|Year : 2015 | Volume
| Issue : 4 | Page : 221-226
Antibiotic administration for prevention or treatment of meconium aspiration syndrome in neonates: A†systematic review
Pharuhad Pongmee1, Gaurav Nagar2, Sandy Campbell3, Manoj Kumar2
1 Department of Pediatrics, Neonatal Division, University of Alberta, Canada; Department of Pediatrics, Neonatal Division, Faculty of Medicine, Ramathibodi Hospital, Mahidol University, Bangkok, Thailand
2 Department of Pediatrics, Neonatal Division, University of Alberta, Edmonton, Canada
3 John W. Scott Health Sciences Library, University of Alberta, Edmonton, Canada
|Date of Web Publication||16-Oct-2015|
Department of Pediatrics, Neonatal Division, Edmonton Clinical Health Academy, Room 3-528, 11405 87 Avenue NW, Edmonton, Alberta T6G1C9
Source of Support: None, Conflict of Interest: None
Objectives: To conduct a systematic review of the clinical trials evaluating the role of antibiotics for prevention or treatment of meconium aspiration syndrome (MAS). Methods: We searched several electronic databases including MEDLINE, EMBASE, CINAHL, SCOPUS (until September 2013), and CENTRAL (until August 2013). Additional citations were retrieved from the bibliographies of the selected articles. Studies were included if they were: Randomized or quasi-randomized trials, compared use of antibiotics with no antibiotics for treatment or prevention of MAS, and reported on clinical outcomes in the neonatal period. Results: Four randomized controlled trials (RCTs) were identified; three studies enrolled subjects for treatment of MAS and one study evaluated the prophylactic use of antibiotics in infants exposed to meconium stained amniotic fluid (MSAF). These trials enrolled 695 infants, with the duration of antibiotics between 3 and 7 days. All studies excluded subjects considered to be at higher risk for neonatal sepsis at onset. There were no differences noted for the outcomes of infection rates (relative risk [RR] [95% confidence interval: 0.85 [0.42, 1.73] for clinical sepsis, and 0.93 [0.36, 2.40] for culture-proven sepsis), need for mechanical ventilation (RR: 1.39 [0.68, 2.82]), air leaks syndrome (RR: 1.65 [0.68, 3.99]), hospital stay (mean difference − 0.34 days [−1.13, 0.45]), or mortality (RR: 1.25 [0.36, 4.39]) between the intervention and control groups. Conclusions: In neonates at low-risk for sepsis, insufficient evidence exists to support the routine use of antibiotics following exposure to MSAF or for the treatment of for suspected MAS. We discuss the implications and limitations of review findings for clinical practice.
Keywords: Antibiotics, meconium aspiration syndrome, meconium-stained amniotic fluid, meta-analysis, systematic review
|How to cite this article:|
Pongmee P, Nagar G, Campbell S, Kumar M. Antibiotic administration for prevention or treatment of meconium aspiration syndrome in neonates: A†systematic review. J Clin Neonatol 2015;4:221-6
|How to cite this URL:|
Pongmee P, Nagar G, Campbell S, Kumar M. Antibiotic administration for prevention or treatment of meconium aspiration syndrome in neonates: A†systematic review. J Clin Neonatol [serial online] 2015 [cited 2019 Nov 18];4:221-6. Available from: http://www.jcnonweb.com/text.asp?2015/4/4/221/165687
| Introduction|| |
Meconium aspiration syndrome (MAS) is a common cause of respiratory distress in neonates, especially in term and postterm infants and is associated with serious respiratory morbidities and mortality. 5–25% of all live births are associated with meconium-stained amniotic fluid (MSAF), but only 4–10% of infants born through MSAF develop MAS.,, MAS is diagnosed in infants exposed to MSAF and presenting as respiratory distress with characteristic radiological findings and whose symptoms cannot be otherwise explained.,
The exact physiology of meconium passage into the amniotic fluid leading to the development MAS is unknown. In addition, MAS could occur in utero or after delivery withinfirst few breaths. Three potential mechanisms of meconium release have been postulated. First, meconium passage is likely related with gut maturation as it typically occurs in term and postterm infants. Second, meconium passage may present in the pathological event such as stress or infection. Finally, fetal hypoxia may reduce the clearance of defecated meconium because of impaired fetal swallowing. It is unclear why some infants born through MSAF develop aspiration syndrome. Fetal hypoxia and acidosis may lead to fetal gasping and result in aspiration in utero.
