Abstract
Purpose
The purpose of this study was to assess the clinical outcomes of adults with invasive meningococcal disease (IMD) and to compare the outcomes of patients with IMD caused by a penicillin susceptible isolate (minimum inhibitory concentration (MIC) ≤ 0.06 mg/L) with patients with IMD caused by an isolate with reduced penicillin susceptibility (MIC > 0.06 mg/L). We also assessed the outcomes of patients with IMD caused by an isolate with reduced penicillin susceptibility who were treated exclusively with intravenous (IV) benzylpenicillin.
Methods
Retrospective study of all culture positive IMD in adult patients (age ≥ 15 years) in the Auckland region from 2004 to 2017.
Results
One hundred and thirty-nine patients were included; 94 had penicillin susceptible isolates (88 cured, 6 died), and 45 had an isolate with reduced penicillin susceptibility (41 cured, 1 possible relapse, 3 died). The median benzylpenicillin/ceftriaxone treatment duration was 3 days for both groups. There was no difference in the patient outcomes of both groups. Eighteen patients with IMD caused by an isolate with reduced penicillin susceptibility received benzylpenicillin alone and were cured.
Conclusions
This study provides further support to existing data that has shown that short duration IV beta-lactam treatment is effective for IMD in adults. Only a small number of patients with meningitis caused by an isolate with reduced penicillin susceptibility received benzylpenicillin alone, limiting its evaluation. For Neisseria meningitidis meningitis, we recommend ceftriaxone as empiric treatment and as definitive treatment when this is caused by an isolate with reduced penicillin susceptibility.
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References
Martin D, Lopez L. The epidemiology of meningococcal disease in New Zealand in 2008. Porirua: Institute of Environmental Science Research; 2009.
The Institute of Environmental Science and Research Ltd (ESR). Notifiable diseases in New Zealand: annual report 2018. Poirura: ESR; 2020.
Clinical and Laboratory Standards Institute. Performance standards for antimicrobial susceptibility testing 28th ed. Wayne: CLSI; 2018.
The European committee on antimicrobial susceptibility testing. Breakpoint tables for interpretation of MICs and zone diameters. Version 10.0. 2020. p. Version 10.0. http://www.eucast.org
Martin D, McDowell R, Garrett N, Baker M. The epidemiology of meningococcal disease in New Zealand in 2001. Porirua: Institute of Environmental Science and Research; 2002.
Institute of Environmental Science and Research (ESR). Antimicrobial susceptibility of invasive neisseria meningitidis, 2017. Porirua: ESR; 2018.
Sáez-Nieto JA, Fontanals D, de Jalon JG, de Artola VM, Peña P, Morera MA, et al. Isolation of neisseria meningitidis strains with increase of penicillin minimal inhibitory concentrations. Epidemiol Infect. 1987;99:463–9.
Pérez-Trallero E, Aldamiz-Echeverria L, Pérez-Yarza E. Meningococci with increased resistance to penicillin. Lancet. 1990;335:1096.
Turner P, Southern K, Spencer N, Pullen H. Treatment failure in meningococcal meningitis. Lancet. 1990;335:732–3.
Vincent JL, Moreno R, Takala J, Willatts S, De Mendonça A, Bruining H, et al. The SOFA (Sepsis-related Organ Failure Assessment) score to describe organ dysfunction/failure. On behalf of the working group on sepsis-related problems of the European society of intensive care medicine. Intensive Care Med. 1996;22:707–10.
Trotter CL, Chandra M, Cano R, Larrauri A, Ramsay ME, Brehony C, et al. A surveillance network for meningococcal disease in Europe. FEMS Microbiol Rev. 2007;31:27–36.
Pace D, Pollard AJ. Meningococcal disease: clinical presentation and sequelae. Vaccine. 2012;30:B3-9.
Dwilow R, Fanella S. Invasive meningococcal disease in the 21st century. An update for the clinician. Curr Neurol Neurosci Rep. 2015. https://doi.org/10.1007/s11910-015-0524-6.
Cabellos C, Pelegrín I, Benavent E, Gudiol F, Tubau F, Garcia-Somoza D, et al. Invasive meningococcal disease: impact of short course therapy. A DOOR/RADAR study. J Infect. 2017;75:420–5. https://doi.org/10.1016/j.jinf.2017.08.009.
Trotter CL, Fox AJ, Ramsay ME, Sadler F, Gray SJ, Mallard R, et al. Fatal outcome from meningococcal disease—An association with meningococcal phenotype but not with reduced susceptibility to benzylpenicillin. J Med Microbiol. 2002;51:855–60.
Ellis-Pegler R, Galler L, Roberts S, Thomas M, Woodhouse A. Three days of intravenous benzyl penicillin treatment of meningococcal disease in adults. Clin Infect Dis. 2003;37:658–62.
Briggs S, Ellis-Pegler R, Roberts S, Thomas M, Woodhouse A. Short course intravenous benzylpenicillin treatment of adults with meningococcal disease. Intern Med J. 2004;34:383–7.
Viladrich PF, Pallares R, Ariza J, Rufi G, Gudiol F. Four days of penicillin therapy for meningococcal meningitis. Arch Intern Med. 1986;146:2380–2.
Martin E, Guggi T, Hohl P, Fernex M, Kayser FH. Short course single daily ceftriaxone monotherapy for acute bacterial meningitis in children: results of a Swiss multicenter study. Part I: clinical results. Infection. 1990;18:70–7.
van de Beek D, Cabellos C, Dzupova O, Esposito S, Klein M, Kloek AT, et al. ESCMID guideline: diagnosis and treatment of acute bacterial meningitis. Clin Microbiol Infect. 2016;22:S37-62.
Masson-Behar V, Jacquier H, Richette P, Ziza JM, Zeller V, Rioux C, et al. Arthritis secondary to meningococcal disease: a case series of 7 patients. Medicine. 2017. https://doi.org/10.1097/MD.0000000000007573.
Schaad UB. Arthritis in disease due to Neisseria meningitidis. Rev Infect Dis. 1980;2:880–8.
Institute of Environmental Science and Research (ESR). Antimicrobial susceptibility of invasive neisseria meningitidis, 2018. Porirua: ESR; 2019.
Burgess DS, Frei CR, Lewis JS, Fiebelkorn KR, Jorgensen JH. The contribution of pharmacokinetic-pharmacodynamic modelling with Monte Carlo simulation to the development of susceptibility breakpoints for Neisseria meningitidis. Clin Microbiol Infect. 2007;13:33–9.
Nasrin D, Collignon PJ, Roberts L, Wilson EJ, Pilotto LS, Douglas RM. Effect of beta lactam antibiotic use in children on pneumococcal resistance to penicillin: prospective cohort study. BMJ. 2002 Jan 5;324:28–28.
Whyler N, Tomlin A, Tilyard M, Thomas M. Ethnic disparities in community antibacterial dispensing in New Zealand, 2015. N Z Med J. 2018 Aug 17;131:50–60.
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A payment of $2000 (USD) was received from the University of Gothenburg, Sweden, to cover the costs of supervision of two elective medical students (SS and MHH).
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Broom, M., Best, E., Heffernan, H. et al. Outcomes of adults with invasive meningococcal disease with reduced penicillin susceptibility in Auckland 2004–2017. Infection 51, 425–432 (2023). https://doi.org/10.1007/s15010-022-01897-6
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DOI: https://doi.org/10.1007/s15010-022-01897-6