Halliday 1984.
Methods | Randomized Single Center Blinding of Randomization: yes (sealed envelope) Complete follow‐up: no Blinding of outcome measurement: yes Blinding of Intervention: attempted (separate staff involved in treatment administration) Long‐term follow‐up: Halliday (1986) 99% of survivors evaluated | |
Participants | Premature infants Gestational age 25 to 33 weeks No evidence of lung maturity No major congenital anomalies Infants randomized: DPPC/HDL = 49 Control = 51 | |
Interventions | Intratracheal administration of dipalmitdylphosphatidylcholine 30mg/ High‐density lipoprotein 3 mg in 5 ml saline vs. manual ventilation | |
Outcomes | Respiratory Distress Syndrome
Complications of prematurity FOLLOW‐UP: Assessed at 2 years |
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Notes | ||
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Allocation concealment? | Low risk | Blinding of Randomization: yes (sealed envelope) |
Blinding? All outcomes | Low risk | Blinding of Intervention: attempted (separate staff involved in treatment administration) Blinding of outcome measurement: yes |
Incomplete outcome data addressed? All outcomes | Unclear risk | Complete follow‐up: no Long‐term follow‐up: Halliday (1986) 99% of survivors evaluated |
Free of selective reporting? | Low risk | |
Free of other bias? | Low risk |