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Original Article

Timing of Elective Repeat Cesarean Delivery at Term and Neonatal Outcomes

Alan T.N. Tita, M.D., Ph.D., Mark B. Landon, M.D., Catherine Y. Spong, M.D., Yinglei Lai, Ph.D., Kenneth J. Leveno, M.D., Michael W. Varner, M.D., Atef H. Moawad, M.D., Steve N. Caritis, M.D., Paul J. Meis, M.D., Ronald J. Wapner, M.D., Yoram Sorokin, M.D., Menachem Miodovnik, M.D., Marshall Carpenter, M.D., Alan M. Peaceman, M.D., Mary J. O'Sullivan, M.D., Baha M. Sibai, M.D., Oded Langer, M.D., John M. Thorp, M.D., Susan M. Ramin, M.D., and Brian M. Mercer, M.D. for the Eunice Kennedy Shriver NICHD Maternal–Fetal Medicine Units Network

N Engl J Med 2009; 360:111-120January 8, 2009

Abstract

Background

Because of increased rates of respiratory complications, elective cesarean delivery is discouraged before 39 weeks of gestation unless there is evidence of fetal lung maturity. We assessed associations between elective cesarean delivery at term (37 weeks of gestation or longer) but before 39 weeks of gestation and neonatal outcomes.

Methods

We studied a cohort of consecutive patients undergoing repeat cesarean sections performed at 19 centers of the Eunice Kennedy Shriver National Institute of Child Health and Human Development Maternal–Fetal Medicine Units Network from 1999 through 2002. Women with viable singleton pregnancies delivered electively (i.e., before the onset of labor and without any recognized indications for delivery before 39 weeks of gestation) were included. The primary outcome was the composite of neonatal death and any of several adverse events, including respiratory complications, treated hypoglycemia, newborn sepsis, and admission to the neonatal intensive care unit (ICU).

Results

Of 24,077 repeat cesarean deliveries at term, 13,258 were performed electively; of these, 35.8% were performed before 39 completed weeks of gestation (6.3% at 37 weeks and 29.5% at 38 weeks) and 49.1% at 39 weeks of gestation. One neonatal death occurred. As compared with births at 39 weeks, births at 37 weeks and at 38 weeks were associated with an increased risk of the primary outcome (adjusted odds ratio for births at 37 weeks, 2.1; 95% confidence interval [CI], 1.7 to 2.5; adjusted odds ratio for births at 38 weeks, 1.5; 95% CI, 1.3 to 1.7; P for trend <0.001). The rates of adverse respiratory outcomes, mechanical ventilation, newborn sepsis, hypoglycemia, admission to the neonatal ICU, and hospitalization for 5 days or more were increased by a factor of 1.8 to 4.2 for births at 37 weeks and 1.3 to 2.1 for births at 38 weeks.

Conclusions

Elective repeat cesarean delivery before 39 weeks of gestation is common and is associated with respiratory and other adverse neonatal outcomes.

Media in This Article

Figure 1Flow Chart Detailing Exclusion Criteria Applied to Identify Elective Cesarean Sections.
Figure 2Timing of Elective Repeat Cesarean Delivery and the Incidence of the Primary Outcome According to the Number of Completed Weeks of Gestation.
Article

Infants born before 39 weeks of gestation are at increased risk for neonatal adverse respiratory outcomes, and the risk increases progressively as gestational age at birth declines.1,2 Thus, prelabor elective delivery (delivery in the absence of a specific maternal or fetal indication) is proscribed before 39 weeks unless fetal lung maturity has been demonstrated.3,4 As compared with infants born vaginally, those born by cesarean section are at increased risk for adverse respiratory outcomes, especially when delivery occurs before the onset of labor.1,2,5-11 This increased risk persists even in infants who are delivered by cesarean section at full term (i.e., at or beyond 37 completed weeks of gestation).

