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. 2021 Oct 4;26(2):328–341. doi: 10.1007/s10995-021-03232-1

Correlates of Early Prenatal Care Access among U.S. Women: Data from the Pregnancy Risk Assessment Monitoring System (PRAMS)

Rebecca A Krukowski 1,, Lisette T Jacobson 2, Jemima John 3, Patricia Kinser 4, Kendra Campbell 5, Tracey Ledoux 6, Kara L Gavin 7, Chi-Yang Chiu 1, Jiajang Wang 1, Abbey Kruper 8
PMCID: PMC8488070  PMID: 34606031

Abstract

Objectives

Early first trimester prenatal counseling could reduce adverse maternal and child health outcomes. Existing literature does not identify the length of time between suspecting pregnancy and attending their first prenatal visit. Identifying this potential window for change is critical for clinical practice, intervention programming and policy change.

Methods

The study sample was composed of women in the United States who responded to the Pregnancy Risk Assessment Monitoring Systems survey in 2016, for the following questions—when they first suspected pregnancy, when they attended their first prenatal visit, were they able to receive prenatal care as early as they wished, and perceived barriers to receiving prenatal care.

Results

On average, participants became certain they were pregnant at 6.0 (SE = 0.1) weeks gestation, while participants reported having their first prenatal care visit at 9.3 (SE = 0.1) weeks, with clear health disparities by race, age, WIC participation, education level, and marital status. About 15% of women reported not receiving prenatal care as early as they wished. Structural or financial barriers in the health care system were common: 38.1% reported that no appointments available, 28.2% reported not having money or insurance to pay for the visit, 27.3% reported that the doctor or health plan would not start care, and 22.5% reported not having a Medicaid card.

Conclusions for Practice

This study illustrates a window for opportunity to provide earlier prenatal care, which would facilitate earlier implementation of prenatal counseling. Strategies to address barriers to care on the patient, provider and systemic levels, particularly among vulnerable population groups, are warranted.

What is already known on this subject?

Seeking prenatal care early is associated with better health outcomes for women and infants. A window of opportunity exists between suspecting pregnancy and attending a first prenatal visit.

What this study adds?

Clear health disparities were apparent in both recognizing their pregnancies, and receiving early prenatal care by race, age, WIC participation, education level, and marital status. About 15% of women reported not receiving prenatal care as early as they wished, and many attributed this later care to structural or financial barriers in the health care system.

Keywords: PRAMS, Pregnancy, Prenatal care, Barriers, Sociodemographic characteristics

Introduction

In the United States, the number of reported maternal pregnancy-related deaths has increased from 7.2 deaths per 100,000 live births in 1987 to 18.0 deaths per 100,000 live births in 2014 (Centers for Disease Control & Prevention, 2019b). This increase may be due in part to increased identification and reporting of maternal deaths, and it may also be due to an increasing number of pregnant women in the U.S. who suffer from chronic health conditions, including hypertension (Kuklina et al., 2009), diabetes (Albrecht et al., 2010), and chronic heart disease (Kuklina & Callaghan, 2011), which increase the likelihood of pregnancy complications and maternal morbidity. Moreover, significant racial and ethnic disparities in pregnancy-related mortality exist with 40.0 deaths per 100,000 live births for Black women and 17.8 deaths per 100,000 live births for women of other races/ethnicities compared to 12.4 deaths per 100,000 live births for white women (Centers for Disease Control & Prevention, 2019b). Prenatal care is essential to optimize women’s and infants’ health outcomes (Academy & of Pediatrics Committee on Fetus & Newborn, 2012). Early prenatal care facilitates appropriate screening for medical conditions and fetal anomalies (American Academy of Pediatrics Committee on Fetus and Newborn, 2012); timely provision of gestational weight gain guidelines (Goldstein et al., 2017); and receipt of education and counseling services on health enhancing behaviors (e.g. getting adequate exercise, eating a balanced diet, use of prenatal vitamins, quitting smoking and eliminating alcohol consumption (Moos et al., 2008).

Early prenatal care presents a critical window for changes to personal and systemic factors that may compromise the health of women and infants. Despite evidence of the positive impact of these health enhancing behaviors on favorable maternal and child health outcomes and about 77% of women initiating prenatal care in the first trimester (Michelle & Osterman, 2016), notable disparities in prenatal care access persist among U.S. women, particularly among younger, less educated, geographically isolated, and racial/ethnic-minority maternal populations (Michelle & Osterman, 2016). Furthermore, although it is well-established that seeking early prenatal care is associated with better health outcomes for women and infants (Stulberg et al., 2017; Yan, 2017), existing literature does not identify the specific time point in pregnancy at which women typically attend their first prenatal visit or the length of time between suspecting pregnancy and attending their first prenatal visit (i.e. the potential window for change). Understanding typical timing along with barriers to accessing early prenatal care is vital for implementing best practice recommendations as well as potential systemic changes aimed at improving health outcomes.

Thus, our study aimed to address these gaps in the literature by determining when women in the 2016 Pregnancy Risk Assessment Monitoring Systems dataset first suspected pregnancy, when they attended their first prenatal visit, and their perceptions around prenatal care initiation (i.e. were they able to receive prenatal care as early as they wished?). Additionally, we examined the prevalence of perceived barriers (e.g. health care system, finances, scheduling, childcare) to receiving prenatal care as early as they wished. In doing so, our study can inform prenatal care policies and clinical practice in racially, ethnically and socioeconomically diverse populations.

Methods

Data from the 2016 PRAMS state-level datasets were aggregated prior to analysis. The goal of PRAMS national surveillance project is to monitor maternal health, identify at-risk populations, and understand the impact of health attitudes, behaviors and experiences in order to better inform and improve maternal and infant care (Centers for Disease Control & Prevention, 2019a). Using stratified sampling, women who delivered a live baby in the previous two to four months are randomly selected from state birth certificate records for participation in PRAMS. Selected individuals are initially contacted via a mailed survey, and by phone if there is no initial response, and all participants received a written informed consent statement. Standardized data collection procedures and measures allow comparisons among states. All states administered the core questions, and a subset of states administered each standard question. For a thorough description of PRAMS study methods, see (Shulman et al., 2006).

Measures

Maternal characteristics obtained from the birth certificate data included ethnicity, race, marital status, educational attainment, maternal age, and participation in the Nutrition Program for Women, Infants, and Children (WIC). All other variables were collected from the PRAMS questionnaire data. Using self-reported anthropometric data (i.e. height, pre-pregnancy weight), a pre-pregnancy body mass index (BMI) variable was created using the standard formula for BMI. A categorical BMI variable was then created using the National Institutes of Health, Heart, Lung, and Blood Institute BMI categories of underweight (< 18.5 kg/m2), normal (18.5–24.9 kg/m2), overweight (25.0–29.9 kg/m2) and obese (≥ 30.0 kg/m2).

