Preoperative care/Catalogs/Beta-blocker evidence table

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Randomized controlled trials with at least 100 total patients and at least one death.[1][2][3][4]
Patients Intervention Comparison Outcome Results
Mortality Stroke Beta-blocker toxicity
Rx Control Rx Control Rx Control

Decrease IV[1]
2009

1066 patients
* Vascular: <1%
* RCRI>2: 0%
Bisoprolol
* Started a median of 34 days preop
* Target HR: >50 bpm
Open label Mortality at 30 days 1.9% 3.0% 0.8% 0.6% Heart failure, clinically significant bradycardia or hypotension
0.6% 0.4%
POISE[2]
2008
8351 patients
* Vascular: 42%
* RCRI>2: uncertain
Metoprolol
* Started day of surgery
* Target HR: >50 bpm
Placebo Mortality at two weeks Overall 1% 0.5% Clinically significant hypotension
3.1% 2.3% 15% 9.7%
Vascular pts
Significant benefit
BBSA[3]
2007
224 patients
*Spinal anesthesia
*Vascular: 1%
* RCRI > 2: 3%
Bisoprolol
* Started day of surgery
Target HR: > 50bpm
Placebo Mortality at one year 0.9 0.9 1.8% 1.8% Hypotension:
0% 2.7%
DIPOM[4]
2006
921 patients
* All had diabetes
* Vascular: 7%
Metoprolol
* Started 0-1 days preop
* Target HR: >55 bpm
Placebo Mortality at a median of 18 months 16% 16% 0.4% 0% Hypotension reported as an ADR
0.4% 0.2%

MaVS
2006

496 patients
* Vascular: 100%
Metoprolol
*Start: day of surgery
* Target HR: > 50 bpm while awake;
>45 bpm while asleep.
Placebo Hospital mortality 0% 1.6% Not reported Intraoperative hypotension treated
46% 34%

POBBLE
2005

103 patients
* Vascular: 100%
Metoprolol
* Start with test dose one day preop
* Target HR: > 50 bpm
Placebo (anesthesiologists were not blinded) Mortality at 30 days 3% 1% 2% 0% Intraoperative inotropes given
92% 64%

Decrease
1999PMID DOI

112 patients
* Vascular surgery: 100%
* Abnl stress echo: 100%
Bisoprolol
* Started a median of 37 days preop
* Target HR: > 50 bpm
Open label Mortality at 30 days 3.4 17.0 Not reported Discontinuation of study drug due to ADRs
0% 0%

Wallace/ MSPI
1996PMID
DOI

200 patients
* Vascular: 41%
Atenolol
* Target HR: > 55 bpm
Placebo 4% 2% Not reported Discontinuation of study drug due to ADRs
0% 0%

References