References

Belfort MB, Drouin K, Riley JF Prevalence and trends in donor milk use in the well-baby nursery: a survey of northeast United States birth hospitals. Breastfeed Med.. 2018; 13:(1)34-41 https://doi.org/10.1089/bfm.2017.0147

Bond DM, Shand AW, Gordon A, Bentley JP, Phipps H, Nassar N Breastfeeding patterns and effects of minimal supplementation on breastfeeding exclusivity and duration in term infants: a prospective sub-study of a randomised controlled trial. J Paediatr Child Health.. 2021; 57:(8)1288-1295 https://doi.org/10.1111/jpc.15464

Bowatte G, Tham R, Allen KJ, Tan DJ, Lau MXZ, Dai X, Lodge CJ Breastfeeding and childhood acute otitis media: a systematic review and meta-analysis. Acta Paediatr.. 2015; 104:(467)85-95 https://doi.org/10.1111/apa.13151

Chowdhury R, Sinha B, Sankar MJ Breastfeeding and maternal health outcomes: a systematic review and meta-analysis. Acta Paediatr.. 2015; 104:(467)96-113 https://doi.org/10.1111/apa.13102

Demirci JR, Glasser M, Himes KP, Sereika SM Structured antenatal milk expression education for nulliparous pregnant people: results of a pilot, randomized controlled trial in the United States. Int Breastfeed J.. 2022; 17:(1) https://doi.org/10.1186/s13006-022-00491-8

European Milk Bank Association. United Kingdon. 2021. https//europeanmilkbanking.com/country/united-kingdom/

Forster DA, Moorhead AM, Jacobs SE Advising women with diabetes in pregnancy to express breastmilk in late pregnancy (Diabetes and Antenatal Milk Expressing [DAME]): a multicentre, unblinded, randomised controlled trial. Lancet.. 2017; 389:(10085)2204-2213 https://doi.org/10.1016/S0140-6736(17)31373-9

Gibbs GOxford: Further Education Unit, Oxford Polytechnic; 1988

Giugliani ERJ, Horta BL, Loret de Mola C, Lisboa BO, Victora CG Effect of breastfeeding promotion interventions on child growth: a systematic review and meta-analysis. Acta Paediatr.. 2015; 104:(467)20-29 https://doi.org/10.1111/apa.13160

Griffin S, Watt J, Wedekind S Establishing a novel community-focussed lactation support service: a descriptive case series. Int Breastfeed J.. 2022; 17:(1)7-7 https://doi.org/10.1186/s13006-021-00446-5

Health Service Executive. National standards for infant feeding in maternity services. 2022. https//www.hse.ie/eng/about/who/acutehospitals-division/woman-infants/nationalreports-on-womens-health/

Horta BL, Loret de Mola C, Victora CG Longterm consequences of breastfeeding on cholesterol, obesity, systolic blood pressure and type 2 diabetes: a systematic review and metaanalysis. Acta Paediatr.. 2015a; 104:(467)30-37 https://doi.org/10.1111/apa.13133

Horta BL, Loret de Mola C, Victora CG Breastfeeding and intelligence: a systematic review and meta-analysis. Acta Paediatr.. 2015b; 104:(467)14-19 https://doi.org/10.1111/apa.13139

Human Milk Foundation. Prioritisation Panel. 2023. https//humanmilkfoundation.org/hearts-milk-bank/prioritisation-panel/

Kair LR, Flaherman VJ Donor milk or formula: a qualitative study of postpartum mothers of healthy newborns. J Hum Lact.. 2017; 33:(4)710-716 https://doi.org/10.1177/0890334417716417

Lodge CJ, Tan DJ, Lau MXZ Breastfeeding and asthma and allergies: a systematic review and meta-analysis. Acta Paediatr.. 2015; 104:(467)38-53 https://doi.org/10.1111/apa.13132

Mantzorou M, Papandreou D, Vasios GK Exclusive breastfeeding for at least four months is associated with a lower prevalence of overweight and obesity in mothers and their children after 2–5 years from delivery. Nutrients.. 2022; 14:(17) https://doi.org/10.3390/nu14173599

Merjaneh N, Williams P, Inman S The impact on the exclusive breastfeeding rate at 6 months of life of introducing supplementary donor milk into the level 1 newborn nursery. J Perinatol.. 2020; 40:(7)1109-1114 https://doi.org/10.1038/s41372-020-0657-6

Miliku K, Azad M Breastfeeding and the developmental origins of asthma: current evidence, possible mechanisms, and future research priorities. Nutrients.. 2018; 10:(8) https://doi.org/10.3390/nu10080995

McGuinness D, Daniel U, O'Brien D, Greene E What are the experiences of antenatal women with diabetes harvesting colostrum?. MIDIRS Midwifery Digest.. 2021; 32:(1)86-91

