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Penggunaan antibiotik untuk neonat yang lahir dengan cecair amniotik bertanda mekonium.

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Abstract

Background

Approximately 1 in 10 pregnancies is affected by meconium passage at delivery, which can result in meconium aspiration syndrome (MAS). MAS can cause respiratory complications and, very rarely, death. Antibiotics have been prescribed for neonates exposed to meconium in amniotic fluid, with the intention of preventing infection due to potential bacterial contaminants.

Objectives

We conducted this review to assess the efficacy and safety of antibiotics for:

1. prevention of infection, morbidity, and mortality among infants born through meconium‐stained amniotic fluid (MSAF) who are asymptomatic at birth; and

2. prevention of infection, morbidity, and mortality among infants born through MSAF who have signs and symptoms compatible with meconium aspiration syndrome (MAS).

Search methods

We performed a literature search using the following databases: MEDLINE (1966 to July 2016); Embase (1980 to July 2016); the Cumulative Index to Nursing and Allied Health Literature (CINAHL; 1982 to July 2016); and the Cochrane Central Register of Controlled Trials (CENTRAL; 2016, Issue 7) in the Cochrane Library. We also searched clinical trials databases, conference proceedings, and reference lists of retrieved articles.

Selection criteria

We included randomised and quasi‐randomised controlled trials that compared antibiotics administered via any route versus placebo or no treatment for prevention of infection among neonates exposed to MSAF, or who developed MAS. We excluded cohort, case control, and any other non‐randomised studies and applied no language restrictions. We included studies of term and preterm infants, and we included studies examining use of any antibacterial antibiotics. We included studies that reported on any outcomes of interest.

Data collection and analysis

We assessed the methodological quality of included trials by reviewing information provided in study reports and obtained by personal communication with study authors. We extracted data on relevant outcomes, estimated effect size, and reported values as risk ratios (RRs), risk differences (RDs), and mean differences (MDs), as appropriate. We conducted subgroup analyses for treatment of MAS and for prophylaxis (asymptomatic neonates exposed to meconium).

Main results

Four randomised controlled studies including a total of 695 participants were eligible for inclusion. Three studies evaluated neonates with MAS, and one study assessed asymptomatic neonates exposed to meconium in amniotic fluid. These studies exhibited varying degrees of methodological rigour: Two studies were at low risk of bias, and two were at unclear risk. We graded evidence derived from these studies as low quality. We downgraded overall evidence owing to the large number of participants lost to follow‐up in one trial, the small sample sizes of all trials, and unclear methodological details provided for two trials.

The primary outcome was risk of early‐ and late‐onset neonatal sepsis. Antibiotics did not decrease the risk of sepsis in neonates with a diagnosis of MAS (RR 1.54, 95% confidence interval (CI) 0.27 to 8.96; RD 0.00, 95% CI ‐0.02 to 0.03; 445 participants, three studies; I² = 0%) nor in asymptomatic neonates exposed to meconium in amniotic fluid (RR 0.76, 95% CI 0.25 to 2.34; RD ‐0.01, 95% CI ‐0.07 to 0.04; 250 participants, one study; I² = 0%). Results show no significant differences in mortality or duration of stay in hospital between groups given antibiotics and control groups of symptomatic and asymptomatic neonates. One study in asymptomatic neonates reported a significant reduction in duration of mechanical ventilation for the control group compared with the antibiotic group (MD 0.26, 95% CI 0.15 to 0.37; 250 participants, one study; I² = 0%).

Authors' conclusions

Upon review of available evidence, we found no differences in infection rates following antibiotic treatment among neonates born through meconium‐stained fluid and those with meconium aspiration syndrome. The overall quality of evidence is low owing to the small number of included studies. Well‐controlled studies of adequate power are needed.

PICO

Population
Intervention
Comparison
Outcome

El uso y la enseñanza del modelo PICO están muy extendidos en el ámbito de la atención sanitaria basada en la evidencia para formular preguntas y estrategias de búsqueda y para caracterizar estudios o metanálisis clínicos. PICO son las siglas en inglés de cuatro posibles componentes de una pregunta de investigación: paciente, población o problema; intervención; comparación; desenlace (outcome).

Para saber más sobre el uso del modelo PICO, puede consultar el Manual Cochrane.

Ringkasan bahasa mudah

Penggunaan antibiotik untuk mengurangkan jangkitan pada bayi yang terdedah kepada mekonium

Apakah isunya?

Kira‐kira 1 dalam setiap 10 kehamilan, bayi akan terdedah kepada mekonium semasa kelahiran. Mekonium ialah najis pertama bayi. Jika bayi mengeluarkan najis sebelum lahir, cecair amniotik yang mengandungi najis boleh memasuki paru‐paru bayi dan mungkin menyebabkan kesukaran bernafas dan membuat bayi berisiko untuk jangkitan dan keradangan paru‐paru dan badan.

Mengapakah isu ini penting?

Jangkitan/radang paru‐paru boleh menyebabkan kesukaran bernafas, kurang paras oksigen dan pneumonia. Antibiotik telah digunakan untuk mencegah jangkitan pada bayi yang terdedah kepada mekonium dalam proses kelahiran.

Apakah bukti yang didapati?

Kami mencari kesusasteraan perubatan kajian‐kajian yang sesuai sehingga Jun 2016. Kami mendapati empat kajian yang membandingkan pengunaan antibiotik berbanding plasebo untuk mengurangkan jangkitan dalam kalangan bayi yang lahir dengan cecair amniotik yang bertanda mekonium. Dua kajian adalah berkualiti baik, dan dua lagi kajian tidak mengandungi beberapa butiran mengenai kaedah kajian. Empat kajian ini melibatkan 695 bayi, yang diberi pelbagai antibiotik atau ditempatkan dalam kumpulan kawalan (tidak diberi antibiotik). Para penyelidik menilai pelbagai jenis antibiotik dan tempoh rawatan. Secara keseluruhan, tiada perbezaan didapati dalam kadar jangkitan atau kematian di antara kedua‐dua kumpulan. Kami menilai bukti tersebut sebagai berkualiti rendah kerana reka bentuk kajian yang berkualiti rendah dan bilangan kecil bayi.

Apakah maksudnya?

Kami tidak pasti sama ada antibiotik mempunyai kesan penting bagi jangkitan pada bayi yang terdedah kepada cecair amniotik yang bertanda mekonium. Keputusan kami adalah tidak jitu, dan lebih banyak kajian diperlukan untuk mengenal pasti peranan antibiotik dalam keadaan ini.

Authors' conclusions

Implications for practice

Given the limited available evidence, we cannot determine whether antibiotics reduce risk of sepsis or death among neonates exposed to meconium through amniotic fluid before birth.

Implications for research

High‐quality multi‐centre placebo‐controlled trials should evaluate the risk‐benefit ratio of antibiotics used to reduce infection among neonates exposed to meconium‐stained amniotic fluid. Such trials should provide long‐term follow‐up to evaluate neurodevelopmental and adverse effects of antibiotic exposure during the immediate neonatal period. Given the low event rate, this would require multi‐centre collaboration. This review highlights variation in antibiotic choices and regimens. An international uniform approach to treatment of neonates exposed to meconium‐stained amniotic fluid would address evident heterogeneity among interventions identified in this review.

