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Which breast pump for which mother: an evidence-based approach to individualizing breast pump technology


The majority of new mothers in the United States use breast pumps in the first 4 months postbirth in order to achieve their personal human milk feeding goals. Although these mothers seek guidance from health-care professionals with respect to the type and use of breast pumps, there are few evidence-based guidelines to guide this professional advice. This paper reviews the evidence to facilitate professional individualization of breast pump recommendations using three categories of literature: the infant as the gold standard to which the pump is compared; the degree of maternal breast pump dependency (for example, the extent to which the breast pump replaces the infant for milk removal and mammary gland stimulation); and the stage of lactation for which the pump replaces the infant. This review can also serve to inform public and private payers with respect to individualizing breast pump type to mother–infant dyad characteristics.


In the United States, approximately 85% of mothers with healthy newborn infants express milk within the first 4 months postbirth, and the majority do so using a breast pump.1 This figure does not include mothers of premature or sick infants or mothers with personal health conditions that necessitate breast pump use.2 These mothers seek guidance from physicians and nurses about the appropriate type and use of breast pumps to help them achieve their personal human milk (HM) feeding goals. Although mothers use breast pumps for different reasons, times and durations after birth, they often receive a ‘one size fits all’ recommendation that reflects the health-care provider's personal breast pump experiences or industry marketing claims, rather than current research in this field.

The most recent Cochrane review on HM expression (defined as any non-infant method for removing HM, including both breast pump use and hand expression) included only 10 studies that enrolled a total of 632 mothers for data analysis.3 These studies included mothers from both industrialized and developing countries (United States, United Kingdom, Malaysia, Brazil, Egypt, Kenya and Nigeria) whose reasons for HM expression varied from one-time participation as a research subject to exclusive use of HM expression owing to a prematurely born infant.3 The major conclusion from this Cochrane review was that the ‘most suitable method’ for HM expression may depend on individual circumstances that were not addressed in the actual report.3 A more recent review on the feeding of expressed HM2 reached a similar conclusion and highlighted the need to tailor the method of HM removal to the mother's purpose for not feeding directly from the breast. Thus the health-care provider is left with the recommendation to individualize the type of breast pump but has few evidence-based guidelines to do so.

This paper addresses this gap in the literature by providing an evidence-based approach to help clinicians individualize breast pump technology to a mother's specific needs and HM feeding goals. Because the breast pump replaces the infant for purposes of HM removal and mammary gland stimulation, the breast pump should mimic the infant's sucking rate, rhythm and pressures to the greatest possible extent. Thus the science of infant feeding is reviewed as a foundation for understanding the role of the breast pump. Second, the extent to which the breast pump replaces the infant for HM removal can serve as an organizing framework for classifying pumping mothers into three categories: minimally, partially or completely breast pump dependent. Finally, the endocrine and autocrine mechanisms that regulate lactation differ by lactation stage (initiation, coming to volume and maintenance of established lactation) and are affected directly by the infant's sucking and HM removal patterns. Thus, the physiological mechanisms underlying these lactation stages are summarized, and implications for appropriate breast pump types and usage for different categories of breast pump dependency during these stages are detailed.

The pump replaces the infant during breastfeeding

A fundamental principle of breast pump use is that the pump replaces the infant for purposes of HM removal and species-specific stimulation of the mammary gland, whether breast pump use is minimal (for example, brief separations) or complete (infant does not feed at breast). Thus, understanding the infant's role in HM removal and mammary gland stimulation is essential. There is remarkable synchrony between effective mammary gland stimulation at different stages of lactation and the sucking and feeding patterns used by healthy infants to extract HM.4, 5, 6, 7, 8, 9, 10, 11, 12, 13 This synchronization provides the infant with adequate nourishment and the mammary gland with adequate stimulation. Additionally, the infant's ability to adapt the sucking rate, rhythm and suction pressure to the variable rates of HM flow during individual feedings at breast is a uniquely human feeding pattern that has not been observed in other mammals.8, 9, 10, 14, 15 This sophisticated plasticity of sucking and feeding patterns is more than simple HM removal, a fact that underscores the importance of adapting the breast pump and its use to the specific situation.8

Infants use a combination of suction (for example, vacuum, negative pressure that occurs with lowering of the mandible) and expression (positive pressure that occurs with closure of the mandible) when feeding from the breast.13, 14, 15, 16, 17, 18, 19 During suction, the infant uses negative pressure to create the elongated nipple shape and transfer HM from the breast.16, 18 In contrast, during expression, the infant compresses the ducts in the mammary gland, which stops or slows HM transfer and allows the infant to safely swallow the bolus of HM and reopen the airway to breathe,16, 17, 18, 20 as opposed to previously held theories that infants transfer HM during expression.16, 18, 21, 22

Hand expression versus breast pump use: the human infant as a model

The distinction between the infant's use of suction and expression has implications for the two broad categories of HM expression techniques. Breast pumps remove HM by use of suction, as does the infant.4, 23 In contrast, hand expression removes HM by compression of HM ducts in the absence of suction.3, 24, 25 Although hand expression is often recommended as an alternative to pumping, the few randomized trials comparing these methods have consistently demonstrated the superiority of electric breast pumps over hand expression for purposes of effective and efficient HM removal.24, 25, 26, 27, 28, 29 In one randomized cross-over study, HM output, serum prolactin and serum oxytocin were compared for 23 mothers of healthy term infants who used five different techniques to remove HM between 28 and 42 days postbirth.24 Of the five methods evaluated, hand expression resulted in the least HM output and significantly lower prolactin and oxytocin responses than the breast pumps.24

Two randomized studies have compared hand expression with electric breast pump use. One study conducted with mothers of ‘sleepy term infants’ who latched and sucked poorly concluded that hand expression is superior to breast pump use during the initiation of lactation, as measured by the fact that more mothers in the hand expression group (96.1%) than in the breast pump group (72.7%) were still likely to be ‘breastfeeding’ (by self-report) at 2 months.30 Of note, all mothers in this study used either hand expression or the breast pump to augment rather than replace the infant, and no measures of HM output were compared. Only one randomized study compared HM output in the mothers of very low birthweight (VLBW; <1500 g birth weight) infants who used exclusive hand expression (n=12) versus a hospital-grade electric breast pump (n=14) during the first 7 days postbirth.25 Cumulative HM output for the first 7 days in hand expression mothers was significantly less than for electric breast pump mothers (456 versus 1317 ml). Hand expression mothers demonstrated lower median HM output throughout the following 8 to 28 days postbirth, despite changing from hand expression to electric breast pump during this time.

