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Nutrition in pregnancy: Assessment and counseling

Nutrition in pregnancy: Assessment and counseling
Literature review current through: Jan 2024.
This topic last updated: Aug 02, 2023.

INTRODUCTION — A healthy dietary pattern during pregnancy promotes fetal growth and development and has been associated with lower risks of pregnancy complications, while unhealthy dietary patterns, undernutrition, and overnutrition have been associated with adverse pregnancy outcomes [1-7]. Thus, it is important to evaluate and monitor maternal nutrition both before and during pregnancy, and when appropriate, make changes to improve maternal nutrition.

Many pregnant individuals in the United States have suboptimal diet quality, which began preconception, and most do not meet dietary recommendations [7]. This is especially true among groups at elevated risk for adverse pregnancy outcomes [8]. National Health and Nutrition Examination Survey (NHANES) data indicate that, on average, pregnant or lactating people consume half the recommended amount of total vegetables and dairy products [9]. In a study of 7511 geographically diverse pregnant people in the United States, the top three sources of calories (energy intake) were soda, pasta dishes, and desserts such as cookies and cakes, which are high in added sugars and unhealthy fats [10]. Furthermore, intake of whole grains, dairy products, and healthy fats was especially low, and people with less education or in minority racial and ethnic groups had lower diet quality.

This topic will discuss assessment of maternal diet and maternal counseling about dietary issues during pregnancy, primarily for pregnant people living in middle- and high-income countries; preconception counseling and basic nutritional requirements in pregnancy in this population are reviewed separately. Issues related to pregnant people who reside in resource-limited areas and experience undernutrition are also reviewed separately.

(See "The preconception office visit", section on 'Core interventions'.)

(See "Nutrition in pregnancy: Dietary requirements and supplements".)

(See "Undernutrition in pregnancy: Evaluation, management, and outcome in resource-limited areas".)

ASSESSMENT OF NUTRITIONAL STATUS — Ideally, nutritional status is initially assessed before pregnancy so dietary changes to optimize maternal and child health can begin well before conception [11]. Nutritional assessment and counseling should continue across pregnancy and during lactation. Where available, these activities are best performed using a team approach, which may include the obstetric provider, health professionals trained in prenatal nutrition counseling and education, and a registered dietitian with perinatal nutritional expertise. (See "Dietary assessment in adults".)

History

Medical and surgical – The medical history can help identify behaviors and medical conditions that pose nutrition-related health risks for the mother and fetus and thus need to be addressed (table 1). For example, use of cigarettes, alcohol, or illicit drugs poses direct health risks but may also affect intake of an adequate and balanced diet: Cigarettes, alcohol, and opioids may suppress appetite while stimulants may increase energy requirements. Some individuals even forget to disclose that they had bariatric surgery, especially if it was laparoscopic and in the distant past. Sequelae of bariatric surgery (eg, micronutrient deficiencies, dumping syndrome) can affect pregnancy management and outcome. (See "Fertility and pregnancy after bariatric surgery".)

Obstetric – The past obstetric history can impact recommendations for nutrition or supplements before or during future pregnancies. As an example, a past history of a neural tube defect (NTD) in offspring would prompt advice to consume a higher dose of supplemental folic acid (4 mg rather than 0.4 mg) prior to conception and in early pregnancy to reduce the risk of recurrence. (See "Preconception and prenatal folic acid supplementation", section on 'Either parent with a personal history of NTD or a previously affected offspring'.)

Dietary – Asking the patient to complete a self-administered questionnaire is helpful for reviewing their typical diet and identifying obvious deficiencies (form 1) [12]. It is important to follow up with specific questions about responses that suggest a possible nutritional issue. Examples of potential problems include skipping meals; limiting food intake; adhering to a self-selected diet; consuming sweetened beverages (eg, soda, sweet tea, sports drinks, energy drinks); low intake of calcium-rich foods, vegetables, or fruits; and high intake of ultra-processed foods with added sugars/fats.

A brief screening questionnaire may be more user-friendly for health professionals in busy practices who are not specifically trained in nutrition (table 2) [12]. This questionnaire has been adapted to assess healthy eating in pregnant people and provides simple tips to improve diet quality. Although this version of the questionnaire has not been validated, a more general version has been validated for assessing diet-related chronic disease risk and has been used successfully in pregnant people [12,13].

Individuals who routinely consume three meals daily that include several servings of vegetables (a variety of green, red/orange, and starchy vegetables), legumes (eg, peas, lentils, beans), fruits, whole grains, low-fat dairy products, and a few sources of protein (eg, meat, poultry, eggs, seafood, nuts, seeds, soy products) likely meet the Daily Recommended Intakes for most nutrients (table 3). However, even nutrient-dense food choices and diets, such as those in the United States Department of Agriculture (USDA) food patterns, may not meet nutrient goals for folate, iron, iodine, vitamin D, and choline during pregnancy [9,14,15]. In a prospective study including approximately 8000 nulliparous participants at eight US medical centers, fewer than one-quarter of the sample consumed a diet that met recommendations for vegetables, fruits, grains, dairy, or protein foods during pregnancy [16].

Physical examination

Body mass index – The physical examination centers on measurements of height and weight to calculate the body mass index (BMI) and assess whether the individual is at a healthy weight (calculator 1). The patient should be asked what they weighed at their last menstrual period (prepregnancy weight) and this weight should be used for baseline calculations. A prepregnancy BMI of 18.5 to 24.9 kg/m2 is normal for White, Hispanic, and Black individuals; for Asian individuals, an upper limit of normal is BMI <23 kg/m2 because in this population, higher body fat and higher health risks (especially type 2 diabetes) exist at lower BMIs compared with other populations [17,18]. BMI tables of appropriate pregnancy-related changes in BMI do not exist.

Signs of a medical disorder or nutritional deficiency – The remainder of the physical examination should screen for signs of nutritional deficiency or a medical disorder. As an example, an eating disorder may cause enlarged parotid glands, eroded tooth enamel, dry skin, and/or hair loss. (See "Eating disorders: Overview of epidemiology, clinical features, and diagnosis".)

Physical signs of gross vitamin deficiency are still observed in areas of the world where diets are very poor due to lack of food. In resource-abundant countries, they occur in special populations, such as individuals with alcohol use disorder, malabsorption, inborn errors of metabolism, and sometimes in those undergoing hemodialysis or receiving parenteral nutrition. (See "Dietary assessment in adults".)

Laboratory

Hemoglobin/hematocrit is routinely checked at the first prenatal visit and in the late second/early third trimester to assess for anemia; some providers also routinely check the ferritin level to assess for iron deficiency in the absence of anemia. (See "Anemia in pregnancy", section on 'Screening during pregnancy' and "Anemia in pregnancy", section on 'Evaluation of anemia' and "Anemia in pregnancy", section on 'Management'.)

Although poor vitamin D status in the perinatal period may have short-term or long-term consequences on bone, the immune system, and general health, the precise threshold defining optimal vitamin D status during pregnancy is not well defined. Most experts agree that it is not necessary to perform broad-based screening of serum 25-hydroxyvitamin D levels in the general population or during pregnancy [19,20]. Measurement is reasonable in pregnant people with obesity, those who have minimal sun exposure of skin, have a history of malabsorption (celiac disease, inflammatory bowel disease), or other risk factors for vitamin D deficiency (eg, live at northern latitudes, consume a vegan diet, have dark skin color). (See "Vitamin D deficiency in adults: Definition, clinical manifestations, and treatment".)

INDICATIONS FOR REFERRAL TO A NUTRITION PROFESSIONAL — Referral to a nutrition professional, such as a registered dietitian, with special training in maternal nutrition is recommended for patients with special nutritional considerations [4,21,22]. Registered dietitians who specialize in maternal nutrition can be found online at Academy for Nutrition and Dietetics website by entering the patient's or provider's zip code, selecting "Search by Expertise" and selecting "Maternal Nutrition" under the Expertise Area; however, the list is not comprehensive. For pregnant individuals who qualify for the Special Supplemental Nutrition Program for Women, Infants, and Children (WIC), nutrition counseling and education should be available at WIC appointments. Participation in WIC has been associated with improved birth and pediatric outcomes [23].

Potential indications for referral include:

Food insecurity or inadequate resources. Individuals with financial constraints regarding the purchase, storage (eg, refrigerator), or preparation (eg, stove) of adequate amounts of appropriate foods require assistance from sources such as the Special Supplemental Food Program for Women, Infants, and Children (WIC) or a social service agency. A short survey form to screen for food insecurity is available from the US Food and Drug Administration (FDA). Food insecurity among pregnant people in 14 states participating in the Pregnancy Risk Assessment Monitoring System (PRAMS) ranged from approximately 6 to 9 percent in recent years [24].

Diabetes, hypertension, inborn metabolic disorders (eg, phenylketonuria, maple syrup urine disease), gastrointestinal disorders that cause malabsorption (eg, Crohn disease, ulcerative colitis, cystic fibrosis), and other disorders that respond to dietary therapy.

Hyperemesis gravidarum. (See "Hyperthyroidism during pregnancy: Clinical manifestations, diagnosis, and causes" and "Nausea and vomiting of pregnancy: Treatment and outcome".)

History of bariatric surgery or other gastrointestinal surgery affecting absorption. (See "Fertility and pregnancy after bariatric surgery".)

Body mass index (BMI) in the overweight or obese range before pregnancy, as over 50 percent of these individuals have been reported to have excessive gestational weight gain [25]. Those with a normal prepregnancy BMI who have inadequate or excessive gestational weight gain (table 4) may benefit from nutritional counseling during pregnancy, as well.

Unhealthy dietary patterns, such as high intake of sweetened beverages or foods with a high level of calories from added sugars or fats (especially solid fats) and/or low intake of calcium-containing foods, vegetables (aside from corn and potatoes), and/or fruits.

Inappropriate food consumption patterns, such as food avoidances, self-selected restrictive diets, skipping meals, as these practices may lead to nutritional deficiencies and inadequate gestational weight gain. (See 'Counseling' below.)

Eating disorders, which may become aggravated by pregnancy or lead to pregnancy complications. (See "Eating disorders in pregnancy".)

Multiple gestation, which increases nutrient requirements and gestational weight gain targets. (See 'Multiple gestation' below.)

Use of substances that may affect nutrition (eg, cigarettes, alcohol, illicit drugs, appetite suppressants or stimulants).

COUNSELING

Nutrition counseling and intervention during pregnancy — Pregnancy is a key opportunity for health care professionals to assess nutrition and provide information and tools to help patients consume a healthy diet, which has both short- and long-term benefits for the mother and child. Pregnancy is considered a "window of opportunity" during which individuals are motivated to make healthy changes. It is also a period of frequent interactions with health professionals. Thus, it is important for health professionals to recognize their role and importance in helping mothers make healthy dietary or lifestyle changes. Dietary and physical activity interventions have been successful at improving outcomes, including reducing excessive gestational weight gain, development of gestational diabetes, and the odds of cesarean birth [26].

