Mamagement of Stenotrophomonas Maltophilia infections in Critically Ill Children

איתי טוקטלי לצר 1 Gideon Paret 2 Marina Rubinstein 2 Nathan Keller 3 Galia Barkai 3 Itai M. Pesach 2
1Department of Pediatrics A, The Edmond and Lily Safra Children’s Hospital, Chaim Sheba Medical Center, Ramat-Gan, Israel, affiliated to the Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
2Pediatric Intensive Care Department, The Edmond and Lily Safra Children’s Hospital, Chaim Sheba Medical Center, Ramat-Gan, Israel, affiliated to the Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv.
3Infectious Diseases Unit, The Edmond and Lily Safra Children’s Hospital, Chaim Sheba Medical Center, Ramat-Gan, Israel, affiliated to the Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv.

Background: Stenotrophomonas maltophilia (S. maltophilia) is a life-threatening nosocomial pathogen with profound multidrug resistant attributes. It is associated with high mortality, particularly in immunocompromised patients. Data on therapy for S. maltophilia infections are scarce, especially in children hospitalized in intensive care settings (PICU).

Methods: A retrospective chart review of pediatric patients with isolates of S. maltophilia hospitalized over a five year period in 2 PICUs.

Results: Thirty-one patients and 91 isolates from blood, respiratory secretions and soft tissues were identified and reviewed. The overall incidence of S. maltophilia infections increased during the study period (P = .003). The all-cause crude mortality was 61%, and the attributed mortality was approximately 16%. Risk factors associated with mortality included longer hospitalization prior to infection (P = .002), septic shock (P = .003), mechanical ventilation (P = .004), an indwelling central vein catheter (P = .03), prior use of steroids (P = .04) and of carbapenems (P = .004). On multivariate analysis, mortality was associated with mechanical ventilation (P = .02) and pre-infection hospitalization days (P = .01). Combination treatment of trimethoprim and sulfamethoxazole (TMP/SMX), ciprofloxacin and/or minocycline significantly extended survival time (P < .001). The method of treatment did not significantly affect the interval between S. maltophilia isolation to resolution of infection (P = .200).

Conclusions: Combinations of TMP-SMX, ciprofloxacin and minocycline are proposed for PICU patients harboring S. maltophilia. Meticulous evaluation of central vascular access and prior treatment with carbapenems are indicated, especially for mechanically ventilated and septic children.

איתי טוקטלי לצר
איתי טוקטלי לצר
Dana-Dwek Children's Hospital, Tel Aviv Medical Center








Powered by Eventact EMS