Assessed as Up-to-date:	20 May 2010
Date of Search:	18 May 2010
Next Stage Expected:	20 May 2012
Protocol First Published:	Issue 3, 1997
Review First Published:	Issue 3, 1997
Last Citation Issue:	Issue 7, 2010

Date / Event	Description
20 May 2010 New citation: conclusions not changed	New co-author William McGuire.
20 May 2010 Updated	This updates the review "Prophylactic intravenous indomethacin for preventing mortality and morbidity in preterm infants" published in the Cochrane Database of Systematic Reviews (Fowlie 2002). No new trials were identified in updated search May 2010. School-age outcomes data from Ment 1994b have been included in this update.

Date / Event	Description
03 November 2008 Amended	Converted to new review format.
26 April 2002 New citation: conclusions changed	Substantive amendment An initial literature search (English only) was undertaken in October 1994 in three databases: MEDLINE at NLM (1980 - September 1994); EMBASE (1974 - 1994) in DIALOG; and the Oxford Database of Perinatal Trials (ODPT) (Version 1.3, Disk issue 7, Spring 1992). A search by first author of any abstracts was done in the Science Citation Index to try and identify any corresponding full manuscripts published. None were identified. The literature search was updated in February 1997 by assessing a trials list supplied by the Cochrane Collaboration Neonatal Review Group and by searching in MEDLINE (September 1994 - January 1997) using a similar strategy to the original search. EMBASE was not searched again as the original search in this database failed to identify any appropriate trials not identified by searching MEDLINE. The search was updated a third time in October 2001, searching in MEDLINE ["indomethacin AND infant AND (prophylactic OR prophylaxis OR prevention)"], and the Cochrane Controlled Trials Register, The Cochrane Library, Issue 3, 2001 ["indomethacin AND (infant OR newborn)"].

Abstract

Background

Persistent patent ductus arteriosus (PDA) is associated with mortality and morbidity in preterm infants. Prostaglandin synthetase inhibitors such as indomethacin promote PDA closure but also have potential side effects. The effect of the prophylactic use of indomethacin, where infants who may not have gone on to develop a symptomatic PDA would be exposed to indomethacin, warrants particular scrutiny.

Objectives

To determine the effect of prophylactic indomethacin on mortality and morbidity in preterm infants.

Search methods

The standard search strategy of the Cochrane Neonatal Review Group was used. This included searches of the Cochrane Central Register of Controlled Trials (CENTRAL, The Cochrane Library, Issue 5, 2010), MEDLINE, EMBASE and CINAHL (until April 2010), conference proceedings, and previous reviews.

Selection criteria

Randomised or quasi-randomised controlled trials that compared prophylactic indomethacin versus placebo or no drug in preterm infants.

Data collection and analysis

The standard methods of the Cochrane Neonatal Review Group were used, with separate evaluation of trial quality and data extraction by two review authors.

Results

Nineteen eligible trials in which 2872 infants participated were identified. Most participants were very low birth weight, but the largest single trial restricted participation to extremely low birth weight infants (N = 1202). The trials were generally of good quality.

The incidence of symptomatic PDA [typical relative risk (RR) 0.44, 95% confidence interval (CI) 0.38 to 0.50] and PDA surgical ligation (typical RR 0.51, 95% CI 0.37,0.71) was significantly lower in treated infants. Prophylactic indomethacin also significantly reduced the incidence of severe intraventricular haemorrhage (typical RR 0.66, 95% CI 0.53 to 0.82). Meta-analyses found no evidence of an effect on mortality (typical RR 0.96, 95% CI 0.81 to 1.12) or on a composite of death or severe neurodevelopmental disability assessed at 18 to 36 months old (typical RR 1.02, 95% CI 0.90, 1.15).

Authors' conclusions

Prophylactic indomethacin has short-term benefits for preterm infants including a reduction in the incidence of symptomatic PDA, PDA surgical ligation, and severe intraventricular haemorrhage. However, there is no evidence of effect on mortality or neurodevelopment.

Plain language summary

Prophylactic intravenous indomethacin for preventing mortality and morbidity in preterm infants

Patent ductus arteriosus (PDA) occurs when an artery near the heart and lungs, which should close off soon after birth, stays open. Babies born preterm (premature) who have a PDA are at higher risk of severe illness and death. Indomethacin, a drug more commonly used for muscle and bone pain in adults, when given to preterm infants can help close a PDA. This review found evidence that giving all preterm infants (especially very preterm infants) indomethacin on the first day after birth reduced their risk of developing a PDA and the complications associated with PDA (including brain damage due to bleeding into the brain). However, despite these short term effects, the trials found evidence that indomethacin does not increase survival or reduce disability in the longer term.

Background

Description of the condition

About one-third of very preterm or very low birth weight (VLBW) (birth weight < 1500 grams) infants develop a haemodynamically-important patent ductus arteriosus (PDA) during the first few days after birth (Evans 1990). The incidence of PDA is inversely related to weight and gestational age at birth and is higher in infants with severe respiratory distress syndrome. PDA is persistent in about one-half of extremely preterm or extremely low birth weight (ELBW) (birth weight < 1000 grams) infants (Evans 1995).

Following the postnatal fall in pulmonary vascular pressures, infants with a haemodynamically-important PDA experience shunting of blood from the aorta to the pulmonary arterial circulation (Evans 1996). This "left to right" shunt alters the blood flow distribution to the lungs and other organs and may contribute to a higher risk of severe and prolonged respiratory distress syndrome, intraventricular haemorrhage (IVH), necrotising enterocolitis (NEC), bronchopulmonary dysplasia (BPD), and death in infants with a PDA compared to similar infants whose PDA has closed (Brown 1979; Lipman 1982).

Description of the intervention

PDA closure may be achieved surgically, by transthoracic ligation or transcatheter occlusion, or pharmacologically using prostaglandin synthetase inhibitors such as indomethacin or ibuprofen (Heymann 1976). Current data are insufficient to determine if surgical or medical treatment is the better initial option for closing a PDA in preterm infants (Malviya 2008; Mosalli 2008). Currently, surgical ligation or transcatheter occlusion is usually reserved for instances in which pharmacological intervention has been unsuccessful.

Three broad strategies of pharmacological therapy for PDA can be considered (Knight 2001):

treatment only when the PDA is judged to be haemodynamically-important based on clinical or echocardiographic assessments ("symptomatic treatment"): see Herrera 2007.
treatment following diagnosis of a PDA (usually by screening echocardiography in first 24 hours after birth) but prior to the development of "left to right" shunting of blood ("targeted treatment"): see Cooke 2003; Ohlsson 2008.
treatment of all at risk infants within the first 24 hours after birth ("prophylactic treatment").

This review focusses on prophylactic treatment of PDA in preterm infants using indomethacin. Another Cochrane review examines ibuprofen prophylaxis (Shah 2006).

How the intervention might work

Prophylactic treatment aims to achieve PDA closure prior to the development of shunting and haemodynamic disturbances that are associated with morbidity and mortality but without the need for screening or surveillance using echocardiography. However, universal prophylaxis exposes a substantial proportion of infants in whom PDA closure would have occurred spontaneously to a pharmacological intervention. This is important because, as well as having potential benefits, treatment with prophylactic indomethacin may have harms related to reducing perfusion of essential organs such as reduced cerebral blood flow which may oppose any neurodevelopmental benefits due to possible reduction in the incidence of IVH (Edwards 1990); reduced gastrointestinal perfusion that potentially limits any effect of PDA closure on reducing the risk of NEC (Coombs 1990); and reduced renal perfusion, glomerular filtration and urine output causing fluid and electrolyte disturbances in the early neonatal period (Cifuentes 1979). Indomethacin may also inhibit platelet function and disrupt haemostasis that may cause clinically-important bleeding e.g. IVH (Friedman 1978).

Why it is important to do this review

Given the uncertainty that exists about the balance between the putative benefits and harms associated with prophylactic indomethacin in preterm neonates, and the potential for this intervention to affect several major outcomes in this population, an attempt to detect, appraise, and synthesise evidence from randomised controlled trials is justified.

Objectives

To determine the effect of prophylactic indomethacin on mortality and morbidity in preterm infants.

Methods

Criteria for considering studies for this review

Types of studies

Randomised or quasi-randomised controlled trials.

Types of participants

Preterm neonates (less than 37 weeks' completed gestation).

Types of interventions

Prophylactic (not guided by knowledge of PDA status) treatment with indomethacin given within 24 hours of birth vs. placebo or no treatment. Specific dose regimens were not pre-specified.

Types of outcome measures

PRIMARY OUTCOMES:

All-cause mortality prior to hospital discharge and at most recent follow-up.
Neurodevelopment: (i) Death or severe neurodevelopmental disability defined as any one or combination of the following: non-ambulant cerebral palsy, developmental delay (developmental quotient less than 70), auditory and visual impairment. Each component will be analysed individually as well as part of the composite outcome, (ii) Neurodevelopmental scores in survivors aged > 12 months measured using validated assessment tools, (iii) Cognitive and educational outcomes measured using validated assessment tools including school examinations.

SECONDARY OUTCOMES:

PDA: (i) symptomatic (clinical signs of heart failure as assessed by individual caregivers and/or receiving anti-failure therapy such as diuretics, and/or receiving non-steroidal anti-inflammatory treatment to close a suspected or confirmed PDA), (ii) all PDA confirmed by echocardiography regardless of other clinical signs (minimum duct dimension not pre-specified), (iii) surgical ligation or transcatheter occlusion of PDA.
IVH: (i) IVH; all grades (grades I-IV), and (ii) severe IVH - grade III (ventricles distended with blood) or IV (parenchymal involvement) (Papile 1978), (iii) other cranial ultrasound abnormalities related to IVH including post-haemorrhagic ventricular dilatation (hydrocephalus), periventricular leukomalacia (PVL), and cystic PVL defined as cysts detected in the periventricular area on ultrasound, computerised tomography or magnetic resonance imaging.
Respiratory outcomes: (i) need for mechanical ventilation, (ii) duration of mechanical ventilation, (iii) duration of supplemental oxygen therapy, (iv) incidence of pneumothorax or pneumopericardium, (v) incidence of bronchopulmonary dysplasia (oxygen requirement beyond (a) 28 postnatal days, (b) 36 weeks' post menstrual age), (vi) pulmonary haemorrhage.
Renal outcomes: (i) anuria or severe oliguria (< 0.5 ml/kg/day), (ii) raised plasma creatinine, (iii) acute electrolyte disturbances, (iv) long term renal impairment (glomerular filtration rate less than 50% of index population mean assessed at > 12 months of age).
Gastrointestinal outcomes: (i) NEC confirmed by at least two of the following features: abdominal radiograph showing pneumatosis intestinalis or gas in the portal venous system or free air in the abdomen; abdominal distension with abdominal radiograph showing gaseous distension or frothy appearance of bowel lumen (or both); blood in stool; lethargy, hypotonia, or apnoea (or combination of these); or a diagnosis confirmed at surgery or autopsy, (ii) isolated gastrointestinal perforation, (iii) feed intolerance: days to establish full enteral feeding independently of parenteral nutrition.
Haemostasis outcomes: (i) "excessive clinical bleeding" (investigator defined) (ii) thrombocytopaenia - platelet count < 50,000 per microlitre, or 'clinically important as defined by clinical investigators'.
Retinopathy of prematurity: (i) all stages, (ii) > stage 3 (ICROP 1984).

Search methods for identification of studies

We used the standard search strategy of the Cochrane Neonatal Review Group.

Electronic searches

Searches were made of the Cochrane Central Register of Controlled Trials (CENTRAL, The Cochrane Library, Issue 5, 2010), MEDLINE (1966 to April 2010), EMBASE (1980 to April 2010), and CINAHL (1982 to April 2010) using combinations of the following text words and MeSH terms: [Infant, Newborn OR Infant, Premature OR Infant, Low Birth Weight OR infan* OR neonat*] AND ["Anti-Inflammatory Agents, Non-Steroidal" OR indomethacin OR indometacin OR indocid OR NSAID]. The search outputs were limited with the relevant search filters for clinical trials. No language restriction was applied.

