Approximately 3500 infants die annually in the United States from sleep-related infant deaths, including sudden infant death syndrome (SIDS), ill-defined deaths, and accidental suffocation and strangulation in bed. After an initial decrease in the 1990s, the overall sleep-related infant death rate has not declined in more recent years. Many of the modifiable and nonmodifiable risk factors for SIDS and other sleep-related infant deaths are strikingly similar. The American Academy of Pediatrics recommends a safe sleep environment that can reduce the risk of all sleep-related infant deaths. Recommendations for a safe sleep environment include supine positioning, use of a firm sleep surface, room-sharing without bed-sharing, and avoidance of soft bedding and overheating. Additional recommendations for SIDS risk reduction include avoidance of exposure to smoke, alcohol, and illicit drugs; breastfeeding; routine immunization; and use of a pacifier. New evidence and rationale for recommendations are presented for skin-to-skin care for newborn infants, bedside and in-bed sleepers, sleeping on couches/armchairs and in sitting devices, and use of soft bedding after 4 months of age. In addition, expanded recommendations for infant sleep location are included. The recommendations and strength of evidence for each recommendation are published in the accompanying policy statement, “SIDS and Other Sleep-Related Infant Deaths: Updated 2016 Recommendations for a Safe Infant Sleeping Environment,” which is included in this issue.

Literature searches with the use of PubMed were conducted for each of the topics in the technical report, concentrating on articles published since 2011 (when the last technical report and policy statement were published1,2). All iterations of the search terms were used for each topic area. For example, the pacifier topic search combined either “SIDS,” “SUID,” “sudden death,” or “cot death” with “pacifier,” “dummy,” “soother,” and “sucking.” A total of 63 new studies were judged to be of sufficiently high quality to be included in this technical report. In addition, because the data regarding bed-sharing have been conflicting, the independent opinion of a biostatistician with special expertise in perinatal epidemiology was solicited. The strength of evidence for recommendations, using the Strength-of-Recommendation Taxonomy,3 was determined by the task force members. A draft version of the policy statement and technical report was submitted to relevant committees and sections of the American Academy of Pediatrics (AAP) for review and comment. After the appropriate revisions were made, a final version was submitted to the AAP Executive Committee for final approval.

Sudden unexpected infant death (SUID), also known as sudden unexpected death in infancy (SUDI), is a term used to describe any sudden and unexpected death, whether explained or unexplained (including sudden infant death syndrome [SIDS] and ill-defined deaths), occurring during infancy. After case investigation, SUID can be attributed to causes of death such as suffocation, asphyxia, entrapment, infection, ingestions, metabolic diseases, and trauma (unintentional or nonaccidental). SIDS is a subcategory of SUID and is a cause assigned to infant deaths that cannot be explained after a thorough case investigation including autopsy, a scene investigation, and review of clinical history.4 (See Table 1 for definitions of terms.) The distinction between SIDS and other SUIDs, particularly those that occur during an unobserved sleep period (ie, sleep-related infant deaths), such as unintentional suffocation, is challenging, cannot be determined by autopsy alone, and may remain unresolved after a full case investigation. A few deaths that are diagnosed as SIDS are found, with further specialized investigations, to be attributable to metabolic disorders or arrhythmia-associated cardiac channelopathies.

TABLE 1

Definitions of Terms

Caregivers: Throughout the document, “parents” are used, but this term is meant to indicate any infant caregivers. 
Bed-sharing: Parent(s) and infant sleeping together on any surface (bed, couch, chair). 
Cosleeping: This term is commonly used, but the task force finds it confusing and it is not used in this document. When used, authors need to make clear whether they are referring to sleeping in close proximity (which does not necessarily entail bed-sharing) or bed-sharing. 
Room-sharing: Parent(s) and infant sleeping in the same room on separate surfaces. 
Sleep-related infant death: SUID that occurs during an observed or unobserved sleep period. 
Sudden infant death syndrome (SIDS): Cause assigned to infant deaths that cannot be explained after a thorough case investigation including a scene investigation, autopsy, and review of the clinical history.4  
Sudden unexpected infant death (SUID), or sudden unexpected death in infancy (SUDI): A sudden and unexpected death, whether explained or unexplained (including SIDS), occurring during infancy. 
Caregivers: Throughout the document, “parents” are used, but this term is meant to indicate any infant caregivers. 
Bed-sharing: Parent(s) and infant sleeping together on any surface (bed, couch, chair). 
Cosleeping: This term is commonly used, but the task force finds it confusing and it is not used in this document. When used, authors need to make clear whether they are referring to sleeping in close proximity (which does not necessarily entail bed-sharing) or bed-sharing. 
Room-sharing: Parent(s) and infant sleeping in the same room on separate surfaces. 
Sleep-related infant death: SUID that occurs during an observed or unobserved sleep period. 
Sudden infant death syndrome (SIDS): Cause assigned to infant deaths that cannot be explained after a thorough case investigation including a scene investigation, autopsy, and review of the clinical history.4  
Sudden unexpected infant death (SUID), or sudden unexpected death in infancy (SUDI): A sudden and unexpected death, whether explained or unexplained (including SIDS), occurring during infancy. 

Although standardized guidelines for conducting thorough case investigations have been developed (http://www.cdc.gov/sids/pdf/suidi-form2-1-2010.pdf),5 these guidelines have not been uniformly adopted across the >2000 US medical examiner and coroner jurisdictions.6 Information from emergency responders, scene investigators, and caregiver interviews may provide additional evidence to assist death certifiers (ie, medical examiners and coroners) in accurately determining the cause of death. However, death certifiers represent a diverse group with varying levels of skill and education. In addition, there are diagnostic preferences. Recently, much attention has focused on reporting differences among death certifiers. On one extreme, some certifiers have abandoned the use of SIDS as a cause-of-death explanation.6 At the other extreme, some certifiers will not classify a death as suffocation in the absence of a pathologic marker of asphyxia at autopsy (ie, pathologic findings diagnostic of oronasal occlusion or chest compression7), even with strong evidence from the scene investigation suggesting a probable unintentional suffocation.

To monitor trends in SIDS and other SUIDs nationally, the United States classifies diseases and injuries according to the International Statistical Classification of Diseases (ICD) diagnostic codes. In the United States, the National Center for Health Statistics assigns a SIDS diagnostic code (International Classification of Diseases, 10th Revision [ICD-10] R95) if the death is classified with terminology such as SIDS (including presumed, probable, or consistent with SIDS), sudden infant death, sudden unexplained death in infancy, sudden unexpected infant death, SUID, or SUDI on the certified death certificate.8,9 A death will be coded “other ill-defined and unspecified causes of mortality” (ICD-10 R99) if the cause of the death is reported as unknown or unspecified.8 A death is coded “accidental suffocation and strangulation in bed” (ICD-10 W75) when the terms asphyxia, asphyxiated, asphyxiation, strangled, strangulated, strangulation, suffocated, or suffocation are reported, along with the terms bed or crib. This code also includes deaths while sleeping on couches and armchairs.

Although SIDS was defined somewhat loosely until the mid-1980s, there was minimal change in the incidence of SIDS in the United States until the early 1990s. In 1992, in response to epidemiologic reports from Europe and Australia, the AAP recommended that infants be placed for sleep in a nonprone position as a strategy to reduce the risk of SIDS.10 The “Back to Sleep” campaign (which is now known as the “Safe to Sleep” campaign11) was initiated in 1994 under the leadership of the National Institute of Child Health and Human Development (now the Eunice Kennedy Shriver National Institute of Child Health and Human Development) as a joint effort of the Maternal and Child Health Bureau of the Health Resources and Services Administration, the AAP, the SIDS Alliance (now First Candle), and the Association of SIDS and Infant Mortality Programs. Between 1992 and 2001, the SIDS rate declined, with the most dramatic declines in the years immediately after the first nonprone sleep position recommendations, and this decline was consistent with the steady increase in the prevalence of supine sleeping (Fig 1).12 The US SIDS rate decreased from 120 deaths per 100 000 live births in 1992 to 56 deaths per 100 000 live births in 2001, representing a reduction of 53% over 10 years. From 2001 to 2008, the rate remained constant (Fig 1) and then declined from 54 per 100 000 live births in 2009 to 40 in 2013 (the latest year that data are available). In 2013, 1561 infants died of SIDS.13 Although SIDS rates have declined by >50% since the early 1990s, SIDS remains the leading cause of postneonatal (28 days to 1 year of age) mortality.

FIGURE 1

Trends in SUID by cause, 1990–2013. Source: Centers for Disease Control and Prevention/National Center for Health Statistics, National Vital Statistics System, compressed mortality file. (Figure duplicated from http://www.cdc.gov/sids/data.htm.)

FIGURE 1

Trends in SUID by cause, 1990–2013. Source: Centers for Disease Control and Prevention/National Center for Health Statistics, National Vital Statistics System, compressed mortality file. (Figure duplicated from http://www.cdc.gov/sids/data.htm.)

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The all-cause postneonatal death rate follows a trend similar to the SIDS and SUID rates, with a 26% decline from 1992 to 2001 (from 314 to 231 per 100 000 live births). From 2001 until 2009, postneonatal mortality rates also remained fairly unchanged (from 231 to 222 per 100 000 live births), and then have declined yearly since 2009 to a rate of 193 per 100 000 live births in 2013.14 Several studies have observed that some deaths previously classified as SIDS (ICD-10 R95) are now being classified as other causes of sleep-related infant death (eg, accidental suffocation and strangulation in bed [ASSB; ICD-10 W75] or other ill-defined or unspecified causes [ICD-10 R99]),15,16 and that at least some of the decline in SIDS rates may be explained by increasing rates of these other assigned causes of SUID.15,17 To account for variations in death certifier classification and to more consistently track SIDS and other sleep-related infant deaths, the National Center for Health Statistics has created the special cause-of-death category SUID. The SUID category captures deaths with an underlying cause coded as ICD-10 R95, R99, and W75.13 In 2013, SIDS accounted for 46% of the 3422 SUIDs in the United States. Similar to the SIDS rate, the SUID rate also declined in the late 2000s, from 99 per 100 000 live births in 2009 to 87 in 2013.