Summary of findings

Open in table viewer
Summary of findings for the main comparison. Antibiotics compared with control (no antibiotics) in symptomatic neonates born through meconium‐stained amniotic fluid

Antibiotics compared with control (no antibiotics) in symptomatic neonates born through meconium‐stained amniotic fluid

Patient or population: symptomatic neonates born through meconium‐stained amniotic fluid
Setting: neonatal intensive care unit
Intervention: antibiotics
Comparison: control (no antibiotics)

Outcomes

Anticipated absolute effects* (95% CI)

Relative effect
(95% CI)

Number of participants
(studies)

Quality of the evidence
(GRADE)

Comments

Risk with control (no antibiotics)

Risk with antibiotics

Incidence of confirmed sepsis in first 28 days

Study population

Not estimable

445
(3 RCTs)

⊕⊕⊝⊝
LOW

Evidence was downgraded owing to unclear risk of bias due to methodological limitations, including a large number of dropouts; and imprecision resulting from a small sample size

9 per 1000

0 per 1000
(0 to 0)

Mortality (before discharge)

Study population

RR 1.69
(0.23 to 12.53)

445
(3 RCTs)

⊕⊕⊝⊝
LOW

Evidence was downgraded owing to unclear risk of bias due to methodological limitations, including a large number of dropouts; and imprecision resulting from a small sample size

5 per 1000

8 per 1000
(1 to 57)

Duration of oxygen therapy, days

Mean duration of oxygen therapy (days) was 0

MD 0.85 days lower
(1.19 lower to 0.52 lower)

405
(2 RCTs)

⊕⊕⊝⊝
LOW

Evidence was downgraded owing to unclear risk of bias due to methodological limitations, including a large number of dropouts; and imprecision resulting from a small sample size

Duration of hospital stay, days

Mean duration of hospital stay (days) was 0

MD 0.16 days higher
(1.15 lower to 1.47 higher)

146
(1 RCT)

⊕⊕⊕⊝
MODERATE

Evidence was downgraded owing to imprecision resulting from a small sample size

Incidence of mechanical ventilation

Study population

RR 1.18
(0.52 to 2.67)

445
(3 RCTs)

⊕⊕⊝⊝
LOW

Evidence was downgraded owing to unclear risk of bias due to methodological limitations, including a large number of dropouts; and imprecision resulting from a small sample size

45 per 1000

53 per 1000
(24 to 121)

Incidence of respiratory failure

Study population

RR 1.20
(0.51 to 2.83)

405
(2 RCTs)

⊕⊕⊝⊝
LOW

Evidence was downgraded owing to unclear risk of bias due to methodological limitations, including a large number of dropouts; and imprecision resulting from a small sample size

41 per 1000

47 per 1000
(20 to 113)

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

Open in table viewer
Summary of findings 2. Antibiotics compared with control (no antibiotics) in asymptomatic neonates born through meconium‐stained amniotic fluid

Antibiotics compared with control (no antibiotics) in asymptomatic neonates born through meconium‐stained amniotic fluid

Patient or population: asymptomatic neonates born through meconium‐stained amniotic fluid
Setting: neonatal intensive care unit
Intervention: antibiotics
Comparison: control (no antibiotics)

Outcomes

Anticipated absolute effects* (95% CI)

Relative effect
(95% CI)

Number of participants
(studies)

Quality of the evidence
(GRADE)

Comments

Risk with control (no antibiotics)

Risk with antibiotics

Incidence of confirmed sepsis in first 28 days

Study population

Not estimable

250
(1 RCT)

⊕⊕⊝⊝
LOW

Evidence was downgraded owing to very serious imprecision, as the results from this study have not been replicated

54 per 1000

0 per 1000
(0 to 0)

Mortality (before discharge)

Study population

RR 1.07
(0.22 to 5.18)

250
(1 RCT)

⊕⊕⊝⊝
LOW

Evidence was downgraded owing to very serious imprecision, as the results from this study have not been replicated

23 per 1000

25 per 1000
(5 to 120)

Duration of oxygen therapy, days

Mean duration of oxygen therapy (days) was 0

MD 0.43 days higher
(0.13 higher to 0.73 higher)

250
(1 RCT)

⊕⊕⊝⊝
LOW

Evidence was downgraded owing to very serious imprecision, as the results from this study have not been replicated

Incidence of suspected sepsis

Study population

Not estimable

250
(1 RCT)

⊕⊕⊝⊝
LOW

Evidence was downgraded owing to very serious imprecision, as the results from this study have not been replicated

109 per 1000

0 per 1000
(0 to 0)

Incidence of mechanical ventilation

Study population

RR 2.13
(0.55 to 8.34)

250
(1 RCT)

⊕⊕⊝⊝
LOW

Evidence was downgraded owing to very serious imprecision, as the results from this study have not been replicated

23 per 1000

50 per 1000
(13 to 194)

Duration of respiratory distress, hours

Mean duration of respiratory distress (hours) was 0

MD 6.87 higher
(4.22 higher to 9.52 higher)

250
(1 RCT)

⊕⊕⊝⊝
LOW

Evidence was downgraded owing to very serious imprecision, as the results from this study have not been replicated

Incidence of MAS

Study population

RR 1.17
(0.67 to 2.04)

250
(1 RCT)

⊕⊕⊝⊝
LOW

Evidence was downgraded owing to very serious imprecision, as the results from this study have not been replicated

155 per 1000

181 per 1000
(104 to 316)

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

Background

Description of the condition

Meconium aspiration syndrome (MAS) is a problem that is commonly encountered in neonates. Meconium is the viscous green material found in the foetal gastrointestinal tract from approximately the tenth week of gestation. Meconium is composed of a mixture of bile, bile acids, mucus, pancreatic secretions, and cellular debris (Wiswell 1993). Approximately 10% to 15% of pregnancies are complicated by passage of meconium around the time of delivery (Wiswell 1993). An adverse intrauterine environment that compromises foetal well‐being can lead to meconium‐stained amniotic fluid (MSAF) (Ahanya 2005). 'Meconium aspiration syndrome' is defined as respiratory distress with compatible chest roentgenographic findings in an infant born through MSAF whose symptoms cannot be otherwise explained (Wiswell 1990). Despite current interventions such as intubation with tracheal suction, it is estimated that 5% to 12% of infants born through MSAF develop MAS (Wiswell 2000). An estimated 25,000 to 30,000 cases and 1000 deaths related to MAS are reported annually in the United States (Gelfand 2004). MAS accounts for roughly 2% of all perinatal deaths (Cleary 1998). Clinical features of MAS include tachypnoea, retractions, grunting, and/or cyanosis with or without radiological features of aspiration pneumonia. Radiological features of MAS consist of areas of atelectasis and consolidation, along with regions of hyperexpansion. Histologically, researchers have observed a significant inflammatory reaction with a diffuse pulmonary infiltrate of polymorphonuclear leucocytes (Burgess 1996). Although initially sterile, meconium can become colonised secondarily by bacteria following rupture of membranes in utero (Florman 1969) or during neonatal interventions such as endotracheal intubation.

Description of the intervention

Antibiotics target bacteria and are prescribed to treat infection or, at times, to prevent infection. Penicillin prevents cross‐linking during the formation of peptidoglycan. Normal healthy human cells do not make or need peptidoglycan, a polymer that makes penicillin selective to bacteria. Loss of peptidoglycan makes the bacterial call wall weak, causing it to burst. Antibiotics are among the treatments most frequently used in the neonatal intensive care unit (NICU) (Warrier 2006).

