Antibiotic treatment strategies for community-acquired pneumonia in adults
- PMID: 25830421
- DOI: 10.1056/NEJMoa1406330
Antibiotic treatment strategies for community-acquired pneumonia in adults
Abstract
Background: The choice of empirical antibiotic treatment for patients with clinically suspected community-acquired pneumonia (CAP) who are admitted to non-intensive care unit (ICU) hospital wards is complicated by the limited availability of evidence. We compared strategies of empirical treatment (allowing deviations for medical reasons) with beta-lactam monotherapy, beta-lactam-macrolide combination therapy, or fluoroquinolone monotherapy.
Methods: In a cluster-randomized, crossover trial with strategies rotated in 4-month periods, we tested the noninferiority of the beta-lactam strategy to the beta-lactam-macrolide and fluoroquinolone strategies with respect to 90-day mortality, in an intention-to-treat analysis, using a noninferiority margin of 3 percentage points and a two-sided 90% confidence interval.
Results: A total of 656 patients were included during the beta-lactam strategy periods, 739 during the beta-lactam-macrolide strategy periods, and 888 during the fluoroquinolone strategy periods, with rates of adherence to the strategy of 93.0%, 88.0%, and 92.7%, respectively. The median age of the patients was 70 years. The crude 90-day mortality was 9.0% (59 patients), 11.1% (82 patients), and 8.8% (78 patients), respectively, during these strategy periods. In the intention-to-treat analysis, the risk of death was higher by 1.9 percentage points (90% confidence interval [CI], -0.6 to 4.4) with the beta-lactam-macrolide strategy than with the beta-lactam strategy and lower by 0.6 percentage points (90% CI, -2.8 to 1.9) with the fluoroquinolone strategy than with the beta-lactam strategy. These results indicated noninferiority of the beta-lactam strategy. The median length of hospital stay was 6 days for all strategies, and the median time to starting oral treatment was 3 days (interquartile range, 0 to 4) with the fluoroquinolone strategy and 4 days (interquartile range, 3 to 5) with the other strategies.
Conclusions: Among patients with clinically suspected CAP admitted to non-ICU wards, a strategy of preferred empirical treatment with beta-lactam monotherapy was noninferior to strategies with a beta-lactam-macrolide combination or fluoroquinolone monotherapy with regard to 90-day mortality. (Funded by the Netherlands Organization for Health Research and Development; CAP-START ClinicalTrials.gov number, NCT01660204.).
Comment in
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[Community acquired pneumonia: antibiotic monotherapy is not inferior to combination therapy].Dtsch Med Wochenschr. 2015 Jun;140(13):964. doi: 10.1055/s-0041-102336. Epub 2015 Jun 26. Dtsch Med Wochenschr. 2015. PMID: 26115125 German. No abstract available.
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Antibiotics for Community-Acquired Pneumonia in Adults.N Engl J Med. 2015 Aug 13;373(7):684-6. doi: 10.1056/NEJMc1506892. N Engl J Med. 2015. PMID: 26267636 No abstract available.
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Antibiotics for Community-Acquired Pneumonia in Adults.N Engl J Med. 2015 Aug 13;373(7):683. doi: 10.1056/NEJMc1506892. N Engl J Med. 2015. PMID: 26267637 No abstract available.
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Antibiotics for Community-Acquired Pneumonia in Adults.N Engl J Med. 2015 Aug 13;373(7):683-4. doi: 10.1056/NEJMc1506892. N Engl J Med. 2015. PMID: 26267638 No abstract available.
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Antibiotics for Community-Acquired Pneumonia in Adults.N Engl J Med. 2015 Aug 13;373(7):684. doi: 10.1056/NEJMc1506892. N Engl J Med. 2015. PMID: 26267639 No abstract available.
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Antibiotics for Community-Acquired Pneumonia in Adults.N Engl J Med. 2015 Aug 13;373(7):684. doi: 10.1056/NEJMc1506892. N Engl J Med. 2015. PMID: 26267640 No abstract available.
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[Beta-lactam monotherapy in hospitalized pneumonia patients is not inferior to a combined therapy].Praxis (Bern 1994). 2015 Aug 19;104(17):929-30. doi: 10.1024/1661-8157/a002108. Praxis (Bern 1994). 2015. PMID: 26286498 German. No abstract available.
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In non-ICU suspected CAP, β-lactam was noninferior to β-lactam-macrolide or fluoroquinolone for 90-d mortality.Ann Intern Med. 2015 Sep 15;163(6):JC5. doi: 10.7326/ACPJC-2015-163-6-005. Ann Intern Med. 2015. PMID: 26370032 No abstract available.
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