The rate of cesarean delivery in the United States rose from 20.7% in 1996 to 31.1% in 2006.12 A major reason for this increase is the decline in the rate of attempted vaginal birth after cesarean delivery. 13 Elective cesarean delivery may be scheduled to accommodate patient and physician convenience, and there is a risk that it may be performed earlier than is appropriate. Because approximately 40% of the 1.3 million cesarean deliveries performed annually in the United States are repeat procedures and the number of cesarean deliveries continues to rise, the timing of elective cesarean delivery has increasingly important public health implications.14,15 Therefore, we undertook the present study of a large, prospectively assembled cohort of women in the United States to describe the timing of elective repeat cesarean deliveries and to assess associations between delivery before 39 weeks and the risk of adverse neonatal outcomes.

Methods

Patients

We selected our study cohort from the cesarean registry of the Eunice Kennedy Shriver National Institute of Child Health and Human Development Maternal–Fetal Medicine Units Network. The registry contains detailed, prospectively collected information on consecutive repeat cesarean deliveries performed at 19 U.S. academic centers from 1999 to 2002.16 Women who underwent cesarean delivery were identified daily by dedicated, trained research personnel at each center, who collected maternal and neonatal information on standardized study forms. The data forms allowed for each woman to have one major and one or two secondary indications for the cesarean delivery from an inclusive list of 20 prespecified options that included “other.”

Using the listed indications for cesarean delivery (a specific focus of the registry), as well as medical and obstetrical history, we defined a group of women who underwent an elective cesarean delivery (i.e., a delivery performed in the absence of labor or other recognized medical or obstetrical indications for delivery) of a viable infant at 37 weeks of gestation or later (Figure 1Figure 1Flow Chart Detailing Exclusion Criteria Applied to Identify Elective Cesarean Sections.). Women who had multiple gestations or a fetus with a major congenital anomaly were excluded, as were women with other medical or obstetrical conditions that would warrant early or immediate delivery. Deliveries were categorized according to the number of completed weeks of gestation. Gestational age was determined by obstetrical providers with the use of standard criteria that took into consideration the clinical history and the results of the earliest ultrasound examination.17 If the findings on ultrasound examination were consistent with a gestational age based on a certain date of the last menstrual period, gestational age was determined according to the date of the last menstrual period; if the date of the last menstrual period was uncertain or the findings on ultrasound examination were inconsistent with a gestational age based on the date of the last menstrual period, gestational age was determined according to the results of the ultrasound examination.

Study Outcomes

The following neonatal outcomes were studied: death, adverse respiratory outcomes (respiratory distress syndrome or transient tachypnea of the newborn), hypoglycemia, newborn sepsis, confirmed seizures, necrotizing enterocolitis, hypoxic–ischemic encephalopathy, cardiopulmonary resuscitation or ventilator support within 24 hours after birth, umbilical-cord-blood arterial pH below 7.0, a 5-minute Apgar score of 3 or below, admission to the neonatal intensive care unit (ICU), and prolonged hospitalization (5 days or longer). The prespecified primary outcome was a composite that included any of the above outcomes. The infants were followed up until discharge from the hospital or 120 days after birth, whichever came first.16

The diagnosis of respiratory distress syndrome required signs of respiratory distress, consistent radiologic features, and oxygen therapy with a fraction of inspired oxygen (FIO2) of 0.40 or greater for at least 24 hours or until death. Transient tachypnea of the newborn was defined by the presence of tachypnea within hours after birth and typical radiologic findings. The diagnosis of necrotizing enterocolitis required confirmation by radiologic findings, surgery, or autopsy. The diagnosis of hypoglycemia required a serum or plasma glucose level of less than 35 mg per deciliter (1.9 mmol per liter) and treatment with intravenous glucose. Newborn sepsis included both suspected infections (with clinical findings suggesting infection) and proved infections (as confirmed in a subgroup of neonates with positive cultures of blood, cerebrospinal fluid, or urine obtained by catheterization or suprapubic aspiration; cardiovascular collapse; or an unequivocal radiograph confirming infection in a neonate with clinical sepsis). Small for gestational age was defined as a birth weight less than or equal to the 10th percentile, and large for gestational age as a birth weight greater than or equal to the 90th percentile derived from sex- and race-specific growth curves.18

