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Table 3 Summary of mortality outcome for pharmacotherapy interventions for a significant difference in mortality

From: Anesthesia interventions that alter perioperative mortality: a scoping review

First author, year

Type of surgery, no. of participants

Intervention/comparison details

Perioperative phase, duration of intervention

Impact on mortality* (outcome definition, timing)

Aronson, 2008

Cardiac, 1506

IV clevidipine at an initial rate of 0.4 mcg/kg/min, titrating to antihypertensive effect to a max dose of 8 mcg/kg/min.

Three comparator groups of common (usual care) perioperative antihypertensives: nitroglycerin, sodium nitroprusside, and nicardipine.

Preoperative, intraoperative, postoperative

Once

Decreased mortality (death at 30 days, primary outcome)

Boyd, 1993

Major surgery, 107

Dopexamine infusion to achieve oxygen delivery (DO2I) of greater than 600 mL/min/m2, perioperatively, in high-risk patients.

Usual care

Preoperative, intraoperative, postoperative

24 h

Decreased mortality (in-hospital mortality, primary outcome)

Comerota, 1993

Vascular, 134

One of three doses of urokinase (125,000, 250,000, or 500,000) infused into the distal circulation before lower extremity bypass for chronic limb ischemia

No treatment

Intraoperative

Once

Increased mortality (death at NR, secondary outcome)

Devereaux, 2008

Non-cardiac, 8351

Extended-release metoprolol 2–4 h before surgery and continued for 30 days

Placebo

Preoperative, postoperative

Once

Increased mortality (cardiovascular death, NR, primary outcome)

Donato, 2007

Vascular, 192

Iloprost (intra-arterial, intraoperative bolus) of 3000 ng, plus intravenous infusion of 0.5–2.0 ng/kg/min.

No treatment

Intraoperative, postoperative

Every day for a time period

Decreased mortality (mortality at 90 days, primary outcome)

Donato, 2006

Vascular, 300

Starting from the first day after surgery, a daily 6-h intravenous infusion of iloprost (or placebo) at doses recommended for chronic critical limb ischemia was performed for 4 to 7 days (7 days recommended).

No treatment

Intraoperative, postoperative

Every day for a time period

Decreased mortality (mortality at 90 days, primary outcome)

Fergusson, 2008

Cardiac, 2331

Aprotinin: test dose of 40,000 KIU administered during a 10-min period after insertion of central venous line and induction of anesthesia. If no anaphylactic reaction remained for loading dose (1.96 million KIU) given followed by maintenance infusion of 500,000 KIU/h and maintained during surgery.

Aminocaproic acid or tranexamic acid

Intraoperative

During most of the intraoperative period

Increased mortality (death from all causes at 30 days, secondary outcome)

Giakoumidakis, 2013

Cardiac, 200

Group 1 received aspirin preoperatively while in group 2, aspirin was stopped at least 7 days before CABG.

No treatment

Preoperative

Once

Decreased mortality (in-hospital mortality, primary outcome)

Hase, 2013

Cardiac, 350

Bolus of sodium bicarbonate (0.5 mmol/kg in 250 mL over 1 h) at induction followed by an infusion over the next 23 h (0.2 mmol/kg/h in 1000 mL).

Intraoperative, postoperative

24 h

Increased mortality (death in-hospital, secondary outcome)

ND (death at 90 days, secondary outcome)

Herr, 2000

NR, 113

Propofol or propofol plus EDTA

Intraoperative

Once

Increased mortality (7-day mortality, primary outcome)

Iliuta, 2009

Cardiac, 1352

Group A: patients with betaxolol postoperative 20 mg once daily

Group B: patients with metoprolol postoperative 200 mg in two equal doses daily

Preoperative, intraoperative postoperative, after discharge from hospital

Every day for a time period

Decreased mortality (30-day mortality, primary outcome)

Illiuta, 2003

Cardiac, 400

Patients received nadroparin 85 U/kg SC q12h.

Usual care: patients received unfractionated heparin IV to maintain APTT at 2.5 the normal value.

Postoperative

Every day for a time period

Decreased mortality (30-day mortality, primary outcome)

Kirdemir, 2008

Cardiac, 200

Continuous insulin infusion titrated per protocol in the perioperative period (Portland protocol) to maintain blood glucose between 100 and 150 mg/dL.

Subcutaneous insulin was injected every 4 h in a directed attempt to maintain blood glucose levels below 200 mg/dL.

