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Table 1 Characteristics of included trials

From: The optimal dose of succinylcholine for rapid sequence induction: a systematic review and meta-analysis of randomized trials

Trial

Country

Experimental regimens [mg kg− 1] (number of patients)

PM

Medications for induction

Rapid Sequence Induction

Cricoid pressure

Adverse effects

Intubation failures

El Orbany 2004

USA

0.3 (n = 23)

0.4 (n = 23)

0.5 (n = 23)

0.6 (n = 23)

1.0 (n = 23)

Yes

Fentanyl 1.5 μg kg− 1

Propofol 2 mg kg− 1

Modified

nr

nr

7 with succinylcholine 0.3 mg kg− 1;

2 with succinylcholine 0.4 mg kg− 1

Luo 2014

China

0.3 (n = 60)

0.5 (n = 60)

1.0 (n = 60)

No

Sevoflurane

True*

nr

“No complications such as cough, laryngospasm, or bronchial spasm attributable to the study”

None

Naguib 2003

Saudi Arabia

0.3 (n = 50)

0.5 (n = 50)

1.0 (n = 50)

Yes

Fentanyl 2 μg kg− 1

Propofol 2 mg kg− 1

True

nr

“Each patient was followed up for any adverse affects”. Results nr.

None

Naguib 2006

USA

0.3 (n = 30)

0.5 (n = 30)

1.0 (n = 30)

1.5 (n = 30)

2.0 (n = 30)

No

Fentanyl 2 μg kg− 1

Propofol 2 mg kg− 1

True

nr

“Each patient was monitored for any adverse event”. Results nr.

None

Prakash 2012

India

0.4 (n = 23)

0.6 (n = 23)

1.0 (n = 23)

No

Fentanyl 2 μg kg− 1

Propofol 2 mg kg− 1

True

yes

Adverse events were recorded and no episodes of laryngospasm, bronchospasm, masseter spasm, generalized rigidity were observed

None

Taxak 2013

India

0.4 (n = 50)

0.6 (n = 50)

0.8 (n = 50)

1.0 (n = 50)

Yes

Meperidine 1 mg kg− 1

Propofol 2 mg kg− 1

Modified

nr

nr

nr

  1. PM premedication, nr not reported, atrue RSI with sevoflurane