Statistical Analysis

Data were analyzed with the use of SAS software, version 8.2. The incidence of adverse neonatal outcomes was calculated for each completed week of gestation at the time of cesarean delivery. The Cochran–Armitage test for trend was used to assess trends in the incidence rates of outcomes. Adjusted odds ratios for the association between neonatal outcomes and gestational age at delivery relative to 39 completed weeks of gestation were derived from logistic-regression models that included maternal age, self-reported race or ethnic group, marital status, the number of previous cesarean deliveries, payor, the presence or absence of smoking during pregnancy, and the presence or absence of diet-controlled gestational diabetes. The attributable risk of the primary outcome was calculated with the use of the following formula: 100×(relative risk−1)÷relative risk, where relative risk is the risk at 37 or 38 weeks divided by the risk at 39 weeks.19 A nominal two-sided P value of less than 0.05 was considered to indicate statistical significance; no adjustments were made for multiple comparisons.

The study was approved by the institutional review boards of each clinical center and the data-coordinating center. The data were transmitted to the coordinating center without patient identification. Informed consent was not required. The staff of the George Washington University Biostatistics Center had complete access to the data and performed the analyses.

Results

Patients

A total of 28,867 women who delivered by repeat cesarean section were enrolled in the registry; 24,077 of the cesarean deliveries were performed at term. After the exclusion of women who had multiple gestations, a fetus with a major congenital anomaly or indications for immediate or early delivery, we identified 13,258 women who underwent an elective cesarean section at term (Figure 1). The week of gestation at delivery was confirmed by a first- or second-trimester ultrasound examination in 76.8% of pregnancies.

Among the women who underwent elective repeat cesarean section at term, 6.3% underwent the procedure at 37 completed weeks of gestation, 29.5% at 38 weeks, 49.1% at 39 weeks, and just over 15% at 40 weeks or later (Figure 2Figure 2Timing of Elective Repeat Cesarean Delivery and the Incidence of the Primary Outcome According to the Number of Completed Weeks of Gestation.). Thus, 35.8% (95% confidence interval [CI], 35.0 to 36.6) of elective repeat cesarean deliveries were performed before 39 weeks of gestation. The median proportion of deliveries performed before 39 weeks of gestation among the 19 centers was 36.5%, and the range was 18.6 to 52.5%.

Maternal and infant characteristics varied according to the number of completed weeks of gestation at delivery (Table 1Table 1Characteristics of Mothers and Infants According to Completed Week of Gestation at Delivery.). As compared with women who delivered at 39 weeks or later, women who delivered before 39 weeks of gestation tended to be older and to have a lower body-mass index at the time of delivery. They were also significantly more likely to be white, to have private insurance, to be married, and to have had a first- or second-trimester ultrasound examination for dating the pregnancy. The mean birth weight of the infants and the prevalence of large-for-gestational-age infants increased with higher gestational age at delivery.

Study Outcomes

There was only one neonatal death, which occurred in an infant born at 39 weeks. Five neonates had seizures, and none had hypoxic–ischemic encephalopathy or necrotizing enterocolitis. The rate of the primary outcome of any neonatal adverse outcome or death varied according to center, with a median of 10.5% (interquartile range, 7.0 to 11.7). Table 2Table 2Incidence of Adverse Neonatal Outcomes According to Completed Week of Gestation at Delivery. shows the incidence rates of neonatal outcomes according to gestational age at birth. The primary outcome was significantly less likely as gestational age at birth increased from 37 to 39 weeks (with rates of 15.3% at 37 weeks and 8.0% at 39 weeks; P for trend <0.001). Similar trends of decreasing incidence with greater gestational age were also noted for any adverse respiratory outcome and its components (transient tachypnea of the newborn or respiratory distress syndrome), admission to the neonatal ICU, need for cardiopulmonary resuscitation or mechanical ventilation within 24 hours after delivery, newborn sepsis, hypoglycemia, and prolonged hospitalization. Three of the four neonates who had cardiopulmonary resuscitation also required mechanical ventilation.