SIDS and SUID mortality rates, like other causes of infant mortality, have notable and persistent racial and ethnic disparities.14 Despite the decline in SIDS and SUIDs in all races and ethnicities, the rate of SUIDs among non-Hispanic black (172 per 100 000 live births) and American Indian/Alaska Native (191 per 100 000 live births) infants was more than double that of non-Hispanic white infants (84 per 100 000 live births) in 2010–2013 (Fig 2). SIDS rates for Asian/Pacific Islander and Hispanic infants were much lower than the rate for non-Hispanic white infants. Furthermore, similar racial and ethnic disparities are seen with deaths attributed to both ASSB and ill-defined or unspecified deaths (Fig 2). Differences in the prevalence of supine positioning and other sleep environment conditions between racial and ethnic populations may contribute to these disparities.18 The prevalence of supine positioning in 2010 data from the National Infant Sleep Position Study in white infants was 75%, compared with 53%, 73%, and 80% among black, Hispanic, and Asian infants, respectively (Fig 3).19 The Pregnancy Risk Assessment Monitoring System also monitors the prevalence of infant sleep position in several states (http://www.cdc.gov/prams/pramstat/index.html). In 2011, 78% of mothers reported that they most often lay their infants on their backs for sleep (26 states reporting and most recent year available), with 80.3% of white mothers and 54% of black mothers reporting supine placement. Parent-infant bed-sharing20,22 and the use of soft bedding are also more common among black families than among other racial/ethnic groups.23,25 

FIGURE 2

SUID by race/ethnicity, 2010–2013. Source: Centers for Disease Control and Prevention/National Center for Health Statistics, National Vital Statistics System, period-linked birth/infant death data. (Figure duplicated from http://www.cdc.gov/sids/data.htm.)

FIGURE 2

SUID by race/ethnicity, 2010–2013. Source: Centers for Disease Control and Prevention/National Center for Health Statistics, National Vital Statistics System, period-linked birth/infant death data. (Figure duplicated from http://www.cdc.gov/sids/data.htm.)

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FIGURE 3

Prevalence of supine sleep positioning by maternal race and ethnic origin, 1992–2010. Source: National Infant Sleep Position Study. Note that data collection for the National Infant Sleep Position Study ended in 2010.

FIGURE 3

Prevalence of supine sleep positioning by maternal race and ethnic origin, 1992–2010. Source: National Infant Sleep Position Study. Note that data collection for the National Infant Sleep Position Study ended in 2010.

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Ninety percent of SIDS cases occur before an infant reaches the age of 6 months.16 SIDS peaks between 1 and 4 months of age. Although SIDS was once considered a rare event during the first month after birth, in 2004–2006 nearly 10% of cases that were coded as SIDS occurred during this period. SIDS is uncommon after 8 months of age.16 A similar age distribution is seen for ASSB.16 

A working model of SIDS pathogenesis includes a convergence of exogenous triggers or “stressors” (eg, prone sleep position, overbundling, airway obstruction), a critical period of development, and dysfunctional and/or immature cardiorespiratory and/or arousal systems (intrinsic vulnerability) that lead to a failure of protective responses (Fig 4).26 The convergence of these factors may ultimately result in a combination of progressive asphyxia, bradycardia, hypotension, metabolic acidosis, and ineffectual gasping, leading to death.27 Thus, death may occur as a result of the interaction between a vulnerable infant and a potentially asphyxiating and/or overheating sleep environment.28 

FIGURE 4

Triple risk model for SIDS. Adapted from Filiano and Kinney.26 

FIGURE 4

Triple risk model for SIDS. Adapted from Filiano and Kinney.26 

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The mechanisms responsible for intrinsic vulnerability (ie, dysfunctional cardiorespiratory and/or arousal protective responses) remain unclear but may be the result of in utero environmental conditions and/or genetically determined maldevelopment or delay in maturation. Infants who die of SIDS are more likely to have been born preterm and/or were growth restricted, which suggests a suboptimal intrauterine environment. Other adverse in utero environmental conditions include exposure to nicotine or other components of cigarette smoke and alcohol.29 

Recent studies have explored how prenatal exposure to cigarette smoke may result in an increased risk of SIDS. In animal models, exposure to cigarette smoke or nicotine during fetal development alters the expression of the nicotinic acetylcholine receptors in areas of the brainstem important for autonomic function and alters the numbers of orexin receptors in piglets,30,31 reduces the number of medullary serotonergic (5-hydroxytryptamine [5-HT]) neurons in the raphe obscurus in mice,32 increases 5-HT and 5-HT turnover in Rhesus monkeys,33 alters neuronal excitability of neurons in the nucleus tractus solitarius (a brainstem region important for sensory integration) in guinea pigs,34 and alters fetal autonomic activity and medullary neurotransmitter receptors, including nicotinic receptors, in baboons.35,37 From a functional perspective, prenatal exposure to nicotine causes hypoventilation and increased apnea38,39; reduces hypercarbia and hypoxia-induced ventilator chemoreflexes in mice, rats,38,40 and lambs41; and blunts arousal in response to hypoxia in rats40 and lambs.41 

In human infants, there are strong associations between nicotinic acetylcholine receptors and serotonergic (5-HT) receptors in the brainstem during development,42 and there is important recent evidence of epigenetic changes in the placentas of infants with prenatal tobacco smoke exposure.43 Prenatal exposure to tobacco smoke attenuates recovery from hypoxia in preterm infants,44 decreases heart rate variability in preterm45 and term46 infants, and abolishes the normal relationship between heart rate and gestational age at birth.45 Moreover, infants of smoking mothers exhibit impaired arousal patterns to trigeminal stimulation in proportion to urinary cotinine concentrations.47 It is important to also note that prenatal exposure to tobacco smoke alters the normal programming of cardiovascular reflexes, such that the increase in blood pressure and heart rate in response to breathing 4% carbon dioxide or a 60° head-up tilt is greater than expected.48 These changes in autonomic function, arousal, and cardiovascular reflexes may all increase an infant’s vulnerability to SIDS.

A recent large systematic review of the neuropathologic features of unexplained SUDI, including only studies that met strict criteria, concluded that “the most consistent findings, and most likely to be pathophysiologically significant, are abnormalities of serotonergic neurotransmission in the caudal brain stem.”49 Brainstem abnormalities that involve the 5-HT system in up to 70% of infants who die of SIDS have now been confirmed in several independent data sets and laboratories.29,50,52 These include decreased 5-hydroxytryptamine 1A (5-HT1A) receptor binding, a relative decreased binding to the 5-HT transporter, increased numbers of immature 5-HT neurons, and decreased tissue levels of 5-HT and the rate-limiting enzyme for 5-HT synthesis, tryptophan hydroxylase.53 Moreover, there is no evidence of excessive serotonin degradation as assessed by levels of 5-hydroxyindoleacetic acid (the main metabolite of serotonin) or ratios of 5-hydroxyindoleacetic acid to serotonin.35 This area of the brainstem plays a key role in coordinating many respiratory, arousal, and autonomic functions, and when dysfunctional, might prevent normal protective responses to stressors that commonly occur during sleep. Importantly, these findings are not confined to nuclei containing 5-HT neurons but also include relevant projection sites. Other abnormalities in brainstem projection sites have been described as well. For example, abnormalities of Phox2B immune-reactive neurons have been reported in the homologous human retrotrapezoid nucleus, a region of the brainstem that receives important 5-HT projections and is critical to carbon dioxide chemoreception and implicated in human congenital central hypoventilation syndrome.54 

The brainstem has important reciprocal connections to the limbic system comprising both cortical and subcortical components, including the limbic cortex, hypothalamus, amygdala, and hippocampus. These areas of the brain are important in the regulation of autonomic function, particularly in response to emotional stimuli. Thus, the brainstem and limbic system constitute a key network in controlling many aspects of autonomic function. Recently, abnormalities in the dentate gyrus (a component of the hippocampus) were observed in 41% of 153 infants who died unexpectedly with no apparent cause and 43% of the subset of deaths classified as SIDS. This finding suggests that dysfunction of other brain regions interconnected with the brainstem may participate in the pathogenesis of SIDS.55 Dentate gyrus bilamination is also found in some cases of temporal lobe epilepsy. A future potential line of investigation is a possible link in brainstem-limbic–related homeostatic instability between SIDS and sudden unexpected death in epilepsy and febrile seizures noted in some cases of sudden unexpected death in childhood.55 

There are significant associations between brainstem 5-HT1A receptor binding abnormalities and specific SIDS risk factors, including tobacco smoking.52 These data confirm results from earlier studies in humans29,53 and are also consistent with studies in piglets that reveal that postnatal exposure to nicotine decreases medullary 5-HT1A receptor immunoreactivity.56 Serotonergic neurons located in the medullary raphe and adjacent paragigantocellularis lateralis play important roles in many autonomic functions, including the control of respiration, blood pressure, heart rate, thermoregulation, sleep and arousal, and upper airway patency. Engineered mice with decreased numbers of 5-HT neurons and rats or piglets with decreased activity secondary to 5-HT1A autoreceptor stimulation show diminished ventilator responses to carbon dioxide, dysfunctional heat production and heat loss mechanisms, and altered sleep architecture.57 The aberrant thermoregulation in these models provides evidence for a biological substrate for the risk of SIDS associated with potentially overheating environments. In addition, mice pups with a constitutive reduction in 5-HT–producing neurons (PET1 knockout) or rat pups in which a large fraction of medullary 5-HT neurons have been destroyed with locally applied neurotoxins have a decreased ability to auto-resuscitate in response to asphyxia.58,59 Moreover, animals with 5-HT neuron deficiency caused by direct injection of a 5-HT–selective neurotoxin had impaired arousal in response to hypoxia.60 

Some cases of SUID have a clear genetic cause, such as medium-chain acyl-coenzyme A dehydrogenase deficiency. A recent study in California showed that the frequency of mutations for undiagnosed inborn errors of metabolism was similar in SIDS and controls and that newborn screening was effectively detecting medium-chain and very-long-chain acyl-coenzyme A dehydrogenase deficiencies that could potentially lead to SUID.61 There is no evidence of a strong heritable contribution for SIDS; however, genetic alterations that may increase the vulnerability to SIDS have been observed. Genetic variation can take the form of common base changes (polymorphisms) that alter gene function or rare base changes (mutations) that often have highly deleterious effects. (For a comprehensive review, see Opdal and Rognum.62) Several categories of physiologic functions relevant to SIDS have been examined for altered genetic makeup. Genes related to the serotonin transporter, cardiac channelopathies, and the development of the autonomic nervous system are the subject of current investigation.63 The serotonin transporter recovers serotonin from the extracellular space and largely serves to regulate overall serotonin neuronal activity. There are reports that polymorphisms in the promoter region that enhance the efficacy of the transporter (L) allele seem to be more prevalent in infants who die of SIDS compared with polymorphisms that reduce efficacy (S)62; however, at least 1 study did not confirm this association.64 It has also been reported that a polymorphism (12-repeat intron 2) of the promoter region of the serotonin transporter, which also enhances serotonin transporter efficiency, was increased in black infants who died of SIDS63 but not in a Norwegian population.62 

It has been estimated that 5% to 10% of infants who die of SIDS have novel mutations in the cardiac sodium or potassium channel genes, resulting in long QT syndrome, as well as in other genes that regulate channel function.63 Some of these mutations may represent an actual cause of death, but others may contribute to causing death when combined with environmental factors, such as acidosis.65 There is molecular and functional evidence that implicates specific SCN5A (sodium channel gene) β subunits in SIDS pathogenesis.66 In addition, 2 rare mutations in connexin 43, a major gap junction protein, have been found in SIDS cases and not in ethnically matched controls.67 In vitro assays of 1 mutation showed a lack of gap junction function, which could lead to ventricular arrhythmogenesis. The other mutation did not appear to have functional consequences. A recent study also adds weight to the need to perform functional assays and morphologic studies of the altered gene products. Several of the missense variants in genes encoding cardiac channels that have been found in SIDS cases had a high prevalence in the National Heart, Lung, and Blood Institute GO Exome Sequencing Project Database.68 A large study in a nonreferred nationwide Danish cohort estimated that up to 7.5% of SIDS cases may be explained by genetic variants in the sodium channel complex.69 These estimates are in the range of those previously reported. However, it is important that for each channelopathy variant discovered, the biological plausibility for pathogenicity is investigated to consider it as a cause of or contributor in SIDS.