The following web sites were searched for completed or ongoing trials:

Searching other resources

The references in studies identified as potentially relevant were examined.

The abstracts from the meetings of the Pediatric Academic Societies (1993 to 2009), the European Society for Pediatric Research (1995 to 2009), and the Royal College of Paediatrics and Child Health (2000 to 2009) were searched.

Trials reported only as abstracts were eligible if sufficient information was available from the report, or from contact with the authors, to fulfil the inclusion criteria.

Data collection and analysis

The standard methods of the Cochrane Neonatal Review Group were used.

Selection of studies

The title and abstract of all studies identified by the above search strategy were screened and the full articles for all potentially relevant trials obtained. The full text of any potentially eligible reports was reassessed and those studies that did not meet all of the inclusion criteria were excluded. Any disagreements were discussed until consensus was achieved.

Data extraction and management

A data collection form was used to aid extraction of relevant information from each included study. Two review authors extracted the data separately. Any disagreements were discussed until consensus was achieved. If data from the trial reports were insufficient, the investigators were contacted for further information.

Assessment of risk of bias in included studies

The criteria and standard methods of the Cochrane Neonatal Review Group were used to assess the methodological quality of any included trials in terms of allocation concealment, blinding of parents or caregivers and assessors to the intervention and completeness of assessment in all randomised individuals. Additional information from the trial authors was requested to clarify methodology and results as necessary. In addition, the following issues were evaluated and entered into the Risk of Bias table:

1. Sequence generation: Was the allocation sequence adequately generated?

2. Allocation concealment: Was allocation adequately concealed?

3. Blinding of participants, personnel and outcome assessors: Was knowledge of the allocated intervention adequately prevented during the study? At study entry? At the time of outcome assessment?

4. Incomplete outcome data: Were incomplete outcome data adequately addressed?

5. Selective outcome reporting: Are reports of the study free of suggestion of selective outcome reporting?

6. Other sources of bias: Was the study apparently free of other problems that could put it at a high risk of bias?

Measures of treatment effect

Relative risk (RR) and risk difference (RD) were calculated for dichotomous data and weighted mean difference (WMD) for continuous data, with respective 95% confidence intervals (CI). The number needed to treat for benefit (NNTB) or harm (NNTH) was determined for a statistically significant difference in the RD.

Unit of analysis issues

The unit on analysis is the participating infant in individually randomised trials and the neonatal unit (or sub-unit) for cluster randomised trials.

Assessment of heterogeneity

If more than one trial was included in a meta-analysis, the treatment effects of individual trials and heterogeneity between trial results were to be examined by inspecting the forest plots. The I² statistic was calculated for each analysis to quantify inconsistency across studies and describe the percentage of variability in effect estimates that may be due to heterogeneity rather than sampling error. If substantial (I² > 50%) heterogeneity was detected, the possible causes (for example, differences in study design, participants, interventions, or completeness of outcome assessments) were explored in sensitivity analyses.

Data synthesis

The fixed effects model was used using RevMan 5 for meta-analysis.

Subgroup analysis and investigation of heterogeneity

The following subgroup analyses were planned:

VLBW (less than 1500 grams) or very preterm (less than 32 weeks' gestation at birth).
ELBW (less than 1000 grams) or extremely preterm (less than 28 weeks' gestation at birth).

Results

Description of studies

Nineteen trials were found to be eligible for inclusion in this review (see table Characteristics of included studies). Overall, the quality of the trials was good, and the results were consistent across trials.

Thirty-two additional studies were excluded (see table Characteristics of excluded studies).

Participants

The size of the trials ranged from single centre studies enrolling less than 50 infants to a large international multi-centre study in which 1202 infants participated (TIPP 2001). Thirteen trials were conducted within North America and the others in Latin America, Europe and Asia. The large international trial included centres in North America, Australasia and Asia (TIPP 2001).

In most trials, participants were very preterm or VLBW infants receiving standard intensive care interventions such as mechanical ventilation. The largest included trial restricted participation to ELBW infants (TIPP 2001). Surfactant was given either as prophylaxis or rescue therapy in seven trials (Couser 1996; Domanico 1994; Ment 1994a; Ment 1994b; Supapannachart 1999; TIPP 2001; Yaseen 1997).

Bada 1989, Hanigan 1988, Krueger 1987, Ment 1985, Ment 1988, Ment 1994b; Morales-Suarez 1994 and Rennie 1986a performed cranial ultrasounds before study entry and excluded infants with IVH. In Ment 1994a, participants were infants with pre-existing grade 1 IVH. The remaining studies enrolled infants without knowledge of pre-existing IVH.

Interventions

All the studies used prophylactic intravenous indomethacin as treatment. The dosage schedules varied from a single dose of 0.2 mg/kg at 24 hours of age to a daily dose of 0.1 mg/kg given for six days. A placebo, typically saline, was used as control in all trials apart from Krueger 1987.

Outcomes

Most trials examined short-term clinical outcomes prior to discharge from hospital. Many of the outcome definitions varied, in particular the definition of BPD. Several studies looked at a variety of measures of renal function including urine output and renal biochemistry but there was little consistency between studies as to which measures and which cut-off points were used. The same issue arose when examining haemostasis when the platelet count, bleeding time and "clinical bleeding" were variably used in different studies.

Data on long-term neurodevelopmental outcomes up to 36 months corrected age were available from five trials (Bandstra 1988; Couser 1996; Ment 1994b; TIPP 2001; Vincer 1987). One trial assessed school age neurodevelopmental outcomes at eight years of age (Ment 1994b).

Risk of bias in included studies

Quality assessments are included in the table, Characteristics of included studies.

The exact method of concealment of randomisation could be determined for twelve of the included studies (Bandstra 1988; Couser 1996; Gutierrez 1987; Hanigan 1988; Mahony 1985; Ment 1985; Ment 1988; Ment 1994a; Ment 1994b; TIPP 2001; Supapannachart 1999; Yaseen 1997). Methods included telephone randomisation, sealed envelopes and coded vials. In the remaining seven studies, it has not been possible to tell how well randomisation was concealed.

Blinding of the intervention to those caring for the infant was explicitly described in nine of the studies (Bandstra 1988; Couser 1996; Domanico 1994; Gutierrez 1987; Hanigan 1988; Mahony 1985; Ment 1985; Ment 1988; Vincer 1987 and TIPP 2001). In Krueger 1987, caregivers were not blinded to the intervention group. Blinding of the intervention is unclear in Puckett 1985 and Rennie 1986a.

In three studies, it is not possible to determine whether or not those responsible for assessing the outcomes of interest were blind to intervention group (Krueger 1987; Puckett 1985; Rennie 1986a). In all the other studies, blinding was adequate.

For all short-term outcome measures prior to discharge, follow-up was more than 90% complete for all the trials. Long-term outcome assessment remained impressive at > 85% in the two trials contributing most data (Ment 1994b; TIPP 2001) and even in smaller trials was still greater than 75% (Couser 1996; Vincer 1987).

Effects of interventions

PROPHYLACTIC INTRAVENOUS INDOMETHACIN VS. PLACEBO OR NO DRUG (COMPARISON 1)

PRIMARY OUTCOMES

Mortality (1.1 - 1.2)

Mortality before hospital discharge (17 trials): Meta-analysis did not detect a statistically significant effect [typical RR 0.82 (95% CI 0.65, 1.03); RD -0.03 (95% CI -0.06, 0.00): (Figure 1)]

Mortality at latest follow-up (18 trials - includes TIPP 2001): Meta-analysis did not detect a statistically significant effect [typical RR 0.96 (95% CI 0.81, 1.12); RD -0.01 (95% CI -0.04, 0.02): (Figure 2)].

There is no evidence of statistical heterogeneity in either of the meta-analyses; I²= 0%.

Neurodevelopment (1.3 - 1.7)

(i) Neurological assessments at 18 - 36 months corrected age:

Death or severe neurodevelopmental disability (3 trials): Meta-analysis did not detect a statistically significant effect [typical RR 1.02 (95% CI 0.90, 1.15); RD 0.01 (95% CI -0.04, 0.06): (Figure 3)].

Cerebral palsy (4 trials): Meta-analysis did not detect a statistically significant effect [typical RR 1.04 (95% CI 0.77, 1.40); RD 0.00 (95% CI -0.03, 0.04): (Figure 4)].

Visual impairment (2 trials): Meta-analysis did not detect a statistically significant effect [typical RR1.26 (95% CI 0.50, 3.18); RD 0.00 (95% CI -0.01, 0.02): (Figure 4)].

Hearing impairment (2 trials): Meta-analysis did not detect a statistically significant effect [typical RR 1.02 (95% CI 0.45, 2.33); RD 0.00 (95% CI -0.01, 0.01): (Figure 4)].

Severe neurodevelopmental impairment (3 trials): The two trials using Bayley examinations at 24 months (TIPP 2001 and Bandstra 1988) found no difference in rates of severe impairment (Mental Developmental Index < 68-70). Ment 1994b did not find a statistically significant difference in the WIPPSI-R (full scale < 70) at 54 months.

Meta-analysis of the three trials did not detect a statistically significant effect [typical RR 0.96 (95% CI 0.79, 1.17); RD -0.01 (95% CI -0.05, 0.04): (Figure 4)].

Cognitive outcomes (1 trial): Ment 1994b did not find a statistically significant difference in either Stanford-Binet IQ scores [WMD 4.6 (95% CI -0.5, 9.7)] or Peabody Picture Vocabulary Test scores [WMD 4.7 (95% CI -0.5, 9.9) assessed at 36 months (Figure 5).

(ii) School-age neurological and developmental assessments:

Ment 1994b did not detect any statistically significant effects on assessment of children aged eight years (Figure 6):

Cerebral palsy: typical RR 1.24 (95% CI 0.59, 2.62); RD 0.02 (95% CI -0.04, 0.08).
Visual impairment: typical RR 0.13 (95% CI 0.01, 2.54); RD -0.02 (95% CI -0.05, 0.01).
Hearing impairment: typical RR 0.78 (95% CI 0.21, 2.86); RD -0.01 (95% CI -0.05, 0.03).
"Abnormal" neurological assessment: RR 1.14 (95% CI 0.59, 2.24); RD 0.01 (95% CI -0.05, 0.08).

Cognitive and educational outcomes: Ment 1994b did not detect statistically significant differences in the risk of scoring < 70 in Wechsler Intelligence Scale for Children - Third Edition (WISC-III) verbal IQ, performance IQ, or full-scale IQ tests, or Peabody Individual Achievement Test-Revised (PIAT-R) assessments. The proportion of infants with a low Peabody Picture Vocabulary Test-Revised (PPVT-R) score (< 70) was statistically significantly lower in the indomethacin group: typical RR 0.54 (95% CI 0.31, 0.93); RD -0.09 (95% CI -0.17, -0.01); NNTB 11 (6, 100) (Figure 7).

SECONDARY OUTCOMES

Patent ductus arteriosus (Outcomes 1.8 - 1.10):

All PDA, echocardiography confirmed (7 trials): Meta-analysis found a statistically significant reduction [typical RR 0.29 (95% CI 0.22, 0.38), RD -0.27 (95% CI -0.32,-0.21), NNTB 4 (95% CI 3, 5) (Figure 8)].

Symptomatic PDA (14 trials): Meta-analysis found a statistically significant reduction [typical RR 0.44 (95% CI 0.38, 0.50); RD -0.24 (95% CI -0.28, -0.21); NNTB 4 (95% CI 3, 5) (Figure 9)].

Surgical PDA ligation (8 trials): Meta-analysis found a statistically significant reduction in risk [typical RR 0.51 (95% CI 0.37, 0.71), RD -0.05 (95% CI -0.08, -0.03), NNTB 20 (95% CI 12, 33) (Figure 10)].