We also assessed the outcomes for deliveries performed beyond 39 completed weeks of gestation. The incidence rates of each neonatal outcome for infants born at 40 weeks were similar to those for infants born at 39 weeks. However, there were significant trends toward an increased incidence of the primary outcome for delivery at more than 40 weeks of gestation (P for trend <0.001). Similar trends were noted for respiratory complications (P=0.002), admission to the neonatal ICU (P<0.001), newborn sepsis (P<0.001), and prolonged hospitalization (P<0.001); the findings for other outcomes were limited by small numbers. Figure 2 shows the overall relationship between gestational age at delivery and the primary outcome.

The trends toward the decreasing incidence of the primary outcome and of individual neonatal complications with increasing gestational age at term birth up to 39 weeks of gestation remained significant in analyses adjusted for potential confounders; the adjusted odds ratios ranged from 1.8 to 4.2 at 37 weeks of gestation and from 1.3 to 2.1 at 38 weeks of gestation, as compared with 1.0 at 39 weeks of gestation (Table 3Table 3Odds Ratios for Adverse Neonatal Outcomes According to Completed Week of Gestation at Delivery.). Delivery at 40 weeks was not associated with significantly increased morbidity as compared with delivery at 39 weeks, but delivery at 41 weeks or at 42 weeks or more was associated with increases in several complications similar in magnitude to those observed for births at 38 weeks and 37 weeks, respectively. Other variables associated with the primary outcome in multivariate analyses were race or ethnic group, number of previous cesarean deliveries, payor, presence or absence of diet-controlled gestational diabetes mellitus, and maternal age (see the Supplementary Appendix, available with the full text of this article at NEJM.org).

Adjusted analyses of the primary outcome restricted to births for which the gestational age was estimated by a first- or second-trimester ultrasound examination yielded similar results. Furthermore, the exclusion of the 1% of infants weighing less than 2500 g at birth did not change the prevalence of delivery before 39 weeks or materially affect the association between earlier gestational age at delivery and the primary outcome. Analyses adjusted for study center gave similar results. Furthermore, when the analysis of deliveries before 39 weeks was restricted to the 51.9% of deliveries (2463 of 4743) that occurred during the last 3 days before week 39 (i.e., from 38 weeks 4 days to 38 weeks 6 days), the risk of the primary outcome remained higher than that for deliveries at 39 completed weeks (relative risk, 1.21; 95% CI, 1.04 to 1.40; P=0.01).

The attributable risk of the primary outcome due to elective delivery before 39 weeks of gestation was 48% at 37 weeks (a result implying that postponing elective delivery to 39 weeks might prevent 48% of cases of the primary outcome among deliveries at 37 weeks of gestation) and 27% at 38 weeks of gestation.

Discussion

In this large, multicenter study in the United States, more than one third of elective repeat cesarean deliveries at term were performed before 39 weeks of gestation. As compared with deliveries at 39 weeks, these early deliveries were associated with a significantly increased risk of a composite outcome that included neonatal death or any adverse outcome, as well as increased risks of individual neonatal adverse outcomes that included respiratory complications and admission to the neonatal ICU. The risks of individual adverse neonatal outcomes were higher for delivery at 37 weeks (by a factor of 1.8 to 4.2) than for delivery at 38 weeks (by a factor of 1.3 to 2.1) relative to delivery at 39 weeks of gestation. Delaying delivery beyond 40 weeks was also associated with increased rates of neonatal adverse outcomes. However, only one neonatal death and no cases of hypoxic–ischemic encephalopathy or necrotizing enterocolitis were observed in this select cohort of low-risk term births.