The identification of polymorphisms in genes pertinent to the embryologic origin of the autonomic nervous system in SIDS cases also lends support to the hypothesis that a genetic predisposition contributes to the etiology of SIDS. The PACAP (pituitary adenylate cyclase-activation polypeptide) gene and the gene of 1 of its receptors (PAC1) have received recent attention because of the apparent racial differences in their expression. For example, there were no associations between PACAP and SIDS found in white infants, but in SIDS cases in black infants a specific allele was significantly associated.70 Although in a recent study, a strong association between variants in the PAC1 gene and SIDS was not found, a number of potential associations between race-specific variants and SIDS were identified; these warrant further study.71 There have also been a number of reports of polymorphisms or mutations in genes regulating inflammation,72,73 energy production,74,76 and hypoglycemia77 in infants who died of SIDS, but these associations require more study to determine their importance.

The recommendations outlined herein were developed to reduce the risk of SIDS and sleep-related suffocation, asphyxia, and entrapment among infants in the general population. As defined by epidemiologists, risk refers to the probability that an outcome will occur given the presence of a particular factor or set of factors. Although all recommendations are intended for all who care for infants, some recommendations are also directed toward health policy makers, researchers, and professionals who care for or work on behalf of infants. In addition, because certain behaviors, such as smoking, can increase risk for the infant, some recommendations are directed toward women who are pregnant or may become pregnant in the near future.

The recommendations, along with the strength of the recommendation, are summarized in the accompanying policy statement.78 It should be noted that there are no randomized controlled trials with regard to SIDS and other sleep-related deaths; instead, case-control studies are the standard.

The recommendations are based on epidemiologic studies that include infants up to 1 year of age. Therefore, recommendations for sleep position and the sleep environment, unless otherwise specified, are for the first year after birth. The evidence-based recommendations that follow are provided to guide health care practitioners in conversations with parents and others who care for infants. Health care practitioners are encouraged to have open and nonjudgmental conversations with families about their sleep practices. Individual medical conditions may warrant that a health care provider make different recommendations after weighing the relative risks and benefits.

To reduce the risk of SIDS, infants should be placed for sleep in the supine position (wholly on the back) for every sleep period by every caregiver until 1 year of age. Side sleeping is not safe and is not advised.

The prone or side sleep position can increase the risk of rebreathing expired gases, resulting in hypercapnia and hypoxia.79,82 The prone position also increases the risk of overheating by decreasing the rate of heat loss and increasing body temperature more than the supine position.83,84 Evidence suggests that prone sleeping alters the autonomic control of the infant cardiovascular system during sleep, particularly at 2 to 3 months of age,85 and may result in decreased cerebral oxygenation.86 The prone position places infants at high risk of SIDS (odds ratio [OR]: 2.3–13.1).87,91 In 1 US study, SIDS risk associated with the side position was similar in magnitude to that associated with the prone position (ORs: 2.0 and 2.6, respectively),88 and a higher population-attributable risk has been reported for the side sleep position than for the prone position.90,92 Furthermore, the risk of SIDS is exceptionally high for infants who are placed on the side and found on the stomach (OR: 8.7).88 The side sleep position is inherently unstable, and the probability of an infant rolling to the prone position from the side sleep position is significantly greater than rolling prone from the back.90,93 Infants who are unaccustomed to the prone position and who are placed prone for sleep are also at greater risk than those usually placed prone (adjusted OR: 8.7–45.4).88,94,95 It is therefore critically important that every caregiver use the supine sleep position for every sleep period. This is particularly relevant in situations in which a new caregiver is introduced: for example, when an infant is placed in foster care or an adoptive home or when an infant enters child care for the first time.

Despite these recommendations, the prevalence of supine positioning has remained stagnant for the past decade.19 One reason often cited by parents for not using the supine sleep position is the perception that the infant is uncomfortable or does not sleep well.96,104 However, an infant who wakes frequently is normal and should not be perceived as a poor sleeper. Physiologic studies show that infants are less likely to arouse when they are sleeping in the prone position.105,113 The ability to arouse from sleep is an important protective physiologic response to stressors during sleep,114,118 and the infant’s ability to sleep for sustained periods may not be physiologically advantageous.

The supine sleep position does not increase the risk of choking and aspiration in infants, even in those with gastroesophageal reflux.

Parents and caregivers continue to be concerned that the infant will choke or aspirate while supine.96,104 Parents often misconstrue coughing or gagging, which is evidence of a normal protective gag reflex, for choking or aspiration. Multiple studies in different countries have not shown an increased incidence of aspiration since the change to supine sleeping.119,121 Parents and caregivers are often concerned about aspiration when the infant has been diagnosed with gastroesophageal reflux. The AAP concurs with the North American Society for Pediatric Gastroenterology and Nutrition that “the risk of SIDS outweighs the benefit of prone or lateral sleep position on GER [gastroesophageal reflux]; therefore, in most infants from birth to 12 months of age, supine positioning during sleep is recommended…. Therefore, prone positioning is acceptable if the infant is observed and awake, particularly in the postprandial period, but prone positioning during sleep can only be considered in infants with certain upper airway disorders in which the risk of death from GERD [gastroesophageal reflux disease] may outweigh the risk of SIDS.”122 Examples of such upper airway disorders are those in which airway-protective mechanisms are impaired, including infants with anatomic abnormalities, such as type 3 or 4 laryngeal clefts, who have not undergone antireflux surgery. There is no evidence that infants receiving nasogastric or orogastric feedings are at increased risk of aspiration if placed in the supine position. Elevating the head of the infant’s crib while the infant is supine is not effective in reducing gastroesophageal reflux123,124; in addition, elevating the head of the crib may result in the infant sliding to the foot of the crib into a position that may compromise respiration and therefore is not recommended.

Preterm infants should be placed supine as soon as possible.

Infants born preterm have an increased risk of SIDS,125,126 and the association between the prone position and SIDS among low birth weight and preterm infants is equal to, or perhaps even stronger than, the association among those born at term.94 Therefore, preterm infants should be placed supine for sleep as soon as clinical status has stabilized. The task force concurs with the AAP Committee on Fetus and Newborn that “preterm infants should be placed supine for sleeping, just as term infants should, and the parents of preterm infants should be counseled about the importance of supine sleeping in preventing SIDS. Hospitalized preterm infants should be kept predominantly in the supine position, at least from the postmenstrual age of 32 weeks onward, so that they become acclimated to supine sleeping before discharge.”127 Furthermore, the task force believes that neonatologists, neonatal nurses, and other health care providers responsible for organizing the hospital discharge of infants from NICUs should be vigilant about endorsing the SIDS risk-reduction recommendations from birth. They should model the recommendations as soon as the infant is medically stable and significantly before the infant’s anticipated discharge from the hospital. In addition, NICUs are encouraged to develop and implement policies to ensure that supine sleeping and other safe sleep practices are modeled for parents beforeo discharge from the hospital.128,129 

As stated in the AAP clinical report, “skin-to-skin care is recommended for all mothers and newborns, regardless of feeding or delivery method, immediately following birth (as soon as the mother is medically stable, awake, and able to respond to her newborn), and to continue for at least an hour.”130Thereafter, or when the mother needs to sleep or take care of other needs, infants should be placed supine in a bassinet.

Placing infants on the side after birth in newborn nurseries or in mother-infant rooms continues to be a concern. The practice likely occurs because of a belief among nursery staff that newborn infants need to clear their airways of amniotic fluid and may be less likely to aspirate while on the side. No evidence that such fluid will be cleared more readily while in the side position exists. Perhaps most importantly, if parents observe health care providers placing infants in the side or prone position, they are likely to infer that supine positioning is not important131 and therefore may be more likely to copy this practice and use the side or prone position at home.101,104,132 Infants who are rooming in with their parents or cared for in a separate newborn nursery should be placed in the supine position as soon as they are ready to be placed in the bassinet. To promote breastfeeding, placing the infant skin-to-skin with mother after delivery, with appropriate observation and/or monitoring, is the best approach. When the mother needs to sleep or take care of other needs, the infant should be placed supine in a bassinet.

Once an infant can roll from supine to prone and from prone to supine, the infant may remain in the sleep position that he or she assumes.

Parents and caregivers are frequently concerned about the appropriate strategy for infants who have learned to roll over, which generally occurs at 4 to 6 months of age. As infants mature, it is more likely that they will roll. In 1 study, 6% and 12% of 16- to 23-week-old infants placed on their backs or sides, respectively, were found in the prone position; among infants ≥24 weeks of age, 14% of those placed on their backs and 18% of those placed on their sides were found in the prone position.133 Repositioning the sleeping infant to the supine position can be disruptive and may discourage the use of the supine position altogether. Because data to make specific recommendations as to when it is safe for infants to sleep in the prone position are lacking, the AAP recommends that all infants continue to be placed supine until 1 year of age. If the infant can roll from supine to prone and from prone to supine, the infant can then be allowed to remain in the sleep position that he or she assumes. One study analyzing sleep-related deaths reported to state child death review teams found that the predominant risk factor for sleep-related deaths in infants 4 to 12 months of age was rolling into objects in the sleep area.134 Thus, parents and caregivers should continue to keep the infant’s sleep environment clear of soft or loose bedding and other objects. Parents may be reassured in being advised that the incidence of SIDS begins to decline after 4 months of age.16 

Infants should be placed on a firm sleep surface (eg, a mattress in a safety-approved crib) covered by a fitted sheet with no other bedding or soft objects to reduce the risk of SIDS and suffocation.

To avoid suffocation, rebreathing, and SIDS risk, infants should sleep on a firm surface (eg, safety-approved crib and mattress). The surface should be covered by a fitted sheet without any soft or loose bedding. A firm surface maintains its shape and will not indent or conform to the shape of the infant’s head when the infant is placed on the surface. Soft mattresses, including those made from memory foam, could create a pocket (or indentation) and increase the chance of rebreathing or suffocation if the infant is placed in or rolls over to the prone position.81,135 

A crib, bassinet, portable crib, or play yard that conforms to the safety standards of the Consumer Product Safety Commission (CPSC) is recommended.

