1578. Back to Bactrim – Utilizing preferred prophylaxis strategies in immunocompromised hosts via a trimethoprim-sulfamethoxazole rechallenge program
Session: Poster Abstract Session: Viruses and Bacteria in Immunocompromised Patients
Friday, October 5, 2018
Room: S Poster Hall
  • ID WEEK 2018_Oral bactrim challenge.pdf (446.8 kB)
  • Background:

    Trimethoprim sulfamethoxazole (TMP-SMX) is the preferred agent for Pneumocystis jirovecii pneumonia prophylaxis in immunocompromised hosts (ICH). However, TMP-SMX is frequently avoided due to an adverse drug reaction (ADR) history. We report on a novel multicentre programmatic approach to TMP-SMX ADRs in ICH.


    We reviewed ICH with a reported TMP-SMX ADR referred to the conjoint antibiotic allergy services at Austin Health (Melb, Aus) and Peter MacCallum Cancer Centre (Melb, Aus) between April 2015 and May 2018. ICH were defined as patients with a history of cancer, transplantation, autoimmune condition or prednisolone use > 20mg day for 1 month. Patients were assessed and managed as per the TMP-SMX ADR protocol (Figure 1).


    Eighteen patients were assessed, of which 16 (89%) underwent allergy testing (6;89% patch testing [PT] and/or 9;56% oral rechallenge [OC]) and 2 (11%) successful desensitization. Of those that underwent allergy testing, 10 (63%) were cancer patients, 4 (25%) solid organ transplant recipients, 1 (6%) HIV and 1 (6%) multiple sclerosis. The median age was 59 (IQR 49.5, 65) and predominate phenotypes were severe cutaneous adverse drug reactions (4; 22%) and maculopapular exanthema [MPE] (11; 61%). Eighty-nine percent (8/9) of OC patients tolerated TMP-SMX challenge. One patient experienced a recurrence of a mild self-resolving localized rash following TMP-SMX OC. Of those 7 patients that did not undergo OC, 2 (29%) were PT positive and 5 (72%) histories of severe or recent T-cell mediated allergy. Three of the 7 patients who did not undergo OC received and tolerated dapsone.


    A novel TMP-SMX ADR protocol was able to identify ICH with severe allergy phenotypes and provide alternative antibiotic sulphonamide therapeutic options, whilst safely rechallenging the majority with low risk TMP-SMX ADR histories.

    Olivia Smibert, Bachelor of Medicine, Bachelor of Surgery1, Karen Urbancic, BPharm2, Abby Douglas, MBBS1, Misha Devchand, BPharm3, Monica Slavin, MBBS FRACP MD4 and Jason Trubiano, MBBS/BBioMed Sci FRACP5, (1)Infectious Diseases and Microbiology, Peter MacCallum Cancer Center, Melbourne, Australia, (2)Austin Health, Heidelberg, Australia, (3)Austin Hospital, Melbourne, Australia, (4)Peter MacCallum Cancer Centre, Melbourne, Australia, (5)Department of Medicine, University of Melbourne, Melbourne, Australia


    O. Smibert, None

    K. Urbancic, None

    A. Douglas, None

    M. Devchand, None

    M. Slavin, None

    J. Trubiano, None

    Findings in the abstracts are embargoed until 12:01 a.m. PDT, Wednesday Oct. 3rd with the exception of research findings presented at the IDWeek press conferences.