Adverse events (AEs; adverse drug reaction): sinus bradycardia · patients with acute myocardial infarction
It is very uncertain whether lidocaine changes adverse events (AEs; adverse drug reaction): sinus bradycardia compared with placebo or no intervention (very low certainty).
1 finding from 1 review
Adverse events (AEs; adverse drug reaction): drowsiness/dizziness · patients with acute myocardial infarction
Lidocaine may leads to higher adverse events (AEs; adverse drug reaction): drowsiness/dizziness compared with placebo or no intervention (low certainty).
1 finding from 1 review
Intervention not reported
Peak IL‐6 (between the end of surgery and 24 hours post‐surgery)
1 finding from 1 review
Intervention not reported
Peak IL‐8 (between the end of surgery and 6 hours post‐surgery)
1 finding from 1 review
Intervention not reported
Hospital or 30‐day mortality
It is very uncertain whether the intervention changes hospital or 30‐day mortality (very low certainty).
1 finding from 1 review
Intervention not reported
Myocardial injury (hospital stay)
It is very uncertain whether the intervention changes myocardial injury (hospital stay) (very low certainty).
1 finding from 1 review
Intervention not reported
Kidney injury (safety outcome) (hospital stay)
The intervention showed no clear difference in kidney injury (safety outcome) (hospital stay) (low certainty).
1 finding from 1 review
Intervention not reported
Surgical Site Infection (hospital stay)
The intervention showed no clear difference in surgical Site Infection (hospital stay) (low certainty).
1 finding from 1 review
Intervention not reported
Duration of hospital length of stay
1 finding from 1 review
Intervention not reported
All‐cause mortality
The intervention showed no clear difference in all‐cause mortality (low certainty).
1 finding from 1 review
Intervention not reported
Cardiovascular‐related mortality
The intervention showed no clear difference in cardiovascular‐related mortality (low certainty).
1 finding from 1 review
Intervention not reported
All‐cause hospital admission (number of events) ‐ not reported
The review found no eligible studies for this question.
1 finding from 1 review
no estimate extracted
Studies not reported
No studies found
Intervention not reported
All‐cause hospital admission (number of participants with at least one event)
The intervention showed no clear difference in all‐cause hospital admission (number of participants with at least… (low certainty).
1 finding from 1 review
Intervention not reported
Cardiovascular‐related hospital admission (number of events)
The intervention may leads to lower cardiovascular‐related hospital admission (number of events) (low certainty).
1 finding from 1 review
Intervention not reported
Cardiovascular‐related hospital admission (number of participants with at least one event)
The intervention showed no clear difference in cardiovascular‐related hospital admission (number of participants… (low certainty).
1 finding from 1 review
Intervention not reported
Health‐related quality of life
1 finding from 1 review
Intervention not reported
Health‐related quality of life
1 finding from 1 review
Intervention not reported
Adverse events ‐ not reported
The review found no eligible studies for this question.
1 finding from 1 review
no estimate extracted
Studies not reported
No studies found
Depression symptoms ‐ short‐term · health problem or population
1 finding from 1 review
Myocardial infarction ‐ short term (end of treatment) ‐ not reported · health problem or population
The review found no eligible studies for this question.
1 finding from 1 review
no estimate extracted
Studies not reported
No studies found