The American College of Obstetricians and Gynecologists (ACOG) endorses counseling at the initial prenatal visit "regarding benefits of appropriate weight gain, nutrition, and exercise" [27]. In a systematic review of 25 studies in resource-abundant countries, pregnant people who received nutrition information from their health care professionals were more likely to follow recommendations that were specific, clearly explained, and repeated at subsequent prenatal visits [28]. Unfortunately, prenatal nutrition counseling is often not provided, resulting in a missed opportunity [28-30]. Many barriers exist, including a lack of time, resources, and training to provide prenatal nutrition education.

Group prenatal care (eg, CenteringPregnancy) is one potential approach to provide nutrition education to more mothers during pregnancy. This model allows for more time with providers with different expertise, including nutrition professionals. One study of group prenatal care in Iran that included a nutrition module reported the individuals receiving group care were significantly more likely to take vitamin and iron supplements during pregnancy [31]. This is consistent with earlier studies reporting that the group prenatal care model improved multiple outcomes, including increased prenatal knowledge [32]. However, more recent systematic reviews have reported limited evidence on the use of group prenatal care for nutrition-related issues, possibly due to lack of rigor in design [33,34]. (See "Group prenatal care".)

General principles of a healthy diet during pregnancy — Pregnant individuals require higher intakes of many micronutrients and macronutrients (see "Nutrition in pregnancy: Dietary requirements and supplements"). To meet increased requirements, the amount consumed from each food group should increase slightly as recommended by the Dietary Guidelines for Americans (table 5) [9]. The exact amount of foods needed from each food group depends on the amount of calories an individual requires.

Energy (calorie) requirements — Energy needs change across the course of pregnancy, with no increase in calories in the first trimester and slight (+340 kcal/day) and moderate (+452 kcal/day) increases in the second and third trimesters, respectively. Energy needs also vary depending on the individual's prepregnancy body mass index (BMI), age, and physical activity level. Typical caloric needs during pregnancy range from 2200 to 2900 kcal/day in the second or third trimester for individuals with prepregnancy BMIs in the normal range (See "Nutrition in pregnancy: Dietary requirements and supplements", section on 'Energy intake'.).

Calorie needs for a pregnant individual can be estimated using an online calculator. Additionally, MyPlate.gov can provide individually tailored calorie estimates and food group requirements. For individuals with overweight, obesity, or other medical conditions that may affect energy needs, referral to a nutrition professional can be helpful. (See 'Indications for referral to a nutrition professional' above.)

Healthy dietary patterns

Overview — To meet the higher nutrient requirements in pregnancy without exceeding caloric needs, pregnant individuals should choose foods that are nutrient-dense (ie, foods that contain high levels of important nutrients compared with the amount of calories, such as fruits and vegetables, legumes, whole grains, nuts/nut butters, unsweetened yogurt, fish, lean meat) and avoid foods that provide little nutritional value beyond calories: processed foods that are high in added sugars (eg, soda, sweet tea, sweets, desserts, flavored yogurt), added fats (eg, fried foods), and solid fats (eg, high-fat and processed meat). (see "Healthy diet in adults", section on 'Dietary components associated with health benefits') Use of a nutrition screening tool can help health professionals identify pregnant people who may be at risk for lower-quality diets. (See 'History' above.)

The table provides the amounts recommended from each food group for a healthy US-style dietary pattern for pregnant individuals based on calorie needs (table 5) [9]. Generally, the increase in nutrient needs during pregnancy should comprise slight increases in each of the food groups. For people who were underweight prior to becoming pregnant, consultation with a nutrition professional may be necessary to develop appropriate, feasible, individualized strategies to consume adequate nutrients.

Additional resources are available online:

MyPlate.gov has customizable plans that allow pregnant individuals to obtain personalized recommendations for dietary patterns.

Tips for Pregnant Moms from the Special Supplemental Nutrition Program for Women, Infants, and Children (WIC) is available in both English and Spanish.

The Food and Information Center of the United States Department of Agriculture (USDA), which provides several online resources for pregnant people, including information on folic acid, food safety, foods to avoid, and nutrition.

Mediterranean diet — A Mediterranean dietary pattern is a way of eating based on the traditional cuisines of countries that border the Mediterranean Sea, such as Greece and Italy. It focuses on plant-based foods, including whole grains, vegetables, fruits, beans, nuts, and seeds, and is higher in fish and olive oil [35]. Dairy and poultry are included in moderation, while red meats and sweets are consumed infrequently.

In nonpregnant adults, this type of dietary pattern has been associated with reduced risks for cardiovascular disease, stroke and cancer, and with improved glycemic control and cognitive function [36-40]. It is notable that many of the studies are observational and thus may be limited by confounding. Research examining the Mediterranean diet during pregnancy, which also tends to be observational, has suggested that this dietary pattern is associated with a reduction in adverse outcome [41], especially gestational diabetes and hypertensive disorders of pregnancy [42,43], and may have favorable effects on offspring, such as possible reductions in wheeze in early childhood and lower waist circumference, but no effect on preterm birth, obesity, or asthma [44,45]. However, data are limited and most of the research was conducted among healthy White females with access to health care, resulting in limited generalizability.

Issues regarding self-imposed dietary restraints — Self-imposed dietary restraints, such as those described in the following sections, can be problematic if essential nutrients are left out of the diet or weight gain is inadequate.

Vegetarian-type diets — Vegetarian diets vary according to the degree of avoidance of foods of animal origin [46]. The nutritional adequacy of a vegetarian diet must be judged individually, based on the type, amount, and variety of nutrients that are consumed [47]. Healthy vegetarian dietary patterns include the same amount of vegetables, fruits, and dairy as a healthy US-style dietary pattern (table 5). To account for the lack of meats, poultry, and seafood, the amount of grains should increase by 0.5 cup per day, with larger increases in the amounts of vegetarian protein sources: nuts and seeds, soy products, beans/peas/lentils, and eggs [9].

Vegetarian diets are frequently grouped as follows (ordered from less restricted to more restricted), and potential deficiencies are described:

Semivegetarian – People who occasionally consume meat, fish, or chicken in their diet. Some people who follow such a diet may not eat red meat but may eat fish and perhaps chicken.

In some Asian cultures, animal protein sources may be consumed only once or twice a week. Although these individuals would not label themselves as vegetarian, in American research studies they would be categorized as semivegetarian, as animal protein intake in the United States tends to be significantly higher than once or twice a week.

Pescatarian – Vegetarians whose diet includes fish on occasion in addition to eggs, milk, and milk products, but no other animal meats. Adequate nutrient consumption is possible.

Lacto-ovo-vegetarian – Eggs, milk, and milk products (lacto = dairy; ovo = eggs) are included, but no meat is consumed. Adequate consumption of most nutrients is possible. Possible inadequate intake of omega-3 (also called n-3) fatty acids.

Lactovegetarian – Milk and milk products are included in the diet, but no eggs or meat are consumed. Possible inadequate intake of choline and omega-3 fatty acids. Likely inadequate intake of iron.

Macrobiotic – Whole grains, especially brown rice, are emphasized, and vegetables, fruits, legumes, and seaweeds are included in the diet. Locally-grown fruits are recommended. Animal foods limited to white meat or white-meat fish may be included in the diet once or twice a week. Likely inadequate intake of vitamin B12, choline, iron, calcium, and omega-3 fatty acids.

Vegan – All animal products, including eggs, milk, and milk products, are excluded from the diet. Some vegans do not use honey. They also may avoid foods that are processed or not organically grown [48]. Likely inadequate intake of vitamin B12, choline, iron, calcium, and omega-3 fatty acids.

Fruitarian – Vegan diet based on fruits, nuts, and seeds. Vegetables classified botanically as fruits (avocado, tomatoes) are commonly included in fruitarian diets; all other vegetables, grains, beans, and animal products are excluded. Likely inadequate intake of multiple micronutrients and possibly protein.

Issues in pregnancy — Although well-planned vegetarian and vegan diets are generally considered safe during pregnancy and lactation, high-quality data are sparse [49-51]. Attention to appropriate intake of key nutrients is essential. Consuming a vegetarian diet does not equate with healthy, as vegetarian diets may include processed foods high in sugar and fat, similar to the diet of omnivores; therefore, individual nutritional assessment of the pregnant person's vegetarian diet with a registered dietitian is advisable [51-54].

Potential concerns include:

Low birth weight/small for gestational age – Some studies have reported lower birth weight and small for gestational age offspring of pregnant individuals consuming a vegetarian or vegan diet [55,56].

Inadequate micronutrient intake – Well-balanced vegetarian diets are similar to well-balanced omnivore diets in that they meet most nutrient goals, with the likely exceptions of iron, vitamin D, vitamin E, and choline for some types of vegetarian diet [15,57] (see 'Vegetarian-type diets' above). Additional potential nutrients of concern, particularly for vegans and diets that completely avoid animal source foods, are calcium, vitamin B12, and omega-3 fatty acids (eicosapentaenoic acid and docosahexaenoic acid) [49,50,58]. In one review, pregnant people on a vegan diet were at higher risk for both iron and vitamin B12 deficiencies [50].

Micronutrient deficiencies can often be resolved with minor dietary alterations or supplements. For example, fortified vegetarian/vegan food products are now widely available and include some nondairy milks (such as fortified soy beverages), calcium-fortified orange juice, meat substitutes (eg, tofu, tempeh), and fortified breakfast cereals. These products can be good sources of key nutrients, such as calcium, iron, zinc, vitamin B12, vitamin D, riboflavin, and omega-3 fatty acids. Of note, some natural food brands are not enriched or fortified to the same degree as mainstream products.

If all animal source foods are excluded and dietary modifications are not possible or unlikely, use of one or more of the following supplements needs to be considered:

Vitamin B12

Omega-3 fatty acids (eg, vegan algae-based supplements [spirulina and chlorella])

Choline

Iron

Vitamin D

Vitamin E

Calcium

Vitamin D, E, and iron are generally provided in sufficient amounts by a standard prenatal vitamin. Other nutrients should be evaluated and provided individually as needed. (See "Nutrition in pregnancy: Dietary requirements and supplements".)

Inadequate macronutrient intake – Limited research in populations outside of the United States showed that the macronutrient intake of pregnant vegetarians was similar to that of pregnant nonvegetarians except the pregnant vegetarians consumed statistically less protein and more carbohydrates; however, none of the studies reported protein deficiency in pregnant vegetarians [59,60]. Protein quality in well-balanced vegetarian diets need not be a concern as long as total energy intake is adequate (because it provides a protein-sparing effect).

