Study: Meropenem could be alternative treatment for bacterial meningitis
New data from a study by Swedish researchers indicates meropenem is an effective alternative empirical treatment option for adults who have community-acquired acute bacterial meningitis (ABM). The findings appeared yesterday in Antimicrobial Agents and Chemotherapy.
The study analyzed data on 623 Swedish adults diagnosed with ABM from 2008 through 2016 who were treated empirically with either cefotaxime plus ampicillin—which is recommended as the first-line treatment for ABM by the Swedish Infectious Disease Association—or meropenem. Propensity score matching was performed to adjust for baseline differences between the two groups. The primary end point was 30-day mortality, and secondary end points were 90-day mortality and unfavorable outcome at follow-up.
Among the 328 patients who received cefotaxime plus ampicillin, the 30-day mortality was 3.4%, compared with 6.4% in the patients treated with meropenem, and the corresponding figures for 90-day mortality were 4.6% and 8.1%, respectively. But the patients who received meropenem were older and more often presented with septic shock, and a lower proportion of them received adequate corticosteroids together with the initiation of antibiotics. In the propensity-matched patients, the 30-day mortality was 3.2% in the cefotaxime plus ampicillin group and 3.4% in the meropenem group.
For matched cases, the odds ratio (OR) for 30-day mortality for meropenem vs cefotaxime plus ampicillin was 1.15 (95% confidence interval [CI], 0.41 to 3.22, P = 0.79). The ORs for 90-day mortality and unfavorable outcome were 1.47 (95% CI, 0.62 to 3.52, P = 0.38) and 1.10 (95% CI, 0.75 to 1.63, P = 0.62).
The authors of the study say that while the findings support meropenem as an effective alternative for empirical treatment of ABM, cefotaxime plus ampicillin should remain the first-line treatment. "However, due to the importance of antibiotic stewardship, and the lack of benefit of meropenem on clinical outcomes in the majority of patients with ABM, third-generation cephalosporins should continue to be the cornerstone of empirical treatment of ABM," they conclude.
Sep 9 Antimicrob Agents Chemother abstract
Oral antibiotics linked to altered immune response to flu vaccine
A small study led by researchers from Stanford University and funded by the National Institutes of Allergy and Infectious Diseases (NIAID) suggests that oral antibiotics may alter the human immune response to the flu vaccine.
In the study, which was published in the journal Cell, the researchers set out to investigate the role of the human gut microbiota in shaping immune responses to the seasonal flu vaccine. They enrolled 22 healthy adults with high pre-existing immunity to the flu during the 2014-15 flu season, then randomized 11 participants to a 5-day oral cocktail of broad-spectrum antibiotics (neomycin, vancomycin, and metronidazole) 3 days prior to and 1 day after vaccination, with the aim of reducing gram-negative and anaerobic bacteria in the gut. They then collected biological samples for the following year and measured key aspects of the gut microbiome and the immune system.
Despite a significant reduction in gut bacterial load and bacterial diversity in the group that received antibiotics, there was no significant difference in antibody responses between the two groups. However, in a second study of 11 adults with low pre-existing flu immunity studied during the 2015-16 flu season, the researchers found a hindered response to the H1N1 A/California-specific strain of flu on day 90 and day 180 in the 5 participants who received antibiotics. No differences were observed for the two other flu strains.
The researchers also found that, in both groups that received antibiotics, there were changes to the immune system that promoted a pro-inflammatory state, similar to that seen in older adults who receive the flu vaccine.
"Here, we have demonstrated the potential for antibiotic-driven perturbation of the microbiome to influence immune responses to vaccination in healthy adults," the authors of the study write. "These findings should inform further research seeking to better understand mechanisms that control the interplay between the gut microbiota and our immune system."
Sep 5 Cell study
Sep 6 NIAID press release