Loading…
PSHP 2026 Residency Conference has ended
Monday May 18, 2026 2:00pm - 2:20pm EDT
Purpose: Bromocriptine is hypothesized to have an antipyretic effect in patients with neurogenic fever, however the evidence is limited to small retrospective studies. This study aimed to evaluate the impact of bromocriptine on neurogenic fever.


Methods: This retrospective chart review included adult patients admitted to the neurological intensive care unit (ICU) who received at least one dose of bromocriptine for suspected neurogenic fever between 6/1/2020 and 6/1/2025. The primary outcome was the change in maximum body temperature (Tmax) from the 24-hour period prior to bromocriptine administration (day 0) to the 48-to-72-hour period after initial administration (day 3). Secondary outcomes included change in Tmax from day 0 compared to 0 to 24 hours after administration (day 1) and 24 to 48 hours after administration (day 2), duration of fever, ICU length of stay (LOS), hospital LOS, and mortality during and 30 days after bromocriptine administration. Outcomes were analyzed by Mann-Whitney U test.


Results: A total of 75 patients were included in the analysis with a median age of 53 years. Administration of bromocriptine resulted in a significant decrease in temperature on day 3 (38.8 ºC vs 38.2 ºC, p < 0.001). The median dose of bromocriptine administered was 15mg on day 1, 30mg on day 2, and 40mg on day 3. Patients with a traumatic injury (n=22) had a greater reduction in fever compared to those with a non-traumatic injury at 72 hours (-0.8 ºC vs -0.5 ºC, p=0.002). The median duration of fever was 2 days. Hypotension occurred in 27 patients after administration, and 20 patients experienced nausea.


Conclusion: In patients with suspected neurogenic fever, bromocriptine may be an option for temperature reduction when added to other antipyretics. Patients with traumatic injury demonstrated a greater reduction in fever, suggesting greater efficacy in this population. Further investigation into dosing strategies is needed


IRB Approval: This study went through IRB approval and received exempt status.
Moderators
JK

Jennifer Kunkel

Medication Safety Officer, Jefferson Health Abington Hospital
Speakers
avatar for Maeghan Biché, PharmD

Maeghan Biché, PharmD

PGY1, St. Luke's University Health Network, Bethlehem Campus
2025 graduate of Duquesne University School of Pharmacy. Current PGY-1 pharmacy resident at St. Luke's University Health Network and incoming PGY-2 in critical care for the network. Interests include surgical/trauma intensive care and transitions of care. 
Monday May 18, 2026 2:00pm - 2:20pm EDT
a.Pavilion Hub WEST

Sign up or log in to save this to your schedule, view media, leave feedback and see who's attending!

Share Modal

Share this link via

Or copy link