NorthernStar Mothers Milk Bank. Order milk. 2020. https//www.northernstarmilkbank.ca/order-milk

Pollard MNew York: Routledge; 2018

Power BD, O'Dea MI, O'Grady MJ Donor human milk use in neonatal units: practice and opinions in the Republic of Ireland. Irish J Med Sci.. 2019; 188:(2)601-605 https://doi.org/10.1007/s11845-018-1873-3

Sen S, Benjamin C, Riley J, Heleba A, Drouin K, Gregory K, Belfort MB Donor milk utilization for healthy infants: experience at a single academic center. Breastfeed Med.. 2018; 13:(1)28-33 https://doi.org/10.1089/bfm.2017.0096

Shenker N, Brown A, Wedekind S, Griffin S Reduction in anxiety and depression scores in parents whose infants receive donor human milk alongside lactation support. Arch Dis Child. 2022; 107:(Suppl 2)A159-A160 https://doi.org/10.1136/archdischild-2022-rcpch.258

Shenker N, Staff M, Vickers A Maintaining human milk bank services throughout the COVID-19 pandemic: a global response. Matern Child Nutr.. 2021; 17:(3) https://doi.org/10.1111/mcn.13131

Tham R, Bowatte G, Dharmage SC Breastfeeding and the risk of dental caries: a systematic review and meta-analysis. Acta Paediatr.. 2015; 104:(467)62-84 https://doi.org/10.1111/apa.13118

Williams T, Nair H, Simpson J, Embleton N Use of donor human milk and maternal breastfeeding rates: a systematic review. J Hum Lact.. 2016; 32:(2)212-220 https://doi.org/10.1177/0890334416632203

Wilson E, Edstedt Bonamy AK, Bonet M Room for improvement in breast milk feeding after very preterm birth in Europe: results from the EPICE cohort. Matern Child Nutr.. 2018; 14:(1) https://doi.org/10.1111/mcn.12485

Western Health and Social Care Trust. Human Milk Bank Newsletter. 2023. https//westerntrust.hscni.net/service/human-milkbank/

World Health Organization. Global nutrition targets 2025 – breastfeeding policy brief. 2015. https//www.who.int/publications/i/item/WHO-NMH-NHD-14.7

World Health Organization, United Nations Children's Fund. Implementation guidance: protecting, promoting and supporting breastfeeding in facilities providing maternity and newborn services: the revised babyfriendly hospital initiative. 2018. https//apps.who.int/iris/handle/10665/272943

Human Donor Milk in Maternity

02 November 2023
Volume 31 · Issue 11

Abstract

Ines Salmoral and Denise McGuinness reflect on whether human donor milk should be made available for healthy term infants in the maternity setting

The World Health Organization (WHO) and United Nations Children's Fund (UNICEF) recommend exclusive breastfeeding for the first 6 months of life and continued breastfeeding with safe and adequate complementary food for up to 2 years and beyond (WHO and UNICEF, 2018).

It is recognised that for term babies, additional milk supplementation may be necessary to support breastfeeding, as a result of medical indications or maternal request during the early postpartum period. Human milk banks provide donor human milk for human babies and operate according to guidelines developed by national bodies or local organisations (Shenker et al, 2021).

Currently, worldwide, donor human milk is reserved primarily for babies in the neonatal setting, preterm babies and critically ill babies (Shenker et al, 2021). Human milk should be offered as first option supplementation for all breastfed babies when additional maternal milk is required (WHO and UNICEF, 2018). The early introduction of commercial formula milk is associated with cessation of breastfeeding (Bond et al, 2021).

Despite the desirable scenario that donor human milk is available in all healthcare settings where care is provided to mothers and their babies, this is far from reality. In this article, the first author reflects on access to donor human milk in an Irish Regional Hospital. Gibb's (1988) reflective cycle has been used to learn from a real life situation in which donor human milk was not available for a term infant requiring supplementation for medical reasons during the early postpartum period. The pseudonyms ‘Elaine’ and ‘baby Tom’ were used to refer to the woman and her baby.

Case study

Elaine was admitted to the postnatal ward following the spontaneous vaginal birth of her firstborn, baby Tom. Elaine had an uncomplicated pregnancy, commenced spontaneous onset of labour and had an uncomplicated birth. Elaine wished to breastfeed.

Baby Tom weighed 4.1kg at birth with an Apgar score of 9 and 10 at 1 and 5 minutes after birth respectively. Baby Tom was placed immediately in skin‑to‑skin contact with his mother, and within a few minutes, he was seeking the breast, latching independently. A deep latch and good attachment were noted and he fed for nearly 1 hour between both breasts. During the feeding episode, rhythmic suckling was noted to be fair, no swallows were heard, and no milk was visible from the breast following hand expression. Additional support with breastfeeding was provided.