Cribs should meet safety standards of the CPSC,136 including those for slat spacing, snugly fitting and firm mattresses, and no drop sides. The AAP recommends the use of new cribs, because older cribs may no longer meet current safety standards, may have missing parts, or may be incorrectly assembled. If an older crib is to be used, care must be taken to ensure that there have been no recalls on the crib model, that all of the hardware is intact, and that the assembly instructions are available.

For some families, the use of a crib may not be possible for financial or space considerations. In addition, parents may be reluctant to place the infant in the crib because of concerns that the crib is too large for the infant or that “crib death” (ie, SIDS) only occurs in cribs. Alternate sleep surfaces, such as portable cribs, play yards, and bassinets that meet safety standards of the CPSC,137,138 can be used and may be more acceptable for some families because they are smaller and more portable.

Bedside sleepers are attached to the side of the parental bed. The CPSC has published safety standards for bedside sleepers,139 and they may be considered by some parents as an option. There are no CPSC safety standards for in-bed sleepers. The task force cannot make a recommendation for or against the use of either bedside sleepers or in-bed sleepers, because there have been no studies examining the association between these products and SIDS or unintentional injury and death, including suffocation. Studies of in-bed sleepers are currently underway, but results are not yet available. Parents and caregivers should adhere to the manufacturer’s guidelines regarding maximum weight of infants who use these products.140,141 In addition, with the use of any of these products, other AAP guidelines for safe sleep outlined in this document, including supine positioning and avoidance of soft objects and loose bedding, should be followed.

Mattresses should be firm and maintain their shape even when the fitted sheet designated for that model is used, such that there are no gaps between the mattress and the wall of the bassinet, playpen, portable crib, play yard, or bedside sleeper. Only mattresses designed for the specific product should be used. Pillows or cushions should not be used as substitutes for mattresses or in addition to a mattress. Soft materials or objects, such as pillows, quilts, comforters, or sheepskins, even if covered by a sheet, should not be placed under a sleeping infant. Mattress toppers, designed to make the sleep surface softer, should not be used for infants younger than 1 year. Any fabric on the crib walls or a canopy should be taut and firmly attached to the frame so as not to create a suffocation risk for the infant.

Infants should not be placed for sleep on adult-sized beds because of the risk of entrapment and suffocation.142 Portable bed rails (railings installed on the side of the bed that are intended to prevent a child from falling off of the bed) should not be used with infants because of the risk of entrapment and strangulation.143 The infant should sleep in an area free of hazards, including dangling cords, electric wires, and window-covering cords, because these may present a strangulation risk.

Recently, special crib mattresses and sleep surfaces that claim to reduce the chance of rebreathing carbon dioxide when the infant is in the prone position have been introduced. Although there are no apparent disadvantages of using these mattresses if they meet the safety standards as described previously, there are no studies that show a decreased risk of SUID/SIDS. (See section entitled “Commercial Devices” for further discussion of special mattresses.)

Sitting devices, such as car seats, strollers, swings, infant carriers, and infant slings, are not recommended for routine sleep in the hospital or at home, particularly for young infants.

Some parents choose to allow their infants to sleep in a car seat or other sitting device. Sitting devices include, but are not restricted to, car seats, strollers, swings, infant carriers, and infant slings. Parents and caregivers often use these devices, even when not traveling, because they are convenient. One study found that the average young infant spends 5.7 hours/day in a car seat or similar sitting device.144 However, there are multiple concerns about the use of sitting devices as a usual infant sleep location. Placing an infant in such devices can potentiate gastroesophageal reflux145 and positional plagiocephaly. Because they still have poor head control and often experience flexion of the head while in a sitting position, infants younger than 4 months in sitting devices may be at increased risk of upper airway obstruction and oxygen desaturation.146,150 A recent retrospective study reviewed deaths involving sitting and carrying devices (car seats, bouncers, swings, strollers, and slings) reported to the CPSC between 2004 and 2008. Of the 47 deaths analyzed, 31 occurred in car seats, 5 occurred in slings, 4 each occurred in swings and bouncers, and 3 occurred in strollers. Fifty-two percent of deaths in car seats were attributed to strangulation from straps; the others were attributed to positional asphyxia.151 In addition, analyses of CPSC data report injuries from falls when car seats are placed on elevated surfaces,152,156 from strangulation on unbuckled or partially buckled car seat straps,151 and from suffocation when car seats overturn after being placed on a bed, mattress, or couch.155 There are also reports of suffocation in infants, particularly those who are younger than 4 months, who are carried in infant sling carriers.151,157,159 When infant slings are used for carrying, it is important to ensure that the infant’s head is up and above the fabric, the face is visible, and the nose and mouth are clear of obstructions. After nursing, the infant should be repositioned in the sling so that the head is up and is clear of fabric and the airway is not obstructed by the adult’s body.151 If an infant falls asleep in a sitting device, he or she should be removed from the product and moved to a crib or other appropriate flat surface as soon as is safe and practical. Car seats and similar products are not stable on a crib mattress or other elevated surfaces.152,156 Infants should not be left unattended in car seats and similar products, nor should they be placed or left in car seats and similar products with the straps unbuckled or partially buckled.151 

Breastfeeding is associated with a reduced risk of SIDS. The protective effect of breastfeeding increases with exclusivity. Furthermore, any breastfeeding is more protective against SIDS than no breastfeeding.

The protective role of breastfeeding on SIDS is enhanced when breastfeeding is exclusive and without formula introduction.160,162 Studies do not distinguish between direct breastfeeding and providing expressed milk. In the Agency for Healthcare Research and Quality’s “Evidence Report on Breastfeeding in Developed Countries,” 6 studies were included in the SIDS-breastfeeding meta-analysis, and ever having breastfed was associated with a lower risk of SIDS (adjusted summary OR: 0.64; 95% confidence interval [CI]: 0.51–0.81).160 The German Study of Sudden Infant Death, the largest and most recent case-control study of SIDS, found that exclusive breastfeeding at 1 month of age halved the risk of SIDS (adjusted OR: 0.48; 95% CI: 0.28–0.82).161 Another meta-analysis of 18 case-control studies found an unadjusted summary OR for any breastfeeding of 0.40 (95% CI: 0.35–0.44) and a pooled adjusted OR of 0.55 (95% CI: 0.44–0.69) (Fig 5).162 The protective effect of breastfeeding increased with exclusivity, with a univariable summary OR of 0.27 (95% CI: 0.24–0.31) for exclusive breastfeeding of any duration.162 

FIGURE 5

Multivariable analysis of any breastfeeding versus no breastfeeding. Adapted from Hauck et al.162 log[ ], logarithm of the OR; Weight: weighting that the study contributed to the meta-analysis (by sample size); IV, Fixed, 95% CI, fixed-effect OR with 95% CI.

FIGURE 5

Multivariable analysis of any breastfeeding versus no breastfeeding. Adapted from Hauck et al.162 log[ ], logarithm of the OR; Weight: weighting that the study contributed to the meta-analysis (by sample size); IV, Fixed, 95% CI, fixed-effect OR with 95% CI.

Close modal

Physiologic sleep studies showed that breastfed infants are more easily aroused from sleep than their formula-fed counterparts.163,164 In addition, breastfeeding results in a decreased incidence of diarrhea, upper and lower respiratory infections, and other infectious diseases165 that are associated with an increased vulnerability to SIDS and provides overall immune system benefits attributable to maternal antibodies and micronutrients in human milk.166,167 Exclusive breastfeeding for 6 months has been found to be more protective against infectious diseases, compared with exclusive breastfeeding to 4 months of age and partial breastfeeding thereafter.165 Furthermore, exclusive breastfeeding results in a gut microbiome that supports a normally functioning immune system and protection from infectious disease, and this commensal microbiome has been proposed as another possible mechanism or marker for protection against SIDS.168 

It is recommended that infants sleep in the parents’ room, close to the parents’ bed, but on a separate surface. The infant’s crib, portable crib, play yard, or bassinet should be placed in the parents’ bedroom, ideally for the first year of life, but at least for the first 6 months.

The terms bed-sharing and cosleeping are often used interchangeably, but they are not synonymous. Cosleeping is when parent and infant sleep in close proximity (on the same surface or different surfaces) so as to be able to see, hear, and/or touch each other.169,170 Cosleeping arrangements can include bed-sharing or sleeping in the same room in close proximity.170,171 Bed-sharing refers to a specific type of cosleeping when the infant is sleeping on the same surface with another person.170 The shared surface can include a bed, sofa, or chair. Because the term cosleeping can be misconstrued and does not precisely describe sleep arrangements, the AAP recommends the use of the terms bed-sharing and room-sharing (when the infant sleeps in the parents’ room but on a separate sleep surface [crib or similar surface] close to the parents’ bed) (see Table 1).

The AAP recommends room-sharing, because this arrangement decreases the risk of SIDS by as much as 50%89,91,172,173 and is safer than bed-sharing89,91,172,173 or solitary sleeping (when the infant is in a separate room).89,172 In addition, room-sharing is most likely to prevent suffocation, strangulation, and entrapment that may occur when the infant is sleeping in the adult bed. Furthermore, this arrangement allows close proximity to the infant, which will facilitate feeding, comforting, and monitoring of the infant. Most of the epidemiologic studies on which these recommendations are based include infants up to 1 year of age. Therefore, the AAP recommends that infants room-share, ideally for the first year after birth, but at least for the first 6 months. Although there is no specific evidence for moving an infant to his or her own room before 1 year of age, room-sharing during the first 6 months is especially critical because the rates of SIDS and other sleep-related deaths, particularly those occurring in bed-sharing situations, are highest during that period.