There is no evidence of statistical heterogeneity in any of the meta-analyses; I²= 0% - 10%.

Intraventicular haemorrhage (1.11- 1.14)

Any IVH (14 trials): Meta-analysis found a statistically significant reduction [typical RR 0.88 (95% CI 0.80, 0.98), RD -0.04 (95% CI -0.08, -0.01), NNTB 25 (95% CI 12, 100) (Figure 11)]. There is evidence that the treatment effect on this outcome is not consistent across all studies; I²= 52%.

Severe IVH - grade >2 (14 trials): Meta-analysis found a statistically significant reduction [typical RR 0.66 (95% CI 0.53, 0.82), RD -0.05 (95% CI -0.07, -0.02), NNTB 20 (95% CI 14, 50) (Figure 12)]. There is no evidence of statistical heterogeneity; I²= 0%.

Ventriculomegaly, periventricular leukomalacia or other white matter echo-abnormalities (6 trials): Meta-analysis found a borderline statistically significant reduction [typical RR 0.80 (95% CI 0.65, 0.97), RD -0.04 (95% CI -0.07, 0.00), NNTB 25 (95% CI 14, infinity) (Figure 13)]. There is no evidence of statistical heterogeneity; I²= 1%.

IVH that progresses (2 trials): Meta-analysis did not detect a statistically significant effect [typical RR 0.80 (95% CI 0.44, 1.47), RD -0.08 (95% CI -0.29, 0.13), (Figure 14).There is no evidence of statistical heterogeneity; I²= 10%.

Respiratory outcomes (1.15 - 1.20)

Duration of assisted ventilation (4 trials): Meta-analysis did not detect a statistically significant effect [WMD -1.83 days (95% CI -5.53, 1.87) (Figure 15)].

Pneumothorax or pneumopericardium (6 trials): Meta-analysis did not detect a statistically significant effect [typical RR 0.75 (95% CI 0.50, 1.13), RD -0.04 (95% CI -0.10, 0.02) (Figure 16)].

Bronchopulmonary dysplasia - oxygen requirement at 28 days (9 trials): Meta-analysis did not detect a statistically significant effect [typical RR 1.08 (95% CI 0.92, 1.26), RD 0.03 (95% CI -0.03, 0.08) (Figure 17)].

Bronchopulmonary dysplasia - oxygen requirement at 36 weeks' postmenstrual age (1 trial): TIPP 2001 did not detect a statistically significant effect [typical RR 1.06 (95% CI 0.92, 1.22), RD 0.03 (95% CI -0.04, 0.09) (Figure 18)].

Duration of supplemental oxygen (4 trials): Meta-analysis did not detect a statistically significant effect [WMD 3.76 days (95% CI -4.23, 11.74) (Figure 19)].

Pulmonary haemorrhage (4 trials): Meta-analysis did not detect a statistically significant effect [typical RR 0.84 (95% CI 0.66, 1.07), RD -0.02 (95% CI -0.06, 0.01) (Figure 20)].

There is no evidence of statistical heterogeneity in any of the meta-analyses; I²= 0%.

Renal outcomes (1.21 - 1.22).

Oliguria/anuria (8 trials): Meta-analysis showed a statistically significantly higher incidence in infants who receive prophylactic indomethacin [typical RR 1.90 (95% CI 1.45, 2.47), RD 0.06 (0.04, 0.08), NNTH 16 (Figure 21)].

Elevated serum creatinine (4 trials): Meta-analysis did not detect a statistically significant difference [typical RR 1.09 (95% CI 0.47, 2.51), RD 0.00 (95% CI -0.03, 0.03) (Figure 22)].

There is no evidence of statistical heterogeneity in either of these meta-analyses; I²= 0%.

Electrolyte disturbances (3 trials): Mahony 1985 reported no statistically significant differences in mean plasma sodium, potassium and creatinine levels on day three. Vincer 1987 reported significantly higher mean plasma sodium levels in the treatment group on days three and four. Rennie 1986a reported no significant differences in mean plasma sodium levels on days one and two following treatment. Data synthesis was not possible because of the differences in the methods of defining these outcomes.

Gastrointestinal outcomes (1.23 - 1.24).

Necrotising enterocolitis (12 trials): Meta-analysis did not detect a statistically significant difference [typical RR 1.09 (95% CI 0.82,1.46), RD 0.01 (95% CI -0.01, 0.03) (Figure 23)].There is no evidence of statistical heterogeneity in the meta-analysis; I²= 0%.

Gastrointestinal perforation (1 trial): TIPP 2001 did not find a statistically significant difference [typical RR 1.12 (0.71,1.79), RD 0.01 (95% CI -0.02, 0.03) (Figure 24)].

Enteral feeds intolerance: Not reported in any of the trials.

Haemostasis outcomes (1.25 - 1.26)

Excessive bleeding (5 trials): Meta-analysis did not detect a statistically significant difference [typical RR 0.74 (95% CI 0.40, 1.38), RD -0.01 (95% CI -0.02, 0.01) (Figure 25)]

Thrombocytopaenia (4 trials): Meta-analysis did not detect a statistically significant difference [typical RR 0.50 (95% CI 0.11, 2.22), RD -0.01 (95%CI -0.03, 0.01) (Figure 26)].

There is no evidence of statistical heterogeneity in either of the meta-analyses; I²= 0%.

Retinopathy of prematurity (1.27 - 1.28)

Any ROP (5 trials): Meta-analysis did not detect a statistically significant difference [typical RR 1.02 (95% CI 0.92, 1.12) (Figure 27)]

Severe ROP (2 trials): Meta-analysis did not detect a statistically significant difference [typical RR 1.75 (95% CI 0.92, 3.34) (Figure 28)].

There is no evidence of statistical heterogeneity in either of the meta-analyses; I²= 0% - 8%.

SUBGROUP ANALYSES

1. Very preterm or VLBW infants: Most trials restricted participation to VLBW infants. Only four small trials allowed infants of higher birth weight (< 1750 grams) to participate. Subgroup analysis excluding only the small number of infants with birth weight 1500 to 1750 grams was not possible.

2. Extremely preterm or ELBW infants: The largest single trial restricted participation to ELBW infants (TIPP 2001). The other trials had upper birth weight bounds between 1250 and 1500 grams (and up to 1750 grams in four small trials). Subgroup analysis of only ELBW infants was not possible for these trials.

Forest plot inspection comparing effect size estimates of TIPP 2001 alone versus the pooled effect sizes of the meta-analyses did not generally reveal major differences in direction or size of effects apart from for the following outcomes related to IVH:

Any IVH (Figure 11): Meta-analysis (14 trials) found a statistically significant reduction: typical RR 0.88 (95% CI 0.80, 0.98), RD -0.04 (95% CI -0.08, -0.01), NNTB 25 (95% CI 12, 100). In comparison, TIPP 2001 did not detect a statistically significant difference: RR 1.01 (95% CI 0.88, 1.16), RD 0.00 (95% CI -0.05, 0.06).

Ventriculomegaly, periventricular leukomalacia or other white matter echo-abnormalities (Figure 13): Meta-analysis (6 trials) found a borderline statistically significant reduction: typical RR 0.80 (95% CI 0.65, 0.97), RD -0.04 (95% CI -0.07, 0.00) NNTB 25 (95% CI 14, infinity). In comparison, TIPP 2001 did not detect a statistically significant difference: RR 0.88 (95% CI 0.71, 1.09), RD -0.03 (95% CI -0.08, 0.02).

Discussion

Summary of main results

This systematic review of 19 randomised controlled trials in which more than 2800 preterm infants participated found evidence that prophylactic indomethacin does not have a substantial effect on mortality or neurodevelopmental outcomes. The homogeneity in the meta-analyses and the narrow confidence intervals around the estimates of effect suggest that small but potentially important effects are unlikely to exist and that further trials of this intervention are not a research priority.

With regard to secondary outcomes, the available evidence indicates that prophylactic administration of indomethacin has short term benefits including a reduction in the incidence of symptomatic PDA, the need for surgical PDA closure, and the incidence of severe IVH. Safety concerns have largely been allayed. The available data indicate that any indomethacin-associated renal impairment is transient and there is no evidence that prophylactic indomethacin affects the risk of NEC or clinically-important bleeding.

Overall completeness and applicability of evidence

The trials were generally of good methodological quality and the effect size estimates consistent between trials suggesting that the meta-analyses were valid. The participants in the included trials reflect the population for which this intervention is currently considered, that is VLBW and particularly ELBW infants. On post hoc inspection of forest plots, the findings appear consistent across trials conducted before surfactant replacement and antenatal corticosteroid therapy were established as standards of care compared with trials undertaken during the later 1990s.

Potential biases in the review process

Most of the trials included in the review were relatively small. Two large multi-centre studies contributed about 60% of the total number of participants (Ment 1994b; TIPP 2001). There is some variation in study design, particularly with regard to birth weight eligibility criteria and the indomethacin dosage regimens used but the meta-analyses did not reveal statistical heterogeneity. The validity of the long term assessment data is enhanced by the impressive completeness of follow-up in the largest trials. TIPP 2001 provided data on more than 95% of survivors at 18 months and showed no statistically significant differences in a variety of neurodevelopmental outcomes. Longer term assessments have not been performed in TIPP 2001 and some caution should perhaps be exercised in applying these findings at 18 months since it has been suggested that assessments done at a relatively young age may be insufficiently predictive of longer term neurodevelopmental outcomes, particularly with regard to cognitive functioning (Roberts 2009). However, Ment 1994b provided data on 85% of survivors at eight years and also failed to detect any statistically significant differences in a range of neurodevelopmental outcomes including educational and cognitive performance.

Authors' conclusions

Implications for practice

Given the lack of evidence of effect on long term outcomes, the decision to use prophylactic indomethacin will depend on the values that families and clinicians attach to the short term benefits. In neonatal units without ready access to cardiac diagnostic and therapeutic services, a reduction in symptomatic PDA and a reduction in the need for surgical closure may be considered a greater benefit than in other units with ready access to these services. Cost implications may need to be considered although economic evaluation of this intervention has been limited to date (TIPP 2001).

Implications for research

Further randomised controlled trials of prophylactic indomethacin versus placebo are unlikely to be considered a research priority. Exploring and evaluating parental perceptions and concerns regarding the use of prophylactic indomethacin may help guide policy and practice development.
Although data are available on long term neurodevelopmental outcomes at the age of 18 months to five years in many children and at eight years in a smaller cohort, continuing follow-up of these children would be justified as more subtle differences in later childhood and adulthood may become apparent (Roberts 2009).

Acknowledgements

The Cochrane Neonatal Review Group has been funded in part with Federal funds from the Eunice Kennedy Shriver National Institute of Child Health and Human Development National Institutes of Health, Department of Health and Human Services, USA, under Contract No. HHSN267200603418C.

Contributions of authors

Peter Fowlie developed the original protocol and undertook the inception review (Fowlie 1997).
Peter Fowlie and Peter Davis updated the review in 2002 (Fowlie 2002).
William McGuire and Peter Fowlie undertook the May 2010 revision and update .

Characteristics of studies

Characteristics of included studies

Bada 1989

Methods	Blinding of randomisation: can't tell Blinding of intervention: yes Blinding of outcome measurement: yes Complete (> 90%) follow-up: yes
Participants	141 VLBW infants. Excluded: IVH > grade 2.
Interventions	Indomethacin (3 iv doses - 0.2; 0.1; 0.1 mg/kg); first dose at 6 hours of age, then 12 hourly thereafter versus placebo (not described).
Outcomes	Death before hospital discharge IVH BPD (oxygen supplementation beyond 28 days) Pulmonary haemorrhage (blood up tube, consistent radiological findings, ventilation required) NEC (Bell stage 2 or 3 disease) Renal dysfunction (low urine output, elevated creatinine and urea)
Notes	Published in abstract form only.

