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Safety and efficacy of antenatal milk expressing for women with diabetes in pregnancy: protocol for a randomised controlled trial
  1. Della A Forster1,2,
  2. Susan Jacobs2,3,4,
  3. Lisa H Amir1,
  4. Peter Davis2,
  5. Susan P Walker4,5,
  6. Kerri McEgan5,
  7. Gillian Opie4,5,
  8. Susan M Donath6,
  9. Anita M Moorhead1,2,
  10. Rachael Ford1,2,
  11. Catharine McNamara5,
  12. Amanda Aylward2,
  13. Lisa Gold7
  1. 1Judith Lumley Centre (formerly Mother & Child Health Research), La Trobe University, Melbourne, Victoria, Australia
  2. 2Royal Women's Hospital, Parkville, Victoria, Australia
  3. 3Clinical Sciences, Murdoch Childrens Research Institute, Parkville, Victoria, Australia
  4. 4Department of Obstetrics and Gynaecology, University of Melbourne, Carlton, Victoria, Australia
  5. 5Mercy Hospital for Women, Heidelberg, Victoria, Australia
  6. 6Clinical Epidemiology and Biostatistics Unit, Murdoch Childrens Research Institute, Parkville, Victoria, Australia
  7. 7Deakin Health Economics, Deakin University, Burwood, Victoria, Australia
  1. Correspondence to Professor Della Forster; d.forster{at}latrobe.edu.au

Abstract

Introduction Many maternity providers recommend that women with diabetes in pregnancy express and store breast milk in late pregnancy so breast milk is available after birth, given (1) infants of these women are at increased risk of hypoglycaemia in the first 24 h of life; and (2) the delay in lactogenesis II compared with women without diabetes that increases their infant's risk of receiving infant formula. The Diabetes and Antenatal Milk Expressing (DAME) trial will establish whether advising women with diabetes in pregnancy (pre-existing or gestational) to express breast milk from 36 weeks gestation increases the proportion of infants who require admission to special or neonatal intensive care units (SCN/NICU) compared with infants of women receiving standard care. Secondary outcomes include birth gestation, breastfeeding outcomes and economic impact.

Methods and analysis Women will be recruited from 34 weeks gestation to a multicentre, two arm, unblinded randomised controlled trial. The intervention starts at 36 weeks. Randomisation will be stratified by site, parity and diabetes type. Women allocated to the intervention will be taught expressing and encouraged to hand express twice daily for 10 min and keep an expressing diary. The sample size of 658 (329 per group) will detect a 10% difference in proportion of babies admitted to SCN/NICU (85% power, α 0.05). Data are collected at recruitment (structured questionnaire), after birth (abstracted from medical record blinded to group), and 2 and 12 weeks postpartum (telephone interview). Data analysis: the intervention group will be compared with the standard care group by intention to treat analysis, and the primary outcome compared using χ2 and ORs.

Ethics and dissemination Research ethics approval will be obtained from participating sites. Results will be published in peer-reviewed journals and presented to clinicians, policymakers and study participants.

Trial registration number Australian Controlled Trials Register ACTRN12611000217909.

  • NEONATOLOGY
  • NUTRITION & DIETETICS

This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/

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Strengths and limitations of this study

  • This will be the first study to provide rigorous evidence regarding the practice of antenatal expression of colostrum in late pregnancy for women with diabetes in pregnancy.

  • It will explore the safety and efficacy for mother, fetus and infant.

  • The conclusions about antenatal expressing will be restricted to women with diabetes in pregnancy, but if this practice is found to be safe and effective for this high-risk group, the conclusions are likely to be applicable to other women as well.

