1 From the Departments of Pediatrics, Obstetrics and Gynecology, The University of Tennessee, Memphis, Tennessee
2 From the Department of Patohology, The University of Tennessee, Memphis, Tennessee
3 From the Department of Mathematical Sciences, Memphis State University, Memphis, Tennessee
Objective. This study was performed to determine prospectively whether, in the presence of proved or presumed bacterial infection, the sensitivity of serum C-reactive protein (CRP) response could be enhanced by serial rather than single determinations. We also sought to assess CRP responses to clinically identified noninfectious disorders.
Design. The CRP responses of 491 infants on 691 occasions of suspected infection were assessed. CRP levels were measured initially and twice again at 12-hour intervals (rate immunonephelometry). Assessments also included a blood culture, complete blood cell count, and chest radiograph and culture of spinal fluid when appropriate. CRP responses were correlated with four designated clinical groups: (1) positive blood or cerebrospinal fluid cultures (n = 190); (2) negative blood culture-definite infection (necrotizing enterocolitis stages 2 and 3, pneumonia, subcutaneous abscess) (n = 52); (3) negative blood culture-possible infection (antenatal risk factors, meconium aspiration, positive urine group B streptococcus antigen, necrotizing enterocolitis stage 1, febrile infants) (n = 287); and (4) negative blood culture-no infection (respiratory distress syndrome, transient tachypnea of the newborn, patent ductus arteriosus, tissue trauma) (n = 160). Diagnoses were made before CRP results were known.
Results. In all, 187 (27%) of the blood cultures were positive. A single organism was recovered from 174 of these; two organisms from 13. Among the single-organism cultures, 50 (29%) were Gram-negative, 120 (69%) were Gram-positive, and 4 (2%) were budding yeasts. CRP levels were elevated in various groups as follows: in the positive blood culture group (by organism), Gram-negative rods, 92% (46/50); group B streptococcus, 92% (12/13); Staphylococcus aureus, 89% (8/9); group D streptococcus, 71% (10/14); Streptococcus viridans, 60% (6/10); Staphylococcus epidermidis, 55% (40/73). In the negative blood culture-definite infection group, CRP levels were abnormal in 88%; in the negative culture-possible infection group, CRP was elevated in 33%; and in the negative blood culture-no infection group, CRP was elevated in 9%. Serial determinations of CRP resulted in enhanced sensitivity in the positive blood culture group, the negative blood culture-definite infection group, and the negative blood culture-possible infection group. Initial determinations by themselves were inadequatey sensitive. Serial determinations did not enhance sensitivity of the negative blood culture-no infection group. High specificity (91%) is suggested by the low incidence of abnormal CRP levels among infants who were not infected.
Conclusions. These data suggest that it would be appropriate to conduct a cautious, controlled trial to assess the safety of discontinuing antibiotic therapy if three serial CRP measurements are normal and if there are no other clinical factors suggestive of infection. The data also indicate the necessity for serial determinations of CRP for optimal sensitivity.
Key Words: C-reactive protein neonatal infection neonatal septicemia
Submitted on July 13, 1992
Accepted on March 29, 1993
This article has been cited by other articles:
![]() |
M. S. Judge Infection and Neuroarthropathy: The Utility of C-reactive Protein as a Screening Tool in the Charcot Foot J Am Podiatr Med Assoc, January 1, 2008; 98(1): 1 - 6. [Abstract] [Full Text] [PDF] |
||||
![]() |
G. Chowdhary, S. Dutta, and A. Narang Randomized Controlled Trial of 7-Day vs. 14-Day Antibiotics for Neonatal Sepsis J Trop Pediatr, December 1, 2006; 52(6): 427 - 432. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. K. Hall and J. A. Lyman Updated Review of Blood Culture Contamination Clin. Microbiol. Rev., October 1, 2006; 19(4): 788 - 802. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Pourcyrous, S. B. Korones, W. Yang, T. F. Boulden, and H. S. Bada C-Reactive Protein in the Diagnosis, Management, and Prognosis of Neonatal Necrotizing Enterocolitis Pediatrics, November 1, 2005; 116(5): 1064 - 1069. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. Kaufman and K. D. Fairchild Clinical Microbiology of Bacterial and Fungal Sepsis in Very-Low-Birth-Weight Infants Clin. Microbiol. Rev., July 1, 2004; 17(3): 638 - 680. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. R. Franz, K. Bauer, A. Schalk, S. M. Garland, E. D. Bowman, K. Rex, C. Nyholm, M. Norman, A. Bougatef, M. Kron, et al. Measurement of Interleukin 8 in Combination With C-Reactive Protein Reduced Unnecessary Antibiotic Therapy in Newborn Infants: A Multicenter, Randomized, Controlled Trial Pediatrics, July 1, 2004; 114(1): 1 - 8. [Abstract] [Full Text] [PDF] |
