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Antenatal magnesium sulphate administration for fetal neuroprotection: a French national survey

  • Clément Chollat1, 2, 3Email author,
  • Lise Le Doussal3,
  • Gaëlle de la Villéon3,
  • Delphine Provost4 and
  • Stéphane Marret2, 3
BMC Pregnancy and ChildbirthBMC series – open, inclusive and trusted201717:304

https://doi.org/10.1186/s12884-017-1489-z

Received: 26 May 2016

Accepted: 8 September 2017

Published: 13 September 2017

Abstract

Background

Magnesium sulphate (MgSO4) is the only treatment approved for fetal neuroprotection. No information on its use is available in the absence of a national registry of neonatal practices. The objective of our study was to evaluate the use of MgSO4 for fetal neuroprotection in French tertiary maternity hospitals (FTMH).

Methods

Online and phone survey of all FTMH between August 2014 and May 2015. A participation was expected from one senior obstetrician, one senior anaesthetist and one senior neonatologist from each FTMH. Information was obtained from 63/63 (100%) FTMH and 138/189 (73%) physicians. Use of MgSO4 for fetal neuroprotection, regimen and injection protocols, reasons for non-use were the main outcome measures.

Results

60.3% of FTMH used MgSO4 for fetal neuroprotection. No significant difference was observed between university and non-university hospitals or according to the annual number of births. Protocols differed especially in terms of the maximum gestational age (3% <28 WG, 71% <33 WG, 18% <34 WG and 8% < 35 WG). Eighty seven percent of centers using MgSO4 prescribed retreatment when necessary, but according to non-consensual modalities in terms of number of treatments or between-treatment intervals. Injections and monitoring were mostly performed in the delivery room (97%) but also in the recovery room in one half of hospitals. Lack of experience (52%), absence of a written protocol (49%) and national guidelines (46%) were the reasons most commonly reported to explain non-use of MgSO4 as a neuroprotective agent.

Conclusions

Sixty percent of FTMH used MgSO4 for fetal neuroprotection, but according to heterogeneous regimens. National guidelines could allow standardization of practices and better MgSO4 coverage.

Keywords

Magnesium sulphate Neuroprotection Neonatology Very preterm infants National survey

Background

Protection of the immature brain of premature infants constitutes a crucial challenge for obstetricians and neonatologists. Although the survival of premature infants is continuously improving [1], their neurological outcome remains a major concern, as preterm birth is associated with neurodevelopmental impairments such as neuromotor deficits, cognitive deficits, learning disabilities, behavioral and psychiatric disorders and neurosensory deficiencies [2]. The prevalence of cerebral palsy (CP) in Europe slowly decreased from 1.90 to 1.77 per 1000 live births between 1980 to 2003, but still remains high [3]. Almost 40% of individuals with CP were born preterm and the risk of CP increases with decreasing gestational age [4]. Neuroprotection in the context of preterm birth is the subject of extensive research, but few strategies have currently been demonstrated to be effective. There is strong evidence to support antenatal magnesium sulphate (MgSO4) infusion in order to prevent CP in context of prematurity [5]. Based on animal and human observational studies that demonstrated a neuroprotective effect of MgSO4 [6, 7], five randomised controlled trials (RCTs) published between 2002 and 2008 were conducted to evaluate its effect [813]. Four meta-analysis of these five trials demonstrated that antenatal MgSO4 treatment significantly reduced the risk of CP in very preterm 2-year-old infants (for the Cochrane meta-analysis: overall RR 0.68; 95%CI 0.54 to 0.87; five trials, 6145 infants) [5, 1417]. Sixty-three women had to be treated in order to prevent CP in one child (95% CI 43 to 155). However, no statistically significant effect on infantile mortality was observed [5]. In the light of these convincing results, several national authorities (USA, Australia and New Zealand, Canada, UK, Belgium and Ireland) have recommended antenatal administration of MgSO4 in women at imminent risk of very preterm birth in order to prevent cerebral palsy [1824].

In France, no guidelines have been drafted in view of the ongoing debate concerning this evidence. No information on the use of MgSO4 in France is available in the absence of a national registry of neonatal practices.

