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. 2024 Nov 13;16(11):e73651. doi: 10.7759/cureus.73651

Tobacco Smoke Exposure and Lactation

Maria Vlachou 1, Giannoula A Kyrkou 2, Victoria Vivilaki 2, Vasiliki E Georgakopoulou 3,, Paraskevi Katsaounou 4, Anastasia Κapetanaki 5, Athina Diamanti 2
Editors: Alexander Muacevic, John R Adler
PMCID: PMC11645517  PMID: 39677116

Abstract

Tobacco smoke exposure remains a significant public health concern, particularly for lactating women and their infants. Despite widespread awareness of the harms of smoking during pregnancy, many women continue to smoke postpartum, directly impacting lactation success and infant health. Studies have shown that nicotine, the primary component of tobacco smoke, inhibits prolactin production and the milk ejection reflex, resulting in a decreased milk supply and poor breastfeeding outcomes. Additionally, the presence of harmful chemicals in tobacco smoke, such as cadmium and lead, can accumulate in breast milk, exposing infants to toxic substances with potential long-term health implications. Maternity professionals play a crucial role in supporting smoking cessation efforts among postpartum women, providing evidence-based counseling, resources, and referrals to cessation programs. This review aims to provide an update for maternity professionals on the effects of tobacco smoke exposure on lactation and breastfeeding outcomes. In this review, we will explore the physiological mechanisms through which tobacco smoke components can interfere with lactation. Furthermore, we will discuss the challenges faced by lactating women who smoke, including increased risk of mastitis, reduced breastfeeding duration, and impaired infant growth and development. Finally, we will highlight emerging research on novel interventions to reduce the adverse effects of tobacco smoke exposure on lactation, including pharmacological treatments and behavioral interventions tailored to postpartum women.

Keywords: breastfeeding support, lactation, maternity professionals, smoking cessation, tobacco smoke exposure

Introduction and background

Breastfeeding improves both maternal and infant health while also promoting a strong bond between them. Infants who are exclusively breastfed for at least three months show reduced incidence of otitis media and respiratory infections and have fewer and less severe episodes of diarrhea [1]. Additionally, exclusive breastfeeding for at least four months is associated with a lower prevalence of allergies, asthma, and atopic dermatitis by the time the child is 2-3 years old, even for children with a family history of allergies [1]. Furthermore, exclusive breastfeeding continues to benefit children and adolescents by reducing the risk of obesity. In adulthood, it is associated with lower blood pressure and cholesterol levels [1]. Breastfeeding women also have a reduced risk of developing breast, ovarian, and endometrial cancers during the premenopausal period, as well as a lower risk of osteoporosis in the postmenopausal period [1]. Moreover, breastfeeding decreases maternal anxiety levels, fosters positive emotions, and strengthens maternal care for the infant [2,3]. Breastfeeding also helps regulate body weight, leading to postpartum weight loss and reducing the likelihood of conditions such as endometriosis, type II diabetes, osteoporosis, hypertension, cardiovascular diseases, metabolic syndrome, autoimmune diseases, multiple sclerosis, and Alzheimer's disease [2].

The World Health Organization (WHO) recommends exclusive breastfeeding for infants until six months of age, followed by age-appropriate complementary foods until two years of age or for as long as the mother-infant pair desires [4, 5]. A lack of education and knowledge about the art of breastfeeding can hinder its initiation, establishment, and continuation, often leading to premature cessation. For this reason, breastfeeding education during prenatal classes, along with support in the first hour after birth, during hospital stays, and through home visits throughout the postpartum period, can significantly increase the number of newborns who are exclusively breastfed in accordance with WHO recommendations [4,5].

Both primary and secondary exposure to cigarette smoke and the harmful substances it contains are responsible for the deaths of more than 8 million people globally each year [6]. Cigarette smoke contains over 4,000 chemicals toxic to the human body, of which more than 40 are known carcinogens [7]. Cigarette smoke contains some of these substances, while combustion produces others that trigger toxic reactions upon inhalation. Notable chemicals include nicotine, carbon monoxide, acetone, arsenic, benzene, cadmium, cyanide, formaldehyde, lead, mercury, nickel, phenol, and styrene [7]. Nicotine, a psychoactive and addictive component of tobacco, and carbon monoxide, when inhaled during the perinatal period through primary, secondary, or tertiary exposure, can cause alterations in the offspring. The placenta and breast milk also transfer these harmful compounds to the offspring [8].

Despite the well-documented research on the harmful effects of smoking on the health of offspring both prenatally and postnatally [9], many expectant and breastfeeding mothers continue to smoke during pregnancy and lactation.

The aim of this paper is to consolidate the scientific data on the effects of smoking during lactation and to serve as a learning resource and tool for providing quality care to midwives and obstetricians during the perinatal period, particularly in the lactation phase.

Review

Detection of substances in breast milk: effects of nicotine and other substances on the components of breast milk

Smoking during lactation transfers substances found in tobacco, such as nicotine, to the breastfeeding infant. Nicotine levels peak within one hour of smoking and then gradually decrease [10]. Nicotine is considered an environmental pollutant capable of contaminating the atmosphere and soil [11]. The harmful effects of nicotine on breast milk depend on the number of cigarettes consumed by the breastfeeding mother and the time elapsed between the last cigarette and the start of breastfeeding [10,12].

The infant's digestive system absorbs nicotine from breast milk, which the liver then metabolizes into cotinine, a byproduct of nicotine metabolism [8]. Researchers have detected cotinine, the main metabolite of nicotine, in the urine of breastfed infants whose mothers smoke [10,13]. As the primary metabolite of nicotine, cotinine is used as a biomarker for tobacco smoke exposure (e.g., measuring cotinine levels in infant urine). Cotinine has a longer half-life (3-4 hours) in infants than in adults [8].

The detection of heavy metals (such as cadmium and lead) in colostrum and mature milk from women who smoke or are exposed to secondhand smoke demonstrates that tobacco use or exposure can alter the composition and nutrient content of human breast milk [14]. Milnerowicz & Chmarek [15] analyzed breast milk samples from smokers and non-smokers. Cadmium levels were found to be four times higher in the milk of smokers compared to non-smokers, while the concentration of total protein and metallothionein levels was lower in the breast milk of smokers. Thus, the researchers concluded that the breast milk of smoking mothers has a lower nutritional value compared to that of non-smoking mothers [15].

Changes in the composition and taste of breast milk due to smoking

Human breast milk is rich in essential components such as lactoferrin, oligosaccharides, polyunsaturated fatty acids, vitamins (vitamin C, vitamin E), minerals, immunoglobulins, enzymes, hormones, and growth factors. These components are crucial for supporting the healthy development of newborns. However, tobacco use and the harmful substances produced by smoking affect the quantity of these valuable components [8].

Researchers collected breast milk samples from breastfeeding mothers who smoke and those who do not and found that smokers' breast milk had lower concentrations of lipids and proteins, suggesting that smoking influences the alteration of breast milk composition [16-19]. Additionally, tobacco use inhibits hepatic lipoprotein lipase activity, impairs lipolysis, and increases maternal blood levels of cholesterol, triglycerides, and low-density lipoproteins [20]. Smokers' breast milk reduces the quantity of polyunsaturated fatty acids, especially omega-3 fatty acids [20]. Lipids are essential for the development of vision, brain, and body weight in infants [20]. The lower lipid content in the breast milk of smokers results in lower body weight, cognitive disorders, and limited physical growth in infants.

Another study notes that smoking reduces the iodine intake through breast milk [8]. Iodine deficiency results in the inability to synthesize thyroid hormones, which the infant's thyroid function depends on. It also causes sleep disturbances due to reduced sleep duration, intracellular oxidative damage, histopathological damage to the liver and lungs, reduced pancreatic beta cells, impaired glucose tolerance, increased body weight, brain damage, and reduced cognitive and motor function [8,21].

Colostrum and full-term milk from breastfeeding mothers have lower amounts of total equivalent antioxidant capacity (TEAC) and higher amounts of thiobarbituric acid-reactive substances (TBARS). They also have more antioxidant defense activity, which can be seen by higher levels of antioxidant enzyme activity [22,23]. As a result, smoking reduces antioxidant properties and alters immunological protections [18].

Finally, smoking and secondhand smoke exposure alter the taste of breast milk, making it difficult for the infant to breastfeed or leading to breastfeeding refusal [12,24]. It remains unknown whether similar taste changes occur in breast milk following cannabis use [25].