Gestational age at first prenatal care visit was measured by the core question, “How many weeks or months pregnant were you when you had your first visit for prenatal care?” with data available from 26 states (i.e. Alaska, Arkansas, Colorado, Delaware, Iowa, Illinois, Louisiana, Massachusetts, Maryland, Maine, Michigan, Missouri, New Hampshire, New Jersey, New Mexico, New York, Oklahoma, Pennsylvania, Rhode Island, Texas, Utah, Vermont, Washington, Wisconsin, West Virginia, and Wyoming) and New York City. Gestational age at pregnancy confirmation was measured by the standard question, “How many weeks or months pregnant were you when you were sure you were pregnant? For example, you had a pregnancy test or a doctor, nurse or other health worker said you were pregnant” with data available from four states (i.e. Delaware, Maine, New Jersey and Oklahoma). Satisfaction with timing of first prenatal care visit was measured by the standard question, “Did you get prenatal care as early in your pregnancy as you wanted?” with data available from 12 states (i.e. Alaska, Delaware, Illinois, Louisiana, Maine, Michigan, Missouri, New Jersey, New Mexico, Pennsylvania, Texas, and Wisconsin). Barriers to receiving early prenatal care were assessed via “yes” or “no” responses to the following prompts: “Did any of these things keep you from getting prenatal care when you wanted it? 1) I couldn’t get an appointment when I wanted one; 2) I didn’t have enough money or insurance to pay for my visits; 3) I didn’t have any transportation to get to the clinic or doctor’s office; 4) The doctor or my health plan would not start care as early as I wanted; 5) I had too many other things going on; 6) I couldn’t take time off from work or school; 7) I didn’t have my Medicaid card; 8) I didn’t have anyone to take care of my children; 9) I didn’t know that I was pregnant; 10) I didn’t want anyone else to know I was pregnant; and 11) I didn’t want prenatal care.” Multiple items could be selected. Data were available for this question from 11 states (i.e. Arkansas, Delaware, Illinois, Louisiana, Michigan, Missouri, New Jersey, New Mexico, Pennsylvania, Texas, and Wisconsin).

Sample

The study sample was composed of women who responded to the PRAMS survey in 2016, for each question that had data available for release. PRAMS had a 55% minimum overall response rate threshold policy for the release of 2016 data. The weighted response rate for the included states ranged from 54.6% to 72.5%. The study was determined to be exempt from University of Tennessee Health Science Center Institutional Review Board approval because no identifiable private information was utilized and have therefore been performed in accordance with the ethical standards laid down in the 1964 Declaration of Helsinki and its later amendments.

Data Analysis and Statistical Methods

Data were analyzed using SAS version 9.4 with survey procedures. In univariate analyses, differences of marginal means and 95% Confidence Intervals (CIs) were generated through one-way ANOVA models; odds ratios and 95% CIs were generated through simple logistic regression. Multiple linear and logistic regression models were used to determine significant factors of continuous and binary outcomes, respectively. Missing data were handled using pairwise deletion. All tests were 2-sided, and significance was set at P < 0.05.

Results

The sample included 31,642 women. Most women were 18–34 years of age, were non-Hispanic white, were married, had at least one previous live birth, and had a high school degree or higher (Table 1).

Table 1.

Socio-demographic Characteristics

Characteristic Mean (Standard Deviation) or Na (%)b
Race
 White 18,616 (71.1%)
 Black 5565 (13.5%)
 Asian (Chinese, Japanese, Filipino, other Asian) 1941 (6.0%)
 Native North American (American Indian, Hawaiian, Alaskan native) 1219 (0.9%)
Other races 1685 (5.9%)
 Mixed race 1310 (2.6%)
Hispanic 6193 (23.9%)
Age (years)
  < 18 456 (1.5%)
 18–24 7335 (22.4%)
 25–34 18,232 (58.6%)
 ≥ 35 5619 (17.4%)
Nutrition program for Women, Infant and Child participation
 No 18,507 (61.3%)
 Yes 12,619 (38.7%)
Maternal years of education
  < 8th grade 996 (3.4%)
 9–12th grade 3313 (10.3%)
 High school graduate/GED 7744 (24.4%)
 Some college/Associate degree 8725 (26.3%)
 Bachelor’s degree or higher 10,448 (35.6%)
Number of previous live births
 0 12,428 (38.2%)
 1–2 15,155 (50.2%)
 ≥ 3 3991(11.6%)
Married 18,942 (61.9%)
Pre-pregnancy BMI (kg/m2) 26.7 (0.06)
Pregnancy BMI category
 Underweight (< 18.5) 1113 (3.6%)
 Normal (18.5–24.9) 14,113 (47.7%)
 Overweight (25–29.9) 7503 (25.5%)
 Obese (≥ 30) 7471 (23.2%)

a Number of women from unweighted sample distribution

b Percentages were weighted to account for deliberate survey oversampling and nonresponse and non-coverage

BMI Body Mass Index

Gestational Age When Certain of Pregnancy

Participants (n = 4677) from four states (i.e. Delaware, Maine, New Jersey, and Oklahoma) responded to when they were certain they were pregnant. Eighty-five percent of respondents were certain they were pregnant at 8 weeks gestation or before (Table 2). On average, participants became certain they were pregnant at 6.0(SE = 0.1), median = 4.5(SE = 0.1) weeks gestation. Significant differences were detected in gestation weeks when certain of pregnancy by race, ethnicity, age, WIC participation, education level, number of previous births and marital status (Table 3). Women who identified as white became aware of their pregnancies significantly earlier (mean(SE) = 5.7(0.1) weeks) than women who identified as Black and Native North American (mean(SE) = 7.2(0.3) weeks and mean(SE) = 7.0(0.3) weeks, respectively). Women who identified as Hispanic reported pregnancy certainty significantly later (mean(SE) = 6.6(0.2) weeks) compared to women who did not identify as Hispanic (mean(SE) = 5.9(0.1) weeks). Women who were receiving WIC benefits were certain of pregnancy significantly later (mean(SE) = 6.6(0.1) weeks) than women who were not (mean(SE) = 5.7(0.1) weeks). Younger women (i.e. 24 years or younger) were certain of their pregnancy significantly later than women who were 35 years or older. In addition, women who reported education levels less than a bachelor’s degree were certain of their pregnancy significantly later than women with a bachelor’s degree. Women who had no previous births or 1–2 previous births were certain of their pregnancy earlier than women with 3 or more previous births. Women who were not married were certain of their pregnancy significantly later (mean(SE) = 7.1(0.2) weeks) than women who were married (mean(SE) = 5.4(0.1) weeks). However, no significant differences were detected in timing of pregnancy certainty by BMI category. In a multiple linear regression model (including all covariates), characteristics significantly associated with the timing of being certain of pregnancy were race, age, education, number of previous births, marital status, and BMI category (Table 4).

Table 2.

