In-hospital mortality among patients with invasive non-group A β-hemolytic Streptococcus treated with clindamycin combination therapy: a nationwide cohort study
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Published on: April 18, 2019
Shoichiro Hamada1,2, Mikio Nakajima1,2,3, Richard H Kaszynski1
1Emergency and Critical Care Center Tokyo Metropolitan Hiroo Hospital Tokyo Japan.
Aim:
Combination treatment with clindamycin is recommended in patients with invasive group A Streptococcus infection; however, whether the same treatment is effective in invasive group B Streptococcus and S. dysgalactiae subspecies equisimilis infections remains unknown. We aimed to investigate whether clindamycin added to standard of care therapy would be effective in patients with invasive non-group A β-hemolytic Streptococcus infections.
Methods:
This was a nationwide retrospective cohort study using the Japanese Diagnosis Procedure Combination inpatient database focusing on the period between 2010 and 2018. We extracted data on patients diagnosed with sepsis due to non-group A β-hemolytic Streptococcus. One-to-four propensity score-matching was undertaken to compare patients who were treated with clindamycin within 2 days of admission (clindamycin group) and those who did not (control group). The primary outcome was in-hospital mortality.
Results:
We identified 3754 eligible patients during the study period. The patients were divided into the clindamycin (n = 296) and control groups (n = 3458). After one-to-four propensity score matching, we compared 289 and 1156 patients with and without clindamycin, respectively. In-hospital mortality did not significantly differ between the two groups (9.7% versus 10.3%; risk difference 0.3%; 95% confidence interval, -3.5% to 4.2%).
Conclusions:
This nationwide database study showed that combination therapy involving the use of clindamycin was not associated with lower in-hospital mortality in patients with invasive non-group A β-hemolytic Streptococcus.
Insights
Clindamycin combination therapy did not reduce in-hospital mortality for invasive non-group A Streptococcus infections. This study examined sepsis patients, finding no significant difference in outcomes between clindamycin and standard care groups.
Area of Science:
- Infectious Diseases
- Clinical Microbiology
- Epidemiology
Background:
- Clindamycin is recommended for invasive group A Streptococcus infections.
- Its efficacy in invasive group B Streptococcus and S. dysgalactiae subspecies equisimilis infections is unknown.
Purpose of the Study:
- To investigate the effectiveness of clindamycin added to standard care for invasive non-group A beta-hemolytic Streptococcus infections.
- To determine if clindamycin reduces in-hospital mortality in these patients.
Main Methods:
- Nationwide retrospective cohort study using Japanese inpatient database (2010-2018).
- Identified patients with sepsis due to non-group A beta-hemolytic Streptococcus.
- Used propensity score matching to compare clindamycin (within 2 days) vs. control groups; primary outcome: in-hospital mortality.
Main Results:
- 3754 eligible patients identified; 296 in clindamycin group, 3458 in control group.
- After matching, 289 patients (clindamycin) and 1156 patients (control) were compared.
- In-hospital mortality rates were similar: 9.7% (clindamycin) vs. 10.3% (control); risk difference: 0.3% (95% CI, -3.5% to 4.2%).
Conclusions:
- Combination therapy with clindamycin was not associated with lower in-hospital mortality in invasive non-group A beta-hemolytic Streptococcus infections.
- Findings suggest clindamycin may not offer survival benefits for these specific streptococcal infections.
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