The validity of these findings depends on our ability to have correctly identified and excluded deliveries for which there were indications for delivery before 39 weeks. Specifically trained and certified personnel scrutinized the charts of all women in the registry and their infants for indications for cesarean delivery. Our criteria for elective cesarean delivery were stringent. Although fetal growth restriction was not captured as a specific indication for cesarean delivery, our results remained unchanged after the exclusion of potentially growth-restricted neonates (birth weight <2500 g). It is possible that some earlier term deliveries may have been performed because of maternal perception of reduced fetal movement (a sign of potential fetal compromise). Although such patients should generally undergo antepartum fetal testing for signs suggesting fetal compromise20 (which would be coded as an indication for delivery), clinicians may forgo fetal testing before delivery at term. This might have affected our results in the unlikely event that more of such deliveries occurred before than after 39 weeks.

Also important is the accuracy with which we assigned gestational age. Our results were materially unchanged in analyses restricted to infants with gestational age estimated by first- or second-trimester ultrasound examination, rather than by third-trimester ultrasound examination or last menstrual period alone. The increase in mean birth weight as the assigned gestational age advanced provides further support for the accuracy of our dating.

Some limitations of the study should be noted. Deliveries that occurred before 39 weeks of gestation but after positive results of tests of lung maturity would not be considered inappropriately early3,4; however, we did not have information about testing for lung maturity. One retrospective study of cesarean delivery at a single U.S. center, although potentially nonrepresentative of the general population, showed that 22% of elective cesarean deliveries were performed early without any tests for fetal lung maturity.21 Further study is warranted to assess whether an increased rate of adverse outcomes in deliveries occurring before 39 weeks is explained entirely by failure to test for fetal lung maturity before delivery, or whether testing indicating “maturity” does not fully protect against an increased rate of adverse outcomes in these early births.

Our study design did not allow us to assess whether there was an increase in stillbirths that was associated with delaying delivery until at least 39 weeks. The risk of unexplained stillbirth has been reported to be no greater than 0.2 of 1000 births at 37 weeks and 0.5 of 1000 births at 38 weeks among Scottish and Canadian cohorts of women who had previous cesarean deliveries.22,23 On the assumption of a higher average risk in our U.S. population of approximately 0.5 of 1000 births per week, we estimate that two or three stillbirths might have been averted in our cohort by delivery before 39 weeks. However, as compared with delivery at 39 weeks, earlier delivery increased the rate of adverse neonatal outcomes in the cohort, including 176 extra cases of the primary outcome, 145 admissions to the neonatal ICU, and 63 cases of respiratory distress syndrome. Although there were no neonatal deaths associated with early delivery in our cohort, the sample size was too small to evaluate an increase in this rare outcome, since more than 20,000 subjects would be needed to measure an incidence of 0.1 to 1.0% with adequate confidence and precision.

Since the vast majority of women with a previous cesarean delivery elect a repeat cesarean delivery,13,14 since more than 25% of primary cesarean deliveries are performed before the onset of labor,24 and since there may be increasing enthusiasm for cesarean delivery on maternal request,25 the timing of cesarean delivery and its effect on infant outcomes have substantial public health importance. We identified a recent systematic review26 and five individual European studies1,2,27-29 that examined the association of the timing of elective cesarean delivery with neonatal outcomes. The rates of elective cesarean delivery before 39 weeks were higher in the European cohorts (ranging from 51 to 83%) than in our study. Because these studies vary considerably in their definitions of “elective” and in their criteria for inclusion and exclusion, their results cannot be directly compared with ours. Even so, the studies consistently demonstrated increased respiratory morbidity with elective cesarean delivery before 39 weeks. These studies focused primarily on respiratory complications, and the combined number of women undergoing elective cesarean deliveries was only about half that of our study.

The composite primary outcome occurred in approximately 10% of all neonates in our study. Although the majority of deliveries before 39 weeks occurred at 38 weeks 4 days through 38 weeks 6 days, deliveries occurring during this period were also associated with increased neonatal morbidity. We also observed a higher risk of neonatal complications with cesarean delivery at 41 weeks or later, although the overall proportion of mothers delivering this late was small (<5%). These findings suggest that in addition to the risk of stillbirth, which is almost doubled at 41 weeks of gestation and increased by a factor of up to five at 42 or more weeks as compared with 39 weeks,22,23 the risk of neonatal complications may also be increased by delaying elective cesarean delivery beyond 39 or 40 completed weeks of gestation.