Meconium may affect infant's lungs in various ways. The pathophysiological mechanisms in MAS include: (1) Acute airway obstruction results in hypoxia, (2) surfactant dysfunction or inactivation, (3) chemical pneumonitis with release of vasoconstrictive and inflammatory mediators, and (4) persistent pulmonary hypertension of the newborn (PPHN)., Hyperinflation or atelectasis may present, depend on the consistency and the amount of meconium aspirated (partial or complete airway obstruction).
Antibiotics are widely used in MAS. Some studies have shown that meconium enhances bacterial growth by increasing the risk of intra-amniotic infection and by reducing host resistance.,, Infection may aggravate stress causing infants to evacuate its bowels in utero and then lead to gasping, and therefore inhalation of meconium. Furthermore, routine use of antibiotics has been supported because the differentiation between MAS and pneumonia may be difficult and because of a risk of secondary infection in these cases.,
On the other hand, meconium itself is sterile and observational studies that assessed the development of sepsis in infants with MAS failed to demonstrate increased risk for bacteremia among meconium-stained neonates. Some studies have proposed that routine antibiotics prophylaxis is not recommended in the management of MAS for those without perinatal risk factors. Antibiotics therapy did not affect the clinical course and outcome related to infection in MAS infants who did not require ventilation and were without risk factors for infection. Nevertheless, antibiotics remain one of the medical therapies which are generously used in the management of MAS often leading to an extended hospital stay, higher health care costs, and the risk of greater antibiotics resistance.
The objective of this systematic review is to determine the role of routine antibiotic administration in the prevention or treatment of MAS for neonatal outcomes.
| Methods|| |
Searches were conducted by a medical librarian (SC) using both controlled vocabularies (MESH, EMTREE, etc.) and keywords (meconium adj3 (aspir* or inhal*) and ((antibiotic* or anti-infect* or anti-infect*) or specific drug names)). We searched the following electronic databases: MEDLINE, EMBASE, CINAHL, SCOPUS, and ProQuest dissertations and theses (until September 23, 2013); CENTRAL (until August 2013), and ACP Journal Club (until September 2013). We also searched database of abstracts of reviews of effects, Health Technology Assessment, and NHS Economic Evaluation Database (all until third-quarter 2013), Cochrane Methodology Register (third-quarter 2012); and International Pharmaceutical Abstracts (until August 2013). Search results were not limited by language. Additional references will be sought from bibliographies of the selected articles.
All citations identified were screened independently by two reviewers (PP, GN). Studies were considered for this review if they satisfied the following criteria: Randomized or quasi-RCT; included term, and postterm neonates who were diagnosed with MAS or exposed to MSAF; compared between antibiotics treatment and no antibiotic treatment; and reported any of the following outcomes: (1) Development of infection (culture proven sepsis or clinical sepsis), (2) need for respiratory support (ventilation and/or oxygen treatment), (3) air leaks syndrome, (4) PPHN, (5) need for extracorporeal membrane oxygenation, (6) need for inhaled nitric oxide, (7) hospital stay, and (8) mortality. Discrepancies regarding inclusion were resolved through discussion among the review team.
Methodological quality of the included studies was assessed using Cochrane risk of bias tool. These assessments were performed independently by two reviewers and discrepancies were resolved by discussion among the review team.
Data were extracted by two reviewers (PP, GN) using a standardized form and check accuracy by a third reviewer (MK). Primary authors for the included studies were contacted for additional information if needed. We extracted the following information: Characteristic of the study population and setting; description of the intervention and comparisons (antibiotics treatment vs. no antibiotics treatment); outcome measures and results.
Assessment of heterogeneity
The I2 statistic was calculated for each analysis to quantify heterogeneity across studies. If substantial (I2 > 50%) heterogeneity was detected, the potential causes for its existence were explored, and further sensitivity analysis undertaken.
| Results|| |
[Figure 1] shows the flow of the studies through the selection process. We identified four randomized controlled trials (RCTs) published between the years 1995 and 2015, enrolling a total of 695 patients. Three studies enrolled subjects for treatment of MAS ,, and one study evaluated prophylactic use of antibiotics in infants exposed to MSAF (initially published as an abstract in 2012 followed by full-text publication listed for 2015). A brief description and salient characteristics of the included studies trials are presented in [Table 1] (studies listed by thefirst author's name and year of publication). All three studies of antibiotics treatment for MAS excluded subjects considered to be at higher risk for neonatal sepsis at the onset due to antenatal risk factors and/or positive sepsis screen. Three studies ,, used a combination of antibiotics from penicillin and aminoglycoside groups whereas one study  used aminoglycoside alone. Duration of antibiotics treatment was 3 to 7 days. Lin et al. study  provided data for infants at 2 months of age without providing data at the time of discharge from the hospital. The study by Goel et al. reported data for the outcome of the prophylactic use of antibiotics in infants exposed to MSAF. In this study, 18.2% of the infants in the prophylactic antibiotic group subsequently developed MAS as compared to 15.5% of the infants not treated with antibiotics.
