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Antimicrob Agents Chemother. 2010 February; 54(2): 924–926.
Published online 2009 November 23. doi:  10.1128/AAC.00836-09
PMCID: PMC2812167

Pharmacokinetics of Ertapenem following Intravenous and Subcutaneous Infusions in Patients[down-pointing small open triangle]

Abstract

Steady-state pharmacokinetics of ertapenem were compared in patients after 1-g intravenous and subcutaneous (s.c.) infusions. Bioavailability was 99% ± 18% after s.c. administration, but peaks were reduced by about (43 ± 29 versus 115 ± 28 μg/ml) and times to peak were delayed. Simulations based on unbound concentrations show that time over the MIC should always be longer than 30% to 40% of the dosing interval, suggesting that s.c. infusion could be an alternative in patients with reduced vascular access.

Ertapenem is a recent long-acting, parenteral carbapenem antibiotic mainly indicated in the treatment of community-acquired infections or hospital-acquired infections without suspicion of Pseudomonas or Acinetobacter (5), as an alternative to penicillin-β-lactamase inhibitor combination (10, 19, 23). The pharmacokinetics of ertapenem has been extensively described (2, 3, 6-8, 15, 16, 18, 21). Ertapenem may be administered intravenously (i.v.) or intramuscularly (i.m.) for several days (13), but for many hospitalized patients the i.m. route might be contraindicated due to anticoagulant therapy. Subcutaneous (s.c.) administration is daily safely used with drugs and fluids mostly for dehydrated elderly patients or patients in palliative care when oral or i.v. administration is impossible (20) and could then appear as an interesting alternative. Advantages for the s.c. route over the i.v. route include a similar number of or even fewer complications, cost savings, greater patient comfort, and less nursing time to start and maintain the infusion (1, 22). The aim of this study was to compare the pharmacokinetics of ertapenem at steady state following 30-min i.v. and s.c. infusions in order to determine if s.c. administration of ertapenem, which is not yet approved, could be a viable alternative for i.v. infusion in patients with limited vascular sites.

The study was conducted at the University Hospital of Poitiers (France) after its approval by the local ethics committee (Region Poitou-Charentes CCPPRB, protocol no. 05.12.26). Written informed consent was obtained from each subject or their closest relative if the patient was unconscious. The study enrolled 6 adult male patients suspected of having an infection due to ertapenem-susceptible bacteria (Table (Table1).1). Ertapenem was the only antibiotic used, sedation was obtained with propofol and sufentanil, and no other drugs that could have been suspected of interacting with ertapenem pharmacokinetics such as vasopressors or midazolam were used. At study enrollment, patients were mechanically ventilated and exhibited a systemic inflammatory response syndrome. Infection sites justifying ertapenem administration were early-onset ventilator-associated pneumonia (n = 5) and surgical wound infection (patient no. 2). The microorganisms isolated at those infection sites were methicillin-susceptible Staphylococcus aureus (n = 2), Haemophilus influenzae (n = 1), Escherichia coli (n = 1), and Klebsiella pneumoniae (n = 2). Local tolerance was assessed during the 24 h following subcutaneous infusion by checking for erythema, pruritus, hematoma, or necrosis at the insertion site. Ertapenem (Invanz) was purchased from the pharmaceutical company Merck Sharp & Dohme-Chibret (Paris, France) as a dry powder and reconstituted in 50 ml normal saline just before being infused with a pump (Orchestra DPS; Fresenius Vial, Brezins, France). The administration sites were a central vein (i.v.) or the anterior side of a thigh (s.c.). Initially 1 g of ertapenem was administered i.v. over 30 min once daily, and blood samples for the i.v. pharmacokinetic study were collected between the 4th day and the 7th day. The next day, treatment was shifted to the s.c. route and a second series of blood samples was collected during the following 24 h for the s.c. pharmacokinetic study. Ertapenem administration was shifted back to the i.v. route until the end of therapy. Blood samples were drawn via an arterial catheter in heparinized tubes and immediately centrifuged for 10 min at 2,500 × g and 4°C to separate plasma, which was then transferred to storage vials and diluted (1:1) with a stabilizing solution consisting of 1:1 ethylene glycol and 2-(4-morpholino) ethylsulfonic acid at 0.1 mol/liter (pH 6.5). Plasma ultrafiltrates were obtained from plasma samples collected at times 0.5 h and 24 h postdosing by centrifugation with a Centrifree system (CF50A model; Amicon, Molsheim, France). Samples were stored at −80°C until analysis. Ertapenem concentrations were measured using a liquid chromatography method with tandem mass spectrometry detection (12). Within- and between-day variability of the method at various concentrations led to coefficients of variation no greater than 16.4% (n = 11) and accuracies ranging between 98.5% and 110.9%. A compartmental pharmacokinetic analysis for total plasma concentrations was conducted with WinNonLin version 4.0.1. (Pharsight Corporation, Mountain View, CA), using a two-open-compartment model with multiple zero order infusions after i.v. administrations followed by a one-open-compartment model with one zero order infusion after s.c. administration. Duration of infusion was set at a fixed value equal to 0.5 h after i.v. administrations, but estimated by the modeling after s.c. administration. A 1/y weight was used for all the analysis. Unbound concentrations were derived from measured total concentrations using a saturable two-class binding site model with one specific binding site and one nonspecific binding site, previously validated for ertapenem (7). The rate constants for specific and nonspecific binding sites were estimated from the 12 pairs of total and unbound concentrations measured at 0.5 and 24 h and using the mean concentration values of albumin (14.1 g/liter) and the remaining proteins (38.7 g/liter) characteristic of these patients. The same compartmental pharmacokinetic analysis as for total concentrations was conducted with unbound concentrations, and simulations were derived for each subject and each route of administration in order to estimate the percentage of dosing interval during which unbound concentrations would be higher than various breakpoint values, chosen as 1, 2, 4, and 8 mg/liter, in agreement with the Clinical Laboratory Standards Institute. Results are presented as means ± standard deviation (SD), and nonparametric Wilcoxon's rank test was used for statistical comparisons, with P < 0.05 considered as significant.