The number of weeks pregnant when participants were certain they were pregnant and when they had their first prenatal visit with a healthcare provider

Characteristic Na (%)b
Gestational age when certain of pregnancy
 ≤ 8 weeks 3902 (85.1%)
 9–13 weeks 569 (11.2%)
 14–27 weeks 174 (2.8%)
 ≥ 28 weeks 32 (0.9%)
Gestational age at 1st prenatal visit
 ≤ 8 weeks 19,486 (64.1%)
 9–13 weeks 8724 (28.4%)
 14–27 weeks 2159 (6.9%)
 ≥ 28 weeks 218(0.7%)

a Number of women from unweighted sample distribution

b Percentages were weighted to account for deliberate survey oversampling and nonresponse and non-coverage

Table 3.

Sociodemographic Characteristics associated with Gestational Age When Certain of Pregnancy and at First Prenatal Visit

Gestational Age when Certain of Pregnancy (weeks) Gestational Age at First Prenatal Visit (weeks)
Weighted Mean (SE) Difference of Marginal Means
(95% CI)
Weighted Mean (SE) Difference of Marginal Means
(95% CI)
Race
 White (ref) 5.7 (0.1) 8.9 (0.1)
 Black 7.2 (0.3) 1.5 (0.9, 2.0) 10.1 (0.4) 1.2 (0.4, 2.0)
 Asian 5.6 (0.3) -0.1 (-0.7, 0.4) 10.9 (0.6) 2.0 (0.8, 3.2)
 Native North American 7.0 (0.3) 1.3 (0.7, 1.9) 10.1 (0.4) 1.2 (0.3, 2.1)
 Other race 6.3 (0.3) 0.6 (0.0, 1.1) 9.5 (0.3) 0.5 (0.0, 1.1)
 Mixed race 7.0 (0.6) 1.3 (0.0, 2.6) 9.6 (0.5) 0.7 (-0.3, 1.6)
Ethnicity
 Non-Hispanic (ref) 5.9 (0.1) 9.1 (0.1)
 Hispanic 6.6 (0.2) 0.7 (0.3, 1.1) 9.6 (0.2) 0.5 (0.0, 0.9)
Maternal Age
  < 18 10.5 (1.0) 4.8 (2.8, 6.7) 17.6 (2.4) 9.1 (4.5, 13.8)
 18–24 6.8 (0.2) 1.0 (0.5, 1.6) 10.6 (0.3) 2.2 (1.6, 2.7)
 25–34 5.7 (0.1) 0.0 (-0.5, 0.4) 8.8 (0.1) 0.3 (0.0, 0.7)
 ≥ 35 (ref) 5.8 (0.2) 8.4 (0.2)
Nutrition program for Women, Infant and Child participation
 Yes 6.6 (0.1) 0.9 (0.6, 1.3) 9.9 (0.2) 1.0 (0.6, 1.4)
 No (ref) 5.7 (0.1) 8.8 (0.1)
Education
  < High school degree 7.7 (0.4) 2.6 (1.9, 3.4) 11.9 (0.4) 4.1 (3.2, 4.9)
 High school graduate/GED 6.7 (0.2) 1.7 (1.2, 2.1) 10.2 (0.2) 2.4 (1.9, 2.8)
 Some college/associate degree 6.0 (0.1) 0.9 (0.6, 1.3) 8.8 (0.1) 1.0 (0.7, 1.3)
 ≥ Bachelor's degree (ref) 5.0 (0.1) 7.8 (0.1)
Previous Births
 0 births 5.8 (0.1) -1.1 (-1.7, -0.5) 9.0 (0.2) -1.8 (-2.5, -1.2)
 1–2 births 6.0 (0.1) -0.9 (-1.6, -0.3) 9.0 (0.1) -1.9 (-2.5, -1.2)
  ≥ 3 births (ref) 6.9 (0.3) 10.9 (0.3)
Marital Status
 Married (ref) 5.4 (0.1) 8.4 (0.1)
 Not married 7.1 (0.2) 1.7 (1.3, 2.0) 10.6 (0.2) 2.1 (1.7, 2.6)
Weight Status
 Underweight 6.7 (0.4) 0.7 (-0.1, 1.5) 9.8 (0.4) 0.7 (-0.1, 1.4)
 Normal Weight (ref) 5.9 (0.1) 9.1 (0.1)
 Overweight 5.5 (0.1) -0.4 (-0.8, 0.0) 9.2 (0.2) 0.1 (-0.4, 0.6)
 Obese 6.4 (0.2) 0.4 (-0.1, 0.9) 9.3 (0.2) 0.2 (-0.3, 0.7)

Bold text indicates the difference between the level of interest and the reference is significant with 95% confidence

Table 4.

Multiple Linear Regression Model of Sociodemographic Characteristics associated with Gestational Age When Certain of Pregnancy and at First Prenatal Visit

Gestational Age when Certain of Pregnancy (weeks) Gestational Age at First Prenatal Visit (weeks)
Estimated Regression Coefficient (95% CI) Tests of Model Effectsa Estimated Regression Coefficient (95% CI) Tests of Model Effectsa
Race
 White (ref) 0.010 0.001
 Black 0.9(0.3, 1.5) − 0.1(− 0.8, 0.5)
 Asian 0.6(0, 1.2) 2.8(1.5, 4.0)
 Native North American 0.8(0.2, 1.4) − 0.1(− 1.2, 1.0)
 Other race 0.1(− 0.7, 0.5) − 0.4(− 1.1, 0.3)
 Mixed race 0.9(− 0.4, 2.1) 0.1(− 0.9, 1.1)
Ethnicity
 Non-Hispanic (ref) 0.671 0.222
 Hispanic 0.1(− 0.5, 0.7) − 0.3(− 0.9, 0.2)
 Maternal Age
  < 18 3.6(1.6, 5.5) 0.001 7.8(2.9, 12.8)  < 0.001
 18–24 0.3(− 0.3, 1.0) 1.7(1.1, 2.3)
 25–34 − 0.1(− 0.6, 0.4) 0.5(0.1, 0.8)
  > 35 (ref)
Nutrition Program for Women, Infant and Child Participation
 Yes − 0.4(− 1.0, 0.2) 0.151 − 0.8(− 1.3, − 0.3) 0.003
 No (ref)
Education
  < High school degree 1.9(0.8, 3.0)  < 0.001 2.9(2.0, 3.9)  < 0.001
 High school graduate/GED 1.2(0.5, 2.0) 1.8(1.2, 2.3)
 Some college/associate degree 0.6(0.2, 1.0) 0.7(0.3, 1.1)
   ≥ Bachelor's degree (ref)
Previous Births
 0 births − 1.0(− 1.6, − 0.4) 0.002 − 2.0(− 2.6, − 1.4)  < 0.001
 1–2 births − 0.6(− 1.2, 0.1) − 1.6(− 2.2, − 1.0)
  ≥ 3 births (ref)
Marital Status
 Married (ref) 0.001  < 0.001
 Not married 0.8(0.3, 1.3) 1.2(0.8, 1.7)
Weight Status
 Underweight 0.2(− 0.5,1.0) 0.002 − 0.5(− 1.4, 0.4) 0.573
 Normal Weight (ref)
 Overweight − 0.6(− 1.0,− 0.2) − 0.1(− 0.6, 0.3)
 Obese 0.1(− 0.5,0.6) 0.1(− 0.4, 0.6)