Background

Diabetes is the second highest contributor to loss of health in Australia.1 Type 2 diabetes and gestational diabetes (GDM) are increasing globally.2 GDM occurs on average in 7% of pregnancies (range 1–14% depending on the population characteristics and diagnostic tests used),2 and is the strongest single population predictor of type 2 diabetes.3 An additional 1% of females aged below 44 years have pre-existing diabetes (type 1 or 2),4 with type 2 diabetes increasing in women of childbearing age.5 Since 2009, women found to have glucose intolerance at the first pregnancy visit are diagnosed as having type 2 diabetes (not GDM).2 In Victoria in 2008, 6.1% of all women giving birth had diabetes in pregnancy (personal communication, A Cooper, Perinatal Data Collection Unit). At the planned original study sites, the Royal Women's Hospital (RWH) and Mercy Hospital for Women (MHW), 7.7% (495/6443) and 10.3% (690/5748) of women, respectively, giving birth in 2009 had diabetes in pregnancy.

Pregnancies affected by diabetes have increased risk of perinatal complications, including increased perinatal mortality for infants of women with type 1 diabetes.6–8 In GDM, poorer glycaemic control is also associated with adverse infant outcomes.9

Infants of women with diabetes in pregnancy are at increased risk of hypoglycaemia (secondary to hyperinsulinism) and other morbidities in the early neonatal period (eg, macrosomia, respiratory distress syndrome, prematurity, congenital anomalies, polycythaemia, jaundice).5 ,10 They are more likely to themselves develop diabetes, and have an increased risk of obesity later in life.5

A strategy to decrease the risk of these infants developing diabetes or impaired glucose tolerance later in life would be one way of interrupting the cycle of diabetes. One such strategy is to increase the rate of exclusive breastfeeding from birth in these infants, given that early exposure to cow's milk protein increases the incidence of both type 1 (juvenile onset) and later onset type 2 diabetes.11–13 However, infants of women with diabetes are at high risk of not being exclusively breastfed for a number of reasons. Studies have found generally that women with diabetes are less likely to breastfeed than other women, and likely to breastfeed for a shorter duration,14–17 although one study has found that where breastfeeding is encouraged and supported, women with diabetes can be just as successful as women without diabetes.18

Lactogenesis II, the onset of copious milk production, usually occurs 30–40 h after birth.19 Women with diabetes experience up to a 24 h delay in lactogenesis II compared with women without diabetes,20–24 as do women with glucose intolerance, increasing their infants’ risk of receiving infant formula.25 Women with diabetes are also at risk of other comorbidities, most commonly obesity.26 ,27 In turn, obese women28 and obese women with diabetes29 are less likely to successfully breastfeed. Separation of mother and infant following caesarean birth (also more likely in women with diabetes in pregnancy27 ,30) and/or admission to special and neonatal intensive care units (SCN/NICU) further decreases the likelihood of establishing breastfeeding.31 ,32

Since infants of women with diabetes are at increased risk of hypoglycaemia,10 they require blood glucose monitoring and are often admitted to the SCN. If infants are hypoglycaemic and their mother is unable to provide a sufficient volume of expressed breast milk in addition to breastfeeding, they may receive supplementation with infant formula or intravenous glucose. This has led to a practice whereby some women with diabetes in pregnancy are being advised to express breast milk before their infant's birth.

Current practice

Increasing numbers of maternity providers are encouraging pregnant women with diabetes to express and store breast milk (colostrum) in the last weeks before their expected delivery date,33–38 so that breast milk is available in the postpartum period, thereby possibly avoiding infant formula if neonatal hypoglycaemia needs management with supplementary formula feeding. Some organisations have implemented guidelines for antenatal expressing of colostrum,39 ,40 and in a recent book for consumers, there is a section entitled “Getting a head start: expressing milk before your baby is born” (ref.41, p.57). This practice presupposes that establishing a supply of colostrum prebirth might ameliorate: (1) the number of infants of women with diabetes who receive infant formula or intravenous glucose if supplementary feeding is required to treat neonatal hypoglycaemia (stored colostrum could be used); (2) the delay in lactogenesis II in women with diabetes and (3) the number of infants of women with diabetes admitted to the SCN. These recommendations for practice have not been investigated and are therefore theoretical, and there is very limited evidence regarding the safety or efficacy of encouraging antenatal expressing of breast milk.