All of the above demonstrate that exposure to cigarette smoke in breastfeeding mothers affects the epithelial cells of the mammary gland, reducing milk production and altering its composition. This results in changes that diminish the protective properties of colostrum and mature milk, which serve as the primary nutrition for infants up to six months of age. These changes may have potential consequences for the health of the newborn and infant and reduce the beneficial effects provided by breastfeeding [8,26].

Effect of smoking on prolactin production

Studies demonstrate the risks associated with maternal smoking during lactation, which leads to a reduction in prolactin levels, decreased milk supply, and changes in both the composition and taste of the milk [12]. These effects often result in early weaning.

Factors related to the mother, the infant, and the environment influence the secretion of prolactin, the hormone responsible for producing breast milk during lactation. Prolactin deficiency can frequently cause lactation issues and disorders [27].

Cigarette smoke and nicotine alter prolactin levels in the bloodstream [18,28]. Consequently, they impair the stimulation of mammary gland development, reduce milk production, and inhibit lactation [24,28]. Additionally, prolactin levels decrease in non-smoking breastfeeding women exposed to secondhand smoke, leading to shorter or premature cessation of breastfeeding [24].

Impact of smoking on the process, duration, and effectiveness of breastfeeding

Among women who smoke, there is evidence of reduced milk production and shorter breastfeeding durations. Research shows that smoking mothers are less likely to initiate breastfeeding, and if they do, they breastfeed for shorter periods [29-31]. Furthermore, despite the intention to breastfeed, younger maternal age, lower educational levels, and smoking during pregnancy are associated with shorter breastfeeding durations [31,32].

Ariz et al. [32] monitored 399 pregnant women intending to breastfeed up to the 12th month postpartum. Results showed that participants who smoked during pregnancy frequently used pacifiers and bottle nipples and had lower rates of exclusive breastfeeding during the first week postpartum. Moreover, those who continued smoking during pregnancy introduced formula feeding earlier, specifically within the first month of life, compared to non-smokers who introduced formula at five months. The same study found that the average breastfeeding duration for smoking mothers was 90 days, while non-smokers breastfed for an average of 177 days, indicating that those who smoked had shorter breastfeeding periods. Additionally, the study noted that occasional smokers had longer breastfeeding durations compared to regular smokers [32]. Researchers concluded that smoking during pregnancy is associated with shorter breastfeeding durations, despite the mother's intention to breastfeed. They observed this association in the short term (up to six months), but not in the long term (up to 12 months when the study ended).

However, smoking cessation before or during pregnancy is associated with longer breastfeeding durations, suggesting that breastfeeding motivates smokers to modify their smoking habits and prevent relapse [32]. Even if they are unable to completely quit, many mothers reduce their smoking habits [33]. In a study by Joseph et al. [34], researchers aimed to assess factors related to breastfeeding intention, initiation, duration, and weaning among pregnant former smokers. The majority of participants quit smoking upon learning of their pregnancy and expressed a positive intention to breastfeed, with their desire to continue breastfeeding serving as motivation to remain smoke-free. However, some participants who relapsed and resumed smoking had shorter breastfeeding durations and weaned early [34].

Secondhand smoke exposure during pregnancy is associated with an increased likelihood of breastfeeding cessation and also affects breastfeeding duration in non-smoking mothers [35]. Additionally, postpartum women exposed to secondhand smoke are less likely to breastfeed [36]. A study by Rosen-Carole et al. [37] examined the effect of secondhand smoke exposure on breastfeeding duration and found that breastfeeding was shorter in these cases. Research links maternal exposure to secondhand smoke to an increased risk of exclusive breastfeeding cessation before six months, as well as reduced breastfeeding intention or cessation within the first two months of the newborn's life [38]. Smoking bans in the home and avoidance of secondhand smoke could potentially improve breastfeeding rates [39].

Researchers at Careggi University Hospital in Florence assessed the breastfeeding behavior, including nipple latch and swallowing, of 35 infants born to smoking mothers and 35 infants born to non-smoking mothers. After three months of follow-up, researchers concluded that infants of smoking mothers exhibited altered neurobehavioral profiles and had difficulty initiating and maintaining breastfeeding, with only 57.1% of infants of smokers successfully breastfeeding compared to 87.5% of infants of non-smokers [40].

These research findings are invaluable as they demonstrate the need for organized interventions aimed at smoking cessation, relapse prevention, increased breastfeeding initiation and duration, and promotion of exclusive breastfeeding, thus improving maternal and infant health [32,34]. Smoking mothers should be informed about the harmful effects of smoking, and the changes it causes in breast milk quantity and composition, and encouraged to change their smoking habits [41,42]. In cases where mothers choose to continue smoking while breastfeeding, they should receive specialized guidance from healthcare professionals to protect their infant's health and promote breastfeeding. Smoking mothers are advised to reduce smoking, ensure several hours pass between smoking and breastfeeding to minimize infant nicotine exposure, smoke in a separate room to protect the infant from secondhand smoke and wear a cover while smoking, which is removed afterward to protect the infant from thirdhand smoke exposure [42,43].

Healthcare providers must support and encourage breastfeeding even if the mother smokes, as the benefits of breastfeeding outweigh those of bottle-feeding and formula. Planning for relapse prevention early in the postpartum period and continuing it for up to three months after birth is ideal [44].

Effects of smoking on offspring

Epigenetics focuses on understanding the regulation of gene expression beyond what is encoded in DNA sequences and how environmental factors influence changes in gene expression. The placenta's epigenetic regulation mediates epigenetic alterations like miRNA imprinting and expression, as well as DNA methylation. Proper placental development and function are crucial for the growth and survival of the developing fetus. Investigating and understanding these epigenetic mechanisms is useful in identifying new biomarkers for exposure, burden, or disease risk [45].

The interaction between genes (during fetal development, the placenta) and the environment can lead to adverse conditions impacting both physical and mental health later in life [45]. The mother's use of cigarette smoke influences the expression of miRNA in the placenta during fetal development [46].

The fetal programming theory [47] identifies gene-environment interactions and explains how the intrauterine environment influences molecular aspects of development. Initially, researchers proposed a hypothesis linking the development of diseases in adulthood to an unfavorable nutritional environment for the fetus (poor maternal dietary choices during pregnancy). However, this risk may change if dietary habits improve postnatally. Beyond poor nutritional exposure, the adverse intrauterine environment is also linked to other health-threatening factors such as influenza, elevated stress levels, medications, maternal smoking, and secondhand smoke exposure [47].

Respiratory issues

Smoking during the perinatal period increases the incidence of respiratory diseases such as asthma, wheezing, bronchiolitis, and pulmonary disorders (e.g., impaired lung development or reduced lung function), leading to more frequent hospitalizations of children with smoking parents [9,48,49]. Maternal smoking and secondhand smoke exposure during pregnancy are associated with the development of asthma in childhood [50]. Vardavas et al. [51] found that children exposed to secondhand smoke during pregnancy were more likely to develop wheezing by age two compared to children not exposed to secondhand smoke. Postnatal exposure to secondhand smoke further increases the risk of wheezing in children.

Prematurity and physical development

Prenatal exposure to cigarette smoke (nicotine and carbon monoxide) hinders the exchange of nutrients and oxygen between the mother and fetus, restricting fetal growth. It has been found that smoking mothers give birth to newborns with low birth weights (with a reduction of 277 g compared to non-smokers or those who quit early in pregnancy) [9,29,38]. Mothers exposed to secondhand smoke during pregnancy are also more likely to give birth to low-birth-weight babies [52-54], smaller head circumferences [52], and premature infants [55].

Secondhand smoke exposure in infancy impacts growth. Baheiraei et al. [39] compared the weight, height, and head circumference of a sample of infants exposed to secondhand smoke with those who were not. Measurements were taken three times (5th-7th day of life, 2 months, and 4 months after birth). The researchers concluded that secondhand smoke exposure in infancy could lead to reduced weight and height during the first four months of life. Another study [56] investigated the interaction between smoking during pregnancy, preeclampsia, and birth weight. Results showed that women who developed preeclampsia and smoked during pregnancy had significantly smaller babies compared to those who did not develop preeclampsia and did not smoke.

Congenital anomalies and cleft palates

The occurrence of congenital anomalies in newborns has been associated with maternal smoking or secondhand smoke exposure during pregnancy [52]. Studies indicate that mothers who smoked or were exposed to secondhand smoke during pregnancy are more likely to have children with neural tube defects (e.g., anencephaly) or cleft lip with or without cleft palate [55,57-59].

