Table 2

Results of the trials

OutcomeNo of studiesIndomethacinControlRelative riskRisk differenceNNT
*In survivors examined.
†Either Bayley mental developmental index (MDI <68 or Wecshler preschool and primary scale of intelligence–revised (WPPSI-R) <70)
‡Number needed to harm.
NNT, Number needed to treat (calculated where significant result obtained); IVH, intraventricular haemorrhage; PDA, patent ductus arteriosus; BPD, bronchopulmonary dysplasia.
Death at latest follow up18231/1372245/13970.96 (0.81 to 1.12)−0.01 (−0.04 to 0.02)
All IVH14422/1258482/12740.88 (0.80 to 0.96)−0.04 (−0.08 to −0.01)25
Severe IVH14115/1285177/13030.66 (0.53 to 0.82)−0.05 (−0.07 to −0.02)20
Symptomatic PDA14204/1093471/11000.44 (0.38 to 0.50)−0.24 (−0.28 to −0.21)4
PDA ligation849/89197/9000.51 (0.37 to 0.71)−0.05 (−0.08 to −0.03)20
Pulmonary haemorrhage4104/795123/7960.84 (0.66 to 1.06)−0.02 (−0.06 to 0.01)
BPD (in oxygen at 28 days)9188/500183/5221.08 (0.92 to 1.26)0.03 (−0.03 to 0.08)
Necrotising enterocolitis1284/118777/12141.09 (0.82 to 1.46)0.01 (−0.01 to 0.03)
Gastrointestinal perforation136/60132/6011.12 (0.71 to 1.79)0.01 (−0.02 to 0.03)
Diminished urine output8131/104570/10701.90 (1.45 to 2.47)0.06 (0.04 to 0.08)16‡
Raised creatinine410/29810/3201.09 (0.47 to 2.51)0.00 (−0.03 to 0.03)
Excessive bleeding516/88023/8960.74 (0.40 to 1.38)−0.01 (−0.02 to 0.01)
Severe developmental delay*†3143/641151/6450.96 (0.79 to 1.17)−0.01 (−0.05 to 0.04)
Cerebral palsy*478/67877/6941.04 (0.77 to 1.40)0.00 (−0.03 to 0.04)
Blindness*210/6358/6391.26 (0.50 to 3.18)0.00 (−0.01 to 0.02)
Deafness*211/62611/6331.02 (0.45 to 2.33)0.00 (−0.01 to 0.01)
Severe neurosensory impairment*3164/682173/7060.98 (0.81 to 1.18)0.00 (−0.05 to 0.04)
Death or severe neurosensory impairment*3304/743299/7481.02 (0.90 to 1.15)0.01 (−0.04 to 0.06)