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. Author manuscript; available in PMC: 2010 Aug 10.
Published in final edited form as: J Clin Pharmacol. 2009 May 5;49(7):758–767. doi: 10.1177/0091270009334375

Table II.

Summary of Included Studies

Author Year Indication Study Setting GIK Formulation, U/kg/h insulin Infusion Duration, h Mortality Timing Treatment, N Control, N Treatment Mortality, n Control Mortality, n Sequence Generationa Allocation Concealmentb Blindingc Selective Outcome Reportingd
Pentecost 1968 AMI ICU Not weight-based 48 In-hospital 100 100 15 16 C C A B
Thys 1974 AMI ICU Not weight-based 168 In-hospital 85 89 14 10 C C C C
Rackley 1976 AMI ICU 0.075 48 In-hospital 8 8 1 2 C C C C
Stanley 1978 AMI Unclear 0.075 48 In-hospital 55 55 4 9 C C A C
Mantle 1981 AMI ICU 0.075 48 In-hospital 41 44 2 4 C C C B
Rogers 1982 AMI ICU 0.075 48 In-hospital 96 94 4 9 C C C B
Oldfield 1986 MVR OR Not weight-based 12 In-hospital 20 23 0 2 C C C C
Coleman 1989 CABG OR 0.08 48 60-d 11 11 1 4 C C A B
Lazar 1997 CABG OR 0.05 12+ In-hospital 16 15 0 0 B C C B
Lazar 2000 CABG OR Not weight-based 12+ In-hospital 20 20 0 0 B C C A
Turkoz 2000 CABG OR 0.14 Othere In-hospital 15 16 1 0 C C C B
Lindholm 2001 CABG±AVR OR Not weight-based Otherg In-hospital 16 14 0 1 C C C C
Smith 2002 CABG OR 0.05 10 30-d 22 22 0 0 A C A B
Lell 2002 CABG OR 0.075 12 In-hospital 21 20 0 0 C A A B
Lazar 2003 CABG OR Not weight-based 12 30-d 72 69 0 0 C C A A
Pache 2004 AMI ICU 0.072 24 30-d 155 157 7 5 A C A A
Krljanac 2005 AMI ICU 0.05 24 1-y 78 40 3 4 C C A C
Koskenkari 2005 CABG+AVR OR 1 6+ In-hospital 20 20 0 1 C C C B
Mehta 2005 AMI ICU 0.075 24 30-d 10 088 10 107 1004 976 A A A A
Ranasinghe 2006 CABG OR 0.0525 6+ In-hospital 157 160 3 3 A A A A
Quinn 2006 CABG OR 0.0525 6+ In-hospital 138 142 3 2 A A A C
Li 2006 AMI ICU 0.075 24 In-hospital 9 12 0 0 C C C C
Zuurbier 2008 CABG OR 0.1 24+ In-hospital 23 21 0 0 A A C C

AMI, acute myocardial infarction; AVR, aortic valve replacement; CABG, coronary artery bypass grafting; GIK, glucose–insulin–potassium; ICU, intensive care unit; MVR, mitral valve replacement; N, number of subjects in each group; n, number of subjects with primary outcome in each group.

a

Sequence generation: grade A = adequate, grade B = inadequate, grade C = unknown.

b

Allocation concealment: grade A = performed, grade B = not performed, grade C = unknown.

c

Blinding: grade A = blinded, grade B = not blinded, grade C = unknown.

d

Selective outcome reporting: grade A = not suggested, grade B = suggested, grade C = unknown.

e

GIK administered from induction of anesthesia until the beginning of cardiopulmonary bypass (CPB).

g

GIK administered from 15 minutes before rewarming until 30 minutes after CPB discontinued.