Risk of bias table

Item	Judgement	Description
Adequate sequence generation?	Unclear
Allocation concealment?	Unclear
Blinding?	Yes	Blinding of intervention - yes Blinding of outcome measurement(s) - yes
Incomplete outcome data addressed?	Yes	Complete (> 90%) follow-up - yes
Free of selective reporting?	Unclear
Free of other bias?	Unclear

Bandstra 1988

Methods	Blinding of randomisation: yes Blinding of intervention: yes Blinding of outcome measurement: yes Complete (> 90%) follow-up: Short term outcomes - yes; Long-term neurodevelopmental outcomes - no (76%).
Participants	199 infants with birthweight <1300 grams. No cranial ultrasound screening before study entry.
Interventions	Indomethacin (3 iv doses - 0.2; 0.1; 0.1 mg/kg), first dose at less than 12 hours of age, 12 hourly thereafter vs. an equal volume of saline placebo.
Outcomes	Death before hospital discharge and death (up to 24 months) IVH Clinically significant PDA; PDA ligation Duration of supplemental oxygen Duration of ventilation Chronic lung disease Pneumothorax Episodes of sepsis NEC ROP: any and severe Renal function (oliguria < 1 ml/kg/hour) IVH grade II - IV; PVL; Long-term outcome assessed as the latest of 6, 12, 18, 24 months visits (numbers not specified). Bayley Mental Development Index (MDI) - Abnormal < 68; Bayley Physical Developmental Index (PDI) - Abnormal < 68; Death or neurosensory impairment (death or Bayley MDI <68); Heamostasis - bleeding time and platelet count
Notes	Data on 149 infants available for long-term follow-up.

Risk of bias table

Item	Judgement	Description
Adequate sequence generation?	Unclear
Allocation concealment?	Yes	Adequate
Blinding?	Yes	Blinding of intervention - yes Blinding of outcome measurement(s) - yes
Incomplete outcome data addressed?	Yes	Complete (> 90%) follow-up: yes
Free of selective reporting?	Unclear
Free of other bias?	Unclear

Couser 1996

Methods	Blinding of randomisation: yes Blinding of intervention: yes Blinding of outcome measurement: yes Complete (> 90%) follow-up: yes for short term outcomes but 77% for long term outcomes.
Participants	90 (of 93 randomised) newborn infants 23 - 29 weeks gestation, birth weight 600 - 1250 grams. No cranial ultrasound screening before study entry. All infants received prophylactic surfactant at initial resuscitation. Follow-up data available on 68 of 88 surviving infants.
Interventions	Indomethacin vs. normal saline placebo. Indomethacin dosage: 0.1 mg/kg, within 24 hours of birth followed by same dose every 24 hours thereafter for a total of 6 doses.
Outcomes	Neurodevelopmental impairment including cerebral palsy at 36 months corrected age Clinically significant PDA IVH grade 3 or 4 Mortality Duration of supplementary oxygen requirement NEC ROP stage 3 Chronic lung disease (supplementary oxygen at 28 days plus chest Xray changes) Urine output reduced to < 1.0 ml/kg/hour at any time during first 7 days
Notes

Risk of bias table

Item	Judgement	Description
Adequate sequence generation?	Yes	Adequate
Allocation concealment?	Yes	Adequate (pharmacy prepared vials)
Blinding?	Yes	Blinding of intervention - yes Blinding of outcome measurement(s) - yes
Incomplete outcome data addressed?	Yes	Complete (> 90%) follow-up: yes
Free of selective reporting?	Unclear
Free of other bias?	Unclear

Domanico 1994

Methods	Blinding of randomisation: can't tell Blinding of intervention: yes Blinding of outcome measurement: Yes Complete (> 90%) follow-up: yes
Participants	100 preterm infants, birth weight < 1250 grams
Interventions	Indomethacin vs. equal volume of placebo (saline). Indomethacin dosage: 3 doses 0.2, 0.1, 0.1 mg/kg; first dose < 12 hours, second dose 12 hours later, final dose 36 hours after first dose
Outcomes	PDA (Diagnosed by echocardiography on day 3-5) Pulmonary haemorrhage IVH grade 3 or 4 Incomplete data on duration of ventilation and duration of supplementary oxygen requirement
Notes	Published in abstract form only.

Risk of bias table

Item	Judgement	Description
Adequate sequence generation?	Unclear
Allocation concealment?	Unclear
Blinding?	Yes	Blinding of intervention - yes Blinding of outcome measurement(s) - yes
Incomplete outcome data addressed?	Yes	Complete (> 90%) follow-up: yes
Free of selective reporting?	Unclear
Free of other bias?	Unclear

Gutierrez 1987

Methods	Blinding of randomisation: yes Blinding of intervention: yes Blinding of outcome measurement: yes Complete (>90%) follow-up: yes
Participants	59 newborn infants less than 34 weeks gestation and less than 1751 grams birth weight
Interventions	IV indomethacin vs. placebo (saline). Indomethacin dosage: 3 doses, 0.2, 0.1, 0.1 mg/kg first dose less than 24 hours of age, then 12 hourly thereafter
Outcomes	Death Symptomatic PDA (Cabal-Siassi score > 3)
Notes	Details were obtained from the trial registration with the Oxford Database of Perinatal Trials.

Risk of bias table

Item	Judgement	Description
Adequate sequence generation?	Yes	Adequate
Allocation concealment?	Yes	Adequate (sealed envelopes)
Blinding?	Yes	Blinding of intervention - yes Blinding of outcome measurement(s) - yes
Incomplete outcome data addressed?	Yes	Complete (> 90%) follow-up: yes
Free of selective reporting?	Unclear
Free of other bias?	Unclear

Hanigan 1988

Methods	Blinding of randomisation: yes Blinding of intervention: yes Blinding of outcome measurement: yes Complete (> 90%) follow-up: yes
Participants	111 VLBW infants. All had normal cranial ultrasound examination before study entry.
Interventions	IV prophylactic indomethacin versus saline placebo. Dose of study drug given before 12 hours of age and then at 24, 48 and 72 hours of age. Indomethacin dosage: 0.1 mg/kg.
Outcomes	Death IVH (Krishnamoorthy classification) PDA Duration of ventilation Pneumothorax
Notes

Risk of bias table

Item	Judgement	Description
Adequate sequence generation?	Yes	Adequate
Allocation concealment?	Yes	Adequate (sealed envelopes)
Blinding?	Yes	Blinding of intervention - yes Blinding of outcome measurement(s) - yes
Incomplete outcome data addressed?	Yes	Complete (> 90%) follow-up: yes
Free of selective reporting?	Unclear
Free of other bias?	Unclear

Krueger 1987

Methods	Blinding of randomisation: can't tell Blinding of intervention: no Blinding of outcome measurement: no Complete (> 90%) follow-up: yes
Participants	32 VLBW infants who were ventilator dependent at 24 hours of age with a diagnosis of RDS. Excluded infants with US or clinical evidence of IVH.
Interventions	IV prophylactic indomethacin, single dose (0.2 mg/kg) at 24 hours of age versus nothing (no placebo used).
Outcomes	Death Symptomatic PDA IVH Duration of ventilation Chronic lung disease NEC Renal insufficiency (Input/output ratio in fixed time period following treatment - 0-24 hour & 25 - 48 hours; serum creatinine)
Notes

Risk of bias table

Item	Judgement	Description
Adequate sequence generation?	Unclear
Allocation concealment?	Unclear
Blinding?	No	Blinding of intervention - no Blinding of outcome measurement(s) - no
Incomplete outcome data addressed?	Yes	Complete (> 90%) follow-up: yes
Free of selective reporting?	Unclear
Free of other bias?	Unclear

Mahony 1985

Methods	Blinding of randomisation: yes Blinding of intervention: yes Blinding of outcome measurement: yes Complete (> 90%) follow-up: yes
Participants	110 infants, birthweight <1300 grams
Interventions	IV prophylactic indomethacin, 3 doses (0.2, 0.1, 0.1 mg/kg), first dose at 12 -18 hours of age, second dose 12 hours after the first and third dose 24 hours after the second versus placebo (unspecified)
Outcomes	Mortality Symptomatic PDA and all PDA IVH Duration of oxygen dependence Duration of mechanical endotracheal ventilation Incidence of sepsis Incidence of NEC Incidence of ROP Parameters of renal function (serum creatinine and electrolytes)
Notes	Six early deaths (3 in each group) which were not included in the denominators of any study outcome in the original article have been included for the purposes of this review.

Risk of bias table

Item	Judgement	Description
Adequate sequence generation?	Yes	Adequate
Allocation concealment?	Yes	Adequate
Blinding?	Yes	Blinding of intervention - yes Blinding of outcome measurement(s) - yes
Incomplete outcome data addressed?	Yes	Complete (> 90%) follow-up: yes
Free of selective reporting?	Unclear
Free of other bias?	Unclear

Ment 1985

Methods	Blinding of randomisation: yes Blinding of intervention: yes Blinding of outcome measurement: yes Complete (> 90%) follow-up: yes
Participants	48 newborn infants, birthweight < 1250 grams. Excluded any IVH on pre-study ultrasound examination.
Interventions	Indomethacin, 5 doses (0.2; 0.1 x 4 mg/kg), first dose at 6 hours, then 12 hourly thereafter versus saline placebo. Study medication stopped if IVH detected, abnormal bleeding, thrombocytopaenia, elevated plasma urea, or urine output <0.5 ml/kg/hr.
Outcomes	Mortality IVH All PDA Parameters of renal function; urine output and serum electrolytes Parameters of haemostasis; platelet abnormalities and bleeding problems
Notes	Dosage schedule changed to 0.1 mg/kg x 5 in trial after concern expressed at diminished urine output in infants receiving indomethacin. On the advice of an advisory committee "the study was terminated when statistical significance was achieved".

Risk of bias table

Item	Judgement	Description
Adequate sequence generation?	Yes	Adequate
Allocation concealment?	Yes	Adequate
Blinding?	Yes	Blinding of intervention - yes Blinding of outcome measurement(s) - yes
Incomplete outcome data addressed?	Yes	Complete (> 90%) follow-up: yes
Free of selective reporting?	Unclear
Free of other bias?	Unclear

Ment 1988

Methods	Blinding of randomisation: yes Blinding of intervention: yes Blinding of outcome measurement: yes Complete (> 90%) follow-up: yes
Participants	36 newborn infants, birthweight < 1250 grams. Excluded infant with IVH on pre-study ultrasound examination.
Interventions	Indomethacin versus saline placebo. Indomethacin dosage: 3 doses (3 x 0.1 mg/kg), first dose 6 - 12 hours of age, 24 hourly thereafter. Study medication stopped if IVH detected, abnormal bleeding, thrombocytopaenia, elevated plasma urea, or urine output <0.5 ml/kg/hr.
Outcomes	Death IVH PDA Renal function (electrolyte abnormality, urine output) Haemostasis (Platelet count, clinical bleeding)
Notes

Risk of bias table

Item	Judgement	Description
Adequate sequence generation?	Yes	Adequate
Allocation concealment?	Yes	Adequate
Blinding?	Yes	Blinding of intervention - yes Blinding of outcome measurement(s) - yes
Incomplete outcome data addressed?	Yes	Complete (> 90%) follow-up: yes
Free of selective reporting?	Unclear
Free of other bias?	Unclear

Ment 1994a

Methods	Blinding of randomisation: yes Blinding of intervention: yes Blinding of outcome measurement: yes Complete (> 90%) follow-up: yes
Participants	61 newborn infants all with non-severe IVH (grade 1) at time of enrolment. Birthweight < 1250 grams
Interventions	Indomethacin versus saline placebo. Indomethacin dosage: 3 doses (3 x 0.1 mg/kg), first dose at 6 - 12 hours of age, 24 hourly thereafter
Outcomes	Death Extension of IVH Closure of PDA NEC Renal function (urine output < 0.5 ml/kg/hour, serum creatinine > 159 micromol/L) Haemostasis (platelet count <50000/mm, clinical bleeding)
Notes

