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- Publisher Website: 10.1016/j.chest.2016.11.012
- Scopus: eid_2-s2.0-85019156178
- PMID: 27884765
- WOS: WOS:000402798000025
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Article: Efficacy of Clarithromycin-Naproxen-Oseltamivir Combination in the Treatment of Patients Hospitalized for Influenza A(H3N2) Infection: An Open-label Randomized, Controlled, Phase IIb/III Trial
Title | Efficacy of Clarithromycin-Naproxen-Oseltamivir Combination in the Treatment of Patients Hospitalized for Influenza A(H3N2) Infection: An Open-label Randomized, Controlled, Phase IIb/III Trial |
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Authors | |
Keywords | A(H3N2) Clarithromycin Hospitalized Naproxen Oseltamivir |
Issue Date | 2017 |
Publisher | Elsevier, co-published with American College of Chest Physicians. The Journal's web site is located at http://www.chestjournal.org |
Citation | Chest, 2017, v. 151 n. 5, p. 1069-1080 How to Cite? |
Abstract | Background:
Influenza causes excessive hospitalizations and deaths. The study assessed the efficacy and safety of a clarithromycin-naproxen-oseltamivir combination for treatment of serious influenza.
Methods:
From February to April 2015, we conducted a prospective open-label, randomized, controlled trial. Adult patients hospitalized for A(H3N2) influenza were randomly assigned to a 2-day combination of clarithromycin 500 mg, naproxen 200 mg, and oseltamivir 75 mg twice daily, followed by 3 days of oseltamivir or to oseltamivir 75 mg twice daily without placebo for 5 days as a control method (1:1). The primary end point was 30-day mortality. The secondary end points were 90-day mortality, serial nasopharyngeal aspirate (NPA) virus titer, percentage of neuraminidase-inhibitor-resistant A(H3N2) virus (NIRV) quasispecies, pneumonia severity index (PSI), and duration of hospital stay.
Results:
Among the 217 patients with influenza A(H3N2) enrolled, 107 were randomly assigned to the combination treatment. The median age was 80 years, and 53.5% were men. Adverse events were uncommon. Ten patients died during the 30-day follow-up. The combination treatment was associated with lower 30-day mortality (P = .01), less frequent high dependency unit admission (P = .009), and shorter hospital stay (P < .0001). The virus titer and PSI (days 1-3; P < .01) and the NPA specimens with NIRV quasispecies ≥ 5% (days 1-2; P < .01) were significantly lower in the combination treatment group. Multivariate analysis showed that combination treatment was the only independent factor associated with lower 30-day mortality (OR, 0.06; 95% CI, 0.004-0.94; P = .04).
Conclusions:
Combination treatment reduced both 30- and 90-day mortality and length of hospital stay. Further study of the antiviral and immunomodulatory effects of this combination treatment of severe influenza is warranted.
Trial Registry:
BioMed Central; No.: ISRCTN11273879 DOI 10.1186/ISRCTN11273879; URL: www.isrctn.com/ISRCTN11273879 |
Persistent Identifier | http://hdl.handle.net/10722/243181 |
ISSN | 2023 Impact Factor: 9.5 2023 SCImago Journal Rankings: 2.123 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Hung, FNI | - |
dc.contributor.author | To, KKW | - |
dc.contributor.author | Chan, JFW | - |
dc.contributor.author | Cheng, CCV | - |
dc.contributor.author | Liu, SHK | - |
dc.contributor.author | Tam, A | - |
dc.contributor.author | Chan, TCI | - |
dc.contributor.author | Zhang, J | - |
dc.contributor.author | Li, PCK | - |
dc.contributor.author | Wong, TL | - |
dc.contributor.author | Zhang, R | - |
dc.contributor.author | Cheung, KSM | - |
dc.contributor.author | Leung, W | - |
dc.contributor.author | Lau, JYN | - |
dc.contributor.author | Fok, M | - |
dc.contributor.author | Chen, H | - |
dc.contributor.author | Chan, KH | - |
dc.contributor.author | Yuen, KY | - |
dc.date.accessioned | 2017-08-25T02:51:14Z | - |
dc.date.available | 2017-08-25T02:51:14Z | - |
dc.date.issued | 2017 | - |
dc.identifier.citation | Chest, 2017, v. 151 n. 5, p. 1069-1080 | - |
dc.identifier.issn | 0012-3692 | - |
dc.identifier.uri | http://hdl.handle.net/10722/243181 | - |
