Treatment with sequential intravenous or oral moxifloxacin was associated with faster clinical improvement than was standard therapy for hospitalized patients with community-acquired pneumonia who received initial parenteral therapy

被引:75
作者
Welte, T
Petermann, W
Schürmann, D
Bauer, TT
Reimnitz, P
机构
[1] Hannover Med Sch, Dept Pulm Med, D-30625 Hannover, Germany
[2] Bruederkrankenhaus St Josef, Med Clin, Paderborn, Germany
[3] Univ Med Berlin, Charite, Dept Internal Med Infect Dis, Berlin, Germany
[4] Ruhr Univ Bochum, Dept Internal Med 3, D-4630 Bochum, Germany
[5] Bayer Vital GmbH, Leverkusen, Germany
关键词
D O I
10.1086/498149
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. Although third-generation cephalosporins, such as ceftriaxone (CTRX), and pneumococcal fluoroquinolones, such as moxifloxacin (MXF), are currently recommended first-line antibiotics for empirical treatment of inpatients with community-acquired pneumonia, CTRX and MXF have never undergone a head-to-head comparison. We therefore compared the efficacy, safety, and speed and quality of defervescence of sequential intravenous or oral MXF and high-dose CTRX with or without erythromycin (CTRX +/- ERY) for patients with community-acquired pneumonia requiring parenteral therapy. Methods. In this prospective, multicenter, randomized, controlled, nonblinded study, 397 patients were randomly assigned to receive either MXF (400 mg once daily intravenously, possibly followed by oral tablets) or CTRX (2 g intravenously once daily) with or without ERY (1 g intravenously every 6-8 h) for 7-14 days. Results. Among 317 patients evaluable for efficacy and safety, 138 (85.7%) of 161 MXF-treated patients and 135 (86.5%) of 156-treated patients (59 [37.8%] of whom received CTRX and ERY) achieved CTRX +/- ERY continued clinical resolution. Defervescence and relief of symptoms, such as chest pain, occurred significantly earlier in the MXF-treated group than in the - treated group. Both regimens were generally well CTRX +/- ERY tolerated. Conclusions. For adult patients hospitalized with community-acquired pneumonia, sequential MXF therapy was clinically equivalent to high-dose therapy but led to a faster clinical improvement.
引用
收藏
页码:1697 / 1705
页数:9
相关论文
共 22 条
[1]  
*AG FRANC SEC SAN, 2003, ANT VOIE GEN PRAT CO
[2]   Evaluation of outcomes in community-acquired pneumonia: a guide for patients, physicians, and policy-makers [J].
Barlow, GD ;
Lamping, DL ;
Davey, PG ;
Nathwani, D .
LANCET INFECTIOUS DISEASES, 2003, 3 (08) :476-488
[3]  
Bartlett John G., 2000, Clinical Infectious Diseases, V31, P347, DOI 10.1086/313954
[4]   Efficacy and safety of oral and early-switch therapy for community-acquired pneumonia:: A randomized controlled trial [J].
Castro-Guardiola, A ;
Viejo-Rodríguez, AL ;
Soler-Simon, S ;
Armengou-Arxé, A ;
Bisbe-Company, V ;
Peñarroja-Matutano, G ;
Bisbe-Company, J ;
García-Bragado, F .
AMERICAN JOURNAL OF MEDICINE, 2001, 111 (05) :367-374
[5]   High-dose, short-course Levofloxacin for community-acquired pneumonia: A new treatment paradigm [J].
Dunbar, LM ;
Wunderink, RG ;
Habib, MP ;
Smith, LG ;
Tennenberg, AM ;
Khashab, MM ;
Wiesinger, BA ;
Xiang, JX ;
Zadeikis, N ;
Kahn, JB .
CLINICAL INFECTIOUS DISEASES, 2003, 37 (06) :752-760
[6]  
EWIG S, 2002, CHEMOTHER J, V11, P12
[7]   Randomized controlled trial of sequential intravenous (i.v.) and oral moxifloxacin compared with sequential i.v. and oral co-amoxiclav with or without clarithromycin in patients with community-acquired pneumonia requiring initial parenteral treatment [J].
Finch, R ;
Schürmann, D ;
Collins, O ;
Kubin, R ;
McGivern, J ;
Bobbaers, H ;
Izquierdo, JL ;
Nikolaides, P ;
Ogundare, F ;
Raz, R ;
Zuck, P ;
Hoeffken, G .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2002, 46 (06) :1746-1754
[8]   A prediction rule to identify low-risk patients with community-acquired pneumonia [J].
Fine, MJ ;
Auble, TE ;
Yealy, DM ;
Hanusa, BH ;
Weissfeld, LA ;
Singer, DE ;
Coley, CM ;
Marrie, TJ ;
Kapoor, WN .
NEW ENGLAND JOURNAL OF MEDICINE, 1997, 336 (04) :243-250
[9]   Community-acquired pneumonia: causes of treatment failure in patients enrolled in clinical trials [J].
Genne, D ;
Kaiser, L ;
Kinge, TN ;
Lew, D .
CLINICAL MICROBIOLOGY AND INFECTION, 2003, 9 (09) :949-954
[10]  
Gibson J, 2013, EUROPEAN LUNG WHITE BOOK: RESPIRATORY HEALTH AND DISEASE IN EUROPE, P64