Intraoperative, postoperative

Immediately preoperatively until postop day 3

Decreased mortality (in-hospital mortality, secondary outcome)

Krestchmer, 1989

Vascular, 252

ASA (1–1.5 g daily)

No treatment

Preoperative, postoperative, after discharge from hospital

Every day for a time period

Decreased mortality (probability of survival at 6 years, primary outcome)

Levin, 2012

Cardiac, 93

Preoperative loading dose of levosimendan (10 μg/kg over 60 min) followed by a continuous 23 h infusion of 0.1 μg/kg/min

No treatment

Preoperative

Every day for a time period

Decreased mortality (30-day mortality, primary outcome)

Levin, 2008

Cardiac, 252

Preoperative loading dose of levosimendan (10 μg/kg over 60 min) followed by a continuous 23 h infusion of 0.1 μg/kg/min

No treatment

Preoperative, intraoperative

Every day for a time period

Decreased mortality (30-day mortality, primary outcome)

Mentzer, 2008

Cardiac, 5761

Intravenous cariporide (180 mg in a 1-h preoperative loading dose, then 40 mg/h over 24 h and 20 mg/h over the subsequent 24 h).

No treatment

Preoperative

Increased mortality (all-cause mortality at day 5, secondary outcome)

Increased mortality (all-cause mortality at day 30, secondary outcome)

ND (all-cause mortality at 6 months, secondary outcome)

Norman, 2009

Thoracic, 16

Aprotinin (IV bonus of 2 million KIU followed by a 0.5 million KIU per but infusion).

No treatment

Intraoperative

Once

Decreased mortality (survival at NR, secondary outcome)

Poldermans, 1999*

Vascular, 112

Beta-blockade with bisoprolol

Usual care with no perioperative blockade

Preoperative, intraoperative postoperative

Until surgery

Decreased mortality (perioperative death, primary outcome)

Reyad, 2013

General, 60

Dobutamine at either 3 mcg/kg/min or 5 mcg/kg/min.

No treatment

Intraoperative

During most of the intraoperative phase

Decreased mortality (death in-hospital, secondary outcome)

Turpie, 2007

General, 467

Injections of fondaparinux 2.5 mg (fondaparinux sodium, Arixtra, GlaxoSmithKline, Research Triangle Park, NC, USA).

No treatment

Postoperative

Every day for a time period: daily for 5–9 days

Decreased mortality (death at 30 days, secondary outcome)

Wallace, 2004

General, 190

0.2 mg oral tablet of clonidine (Catapres; Boehringer Ingelheim, Ridgefield, CT), a 7.0-cm2 transdermal patch of clonidine (Catapres-TTS-2; Boehringer Ingelheim), providing continuous systemic delivery of 0.2 mg/day, and an oral loading dose of clonidine, 0.2-mg tablet (Catapres).

No treatment

Preoperative, intraoperative, postoperative

Every day for a time period: 4 days

Decreased mortality (30-day mortality, NR)

Decreased mortality (2-year mortality, NR)

Wilson, 1999

General, 138

1 L of Hartmann’s solution during line insertion. Human albumin solution 4.5% was then infused until a pulmonary artery occlusion pressure of 12 mmHg was achieved. If hemoglobin concentration was < 110 g/L, red blood cells were transfused instead of the albumin solution. If oxygen saturation was < 94%, supplemental oxygen was provided. Inotrope was commenced at a rate (mL/h) calculated from a chart according to the patient’s weight and equated to 0.025 ìg/kg/min for adrenaline. The infusion was increased by single multiples of the initial rate until the target oxygen delivery of > 600 ml/min/m2 was achieved or the onset of side effects was noted (increase in heart rate > 30% above baseline or development of chest pain or a new dysrhythmia). All patients were started on the study inotrope even if the target oxygen delivery had been achieved after the fluid phase.

Usual care

Preoperative, intraoperative, postoperative

Minimum of 4 h before surgery, continued for at least 12 h afterwards.

Decreased mortality (in-hospital mortality, primary outcome)

  1. Anesthesia-related intervention refers to the interventions provided in the perioperative period that was or could be performed, organized, or initiated by a healthcare professional with specific training in anesthesia
  2. ND no significant change, NR not reported
  3. *This study was part of an investigation of academic integrity. The investigating committee was unable to confirm or deny any doubts surrounding the conduct of the study, and it thus not retracted from the journal where it was published. We therefore did not exclude the study from our scoping review