Parent-infant bed-sharing for all or part of sleep duration is common. In 1 national survey for the period 2001–2010, 46% of parents responded that they had shared a bed with their infant (8 months or younger) at some point in the preceding 2 weeks, and 13.5% reported that they usually bed-shared.174 In another national survey, any bed-sharing was reported by 42% of mothers at 2 weeks of infant age and 27% of mothers at 12 months of infant age.175 In a third study, almost 60% of mothers of infants from birth to 12 months of age reported bed-sharing at least once.176 The rate of routine bed-sharing is higher among some racial/ethnic groups, including black, Hispanic, and American Indian/Alaska Native parents/infants.20,22,174 There are often cultural and personal reasons why parents choose to bed-share, including convenience for feeding (breast or formula), comforting a fussy or sick infant, helping the infant and/or mother sleep better, bonding and attachment, and because it is a family tradition.175,177 In addition, many parents may believe that their own vigilance is the only way that they can keep their infant safe and that the close proximity of bed-sharing allows them to maintain vigilance, even while sleeping.178 Some parents will use bed-sharing specifically as a safety strategy if the infant sleeps in the prone position23,178 or there is concern about environmental dangers, such as vermin or stray gunfire.178 

Parent-infant bed-sharing continues to be highly controversial. Although electrophysiologic and behavioral studies offer a strong case for its effect in facilitating breastfeeding,179,181 and although many parents believe that they can maintain vigilance of the infant while they are asleep and bed-sharing,178 epidemiologic studies have shown that bed-sharing is associated with a number of conditions that are risk factors for SIDS, including soft bedding,182,185 head covering,186,189 and, for infants of smokers, increased exposure to tobacco smoke.190 In addition, bed-sharing is associated with an increased risk of SIDS; a recent meta-analysis of 11 studies investigating the association of bed-sharing and SIDS showed a summary OR of 2.88 (95% CI: 1.99–4.18) with bed-sharing.191 Furthermore, bed-sharing in an adult bed not designed for infant safety, especially when associated with other risk factors, exposes the infant to additional risks for unintentional injury and death, such as suffocation, asphyxia, entrapment, falls, and strangulation.192,193 Infants younger than 4 months194 and those born preterm and/or with low birth weight195 are at the highest risk, possibly because immature motor skills and muscle strength make it difficult to escape potential threats.191 In recent years, the concern among public health officials about bed-sharing has increased, because there have been increased reports of SUIDs occurring in high-risk sleep environments, particularly bed-sharing and/or sleeping on a couch or armchair.196,198 

On the other hand, some breastfeeding advocacy groups encourage safer bed-sharing to promote breastfeeding,199 and debate continues as to the safety of this sleep arrangement for low-risk, breastfed infants. In an analysis from 2 case-control studies in England (1993–1996 and 2003–2006), Blair et al200 reported an adjusted OR of bed-sharing (excluding bed-sharing on a sofa) for infants in the absence of parental alcohol or tobacco use of 1.1 (95% CI: 0.6–2.9). For infants younger than 98 days, the OR was 1.6 (95% CI: 0.96–2.7).200 These findings were independent of feeding method. The study lacked power to examine this association in older infants, because there was only 1 SIDS case in which bed-sharing was a factor in the absence of other risk factors. Breastfeeding was more common among bed-sharing infants, and the protective effect of breastfeeding was found only for infants who slept alone. The controls in these analyses were infants who were not bed-sharing/sofa-sharing regardless of room location; thus, they included infants who were room-sharing or sleeping in a separate room. In addition, the control infants included those whose parent(s) smoked or used alcohol. It is possible that this choice of controls overestimated their risk, leading to smaller ORs for risk among the cases (ie, biasing the results toward the null).

Carpenter et al201 analyzed data from 19 studies across the United Kingdom, Europe, and Australasia to determine the risk of SIDS from bed-sharing when an infant is breastfed, the parents do not smoke, and the mother has not taken alcohol or drugs. When neither parent smoked, in the absence of other risk factors, the adjusted OR for bed-sharing versus room-sharing for all breastfed infants was 2.7 (95% CI: 1.4–5.3).201 For breastfed infants younger than 3 months, in the absence of other risk factors, the adjusted OR for bed-sharing versus room-sharing was 5.1 (95% CI: 2.3–11.4). The study lacked power to examine this association in breastfed infants 3 months and older. Moreover, the large proportion of missing data for maternal alcohol and drug use is a limitation, although the authors used appropriate multiple imputation techniques for addressing these missing data.

The task force, recognizing the controversial nature of the recommendations about bed-sharing and the different methods and interpretations of these 2 sets of analyses outlined previously, requested an independent review of both articles by Dr Robert Platt, a biostatistician with expertise in perinatal epidemiology from McGill University in Canada. Dr Platt has no connection to the task force, nor does he have a vested interest in the recommendations. Dr Platt provided the following conclusion:

The fundamental difference in conclusions is that Blair et al conclude that bed-sharing in the absence of other risk factors (smoking, alcohol) does not convey an increased risk of SIDS, while Carpenter et al conclude the opposite. In both studies, the no-other-risk-factors group is limited in size, and the number of exposed cases is very small. In Blair et al, there are only 24 cases who bed-shared in the absence of these hazards. In Carpenter et al, although the total number of SIDS cases (1472) is more than 3 times the number of cases in the Blair study (400), the number of cases who bed-shared in the absence of these hazards was only 12 (personal communication, Professor Robert Carpenter, January 25, 2016). Therefore, the Carpenter results should be interpreted with some caution as well. In conclusion, both studies have strengths and weaknesses, and while on the surface the studies appear to contradict each other, I do not believe that their data support definitive differences between the 2 studies. There is some evidence of an increased risk in the no-other-risk-factor setting, in particular in the youngest age groups. However, based on concerns about sample size limitations, we are not able to say how large that increased risk is. Clearly, these data do not support a definitive conclusion that bed-sharing in the youngest age group is safe, even under less hazardous circumstances.

There is insufficient evidence to recommend for or against the use of devices promoted to make bed-sharing “safe.”

There is no evidence that devices marketed to make bed-sharing “safe” reduce the risk of SIDS or suffocation or are safe. Several products designed for in-bed use are currently under study, but results are not yet available. Bedside sleepers, which attach to the side of the parental bed and for which the CPSC published standards in 2013, may be considered by some parents as an option. The task force cannot make a recommendation for or against the use of either bedside sleepers or in-bed sleepers, because there have been no studies examining the association between these products and SIDS or unintentional injury and death, including suffocation. (See section entitled “Sleep Surfaces” for further discussion of sleepers.)

Infants who are brought into the bed for feeding or comforting should be returned to their own crib or bassinet when the parent is ready to return to sleep.

Studies have found an association between bed-sharing and longer duration of breastfeeding,202 but most of these were cross-sectional studies, which do not enable the determination of a temporal relationship: that is, whether bed-sharing promotes breastfeeding or whether breastfeeding promotes bed-sharing, and whether women who prefer one practice are also likely to prefer the other.203 However, a more recent longitudinal study provides strong evidence that bed-sharing promotes breastfeeding duration, with the greatest effect among frequent bed-sharers.202 Another recent study has shown that, compared with mothers who room-shared without bed-sharing, mothers who bed-shared were more likely to report exclusive breastfeeding (adjusted OR: 2.46; 95% CI: 1.76–3.45) or partial breastfeeding (adjusted OR: 1.75; 95% CI: 1.33–2.31).204 Although bed-sharing may facilitate breastfeeding,175 there are other factors, such as intent, that influence successful breastfeeding.205 Furthermore, 1 case-control study found that the risk of SIDS while bed-sharing was similar among infants in the first 4 months of life, regardless of breastfeeding status, implying that the benefits of breastfeeding do not outweigh the increased risk associated with bed-sharing for younger infants.194 The risk of bed-sharing is higher the longer the duration of bed-sharing during the night,91 especially when associated with other risks.89,90,206,207 Returning the infant to the crib after bringing the infant into the bed for a short period of time is not associated with increased risk.90,207 Therefore, after the infant is brought into the bed for feeding, comforting, and bonding, the infant should be returned to the crib when the parent is ready for sleep.

Couches and armchairs are extremely dangerous places for infants.

Sleeping on couches and armchairs places infants at an extraordinarily high risk of infant death, including SIDS,87,89,90,173,200,207 suffocation through entrapment or wedging between seat cushions, or overlay if another person is also sharing this surface.197 Therefore, parents and other caregivers should be especially vigilant as to their wakefulness when feeding infants or lying with infants on these surfaces. It is important to emphasize this point to mothers, because 25% of mothers in 1 study reported falling asleep during the night when breastfeeding their infant on one of these surfaces.176 Infants should never be placed on a couch or armchair for sleep.

Guidance for parents who fall asleep while feeding their infant.

The safest place for an infant to sleep is on a separate sleep surface designed for infants close to the parent’s bed. However, the AAP acknowledges that parents frequently fall asleep while feeding the infant. Evidence suggests that it is less hazardous to fall asleep with the infant in the adult bed than on a sofa or armchair, should the parent fall asleep.87,89,90,173,200,207 It is important to note that a large percentage of infants who die of SIDS are found with their head covered by bedding.186 Therefore, there should be no pillows, sheets, blankets, or any other items in the bed that could obstruct infant breathing87,182 or cause overheating.208,211 Parents should follow safe sleep recommendations outlined elsewhere in this statement. Because there is evidence that the risk of bed-sharing is higher with longer duration, if the parent falls asleep while feeding the infant in bed the infant should be placed back on a separate sleep surface as soon as the parent awakens.89,90,206,207 

There are specific circumstances that, in case-control studies and case series, have been shown to substantially increase the risk of SIDS or unintentional injury or death while bed-sharing, and these should be avoided at all times.

The task force emphasizes that certain circumstances greatly increase the risk of bed-sharing for both breastfed and formula-fed infants. Bed-sharing is especially dangerous in the following circumstances, and these should be avoided at all times:

  • when one or both parents are smokers, even if they are not smoking in bed (OR: 2.3–21.6)89,90,191,200,201,206,212;

  • when the mother smoked during pregnancy89,90,191,206,212;

  • when the infant is younger than 4 months of age, regardless of parental smoking status (OR: 4.7–10.4)89,91,173,191,201,207,213,214;

  • when the infant is born preterm and/or with low birth weight195;

  • when the infant is bed-sharing on excessively soft or small surfaces, such as waterbeds, sofas, and armchairs (OR: 5.1–66.9)87,89,90,173,200,207;

  • when soft bedding accessories such as pillows or blankets are used (OR: 2.8–4.1)87,215;

  • when there are multiple bed-sharers (OR: 5.4)87;

  • when the parent has consumed alcohol (OR: 1.66–89.7)91,196,200,201 and/or illicit or sedating drugs201; and

  • when the infant is bed-sharing with someone who is not a parent (OR: 5.4).87 

A retrospective series of SIDS cases reported that mean maternal body weight was higher for bed-sharing mothers than for non–bed-sharing mothers.216 The only case-control study to investigate the relationship between maternal body weight and bed-sharing did not find an increased risk of bed-sharing with increased maternal weight.217 

The safety and benefits of cobedding twins and higher-order multiples have not been established. It is prudent to provide separate sleep areas and avoid cobedding (sleeping on the same sleep surface) for twins and higher-order multiples in the hospital and at home.

Cobedding of twins and other infants of multiple gestation is a frequent practice, both in the hospital setting and at home.218 However, the benefits of cobedding twins and higher-order multiples have not been established.219,221 Twins and higher-order multiples are often born preterm and with low birth weights, so they are at increased risk of SIDS.125,126 Furthermore, cobedding increases the potential for overheating and rebreathing, and size discordance between multiples may increase the risk of unintentional suffocation.220 Most cobedded twins are placed on the side rather than supine.218 Finally, cobedding of twins and higher-order multiples in the hospital setting may encourage parents to continue this practice at home.220 Because the evidence for the benefits of cobedding twins and higher-order multiples is not compelling and because of the increased risk of SIDS and suffocation, the AAP believes that it is prudent to provide separate sleep areas for these infants to decrease the risk of SIDS and unintentional suffocation.

