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Amoxicillin-non-susceptible Streptococcus pneumoniae causing invasive pneumonia: serotypes, clones, and clinical
Jordi Càmara1,2, Inmaculada Grau2,3, Aida González-Díaz1,2
1Department of Clinical Microbiology, Hospital Universitari de Bellvitge-IDIBELL, L'Hospitalet de Llobregat, Spain.
Abstract:
Amoxicillin is one of the most commonly used antibiotics to treat pneumococcal infections. We analyzed the epidemiology and clinical impact of amoxicillin non-susceptibility in invasive pneumococcal pneumonia. This is an observational study based on prospectively collected data at Bellvitge University Hospital (Barcelona, Spain) from 1994 to 2020. Isolates were tested for antibiotic susceptibility, serotyped, and genotyped. Clinical characteristics and 30 day mortality were evaluated using independent Cox proportional hazards models. We analyzed 1,663 episodes. While the proportion of isolates susceptible to amoxicillin increased from 72.9% (1994-2001) to 91.4% (2016-2020), the proportion of isolates with MIC > 2 mg/L remained stable (4.8% and 5.3%, respectively). A single lineage (GPSC6; serotypes 9V, 14, and 11A) accounted for 56.5% of non-susceptible strains. High McCabe scores (ultimately fatal: HR 2.87 [2.10-3.92] and rapidly fatal: HR 4.98 [3.50-7.09]), along with parameters linked to disease severity such as leukopenia (HR 2.14 [1.63-2.82]), shock (HR 3.47 [2.63-4.57]), respiratory failure (HR 4.26 [2.63-6.89]), and bilobar pneumonia (HR 1.44 [1.09-1.90]), were associated with 30 day mortality. The risk of mortality was higher in episodes treated with amoxicillin than with third-generation cephalosporins (HR 1.81 [1.28-2.56]), especially in episodes with amoxicillin MIC > 2 mg/L (HR 6.14 [1.65-22.80]). Amoxicillin therapy was not associated with increased mortality in patients with a non-fatal McCabe score (HR 1.49 [0.62-3.55]), but it was in the ultimately fatal/rapidly fatal group (HR 1.97 [1.34-2.90]). In addition to the crucial importance of host factors in the outcome of invasive pneumococcal pneumonia, our data indicate that amoxicillin yields poorer outcomes compared to third-generation cephalosporins, particularly in patients with a worse prognosis.
Insights
Amoxicillin non-susceptibility in invasive pneumococcal pneumonia remains stable. Amoxicillin treatment was linked to higher mortality than cephalosporins, especially in severe cases.
Area of Science:
- Infectious Diseases
- Clinical Microbiology
- Epidemiology
Background:
- Amoxicillin is a primary antibiotic for pneumococcal infections.
- Understanding amoxicillin non-susceptibility is crucial for effective treatment of invasive pneumococcal pneumonia.
- Long-term data on amoxicillin resistance trends and clinical outcomes are needed.
Purpose of the Study:
- To analyze the epidemiology of amoxicillin non-susceptibility in invasive pneumococcal pneumonia.
- To evaluate the clinical impact and mortality associated with amoxicillin non-susceptibility.
- To compare outcomes of amoxicillin versus third-generation cephalosporins in treating these infections.
Main Methods:
- Observational study using prospectively collected data from 1994-2020.
- Analysis of 1,663 episodes of invasive pneumococcal pneumonia.
- Evaluation of antibiotic susceptibility, serotyping, genotyping, clinical characteristics, and 30-day mortality using Cox proportional hazards models.
Main Results:
- Amoxicillin susceptibility increased from 72.9% to 91.4%, but MIC > 2 mg/L remained stable (4.8%-5.3%).
- A single lineage (GPSC6) dominated non-susceptible strains.
- High McCabe scores, leukopenia, shock, respiratory failure, and bilobar pneumonia were associated with mortality.
- Amoxicillin treatment showed higher mortality risk than cephalosporins, particularly with MIC > 2 mg/L and in severe cases.
Conclusions:
- Despite increasing amoxicillin susceptibility, a stable proportion of non-susceptible strains persist.
- Host factors significantly influence invasive pneumococcal pneumonia outcomes.
- Amoxicillin may yield poorer outcomes compared to third-generation cephalosporins, especially in patients with severe disease or high MIC values.
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