One observational study31 and one randomized clinical trial27 have suggested that the combination of simultaneous pumping (for example, both breasts at the same time) with an electric breast pump and breast massage, either with31 or without27 hand expression, increases HM output during pumping. However, neither of these studies tested only hand expression in the absence of simultaneous electric breast pump use. Thus hand expression alone should not be used routinely, especially for mothers of VLBW infants who use a breast pump to replace—not to supplement—the breastfeeding infant.

Evaluating breast pumps: the breastfeeding infant as the gold standard

Whereas earlier breast pump evaluations primarily compared pumped HM volume and mothers' preferences in observational or randomized designs,24, 32, 33 the early 2000s ushered in new state-of-the art technologies that redefined these simplistic measures. These technologies included ultrasound imaging of the term infant during breastfeeding, computerized tomography of breast fullness and the use of accurate weighing scales to depict and measure HM ejection and flow rates.4, 6, 12, 22, 34, 35, 36, 37 These technologies moved the research question from ‘Does the mother like the breast pump?’ to ‘How does the breast pump compare to the healthy term infant during breastfeeding?’

Subsequent studies have evaluated the effectiveness, efficiency, comfort and convenience of breast pumps and breast pump suction patterns (BPSPs; computer programs embedded in the pump that integrate changes in sucking rates, rhythms and pressures), using the infant as the ‘gold standard’ to which the pump technologies are compared.4, 6, 8, 12, 22, 34, 35, 36, 38, 39 Additionally, researchers have begun to control for extraneous factors that directly impact outcome variables but were unappreciated in earlier studies. These factors include the sizing and temperature of breast shields (the part of the collection kit that fits over the breast, which varies from a 21-mm to 40-mm tunnel), vacuum pressure and the interval since the last pumping or breastfeeding.4, 8, 32, 38, 40, 41

In particular, a new metric, the percentage of available milk removed (PAMR), provided a much-improved measure for the effectiveness of HM removal, as it standardized the volume of HM removed by the breast pump to the baseline HM volume in the breast prior to pumping.5, 7, 12, 35, 36, 38 Expressed as a percentage or proportion, the PAMR controls for the fact that there is substantial within- and between-mother variability in baseline HM at any single time point, and a PAMR=80% might be 150 ml for one mother and 50 ml for another (or the same mother at a different time).4, 42 However, the measurement of PAMR requires additional subject procedures, researcher time and research equipment (for example, collection of prepumping and postpumping HM samples, creamatocrit measures and use of the PAMR algorithm) than measurement of absolute pumped HM volume.38 Thus, while it is the gold standard measure of the effectiveness of HM removal, the PAMR has not been routinely incorporated into current breast pump evaluation studies.

The efficiency of HM removal is measured by milliliters of HM removed per unit of time spent pumping and has been reported in numerous breast pump studies.6, 8, 32, 33, 36, 38, 43, 44, 45 A healthy breastfeeding infant removes approximately 80% of the total ingested HM volume in 5 min,46 and an efficient breast pump removes 85% of the available HM in the breast in 15 min.38 Although the efficiency of HM removal is not routinely evaluated in breast pump studies, it is an important consideration for mothers, especially those who must pump HM during time-restricted work breaks or several times daily for a neonatal intensive care unit (NICU) infant.8, 38 In addition to breast pump type, simultaneous versus serial pumping,27, 47 BPSPs that mimic the human infant during breastfeeding6, 8, 36, 38, 43 and warmed breast shields41 improve the efficiency of HM removal during pumping.

Several studies have compared the comfort and convenience of breast pumps and BPSPs in randomized6, 8, 32, 33, 38 and non-randomized44 designs. Mothers commonly prefer one breast pump or BPSP type over another, despite the fact that the same maximum absolute negative pressure (for example, suction) is achieved by both. Although often minimized in marketing claims, this is a real perception and is a function of the shape and timing of the suction curve during each cycling of the breast pump.6, 8, 36, 38, 43 These curves determine how quickly the maximum absolute negative pressure is reached, how long it is held and how quickly it returns to baseline during each cycle. These differences impact not only comfort but also the effectiveness and efficiency of HM removal.6, 8, 36, 38, 43, 44 Finally, mothers also value highly individual features in a breast pump such as portability, quietness, ease of use and discreet carrying cases, which allow them to fit HM removal into their daily activities.32, 33, 38, 44

Although there is a variety of brands and models of breast pumps, they can be categorized into three primary types: manual, battery-operated, and mini-electric; double electric; and hospital-grade electric. Table 1 summarizes the primary characteristics and highlights the differences among these breast pump types.

Table 1 Characteristics of commonly used breast pumps

Minimal, partial and complete breast pump dependency

The extent to which the breast pump replaces the infant for feedings is a major consideration in the selection of a breast pump because either the infant or the pump must serve as the primary regulator of lactation.48 Thus a first step for the health-care provider is to ascertain whether the infant or the pump is primarily responsible for HM removal and mammary gland stimulation over the course of a day. For mothers who feed healthy term infants directly from the breast, a breast pump is needed for occasional or routine brief separations from the infant, potentially including the mother's return to the workplace based on the duration of the workday. In these instances, the breast pump replaces the infant for fewer than half of daily feedings, and the infant removes HM effectively and efficiently during the remaining daily breastfeedings. These mothers are minimally breast pump dependent and the breastfeeding infant remains the regulator of lactation.