One hour post‑feed, Tom was awake and slightly jittery; therefore, a blood glucose level was taken, with a result recorded as 1.8mmol/L. Elaine and Baby Tom were supported to breastfeed again. The paediatric team on call were informed and a full infant consultation was completed. Baby Tom was admitted to the neonatal unit, as per the hospital guidelines. Manual hand expression of colostrum was commenced by Elaine with assistance from the midwife, to use as a supplement. Unfortunately, no colostrum was obtained, and so Elaine consented for her baby Tom to receive commercial milk formula for supplementation in the neonatal unit. Elaine was subsequently transferred to the maternity ward.

Description

Elaine was a postnatal mother on the maternity ward, in my care. Elaine wished to breastfeed her baby exclusively; however, following an episode of hypoglycaemia post‑birth, her baby received commercial formula milk. Elaine felt disappointed that she had consented to commercial formula milk supplementation, and she subsequently requested for her baby to receive donor human milk instead. I agreed to speak with the staff in the neonatal unit, who explained that in the regional hospital, donor human milk was not provided for any term baby, as there is no policy to regulate it.

I informed Elaine about the outcome of my conversation with the neonatal staff and she agreed to feed her baby with commercial formula milk if supplementation was required. A plan of action was established for the following 24‑hour period; Elaine would hand express colostrum every 3 hours while she was separated from her baby and would also visit the neonatal unit to stay close to her baby, with skin‑to‑skin contact as much as possible. Elaine would offer the breast regularly and supplement with commercial formula milk when medically indicated.

For the first 24 hours, baby Tom was mostly offered commercial formula milk when supplementation was indicated. Elaine only could obtain 1–2ml of colostrum in total by hand expression. A conversation with Elaine identified that she never received information on antenatal colostrum harvesting from 37 weeks’ gestation, and so could not provide extra expressed milk. Despite the challenges at this early postnatal stage, baby Tom latched to the breast for most feeds and received small quantities of expressed breast milk. However, the baby needed commercial formula milk top‑ups of 30–35ml to maintain adequate blood glucose levels.

Feelings

As a breastfeeding advocate, I was very disheartened for Elaine. Baby Tom was restricted from receiving donor human milk, despite his mother's wish to breastfeed and the well‑known recommendations that human milk should be prioritised when supplementation is needed (WHO and UNICEF, 2018). I felt frustrated both ethically and morally, as I was aware of the lack of availability of donor human milk in the hospital. I felt that we were not providing the best care because of the restricted access to donor human milk, especially as the maternity hospital is very supportive of breastfeeding. Healthcare professionals offering commercial formula milk is not supportive of exclusive breastfeeding, and this has been highlighted by the WHO (2015) as a cause of low breastfeeding rates.

Evaluation

Elaine was feeling guilty and emotional that her baby was receiving commercial formula milk. Her plan was to exclusively breastfeed. Emotional support was provided, and reassurance was given.

She was determined to breastfeed her baby. An individualised feeding plan was developed and Elaine was very thankful to the neonatal team and myself as we identified solutions to the breastfeeding challenges of the early postnatal period. The plan was in‑keeping with the Health Service Executive (2022) national standards for infant feeding in maternity services, whereby mothers are supported to breastfeed and then hand express at least eight times within 24 hours, in addition to safe skin‑to‑skin contact. At this stage, baby Tom was alert and feeding responsively. Hand expressing of colostrum is an essential tool to teach mothers to facilitate supplementation with their own milk, if this is required (Pollard, 2018).

I was disappointed that further efforts were not followed to obtain donor human milk for baby Tom. Additionally, Elaine had not been made aware of colostrum harvesting during the antenatal period. Antenatal colostrum harvesting can commence from 36 gestational weeks if there are no risks for preterm labour, multiple pregnancy, cervical incompetence or cervical sutures (Pollard, 2018). In the DAME study, it was found that antenatal colostrum harvesting by hand expressing twice a day from 36 gestational weeks in diabetic mothers with low‑risk pregnancy was an intervention of no harm that may increase the chances of exclusive breastfeeding and avoid commercial formula milk (Forster et al, 2017).

Analysis

The importance of breastfeeding for maternal and infant health is unrivalled. Breastfeeding supports infants’ health and offers a protective effect against developing asthma (Lodge et al, 2015; Miliku and Azad, 2018), obesity (Giugliani et al, 2015), type 2 diabetes in adulthood (Horta et al, 2015a), dental cavities (Tham et al, 2015) and infections such as acute otitis media (Bowatte et al, 2015), and also produce better results on intelligence tests (Horta et al, 2015b). Women who breastfeed also benefit, having a lower risk of developing type 2 diabetes or breast and ovarian cancer (Chowdhury et al, 2015) and a reduced body mass index postnatally (Mantzorou et al, 2022).