How the intervention might work

Proposed explanations for widespread use of antibiotics in patients with MAS include difficulty differentiating aspiration pneumonia from bacterial pneumonia radiologically (Lee 2004); the possibility of meconium‐induced inhibition of phagocytic activity and respiratory burst response by alveolar macrophages, rendering infants with MAS susceptible to pulmonary infection (Craig 2005); in vitro enhancement of bacterial growth in the presence of meconium in amniotic fluid (Florman 1969; Lembet 2003); in vivo inflammatory response aggravated by the combination of meconium and bacteria (Speer 1998); the likelihood of foetal bacterial infection causing in utero meconium passage (Blot 1983; Bortolucci 1990); and apprehension about complications associated with untreated bacterial pneumonia (Wiswell 1992). Several study authors have reported increased rates of chorioamnionitis associated with MSAF (Mazor 1995; Rao 2001; Romero 1991; Usta 1995), although it is unclear whether chorioamnionitis is a cause or a secondary effect of meconium passage. In a retrospective study of 215 well term babies born through MSAF (88 of whom required tracheal meconium aspiration at birth), researchers noted no significant differences in the incidence of culture‐positive sepsis (1 (1.1%) vs 2 (1.6%); P > 0.05) when comparing 127 control infants not requiring tracheal suctioning of meconium passage (Krishnan 1995). Administration of intravenous ampicillin‐sulbactam therapy or cefazolin infusion into the amniotic cavity during amnioinfusion in mothers with MSAF has not been beneficial in reducing neonatal sepsis (Adair 1996; Edwards 1999).

Why it is important to do this review

Widespread use of antibiotics in neonates is a matter of some concern (CDC 2004). Excessive use of antibiotics in neonatal units can lead to emergence of resistant bacterial strains (Tom‐Revzon 2004). Fanos 1999 reported nephrotoxicity in newborns even after brief periods of antibacterial treatment. McCracken 1986 observed ototoxicity in neonates following aminoglycoside treatment. Researchers have not systematically evaluated the role of antibiotics in infants born through MSAF.

Objectives

We conducted this review to assess the efficacy and safety of antibiotics for:

  1. prevention of infection, morbidity, and mortality among infants born through meconium‐stained amniotic fluid (MSAF) who are asymptomatic at birth; and

  2. prevention of infection, morbidity, and mortality among infants born through MSAF who have signs and symptoms compatible with meconium aspiration syndrome (MAS).

Methods

Criteria for considering studies for this review

Types of studies

We considered for inclusion in this review randomised and quasi‐randomised controlled trials of antibiotic administration in infants born through MSAF. We excluded non‐randomised studies, editorials, letter to editors, and commentaries.

Types of participants

We studied two sets of infants.

  1. Term (≥ 37 weeks' gestational age) and preterm (< 37 weeks' gestational age) newborn infants with a history of meconium‐stained amniotic fluid and asymptomatic at birth.

  2. Term (≥ 37 weeks' gestational age) and preterm (< 37 weeks' gestational age) newborn infants with a history of meconium‐stained amniotic fluid and clinical findings of tachypnoea, retractions, grunting, and cyanosis with or without radiological findings of atelectasis, consolidation, and hyperinflation.

If studies included a mixed population of term and preterm infants born with a history of meconium‐stained amniotic fluid who may or may not have had symptoms and signs (clinical or radiological) of MAS, we contacted study authors to request individual data for symptomatic and asymptomatic infants. We incorporated these data into appropriate subgroup comparisons, as noted above.

Types of interventions

We studied two intervention strategies.

  1. Administration of antibiotics started immediately after birth compared with no antibiotics or placebo in infants born through MSAF and asymptomatic at birth.

  2. Administration of antibiotics compared with no antibiotics or placebo started at the time of initial clinical suspicion of MAS in infants born through MSAF.

Types of outcome measures

Outcomes were similar across sets of interventions/populations.

Primary outcome

The primary outcome was incidence of sepsis in the first 28 days (symptomatic neonate was considered to have sepsis if blood or cerebrospinal fluid (CSF) culture was positive for bacterial organisms). We planned to classify this outcome into two groups.

  1. Early‐onset neonatal sepsis (symptomatic before 72 hours).

  2. Late‐onset neonatal sepsis (symptomatic at 72 hours or later).

Secondary outcomes

  1. Mortality before discharge

  2. Duration of mechanical ventilation (days)

  3. Maximum ventilatory requirements (oxygenation index (OI), mean airway pressure (MAP), fraction of inspired oxygen (FiO2)) during first seven days of life

  4. Duration of oxygen therapy (days)

  5. Treatment with high‐frequency ventilation (HFV)

  6. Treatment with inhaled nitric oxide

  7. Treatment with surfactant lavage

  8. Treatment with bolus surfactant administration

  9. Treatment with extracorporeal membrane oxygenation (ECMO)

  10. Incidence of pulmonary air leak syndrome (pneumothorax, pulmonary interstitial emphysema)

  11. Incidence of intracranial haemorrhage

  12. Incidence of intraventricular haemorrhage

  13. Incidence of periventricular leucomalacia

  14. Duration of hospital stay until discharge home among survivors (days)

  15. Incidence of oliguria (< 1 mL/kg/h)

  16. Incidence of azotaemia (> 1.5 mg/dL)

  17. Incidence of diarrhoea

  18. Incidence of hearing impairment associated with antibiotics

  19. Incidence of suspected sepsis (neonate was suspected to have sepsis if one or a combination of the following markers of sepsis was abnormal: total white blood cell count, absolute neutrophil count, immature‐to‐total neutrophil ratio, C‐reactive protein, cytokines, interleukin (IL)‐6, gastric aspirates for neutrophils or bacteria)

  20. Proportion of infants born through MSAF starting antibiotics before discharge

Subgroup analysis

For both of the comparisons above, we planned to perform subgroup analyses to assess effects of the antibiotic regimen, duration of antibiotics, and gestational age.

Search methods for identification of studies

We searched MEDLINE (1966 to July 2016) using the following terms, with all subheadings connected by "AND".

  1. Population: infant‐newborn (MeSH) OR infant, newborn, meconium aspiration (MeSH) OR infant, newborn, MAS (MeSH) OR newborn (text word) OR infant (text word) OR neonate (text word) OR meconium aspiration (text word) OR MAS.

  2. Intervention: antibacterial agents (MeSH), antibiotics (text word).

  3. Comparison: clinical trial (MeSH) OR controlled clinical trial (MeSH) OR randomized controlled trial (MeSH).

Electronic searches  We searched other databases including Embase (1980 to July 2016); the Cumulative Index to Nursing and Allied Health Literature (CINAHL; 1982 to July 2016); the Cochrane Central Register of Controlled Trials (CENTRAL; 2016, Issue 7) in the Cochrane Library; and reference lists of identified trials and abstracts from annual meetings of the Society for Pediatric Research, the American Pediatric Society, and Pediatric Academic Societies, published in Pediatric Research (2002 to 2016). We included editorials, commentaries, reviews, lectures, abstracts, and letters to the editor only if they included original data. We applied no language restrictions. We contacted study authors for additional/missing information. We have appended below the detailed search strategy developed by the Cochrane Neonatal Review Group (Appendices).

Electronic searches

We searched other databases including Embase (1980 to July 2016); the Cumulative Index to Nursing and Allied Health Literature (CINAHL; 1982 to July 2016); and the Cochrane Central Register of Controlled Trials (CENTRAL; 2016, Issue 7) in the Cochrane Library; as well as reference lists of identified trials and abstracts from annual meetings of the Society for Pediatric Research, the American Pediatric Society, and Pediatric Academic Societies, published in Pediatric Research (2002 to 2016). We included editorials, commentaries, reviews, lectures, abstracts, and letters to the editor only if they included original data. We applied no language restrictions. We contacted study authors to ask for additional/missing information. We have appended below the detailed search strategy developed by the Cochrane Neonatal Review Group (Appendices).

Searching other resources

We searched multiple clinical trials registries (clinicaltrials.gov; controlled‐trials.com; who.int/ictrp) to identify past, current, and planned clinical studies evaluating antibiotic use in neonates exposed to meconium‐stained amniotic fluid.

