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Observational Study
. 2022 Dec 20;66(12):e0082022.
doi: 10.1128/aac.00820-22. Epub 2022 Nov 3.

Penicillin- and Cephalosporin-Resistant Pneumococcal Meningitis: Treatment in the Real World and in Guidelines

Affiliations
Observational Study

Penicillin- and Cephalosporin-Resistant Pneumococcal Meningitis: Treatment in the Real World and in Guidelines

Carmen Cabellos et al. Antimicrob Agents Chemother. .

Abstract

To report on the therapy used for penicillin- and cephalosporin-resistant pneumococcal meningitis, we conducted an observational cohort study of patients admitted to our hospital with pneumococcal meningitis between 1977 and 2018. According to the European Committee on Antimicrobial Susceptibility Testing (EUCAST) recommendations, we defined pneumococci as susceptible and resistant to penicillin with MIC values of ≤0.06 mg/L and > 0.06 mg/L, respectively; the corresponding values for cefotaxime (CTX) were ≤0.5 mg/L and >0.5 mg/L. We treated 363 episodes of pneumococcal meningitis during the study period. Of these, 24 had no viable strain, leaving 339 episodes with a known MIC for inclusion. Penicillin-susceptible strains accounted for 246 episodes (73%), penicillin-resistant strains for 93 (27%), CTX susceptible for 58, and CTX resistant for 35. Nine patients failed or relapsed and 69 died (20%), of whom 22% were among susceptible cases and 17% were among resistant cases. During the dexamethasone period, mortality was equal (12%) in both susceptible and resistant cases. High-dose CTX (300 mg/Kg/day) helped to treat failed or relapsed cases and protected against failure when used as empirical therapy (P = 0.02), even in CTX-resistant cases. High-dose CTX is a good empirical therapy option for pneumococcal meningitis in the presence of a high prevalence of penicillin and cephalosporin resistance, effectively treating pneumococcal strains with MICs up to 2 mg/L for either penicillin or CTX.

Keywords: antibiotic resistance; bacterial meningitis; cefotaxime; ceftriaxone.

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Conflict of interest statement

The authors declare a conflict of interest. C.A. has participated as scientific advisor of Pfizer and MSD, and has received research funding from MSD, unrelated to the present study. All other authors declare no conflicts of interest.

Figures

FIG 1
FIG 1
Evolution of penicillin and cefotaxime resistance and total number of episodes of S. pneumoniae meningitis.
FIG 2
FIG 2
Number of meningitis episodes caused by PCV7 serotypes, additional PCV13 serotypes, additional PPSV23 serotypes, and nonvaccine types (other).

Comment in

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