Our combined study population reflects the socioeconomic and demographic spectrum of the United States.30 Although we studied only repeat procedures, which constitute the majority of elective cesarean deliveries, previous studies that included primary cesarean deliveries have shown similar increases in respiratory complications with delivery before 39 weeks of gestation.28,29

Our results indicate that a high proportion of elective cesarean deliveries in the United States are performed before 39 weeks. This may be driven by several factors, including a woman's desire to give birth once term is attained and an obstetrician's desire to schedule the procedure at a convenient time.25 These early deliveries are associated with a preventable increase in neonatal morbidity and admissions to the neonatal ICU, which carry a high economic cost. These findings support recommendations to delay elective delivery until 39 weeks of gestation and should be helpful in counseling.

Presented in part at the 28th Annual Meeting of the Society for Maternal–Fetal Medicine, Dallas, January 28–February 2, 2008.

Supported by grants (HD21410, HD21414, HD27860, HD27861, HD27869, HD27905, HD27915, HD27917, HD34116, HD34122, HD34136, HD34208, HD34210, HD40500, HD40485, HD40544, HD40545, HD40560, HD40512, HD36801) from the National Institute of Child Health and Human Development (NICHD). Dr. Tita is supported by NICHD grant HD001258 as a Women's Reproductive Health Research Scholar. No potential conflict of interest relevant to this article was reported.

We thank Dwight J. Rouse, M.D., M.S.P.H., for contributing to the development of this study concept and critically reviewing earlier drafts of the manuscript; Dr. Steven G. Gabbe, Vanderbilt University, Nashville, chair of the Maternal–Fetal Medicine Units Network Steering Committee for the study; and the following core committee members: Francee Johnson, B.S.N., Ohio State University, and Julia McCampbell, R.N., University of Texas Southwestern Medical Center, for primary protocol development and coordination between clinical research centers; Elizabeth Thom, Ph.D., and Sharon Gilbert, M.S., M.B.A., George Washington University Biostatistics Center, for protocol and data management and statistical analysis; and John C. Hauth, M.D., University of Alabama at Birmingham, for protocol development and oversight.

Source Information

From the University of Alabama at Birmingham, Birmingham (A.T.N.T.); Ohio State University, Columbus (M.B.L.); Eunice Kennedy Shriver National Institute of Child Health and Human Development, Bethesda, MD (C.Y.S.); George Washington University Biostatistics Center, Washington, DC (Y.L.); the University of Texas Southwestern Medical Center, Dallas (K.J.L.); University of Utah, Salt Lake City (M.W.V.); University of Chicago, Chicago (A.H.M.); University of Pittsburgh, Pittsburgh (S.N.C.); Wake Forest University School of Medicine, Winston-Salem, NC (P.J.M.); Thomas Jefferson University, Philadelphia (R.J.W.); Wayne State University, Detroit (Y.S.); University of Cincinnati, Cincinnati, and Columbia University, New York (M.M.); Brown University, Providence, RI (M.C.); Northwestern University, Chicago (A.M.P.); University of Miami, Miami (M.J.O.); University of Tennessee, Memphis (B.M.S.); University of Texas Health Science Center, San Antonio (O.L.); the University of North Carolina, Chapel Hill (J.M.T.); University of Texas Health Science Center, Houston (S.M.R.); and Case Western Reserve University, Cleveland (B.M.M.).

Address reprint requests to Dr. Tita at the Department of Obstetrics and Gynecology, Division of Maternal–Fetal Medicine, University of Alabama at Birmingham, 619 19th St. South, Birmingham, AL 35249, or at .

The other members of the Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) Maternal–Fetal Medicine Units Network are listed in the Appendix.