Data collection and analysis

Two review authors (LEK, PSS) independently searched for and assessed trials for inclusion and for methodological quality. We resolved discrepancies by consensus. We assessed the quality of studies by using the Cochrane 'Risk of bias' assessment tool (Review Manager 5.3). We evaluated domains of bias that included the following criteria: masking of randomisation, masking of intervention, completeness of follow‐up, and blinding of outcome measurement. Two review authors (LEK, PSS) independently extracted data. We resolved discrepancies or differences by discussion and consensus. We performed meta‐analysis by using RevMan 5.3. We reported mean differences (MDs) for continuous variables, and risk ratios (RRs) and risk differences (RDs) for categorical outcomes. For significant findings, we calculated the number needed to treat for an additional beneficial outcome (NNTB) along with 95% confidence intervals (CIs). We estimated treatment effects of individual trials and examined heterogeneity between trial results by inspecting forest plots and quantifying the impact of heterogeneity in any meta‐analysis using I² as a measure of inconsistency in study results. When we detected statistical heterogeneity, we explored possible causes. We used a fixed‐effect model for meta‐analysis.

Selection of studies

Two review authors (LEK, PSS) independently searched for and assessed trials for inclusion and for methodological quality. We resolved discrepancies by consensus.

Data extraction and management

Two review authors (LEK, PSS) independently extracted and managed data from full‐text publications using Review Manager 5.3.

Assessment of risk of bias in included studies

We assessed the quality of studies by using the Cochrane 'Risk of bias' assessment tool (Review Manager 5.3). We evaluated the following criteria for domains of bias: masking of randomisation, masking of intervention, completeness of follow‐up, and blinding of outcome measurement. Two review authors (LEK, PSS) independently extracted data and resolved discrepancies or differences by discussion and consensus.

Measures of treatment effect

We performed meta‐analysis using RevMan 5.3. We reported mean differences (MDs) for continuous variables, and risk ratios (RRs) and risk differences (RDs) for categorical outcomes. For significant findings, we calculated the number needed to treat for an additional beneficial outcome (NNTB) along with 95% confidence intervals (CIs).

Unit of analysis issues

The unit of analysis in each included study is the individual neonate; we identified no cluster‐randomised studies.

Dealing with missing data

When study data were missing, we contacted corresponding study authors to request further information. We performed all analyses by intention‐to‐treat, including all randomised participants.

Assessment of heterogeneity

We estimated treatment effects of individual trials and examined heterogeneity between trial results by inspecting forest plots and quantifying the impact of heterogeneity in any meta‐analysis using I² to measure inconsistency in study results. When we detected statistical heterogeneity, we explored possible causes. We used a fixed‐effect model for meta‐analysis.

Assessment of reporting biases

We were unable to identify study protocols or clinical trial registrations for all four studies. We reported these findings in the 'Risk of bias' tables.

Data synthesis

We performed data synthesis according to recommendations provided by the Cochrane Neonatal Review Group. We randomly assigned all neonates and performed intention‐to‐treat analysis. If results were presented as medians and interquartile ranges (IQRs), we transformed the data into means and standard deviations using the formulas provided by Wan 2014.

Sensitivity analysis

All included studies evaluated different antibiotic treatment protocols for neonatal exposure to meconium in amniotic fluid; therefore, a sensitivity analysis was not indicated.

Results

Description of studies

See Characteristics of included studies and Characteristics of excluded studies tables. No included studies included mixed populations of symptomatic and asymptomatic neonates at the time of randomisation.

Results of the search

We identified 116 citations from the literature and 41 trials from clinical trials registries. We have presented the process of selection of studies for inclusion in the PRISMA (Preferred Reporting Items for Systematic Reviews and Meta‐Analyses) flow diagram (Figure 1). We included in this review four eligible studies (Basu 2007; Goel 2015; Lin 2005; Shankar 1995) conducted in India and Taiwan with a total of 695 participants. We have presented the demographics of participants and details of interventions, study design, and outcomes in the Characteristics of included studies table.


Figure 1. Study flow diagram.

Figure 1. Study flow diagram.

Included studies

In summary, three studies (Basu 2007; Lin 2005; Shankar 1995) enrolled infants with a diagnosis of MAS (symptomatic).

Shankar 1995 randomised infants (N = 40) with a diagnosis of MAS to antibiotics (gentamicin) for seven days or to no treatment. Shankar 1995 included no predefined primary outcome.

Lin 2005 randomised 259 neonates with a diagnosis of MAS to antibiotics (ampicillin and gentamicin) for three days or no treatment. Lin 2005 included no predefined primary outcome.

Basu 2007 randomised neonates (N = 146) with MAS to antibiotics (ampicillin and amikacin) for seven days or no treatment. The primary outcome in Basu 2007 was the incidence of sepsis.

The fourth included study (Goel 2015) compared the prophylactic effectiveness of antibiotics given for three days versus no treatment in terms of the incidence of sepsis among neonates (N = 250) born through meconium‐stained amniotic fluid. Goel 2015 excluded infants with congenital malformations and those for whom consent could not be obtained. Both groups reported subsequent development of MAS, along with infection.

With respect to heterogeneity between included studies, the diagnostic criteria for MAS (born through meconium‐stained amniotic fluid, respiratory distress for longer than four hours after birth, and radiographic evidence of meconium in the trachea) were consistent among studies. All four trials used positive blood culture screens to define the primary outcome of this review ‐ culture‐proven (confirmed) sepsis. Review authors observed heterogeneity in study design and antibiotic treatment regimens among included studies and noted that investigators evaluated various antibiotics. The following were evaluated (each by two trials): amikacin, gentamicin, and ampicillin.Treatment timelines varied from three days (Goel 2015; Lin 2005) to seven days (Basu 2007; Shankar 1995).

Excluded studies

We excluded studies that did not prospectively evaluate antibiotic use using a randomised clinical design.

Risk of bias in included studies

Included studies showed varying degrees of bias. We have presented risk of bias details for each study in Figure 2. Two included studies (Lin 2005; Shankar 1995) were at overall unclear or high risk of bias, and two included studies (Basu 2007; Goel 2015) were at low risk of bias.


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

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

Allocation

Lin 2005 and Shankar 1995 provided no data on allocation concealment, resulting in unclear risk of bias. Basu 2007 and Goel 2015 appropriately concealed treatment allocation.

Blinding

Shankar 1995 did not blind nursery staff, resulting in high risk of bias. Lin 2005 described no blinding of participants, personnel, or outcome assessors. Basu 2007 reported that parents, attendants, radiologists, and statisticians were blinded. Goel 2015 blinded treating clinicians and nursery personnel but did not indicate how the treating clinician could be blinded, as the control group was provided no intervention, resulting in unclear risk of bias.

Incomplete outcome data

Lin 2005 described significant post‐randomisation exclusions, resulting in high risk of bias. Basu 2007,Goel 2015, and Shankar 1995 reported data for all randomised participants.

Selective reporting

Lin 2005 and Shankar 1995 did not provide data points for primary or secondary outcomes. We could not access a protocol or a clinical trials registry for Lin 2005 or Shankar 1995, nor a protocol for Basu 2007, creating unclear risk of bias, as we could not identify planned outcomes. For Goel 2015, reported outcomes matched those in the clinical trial registry.

Other potential sources of bias

We identified no other potential sources of bias in Basu 2007, Goel 2015, Lin 2005, or Shankar 1995.

