Treatment of severe nosocomial pneumonia: a prospective randomised comparison of intravenous ciprofloxacin with imipenem/cilastatin
A Torresa, T T Bauerb, C León-Gilc, F Castillof, F Alvarez-Lermad, A Martínez-Pellúse, S R Leal-Novalf, P Nadalg, M Palomarh, J Blanqueri, F Rosj
a Institut Clinic de
Pneumologia i Cirurgia Toràcica, Servei de Pneumologia, UVIR,
Universitat de Barcelona, IDIBAPS, Barcelona, Spain, b Medizinische Klinik, Department of Pneumology,
Allergology and Sleep Medicine, Bergmannsheil Klinikum der
Ruhr-Universität, Bochum, Germany, c Servicio de Medicina Intensiva y Urgencias,
Hospital, Universitario de Valme, Sevilla, Spain, d Hospital
Del Mar, Barcelona, Spain, e Hospital Virgen de la Arrixaca, Murcia, Spain, f Hospital Virgen
del Rocío, Sevilla, Spain, g Area de Vigilancia Intensiva, Hospital Clinic,
Universitat de Barcelona, Barcelona, Spain, h Servei Cures Intensives, Hospital Vall
d'Hebrón, Barcelona, Spain, i Respiratory Intensive Care Unit, Hospital
Clínico Universitario de Valencia, Spain, j Quimica Farmacéutica Bayer SA, Spain
Correspondence to: Dr A Torres atorres{at}medicina.ub.es
Received 5 January 2000; Returned to authors 3 March 2000; Revised version received 26 June 2000; Accepted for publication 8 August 2000
BACKGROUND
A
prospective multicentre study was undertaken to compare the efficacy of
intravenous ciprofloxacin or imipenem in the treatment of severe
nosocomial pneumonia requiring mechanical ventilation.
METHODS
Patients with
a clinical suspicion of pneumonia were randomised to receive either
ciprofloxacin (800-1200 mg/day) or imipenem (2-4 g/day) in doses
adjusted for renal function and specimens of the lower respiratory
tract were taken. Patients were included in the study when specimens
showed significant growth for potentially pathogenic microorganisms in
quantitative bacterial cultures (n = 75, ciprofloxacin 41/75 (55%);
imipenem 34/75 (45%)). The clinical and bacteriological success rates
were the primary and secondary efficacy variables. An intent-to-treat
analysis was performed for all randomised patients who received at
least one dose of the study medication (n = 149, ciprofloxacin 72/149
(48%), imipenem 77/149 (52%)).
RESULTS
The success
rates were generally good, but neither the clinical success rates
(ciprofloxacin, 29/41 (71%), imipenem, 27/34 (79%); 95% CI -10.8 to
28.1; p = 0.435) nor the bacteriological response rate (ciprofloxacin,
20/41 (49%), imipenem, 17/34 (50%); 95% CI -21.5 to 23.9; p = 1.0) were significantly different between the study arms.
Pseudomonas aeruginosa was recovered in
26/75 patients (35%) and clinical (ciprofloxacin, 10/14 (71%),
imipenem, 8/12 (67%); 95% CI -40.4 to 30.9; p = 1.0) and
bacteriological response rates (ciprofloxacin, 7/14 (50%), imipenem,
3/12 (25%), 95% CI -60.9 to 10.9, p = 0.247) were not significantly
different in this subgroup of patients. Resistance of
Pseudomonas aeruginosa developed in 5/26
cases (19%), 1/14 (7%) to ciprofloxacin and 4/12 (33%) to imipenem
(p = 0.147), and the mortality was 12/75 (16%) with no difference
between treatment groups (ciprofloxacin, 8/41(24%), imipenem 4/34
(17%); p = 0.362). The clinical response was evaluable in 109/149
patients (73%) in the intent-to-treat analysis and was successful in
74/109 patients (68%). The clinical response rates were also not
significantly different in the intent-to-treat analysis (ciprofloxacin,
34/52 (65%), imipenem, 40/57 (70%); 95% CI -12.8 to 22.3; p = 0.746).
CONCLUSIONS
Treatment
with either ciprofloxacin or imipenem was effective in a selected group
of patients with microbiologically confirmed, severe nosocomial
pneumonia requiring mechanical ventilation. Although no differences
between the study medication could be documented in this trial, smaller
differences between treatment arms may have been missed because of
sample size limitations.
Keywords: pneumonia; treatment; ciprofloxacin; imipenem
© 2000 by Thorax
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