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Association of Early Beta-Blocker Exposure and Functional Outcomes in Critically Ill Patients With Moderate to Severe Traumatic Brain Injury: A Transforming Clinical Research and Knowledge in Traumatic Brain Injury Study
- Kelly-Hedrick, Margot;
- Liu, Sunny Yang;
- Temkin, Nancy;
- Barber, Jason;
- Komisarow, Jordan;
- Manley, Geoffrey;
- Ohnuma, Tetsu;
- Colton, Katharine;
- Treggiari, Miriam M;
- Monson, Eric E;
- Vavilala, Monica S;
- Grandhi, Ramesh;
- Laskowitz, Daniel T;
- Mathew, Joseph P;
- Hernandez, Adrian;
- James, Michael L;
- Raghunathan, Karthik;
- Goldstein, Ben;
- Markowitz, Amy J;
- Krishnamoorthy, Vijay;
- Badjatia, Neeraj;
- Ferguson, Adam R;
- Foreman, Brandon;
- McCrea, Michael;
- Merchant, Randall;
- Ngwenya, Laura B;
- Okonkwo, David;
- Schnyer, David;
- Yue, John K;
- Zafonte, Ross
Published Web Location
https://doi.org/10.1097/cce.0000000000000958Abstract
OBJECTIVES: We aimed to 1) describe patterns of beta-blocker utilization among critically ill patients following moderate-severe traumatic brain injury (TBI) and 2) examine the association of early beta-blocker exposure with functional and clinical outcomes following injury. DESIGN: Retrospective cohort study. SETTING: ICUs at 18 level I, U.S. trauma centers in the Transforming Clinical Research and Knowledge in TBI (TRACK-TBI) study. PATIENTS: Greater than or equal to 17 years enrolled in the TRACK-TBI study with moderate-severe TBI (Glasgow Coma Scale of <13) were admitted to the ICU after a blunt TBI. INTERVENTIONS: None. MEASUREMENTS: Primary exposure was a beta blocker during the first 7 days in the ICU, with a primary outcome of 6-month Glasgow Outcome Scale-Extended (GOSE). Secondary outcomes included: length of hospital stay, in-hospital mortality, 6-month and 12-month mortality, 12-month GOSE score, and 6-month and 12-month measures of disability, well-being, quality of life, and life satisfaction. MAIN RESULTS: Of the 450 eligible participants, 57 (13%) received early beta blockers (BB+ group). The BB+ group was on average older, more likely to be on a preinjury beta blocker, and more likely to have a history of hypertension. In the BB+ group, 34 participants (60%) received metoprolol only, 19 participants (33%) received propranolol only, 3 participants (5%) received both, and 1 participant (2%) received atenolol only. In multivariable regression, there was no difference in the odds of a higher GOSE score at 6 months between the BB+ group and BB- group (odds ratio = 0.86; 95% CI, 0.48-1.53). There was no association between BB exposure and secondary outcomes. CONCLUSIONS: About one-sixth of subjects in our study received early beta blockers, and within this group, dose, and timing of beta-blocker administration varied substantially. No significant differences in GOSE score at 6 months were demonstrated, although our ability to draw conclusions is limited by overall low total doses administered compared with prior studies.
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