TY - JOUR
T1 - Clinical implications of Stenotrophomonas maltophilia resistant to trimethoprim-sulfamethoxazole
T2 - A study of 69 patients at 2 University Hospitals
AU - Tsiodras, S.
AU - Pittet, D.
AU - Carmeli, Y.
AU - Eliopoulos, G.
AU - Boucher, H.
AU - Harbarth, S.
N1 - Funding Information:
We thank Peter Rohner for technical asissnce.tSaT. rasswisoad supported by a Lilian Voudouri Institute scholarship and is a fellow with the Clinical Investigator Training Program (upposrted byP® zerInc.)attheHarvard-MasacshusettsInstituteofTechnol-ogy, Division of Health Sciences and Technology. S. Harbarth is currntlyea recipient of the Max-Kade-ScholarhipsatHarvard Children’s Hospital, Boston. Y. Carmeli is currntlyeat the Division of Infectious Diseases, Soarasky Medical Center, Tel Aviv, IrselaanSHd.rbaiasttrhIthncetifoDeieasusesDsisiaivot n Children’sHospitalandHarvardMicalSehdcloB, oo,MstAon This work ws preasented in part at the 39th Interscience Conference on Antimicrobial Agents and Chemotherapy, September 1999, San Francisco, California, USA.
PY - 2000
Y1 - 2000
N2 - We conducted a retrospective case study at 2 tertiary care centers to determine the clinical implications of trimethoprim-sulfamethoxazole resistant Stenotrophomonas maltophilia (TSRSM). Of 69 reviewed cases (mean age, 57 y; male gender, 70%), 40 (58%) were classified as infections associated with TSRSM (respiratory tract, 14; soft tissue, 11; bloodstream, 8; other sites, 7). Severe underlying comorbidities (86%) and previous antibiotic exposure (99%) were common. Cefotetan (susceptibility, 55%), chloramphenicol (49%) and ticarcillin-clavulanate (45%) showed the highest in vitro activity against TSRSM, but were seldom used for therapy (7%). Among the 40 infected cases, 8 developed sepsis disorders and 8 died. Only 1 death could be directly attributed to autopsy-proven TSRSM infection (pneumonia). McCabe score (p = 0.03) and organ dysfunction (p = 0.006) were associated with an increased risk of death in infected patients; exposure to appropriate therapy tended to be protective against death (p = 0.08). 22 infected patients were treated medically; an additional procedure was necessary to clear the infection in 18 cases (surgery, 13; catheter removal, 5). Isolation precautions were rarely exercised, even in the presence of panresistant isolates. In summary, TSRSM-related infections occurred in severely ill patients with extensive exposure to the health-care system, and often required invasive procedures for cure. Infections were directly associated with severe morbidity, and tended to have an indirect rather than a direct impact on mortality.
AB - We conducted a retrospective case study at 2 tertiary care centers to determine the clinical implications of trimethoprim-sulfamethoxazole resistant Stenotrophomonas maltophilia (TSRSM). Of 69 reviewed cases (mean age, 57 y; male gender, 70%), 40 (58%) were classified as infections associated with TSRSM (respiratory tract, 14; soft tissue, 11; bloodstream, 8; other sites, 7). Severe underlying comorbidities (86%) and previous antibiotic exposure (99%) were common. Cefotetan (susceptibility, 55%), chloramphenicol (49%) and ticarcillin-clavulanate (45%) showed the highest in vitro activity against TSRSM, but were seldom used for therapy (7%). Among the 40 infected cases, 8 developed sepsis disorders and 8 died. Only 1 death could be directly attributed to autopsy-proven TSRSM infection (pneumonia). McCabe score (p = 0.03) and organ dysfunction (p = 0.006) were associated with an increased risk of death in infected patients; exposure to appropriate therapy tended to be protective against death (p = 0.08). 22 infected patients were treated medically; an additional procedure was necessary to clear the infection in 18 cases (surgery, 13; catheter removal, 5). Isolation precautions were rarely exercised, even in the presence of panresistant isolates. In summary, TSRSM-related infections occurred in severely ill patients with extensive exposure to the health-care system, and often required invasive procedures for cure. Infections were directly associated with severe morbidity, and tended to have an indirect rather than a direct impact on mortality.
UR - http://www.scopus.com/inward/record.url?scp=0034525349&partnerID=8YFLogxK
U2 - 10.1080/003655400459577
DO - 10.1080/003655400459577
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C2 - 11200376
AN - SCOPUS:0034525349
SN - 0036-5548
VL - 32
SP - 651
EP - 656
JO - Scandinavian Journal of Infectious Diseases
JF - Scandinavian Journal of Infectious Diseases
IS - 6
ER -