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Published in: International Journal of Clinical Pharmacy 3/2014

01-06-2014 | Research Article

Outcome evaluation of an intervention to improve the effective and safe use of meropenem

Authors: Yusuke Yagi, Masafumi Okazaki, Hiromi Higaki, Megumi Nakai, Ayumu Hirata, Mitsuhiko Miyamura

Published in: International Journal of Clinical Pharmacy | Issue 3/2014

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Abstract

Background Pharmacists have been involved in promoting the proper and safe use of antimicrobial drugs in our institution since 2010. Setting Kochi Medical School Hospital, Japan. Objective To design and evaluate a plan of administration of meropenem (MEPM) based on its pharmacokinetics and pharmacodynamics, drug sensitivity, bacterial cultures, patient condition and renal function. Method A total of 547 patients admitted between April 2010 and March 2013 with serious infections who were successfully treated with MEPM for three or more days were analysed. Patients were initially divided into two groups according to renal function: group A consisted of patients with mild renal dysfunction [creatinine clearance (CLcr) > 50 mL/min] while group B consisted of patients with moderate to severe renal dysfunction (CLcr ≤ 50 mL/min). These groups were then subdivided into two groups according to the implementation of pharmacist intervention. Main outcome measures Daily dose, frequency of administration, dose interval, duration of therapy, adverse events and cost reduction. Results In the non-intervention subgroup within group A, the daily dose was 1,000 mg/day, the frequency of administration was 1.8 ± 0.6 times/day, and the duration of therapy was 9.4 ± 5.4 days. In the intervention subgroup within group A, the daily dose was 1,500 mg/day, the administration frequency was 2.5 ± 0.6 times/day, and the duration of therapy was 7.4 ± 3.7 days. Although the dose was higher (P < 0.05) and the duration of therapy was an average of 2 days shorter (P < 0.05) in the intervention subgroup, there was no significant difference in the rate of adverse events between the two subgroups. In group B, there were no significant differences between the two subgroups in the daily dose, administration frequency, or duration of therapy. However, liver dysfunction was significantly more common in the non-intervention subgroup than in the intervention subgroup (P < 0.05). The total reduction in drug cost in the intervention groups was estimated to be US$17,490 over 3 years. Conclusion Pharmacist intervention was associated with a shorter duration of therapy, lower drug costs, and decreased adverse effect. We believe that our intervention is beneficial in terms of effectiveness and safety, and supports proper antimicrobial use.
Literature
1.
go back to reference Edwards JR, Turner PJ, Wannop C, Withnell ES, Grindey AJ, Nairn K. In vitro antibacterial activity of SM-7338, a carbapenem antibiotic with stability to dehydropeptidase I. Antimicrob Agents Chemother. 1989;33:215–22.PubMedCentralPubMedCrossRef Edwards JR, Turner PJ, Wannop C, Withnell ES, Grindey AJ, Nairn K. In vitro antibacterial activity of SM-7338, a carbapenem antibiotic with stability to dehydropeptidase I. Antimicrob Agents Chemother. 1989;33:215–22.PubMedCentralPubMedCrossRef
2.
go back to reference Jones RN, Aldridge KE, Allen SD, Barry AL, Fuchs PC, Gerlach EH, Pfaller MA. Multicenter in vitro evaluation of SM-7338, a new carbapenem. Antimicrob Agents Chemother. 1989;33:562–5.PubMedCentralPubMedCrossRef Jones RN, Aldridge KE, Allen SD, Barry AL, Fuchs PC, Gerlach EH, Pfaller MA. Multicenter in vitro evaluation of SM-7338, a new carbapenem. Antimicrob Agents Chemother. 1989;33:562–5.PubMedCentralPubMedCrossRef
3.
go back to reference Neu HC, Novelli A, Chin NX. In vitro activity and beta-lactamase stability of a new carbapenem, SM-7338. Antimicrob Agents Chemother. 1989;33:1009–18.PubMedCentralPubMedCrossRef Neu HC, Novelli A, Chin NX. In vitro activity and beta-lactamase stability of a new carbapenem, SM-7338. Antimicrob Agents Chemother. 1989;33:1009–18.PubMedCentralPubMedCrossRef
4.
go back to reference Sentochnik DE, Eliopoulos GM, Ferraro MJ, Moellering RC Jr. Comparative in vitro activity of SM-7338, a new carbapenem antimicrobial agent. Antimicrob Agents Chemother. 1989;33:1232–6.PubMedCentralPubMedCrossRef Sentochnik DE, Eliopoulos GM, Ferraro MJ, Moellering RC Jr. Comparative in vitro activity of SM-7338, a new carbapenem antimicrobial agent. Antimicrob Agents Chemother. 1989;33:1232–6.PubMedCentralPubMedCrossRef
