Cefdinir: an oral cephalosporin for the treatment of respiratory tract infections and skin and skin structure infections

被引:19
作者
Sader, Helio S. [1 ,2 ]
Jones, Ronald N. [1 ,3 ]
机构
[1] JMI Labs, N Liberty Iowa, IA 52317 USA
[2] Univ Fed Sao Paulo, Sao Paulo, Brazil
[3] Tufts Univ, Sch Med, Boston, MA 02111 USA
关键词
acute otitis media; cefdinir; group A streptococcal pharyngitis; Haemophilus influenzae; oral cephalosporin; palatability; respiratory tract infections; skin and skin structure infections; Streptococcus pneumoniae; toleration; uSSTI;
D O I
10.1586/14787210.5.1.29
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Cefdinir is an oral third-generation cephalosporin (also known as an advanced-spectrum or generation cephem) with good in vitro activity against the pathogens responsible for community-acquired respiratory tract infections and uncomplicated skin and skin structure infections. The drug distributes very well in respiratory tract tissues and fluids, as well as skin blisters and ear fluids; its pharmacokinetic profile allows once- or twice-daily administration. Oral cefdinir 300 mg twice daily or 600 mg once daily in adults and adolescents, or 14 mg/kg/day in one or two daily doses in pediatric patients, administered for 5 or 10 days, has shown good clinical and bacteriological efficacy, at least equivalent to that of other oral agents in randomized controlled trials conducted in patients with community-acquired pneumonia, acute bacterial exacerbation of chronic bronchitis, sinusitis, acute otitis media, pharyngitis and uncomplicated skin and skin structure infections. Cefdinir is well tolerated and the oral suspension has shown superior taste or palatability over other comparator oral antimicrobial agents. Thus, cefdinir continues to represent an important cephalosporin option for the treatment of adult, adolescent and pediatric patients with mild or moderate respiratory tract or cutaneous infections, especially in areas with elevated rates of beta-lactamase production in Haemophilus influenzae and where resistance to other commonly used agents has emerged (e.g., macrolides, penicillins, tetracyclines, fluoroquinolones and trimethoprim-sulfamethoxazole).
引用
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页码:29 / 43
页数:15
相关论文
共 65 条
[1]  
*ABB LAB, 2006, OMN CEFD PACK INS
[2]   Cefdinir vs. amoxicillin/clavulanic acid in the treatment of suppurative acute otitis media in children [J].
Adler, M ;
McDonald, PJ ;
Trostmann, U ;
Keyserling, C ;
Tack, K .
PEDIATRIC INFECTIOUS DISEASE JOURNAL, 2000, 19 (12) :S166-S170
[3]  
[Anonymous], 2004, Archives of Surgery Chicago, Ill
[4]   A multicenter, open label, double tympanocentesis study of high dose cefdinir in children with acute otitis media at high risk of persistent or recurrent infection [J].
Arguedas, A ;
Dagan, R ;
Leibovitz, E ;
Hoberman, A ;
Pichichero, M ;
Paris, M .
PEDIATRIC INFECTIOUS DISEASE JOURNAL, 2006, 25 (03) :211-218
[5]   Comparison of five-day cefdinir treatment with ten-day low dose amoxicillin/clavulanate treatment for acute otitis media [J].
Block, SL ;
Busman, TA ;
Paris, MM ;
Bukofzer, S .
PEDIATRIC INFECTIOUS DISEASE JOURNAL, 2004, 23 (09) :834-838
[6]   Comparative safety and efficacy of cefdinir vs. amoxicillin/clavulanate for treatment of suppurative acute otitis media in children [J].
Block, SL ;
McCarty, JM ;
Hedrick, JA ;
Nemeth, MA ;
Keyserling, CH ;
Tack, KJ .
PEDIATRIC INFECTIOUS DISEASE JOURNAL, 2000, 19 (12) :S159-S165
[7]   Five-day cefdinir course vs. ten-day cefprozil course for treatment of acute otitis media [J].
Block, SL ;
Kratzer, J ;
Nemeth, MA ;
Tack, KJ .
PEDIATRIC INFECTIOUS DISEASE JOURNAL, 2000, 19 (12) :S147-S152
[8]   Efficacy, tolerability, and parent reported outcomes for cefdinir vs. high-dose amoxicillin/clavulanate oral suspension for acute otitis media in young children [J].
Block, Stan L. ;
Schmier, Jordana K. ;
Notario, Gerard F. ;
Akinlade, Bolanle K. ;
Busman, Todd A. ;
MacKinnon, George E., III ;
Halpern, Michael T. ;
Nilius, Angela M. .
CURRENT MEDICAL RESEARCH AND OPINION, 2006, 22 (09) :1839-1847
[9]   Cefdinir pharmacokinetics and tolerability in children receiving 25 mg/kg once daily [J].
Bowlware, KL ;
McCracken, GH ;
Lozano-Hernandez, J ;
Ghaffar, F .
PEDIATRIC INFECTIOUS DISEASE JOURNAL, 2006, 25 (03) :208-210
[10]   INVITRO ACTIVITY EVALUATIONS OF CEFDINIR (FK482, CI-983, AND PD134393) - A NOVEL ORALLY-ADMINISTERED CEPHALOSPORIN [J].
BRIGGS, BM ;
JONES, RN ;
ERWIN, ME ;
BARRETT, MS ;
JOHNSON, DM .
DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 1991, 14 (05) :425-434