Elsevier

Early Human Development

Volume 85, Issue 10, October 2009, Pages 611-615
Early Human Development

Best Practice Guideline article
What (not) to do before delivery? Prevention of fetal meconium release and its consequences

https://doi.org/10.1016/j.earlhumdev.2009.09.010Get rights and content

Abstract

Background

Meconium-stained amniotic fluid is a common occurrence which places the mother at risk of escalating obstetric interventions, and the baby at risk of meconium aspiration syndrome.

Methods

The Cochrane Library was searched for interventions related to care before delivery with useful evidence on the outcomes ‘meconium-stained amniotic fluid’ and ‘meconium aspiration syndrome’.

Findings

Curtailment of post-term pregnancy reduces the occurrence of meconium-stained amniotic fluid, and meconium aspiration syndrome.

Uterine stimulants, particularly misoprostol, are associated with occurrence of meconium-stained amniotic fluid.

Amniotomy during labour may be a risk factor for meconium aspiration syndrome.

There is little research evidence on the benefits or otherwise of obstetric interventions such as expedited delivery for meconium-stained liquor without other evidence of fetal distress. Amnioinfusion for meconium-stained amniotic fluid improves neonatal outcome only in settings with limited peripartum surveillance. There is insufficient evidence to support the use of amnioinfusion for meconium-stained liquor in settings with adequate peripartum surveillance.

Introduction

The appearance of meconium in the amniotic fluid before or during labour is often a source of anxiety for health workers. It has the potential to cause both direct harm to the newborn child, and indirect benefit or harm to mother or child by eliciting appropriate or inappropriate obstetric interventions.

Meconium staining of the amniotic fluid is a common occurrence, and increases with increasing gestational age, from 7% to 22% of term deliveries overall [1], [2], to 23% to 52% after 42 weeks [3], [4], [5], [6]. It is more common in babies of black African descent, [7] and is associated with reduced amniotic fluid index (< 5 cm) [8], with reduced middle cerebral artery pulsatility index [9], with maternal fever, [10] with opiate and cocaine use, [11] and with multiple nuchal cord loops in postdate pregnancies [12]. It may be associated with fetal compromise, but is also common in uncompromised labours. Thick but not thin meconium staining of the amniotic fluid is associated with poor perinatal outcome [13], [14].

The most important consequence of meconium staining of the amniotic fluid is meconium aspiration syndrome which occurs in 1% to 3% of pregnancies [15], [16], [17]. Meconium aspiration may occur before birth, or during the birth process, and is associated with significant morbidity. Meconium aspiration syndrome is an important cause of neonatal mortality in otherwise healthy term or post-term infants, with a case fatality rate of 5%-40% [16], [18], [19], [20].

Airways suctioning of the neonate may reduce, but does not eliminate the occurrence of meconium aspiration (see Vain NE, chapter 4). Strategies have therefore been sought to reduce fetal meconium aspiration before birth.

This review will attempt to provide a balanced view of the significance of meconium staining of the amniotic fluid, and evidence regarding strategies which may reduce either its occurrence or its impact on the pregnancy outcome. Particular attention will be paid to the following strategies:

  • curtailing the duration of pregnancy

  • avoiding harmful medication

  • appropriate use of amniotomy

  • clinical response to observed meconium staining of the amniotic fluid

  • amnioinfusion.

Section snippets

Methods of the review

In order to identify pregnancy interventions before birth which might reduce or increase the risk of meconium passage or meconium aspiration syndrome, the Cochrane Library was searched on the term ‘meconium’. Those interventions identified which related to care before delivery were searched for any useful evidence on the outcomes ‘meconium-stained amniotic fluid’ and ‘meconium aspiration syndrome’. Where evidence from Cochrane reviews was not available, other review data were used. These data

Curtailing the duration of pregnancy

The physiological propensity of the fetus to pass meconium, and thus the incidence of meconium-stained amniotic fluid, increases with increasing gestational age (see Ghidini A, chapter 1). Preventing prolonged pregnancy by labour induction might reduce the risk of meconium-stained amniotic fluid. On the other hand, the process of labour induction might increase the risk of meconium passage by causing fetal hypoxia or by other mechanisms such as a direct effect of the induction agent on the

Avoiding harmful medication

In 1987 we reported an association between meconium-stained amniotic fluid and the ingestion of traditional herbal uterine stimulants (‘isihlambezo’) or castor oil [41]. We showed that isihlambezo stimulated both rat uterine and ileal smooth muscle in vitro [42], and postulated that smooth uterine stimulants might cross from mother to the fetus and cause meconium passage by direct stimulation of the bowel. We subsequently showed that misoprostol, a prostaglandin E1 analogue, and dinoprostone

Appropriate use of amniotomy

Amniotomy might in theory increase the risk of meconium-stained amniotic fluid by causing increased uterine contractions, increased direct pressure on the baby's head, or increased umbilical cord compression due to reduced amniotic fluid volume. Amniotomy (plus oxytocin) used for labour induction versus expectant management was associated with reduced meconium-stained amniotic fluid, presumably by curtailing prolonged pregnancy (Table 1 — see above).

In a review of two randomized trials of

Clinical response to observed meconium staining of the amniotic fluid

Meconium may be passed in response to fetal distress. The presence of meconium-stained amniotic fluid is thus commonly taken as an indication of possible fetal distress [1], [44].

However, the predictive values of meconium-stained amniotic fluid for fetal distress are poor [45], [46], [47], [48]. As with any diagnostic test with low predictive values, the potential exists for medical interventions in response to meconium-stained amniotic fluid to do more harm than good. In the absence of direct

Amnioinfusion

Amnioinfusion has been described as a method of preventing or relieving umbilical cord compression during labour [35], or of diluting meconium in the amniotic fluid to try to reduce the risk of meconium aspiration [49]. The technique is well described by Weismiller [50]. Saline or Ringer's lactate is usually infused through a purpose-designed intrauterine pressure catheter using an infusion pump. Studies from low-income countries where such catheters are unaffordable have demonstrated that

Oral hydration

Oral hydration has been shown to increase amniotic fluid volume in the short term [54]. Whether this strategy would dilute meconium and improve labour outcomes has not been assessed.

Other interventions during labour

Home-like versus conventional institutional settings for birth, epidural vs parental opioid analgesia, and immersion in water vs no immersion during 1st stage of labour have not been found to have any effect on the occurrence of meconium-stained amniotic fluid (Table 1).

Key guidelines

  • Curtailment of prolonged pregnancy reduces the risk of meconium-stained amniotic fluid and meconium aspiration syndrome.

  • Labour induction with prostaglandins, particularly misoprostol, appears to be associated with the occurrence of meconium-stained amniotic fluid.

  • Amniotomy during labour may increase the risk for meconium aspiration syndrome.

  • No evidence as to whether expediting delivery because of meconium-stained amniotic fluid alone improves outcome.

  • Amnioinfusion for suspected umbilical cord

Research directions

  • Specific research to determine the relationship between prostaglandin administration and meconium-stained amniotic fluid.

  • Research to confirm the effect of amniotomy during labour on meconium aspiration syndrome.

  • Research to determine the appropriate clinical response to meconium staining of the amniotic fluid.

  • Research to determine the effect of oral or parenteral hydration on thick meconium staining of the amniotic fluid.

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