5.
go back to reference Sumita Y, Inoue M, Mitsuhashi S. In vitro antibacterial activity and beta-lactamase stability of the new carbapenem SM-7338. Eur Clin Microbiol Infect Dis. 1989;8:908–16.CrossRef Sumita Y, Inoue M, Mitsuhashi S. In vitro antibacterial activity and beta-lactamase stability of the new carbapenem SM-7338. Eur Clin Microbiol Infect Dis. 1989;8:908–16.CrossRef
6.
go back to reference Tsuji A, Kobayashi I, Oguri T, Inoue M, Yabuuchi E, Goto S. An epidemiological study of the susceptibility and frequency of multiple-drug-resistant strains of Pseudomonas aeruginosa isolated at medical institutes nationwide in Japan. J Infect Chemother. 2005;11:64–70.PubMedCrossRef Tsuji A, Kobayashi I, Oguri T, Inoue M, Yabuuchi E, Goto S. An epidemiological study of the susceptibility and frequency of multiple-drug-resistant strains of Pseudomonas aeruginosa isolated at medical institutes nationwide in Japan. J Infect Chemother. 2005;11:64–70.PubMedCrossRef
7.
go back to reference Sumita Y, Tada E, Nouda H, Okuda T, Fukasawa M. Mode of action of meropenem, a new carbapenem antibiotic. Chemotherapy. 1992;40:90–102. Sumita Y, Tada E, Nouda H, Okuda T, Fukasawa M. Mode of action of meropenem, a new carbapenem antibiotic. Chemotherapy. 1992;40:90–102.
8.
go back to reference Nakamura H, Fukui T, Katsu M, Torikai K, Tomii M, Kawai K. Bacteriological and clinical studies on meropenem. Chemotherapy. 1992;40:312–25. Nakamura H, Fukui T, Katsu M, Torikai K, Tomii M, Kawai K. Bacteriological and clinical studies on meropenem. Chemotherapy. 1992;40:312–25.
9.
go back to reference The Japanese Society of Intensive Care Medicine Sepsis Registry Committee. The Japanese Guidelines for the Management of Sepsis. J Jpn Soc Intensive Care Med. 2013;20:124–73.CrossRef The Japanese Society of Intensive Care Medicine Sepsis Registry Committee. The Japanese Guidelines for the Management of Sepsis. J Jpn Soc Intensive Care Med. 2013;20:124–73.CrossRef
10.
go back to reference Mikamo H. Optimizing meropenem therapy based on pharmacokinetics/pharmacodynamics (PK/PD) for severe infectious disease. Antibiot Chemother. 2005;21:405–13. Mikamo H. Optimizing meropenem therapy based on pharmacokinetics/pharmacodynamics (PK/PD) for severe infectious disease. Antibiot Chemother. 2005;21:405–13.
11.
go back to reference Mitsuo K. Attempt of host disease state levelling. Basic concept and clinical application. Jpn J Antibiot. 1998;51:532–4. Mitsuo K. Attempt of host disease state levelling. Basic concept and clinical application. Jpn J Antibiot. 1998;51:532–4.
12.
go back to reference Noda K, Ueda A, Kuronuma H, Iwai S, Ito K, Saitoh Y, et al. Long-term monitoring and analysis for changing of selectivity and consumption of antimicrobial drugs estimated with AUD in our hospital I. Jpn J Environ Infect. 2009;24:332–6.CrossRef Noda K, Ueda A, Kuronuma H, Iwai S, Ito K, Saitoh Y, et al. Long-term monitoring and analysis for changing of selectivity and consumption of antimicrobial drugs estimated with AUD in our hospital I. Jpn J Environ Infect. 2009;24:332–6.CrossRef
14.
go back to reference Chimata M, Nagase M, Suzuki Y, Shimomura M, Kakuta S. Pharmacokinetics of meropenem in patients with various degrees of renal function, including patients with end-stage renal disease. Antimicrob Agents Chemother. 1993;37:229–33.PubMedCentralPubMedCrossRef Chimata M, Nagase M, Suzuki Y, Shimomura M, Kakuta S. Pharmacokinetics of meropenem in patients with various degrees of renal function, including patients with end-stage renal disease. Antimicrob Agents Chemother. 1993;37:229–33.PubMedCentralPubMedCrossRef
15.
go back to reference Takikawa H, Onji M. A proposal of the diagnostic scale of drug induced liver injury. Hepatol Res. 2005;32:250–1.PubMedCrossRef Takikawa H, Onji M. A proposal of the diagnostic scale of drug induced liver injury. Hepatol Res. 2005;32:250–1.PubMedCrossRef
16.
go back to reference Mehta RL, Kellum JA, Shah SV, Molitoris BA, Ronco C, Warnock DG, et al. Acute Kidney Injury Network: report of an initiative to improve outcomes in acute kidney injury. Crit Care. 2007;11:1–8. Mehta RL, Kellum JA, Shah SV, Molitoris BA, Ronco C, Warnock DG, et al. Acute Kidney Injury Network: report of an initiative to improve outcomes in acute kidney injury. Crit Care. 2007;11:1–8.
