- Research article
- Open Access
Use of rifampin in persistent coagulase negative staphylococcal bacteremia in neonates
BMC Pediatrics volume 10, Article number: 84 (2010)
Coagulase negative staphylococci (CoNS) are the most common cause of neonatal sepsis in the Neonatal Intensive Care Unit (NICU). A minority of neonates does not respond to vancomycin therapy and develops persistent bacteremia, which may be treated with rifampin. We evaluated the use of rifampin in persistent CoNS bacteremia.
Retrospective study of 137 neonates with CoNS bacteremia during admission to a tertiary NICU between July 2006 and July 2009. Main outcome measures were total duration of bacteremia and the adequacy of vancomycin and rifampin therapy.
137/1696 (8.0%) neonates developed a CoNS bacteremia. Eighteen were treated with rifampin because of persistent bacteremia (3 positive blood cultures at least 48 hours apart with clinical symptoms) or (a serious suspicion of) an intravascular thrombus. Duration of bacteremia prior to rifampin therapy (8.0 ± 3.6 days) was positively correlated (p < 0.001) to the total duration of bacteremia (10.3 ± 3.7 days). After starting rifampin therapy C-reactive protein (CRP) levels of all neonates declined and blood cultures became sterile after 2.3 ± 1.6 days. Vancomycin levels were not consistently measured in all neonates, resulting in late detection of subtherapeutic trough levels.
Rifampin may be effective in the treatment of persistent CoNS infections in neonates. Outcome may be improved by adequate monitoring of vancomycin trough levels.
Sepsis due to coagulase negative staphylococci (CoNS) is common in the neonatal intensive care unit (NICU). The incidence of CoNS sepsis varies between 1.3 and 19.9%, depending on birth weight and gestational age [1–5]. Most of these infections respond well to vancomycin, the first drug of choice. A minority of neonates develops a persistent staphylococcal bacteremia, which does not respond to vancomycin. For these neonates rifampin may be a safe and effective additive treatment to vancomycin [1, 6–8]. Interaction between vancomycin and rifampin in treatment of staphylococcal infections is ambiguous, as some studies demonstrate antagonism and others synergism or indifference [9–12]. High concentrations of rifampin may result in antagonism [13, 14]. Rifampin is only effective as combination therapy, because resistance develops when rifampin is used as monotherapy .
Through its highly lipophilic character, rifampin molecules can easily cross biological membranes, resulting in a wide tissue distribution [6, 16]. The efficacy of rifampin in persistent staphylococcal bacteremia is due to its abilities to enhance serum bactericidal activity and to penetrate phagocytic leukocytes for intraleukocytic killing of staphylococci .
Pharmacokinetic research has demonstrated a positive correlation between the duration of rifampin therapy and its clearance, the equilibrium clearance is achieved after one to two weeks. The increase in clearance and decrease in half-life are probably due to auto-induction of the metabolism of rifampin and require caution to maintain serum levels within the therapeutic range by adjusting the dose of rifampin, when necessary [6, 16, 18].
Although CoNS bacteremia is common in NICUs and the treatment of persistent CoNS bacteremia with rifampin seems successful, previous studies were only small case reports or studies focusing on pharmacokinetics. The aim of this study was to evaluate the existing local guidelines for the use of rifampin therapy in persistent CoNS infection, checking the current indications to start rifampin therapy and estimating its efficacy.
The study population of this retrospective chart review consisted of all neonates admitted to the neonatology department of the Leiden University Medical Center (LUMC) between July 2006 and July 2009. The Medical Ethics Committee of the LUMC did not require approval of this study because it consisted of retrospective chart review, nor did the medical ethics committee require written consent by the parents for their infant's information to be stored in the hospital database and used for research. Approval by the ethics committee and informed consent was not necessary as the patient data were analyzed anonymously.
Inclusion criterion was the presence of a positive blood culture for CoNS. Persistent CoNS bacteremia was defined as 3 positive blood cultures, spaced at least 48 hours apart, in combination with clinical symptoms of sepsis. The indication to start rifampin treatment was persistent CoNS bacteremia despite treatment with vancomycin and removal of indwelling catheters, or a non-persistent CoNS bacteremia in combination with a proven intravascular thrombus. Starting dose of rifampin was 10 mg/kg/day intravenously.
Data on demographic, perinatal and postnatal clinical characteristics were collected to provide an overview of baseline characteristics and included birth weight, gestational age, gender, exposure to prenatal and postnatal steroids, presence of chorioamnionitis, hyperglycemia, prolonged rupture of membranes (PROM), asphyxia, respiratory distress syndrome (RDS), bronchopulmonary dysplasia (BPD), necrotizing enterocolitis (NEC), cystic periventricular leukomalacia (PVL) and intraventricular hemorrhage (IVH)[23, 24]. These data were collected from the neonatal charts and used to compare neonates with non-persistent and persistent CoNS bacteremia.