In contrast, completely and partially breast pump-dependent mothers rely upon the breast pump to regulate lactation either temporarily or long term owing to a variety of reasons: the inability of the infant to remove HM effectively and efficiently, lengthy separation from the infant, and maternal health problems or preferences for feeding some or all pumped HM by bottle.48, 49 Mothers who are partially breast pump dependent include those with late preterm, early term and discharged NICU infants who consume small volumes of HM at the breast, slip off of the nipple frequently, fall asleep quickly after the feeding starts and do not awaken to feed at regular intervals.48, 50 If these mothers did not use a breast pump to complement HM removal and mammary gland stimulation, HM synthesis would be impaired.48, 50 Thus the pump preserves and regulates lactation so that the infant continues to consume partial and eventually complete feedings at the breast.48, 50 Other mothers are partially breast pump dependent owing to their own health issues. For mothers who are completely breast pump dependent, such as mothers of extremely premature infants, the pump replaces the infant as the primary regulator of HM removal and mammary gland stimulation and often does so for weeks or months after birth.8, 38, 50, 51 Mothers whose term infants are unable to breastfeed (for example, craniofacial anomalies, hypotonia) or choose to provide exclusive HM by bottle are also completely breast pump dependent.

Mothers can move among the categories of breast pump dependency, so the type of breast pump they need may change. For example, a completely breast pump-dependent mother with a 1000-g infant typically progresses from complete to partial breast pump dependency during and immediately following the NICU hospitalization. However, she can progress to exclusive breastfeeding and/or minimal breast pump dependency after effective and efficient feeding at the breast has been established.48, 50 Conversely, a minimally breast pump-dependent mother with a healthy breastfeeding infant can move from minimally to completely breast pump dependent if she or her infant is hospitalized or the mother–infant dyad is otherwise separated later in lactation.

In general, the more intensive and longer the breast pump dependency, the more important is the pump's effectiveness, efficiency, comfort and convenience. Hospital-grade electric pumps that accommodate different sizes of breast shields, the ability to warm breast shields and the use of simultaneous versus sequential pumping meet these criteria.8, 27, 38, 41, 47, 50 In contrast, personal use electric, battery and manual-operated pumps, especially those restricted to sequential versus simultaneous pumping and only one breast shield size, do not meet these same criteria. Additionally, personal use pumps are not designed to be sufficiently durable for partially and completely breast pump-dependent women.

Stages of lactation: regulatory mechanisms and implications for breast pump use

The processes that regulate HM synthesis and secretion vary over the course of lactation, and these variations have important implications for breast pump use in addition to type. These phases of lactation include initiation, coming to volume and the maintenance of established lactation.8, 11, 50, 52, 53 The early postbirth phases of initiation and coming to volume, while time-limited, are especially important because their achievement is critical to the maintenance of established lactation and eventual exclusive HM feeding. Table 2 (supplementary) integrates the degree of breast pump dependency and stage of lactation and provides clinical examples of mother–infant dyads in each category.

Table 2 Examples of mother–infant dyads with differing degrees of breast pump dependency during the three stages of lactation

Initiation stage

The initiation stage, otherwise known as the transition from lactogenesis I (secretory differentiation) to lactogenesis II (secretory activation; the milk coming in; the onset of copious HM production), is an extraordinarily complex series of hormonal, anatomical and HM compositional changes that occur in the first days postbirth.11, 52, 53 Hormonally, the initiation of lactation in all mammals is triggered by the rapid decline in serum progesterone that accompanies the birth of the placenta, freeing prolactin, inhibited prebirth by progesterone, to begin the regulation of HM synthesis.52, 53, 54, 55, 56 Prolactin, in combination with infant suckling, catalyzes the closure of paracellular pathways between mammary epithelial cells, with resulting retention of HM lactose in the gland.52, 53, 57 The rapid increase in HM lactose draws water into the lactocytes and corresponds with mothers' perceptions of the HM coming in.53, 58 This extraordinary series of events occurs within 72 h postbirth in healthy mothers with breastfeeding infants58 and is a one-time event that is critical to continued HM synthesis.

Human infants use different sucking patterns during the initiation of lactation

During the initiation stage, the infant feeds at the breast using a different sucking pattern than during the coming to volume and maintenance of lactation phases.8, 15 Studies of healthy term infants who served as their own controls for breastfeeding and bottle feeding of expressed HM during the first 4 days postbirth demonstrated that infants sucked ‘differently’ during breastfeeding (rapid sucks with intermittent, lengthy pauses between sucking bursts) than bottle feeding, attributed to the small volume of HM available to the infant during the initiation phase.14, 15, 19 Using accurate test-weighing to measure HM intake during the first 24 h of life in exclusively breastfed healthy infant, researchers recently confirmed that infants consumed an average of 15 ml of HM during the entire first 24 h of life, feeding 10.2 times and transferring only 1.5 ml per breastfeed.59 During the next 2 to 3 days, the maternal HM volume increases, but the overall flow of HM remains less rapid and less consistent than during established lactation60 and the term infant responds by sucking faster, using stronger pressures and more pauses than when HM flow is more regular and rapid, as during bottle feeding or established breastfeeding.8, 9, 10, 13, 14, 15 There is some evidence that this human-specific sucking pattern has a programming impact on the mammary gland during the initiation phase and may be important to recreate in BPSPs.8, 39

Integrating the initiation stage and breast pump-dependency categories

The majority of mothers who use a breast pump during the initiation phase are either partially or completely breast pump dependent and often have health problems that increase the risk for delayed and/or failed lactogenesis II.48, 50, 51, 58, 61, 62, 63 During delayed lactogenesis II, the paracellular pathways do not close in a timely manner, so HM lactose is not retained in the mammary gland, resulting in minimal HM output.61 Although by definition delayed lactogenesis II is temporary, mothers who are partially or completely breast pump dependent require effective and efficient mammary gland stimulation during this time so that delayed lactogenesis II does not segue into irreversible low HM volume. A hospital-grade electric breast offers effectiveness, efficiency, comfort and convenience to these mothers.8, 38, 50

Integrating guidelines for breast pump use with breast pump type in completely breast pump-dependent mothers

The timing of first breast pump use in mothers of VLBW infants has been studied in recent randomized and non-randomized studies.64, 65 In a randomized study, mothers who used a hospital-grade electric breast pump within the first hour postbirth produced significantly greater cumulative HM output at Day 7 and Week 3 compared with mothers who used the same breast pump after the first hour postbirth.65 Recently, Parker et al.64 again found that breast pump use in the first hour postbirth explained the greater HM output in breast pump-dependent mothers of VLBW infants whose first breast pump use was 6 versus >6 h postbirth.