The evidence

A retrospective cohort study from the UK included 94 women, and found that infants of women with diabetes who expressed were born 1 week earlier on average (37.1 weeks (SD 2.6), compared with 38.2 weeks (SD 2.2), p=0.06), and were more likely to be admitted to the SCN.42 We conducted a pilot study in 2007 that also provided some evidence, and provided the baseline data to undertake the proposed randomised controlled trial (RCT).43 We recruited 43 women with diabetes in pregnancy who agreed to undertake antenatal expressing (35% of those eligible agreed to participate when invited) and we conducted a concurrent audit of clinical outcomes in a group of infants of similar women (with diabetes in pregnancy) to provide ‘control’ data. Women in the expressing pilot completed a demographic questionnaire, were then taught how to express colostrum and encouraged to do so for 10 min twice daily from 36 weeks gestation. They were advised on the safe storage of colostrum, which they froze for their baby's use after birth. Women kept a diary documenting their expressing and completed telephone interviews at 6 and 12 weeks postpartum. We found that 30% of infants in the pilot were admitted to SCN compared with 17% of ‘control’ infants, and that reasons for admission to SCN were similar in the two groups.43 Intravenous glucose use was 14% for pilot infants and 8% for control infants (RR=1.77; 95% CI 0.63 to 4.96). There was no evidence of any fetal compromise based on cardiotocographs (CTGs) undertaken after the first expressing episode. Women recorded blood sugar levels (BSLs) following their first three expressing episodes. Although the median BSLs were normal and suggested no evidence of hypoglycaemia at a group level, 10% (2/20) of women had a BSL <3.5 mmol/L after the first expressing episode, and seven women (27%; 7/29) reported they experienced tightenings or Braxton Hicks contractions as a result of antenatal expressing, and one ceased the intervention for this reason.

The amount of colostrum women obtained varied according to number of expressions, length of time between onset of expressing and birth and the time spent expressing, with a median of 14 days expressing and 40 mL (range 5–310 mL) obtained. Although some women found expressing difficult (31%), the intervention was positively received overall, and 95% (38/40) of women would express antenatally again if the practice was proven beneficial. More infants in the pilot received exclusive breast milk during their postpartum hospital stay (37%) compared with the ‘control’ group (27%; RR=1.38; 95% CI 0.82 to 2.31).

In January 2010, we conducted a telephone survey of 48 tertiary and large metropolitan and regional maternity hospitals across Australia providing care for 109 465 births per year and found that 30 of these services (63%; 65 478 births) recommend antenatal milk expressing.44 Of these, 21 (70%) recommended antenatal expressing primarily to women with diabetes in pregnancy (although the practice is also being recommended to women with other high-risk pregnancies), and 11 (37%) had a policy or guideline for antenatal milk expressing. Across the 11 services with a policy or guideline for antenatal milk expressing, the mean gestation recommended for start of expressing was 36 weeks (range 30–37 weeks). Of the 18 services (38%; 43 987 births) who did not recommend this practice, 5 (28%) discontinued antenatal expressing based on the recommendations of our pilot observational study,43 and await evidence to inform this practice.44

A recent Cochrane review identified no RCTs that investigated the practice of expressing and storing breast milk during pregnancy, and concluded that there is no high-level systematic evidence to inform the safety and efficacy of this practice.38 Rigorous evidence is urgently required to inform the clinical practice of antenatal expression of colostrum.44 This paper describes the protocol for an adequately powered RCT exploring the practice of advising women with diabetes in pregnancy to express breast milk from 36 weeks gestation.

Methods

A multicentre, two arm, unblinded RCT design will be used to compare the practice of antenatal milk expressing with standard care, for women with pre-existing or GDM. In the original trial design we included only women with diabetes in pregnancy who required insulin, choosing this group because they are the women for whom antenatal expressing is most often suggested, yet are at the highest risk of perinatal complications, particularly if glycaemic control is poor. This inclusion criterion changed, as detailed below in the sample size section.

Aims

Primary aim

To establish whether the practice of antenatal expressing of colostrum from 36 weeks gestation, for women with diabetes in pregnancy, increases the proportion of infants who require admission to the SCN or NICU compared with the infants of similar women receiving standard care.