Effects of interventions

See: Summary of findings for the main comparison Antibiotics compared with control (no antibiotics) in symptomatic neonates born through meconium‐stained amniotic fluid; Summary of findings 2 Antibiotics compared with control (no antibiotics) in asymptomatic neonates born through meconium‐stained amniotic fluid

Antibiotics versus control (no treatment with antibiotics) in neonates with a diagnosis of MAS

Three studies (Basu 2007; Lin 2005; Shankar 1995) evaluated effects of antibiotics in neonates with MAS. We graded evidence showing effects of antibiotics in neonates with a diagnosis of MAS as low owing to the small sample size (of only one study) and unclear risk of bias in the design of included studies.

Primary outcome
Outcome 1.1. Incidence of sepsis within first 28 days of life (Analysis 1.1)

We found no significant differences in risk of culture‐proven, confirmed sepsis (RR 1.54, 95% CI 0.27 to 8.96; RD 0.00, 95% CI ‐0.02 to 0.03; 445 participants, three studies; I² = 0%) (Figure 3). Of note, two of the three included studies (Lin 2005; Shankar 1995) reported a confirmed sepsis event rate of zero in both groups. Owing to low infection rates and limited information on the time of onset, we could not evaluate early‐onset versus late‐onset neonatal sepsis. None of the three studies included in this analysis reported the incidence of suspected sepsis.


Forest plot of comparison: Incidence of confirmed sepsis in symptomatic neonates within the first 28 days.

Forest plot of comparison: Incidence of confirmed sepsis in symptomatic neonates within the first 28 days.

Secondary outcomes
Outcome 1.2. Mortality before discharge (Analysis 1.2)

We found no statistically significant differences in mortality between groups (RR 1.69, 95% CI 0.23 to 12.53; RD 0.00, 95% CI ‐0.01 to 0.02; 445 participants, three studies; I² = 0%) (Figure 4).


Forest plot of comparison: Mortality in symptomatic neonates (before discharge).

Forest plot of comparison: Mortality in symptomatic neonates (before discharge).

Outcome 1.3. Duration of oxygen therapy (days) (Analysis 1.3)

Duration of oxygen therapy, as evaluated in two studies, was significantly less in the antibiotics group than in the control group (MD ‐0.85, 95% CI ‐1.19 to ‐0.52; 405 participants, two studies; I² = 73%; P < 0.00001).

Outcome 1.4. Duration of hospital stay (days) (Analysis 1.4)

Basu 2007 noted no statistically significant differences in mean duration of hospital stay between neonates who received antibiotics and those in the control group (MD 0.16, 95% CI ‐1.15 to 1.47; 146 participants, one study; I² = 0%).

Outcome 1.5. Incidence of pulmonary air leak syndrome (Analysis 1.5)

Trial authors noted no statistically significant differences in pulmonary air leak syndrome between groups (RR 1.50, 95% CI 0.62 to 3.67; RD 0.02, 95% CI ‐0.02 to 0.05; 445 participants, three studies; I² = 38%).

Post hoc outcomes in neonates with MAS

We added post hoc outcomes after reviewing included studies.

Incidence of mechanical ventilation (outcome 1.6) (Analysis 1.6)

Three studies reported the incidence of mechanical ventilation. Results show no statistically significant differences in the requirement for mechanical ventilation between antibiotic and control groups (RR 1.18, 95% CI 0.52 to 2.67; RD 0.01, 95% CI ‐0.03 to 0.05; 445 participants, three studies; I² = 0%).

Time to clear chest radiograph (days) (outcome 1.7) (Analysis 1.7)

Basu 2007 evaluated the time it took to obtain a clear chest radiograph in neonates with the diagnosis of MAS. Results show no statistically significant differences in both antibiotic and control groups (MD ‐1.31 days, 95% CI ‐3.04 to 0.42 days; 146 participants, one study; I² = 0%; P = 0.14).

Incidence of respiratory failure (outcome 1.8) (Analysis 1.8)

Two studies (Basu 2007; Lin 2005) reported the incidence of respiratory failure. Data show no statistically significant differences in risk between antibiotic and control groups (RR 1.20, 95% CI 0.51 to 2.83; RD 0.01, 95% CI ‐0.03 to 0.05; 405 participants, two studies; I² = 0%).

Duration of respiratory distress (hours) (outcome 1.9) Analysis 1.9

Neonates with MAS randomised to receive antibiotics did not experience different durations of respiratory distress (MD ‐1.20 hours, 95% CI ‐25.59 to 23.19 hours; 40 participants, one study; I² = 0%).

Antibiotics versus control (no treatment with antibiotics) in asymptomatic neonates

Only one study contributed data for this comparison (Goel 2015). We graded the evidence for effects of antibiotics in neonates who appear asymptomatic as low owing to the small sample size (of only one study). We were unable to assess the generalisability and impact of these findings.

Primary outcome
Outcome 2.1. Incidence of confirmed sepsis in first 28 days (Analysis 2.1)

Results show no significant differences in risk of culture‐proven, confirmed sepsis between groups (RR 0.76, 95% CI 0.25 to 2.34; RD ‐0.01, 95% CI ‐0.07 to 0.04; 250 participants, one study; I² = 0%). As only one study evaluated infection prevention in asymptomatic neonates, and given that infection rates were low and information on time of onset was limited, we could not evaluate early‐onset versus late‐onset neonatal sepsis.

Secondary outcomes
Outcome 2.2. Mortality (before discharge) (Analysis 2.2)

We noted no significant differences in mortality before discharge from hospital between groups (RR 1.07, 95% CI 0.22 to 5.18; RD 0.00, 95% CI ‐0.04 to 0.04; 250 participants, one study; I² = 0%).

Outcome 2.3. Duration of mechanical ventilation (days) (Analysis 2.3)

Duration of mechanical ventilation was significantly longer in the antibiotics group than in the placebo group (MD 0.26 days, 95% CI 0.15 to 0.37 days; 250 participants; one study; I² = 0%; P < 0.00001).

Outcome 2.4. Duration of oxygen therapy (days) (Analysis 2.4)

Neonates in the antibiotic arm required oxygen for a significantly longer time than those in the control group (MD 0.43 days, 95% CI 0.13 to 0.73 days; 250 participants, one study; I² = 0%; P = 0.004) (Analysis 2.4).

Outcome 2.5. Incidence of suspected sepsis (Analysis 2.5)

Suspected sepsis was confirmed in 50% of cases in both antibiotic and control groups. Results show no significant differences in the incidence of suspected sepsis between groups (RR 0.76, 95% CI 0.35 to 1.65; RD ‐0.03, 95% CI ‐0.10 to 0.05; 250 participants, one study; I² = 0%).

Outcome 2.6. Incidence of intracranial haemorrhage (Analysis 2.6)

Investigators identified only one case of intracranial haemorrhage in the control group, making this finding not significantly different from that in the antibiotic group (RR 0.36, 95% CI 0.01 to 8.64; RD ‐0.01, 95% CI ‐0.03 to 0.01; 250 participants; one study; I² = 0%).

Outcome 2.7. Incidence of azotaemia (Analysis 2.7)

Goel 2015 detected azotaemia in one infant treated with antibiotics. Data show no statistically significant differences in the incidence of azotaemia between groups (RR 3.20, 95% CI 0.13 to 77.73; RD 0.01, 95% CI ‐0.01 to 0.03; 250 participants, one study; I² = 0%).

Outcome 2.8. Incidence of oliguria (Analysis 2.8)

Goel 2015 detected only one case of oliguria in the antibiotics group. Study results show no statistically significant differences in the incidence of oliguria between groups (RR 3.20, 95% CI 0.13 to 77.73; RD 0.01, 95% CI ‐0.01 to 0.03; 250 participants, one study; I² = 0%).