Although individual plant sources of protein tend to be incomplete in their provision of all essential amino acids, eating a variety of types of plant protein sources (grains, legumes, nuts) over the course of a day can provide all essential amino acids [61].

Effect of phytoestrogens – Phytoestrogen consumption tends to be higher among vegetarians than among omnivores. Although concerns have been raised regarding phytoestrogen intake and reproductive development (hypospadias [62]), subsequent research found no correlation [63]. Available evidence does not support an association between vegetarian diets and risk of disrupted reproductive development. (See "Endocrine-disrupting chemicals".)

Gluten-free diet — Gluten-free grains often do not contain the same levels of added folate, calcium, and iron compared with wheat products; therefore, elimination of gluten-rich foods during pregnancy could result in inadequate intakes of these nutrients as well as thiamin, riboflavin, and niacin. However, use of other whole grain foods (eg, quinoa, brown rice, buckwheat, gluten-free oats, plus amaranth or sorghum for iron), in addition to standard folic acid supplementation of 400 to 800 mcg/day, should prevent any nutritional deficiency and these diets are generally considered safe. (See "Nutrition in pregnancy: Dietary requirements and supplements".)

Patients with celiac disease – Patients with celiac disease benefit from following a gluten-free diet. In systematic reviews of case-control and cohort studies, females with untreated celiac disease were at increased risk of reproductive failure compared with females in the general population and treatment with a gluten-free diet eliminated the excess risk of complications [64-66]. (See "Epidemiology, pathogenesis, and clinical manifestations of celiac disease in adults", section on 'Menstrual and reproductive issues'.)

Patients without celiac disease – Gluten-free diets are now also popular in the general population and are promoted in the lay press as having health benefits despite a lack of evidence to support this claim in patients without celiac disease or gluten sensitivity [67,68]. While there is no evidence to support their use in the absence of celiac disease or documented gluten sensitivity, gluten-free diets can provide adequate nutrition.

Low-carbohydrate diet — The recommended minimum carbohydrate requirements for nonpregnant and pregnant females is to consume a minimum of 130 and 175 grams per day, respectively [9,69]. Nonpregnant individuals may choose to follow a low-carbohydrate diet for a variety of reasons, in particular management of type 2 diabetes and weight loss [70].

"Low-carb" diets vary greatly in the amount of carbohydrates consumed. Technically, any diet that provides less than 45 percent of energy from carbohydrates may be considered "low carb." For a 2000 calorie diet, this would be less than 225 grams per day. However, low-carb diets may limit carbohydrate intake to as little as 50 grams per day (see 'Ketogenic diet' below). Pregnant patients should consult with a health professional before restricting carbohydrates below the daily recommended intake of 175 grams per day and we recommend avoiding extremely low-carbohydrate diets during pregnancy. Moderate carbohydrate restriction may be acceptable, particularly in patients with gestational diabetes, but this should take place under the care of a health professional trained in management of gestational diabetes.

Possible relationship with neural tube defects – In a review of data from the National Birth Defects Prevention Study, pregnant people with restricted carbohydrate intake had less than half the folate intake of pregnant people with nonrestricted carbohydrate intake and also appeared to be at slightly increased risk of having an infant with a neural tube defect (NTD; odds ratio 1.30, 95% CI 1.02-1.67) [71]. A subsequent study using prefolic acid food fortification data also noted this association between low-carbohydrate diets and NTDs, suggesting that the increased risk may not be related solely to low folic acid intake in the postfortification era [72]. Although a causal role between restricted carbohydrate intake (≤5th percentile or 95 g/day) and NTDs has not been established, for females who follow low-carbohydrate diets, it is prudent to emphasize the importance of the standard recommendation that all reproductive-age females take a 0.4 to 0.8 mg folic acid supplement one month before and for the first two to three months after conception. Further investigation between low-carbohydrate diets and NTDs is needed. (See "Nutrition in pregnancy: Dietary requirements and supplements", section on 'Folate/folic acid'.)

Ketogenic diet — The ketogenic diet is one type of very low-carbohydrate diet, classically consisting of high-fat, moderate-protein, and extremely low-carbohydrate consumption that produces metabolic changes associated with the starvation state. These diets were initially developed to treat seizure disorders, but have since been promoted for weight loss and other health reasons, and can be either hypocaloric or normocaloric [73]. Ketogenic diets typically restrict carbohydrate consumption to 5 to 10 percent of energy needs, which would provide only 25 to 50 grams per day of carbohydrate. (See 'Low-carbohydrate diet' above.)

There is minimal information on the fetal effects of the ketogenic diet in human pregnancy [74,75], which is concerning since maternal changes in plasma ketones, insulin, glucose, glucagon, and free fatty acids can be quite profound. Rodent studies have reported potentially adverse fetal effects, such as fetal overgrowth, and changes in organ (heart) size and brain structures [76,77]. Furthermore, rodent mothers fed a ketogenic diet exhibited reduction in fertility, litter size, and high risk of fatal ketoacidosis during lactation [78]. Given these animal data, a lack of evidence of the effects in humans, and concerns about a very low-carbohydrate diet in the absence of folic acid supplementation, we and others recommend avoiding ketogenic diets during pregnancy [7].

Paleolithic diet — The "Paleo" diet was developed based on an idea that foods from the paleolithic era, a hunter-gatherer period prior to farming and cultivation, may promote greater health. This diet generally includes nuts, fish, meat, eggs, and some fruits and vegetables and excludes dairy, grain-based foods, legumes, refined sugar, table salt, and processed foods [79]. It tends to be high in protein, moderate in fat (mainly unsaturated fats), low to moderate in carbohydrates, and low in sodium. It may be low in folate, certain types of fiber, and calcium due to the exclusion of grains, legumes, and dairy [80,81]. One study among nonpregnant females reported a rise in iodine deficiency after six months of consuming a Paleo diet [82].

There is limited research about the Paleo diet in pregnant people. In one retrospective cohort study comparing 37 pregnant people with low-risk pregnancies who adhered to this diet before and throughout gestation with 39 similar low-risk pregnant people who consumed a regular diet, the Paleo diet was associated with lower glucose challenge test results (one hour glucose level: 95.8 versus 123.1 mg/dL), higher hemoglobin levels (12.10 versus 11.05 g/dL) and ferritin (32.1 versus 21.3 mg/mL), lower gestational weight gain (9.3 versus 10.8 kg), and lower birth weight (3098 versus 3275 g), with no differences in adverse neonatal outcomes [83].

A Paleo diet during pregnancy may be acceptable, as it includes vegetables, fruits, and healthy proteins, while also excluding or limiting added sugars, certain processed foods, and processed meats. However, it is likely to provide insufficient amounts of key nutrients.

For pregnant people on Paleo diets, we suggest a prenatal vitamin containing at least 400 to 800 micrograms of folic acid and 150 to 250 micrograms of iodine (if they do not consume iodized table salt) and calcium supplements of 1000 mg divided into two or three doses throughout the day. Some authors have advised against the Paleo diet because of the dairy restriction [7]. (See "Nutrition in pregnancy: Dietary requirements and supplements", section on 'Micronutrients'.)

Intermittent fasting — Intermittent fasting may involve fasting for several hours during the day or for one or more days. Fasting may occur for religious reasons or to promote weight loss [84]. The effects of intermittent fasting in otherwise healthy pregnant people are not well defined. Some authors have hypothesized that prolonged daytime fasting during pregnancy, such as during Ramadan (see 'Ramadan fasting' below), can lead to permanent epigenetic alterations in fetal physiology (fetal programming) that have adverse consequences in adult life [84]. In ovine and human studies, the most consistently reported effect of daytime fasting is reduction in fetal breathing movements, with resolution in the fed state [85-89]. There is no information on the effect of ketonuria on fetal/neonatal outcome in the absence of ketoacidosis.

Nighttime fasting is better understood. During an overnight 12- to 18-hour fast, plasma glucose, insulin, and alanine levels fall, and plasma-free fatty acids and beta-hydroxybutyrate levels rise, a phenomenon termed "accelerated starvation" [90]. With early conversion to fat metabolism, other fuels, such as glucose and amino acids, are more available for the fetus. Free fatty acids and beta-hydroxybutyrate are also transferred across the placenta and metabolized by the fetus.

Ramadan fasting — Refraining from food and drink during daylight hours for the month of Ramadan is a religious practice that is observed by between 30 and 85 percent of pregnant Muslim individuals [91]. A meta-analysis of 22 studies of short-term pregnancy outcome in nearly 19,000 pregnancies exposed to Ramadan fasting (during which fasting occurs from sunrise to sunset) observed no adverse effects on birth weight or preterm birth rate, but a reduction in placental weight in one of the three studies that reported this outcome [92]. Rare outcomes such as stillbirth and neonatal death could not be assessed. A limitation of these data is that the practice of Ramadan varies within and among Muslim communities.

A literature review found that Ramadan fasting probably did not affect fetal antenatal testing, although dehydration may affect amniotic fluid volume as a component of the biophysical profile [91]. It also noted a minimal yet significant decrease (<1 lb [0.45 kg]) in gestational weight and signs and symptoms that make pregnancy more difficult, including vomiting, diarrhea, dizziness, ketosis, weakness, and low energy.

One of the few longer-term studies on exposure to Ramadan in early pregnancy found that it may have adverse effects on childhood mortality [93]. In this study of 20 years of data from Burkina Faso (>40,000 children, >25,000 mothers), when Ramadan occurred during conception, the first trimester, or the second trimester, the under-age-five mortality rates of children born to Muslim mothers were 33, 29, and 22 percent higher, respectively, than in children of non-Muslim mothers born at the same time. Childhood mortality in offspring of Muslim mothers was not increased with exposure during the third trimester or in the absence of in utero exposure. However, it should be noted that most of the population of Burkina Faso lives by subsistence farming and has seasonal food insecurity and the pregnant people may have been nutritionally deprived in addition to fasting; many young children are chronically nutritionally deprived. Thus, the findings in this study may not apply to Muslim females in other countries where food insecurity is not prevalent. Other lifestyle changes also occur during Ramadan, such as increases in fat and sugar consumption, which may also play a role in the observed association.

Additional studies are needed to determine the effects of factors, such as the trimester of pregnancy when Ramadan fasting occurs, coexistence of medical conditions and pregnancy complications, the geographic location of the population, and dietary intake outside of fasting hours. Some small studies have reported an impact from these factors [94]. Information on the long-term development of offspring would also be useful.

A clinical opinion and literature review provided guidance for counseling pregnant Muslim patients, including specific information for counseling and monitoring those with diabetes [91].

