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. 2015 Sep 4;2015(9):CD009106. doi: 10.1002/14651858.CD009106.pub2

Summary of findings for the main comparison. Standardised formal neonatal resuscitation programme (SFNRT) compared with no SFNRT.

Standardised formal neonatal resuscitation programme (SFNRT) compared with no SFNRT
Patient or population: birth attendants
Settings: hospitals in Canada
Intervention: SFNRT
Comparison: no SFNRT
Outcomes Illustrative comparative risks* (95% CI) Relative effect
 (95% CI) No of participants
 (studies) Quality of the evidence
 (GRADE) Comments
Assumed risk Corresponding risk
No SFNRT SFNRT
Knowledge acquisition
(Immediately after SFNRT)
Population at risk RR 5.96 (3.60 to 9.87) 166 participants
(1 study)
⊕⊝⊝⊝
 very low The quality of evidence was downgraded 3 levels because of serious risk of bias (high risk of selection bias, unit of analysis error and serious imprecision (evidence available from a single small study))
153 per 1000 911 per 1000
(551 to 1510)
Skills Acquisition
(Immediately after SFNRT)
Population at risk RR 170.93 (10.78 to 2710.85) 166 participants
(1 study)
⊕⊝⊝⊝
 very low The quality of evidence was downgraded 3 levels because of serious risk of bias (high risk of selection bias, unit of analysis error and serious imprecision (evidence available from a single small study))
0 per 1000 Not estimable
Knowledge retention
(6 months after SFNRT)
Population at risk RR 3.60 (2.43 to 5.35) 166 participants
(1 study)
⊕⊝⊝⊝
 very low The quality of evidence was downgraded 3 levels because of serious risk of bias (high risk of selection bias, unit of analysis error and serious imprecision (evidence available from a single small study))
235 per 1000 846 per 1000
(571 to 1257)
Skills retention
(6 months after SFNRT)
Population at risk RR not estimable as there were no events in the control or the intervention groups 166 participants
(1 study)
⊕⊝⊝⊝
 very low The quality of evidence was downgraded 3 levels because of serious risk of bias (high risk of selection bias, unit of analysis error and serious imprecision (evidence available from a single small study))
0 per 1000 Not estimable
*The basis for the assumed risk (e.g. the median control group risk across studies) is provided in footnotes. The corresponding risk (and its 95% confidence interval) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI).
 CI: confidence interval; RR: risk ratio; SFNRT: standardised formal neonatal resuscitation programme.
GRADE Working Group grades of evidence
 High quality: Further research is very unlikely to change our confidence in the estimate of effect.
 Moderate quality: Further research is likely to have an important impact on our confidence in the estimate of effect and may change the estimate.
 Low quality: Further research is very likely to have an important impact on our confidence in the estimate of effect and is likely to change the estimate.
 Very low quality: We are very uncertain about the estimate.