Bold text indicates the difference between the level of interest and the reference is significant with 95% confidence

aP value based on F-test for Type 3 Analysis of Effects

Gestation Age at First Prenatal Care Visit

Sixty-four percent of respondents received prenatal care prior to 8 weeks gestation, and 28% of women received prenatal care between 9 and 13 weeks gestation (Table 2). On average, participants reported having their first prenatal care visit at 9.3 (SE = 0.1, median = 7.3(SE = 0.0) weeks gestation (data from 26 states and New York City, n = 30,087). With a similar pattern of results to the certainty of pregnancy data, significant differences were shown in gestation weeks at which prenatal care was received by race, age, WIC participation, education level, number of previous births and marital status (Table 3). Women who identified as white received prenatal care significantly earlier (mean(SE) = 8.9(0.1) weeks) than women who identified as Black and Native North American (mean(SE) = 10.1(0.4) weeks and mean(SE) = 10.1(0.4) weeks, respectively). Women who were participating in WIC received prenatal care significantly later (mean(SE) = 9.9(0.2) weeks) than women who were not (mean(SE) = 8.8(0.1) weeks). Women who were 24 years or younger received prenatal care significantly later than women who were 35 years or older. In addition, women who reported education levels less than a bachelor’s degree received prenatal care significantly later than women with a bachelor’s degree. Women who had 3 or more previous births received prenatal care significantly earlier than women who had no previous births or 1–2 previous births. Women who were not married received prenatal care significantly later (mean(SE) = 10.6(0.2) weeks) than women who were married (mean(SE) = 8.4(0.1) weeks). Finally, no significant differences were detected in timing of prenatal care by ethnicity or BMI category. In a multiple linear regression model (including all covariates), characteristics significantly associated with gestational age at first prenatal care visit were race, age, WIC participation, education, number of previous births, and marital status (Table 4).

Predictors of Not Getting Prenatal Care as Early as Desired

Participants (n = 14,330) in 12 states comprised the sample responding to whether they received prenatal care as early as they wished. While 84.8% (n = 12,164) of women received prenatal care as early in their pregnancy as they wanted, 15.2% of women (n = 2166) did not. Women who received prenatal care as early as they wanted reported they received care at mean(SE) = 7.7(0.1) weeks, after being sure they were pregnant at mean(SE) = 5.4(0.1) weeks. In comparison, women who did not receive prenatal care as early as they wanted reported they received care at mean(SE) = 12.8(0.2) weeks, after being sure they were pregnant at mean(SE) = 8.3(0.4) weeks. Clear differences across race, ethnicity, age, education, WIC participation, number of previous births, marital status, and weight status were observed (Table 5). Specifically, in the univariate analyses, Black women, Native North American, women of other races, Hispanic women, women younger than 24 years old, women participating in WIC, women with less than a bachelor’s degree, women with 1–2 previous births, women who were unmarried, and women with underweight were significantly more likely to report not receiving prenatal care as early as they wanted. In a multiple logistic regression model (including all covariates), characteristics associated with reporting not getting prenatal care as early as desired were ethnicity, age, education, number of previous births, and marital status (Table 6).

Table 5.

Socio-demographic Characteristics by Receiving Prenatal Care as Early as would have Liked or Not

Characteristic Received Prenatal Care as Early as would have Like
Na (%)b
Did not Receive Prenatal Care as Early as would have Liked
N (%)
Race
 White 7549 (61.7%) 1156 (10.4%)
 Black 2450 (11.6%) 540 (2.4%)

 Asian (Chinese, Japanese, Filipino, other

Asian)

691 (4.4%) 106 (0.6%)
 Native North American (American Indian, Hawaiian, Alaskan native) 389 (0.6%) 133 (0.2%)
 Other races 421 (4.4%) 104 (1.3%)
 Mixed race 487 (2.0%) 100 (0.3%)
Ethnicity
 Hispanic 1955 (20.9%) 412 (5.0%)
 Non-Hispanic 10,150 (63.9%) 1740 (10.2%)
Age (years)
  < 18 170 (1.1%) 63 (0.5%)
 18–24 2728 (18.4%) 695 (5.3%)
 25–34 7186 (51.2%) 1132 (7.6%)
  ≥ 35 2080 (14.0%) 276 (1.8%)
Nutrition program for Women, Infant and Child participation
 Yes 4525 (31.5%) 1027 (7.1%)
 No 7459 (53.3%) 1106 (8.1%)
Maternal years of education
 Less than a high school degree 1586 (11.4%) 378 (2.5%)
 High school graduate/GED 2941 (20.5%) 692 (5.2%)
 Some college/Associate degree 3364 (22.2%) 684 (4.3%)
 Bachelor’s degree or higher 4184 (30.7%) 398 (3.2%)
Number of previous live births
 0 4614 (30.8%) 889 (6.5%)
 1–2 6008 (44.5%) 930 (6.7%)
  ≥ 3 1525 (9.5%) 342 (1.9%)
Married
 Yes 7204 (52.9%) 886 (7.3%)
 No 4949 (31.9%) 1278 (7.9%)
BMI category
 Underweight (< 18.5)
 Normal (18.5–24.9) 395 (2.7%) 92 (0.7%)
 Overweight (25–29.9) 5316 (39.8%) 936 (7.0%)
 Obese (≥ 30) 2916 (22.1%) 485 (3.4%)
3049 (20.4%) 558 (3.9%)

a Number of women from unweighted sample distribution

b Percentages were weighted to account for deliberate survey oversampling and nonresponse and non-coverage

Table 6.

Sociodemographic Characteristics associated with not Receiving Prenatal Care as Early as Would have Liked

Did not receive prenatal care as early as would have liked
Univariate Multivariate
Odds Ratio 95% CI Tests of Model Effectsa Odds Ratio 95% CI Tests of Model Effectsa
Race
 White (ref)  < 0.001 0.625
 Black 1.2 1.0–1.5 1.0 0.8–1.2
 Asian 0.8 0.5–1.2 1.2 0.7–1.8
 Native North American 1.6 1.2–2.3 1.3 0.8–2.0
 Other race 1.7 1.3–2.4 1.3 0.9–1.8
 Mixed race 1.0 0.7–1.5 0.9 0.6–1.3
Ethnicity
 Non-Hispanic (ref)  < 0.001 0.033
 Hispanic 1.5 1.3–1.8 1.3 1.0–1.5
Maternal Age
  < 18 3.4 2.0–5.8  < 0.001 1.9 1.0–3.6 0.004
 18–24 2.2 1.7–2.8 1.4 1.1–1.9
 25–34 1.1 0.9–1.4 1.0 0.8–1.3
  > 35 (ref)
Nutrition Program for Women, Infant and Child Participation
 Yes 1.5 1.3–1.7  < 0.001 1.0 0.8–1.2 0.989
 No (ref)
Education
  < High school degree 2.1 1.6–2.8  < 0.001 1.5 1.0–2.1  < 0.001
 High school graduate/GED 2.4 2.0–3.0 1.8 1.4–2.4
 Some college/associate degree 1.9 1.5–2.3 1.6 1.2–2.0
  ≥ Bachelor's degree (ref)
Previous Births
 0 births 1.0 0.8–1.3  < 0.001 0.9 0.7–1.2 0.002
 1–2 births 0.7 0.6–0.9 0.7 0.6–0.9
  ≥ 3 births (ref)
Marital Status
 Married (ref)  < 0.001 0.017
 Not married 1.8 1.5–2.1 1.3 1.0–1.6
Weight Status
 Underweight 1.5 1.0–2.3 0.034 1.2 0.8–1.8 0.115
 Normal Weight (ref)
 Overweight 0.9 0.7–1.1 0.8 0.7–1.0
 Obese 1.1 0.9–1.3 1.0 0.8–1.2