Other dietary issues

Lactose intolerance — Lactose intolerant patients who are unable to consume adequate amounts of calcium through dairy and other dietary components can take calcium supplements or consume calcium-fortified foods and beverages, such as fortified soy beverages. There are no data on the safety of commercially available "lactase" preparations during pregnancy; however, beta-galactosidases are normal constituents of human tissues. (See "Lactose intolerance and malabsorption: Clinical manifestations, diagnosis, and management".)

Of note, pregnant people with lactose maldigestion have improved lactose tolerance in late pregnancy [95,96]. This has been attributed to slower intestinal transit during pregnancy and bacterial adaptation to increased lactose intake.

Food avoidance/consumption to prevent atopic disease in offspring — Both avoidance and ingestion of specific antigens, such as peanuts, milk, and eggs, during pregnancy have been hypothesized to reduce the frequency of atopic disease in offspring, but the bulk of evidence does not support either approach and early postnatal exposure may be the modifiable determinant. These diets are not recommended. (See "Primary prevention of allergic disease: Maternal diet in pregnancy and lactation".)

On the other hand, breastfeeding may reduce the risk of allergic disease in offspring and is recommended. (See "The impact of breastfeeding on the development of allergic disease".)

Consumption of nonfluoridated bottled or tap water — Theoretically, pregnant people who live in areas where water is not fluoridated or who only consume bottled water not containing fluoride may not achieve adequate intake of fluoride, which is 3 mg/day in nonpregnant, pregnant, and breastfeeding people [97,98]. Fluoride intake is difficult to determine, given that fluoride may be present in liquids used for bottled beverages and prepared foods (eg, soups, canned vegetables) and is present in tea and seafood that contains edible bones or shells.

The United States Centers for Disease Control and Prevention (CDC) recommends not supplementing fluoride during pregnancy [99] because prenatal fluoride supplementation is not incorporated into primary teeth [100] and did not reduce caries in offspring in the only randomized trial of this intervention [101,102]. The benefits of fluoride occur almost entirely after tooth eruption as a direct topical effect on teeth; earlier hypotheses that ingested fluoride is systemically incorporated into developing tooth enamel have been largely discredited as a primary mechanism of fluoride action [103,104]. On the other hand, there is good evidence that postnatal exposure of newly erupted teeth to topical fluoride from water or dentifrice is efficacious [103,104].

Excessive ingestion of fluoride during pregnancy does not appear to produce fluorosis in offspring [105]. Although fluoride readily crosses the placenta, the placenta may provide a partial barrier to transfer of excess fluoride when maternal levels are high [106]. However, a possible association with neurodevelopmental effects has been reported in ecological studies in China and Mexico and a multicenter birth cohort study in Canada [107-110]. The source of fluoride in the Canadian and Mexican studies was optimally fluoridated water consumed as tap water and other water-based beverages. The Canadian study also adjusted for tea consumption, which has a high-fluoride content. The source of fluoride in the Chinese study was well water; there was no adjustment for tea consumption. The observed association may be related to bias, imprecision, and unmeasured confounding; further investigation is warranted before fluoride can be considered a neurodevelopmental toxicant [111]. (See "Overview of dietary trace elements" and "Preventive dental care and counseling for infants and young children".)

Use of non-nutritive sweeteners — The US Food and Drug Administration (FDA), which regulates nutritive and non-nutritive sweeteners in the United States, has deemed acesulfame potassium (eg, Sunett, Sweet One), advantame, aspartame (eg, NutraSweet, Equal), neotame (eg, Newtame), saccharin (eg, Sweet'N Low), luo han guo fruit extract (Siraitia grosvenorii Swingle fruit extract), >95 percent purity steviol glycosides (eg, Stevia, Truvia, SweetLeaf), and sucralose (eg, Splenda) to be safe for use by the general public, including during pregnancy [112]. Saccharin, acesulfame, and sucralose cross the placenta whereas aspartame does not because it is fully digested in the gastrointestinal tract [113].

Intake of non-nutritive sweeteners is common and has increased dramatically among pregnant people in the United States over the last decade [114,115]. Although clinical studies on the short- and long-term effects of consumption of these substances during pregnancy are limited, no data suggest that use of aspartame, sucralose, saccharin, acesulfame potassium, or stevioside by pregnant people increases the risk of congenital anomalies above the baseline risk in the general population [116]. However, other issues, including increased infant BMI, childhood obesity, a small increase in preterm birth, and an altered childhood preference for sweet taste, have been observed, and the effects appear to be independent of overall diet quality, energy intake, or other obesity risk factors [117-123]. Pregnant people with phenylketonuria should avoid aspartame because it is converted into phenylalanine in the body.

We consider consumption of small amounts of non-nutritive sweeteners during pregnancy acceptable, particularly to replace sugar, such as in patients with gestational diabetes where refined sugar consumption can be detrimental. The acceptable daily intake (ADI) is defined as an estimate of the amount of a food additive that can be ingested daily over a lifetime without appreciable health risk. Average use of non-nutritive sweeteners is usually below this limit. For example, the ADI for aspartame is 50 mg/kg/day; Diet Coke contains 131 mg aspartame per 355 mL can and one packet of Equal contains 33 mg of aspartame. The ADI for saccharin and sucralose is 5 mg/kg/day, for acesulfame potassium it is 15 mg/kg/day, and for stevioside it is 4 mg/kg/day.

An overview of issues related to use of non-nutritive sweeteners is available separately. (See "Overview of nonnutritive sweeteners".)

Consumption of sugar-sweetened beverages — Sugar-sweetened beverages include soda, sweet tea, sports drinks, and juices. These drinks tend to be high in calories and low in nutritive value; therefore, more than occasional intake of sugar-sweetened beverages is discouraged in all populations. National Health and Nutrition Examination Survey (NHANES) data indicate that pregnant females in the United States consume an average of 1.3 sugar sweetened beverages per day, with the highest intake among those with incomes below the federal poverty level, a group with other social determinants of poorer health [124].

Concerns have been raised about consumption of these beverages by pregnant people. Consumption can lead to large spikes in blood glucose, which can be particularly problematic during pregnancy, when insulin resistance is naturally increased to promote adequate nutrient availability to the fetus. In addition, sugar-sweetened beverage consumption has been associated with poorer diet quality and extra calories (estimated to be an extra 203 kcal/day), which may contribute to excess gestational weight gain [124]. Maternal sugary beverage intake has also been associated with risk for preeclampsia [125], conflicting findings regarding risk for preterm birth [122,126], and increased adiposity in school-aged children. With respect to offspring, one study reported that for each additional serving of a sugary beverage consumed by a mother during the second trimester, fat mass in offspring increased by 0.15 kg/m2 [127]. The association persisted after adjustment for multiple confounding variables and was independent of the offsprings' beverage intake, and no such association was found for maternal intakes of diet soda or water. These findings add to an increasing body of data supporting prenatal programming of susceptibility to obesity.

FOOD SAFETY

Avoidance of foodborne infections — Foodborne illnesses can cause maternal disease as well as congenital disease, miscarriage, preterm labor, and fetal death. To reduce the risk of foodborne illness [128]:

Practice good personal hygiene (frequent hand washing).

Consume only meats, fish, and poultry (including eggs) that are fully cooked.

Avoid deli meats, hot dogs, and smoked seafood. Alternatively, cook them until they steam to destroy bacteria (particularly listeria).

Avoid unpasteurized dairy products and fruit/vegetable juices.

Thoroughly rinse fresh fruits and vegetables under running water (approximately 30 seconds) before eating.

Avoid eating raw sprouts (including alfalfa, clover, radish, and mung bean). Bacteria can get into sprout seeds through cracks in the shell; these bacteria are nearly impossible to wash out.

Wash hands, food preparation surfaces, cutting boards, dishes, and utensils that come in contact with raw meat, poultry, or fish with hot, soapy water. Countertops can be sanitized by wiping with a solution of one teaspoon liquid chlorine bleach per quart of water and leaving to dry over 10 minutes.

In the United States, FoodSafety.gov provides detailed advice on food safety for people who are pregnant or planning pregnancy.

The following foodborne infections can have adverse effects on pregnancy. These infections and strategies for avoiding them are described in detail separately:

Toxoplasmosis – Toxoplasmosis is caused by ingestion of undercooked or cured meat or meat products, fruit or vegetables contaminated by infected soil, and contaminated unfiltered water. (See "Toxoplasmosis and pregnancy".)

Listeriosis – Listeria monocytogenes is a common low-level bacterial contaminant of both processed and unprocessed foods of plant and animal origin; hot cooked foods are not a vehicle for its transmission. L. monocytogenes is most associated with processed/delicatessen meats, hot dogs, soft cheeses, smoked seafood, meat spreads, and pâté, but has also been transmitted by fresh fruits and vegetables that are commonly eaten uncooked. (See "Clinical manifestations and diagnosis of Listeria monocytogenes infection".)

Brucellosis – Brucellosis is caused by ingestion of contaminated food such as raw milk, cheeses made from unpasteurized (raw) milk, or raw meat. (See "Brucellosis: Epidemiology, microbiology, clinical manifestations, and diagnosis".)

Information about current foodborne illness outbreaks in the United States can be found at the Centers for Disease Control and Prevention website.

Guidelines for safe seafood consumption — Pregnant people are advised to eat only cooked fish to avoid potentially harmful organisms [129]. However, pregnant people who have consumed "sushi grade" raw fish can be reassured that this is generally safe [130], as long as the raw fish was frozen appropriately [131], as this eliminates most parasites and bacteria. These individuals should be advised to discontinue future raw fish consumption. A variety of marine toxins (eg, ciguatoxin) can be ingested via fish consumption (cooked or raw), but there are only rare reports of adverse effects on pregnancy or the fetus. (See "Overview of shellfish, pufferfish, and other marine toxin poisoning".)

Fish may be contaminated by environmental pollutants, such as methylmercury. Methylmercury exposure, primarily through ingestion of contaminated fish, can cause severe fetal central nervous system damage, as well as milder intellectual, motor, and psychosocial impairment. For this reason, the FDA and the Environmental Protection Agency (EPA) recommend that pregnant people (or people who might become pregnant or who are nursing) should [129]:

Avoid eating any shark, swordfish, king mackerel, marlin, orange roughy, tilefish (Gulf of Mexico), or bigeye tuna (other kinds of tuna are acceptable) because they may contain high levels of mercury; an online table of mercury content in commercial fish and shellfish is available.

Eat two to three servings (8 to 12 oz total) per week of seafood that is likely very low in mercury or other contaminants ("best choices") or one serving of seafood (4 oz) that is likely low in mercury or other contaminants ("good choices"). A chart to help consumers make appropriate choices is available online. Additional information on specific levels of methylmercury and other contaminants is available through the FDA food safety website and the EPA website.

Check local advisories about the safety of fish caught in local lakes, rivers, and coastal areas.

