Perioperative β-Blocker Therapy and Survival

Study
N
Drug
Onset and duration
Surgery
Results
Mangano/1966
200
Atenolol 50–100 mg
Before induction—7-d postop
Noncardiac surgery
Reduced mortality at 6 m (0 vs. 8 %, p < 0.001), at 1 y (3 vs. 14 %, p = 0.005), and at 2 y (10 vs. 21 % p = 0.019)
DECREASE1/1999
112
Bisoprolol 5–10 mg
1-w preop—30 d postop
Major vascular surgery
Decreased cardiac mortality (3.4 vs. 17 %, p = 0.02) and nonfatal MI (0 vs. 17 %, p < 0.001) in the BB group
Lindenauer/2005
122,338
Undetermined
Hospital day 2
Major noncardiac surgery
With RCRI score 0 or 1, there is no benefit and possible harm. With RCRI score 2, 3, and 4 or more, the adjusted OR for inhospital death is 0.88, 0.71, and 0.58, respectively
POBBLE/2005
103
Metoprolol 50 mg BID
1 d before surgery—7-d postop
Infrarenal vascular surgery
No difference in 30-d CV events (32 vs. 34 %) in the BB and placebo group, respectively
MAVS/2006
496
Metoprolol 25–100 mg
2-h preop—5 d or discharge
Vascular surgery
No significant difference in primary outcomea at 30 d (10.2 vs. 12.0 %) in BB and placebo groups, respectively, (p = 0.57) and at 6 m (p = 0.81)
DIPOM/2006
921
Metoprolol 100 mg ER
1-d preop—8-d postop
Major noncardiac surgery
Primary outcomeb occurred in 21 and 20 % in BB and placebo, respectively (CI 0.80–1.41). All-cause mortality was 16 % in both groups (CI 0.74–1.42 p = 0.88)
BBSA/2007
219
Bisoprolol 5 mg
3-h preop—10 d or discharge
Surgery with spinal block
Primary outcomec was 22.7 vs. 22.0 % in BB and placebo group, respectively, at 1 y (p = 0.90)
POISE/2008
8,331
Metoprolol ER 200 mg
2–4-h preop—30-d postop
Noncardiac surgery
MI occurred in 4.2 vs. 5.7 % in BB and placebo, respectively, p = 0.017. Mortality was higher in the metoprolol group (3.1 vs. 2.3 %, p = 0.0317). Stroke was more in the metoprolol group (1 vs. 0.5 %, p = 0.0053)
Look to references for expansion of study abbreviations. ER extended release, preop preoperative, postop postoperative, d day, w week, m month, y year, RCRI revised cardiac risk index, MI myocardial infarction, CV cardiovascular, BB β-blocker, OR odds ratio, BID twice a day. aPrimary outcome was postoperative 30-day composite incidence of nonfatal myocardial infarction, unstable angina, new congestive heart failure, new atrial or ventricular dysrhythmia requiring treatment, or cardiac death. bPrimary outcomes were time to all-cause mortality, acute myocardial infarction, unstable angina, or congestive heart failure. cPrimary outcomes were cardiovascular mortality, nonfatal myocardial infarction, unstable angina, congestive heart failure, and cerebrovascular insult

9.2.2 AHA and ESC Guideline Controversies

The conflicting results of these major BB trials and especially the POISE led to several controversies between the ESC [9] and AHA [10] guidelines on perioperative beta blockade. These guidelines were updated after the POISE trial showed increased all-cause mortality and the risk of disabling stroke. Table 9.2 lists the differences in guideline recommendation between the ESC and the AHA. As evident, the AHA adapted a more restrictive approach in contrast to the ESC, which has been more liberal with the administration of perioperative BB. Below is a summary of the main similarities and differences between both societies.
Table 9.2
Summary of recommendations on perioperative β-blockers by the ESC and the AHA
 
ESC guideline (August 2009)
ACC/AHA guideline (November 2009)
Class I
BB recommended in patients
-with known IHD or myocardial ischemia on preoperative testing (I B)
-Undergoing high-risk surgery (I B)
-Who were previously treated with BB for IHD, arrhythmias, or hypertension (I C)
BB recommended in patients
-Who are receiving BB for treatment of conditions with ACC/AHA Class I indication for the drug (I C)
Class II
BB should be considered in patients
-Undergoing intermediate-risk surgery (IIa B)
-Previously treated with BB because of chronic heart failure with systolic dysfunction (IIa C)
-Scheduled for low-risk surgery with risk factor(s) (IIb B)
BB are probably recommended in patients
-Undergoing vascular surgery who suffer from IHD or show ischemia on preoperative testing (IIa B)
-In the presence of CAD or high cardiac risk (more than one risk factor) who are undergoing intermediate-risk surgery (IIa B)
-Where preoperative assessment for vascular surgery identifies high cardiac risk (more than one risk factor; IIa C)
The usefulness of BB is uncertain in patients
-Undergoing vascular surgery with no risk factors who are not currently taking BB (IIb B)
–Undergoing either intermediate-risk procedures or vascular surgery with a single clinical risk factor in the absence of CAD (IIb C)
Class III

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Apr 6, 2017 | Posted by in CRITICAL CARE | Comments Off on Perioperative β-Blocker Therapy and Survival

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