Risk of bias assessments
[Table 2] shows the risk of bias assessments of the included studies. Two studies did not adequately describe the methods used to generate the random sequence for participants., Only one of the included studies described satisfactorily the method of allocation concealment. None of the studies used a placebo in the control group or blinded intervention from the caregivers. Most studies were classified as "unclear" for the criterion of free of selective reporting, because it was difficult to make this judgment in the absence of availability of study protocols. Only one study registered its protocol online at clinicaltrials.gov. The study by Lin et al. had a large number of infants excluded (47 infants) following randomization.
Development of Infections
All studies reported the outcome of culture-proven sepsis whereas three studies also reported the rates of clinical sepsis. Figure 2] and [Figure 3] show the results of a meta-analysis of culture-proven and clinical sepsis, respectively. There was no difference between the treatment and the control groups in the rates of culture-proven sepsis (relative risk [RR]: 0.93 [0.36, 2.40]) or for clinical sepsis (0.85 [0.42, 1.73]). There was no heterogeneity in the estimates from the individual studies.
|Figure 2: Antibiotics versus control. Pooled estimates for culture-proven sepsis rates|
Click here to view
|Figure 3: Antibiotics versus control. Pooled estimates of the clinical sepsis rates|
Click here to view
There were no differences in any of the respiratory morbidities studied [Table 3]: The need for mechanical ventilation (RR: 1.39 [0.68, 2.82]) [Figure 4], the need for noninvasive ventilation (RR: 1.09 [0.71, 1.69]), and the incidence of air leaks syndromes (RR: 1.65 [0.68, 3.99]). The duration of respiratory support (ventilation or oxygen alone) was also not different between the intervention groups for studies that provided those data. One study  reported one infant in the antibiotics treatment group developed PPHN whereas two infants who were in control group diagnosed with PPHN.
|Table† 3: Pooled estimates of the study outcomes measured in the included studies|
Click here to view
|Figure 4: Meta-analysis for the outcome of need for mechanical ventilation|
Click here to view
There was no significant difference in the outcome of mortality (RR: 1.25 [0.36, 4.39]) between the antibiotics treatment group as compared to the control group [Figure 5]. Similarly, there was no difference in the duration of hospital stay (mean difference −0.34 days [−1.13, 0.45]) between two groups.
| Discussion|| |
Through this systematic review of the RCTs, we evaluated the role of antibiotics treatment in prevention or treatment of MAS in neonates. The main outcomes studied were the development of neonatal sepsis which included culture positive sepsis and clinical sepsis, respiratory morbidities, duration of hospital stay, and mortality. The included studies were assessed at high-risk of bias due to lack of blinding. The three trials ,, that enrolled subjects for treatment of established MAS, excluded infants with higher baseline risk for neonatal sepsis assessed based on presence of antenatal risk factors and/or positive sepsis screen following birth. We did not find any difference between antibiotics treatment and control groups for any of the outcomes evaluated. There was no heterogeneity in the pooled estimates of data from the individual trials.
The results of this review show insufficient evidence to support the practice of routine use of antibiotics in neonates exposed to MSAF or with MAS, who are otherwise considered at low-risk for neonatal sepsis. Based on these data, we suggest that the use of antibiotics in asymptomatic infants merely exposed to MSAF is not needed. This would prevent delay in hospital discharge for these otherwise healthy infants and result in saving health care resources.
However, similar recommendation for symptomatic neonates with respiratory distress could be problematic, as pneumonia is usually considered in the differential diagnosis and cannot be excluded with certainly based on normal blood counts, or unremarkable sepsis screen and/or the lack of characteristic chest X-ray findings. In addition, the wide confidence intervals (CIs) for point estimates of the outcomes studied in this review mean that a definite statement in favor of withholding antibiotics in these symptomatic infants would not be feasible based on current evidence. For such infants, we suggest that the use of antibiotics could be restricted to a shorter duration lasting 48–72 h if appropriate investigations for infection are negative.