Outcome 2.9. Incidence of diarrhoea (Analysis 2.9)

Researchers documented diarrhoea in four infants in the control group. Data show no statistically significant differences in the rate of diarrhoea between antibiotic and control groups (RR 0.12, 95% CI 0.01 to 2.18; RD ‐0.03, 95% CI ‐0.06 to 0.00; 250 participants, one study; I² = 0%).

Additional Outcome: Length of stay

Goel 2015 reported duration of stay in hospital at a median of three days (range three to three days) in both groups. As the range is 0, and the mean/standard deviation was not reported or was not available from the corresponding author, we could perform no further analysis on this outcome.

Post hoc outcomes in asymptomatic neonates

We added post hoc outcomes after reviewing included studies.

Outcome 2.10. Incidence of mechanical ventilation (Analysis 2.10)

Data show no significant differences in the number of neonates requiring mechanical ventilation between groups (RR 2.13, 95% CI 0.55 to 8.34; RD 0.03, 95% CI ‐0.02 to 0.07; 250 participants, one study; I² = 0%).

Outcome 2.11. Incidence of respiratory distress (Downe's score) (Analysis 2.11)

Results show no differences in risk of respiratory distress between antibiotic and control groups (RR 1.18, 95% CI 0.81 to 1.72; RD 0.05, 95% CI ‐0.06 to 0.17; 250 participants, one study; I² = 0%).

Outcome 2.12. Duration of respiratory distress (hours) (Analysis 2.12)

Neonates randomised to antibiotics had a significantly longer duration of respiratory distress than those in the control group (MD 6.87 hours, 95% CI 4.22 to 9.52 hours; 250 participants, one study; I² = 0%; P < 0.00001).

Outcome 2.13. Incidence of MAS (Analysis 2.13)

Goel 2015 treated neonates exposed to meconium but without a diagnosis of MAS before enrolment. Data show no significant differences in development of MAS between antibiotic and control groups (RR 1.17, 95% CI 0.67 to 2.04; RD 0.03, 95% CI ‐0.07 to 0.12; 250 participants, one study; I² = 0%).

Subgroup analysis

We could not complete comparisons planned to evaluate effects of antibiotic regimens, duration of antibiotics, and gestational age owing to limited information provided by few studies.

Discussion

Summary of main results

Clinicians have used various antibiotics and antibiotic regimens to treat neonates exposed to meconium during delivery. We identified four randomised controlled trials that enrolled 695 individuals to evaluate effectiveness of antibiotics in reducing infection following meconium exposure or diagnosis of meconium aspiration syndrome (MAS). Upon review of available evidence, we identified no differences in risk of infection (confirmed sepsis) among neonates receiving antibiotics (3/224) and controls (2/221) following MAS diagnosis. Evidence does not allow us to corroborate differences in the incidence of confirmed sepsis among asymptomatic neonates receiving antibiotics. Data show that in symptomatic neonates, antibiotics significantly lowered the duration of oxygen therapy, but in asymptomatic neonates, antibiotics were significantly associated with increased duration of oxygen therapy, mechanical ventilation, and respiratory distress. Given these inconsistent findings and the small numbers of neonates enrolled in these studies, we cannot present conclusions regarding the efficacy or safety of antibiotics in preventing infection following meconium exposure.

Overall completeness and applicability of evidence

All four included trials consistently reported no significant improvement in infection reduction with antibiotic treatment or prophylaxis despite use of different antibiotics and treatment durations. Studies were of mixed quality, included small sample sizes, and differed marginally in types of antibiotics and duration of therapy examined. Differences in antibiotic type and in treatment timelines (three to seven days) created heterogeneity in the intervention arms of included studies.

Quality of the evidence

All four trials compared antibiotics versus no treatment and did not include a placebo control. The lack of placebo control may have resulted in biased reporting; however, each study objectively defined criteria for sepsis. Limitations of this review include that the methodological quality of some included studies was poor, and that none of these studies included a placebo arm and full blinding of treating clinicians. Types of outcome measures reported showed some inconsistency, with only one trial evaluating the duration of mechanical ventilation, and with various measures of respiratory morbidity used across studies. We downgraded evidence owing to imprecision related to small sample sizes and unclear methodological features in some trials.

Potential biases in the review process

When interpreting the results of this review, one must consider the overall low event rate for sepsis in both intervention and control arms of all four trials. Variation in study design, including the addition of post hoc outcomes, could present a potential source of bias. After searching the literature, the review authors believed that relevant clinical outcomes should be added, but outcomes evaluated post hoc did not influence overall recommendations provided in this review. Although dogma suggests that meconium (comprising mostly water) is sterile, this paradigm is shifting, as several studies have identified bacterial contaminants in meconium samples (Jiménez 2008; Madan 2012; Mshvildadze 2010). Further investigation into the variable degree of bacterial colonisation observed in meconium and characterisation of organisms as pathogenic or non‐pathogenic may allow clinicians to better predict which neonates are at greatest risk for infection.

Agreements and disagreements with other studies or reviews

Similar to reviews published in 2015 (Pongmee 2015) and 2016 (Natarajan 2016), we did not identify a change in risk of infection (confirmed sepsis) among neonates receiving antibiotics following exposure to meconium.

Figure 1. Study flow diagram.
Figuras y tablas -
Figure 1

Figure 1. Study flow diagram.

Figure 2. Risk of bias summary: review authors' judgements about each risk of bias item for each included study.
Figuras y tablas -
Figure 2

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

Forest plot of comparison: Incidence of confirmed sepsis in symptomatic neonates within the first 28 days.
Figuras y tablas -
Figure 3

Forest plot of comparison: Incidence of confirmed sepsis in symptomatic neonates within the first 28 days.

Forest plot of comparison: Mortality in symptomatic neonates (before discharge).
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Figure 4

Forest plot of comparison: Mortality in symptomatic neonates (before discharge).

Comparison 1 Antibiotics versus control (no antibiotics) in symptomatic neonates, Outcome 1 Incidence of confirmed sepsis in first 28 days.
Figuras y tablas -
Analysis 1.1

Comparison 1 Antibiotics versus control (no antibiotics) in symptomatic neonates, Outcome 1 Incidence of confirmed sepsis in first 28 days.

Comparison 1 Antibiotics versus control (no antibiotics) in symptomatic neonates, Outcome 2 Mortality (before discharge).
Figuras y tablas -
Analysis 1.2

Comparison 1 Antibiotics versus control (no antibiotics) in symptomatic neonates, Outcome 2 Mortality (before discharge).

Comparison 1 Antibiotics versus control (no antibiotics) in symptomatic neonates, Outcome 3 Duration of oxygen therapy, days.
Figuras y tablas -
Analysis 1.3

Comparison 1 Antibiotics versus control (no antibiotics) in symptomatic neonates, Outcome 3 Duration of oxygen therapy, days.

Comparison 1 Antibiotics versus control (no antibiotics) in symptomatic neonates, Outcome 4 Duration of hospital stay, days.
Figuras y tablas -
Analysis 1.4

Comparison 1 Antibiotics versus control (no antibiotics) in symptomatic neonates, Outcome 4 Duration of hospital stay, days.

Comparison 1 Antibiotics versus control (no antibiotics) in symptomatic neonates, Outcome 5 Incidence of pulmonary air leak syndrome.
Figuras y tablas -
Analysis 1.5

Comparison 1 Antibiotics versus control (no antibiotics) in symptomatic neonates, Outcome 5 Incidence of pulmonary air leak syndrome.

Comparison 1 Antibiotics versus control (no antibiotics) in symptomatic neonates, Outcome 6 Incidence of mechanical ventilation.
Figuras y tablas -
Analysis 1.6

Comparison 1 Antibiotics versus control (no antibiotics) in symptomatic neonates, Outcome 6 Incidence of mechanical ventilation.