Bold text indicates the difference between the level of interest and the reference is significant with 95% confidence

aP value based on F-test for Type 3 Analysis of Effects

Reasons for Not Receiving Early Prenatal Care

Participants in 11 states comprised the sample responding to barriers to receiving early prenatal care. Of the women who did not receive early prenatal care, 42.3% reported the reason was not being aware they were pregnant (Table 7). Other common reasons for not receiving early prenatal care were structural or financial barriers in the health care system, with 38.1% reporting no appointments available, 28.2% reporting not having money or insurance to pay for the visit, 27.3% reporting the doctor/health plan would not start care, and 22.5% not having a Medicaid card. Reasons women reported not receiving prenatal care as early as they desired differed depending on race, age, WIC participation, education, number of previous births, marital status, and weight status (Table 8). Younger women, women receiving WIC benefits and women who had less education were more likely to report financial barriers to early prenatal care (i.e. not being able to afford care, not having transportation, not yet having a Medicaid card). Women participating in WIC, women who were not married, and women with less than a bachelor’s degree were less likely to report health care structural barriers to early prenatal care (i.e. not having appointments available, doctor/health care plan not being willing to start care).

Table 7.

Perceived barriers to receiving early prenatal care

Perceived barrier Na (%)b
Was not aware of pregnancy status 917 (42.3%)
No appointments available when they wanted one 755 (38.1%)
Unable to afford the visits 452 (28.2%)
Doctor or health plan would not start prenatal care as early as they wanted 463 (27.3%)
No Medicaid card 392 (22.5%)
Too busy 326 (15.4%)
Lack of transportation 238 (10.7%)
Did not want to disclose pregnancy status 221 (9.5%)
No leave at work/school 184 (8.2%)
Lack of child care did not want prenatal care

134 (7.0%)

92 (3.2%)

a Number of women from unweighted sample distribution

b Percentages were weighted to account for deliberate survey oversampling and nonresponse and non-coverage

Table 8.

Odds of reasons for not receiving early prenatal care by sociodemographic characteristic and body mass index category

No appointment available Could not afford No transportation Doctor/health plan would not start prenatal care Too busy No leave from work/school No medicaid card No child care Not aware of pregnancy Keeping pregnancy secret Did not want prenatal care
Odds Ratio (95% CI) Odds Ratio (95% CI) Odds Ratio (95% CI) Odds Ratio (95% CI) Odds Ratio (95% CI) Odds Ratio (95% CI)

Odds Ratio

(95% CI)

Odds Ratio (95% CI)

Odds Ratio

(95% CI)

Odds Ratio (95% CI)

Odds Ratio

(95% CI)

Race
 White (ref)
 Black

0.8

(0.5–1.2)

0.8

(0.5–1.2)

2.9

(1.7–5.2)

0.5

(0.3–0.8)

2.2

(1.3–3.5)

1.0

(0.6–1.8)

1.0

(0.7–1.6)

1.8

(0.9–3.7)

1.6

(1.1–2.3)

2.0

(1.1–3.8)

1.5

(0.7–3.3)

 Asian

0.9

(0.4–1.9)

0.9

(0.4–2.4)

0.8

(0.3–2.0)

0.5

(0.2–1.3)

1.2

(0.4–3.4)

0.6

(0.2–1.8)

1.2

(0.5–2.8)

2.7

(0.9–8.4)

0.9

(0.4–1.8)

0.3

(0.1–0.7)

6.4

(1.8–22.4)

 Native North American

0.5

(0.3–0.9)

0.1

(0.0–0.2)

1.4

(0.7–2.9)

1.3

(0.5–3.4)

2.1

(1.0–4.2)

1.6

(0.7–3.8)

0.1

(0.1–0.3)

1.1

(0.5–2.5)

2.3

(1.3–4.1)

1.9

(0.9–3.9)

1.9

(0.6–6.9)

 Other race

0.6

(0.3–1.2)

1.2

(0.7–2.3)

1.4

(0.5–3.6)

1.1

(0.6–2.1)

1.3

(0.6–3.2)

0.8

(0.3–2.3)

1.8

(1.0–3.5)

1.2

(0.3–4.8)

1.3

(0.7–2.4)

1.9

(0.7–4.7)

3.3

(0.9–12.3)

 Mixed race

0.6

(0.3–1.2)

0.7

(0.3–1.9)

3.2

(1.2–8.8)

0.9

(0.4–1.9)

1.9

(0.8–4.9)

0.5

(0.1–2.2)

0.3

(0.1–1.0)

1.0

(0.3–2.9)

1.8

(0.9–3.7)

2.5

(0.9–6.7)

2.3

(0.4–14.9)

Ethnicity
 Non–Hispanic (ref)
 Hispanic

0.7

(0.5–1.1)

2.2

(1.6–3.2)

0.7

(0.4–1.3)

1.1

(0.7–1.6)

0.8

(0.5–1.4)

1.3

(0.7–2.2)

2.3

(1.6–3.4)

1.3

(0.7–2.6)

1.2

(0.9–1.7)

1.3

(0.7–2.2)

1.7

(0.7–3.9)

Age
  < 18

0.9

(0.3–2.7)

0.3

(0.1–1.2)

7.5

(1.9–30.7)

0.4

(0.1–1.5)

2.6

(0.8–8.8)

1.2

(0.2–5.9)

0.1

(0.0–0.3)

0.4

(0.0–3.4)

1.9

(0.8–4.9)

5.0

(1.3–18.4)

2.6

(0.3–26.9)

 18–24

1.0

(0.6–1.5)

1.2

(0.7–2.0)

3.6

(1.5–8.6)

0.9

(0.5–1.5)

1.4

(0.7–2.8)

1.1

(0.5–2.6)

1.8

(1.0–3.3)

1.1

(0.4–3.1)

1.6

(1.0–2.5)

2.3

(1.1–5.0)

1.0

(0.2–5.7)

 25–34

1.7

(1.1–2.7)

0.8

(0.5–1.4)

2.5

(1.0–5.9)

1.3

(0.8–2.2)

1.1

(0.6–2.2)

0.9

(0.4–1.9)

0.9

(0.5–1.6)

0.9

(0.4–2.4)

0.7

(0.5–1.1)

1.4

(0.6–3.1)

0.9

(0.2–4.7)

  > 35 (ref)
Nutrition Program for Women, Infant and Child participation
 Yes

0.8

(0.6–1.0)

1.4

(1.0–2.0)

2.3

(1.4–3.7)

0.7

(0.5–0.9)

1.6

(1.1–2.4)

1.3

(0.8–2.3)

1.8

(1.2–2.6)

1.7

(1.0–3.3)

1.8

(1.4–2.4)

1.9

(1.2–3.2)

1.4

(0.7–3.1)

 No (ref)
Education
  < High school degree

0.5

(0.3–0.8)

2.7

(1.3–5.6)

45.2

(10.2–200.1)

0.3

(0.2–0.5)

4.5

(2.1–9.9)

2.1

(0.8–5.3)

4.8

(2.1–10.6)

6.6

(2.2–19.3)

1.9

(1.1–3.1)

4.2

(1.4–13.1)

3.8

(1.0–15.1)

 High school graduate/GED

0.6

(0.4–0.9)

3.9

(2.0–7.7)

22.5

(5.2–97.6)

0.4

(0.2–0.6)

2.2

(1.0–4.5)

1.8

(0.8–4.2)

5.0

(2.4–10.3)

5.2

(2.0–13.6)

2.0

(1.3–3.0)

2.8

(1.0–8.0)

1.7

(0.4–6.6)

 Some college/ associate degree

0.6

(0.4–0.9)

3.0

(1.5–6.0)

7.3

(1.6–33.0)

0.5

(0.3–0.8)

2.3

(1.1–4.6)

1.8

(0.8–4.1)

3.4

(1.6–7.0)

3.1

(1.1–9.2)

1.9

(1.3–3.0)

2.2

(0.8–6.3)

0.3

(0.1–1.4)

  > Bachelor's degree (ref)
Previous Births
 0 births

1.1

(0.7–1.8)

0.5

(0.3–0.9)

0.3

(0.2–0.6)

1.4

(0.8–2.5)

0.4

(0.2–0.7)

0.5

(0.2–1.0)

0.5

(0.3–0.9)

0.0

(0.0–0.1)

1.7

(1.1–2.7)

0.4

(0.2–0.7)

0.4

(0.1–1.0)

 1–2 births

1.0

(0.7–1.6)

0.8

(0.5–1.2)

0.3

(0.2–0.6)

1.5

(0.8–2.6)

0.6

(0.4–1.0)

0.6

(0.3–1.2)

0.5

(0.3–0.9)

0.3

(0.2–0.6)

1.2

(0.7–1.8)

0.3

(0.1–0.5)

0.8

(0.3–1.7)

  > 3 births (ref)
Marital Status
 Married (ref)
 Other

0.6

(0.4–0.8)

1.0

(0.7–1.4)

3.9

(2.2–6.7)

0.4

(0.3–0.6)

1.9

(1.2–2.9)

2.0

(1.1–3.5)

1.2

(0.9–1.8)

1.2

(0.6–2.2)

2.3

(1.7–3.1)

3.2

(1.7–5.9)

1.0

(0.5–2.3)

Weight Status
 Underweight

0.6

(0.3–1.4)

2.6

(1.2–5.6)

1.8

(0.6–4.9)

0.7

(0.2–1.8)

1.0

(0.4–2.8)

0.8

(0.2–3.2)

1.9

(0.8–4.6)

1.5

(0.3–6.4)

2.1

(1.0–4.2)

1.1

(0.4–3.2)

2.6

(0.4–17.2)

 Normal Weight (ref)
 Overweight

0.8

(0.5–1.1)

1.0

(0.6–1.5)

0.5

(0.3–1.0)

1.0

(0.6–1.5)

0.7

(0.4–1.3)

0.9

(0.4–1.8)

1.6

(1.0–2.5)

0.5

(0.3–1.1)

1.1

(0.7–1.6)

0.7

(0.4–1.4)

1.9

(0.7–4.7)

 Obese

0.6

(0.4–0.8)

0.9

(0.6–1.4)

0.7

(0.4–1.4)

0.8

(0.5–1.3)

1.1

(0.6–1.8)

0.9

(0.5–1.7)

1.3

(0.8–2.1)

0.6

(0.2–1.3)

1.1

(0.8–1.6)

0.8

(0.4–1.6)

0.7

(0.3–2.0)

Bold text indicates the difference between the level of interest and the reference is significant with 95% confidence

Discussion

While preconception counseling is the gold standard for care to prepare women for a healthy pregnancy by detecting or treating co-morbidities or assisting women with changing health behaviors, 50% of pregnancies are unplanned (Finer & Zolna, 2014) and so many women miss this opportune time for counseling. Therefore, optimizing the delivery of prenatal care as early as possible is essential to support the health of women and infants. The majority of the sample (92%) was able to receive prenatal care in the first trimester, with participants reporting having their first prenatal care appointment around 9 weeks gestation, on average. However, the data demonstrated a two-week gap among women between being certain of their pregnancy and receiving their first prenatal care appointment, with a larger gap among the 15% of women (almost 600,000 women (Centers for Disease Control & Prevention, 2017) in the United States each year) who reported not receiving prenatal care as early as they wished. Significant systemic and socioeconomic barriers to initial prenatal care visits were identified such as no available appointments, not having money/insurance to pay for the visit, doctor/health plan being unwilling to start care until later in pregnancy, and not having a Medicaid card.

The data also showed clear health disparities in how early prenatal care is received by vulnerable populations of women who are at highest risk for pregnancy-related mortality (Creanga et al., 2017). Specifically, women who identified as Black and Native American learned of pregnancy significantly later and established prenatal care later compared to women who identified as white. Given the higher burden of adverse outcomes among Black and Native American women (Heck et al., 2021; Kuehn, 2019; Kuriya et al., 2016; Singh, 2021), changes in policy (e.g. recommendations for a specific week to start prenatal care from professional organization) and insurance coverage will be necessary to prioritize early prenatal care in these populations. Women who were 24 years or younger, women who were not married, women with lower educational attainment, and women who were receiving WIC benefits similarly confirmed their pregnancies later and also received prenatal care later. Given the most common barrier to timely prenatal care was lack of early identification of pregnancy, it may be helpful to enhance efforts reducing rates of unintended pregnancies through facilitating birth control access (Kallner & Danielsson, 2016). In addition, increasing awareness of the importance of receiving prenatal care early may encourage women of childbearing age to act quickly to access care when they suspect they are pregnant. However, early recognition of pregnancy may not eliminate the issue of accessing early prenatal care, since women in disadvantaged populations reported that lack of appointments and reluctance of providers to provide early prenatal appointments were key barriers to receiving early prenatal care.