In a separate randomized trial of 105 breast pump-dependent mothers of premature infants, the type of BPSP used during the initiation of lactation determined the mean cumulative pumped HM volume and the efficiency of HM removal over the first 14 days postbirth.8 An experimental initiation BPSP, created to mimic the sucking pattern of the healthy term infant during the initiation of lactation, was used only until the onset of lactogenesis II (mean=3.1 days) in the experimental group while the control mothers used the standard BPSP that was designed to maintain established lactation.38 All mothers used the standard BPSP after lactogenesis II. Over the first 14 days postbirth, experimental BPSP mothers produced 7000 ml of HM versus 4000 ml for control mothers. Thus interventions during the initiation phase of lactation appear to have a long-lasting programming impact on subsequent HM output in vulnerable breast pump-dependent mothers.8, 25, 64, 65

Coming to volume stage

Coming to volume is the period between the onset of lactogenesis II and the achievement of a threshold HM volume of 500 to 600 ml day−1,50, 51 typically between 4 and 7 days postbirth in healthy populations of mothers and infants who breastfeed exclusively.8, 60, 66 Coming to volume is the stage associated with the greatest risk of suboptimal breastfeeding and early, unplanned weaning in otherwise healthy populations8, 11, 50, 67, 68 and is fraught with problems for partially and completely breast pump-dependent mothers with lactation risk factors.8, 50, 66, 68 These adverse outcomes are understandable given that the mechanisms regulating lactation change completely during this time.

Coming to volume ushers in the remarkable transition from the endocrine to the autocrine control of lactation, meaning that HM must be removed effectively from the breasts in order to be replaced.7, 8, 11, 60, 69, 70, 71 Two primary mechanisms regulate coming to volume and its segue into the maintenance of lactation: the suckling-induced prolactin surge72, 73, 74, 75 and the feedback inhibitor of lactation (FIL).69, 76, 77, 78 The suckling-induced prolactin surge, wherein the anterior pituitary secretes prolactin in concentrations up to threefold over baseline values within 30 to 45 min after the beginning of feeding or pumping, is triggered only in response to suckling and HM removal.72, 73, 74, 75 FIL is a HM protein-mediated mechanism that functions to downregulate sensitivity of the alveolar membrane to prolactin when HM remains in the breasts after feeding or pumping.69, 76, 77, 78 FIL functions at the level of the individual breast, meaning that HM not removed from the same breast over time reduces HM synthesis in the individual breast but not necessarily the other breast.76

For unseparated healthy mothers with exclusively breastfed infants, the suckling-induced prolactin surge and the FIL begin to tailor maternal HM output to the individual infant's HM intake during coming to volume. In contrast, mothers who are partially or completely breast pump dependent are at risk during coming to volume.48, 50, 51 These women need a hospital-grade electric breast pump that removes HM effectively and efficiently during this important phase, even if the mother and infant are not separated. Among the women most frequently overlooked for breast pump use during coming to volume are mothers of late preterm and early term infants who are not separated in the maternity unit and are discharged home within 2 to 3 days postbirth. The literature is replete with studies demonstrating that these infants are at risk for inadequate HM intake during breastfeeding, compromising both the suckling-induced prolactin surge and FIL and predisposing to permanent inadequate HM output.48

Similarly, completely breast pump-dependent NICU mothers are at risk during coming to volume but for different reasons.8, 38, 50, 51 The stress, fatigue, pain, serious maternal illness and medications that accompany preterm/high-risk birth can inhibit prolactin, and these mothers are especially vulnerable to non-evidence-based practices (for example, use of hand expression, setting an alarm clock to pump HM during the night) that further exacerbate this critical lactation transition.8, 40, 50, 51 An ineffective breast pump, improperly fitted breast shields, insufficient time spent pumping and improper suction pressures are common problems that compromise coming to volume.8, 38, 40, 50, 51 Use of the coming to volume assessment tool can prevent and/or identify these common problems in breast pump-dependent mothers.50, 51

Maintenance of established lactation stage

The autocrine mechanisms that control HM secretion become more mother–infant specific and efficient as lactation progresses.79 In particular, HM storage capacity, the ability of the mammary gland to store synthesized HM without triggering the FIL, becomes highly individualized.5 This individuality explains why some mothers can feed or pump significantly less frequently than others and still maintain an adequate HM output over time.79 Similarly, although daily HM intake (mean=808 ml) remains relatively stable in the individual breastfed infant between 1 and 6 months of age, the between-infant variability is striking (463 to 1370 ml).42 Furthermore, during this time, exclusively breastfed infants consume markedly different volumes of HM during individual feeds over the course of a day (0 to 240 ml), with most mothers having a ‘more productive and a less productive breast’.79 If a mother is not made aware of these normal fluctuations in pumped HM, it limits her ability to evaluate the suitability of a breast pump for her personal situation. This situation is especially common for minimally breast pump-dependent mothers who have had limited opportunities to visualize pumped HM volume prior their return to employment outside the home.