Risk of bias table

Item	Judgement	Description
Adequate sequence generation?	Yes	Adequate
Allocation concealment?	Yes	Adequate
Blinding?	Yes	Blinding of intervention - yes Blinding of outcome measurement(s) - yes
Incomplete outcome data addressed?	Yes	Complete (> 90%) follow-up - yes for in hospital outcomes, no for longer term neurodevelopmental outcomes
Free of selective reporting?	Unclear
Free of other bias?	Unclear

Ment 1994b

Methods	Blinding of randomisation: yes Blinding of intervention: yes Blinding of outcome measurement: yes Complete (> 90%) follow-up: Outcomes prior to hospital discharge - yes; long-term neurodevelopmental outcomes - no.
Participants	431 newborn infants, birthweight < 1250 grams. Excluded infants with any IVH on pre-study cranial ultrasound.
Interventions	IV prophylactic indomethacin versus saline placebo. Indomethacin dosage: 3 doses (3 x 0.1 mg/kg), first dose at 6 - 12 hours of age, 24 hourly thereafter by slow infusion (5 - 10 minutes)
Outcomes	Death IVH PDA NEC Renal impairment (serum creatinine > 1.8 mg/dL) Impaired haemostasis (platelet count < 50000/mm, clinical bleeding) Stanford-Binet Intelligence Scale Peabody Picture Vocabulary Test- Revised Cerebral palsy on clinical examination - spastic diplegia, tetraplegia, hemiplegia Blindness (not further defined) Deafness (not further defined)
Notes	431 infants were randomised. 45 died before hospital discharge and their group of allocation is known. At 36 months follow-up, 343 (89% of survivors) were assessed for the presence or absence of cerebral palsy. Fewer were formally assessed for hearing impairment (135) and visual impairment (158). 251 infants underwent objective cognitive function testing. Cognitive function testing was limited to children who spoke English as their first and only language because of concerns that the instruments used were not valid in non-English speaking or multilingual children. The proportions of survivors who were tested for cognitive function at follow-up were similar for the indomethacin and placebo groups. However, no data were provided on those children not assessed. At 54-months follow-up, vision and hearing were assessed in 337 infants, presence or absence of cerebral palsy in 323 and cognitive testing in 233. For the purposes of this review, we used the 54-month outcomes for vision and hearing and the 36-month outcome for cerebral palsy to minimise loss to follow-up. Follow-up neurodevelopmental and/or educational outcomes assessments at aged 8 years were reported for 328 of 384 surviving children (85%).

Risk of bias table

Item	Judgement	Description
Adequate sequence generation?	Yes	Adequate
Allocation concealment?	Yes	Adequate
Blinding?	Yes	Blinding of intervention - yes Blinding of outcome measurement(s) - yes
Incomplete outcome data addressed?	Yes	Complete (> 90%) follow-up - yes for in hospital outcomes, no for longer term neurodevelopmental outcomes
Free of selective reporting?	Unclear
Free of other bias?	Unclear

Morales-Suarez 1994

Methods	Blinding of randomisation: can't tell Blinding of intervention: yes Complete follow-up: yes Blind outcome assessment: yes
Participants	80 preterm infants with gestational ages between 28 and 36 weeks, intubated in the delivery room and requiring ventilation in ICU. Excluded those with IVH on admission US, platelet count < 50,000, oliguria and pneumothorax
Interventions	IV prophylactic indomethacin 0.1 mg/kg in first 12 hours then 2 further doses 12 hours apart versus equal volume of normal saline placebo.
Outcomes	Death to hospital discharge IVH - all and severe Symptomatic PDA Pneumothorax
Notes

Risk of bias table

Item	Judgement	Description
Adequate sequence generation?	Unclear
Allocation concealment?	Unclear
Blinding?	Yes	Blinding of intervention - yes Blinding of outcome measurement(s) - yes
Incomplete outcome data addressed?	Yes	Complete follow-up: yes
Free of selective reporting?	Unclear
Free of other bias?	Unclear

Puckett 1985

Methods	Blinding of randomisation: can't tell Blinding of intervention: can't tell Blinding of outcome measurement: can't tell Complete (> 90%) follow-up: no
Participants	32 newborn infants, birthweight < 1400 grams
Interventions	Indomethacin vs. placebo (unspecified). Indomethacin dosage: 3 doses (3 x 0.2 mg/kg), first dose at less than 24 hours, 12 hourly thereafter
Outcomes	Death PDA IVH Duration of mechanical ventilation Duration of supplemental oxygen requirement
Notes	Details of this study are available in abstract only.

Risk of bias table

Item	Judgement	Description
Adequate sequence generation?	Unclear
Allocation concealment?	Unclear
Blinding?	Unclear	Blinding of intervention - unclear Blinding of outcome measurement(s) - unclear
Incomplete outcome data addressed?	No	Complete follow-up: no
Free of selective reporting?	Unclear
Free of other bias?	Unclear

Rennie 1986a

Methods	Blinding of randomisation: can't tell Blinding of intervention: can't tell Blinding of outcome measurement: can't tell. Complete (> 90%) follow-up: yes
Participants	50 newborn infants, birthweight < 1750 grams. Excluded infants with IVH on pre-study US.
Interventions	Indomethacin versus an equal volume of saline placebo. Indomethacin dosage: 3 doses (3 x 0.2 mg/kg), first dose at less than 24 hours, 24 hourly thereafter
Outcomes	Death Clinical PDA requiring treatment IVH Duration of ventilation Duration of oxygen supplementation Chronic lung disease Pneumothorax Renal impairment (peak serum creatinine, "renal impairment", serum sodium on days 1 and 2) Impaired haemostasis ("GI bleed", bleeding time)
Notes

Risk of bias table

Item	Judgement	Description
Adequate sequence generation?	Unclear
Allocation concealment?	Unclear
Blinding?	Unclear	Blinding of intervention - unclear Blinding of outcome measurement(s) - unclear (one member of nursing staff prepared study drug vials)
Incomplete outcome data addressed?	Yes	Complete (> 90%) follow-up: yes
Free of selective reporting?	Unclear
Free of other bias?	Unclear

Supapannachart 1999

Methods	Blinding of randomisation: yes (sealed envelopes) Blinding of intervention: yes Complete follow-up: yes Blind outcome assessment: yes.
Participants	30 newborn infants with birth weights < 1250g and <24 hours old. Excluded: thrombocytopenia, elevated creatinine, overt bleeding, poor urine output and major congenital anomalies.
Interventions	IV prophylactic indomethacin 0.2 mg/kg initially, then 0.1 mg/kg x 2 doses, 12 hours apart versus an equal volume of saline placebo.
Outcomes	Death Symptomatic PDA PDA ligation BPD IVH: all and severe NEC Diminished urine output Any ROP
Notes

Risk of bias table

Item	Judgement	Description
Adequate sequence generation?	Yes	Adequate
Allocation concealment?	Yes	Adequate
Blinding?	Yes	Blinding of intervention - yes Blinding of outcome measurement(s) - yes
Incomplete outcome data addressed?	Yes	Complete (> 90%) follow-up: yes
Free of selective reporting?	Unclear
Free of other bias?	Unclear

TIPP 2001

Methods	Blinding of randomisation: yes Blinding of intervention: yes Blind outcome assessment: yes Complete follow-up (>90%): yes
Participants	1202 ELBW infants, birthweight 500-999 grams between 2 and 6 hours of age. Excluded known cardiac or renal disease, dysmorphic features, platelet count < 50,000/ml, maternal indomethacin therapy or overt bleeding. No screening for IVH before study entry.
Interventions	Indomethacin versus an equal volume of normal saline placebo (both masked using yellow tape). Indomethacin dose: 0.1 mg/kg every 24 hours for 3 doses starting between 2 and 6 hours of age.
Outcomes	Death PDA PDA ligation BPD (36 weeks) IVH White matter injury on cranial ultrasound Bayley Mental Developmental Index Blindness Deafness Cerebral palsy Death or major impairment NEC and gastrointestinal perforation Diminished urine output Excessive clinical bleeding Pulmonary haemorrhage ROP (any and grade 3 or worse)
Notes	Follow-up outcomes assessed at 18 months.

Risk of bias table

Item	Judgement	Description
Adequate sequence generation?	Yes	Adequate
Allocation concealment?	Yes	Adequate
Blinding?	Yes	Blinding of intervention - yes Blinding of outcome measurement(s) - yes
Incomplete outcome data addressed?	Yes	Complete follow-up (>90%): yes
Free of selective reporting?	Unclear
Free of other bias?	Unclear

Vincer 1987

Methods	Blinding of randomisation: can't tell Blinding of intervention: yes Blinding of outcome measurement: yes Complete (> 90%) follow-up: yes
Participants	30 newborn infants, birthweight < 1500 grams
Interventions	IV prophylactic indomethacin vs. an equal volume of normal saline. Indomethacin dosage: 3 doses (3 x 0.2 mg/kg), first dose at 12 hours of age, 12 hourly thereafter
Outcomes	Cerebral palsy at 2 years corrected age Death IVH Symptomatic PDA Evolving chronic lung disease (clinical signs, pCO2 > 60 mm Hg at 2 weeks of age) NEC ROP Renal impairment
Notes

Risk of bias table

Item	Judgement	Description
Adequate sequence generation?	Unclear
Allocation concealment?	Unclear
Blinding?	Yes	Blinding of intervention - yes Blinding of outcome measurement(s) - yes
Incomplete outcome data addressed?	Yes	Complete (> 90%) follow-up: yes
Free of selective reporting?	Unclear
Free of other bias?	Unclear

Yaseen 1997

Methods	Blinding of randomisation: yes - sealed, sequentially numbered and coded envelopes Blinding of intervention: yes Blind outcome assessment: yes Complete follow-up (>90%): yes
Participants	27 preterm infants, birthweight <1750g, RDS requiring ventilation with > 30% oxygen. Excluded if platelets < 75,000/ml, creatinine >180 micromol/L, serum bilirubin > 90 micromol/L in first 8 hours
Interventions	IV prophylactic indomethacin versus an equal volume of saline. First dose 0.2 mg/kg at 12 hours then repeated twice at 24 hour intervals.
Outcomes	Death before hospital discharge; IVH grades 3 and 4: BPD at 28 days; duration of supplemental oxygen; NEC; duration of hospital stay.
Notes

Risk of bias table

Item	Judgement	Description
Adequate sequence generation?	Yes	Adequate
Allocation concealment?	Yes	Adequate
Blinding?	Yes	Blinding of intervention - yes Blinding of outcome measurement(s) - yes
Incomplete outcome data addressed?	Yes	Complete (> 90%) follow-up: yes
Free of selective reporting?	Unclear
Free of other bias?	Unclear

ROP=retinopathy of prematurity
CP=cerebral palsy
BPD=bronchopulmonary dysplasia
NEC=necrotising enterocolitis
PDA=patent ductus arteriosus

Characteristics of excluded studies

Bada 1996

Reason for exclusion	These data are presented in abstract only. From the limited published information, it is not possible to determine if this is follow-up of an RCT or not, hence the data are not included in the review. However, it seems likely it may relate to the study listed in the "included studies" - Bada 1989.

Cotton 1980

Reason for exclusion	Not a study of indomethacin given prophylactically.

Cotton 1983

Reason for exclusion	No original data on prophylactic indomethacin.

Gersony 1983

Reason for exclusion	Not a study of indomethacin given prophylactically.

Hammerman 1986

Reason for exclusion	Not an RCT.

Hammerman 1987

Reason for exclusion	Not a study of indomethacin used prophylactically. All the infants enrolled had echocardiographic evidence of a PDA at 48-72 hours of life.

Hammerman 1990

Reason for exclusion	Not a study of indomethacin used prophylactically.

Hammerman 1995

Reason for exclusion	Not an RCT.

Kaapa 1983

Reason for exclusion	Not a study of indomethacin used prophylactically.

Krauss 1989

Reason for exclusion	Not a study of indomethacin used prophylactically.