Methods

Study design

This study was designed to evaluate the use of MgSO4 prior to preterm birth in all French tertiary maternity hospitals (FTMH) to describe the various protocols used and to analyze the reasons for non-use. This questionnaire-based study was conducted between August 2014 and May 2015 among all FTMH. Sixty-three FTMH were identified (61 in metropolitan France and two in overseas territories). In France, MgSO4 is usually prescribe by obstetricians. Midwives or nurses administer it under the responsibility of the anaesthetists, in case of side effects. Paediatricians, on the other hand, are most often initiators of the MgSO4 protocol at maternity. The point of view of theses three medical specialists is therefore crucial to adress this issue in a holistic way. Accordingly, in each center, the Heads of Departments of Obstetrics, Anaesthesia and Neonatology were contacted by mail and/or phone. Surveys were completed by the Head of Department or a senior physician. Each participant was able to answer the survey online, by e-mail or by phone. The Local Ethics Committee of Rouen University Hospital ruled that no formal ethics approval was required for such a current practice survey. Informed consent to participate was obtained from all participants involved in this study. The survey was designed and conducted using Google Forms software (https://www.google.com, Mountain View, CA, USA).

Collected data

The first part of the questionnaire comprised three general questions:
  1. 1)

    In your opinion, what are the advantages of administering MgSO4 to the mother before preterm birth?

     
  2. 2)

    Have you ever read one or more scientific articles on this topic?

     
  3. 3)

    Do you use MgSO4 in your center for neuroprotection prior to very preterm birth?

     

The second part of the questionnaire focused on MgSO4 users. Participants answered 20 questions about their MgSO4 administration protocol and their patterns of use.

The third part concerned MgSO4 non-users. Participants had to indicate their reasons for not using MgSO4:
  • lack of knowledge on the subject

  • lack of scientific evidence

  • expected benefit/risk balance not in favor of the use of MgSO4

  • lack of local experience

  • no written protocol in the department

  • reluctance of obstetricians or anaesthetists or paediatricians or all three.

Data analysis

Data were recorded on an Excel database. Results were analyzed descriptively. Statistical analysis was performed with Statview 5.0 (SAS Institute Inc.). Statistical analysis was done with the chi-squared test. A value of p < 0.05 was considered statistically significant.

Results

A total of 138 responses were obtained from the 189 physicians contacted (73%). A response to the survey was obtained from all 63 FTMH (100%) and from 54% of anaesthetists (34/63), 76% of obstetricians (48/63) and 89% of paediatricians (56/63). Respondents were distributed as follows: 40% (56/138) from paediatricians, 35% (48/138) from obstetricians and 25% (34/138) from anaesthetists. Respondents were distributed equally between university hospitals and non-university hospitals and according to the annual number of births per center. Among the respondents, 91% were familiar with the neuroprotective effect of MgSO4 and 79% had read at least one scientific article on this topic, with no significant difference between specialities (Table 1). Thirty-eight (60%) of the 63 centers used MgSO4 prior to preterm birth in order to protect the infant’s immature brain. No significant difference was observed according to the type of hospital (university hospital or non-university hospital, P = .47) or the annual number of births in each hospital (<3000 births per year or >3000 births per year, P = .71). Among the FTMH that routinely used MgSO4, 95% had a written administration protocol per hospital. The maximum gestational age for MgSO4 administration ranged between 32 (27/38 centers, 71%) and 33 WG (7/38 centers, 18%), while three centers continued to administer MgSO4 up to 34 WG. However, one center did not prescribe MgSO4 after 28 WG. The majority of centers (35/38, 92%) prescribed a loading dose of 4 g followed by maintenance treatment at a dose of 1 g per hour for 12 h. Thirty-three FTMH repeated the regimen when necessary. The modalities of subsequent courses were less clearly defined: 50% of written protocols did not specify the minimum interval between two doses and 76% did not specify the maximum number of doses. Nevertheless, the subsequent course was started within 24 h for 26% of centers, between 24 and 48 h for 16% of centers, and after 48 h for 8% of centers. Seven FTMH (18%) repeated the infusion once, one center repeated the infusion twice, and one center did not set any limits. Calcium channel blockers were coprescribed by 33 centers (87%) (Table 2). Contraindications and criteria for discontinuation of the MgSO4 infusion are shown in Table 3. MgSO4 was administered in the delivery room (97%), but also in the recovery room (50%), intensive care unit (24%) or obstetrics unit (21%). The reasons for non-use of MgSO4 are described in Table 4. None of the anaesthetists who did not use MgSO4 answered the question of non-use of MgSO4 (0/4). Lack of experience (52%), lack of a written protocol (49%) and the absence of national guidelines (46%) were the reasons most commonly reported by respondents to explain the absence of use of MgSO4 as a neuroprotective agent in their unit.
Table 1