For minimally breast pump-dependent mothers, the efficiency and convenience of the breast pump often takes priority over its effectiveness and comfort, especially if the pump is chosen for employment outside the home. For most mothers, the mini-electric or double electric breast pump fulfills these criteria because the breastfeeding infant regulates lactation processes, compensating for unremoved HM by feeding effectively and efficiently during remaining daily breastfeeds.48 The clinician should be aware that some portable, battery-operated breast pumps incorporate a double collection kit (for example, breast shields and containers for the two breasts) but in fact operate sequentially rather than simultaneously by alternating suction between the breasts.

Partially breast pump-dependent mothers must be reminded that the pump—not the infant—provides effective and efficient HM removal and regulates lactation processes until the infant is capable of doing so. For late preterm, early term and discharged NICU infants, this transition can occur as late as 44 weeks, corrected age.48, 50, 51, 80 Thus these mothers should continue the use of a hospital-grade electric breast pump because of its effectiveness, efficiency and comfort to complement feedings at breast until infants consume adequate volumes of HM from the breast routinely and demonstrate adequate weight gain without additional daily bottle feeds of expressed HM. Completely breast pump-dependent women are typically those with a NICU or other special needs infant or those who have decided to feed expressed HM exclusively by bottle.49, 81, 82 These mothers require the maximum effectiveness, efficiency, comfort and convenience provided by a hospital-grade electric breast pump, especially if their individual HM feeding goal is to provide HM via pumping for several months.


Given the prevalence of breast pump use in the United States, it is important that perinatal health-care providers are able to provide evidence-based recommendations about breast pump types in order to help mothers meet their individual HM feeding goals. This advice should integrate the three abovementioned categories: the ability of the pump to mimic the human infant during breastfeeding, the degree of maternal breast pump dependency, and the stage of lactation for which the pump replaces the infant. This review provides extensive evidence for each of these categories and can serve as a reference for individualizing the breast pump type and use to the specific mother–infant dyad. This information can also serve as an evidence-based guide for public and private payers to insure that mothers receive a breast pump that is individualized to their specific HM expression needs.


  1. 1

    Labiner-Wolfe J, Fein SB, Shealy KR, Wang C . Prevalence of breast milk expression and associated factors. Pediatrics 2008; 122 (Suppl 2): S63–S68.

    PubMed  Article  Google Scholar 

  2. 2

    Flaherman VJ, Lee HC . ‘Breastfeeding’ by feeding expressed mother's milk. Pediatr Clin North Am 2013; 60 (1): 227–246.

    PubMed  PubMed Central  Article  Google Scholar 

  3. 3

    Becker GE, Cooney F, Smith HA . Methods of milk expression for lactating women. Cochrane Database Syst Rev 2011 Dec 7;(12):CD006170.

  4. 4

    Kent JC, Mitoulas LR, Cregan MD, Geddes DT, Larsson M, Doherty DA et al. Importance of vacuum for breastmilk expression. Breastfeed Med 2008; 3 (1): 11–19.

    PubMed  PubMed Central  Article  Google Scholar 

  5. 5

    Kent JC . How breastfeeding works. J Midwifery Womens Health 2007; 52 (6): 564–570.

    Article  Google Scholar 

  6. 6

    Kent JC, Ramsay DT, Doherty D, Larsson M, Hartmann PE . Response of breasts to different stimulation patterns of an electric breast pump. J Hum Lact 2003; 19 (2): 179–186.

    Article  Google Scholar 

  7. 7

    Daly SE, Kent JC, Owens RA, Hartmann PE . Frequency and degree of milk removal and the short-term control of human milk synthesis. Exp Physiol 1996; 81 (5): 861–875.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  8. 8

    Meier PP, Engstrom JL, Janes JE, Jegier BJ, Loera F . Breast pump suction patterns that mimic the human infant during breastfeeding: greater milk output in less time spent pumping for breast pump-dependent mothers with premature infants. J Perinatol 2012; 32 (2): 103–110.

    CAS  Article  Google Scholar 

  9. 9

    Wolff PH . Sucking patterns of infant mammals. Brain Behav Evol 1968; 1 (4): 354–367.

    Article  Google Scholar 

  10. 10

    Wolff PH . The serial organization of sucking in the young infant. Pediatrics 1968; 42 (6): 943–956.

    CAS  Google Scholar 

  11. 11

    Neville MC . Anatomy and physiology of lactation. Pediatr Clin North Am 2001; 48 (1): 13–34.

    CAS  Article  Google Scholar 

  12. 12

    Mitoulas LR, Ramsay DT, Kent JC, Larsson M, Hartmann PE . Identification of factors affecting breast pump efficacy. Adv Exp Med Biol 2004; 554: 325–327.

    CAS  PubMed  Article  Google Scholar 

  13. 13

    Mizuno K, Ueda A . Changes in sucking performance from nonnutritive sucking to nutritive sucking during breast- and bottle-feeding. Pediatr Res 2006; 59 (5): 728–731.

    Article  Google Scholar 

  14. 14

    Bowen-Jones A, Thompson C, Drewett RF . Milk flow and sucking rates during breast-feeding. Dev Med Child Neurol 1982; 24 (5): 626–633.

    CAS  Google Scholar 

  15. 15

    Drewett RF, Woolridge M . Sucking patterns of human babies on the breast. Early Hum Dev 1979; 3 (4): 315–321.

    CAS  Article  Google Scholar 

  16. 16

    Elad D, Kozlovsky P, Blum O, Laine AF, Po MJ, Botzer E et al. Biomechanics of milk extraction during breast-feeding. Proc Natl Acad Sci USA 2014; 111 (14): 5230–5235.

    CAS  PubMed  Article  Google Scholar 

  17. 17

    Meier PP . Suck-breathe patterning during bottle and breast feeding for preterm infants. In: David TJ (ed). Major Controversies in Infant Nutrition. International Congress and Symposium Series 215. Royal Society of Medicine Press: London, England, 1996; 9–20.