Lai 1990

Reason for exclusion	This is an RCT of ORAL indomethacin used prophylactically.

Mahony 1982

Reason for exclusion	Not a study of prophylactic indomethacin - all infants had "subclinical PDA".

Mardoum 1991

Reason for exclusion	Not an RCT of indomethacin given prophylactically.

Ment 1987

Reason for exclusion	This is probably the same study as Ment 1994b. Because it is not possible to determine this with certainty from the published information it has been labelled as a separate study. However, it probably reports interim analyses of the data included in this review taken from Ment 1994b and would not contribute any unique data.

Ment 1993

Reason for exclusion	From the published information, it is unclear if this was truly prophylactic indomethacin so the data presented cannot be included in this review. In fact, this might well be an analysis of a selected population from two studies that are included in this review - Ment 1994a and Ment 1994b. It is therefore likely that the findings are already incorporated into the review.

Merritt 1981

Reason for exclusion	Not a study of indomethacin used prophylactically.

Monset-Couchard 1983

Reason for exclusion	Not a trial of indomethacin used prophylactically: all infants had symptomatic PDA.

Mullett 1982

Reason for exclusion	This is an RCT of oral indomethacin and the treatment is not used prophylactically: all infants had clinical evidence of a PDA.

Nestrud 1980

Reason for exclusion	Not a trial of indomethacin given prophylactically: all the infants had PDA.

Neu 1980

Reason for exclusion	Not a study of indomethacin given prophylactically.

Rennie 1991

Reason for exclusion	Intervention was not indomethacin given prophylactically.

Rhodes 1988

Reason for exclusion	Not a trial of indomethacin used prophylactically.

Rudd 1983

Reason for exclusion	Not a study of indomethacin used prophylactically.

Valaes 1980

Reason for exclusion	Not a study of indomethacin used prophylactically.

van Overmeire 1995

Reason for exclusion	Not an RCT of indomethacin used prophylactically.

Vogtmann 1988

Reason for exclusion	This is a trial of oral prophylactic indomethacin.

Wagner 1984

Reason for exclusion	Not an RCT of prophylactic indomethacin.

Weesner 1987

Reason for exclusion	Not a study of prophylactic therapy - all infants enrolled had an asymptomatic PDA.

Wurtzel 1990

Reason for exclusion	This is a trial examining the effects of maternal antenatal indomethacin on the renal function of the newborn infant.

Yanagi 1981

Reason for exclusion	Not a study of indomethacin used prophylactically.

Yeh 1981

Reason for exclusion	Not an RCT of indomethacin given prophylactically - all infants had a documented PDA at entry to the trial.

Zamboni 1993

Reason for exclusion	Not an RCT of indomethacin.

References to studies

Included studies

Bada 1989

*Bada HS, Green RS, Pourcyrous M, et al. Indomethacin reduces the risks of severe intraventricular hemorrhage. Journal of Pediatrics 1989;115:631-7.

Bada HS, Green RS, Pourcyrous M, Leffler CW, Korones SB, Arheart K. Indomethacin reduces relative risks of severe intraventricular hemorrhage [Abstract]. Pediatric Research 1989;25:353A.

Pourcyrous M, Bada HS, Green RS, Korones SB. Safety of indomethacin use for newborn infants [Abstract]. Pediatric Research 1988;23:422A.

Bandstra 1988

*Bandstra ES, Montalvo BM, Goldberg RN, et al. Prophylactic indomethacin for prevention of intraventricular hemorrhage in premature infants. Pediatrics 1988;82:533-542.

Bandstra ES, Bauer CR, Duenas ML, Chao H, Montalvo BM, Bancalari E. Prophylactic indomethacin for prevention of intraventricular hemorrhage: neurodevelopmental follow-up [Abstract]. Annals of Neurology 1987;22:427A.

Bandstra ES, Duenas ML, Rodriguez I, et al. Prophylactic indomethacin for the prevention of intraventricular hemorrhage (IVH): neurodevelopmental follow-up [Abstract]. Pediatric Research 1987;21:391.

Setzer ES, Morse BM, Goldberg RN, Smith M, Bancalari E. Prophylactic indomethacin and intraventricular hemorrhage in the premature [Abstract]. Pediatric Research 1984;18:345A.

Setzer ES, Smith M, Goulding PJ, Bandstra TE. Severity of platelet dysfunction induced by prophylactic indomethacin in the premature [Abstract]. Pediatric Research 1984;18:346A.

Setzer ES, Torres-Arraut E, Gomez-del-Rio M, Young ML, Pacheco I, Ferrer PL, et al. Cardiopulmonary effects of prophylactic indomethacin in the very low birth weight infant [Abstract]. Pediatric Research 1984;18:346A.

Couser 1996

*Couser RJ, Ferrara TB, Wright GB, Cabalka AK, Schilling CG, et al. Prophylactic indomethacin therapy in the first 24 hours of life for the prevention of patent ductus arteriosus in preterm infants treated prophylactically with surfactant in the delivery room. Journal of Pediaitrcs 1996;128:631-7.

Couser RJ, Hoekstra RE, Ferrara B, Wright GB, Cabalka AK, Connet JE. Neurodevelopmental follow-up at 36 months' corrected age of preterm infants treated with prophylactic indomethacin. Archives of Pediatric and Adolescent Medicine 2000;154:598-602.

Domanico 1994

Domanico RS, Waldman JD, Lester LA, McPhillips HA, Catrambone JE, Covert RF. Prophylactic indomethacin reduces the incidence of pulmonary hemorrhage and patent ductus arteriosus in surfactant-treated infants < 1250 grams. Pediatric Research 1994;35:331A.

Gutierrez 1987

Gutierrez NG, Lapasset M. Prophylactic indomethacin and the incidence of patent ductus arteriosus in preterm neonates. In: Proceedings of the 3rd Argentinian Congress of Perinatology, Buenos Aires. Vol. 62. 1987.

Hanigan 1988

Hanigan WC, Kennedy G, Roemisch F, et al. Administration of indomethacin for the prevention of periventricular haemorrhage in high-risk neonates. Journal of Pediatrics 1988;112:941-7.

Krueger 1987

Krueger E, Mellander M, Bratton D, Cotton R. Prevention of symptomatic patent ductus arteriosus with a single dose of indomethacin. Journal of Pediatrics 1987;111:749-54.

Mahony 1985

Mahony L, Caldwell RL, Girod DA, et al. Indomethacin therapy on the first day of life in infants with very low birth weight. Journal of Pediatrics 1985;106:801-5.

Ment 1985

Ment LR, Duncan CC, Ehrenkranz RA, et al. Randomized indomethacin trial for prevention of intraventricular hemorrhage in very low birth weight infants. Journal of Pediatrics 1985;107:937-43.

Ment 1988

Ment LR, Duncan CC, Ehrenkranz RA, et al. Randomized low-dose indomethacin trial for prevention of intraventricular hemorrhage in very low birth weight neonates. Journal of Pediatrics 1988;112:948-55.

Ment 1994a

Ment LR, Oh W, Ehrenkranz, Phillip AGS et al. Low-dose indomethacin therapy and extension of intraventricular hemorrhage: a multicenter randomized trial. Journal of Pediatrics 1994;124:951-5.

Ment 1994b

Ment LR, Duncan CC, Ehrenkranz RA, Kleinman CS, Taylor KJW, Scott DT. Randomized low-dose indomethacin trial for the prevention of intraventricular hemorrhage in very low birth weight neonates [Abstract]. Annals of Neurology 1987;22:406-7.

Ment LR, Oh W, Ehrenkranz RA, Phillip AG, Vohr B, Allan W, et al. Low-dose indomethacin and prevention of intraventricular hemorrhage: a multicenter randomized trial. Pediatrics 1994;93:543-50.

Ment LR, Peterson BS, Meltzer JA, Vohr B, Allan W, Katz KH. A functional magnetic resonance imaging study of the long-term influences of early indomethacin exposure on language processing in the brains of prematurely born children. Pediatrics 2006;118:961-70.

Ment LR, Vohr B, Allan W, Westerveld M, Sparrow SS, Schneider KC, et al. Outcome of children in the indomethacin intraventricular hemorrhage prevention trial. Pediatrics 2000;105:485-91.

Ment LR, Vohr B, Oh W, Scott DT, Allen WC, Westerveld M, et al. Neurodevelopmental outcome at 36 months corrected age of preterm infants in the Multicenter Indomethacin Intraventricular Hemorrhage Prevention Trial. Pediatrics 1996;98:714-8.

Vohr BR, Allan WC, Westerveld M, et al. School-age outcomes of very low birth weight infants in the indomethacin intraventricular hemorrhage prevention trial. Pediatrics 2003;111:e340- 6.

Morales-Suarez 1994

Morales-Suarez M, Lemus-Varella L, Udaeta-Mora E, Cardiel-Marmolejo L, Rodriguez-Balderrama I, Liz-Cedilla RE. Indomethacin in the prevention of subependymal-intraventricular hemorrhage in preterm newborns with conventional mechanical ventilation. Boletin Medico del Hospital Infantil de Mexico 1992;49:217-24.

Morales-Suarez M, Sanchez-Gil T, Lemus-Varela L. Low dose indomethacin for prevention of intraventricular hemorrhage in the preterm infant with mechanical ventilation: Final report of a randomized study [Estudio comparavito de dosis baja de indometacina profilactica para hemorragia subependimaria/intraventricular en neonatos pretermino con ventilation mecanica]. Boletin Medico del Hospital Infantil de Mexico 1994;51:389 -394.

Puckett 1985

Puckett CG, Cox MA, Haskins KS, Fisher DJ. Prophylactic indomethacin (I) for the prevention of patent ductus arteriosus (PDA) [Abstract]. Pediatric Research 1985;19:358.

Rennie 1986a

Rennie JM, Doyle J, Cooke RWI. Early administration of indomethacin to preterm infants. Archives of Disease in Childhood 1986;61:233-8.

Supapannachart 1999

Supapannachart S, Khowsathit P, Patchakapati B. Indomethacin prophylaxis for patent ductus arteriosus (PDA) in infants with a birth weight of less than 1250 grams. Journal of the Medical Associaition of Thailand 1999;82:S87-S91.

TIPP 2001

Ohlsson A, Roberts RS, Schmidt B, Davis P, Moddeman D, Saigal S, et al. Male/female differences in indomethacin effects in preterm infants. Journal of Pediatrics 2005;147:860-2. [PubMed: 16356449]

* Schmidt B, Davis P, Moddemann D, Ohlsson A, Roberts RS, Saigal S, et al. Long-term effects of indomethacin prophylaxis in extremely-low-birth-weight infants. New England Journal of Medicine 2001;344:1966-72.

Schmidt B, Roberts RS, Fanaroff A, Davis P, Kirpalani HM, Nwaesei C, et al. Indomethacin prophylaxis, patent ductus arteriosus, and the risk of bronchopulmonary dysplasia: further analyses from the Trial of Indomethacin Prophylaxis in Preterms (TIPP). Journal of Pediatrics 2006;148:730-4.

Zupancic JA, Richardson DK, O'Brien BJ, Cronin CG, Schmidt B, Roberts R, et al. Retrospective economic evaluation of a controlled trial of indomethacin prophylaxis for patent ductus arteriosus in premature infants. Early Human Development 2006;82:97-103.

Vincer 1987

* Vincer M, Allen A, Evans J, Nwaesei C, Stinson D, Rees E, et al. Early intravenous indomethacin prolongs respiratory support in very low birth weight infants. Acta Paediatrica Scandinavica 1987;76:894-7.

Vincer M, Allen A. Does prophylactic indomethacin in VLBW (<1500 grams birth weight) infants cause cerebral palsy (CP)? Pediatric Research 1998;43:232.

Yaseen 1997

Yaseen H, al Umran K, Ali H, Rustum M, Darwich M, al-Faraidy A. Effects of early indomethacin administration on oxygenation and surfactant requirement in low birth weight infants. Journal of Tropical Pediatrics 1997;43:42-6.

