Pregled bibliografske jedinice broj: 732956
Efficacy and safety of moxifloxacin in community acquired pneumonia:A prospective, multicenter, observational study (CAPRIVI)
Efficacy and safety of moxifloxacin in community acquired pneumonia:A prospective, multicenter, observational study (CAPRIVI) // BMC Pulmonary Medicine, 14 (2014), 105-1 doi:10.1186/1471-2466-14-105 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 732956 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Efficacy and safety of moxifloxacin in community acquired pneumonia:A prospective, multicenter, observational study (CAPRIVI)
Autori
Kuzman, Ilija ; Bezlepko, Alexander ; Topuzovska Tondova, Irena ; Rokusz, Laszlo ; Ludina, Ludmyla ; Marschall, Hans-Peter ; Petri, Thomas.
Izvornik
BMC Pulmonary Medicine (1471-2466) 14
(2014);
105-1
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
Antibiotics; Pneumonia; Community acquired; CAP; Moxifloxacin
Sažetak
CAPRIVI (Community Acquired Pneumonia: tReatment wIth AVelox® in hospItalized patients) was a prospective observational study in 12 countries: Croatia, France, Hungary, Kazakhstan, Jordan, Kyrgyzstan, Lebanon, Republic of Moldova, Romania, Russia, Ukraine, and Macedonia. Patients aged >18 years were treated with moxifloxacin 400 mg daily following hospitalization with a CAP diagnosis. In addition to efficacy and safety outcomes, data were collected on patient history and disease severity measured by CRB-65 score. 2733 patients were enrolled. A low severity index (i.e., CRB-65 score <2) was reported in 87.5% of CAP patients assessed (n = 1847), an unexpectedly high proportion for hospitalized patients. Moxifloxacin administered for a mean of 10.0 days (range: 2.0 to 39.0 days) was highly effective: 96.7% of patients in the efficacy population (n = 2152) improved and 93.2% were cured of infection during the study. Severity of infection changed from “moderate” or “severe” in 91.8% of patients at baseline to “no infection” or “mild” in 95.5% at last visit. In the safety population (n = 2595), 127 (4.9%) patients had treatment-emergent adverse events (TEAEs) and 40 (1.54%) patients had serious TEAEs ; none of these 40 patients died. The safety results were consistent with the known profile of moxifloxacin. The efficacy and safety profiles of moxifloxacin at the recommended dose of 400 mg daily are characterized in this large observational study of hospitalized CAP patients from Eastern and Central Europe and the Middle East. The high response rate in this study, which included patients with a range of disease severities, suggests that treatment with broader-spectrum drugs such as moxifloxacin is appropriate for patients with CAP who are managed in hospital
Izvorni jezik
Engleski
Znanstvena područja
Kliničke medicinske znanosti
POVEZANOST RADA
Projekti:
108-0000000-3491 - ISTRAŽIVANJE ETIOLOGIJE I PATOGENEZE PNEUMONIJA (Kuzman, Ilija, MZOS ) ( CroRIS)
Ustanove:
Medicinski fakultet, Zagreb
Profili:
Ilija Kuzman
(autor)
Citiraj ovu publikaciju:
Časopis indeksira:
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE