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Nasal intermittent positive pressure ventilation (NIPPV) versus nasal continuous positive airway pressure (NCPAP) for preterm neonates after extubation

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Abstract

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Background

Previous randomised trials and meta‐analyses have shown that nasal continuous positive airway pressure (NCPAP) is a useful method for providing respiratory support after extubation. However, this treatment sometimes 'fails' in infants, and they may require endotracheal re‐intubation with its attendant risks and expense. Nasal intermittent positive pressure ventilation (NIPPV) can augment NCPAP by delivering ventilator breaths via nasal prongs. Older children and adults with chronic respiratory failure benefit from NIPPV, and the technique has been applied to neonates. However, serious side effects including gastric perforation have been reported with older methods of providing NIPPV.

Objectives

Primary objective

To compare effects of management with NIPPV versus NCPAP on the need for additional ventilatory support in preterm infants whose endotracheal tube was removed after a period of intermittent positive pressure ventilation.

Secondary objectives

To compare rates of gastric distension, gastrointestinal perforation, necrotising enterocolitis and chronic lung disease; duration of hospitalisation; and rates of apnoea, air leak and mortality for NIPPV and NCPAP.

Search methods

We used the standard search strategy of the Cochrane Neonatal Review Group to search the Cochrane Central Register of Controlled Trials (CENTRAL; 2015, Issue 9), MEDLINE via PubMed (1966 to 28 September 2015), Embase (1980 to 28 September 2015) and the Cumulative Index to Nursing and Allied Health Literature (CINAHL; 1982 to 28 September 2015). We also searched clinical trials databases, conference proceedings and reference lists of retrieved articles for randomised controlled trials and quasi‐randomised trials.

Selection criteria

We included randomised and quasi‐randomised trials comparing use of NIPPV versus NCPAP in extubated preterm infants. NIPPV included non‐invasive support delivered by a mechanical ventilator or a bilevel device in a synchronised or non‐synchronised way. Participants included ventilated preterm infants who were ready to be extubated to non‐invasive respiratory support. Interventions compared were NIPPV, delivered by short nasal prongs or nasopharyngeal tube, and NCPAP, delivered by the same methods.

Types of outcomes measures included failure of therapy (respiratory failure, rates of endotracheal re‐intubation); gastrointestinal complications (i.e. abdominal distension requiring cessation of feeds, gastrointestinal perforation or necrotising enterocolitis); pulmonary air leak; chronic lung disease (oxygen requirement at 36 weeks' postmenstrual age) and mortality.

Data collection and analysis

Three review authors independently extracted data regarding clinical outcomes including extubation failure; endotracheal re‐intubation; rates of apnoea, gastrointestinal perforation, feeding intolerance, necrotising enterocolitis, chronic lung disease and air leak; and duration of hospital stay. We analysed trials using risk ratio (RR), risk difference (RD) and the number needed to treat for an additional beneficial outcome (NNTB) or an additional harmful outcome (NNTH) for dichotomous outcomes, and mean difference (MD) for continuous outcomes. We used the Grading of Recommendations Assessment, Development and Evaluation (GRADE) approach to assess the quality of evidence.

Main results

Through the search, we identified 10 trials enrolling a total of 1431 infants and comparing extubation of infants to NIPPV or NCPAP. Three trials had methodological limitations and possible selection bias.

Five trials used the synchronised form of NIPPV, four used the non‐synchronised form and one used both methods. Eight studies used NIPPV delivered by a ventilator, one used a bilevel device and one used both methods. When all studies were included, meta‐analysis demonstrated a statistically and clinically significant reduction in the risk of meeting extubation failure criteria (typical RR 0.70, 95% CI 0.60 to 0.80; typical RD ‐0.13, 95% CI ‐0.17 to ‐0.08; NNTB 8, 95% CI 6 to 13; 10 trials, 1431 infants) and needing re‐intubation (typical RR 0.76, 95% CI 0.65 to 0.88; typical RD ‐0.10, 95% CI ‐0.15 to ‐0.05; NNTB 10, 95% CI 7 to 20; 10 trials, 1431 infants). We graded evidence for these outcomes as moderate, as all trial interventions were unblinded. Although methods of synchronisation varied (Graseby capsule or pneumotachograph/flow‐trigger), the five trials that synchronised NIPPV showed a statistically significant benefit for infants extubated to NIPPV in terms of prevention of extubation failure up to one week after extubation.

Unsynchronised NIPPV also reduced extubation failure. NIPPV provided via a ventilator is more beneficial than that provided by bilevel devices in reducing extubation failure during the first week. When comparing interventions, investigators found no significant reduction in rates of chronic lung disease (typical RR 0.94, 95% CI 0.80 to 1.10; typical RD ‐0.02, 95% CI ‐0.08 to 0.03) or death, and no difference in the incidence of necrotising enterocolitis. Air leaks were reduced in infants randomised to NIPPV (typical RR 0.48, 95% CI 0.28 to 0.82; typical RD ‐0.03, 95% CI ‐0.05 to ‐0.01; NNTB 33, 95% CI 20 to 100). We graded evidence quality as moderate (unblinded studies) or low (imprecision) for secondary outcomes.

Authors' conclusions

Implications for practice

NIPPV reduces the incidence of extubation failure and the need for re‐intubation within 48 hours to one week more effectively than NCPAP; however, it has no effect on chronic lung disease nor on mortality. Synchronisation may be important in delivering effective NIPPV. The device used to deliver NIPPV may be important; however, data are insufficient to support strong conclusions. NIPPV does not appear to be associated with increased gastrointestinal side effects.

Implications for research

Large trials should establish the impact of synchronisation of NIPPV on safety and efficacy of the technique and should compare the efficacy of bilevel devices versus a ventilator for providing NIPPV.

PICOs

Population
Intervention
Comparison
Outcome

The PICO model is widely used and taught in evidence-based health care as a strategy for formulating questions and search strategies and for characterizing clinical studies or meta-analyses. PICO stands for four different potential components of a clinical question: Patient, Population or Problem; Intervention; Comparison; Outcome.

See more on using PICO in the Cochrane Handbook.

Plain language summary

Nasal intermittent positive pressure ventilation (NIPPV) versus nasal continuous positive airway pressure (NCPAP) for preterm neonates after extubation

Review question

Does nasal intermittent positive pressure ventilation (NIPPV) confer short‐term and long‐term benefits without causing harm to premature infants coming off a ventilator? How does it compare with nasal continuous positive airway pressure (NCPAP)?

Background

Evidence suggests that NIPPV increases the effectiveness of NCPAP in preterm babies who no longer need an endotracheal tube (tube in the windpipe). Preterm babies with breathing problems often require help from a machine (ventilator) that provides regular breaths through a tube in the windpipe. The process of extubation or removal of this tube does not always go smoothly, and the tube may need to be re‐inserted if the baby cannot manage without assistance. NCPAP and NIPPV are ways of supporting babies' breathing in a minimally invasive way ‐ the tubes are short and reach only to the back of the nose, thus causing minimal damage to the lungs. NCPAP and NIPPV may be used after extubation to reduce the number of babies who need re‐insertion of the endotracheal tube. NCPAP provides steady pressure to the back of the nose that is transmitted to the lungs, helping the baby breathe more comfortably. NIPPV provides the same support along with some breaths via the ventilator.

Study characteristics

We searched scientific databases for studies comparing NCPAP versus NIPPV in preterm infants (born before 37 completed weeks of pregnancy) who no longer need an endotracheal tube. We looked at breathing problems, the need for the endotracheal tube to be re‐instated and side effects. Evidence is current to September 2015.

Key results

We found ten trials comparing NCPAP versus NIPPV. Six of ten studies that compared NCPAP and NIPPV showed that NIPPV reduced the need for re‐insertion of the endotracheal tube. Future studies must determine how NIPPV can best be delivered to infants.

Quality of the evidence

In clinical trials, clinicians and investigators were aware of the intervention received by each infant (NIPPV or NCPAP). Therefore, we graded the quality of evidence for the primary outcome (breathing problems and need for re‐insertion of the endotracheal tube) as moderate.

Authors' conclusions

Implications for practice

Use of nasal intermittent positive pressure ventilation (NIPPV) and nasal continuous positive airway pressure (NCPAP) after extubation reduces the incidence of extubation failure within 48 hours to seven days. Studies using synchronised NIPPV and delivering NIPPV to infants by a ventilator observed benefits more consistently. Investigators noted no overall reduction in chronic lung disease among infants randomised to NIPPV and reported a reassuring absence of the gastrointestinal side effects that had been reported in previous case series.

Implications for research

Future trials should enrol sufficient infants to detect differences in important outcomes such as death or chronic lung disease and should compare different categories of devices. These trials should establish the impact of synchronisation of NIPPV on safety and efficacy of the technique as well as the best combination of settings for NIPPV (rate, peak pressure and positive end expiratory pressure).

Summary of findings

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Summary of findings for the main comparison. NIPPV versus NCPAP

NIPPV versus NCPAP

Patient or population: preterm neonates after extubation
Setting: neonatal intensive care unit
Intervention: NIPPV
Comparison: NCPAP

Outcomes

Anticipated absolute effects* (95% CI)

Relative effect
(95% CI)

Number of participants
(studies)

Quality of the evidence
(GRADE)

Comments

Risk with NCPAP

Risk with NIPPV

Respiratory failure post extubation

Study population

RR 0.70
(0.60 to 0.80)

1431
(10 studies)

Moderatea

Risk of bias: intervention unblinded

OIS 554

413 per 1000

289 per 1000
(248 to 330)

Endotracheal re‐intubation during the week post extubation

Study population

RR 0.76
(0.65 to 0.88)

1301

(8 studies)

Moderatea

Risk of bias: intervention unblinded

OIS 724

396 per 1000

301 per 1000
(257 to 348)

Abdominal distension requiring cessation of feeds

Study population

RR 1.27
(0.64 to 2.53)

199

(4 studies)

Lowa,b

Risk of bias: intervention unblinded Imprecision: wide confidence intervals

112 per 1000

143 per 1000
(72 to 284)

Gastrointestinal perforation

Study population

RR 0.94
(0.60 to 1.48)

1066

(5 studies)

Moderatea

Risk of bias: intervention unblinded

66 per 1000

62 per 1000
(40 to 98)

Necrotising enterocolitis

Study population

RR 0.87
(0.64 to 1.19)

1214
(6 studies)

Moderatea

Risk of bias: intervention unblinded

127 per 1000

110 per 1000
(81 to 151)

Chronic lung disease (oxygen supplementation at 36 weeks)

Study population

RR 0.94
(0.80 to 1.10)

1140

(6 studies)

Moderatea

Risk of bias: intervention unblinded

355 per 1000

334 per 1000
(284 to 391)

Pulmonary air leak

Study population

RR 0.48
(0.28 to 0.82)

1229
(6 studies)

Moderatea

Risk of bias: intervention unblinded

OIS 749

61 per 1000

29 per 1000
(17 to 50)

Duration of hospitalisation (days)

Mean duration of hospitalisation (days) was 0

Mean duration of hospitalisation (days) in the intervention group was 2.77 higher (0.04 to 5.51 higher)

238
(4 studies)

Lowa,b

Risk of bias: intervention unblinded Imprecision: wide confidence intervals

Death before discharge

Study population

RR 0.69
(0.48 to 0.99)

1237
(6 studies)

Moderatea

Risk of bias: intervention unblinded

Imprecision

OIS 1844

104 per 1000

72 per 1000
(50 to 103)

*The risk in the intervention group (and its 95% confidence interval) is based on assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI).

CI: confidence interval; OR: odds ratio; RR: risk ratio.

GRADE Working Group grades of evidence.
High quality: We are very confident that the true effect lies close to the estimate of effect.
Moderate quality: We are moderately confident in the effect estimate: The true effect is likely to be close to the estimate of effect but may be substantially different.
Low quality: Our confidence in the effect estimate is limited: The true effect may be substantially different from the estimate of effect.
Very low quality: We have very little confidence in the effect estimate: The true effect is likely to be substantially different from the estimate of effect.

aIntervention unblinded.

bImprecise estimate (wide confidence intervals).

Background

Description of the condition

Preterm infants may experience difficulty with spontaneous, unassisted breathing for a variety of reasons, including lung immaturity, chest wall instability, upper airway obstruction and poor central respiratory drive. Historically, the primary method of support for these infants has consisted of endotracheal intubation and intermittent positive pressure ventilation. Although this method is effective, it is accompanied by complications (upper airway damage, bronchopulmonary dysplasia, sepsis) and is associated with considerable economic cost. Minimising the duration of endotracheal intubation or avoiding it completely has been a goal of neonatal intensive care. Nasal continuous positive airway pressure (NCPAP) is a less invasive way of providing respiratory support for neonates at risk of, or actually experiencing, respiratory failure. One systematic review of trials comparing NCPAP versus treatment with oxyhood concluded that NCPAP begun immediately after a period of endotracheal intubation reduced the rate of adverse events (apnoea, respiratory acidosis and increased oxygen requirements) leading to re‐intubation (Bancalari 2013; Davis 2003b). In this systematic review, approximately 25% of all preterm infants allocated to NCPAP failed extubation; therefore, the need exists to improve outcomes further for infants thought to no longer require an endotracheal tube.

Adults and older children with acute or chronic ventilatory failure of various origins, including chronic obstructive pulmonary disease (Bott 1993), severe kyphoscoliosis (Ellis 1988) and pre‐lung transplantation cystic fibrosis (Piper 1992), have been treated with intermittent positive pressure ventilation delivered via a nasal interface. Clinicians have reported improvements in respiratory function.

Description of the intervention

Nasal intermittent positive pressure ventilation (NIPPV) is a simple, effective mode of respiratory support. NIPPV augments continuous positive airway pressure (CPAP) with superimposed inflations to a set peak pressure (typically 15 to 22 cmH2O). NIPPV may be delivered by nasal mask or prongs, which may be short or long, single or binasal. Some devices attempt to synchronise inflations with the infant's respiratory efforts (Owen 2007). Synchronisation can occur via pneumatic capsules detecting abdominal wall movements or by airway‐derived flow signals. Trigger delays occur, and trigger response is less consistent at high spontaneous breathing rates (Owen 2016).

How the intervention might work

NIPPV has been used in neonates for a variety of indications. About 53% of Canadian tertiary care nurseries reported using NIPPV in the mid‐1980s (Ryan 1989). More recently, 44 of 91 (48%) neonatal units in the UK reported using NIPPV (Owen 2008). The physiological benefits of this technique have been evaluated. NIPPV reduces asynchronous thoracoabdominal motion, perhaps by reducing tube resistance or providing better stabilisation of the chest wall, or both (Kiciman 1998). Its use improves tidal and minute volumes and decreases the inspiratory effort required by neonates compared with NCPAP (Moretti 1999). NIPPV has not been provided without problems in neonates; Garland 1985 reported an association between use of ventilation via nasal prongs and increased risk of gastrointestinal perforation. In the past, lack of high‐quality evidence has led to variability in practice between neonatal intensive care units with respect to NIPPV.

Newer devices now on the market, which are not ventilators, provide bilevel respiratory support (higher positive pressure followed by lower pressure); however, they have limited peak pressure capabilities (i.e. they generally cannot provide more than 10 cmH2O of peak positive pressure). Some devices have the ability to synchronise higher pressure with the infant's own breaths by using a trigger biphasic mode. Whether these devices are comparable with more conventional NIPPV delivered via a ventilator is unclear, as they cannot attain peak inspiratory pressure (PIP) similar to that achieved by NIPPV delivered via a ventilator. Whether synchronisation adds clinical benefit remains unclear (Davis 2009). For the purposes of this review, we will use the term 'NIPPV' to describe all forms of non‐invasive ventilation that intermittently provide supportive breaths or higher pressure.

Why it is important to do this review

Avoiding or reducing time spent on invasive ventilation is a goal of treatment for all premature infants. Many published studies have reported use of various forms of NIPPV or bilevel support, often including a small number of infants or a single centre. We are conducting this review to provide bedside clinicians with the best available evidence regarding their choice of non‐invasive support.

Objectives

Primary objective

To determine effects of management with NIPPV versus NCPAP on the need for additional ventilatory support in preterm infants whose endotracheal tube was removed after a period of intermittent positive pressure ventilation.

Secondary objectives

To compare rates of gastric distension, gastrointestinal perforation, necrotising enterocolitis and chronic lung disease; duration of hospitalisation; and rates of apnoea, air leak and mortality for NIPPV and NCPAP.

Methods

Criteria for considering studies for this review

Types of studies

Randomised and quasi‐randomised trials.

Types of participants

Preterm infants (i.e. those born before 37 completed weeks' gestation) extubated after a period of endotracheal intubation.

Types of interventions

Intermittent positive pressure ventilation provided by a ventilator or a bilevel device and administered via the nasal route by short nasal prongs or nasopharyngeal tubes versus NCPAP delivered by the same methods. NIPPV included non‐invasive support delivered by a mechanical ventilator or a bilevel device in a synchronised or non‐synchronised way.

Types of outcome measures

Primary outcomes

  • Respiratory failure defined by respiratory acidosis, increased oxygen requirement or apnoea that was frequent or severe, leading to additional ventilatory support during the week post extubation

Secondary outcomes

  • Endotracheal re‐intubation during the week post extubation

  • Rates of abdominal distension requiring cessation of feeds

  • Rates of gastrointestinal perforation diagnosed radiologically or at operation

  • Rates of necrotising enterocolitis (NEC), defined according to modified Bell's criteria (stage 2 to 3)

  • Rates of chronic lung disease (CLD), defined as requirement for supplemental oxygen at 28 days of life or at 36 weeks' postmenstrual age

  • Duration of hospitalisation

  • Rates of apnoea and bradycardia expressed as events per hour

  • Rates of pulmonary air leak

  • Mortality

  • Neurodevelopmental status at 18 to 24 months (post hoc, 2015 update)

Search methods for identification of studies

We used the criteria and standard methods of Cochrane and the Cochrane Neonatal Review Group (see the Cochrane Neonatal Group search strategy for specialized register).

We conducted a comprehensive search including the Cochrane Central Register of Controlled Trials (CENTRAL; 2015, Issue 9) in the Cochrane Library; MEDLINE via PubMed (1966 to 28 September 2015); Embase (1980 to 28 September 2015); and the Cumulative Index to Nursing and Allied Health Literature (CINAHL; 1982 to 28 September 2015) using the following search terms: (nasal continuous positive airway pressure OR NCPAP OR nasal intermittent positive pressure ventilation OR NIPPV OR nasal intermittent mandatory ventilation OR NIMV OR nasal distending pressure OR nasal positive pressure OR nasal ventilation OR non‐invasive positive pressure ventilation OR synchronized intermittent mandatory ventilation OR SIMV OR nasopharyngeal synchronized intermittent mandatory ventilation OR bilevel CPAP OR BiCPAP OR BiPAP OR SiPAP), plus database‐specific limiters for randomised controlled trials (RCTs) and neonates (see Appendix 1 for the full search strategies used for each database). We applied no language restrictions.

We searched clinical trials registries for ongoing and recently completed trials (clinicaltrials.gov; the World Health Organization International Trials Registry and Platform (www.whoint/ictrp/search/en/) and the ISRCTN Registry).

Data collection and analysis

Three review authors (BL, PGD and HK) used standard methods of Cochrane and the Cochrane Neonatal Review Group to assess the methodological quality of trials.

Selection of studies

We included all randomised and quasi‐randomised controlled trials of NIPPV compared with NCPAP in ventilated preterm infants ready for extubation. Three review authors (BL, PGD and HK) independently reviewed results of the updated search and selected studies for inclusion. We resolved disagreements by discussion.

Data extraction and management

Three review authors (BL, PGD and HK) independently extracted data, compared entries and resolved differences by discussion. For the 2015 update, one review author (BL) and the Cochrane Neonatal Review Group Editor extracted data, compared entries and resolved differences.

Assessment of risk of bias in included studies

Three review authors (BL, PGD and HK) independently assessed the quality of studies using the following criteria: blinding of randomisation, blinding of intervention, completeness of follow‐up and blinding of outcome measurement. We sought additional information from study authors when required.

For the update, we assessed risk of bias using the criteria outlined in the Cochrane Handbook for Systematic Reviews of Interventions (Higgins 2011) and presented this information in the 'Risk of bias tables'.

We assessed the methodological quality of studies by using the following criteria.

  • Sequence generation (checking for possible selection bias): For each included study, we categorised the method used to generate the allocation sequence as:

    • low risk (any truly random process, e.g. random number table; computer random number generator);

    • high risk (any non‐random process, e.g. odd or even date of birth; hospital or clinic record number); or

    • unclear risk.

  • Allocation concealment (checking for possible selection bias): For each included study, we categorised the method used to conceal the allocation sequence as:

    • low risk (e.g. telephone or central randomisation; consecutively numbered sealed opaque envelopes);

    • high risk (open random allocation; unsealed or non‐opaque envelopes, alternation; date of birth); or

    • unclear risk.

  • Blinding (checking for possible performance bias): For each included study, we categorised the methods used to blind study participants and personnel from knowledge of which intervention a participant received. We assessed blinding separately for different outcomes or classes of outcomes. We categorised methods as:

    • low risk for participants, personnel and outcome assessors;

    • high risk for participants, personnel and outcome assessors; or

    • unclear risk for participants, personnel and outcome assessors.

  • Incomplete outcome data (checking for possible attrition bias through withdrawals, drop‐outs, protocol deviations): For each included study and for each outcome, we described completeness of data including attrition and exclusions from the analysis. We noted whether attrition and exclusions were reported, numbers included in the analysis at each stage (compared with the total number of randomised participants), reasons for attrition or exclusion when reported and whether missing data were balanced across groups or were related to outcomes. When sufficient information was reported or supplied by trial authors, we re‐included missing data in the analyses. We categorised methods as:

    • low risk (less than 20% missing data);

    • high risk (20% or more missing data); or

    • unclear risk.

  • Selective reporting bias: For each included study, we described how we investigated the possibility of selective outcome reporting bias and what we found. We assessed methods as:

    • low risk (when it was clear that all of the study's prespecified outcomes and all expected outcomes of interest to the review had been reported);

    • high risk (when not all of the study's prespecified outcomes had been reported; one or more reported primary outcomes were not prespecified; outcomes of interest were reported incompletely and so could not be used; or study did not include results of a key outcome that would have been expected to have been reported); or

    • unclear risk.

  • Other sources of bias: For each included study, we described any important concerns that we had about other possible sources of bias (e.g. whether a potential source of bias was related to the specific study design, whether the trial was stopped early owing to some data‐dependent process). We assessed whether each study was free of other problems that could put it at risk of bias as:

    • low risk;

    • high risk; or

    • unclear risk.

We made explicit judgements regarding whether studies were at high risk of bias, according to the criteria given in the Cochrane Handbook for Systematic Reviews of Interventions (Higgins 2011). We assessed the likely magnitude and direction of the bias, and whether we considered it likely to impact findings. If needed, we planned to explore the impact of the level of bias by undertaking sensitivity analyses (see Sensitivity analysis).

Quality of evidence

We assessed the quality of evidence for the main comparison at the outcome level using the Grading of Recommendations Assessment, Development and Evaluation (GRADE) approach (Guyatt 2011a). This methodological approach considers evidence from RCTs as high quality that may be downgraded on the basis of consideration of any of five areas: design (risk of bias), consistency across studies, directness of the evidence, precision of estimates and presence of publication bias (Guyatt 2011a). The GRADE approach results in an assessment of the quality of a body of evidence according to one of the following four grades. High: We are very confident that the true effect lies close to that of the estimate of effect. Moderate: We are moderately confident in the effect estimate: The true effect is likely to be close to the estimate of effect but may be substantially different. Low: Our confidence in the effect estimate is limited: The true effect may be substantially different from the estimate of effect. Very low: We have very little confidence in the effect estimate: The true effect is likely to be substantially different from the estimate of effect (Schünemann 2013).

Review authors independently assessed the quality of the evidence found for outcomes identified as critical or important for clinical decision making. These outcomes included:

  • Respiratory failure (defined by respiratory acidosis, increased oxygen requirement or apnoea that was frequent or severe, leading to additional ventilatory support during the week post extubation);

  • Endotracheal re‐intubation during the week post extubation;

  • Rates of CLD, defined as requirement for supplemental oxygen at 36 weeks' postmenstrual age;

  • Rates of pulmonary air leak;

  • Rates of NEC, defined according to modified Bell's criteria (stage 2 to 3);

  • Mortality; and

  • Neurodevelopmental outcomes at 18 to 24 months.

When we considered risk of bias arising from inadequate concealment of allocation, randomised assignment, complete follow‐up or blinded outcome assessment to reduce our confidence in effect estimates, we downgraded the quality of evidence accordingly (Guyatt 2011b). We evaluated consistency by examining similarity of point estimates, extent of overlap of confidence intervals and statistical criteria including measurement of heterogeneity (I2). We downgraded the quality of evidence when large and unexplained inconsistency across study results was present (i.e. some studies suggest important benefit and others no effect or harm without a clinical explanation) (Guyatt 2011d). We assessed precision on the basis of the width of the 95% confidence interval (CI) and calculation of the optimal information size (OIS). If the total number of participants included in the pooled effect estimation was less than the number of participants generated by a conventional sample size calculation for a single adequately powered trial, we considered rating down for imprecision (Guyatt 2011c). When trials were conducted in populations other than the target population, we downgraded the quality of evidence because of indirectness (Guyatt 2011e).

We entered data (i.e. pooled estimates of effects and corresponding 95% confidence Intervals) and explicit judgements for each of the above aspects assessed into the Guideline Development Tool ‐ the software used to create ‘Summary of findings’ tables (GRADEpro 2008). We explained in footnotes or comments in the ‘Summary of findings’ table all judgements involving assessment of the study characteristics described above.

Measures of treatment effect

We analysed categorical data (proportion requiring re‐intubation) using risk ratio (RR), risk difference (RD) and number needed to treat for an additional beneficial outcome (NNTB) or an additional harmful outcome (NNTH). We reported 95% confidence intervals (CIs) on all estimates. We analysed continuous data (frequency of apnoea) using mean difference (MD). We applied the fixed‐effect model.

Assessment of heterogeneity

We examined heterogeneity between trials by inspecting forest plots and quantifying the impact of heterogeneity using the I2 statistic. If noted, we planned to explore possible causes of statistical heterogeneity by performing prespecified subgroup analyses (e.g. differences in study quality, participants, intervention regimens or outcome assessments).

Data synthesis

We used the Mantel‐Haenszel method for estimates of typical RR and RD. We analysed continuous outcomes using the inverse variance method. We applied the fixed‐effect model for all meta‐analyses.

Subgroup analysis and investigation of heterogeneity

We planned to perform subgroup analyses using the same methods to determine whether responses differed according to methods of NIPPV delivery and whether or not methylxanthines were used concurrently. We planned subgroup analyses on the basis of characteristics of participants, including birth weight (e.g. infants weighing less than 1000 grams) and corrected age at the time of intervention (e.g. infants less than 28 weeks' gestation).

Sensitivity analysis

We planned sensitivity analyses for situations for which this might affect interpretation of significant results (e.g. when risk of bias was associated with the quality of some included trials or missing outcome data). We judged none to be necessary in this review.

Results

Description of studies

Included studies

We identified ten trials that met the inclusion criteria of this review (1431 infants) (Figure 1) (Barrington 2001; Friedlich 1999; Gao 2010; Jasani 2016; Kahramaner 2014; Khalaf 2001; Khorana 2008; Kirpalani 2013; Moretti 2008; O'Brien 2012). We provided details in the Characteristics of included studies table.


Study flow diagram: review update.

Study flow diagram: review update.

Inclusion criteria varied somewhat between trials; seven trials enrolled very low birth weight (VLBW) infants (i.e. infants at moderate risk of requiring endotracheal re‐intubation), one trial exclusively enrolled extremely low birth weight infants (ELBW) and two trials enrolled premature infants at less than 35 or 36 weeks' gestation. In six trials, use of methylxanthines was mandatory (Barrington 2001; Jasani 2016; Kahramaner 2014; Khalaf 2001; Khorana 2008; Moretti 2008), and in three other trials, it was extensively prescribed (Friedlich 1999; Kirpalani 2013; O'Brien 2012). Infants were extubated from generally low levels of ventilator support (ventilator rates less than 25 breaths per minute and oxygen concentrations less than 40%). Differences in settings between studies were small. An interesting variation in ventilatory strategies was noted between centres, in spite of little variation in enrolment criteria. Barrington 2001,Gao 2010,Jasani 2016, Kahramaner 2014,Khalaf 2001,Moretti 2008 and O'Brien 2012 extubated infants at a median age of less than one week, whereas Friedlich 1999 and Khorana 2008 extubated infants later (median age of 18.5 days and 21 days in the two groups in Friedlich 1999; mean age of 12.9 days and 6.9 days in the two groups in Khorana 2008).

Five trials synchronised NIPPV delivery; three trials used the Infant Star ventilator with Star Synch abdominal capsule (Barrington 2001; Friedlich 1999; Khalaf 2001), and two used more recent ventilators (Gao 2010; Moretti 2008). One trial used bilevel devices (SiPAP) to deliver non‐synchronised intermittent positive pressure ventilation (O'Brien 2012), two trials used ventilators to deliver non‐synchronised NIPPV (Jasani 2016; Kahramaner 2014) and another permitted use of ventilator‐driven NIPPV (synchronised or not) or bilevel devices (synchronised or not) (Kirpalani 2013).

Ventilator settings applied after extubation varied between studies. Intermittent mechanical ventilation rates varied between 10 per minute and 40 per minute, and PIP from that used before extubation to 2 cmH2O to 4 cmH2O above that used before extubation. Levels used in NCPAP groups also varied between studies (between 3 cmH2O and 8 cmH2O). No attempt was made to match NIPPV and NCPAP groups with respect to mean airway pressure delivered. Different prongs were used to deliver NCPAP and NIPPV; three studies used nasopharyngeal prongs (single or binasal) (Friedlich 1999; Kahramaner 2014; Khorana 2008), and the others used short nasal prongs. Barrington 2001, Jasani 2016, Khalaf 2001 and Moretti 2008 assessed the primary outcome (respiratory failure) over 72 hours post extubation, Friedlich 1999 and Kahramaner 2014 over 48 hours and Khorana 2008,Kirpalani 2013 and O'Brien 2012 over seven days. The assessment period was unclear in Gao 2010.

Three studies (Barrington 2001; Friedlich 1999; Khalaf 2001) permitted rescue NIPPV for infants not responding to NCPAP but analysed the primary outcome on an intention‐to‐treat basis. Criteria for offering rescue treatment varied; some trials proposed more stringent guidelines for extubation, and duration of follow‐up to endpoints for re‐intubation differed from 48 hours to discharge from the neonatal intensive care unit. Therefore, the term 'need for endotracheal re‐intubation', although available for each of the trials, assumed a clinically different meaning for each.

Excluded studies

We excluded 14 studies (see Characteristics of excluded studies table) for the following reasons.

Ongoing studies and studies awaiting clarification include El‐Farash 2013,Estay 2013,Shi 2013,Silveira 2015 and Victor 2011.

Risk of bias in included studies

We assessed methodological quality using the criteria of the Cochrane Neonatal Review Group (Figure 2).


Risk of bias summary: review authors' judgements about each risk of bias item for each included study.

Risk of bias summary: review authors' judgements about each risk of bias item for each included study.

  • Random sequence generation: Eight of the included trials met this criterion. This was unclear in two trials (Gao 2010; Kahramaner 2014).

  • Allocation concealment: This was adequate in eight trials and unclear in two (Gao 2010; Khorana 2008).

  • Blinding of participants and personnel: No study attempted to blind participants and personnel.

  • Blinding of outcome assessments: No study attempted this.

  • Incomplete outcome data: Risk was low in eight trials and unclear in two (Gao 2010; Kahramaner 2014).

  • Selective reporting: Five trials did not have clearly specified outcomes (Barrington 2001; Friedlich 1999; Gao 2010; Kahramaner 2014; Khalaf 2001).

  • Other sources of bias: We found no major sources of other bias in the included trials.

Effects of interventions

See: Summary of findings for the main comparison NIPPV versus NCPAP

Discussion between review authors resulted in no disagreement regarding quality assessment and data extraction from the ten identified trials.

Nasal intermittent positive pressure ventilation versus nasal continuous positive airway pressure to prevent extubation failure

Primary outcome
Respiratory failure post extubation (outcomes 1.1, 1.2 and 1.3)

Six of the ten trials showed statistically significant benefit in terms of respiratory failure 48 hours to seven days post extubation for infants extubated to NIPPV: typical risk ratio (RR) 0.70, 95% confidence interval (CI) 0.60 to 0.80; typical risk difference (RD) ‐0.13, 95% CI ‐0.17 to ‐0.08, with eight infants (95% CI 6 to 13) needing to be treated with NIPPV to prevent one extubation failure (Analysis 1.1). Only one study followed the number of re‐intubations to discharge (Kirpalani 2013) and found no differences between groups. We graded the quality of evidence for this outcome as moderate (unblinded intervention).

Seven trials used short binasal prongs (Barrington 2001; Gao 2010; Jasani 2016; Khalaf 2001; Kirpalani 2013; Moretti 2008; O'Brien 2012), two used bi‐nasopharyngeal prongs (Friedlich 1999; Khorana 2008) and one used a shortened endotracheal tube in one nostril (Kahramaner 2014). Both prongs and tube were effective (post hoc analysis).

Owing to methodological limitations (risk of selection bias) in three studies (Gao 2010; Kahramaner 2014; Khorana 2008), we performed a post hoc analysis for the outcome respiratory failure post extubation, including only higher‐quality studies in the analysis (Analysis 1.3). Results were largely unchanged: typical RR 0.73, 95% CI 0.63 to 0.85; typical RD ‐0.11, 95% CI ‐0.16 to ‐0.06.

Secondary outcomes
Endotracheal re‐intubation (outcome 1.2)

Not all NCPAP infants reaching extubation failure criteria were re‐intubated, because a varying proportion of infants in each trial were offered rescue therapy with NIPPV. The pooled estimate of rates of endotracheal re‐intubation favoured NIPPV (typical RR 0.76, 95% CI 0.65 to 0.88; typical RD ‐0.10, 95% CI ‐0.15 to ‐0.05; number needed to treat for an additional beneficial outcome (NNTB) 10, 95% CI 7 to 20; Analysis 1.2). We graded the quality of evidence for this outcome as moderate (unblinded intervention).

Gastrointestinal side effects (outcomes 2.1, 2.2 and 2.3)

Friedlich 1999, Barrington 2001 and Jasani 2016 reported rates of feeding cessation, and Khalaf 2001 provided unpublished data for this outcome. Other studies reported feeding intolerance. Investigators reported no significant differences between groups (typical RR 1.27, 95% CI 0.64 to 2.53; typical RD 0.03, 95% CI ‐0.06 to 0.12; Analysis 2.1). We graded the quality of evidence for this outcome as low (unblinded intervention and imprecision of results).

Results showed no significant differences between groups in the incidence of gastrointestinal perforation (typical RR 0.94, 95% CI 0.60 to 1.48; Analysis 2.2). Six trials reported rates of NEC (Friedlich 1999; Kahramaner 2014; Khorana 2008; Kirpalani 2013; Moretti 2008; O'Brien 2012) and revealed no differences between groups (typical RR 0.87, 95% CI 0.64 to 1.19; Analysis 2.3). We graded the quality of evidence for these outcomes as moderate (unblinded intervention).

Pulmonary outcomes (outcomes 3.1, 3.2 and 3.3)

Six trials reported oxygen need at 36 weeks' corrected gestational age (Barrington 2001; Jasani 2016; Khalaf 2001; Kirpalani 2013; Moretti 2008; O'Brien 2012). Infants randomised to NIPPV did not have significantly lower rates of CLD compared with infants randomised to NCPAP (typical RR 0.94, 95% CI 0.80 to 1.10; typical RD ‐0.02, 95% CI ‐0.08 to 0.03; Analysis 3.1). We graded the quality of evidence for this outcome as moderate (unblinded intervention). Heterogeneity between trials was also moderate (I2= 51%).

In view of new trials added to the review since its first publication, we added the outcome of air leaks to the review. Six trials reported this outcome (Gao 2010; Jasani 2016; Kahramaner 2014; Kirpalani 2013; Moretti 2008; O'Brien 2012) and described reduced air leaks among infants randomised to NIPPV (typical RR 0.48, 95% CI 0.28 to 0.82; typical RD ‐0.03, 95% CI ‐0.05 to ‐0.01; NNTB 33, 95% CI 20 to 100; Analysis 3.2). We rated the quality of evidence for this outcome as moderate (unblinded intervention).

Mortality (outcome 4.1)

Six trials (1237 infants) reported mortality (Jasani 2016; Kahramaner 2014; Khorana 2008; Kirpalani 2013; Moretti 2008; O'Brien 2012). Khorana 2008 reported no deaths, and meta‐analysis revealed a small difference between treatment groups (typical RR 0.69, 95% CI 0.48 to 0.99; typical RD ‐0.03, 95% CI ‐0.06 to 0.00; Analysis 4.1). We graded evidence for this outcome as moderate (unblinded intervention).

Duration of hospitalisation (outcome 5.1)

Meta‐analysis of the four studies that reported this outcome showed that duration of hospitalisation was longer in infants who were randomised to NIPPV (Analysis 5.1). However, these results should be viewed with caution because liberal use of rescue NIPPV for infants not responding to NCPAP within the first days of extubation makes a difference, and longer‐term outcomes, should they exist, are more difficult to establish. We graded the quality of evidence for this outcome as low (unblinded intervention and imprecision of results).

Rates of apnoea (outcome 6.1)

Barrington 2001 used continuous multi‐channel recording to detect apnoeic events and noted a trend towards fewer apnoeic episodes per day in the NIPPV group, which did not reach statistical significance (mean difference (MD) ‐3.10, 95% CI ‐7.92 to 1.72; Analysis 6.1).

Subgroup analyses

We planned to perform subgroup analyses to determine whether responses differed according to the modality used to deliver NIPPV (synchronised or not, bilevel devices or NIPPV provided by a ventilator).

Synchronised versus non‐synchronised NIPPV

Five studies used synchronised NIPPV (Barrington 2001; Friedlich 1999; Gao 2010; Khalaf 2001; Moretti 2008), and four did not (Jasani 2016; Kahramaner 2014; Khorana 2008; O'Brien 2012); one study did not prescribe use of either synchronised or non‐synchronised NIPPV (Kirpalani 2013). Both synchronised (typical RR 0.25, 95% CI 0.15 to 0.41) and non‐synchronised studies (typical RR 0.65, 95% CI 0.46 to 0.93) showed overall benefit, and the trial using both methods (typical RR 0.86, 95% CI 0.72 to 1.01) showed no benefit of NIPPV for preventing extubation failure (Analysis 7.1). Heterogeneity was high in this subgroup analysis.

When CLD was examined by method of delivery of NIPPV, synchronised NIPPV was associated with a reduction in CLD in three trials (181 infants) that could be pooled for this analysis (typical RR 0.64, 95% CI 0.44 to 0.95; typical RD ‐0.15, 95% CI ‐0.28 to 0.02; Analysis 7.6). Air leaks were also reduced in the two trials that used synchronised NIPPV and reported this outcome (typical RR 0.35, 95% CI 0.14 to 0.90; Analysis 7.7).

NIPPV provided by a ventilator versus bilevel devices

Eight trials used NIPPV delivered via a ventilator, one used bilevel devices (O'Brien 2012) and another used both a ventilator and bilevel devices (Kirpalani 2013). Six of the eight trials using a ventilator to generate NIPPV showed benefit of NIPPV in preventing respiratory failure post extubation (typical RR 0.32, 95% CI 0.22 to 0.47); the two trials that used bilevel (typical RR 0.78, 95% CI 0.50 to 1.21) or both ventilator and bilevel (typical RR 0.86, 95% CI 0.72 to 1.01) showed no benefit (Analysis 8.1). Heterogeneity was high in this subgroup analysis.

When CLD was examined by device delivering NIPPV, NIPPV delivered by a ventilator was associated with a reduction in CLD in the five trials (298 infants) that could be pooled for this analysis (typical RR 0.69, 95% CI 0.50 to 0.95; typical RD ‐0.12, 95% CI ‐0.22 to ‐0.02; Analysis 8.6). Air leaks were also reduced in the four trials that reported this outcome (typical RR 0.35, 95% CI 0.16 to 0.79; Analysis 8.7).

We had planned to perform subgroup analysis to determine whether use of methylxanthines alters response. Almost all infants received methylxanthines before extubation, so we did not perform the planned subgroup analysis. We could not perform planned subgroup analyses based on birth weight and age at randomisation, as trial authors did not present data in ways that would allow us to ascertain this information.

Discussion

Meta‐analysis performed for this updated review showed a strong effect of non‐invasive positive pressure ventilation (NIPPV) on extubation failure but no overall effect on chronic lung disease (CLD). Asymmetrical funnel plots for the primary outcome suggest possible small study bias. When outcomes were examined by subgroups, synchronised NIPPV and NIPPV delivered by a ventilator demonstrated short‐term benefit for extubation failure and long‐term pulmonary effects for CLD and pulmonary air leaks. These subgroup analyses included a smaller number of infants and high heterogeneity; thus results should be interpreted with caution. Individual neonatal intensive care units may interpret these results differently.

Most trials included in this review were small, single‐centre studies, and some used devices no longer available on the market. Additional data from one large pragmatic study increased heterogeneity in the meta‐analysis, likely as the result of broader inclusion criteria, multi‐centre status and examination of many devices providing NIPPV. Generalisation of these results to many currently available devices may not be appropriate.

Six of the ten trials identified in this review had no major methodological limitations. Three trials had potential selection bias (Gao 2010; Kahramaner 2014; Khorana 2008), and one was terminated early owing to enrolment difficulties (O'Brien 2012). Because of the nature of the interventions, it has been impossible to blind carers, and bias may have arisen through uneven use of co‐interventions. Investigators dealt with potential confounders, such as methylxanthine usage and weaning strategies, by having management protocols in place; use of objective failure criteria in these extubation trials enhances our confidence in their findings.

Provision of synchronised NIPPV requires a ventilator capable of delivering this mode of support. Few such ventilators are available on the market. Further research should define whether this modality is definitely superior to non‐synchronised NIPPV, and which type of synchronisation is optimal. Similarly, the effect of bilevel or bilevel positive airway pressure devices deserves more study. In preparing this review, we could not determine benefits for a subgroup of infants (smaller and more immature). A newly available method (neurally adjusted ventilatory assist, or NAVA) has shown promise in small case series (Lee 2015; Stein 2012), but further assessment is needed.

Study flow diagram: review update.
Figures and Tables -
Figure 1

Study flow diagram: review update.

Risk of bias summary: review authors' judgements about each risk of bias item for each included study.
Figures and Tables -
Figure 2

Risk of bias summary: review authors' judgements about each risk of bias item for each included study.

Comparison 1 NIPPV versus NCPAP to prevent extubation failure, Outcome 1 Respiratory failure post extubation.
Figures and Tables -
Analysis 1.1

Comparison 1 NIPPV versus NCPAP to prevent extubation failure, Outcome 1 Respiratory failure post extubation.

Comparison 1 NIPPV versus NCPAP to prevent extubation failure, Outcome 2 Endotracheal re‐intubation.
Figures and Tables -
Analysis 1.2

Comparison 1 NIPPV versus NCPAP to prevent extubation failure, Outcome 2 Endotracheal re‐intubation.

Comparison 1 NIPPV versus NCPAP to prevent extubation failure, Outcome 3 Post hoc analysis (high‐quality studies): respiratory failure post extubation.
Figures and Tables -
Analysis 1.3

Comparison 1 NIPPV versus NCPAP to prevent extubation failure, Outcome 3 Post hoc analysis (high‐quality studies): respiratory failure post extubation.

Comparison 2 NIPPV versus NCPAP and gastrointestinal complications, Outcome 1 Abdominal distension leading to cessation of feeds.
Figures and Tables -
Analysis 2.1

Comparison 2 NIPPV versus NCPAP and gastrointestinal complications, Outcome 1 Abdominal distension leading to cessation of feeds.

Comparison 2 NIPPV versus NCPAP and gastrointestinal complications, Outcome 2 Gastrointestinal perforation.
Figures and Tables -
Analysis 2.2

Comparison 2 NIPPV versus NCPAP and gastrointestinal complications, Outcome 2 Gastrointestinal perforation.

Comparison 2 NIPPV versus NCPAP and gastrointestinal complications, Outcome 3 Necrotising enterocolitis.
Figures and Tables -
Analysis 2.3

Comparison 2 NIPPV versus NCPAP and gastrointestinal complications, Outcome 3 Necrotising enterocolitis.

Comparison 3 NIPPV versus NCPAP to improve pulmonary outcomes, Outcome 1 Chronic lung disease (oxygen supplementation at 36 weeks).
Figures and Tables -
Analysis 3.1

Comparison 3 NIPPV versus NCPAP to improve pulmonary outcomes, Outcome 1 Chronic lung disease (oxygen supplementation at 36 weeks).

Comparison 3 NIPPV versus NCPAP to improve pulmonary outcomes, Outcome 2 Air leaks.
Figures and Tables -
Analysis 3.2

Comparison 3 NIPPV versus NCPAP to improve pulmonary outcomes, Outcome 2 Air leaks.

Comparison 4 NIPPV versus NCPAP and mortality, Outcome 1 Death before discharge.
Figures and Tables -
Analysis 4.1

Comparison 4 NIPPV versus NCPAP and mortality, Outcome 1 Death before discharge.

Comparison 5 NIPPV versus NCPAP and duration of hospital admission, Outcome 1 Duration of hospital admission (days).
Figures and Tables -
Analysis 5.1

Comparison 5 NIPPV versus NCPAP and duration of hospital admission, Outcome 1 Duration of hospital admission (days).

Comparison 6 NIPPV versus NCPAP and apnoea, Outcome 1 Rates of apnoea (episodes/24 h).
Figures and Tables -
Analysis 6.1

Comparison 6 NIPPV versus NCPAP and apnoea, Outcome 1 Rates of apnoea (episodes/24 h).

Comparison 7 NIPPV versus NCPAP (synchronised vs non‐synchronised), Outcome 1 Respiratory failure post extubation.
Figures and Tables -
Analysis 7.1

Comparison 7 NIPPV versus NCPAP (synchronised vs non‐synchronised), Outcome 1 Respiratory failure post extubation.

Comparison 7 NIPPV versus NCPAP (synchronised vs non‐synchronised), Outcome 2 Endotracheal re‐intubation during the week post extubation.
Figures and Tables -
Analysis 7.2

Comparison 7 NIPPV versus NCPAP (synchronised vs non‐synchronised), Outcome 2 Endotracheal re‐intubation during the week post extubation.

Comparison 7 NIPPV versus NCPAP (synchronised vs non‐synchronised), Outcome 3 Abdominal distension requiring cessation of feeds.
Figures and Tables -
Analysis 7.3

Comparison 7 NIPPV versus NCPAP (synchronised vs non‐synchronised), Outcome 3 Abdominal distension requiring cessation of feeds.

Comparison 7 NIPPV versus NCPAP (synchronised vs non‐synchronised), Outcome 4 Gastrointestinal perforation.
Figures and Tables -
Analysis 7.4

Comparison 7 NIPPV versus NCPAP (synchronised vs non‐synchronised), Outcome 4 Gastrointestinal perforation.

Comparison 7 NIPPV versus NCPAP (synchronised vs non‐synchronised), Outcome 5 Necrotising enterocolitis.
Figures and Tables -
Analysis 7.5

Comparison 7 NIPPV versus NCPAP (synchronised vs non‐synchronised), Outcome 5 Necrotising enterocolitis.

Comparison 7 NIPPV versus NCPAP (synchronised vs non‐synchronised), Outcome 6 Chronic lung disease (oxygen supplementation at 36 weeks).
Figures and Tables -
Analysis 7.6

Comparison 7 NIPPV versus NCPAP (synchronised vs non‐synchronised), Outcome 6 Chronic lung disease (oxygen supplementation at 36 weeks).

Comparison 7 NIPPV versus NCPAP (synchronised vs non‐synchronised), Outcome 7 Pulmonary air leak.
Figures and Tables -
Analysis 7.7

Comparison 7 NIPPV versus NCPAP (synchronised vs non‐synchronised), Outcome 7 Pulmonary air leak.

Comparison 7 NIPPV versus NCPAP (synchronised vs non‐synchronised), Outcome 8 Rates of apnoea (episodes/24 h).
Figures and Tables -
Analysis 7.8

Comparison 7 NIPPV versus NCPAP (synchronised vs non‐synchronised), Outcome 8 Rates of apnoea (episodes/24 h).

Comparison 7 NIPPV versus NCPAP (synchronised vs non‐synchronised), Outcome 9 Duration of hospitalisation (days).
Figures and Tables -
Analysis 7.9

Comparison 7 NIPPV versus NCPAP (synchronised vs non‐synchronised), Outcome 9 Duration of hospitalisation (days).

Comparison 7 NIPPV versus NCPAP (synchronised vs non‐synchronised), Outcome 10 Death before discharge.
Figures and Tables -
Analysis 7.10

Comparison 7 NIPPV versus NCPAP (synchronised vs non‐synchronised), Outcome 10 Death before discharge.

Comparison 8 NIPPV versus NCPAP (ventilator‐generated NIPPV vs bilevel NIPPV), Outcome 1 Respiratory failure post extubation.
Figures and Tables -
Analysis 8.1

Comparison 8 NIPPV versus NCPAP (ventilator‐generated NIPPV vs bilevel NIPPV), Outcome 1 Respiratory failure post extubation.

Comparison 8 NIPPV versus NCPAP (ventilator‐generated NIPPV vs bilevel NIPPV), Outcome 2 Endotracheal re‐intubation during the week post extubation.
Figures and Tables -
Analysis 8.2

Comparison 8 NIPPV versus NCPAP (ventilator‐generated NIPPV vs bilevel NIPPV), Outcome 2 Endotracheal re‐intubation during the week post extubation.

Comparison 8 NIPPV versus NCPAP (ventilator‐generated NIPPV vs bilevel NIPPV), Outcome 3 Abdominal distension requiring cessation of feeds.
Figures and Tables -
Analysis 8.3

Comparison 8 NIPPV versus NCPAP (ventilator‐generated NIPPV vs bilevel NIPPV), Outcome 3 Abdominal distension requiring cessation of feeds.

Comparison 8 NIPPV versus NCPAP (ventilator‐generated NIPPV vs bilevel NIPPV), Outcome 4 Gastrointestinal perforation.
Figures and Tables -
Analysis 8.4

Comparison 8 NIPPV versus NCPAP (ventilator‐generated NIPPV vs bilevel NIPPV), Outcome 4 Gastrointestinal perforation.

Comparison 8 NIPPV versus NCPAP (ventilator‐generated NIPPV vs bilevel NIPPV), Outcome 5 Necrotising enterocolitis.
Figures and Tables -
Analysis 8.5

Comparison 8 NIPPV versus NCPAP (ventilator‐generated NIPPV vs bilevel NIPPV), Outcome 5 Necrotising enterocolitis.

Comparison 8 NIPPV versus NCPAP (ventilator‐generated NIPPV vs bilevel NIPPV), Outcome 6 Chronic lung disease (oxygen supplementation at 36 weeks).
Figures and Tables -
Analysis 8.6

Comparison 8 NIPPV versus NCPAP (ventilator‐generated NIPPV vs bilevel NIPPV), Outcome 6 Chronic lung disease (oxygen supplementation at 36 weeks).

Comparison 8 NIPPV versus NCPAP (ventilator‐generated NIPPV vs bilevel NIPPV), Outcome 7 Pulmonary air leak.
Figures and Tables -
Analysis 8.7

Comparison 8 NIPPV versus NCPAP (ventilator‐generated NIPPV vs bilevel NIPPV), Outcome 7 Pulmonary air leak.

Comparison 8 NIPPV versus NCPAP (ventilator‐generated NIPPV vs bilevel NIPPV), Outcome 8 Rates of apnoea (episodes/24 h).
Figures and Tables -
Analysis 8.8

Comparison 8 NIPPV versus NCPAP (ventilator‐generated NIPPV vs bilevel NIPPV), Outcome 8 Rates of apnoea (episodes/24 h).

Comparison 8 NIPPV versus NCPAP (ventilator‐generated NIPPV vs bilevel NIPPV), Outcome 9 Duration of hospitalisation (days).
Figures and Tables -
Analysis 8.9

Comparison 8 NIPPV versus NCPAP (ventilator‐generated NIPPV vs bilevel NIPPV), Outcome 9 Duration of hospitalisation (days).

Comparison 8 NIPPV versus NCPAP (ventilator‐generated NIPPV vs bilevel NIPPV), Outcome 10 Death before discharge.
Figures and Tables -
Analysis 8.10

Comparison 8 NIPPV versus NCPAP (ventilator‐generated NIPPV vs bilevel NIPPV), Outcome 10 Death before discharge.

Summary of findings for the main comparison. NIPPV versus NCPAP

NIPPV versus NCPAP

Patient or population: preterm neonates after extubation
Setting: neonatal intensive care unit
Intervention: NIPPV
Comparison: NCPAP

Outcomes

Anticipated absolute effects* (95% CI)

Relative effect
(95% CI)

Number of participants
(studies)

Quality of the evidence
(GRADE)

Comments

Risk with NCPAP

Risk with NIPPV

Respiratory failure post extubation

Study population

RR 0.70
(0.60 to 0.80)

1431
(10 studies)

Moderatea

Risk of bias: intervention unblinded

OIS 554

413 per 1000

289 per 1000
(248 to 330)

Endotracheal re‐intubation during the week post extubation

Study population

RR 0.76
(0.65 to 0.88)

1301

(8 studies)

Moderatea

Risk of bias: intervention unblinded

OIS 724

396 per 1000

301 per 1000
(257 to 348)

Abdominal distension requiring cessation of feeds

Study population

RR 1.27
(0.64 to 2.53)

199

(4 studies)

Lowa,b

Risk of bias: intervention unblinded Imprecision: wide confidence intervals

112 per 1000

143 per 1000
(72 to 284)

Gastrointestinal perforation

Study population

RR 0.94
(0.60 to 1.48)

1066

(5 studies)

Moderatea

Risk of bias: intervention unblinded

66 per 1000

62 per 1000
(40 to 98)

Necrotising enterocolitis

Study population

RR 0.87
(0.64 to 1.19)

1214
(6 studies)

Moderatea

Risk of bias: intervention unblinded

127 per 1000

110 per 1000
(81 to 151)

Chronic lung disease (oxygen supplementation at 36 weeks)

Study population

RR 0.94
(0.80 to 1.10)

1140

(6 studies)

Moderatea

Risk of bias: intervention unblinded

355 per 1000

334 per 1000
(284 to 391)

Pulmonary air leak

Study population

RR 0.48
(0.28 to 0.82)

1229
(6 studies)

Moderatea

Risk of bias: intervention unblinded

OIS 749

61 per 1000

29 per 1000
(17 to 50)

Duration of hospitalisation (days)

Mean duration of hospitalisation (days) was 0

Mean duration of hospitalisation (days) in the intervention group was 2.77 higher (0.04 to 5.51 higher)

238
(4 studies)

Lowa,b

Risk of bias: intervention unblinded Imprecision: wide confidence intervals

Death before discharge

Study population

RR 0.69
(0.48 to 0.99)

1237
(6 studies)

Moderatea

Risk of bias: intervention unblinded

Imprecision

OIS 1844

104 per 1000

72 per 1000
(50 to 103)

*The risk in the intervention group (and its 95% confidence interval) is based on assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI).

CI: confidence interval; OR: odds ratio; RR: risk ratio.

GRADE Working Group grades of evidence.
High quality: We are very confident that the true effect lies close to the estimate of effect.
Moderate quality: We are moderately confident in the effect estimate: The true effect is likely to be close to the estimate of effect but may be substantially different.
Low quality: Our confidence in the effect estimate is limited: The true effect may be substantially different from the estimate of effect.
Very low quality: We have very little confidence in the effect estimate: The true effect is likely to be substantially different from the estimate of effect.

aIntervention unblinded.

bImprecise estimate (wide confidence intervals).

Figures and Tables -
Summary of findings for the main comparison. NIPPV versus NCPAP
Comparison 1. NIPPV versus NCPAP to prevent extubation failure

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Respiratory failure post extubation Show forest plot

10

1431

Risk Ratio (M‐H, Fixed, 95% CI)

0.70 [0.60, 0.80]

1.1 Short (nasal) prongs

7

1275

Risk Ratio (M‐H, Fixed, 95% CI)

0.73 [0.63, 0.84]

1.2 Long (nasopharyngeal) prongs

3

156

Risk Ratio (M‐H, Fixed, 95% CI)

0.31 [0.14, 0.65]

2 Endotracheal re‐intubation Show forest plot

8

1301

Risk Ratio (M‐H, Fixed, 95% CI)

0.76 [0.65, 0.88]

3 Post hoc analysis (high‐quality studies): respiratory failure post extubation Show forest plot

7

1266

Risk Ratio (M‐H, Fixed, 95% CI)

0.73 [0.63, 0.85]

Figures and Tables -
Comparison 1. NIPPV versus NCPAP to prevent extubation failure
Comparison 2. NIPPV versus NCPAP and gastrointestinal complications

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Abdominal distension leading to cessation of feeds Show forest plot

4

199

Risk Ratio (M‐H, Fixed, 95% CI)

1.27 [0.64, 2.53]

2 Gastrointestinal perforation Show forest plot

5

1066

Risk Ratio (M‐H, Fixed, 95% CI)

0.94 [0.60, 1.48]

3 Necrotising enterocolitis Show forest plot

6

1214

Risk Ratio (M‐H, Fixed, 95% CI)

0.87 [0.64, 1.19]

Figures and Tables -
Comparison 2. NIPPV versus NCPAP and gastrointestinal complications
Comparison 3. NIPPV versus NCPAP to improve pulmonary outcomes

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Chronic lung disease (oxygen supplementation at 36 weeks) Show forest plot

6

1140

Risk Ratio (M‐H, Fixed, 95% CI)

0.94 [0.80, 1.10]

2 Air leaks Show forest plot

6

1229

Risk Ratio (M‐H, Fixed, 95% CI)

0.48 [0.28, 0.82]

Figures and Tables -
Comparison 3. NIPPV versus NCPAP to improve pulmonary outcomes
Comparison 4. NIPPV versus NCPAP and mortality

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Death before discharge Show forest plot

6

1237

Risk Ratio (M‐H, Fixed, 95% CI)

0.69 [0.48, 0.99]

Figures and Tables -
Comparison 4. NIPPV versus NCPAP and mortality
Comparison 5. NIPPV versus NCPAP and duration of hospital admission

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Duration of hospital admission (days) Show forest plot

4

238

Mean Difference (IV, Fixed, 95% CI)

2.77 [0.04, 5.51]

Figures and Tables -
Comparison 5. NIPPV versus NCPAP and duration of hospital admission
Comparison 6. NIPPV versus NCPAP and apnoea

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Rates of apnoea (episodes/24 h) Show forest plot

1

54

Mean Difference (IV, Fixed, 95% CI)

‐3.10 [‐7.92, 1.72]

Figures and Tables -
Comparison 6. NIPPV versus NCPAP and apnoea
Comparison 7. NIPPV versus NCPAP (synchronised vs non‐synchronised)

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Respiratory failure post extubation Show forest plot

10

1431

Risk Ratio (M‐H, Fixed, 95% CI)

0.70 [0.60, 0.80]

1.1 Synchronised NIPPV

5

272

Risk Ratio (M‐H, Fixed, 95% CI)

0.25 [0.15, 0.41]

1.2 Non‐synchronised NIPPV

4

314

Risk Ratio (M‐H, Fixed, 95% CI)

0.65 [0.46, 0.93]

1.3 Mixed NIPPV devices

1

845

Risk Ratio (M‐H, Fixed, 95% CI)

0.86 [0.72, 1.01]

2 Endotracheal re‐intubation during the week post extubation Show forest plot

10

1431

Risk Ratio (M‐H, Fixed, 95% CI)

0.74 [0.64, 0.85]

2.1 Synchronised NIPPV

5

272

Risk Ratio (M‐H, Fixed, 95% CI)

0.33 [0.19, 0.57]

2.2 Non‐synchronised NIPPV

4

314

Risk Ratio (M‐H, Fixed, 95% CI)

0.65 [0.46, 0.93]

2.3 Mixed NIPPV devices

1

845

Risk Ratio (M‐H, Fixed, 95% CI)

0.86 [0.72, 1.01]

3 Abdominal distension requiring cessation of feeds Show forest plot

3

136

Risk Ratio (M‐H, Fixed, 95% CI)

1.76 [0.77, 4.05]

3.1 Synchronised NIPPV

3

136

Risk Ratio (M‐H, Fixed, 95% CI)

1.76 [0.77, 4.05]

3.2 Non‐synchronised NIPPV

0

0

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

3.3 Mixed NIPPV devices

0

0

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

4 Gastrointestinal perforation Show forest plot

5

1052

Risk Ratio (M‐H, Fixed, 95% CI)

0.86 [0.72, 1.01]

4.1 Synchronised NIPPV

3

159

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

4.2 Non‐synchronised NIPPV

1

48

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

4.3 Mixed NIPPV devices

1

845

Risk Ratio (M‐H, Fixed, 95% CI)

0.86 [0.72, 1.01]

5 Necrotising enterocolitis Show forest plot

6

1214

Risk Ratio (M‐H, Fixed, 95% CI)

0.87 [0.64, 1.19]

5.1 Synchronised NIPPV

5

1147

Risk Ratio (M‐H, Fixed, 95% CI)

0.88 [0.64, 1.20]

5.2 Non‐synchronised NIPPV

1

67

Risk Ratio (M‐H, Fixed, 95% CI)

0.72 [0.11, 4.79]

5.3 Mixed NIPPV devices

0

0

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

6 Chronic lung disease (oxygen supplementation at 36 weeks) Show forest plot

6

1108

Risk Ratio (M‐H, Fixed, 95% CI)

0.93 [0.79, 1.10]

6.1 Synchronised NIPPV

3

181

Risk Ratio (M‐H, Fixed, 95% CI)

0.64 [0.44, 0.95]

6.2 Non‐synchronised NIPPV

2

185

Risk Ratio (M‐H, Fixed, 95% CI)

0.74 [0.47, 1.16]

6.3 Mixed NIPPV devices

1

742

Risk Ratio (M‐H, Fixed, 95% CI)

1.07 [0.88, 1.30]

7 Pulmonary air leak Show forest plot

6

1222

Risk Ratio (M‐H, Fixed, 95% CI)

0.67 [0.44, 1.02]

7.1 Synchronised NIPPV

2

113

Risk Ratio (M‐H, Fixed, 95% CI)

0.35 [0.14, 0.90]

7.2 Non‐synchronised NIPPV

3

259

Risk Ratio (M‐H, Fixed, 95% CI)

1.10 [0.58, 2.08]

7.3 Mixed NIPPV devices

1

850

Risk Ratio (M‐H, Fixed, 95% CI)

0.61 [0.29, 1.28]

8 Rates of apnoea (episodes/24 h) Show forest plot

1

54

Mean Difference (IV, Fixed, 95% CI)

‐3.10 [‐7.92, 1.72]

8.1 Synchronised NIPPV

1

54

Mean Difference (IV, Fixed, 95% CI)

‐3.10 [‐7.92, 1.72]

8.2 Non‐synchronised NIPPV

0

0

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

8.3 Mixed NIPPV devices

0

0

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

9 Duration of hospitalisation (days) Show forest plot

4

244

Mean Difference (IV, Fixed, 95% CI)

2.72 [‐0.01, 5.44]

9.1 Synchronised NIPPV

3

181

Mean Difference (IV, Fixed, 95% CI)

3.39 [0.52, 6.25]

9.2 Non‐synchronised NIPPV

1

63

Mean Difference (IV, Fixed, 95% CI)

‐3.48 [‐12.20, 5.24]

9.3 Mixed NIPPV devices

0

0

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

10 Death before discharge Show forest plot

6

1237

Risk Ratio (M‐H, Fixed, 95% CI)

0.69 [0.48, 0.99]

10.1 Synchronised NIPPV

2

111

Risk Ratio (M‐H, Fixed, 95% CI)

0.97 [0.21, 4.44]

10.2 Non‐synchronised NIPPV

3

266

Risk Ratio (M‐H, Fixed, 95% CI)

0.35 [0.16, 0.75]

10.3 Mixed NIPPV devices

1

860

Risk Ratio (M‐H, Fixed, 95% CI)

0.85 [0.55, 1.31]

Figures and Tables -
Comparison 7. NIPPV versus NCPAP (synchronised vs non‐synchronised)
Comparison 8. NIPPV versus NCPAP (ventilator‐generated NIPPV vs bilevel NIPPV)

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Respiratory failure post extubation Show forest plot

10

1431

Risk Ratio (M‐H, Fixed, 95% CI)

0.70 [0.60, 0.80]

1.1 Ventilator‐generated NIPPV

8

450

Risk Ratio (M‐H, Fixed, 95% CI)

0.32 [0.22, 0.47]

1.2 Bilevel NIPPV

1

136

Risk Ratio (M‐H, Fixed, 95% CI)

0.78 [0.50, 1.21]

1.3 Mixed NIPPV devices

1

845

Risk Ratio (M‐H, Fixed, 95% CI)

0.86 [0.72, 1.01]

2 Endotracheal re‐intubation during the week post extubation Show forest plot

10

1431

Risk Ratio (M‐H, Fixed, 95% CI)

0.74 [0.64, 0.85]

2.1 Ventilator‐generated NIPPV

8

450

Risk Ratio (M‐H, Fixed, 95% CI)

0.39 [0.26, 0.59]

2.2 Bilevel NIPPV

1

136

Risk Ratio (M‐H, Fixed, 95% CI)

0.78 [0.50, 1.21]

2.3 Mixed NIPPV devices

1

845

Risk Ratio (M‐H, Fixed, 95% CI)

0.86 [0.72, 1.01]

3 Abdominal distension requiring cessation of feeds Show forest plot

3

136

Risk Ratio (M‐H, Fixed, 95% CI)

1.76 [0.77, 4.05]

3.1 Ventilator‐generated NIPPV

3

136

Risk Ratio (M‐H, Fixed, 95% CI)

1.76 [0.77, 4.05]

3.2 Bilevel NIPPV

0

0

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

3.3 Mixed NIPPV devices

0

0

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

4 Gastrointestinal perforation Show forest plot

6

1133

Risk Ratio (M‐H, Fixed, 95% CI)

0.94 [0.60, 1.48]

4.1 Ventilator‐generated NIPPV

6

1133

Risk Ratio (M‐H, Fixed, 95% CI)

0.94 [0.60, 1.48]

4.2 Bilevel NIPPV

0

0

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

4.3 Mixed NIPPV devices

0

0

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

5 Necrotising enterocolitis Show forest plot

6

1214

Risk Ratio (M‐H, Fixed, 95% CI)

0.87 [0.64, 1.19]

5.1 Ventilator‐generated NIPPV

4

219

Risk Ratio (M‐H, Fixed, 95% CI)

0.63 [0.21, 1.93]

5.2 Bilevel NIPPV

1

136

Risk Ratio (M‐H, Fixed, 95% CI)

1.03 [0.38, 2.78]

5.3 Mixed NIPPV devices

1

859

Risk Ratio (M‐H, Fixed, 95% CI)

0.89 [0.63, 1.24]

6 Chronic lung disease (oxygen supplementation at 36 weeks) Show forest plot

7

1168

Risk Ratio (M‐H, Fixed, 95% CI)

0.95 [0.81, 1.11]

6.1 Ventilator‐generated NIPPV

5

298

Risk Ratio (M‐H, Fixed, 95% CI)

0.69 [0.50, 0.95]

6.2 Bilevel NIPPV

1

128

Risk Ratio (M‐H, Fixed, 95% CI)

0.95 [0.59, 1.55]

6.3 Mixed NIPPV devices

1

742

Risk Ratio (M‐H, Fixed, 95% CI)

1.07 [0.88, 1.30]

7 Pulmonary air leak Show forest plot

6

1229

Risk Ratio (M‐H, Fixed, 95% CI)

0.48 [0.28, 0.82]

7.1 Ventilator‐generated NIPPV

4

243

Risk Ratio (M‐H, Fixed, 95% CI)

0.35 [0.16, 0.79]

7.2 Bilevel NIPPV

1

136

Risk Ratio (M‐H, Fixed, 95% CI)

0.0 [0.0, 0.0]

7.3 Mixed NIPPV devices

1

850

Risk Ratio (M‐H, Fixed, 95% CI)

0.61 [0.29, 1.28]

8 Rates of apnoea (episodes/24 h) Show forest plot

1

54

Mean Difference (IV, Fixed, 95% CI)

‐3.10 [‐7.92, 1.72]

8.1 Ventilator‐generated NIPPV

1

54

Mean Difference (IV, Fixed, 95% CI)

‐3.10 [‐7.92, 1.72]

8.2 Bilevel NIPPV

0

0

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

8.3 Mixed NIPPV devices

0

0

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

9 Duration of hospitalisation (days) Show forest plot

4

244

Mean Difference (IV, Fixed, 95% CI)

2.72 [‐0.01, 5.44]

9.1 Ventilator‐generated NIPPV

4

244

Mean Difference (IV, Fixed, 95% CI)

2.72 [‐0.01, 5.44]

9.2 Bilevel NIPPV

0

0

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

9.3 Mixed NIPPV devices

0

0

Mean Difference (IV, Fixed, 95% CI)

0.0 [0.0, 0.0]

10 Death before discharge Show forest plot

6

1237

Risk Ratio (M‐H, Fixed, 95% CI)

0.69 [0.48, 0.99]

10.1 Ventilator‐generated NIPPV

4

241

Risk Ratio (M‐H, Fixed, 95% CI)

0.38 [0.18, 0.81]

10.2 Bilevel NIPPV

1

136

Risk Ratio (M‐H, Fixed, 95% CI)

0.62 [0.15, 2.48]

10.3 Mixed NIPPV devices

1

860

Risk Ratio (M‐H, Fixed, 95% CI)

0.85 [0.55, 1.31]

Figures and Tables -
Comparison 8. NIPPV versus NCPAP (ventilator‐generated NIPPV vs bilevel NIPPV)