Primary hypothesis

Infants of women with diabetes in pregnancy who start antenatal expressing of colostrum from 36 weeks gestation will be more likely to be admitted to the SCN or NICU during the primary hospitalisation after birth compared with the infants of women with diabetes in pregnancy receiving standard care.

Secondary aims

To determine whether antenatal expressing of colostrum from 36 weeks gestation for women with diabetes in pregnancy, compared with similar women receiving standard care:

  1. Increases the proportion of infants receiving exclusive breast milk at 3 months of age (ie, is effective in promoting exclusive breastfeeding);

  2. Decreases the mean gestation at birth (ie, is harmful);

  3. Increases the proportion of infants receiving exclusive breast milk during initial hospital stay (ie, is effective).

We will also:

  • Test the cost and cost-effectiveness of this intervention compared with standard care;

  • Explore the views and experiences of women participating in this trial;

  • Collect data on other outcomes—for example, fetal well-being associated with expressing; volumes of antenatal colostrum obtained; time to onset of lactogenesis II (onset of copious milk production).

Table 1 summarises the potential harms and benefits of antenatal expressing of colostrum.

Table 1

Potential harms and benefits of antenatal breast milk expressing

Study sample

All eligible women booking for maternity care at the trial sites during the recruitment period will be offered study participation.

Inclusion criteria: Any woman

  1. With pre-existing or GDM;

  2. Between 34 and 36 weeks gestation (but not more than 37 weeks);

  3. With a singleton pregnancy in a cephalic presentation;

  4. Attending the study sites for pregnancy care as a public patient;

  5. Planning to breastfeed and

  6. Able to speak and read in English.

Exclusion criteria: Women with

  1. Any history of antepartum haemorrhage, or placenta praevia (even in the absence of any antenatal bleeding);

  2. An unknown or classical caesarean section scar or more than one lower segment caesarean section scar;

  3. Any suspicion of fetal compromise including known or suspected intrauterine growth restriction, documented macrosomia (estimated fetal weight ≥95th centile) with abdominal circumference >97th centile, polyhydramnios or any abnormal tests of fetal well-being (whether clinically, ultrasound or CTG based);

  4. A known fetal anomaly;

  5. Hypertension and proteinuria—if any concerns about fetal well-being;

  6. A serious maternal mental health issue, other severe maternal obstetric/medical issue.

In some sites there are small proportions of infants who are automatically admitted to the SCN after birth, for example, infants of women who have type 1 or 2 diabetes, or women on higher doses of insulin. In these sites, given the primary outcome is SCN/NICU admission, the women in those groups will be ineligible for inclusion in the trial.

Recruitment

Eligible women will be identified and offered participation by a study midwife at 34–36 weeks gestation, to maximise the opportunity to recruit women. If the woman is interested she will provide written consent and complete a questionnaire regarding demographic details and breastfeeding intentions. Randomisation occurs at 36 weeks gestation, so recruitment and randomisation will often be a two-stage process. Prior to randomisation women will have a preliminary 20 min CTG, and if the CTG is assessed as reactive and without significant uterine activity, the woman will be randomised to one of the two trial arms. Women allocated to the intervention will be taught hand expressing at that time (detailed more fully below), with a CTG during this first 10 min expressing episode and for 20 min after. The schedule of participant enrolment, intervention and assessments is shown in figure 1.

Figure 1

Schedule of enrolment, intervention and assessments for the DAME (Diabetes and Antenatal Expressing) trial.

Randomisation procedure

Randomisation is stratified by site, first baby or not, and diabetes type (ie, pre-existing (type 1 or 2), gestational requiring insulin or gestational not requiring insulin). A computerised random number generator was used to select random permuted blocks with at least three different block sizes. A system designed and administered by the Clinical Epidemiology and Biostatistics Unit at Murdoch Childrens Research Institute is accessed by the internet to ascertain women's allocation.

The intervention

Women randomised to the intervention will receive all standard advice and care (guided by existing hospital protocols) as well as receiving instructions on the intervention. They will be taught how to hand express colostrum (see online supplementary file 1). Women will be encouraged to express twice daily for no more than 10 min until being admitted to hospital to give birth, unless any concerns arise which indicate that the intervention should cease (see below).