||||
![]() |
P C Ng Diagnostic markers of infection in neonates Arch. Dis. Child. Fetal Neonatal Ed., May 1, 2004; 89(3): F229 - F235. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. Chiesa, A. Panero, J. F. Osborn, A. F. Simonetti, and L. Pacifico Diagnosis of Neonatal Sepsis: A Clinical and Laboratory Challenge Clin. Chem., February 1, 2004; 50(2): 279 - 287. [Full Text] [PDF] |
||||
![]() |
A. G. S. Philip Neonatal Meningitis in the New Millennium NeoReviews, March 1, 2003; 4(3): e73 - 80. [Full Text] [PDF] |
||||
![]() |
A. Madan, M. M. Adams, and A. G. S. Philip Frequency and Timing of Symptoms in Infants Screened for Sepsis: Effectiveness of a Sepsis-Screening Pathway Clinical Pediatrics, January 1, 2003; 42(1): 11 - 18. [Abstract] [PDF] |
||||
![]() |
C. Chiesa, G. Pellegrini, A. Panero, J. F. Osborn, F. Signore, M. Assumma, and L. Pacifico C-Reactive Protein, Interleukin-6, and Procalcitonin in the Immediate Postnatal Period: Influence of Illness Severity, Risk Status, Antenatal and Perinatal Complications, and Infection Clin. Chem., January 1, 2003; 49(1): 60 - 68. [Abstract] [Full Text] [PDF] |
||||
![]() |
L. G. Rubin, P. J. Sanchez, J. Siegel, G. Levine, L. Saiman, and W. R. Jarvis Evaluation and Treatment of Neonates With Suspected Late-Onset Sepsis: A Survey of Neonatologists' Practices Pediatrics, October 1, 2002; 110(4): e42 - 42. [Abstract] [Full Text] [PDF] |
||||
![]() |
B. J. Stoll, N. Hansen, A. A. Fanaroff, L. L. Wright, W. A. Carlo, R. A. Ehrenkranz, J. A. Lemons, E. F. Donovan, A. R. Stark, J. E. Tyson, et al. Changes in Pathogens Causing Early-Onset Sepsis in Very-Low-Birth-Weight Infants N. Engl. J. Med., July 25, 2002; 347(4): 240 - 247. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Ishibashi, Y. Takemura, H. Ishida, K. Watanabe, and T. Kawai C-Reactive Protein Kinetics in Newborns: Application of a High-Sensitivity Analytic Method in Its Determination Clin. Chem., July 1, 2002; 48(7): 1103 - 1106. [Full Text] [PDF] |
||||
![]() |
G. J. Escobar, D.-k. Li, M. A. Armstrong, M. N. Gardner, B. F. Folck, J. E. Verdi, B. Xiong, R. Bergen, and for the Neonatal Infection Study Group Neonatal Sepsis Workups in Infants >= 2000 Grams at Birth: A Population-Based Study Pediatrics, August 1, 2000; 106(2): 256 - 263. [Abstract] [Full Text] |
||||
![]() |
A. G. S. Philip and P. C. Mills Use of C-Reactive Protein in Minimizing Antibiotic Exposure: Experience With Infants Initially Admitted to a Well-Baby Nursery Pediatrics, July 1, 2000; 106(1): 4e - 4. [Abstract] [Full Text] |
||||
![]() |
A. R. Franz, G. Steinbach, M. Kron, and F. Pohlandt Reduction of Unnecessary Antibiotic Therapy in Newborn Infants Using Interleukin-8 and C-Reactive Protein as Markers of Bacterial Infections Pediatrics, September 1, 1999; 104(3): 447 - 453. [Abstract] [Full Text] [PDF] |
||||
![]() |
B. S. Dahler-Eriksen, T. Lauritzen, J. F. Lassen, E. D. Lund, and I. Brandslund Near-Patient Test for C-Reactive Protein in General Practice: Assessment of Clinical, Organizational, and Economic Outcomes Clin. Chem., April 1, 1999; 45(4): 478 - 485. [Abstract] [Full Text] [PDF] |
||||
![]() |
W. E. Benitz, M. Y. Han, A. Madan, and P. Ramachandra Serial Serum C-Reactive Protein Levels in the Diagnosis of Neonatal Infection Pediatrics, October 1, 1998; 102(4): e41 - 41. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Pourcyrous, S. B. Korones, D. Crouse, and H. S. Bada Interleukin-6, C-Reactive Protein, and Abnormal Cardiorespiratory Responses to Immunization in Premature Infants Pediatrics, March 1, 1998; 101 (3): e3 - e3. [Abstract] [Full Text] [PDF] |
||||
![]() |
P W Fowlie and B Schmidt Diagnostic tests for bacterial infection from birth to 90 days---a systematic review Arch. Dis. Child. Fetal Neonatal Ed., March 1, 1998; 78(2): 92F - 98. [Abstract] [Full Text] |
||||
![]() |
S. R. Allen Management of Asymptomatic Term Neonates Whose Mothers Received Intrapartum Antibiotics--Part 2: Diagnostic Tests and Management Strategies Clinical Pediatrics, November 1, 1997; 36(11): 617 - 624. [Abstract] [PDF] |
||||
![]() |
M. J. Grella;, S. Ehl, and F. Pohlandt C-Reactive Protein to Determine the Duration of Antibiotic Therapy in Infants With Suspected Sepsis Pediatrics, November 1, 1997; 100(5): 900 - 900. [Full Text] |
||||
![]() |
S. Ehl, B. Gering, P. Bartmann, J. Hogel, and F. Pohlandt C-Reactive Protein Is a Useful Marker for Guiding Duration of Antibiotic Therapy in Suspected Neonatal Bacterial Infection Pediatrics, February 1, 1997; 99(2): 216 - 221. [Abstract] [Full Text] [PDF] |
||||