Efficacy and safety of azithromycin versus placebo to treat lower respiratory tract infections associated with low procalcitonin: a randomised, placebo-controlled, double-blind, non-inferiority trial.
| dc.contributor.author | Tsalik, Ephraim L | |
| dc.contributor.author | Rouphael, Nadine G | |
| dc.contributor.author | Sadikot, Ruxana T | |
| dc.contributor.author | Rodriguez-Barradas, Maria C | |
| dc.contributor.author | McClain, Micah T | |
| dc.contributor.author | Wilkins, Dana M | |
| dc.contributor.author | Woods, Christopher W | |
| dc.contributor.author | Swamy, Geeta K | |
| dc.contributor.author | Walter, Emmanuel B | |
| dc.contributor.author | El Sahly, Hana M | |
| dc.contributor.author | Keitel, Wendy A | |
| dc.contributor.author | Mulligan, Mark J | |
| dc.contributor.author | Tuyishimire, Bonifride | |
| dc.contributor.author | Serti, Elisavet | |
| dc.contributor.author | Hamasaki, Toshimitsu | |
| dc.contributor.author | Evans, Scott R | |
| dc.contributor.author | Ghazaryan, Varduhi | |
| dc.contributor.author | Lee, Marina S | |
| dc.contributor.author | Lautenbach, Ebbing | |
| dc.contributor.author | TRAP-LRTI Study Group | |
| dc.contributor.author | Antibacterial Resistance Leadership Group | |
| dc.date.accessioned | 2023-04-01T16:17:20Z | |
| dc.date.available | 2023-04-01T16:17:20Z | |
| dc.date.issued | 2023-04 | |
| dc.date.updated | 2023-04-01T16:17:19Z | |
| dc.description.abstract | BackgroundLower respiratory tract infections are frequently treated with antibiotics, despite a viral cause in many cases. It remains unknown whether low procalcitonin concentrations can identify patients with lower respiratory tract infection who are unlikely to benefit from antibiotics. We aimed to compare the efficacy and safety of azithromycin versus placebo to treat lower respiratory tract infections in patients with low procalcitonin.MethodsWe conducted a randomised, placebo-controlled, double-blind, non-inferiority trial at five health centres in the USA. Adults aged 18 years or older with clinically suspected non-pneumonia lower respiratory tract infection and symptom duration from 24 h to 28 days were eligible for enrolment. Participants with a procalcitonin concentration of 0·25 ng/mL or less were randomly assigned (1:1), in blocks of four with stratification by site, to receive over-encapsulated oral azithromycin 250 mg or matching placebo (two capsules on day 1 followed by one capsule daily for 4 days). Participants, non-study clinical providers, investigators, and study coordinators were masked to treatment allocation. The primary outcome was efficacy of azithromycin versus placebo in terms of clinical improvement at day 5 in the intention-to-treat population. The non-inferiority margin was -12·5%. Solicited adverse events (abdominal pain, vomiting, diarrhoea, allergic reaction, or yeast infections) were recorded as a secondary outcome. This trial is registered with ClinicalTrials.gov, NCT03341273.FindingsBetween Dec 8, 2017, and March 9, 2020, 691 patients were assessed for eligibility and 499 were enrolled and randomly assigned to receive azithromycin (n=249) or placebo (n=250). Clinical improvement at day 5 was observed in 148 (63%, 95% CI 54 to 71) of 238 participants with full data in the placebo group and 155 (69%, 61 to 77) of 227 participants with full data in the azithromycin group in the intention-to-treat analysis (between-group difference -6%, 95% CI -15 to 2). The 95% CI for the difference did not meet the non-inferiority margin. Solicited adverse events and the severity of solicited adverse events were not significantly different between groups at day 5, except for increased abdominal pain associated with azithromycin (47 [23%, 95% CI 18 to 29] of 204 participants) compared with placebo (35 [16%, 12 to 21] of 221; between-group difference -7% [95% CI -15 to 0]; p=0·066).InterpretationPlacebo was not non-inferior to azithromycin in terms of clinical improvement at day 5 in adults with lower respiratory tract infection and a low procalcitonin concentration. After accounting for both the rates of clinical improvement and solicited adverse events at day 5, it is unclear whether antibiotics are indicated for patients with lower respiratory tract infection and a low procalcitonin concentration.FundingNational Institute of Allergy and Infectious Diseases, bioMérieux. | |
| dc.identifier | S1473-3099(22)00735-6 | |
| dc.identifier.issn | 1473-3099 | |
| dc.identifier.issn | 1474-4457 | |
| dc.identifier.uri | ||
| dc.language | eng | |
| dc.publisher | Elsevier BV | |
| dc.relation.ispartof | The Lancet. Infectious diseases | |
| dc.relation.isversionof | 10.1016/s1473-3099(22)00735-6 | |
| dc.subject | TRAP-LRTI Study Group | |
| dc.subject | Antibacterial Resistance Leadership Group | |
| dc.subject | Humans | |
| dc.subject | Respiratory Tract Infections | |
| dc.subject | Azithromycin | |
| dc.subject | Anti-Bacterial Agents | |
| dc.subject | Treatment Outcome | |
| dc.subject | Double-Blind Method | |
| dc.subject | Adult | |
| dc.subject | Procalcitonin | |
| dc.title | Efficacy and safety of azithromycin versus placebo to treat lower respiratory tract infections associated with low procalcitonin: a randomised, placebo-controlled, double-blind, non-inferiority trial. | |
| dc.type | Journal article | |
| duke.contributor.orcid | Tsalik, Ephraim L|0000-0002-6417-2042 | |
| duke.contributor.orcid | Woods, Christopher W|0000-0001-7240-2453 | |
| duke.contributor.orcid | Swamy, Geeta K|0000-0001-5092-6993 | |
| pubs.begin-page | 484 | |
| pubs.end-page | 495 | |
| pubs.issue | 4 | |
| pubs.organisational-group | Duke | |
| pubs.organisational-group | School of Medicine | |
| pubs.organisational-group | Clinical Science Departments | |
| pubs.organisational-group | Institutes and Centers | |
| pubs.organisational-group | Medicine | |
| pubs.organisational-group | Obstetrics and Gynecology | |
| pubs.organisational-group | Pediatrics | |
| pubs.organisational-group | Medicine, Infectious Diseases | |
| pubs.organisational-group | Obstetrics and Gynecology, Maternal Fetal Medicine | |
| pubs.organisational-group | Duke Clinical Research Institute | |
| pubs.organisational-group | Duke Human Vaccine Institute | |
| pubs.organisational-group | Institutes and Provost's Academic Units | |
| pubs.organisational-group | University Institutes and Centers | |
| pubs.organisational-group | Duke Global Health Institute | |
| pubs.organisational-group | Pediatrics, General Pediatrics and Adolescent Health | |
| pubs.organisational-group | Duke Center for Applied Genomics and Precision Medicine | |
| pubs.publication-status | Published | |
| pubs.volume | 23 |
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