Comparison 1 Antibiotics versus control (no antibiotics) in symptomatic neonates, Outcome 7 Time to clear chest radiograph, days.
Figuras y tablas -
Analysis 1.7

Comparison 1 Antibiotics versus control (no antibiotics) in symptomatic neonates, Outcome 7 Time to clear chest radiograph, days.

Comparison 1 Antibiotics versus control (no antibiotics) in symptomatic neonates, Outcome 8 Incidence of respiratory failure.
Figuras y tablas -
Analysis 1.8

Comparison 1 Antibiotics versus control (no antibiotics) in symptomatic neonates, Outcome 8 Incidence of respiratory failure.

Comparison 1 Antibiotics versus control (no antibiotics) in symptomatic neonates, Outcome 9 Duration of respiratory distress, hours.
Figuras y tablas -
Analysis 1.9

Comparison 1 Antibiotics versus control (no antibiotics) in symptomatic neonates, Outcome 9 Duration of respiratory distress, hours.

Comparison 2 Antibiotics versus control (no antibiotics) for prevention in asymptomatic neonates, Outcome 1 Incidence of confirmed sepsis in first 28 days.
Figuras y tablas -
Analysis 2.1

Comparison 2 Antibiotics versus control (no antibiotics) for prevention in asymptomatic neonates, Outcome 1 Incidence of confirmed sepsis in first 28 days.

Comparison 2 Antibiotics versus control (no antibiotics) for prevention in asymptomatic neonates, Outcome 2 Mortality (before discharge).
Figuras y tablas -
Analysis 2.2

Comparison 2 Antibiotics versus control (no antibiotics) for prevention in asymptomatic neonates, Outcome 2 Mortality (before discharge).

Comparison 2 Antibiotics versus control (no antibiotics) for prevention in asymptomatic neonates, Outcome 3 Duration of mechanical ventilation, days.
Figuras y tablas -
Analysis 2.3

Comparison 2 Antibiotics versus control (no antibiotics) for prevention in asymptomatic neonates, Outcome 3 Duration of mechanical ventilation, days.

Comparison 2 Antibiotics versus control (no antibiotics) for prevention in asymptomatic neonates, Outcome 4 Duration of oxygen therapy, days.
Figuras y tablas -
Analysis 2.4

Comparison 2 Antibiotics versus control (no antibiotics) for prevention in asymptomatic neonates, Outcome 4 Duration of oxygen therapy, days.

Comparison 2 Antibiotics versus control (no antibiotics) for prevention in asymptomatic neonates, Outcome 5 Incidence of suspected sepsis.
Figuras y tablas -
Analysis 2.5

Comparison 2 Antibiotics versus control (no antibiotics) for prevention in asymptomatic neonates, Outcome 5 Incidence of suspected sepsis.

Comparison 2 Antibiotics versus control (no antibiotics) for prevention in asymptomatic neonates, Outcome 6 Incidence of intracranial haemorrhage.
Figuras y tablas -
Analysis 2.6

Comparison 2 Antibiotics versus control (no antibiotics) for prevention in asymptomatic neonates, Outcome 6 Incidence of intracranial haemorrhage.

Comparison 2 Antibiotics versus control (no antibiotics) for prevention in asymptomatic neonates, Outcome 7 Incidence of azotaemia.
Figuras y tablas -
Analysis 2.7

Comparison 2 Antibiotics versus control (no antibiotics) for prevention in asymptomatic neonates, Outcome 7 Incidence of azotaemia.

Comparison 2 Antibiotics versus control (no antibiotics) for prevention in asymptomatic neonates, Outcome 8 Incidence of oliguria.
Figuras y tablas -
Analysis 2.8

Comparison 2 Antibiotics versus control (no antibiotics) for prevention in asymptomatic neonates, Outcome 8 Incidence of oliguria.

Comparison 2 Antibiotics versus control (no antibiotics) for prevention in asymptomatic neonates, Outcome 9 Incidence of diarrhoea.
Figuras y tablas -
Analysis 2.9

Comparison 2 Antibiotics versus control (no antibiotics) for prevention in asymptomatic neonates, Outcome 9 Incidence of diarrhoea.

Comparison 2 Antibiotics versus control (no antibiotics) for prevention in asymptomatic neonates, Outcome 10 Incidence of mechanical ventilation.
Figuras y tablas -
Analysis 2.10

Comparison 2 Antibiotics versus control (no antibiotics) for prevention in asymptomatic neonates, Outcome 10 Incidence of mechanical ventilation.

Comparison 2 Antibiotics versus control (no antibiotics) for prevention in asymptomatic neonates, Outcome 11 Incidence of respiratory distress (Downe's score).
Figuras y tablas -
Analysis 2.11

Comparison 2 Antibiotics versus control (no antibiotics) for prevention in asymptomatic neonates, Outcome 11 Incidence of respiratory distress (Downe's score).

Comparison 2 Antibiotics versus control (no antibiotics) for prevention in asymptomatic neonates, Outcome 12 Duration of respiratory distress, hours.
Figuras y tablas -
Analysis 2.12

Comparison 2 Antibiotics versus control (no antibiotics) for prevention in asymptomatic neonates, Outcome 12 Duration of respiratory distress, hours.

Comparison 2 Antibiotics versus control (no antibiotics) for prevention in asymptomatic neonates, Outcome 13 Incidence of MAS.
Figuras y tablas -
Analysis 2.13

Comparison 2 Antibiotics versus control (no antibiotics) for prevention in asymptomatic neonates, Outcome 13 Incidence of MAS.

Summary of findings for the main comparison. Antibiotics compared with control (no antibiotics) in symptomatic neonates born through meconium‐stained amniotic fluid

Antibiotics compared with control (no antibiotics) in symptomatic neonates born through meconium‐stained amniotic fluid

Patient or population: symptomatic neonates born through meconium‐stained amniotic fluid
Setting: neonatal intensive care unit
Intervention: antibiotics
Comparison: control (no antibiotics)

Outcomes

Anticipated absolute effects* (95% CI)

Relative effect
(95% CI)

Number of participants
(studies)

Quality of the evidence
(GRADE)

Comments

Risk with control (no antibiotics)

Risk with antibiotics

Incidence of confirmed sepsis in first 28 days

Study population

Not estimable

445
(3 RCTs)

⊕⊕⊝⊝
LOW

Evidence was downgraded owing to unclear risk of bias due to methodological limitations, including a large number of dropouts; and imprecision resulting from a small sample size

9 per 1000

0 per 1000
(0 to 0)

Mortality (before discharge)

Study population

RR 1.69
(0.23 to 12.53)

445
(3 RCTs)

⊕⊕⊝⊝
LOW

Evidence was downgraded owing to unclear risk of bias due to methodological limitations, including a large number of dropouts; and imprecision resulting from a small sample size

5 per 1000

8 per 1000
(1 to 57)

Duration of oxygen therapy, days

Mean duration of oxygen therapy (days) was 0

MD 0.85 days lower
(1.19 lower to 0.52 lower)

405
(2 RCTs)

⊕⊕⊝⊝
LOW

Evidence was downgraded owing to unclear risk of bias due to methodological limitations, including a large number of dropouts; and imprecision resulting from a small sample size

Duration of hospital stay, days

Mean duration of hospital stay (days) was 0

MD 0.16 days higher
(1.15 lower to 1.47 higher)

146
(1 RCT)

⊕⊕⊕⊝
MODERATE

Evidence was downgraded owing to imprecision resulting from a small sample size

Incidence of mechanical ventilation

Study population

RR 1.18
(0.52 to 2.67)

445
(3 RCTs)