Excluded studies

Bada 1996

Bada HS, Yolton KA, Duncan C, Wong SP, Pourcyrous M, Korones SB. Indomethacin (INDO) prophylaxis and outcome at school age [abstract]. Pediatric Research 1996;39:373A.

Cotton 1980

Cotton RB, Hickey DE, Graham TP, Stahlman MT. Effects of early indomethacin (I) on ventilatory status of preterm infants with symptomatic patent ductus arteriosus (sPDA) [abstract]. Pediatric Research 1980;14:442A.

Cotton 1983

Cotton L, Hickey D, Stahlman MT. Management of premature infants with symptomatic patent ductus arteriosus Intensive. In: Stern L, editor(s). Care in the Newborn. IV edition. New York: Masson Publishing Co, 1983:225-31.

Gersony 1983

Gersony WM, Peckham GJ, Ellison RC, Miettinen OS, Nadas AS. Effects of indomethacin in premature infants with patent ductus arteriosus: results of a national collaborative study. Journal of Pediatrics 1983;102:895-906.

Peckham GJ, Miettinen OS, Ellison RC, Kraybill EN, Gersony WM, Zeirler S, Nadas AS. Clinical course to 1 year if age in premature infants with patent ductus arteriosus: results of a multicenter randomized trial of indomethacin. Journal of Pediatrics 1984;104:285-91.

Hammerman 1986

Hammerman C, Strates E, Valaitis S. The silent ductus: its precursors and its aftermath. Pediatric Cardiology 1986;7:121-7.

Hammerman 1987

Hammerman C, Strates E, Komar K, Bui K. Failure of prophylactic indomethacin to improve the outcome of the very low birth weight infant. Developmental Pharmacology and Therapeutics 1987;10:393-404.

Hammerman 1990

Hammerman C, Aramburo MJ. Prolonged indomethacin therapy for the prevention of recurrences of patent ductus arteriosus. Journal of Pediatrics 1990;117:771-6.

Hammerman 1995

Hammerman C, Glaser J, Schimmel MS, Ferber B, Kaplan M, Eidelman AI. Continuous versus multiple rapid infusions of indomethacin: effects on cerebral blood flow velocity. Pediatrics 1995;95:244-8.

Kaapa 1983

Kaapa P, Lanning P, Koivisto M. Early closure of patent ductus arteriosus with indomethacin in preterm infants with idiopathic respiratory distress syndrome. Acta Paediatrica Scandanavia 1983;72:179-84.

Krauss 1989

Krauss AN, Fatica N, Lewis BS, Cooper R, Thaler HT, Cirrincione C, O'Loughlin J, Levin A, Engle MA, Auld PAM. Pulmonary function in preterm infants following treatment with intravenous indomethacin. American Journal of Diseases of Children 1989;143:78-81.

Lai 1990

Lai TH, Soong WJ, Hwang B. Indomethacin for the prevention of symptomatic patent ductus arteriosus in very low birth weight infants. Acta Paediatrica Sinica 1990;31:17-23.

Mahony 1982

*Mahony L, Carnero V, Brett C, Heymann MA, Clyman RI. Prophylactic indomethacin therapy for patent ductus arteriosus in very low birth weight infants. New England Journal of Medicine 1982;306:506-10.

Mahony L, Heymann MA, Carnero V, Brett C, Clyman RI. When to treat the patent ductus arteriosus with indomethacin in very low birth weight infants. Advances in Prostaglandin, Thromboxane, and Leukotriene Research 1983;12:491-4.

Mardoum 1991

Mardoum R, Bejar R, McFeely E, Peterson B, Merritt TA. Controlled study of the effects of indomethacin (INDO) on the cerebral blood flow velocities in the newborn infant [Abstract]. Pediatric Research 1988;23:554.

* Mardoum R, Bejar R, Merritt A, Berry C. Controlled study of the effects of indomethacin on cerebral blood flow velocities in newborn infants. Journal of Pediatrics 1991;118:112-5.

Ment 1987

Ment 1993

Ment LR, Oh W, Ehrenkrantz RA, Philip AGS, Schneider K, Katz KH, Taylor KJW, Duncan CC, Makuch. Risk period for intraventricular hemorrhage of the preterm neonate is independent of gestational age. Seminars in Perinatology 1993;17:338-41.

Merritt 1981

Merritt TA, Harris JP, Roghmann K, Wood B, Campanella V, Alexzon C, Manning J, Shapiro DL. Early closure of patent ductus arteriosus in very low birth weight infants: a controlled trial. Journal of Pediatrics 1981;99:281-6.

Monset-Couchard 1983

Monset-Couchard M, Dias-Mancano D, Murat I, Relier JP. Controlled trial of intravenous lyophilized indomethacin in the treatment of persistent ductus arteriosus in premature infants [French]. Pediatrie 1983;38:365-77.

Mullett 1982

*Mullett MD, Croghan TW, Myerberg DZ, Krall JM, Neal WA. Indomethacin closure of patent ductus arteriosus in prematures. Clinica Pediatrica 1982;21:217-20.

Mullett MD, Crogan TW, Myerberg DZ, Neal WA. Administration of oral indomethacin (I) to prematures with patent ductus arteriosus (PDA): a randomized double blind study [Abstract]. Pediatric Research 1980;14:606.

Nestrud 1980

Nestrud RM, Hill DE, Arrington RW, Beard AG, Dungan WT, Norton JB, Radinger RI. Indomethacin treatment in patent ductus arteriosus. A double blind study utilizing indomethacin plasma levels. Developmental Pharmacology and Therapeutics 1980;1:125-36.

Neu 1980

Neu J, Ariagno RL, Johnson JD, Pitlick PT, Cohen JS, Beets CL. A double blind study of the effects of oral indomethacin (IN) in preterm infants with patent ductus arteriosus (PDA) who failed medical management [Abstract]. Pediatric Research 1980;14:607.

Rennie 1991

Rennie JM, Cooke RWI. Prolonged low dose indomethacin for persistent ductus arteriosus of prematurity. Archives of Disease in Childhood 1991;66:55-8.

Rhodes 1988

Rhodes PG, Ferguson MG, Reddy NS, Joransen JA, Gibson J. Effects of prolonged versus acute indomethacin therapy in very low birth weight infants with patent ductus arteriosus. European Journal of Paediatrics 1988;147:481-4.

Rudd 1983

Rudd P, Montanez P, Hallidie-Smith K, Silverman M. Indomethacin treatment for patent ductus arteriosus in very low birthweight infants: double blind trial. Archives of Disease in Childhood 1983;58:267-70.

Valaes 1980

Valaes T, Moylan FMB, Cohn H, Chung K, Nagpaul K, Chrenoff HL, Kreidberg MB. Incidence and significance of PDA in preterm infants (PTI) and controlled blind trial of indomethacin (IND) [Abstract]. Pediatric Research 1980;14:452.

van Overmeire 1995

Van Overmeire B, Brus F, Van Acker KJ et al. Aspirin versus indomethacin treatment of patent ductus arteriosus in preterm infants with respiratory distress syndrome. Pediatric Research 1995;38:886-91.

Vogtmann 1988

Vogtmann C, Grubbe G, Ruckhaberle KE, Bottcher H, Ockert C. Effects of early therapy with indomethacin on the manifestation of a persistent ductus arteriosus in extremely underweight premature infants [German]. Monatsschrift Kinderheilkunde 1988;136:636-9.

Wagner 1984

Wagner HR, Ellison C, Zierler S, Lang P, Purohit DM, Behrendt D, Waldhausen JA. Surgical closure of patent ductus arteriosus in 268 preterm infants. Journal of Thoracic and Cardiovascular Surgery 1984;87:870-5.

Weesner 1987

Weesner KM, Dillard RG, Boyle RJ, Block SM. Prophylactic treatment of asymptomatic ductus arteriosus in premature infants with respiratory distress syndrome. Southern Medical Journal 1987;80:706-8.

Wurtzel 1990

Wurtzel D. Prenatal administration of indomethacin as a tocolytic agent: effect on neonatal renal function. Obstetrics and Gynecology 1990;76:689-92.

Yanagi 1981

Yanagi RM, Wilson A, Newfeld EA, Aziz KU, Hubt CE. Indomethacin treatment for symptomatic patent ductus arteriosus: a double blind control study. Pediatrics 1981;67:647-52.

Yeh 1981

*Yeh TF, Luken JA, Thalji A, Raval D, Carr I, Pildes RS. Intravenous indomethacin therapy in premature infants with persistent ductus arteriosus - a double blind controlled study. Journal of Pediatrics 1981;98:137-45.

Betkerur MV, Yeh TF, Miller K, Glasser RJ, Pildes RS. Indomethacin and its effect on renal function and urinary kallikrein excretion in premature infants with patent ductus arteriosus. Pediatrics 1981;68:99-102.

Yeh TF, Goldbarg HR, Henek T, Thalji A, Pildes RS. Intravenous indomethacin therapy in premature infants with patent ductus arteriosus. Causes of death and one year follow-up. American Journal of Diseases of Children 1982;136:803-7.

Yeh TF, Raval D, Pyati S, Pildes RS. Retinopathy of prematurity (ROP) and indomethacin therapy in premature infants with patent ductus arteriosus (PDA). Prostaglandins 1983;25:385-91.

Yeh TF, Thalji A, Luken L, Lilien L, Carr I, Pildes RS. Improved lung compliance following indomethacin therapy in premature infants with patent ductus arteriosus. Chest 1981;80:698-700.

Yeh TF, Wilks A, Singh J, Betkerur M, Lilien L, Pildes RS. Furosemide prevents the renal side effects of indomethacin therapy in premature infants with patent ductus arteriosus. Journal of Pediatrics 1982;101:433-7.

Zamboni 1993

Zamboni G, Piemonte G, Boner A et al. Influence of dietary taurine on vitamin D absorption. Acta Paediatrica 1993;82:811-5.

Other references

Additional references

Brown 1979

Brown ER. Increased risk of bronchopulmonary dysplasia in infants with patent ductus arteriosus. Journal of Pediatrics 1979;95:865.

Cifuentes 1979

Cifuentes RF, Olley PM, Balfe JW et al. Indomethacin and renal function in premature infants with persistent patent ductus arteriosus. Journal of Pediatrics 1979;95:583-7.

Cooke 2003

Cooke L, Steer P, Woodgate P. Indomethacin for asymptomatic patent ductus arteriosus in preterm infants. Cochrane Database of Systematic Reviews 2003, Issue 1. Art. No.: CD003745. DOI: 10.1002/14651858.CD003745.

Coombs 1990

Coombs RC, Morgan MEI, Durbin GM et al. Gut blood flow velocities in the newborn: effects of patent ductus arteriosus and parenteral indomethacin. Archives of Disease in Childhood 1990;65:1067-71.

Edwards 1990

Edwards AD, Wyatt JS, Richardson C et al. Effects of indomethacin on cerebral haemodynamics in very preterm infants. Lancet 1990;335:1491-5.

Evans 1990

Evans NJ, Archer LN. Postnatal circulatory adaptation in healthy term and preterm neonates. Archives of Disease in Childhood 1990;65:24-6.

Evans 1995

Evans N, Iyer P. Longitudinal changes in the diameter of the ductus arteriosus in ventilated preterm infants: correlation with respiratory outcomes. Archives of Disease in Childhood. Fetal and Neonatal Edition 1995;72:F156-61.

Evans 1996

Evans N, Kluckow M. Early determinants of right and left ventricular output in ventilated preterm infants. Archives of Disease in Childhood. Fetal and Neonatal Edition 1996;74:F88-94.

Fowlie 1996

Fowlie PW. Prophylactic indomethacin: systematic review and meta-analysis. Archives of Disease in Childhood 1996;74:F81-7.

Friedman 1978

Friedman Z, Whitman V, Maisels MJ et al. Indomethacin disposition and indomethacin-induced platelet dysfunction in premature infants. Journal of Clinical Pharmacology 1978;18:272-9.