Women who were participating in WIC (a proxy for lower income) and had less educational attainment were more likely to report both financial barriers (i.e. inability to afford medical care, not having transportation, not yet having her Medicaid card) and systemic barriers (i.e. doctor/health plan not offering early care or appointment availability) compared to women with higher incomes and more education. Understanding and intervening on these barriers is crucial in facilitating prenatal care as early as possible in pregnancy, in order to reduce morbidity and mortality for both maternal and fetal health (Bingham et al., 2011; Maternal Health Task Force). Potential considerations to facilitate early prenatal care include: 1) facilitating early prenatal care appointments among Medicaid-eligible women prior to receiving their card (Palmer, 2020; Piper et al., 1994), 2) increasing awareness among pregnant women that a variety of providers can offer the initial prenatal care visit (including family physicians) (Kozhimannil et al., 2012), and 3) supporting technology-based prenatal care visits (Marko et al., 2019; Peahl et al., 2020). In addition, dividing the global obstetrics fee into components, including an “initial prenatal care visit” component, could provide appropriate incentives for clinics to provide early prenatal care, even if there is a first trimester pregnancy loss (Applegate et al., 2014). Further, onsite childcare or child-friendly clinic spaces could address the challenge of lack of child care during these medical appointments (Phillippi, 2009). Lastly, ensuring the scheduling process is simple for those with the lowest levels of literacy or of experience with the medical community may remove barriers for young women and those with low levels of education.

Consistent with previous research (Lynch et al., 2014), it is notable that no disparities were detected in gestational age at the first prenatal care visit by pre-gravid BMI category, despite the prevalence of weight stigma in health care settings and health care avoidance among individuals with overweight or obesity (Mensinger et al., 2018). Despite the greater likelihood of excessive gestational weight gain (Deputy et al., 2015) and the increased prevalence of maternal health complications among women with overweight and obesity (Wei et al., 2016), we found no differences in the timing of prenatal care based on BMI category. Nonetheless, since gestational weight gain in the first trimester appears to have a disproportionate impact on the development of gestational diabetes (MacDonald et al., 2017), it may be beneficial for all women to receive prenatal care with clear recommendations for gestational weight gain earlier in the first trimester.

This study has several key strengths and limitations. First, our research has the strength of using a large, national dataset, allowing for an adequate sample size for examining the effects of several sociodemographic variables. However, due to the large sample size, some differences detected may be statistically significant but not clinically meaningful. While we utilized a national data set, which recruited a representative sample within each state, not all states administered every question that we utilized in these analyses and one question (i.e. gestational age at pregnancy confirmation) was only administered by four states; thus the degree to which the results are generalizable is unknown. Furthermore, women who respond to the PRAMS survey may differ from the general population (e.g. characteristics like conscientiousness and altruism). In addition, data utilized in these analyses were based on maternal self-report and are therefore subject to the typical limitations of self-reported data (e.g. ability to recall accurate information about their prenatal care, providing social acceptable rather than entirely accurate responses). Thus, delayed prenatal care and barriers may be even more common than was reported in this article. Finally, the COVID-19 pandemic has led to many dramatic changes in the provision of health care (e.g. telehealth), and future research should examine whether the timing of the initial prenatal care visit or the prevalence of barriers has changed.

In summary, this study illustrates a window of opportunity to provide earlier prenatal care. Early prenatal care is preferred by many women and would facilitate important medical and behavioral treatments critical for maternal and fetal health to be addressed as early as possible. This study also identified common barriers to care, overall and among specific vulnerable population groups. Strategies to address these barriers on the patient, provider and systemic levels is warranted.

Acknowledgements

We would like to acknowledge the Pregnancy Risk Assessment Monitoring System (PRAMS) working group and the Centers for Disease Control and Prevention for providing access to the PRAMS dataset for this analysis. We would also like to acknowledge Christina M. Frank, University of Kansas, School of Medicine-Wichita, for her work on in-text citations and references.

Authors' contributions

All authors contributed to study design, drafting of the manuscript, and review of the final manuscript. C.Y.C. & J. W. conducted the data analyses.

Funding

Not applicable.

Data availability

The data are available from Pregnancy Risk Assessment Monitoring System (PRAMS) working group and the Centers for Disease Control and Prevention.

Code availability

Not applicable.

Declarations

Conflict of interest

The authors declare that they have no conflict of interest.

Ethical Approval

The study was determined to be exempt from University of Tennessee Health Science Center Institutional Review Board approval because no identifiable private information was utilized and have therefore been performed in accordance with the ethical standards laid down in the 1964 Declaration of Helsinki and its later amendments;

Consent to Participate

All participants received a written informed consent statement.

Consent for Publication

Not applicable.