Women will be provided with written and verbal instructions on the safe storage and transportation of colostrum (see online supplementary file 1). Expressed colostrum will be labelled with the woman's hospital medical record number and kept in syringes in her home freezer. Women will be asked to bring the frozen colostrum in an ‘esky’ (cold storage box) when they are admitted for the birth. Women will be provided with all the equipment they require for this intervention: syringes (2 and 5 mL), small eskies, ice pack and specimen bags, labels with medical record number and diaries to document each episode of expressing.

A dedicated freezer will be available at each trial site for storage of antenatally expressed frozen colostrum. Midwifery and neonatal staff will receive education about the trial and be informed as to where to store the frozen expressed breast milk.

Ensuring maternal and fetal well-being

Surveillance in hospital

Women in the intervention group will undertake an expressing episode under CTG surveillance at the time they are taught expressing (immediately after randomisation). If a woman requires further CTGs during their pregnancy care she will be asked to do one of her expressing episodes during those CTGs, as the uterus may become more sensitive to the resultant oxytocin surge with advancing gestation. The protocol for subsequent CTGs and expressing will be identical to that of the initial expressing episode, that is, preliminary CTG, express for 10 min, then continue the CTG for 20 min postexpression. The CTG must be reactive prior to starting expressing. Immediate discontinuation of expressing will occur if there are any signs of fetal compromise (fetal tachycardia, reduced variability, late decelerations), or if there is excessive uterine activity (either a hypertonic contraction (one lasting longer than 90 s), or tachysystole (>5 contractions per 10 min period)). Each participating centre will follow their existing protocol for management of fetal distress, including availability of acute tocolysis and on-site obstetric support.

Surveillance at home

Women will be advised of precautions related to expressing in the antenatal period and informed that if they have concerns regarding any of these issues they should telephone the study midwife, or the emergency department/birth suite of their relevant hospital after hours. Instructions will be given regarding the importance of:

  1. Noting normal fetal activity prior to expressing.

  2. Reporting any complications after expressing, such as excessive uterine activity, vaginal blood loss, decreased fetal movements or signs of hypoglycaemia.

  3. Measuring BSLs after the first three episodes of expressing, to ensure that the expressing is not causing hypoglycaemia (which can occur with breastfeeding).45 A consultant endocrinologist will advise the research team on maternal diabetes care as needed, and assist with interpretation of relevant outcomes.

Standard care

All women with pre-existing or GDM are seen by a diabetes educator for management of their diabetes. Additionally, all women discuss breastfeeding with midwives during pregnancy, and at all sites women can ask to see a lactation consultant in the antenatal period if they wish. No site can participate in the trial if they recommend that women express colostrum in the antenatal period.

Management of neonatal hypoglycaemia

The intervention being tested is not aimed at preventing hypoglycaemia; however, in practice the aim of many clinicians who advise antenatal milk expressing for this group is to avoid the use of formula for supplementary feeding if/when neonatal hypoglycaemia occurs. Based on our pilot data, approximately half of the admissions to SCN or NICU will be for neonatal hypoglycaemia.43 We will measure the incidence and duration of neonatal hypoglycaemia; however, it is not expected that encouraging women to express prior to birth could of itself prevent neonatal hypoglycaemia.

Existing guidelines for management of newborn infants at risk of hypoglycaemia, including infants of women with diabetes in pregnancy, will be followed. While there may be slight variations in guidelines by trial site, for the purposes of data analysis neonatal hypoglycaemia is defined as a true blood glucose (TBG) <2.6 mmol/L as measured on a blood gas analyser (or portable point of care TBG analyser) or in the laboratory. Sites whose guidelines for management of newborn infants at risk of hypoglycaemia are too different from this are not eligible to participate in the trial, and site guidelines are reviewed by the trial neonatologist prior to a decision about any site's suitability for inclusion. Although bedside testing with a glucometer is possible (providing BSLs), this method is not accurate at low blood glucose levels, when a TBG is mandatory. Prompt, standardised and accurate blood glucose measurement of TBG is optimal,46 ,47 and in the trial will eliminate measurement bias in either trial arm. A portable point of care TBG analyser will facilitate prompt, accurate TBG measurement at the bedside without separation of mother and baby—crucial in supporting early breastfeeding.

Stratification by site ensures that any slight variation in infant glucose management will not affect trial outcomes. Regardless of group assignment, mothers will breastfeed their infants, and express their milk postpartum if required. The first response to hypoglycaemia (as per existing clinical guidelines at the two primary trial sites, RWH and MHW) is a prescribed volume (30–60 mL/kg/day of supplemental feed of expressed breast milk or infant formula, or glucose gel (0.5 mL/kg of 40%)) massaged into buccal mucosa. Hypoglycaemia unresponsive to supplemental feeding triggers admission to SCN/NICU, more frequent, larger supplemental feeds, further glucose gel or intravenous glucose therapy, to achieve normal TBGs.

Process evaluation

Adherence to the study protocol and intervention fidelity will be monitored.

  1. Measures of intervention exposure: Women in the intervention group will keep a diary of antenatal expressing, noting: date and time of day each expressing episode takes place, length of each expressing episode and volume of colostrum expressed. Women in the control group will be asked at the 1–2 week interview if they expressed antenatally, to check for any cross-over.

  2. Monthly meetings with all project staff will include discussion of protocol adherence, measurement and documentation.

  3. Intervention evaluation by participants: The telephone interview at 12 weeks postpartum will include questions regarding women's views and experiences of being in the trial.

Sample size

Given the aim of antenatal expressing of breast milk is to benefit infants of women with diabetes in pregnancy, we debated whether our primary outcome should test efficacy or safety. Because our pilot data suggested potential harm, we chose the primary hypothesis to test safety. We are also powered to test the listed secondary outcomes.

Primary outcome

As aforementioned, when we designed the trial originally, we included only women with diabetes in pregnancy who required insulin, and our sample size calculations were based on estimates of this group. With that population we needed an estimated sample size of 658 women (329 in each group) based on 80% power (α 0.05), and allowing 5% loss to follow-up. This allowed the detection of an increase in the proportion of infants of women (requiring insulin in pregnancy) who are admitted to SCN or NICU in the primary hospital admission following birth, from 20% in the control group to 30% in the intervention group. This estimate was derived from the pilot and audit data presented above.

Secondary outcomes

This sample size also allows detection of:

  1. A difference in exclusive breastfeeding at 3 months of 12% (40% in the control group compared with 52% in the intervention group; assuming the infants in the intervention achieve the same rate as the statewide data and as per our pilot, ie, 52%; requires n=254);

  2. A difference in the mean duration of pregnancy (38 weeks in the control group compared with 37 weeks in the intervention group; requires n=184; means, SDs derived from Soltani study42) and

  3. A difference in exclusive breastfeeding during initial hospital stay of 12% (25% in the control group compared with 37% in the intervention group).

Sample size revision May 2012

Recruitment to the trial as per the original criteria started in July 2011. In May 2012, it was agreed to amend our inclusion criteria to include all women with diabetes in pregnancy. This was due to two factors (A) the slow recruitment rate due to smaller numbers of eligible women than anticipated, and (B) expert advice from outside the research group recommending that the external validity of the trial would be increased if the criteria were broadened to also include women with diabetes in pregnancy who did not require insulin.

The change of inclusion criteria meant that a baseline rate of admission to the SCN or NICU would be 17% rather than 20% as per our original sample size calculations (based on a review of all 2011 outcome data for women with diabetes in pregnancy at the RWH). We undertook various recalculations to address this. Regarding the sample size with the altered baseline:

  • To detect 10% absolute difference (as in the original calculation) we would need 289 per group—this would be a decrease in sample size—which none of the team considered optimal;

  • To detect a 50% relative increase to 25.7% would need 379 per group, that is, 758 (100 more than current sample of 658)—again this is not ideal as the study is not funded for this and we did not use this difference in our original calculations;

  • Or we could maintain current sample size (658) and describe the study power to detect a 10% absolute difference.