Primary outcome measures were the total duration of bacteremia and the adequacy of vancomycin treatment, estimated by following trough levels obtained after the initiation of vancomycin therapy until the tenth day of rifampin therapy. The desired range of trough levels of vancomycin was 5-10 mg/L, trough levels <5 mg/L were considered to be subtherapeutic and the desired range for peak levels was 20-30 mg/L. Other variables studied included plasma urea and creatinine levels and duration of vancomycin therapy.
Main outcomes for analysis of the group of rifampin treated neonates were total duration of bacteremia and rapidity of sterilization of blood cultures after the start of rifampin. Age at start of infection, CRP levels from the first day of CoNS positive blood culture until the tenth day of rifampin treatment, and duration and dose of rifampin treatment were additional variables among rifampin treated neonates.
Identification of CoNS isolates was performed by the microbiology department using Bactec Peds Plus bottles (Becton and Dickinson, Franklin Lakes, NJ USA). Blood cultures, complete blood count and CRP were drawn upon clinical suspicion of sepsis. CRP levels were determined daily during therapy with antibiotics. Vancomycin serum samples were drawn just before the third dose and 1 hour after administration of the third dose. When the dosage of vancomycin was changed, another serum sample was drawn around the second dose after the change. CRP levels were measured using a immunoturbidimetric assay (imCRP, detection limit ≥3 mg/L ) and serum vancomycin levels by a fluorescence polarization assay .
CoNS bacteremia was an indication for removal of central venous lines and sonography for a remaining vascular thrombus.
Data are reported as mean values ± standard deviation, minimum and maximum, numerical values or categories. Analyses were performed with SPSS Version 16.0 (SPSS Inc., Chicago, IL). Numerical data were analyzed by bivariate Pearson correlation and unpaired T-tests, categorical data were analyzed using a chi-squared test. To correct for potential confounding effects, logistic regression analysis was done.
In the period between July 2006 and July 2009 1696 neonates were admitted to the NICU with a mean birth weight of 1271 ± 663 gram and a gestational age of 29.2 ± 3.2 weeks. The incidence of CoNS bacteremia was 137/1696 (8%), 17 (12%) of these neonates developed a persistent CoNS bacteremia and in 3 of them an intravascular thrombus was identified. One neonate with a CoNS sepsis also had a S. aureus sepsis.
A flowchart of the included patients can be seen in figure 1. Baseline characteristics of the included patients are listed in table 1. Newborn infants with persistent CoNS bacteremia had lower birth weights (p = 0.008) and, independent of birth weight, more often hyperglycemia (p = 0.007), than infants with non-persistent CoNS bacteremia. Subtherapeutic vancomycin trough levels were equally divided among the groups with persistent and non-persistent CoNS bacteremia (p = 0.712).
Eighteen of the 137 neonates received rifampin treatment, started after 8.0 ± 3.6 (mean ± SD) days of CoNS bacteremia. 13/18 neonates had persistent CoNS bacteremia (in three of them an intravascular thrombus was found), 3/18 had an intravascular thrombus with a non-persistent CoNS bacteremia, 2/18 received rifampin because of increasing CRP levels during vancomycin therapy in combination with severe thrombocytopenia and a serious suspicion of an intravascular thrombus.
Figure 2 shows the course of the CRP levels before and after the first CoNS positive blood culture, for both infants treated with and without rifampin (start of rifampin is marked, dotted lines represent infants without rifampin therapy).
CRP levels from the first day of a CoNS positive blood culture until the tenth day of rifampin therapy demonstrate a serious decline in CRP levels after starting rifampin therapy (figure 3). Indwelling catheters were removed before the first CoNS positive blood culture (6 times), on the day of the first CoNS positive blood culture (3 times) or after the first CoNS blood culture (6 times, although in all these infants maximum CRP was achieved after removal of the catheter). The most important decline in CRP occurred during the first 3 days after the start of rifampin. In these first 3 days the blood culture of most neonates became sterile, with a mean duration of 2.3 ± 1.6 days. Values of other infection- and pharmacokinetic parameters of the neonates treated with rifampin are listed in table 2.
Before the start of rifampin all neonates received vancomycin as monotherapy (n = 1) or in combination with ceftazidim (until definitive identification and antimicrobial susceptibility testing of gram-positive cocci in clusters) (n = 17). The duration of vancomycin therapy was 8.9 ± 4.5 days. Ten neonates had adequate initial vancomycin levels, in 8 infants vancomycin dosage had to be readjusted. Vancomycin trough levels between the first day of CoNS positive blood culture and the tenth day of rifampin treatment are presented in figure 4. In contrast to vancomycin levels, rifampin levels were never obtained.
