Cefonicid (Smith Kline & French Laboratories; D-75073) is a new parenteral
cephalosporin with a markedly long half-life, high serum levels, and good in vitro activity against Haemophilus influenzae. Patients with community-acquired
pneumonia were randomized 2:1 to receive
cefonicid, 1 g daily (21 cases) or
cefamandole, 1 g every 6 h (12 cases). The two groups were similar, except that the
cefonicid patients were older (mean 42 versus 31 years). Peak serum levels of
cefonicid averaged 133 microgram/ml after intravenous and 83 microgram/ml after intramuscular administration compared with 55 microgram/ml with intravenous
cefamandole. All 9 patients on intramuscular
cefonicid and 8 or 12 patients on intravenous
cefonicid had trough serum levels of greater than 2.0 microgram/ml at 24 h. Sputum levels of
cefonicid were usually between 2.0 and 4.0 microgram/ml and did not correlate with serum levels.
Cefonicid was well tolerated, and all
cefonicid patients responded clinically. Sputum cultures for H. influenzae or Streptococcus pneumoniae became negative in 6 of 7
cefamandole patients and 13 or 15
cefonicid patients. In in vitro studies,
cefonicid inhibited 90% of
beta-lactamase-negative h. influenzae at 0.5 microgram/ml and
beta-lactamase-positive strains at 2.0 microgram/ml.
Cefonicid inhibited 50% of S. pneumoniae at 1.6 microgram/ml, but required 6.4 microgram/ml to inhibit 90%.
Cefonicid once a day appears to be as safe and as effective as
cefamandole four times a day for
therapy of community-acquired
pneumonia.