Publication:
Stenotrophomonas maltophilia infections in intensive care units: a prospective and international ID-IRI study

dc.contributor.authorÇaşkurlu H.
dc.contributor.authorÇağ Y.
dc.contributor.authorAnkaralı H.
dc.contributor.authorTahmaz A.
dc.contributor.authorVatansever G.
dc.contributor.authorBilir Y. A.
dc.contributor.authorAtasoy P. Y.
dc.contributor.authorTaşbakan M.
dc.contributor.authorKarlıdağ G. E.
dc.contributor.authorŞenol A.
dc.contributor.authoret al.
dc.date.accessioned2026-05-13T21:37:13Z
dc.date.issued2026-03-01
dc.description.abstractIntroduction: Stenotrophomonas maltophilia (S. Maltophilia) is a multidrug-resistant pathogen causing severe infections in intensive care units (ICUs). This study aimed to identify the risk factors influencing 30-day mortality and evaluate antimicrobial susceptibility patterns in ICU patients with S. maltophilia infections. Methodology: A prospective, multicenter, international observational study was conducted between 15 October 2023 and 15 April 2024, in 36 ICUs across 12 countries. Adult patients (≥ 18 years) with S. maltophilia isolated from blood, urine, or respiratory cultures were included if isolates were considered clinically consistent with infection. Colonized or coinfected patients were excluded. Clinical, laboratory data were collected prospectively. Thirty-day outcome was defined as survival or death after the first positive culture. Results: A total of 207 patients were included; 109 (52.7%) died within 30 days. The primary infection sites were pneumonia (28.5%) and bloodstream infections (38.0%). Resistance rates were 7.2% for trimethoprim-sulfamethoxazole (TMP-SMX), 10.4% for levofloxacin, and 27% for ceftazidime. None of the patients received effective empiric therapy. Older age (p = 0.030), acute renal failure (p = 0.016), chronic obstructive pulmonary disease (COPD; p = 0.008), malignancy (p = 0.001), and sequential organ failure assessment (qSOFA) ≥ 2 (p = 0.001) were independently associated with higher mortality. Repeat culturing and antimicrobial modification according to susceptibility testing reduced mortality (p = 0.017). Conclusions: S. maltophilia remains a lethal ICU pathogen. Early risk assessment, cultures, susceptibility testing, and therapy changes are vital. TMP-SMX and levofloxacin stay effective; but surveillance, infection control, and prudent antibiotic use remain essential.
dc.identifier.citationÇaşkurlu H., Çağ Y., Ankaralı H., Tahmaz A., Vatansever G., Bilir Y. A., Atasoy P. Y., Taşbakan M., Karlıdağ G. E., Şenol A., et al., "Stenotrophomonas maltophilia infections in intensive care units: a prospective and international ID-IRI study", Journal of Infection in Developing Countries, cilt.20, sa.3, ss.398-406, 2026
dc.identifier.doi10.3855/jidc.22056
dc.identifier.issn2036-6590
dc.identifier.issue3
dc.identifier.pubmed41990058
dc.identifier.scopus105035824217
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=105035824217&origin=inward
dc.identifier.urihttps://hdl.handle.net/20.500.12645/42012
dc.identifier.volume20
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectTıp
dc.subjectMikrobiyoloji ve Klinik Mikrobiyoloji
dc.subjectViroloji
dc.subjectParazitoloji
dc.subjectYaşam Bilimleri
dc.subjectSağlık Bilimleri
dc.subjectTemel Tıp Bilimleri
dc.subjectBiyokimya
dc.subjectTemel Bilimler
dc.subjectMedicine
dc.subjectMicrobiology and Clinical Microbiology
dc.subjectVirology
dc.subjectParasitology
dc.subjectLife Sciences
dc.subjectHealth Sciences
dc.subjectFundamental Medical Sciences
dc.subjectBiochemistry
dc.subjectNatural Sciences
dc.subjectYaşam Bilimleri (Life)
dc.subjectBiyoloji ve Biyokimya
dc.subjectİmmünoloji
dc.subjectMikrobiyoloji
dc.subjectBulaşıcı Hastalıklar
dc.subjectLife Sciences (Life)
dc.subjectBiology & Biochemistry
dc.subjectImmunology
dc.subjectMicrobiology
dc.subjectInfectious Diseases
dc.subjectBulaşıcı hastalıklar
dc.subjectintensive care unit (ICU)
dc.subjectmaltophilia
dc.subjectmortality
dc.subjectrisks
dc.titleStenotrophomonas maltophilia infections in intensive care units: a prospective and international ID-IRI study
dc.typearticle
dspace.entity.typePublication
local.avesis.ided9edf69-88dc-42d6-aece-bc2de3152daa

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