Litcius/Paper detail

Vancomycin loading dose is associated with increased early clinical response without attainment of initial target trough concentration at a steady state in patients with methicillin‐resistant <i>Staphylococcus aureus</i> infections

Takashi Ueda, Yoshio Takesue, Kazuhiko Nakajima, Kaoru Ichiki, Kaori Ishikawa, Y. Takai, Kumiko Yamada, Yasunao Wada, Toshie Tsuchida, Naruhito Otani, Yoshiko Takahashi, Mika Ishihara, Sumiyo Shibata, Hiroki Ikeuchi, Motoi Uchino, Takeshi Kimura

2020Journal of Clinical Pharmacy and Therapeutics21 citationsDOI

Abstract

What is known and objective Vancomycin therapeutic guidelines suggest a loading dose of 25-30 mg/kg for seriously ill patients. However, high-quality data to guide the use of loading doses are lacking. We aimed to evaluate whether a loading dose (a) achieved a target trough concentration at steady state and (b) improved early clinical response. Methods Patients with an estimated glomerular filtration rate ≥ 90 mL/min/1.73 m2 were included. A loading dose of 25 mg/kg vancomycin followed by 15 mg/kg twice daily was compared with traditional dosing. A Cmin sample was obtained before the fifth dose. An early clinical response 48-72 hours after the start of therapy and clinical success at end of therapy (EOT) was evaluated in patients with methicillin-resistant Staphylococcus aureus (MRSA), methicillin-resistant coagulase-negative Staphylococci or Enterococcus faecium. Results There was no significant difference in Cmin between the regimen with and without a loading dose (median: 10.4 and 10.2 µg/mL, P = .54). Proportions of patients achieving 10-20 and 15-20 µg/mL were 56.9% and 5.6%, respectively, in patients with a loading dose. Although there was no significant difference in success rate at EOT between groups, a loading dose was associated with increased early clinical response for all infections (adjusted odds ratio [OR]: 4.588, 95% confidence interval [CI]: 1.373-15.330) and MRSA infections (OR: 12.065, 95% CI: 1.821-79.959). Study limitations included no Cmin measurements within 24 hours and the inclusion of less critically ill patients. What is new and conclusion A loading dose of 25 mg/kg followed by 15 mg/kg twice daily did not achieve the optimal Cmin at steady state in patients with normal renal function. However, more early clinical responses were obtained with a loading dose compared with traditional dosing, possibly because of a prompt albeit temporary achievement of a more effective concentration.

Topics & Concepts

CminMedicineLoading doseVancomycinEnterococcus faeciumMethicillin-resistant Staphylococcus aureusTrough ConcentrationDosingInternal medicineConfidence intervalStaphylococcus aureusMaintenance doseTherapeutic drug monitoringAntibioticsPharmacokineticsCmaxMicrobiologyBiologyGeneticsBacteriaAntimicrobial Resistance in StaphylococcusClostridium difficile and Clostridium perfringens researchAntibiotics Pharmacokinetics and Efficacy