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. 2016 Dec 15;2016(12):CD005384. doi: 10.1002/14651858.CD005384.pub2

Summary of findings for the main comparison. NIPPV versus NCPAP (by population).

NIPPV versus NCPAP (by population)
Patient or population: preterm infants
 Setting: neonatal intensive care units
 Intervention: NIPPV
 Comparison: NCPAP
Outcomes Anticipated absolute effects* 
 (95% CI) Relative effect
 (95% CI) Number of participants
 (studies) Quality of the evidence
 (GRADE) Comments
Risk with NCPAP Risk with NIPPV
Respiratory failure Study population RR 0.62
 (0.47 to 0.82) 876
 (9 RCTs) Moderatea Risk of bias: unblinded intervention
Meets optimal information size (OIS) (N = 377)
251 per 1000 155 per 1000
 (120 to 200)
Moderate
175 per 1000 109 per 1000
 (84 to 140)
Need for intubation Study population RR 0.79
 (0.64 to 0.97) 766
 (8 RCTs) Moderatea Risk of bias: unblinded intervention
Does not meet OIS (N = 838)
300 per 1000 237 per 1000
 (192 to 291)
Moderate
175 per 1000 138 per 1000
 (112 to 170)
Pneumothorax Study population RR 0.69
 (0.35 to 1.34) 876
 (9 RCTs) Lowa,b Risk of bias: unblinded intervention 
 Imprecision: wide confidence intervals
43 per 1000 29 per 1000
 (15 to 57)
Moderate
44 per 1000 30 per 1000
 (15 to 58)
Severe intraventricular hemorrhage (grade III/IV) Study population RR 1.26
 (0.53 to 3.01) 430
 (4 RCTs) Very lowa,b Risk of bias: unblinded intervention 
 Imprecision: extremely wide confidence intervals
37 per 1000 46 per 1000
 (19 to 110)
Moderate
49 per 1000 61 per 1000
 (26 to 147)
Chronic lung disease Study population RR 0.67
 (0.47 to 0.94) 727
 (8 RCTs) Moderatea Risk of bias: unblinded intervention
Does not meet OIS (N = 1250)
179 per 1000 120 per 1000
 (84 to 168)
Moderate
170 per 1000 114 per 1000
 (80 to 160)
Mortality during study period Study population RR 0.77
 (0.51 to 1.17) 876
 (9 RCTs) Lowa,b Risk of bias: unblinded intervention 
 Imprecision: wide confidence intervals
89 per 1000 69 per 1000
 (46 to 105)
Low
0 per 1000 0 per 1000
 (0 to 0)
Moderate
26 per 1000 20 per 1000
 (13 to 30)
*The risk in the intervention group (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; RCT: randomized controlled trial; RR: risk ratio.
GRADE Working Group grades of evidenceHigh quality: We are very confident that the true effect lies close to that of the estimate of effect.
 Moderate quality: We are moderately confident in the effect estimate: The true effect is likely to be close to the estimate of effect but may be substantially different.
 Low quality: Our confidence in the effect estimate is limited: The true effect may be substantially different from the estimate of effect.
 Very low quality: We have very little confidence in the effect estimate: The true effect is likely to be substantially different from the estimate of effect.

aUnblinded intervention.

bImprecision: wide confidence intervals.