Donor human milk has been prioritised in neonatal units and is available to the most premature and ill babies (Shenker et al. 2021). Human milk should be available for all newborn infants when medically indicated. There are 15 human milk banks in the UK (European Milk Bank Association 2021), one located in Northern Ireland, which was opened in 2000. In 2022, the milk bank provided donor human milk for approximately 844 babies across Ireland (Western Health and Social Care Trust, 2023).

In 2017, the Hearts Milk Bank was opened as an independent human milk bank, the first of its kind in the UK. The Hearts Milk Bank's initial purpose was to provide donor human milk to hospitals with no human milk bank; however, because of the large number of donors, they could also provide donor human milk to families outside of the hospital (Griffin et al, 2022). The growth of this independent milk bank has been achieved in association with charitable activity, as part of the Human Milk Foundation (Griffin et al, 2022).

In 2019, the Human Milk Foundation developed a prioritising panel, with the advice of volunteer experts, to provide donor human milk to families both inside and outside of the hospital. In this regard, they established four pillars of prioritisation: infant vulnerability (babies in intensive care units are always prioritised), maternal breastfeeding, maternal psychological health and milk bank supply/logistics (Human Milk Foundation, 2023). In Canada, donor human milk can be obtained in some pharmacies, via prescription or by buying it without prescription (NorthernStar Mothers Milk Bank, 2023).

There is evidence to suggest that the use of donor human milk for supplementation can support achievement of successful breastfeeding compared with the use of formula supplementation (Shenker et al, 2021). In a study in the USA, 30 women were interviewed after their healthy newborns required supplementation; the parents reported that donor milk was seen as a temporary plan versus the use of commercial formula milk which, once used for supplementation, was seen mostly as a long‑term plan (Kair and Flaherman, 2017). The use of donor human milk in neonatal units has been reported to increase breastfeeding rates on discharge (Williams et al, 2016;Wilson et al, 2018) and at 6 months of age (Merjaneh et al, 2020).

There is a trend in the USA towards the use of donor milk for healthy term babies, when supplementation is required, with reported higher exclusive breastfeeding rates (Belfort et al, 2017; Sen et al, 2018). It is important that mothers and healthcare professionals are aware of the negative impact that supplementation with commercial formula milk causes to the breastfeeding relationship.

Additionally, the impact of donor human milk use on maternal mental health was researched by Shenker at al (2022), who reported that most mothers of babies receiving donor human milk reported that it had a positive impact on their mental and physical health, and general family wellbeing. The use of donor human milk acted as a motivation to continue breastfeeding as women worked on increasing their breastmilk supply (Shenker et al, 2022).

Should donor human milk be used for supplementation of term healthy infants instead of commercial formula milk when supplementation is medically indicated? Power et al (2019) identified that in the Republic of Ireland, 38 (86%) respondents (paediatricians and neonatologists) were opposed to the use of donor milk supplementation of otherwise healthy term neonates. In light of the success of the WHO ‘ten steps to successful breastfeeding’, donor human milk should be available for all newborn infants as it provides an equitable and supportive environment (WHO and UNICEF, 2018).

In the absence of donor human milk availability, colostrum harvesting is a feasible option. Antenatal milk expression after 37 weeks’ gestation has been shown as a safe tool to minimise the use of formula supplementation (Demirci et al, 2022). Forster et al (2017) offered the opinion that colostrum harvesting can commence at 36 weeks’ gestation for women with diabetes and low‑risk pregnancies. Antenatal colostrum harvesting has been described by women as empowering in a qualitative study (McGuinness et al, 2021) in which women with diabetes harvested colostrum in preparation for any breastfeeding challenges. Interestingly, the fact that commercial formula milk supplementation was less likely to be needed was highlighted by the women in this study (McGuinness et al, 2021).

Action plan

Further education in relation to antenatal colostrum harvesting is imperative in the maternity setting and is an important midwife‑led initiative. Antenatal colostrum harvesting is available for all low‑risk pregnant women after 37 weeks’ gestation at the authors’ hospital.

A policy and guideline are indicated to support supplementation with donor human milk for all newborn infants. The development of a human milk bank in the Republic of Ireland would be welcomed.

Conclusions

Further measures are needed to improve access to donor human milk in all maternity hospitals, including the development of evidence‑based policies. Antenatal colostrum harvesting can be encouraged when pregnant women express their wish to breastfeed and no contraindications are identified, in view of the restrictions on donor human milk at present in Irish and UK hospitals.

There is a lack of research on the use of donor human milk for healthy term babies to support exclusive breastmilk feeding. Further research is indicated, as breastfeeding mothers of healthy term babies may face delayed or low milk supply because of multiple clinical factors. The availability of donor human milk will support an enjoyable breastfeeding journey and early motherhood.