Allergies

Secondhand smoke exposure may contribute to the development of childhood allergies due to disruptions in the immune system [60]. Damage to the epithelial cells of the nasal cavity, airways, and skin barrier can cause these disorders to affect the skin, such as atopic dermatitis, or the respiratory system, such as allergic rhinitis [60].

Obesity, metabolic syndrome, and overweight infants

Early and involuntary exposure of the fetus and newborn to cigarette smoke and nicotine (during pregnancy and breastfeeding) is linked to metabolic syndrome and obesity in childhood and adulthood [61]. The mechanism by which smoking during breastfeeding causes metabolic dysfunctions is not fully understood. Researchers concluded in a study of 378 adolescents prenatally exposed to maternal smoking that changes in brain synapses and reduced amygdala volume promote obesity [62].

Secondhand smoke exposure and non-exclusive breastfeeding are associated with infant obesity, while exclusive breastfeeding reduces the likelihood of obesity resulting from passive smoking [61]. Children exposed to smoke prenatally, whether through maternal smoking or secondhand exposure, exhibit a higher body mass index (BMI) in early childhood [63]. Teenagers whose mothers smoked or were exposed to secondhand smoke during pregnancy have a higher prevalence of obesity during adolescence [64]. The study found that not breastfeeding, maternal obesity, and excessive screen time contributed to adolescent obesity [64].

A study by Wen et al. [65] explored the relationship between cigarette smoke exposure through breast milk and weight gain risk. Wen et al. [65] used a sample of 21,063 mother-infant pairs, categorizing mothers by their smoking status (non-smokers, light smokers, moderate smokers, and heavy smokers) and recording the infants' feeding type (exclusive breastfeeding or bottle feeding) during daycare. After tracking the children's weight and height up to age seven and considering additional factors (maternal smoking, diet), the researchers concluded that cigarette smoke exposure through breast milk contributes to moderate weight gain by age seven, resulting in overweight children.

Sleep disorders

Sleep disturbances arise from nicotine's effects on brain function, its stimulating properties, and the inhibitory function of neurons that promote sleep, manifesting in irritability and crying [8]. Mennella et al. [12] observed that infants breastfed by mothers who had recently smoked had shorter sleep durations (53.4 minutes) compared to infants breastfed by mothers who abstained from smoking (84.5 minutes of sleep). The researchers concluded that the infant's sleep duration was shorter the higher the dose of nicotine the infant ingested through breastfeeding, depending on how close the mother had smoked to feeding.

Other problems

Additional problems for offspring resulting from maternal smoking and cigarette smoke exposure during the perinatal period include hearing loss [66], early childhood leukemia [67], cardiac rhythm disturbances [8,68], anemia, rickets [14], frequent colic episodes [8,9,69], sudden infant death syndrome (SIDS), excessive crying [70], paleness [8], hyperactivity and attention deficit disorder [71], memory deficits, and learning difficulties [8].

Cannabis and marijuana use during lactation

The legalization of cannabis (and marijuana) in many countries has led to the production of a wide variety of products for ingestion, topical application, inhalation, or vaping, with significantly higher potency than in the past [72]. Furthermore, the widespread belief in the safety of cannabis use has led to health issues in infants and children whose parents use it, as they are susceptible to its effects through breastfeeding and indirect exposure.

Research data indicate that the use of both tobacco and cannabis (either individually or together) during breastfeeding negatively impacts the developing brain of the newborn and infant [73]. It is associated with adverse pregnancy outcomes and health problems in infants and children, such as reduced muscle tone, decreased sucking reflexes [74,75], low body weight, reduced head circumference [66], increased likelihood of admission to neonatal intensive care units (NICUs) [76], delayed development [66], neurobiological development disorders, changes in normal brain function [66], sleep disorders, psychotic symptoms, learning difficulties, behavioral disorders (aggression, impulsivity), hyperactivity (ADHD), autism spectrum disorders [77], reduced cognitive ability, decreased gray matter [73,78], and increased risk of marijuana, alcohol, and opioid use during adolescence and young adulthood [73,79]. Furthermore, there are reports of negative academic performance [80]. The American Academy of Pediatrics and the American College of Obstetricians recommend avoiding the use of cannabis and cannabis-containing products throughout lactation due to potential neurodevelopmental issues in newborns and infants [81,82].

Researchers have detected delta-9-tetrahydrocannabinol (THC), a lipid-soluble psychoactive chemical in cannabis, in breast milk, with concentrations peaking one hour after cannabis inhalation and gradually decreasing over the next four hours [83]. Mothers who smoked cannabis detected THC in breast milk at concentrations 7.5 times higher than in their plasma, and these mothers also detected it in the feces and urine of their breastfed infants [84]. Other studies [85,86] have similarly confirmed THC in breast milk, thus showing its transfer to breastfeeding infants.

Further research is necessary to assess the safety of cannabis use during pregnancy and breastfeeding in order to reduce unintended health consequences for infants and children from cannabis use. This research should investigate its impact on neurodevelopment, sleep, feeding, and cognitive development beyond the first year of life [73-75]. Avoid using cannabis as a treatment for hyperemesis gravidarum (severe morning sickness) [87].

Healthcare professionals hold varying opinions regarding the breastfeeding practices of mothers who use cannabis. Scientific guidelines recommend avoiding cannabis use during lactation. Additionally, mothers who use cannabis should receive full disclosure about the negative effects (such as developmental disorders and increased risk of infant death) of exposing a breastfeeding infant to cannabis through breast milk and secondhand exposure, including from a father or other household members [81,88-90].

There is currently a lack of scientific and research data on the transfer of cannabis to amniotic fluid and human breast milk [87,91], and we do not yet know the safe levels of use during the perinatal period [87]. Healthcare professionals should equip themselves with the necessary knowledge to provide expectant parents and breastfeeding women with appropriate, evidence-based recommendations about the risks of intrauterine exposure and potential harm to the developing brain. These professionals should also encourage pregnant and breastfeeding women to avoid cannabis use throughout the perinatal and lactation periods or reduce usage if complete cessation is not feasible [91]. To minimize cannabis exposure through breast milk, breastfeeding should be avoided within one hour of cannabis use [91], and efforts should be made to prevent infants and children from being exposed to such substances [87,92-94].

New Tobacco Products

Vaping Devices: E-Cigarettes and ENDS

E-cigarettes and other electronic nicotine delivery systems (ENDS) are battery-operated devices that heat a liquid (usually glycerin or propylene glycol), creating vapor. The liquid often contains nicotine, flavorings (fruity or sweet), additives, and various pollutants and carcinogenic substances [42,95]. The tobacco residues from e-cigarettes can be deposited on surfaces in the environment, creating thirdhand exposure risks for offspring with potentially harmful health consequences [96]. Similar risks arise from secondhand exposure to e-cigarette vapor, which children can inhale, ingest, or absorb through the skin long after the device's use [96].

Despite these risks, people frequently use these devices as smoking cessation tools to switch from conventional cigarettes [97]. Additionally, breastfeeding smokers may believe that e-cigarettes are safer during lactation compared to conventional cigarettes, which leads them to continue breastfeeding while using them [98].

Heated Tobacco Products

Currently, no research has examined the relationship between heated tobacco use and breastfeeding. However, concerns about breastfeeding as a smoker, especially regarding the potential contamination of breast milk with heated tobacco, and related chemicals-are not entirely unwarranted. Although smoking mothers are advised that it is safer to breastfeed than to use formula, exposure to harmful toxins remains a risk, as these may transfer to infants through breast milk. This transfer occurs due to the specific mechanisms involved in breast milk production and secretion. While heated tobacco products contain significantly fewer toxicants than traditional cigarettes, assessing how these substances might transfer to breast milk compared to traditional cigarettes could provide women with the clear, straightforward information they seek [99]. 

Smokeless Tobacco (SLT)

The term "smokeless tobacco" (SLT) refers to tobacco products that do not produce smoke when smoked or burned [99]. It is used in various forms, such as chewing, nasal inhalation, or placement between the gums, cheeks, or lips [99]. SLT contains nicotine and other harmful and carcinogenic chemicals, leading to addiction [100].

Researchers observed that different life stages, including adolescence, pre- and post-marriage periods, as well as familial and social environments, influence the use of SLT in a study by Singh et al. [101], which involved 20 pregnant and 22 breastfeeding women. The study also revealed that participants were aware of the harmful effects of SLT during pregnancy but were unaware of its consequences during breastfeeding. Many of the participants expressed a desire to quit smoking but noted a lack of knowledge on how to do so. These findings highlight the need for smoking cessation intervention tools specifically tailored for groups such as pregnant and breastfeeding women.