Herrera 2007

Herrera C, Holberton J, Davis P. Prolonged versus short course of indomethacin for the treatment of patent ductus arteriosus in preterm infants. Cochrane Database of Systematic Reviews 2007, Issue 2. Art. No.: CD003480. DOI: 10.1002/14651858.CD003480.pub3 .

Heymann 1976

Heymann MA, Rudolph AM, Silverman NH. Closure of the ductus arteriosus in premature infants by inhibition of prostaglandin synthesis. New England Journal of Medicine 1976;295:530-3.

ICROP 1984

ICROP. An International Classification of Retinopathy of Prematurity. Pediatrics 1984;74:127-133.

Knight 2001

Knight DB. The treatment of patent ductus arteriosus in preterm infants. A review and overview of randomized trials. Seminars in Neonatology 2001;6:63-73.

Lipman 1982

Lipman B, Server GA, Brazy JE. Abnormal cerebral haemodynamics in preterm infants with patent ductus arteriosus. Pediatrics 1982;69:778-781.

Malviya 2008

Malviya M, Ohlsson A, Shah S. Surgical versus medical treatment with cyclooxygenase inhibitors for symptomatic patent ductus arteriosus in preterm infants. Cochrane Database of Systematic Reviews 2008, Issue 1. Art. No.: CD003951. DOI: 10.1002/14651858.CD003951.pub2 .

Mosalli 2008

Mosalli R, Alfaleh K. Prophylactic surgical ligation of patent ductus arteriosus for prevention of mortality and morbidity in extremely low birth weight infants. Cochrane Database of Systematic Reviews 2008, Issue 1. Art. No.: CD006181. DOI: 10.1002/14651858.CD006181.pub2 .

Ohlsson 2008

Ohlsson A, Walia R, Shah S. Ibuprofen for the treatment of patent ductus arteriosus in preterm and/or low birth weight infants. Cochrane Database of Systematic Reviews 2010, Issue 4. Art. No.: CD003481. DOI: 10.1002/14651858.CD003481.pub4 .

Papile 1978

Papile LA, Burstein J, Burstein R, Koffler H. Incidence and evolution of subependymal and intraventricular hemorrhage: a study of infants with birthweights less than 1,500 grams. Journal of Pediatrics 1978;92:529-34.

Roberts 2009

Roberts G, Doyle LW, Anderson PJ. The stability of the diagnosis of developmental disability between age 2 and 8 in a geographic cohort of very preterm children born In 1997. Archives of Disease in Childhood 2009;October 14:[Epub ahead of print].

Shah 2006

Ohlsson A, Shah SS. Ibuprofen for the prevention of patent ductus arteriosus in preterm and/or low birth weight infants. Cochrane Database of Systematic Reviews 2006, Issue 1. Art. No.: CD004213. DOI: 10.1002/14651858.CD004213.pub2 .

Other published versions of this review

Fowlie 1997

Fowlie PW. Intravenous indomethacin for preventing mortality and morbidity in very low birth weight infants. Cochrane Database of Systematic Reviews 1997, Issue 3. Art. No.: CD000174. DOI: 10.1002/14651858.CD000174.

Fowlie 2002

Fowlie PW, Davis PG. Prophylactic intravenous indomethacin for preventing mortality and morbidity in preterm infants. Cochrane Database of Systematic Reviews 2002, Issue 3. Art. No.: CD000174. DOI: 10.1002/14651858.CD000174 .

Outcome or Subgroup	Studies	Participants	Statistical Method	Effect Estimate
1.1 Death to hospital discharge	17	1567	Risk Ratio (M-H, Fixed, 95% CI)	0.82 [0.65, 1.03]
1.2 Death at latest follow-up	18	2769	Risk Ratio (M-H, Fixed, 95% CI)	0.96 [0.81, 1.12]
1.3 Death or severe neurosensory impairment	3	1491	Risk Ratio (M-H, Fixed, 95% CI)	1.02 [0.90, 1.15]
1.4 Neurological assessments (18-54 months)	5		Risk Ratio (M-H, Fixed, 95% CI)	Subtotals only
1.4.1 Cerebral palsy	4	1372	Risk Ratio (M-H, Fixed, 95% CI)	1.04 [0.77, 1.40]
1.4.2 Visual impairment	2	1274	Risk Ratio (M-H, Fixed, 95% CI)	1.26 [0.50, 3.18]
1.4.3 Hearing impairment	2	1259	Risk Ratio (M-H, Fixed, 95% CI)	1.02 [0.45, 2.33]
1.4.4 Severe neurodevelopmental impairment	3	1286	Risk Ratio (M-H, Fixed, 95% CI)	0.96 [0.79, 1.17]
1.5 Cognitive assessments (18-36 months)	1		Mean Difference (IV, Fixed, 95% CI)	Subtotals only
1.5.1 Stanford-Binet IQ score	1	233	Mean Difference (IV, Fixed, 95% CI)	4.60 [-0.51, 9.71]
1.5.2 Peabody Picture Vocabulary Test scores	1	233	Mean Difference (IV, Fixed, 95% CI)	4.70 [-0.54, 9.94]
1.6 School age neurological assessments	1		Risk Ratio (M-H, Fixed, 95% CI)	Subtotals only
1.6.1 Cerebral palsy aged 8 years	1	304	Risk Ratio (M-H, Fixed, 95% CI)	1.24 [0.59, 2.62]
1.6.2 Blind (receipt of services) aged 8 years	1	306	Risk Ratio (M-H, Fixed, 95% CI)	0.13 [0.01, 2.54]
1.6.3 Hearing impairment (requiring amplification) aged 8 years	1	295	Risk Ratio (M-H, Fixed, 95% CI)	0.78 [0.21, 2.86]
1.6.4 Abnormal neurological examination aged 8 years	1	305	Risk Ratio (M-H, Fixed, 95% CI)	1.14 [0.59, 2.24]
1.7 School age cognitive and educational outcomes	1		Risk Ratio (M-H, Fixed, 95% CI)	Subtotals only
1.7.1 WISC-III verbal IQ (<70)	1	328	Risk Ratio (M-H, Fixed, 95% CI)	0.92 [0.46, 1.85]
1.7.2 WISC-III performance IQ (<70)	1	328	Risk Ratio (M-H, Fixed, 95% CI)	0.99 [0.58, 1.69]
1.7.3 WISC-III full-scale IQ (<70)	1	328	Risk Ratio (M-H, Fixed, 95% CI)	1.16 [0.63, 2.14]
1.7.4 PPVT-R (<70)	1	321	Risk Ratio (M-H, Fixed, 95% CI)	0.54 [0.31, 0.93]
1.7.5 PIAT-R reading recognition (<70)	1	314	Risk Ratio (M-H, Fixed, 95% CI)	0.84 [0.39, 1.81]
1.7.6 PIAT-R reading comprehension (<70)	1	315	Risk Ratio (M-H, Fixed, 95% CI)	0.94 [0.52, 1.70]
1.7.7 PIAT-R mathematics (<70)	1	313	Risk Ratio (M-H, Fixed, 95% CI)	0.91 [0.56, 1.48]
1.8 All PDA (echo-diagnosed, symptomatic or not)	7	965	Risk Ratio (M-H, Fixed, 95% CI)	0.29 [0.22, 0.38]
1.9 Symptomatic PDA	14	2193	Risk Ratio (M-H, Fixed, 95% CI)	0.44 [0.38, 0.50]
1.10 PDA ligation	8	1791	Risk Ratio (M-H, Fixed, 95% CI)	0.51 [0.37, 0.71]
1.11 All IVH	14	2532	Risk Ratio (M-H, Fixed, 95% CI)	0.88 [0.80, 0.98]
1.12 Severe IVH (grades III - IV)	14	2588	Risk Ratio (M-H, Fixed, 95% CI)	0.66 [0.53, 0.82]
1.13 Ventriculomegaly, periventricular leukomalacia or other white matter echo-abnormalities	6	2013	Risk Ratio (M-H, Fixed, 95% CI)	0.80 [0.65, 0.97]
1.14 IVH that progresses	2	83	Risk Ratio (M-H, Fixed, 95% CI)	0.80 [0.44, 1.47]
1.15 Duration of assisted ventilation	4	417	Mean Difference (IV, Fixed, 95% CI)	-1.83 [-5.53, 1.87]
1.16 Pneumothorax and pneumopericardium	6	524	Risk Ratio (M-H, Fixed, 95% CI)	0.75 [0.50, 1.13]
1.17 Bronchopulmonary dysplasia (28 days)	9	1022	Risk Ratio (M-H, Fixed, 95% CI)	1.08 [0.92, 1.26]
1.18 Bronchopulmonary dysplasia (36 weeks' PMA)	1	999	Risk Ratio (M-H, Fixed, 95% CI)	1.06 [0.92, 1.22]
1.19 Duration of supplementary oxygen requirement	4	342	Mean Difference (IV, Fixed, 95% CI)	3.76 [-4.23, 11.74]
1.20 Pulmonary haemorrhage	4	1591	Risk Ratio (M-H, Fixed, 95% CI)	0.84 [0.66, 1.07]
1.21 Oliguria/anuria	8	2115	Risk Ratio (M-H, Fixed, 95% CI)	1.90 [1.45, 2.47]
1.22 Elevated serum creatinine	4	618	Risk Ratio (M-H, Fixed, 95% CI)	1.09 [0.47, 2.51]
1.23 Necrotising enterocolitis	12	2401	Risk Ratio (M-H, Fixed, 95% CI)	1.09 [0.82, 1.46]
1.24 Gastointestinal perforation	1	1202	Risk Ratio (M-H, Fixed, 95% CI)	1.13 [0.71, 1.79]
1.25 Excessive clinical bleeding (investigator defined)	5	1776	Risk Ratio (M-H, Fixed, 95% CI)	0.74 [0.40, 1.38]
1.26 Thrombocytopaenia (investigator defined)	4	618	Risk Ratio (M-H, Fixed, 95% CI)	0.50 [0.11, 2.22]
1.27 Any retinopathy of prematurity	5	1571	Risk Ratio (M-H, Fixed, 95% CI)	1.02 [0.92, 1.12]
1.28 Severe retinopathy of prematurity (stage 3 or more)	2	289	Risk Ratio (M-H, Fixed, 95% CI)	1.75 [0.92, 3.34]

Prophylactic intravenous indomethacin for preventing mortality and morbidity in preterm infants

Authors

Contact person

Peter W Fowlie

Dates

What's new

History

Abstract

Background

Objectives

Search methods

Selection criteria

Data collection and analysis

Results

Authors' conclusions

Plain language summary

Prophylactic intravenous indomethacin for preventing mortality and morbidity in preterm infants

Background

Description of the condition

Description of the intervention

How the intervention might work

Why it is important to do this review

Objectives

Methods

Criteria for considering studies for this review

Types of studies

Types of participants

Types of interventions

Types of outcome measures

Search methods for identification of studies

Electronic searches

Searching other resources

Data collection and analysis

Selection of studies

Data extraction and management

Assessment of risk of bias in included studies

Measures of treatment effect

Unit of analysis issues

Assessment of heterogeneity

Data synthesis

Subgroup analysis and investigation of heterogeneity

Results

Description of studies

Risk of bias in included studies

Effects of interventions

Discussion

Summary of main results

Overall completeness and applicability of evidence

Potential biases in the review process

Authors' conclusions

Implications for practice

Implications for research

Acknowledgements

Contributions of authors

Characteristics of studies

Characteristics of included studies

Bada 1989

Risk of bias table

Bandstra 1988

Risk of bias table

Couser 1996

Risk of bias table

Domanico 1994

Risk of bias table

Gutierrez 1987

Risk of bias table

Hanigan 1988

Risk of bias table

Krueger 1987

Risk of bias table

Mahony 1985

Risk of bias table

Ment 1985

Risk of bias table

Ment 1988

Risk of bias table

Ment 1994a

Risk of bias table

Ment 1994b

Risk of bias table