TABLE 1.
Patient characteristics and individual and mean ± SD pharmacokinetic parameters based on total ertapenem concentrations measured after i.v. and s.c. 30-min infusions of ertapenem (1 g/24 h) to 6 adult patients

All patients completed the study without any local or systemic adverse effect attributable to ertapenem administration, and signs of infection had disappeared by the end of treatment. Ertapenem plasma concentration-time profiles were shifted to the right after s.c. infusion, with an approximately 3-fold reduction of peak concentrations (Cmax) and 5-fold increase of time to peak concentration (tmax) (Table (Table1).1). However, after 3 h postdosing on average, plasma concentrations became higher following s.c. infusion (Fig. (Fig.1),1), and AUCs were virtually identical after both routes of administration, attesting for complete bioavailability following s.c. infusion. However, because only unbound drug has the ability to distribute and to exert antimicrobial activity at the target site of infection, unbound concentrations should be considered to predict efficacy (4, 14). In this study, ertapenem protein binding demonstrated no sign of nonlinearity and was relatively limited, with unbound fractions (fu) ranging from 40.4% ± 2.8% to 51.4% ± 5.5% (Table (Table1),1), consistent with the value (fu = 54.8% ± 19.1%) recently reported by Burkhardt et al. in critical care patients (7), but much higher than the average value (16% unbound corresponding to 84% bound) currently reported in healthy volunteers (15, 20). Because ertapenem antimicrobial activity is considered to be time dependent (9), a peak reduction after s.c. administration may not have major consequences on its clinical efficacy. Instead, the dosing interval during which unbound drug concentration exceeds the MIC (t > MIC), represents the most relevant pharmacokinetics/pharmacodynamics parameter (17), and a t > MIC of 30 to 40% of the dosing interval should be effective (11). Conducted simulations suggested that for susceptible and intermediately susceptible microorganisms (MIC ≤ 4 mg/liter), t > MIC based upon unbound ertapenem concentrations should always be longer than 30% to 40% of the dosing interval, independently of the route of administration. In conclusion, this study suggests that s.c. infusion of ertapenem should be equivalent to i.v. infusions in terms of efficacy and could therefore represent an interesting alternative for patients with reduced vascular access, such as dehydrated elderly patients or patients in palliative care. However, this should be confirmed in a larger population of such patients.

FIG. 1.
Mean ± SD total ertapenem concentrations in plasma after multiple daily intravenous infusions (1 g over 30 min) followed by a subcutaneous infusion (1 g over 30 min) in 6 patients. Closed symbols and the solid line correspond to intravenous infusion, ...

Acknowledgments

Vipul Kumar from the Medical School of Hannover (Germany) is gratefully acknowledged for providing information required to perform the binding modeling of ertapenem. We thank Pharsight Corporation for supplying WinNonLin through the PAL program.

Footnotes

[down-pointing small open triangle]Published ahead of print on 23 November 2009.

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