The risks and benefits of fish consumption and fish oil supplements during pregnancy are reviewed in detail separately. (See "Fish consumption and marine omega-3 fatty acid supplementation in pregnancy".)

Guidelines for safe caffeine intake — Females who are attempting to conceive or who are pregnant are generally advised to limit caffeine consumption to less than 200 to 300 mg per day (table 6). A short list of the caffeine content of beverages and foods is available in the table (table 7); a longer list is available online.

Available data on the safety of any caffeine intake is of low quality. The effect of extraneous variables and possible misclassification of exposure and outcome variables remains a limitation of observational studies. These data and the effects of caffeine on pregnancy outcomes are discussed in detail separately. (See "Caffeine: Effects on reproductive outcomes in females".)

Avoidance of herbal products (except ginger) — Herbal medicines and supplements should generally be avoided during pregnancy [132-134], except for ginger (see "Nausea and vomiting of pregnancy: Treatment and outcome", section on 'Ginger supplements'). The practitioner has no control over the strength or purity of the individual herbs; herbal preparations can interact with commonly prescribed medications and lead to dangerous side effects [135,136]; and several cases of potentially harmful effects to the pregnancy have been reported [134,137-141]. In the United States, makers of supplements are not required to prove efficacy, safety, or quality of a product before it is on the market, and numerous recalls of supplements have taken place due to product adulteration. (See "Overview of herbal medicine and dietary supplements", section on 'Regulation in the United States'.)

Consumption of herbal products is common. In the United States, 5 to 10 percent of pregnant people reported herbal intake during pregnancy [142,143] and 15 percent reported using an herbal product or nonvitamin supplement, most commonly fish oil, melatonin, probiotics or prebiotics, acai, and cranberry [144]. Estimates of herbal intake have been higher in Europe and Australia, as high as 58 percent of pregnant people in one United Kingdom sample [145]. The most common products were herbal teas, chamomile, ginger, cranberry, raspberry leaf, echinacea, and ephedra.

There is a paucity of high-quality randomized trials evaluating the efficacy and safety of traditional herbal preparations in pregnancy [146]. In a 2016 systematic review that examined the effects of herbal medicines on miscarriage, none of nine randomized trials compared herbal medicines with either placebo or bed rest; thus, the authors concluded that there were insufficient data to make recommendations [147]. Some studies have reported lack of positive effects of herbal remedies [148], while others have reported negative effects on pregnancy and infant outcomes (eg, almond oil, licorice, and chamomile have been associated with preterm birth; mwanaphepo has been associated with maternal and neonatal morbidity) [134,141]. One systematic review found that raspberry leaf was associated with cesarean birth, while another concluded that it resulted in neither harm nor benefit [134,149]. A meta-analysis of nine studies found evening primrose oil was associated with a shorter duration of first- and second-stage labor and a reduction in cesarean birth, however, further research was recommended due to the low quality of the studies [150].

Caution regarding consumption of liver-based foods — High consumption of liver or liver-based foods (eg, liver patties or sausage) may be harmful in pregnancy because of excessive intake of vitamin A. Some groups have recommended limiting or avoiding liver consumption in pregnancy for this reason. (See "Nutrition in pregnancy: Dietary requirements and supplements", section on 'Supplements and dietary intake that can be harmful'.)

Limiting exposure to environmental toxins — Reducing exposure to toxic environmental agents is a critical area for intervention because of effects of toxins on the developing fetus [151]. Good nutrition is one way to buffer exposure to toxic agents [152,153]. Pregnant people should be encouraged to eat plenty of fruits and vegetables (either conventional or organic), legumes, and whole grains every day, and to avoid processed foods and fast foods.

Bisphenol A and phthalates – Food can be a source of exposure to environmental toxins, such as bisphenol A (BPA), phthalates, and pesticides. BPA enters into food and beverages from containers that are made with BPA (eg, lining of canned foods, polycarbonate plastics heated in a microwave oven or dishwasher). Phthalates are used in food production and storage containers (such as conveyer belts, jar lids, tubing, gloves, and packaging) and can seep into a wide variety of foods and beverages during processing and packaging [154]. Exposure is a concern during pregnancy because of potential increase in preterm birth and neural and behavioral effects in offspring.

Pregnant people should be encouraged to avoid use of plastics for food and beverage containers that contain BPA and avoid canned goods that use BPA linings (BPA-free canned goods are increasingly available). (See "Occupational and environmental risks to reproduction in females: Specific exposures and impact", section on 'Bisphenol A and other phenols' and "Overview of occupational and environmental risks to reproduction in females", section on 'Interference with fetal development'.)

Pesticide and antibiotic residues – The effects of pesticide exposure from foods are unclear. The American Academy of Pediatrics recognizes that early pesticide exposure may adversely impact birth weight, risk of pediatric cancers, and cognitive function and behavior [155]. The EPA sets a maximum residue limit, which is the amount of pesticide residue allowed to remain on each food or product [156]. This limit is set to ensure that "there is reasonable certainty of no harm." Much of the public, however, is still concerned about pesticides in food.

Consumption of organic foods may reduce exposure to pesticide residues and antibiotics (which can promote antibiotic resistant bacteria) [157]. On the other hand, organic foods have not been found to be nutritionally superior and tend to be more expensive and less accessible, particularly for disadvantaged populations. (See "Overview of occupational and environmental risks to reproduction in females", section on 'Interference with fetal development'.)

Tips to help reduce pesticide residues on foods include [158]:

Eat a variety of fruits and vegetables to minimize exposure to a single pesticide

Thoroughly wash all produce, even organic produce and produce that is peeled before consumption

Wash produce under running water rather than dunking or soaking it

Scrub produce that is firm (eg, melons, root vegetables)

Dry produce with clean cloth or towel, if possible

Discard outer layer of lettuce or cabbage

Trim fat and skin from meat, poultry, and fish to minimize pesticide residues that accumulate in fat

SPECIAL POPULATIONS

Multiple gestation — Nutritional requirements and weight gain recommendations are higher in multiple gestations. Guidelines are provided separately. (See "Twin pregnancy: Routine prenatal care", section on 'Nutrition and supplements' and "Twin pregnancy: Routine prenatal care", section on 'Gestational weight gain' and "Triplet pregnancy", section on 'Weight gain'.)

Pregnant people with diabetes — Medical nutritional therapy for patients with pregestational or gestation diabetes is reviewed separately. (See "Pregestational (preexisting) diabetes mellitus: Antenatal glycemic control", section on 'Medical nutrition therapy' and "Gestational diabetes mellitus: Glucose management and maternal prognosis", section on 'Medical nutritional therapy'.)

Postpartum and breastfeeding — An adequate, balanced diet is important for replenishing maternal stores that are expended during the pregnancy, promoting loss of excess weight, and nourishing the breastfed infant. Maternal nutrition in the postpartum period, including during lactation, is discussed separately. (See "Maternal nutrition during lactation" and "Overview of the postpartum period: Disorders and complications", section on 'Postpartum weight retention'.)

Pregnant people with undernutrition living in resource-limited areas — Pregnant people with potentially severe undernutrition living in resource-limited areas require careful assessment and a different approach to treatment, which is reviewed separately. (See "Undernutrition in pregnancy: Evaluation, management, and outcome in resource-limited areas".)

SOCIETY GUIDELINE LINKS — Links to society and government-sponsored guidelines from selected countries and regions around the world are provided separately. (See "Society guideline links: Nutrition and supplements in pregnancy".)

INFORMATION FOR PATIENTS — UpToDate offers two types of patient education materials, "The Basics" and "Beyond the Basics." The Basics patient education pieces are written in plain language, at the 5th to 6th grade reading level, and they answer the four or five key questions a patient might have about a given condition. These articles are best for patients who want a general overview and who prefer short, easy-to-read materials. Beyond the Basics patient education pieces are longer, more sophisticated, and more detailed. These articles are written at the 10th to 12th grade reading level and are best for patients who want in-depth information and are comfortable with some medical jargon.

Here are the patient education articles that are relevant to this topic. We encourage you to print or e-mail these topics to your patients. (You can also locate patient education articles on a variety of subjects by searching on "patient info" and the keyword(s) of interest.)

Basics topics (see "Patient education: Nutrition before and during pregnancy (The Basics)" and "Patient education: Health and nutrition during breastfeeding (The Basics)" and "Patient education: Vegetarian diet (The Basics)")

Beyond the Basics topic (see "Patient education: Health and nutrition during breastfeeding (Beyond the Basics)")

SUMMARY AND RECOMMENDATIONS

Assessment and referral – Ideally, a female patient's nutritional status is initially assessed before pregnancy so dietary changes to optimize maternal and child health can begin well before conception. Nutritional assessment and counseling should continue across pregnancy and during lactation. Completion of a self-administered dietary questionnaire prior to seeing the clinician can be helpful (form 1 and table 2). (See 'Assessment of nutritional status' above.):

Consultation with a trained specialist in maternal nutrition, such as a registered dietitian, is recommended for pregnant people with high-nutrition risk. Some examples are listed in the table (table 1). (See 'Indications for referral to a nutrition professional' above.)

Counseling

Healthy diet – Pregnant people should be counseled to eat a healthy dietary pattern during pregnancy, consistent with the Dietary Guidelines for Americans (table 5). This includes plenty of fruits and vegetables, whole grains, low-fat dairy, and a variety of proteins. Nutrient-dense foods should be encouraged, and empty calories should be minimized or avoided. The exact amount of foods needed from each food group depends on a combination of factors, including the individual's prepregnancy body mass index (BMI), physical activity level, age (adolescent versus adult), and trimester (first versus second and third trimesters). (See 'General principles of a healthy diet during pregnancy' above.)

Avoiding foodborne infections – Patients should be educated about the risk for and prevention of foodborne infections. (See 'Avoidance of foodborne infections' above.)

Avoiding potentially toxic foods – Certain foods should be limited or avoided during pregnancy because of potentially toxic effects. These include consumption of fish high in mercury or environmental toxins, high-caffeine intake, unwashed fruits/vegetables, unpasteurized dairy and fruit juices products, herbal products, liver-based foods, and undercooked meats. (See 'Guidelines for safe seafood consumption' above and 'Guidelines for safe caffeine intake' above and 'Avoidance of herbal products (except ginger)' above and 'Caution regarding consumption of liver-based foods' above and 'Limiting exposure to environmental toxins' above.)

Patients with self-imposed dietary restrictions – Self-imposed dietary restraints (eg, vegetarian-type diet, gluten-free diet, paleolithic diet) can be problematic if essential nutrients are left out of the diet or weight gain is inadequate. (See 'Issues regarding self-imposed dietary restraints' above and 'Other dietary issues' above.)