The final option was chosen, that is, we agreed to maintain the current sample size and assume increased power to detect 10% absolute difference. Allowing for 5% loss to follow-up, the original sample size of 658 would provide 625 women at primary outcome measurement. This would detect a change in primary outcome from 17% to 27% with a power of 85%. All the original secondary outcome comparisons described above will be maintained given the sample size has not altered.

Outcome variables

Primary outcome

Proportion of infants admitted to SCN or NICU.

Secondary outcomes

  1. Proportion of infants receiving exclusive breast milk at 3 months of age;

  2. Gestational age at birth;

  3. Proportion of infants receiving exclusive breast milk during initial hospital stay;

  4. Cost of the intervention to hospitals and to women and cost-effectiveness against breastfeeding outcomes;

  5. Women's views and experiences;

  6. Fetal well-being associated with expressing (assessed by CTG at initial then subsequent opportunistic CTG episodes); antenatal expression episodes, timing and volumes collected (intervention group only); time to lactogenesis II.

Potential explanatory variables

  • Reasons for SCN/NICU admissions;

  • Hypoglycaemia treatments in maternity or SCN/NICU including glucose gel, intravenous glucose, glucagon, hydrocortisone;

  • Length of time until three consecutive infant TBG levels ≥2.6 mmol/L;

  • Maternal blood glucose levels following first three expressing episodes;

  • Maternal morbidity that could be related to expressing, for example, premature labour.

Data collection

Maternal and infant

Demographic data (including age, education, marital status, ethnic background, smoking) will be collected by questionnaire at recruitment, prior to randomisation.

Obstetric/neonatal medical outcomes will be abstracted from the medical record following the birth by researchers blinded to group allocation.

Other outcome data will be collected by telephone administered questionnaire at 1–2 and 12 weeks postpartum. Women in the intervention arm will complete a diary of their expressing activity.

Economic evaluation

Resource use data will be collected from the medical record following birth and from women’s self-reported use of health care and other resources in the 12 weeks after the birth. Costs included in the economic evaluation are those relating to care provided by the hospital (including admission to SCN/NICU) and women’s (infants’) use of healthcare and other societal resources over the period of the evaluation. Measured resource use will be valued using existing unit cost estimates (eg, Diagnosis Related Groups cost weights for hospital admissions for mother and infant48 and Medicare fee schedules for any attendances at the women's local doctor).49 As the primary outcome measure is itself a resource use item, economic evaluation will be expressed as cost-effectiveness analysis against exclusive breastfeeding at 3 months.

Blinding: The nature of the trial necessitates non-blinding of participants assigned to the intervention group, so that staff know to look for expressed breast milk in the freezer if it is available and required, and at most sites both the intervention and control groups need to be non-blinded to ensure that point of care TBGs are performed rather than BSLs, as most sites do BSLs unless indicated (rather than the TBGs required by this trial). Staff at sites that routinely undertake TBGs for all infants of women with diabetes in pregnancy will be blinded to women in the control group. Abstraction of medical record data will be undertaken blinded to group allocation; data will be presented to the data monitoring committee for the interim analysis in unlabelled study groups; and the research team will remain blinded to group allocation at all stages prior to final data analysis.

Data analysis

Data will be collected to meet the CONSORT guidelines for reporting of randomised trials,50 including data on eligible non-participants. The first stage of analysis will check the comparability of participants allocated to the two groups. The intervention group will be compared with the standard care group by intention to treat analysis. The primary outcome measure will be compared using χ2 tests and ORs. Comparison of means will be undertaken for continuous variables using t tests where data are normally distributed or Mann-Whitney U tests will compare medians otherwise. Ranked or Likert-type scales will be analysed using cumulative ORs. Where there are differences in baseline characteristics of the women in the two groups which might be associated with outcomes, an additional multivariate analysis will be carried out. Duration of breastfeeding will be compared using Kaplan-Meier statistics. Content analysis will be used to summarise open-ended comments.51

Data and Safety Monitoring Committees: A Data Monitoring Committee including a statistician, a midwife and an obstetrician (experienced in conducting RCTs) will undertake an interim analysis after half the women have given birth. A Safety Committee including a neonatologist, a midwife and an obstetrician (all experienced clinicians and researchers) will review reports of any adverse events, for example, an excess of any of the predefined adverse events for women or infants, blinded to group allocation (see online supplementary file 2 for list of events). Terms of reference for each of these committees will guide frequency of reviews and the conditions under which either committee would advise the research team that enrolment to the trial should cease.