The presence of an intravascular thrombus did not correlate with the total duration of CoNS bacteremia or with the rapidity of sterilization of blood cultures after the start of rifampin treatment.
Comparing our incidence of CoNS bacteremia (8%) with other studies is difficult, as the composition of study populations vary. Most studies report a lower incidence, probably due to higher birth weights and gestational ages in these populations [2–4]. One study reported an incidence of 19.9%, but neonates in this study had a lower gestational age . Effectiveness of rifampin treatment in persistent staphylococcal bacteremia in neonates has been demonstrated in several case reports and pharmacokinetic studies, in which speed of sterilization of the blood culture was the main outcome [1, 6–8]. Our data also show a substantial decline in CRP during the first days of rifampin treatment. To our knowledge, studies evaluating the treatment of CoNS bacteremia, focusing on the adequacy of monitoring and responding to vancomycin trough levels and the compliance with starting rifampin after 3 positive blood cultures with an interval of 48 hours, have not been reported earlier.
This retrospective study has several limitations. The most important one is the small size of the study population (18 patients) available for evaluation of rifampin treatment. As most neonates with a CoNS bacteremia respond well to vancomycin, rifampin is given only incidentally. Another limitation is the absence of an appropriate control group. As 4 patients with a persistent CoNS bacteremia did not receive rifampin, this group was too small for comparison purposes. Comparison of the occurrence of vancomycin levels below the therapeutic margin between persistent and non persistent bacteremia appeared difficult, as vancomycin levels were not regularly assessed in all neonates, especially in neonates with a non-persistent bacteremia.
Comparing the groups with and without persistent CoNS bacteremia, significant differences were seen for birth weight and the presence of hyperglycemia. Hyperglycemia is caused by relative insulin deficiency and resistance, due to high levels of circulating cytokines and inflammatory markers during sepsis . Persistent bacteremia may increase the risk for developing co-morbidity such as hyperglycemia.
No clear statements can be made about the possible influence of adequate monitoring and the response to vancomycin trough levels on the risk of developing a persistent CoNS bacteremia. Because vancomycin levels were not consistently obtained in all neonates (especially in those without persistent CoNS-bacteremia), an accurate comparison of the occurrence of subtherapeutic vancomycin trough levels of infants with and without a persistent CoNS bacteremia was not possible.
Our results suggest that the treatment strategy for persistent staphylococcal bacteremia with rifampin may be effective, but can be optimized by improving the monitoring of vancomycin trough levels and minimizing the delay in starting rifampin treatment. If, in spite of adequate vancomycin levels, CoNS bacteremia becomes persistent, rifampin therapy may be started after 6 days of bacteremia (3 positive blood cultures with a 48 hours interval after each).
Neonatal intensive care unit
Prolonged rupture of membranes
Respiratory distress syndrome
Coagulase negative staphylococci
Tan TQ, Mason EO, Ou CN, Kaplan SL: Use of intravenous rifampin in neonates with persistent staphylococcal bacteremia. Antimicrob Agents Chemother. 1993, 37: 2401-2406.
Orsi GB, d'Ettorre G, Panero A, Chiarini F, Vullo V, Venditti M: Hospital-acquired infection surveillance in a neonatal intensive care unit. Am J Infect Control. 2009, 37: 201-203. 10.1016/j.ajic.2008.05.009.
Wu JH, Chen CY, Tsao PN, Hsieh WS, Chou HC: Neonatal sepsis: a 6-year analysis in a neonatal care unit in Taiwan. Pediatr Neonatol. 2009, 50: 88-95. 10.1016/S1875-9572(09)60042-5.
Auriti C, Maccallini A, Di LG, Di C, Ronchetti MP, Orzalesi M: Risk factors for nosocomial infections in a neonatal intensive-care unit. J Hosp Infect. 2003, 53: 25-30. 10.1053/jhin.2002.1341.
Lahra MM, Beeby PJ, Jeffery HE: Intrauterine inflammation, neonatal sepsis, and chronic lung disease: a 13-year hospital cohort study. Pediatrics. 2009, 123: 1314-1319. 10.1542/peds.2008-0656.
Pullen J, Stolk LM, Degraeuwe PL, van Tiel FH, Neef C, Zimmermann LJ: Pharmacokinetics of intravenous rifampicin (rifampin) in neonates. Ther Drug Monit. 2006, 28: 654-661. 10.1097/01.ftd.0000245382.79939.a4.
Shama A, Patole SK, Whitehall JS: Intravenous rifampicin in neonates with persistent staphylococcal bacteraemia. Acta Paediatr. 2002, 91: 670-673. 10.1080/080352502760069098.
Soraisham AS, Al-Hindi MY: Intravenous rifampicin for persistent staphylococcal bacteremia in premature infants. Pediatr Int. 2008, 50: 124-126. 10.1111/j.1442-200X.2007.02519.x.
