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March 6, 2026Antibiotics0 citationsOpen Access

Hemodialysis Central Venous Catheter-Associated Bloodstream Infection Caused by Stenotrophomonas maltophilia Treated with Cefiderocol and Levofloxacin After Failure of Trimethoprim–Sulfamethoxazole Monotherapy and Device Replacement

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SMSimone MeiniAAAlberto AntonelliBLBenedetta Longo

Key Points

  • To explore effective treatment options for bloodstream infections caused by Stenotrophomonas maltophilia, particularly after trimethoprim-sulfamethoxazole failure.
  • Described a clinical case of a 55-year-old female patient
  • Documented hemodialysis central venous catheter-associated bloodstream infection
  • Administered cefiderocol and levofloxacin after device replacement and SXT failure
  • Successful treatment with cefiderocol and levofloxacin after trimethoprim-sulfamethoxazole failure
  • Improved outcomes following central venous catheter replacement
  • Combination therapy potentially beneficial in biofilm-associated infections

Abstract

Background: Stenotrophomonas maltophilia infections represent a clinical challenge in treating frail and immunocompromised patients. Alternatives to trimethoprim–sulfamethoxazole (SXT) are needed, with cefiderocol (FDC) representing a promising option, but clinical evidence is limited; moreover, data to support the superiority of mono or combination therapy are lacking. Case presentation: We describe the case of a 55-year-old female patient with a tunneled hemodialysis central venous catheter (HD-CVC)-associated bloodstream infection caused by S. maltophilia that, after failure of a prolonged SXT monotherapy, was successfully treated by HD-CVC replacement followed by intravenous cefiderocol (FDC) and levofloxacin (LVX). Conclusions: FDC represents an interesting option for complex cases of S. maltophilia bloodstream infections, and the combination with LVX might add benefit in cases associated with biofilm formation on intravascular devices.

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Cite This Study

Meini et al. (2026) studied this question.

synapsesocial.com/papers/69aa7008531e4c4a9ff59798https://doi.org/10.3390/antibiotics15030265
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