Keep soft objects, such as pillows, pillow-like toys, quilts, comforters, sheepskins, and loose bedding, such as blankets and nonfitted sheets, away from the infant’s sleep area to reduce the risk of SIDS, suffocation, entrapment, and strangulation.

Soft objects and loose bedding can obstruct an infant’s airway and increase the risk of SIDS,87,182 suffocation, and rebreathing.79,81,82,135,222,224 In the United States, nearly 55% of infants are placed to sleep underneath or on top of bedding such as thick blankets, quilts, and pillows.25 The prevalence of bedding use is highest among infants whose mothers are teenagers, from minority racial groups, and among those without a college education.

Pillows, quilts, comforters, sheepskins, and other soft bedding can be hazardous when placed under the infant87,182,210,225,229 or left loose in the infant’s sleep area.90,182,215,224,228,234 Bedding in the sleeping environment increases SIDS risk fivefold, independent of sleep position,87,182 and this risk increases to 21-fold when the infant is placed prone.87,182 Many infants who die of SIDS are found in the supine position but with their heads covered by loose bedding.90,225,226,230 In addition, infants who bed-share (share a sleep surface) have a higher SIDS risk when sleeping on a soft as opposed to a firm surface.215 

In addition to SIDS risk, soft objects and loose bedding in the sleeping environment may also lead to unintentional suffocation.134,224,235 A review of 66 SUID case investigations in 2011 showed that soft bedding was the most frequently reported factor among deaths classified as possible and explained unintentional suffocation deaths.224 In addition, a CPSC report of sleep-related infant deaths in 2009–2011 found that most deaths attributed to suffocation (regardless of whether infant was sleeping in a crib, on a mattress, or in a play yard) involved extra bedding, such as pillows or blankets.235 Soft bedding (eg, blankets and stuffed animals) may also be a stronger risk factor for sleep-related deaths among infants older than 3 months than it is for their younger counterparts, especially when infants are placed in or roll to the prone position.134 

Parents and caregivers are likely motivated by good intentions and perceived cultural norms when they opt to use bedding for infant sleep. Qualitative studies show that parents who use bedding want to provide a comfortable and safe environment for their infant.236 For comfort, parents may use blankets to provide warmth or to soften the sleep surface. For safety, parents may use pillows as barriers to prevent falls from adult beds or sofas or as a prop to keep their infant on the side.236 Images of infants sleeping with blankets, pillows, and other soft objects are widespread in popular magazines targeted to families with newborn infants.237 Parents and caregivers who see these images may perceive the use of these items as the norm, both favorable and the ideal, for infant sleep.

To avoid suffocation, rebreathing, and SIDS risk, infants should sleep on a firm surface (see section entitled “Sleep Surfaces” for a definition of a firm surface).135 Because pillows, quilts, and comforters can obstruct the infant’s airway (nose or mouth), they should never be used in the infant’s sleeping environment. Infant sleep clothing, such as sleeping sacks, are designed to keep the infant warm and can be used in place of blankets to prevent the possibility of head covering or entrapment. However, care must be taken to select appropriately sized clothing and to avoid overheating. Nursing and hospital staff should model safe sleep arrangements to new parents after delivery.

Bumper pads are not recommended; they have been implicated in deaths attributable to suffocation, entrapment, and strangulation and, with new safety standards for crib slats, are not necessary for safety against head entrapment.

Bumper pads and similar products attaching to crib slats or sides are frequently used with the thought of protecting infants from injury. Initially, bumper pads were developed to prevent head entrapment between crib slats.238 However, newer crib standards requiring crib slat spacing to be <2-3/8 inches have obviated the need for crib bumpers. In addition, infant deaths have occurred because of bumper pads. A case series by Thach et al,239 which used 1985–2005 CPSC data, found that deaths attributed to bumper pads occurred as a result of 3 mechanisms: (1) suffocation against soft, pillow-like bumper pads; (2) entrapment between the mattress or crib and firm bumper pads; and (3) strangulation from bumper pad ties. However, a 2010 CPSC white paper that reviewed the same cases concluded that there were other confounding factors, such as the presence of pillows and/or blankets, that may have contributed to many of the deaths in this report.240 The white paper pointed out that available data from the scene investigations, autopsies, law enforcement records, and death certificates often lacked sufficiently detailed information to conclude how or whether bumper pads contributed to the deaths. Two more recent analyses of CPSC data also came to different conclusions. The CPSC review concluded again that there was insufficient evidence to support that bumper pads were primarily responsible for infant deaths when bumper pads were used per the manufacturer’s instructions and in the absence of other unsafe sleep risk factors.241 Scheers et al,242 in their re-analysis, concluded that the rate of bumper pad–related deaths has increased, recognizing that changes in reporting may account for the increase, and that 67% of the deaths could have been prevented if the bumper pads had not been present. Limitations of CPSC data collection processes contribute to the difficulty in determining the risk of bumper pad use.

However, others239,243 have concluded that the use of bumper pads only prevents minor injuries, and that the potential benefits of preventing minor injury with bumper pad use are far outweighed by the risk of serious injury, such as suffocation or strangulation. In addition, most bumper pads obscure infant and parent visibility, which may increase parental anxiety.236,238 Other products exist that attach to crib sides or crib slats and claim to protect infants from injury; however, there are no published data that support these claims. Because of the potential for suffocation, entrapment, and strangulation and lack of evidence to support that bumper pads or similar products that attach to crib slats or sides prevent injury in young infants, the AAP does not recommend their use.

Consider offering a pacifier at naptime and bedtime.

Multiple case-control studies87,91,207,244,250 and 2 meta-analyses251,252 have reported a protective effect of pacifiers on the incidence of SIDS, particularly when used at the time of the last sleep period, with decreased risk of SIDS ranging from 50% to 90%. Furthermore, 1 study found that pacifier use favorably modified the risk profile of infants who sleep in the prone/side position, bed-share, or use soft bedding.253 The mechanism for this apparent strong protective effect is still unclear, but favorable modification of autonomic control during sleep254 and maintaining airway patency during sleep255 have been proposed. Physiologic studies of the effect of pacifier use on arousal are conflicting; 1 study found that pacifier use decreased arousal thresholds,163 but others have found no effects on arousability with pacifier use.256,257 It is common for the pacifier to fall from the mouth soon after the infant falls asleep; even so, the protective effect persists throughout that sleep period.163,258 Two studies have shown that pacifier use is most protective when used for all sleep periods.207,250 However, these studies also showed an increased risk of SIDS when the pacifier was usually used but not used the last time the infant was placed for sleep; the significance of these findings is yet unclear.

Although some SIDS experts and policy makers endorse pacifier use recommendations that are similar to those of the AAP,259,260 concerns about possible deleterious effects of pacifier use have prevented others from making a recommendation for pacifier use as a risk-reduction strategy.261 Although several observational studies262,264 have shown a correlation between pacifiers and reduced breastfeeding duration, a recent Cochrane review comparing pacifier use and nonuse in healthy term infants who had initiated breastfeeding found that pacifier use had no effects on partial or exclusive breastfeeding rates at 3 and 4 months.265 Furthermore, a systematic review found that the highest level of evidence (ie, from clinical trials) does not support an adverse relationship between pacifier use and breastfeeding duration or exclusivity.266 The association between shortened duration of breastfeeding and pacifier use in observational studies likely reflects a number of complex factors, such as breastfeeding difficulties or intent to wean.266,267 However, some have also raised the concern that studies that show no effect of pacifier introduction on breastfeeding duration or exclusivity may not account for early weaning or failure to establish breastfeeding.268 The AAP policy statement “Breastfeeding and the Use of Human Milk” includes a recommendation that pacifiers can be used during breastfeeding but that implementation should be delayed until breastfeeding is well established.269 Infants who are not being directly breastfed can begin pacifier use as soon as desired.

Some dental malocclusions have been found more commonly among pacifier users than nonusers, but the differences generally disappeared after pacifier cessation.270 The American Academy of Pediatric Dentistry policy statement on oral habits states that nonnutritive sucking behaviors (ie, fingers or pacifiers) are considered normal in infants and young children and that, in general, sucking habits in children to the age of 3 years are unlikely to cause any long-term problems.271 Pacifier use is associated with an approximate 1.2- to 2-fold increased risk of otitis media, particularly between 2 and 3 years of age.272,273 The incidence of otitis media is generally lower in the first year after birth, especially the first 6 months, when the risk of SIDS is the highest.274,279 However, pacifier use, once established, may persist beyond 6 months, thus increasing the risk of otitis media. Gastrointestinal tract infections and oral colonization with Candida species were also found to be more common among pacifier users than nonusers.275,277 

Because of the risk of strangulation, pacifiers should not be hung around the infant’s neck. Pacifiers that attach to the infant’s clothing should not be used with sleeping infants. Objects, such as stuffed toys, that may present a suffocation or choking risk, should not be attached to pacifiers.

There is insufficient evidence that finger sucking is protective against SIDS.

The literature on infant finger sucking and SIDS is extremely limited. Only 2 case-control studies have reported these results.248,249 One study from the United States showed a protective effect of infant finger sucking (reported as “thumb sucking”) against SIDS (adjusted OR: 0.43; 95% CI: 0.25–0.77), but it was less protective than pacifier use (adjusted OR: 0.07 [95% CI: 0.01–0.64] if the infant also sucked the thumb; adjusted OR: 0.08 [95% CI: 0.03–0.23] if the infant did not suck the thumb).249 Another study from The Netherlands did not show an association between usual finger sucking (reported as “thumb sucking”) and SIDS risk (OR: 1.38; 95% CI: 0.35–1.51), but the wide CI suggests that there was insufficient power to detect a significant association.248 

Pregnant women should obtain regular prenatal care.

There is substantial epidemiologic evidence linking a lower risk of SIDS for infants whose mothers obtain regular prenatal care.280,283 Women should obtain prenatal care from early in the pregnancy, according to established guidelines for frequency of prenatal visits.284 

Smoking during pregnancy, in the pregnant woman’s environment, and in the infant’s environment should be avoided.

Maternal smoking during pregnancy has been identified as a major risk factor in almost every epidemiologic study of SIDS.285,288 Smoke in the infant’s environment after birth has been identified as a separate major risk factor in a few studies,286,289 although separating this variable from maternal smoking before birth is problematic. Third-hand smoke refers to residual contamination from tobacco smoke after the cigarette has been extinguished290; there is no research to date on the significance of third-hand smoke with regard to SIDS risk. Smoke exposure adversely affects infant arousal291,297; in addition, smoke exposure increases the risk of preterm birth and low birth weight, both risk factors for SIDS. The effect of tobacco smoke exposure on SIDS risk is dose-dependent. The risk of SIDS is particularly high when the infant bed-shares with an adult smoker (OR: 2.3–21.6), even when the adult does not smoke in bed.89,90,191,200,201,206,212,298 It is estimated that one-third of SIDS deaths could be prevented if all maternal smoking during pregnancy was eliminated.299,300 The AAP supports the elimination of all tobacco smoke exposure, both prenatally and environmentally.

