TY - JOUR
T1 - A study evaluating the efficacy, safety, and tolerability of ertapenem versus ceftriaxone for the treatment of community-acquired pneumonia in adults
AU - Protocol 018 Ertapenem Community-Acquired Pneumonia Study Group
AU - Ortiz-Ruiz, Guillermo
AU - Caballero-Lopez, Jose
AU - Friedland, Ian R.
AU - Woods, Gail L.
AU - Carides, Alexandra
AU - Beneitone, Roger
AU - Boylen, C. Thomas
AU - Bremner, Peter Reid
AU - Cipullo, Jose
AU - Correa da Silva, Luiz Carlos
AU - Dalhoff, Klaus
AU - Dunbar, Lala
AU - Farkas, Stephen
AU - Filler, Scott
AU - Fogarty, Charles
AU - Frank, Elliot
AU - Geckler, Ronald
AU - Godfrey, Catherine
AU - Gonzalez-Fuenzalida, Fernando
AU - Gremillion, David H.
AU - Hawes, Stephen J.
AU - Herrera, Maria
AU - Hincapie, Gustavo
AU - Jasovich, Abel
AU - Koffler, Howard
AU - Lampasso, James G.
AU - Langton, David
AU - Levison, Matthew E.
AU - Lopardo, Gustavo
AU - Caballero Lopez, Jose
AU - Lorena, Gifford
AU - Many, Wycliffe J.
AU - Maslow, Melanie J.
AU - De Oca, Maria Montes
AU - Morales-Reyes, Juan
AU - Moser, Roy
AU - Nelson, Michael
AU - Noriega-Ricalde, Luis
AU - Nicholas Parkes, Scott
AU - Phillips, Martin J.
AU - Player, Rick
AU - Ramirez, Julio
AU - Reed, Kevin D.
AU - Reinhardt, John F.
AU - Richards, Guy Anthony
AU - Rubinfeld, Abraham R.
AU - Ruiz, Guillermo Ortiz
AU - Santiago, Silverio
AU - Siami, Ghodrat A.
AU - Singh, Gagrath P.
PY - 2002/4/15
Y1 - 2002/4/15
N2 - In a double-blind, multicenter trial, 502 patients hospitalized with community-acquired pneumonia were randomized to receive therapy with either ertapenem or ceftriaxone (for each, 1 g given intravenously once daily). After a minimum of 3 days, therapy could be switched to oral amoxicillin-clavulanate. The median duration of intravenously administered therapy for the 383 clinically evaluable patients was 4 days for both treatment groups; 345 patients (90.1%) had their treatment switched to orally administered therapy. Of the clinically evaluable patients, 168 (92.3%) in the ertapenem group and 183 (91.0%) in the ceftriaxone group had a favorable clinical response. Streptococcus pneumoniae was the most commonly isolated pathogen, and high cure rates were observed both for penicillin-susceptible and -nonsusceptible infections in the ertapenem group (28 [87.5%] of 32 patients versus 17 [100%] of 17 patients, respectively). Both treatment regimens were generally well tolerated; the most common drug-related adverse events reported were diarrhea (2.9% versus 2.7%) and nausea (0.8% versus 2.0%) in the ertapenem and ceftriaxone groups, respectively. These results suggest that ertapenem and ceftriaxone therapy have similar efficacy and safety in hospitalized patients with community-acquired pneumonia.
AB - In a double-blind, multicenter trial, 502 patients hospitalized with community-acquired pneumonia were randomized to receive therapy with either ertapenem or ceftriaxone (for each, 1 g given intravenously once daily). After a minimum of 3 days, therapy could be switched to oral amoxicillin-clavulanate. The median duration of intravenously administered therapy for the 383 clinically evaluable patients was 4 days for both treatment groups; 345 patients (90.1%) had their treatment switched to orally administered therapy. Of the clinically evaluable patients, 168 (92.3%) in the ertapenem group and 183 (91.0%) in the ceftriaxone group had a favorable clinical response. Streptococcus pneumoniae was the most commonly isolated pathogen, and high cure rates were observed both for penicillin-susceptible and -nonsusceptible infections in the ertapenem group (28 [87.5%] of 32 patients versus 17 [100%] of 17 patients, respectively). Both treatment regimens were generally well tolerated; the most common drug-related adverse events reported were diarrhea (2.9% versus 2.7%) and nausea (0.8% versus 2.0%) in the ertapenem and ceftriaxone groups, respectively. These results suggest that ertapenem and ceftriaxone therapy have similar efficacy and safety in hospitalized patients with community-acquired pneumonia.
UR - https://www.scopus.com/pages/publications/0037090185
U2 - 10.1086/339543
DO - 10.1086/339543
M3 - Article
C2 - 11914996
AN - SCOPUS:0037090185
SN - 1058-4838
VL - 34
SP - 1076
EP - 1083
JO - Clinical Infectious Diseases
JF - Clinical Infectious Diseases
IS - 8
ER -