17.
go back to reference Ogasahara Y, Ohno K, Harino T, Funahara H, Gotou C, Nagasaki N, et al. Promotion of correct use of antibiotics utilizing the antibiotics PK/PD check sheet by clinical pharmacists. Jpn J Environ Infect. 2008;23:117–23.CrossRef Ogasahara Y, Ohno K, Harino T, Funahara H, Gotou C, Nagasaki N, et al. Promotion of correct use of antibiotics utilizing the antibiotics PK/PD check sheet by clinical pharmacists. Jpn J Environ Infect. 2008;23:117–23.CrossRef
18.
go back to reference Scaglione F. Can PK/PD be used in everyday clinical practice. Int J Antimicrob Agents. 2002;19:349–53.PubMedCrossRef Scaglione F. Can PK/PD be used in everyday clinical practice. Int J Antimicrob Agents. 2002;19:349–53.PubMedCrossRef
19.
go back to reference Linden P. Safety profile of meropenem: an updated review of over 6000 patients treated with meropenem. Drug Saf. 2007;30:657–68.PubMedCrossRef Linden P. Safety profile of meropenem: an updated review of over 6000 patients treated with meropenem. Drug Saf. 2007;30:657–68.PubMedCrossRef
20.
go back to reference Drusano GL. Prevention of resistance: a goal for dose selection for antimicrobial agents. Clin Infect Dis. 2003;36:S42–50.PubMedCrossRef Drusano GL. Prevention of resistance: a goal for dose selection for antimicrobial agents. Clin Infect Dis. 2003;36:S42–50.PubMedCrossRef
21.
go back to reference Craigh WA. The role of pharmacodynamics in effective treatment of community-acquired pathogens. Adv Stud Med. 2002;2:126–34. Craigh WA. The role of pharmacodynamics in effective treatment of community-acquired pathogens. Adv Stud Med. 2002;2:126–34.
22.
go back to reference Shimada J, Hori S, Kanemitsu K, Shoji Y, Nakashio S, Yanagawa A. A comparative study on the convulsant activity of carbapenems and beta-lactams. Drugs Exp Clin Res. 1992;18:377–81.PubMed Shimada J, Hori S, Kanemitsu K, Shoji Y, Nakashio S, Yanagawa A. A comparative study on the convulsant activity of carbapenems and beta-lactams. Drugs Exp Clin Res. 1992;18:377–81.PubMed
23.
go back to reference Calandra G, Lydick E, Carrigan J, Weiss L, Guess H. Factors predisposing to seizures in seriously ill, infected patients receiving antibiotics: experience with imipenem/cilastatin. Am J Med. 1988;84:911–8.PubMedCrossRef Calandra G, Lydick E, Carrigan J, Weiss L, Guess H. Factors predisposing to seizures in seriously ill, infected patients receiving antibiotics: experience with imipenem/cilastatin. Am J Med. 1988;84:911–8.PubMedCrossRef
24.
go back to reference Norrby SR, Newell PA, Faulkner KL, Lesky W. Safety profile of meropenem: international clinical experience based on the first 3125 patients treated with Meropenem. J Antimicrob Chemother. 1995;36(Suppl A):207–23.PubMedCrossRef Norrby SR, Newell PA, Faulkner KL, Lesky W. Safety profile of meropenem: international clinical experience based on the first 3125 patients treated with Meropenem. J Antimicrob Chemother. 1995;36(Suppl A):207–23.PubMedCrossRef
25.
go back to reference Leroy A, Fillastre JP, Borsa-Lebas F, Etienne I, Humbert G. Pharmacokinetics of meropenem (ICI 194,660) and its metabolite (ICI 213,689) in healthy subjects and in patients with renal impairment. Antimicrob Agents Chemother. 1992;36:2794–8.PubMedCentralPubMedCrossRef Leroy A, Fillastre JP, Borsa-Lebas F, Etienne I, Humbert G. Pharmacokinetics of meropenem (ICI 194,660) and its metabolite (ICI 213,689) in healthy subjects and in patients with renal impairment. Antimicrob Agents Chemother. 1992;36:2794–8.PubMedCentralPubMedCrossRef
26.
go back to reference Leroy A, Fillastre JP, Etienne I, Borsa-Lebas F, Humbert G. Pharmacokinetics of meropenem in subjects with renal insufficiency. Eur J Clin Pharmacol. 1992;42:535–8.PubMedCrossRef Leroy A, Fillastre JP, Etienne I, Borsa-Lebas F, Humbert G. Pharmacokinetics of meropenem in subjects with renal insufficiency. Eur J Clin Pharmacol. 1992;42:535–8.PubMedCrossRef
Metadata
Title
Outcome evaluation of an intervention to improve the effective and safe use of meropenem
Authors
Yusuke Yagi
Masafumi Okazaki
Hiromi Higaki
Megumi Nakai
Ayumu Hirata
Mitsuhiko Miyamura
Publication date
01-06-2014
Publisher
Springer Netherlands
Published in
International Journal of Clinical Pharmacy / Issue 3/2014
Print ISSN: 2210-7703
Electronic ISSN: 2210-7711
DOI
https://doi.org/10.1007/s11096-014-9949-2

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