Avoid alcohol and illicit drug use during pregnancy and after the infant’s birth.

Several studies have specifically investigated the association of SIDS with prenatal and postnatal exposure to alcohol or illicit drug use, although substance abuse often involves more than one substance and it is often difficult to separate out these variables from each other and from smoking. However, 1 study in Northern Plains American Indian infants found that periconceptional maternal alcohol use (adjusted OR: 6.2; 95% CI: 1.6–23.3) and maternal first-trimester binge drinking (adjusted OR: 8.2; 95% CI: 1.9–35.3)211 were associated with increased SIDS risk, independent of prenatal cigarette smoking exposure. A retrospective study from Western Australia found that a maternal alcoholism diagnosis recorded during pregnancy (adjusted hazard ratio: 6.92; 95% CI: 4.02–11.90) or within 1 year postpregnancy (adjusted hazard ratio: 8.61; 95% CI: 5.04–14.69) was associated with increased SIDS risk, and the authors estimated that at least 16.41% of SIDS deaths were attributable to maternal alcohol use disorder.301 Another study from Denmark, based on prospective data on maternal alcohol use, has also shown a significant relationship between maternal binge drinking and postneonatal infant mortality, including SIDS.302 Parental alcohol and/or illicit drug use in combination with bed-sharing places the infant at particularly high risk of SIDS and unintentional suffocation.91,196 

Rat models have shown increased arousal latency to hypoxia in rat pups exposed to prenatal alcohol.303 Furthermore, postmortem studies in Northern Plains American Indian infants showed that prenatal cigarette smoking was significantly associated with decreased serotonin receptor binding in the brainstem. In this study, the association of maternal alcohol drinking in the 3 months before or during pregnancy was of borderline significance on univariate analysis but was not significant when prenatal smoking and case versus control status was in the model.29 However, this study had limited power for multivariate analysis because of the small sample size. One study found an association of SIDS with heavy alcohol consumption in the 2 days before the death.304 Several studies have found a particularly strong association when alcohol consumption or illicit drug use occurs in combination with bed-sharing.89,91,305 

Studies investigating the relationship of illicit drug use and SIDS have focused on specific drugs or illicit drug use in general. One study found maternal cannabis use to be associated with an increased risk of SIDS (adjusted OR: 2.35; 95% CI: 1.36–4.05) at night but not during the day.306 In utero exposure to opiates (primarily methadone and heroin) has been shown in retrospective studies to be associated with an increased risk of SIDS.307,308 With the exception of 1 study that did not show an increased risk,309 population-based studies have generally shown an increased risk with in utero cocaine exposure.310,312 However, these studies did not control for confounding factors. A prospective cohort study found the SIDS rate to be significantly increased for infants exposed in utero to methadone (OR: 3.6; 95% CI: 2.5–5.1), heroin (OR: 2.3; 95% CI: 1.3–4.0), methadone and heroin (OR: 3.2; 95% CI: 1.2–8.6), and cocaine (OR: 1.6; 95% CI: 1.2–2.2), even after controlling for race/ethnicity, maternal age, parity, birth weight, year of birth, and maternal smoking.313 In addition, a meta-analysis of studies investigating an association between in utero cocaine exposure and SIDS found an increased risk of SIDS to be associated with prenatal exposure to cocaine and illicit drugs in general.314 

Avoid overheating and head covering in infants.

The amount of clothing or blankets covering an infant and the room temperature are associated with an increased risk of SIDS.208,211 Infants who sleep in the prone position have a higher risk of overheating than supine sleeping infants.210 However, the definition of overheating in the studies that found an increased risk of SIDS varies. It is therefore difficult to provide specific room temperature guidelines to avoid overheating.

It is unclear whether the relationship to overheating is an independent factor or merely a reflection of the increased risk of SIDS and suffocation with blankets and other potentially asphyxiating objects in the sleeping environment. Head covering during sleep is of particular concern. In 1 systematic review, the pooled mean prevalence of head covering among SIDS victims was 24.6%, compared with 3.2% among control infants.186 It is not known whether the risk related to head covering is due to overheating, hypoxia, or rebreathing.

Some have suggested that room ventilation may be important. One study found that bedroom heating, compared with no bedroom heating, increases SIDS risk (OR: 4.5),315 and another study showed a decreased risk of SIDS in a well-ventilated bedroom (windows and doors open; OR: 0.4).316 In 1 study, the use of a fan appeared to reduce the risk of SIDS (adjusted OR: 0.28; 95% CI: 0.10–0.77).317 However, because of the possibility of recall bias, the small sample size of controls who used fans (n = 36), a lack of detail about the location and types of fans used, and the weak link to a mechanism, this study should be interpreted with caution. On the basis of available data, the task force cannot make a recommendation on the use of a fan as a SIDS risk-reduction strategy.

Infants should be immunized in accordance with AAP and Centers for Disease Control and Prevention recommendations.

The incidence of SIDS peaks at a time when infants are receiving numerous immunizations. Case reports of a cluster of deaths shortly after immunization with diphtheria-tetanus toxoids-pertussis vaccine in the late 1970s created concern of a possible causal relationship between vaccinations and SIDS.318,321 Case-control studies were performed to evaluate this temporal association. Four of the 6 studies showed no relationship between diphtheria-tetanus toxoids-pertussis vaccination and subsequent SIDS322,325; the other 2 suggested a temporal relationship, but only in specific subgroup analysis.326,327 In 2003, the Institute of Medicine reviewed available data and concluded the following: “The evidence favors rejection of a causal relationship between exposure to multiple vaccinations and SIDS.”328 Several analyses of the US Vaccine Adverse Event Reporting System database have shown no relationship between vaccines and SIDS.329,331 In addition, several large-population case-control trials consistently have found vaccines to be protective against SIDS332,335; however, confounding factors (social, maternal, birth, and infant medical history) may account for this protective effect.336 It also has been theorized that the decreased SIDS rate immediately after vaccination was attributable to infants being healthier at the time of immunization, or “the healthy vaccinee effect.”337 Recent illness would both place infants at higher risk of SIDS and make them more likely to have immunizations deferred.338 

Recent studies have attempted to control for confounding by social, maternal, birth, and infant medical history.332,334,338 A meta-analysis of 4 studies found a multivariate summary OR for immunizations and SIDS to be 0.54 (95% CI: 0.39–0.76), indicating that the risk of SIDS is halved by immunization.338 The evidence continues to show no causal relationship between immunizations and SIDS and suggests that vaccination may have a protective effect against SIDS.

Avoid the use of commercial devices that are inconsistent with safe sleep recommendations.

Risk-reduction strategies are based on the best-available evidence in large epidemiologic studies. These studies have been largely focused on the correlations between the sleep environment and SIDS. Our current understanding is that the cause of SIDS is multifactorial and that death results from the interaction between a vulnerable infant and a potentially asphyxiating sleep environment. Thus, claims that sleep devices, mattresses, or special sleep surfaces reduce the risk of SIDS must therefore be supported by epidemiologic evidence. At a minimum, any devices used should meet safety standards of the CPSC, the Juvenile Product Manufacturers Association, and ASTM International (known previously as the American Society for Testing and Materials). The AAP concurs with the US Food and Drug Administration and CPSC that manufacturers should not claim that a product or device protects against SIDS unless there is scientific evidence to that effect.

Wedges and positioning devices are often used by parents to maintain the infant in the side or supine position because of claims that these products reduce the risk of SIDS, suffocation, or gastroesophageal reflux. However, these products are frequently made with soft, compressible materials, which might increase the risk of suffocation. The CPSC has received reports of deaths attributable to suffocation and entrapment associated with wedges and positioning devices. Most of these deaths occurred when infants were placed in the prone or side position with these devices339; other incidents have occurred when infants have slipped out of the restraints or rolled into a prone position while using the device.240,340 Because of the lack of evidence that they are effective against SIDS, suffocation, or gastroesophageal reflux and because of the potential for suffocation and entrapment risk, the AAP concurs with the CPSC and the US Food and Drug Administration in warning against the use of these products. If positioning devices are used in the hospital as part of physical therapy, they should be removed from the infant sleep area well before discharge from the hospital.

Certain crib mattresses have been designed with air-permeable materials to reduce rebreathing of expired gases, in the event that an infant ends up in the prone position during sleep, and these may be preferable to those with air-impermeable materials. With the use of a head box model, Bar-Yishay et al341 found that a permeable sleeping surface exhibited significantly better aeration properties in dispersing carbon dioxide and in preventing its accumulation. They also found the measured temperature within the head box to be substantially lower with the more permeable mattress, concluding that it was due to faster heat dissipation. This finding could be potentially protective against overheating, which has been identified as a risk factor for SIDS. Colditz et al342 also performed studies both in vitro and in vivo, showing better diffusion and less accumulation of carbon dioxide with a mesh mattress. However, Carolan et al343 found that even porous surfaces are associated with carbon dioxide accumulation and rebreathing thresholds unless there is an active carbon dioxide dispersal system. In addition, although rebreathing has been hypothesized to contribute to death in SIDS, particularly if the head is covered or when the infant is face down, there is no evidence that rebreathing, per se, causes SIDS and no epidemiologic evidence that these mattresses reduce the risk of SIDS. The use of “breathable” mattresses can be an acceptable alternative as long as the other manufacturing requirements are met, including being designed for a particular crib, having a firm surface, and maintaining its shape even when the fitted sheet designated for that model is used, such that there are no gaps between the mattress and the side of the crib, bassinet, portable crib, or play yard.

There is no evidence that apparent life-threatening events are precursors to SIDS. Furthermore, infant home cardiorespiratory monitors should not be used as a strategy to reduce the risk of SIDS.

For many years, it was believed that brief resolved unexplained events (BRUEs; formerly known as apparent life-threatening events [ALTEs]) were the predecessors of SIDS, and home apnea monitors were used as a strategy for preventing SIDS.344 However, the use of home cardiorespiratory monitors has not been documented to decrease the incidence of SIDS.345,348 Home cardiorespiratory monitors are sometimes prescribed for use at home to detect apnea and bradycardia and, when pulse oximetry is used, decreases in oxyhemoglobin saturation for infants at risk of these conditions.349 Routine in-hospital cardiorespiratory monitoring before discharge from the hospital has not been shown to detect infants at risk of SIDS. There are no data that other commercial devices that are designed to monitor infant vital signs reduce the risk of SIDS.