Our systematic review has a few limitations. First, the individual studies included for this review were relatively small trials with a low event rate for the important binary outcomes assessed such as sepsis rates, need for ventilation or mortality. Thus, as discussed above, the estimates for those outcomes are imprecise (as reflected in their wide 95% CIs) and we could have missed a clinical significant effect that may have existed due to a β-error. Second, the included studies were methodologically of poor quality with none employing blinding of interventions through the use of placebo in the control arm. In addition, one of the included studies  reported a large dropout rate postrandomization, a potential source of additional bias. Lastly, we could have missed an important study that may have changed the results of this review. However, it seems unlikely as our search strategy, undertaken with the help of a research librarian was broad, and we did not use any language restrictions. We could not assess for publication bias using a formal test or through funnel plots, in view of a small number of trials included in this review.
| Conclusions|| |
In summary, the neonates who are otherwise at low risk for neonatal sepsis, there is insufficient evidence to support the routine use of antibiotics for treatment of MAS or for prophylaxis in infants exposed to MSAF. The use of antibiotics in asymptomatic infants exposed to MSAF should thus be avoided. For symptomatic infants with a diagnosis of probable MAS, if appropriate investigations for infection are negative the use of antibiotics could be restricted to a short course of 2–3 days. Further, placebo control RCTs are warranted to elucidate the risk-benefit of antibiotics administration to infants with established MAS.
Financial support and sponsorship
Conflicts of interest
There are no conflicts of interest.
| References|| |
Wiswell TE, Bent RC. Meconium staining and the meconium aspiration syndrome. Unresolved issues. Pediatr Clin North Am 1993;40:955-81.
Cleary GM, Wiswell TE. Meconium-stained amniotic fluid and the meconium aspiration syndrome. An update. Pediatr Clin North Am 1998;45:511-29.
Wiswell TE. Advances in the treatment of the meconium aspiration syndrome. Acta Paediatr Suppl 2001;90:28-30.
Walsh MC, Fanaroff JM. Meconium stained fluid: Approach to the mother and the baby. Clin Perinatol 2007;34:653-65, viii.
Swarnam K, Soraisham AS, Sivanandan S. Advances in the management of meconium aspiration syndrome. Int J Pediatr 2012;2012:359571.
Poggi SH, Ghidini A. Pathophysiology of meconium passage into the amniotic fluid. Early Hum Dev 2009;85:607-10.
Yurdakök M. Meconium aspiration syndrome: Do we know? Turk J Pediatr 2011;53:121-9.
van Ierland Y, de Beaufort AJ. Why does meconium cause meconium aspiration syndrome? Current concepts of MAS pathophysiology. Early Hum Dev 2009;85:617-20.
Romero R, Hanaoka S, Mazor M, Athanassiadis AP, Callahan R, Hsu YC, et al.
Meconium-stained amniotic fluid: A risk factor for microbial invasion of the amniotic cavity. Am J Obstet Gynecol 1991;164:859-62.
Wen TS, Eriksen NL, Blanco JD, Graham JM, Oshiro BT, Prieto JA. Association of clinical intra-amniotic infection and meconium. Am J Perinatol 1993;10:438-40.
Eidelman AI, Nevet A, Rudensky B, Rabinowitz R, Hammerman C, Raveh D, et al.
The effect of meconium staining of amniotic fluid on the growth of Escherichia coli
and group B streptococcus. J Perinatol 2002;22:467-71.
Basu S, Kumar A, Bhatia BD. Role of antibiotics in meconium aspiration syndrome. Ann Trop Paediatr 2007;27:107-13.
Lin HC, Su BH, Tsai CH, Lin TW, Yeh TF. Role of antibiotics in management of non-ventilated cases of meconium aspiration syndrome without risk factors for infection. Biol Neonate 2005;87:51-5.
Wiswell TE, Henley MA. Intratracheal suctioning, systemic infection, and the meconium aspiration syndrome. Pediatrics 1992;89:203-6.
Higgins JP, Altman DG, Sterne JA. Assessing risk of bias in included studies. In: Higgins JP, Green S, editors. Cochrane Handbook for Systematic Reviews of Interventions. Ch. 8. Version 5.1.0. Copenhagen, Denmark: The Cochrane Collaboration; 2011. Available from: http://www.cochrane-handbook.org
. [Last updated on 2011 Mar].
Shankar V, Paul VK, Deorari AK, Singh M. Do neonates with meconium aspiration syndrome require antibiotics? Indian J Pediatr 1995;62:327-31.
Goel A, Nangia S, Saili A, Garg A, Sharma S, Randhawa VS. Role of prophylactic antibiotics in neonates born through a meconium-stained amniotic fluid (MSAF) – A randomized controlled trial. Eur J Pediatr 2015;174:237-43.
[Figure 1], [Figure 2], [Figure 3], [Figure 4], [Figure 5]
[Table 1], [Table 2], [Table 3]