Description of respondents

 

Speciality

Center n/N (%)

 

Anaesthetists n/N (%)

Obstetricians n/N (%)

Paediatricians n/N (%)

Total n/N (%)

P

Number of respondents

34/63 (54)

48/63 (76)

56/63 (89)

138/138 (100)

<.001

63/63 (100)

University Hospital

25/41 (61)

32/41 (78)

36/41 (88)

93/123 (76)

.66

41/63 (65)

Non-university Hospital

9/22 (41)

16/22 (73)

20/22 (91)

45/66 (68)

22/63 (35)

Annual number of births

<3000

17/36 (47)

23/36 (64)

33/36 (92)

73/108 (68)

.49

36/63 (57)

>3000

17/27 (63)

25/27 (93)

23/27 (85)

65/81 (80)

27/63 (43)

Familiar with the neuroprotective value of MgSO4

30/34 (88)

44/48 (92)

51/56 (91)

125/138 (91)

.76

N/A

Had read at least one article on this topic

24/34 (71)

40/48 (83)

45/56 (80)

109/138 (79)

.36

N/A

Values are n/N (%)

Percentages may not sum to 100 because of rounding

Table 2

MgSO4 protocols

MgSO4 indications

n/N (%)

Pre-eclampsia

46/63 (73)

Neuroprotection

38/63 (60)

Pre-eclampsia and neuroprotection

37/63 (59)

None

17/63 (27)

Written protocol for indication and administration

36/38 (95)

Maximum gestational age

 

 34

3/38 (8)

 33

7/38 (18)

 32

27/38 (71)

 31

0/38 (0)

 30

0/38 (0)

 29

0/38 (0)

 28

1/38 (3)

MgSO4 regimen

 

Loading dose of 4 g then maintenance with 1 g/h for 12 h

35/38 (92)

Loading dose of 4 g then maintenance with 2 g/h for 12 h

1/38 (3)

Only maintenance with 1 g/h for 12 h

2/38 (5)

Repeat MgSO4 if birth does not occur after the first course of MgSO4

33/38 (87)

Minimum interval between 2 treatments

 

 < 24 h

10/38 (26)

 24 to 48 h

6/38 (16)

 > 48 h

3/38 (8)

Not specified by protocol

19/38 (50)

Maximum number of treatments

 

 2

7/38(18)

 3

1/38 (3)

No maximum number

1/38 (3)

Not specified by the protocol

29/38 (76)

Start of MgSO4 administration in the case of imminent delivery < 4 h (without delaying obstetric management)

34/38 (90)

Coprescription of calcium channel blockers

33/38 (87)

Values are n/N (%)

Percentages may not sum to 100 because of rounding

Table 3

Contraindications, criteria for discontinuation of the infusion and place of administration and monitoring

Contraindications

n/N (%)

Renal failure

33/38 (87)

Electrolyte disorders

19/38 (50)

Cardiovascular disease

27/38 (71)

Respiratory distress

2/38 (5)

Myasthenia gravis

23/38 (61)

Delivery <30 min

18/38 (47)

Digitalis interaction

22/38 (58)

MgSO4 intolerance

1/38 (3)

Stop the infusion if

 

 Oliguria <120 mL/4 h

2/38 (5)

 Oliguria <100 mL/4 h

29/38 (76)

 Hemodynamic instability

31/38 (82)

 Respiratory rate < 12/min

6/38 (16)

 Respiratory rate < 10/min

28/38 (74)

 Hyporeflexia

35/38 (92)

 Disorders of consciousness

33/38 (87)

 Other

4/38 (1)

Place of administration

 

 Delivery room

37/38 (97)

 Recovery room

19/38 (50)

 Intensive care unit

9/38 (24)

 Obstetrics unit

8/38 (21)

Values are n/N (%)

Multiple answers were possible

Table 4

Reasons why MgSO4 was not used

 

Speciality

Center n/N (%)