Antigen avoidance/ingestion and allergy in offspring – Neither avoidance nor ingestion of specific antigens, such as peanuts, milk, and eggs, during pregnancy impact the frequency of atopic disease in offspring. (See "Primary prevention of allergic disease: Maternal diet in pregnancy and lactation".)

ACKNOWLEDGMENT — The UpToDate editorial staff acknowledges Edmund F Funai, MD, Jonathan Gillen-Goldstein, MD, Henry Roque, MD, MS, and Jean M Ruvel, RD, CDE, CDN who contributed to an earlier version of this topic review.

  1. Feodor Nilsson S, Andersen PK, Strandberg-Larsen K, Nybo Andersen AM. Risk factors for miscarriage from a prevention perspective: a nationwide follow-up study. BJOG 2014; 121:1375.
  2. Shaw GM, Wise PH, Mayo J, et al. Maternal prepregnancy body mass index and risk of spontaneous preterm birth. Paediatr Perinat Epidemiol 2014; 28:302.
  3. Ramakrishnan U, Grant F, Goldenberg T, et al. Effect of women's nutrition before and during early pregnancy on maternal and infant outcomes: a systematic review. Paediatr Perinat Epidemiol 2012; 26 Suppl 1:285.
  4. American College of Obstetricians and Gynecologists. ACOG Committee opinion no. 549: obesity in pregnancy. Obstet Gynecol 2013; 121:213.
  5. Nutrition during pregnancy: Part 1: Weight gain, Part 2: Nutrient supplements. Institute of Medicine. Available at: http://nationalacademies.org/hmd/reports/1990/nutrition-during-pregnancy-part-i-weight-gain-part-ii-nutrient-supplements.aspx (Accessed on April 05, 2016).
  6. Li M, Grewal J, Hinkle SN, et al. Healthy dietary patterns and common pregnancy complications: a prospective and longitudinal study. Am J Clin Nutr 2021; 114:1229.
  7. Marshall NE, Abrams B, Barbour LA, et al. The importance of nutrition in pregnancy and lactation: lifelong consequences. Am J Obstet Gynecol 2022; 226:607.
  8. Carmichael SL, Ma C, Feldkamp ML, et al. Comparing Usual Dietary Intakes Among Subgroups of Mothers in the Year Before Pregnancy. Public Health Rep 2019; 134:155.
  9. Dietary Guidelines for Americans, 2020-2025 9th Edition. U.S. Department of Agriculture and U.S. Department of Health and Human Services, 2020. https://www.dietaryguidelines.gov/sites/default/files/2021-03/Dietary_Guidelines_for_Americans-2020-2025.pdf
  10. Bodnar LM, Simhan HN, Parker CB, et al. Racial or Ethnic and Socioeconomic Inequalities in Adherence to National Dietary Guidance in a Large Cohort of US Pregnant Women. J Acad Nutr Diet 2017; 117:867.
  11. Stephenson J, Heslehurst N, Hall J, et al. Before the beginning: nutrition and lifestyle in the preconception period and its importance for future health. Lancet 2018; 391:1830.
  12. Widen E, Siega-Riz AM. Prenatal nutrition: a practical guide for assessment and counseling. J Midwifery Womens Health 2010; 55:540.
  13. Paxton AE, Ammerman AS, Gizlice Z, et al. Validation of a very brief diet assessment tool designed to guide counseling for chronic disease prevention. Abstract presented at: International Society for Behavior, Nutrition, and Physical Activity, 2007, Oslo, Norway.
  14. Center for Nutrition Policy and Promotion. Nutrients in 2010 USDA food patterns at all calorie levels. http://www.cnpp.usda.gov/sites/default/files/usda_food_patterns/Nutrientsin2010USDAFoodPatternsatAllCalorieLevels.pdf (Accessed on March 25, 2016).
  15. Academy of Nutrition and Dietetics. Practice Paper of the Academy of Nutrition and Dietetics Abstract: Nutrition and Lifestyle for a Healthy Pregnancy Outcome 2014. http://www.eatright.org/members/practicepapers/ (Accessed on March 23, 2016).
  16. Bodnar LM, Petersen JM, Naimi AI, Kirkpatrick SI. Pregnant people in a large United States cohort study do not meet federal nutrition guidelines. Am J Obstet Gynecol MFM 2023; 5:100772.
  17. WHO Expert Consultation. Appropriate body-mass index for Asian populations and its implications for policy and intervention strategies. Lancet 2004; 363:157.
  18. Hsu WC, Araneta MR, Kanaya AM, et al. BMI cut points to identify at-risk Asian Americans for type 2 diabetes screening. Diabetes Care 2015; 38:150.
  19. Holick MF, Binkley NC, Bischoff-Ferrari HA, et al. Evaluation, treatment, and prevention of vitamin D deficiency: an Endocrine Society clinical practice guideline. J Clin Endocrinol Metab 2011; 96:1911.
  20. ACOG Committee on Obstetric Practice. ACOG Committee Opinion No. 495: Vitamin D: Screening and supplementation during pregnancy. Obstet Gynecol 2011; 118:197. Reaffirmed 2019.
  21. Stang J, Huffman LG. Position of the Academy of Nutrition and Dietetics: Obesity, Reproduction, and Pregnancy Outcomes. J Acad Nutr Diet 2016; 116:677.
  22. Cox JT, Phelan ST. Nutrition during pregnancy. Obstet Gynecol Clin North Am 2008; 35:369.
  23. Venkataramani M, Ogunwole SM, Caulfield LE, et al. Maternal, Infant, and Child Health Outcomes Associated With the Special Supplemental Nutrition Program for Women, Infants, and Children : A Systematic Review. Ann Intern Med 2022; 175:1411.
  24. Hinkle SN, Dolin CD, Keddem S, Kinsey EW. Patterns in Food Insecurity During Pregnancy, 2004 to 2020. JAMA Netw Open 2023; 6:e2324005.
  25. Deputy NP, Sharma AJ, Kim SY. Gestational Weight Gain - United States, 2012 and 2013. MMWR Morb Mortal Wkly Rep 2015; 64:1215.
  26. International Weight Management in Pregnancy (i-WIP) Collaborative Group. Effect of diet and physical activity based interventions in pregnancy on gestational weight gain and pregnancy outcomes: meta-analysis of individual participant data from randomised trials. BMJ 2017; 358:j3119.
  27. American College of Obstetricians and Gynecologists. ACOG Committee opinion no. 548: weight gain during pregnancy. Obstet Gynecol 2013; 121:210. Reaffirmed 2023.
  28. Lucas C, Charlton KE, Yeatman H. Nutrition advice during pregnancy: do women receive it and can health professionals provide it? Matern Child Health J 2014; 18:2465.
  29. Whitaker KM, Wilcox S, Liu J, et al. Provider Advice and Women's Intentions to Meet Weight Gain, Physical Activity, and Nutrition Guidelines During Pregnancy. Matern Child Health J 2016; 20:2309.
  30. Vander Wyst KB, Quintana G, Balducci J, Whisner CM. Comparison and Characterization of Prenatal Nutrition Counseling among Large-for-Gestational Age Deliveries by Pre-Pregnancy BMI. Nutrients 2019; 11.
  31. Jafari F, Eftekhar H, Fotouhi A, et al. Comparison of maternal and neonatal outcomes of group versus individual prenatal care: a new experience in Iran. Health Care Women Int 2010; 31:571.
  32. Ickovics JR, Kershaw TS, Westdahl C, et al. Group prenatal care and perinatal outcomes: a randomized controlled trial. Obstet Gynecol 2007; 110:330.
  33. Kominiarek MA, Lewkowitz AK, Carter E, et al. Gestational weight gain and group prenatal care: a systematic review and meta-analysis. BMC Pregnancy Childbirth 2019; 19:18.
  34. Carter EB, Temming LA, Akin J, et al. Group Prenatal Care Compared With Traditional Prenatal Care: A Systematic Review and Meta-analysis. Obstet Gynecol 2016; 128:551.
  35. Davis C, Bryan J, Hodgson J, Murphy K. Definition of the Mediterranean Diet; a Literature Review. Nutrients 2015; 7:9139.
  36. Rosato V, Temple NJ, La Vecchia C, et al. Mediterranean diet and cardiovascular disease: a systematic review and meta-analysis of observational studies. Eur J Nutr 2019; 58:173.
  37. Liyanage T, Ninomiya T, Wang A, et al. Effects of the Mediterranean Diet on Cardiovascular Outcomes-A Systematic Review and Meta-Analysis. PLoS One 2016; 11:e0159252.
  38. Schwingshackl L, Schwedhelm C, Galbete C, Hoffmann G. Adherence to Mediterranean Diet and Risk of Cancer: An Updated Systematic Review and Meta-Analysis. Nutrients 2017; 9.
  39. Esposito K, Maiorino MI, Bellastella G, et al. A journey into a Mediterranean diet and type 2 diabetes: a systematic review with meta-analyses. BMJ Open 2015; 5:e008222.
  40. Petersson SD, Philippou E. Mediterranean Diet, Cognitive Function, and Dementia: A Systematic Review of the Evidence. Adv Nutr 2016; 7:889.
  41. Makarem N, Chau K, Miller EC, et al. Association of a Mediterranean Diet Pattern With Adverse Pregnancy Outcomes Among US Women. JAMA Netw Open 2022; 5:e2248165.
  42. Mijatovic-Vukas J, Capling L, Cheng S, et al. Associations of Diet and Physical Activity with Risk for Gestational Diabetes Mellitus: A Systematic Review and Meta-Analysis. Nutrients 2018; 10.
  43. Raghavan R, Dreibelbis C, Kingshipp BL, et al. Dietary patterns before and during pregnancy and maternal outcomes: a systematic review. Am J Clin Nutr 2019; 109:705S.
  44. Zhang Y, Lin J, Fu W, et al. Mediterranean diet during pregnancy and childhood for asthma in children: A systematic review and meta-analysis of observational studies. Pediatr Pulmonol 2019; 54:949.
  45. Amati F, Hassounah S, Swaka A. The Impact of Mediterranean Dietary Patterns During Pregnancy on Maternal and Offspring Health. Nutrients 2019; 11.
  46. Leitzmann C. Vegetarian diets: what are the advantages? Forum Nutr 2005; :147.
  47. Haddad EH, Tanzman JS. What do vegetarians in the United States eat? Am J Clin Nutr 2003; 78:626S.
  48. Johnston PK, Sabate J. Nutritional implications of vegetarian diets. In: Modern nutrition in health and disease, 10, Shils ME, Shike M, Ross AC, et al (Eds), Lippincott Williams & Wilkins, 2006. p.1638.
  49. Sebastiani G, Herranz Barbero A, Borrás-Novell C, et al. The Effects of Vegetarian and Vegan Diet during Pregnancy on the Health of Mothers and Offspring. Nutrients 2019; 11.
  50. Piccoli GB, Clari R, Vigotti FN, et al. Vegan-vegetarian diets in pregnancy: danger or panacea? A systematic narrative review. BJOG 2015; 122:623.
  51. Melina V, Craig W, Levin S. Position of the Academy of Nutrition and Dietetics: Vegetarian Diets. J Acad Nutr Diet 2016; 116:1970.
  52. Koebnick C, Hoffmann I, Dagnelie PC, et al. Long-term ovo-lacto vegetarian diet impairs vitamin B-12 status in pregnant women. J Nutr 2004; 134:3319.
  53. Cox SR. Staying healthy on a vegetarian diet during pregnancy. J Midwifery Womens Health 2008; 53:91.
  54. Penney DS, Miller KG. Nutritional counseling for vegetarians during pregnancy and lactation. J Midwifery Womens Health 2008; 53:37.
  55. Avnon T, Paz Dubinsky E, Lavie I, et al. The impact of a vegan diet on pregnancy outcomes. J Perinatol 2021; 41:1129.
  56. Tan C, Zhao Y, Wang S. Is a vegetarian diet safe to follow during pregnancy? A systematic review and meta-analysis of observational studies. Crit Rev Food Sci Nutr 2019; 59:2586.
  57. Center for Nutrition Policy and Promotion. Nutrients in 2010 USDA Lacto-Ovo Vegetarian Food Patterns at all calorie levels. http://www.cnpp.usda.gov/sites/default/files/usda_food_patterns/Nutrientsin2010USDALacto-OvoFoodPatternsatAllCalorieLevels.pdf (Accessed on April 05, 2016).
  58. Burns-Whitmore B, Froyen E, Heskey C, et al. Alpha-Linolenic and Linoleic Fatty Acids in the Vegan Diet: Do They Require Dietary Reference Intake/Adequate Intake Special Consideration? Nutrients 2019; 11.
  59. Ganpule A, Yajnik CS, Fall CH, et al. Bone mass in Indian children--relationships to maternal nutritional status and diet during pregnancy: the Pune Maternal Nutrition Study. J Clin Endocrinol Metab 2006; 91:2994.
  60. Drake R, Reddy S, Davies J. Nutrient intake during pregnancy and pregnancy outcome of lacto-ovo-vegetarians, fish-eaters and non-vegetarians. Veg Nutr 1988; 2:45.
  61. Craig WJ, Mangels AR, American Dietetic Association. Position of the American Dietetic Association: vegetarian diets. J Am Diet Assoc 2009; 109:1266.
  62. North K, Golding J. A maternal vegetarian diet in pregnancy is associated with hypospadias. The ALSPAC Study Team. Avon Longitudinal Study of Pregnancy and Childhood. BJU Int 2000; 85:107.
  63. Carmichael SL, Ma C, Feldkamp ML, et al. Nutritional factors and hypospadias risks. Paediatr Perinat Epidemiol 2012; 26:353.
  64. Tersigni C, Castellani R, de Waure C, et al. Celiac disease and reproductive disorders: meta-analysis of epidemiologic associations and potential pathogenic mechanisms. Hum Reprod Update 2014; 20:582.
  65. Lasa JS, Zubiaurre I, Soifer LO. Risk of infertility in patients with celiac disease: a meta-analysis of observational studies. Arq Gastroenterol 2014; 51:144.
  66. Saccone G, Berghella V, Sarno L, et al. Celiac disease and obstetric complications: a systematic review and metaanalysis. Am J Obstet Gynecol 2016; 214:225.
  67. Marcason W. Is there evidence to support the claim that a gluten-free diet should be used for weight loss? J Am Diet Assoc 2011; 111:1786.
  68. Gaesser GA, Angadi SS. Gluten-free diet: imprudent dietary advice for the general population? J Acad Nutr Diet 2012; 112:1330.
  69. Institute of Medicine. Dietary Reference Intakes: The Essential Guide to Nutrient Requirements. Washington, DC. National Academies Press 2006.
  70. Barber TM, Hanson P, Kabisch S, et al. The Low-Carbohydrate Diet: Short-Term Metabolic Efficacy Versus Longer-Term Limitations. Nutrients 2021; 13.
  71. Desrosiers TA, Siega-Riz AM, Mosley BS, et al. Low carbohydrate diets may increase risk of neural tube defects. Birth Defects Res 2018; 110:901.
  72. Shaw GM, Yang W. Women's periconceptional lowered carbohydrate intake and NTD-affected pregnancy risk in the era of prefortification with folic acid. Birth Defects Res 2019; 111:248.
  73. Barry D, Ellul S, Watters L, et al. The ketogenic diet in disease and development. Int J Dev Neurosci 2018; 68:53.
  74. van der Louw EJ, Williams TJ, Henry-Barron BJ, et al. Ketogenic diet therapy for epilepsy during pregnancy: A case series. Seizure 2017; 45:198.
  75. Husari KS, Cervenka MC. The ketogenic diet all grown up-Ketogenic diet therapies for adults. Epilepsy Res 2020; 162:106319.
  76. Sussman D, van Eede M, Wong MD, et al. Effects of a ketogenic diet during pregnancy on embryonic growth in the mouse. BMC Pregnancy Childbirth 2013; 13:109.
  77. Sussman D, Germann J, Henkelman M. Gestational ketogenic diet programs brain structure and susceptibility to depression & anxiety in the adult mouse offspring. Brain Behav 2015; 5:e00300.
  78. Sussman D, Ellegood J, Henkelman M. A gestational ketogenic diet alters maternal metabolic status as well as offspring physiological growth and brain structure in the neonatal mouse. BMC Pregnancy Childbirth 2013; 13:198.
  79. Manheimer EW, van Zuuren EJ, Fedorowicz Z, Pijl H. Paleolithic nutrition for metabolic syndrome: systematic review and meta-analysis. Am J Clin Nutr 2015; 102:922.
  80. Churuangsuk C, Griffiths D, Lean MEJ, Combet E. Impacts of carbohydrate-restricted diets on micronutrient intakes and status: A systematic review. Obes Rev 2019; 20:1132.
  81. Chenard CA, Rubenstein LM, Snetselaar LG, Wahls TL. Nutrient Composition Comparison between a Modified Paleolithic Diet for Multiple Sclerosis and the Recommended Healthy U.S.-Style Eating Pattern. Nutrients 2019; 11.
  82. Manousou S, Stål M, Larsson C, et al. A Paleolithic-type diet results in iodine deficiency: a 2-year randomized trial in postmenopausal obese women. Eur J Clin Nutr 2018; 72:124.
  83. Lavie M, Lavie I, Maslovitz S. Paleolithic diet during pregnancy-A potential beneficial effect on metabolic indices and birth weight. Eur J Obstet Gynecol Reprod Biol 2019; 242:7.
  84. van Ewijk RJ, Painter RC, Roseboom TJ. Associations of prenatal exposure to Ramadan with small stature and thinness in adulthood: results from a large Indonesian population-based study. Am J Epidemiol 2013; 177:729.
  85. Fox HE, Hohler CW, Steinbrecher M. Human fetal breathing movements after carbohydrate ingestion in fasting and nonfasting subjects. Am J Obstet Gynecol 1982; 144:213.
  86. Mirghani HM, Weerasinghe SD, Smith JR, Ezimokhai M. The effect of intermittent maternal fasting on human fetal breathing movements. J Obstet Gynaecol 2004; 24:635.
  87. Abd-El-Aal DE, Shahin AY, Hamed HO. Effect of short-term maternal fasting in the third trimester on uterine, umbilical, and fetal middle cerebral artery Doppler indices. Int J Gynaecol Obstet 2009; 107:23.
  88. Richardson B, Hohimer AR, Mueggler P, Bissonnette J. Effects of glucose concentration on fetal breathing movements and electrocortical activity in fetal lambs. Am J Obstet Gynecol 1982; 142:678.
  89. Schreyer P, Sherman DJ, Ervin MG, et al. Ovine fetal breathing and swallowing activity in response to plasma glucose changes. Gynecol Obstet Invest 1991; 32:15.
  90. Metzger BE, Ravnikar V, Vileisis RA, Freinkel N. "Accelerated starvation" and the skipped breakfast in late normal pregnancy. Lancet 1982; 1:588.
  91. Shahawy S, Al Kassab L, Rattani A. Ramadan fasting and pregnancy: an evidence-based guide for the obstetrician. Am J Obstet Gynecol 2023; 228:689.
  92. Glazier JD, Hayes DJL, Hussain S, et al. The effect of Ramadan fasting during pregnancy on perinatal outcomes: a systematic review and meta-analysis. BMC Pregnancy Childbirth 2018; 18:421.
  93. Schoeps A, van Ewijk R, Kynast-Wolf G, et al. Ramadan Exposure In Utero and Child Mortality in Burkina Faso: Analysis of a Population-Based Cohort Including 41,025 Children. Am J Epidemiol 2018; 187:2085.
  94. Pradella F, Leimer B, Fruth A, et al. Ramadan during pregnancy and neonatal health-Fasting, dietary composition and sleep patterns. PLoS One 2023; 18:e0281051.
  95. Szilagyi A, Salomon R, Martin M, et al. Lactose handling by women with lactose malabsorption is improved during pregnancy. Clin Invest Med 1996; 19:416.
  96. Villar J, Kestler E, Castillo P, et al. Improved lactose digestion during pregnancy: a case of physiologic adaptation? Obstet Gynecol 1988; 71:697.
  97. Standing Committee on the Scientific Evaluation of Dietary Reference Intakes, Food and Nutrition Board of the Institute of Medicine. Dietary reference intakes for calcium, phosphorus, magnesium, vitamin D, and fluoride. 1997.
  98. National Academy of Sciences. Dietary reference intakes: The essential guide to nutrient requirements. Otten JJ, Hellwig JP, Meyers LD (Eds), The National Academies Press, Washington, DC 2006. pp. 530-541.
  99. Recommendations for using fluoride to prevent and control dental caries in the United States. Centers for Disease Control and Prevention. MMWR Recomm Rep 2001; 50:1.
  100. Sá Roriz Fonteles C, Zero DT, Moss ME, Fu J. Fluoride concentrations in enamel and dentin of primary teeth after pre- and postnatal fluoride exposure. Caries Res 2005; 39:505.
  101. Leverett DH, Adair SM, Vaughan BW, et al. Randomized clinical trial of the effect of prenatal fluoride supplements in preventing dental caries. Caries Res 1997; 31:174.
  102. Takahashi R, Ota E, Hoshi K, et al. Fluoride supplementation (with tablets, drops, lozenges or chewing gum) in pregnant women for preventing dental caries in the primary teeth of their children. Cochrane Database Syst Rev 2017; 10:CD011850.
  103. Hellwig E, Lennon AM. Systemic versus topical fluoride. Caries Res 2004; 38:258.