  18. 18

    Ramsay DT, Hartmann PE . Milk removal from the breast. Breastfeed Rev 2005; 13 (1): 5–7.

    Google Scholar 

  19. 19

    Mathew OP, Bhatia J . Sucking and breathing patterns during breast- and bottle-feeding in term neonates. Effects of nutrient delivery and composition. Am J Dis Child 1989; 143 (5): 588–592.

    CAS  Article  Google Scholar 

  20. 20

    Geddes DT, Chadwick LM, Kent JC, Garbin CP, Hartmann PE . Ultrasound imaging of infant swallowing during breast-feeding. Dysphagia 2010; 25 (3): 183–191.

    PubMed  Article  Google Scholar 

  21. 21

    Ramsay DT, Kent JC, Hartmann RA, Hartmann PE . Anatomy of the lactating human breast redefined with ultrasound imaging. J Anat 2005; 206 (6): 525–534.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  22. 22

    Ramsay DT, Mitoulas LR, Kent JC, Larsson M, Hartmann PE . The use of ultrasound to characterize milk ejection in women using an electric breast pump. J Hum Lact 2005; 21 (4): 421–428.

    PubMed  PubMed Central  Article  Google Scholar 

  23. 23

    Geddes DT, Kent JC, Mitoulas LR, Hartmann PE . Tongue movement and intra-oral vacuum in breastfeeding infants. Early Hum Dev 2008; 84 (7): 471–477.

    PubMed  PubMed Central  Article  Google Scholar 

  24. 24

    Zinaman MJ, Hughes V, Queenan JT, Labbok MH, Albertson B . Acute prolactin and oxytocin responses and milk yield to infant suckling and artificial methods of expression in lactating women. Pediatrics 1992; 89 (3): 437–440.

    CAS  PubMed  Google Scholar 

  25. 25

    Lussier MM, Brownell EA, Proulx TA, Bielecki DM, Marinelli KA, Bellini SL et al. Daily breastmilk volume in mothers of very low birth weight neonates: a repeated-measures randomized trial of hand expression versus electric breast pump expression. Breastfeed Med 2015; 10: 312–317.

    PubMed  Article  Google Scholar 

  26. 26

    Paul VK, Singh M, Deorari AK, Pacheco J, Taneja U . Manual and pump methods of expression of breast milk. Indian J Pediatr 1996; 63 (1): 87–92.

    CAS  PubMed  Article  Google Scholar 

  27. 27

    Jones E, Dimmock PW, Spencer SA . A randomised controlled trial to compare methods of milk expression after preterm delivery. Arch Dis Child Fetal Neonatal Ed 2001; 85 (2): F91–F95.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  28. 28

    Slusher T, Slusher IL, Biomdo M, Bode-Thomas F, Curtis BA, Meier P . Electric breast pump use increases maternal milk volume in African nurseries. J Trop Pediatr 2007; 53 (2): 125–130.

    PubMed  PubMed Central  Article  Google Scholar 

  29. 29

    Green D, Moye L, Schreiner RL, Lemons JA . The relative efficacy of four methods of human milk expression. Early Hum Dev 1982; 6 (2): 153–159.

    CAS  PubMed  Article  Google Scholar 

  30. 30

    Flaherman VJ, Gay B, Scott C, Avins A, Lee KA, Newman TB . Randomised trial comparing hand expression with breast pumping for mothers of term newborns feeding poorly. Arch Dis Child Fetal Neonatal Ed 2012; 97 (1): F18–F23.

    PubMed  Article  Google Scholar 

  31. 31

    Morton J, Hall JY, Wong RJ, Thairu L, Benitz WE, Rhine WD . Combining hand techniques with electric pumping increases milk production in mothers of preterm infants. J Perinatol 2009; 29 (11): 757–764.

    CAS  Article  Google Scholar 

  32. 32

    Hopkinson J, Heird W . Maternal response to two electric breast pumps. Breastfeed Med 2009; 4 (1): 17–23.

    PubMed  Article  Google Scholar 

  33. 33

    Fewtrell MS, Lucas P, Collier S, Singhal A, Ahluwalia JS, Lucas A . Randomized trial comparing the efficacy of a novel manual breast pump with a standard electric breast pump in mothers who delivered preterm infants. Pediatrics 2001; 107 (6): 1291–1297.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  34. 34

    Ramsay DT, Mitoulas LR, Kent JC, Cregan MD, Doherty DA, Larsson M et al. Milk flow rates can be used to identify and investigate milk ejection in women expressing breast milk using an electric breast pump. Breastfeed Med 2006; 1 (1): 14–23.

    PubMed  PubMed Central  Article  Google Scholar 

  35. 35

    Mitoulas LR, Lai CT, Gurrin LC, Larsson M, Hartmann PE . Effect of vacuum profile on breast milk expression using an electric breast pump. J Hum Lact 2002; 18 (4): 353–360.

    PubMed  PubMed Central  Article  Google Scholar 

  36. 36

    Mitoulas LR, Lai CT, Gurrin LC, Larsson M, Hartmann PE . Efficacy of breast milk expression using an electric breast pump. J Hum Lact 2002; 18 (4): 344–352.

    PubMed  PubMed Central  Article  Google Scholar 

  37. 37

    Prime DK, Geddes DT, Hepworth AR, Trengove NJ, Hartmann PE . Comparison of the patterns of milk ejection during repeated breast expression sessions in women. Breastfeed Med 2011; 6 (4): 183–190.

    PubMed  PubMed Central  Article  Google Scholar 

  38. 38

    Meier PP, Engstrom JL, Hurst NM, Ackerman B, Allen M, Motykowski JE et al. A comparison of the efficiency, efficacy, comfort, and convenience of two hospital-grade electric breast pumps for mothers of very low birthweight infants. Breastfeed Med 2008; 3 (3): 141–150.

    Article  Google Scholar 

  39. 39

    Post ED, Stam G, Tromp E . Milk production after preterm, late preterm and term delivery; effects of different breast pump suction patterns. J Perinatol 2015; 36 (1): 47–51.