Supervised, awake tummy time is recommended to facilitate development and to minimize development of positional plagiocephaly.

Positional plagiocephaly, or plagiocephaly without synostosis (PWS), can be associated with a supine sleeping position (OR: 2.5).350 It is most likely to result if the infant’s head position is not varied when placed for sleep; if the infant spends little or no time in awake, supervised tummy time; and if the infant is not held in the upright position when not sleeping.350,352 Children with developmental delay and/or neurologic injury have increased rates of PWS, although a causal relationship has not been shown.350,353,356 In healthy normal children, the incidence of PWS decreases spontaneously from 20% at 8 months to 3% at 24 months of age.351 Although data to make specific recommendations as to how often and how long tummy time should be undertaken are lacking, the task force concurs with the AAP Section on Neurologic Surgery that “a certain amount of prone positioning, or ‘tummy time,’ while the infant is awake and being observed is recommended to help prevent the development of flattening of the occiput and to facilitate development of the upper shoulder girdle strength necessary for timely attainment of certain motor milestones.”357 The AAP clinical report “Prevention and Management of Positional Skull Deformities in Infants”357 provides additional detail on the prevention, diagnosis, and management of positional plagiocephaly.

There is no evidence to recommend swaddling as a strategy to reduce the risk of SIDS. Infants who are swaddled have an increased risk of death if they are placed in or roll to the prone position. If swaddling is used, infants should always be placed on the back. When an infant exhibits signs of attempting to roll, swaddling should no longer be used.

Many cultures and newborn nurseries have traditionally used swaddling, or wrapping the infant in a light blanket, as a strategy to soothe infants and, in some cases, to encourage sleep in the supine position. Swaddling, when done correctly, can be an effective technique to help calm infants and promote sleep.358,359 

Some have argued that swaddling can alter certain risk factors for SIDS, thus reducing the risk of SIDS. For instance, it has been suggested that the physical restraint associated with swaddling may prevent infants placed supine from rolling to the prone position.358 One study suggested a decrease in SIDS rate with swaddling if the infant was supine, but notably, there was an increased risk of SIDS if the infant was swaddled and placed in the prone position.210 Although another study found a 31-fold increase in SIDS risk with swaddling, the analysis was not stratified by sleep position.196 Although it may be more likely that parents will initially place a swaddled infant supine, this protective effect may be offset by the 12-fold increased risk of SIDS if the infant is either placed or rolls to the prone position when swaddled.210,359 In addition, an analysis of CPSC data found that deaths associated with swaddling were most often attributed to positional asphyxia related to prone sleeping, and a large majority of sleep environments had soft bedding.360 Thus, if swaddling is used, the infant should be placed wholly supine, and swaddling should be discontinued as soon as the infant begins to attempt to roll. Commercially available swaddle sacks are an acceptable alternative, particularly if the parent or caregiver does not know how to swaddle an infant with a conventional thin blanket. There is no evidence with regard to SIDS risk related to the arms swaddled in or out.

There is some evidence that swaddling may cause detrimental physiologic consequences. For example, it can cause an increase in respiratory rate,361 and tight swaddling can reduce the infant’s functional residual lung capacity.358,362,363 Tight swaddling can also exacerbate hip dysplasia if the hips are kept in extension and adduction,364,367 which is particularly important because some have advocated that the calming effects of swaddling are related to the “tightness” of the swaddling. In contrast, “loose” or incorrectly applied swaddling could result in head covering and, in some cases, strangulation if the blankets become loose in the bed. Swaddling may also possibly increase the risk of overheating in some situations, especially when the head is covered or there is infection.368,369 However, 1 study found no increase in abdominal skin temperature when infants were swaddled in a light cotton blanket from the shoulders down.362 

Impaired arousal has often been postulated as a mechanism contributing to SIDS, and several studies have investigated the relationship between swaddling and arousal and sleep patterns in infants. Physiologic studies have shown that, in general, swaddling decreases startling,361 increases sleep duration, and decreases spontaneous awakenings.370 Swaddling also decreases arousability (ie, increases cortical arousal thresholds) to a nasal pulsatile air-jet stimulus, especially in infants who are easily arousable when not swaddled.361 One study found decreased arousability in infants at 3 months of age who were not usually swaddled and then were swaddled but no effect on arousability in routinely swaddled infants.361 In contrast, another study has shown infants to be more easily arousable370 and to have increased autonomic (subcortical) responses371 to an auditory stimulus when swaddled.371 Thus, although swaddling clearly promotes sleep and decreases the number of awakenings, the effects on arousability to an external stimulus remain unclear. Accumulating evidence suggests, however, that routine swaddling has only minimal effects on arousal. In addition, there have been no studies investigating the effects of swaddling on arousal to more relevant stimuli such as hypoxia or hypercapnia. Finally, there is no evidence with regard to SIDS risk related to the arms swaddled in or out.

In summary, it is recognized that swaddling is one of many child care practices that can be used to calm infants, promote sleep, and encourage the use of the supine position. However, there is no evidence to recommend routine swaddling as a strategy to reduce the risk of SIDS. The risk of death is high if a swaddled infant is placed in or rolls to the prone position. If infants are swaddled, they should always be placed on the back. When an infant exhibits signs of attempting to roll, swaddling should no longer be used. Moreover, as many have advocated, swaddling must be correctly applied to avoid the possible hazards, such as hip dysplasia, head covering, and strangulation. Importantly, swaddling does not reduce the necessity to follow recommended safe sleep practices.

There is no evidence substantiating a causal relationship between various toxicants to SIDS.

Many theories link various toxicants and SIDS.372,374 Although 1 ecological study found a correlation of the maximal recorded nitrate levels of drinking water with local SIDS rates in Sweden,375 no case-control study has shown a relationship between nitrates in drinking water and SIDS. Furthermore, an expert group in the United Kingdom analyzed data pertaining to a hypothesis that SIDS is related to toxic gases, such as antimony, phosphorus, or arsenic, being released from mattresses376,377 and found the toxic gas hypothesis unsubstantiated.378 Finally, 2 case-control studies found that wrapping mattresses in plastic to reduce toxic gas emission did not protect against SIDS.230,379 

Current data do not support the use of newborn hearing screens as screening tests for SIDS.

One retrospective case-control study examined the use of newborn transient evoked otoacoustic emission hearing screening tests as a tool to identify infants at subsequent risk of SIDS.380 Infants who subsequent died of SIDS did not fail their hearing tests but, compared with controls, showed a decreased signal-to-noise ratio score in the right ear only, at frequencies of 2000, 3000, and 4000 Hz. Methodologic concerns have been raised about the validity of the study methods used in this study,381,382 and these results have not been substantiated by others. A larger, but non–peer-reviewed, report of hearing screening data in Michigan383 and a peer-reviewed retrospective study in Hong Kong383,384 showed no relationship between hearing screening test results and SIDS cases. Until additional data are available, hearing screening should not be considered as a valid screening tool to determine which infants may be at subsequent risk of SIDS. Furthermore, an increased risk of SIDS should not be inferred from an abnormal hearing screen result.

Educational and intervention campaigns are often effective in altering practice.

Intervention campaigns for SIDS have been extremely effective, especially with regard to the avoidance of prone positioning.385 Furthermore, primary care–based educational interventions, particularly those that address caregiver concerns and misconceptions about safe sleep recommendations, can be effective in altering practice. For instance, addressing concerns about infant comfort, choking, and aspiration while the infant is sleeping supine is helpful.19,96,97,386 However, many families report not receiving information consistent with AAP recommendations. When a nationally representative sample of mothers of young infants were asked about information received from their pediatricians, only 54.5% had received a recommendation to place their infant supine for sleep, 19.9% had received information about appropriate sleep location, and 11.0% had received information about pacifier use.387 Primary care providers should be encouraged to develop quality-improvement initiatives to improve adherence to safe sleep recommendations among their patients.

In addition, modeling of unsafe sleep practices by health care and child care providers may increase the prevalence of these unsafe practices.388,390 Modeling of unsafe practices may occur because professionals are not convinced of the utility of the safe sleep recommendations or have concerns about the supine sleep position, particularly with regard to infant comfort, choking, and aspiration.391,395 Interventions that address provider concerns are effective in improving behavior.391,396,398 

Media and manufacturers should follow safe sleep guidelines in their messaging and advertising.

A recent study found that, in magazines targeted toward childbearing women, more than one-third of pictures of sleeping infants and two-thirds of pictures of infant sleep environments portrayed unsafe sleep positions and sleep environments.237 Media exposures (including movie, television, magazines, newspapers, and Web sites), manufacturer advertisements, and store displays affect individual behavior by influencing beliefs and attitudes. Frequent exposure to health-related media messages can affect individual health decisions,399,400 and media messages have been very influential in decisions regarding sleep position.101,104 Media and advertising messages contrary to safe sleep recommendations may create misinformation about safe sleep practices.

Media and manufacturer messaging and advertising should follow safe sleep guidelines in text, photos, and illustrations. In addition, public health departments and organizations that provide safe sleep information should review, revise, and reissue this information at least every 5 years to ensure that each generation of new parents receives appropriate information.

The recommendations for a safe infant sleeping environment to reduce the risk of both SIDS and other sleep-related infant deaths are specified in the accompanying policy statement.78 

AAP

American Academy of Pediatrics

ASSB

accidental suffocation or strangulation in bed

CI

confidence interval

CPSC

Consumer Product Safety Commission

ICD

International Statistical Classification of Diseases and Related Health Problems

ICD-10

International Classification of Diseases, 10th Revision

OR

odds ratio

PWS

plagiocephaly without synostosis

SIDS

sudden infant death syndrome

SUDI

sudden unexpected death in infancy

SUID

sudden unexpected infant death

5-HT

5-hydroxytryptamine (serotonin)

5-HT1A

5-hydroxytryptamine 1A (serotonin 1A)

This document is copyrighted and is property of the American Academy of Pediatrics and its Board of Directors. All authors have filed conflict of interest statements with the American Academy of Pediatrics. Any conflicts have been resolved through a process approved by the Board of Directors. The American Academy of Pediatrics has neither solicited nor accepted any commercial involvement in the development of the content of this publication.

Technical reports from the American Academy of Pediatrics benefit from expertise and resources of liaisons and internal (AAP) and external reviewers. However, technical reports from the American Academy of Pediatrics may not reflect the views of the liaisons or the organizations or government agencies that they represent.

The guidance in this report does not indicate an exclusive course of treatment or serve as a standard of medical care. Variations, taking into account individual circumstances, may be appropriate.

All technical reports from the American Academy of Pediatrics automatically expire 5 years after publication unless reaffirmed, revised, or retired at or before that time.

FUNDING: No external funding.

We acknowledge the contributions provided by others to the collection and interpretation of data examined in preparation of this report. We are particularly grateful for the independent biostatistical report submitted by Robert W. Platt, PhD.

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