⊕⊕⊝⊝
LOW

Evidence was downgraded owing to unclear risk of bias due to methodological limitations, including a large number of dropouts; and imprecision resulting from a small sample size

45 per 1000

53 per 1000
(24 to 121)

Incidence of respiratory failure

Study population

RR 1.20
(0.51 to 2.83)

405
(2 RCTs)

⊕⊕⊝⊝
LOW

Evidence was downgraded owing to unclear risk of bias due to methodological limitations, including a large number of dropouts; and imprecision resulting from a small sample size

41 per 1000

47 per 1000
(20 to 113)

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

Figuras y tablas -
Summary of findings for the main comparison. Antibiotics compared with control (no antibiotics) in symptomatic neonates born through meconium‐stained amniotic fluid
Summary of findings 2. Antibiotics compared with control (no antibiotics) in asymptomatic neonates born through meconium‐stained amniotic fluid

Antibiotics compared with control (no antibiotics) in asymptomatic neonates born through meconium‐stained amniotic fluid

Patient or population: asymptomatic neonates born through meconium‐stained amniotic fluid
Setting: neonatal intensive care unit
Intervention: antibiotics
Comparison: control (no antibiotics)

Outcomes

Anticipated absolute effects* (95% CI)

Relative effect
(95% CI)

Number of participants
(studies)

Quality of the evidence
(GRADE)

Comments

Risk with control (no antibiotics)

Risk with antibiotics

Incidence of confirmed sepsis in first 28 days

Study population

Not estimable

250
(1 RCT)

⊕⊕⊝⊝
LOW

Evidence was downgraded owing to very serious imprecision, as the results from this study have not been replicated

54 per 1000

0 per 1000
(0 to 0)

Mortality (before discharge)

Study population

RR 1.07
(0.22 to 5.18)

250
(1 RCT)

⊕⊕⊝⊝
LOW

Evidence was downgraded owing to very serious imprecision, as the results from this study have not been replicated

23 per 1000

25 per 1000
(5 to 120)

Duration of oxygen therapy, days

Mean duration of oxygen therapy (days) was 0

MD 0.43 days higher
(0.13 higher to 0.73 higher)

250
(1 RCT)

⊕⊕⊝⊝
LOW

Evidence was downgraded owing to very serious imprecision, as the results from this study have not been replicated

Incidence of suspected sepsis

Study population

Not estimable

250
(1 RCT)

⊕⊕⊝⊝
LOW

Evidence was downgraded owing to very serious imprecision, as the results from this study have not been replicated

109 per 1000

0 per 1000
(0 to 0)

Incidence of mechanical ventilation

Study population

RR 2.13
(0.55 to 8.34)

250
(1 RCT)

⊕⊕⊝⊝
LOW

Evidence was downgraded owing to very serious imprecision, as the results from this study have not been replicated

23 per 1000

50 per 1000
(13 to 194)

Duration of respiratory distress, hours

Mean duration of respiratory distress (hours) was 0

MD 6.87 higher
(4.22 higher to 9.52 higher)

250
(1 RCT)

⊕⊕⊝⊝
LOW

Evidence was downgraded owing to very serious imprecision, as the results from this study have not been replicated

Incidence of MAS

Study population

RR 1.17
(0.67 to 2.04)

250
(1 RCT)

⊕⊕⊝⊝
LOW

Evidence was downgraded owing to very serious imprecision, as the results from this study have not been replicated

155 per 1000

181 per 1000
(104 to 316)

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

Figuras y tablas -
Summary of findings 2. Antibiotics compared with control (no antibiotics) in asymptomatic neonates born through meconium‐stained amniotic fluid
Comparison 1. Antibiotics versus control (no antibiotics) in symptomatic neonates

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Incidence of confirmed sepsis in first 28 days Show forest plot

3

445

Risk Difference (M‐H, Fixed, 95% CI)

0.00 [‐0.02, 0.03]

2 Mortality (before discharge) Show forest plot

3

445

Risk Difference (M‐H, Fixed, 95% CI)

0.00 [‐0.01, 0.02]

3 Duration of oxygen therapy, days Show forest plot

2

405

Mean Difference (IV, Fixed, 95% CI)

‐0.85 [‐1.19, ‐0.52]

4 Duration of hospital stay, days Show forest plot

1

146

Mean Difference (IV, Fixed, 95% CI)

0.16 [‐1.15, 1.47]

5 Incidence of pulmonary air leak syndrome Show forest plot

3

445

Risk Ratio (M‐H, Fixed, 95% CI)

1.50 [0.62, 3.67]

6 Incidence of mechanical ventilation Show forest plot

3

445

Risk Ratio (M‐H, Fixed, 95% CI)

1.18 [0.52, 2.67]

7 Time to clear chest radiograph, days Show forest plot

1

146

Mean Difference (IV, Fixed, 95% CI)

‐1.31 [‐3.04, 0.42]

8 Incidence of respiratory failure Show forest plot

2

405

Risk Difference (M‐H, Fixed, 95% CI)

0.01 [‐0.03, 0.05]

9 Duration of respiratory distress, hours Show forest plot

1

40

Mean Difference (IV, Random, 95% CI)

‐1.20 [‐25.59, 23.19]

Figuras y tablas -
Comparison 1. Antibiotics versus control (no antibiotics) in symptomatic neonates
Comparison 2. Antibiotics versus control (no antibiotics) for prevention in asymptomatic neonates

Outcome or subgroup title

No. of studies

No. of participants

Statistical method

Effect size

1 Incidence of confirmed sepsis in first 28 days Show forest plot

1

250

Risk Difference (M‐H, Fixed, 95% CI)

‐0.01 [‐0.07, 0.04]

2 Mortality (before discharge) Show forest plot

1

250

Risk Ratio (M‐H, Fixed, 95% CI)

1.07 [0.22, 5.18]

3 Duration of mechanical ventilation, days Show forest plot

1

250

Mean Difference (IV, Fixed, 95% CI)

0.26 [0.15, 0.37]

4 Duration of oxygen therapy, days Show forest plot

1

250

Mean Difference (IV, Fixed, 95% CI)

0.43 [0.13, 0.73]

5 Incidence of suspected sepsis Show forest plot

1

250

Risk Difference (M‐H, Fixed, 95% CI)

‐0.03 [‐0.10, 0.05]

6 Incidence of intracranial haemorrhage Show forest plot

1

250

Risk Ratio (M‐H, Fixed, 95% CI)

0.36 [0.01, 8.64]

7 Incidence of azotaemia Show forest plot

1

250

Risk Ratio (M‐H, Fixed, 95% CI)

3.20 [0.13, 77.73]

8 Incidence of oliguria Show forest plot

1

250

Risk Ratio (M‐H, Fixed, 95% CI)

3.20 [0.13, 77.73]

9 Incidence of diarrhoea Show forest plot

1

250

Risk Ratio (M‐H, Fixed, 95% CI)

0.12 [0.01, 2.18]

10 Incidence of mechanical ventilation Show forest plot

1

250

Risk Ratio (M‐H, Fixed, 95% CI)

2.13 [0.55, 8.34]

11 Incidence of respiratory distress (Downe's score) Show forest plot

1

250

Risk Ratio (M‐H, Fixed, 95% CI)

1.18 [0.81, 1.72]

12 Duration of respiratory distress, hours Show forest plot

1

250

Mean Difference (IV, Fixed, 95% CI)

6.87 [4.22, 9.52]

13 Incidence of MAS Show forest plot

1

250

Risk Ratio (M‐H, Fixed, 95% CI)

1.17 [0.67, 2.04]

Figuras y tablas -
Comparison 2. Antibiotics versus control (no antibiotics) for prevention in asymptomatic neonates