Watanakunakorn C, Guerriero JC: Interaction between vancomycin and rifampin against Staphylococcus aureus. Antimicrob Agents Chemother. 1981, 19: 1089-1091.
Varaldo PE, Debbia E, Schito GC: In vitro activity of teichomycin and vancomycin alone and in combination with rifampin. Antimicrob Agents Chemother. 1983, 23: 402-406.
Bayer AS, Morrison JO: Disparity between timed-kill and checkerboard methods for determination of in vitro bactericidal interactions of vancomycin plus rifampin versus methicillin-susceptible and -resistant Staphylococcus aureus. Antimicrob Agents Chemother. 1984, 26: 220-223.
Tuazon CU, Lin MY, Sheagren JN: In vitro activity of rifampin alone and in combination with nafcillin and Vancomycin against pathogenic strains of Staphylococcus aureus. Antimicrob Agents Chemother. 1978, 13: 759-761.
Acar JF, Goldstein FW, Duval J: Use of rifampin for the treatment of serious staphylococcal and gram-negative bacillary infections. Rev Infect Dis. 1983, 5 (Suppl 3): S502-S506.
Zinner SH, Lagast H, Klastersky J: Antistaphylococcal activity of rifampin with other antibiotics. J Infect Dis. 1981, 144: 365-371.
Wehrli W: Rifampin: mechanisms of action and resistance. Rev Infect Dis. 1983, 5 (Suppl 3): S407-S411.
Acocella G: Pharmacokinetics and metabolism of rifampin in humans. Rev Infect Dis. 1983, 5 (Suppl 3): S428-S432.
Mandell GL, Vest TK: Killing of intraleukocytic Staphylococcus aureus by rifampin: in-vitro and in-vivo studies. J Infect Dis. 1972, 125: 486-490.
Koup JR, Williams-Warren J, Weber A, Smith AL: Pharmacokinetics of rifampin in children. I. Multiple dose intravenous infusion. Ther Drug Monit. 1986, 8: 11-16. 10.1097/00007691-198603000-00003.
Giedion A, Haefliger H, Dangel P: Acute pulmonary X-ray changes in hyaline membrane disease treated with artificial ventilation and positive end-expiratory pressure (PEP). Pediatr Radiol. 1973, 1: 145-152. 10.1007/BF00974058.
Martin RJ, Fanaroff AA, Walsh MC: Fanaroff and Martin's Neonatal-Perinatal Medicine: Diseases of the Fetus and Infant. 2005, Philadelphia: Elsevier
Walsh MC, Kliegman RM: Necrotizing enterocolitis: treatment based on staging criteria. Pediatr Clin North Am. 1986, 33: 179-201.
Sie LT, van der Knaap MS, van Wezel-Meijler G, Taets van Amerongen AH, Lafeber HN, Valk J: Early MR features of hypoxic-ischemic brain injury in neonates with periventricular densities on sonograms. AJNR Am J Neuroradiol. 2000, 21: 852-861.
Volpe JJ: Neurology of the Newborn. 2008, Philadelphia: Saunders
Papile LA, Burstein J, Burstein R, Koffler H: Incidence and evolution of subependymal and intraventricular hemorrhage: a study of infants with birth weights less than 1,500 gm. J Pediatr. 1978, 92: 529-534. 10.1016/S0022-3476(78)80282-0.
Grootendorst DC, de Jager DJ, Brandenburg VM, Boeschoten EW, Krediet RT, Dekker FW, NECOSAD Study Group: Excellent agreement between C-reactive protein measurement methods in end-stage renal disease patients--no additional power for mortality prediction with high-sensitivity CRP. Nephrol Dial Transplant. 2007, 22: 3277-3284. 10.1093/ndt/gfm381.
de Hoog M, Schoemaker RC, Mouton JW, van den Anker JN: Vancomycin population pharmacokinetics in neonates. Clin Pharmacol Ther. 2000, 67: 360-367. 10.1067/mcp.2000.105353.
Beardsall K, Dunger D: Insulin therapy in preterm newborns. Early Hum Dev. 2008, 84: 839-842. 10.1016/j.earlhumdev.2008.09.013.
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The authors declare that they have no competing interests.
NMvdL participated in the design of the study, collected the data, performed the statistical analysis and drafted the manuscript. SJS conceived of the study and helped to correct the manuscript. FJW conceived of the study, participated in its design and coordination and helped to draft the manuscript. All authors read and approved the final manuscript.
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van der Lugt, N.M., Steggerda, S.J. & Walther, F.J. Use of rifampin in persistent coagulase negative staphylococcal bacteremia in neonates. BMC Pediatr 10, 84 (2010). https://doi.org/10.1186/1471-2431-10-84
- Neonatal Intensive Care Unit
- Positive Blood Culture
- Periventricular Leukomalacia