Snus (Nicotine Pouches)

Snus is a smokeless tobacco product consumed orally by placing it behind the lips. It contains nicotine, causes addiction, and has harmful health effects. Its use during pregnancy and lactation can result in adverse effects on the developing fetus and newborn, such as premature birth, fetal and neonatal mortality, and small-for-gestational-age infants [43]. The use of snus before and during pregnancy increases the likelihood of continued use during breastfeeding [102].

Researchers discovered through ultrasound that children exposed to snus in utero, due to maternal use, had increased carotid artery thickness and stiffness during preschool years in the study by Nordenstam et al. [102]. Due to the nicotine content, snus can disrupt prolactin secretion, leading to breastfeeding duration issues and affecting the quantity and composition of breast milk [8]. However, the study by Kreyberg et al. [43] found no significant results regarding the impact of snus use on breastfeeding.

Waterpipe (Hookah)

A study analyzing data from two national health surveys in Jordan involved a total of 6,726 mother-infant pairs (infants under 25 months) [103]. Among infants aged 0-6 months, 87% were breastfed, compared to 19.4% of infants aged 18-24 months. Of the mothers who participated in the study, 4.4% smoked conventional cigarettes, 5.4% smoked hookah, and 1.6% smoked both. In Jordan, people commonly use hookah, either in conjunction with conventional cigarettes or on its own. The researchers found that 57.7% of breastfed infants had non-smoking mothers, while wives who smoked conventional cigarettes, hookah, or both breastfed at lower rates [103]. Therefore, smoking was associated with lower breastfeeding rates up to two years of age [103].

Nicotine replacement therapy (NRT) and pharmacotherapy

NRT, a non-pharmacological method, aids in the cessation of smoking. There are short-acting and long-acting formulations available, and smokers can access them in the form of patches, gum, oral sprays, or inhalers [42]. However, research data regarding the use of NRT during breastfeeding is limited. In the study by Kreyberg et al. [43], the researchers did not find significant results regarding the use of nicotine substitutes during breastfeeding.

Nicotine and cotinine, the primary metabolites of nicotine, are detectable in breast milk. Additionally, cigarette smoke contains a variety of potentially harmful substances that can pass through breast milk, causing harm to infants [8]. Given this, using nicotine substitutes can shield infants from the harmful substances present in cigarette smoke [104].

Nicotine absorption from NRT appears to be at lower concentrations in the circulation of breastfeeding smokers compared to nicotine from smoking, and these concentrations are likely proportionally lower in breast milk [42]. However, this does not hold true for nicotine patches, as they seem to increase the levels of nicotine in the blood of breastfeeding women to a level comparable to smoking [42].

For smoking cessation, doctors also prescribe bupropion, an antidepressant, and varenicline, another pharmaceutical agent. Breastfeeding contraindicates the use of both medications [33].

The role of healthcare professionals

Healthcare professionals should advise breastfeeding mothers to quit smoking and protect themselves from secondhand and thirdhand smoke, given the potential risks of cigarette smoke exposure to infants and the changes in breast milk composition caused by smoking. In cases where breastfeeding smokers are unable to quit, healthcare professionals should provide guidance on reducing or adjusting smoking habits during breastfeeding.

Healthcare professionals who specialize in perinatal care play a critical role in protecting pregnant women, postpartum mothers, and their infants from smoking-related harm [105]. Understanding healthcare professionals' experiences with providing smoking cessation support during the perinatal period can help inform intervention design and improve routine care [106].

Midwives, in particular, are the primary healthcare providers responsible for caring for the mother-infant dyad throughout the perinatal period. Through frequent contact with midwives, women have opportunities to receive information about the harms of smoking for both their health and their baby’s health. Midwives can support them in their efforts to quit smoking without compromising their overall perinatal care [105]. Midwives are also essential in promoting maternal and child health through actions that support breastfeeding, smoking cessation, and relapse prevention [38].

Smoking cessation interventions provided by midwives in the context of perinatal care can help women reduce their smoking initially and eventually quit altogether while also facilitating breastfeeding initiation and continuation.

The research team of Naughton et al. [107] aimed to evaluate the interest, use, and attitudes toward smoking cessation support during pregnancy and postpartum among women who smoke or had recently quit. Their results indicated that interest in attending a smoking cessation intervention program was high during the later stages of pregnancy and immediately after birth but significantly decreased by three months postpartum. Additionally, fewer than half of the women who smoked reported speaking with a midwife about smoking cessation early in pregnancy, revealing a lack of healthcare professional training in this area [107].

In the study by Philips et al. [108], semi-structured phone interviews were conducted to identify barriers reported by pregnant and postpartum smokers and former smokers that made it difficult for them to quit smoking or led to relapse. Among the barriers mentioned was the lack of support from healthcare professionals.

It was also evident that although healthcare professionals working in the perinatal period typically ask about tobacco use during initial history taking, they do not provide systematic counseling for smoking cessation throughout the perinatal period. As a result, women who want to change their smoking habits may not find adequate support [109].

Some women expressed concerns and were reluctant to use nicotine replacement therapy for relapse prevention, fearing that their nicotine addiction would persist [108]. However, they appeared more open to the idea if a healthcare professional recommended it.

Thus, smoking cessation and relapse prevention support from healthcare professionals should continue during the postpartum period, extending to the entire family [108,110]. Smoking cessation programs tailored specifically for the perinatal period should be implemented to ensure relapse prevention and the identification of motivating factors [111].

From the perspective of healthcare professionals, barriers to smoking cessation support include the need to protect the professional-client relationship, lack of knowledge and confidence regarding smoking cessation interventions during the perinatal period, unfamiliarity with tools (such as the Fagerstrom test), time constraints, service priorities, limited or nonexistent funding for intervention programs, resistance from women to quitting smoking, and difficulty in approaching the topic [112-115].

Despite these challenges, healthcare professionals generally encourage women to quit smoking early in pregnancy during their initial history-taking, emphasizing the potential harm to both mother and baby. However, professionals often feel they lack the necessary training and knowledge to provide ongoing support or interventions during pregnancy or postpartum [107,112,113,115,116].

A study of 296 pediatricians revealed that while over half felt confident in advising mothers on breastfeeding, they lacked the knowledge to counsel breastfeeding smokers, underscoring the need for pediatricians to receive training in topics related to lactation, tobacco use, and smoking cessation programs [117].

Conclusions

Researchers have detected nicotine in the breast milk of smoking mothers during lactation. This finding indicates that there may be critical health impacts on the newborn and infant, as breast milk serves as the primary source of nutrition for the first six months of life. Furthermore, not only can breast milk expose an infant to cigarette smoke compounds, but also secondhand and thirdhand smoke, both of which carry negative health implications.

The majority of research findings underscore the need for policies that implement specific educational programs aimed at minimizing smoke exposure and promoting smoking cessation during pregnancy and breastfeeding. These programs should address cessation motivations, the challenges posed by the limited availability of pharmacotherapy during lactation, and the impacts of smoking on breastfeeding.

Disclosures

Conflicts of interest: In compliance with the ICMJE uniform disclosure form, all authors declare the following:

Payment/services info: All authors have declared that no financial support was received from any organization for the submitted work.

Financial relationships: All authors have declared that they have no financial relationships at present or within the previous three years with any organizations that might have an interest in the submitted work.

Other relationships: All authors have declared that there are no other relationships or activities that could appear to have influenced the submitted work.