dc.description.abstract | Background: Influenza causes excessive hospitalizations and deaths. The study assessed the efficacy and safety of a clarithromycin-naproxen-oseltamivir combination for treatment of serious influenza. Methods: From February to April 2015, we conducted a prospective open-label, randomized, controlled trial. Adult patients hospitalized for A(H3N2) influenza were randomly assigned to a 2-day combination of clarithromycin 500 mg, naproxen 200 mg, and oseltamivir 75 mg twice daily, followed by 3 days of oseltamivir or to oseltamivir 75 mg twice daily without placebo for 5 days as a control method (1:1). The primary end point was 30-day mortality. The secondary end points were 90-day mortality, serial nasopharyngeal aspirate (NPA) virus titer, percentage of neuraminidase-inhibitor-resistant A(H3N2) virus (NIRV) quasispecies, pneumonia severity index (PSI), and duration of hospital stay. Results: Among the 217 patients with influenza A(H3N2) enrolled, 107 were randomly assigned to the combination treatment. The median age was 80 years, and 53.5% were men. Adverse events were uncommon. Ten patients died during the 30-day follow-up. The combination treatment was associated with lower 30-day mortality (P = .01), less frequent high dependency unit admission (P = .009), and shorter hospital stay (P < .0001). The virus titer and PSI (days 1-3; P < .01) and the NPA specimens with NIRV quasispecies ≥ 5% (days 1-2; P < .01) were significantly lower in the combination treatment group. Multivariate analysis showed that combination treatment was the only independent factor associated with lower 30-day mortality (OR, 0.06; 95% CI, 0.004-0.94; P = .04). Conclusions: Combination treatment reduced both 30- and 90-day mortality and length of hospital stay. Further study of the antiviral and immunomodulatory effects of this combination treatment of severe influenza is warranted. Trial Registry: BioMed Central; No.: ISRCTN11273879 DOI 10.1186/ISRCTN11273879; URL: www.isrctn.com/ISRCTN11273879 | - |
dc.language | eng | - |
dc.publisher | Elsevier, co-published with American College of Chest Physicians. The Journal's web site is located at http://www.chestjournal.org | - |
dc.relation.ispartof | Chest | - |
dc.subject | A(H3N2) | - |
dc.subject | Clarithromycin | - |
dc.subject | Hospitalized | - |
dc.subject | Naproxen | - |
dc.subject | Oseltamivir | - |
dc.title | Efficacy of Clarithromycin-Naproxen-Oseltamivir Combination in the Treatment of Patients Hospitalized for Influenza A(H3N2) Infection: An Open-label Randomized, Controlled, Phase IIb/III Trial | - |
dc.type | Article | - |
dc.identifier.email | Hung, FNI: ivanhung@hkucc.hku.hk | - |
dc.identifier.email | To, KKW: kelvinto@hkucc.hku.hk | - |
dc.identifier.email | Chan, JFW: jfwchan@hku.hk | - |
dc.identifier.email | Cheng, CCV: vcccheng@hkucc.hku.hk | - |
dc.identifier.email | Liu, SHK: drkliu@hku.hk | - |
dc.identifier.email | Chan, TCI: tuenchin@hku.hk | - |
dc.identifier.email | Zhang, J: zhangajx@hkucc.hku.hk | - |
dc.identifier.email | Li, PCK: drckli@hku.hk | - |
dc.identifier.email | Cheung, KSM: cks634@hku.hk | - |
dc.identifier.email | Chen, H: hlchen@hku.hk | - |
dc.identifier.email | Chan, KH: chankh2@hkucc.hku.hk | - |
dc.identifier.email | Yuen, KY: kyyuen@hkucc.hku.hk | - |
dc.identifier.authority | Hung, FNI=rp00508 | - |
dc.identifier.authority | To, KKW=rp01384 | - |
dc.identifier.authority | Chan, JFW=rp01736 | - |
dc.identifier.authority | Zhang, J=rp00413 | - |
dc.identifier.authority | Cheung, KSM=rp02532 | - |
dc.identifier.authority | Chen, H=rp00383 | - |
dc.identifier.authority | Chan, KH=rp01921 | - |
dc.identifier.authority | Yuen, KY=rp00366 | - |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1016/j.chest.2016.11.012 | - |
dc.identifier.pmid | 27884765 | - |
dc.identifier.scopus | eid_2-s2.0-85019156178 | - |
dc.identifier.hkuros | 275459 | - |
dc.identifier.volume | 151 | - |
dc.identifier.issue | 5 | - |
dc.identifier.spage | 1069 | - |
dc.identifier.epage | 1080 | - |
dc.identifier.isi | WOS:000402798000025 | - |
dc.publisher.place | United States | - |
dc.identifier.issnl | 0012-3692 | - |