp, Med Fac 2, Dept Obstet & Gynocol, Prague, Czech Republic
[7] First Med Fac, Prague, Czech Republic
[8] Inst Pathol Physiol, Prague, Czech Republic
[9] Reinier de Graaf Gasthuis, Dept Neonatol, Delft, Netherlands
[10] Zuyderland Med Ctr, Dept Neonatol, Heerlen, Netherlands
[11] Vrije Univ Amsterdam, Amsterdam Univ Med Ctr, Dept Neonatol, Amsterdam, Netherlands
[12] Jeroen Bosch Hosp, Dept Paediat, Shertogenbosch, Netherlands
[13] Maxima Med Ctr, Dept Paediat, Veldhoven, Netherlands
[14] Kantonsspital Winterthur, Dept Paediat, Winterthur, Switzerland
[15] Univ Queensland, Child Hlth Res Ctr, Paediat Crit Care Res Grp, Brisbane, Qld, Australia
[16] Queensland Childrens Hosp, Padiaitr Intens Care Unit, Brisbane, Qld, Australia
[17] Univ Childrens Hosp Zurich, Zurich, Switzerland
[18] Univ Zurich, Zurich, Switzerland
[19] Albert Schweitzer Hosp, Dept Neonatol, Dordrecht, Netherlands
[20] St Franciscus Gasthuis, Dept Neonatol, Rotterdam, Netherlands
[21] St Josephs Healthcare, Hamilton Hlth Sci, Dept Neonatol, Hamilton, ON, Canada
[22] Stadtspital Triemli, Dept Paediat, Zurich, Switzerland
[23] Erasmus MC, Univ Med Ctr, Dept Paediat, Div Neonatol,Sophia Childrens Hosp, Rotterdam, Netherlands
[24] Therapeuticum Utrecht, Utrecht, Netherlands
[25] Tergooi Hosp, Dept Pediat, Blaricum, Netherlands
[26] St Georges Univ Hosp, Dept Paediat Infect Dis, London, England
[27] Univ Lucerne, Dept Hlth Sci & Med, Head Biostat & Methodol, Luzern, Switzerland
关键词
neonatal early-onset sepsis; C-reactive protein; procalcitonin; white blood count; negative predictive value; RISK; DURATION; NEWBORNS; THERAPY;
D O I
10.1093/cid/ciaa876
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. Neonatal early-onset sepsis (EOS) is one of the main causes of global neonatal mortality and morbidity, and initiation of early antibiotic treatment is key. However, antibiotics may be harmful. Methods. We performed a secondary analysis of results from the Neonatal Procalcitonin Intervention Study, a prospective, multicenter, randomized, controlled intervention study. The primary outcome was the diagnostic accuracy of serial measurements of C-reactive protein (CRP), procalcitonin (PCT), and white blood count (WBC) within different time windows to rule out culture-positive EOS (proven sepsis). Results. We analyzed 1678 neonates with 10 899 biomarker measurements (4654 CRP, 2047 PCT, and 4198 WBC) obtained within the first 48 hours after the start of antibiotic therapy due to suspected EOS. The areas under the curve (AUC) comparing no sepsis vs proven sepsis for maximum values of CRP, PCT, and WBC within 36 hours were 0.986, 0.921, and 0.360, respectively. The AUCs for CRP and PCT increased with extended time frames up to 36 hours, but there was no further difference between start to 36 hours vs start to 48 hours. Cutoff values at 16 mg/L for CRP and 2.8 ng/L for PCT provided a sensitivity of 100% for discriminating no sepsis vs proven sepsis. Conclusions. Normal serial CRP and PCT measurements within 36 hours after the start of empiric antibiotic therapy can exclude the presence of neonatal EOS with a high probability. The negative predictive values of CRP and PCT do not increase after 36 hours.
引用
收藏
页码:E383 / E390
页数:8
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