    PubMed  Article  Google Scholar 

  40. 40

    Meier PP, Engstrom JL . Evidence-based practices to promote exclusive feeding of human milk in very low-birthweight infants. Neoreviews 2007; 8 (11): e467–e477.

    Article  Google Scholar 

  41. 41

    Kent JC, Geddes DT, Hepworth AR, Hartmann PE . Effect of warm breastshields on breast milk pumping. J Hum Lact 2011; 27 (4): 331–338.

    PubMed  Article  Google Scholar 

  42. 42

    Kent JC, Hepworth AR, Sherriff JL, Cox DB, Mitoulas LR, Hartmann PE . Longitudinal changes in breastfeeding patterns from 1 to 6 months of lactation. Breastfeed Med 2013; 8 (4): 401–407.

    PubMed  Article  Google Scholar 

  43. 43

    Smith MM, Durkin M, Hinton VJ, Bellinger D, Kuhn L . Initiation of breastfeeding among mothers of very low birth weight infants. Pediatrics 2003; 111 (6): 1337–1342.

    PubMed  PubMed Central  Article  Google Scholar 

  44. 44

    Larkin T, Kiehn T, Murphy PK, Uhryniak J . Examining the use and outcomes of a new hospital-grade breast pump in exclusively pumping NICU mothers. Adv Neonatal Care 2013; 13 (1): 75–82.

    PubMed  Article  Google Scholar 

  45. 45

    Alekseev NP, Ilyin VI, Yaroslavski VK, Gaidukov SN, Tikhonova TK, Specivcev YA et al. Compression stimuli increase the efficacy of breast pump function. Eur J Obstet Gynecol Reprod Biol 1998; 77 (2): 131–139.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  46. 46

    Howie PW, Houston MJ, Cook A, Smart L, McArdle T, McNeilly AS . How long should a breast feed last? Early Hum Dev 1981; 5 (1): 71–77.

    CAS  PubMed  Article  Google Scholar 

  47. 47

    Hill PD, Aldag JC, Chatterton RT . The effect of sequential and simultaneous breast pumping on milk volume and prolactin levels: a pilot study. J Hum Lact 1996; 12 (3): 193–199.

    CAS  PubMed  Article  Google Scholar 

  48. 48

    Meier P, Patel AL, Wright K, Engstrom JL . Management of breastfeeding during and after the maternity hospitalization for late preterm infants. Clin Perinatol 2013; 40 (4): 689–705.

    PubMed  PubMed Central  Article  Google Scholar 

  49. 49

    Felice JP, Rasmussen KM . Breasts pumps and bottles, and unanswered questions. Breastfeed Med 2015; 10: 412–415.

    PubMed  Article  Google Scholar 

  50. 50

    Meier PP, Engstrom JL, Patel AL, Jegier BJ, Bruns N . Improving the use of human milk during and after the NICU stay. Clin Perinatol 2010; 37 (1): 217–245.

    PubMed  PubMed Central  Article  Google Scholar 

  51. 51

    Meier PP, Patel AL, Bigger HR, Rossman B, Engstrom JL . Supporting breastfeeding in the neonatal intensive care unit: Rush mother's milk club as a case study of evidence-based care. Pediatr Clin North Am 2013; 60 (1): 209–226.

    PubMed  Article  Google Scholar 

  52. 52

    Neville MC, Morton J . Physiology and endocrine changes underlying human lactogenesis II. J Nutr 2001; 131 (11): 3005S–3008S.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  53. 53

    Pang WW, Hartmann PE . Initiation of human lactation: secretory differentiation and secretory activation. J Mammary Gland Biol Neoplasia 2007; 12 (4): 211–221.

    PubMed  Article  Google Scholar 

  54. 54

    Nguyen DA, Parlow AF, Neville MC . Hormonal regulation of tight junction closure in the mouse mammary epithelium during the transition from pregnancy to lactation. J Endocrinol 2001; 170 (2): 347–356.

    CAS  PubMed  Article  Google Scholar 

  55. 55

    Kuhn NJ . Progesterone withdrawal as the lactogenic trigger in the rat. 1969. J Mammary Gland Biol Neoplasia 2009; 14 (3): 327–342.

    CAS  PubMed  Article  Google Scholar 

  56. 56

    Hartmann PE, Trevethan P, Shelton JN . Progesterone and oestrogen and the initiation of lactation in ewes. J Endocrinol 1973; 59 (2): 249–259.

    CAS  PubMed  Article  Google Scholar 

  57. 57

    Neville MC, Morton J, Umemura S . Lactogenesis. the transition from pregnancy to lactation. Pediatr Clin North Am 2001; 48 (1): 35–52.

    CAS  Article  Google Scholar 

  58. 58

    Nommsen-Rivers LA, Chantry CJ, Peerson JM, Cohen RJ, Dewey KG . Delayed onset of lactogenesis among first-time mothers is related to maternal obesity and factors associated with ineffective breastfeeding. Am J Clin Nutr 2010; 92 (3): 574–584.

    CAS  PubMed  Article  Google Scholar 

  59. 59

    Santoro W Jr, Martinez FE, Ricco RG, Jorge SM . Colostrum ingested during the first day of life by exclusively breastfed healthy newborn infants. J Pediatr 2010; 156 (1): 29–32.

    Article  Google Scholar 

  60. 60

    Neville M, Keller R, Seacat J, Lutes V, Neifert M, Casey C et al. Studies in human lactation: milk volumes in lactating women during the onset of lactation and full lactation. Am J Clin Nutr 1988; 48: 1375–1386.

    CAS  Article  Google Scholar 

  61. 61

    Hurst NM . Recognizing and treating delayed or failed lactogenesis II. J Midwifery Womens Health 2007; 52 (6): 588–594.