Author Contributions

Concept and design:  Vasiliki E. Georgakopoulou, Athina Diamanti, Maria Vlachou, Paraskevi Katsaounou, Anastasia Κapetanaki, Victoria Vivilaki, Giannoula A. Kyrkou

Acquisition, analysis, or interpretation of data:  Vasiliki E. Georgakopoulou, Athina Diamanti, Maria Vlachou, Paraskevi Katsaounou, Anastasia Κapetanaki, Victoria Vivilaki, Giannoula A. Kyrkou

Drafting of the manuscript:  Vasiliki E. Georgakopoulou, Athina Diamanti, Maria Vlachou, Paraskevi Katsaounou, Anastasia Κapetanaki, Victoria Vivilaki, Giannoula A. Kyrkou

Critical review of the manuscript for important intellectual content:  Vasiliki E. Georgakopoulou, Athina Diamanti, Maria Vlachou, Paraskevi Katsaounou, Anastasia Κapetanaki, Victoria Vivilaki, Giannoula A. Kyrkou

Supervision:  Vasiliki E. Georgakopoulou, Athina Diamanti

References

  • 1.Allaitement maternel: les bénéfices pour la santé de l'enfant et de sa mère [Breastfeeding health benefits for child and mother] Turck D, Vidailhet M, Bocquet A, et al. Arch Pediatr. 2013;20:0–48. doi: 10.1016/S0929-693X(13)72251-6. [DOI] [PubMed] [Google Scholar]
  • 2.Breastfeeding and the benefits of lactation for women's health. Del Ciampo LA, Del Ciampo IR. Rev Bras Ginecol Obstet. 2018;40:354–359. doi: 10.1055/s-0038-1657766. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.Psychological effects of breastfeeding on children and mothers. Krol KM, Grossmann T. Bund Gesun Gesun. 2018;61:977–985. doi: 10.1007/s00103-018-2769-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.World Health Organization: Global strategy for infant and young child feeding. [ Nov; 2024 ]. 2003. https://iris.who.int/bitstream/handle/10665/42590/9241562218.pdf?sequence=1 https://iris.who.int/bitstream/handle/10665/42590/9241562218.pdf?sequence=1
  • 5.World Health Organization (2023) Infant and young child feeding. (20 December 2023. World Health Organization: Infant and young child feeding. [ Dec; 2023 ]. 2023. https://www.who.int/news-room/fact-sheets/detail/infant-and-young-child-feeding https://www.who.int/news-room/fact-sheets/detail/infant-and-young-child-feeding
  • 6.World Health Organization (2019. World Health Organization: WHO report on the global tobacco epidemic 2019: offer help to quit tobacco use. [ Nov; 2024 ]. 2019. https://www.who.int/publications/i/item/9789241516204 https://www.who.int/publications/i/item/9789241516204
  • 7.IARC Working Group on the Evaluation of Carcinogenic Risks to Humans. IARC monographs on the evaluation of carcinogenic risks to humans. 100E. International Agency for Research on Cancer; 2012. Personal habits and indoor combustions, a review of human carcinogens; pp. 1–538. [PMC free article] [PubMed] [Google Scholar]
  • 8.Tobacco smoking and breastfeeding: Effect on the lactation process, breast milk composition and infant development. A critical review. Napierala M, Mazela J, Merritt TA, Florek E. Environ Res. 2016;151:321–338. doi: 10.1016/j.envres.2016.08.002. [DOI] [PubMed] [Google Scholar]
  • 9.Negative influence of maternal smoking during pregnancy on infant outcomes. Olives JP, Elias-Billon I, Barnier-Ripet D, Hospital V. Arch Pediatr. 2020;27:189–195. doi: 10.1016/j.arcped.2020.03.009. [DOI] [PubMed] [Google Scholar]
  • 10.Effects of maternal nicotine on breastfeeding infants. Primo CC, Ruela PB, Brotto LD, Garcia TR, Lima Ede F. Rev Paul Pediatr. 2013;31:392–397. doi: 10.1590/S0103-05822013000300018. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Uptake of nicotine from discarded cigarette butts - A so far unconsidered path of contamination of plant-derived commodities. Selmar D, Radwan A, Abdalla N, et al. Environ Pollut. 2018;238:972–976. doi: 10.1016/j.envpol.2018.01.113. [DOI] [PubMed] [Google Scholar]
  • 12.Breastfeeding and smoking: short-term effects on infant feeding and sleep. Mennella JA, Yourshaw LM, Morgan LK. Pediatrics. 2007;120:497–502. doi: 10.1542/peds.2007-0488. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.The urinary cotinine levels of infants and the determinants. Yilmaz G, Karacan C, Besler HT, Yurdakök K, Coşkun T. https://pubmed.ncbi.nlm.nih.gov/20718188/ Turk J Pediatr. 2010;52:294–300. [PubMed] [Google Scholar]
  • 14.Cadmium, lead, copper and zinc in breast milk in Poland. Winiarska-Mieczan A. Biol Trace Elem Res. 2014;157:36–44. doi: 10.1007/s12011-013-9870-x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Influence of smoking on metallothionein level and other proteins binding essential metals in human milk. Milnerowicz H, Chmarek M. Acta Paediatr. 2005;94:402–406. doi: 10.1111/j.1651-2227.2005.tb01908.x. [DOI] [PubMed] [Google Scholar]
  • 16.Effects of smoking, mother's age, body mass index, and parity number on lipid, protein, and secretory immunoglobulin A concentrations of human milk. Bachour P, Yafawi R, Jaber F, Choueiri E, Abdel-Razzak Z. Breastfeed Med. 2012;7:179–188. doi: 10.1089/bfm.2011.0038. [DOI] [PubMed] [Google Scholar]
  • 17.The effects of maternal passive smoking on maternal milk lipid. Baheiraei A, Shamsi A, Khaghani S, Shams S, Chamari M, Boushehri H, Khedri A. https://pubmed.ncbi.nlm.nih.gov/24901858/ Acta Med Iran. 2014;52:280–285. [PubMed] [Google Scholar]
  • 18.The effect of tobacco smoking during pregnancy and breastfeeding on human milk composition-a systematic review. Macchi M, Bambini L, Franceschini S, Alexa ID, Agostoni C. Eur J Clin Nutr. 2021;75:736–747. doi: 10.1038/s41430-020-00784-3. [DOI] [PubMed] [Google Scholar]
  • 19.The effects of maternal exposure to second-hand smoke on breast-feeding duration: A prospective cohort study. Baheiraei A, Ghafoori F, Rahimi Foroushani A, Nedjat S. Journal of Public Health. 2014;22:13–22. [Google Scholar]
  • 20.Earlier smoking habits are associated with higher serum lipids and lower milk fat and polyunsaturated fatty acid content in the first 6 months of lactation. Agostoni C, Marangoni F, Grandi F, Lammardo AM, Giovannini M, Riva E, Galli C. Eur J Clin Nutr. 2003;57:1466–1472. doi: 10.1038/sj.ejcn.1601711. [DOI] [PubMed] [Google Scholar]
  • 21.Iodine nutrition in breast-fed infants is impaired by maternal smoking. Laurberg P, Nøhr SB, Pedersen KM, Fuglsang E. J Clin Endocrinol Metab. 2004;89:181–187. doi: 10.1210/jc.2003-030829. [DOI] [PubMed] [Google Scholar]
  • 22.Maternal smoking decreases antioxidative status of human breast milk. Zagierski M, Szlagatys-Sidorkiewicz A, Jankowska A, Krzykowski G, Korzon M, Kaminska B. J Perinatol. 2012;32:593–597. doi: 10.1038/jp.2011.156. [DOI] [PubMed] [Google Scholar]
  • 23.The effect of maternal tobacco smoking and second-hand tobacco smoke exposure on human milk oxidant-antioxidant status. Napierala M, Merritt TA, Miechowicz I, Mielnik K, Mazela J, Florek E. Environ Res. 2019;170:110–121. doi: 10.1016/j.envres.2018.12.017. [DOI] [PubMed] [Google Scholar]
  • 24.Relationship of nicotine levels with prolactant hormones in passive smoking postpartum mom. Amran A, Sulastri D, Susilasastri S. Jr Mid. 2019;4:7–14. [Google Scholar]
  • 25.Infant factors that impact the ecology of human milk secretion and composition-a report from "Breastmilk Ecology: Genesis of Infant Nutrition (BEGIN)" Working Group 3. Krebs NF, Belfort MB, Meier PP, Mennella JA, O'Connor DL, Taylor SN, Raiten DJ. Am J Clin Nutr. 2023;117 Suppl 1:0–60. doi: 10.1016/j.ajcnut.2023.01.021. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26.Toxic metals in human milk in relation to tobacco smoke exposure. Szukalska M, Merritt TA, Lorenc W, et al. Environ Res. 2021;197:111090. doi: 10.1016/j.envres.2021.111090. [DOI] [PubMed] [Google Scholar]
