TY - JOUR
T1 - Ceftolozane/tazobactam for the treatment of XDR Pseudomonas aeruginosa infections
AU - Escolà-Vergé, Laura
AU - Pigrau, Carles
AU - Los-Arcos, Ibai
AU - Arévalo, Ángel
AU - Viñado, Belen
AU - Campany, David
AU - Larrosa, Nieves
AU - Nuvials, Xavier
AU - Ferrer, Ricard
AU - Len, Oscar
AU - Almirante, Benito
PY - 2018/8/1
Y1 - 2018/8/1
N2 - © 2018, Springer-Verlag GmbH Germany, part of Springer Nature. Purpose: The aim of this study was to evaluate the effectiveness of ceftolozane/tazobactam (C/T) for treating extensively drug-resistant Pseudomonas aeruginosa (XDR-PA) infections, and to analyze whether high C/T dosing (2 g ceftolozane and 1 g tazobactam every 8 h) and infection source control have an impact on outcome. Methods: Retrospective study of all consecutive patients treated with C/T for XDR-PA infection at a tertiary referral hospital (November 2015–July 2017). Main clinical and microbiological variables were analyzed. Results: Thirty-eight patients were included. Median age was 59.5 years and Charlson Comorbidity Index was 3.5. Fourteen (36.8%) patients had respiratory tract infection, six (15.8%) soft tissue, and six (15.8%) urinary tract infection. Twenty-three (60.5%) received high-dose C/T and in 24 (63.2%) C/T was combined with other antibiotics. At completion of treatment, 33 (86.8%) patients showed clinical response. At 90 days of follow-up, 26 (68.4%) achieved clinical cure, and 12 (31.6%) had clinical failure because of persistent infection in one patient, death attributable to the XDR-PA infection in four, and clinical recurrence in seven. All-cause mortality was 5 (13.2%). Lower C/T MIC and adequate infection source control were the only variables significantly associated with clinical cure. Conclusions: C/T should be considered for treating XDR-PA infections, with infection source control being an important factor to avoid failure and resistance.
AB - © 2018, Springer-Verlag GmbH Germany, part of Springer Nature. Purpose: The aim of this study was to evaluate the effectiveness of ceftolozane/tazobactam (C/T) for treating extensively drug-resistant Pseudomonas aeruginosa (XDR-PA) infections, and to analyze whether high C/T dosing (2 g ceftolozane and 1 g tazobactam every 8 h) and infection source control have an impact on outcome. Methods: Retrospective study of all consecutive patients treated with C/T for XDR-PA infection at a tertiary referral hospital (November 2015–July 2017). Main clinical and microbiological variables were analyzed. Results: Thirty-eight patients were included. Median age was 59.5 years and Charlson Comorbidity Index was 3.5. Fourteen (36.8%) patients had respiratory tract infection, six (15.8%) soft tissue, and six (15.8%) urinary tract infection. Twenty-three (60.5%) received high-dose C/T and in 24 (63.2%) C/T was combined with other antibiotics. At completion of treatment, 33 (86.8%) patients showed clinical response. At 90 days of follow-up, 26 (68.4%) achieved clinical cure, and 12 (31.6%) had clinical failure because of persistent infection in one patient, death attributable to the XDR-PA infection in four, and clinical recurrence in seven. All-cause mortality was 5 (13.2%). Lower C/T MIC and adequate infection source control were the only variables significantly associated with clinical cure. Conclusions: C/T should be considered for treating XDR-PA infections, with infection source control being an important factor to avoid failure and resistance.
KW - Ceftolozane/tazobactam
KW - Extensively drug-resistant
KW - Infection source control
KW - Pseudomonas aeruginosa
UR - https://www.scopus.com/pages/publications/85044459043
U2 - 10.1007/s15010-018-1133-5
DO - 10.1007/s15010-018-1133-5
M3 - Article
SN - 0300-8126
VL - 46
SP - 461
EP - 468
JO - Infection
JF - Infection
IS - 4
ER -