    PubMed  PubMed Central  Article  Google Scholar 

  62. 62

    Nommsen-Rivers LA, Dolan LM, Huang B . Timing of stage II lactogenesis is predicted by antenatal metabolic health in a cohort of primiparas. Breastfeed Med 2012; 7 (1): 43–49.

    PubMed  PubMed Central  Article  Google Scholar 

  63. 63

    Rasmussen KM . Association of maternal obesity before conception with poor lactation performance. Annu Rev Nutr 2007; 27: 103–121.

    CAS  PubMed  Article  Google Scholar 

  64. 64

    Parker LA, Sullivan S, Krueger C, Mueller M . Association of timing of initiation of breastmilk expression on milk volume and timing of lactogenesis stage II among mothers of very low-birth-weight infants. Breastfeed Med 2015; 10 (2): 84–91.

    PubMed  PubMed Central  Article  Google Scholar 

  65. 65

    Parker LA, Sullivan S, Krueger C, Kelechi T, Mueller M . Effect of early breast milk expression on milk volume and timing of lactogenesis stage II among mothers of very low birth weight infants: a pilot study. J Perinatol 2012; 32 (3): 205–209.

    CAS  Article  Google Scholar 

  66. 66

    Hill PD, Aldag JC, Chatterton RT, Zinaman M . Comparison of milk output between mothers of preterm and term infants: the first 6 weeks after birth. J Hum Lact 2005; 21 (1): 22–30.

    PubMed  PubMed Central  Article  Google Scholar 

  67. 67

    Chapman Donna J, Perez-Escamilla R . Lactogenesis stage II: hormonal regulation, determinants and public health consequences. Recent Res Dev Nutr 2000; 3: 43–63.

    Google Scholar 

  68. 68

    Brownell E, Howard CR, Lawrence RA, Dozier AM . Delayed onset lactogenesis II predicts the cessation of any or exclusive breastfeeding. J Pediatr 2012; 161 (4): 608–614.

    PubMed  PubMed Central  Article  Google Scholar 

  69. 69

    Knight CH, Peaker M, Wilde CJ . Local control of mammary development and function. Rev Reprod 1998; 3 (2): 104–112.

    CAS  PubMed  Article  Google Scholar 

  70. 70

    Daly SE, Hartmann PE . Infant demand and milk supply. Part 2: The short-term control of milk synthesis in lactating women. J Hum Lact 1995; 11 (1): 27–37.

    CAS  PubMed  Article  Google Scholar 

  71. 71

    Daly SE, Owens RA, Hartmann PE . The short-term synthesis and infant-regulated removal of milk in lactating women. Exp Physiol 1993; 78 (2): 209–220.

    CAS  Article  Google Scholar 

  72. 72

    Battin DA, Marrs RP, Fleiss PM, Mishell DR Jr. . Effect of suckling on serum prolactin, luteinizing hormone, follicle-stimulating hormone, and estradiol during prolonged lactation. Obstet Gynecol 1985; 65 (6): 785–788.

    CAS  PubMed  Google Scholar 

  73. 73

    Hill PD, Chatterton RT Jr, Aldag JC . Serum prolactin in breastfeeding: state of the science. Biol Res Nurs 1999; 1 (1): 65–75.

    CAS  PubMed  Article  Google Scholar 

  74. 74

    Glasier A, McNeilly AS, Howie PW . The prolactin response to suckling. Clin Endocrinol (Oxf) 1984; 21 (2): 109–116.

    CAS  Article  Google Scholar 

  75. 75

    Howie PW, McNeilly AS, McArdle T, Smart L, Houston M . The relationship between suckling-induced prolactin response and lactogenesis. J Clin Endocrinol Metab 1980; 50 (4): 670–673.

    CAS  PubMed  Article  Google Scholar 

  76. 76

    Blatchford DR, Hendry KA, Wilde CJ . Autocrine regulation of protein secretion in mouse mammary epithelial cells. Biochem Biophys Res Commun 1998; 248 (3): 761–766.

    CAS  PubMed  Article  Google Scholar 

  77. 77

    Wilde CJ, Addey CV, Casey MJ, Blatchford DR, Peaker M . Feed-back inhibition of milk secretion: the effect of a fraction of goat milk on milk yield and composition. Q J Exp Physiol 1988; 73 (3): 391–397.

    CAS  PubMed  Article  Google Scholar 

  78. 78

    Wilde CJ, Blatchford DR, Knight CH, Peaker M . Metabolic adaptations in goat mammary tissue during long-term incomplete milking. J Dairy Res 1989; 56 (1): 7–15.

    CAS  PubMed  Article  Google Scholar 

  79. 79

    Kent JC, Mitoulas LR, Cregan MD, Ramsay DT, Doherty DA, Hartmann PE . Volume and frequency of breastfeedings and fat content of breast milk throughout the day. Pediatrics 2006; 117 (3): e387–e395.

    PubMed  PubMed Central  Article  Google Scholar 

  80. 80

    Lau C, Alagugurusamy R, Schanler RJ, Smith EO, Shulman RJ . Characterization of the developmental stages of sucking in preterm infants during bottle feeding. Acta Paediatr 2000; 89 (7): 846–852.

    CAS  PubMed  Article  Google Scholar 

  81. 81

    Martino K, Wagner M, Froh EB, Hanlon AL, Spatz DL . Postdischarge breastfeeding outcomes of infants with complex anomalies that require surgery. J Obstet Gynecol Neonatal Nurs 2015; 44 (3): 450–457.

    PubMed  Article  Google Scholar 

  82. 82

    Froh EB, Hallowell S, Spatz DL . The use of technologies to support human milk & breastfeeding. J Pediatr Nurs 2015; 30 (3): 521–523.

    PubMed  Article  Google Scholar 

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This study was funded by NIH grants: NR010009 and NICHD R03HD081412.

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Correspondence to P P Meier.

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Meier, P., Patel, A., Hoban, R. et al. Which breast pump for which mother: an evidence-based approach to individualizing breast pump technology. J Perinatol 36, 493–499 (2016).

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