  • 27.Prolactin biology and laboratory measurement: an update on physiology and current analytical issues. Saleem M, Martin H, Coates P. https://pubmed.ncbi.nlm.nih.gov/30072818/ Clin Biochem Rev. 2018;39:3–16. [PMC free article] [PubMed] [Google Scholar]
  • 28.Hypothesis: smoking decreases breast feeding duration by suppressing prolactin secretion. Bahadori B, Riediger ND, Farrell SM, Uitz E, Moghadasian MF. Med Hypotheses. 2013;81:582–586. doi: 10.1016/j.mehy.2013.07.007. [DOI] [PubMed] [Google Scholar]
  • 29.Maternal smoking and newborn sex, birth weight and breastfeeding: a population-based study. Timur Taşhan S, Hotun Sahin N, Omaç Sönmez M. J Matern Fetal Neonatal Med. 2017;30:2545–2550. doi: 10.1080/14767058.2016.1256986. [DOI] [PubMed] [Google Scholar]
  • 30.Factors associated with breastfeeding initiation and continuation: a meta-analysis. Cohen SS, Alexander DD, Krebs NF, et al. J Pediatr. 2018;203:190–196. doi: 10.1016/j.jpeds.2018.08.008. [DOI] [PubMed] [Google Scholar]
  • 31.Maternal smoking and psychosocial functioning: impact on subsequent breastfeeding practices. Godleski SA, Shisler S, Eiden RD, Schuetze P. Breastfeed Med. 2020;15:246–253. doi: 10.1089/bfm.2019.0148. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 32.Despite intention to breastfeed, smoking during pregnancy is associated with shorter breastfeeding duration. Ariz U, Gutierrez-De-Terán-Moreno G, Fernández-Atutxa A, et al. Jr Neo Nur. 2023;29:334–340. [Google Scholar]
  • 33.[Smoking and breastfeeding - CNGOF-SFT expert report and guidelines on the management for smoking management during pregnancy] Le Lous M, Torchin H. Gynecol Obstet Fertil Senol. 2020;48:612–618. doi: 10.1016/j.gofs.2020.03.032. [DOI] [PubMed] [Google Scholar]
  • 34.The influence of smoking on breast feeding among women who quit smoking during pregnancy. Joseph HM, Emery RL, Bogen DL, Levine MD. Nicotine Tob Res. 2017;19:652–655. doi: 10.1093/ntr/ntw254. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 35.Secondhand smoke exposure during pregnancy and mothers' subsequent breastfeeding outcomes: a systematic review and meta-analysis. Suzuki D, Wariki WM, Suto M, Yamaji N, Takemoto Y, Rahman M, Ota E. Sci Rep. 2019;9:8535. doi: 10.1038/s41598-019-44786-z. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 36.Association between exposure to environmental tobacco smoke (ETS) and breastfeeding behaviour. Chou SY, Hsu HH, Kuo HH, Kuo HW. Acta Paediatr. 2008;97:76–80. doi: 10.1111/j.1651-2227.2007.00593.x. [DOI] [PubMed] [Google Scholar]
  • 37.Low-level prenatal toxin exposures and breastfeeding duration: a prospective cohort study. Rosen-Carole CB, Auinger P, Howard CR, Brownell EA, Lanphear BP. Matern Child Health J. 2017;21:2245–2255. doi: 10.1007/s10995-017-2346-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 38.[Effects of active and/or passive smoking during pregnancy and the postpartum period] Míguez MC, Pereira B. An Pediatr (Engl Ed) 2020 doi: 10.1016/j.anpede.2020.07.021. [DOI] [PubMed] [Google Scholar]
  • 39.The effects of secondhand smoke exposure on infant growth: a prospective cohort study. Baheiraei A, Shamsi A, Mohsenifar A, Kazemnejad A, Hatmi Z, Milani M, Keshavarz A. https://pubmed.ncbi.nlm.nih.gov/25597604/ Acta Med Iran. 2015;53:39–45. [PubMed] [Google Scholar]
  • 40.Abnormal neurological soft signs in babies born to smoking mothers were associated with lower breastfeeding for first three months. Bertini G, Elia S, Lori S, Dani C. Acta Paediatr. 2019;108:1256–1261. doi: 10.1111/apa.14762. [DOI] [PubMed] [Google Scholar]
  • 41.Centers for Disease Control and Prevention: Division of nutrition, physical activity and obesity, National Center for Chronic Disease Prevention and Health Promotion, Breastfeeding and Special Circumstances. [ Nov; 2024 ]. 2019. https://www.cdc.gov/nccdphp/index.html https://www.cdc.gov/nccdphp/index.html
  • 42.Breastfeeding with smoking cessation products. Anderson PO. Breastfeed Med. 2021;16:766–768. doi: 10.1089/bfm.2021.0230. [DOI] [PubMed] [Google Scholar]
  • 43.An update on prevalence and risk of snus and nicotine replacement therapy during pregnancy and breastfeeding. Kreyberg I, Nordhagen LS, Bains KE, et al. Acta Paediatr. 2019;108:1215–1221. doi: 10.1111/apa.14737. [DOI] [PubMed] [Google Scholar]
  • 44.Predictors of changes in smoking from third trimester to 9 months postpartum. Shisler S, Homish GG, Molnar DS, Schuetze P, Colder CR, Eiden RD. Nicotine Tob Res. 2016;18:84–87. doi: 10.1093/ntr/ntv057. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 45.Epigenetics in the placenta. Maccani MA, Marsit CJ. Am J Reprod Immunol. 2009;62:78–89. doi: 10.1111/j.1600-0897.2009.00716.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 46.Maternal cigarette smoking during pregnancy is associated with downregulation of miR-16, miR-21, and miR-146a in the placenta. Maccani MA, Avissar-Whiting M, Banister CE, McGonnigal B, Padbury JF, Marsit CJ. Epigenetics. 2010;5:583–589. doi: 10.4161/epi.5.7.12762. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 47.Fetal undernutrition and disease in later life. Barker DJ, Clark PM. Rev Reprod. 1997;2:105–112. doi: 10.1530/ror.0.0020105. [DOI] [PubMed] [Google Scholar]
  • 48.Effects of environmental tobacco smoke on the respiratory health of children. Cinar ND, Dede C. https://www.pjms.com.pk/issues/janmar2010/pdf/ReviewArticle1.pdf Paki Jr Med Sci. 2010;26:223–228. [Google Scholar]
  • 49.Perinatal exposure to nicotine and implications for subsequent obstructive lung disease. Maritz GS. Paediatr Respir Rev. 2013;14:3–8. doi: 10.1016/j.prrv.2012.03.006. [DOI] [PubMed] [Google Scholar]
  • 50.Maternal second-hand smoke exposure in pregnancy is associated with childhood asthma development. Simons E, To T, Moineddin R, Stieb D, Dell SD. J Allergy Clin Immunol Pract. 2014;2:201–207. doi: 10.1016/j.jaip.2013.11.014. [DOI] [PubMed] [Google Scholar]
  • 51.The independent role of prenatal and postnatal exposure to active and passive smoking on the development of early wheeze in children. Vardavas CI, Hohmann C, Patelarou E, et al. Eur Respir J. 2016;48:115–124. doi: 10.1183/13993003.01016-2015. [DOI] [PubMed] [Google Scholar]
  • 52.Environmental tobacco smoke exposure and perinatal outcomes: a systematic review and meta-analyses. Salmasi G, Grady R, Jones J, McDonald SD. Acta Obstet Gynecol Scand. 2010;89:423–441. doi: 10.3109/00016340903505748. [DOI] [PubMed] [Google Scholar]
  • 53.Association between exposure to secondhand smoke during pregnancy and low birthweight: a narrative review. Hawsawi AM, Bryant LO, Goodfellow LT. Respir Care. 2015;60:135–140. doi: 10.4187/respcare.02798. [DOI] [PubMed] [Google Scholar]
  • 54.Low birthweight of children is positively associated with mother's prenatal tobacco smoke exposure in Shanghai: a cross-sectional study. Wang R, Sun T, Yang Q, et al. BMC Pregnancy Childbirth. 2020;20:603. doi: 10.1186/s12884-020-03307-x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 55.Does maternal exposure to secondhand tobacco smoke during pregnancy increase the risk for preterm or small-for-gestational age birth? Hoyt AT, Canfield MA, Romitti PA, Botto LD, Anderka MT, Krikov SV, Feldkamp ML. Matern Child Health J. 2018;22:1418–1429. doi: 10.1007/s10995-018-2522-1. [DOI] [PubMed] [Google Scholar]
  • 56.Effects of smoking and preeclampsia on birth weight for gestational age. Spracklen CN, Ryckman KK, Harland K, Saftlas AF. J Matern Fetal Neonatal Med. 2015;28:679–684. doi: 10.3109/14767058.2014.928853. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 57.Maternal passive smoking and risk of cleft lip with or without cleft palate. Li Z, Liu J, Ye R, Zhang L, Zheng X, Ren A. Epidemiology. 2010;21:240–242. doi: 10.1097/EDE.0b013e3181c9f941. [DOI] [PubMed] [Google Scholar]
  • 58.Maternal tobacco exposure and development of orofacial clefts in the child: a case-control study conducted in Pakistan. Bui AH, Ayub A, Ahmed MK, Taioli E, Taub PJ. Ann Plast Surg. 2018;81:708–714. doi: 10.1097/SAP.0000000000001665. [DOI] [PubMed] [Google Scholar]
  • 59.Secondhand smoke during the periconceptional period increases the risk for orofacial clefts in offspring. Pi X, Li Z, Jin L, et al. Paediatr Perinat Epidemiol. 2018;32:423–427. doi: 10.1111/ppe.12497. [DOI] [PubMed] [Google Scholar]
  • 60.Impact of perinatal environmental tobacco smoke on the development of childhood allergic diseases. Yang HJ. Korean J Pediatr. 2016;59:319–327. doi: 10.3345/kjp.2016.59.8.319. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 61.Exposure to secondhand smoke, exclusive breastfeeding and infant adiposity at age 5 months in the Healthy Start study. Moore BF, Sauder KA, Starling AP, Ringham BM, Glueck DH, Dabelea D. Pediatr Obes. 2017;12 Suppl 1:111–119. doi: 10.1111/ijpo.12233. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 62.Prenatal exposure to maternal cigarette smoking, amygdala volume, and fat intake in adolescence. Haghighi A, Schwartz DH, Abrahamowicz M, et al. JAMA Psychiatry. 2013;70:98–105. doi: 10.1001/archgenpsychiatry.2012.1101. [DOI] [PubMed] [Google Scholar]
  • 63.Prenatal environmental tobacco smoke exposure and early childhood body mass index. Braun JM, Daniels JL, Poole C, et al. Paediatr Perinat Epidemiol. 2010;24:524–534. doi: 10.1111/j.1365-3016.2010.01146.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 64.Independent and joint effects of prenatal maternal smoking and maternal exposure to second-hand smoke on the development of adolescent obesity: a longitudinal study. Wang L, Mamudu HM, Alamian A, Anderson JL, Brooks B. J Paediatr Child Health. 2014;50:908–915. doi: 10.1111/jpc.12667. [DOI] [PubMed] [Google Scholar]
  • 65.Maternal smoking, breastfeeding, and risk of childhood overweight: findings from a national cohort. Wen X, Shenassa ED, Paradis AD. Matern Child Health J. 2013;17:746–755. doi: 10.1007/s10995-012-1059-y. [DOI] [PubMed] [Google Scholar]
  • 66.Toxic effects of prenatal exposure to alcohol, tobacco and other drugs. Scott-Goodwin AC, Puerto M, Moreno I. Reprod Toxicol. 2016;61:120–130. doi: 10.1016/j.reprotox.2016.03.043. [DOI] [PubMed] [Google Scholar]
  • 67.Pregnancy, maternal tobacco smoking, and early age leukemia in Brazil. Ferreira JD, Couto AC, Pombo-de-Oliveira MS, Koifman S. Front Oncol. 2012;2:151. doi: 10.3389/fonc.2012.00151. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 68.Nicotine in breast milk influences heart rate variability in the infant. Dahlström A, Ebersjö C, Lundell B. Acta Paediatr. 2008;97:1075–1079. doi: 10.1111/j.1651-2227.2008.00785.x. [DOI] [PubMed] [Google Scholar]
  • 69.Infantile colic: maternal smoking as potential risk factor. Reijneveld SA, Brugman E, Hirasing RA. Arch Dis Child. 2000;83:302–303. doi: 10.1136/adc.83.4.302. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 70.Exposure to tobacco smoke and infant crying. Reijneveld SA, Lanting CI, Crone MR, Van Wouwe JP. Acta Paediatr. 2005;94:217–221. doi: 10.1111/j.1651-2227.2005.tb01894.x. [DOI] [PubMed] [Google Scholar]
  • 71.Passive smoking and behavioural problems in children: results from the LISAplus prospective birth cohort study. Tiesler CM, Chen CM, Sausenthaler S, et al. Environ Res. 2011;111:1173–1179. doi: 10.1016/j.envres.2011.06.011. [DOI] [PubMed] [Google Scholar]
  • 72.Adverse health effects of marijuana use. Volkow ND, Baler RD, Compton WM, Weiss SR. N Engl J Med. 2014;370:2219–2227. doi: 10.1056/NEJMra1402309. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 73.Cannabis use in pregnant and breastfeeding women: behavioral and neurobiological consequences. Navarrete F, García-Gutiérrez MS, Gasparyan A, Austrich-Olivares A, Femenía T, Manzanares J. Front Psychiatry. 2020;11:586447. doi: 10.3389/fpsyt.2020.586447. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 74.Is breast best? Examining the effects of alcohol and cannabis use during lactation. Brown RA, Dakkak H, Seabrook JA. J Neonatal Perinatal Med. 2018;11:345–356. doi: 10.3233/NPM-17125. [DOI] [PubMed] [Google Scholar]
  • 75.Cannabis and breastfeeding. Graves L. Paediatr Child Health. 2020;25:0–8. doi: 10.1093/pch/pxaa037. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 76.Prenatal exposure to cannabis and maternal and child health outcomes: a systematic review and meta-analysis. Gunn JK, Rosales CB, Center KE, Nuñez A, Gibson SJ, Christ C, Ehiri JE. BMJ Open. 2016;6:0. doi: 10.1136/bmjopen-2015-009986. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 77.Prenatal cannabis use and the risk of attention deficit hyperactivity disorder and autism spectrum disorder in offspring: A systematic review and meta-analysis. Tadesse AW, Dachew BA, Ayano G, Betts K, Alati R. J Psychiatr Res. 2024;171:142–151. doi: 10.1016/j.jpsychires.2024.01.045. [DOI] [PubMed] [Google Scholar]
  • 78.Associations between prenatal cannabis exposure and childhood outcomes: results from the ABCD study. Paul SE, Hatoum AS, Fine JD, et al. JAMA Psychiatry. 2021;78:64–76. doi: 10.1001/jamapsychiatry.2020.2902. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 79.Associations of parental marijuana use with offspring marijuana, tobacco, and alcohol use and opioid misuse. Madras BK, Han B, Compton WM, Jones CM, Lopez EI, McCance-Katz EF. JAMA Netw Open. 2019;2:0. doi: 10.1001/jamanetworkopen.2019.16015. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 80.Drinking or smoking while breastfeeding and later academic outcomes in children. Gibson L, Porter M. Nutrients. 2020;12 doi: 10.3390/nu12030829. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 81.Policy statement: Breastfeeding and the use of human milk. Meek JY, Noble L. Pediatrics. 2022;150 doi: 10.1542/peds.2022-057988. [DOI] [PubMed] [Google Scholar]
  • 82.Marijuana use during pregnancy and lactation. ACOG Committee Opinion No. 722. Obstet Gynecol. 2017;130:0–9. doi: 10.1097/AOG.0000000000002354. [DOI] [PubMed] [Google Scholar]
  • 83.Transfer of inhaled cannabis into human breast milk. Baker T, Datta P, Rewers-Felkins K, Thompson H, Kallem RR, Hale TW. Obstet Gynecol. 2018;131:783–788. doi: 10.1097/AOG.0000000000002575. [DOI] [PubMed] [Google Scholar]
  • 84.Persistence of Δ-9-tetrahydrocannabinol in human breast milk. Wymore EM, Palmer C, Wang GS, Metz TD, Bourne DW, Sempio C, Bunik M. JAMA Pediatr. 2021;175:632–634. doi: 10.1001/jamapediatrics.2020.6098. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 85.Marijuana use by breastfeeding mothers and cannabinoid concentrations in breast milk. Bertrand KA, Hanan NJ, Honerkamp-Smith G, Best BM, Chambers CD. Pediatrics. 2018;142 doi: 10.1542/peds.2018-1076. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 86.Cannabis use and measurement of cannabinoids in plasma and breast milk of breastfeeding mothers. Moss MJ, Bushlin I, Kazmierczak S, Koop D, Hendrickson RG, Zuckerman KE, Grigsby TM. Pediatr Res. 2021;90:861–868. doi: 10.1038/s41390-020-01332-2. [DOI] [PubMed] [Google Scholar]
  • 87.Cannabis use during pregnancy and postpartum. Badowski S, Smith G. https://pubmed.ncbi.nlm.nih.gov/32060189/ Can Fam Physician. 2020;66:98–103. [PMC free article] [PubMed] [Google Scholar]