  104. Limeback H. A re-examination of the pre-eruptive and post-eruptive mechanism of the anti-caries effects of fluoride: is there any anti-caries benefit from swallowing fluoride? Community Dent Oral Epidemiol 1999; 27:62.
  105. Gupta S, Seth AK, Gupta A, Gavane AG. Transplacental passage of fluorides. J Pediatr 1993; 123:139.
  106. US Department of Health and Human Services. Public Health Service. Agnecy for Toxic Substances and Disease Registry. Toxicological Profile for Fluorides, Hydrogen Fluoride, and Fluorine. September 2003. Available at https://www.atsdr.cdc.gov/toxprofiles/tp11.pdf.
  107. Green R, Lanphear B, Hornung R, et al. Association Between Maternal Fluoride Exposure During Pregnancy and IQ Scores in Offspring in Canada. JAMA Pediatr 2019; 173:940.
  108. Bashash M, Marchand M, Hu H, et al. Prenatal fluoride exposure and attention deficit hyperactivity disorder (ADHD) symptoms in children at 6-12 years of age in Mexico City. Environ Int 2018; 121:658.
  109. Bashash M, Thomas D, Hu H, et al. Prenatal Fluoride Exposure and Cognitive Outcomes in Children at 4 and 6-12 Years of Age in Mexico. Environ Health Perspect 2017; 125:097017.
  110. Choi AL, Zhang Y, Sun G, et al. Association of lifetime exposure to fluoride and cognitive functions in Chinese children: a pilot study. Neurotoxicol Teratol 2015; 47:96.
  111. Bellinger DC. Is Fluoride Potentially Neurotoxic? JAMA Pediatr 2019; 173:915.
  112. US Food and Drug Administration. Additional Information about High-Intensity Sweeteners Permitted for Use in Food in the United States. https://www.fda.gov/food/food-additives-petitions/additional-information-about-high-intensity-sweeteners-permitted-use-food-united-states (Accessed on February 21, 2020).
  113. Palatnik A, Moosreiner A, Olivier-Van Stichelen S. Consumption of non-nutritive sweeteners during pregnancy. Am J Obstet Gynecol 2020; 223:211.
  114. Malek AM, Hunt KJ, DellaValle DM, et al. Reported Consumption of Low-Calorie Sweetener in Foods, Beverages, and Food and Beverage Additions by US Adults: NHANES 2007-2012. Curr Dev Nutr 2018; 2:nzy054.
  115. Sylvetsky AC, Figueroa J, Rother KI, et al. Trends in Low-Calorie Sweetener Consumption Among Pregnant Women in the United States. Curr Dev Nutr 2019; 3:nzz004.
  116. Pope E, Koren G, Bozzo P. Sugar substitutes during pregnancy. Can Fam Physician 2014; 60:1003.
  117. Azad MB, Sharma AK, de Souza RJ, et al. Association Between Artificially Sweetened Beverage Consumption During Pregnancy and Infant Body Mass Index. JAMA Pediatr 2016; 170:662.
  118. Ali F. Consumption of artificial sweeteners in pregnancy increased overweight risk in infants. Arch Dis Child Educ Pract Ed 2017; 102:277.
  119. Archibald AJ, Dolinsky VW, Azad MB. Early-Life Exposure to Non-Nutritive Sweeteners and the Developmental Origins of Childhood Obesity: Global Evidence from Human and Rodent Studies. Nutrients 2018; 10.
  120. Mullie P, Clarys P. Consumption of artificially sweetened beverages during pregnancy is associated with a twofold higher risk of infant being overweight at 1 year. Evid Based Nurs 2017; 20:11.
  121. Zhu Y, Olsen SF, Mendola P, et al. Maternal consumption of artificially sweetened beverages during pregnancy, and offspring growth through 7 years of age: a prospective cohort study. Int J Epidemiol 2017; 46:1499.
  122. Englund-Ögge L, Brantsæter AL, Haugen M, et al. Association between intake of artificially sweetened and sugar-sweetened beverages and preterm delivery: a large prospective cohort study. Am J Clin Nutr 2012; 96:552.
  123. Maslova E, Strøm M, Olsen SF, Halldorsson TI. Consumption of artificially-sweetened soft drinks in pregnancy and risk of child asthma and allergic rhinitis. PLoS One 2013; 8:e57261.
  124. Gamba RJ, Leung CW, Petito L, et al. Sugar sweetened beverage consumption during pregnancy is associated with lower diet quality and greater total energy intake. PLoS One 2019; 14:e0215686.
  125. Borgen I, Aamodt G, Harsem N, et al. Maternal sugar consumption and risk of preeclampsia in nulliparous Norwegian women. Eur J Clin Nutr 2012; 66:920.
  126. Halldorsson TI, Strøm M, Petersen SB, Olsen SF. Intake of artificially sweetened soft drinks and risk of preterm delivery: a prospective cohort study in 59,334 Danish pregnant women. Am J Clin Nutr 2010; 92:626.
  127. Gillman MW, Rifas-Shiman SL, Fernandez-Barres S, et al. Beverage Intake During Pregnancy and Childhood Adiposity. Pediatrics 2017; 140.
  128. FoodSafety.gov. People at Risk: Pregnant Women. https://www.foodsafety.gov/people-at-risk/pregnant-women (Accessed on April 20, 2021).
  129. US Food and Drug Administration. Eating Fish: What Pregnant Women and Parents Should Know http://www.fda.gov/Food/FoodborneIllnessContaminants/Metals/ucm393070.htm (Accessed on January 19, 2017).
  130. Spogen D, Passalacqua B. Evidence-Based Practice 2008; 11:5. http://www.fpin.org/wp/wp-content/uploads/2014/10/759-EBP-December-2008.pdf (Accessed on June 22, 2015).
  131. http://www.fda.gov/downloads/Food/GuidanceRegulation/UCM252393.pdf (Accessed on January 19, 2017).
  132. Marcus DM, Snodgrass WR. Do no harm: avoidance of herbal medicines during pregnancy. Obstet Gynecol 2005; 105:1119.
  133. Friedman JM. Teratology society: presentation to the FDA public meeting on safety issues associated with the use of dietary supplements during pregnancy. Teratology 2000; 62:134.
  134. Muñoz Balbontín Y, Stewart D, Shetty A, et al. Herbal Medicinal Product Use During Pregnancy and the Postnatal Period: A Systematic Review. Obstet Gynecol 2019; 133:920.
  135. Fugh-Berman A. Herbal medicinals: selected clinical considerations, focusing on known or potential drug-herb interactions. Arch Intern Med 1999; 159:1957.
  136. Buehler BA. Interactions of herbal products with conventional medicines and potential impact on pregnancy. Birth Defects Res B Dev Reprod Toxicol 2003; 68:494.
  137. Facchinetti F, Pedrielli G, Benoni G, et al. Herbal supplements in pregnancy: unexpected results from a multicentre study. Hum Reprod 2012; 27:3161.
  138. Mabina MH, Pitsoe SB, Moodley J. The effect of traditional herbal medicines on pregnancy outcome. The King Edward VIII Hospital experience. S Afr Med J 1997; 87:1008.
  139. Jones TK, Lawson BM. Profound neonatal congestive heart failure caused by maternal consumption of blue cohosh herbal medication. J Pediatr 1998; 132:550.
  140. Ernst E. Herbal medicinal products during pregnancy: are they safe? BJOG 2002; 109:227.
  141. Trabace L, Tucci P, Ciuffreda L, et al. "Natural" relief of pregnancy-related symptoms and neonatal outcomes: above all do no harm. J Ethnopharmacol 2015; 174:396.
  142. Broussard CS, Louik C, Honein MA, et al. Herbal use before and during pregnancy. Am J Obstet Gynecol 2010; 202:443.e1.
  143. Louik C, Gardiner P, Kelley K, Mitchell AA. Use of herbal treatments in pregnancy. Am J Obstet Gynecol 2010; 202:439.e1.
  144. Chung S, Yeh T, Wu CH. Trend and pattern of herb and supplement use among pregnant women in the United States: findings from the 2002, 2007, and 2012 US National Health Interview Surveys. Am J Obstet Gynecol 2017; 216:189.
  145. Holst L, Wright D, Haavik S, Nordeng H. Safety and efficacy of herbal remedies in obstetrics-review and clinical implications. Midwifery 2011; 27:80.
  146. Conover EA. Herbal agents and over-the-counter medications in pregnancy. Best Pract Res Clin Endocrinol Metab 2003; 17:237.
  147. Li L, Dou L, Leung PC, et al. Chinese herbal medicines for unexplained recurrent miscarriage. Cochrane Database Syst Rev 2016; :CD010568.
  148. Dante G, Pedrielli G, Annessi E, Facchinetti F. Herb remedies during pregnancy: a systematic review of controlled clinical trials. J Matern Fetal Neonatal Med 2013; 26:306.
  149. Bowman R, Taylor J, Muggleton S, Davis D. Biophysical effects, safety and efficacy of raspberry leaf use in pregnancy: a systematic integrative review. BMC Complement Med Ther 2021; 21:56.
  150. Hemmatzadeh S, Mohammad Alizadeh Charandabi S, Veisy A, Mirghafourvand M. Evening primrose oil for cervical ripening in term pregnancies: a systematic review and meta-analysis. J Complement Integr Med 2023; 20:328.
  151. ACOG Committee Opinion No. 575. Exposure to toxic environmental agents. Obstet Gynecol 2013; 122:931. Reaffirmed 2018.
  152. Kordas K. Iron, Lead, and Children's Behavior and Cognition. Annu Rev Nutr 2010; 30:123.
  153. Companion piece to Committee Opinion #575, exposure to toxic environmental agents. www.acog.org/goto/underserved (Accessed on April 15, 2016).
  154. Giuliani A, Zuccarini M, Cichelli A, et al. Critical Review on the Presence of Phthalates in Food and Evidence of Their Biological Impact. Int J Environ Res Public Health 2020; 17.
  155. Council On Environmental Health. Pesticide exposure in children. Pediatrics 2012; 130:e1757.
  156. Setting tolerances for pesticide residues in food. US Environmental Protection Agency. Updated March 14, 2016. http://www2.epa.gov/pesticide-tolerances/setting-tolerances-pesticide-residues-foods (Accessed on April 15, 2016).
  157. Smith-Spangler C, Brandeau ML, Hunter GE, et al. Are organic foods safer or healthier than conventional alternatives?: a systematic review. Ann Intern Med 2012; 157:348.
  158. Minimizing pesticide residues in food. National Pesticide Information Center. http://npic.orst.edu/health/foodprac.html (Accessed on October 22, 2021).
Topic 130920 Version 16.0

References

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