Footnotes

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

References

  1. American Academy of Pediatrics Committee on Fetus and Newborn. (2012). Guidelines for Perinatal Care (7th edition ed.).
  2. Albrecht SS, Kuklina EV, Bansil P, Jamieson DJ, Whiteman MK, Kourtis AP, Posner SF, Callaghan WM. Diabetes trends among delivery hospitalizations in the US, 1994–2004. Diabetes Care. 2010;33(4):768–773. doi: 10.2337/dc09-1801. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Applegate M, Gee RE, Martin JN. Improving maternal and infant health outcomes in Medicaid and the children's health insurance program. Obstetrics & Gynecology. 2014;124(1):143–149. doi: 10.1097/AOG.0000000000000320. [DOI] [PubMed] [Google Scholar]
  4. Bingham D, Strauss N, Coeytaux F. Maternal mortality in the United States: A human rights failure. Contraception. 2011;83(3):189–193. doi: 10.1016/j.contraception.2010.11.013. [DOI] [PubMed] [Google Scholar]
  5. Centers for Disease Control and Prevention. (2017). National Center for Health Statistics. Retrieved November 4, 2019 from https://www.cdc.gov/nchs/fastats/births.htm.
  6. Centers for Disease Control and Prevention. (2019b). Reproductive Health. Retrieved December 1, 2019 from https://www.cdc.gov/reproductivehealth/maternalinfanthealth/pregnancy-mortality-surveillance-system.htm.
  7. Centers for Disease Control and Prevention. (2019a). Pregnancy Risk Assessment Monitoring Survey. Retrieved October 22, 2019 from https://www.cdc.gov/prams/.
  8. Creanga AA, Syverson C, Seed K, Callaghan WM. Pregnancy-related mortality in the United States, 2011–2013. Obstetrics and Gynecology. 2017;130(2):366. doi: 10.1097/AOG.0000000000002114. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Deputy NP, Sharma AJ, Kim SY. Gestational weight gain—United States, 2012 and 2013. MMWR. Morbidity and Mortality Weekly Report. 2015;64(43):1215. doi: 10.15585/mmwr.mm6443a3. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Finer LB, Zolna MR. Shifts in intended and unintended pregnancies in the United States, 2001–2008. American Journal of Public Health. 2014;104(S1):S43–S48. doi: 10.2105/AJPH.2013.301416. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Goldstein RF, Abell SK, Ranasinha S, Misso M, Boyle JA, Black MH, Li N, Hu G, Corrado F, Rode L. Association of gestational weight gain with maternal and infant outcomes: A systematic review and meta-analysis. Journal of the American Medical Association. 2017;317(21):2207–2225. doi: 10.1001/jama.2017.3635. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Heck JL, Jones EJ, Bohn D, McCage S, Parker JG, Parker M, Pierce SL, Campbell J. Maternal mortality among American Indian/Alaska Native women: A scoping review. Journal of Women's Health. 2021;30(2):220–229. doi: 10.1089/jwh.2020.8890. [DOI] [PubMed] [Google Scholar]
  13. Kallner HK, Danielsson KG. Prevention of unintended pregnancy and use of contraception—important factors for preconception care. Upsala Journal of Medical Sciences. 2016;121(4):252–255. doi: 10.1080/03009734.2016.1208310. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Kozhimannil KB, Avery MD, Terrell CA. Recent trends in clinicians providing care to pregnant women in the United States. Journal of Midwifery & Women’s Health. 2012;57(5):433–438. doi: 10.1111/j.1542-2011.2012.00171.x. [DOI] [PubMed] [Google Scholar]
  15. Kuehn B. Disparities in maternal mortality. Journal of the American Medical Association. 2019;322(16):1545–1545. doi: 10.1001/jama.2019.16156. [DOI] [PubMed] [Google Scholar]
  16. Kuklina EV, Callaghan WM. Chronic heart disease and severe obstetric morbidity among hospitalisations for pregnancy in the USA: 1995–2006. BJOG: an International Journal of Obstetrics & Gynaecology. 2011;118(3):345–352. doi: 10.1111/j.1471-0528.2010.02743.x. [DOI] [PubMed] [Google Scholar]
  17. Kuklina EV, Ayala C, Callaghan WM. Hypertensive disorders and severe obstetric morbidity in the United States. Obstetrics & Gynecology. 2009;113(6):1299–1306. doi: 10.1097/AOG.0b013e3181a45b25. [DOI] [PubMed] [Google Scholar]
  18. Kuriya A, Piedimonte S, Spence AR, Czuzoj-Shulman N, Kezouh A, Abenhaim HA. Incidence and causes of maternal mortality in the USA. Journal of Obstetrics and Gynaecology Research. 2016;42(6):661–668. doi: 10.1111/jog.12954. [DOI] [PubMed] [Google Scholar]
  19. Lynch CD, Tumin R, Prasad MR. Association between body mass index and the timing of pregnancy recognition and entry into prenatal care. Obstetrics & Gynecology. 2014;124(5):911–918. doi: 10.1097/AOG.0000000000000516. [DOI] [PubMed] [Google Scholar]
  20. MacDonald SC, Bodnar LM, Himes KP, Hutcheon JA. Patterns of gestational weight gain in early pregnancy and risk of gestational diabetes mellitus. Epidemiology (cambridge, Mass.) 2017;28(3):419. doi: 10.1097/EDE.0000000000000629. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Marko KI, Ganju N, Krapf JM, Gaba ND, Brown JA, Benham JJ, Oh J, Richards LM, Meltzer AC. A mobile prenatal care app to reduce in-person visits: prospective controlled trial. JMIR mHealth and uHealth. 2019;7(5):e10520. doi: 10.2196/10520. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Maternal Health Task Force. Maternal Health in the United States. Retrieved November 4, 2019 from https://www.mhtf.org/topics/maternal-health-in-the-united-states/.
  23. Mensinger JL, Tylka TL, Calamari ME. Mechanisms underlying weight status and healthcare avoidance in women: A study of weight stigma, body-related shame and guilt, and healthcare stress. Body Image. 2018;25:139–147. doi: 10.1016/j.bodyim.2018.03.001. [DOI] [PubMed] [Google Scholar]
  24. Michelle J, Osterman M. Timing and adequacy of prenatal care in the United States. National Vital Statistics Report. 2016;67:1–14. [PubMed] [Google Scholar]
  25. Moos M-K, Dunlop AL, Jack BW, Nelson L, Coonrod DV, Long R, Boggess K, Gardiner PM. Healthier women, healthier reproductive outcomes: Recommendations for the routine care of all women of reproductive age. American Journal of Obstetrics and Gynecology. 2008;199(6):S280–S289. doi: 10.1016/j.ajog.2008.08.060. [DOI] [PubMed] [Google Scholar]
  26. Palmer M. Preconception subsidized insurance: Prenatal care and birth outcomes by race/ethnicity. Health Economics. 2020;29(9):1013–1030. doi: 10.1002/hec.4116. [DOI] [PubMed] [Google Scholar]
  27. Peahl AF, Smith RD, Moniz MH. Prenatal care redesign: creating flexible maternity care models through virtual care. American Journal of Obstetrics and Gynecology. 2020;223(3):389. doi: 10.1016/j.ajog.2020.05.029. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Phillippi JC. Women's perceptions of access to prenatal care in the United States: A literature review. Journal of Midwifery & Women's Health. 2009;54(3):219–225. doi: 10.1016/j.jmwh.2009.01.002. [DOI] [PubMed] [Google Scholar]
  29. Piper JM, Mitchel EF, Jr, Ray W. Presumptive eligibility for pregnant Medicaid enrollees: Its effects on prenatal care and perinatal outcome. American Journal of Public Health. 1994;84(10):1626–1630. doi: 10.2105/AJPH.84.10.1626. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Shulman HB, Gilbert BC, Lansky A. The Pregnancy Risk Assessment Monitoring System (PRAMS): Current methods and evaluation of 2001 response rates. Public Health Reports. 2006;121(1):74–83. doi: 10.1177/003335490612100114. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Singh GK. Trends and social inequalities in maternal mortality in the United States, 1969–2018. International Journal of Maternal and Child Health and AIDS. 2021;10(1):29. doi: 10.21106/ijma.444. [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. Stulberg DB, Cain L, HashamDahlquist I, Lauderdale DS. Pre-pregnancy and Early Prenatal Care are Associated with Lower Risk of Ectopic Pregnancy Complications in the Medicaid Population: 2004–08. Paediatric and Perinatal Epidemiology. 2017;31(1):4–10. doi: 10.1111/ppe.12327. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Wei Y-M, Yang H-X, Zhu W-W, Liu X-Y, Meng W-Y, Wang Y-Q, Shang L-X, Cai Z-Y, Ji L-P, Wang Y-F. Risk of adverse pregnancy outcomes stratified for pre-pregnancy body mass index. The Journal of Maternal-Fetal & Neonatal Medicine. 2016;29(13):2205–2209. doi: 10.3109/14767058.2015.1081167. [DOI] [PubMed] [Google Scholar]
  34. Yan J. The effects of prenatal care utilization on maternal health and health behaviors. Health Economics. 2017;26(8):1001–1018. doi: 10.1002/hec.3380. [DOI] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Data Availability Statement

The data are available from Pregnancy Risk Assessment Monitoring System (PRAMS) working group and the Centers for Disease Control and Prevention.

Not applicable.


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