  • 88.Marijuana use in pregnancy and while breastfeeding. Metz TD, Borgelt LM. Obstet Gynecol. 2018;132:1198–1210. doi: 10.1097/AOG.0000000000002878. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 89.Marijuana use during pregnancy and breastfeeding: implications for neonatal and childhood outcomes. Ryan SA, Ammerman SD, O'Connor ME. Pediatrics. 2018;142 doi: 10.1542/peds.2018-1889. [DOI] [PubMed] [Google Scholar]
  • 90.Academy of breastfeeding medicine clinical protocol #21: breastfeeding in the setting of substance use and substance use disorder (revised 2023) Harris M, Schiff DM, Saia K, Muftu S, Standish KR, Wachman EM. Breastfeed Med. 2023;18:715–733. doi: 10.1089/bfm.2023.29256.abm. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 91.Cannabis use during lactation: literature review and clinical recommendations. Ordean A, Kim G. J Obstet Gynaecol Can. 2020;42:1248–1253. doi: 10.1016/j.jogc.2019.11.003. [DOI] [PubMed] [Google Scholar]
  • 92.Cannabidiol exposure through maternal marijuana use: predictions in breastfed infants. Yeung CH, Bertrand KA, Best BM, et al. Clin Pharmacokinet. 2023;62:1611–1619. doi: 10.1007/s40262-023-01307-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 93.Marijuana and the pediatric population. Dharmapuri S, Miller K, Klein JD. Pediatrics. 2020;146 doi: 10.1542/peds.2019-2629. [DOI] [PubMed] [Google Scholar]
  • 94.Women's questions about perinatal cannabis use and health care providers' responses. Young-Wolff KC, Gali K, Sarovar V, Rutledge GW, Prochaska JJ. J Womens Health (Larchmt) 2020;29:919–926. doi: 10.1089/jwh.2019.8112. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 95.E-cigarettes: a scientific review. Grana R, Benowitz N, Glantz SA. Circulation. 2014;129:1972–1986. doi: 10.1161/CIRCULATIONAHA.114.007667. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 96.Nicotine and the developing human: a neglected element in the electronic cigarette debate. England LJ, Bunnell RE, Pechacek TF, Tong VT, McAfee TA. Am J Prev Med. 2015;49:286–293. doi: 10.1016/j.amepre.2015.01.015. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 97.A systematic review of randomized controlled trials and network meta-analysis of e-cigarettes for smoking cessation. Chan GC, Stjepanović D, Lim C, et al. Addict Behav. 2021;119:106912. doi: 10.1016/j.addbeh.2021.106912. [DOI] [PubMed] [Google Scholar]
  • 98.Perinatal smoking and e-cigarette use and their relationship with breastfeeding: PRAMS 2015-2020. Hamilton WN, Masud N, Kouambo C, Tarasenko YN. Breastfeed Med. 2023;18:855–863. doi: 10.1089/bfm.2023.0152. [DOI] [PubMed] [Google Scholar]
  • 99.Johnston E. University of Nottingham; 2020. E-cigarettes: an acceptable alternative to smoking for breastfeeding mothers? [Google Scholar]
  • 100.IARC Working Group on the Evaluation of Carcinogenic Risks to Humans. Lyon (FR): International Agency for Research on Cancer; 2007. Smokeless Tobacco and Some Tobacco-specific N-Nitrosamines. [Google Scholar]
  • 101.Determinants of initiation, continuation and cessation of smokeless tobacco use among pregnant and lactating women: a qualitative study from low-income communities in urban India. Singh S, Jain R, Joshi I, Chandra R, Singh L, Singh PK. Health Policy Plan. 2023;38:907–915. doi: 10.1093/heapol/czad056. [DOI] [PubMed] [Google Scholar]
  • 102.Maternal use of nicotine products and breastfeeding 3 months postpartum. Nordhagen LS, Kreyberg I, Bains KE, et al. Acta Paediatr. 2020;109:2594–2603. doi: 10.1111/apa.15299. [DOI] [PubMed] [Google Scholar]
  • 103.Is maternal cigarette or water pipe use associated with stopping breastfeeding? Evidence from the Jordan population and family health surveys 2012 and 2017-18. Can Özalp E, Yalçın SS. Int Breastfeed J. 2021;16:43. doi: 10.1186/s13006-021-00387-z. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 104.Use of nicotine patches in breast-feeding mothers: transfer of nicotine and cotinine into human milk. Ilett KF, Hale TW, Page-Sharp M, Kristensen JH, Kohan R, Hackett LP. Clin Pharmacol Ther. 2003;74:516–524. doi: 10.1016/j.clpt.2003.08.003. [DOI] [PubMed] [Google Scholar]
  • 105.Barriers and facilitators to smoking cessation in pregnancy and in the post-partum period: The health care professionals' perspective. Naughton F, Hopewell S, Sinclair L, McCaughan D, McKell J, Bauld L. Br J Health Psychol. 2018;23:741–757. doi: 10.1111/bjhp.12314. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 106.Health professionals' perceptions of the barriers and facilitators to providing smoking cessation advice to women in pregnancy and during the post-partum period: a systematic review of qualitative research. Flemming K, Graham H, McCaughan D, Angus K, Sinclair L, Bauld L. BMC Public Health. 2016;16:290. doi: 10.1186/s12889-016-2961-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 107.Interest in and use of smoking cessation support across pregnancy and postpartum. Naughton F, Vaz LR, Coleman T, et al. Nicotine Tob Res. 2020;22:1178–1186. doi: 10.1093/ntr/ntz151. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 108.Barriers and facilitators to staying smoke-free after having a baby, a qualitative study: women's views on support needed to prevent returning to smoking postpartum. Phillips L, Campbell KA, Coleman T, Ussher M, Cooper S, Lewis S, Orton S. Int J Environ Res Public Health. 2021;18 doi: 10.3390/ijerph182111358. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 109.Quitting smoking before and after pregnancy: study methods and baseline data from a prospective cohort study. Cruvinel E, Richter KP, Pollak KI, et al. Int J Environ Res Public Health. 2022;19 doi: 10.3390/ijerph191610170. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 110.Re-configuring identity postpartum and sustained abstinence or relapse to tobacco smoking. Brown TJ, Bauld L, Hardeman W, et al. Int J Environ Res Public Health. 2019;16 doi: 10.3390/ijerph16173139. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 111.The changing process of women's smoking status triggered by pregnancy. Itai M, Sasaki A, Mori M, Tsuda S, Matsumoto-Murakoso A. Int J Environ Res Public Health. 2019;16 doi: 10.3390/ijerph16224424. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 112.Exploring the adequacy of smoking cessation support for pregnant and postpartum women. Borland T, Babayan A, Irfan S, Schwartz R. BMC Public Health. 2013;13:472. doi: 10.1186/1471-2458-13-472. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 113.Activities of the healthcare team for women who smoke during pregnancy and the puerperium. Teixeira Cde C, Lucena Ade F, Echer IC. Rev Lat Am Enfermagem. 2014;22:621–628. doi: 10.1590/0104-1169.3361.2460. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 114.Smoking cessation care during pregnancy: A qualitative exploration of midwives' challenging role. Kalamkarian A, Hoon E, Chittleborough CR, Dekker G, Lynch JW, Smithers LG. Women Birth. 2023;36:89–98. doi: 10.1016/j.wombi.2022.03.005. [DOI] [PubMed] [Google Scholar]
  • 115.Artificial intelligence for smoking cessation in pregnancy. Georgakopoulou VE, Diamanti A. Cureus. 2024;16:0. doi: 10.7759/cureus.63732. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 116.Smoking cessation intervention in puerperium: A systematic review and meta-analysis. Vlachou M, Kirkou G, Vivilaki V, Katsaounou P, Georgakopoulou VE, Diamanti A. Pneumon. 2024;37:33. [Google Scholar]
  • 117.An examination of attitudes, knowledge, and clinical practices among Pennsylvania pediatricians regarding breastfeeding and smoking. Lucero CA, Moss DR, Davies ED, Colborn K, Barnhart WC, Bogen DL. Breastfeed Med. 2009;4:83–89. doi: 10.1089/bfm.2008.0119. [DOI] [PMC free article] [PubMed] [Google Scholar]

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