Appendix

In addition to the authors, the members of the Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) Maternal–Fetal Medicine Units Network are as follows: Ohio State University — J. Iams, F. Johnson, S. Meadows, H. Walker; University of Alabama at Birmingham — D. Rouse, J. Hauth, A. Northen, S. Tate; University of Texas Southwestern Medical Center — S. Bloom, J. McCampbell, D. Bradford; University of Utah — M. Belfort, F. Porter, B. Oshiro, K. Anderson, A. Guzman; University of Chicago — J. Hibbard, P. Jones, M. Ramos-Brinson, M. Moran, D. Scott; University of Pittsburgh — K. Lain, M. Cotroneo, D. Fischer, M. Luce; Wake Forest University — M. Harper, M. Swain, C. Moorefield, K. Lanier, L. Steele; Thomas Jefferson University — A. Sciscione, M. DiVito, M. Talucci, M. Pollock; Wayne State University — M. Dombrowski, G. Norman, A. Millinder, C. Sudz, B. Steffy; University of Cincinnati — T. Siddiqi, H. How, N. Elder; Columbia University — F. Malone, M. D'Alton, V. Pemberton, V. Carmona, H. Husami; Brown University — H. Silver, J. Tillinghast, D. Catlow, D. Allard; Northwestern University — M. Socol, D. Gradishar, G. Mallett; University of Miami — G. Burkett, J. Gilles, J. Potter, F. Doyle, S. Chandler; University of Tennessee — W. Mabie, R. Ramsey; University of Texas at San Antonio — O. Langer, S. Barker, M. Rodriguez; University of North Carolina — K. Moise, K. Dorman, S. Brody, J. Mitchell; University of Texas at Houston — L. Gilstrap, M. Day, M. Kerr, E. Gildersleeve; Case Western Reserve University — P. Catalano, C. Milluzzi, B. Slivers, C. Santori; George Washington University Biostatistics Center — E. Thom, S. Gilbert, H. Juliussen-Stevenson, M. Fischer; Eunice Kennedy Shriver NICHD — D. McNellis, K. Howell, S. Pagliaro.