Discussion

This will be the first study to provide rigorous evidence regarding the practice of antenatal expression of colostrum in late pregnancy for women with diabetes in pregnancy. It will explore the safety and efficacy for mother, fetus and infant.

There remains widespread national and international interest in the outcomes of this trial, and the controversy can be seen in a recent review which concluded antenatal expressing should be encouraged: “Although Forster et al43 have argued the teaching of [antenatal expressing] should cease until the practice is proven to be safe and effective…an ethical dilemma now exists…as to whether the benefits of early colostrum feedings in at-risk babies outweighs the unproven side effect of premature labour.52 In the absence of evidence, the clear benefits of early feedings of colostrum should outweigh the unsupported risks of ceasing [antenatal expressing] education.”53

Trial status

Approval has been granted from the following Human Research Ethics Committees (reference number in brackets): RWH (11/07); MHW (11/06); La Trobe University (11-004); Monash Medical Centre (12181-B); Barwon Health (13/06); Peninsula Health (14/PH/21).

Recruitment started at RWH in June 2011, followed by MHW in July 2011. In May 2012, due to (A) the slow recruitment rate resulting from low numbers of eligible women, and (B) external expert advice to include women with diabetes in pregnancy who did not require insulin, thereby increasing the trial's external validity, it was agreed to amend our inclusion criteria to include all women with diabetes in pregnancy (not just those requiring insulin) and to identify and recruit further trial sites. Monash Medical Centre started in October 2012 and Barwon Health (Geelong Hospital) in April 2013. The last site, Frankston Hospital, had ethics approval from Peninsula Health in July 2014 and recruitment will start soon.

In the original protocol women who had a history of spontaneous preterm birth or who had threatened preterm birth in the current pregnancy were excluded, however following the Safety Committee review of the first 100 births, which found no evidence of contractions following expressing, and because no woman is randomised prior to 36 weeks gestation, this exclusion criterion was removed.

Monitoring CTGs

The CTGS for all of the first 100 women who have given birth (prerandomisation, during and postexpressing) have been assessed by investigator SPW, with no sign of fetal compromise or increase in contractions as a result of expressing.

Substudies

  1. Onset of lactation: In order to determine if the onset of lactation is delayed in women with diabetes, we are recruiting a comparison group of 200 women without diabetes. Women are being recruited in the postnatal wards at the RWH in 2014, and followed by telephone at 1–2 weeks postpartum, using identical questions to the DAME interview.

  2. Antenatal colostrum: We plan to conduct a biochemical analysis of some excess samples of antenatal colostrum that infants have not required.

Acknowledgments

The authors are grateful to all the trial sites for their support of the DAME trial. They also thank the women and their babies participating in this trial.

References

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  • Supplementary Data

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Footnotes

  • Contributors DAF, AMM and KM conceptualised the study, and SJ, LHA, PD, SPW, GO, SMD, RF, CM, AA and LG contributed to study design. DAF, LHA, AMM, KM drafted protocol and all authors contributed to protocol revision and application of grant. DAF, LHA, AMM developed data collection tools and all authors contributed to refinement, piloting and completion of tools. AMM, KM, LHA, GO, SJ and DAF piloted and refined the intervention. AMM, DAF, AA and CM developed the recruitment processes. DAF, AMM and LHA developed the data collection process. DAF and LHA drafted the trial protocol manuscript, and all authors read and contributed to drafts, and read and approved final manuscript.

  • Funding This trial is funded by a project grant from the National Health and Medical Council of Australia (no. 1005345). We have also received equipment grants from the National Health and Medical Council of Australia.

  • Competing interests None.

  • Ethics approval La Trobe University and participating hospital sites.

  • Provenance and peer review Not commissioned; externally peer reviewed.

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