Anaesthetists n/N (%)

Obstetricians n/N (%)

Paediatricians n/N (%)

Total n/N (%)

P a

Lack of knowledge

0/4

2/12 (17)

4/21 (19)

6/37 (16)

.95

6/25 (24)

Lack of scientific evidence

0/4

2/12 (17)

2/21 (10)

4/37 (11)

.55

3/25 (12)

Lack of guidelines

0/4

4/12 (33)

11/21 (52)

15/37 (41)

.29

13/25 (52)

Benefit-risk balance

0/4

2/12 (17)

3/21 (14)

5/37 (14)

.85

5/25 (20)

Lack of experience

0/4

7/12 (58)

10/21 (48)

17/37 (46)

.55

17/25 (68)

Lack of written protocol

0/4

7/12 (58)

9/21 (43)

16/37 (43)

.39

13/25 (52)

Reluctance of obstetricians

0/4

2/12 (17)

2/21 (10)

4/37 (11)

.55

3/25 (12)

Reluctance of anesthesiologists

0/4

2/12 (17)

3/21 (14)

5/37 (14)

.85

5/25 (20)

Reluctance of pediatricians

0/4

2/12 (17)

2/21 (10)

4/37 (11)

.55

4/25 (16)

Values are n/N (%)

Multiple answers were possible

aComparison between the answers provided by obstetricians and pediatricians, as anesthesiologists did not answer this question when they did not use MgSO4

Discussion

Main findings

This study provides an update on the reported use of MgSO4 for fetal neuroprotection in France, in the absence of a national registry of neonatal practices in France. Our survey showed that 60% (38/63) of FTMH stated that they used MgSO4 for fetal neuroprotection. This practice is not widespread and remains heterogeneous in France, despite a good knowledge by respondents of the scientific evidence and the benefits of MgSO4 in this context.

Another important finding is that the absence of national guidelines is one of reasons for non use MgSO4 for fetal neuroprotection.

Strenghts and limitations

This study presents a number of limitations: 1) our findings are based on physicians’ statements and not on written protocols; 2) only one representative of each speciality in each hospital was asked to complete the survey, which may not be representative of the whole team; 3) although at least one response was obtained from each FTMH, the various specialities were not equally represented (anaesthetists: 54%, obstetricians: 76% and paediatricians: 89%, P < .001); 4) albeit we have a clear idea of the number of tertiary maternity units that use MgSO4, actual coverage remains unknown as data for each center were not available (i.e number of preterm birth and number of fetuses exposed to MgSO4). We took into account only the reported policies and not the actual use of MgSO4.

Despite these major limitations, this survey is useful to describe the conditions of use of MgSO4 in real-life practice and to understand the lack of generalisation of such a protocol in France.

Interpretation

Our findings cannot be compared with others because there are no previous surveys about the use of MgSO4 for fetal neuroprotection. Our study highlighted the diversity of regimens and protocols in France. According to international guidelines, the most consensual regimen consisted of a 4 g loading dose following by 1 g/h maintenance treatment. However, heterogeneous practices were observed for several procedures, particularly the possibility of retreatment and the minimum interval between two treatments, as these particular issues are not clearly discussed in the scientific literature (especially in the five randomised controlled trials and meta-analysis). Meta-analysis of the individual data of participants in these five RCT is currently underway and could clarify these issues [25]. In our study, only one center (3%) prescribed MgSO4 up until 28 WG, whereas 71% of centers prescribed MgSO4 up until 32 WG. This difference could be explained by the number of women who need to be treated to avoid one case of cerebral palsy: 29 before 28 WG and 63 before 32 WG [5]. No data are available in the literature concerning the indication for MgSO4 after a gestational age of 32 WG, but a randomised controlled trial is ongoing (MAGENTA study protocol) [26]. However, in France, 18% and 8% of MgSO4 users centers prescribed this agent up until 33 WG and 34 WG, respectively. A similar heterogeneity is also observed in international guidelines. For example, the Australia and New Zealand Binational Clinical Practice guidelines established 30 WG as a limit [27]. Canadian, Belgian and Irish guidelines recommend that MgSO4 administration be proposed before 32 WG [21, 23, 24]. UK guidelines proposed the use of MgSO4 up until 30 WG and indicated that it should be considered up until 34 WG [22]. The American College of Obstetricians and Gynecologists recommended the development of specific guidelines, especially concerning gestational age, “in accordance with one of the larger trials” but with no specific details [18].

Contraindications and criteria for discontinuation of the infusion seem to be more consensual in our survey, with minor differences for oliguria or bradypnea cut-off values. Almost all units administered MgSO4 in the delivery room, while one half of units administered MgSO4 also in the recovery room. Administration of this treatment obviously requires close cardiorespiratory monitoring and the place of administration should be determined according to the unit’s usual practice and the possibility of close monitoring by appropriate staff (nurse, midwife and/or anaesthetist). Drafting a written protocol seems essential to define the treatment regimen and to optimise its implementation. A few studies have demonstrated the feasibility of this type of protocol, with adequate selection of women at high risk of imminent preterm birth, ensuring optimal MgSO4 coverage for infants born preterm with a minimum of unnecessary maternal exposure [2831]. The American College of Obstetricians and Gynecologists published a patient safety checklist, which could be used to improve targeting and safety of MgSO4 administration [32].

Non-users reported lack of experience and the absence of a written protocol to explain their practice. Only a few respondents reported a low level of scientific evidence (4/37, 11%, representing 3/25 maternity units, 12%), suggesting that the majority of respondents consider that MgSO4 is beneficial for fetal neuroprotection. In contrast, the absence of national guidelines was reported by 46% of non-users, representing 13/25 maternity units, 52%. In France, national guidelines are necessary to ensure more widespread use of MgSO4. At the present time, MgSO4 is the only specific fetal neuroprotective medical treatment able to improve the neurodevelopment of preterm infants. As the development of preterm children is a long process which can be influenced by several environmental factors, optimal brain neuroprotective strategies comprising pharmacological interventions associated with educational measures need to be determined.

Conclusions

Sixty percent of FTMH used MgSO4 for fetal neuroprotection. Administration protocols differed from one center to another, particularly concerning the maximum gestational age, the possibility of retreatment, and the place of administration and monitoring. National guidelines could allow standardization of practices and better MgSO4 coverage. In the future, the use of MgSO4 should be as systematic as that of corticosteroids, allowing paediatricians to rightfully ask obstetricians: “Have you injected both corticosteroids and MgSO4?” in case of preterm birth.

Abbreviations

CP: 

Cerebral palsy

FTMH: 

French tertiary maternity hospitals

MgSO4

Magnesium sulphate

Declarations

Acknowledgments

We are grateful to Anthony Saul for editorial assistance and linguistic support.

Funding

This follow-up study was funded by a grant from the European Regional Development Fund (ERDF) and by a grant from the Upper-Normandy region. The funding sponsors had no role in the design of the study; in the collection, analyses or interpretation of data; and in the writing of the manuscript.

Availability of data and materials

Please contact Doctor Clement Chollat (clement.chollat@gmail.com) or Professor Marret (stephane.marret@chu-rouen.fr) for data requests.

Authors’ contributions

CC, LLD, and SM are responsible for the conception, design, and planning of the study. CC, LLD, GDV and DP carried out data extraction and analyses,. CC, LLD, and SM drafted the article; GDV and DP revised the article for important intellectual content. All authors revised and approved the final version of the article for publication.

Ethics approval and consent to participate

No patient or doctor identifiers were provided to the authors for this survey. The Local Ethics Committee of Rouen University Hospital ruled that no formal ethics approval was required for such a current practice survey. Informed consent to participate was obtained from all participants involved in this study. The consent was obtained online or in written according to the method of response to the questionnaire (online, email or phone).

Consent for publication

Not applicable.

Competing interests

The authors and the individuals referenced in the Acknowledments section have no conflicts of interest to disclose.

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Authors’ Affiliations

(1)
Assistance Publique - Hôpitaux de Paris, Service de Médecine et Réanimation Néonatales de Port-Royal, Groupe Hospitalier Cochin, Broca, Hôtel-Dieu
(2)
INSERM U1245, Team “Genetics and Pathophysiology of Neurodevelopmental Disorders”, Rouen University, Normandie University, Faculty of Medicine
(3)
Department of Neonatal Paediatrics and Intensive Care – Neuropaediatrics, Rouen University Hospital
(4)
Department of Anaesthetics and Intensive Care, Rouen University Hospital

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