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Citing Articles

  1. 1

    Steven L. Clark, Janet A. Meyers, Jonathan B. Perlin. (2012) Oversight of elective early term deliveries: avoiding unintended consequences. American Journal of Obstetrics and Gynecology 206:5, 387-389
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    M K Barger, A Nannini, J Weiss, E R Declercq, P Stubblefield, M Werler, S Ringer. (2012) Severe maternal and perinatal outcomes from uterine rupture among women at term with a trial of labor. Journal of Perinatology
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    Lee T. Dresang, Lawrence Leeman. (2012) Cesarean Delivery. Primary Care: Clinics in Office Practice 39:1, 145-165
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    Clarissa Bonanno, Ronald J. Wapner. (2012) Antenatal Corticosteroids in the Management of Preterm Birth: Are We Back Where We Started?. Obstetrics and Gynecology Clinics of North America 39:1, 47-63
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    J S Anadkat, M W Kuzniewicz, B P Chaudhari, F S Cole, A Hamvas. (2012) Increased risk for respiratory distress among white, male, late preterm and term infants. Journal of Perinatology
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    J. B. Warren, C. A. Phillipi. (2012) Care of the Well Newborn. Pediatrics in Review 33:1, 4-18
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    James A. Taylor, Jeffrey A. Wright, David Woodrum. 2012. Routine Newborn Care. , 300-315.
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    Sarah A. Waller, Sameer Gopalani, Thomas J. Benedetti. 2012. Complicated Deliveries. , 146-158.
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    Luisa Wetta, Alan T.N. Tita. (2012) Early Term Births: Considerations in Management. Obstetrics and Gynecology Clinics of North America
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    William A. Grobman, Jennifer L. Bailit. 2012. Patient Safety and Quality Measurement in Obstetrical Care. , 1191-1199.
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    Mara B. Greenberg, Maurice L. Druzin, Steven G. Gabbe. 2012. Antepartum Fetal Evaluation. , 237-263.
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    Vincenzo Berghella, Mark B. Landon. 2012. Cesarean Delivery. , 445-478.
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    Lawrence M. Nogee, Bruce C. Trapnell. 2012. Lung Diseases Associated with Disruption of Pulmonary Surfactant Homeostasis. , 810-821.
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    Alan H. Jobe, Suhas G. Kallapur, Boris W. Kramer. 2012. Perinatal Events and Their Influence on Lung Development and Function. , 57-89.
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    T Boutsikou, A Malamitsi-Puchner. (2011) Caesarean section: impact on mother and child. Acta Paediatrica 100:12, 1518-1522
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    Robert M. Silver, D. Ware Branch, Robert Goldenberg, Jay D. Iams, Mark A. Klebanoff. (2011) Nomenclature for Pregnancy Outcomes. Obstetrics & Gynecology 118:6, 1402-1408
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    Josje Langenveld, Anita C.J. Ravelli, Anton H. van Kaam, David P. van der Ham, Maria G. van Pampus, Martina Porath, Ben Willem Mol, Wessel Ganzevoort. (2011) Neonatal outcome of pregnancies complicated by hypertensive disorders between 34 and 37 weeks of gestation: a 7 year retrospective analysis of a national registry. American Journal of Obstetrics and Gynecology 205:6, 540.e1-540.e7
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    KS Joseph. (2011) The natural history of pregnancy: diseases of early and late gestation. BJOG: An International Journal of Obstetrics & Gynaecology 118:13, 1617-1629
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    Alan Thevenet N. Tita, Yinglei Lai, Steven L. Bloom, Catherine Y. Spong, Michael W. Varner, Susan M. Ramin, Steve N. Caritis, William A. Grobman, Yoram Sorokin, Anthony Sciscione, Marshall W. Carpenter, Brian M. Mercer, John M. Thorp, Fergal D. Malone, Margaret Harper, Jay D. Iams. (2011) Timing of delivery and pregnancy outcomes among laboring nulliparous women. American Journal of Obstetrics and Gynecology
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    Deborah B. Ehrenthal, Matthew K. Hoffman, Xiaozhang Jiang, Gordon Ostrum. (2011) Neonatal Outcomes After Implementation of Guidelines Limiting Elective Delivery Before 39 Weeks of Gestation. Obstetrics & Gynecology 118:5, 1047-1055
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    P. Lopes, E. Misbert. (2011) Les 10 commandements pour l’intervention césarienne. Gynécologie Obstétrique & Fertilité 39:11, 601-602
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    2011. Cesarean Delivery. , 227-249.
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    Cynthia Gyamfi-Bannerman. (2011) The Scope of the Problem: The Epidemiology of Late Preterm and Early-Term Birth. Seminars in Perinatology 35:5, 246-248
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    Robert M. Silver. (2011) Previous Stillbirth, Late Preterm, and Early-Term Birth. Seminars in Perinatology 35:5, 302-308
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    Mark B. Landon, Courtney D. Lynch. (2011) Optimal Timing and Mode of Delivery After Cesarean with Previous Classical Incision or Myomectomy: A Review of the Data. Seminars in Perinatology 35:5, 257-261
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    Jay D. Iams, Edward F. Donovan. (2011) Spontaneous Late Preterm Births: What Can Be Done to Improve Outcomes?. Seminars in Perinatology 35:5, 309-313
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    Robert L. Goldenberg, Michael G. Gravett, Jay Iams, Aris T. Papageorghiou, Sarah A. Waller, Michael Kramer, Jennifer Culhane, Fernando Barros, Augustin Conde-Agudelo, Zulfiqar A. Bhutta, Hannah E. Knight, Jose Villar. (2011) The preterm birth syndrome: issues to consider in creating a classification system. American Journal of Obstetrics and Gynecology
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    Howard Blanchette. (2011) The Rising Cesarean Delivery Rate in America. Obstetrics & Gynecology 118:3, 687-690
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    Pathik D. Wadhwa, Sonja Entringer, