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Clinical Outcomes in Patients With Ceftriaxone-Resistant Streptococcus pneumoniae Pneumonia

Wenzler, Eric PharmD, BCPS*; Goff, Debra A. PharmD, FCCP*; Bazan, Jose A. DO; Bauer, Karri A. PharmD, BCPS*

Infectious Diseases in Clinical Practice: September 2014 - Volume 22 - Issue 5 - p 263–266
doi: 10.1097/IPC.0000000000000134
Original Article

Background Multiple in vitro studies have demonstrated Streptococcus pneumoniae resistance to β-lactams, including ceftriaxone. The clinical impact of resistance has not been fully evaluated in patients with pneumonia caused by drug-resistant strains of S. pneumoniae.

Methods Adult inpatients 18 or older and younger than 89 years with a diagnosis of pneumonia plus a respiratory culture positive for S. pneumoniae between January 2007 and September 2012 were evaluated. Patients with pneumonia due to ceftriaxone-resistant (minimum inhibitory concentration >1 µg/mL) S. pneumoniae (CRSP) were compared with those with ceftriaxone-susceptible S. pneumoniae (CSSP). Statistical significance was ascertained using 2-tailed χ2 or Fisher exact test.

Results Thirty patients were evaluated: 10 with CRSP and 20 with CSSP. No patient with CRSP had prior ceftriaxone exposure. Seven CRSP patients (70%) achieved a clinical cure compared with 14 CSSP patients (70%) (P = 1.00). Time to clinical cure for CRSP was 4 (1–5) days compared with 8 (3–12) days for CSSP (P = 0.51). Length of stay and infection-related length of stay were 17 days (9–23) and 9 days (7–13) for patients with CRSP, respectively, compared with 15 (8–20) days and 8 (7–13) days for patients with CSSP (P = 0.46, 0.74). No patient with CRSP died or was readmitted for pneumonia. Of the 10 CRSP isolates, 100% were resistant to azithromycin, 90% to penicillin, and 70% to cefepime.

Conclusions Although differences in clinical outcomes were not observed, isolates resistant to ceftriaxone were more likely to be multidrug resistant. As the proportion of pneumococcal isolates with elevated minimum inhibitory concentrations to β-lactams continues to rise, treatment options may become more limited.

From the Departments of *Pharmacy and †Internal Medicine, Division of Infectious Diseases, The Ohio State University Wexner Medical Center.

Correspondence to: Karri A. Bauer, PharmD, BCPS, Infectious Diseases, The Ohio State University Wexner Medical Center, 410 W 10th Ave, Room 368 Doan Hall, Columbus, OH 43210. E-mail:

D.A.G. serves on the advisory boards of Astellas, Nanosphere, Cubist, Forest, and Merck and has received grants from Cubist and Merck. K.A.B. has attended speakers’ bureau for Merck, Astellas, and Forest and has received grants from Cubist and Merck.

The other authors have no funding or conflicts of interest to disclose.

© 2014 by Lippincott Williams & Wilkins.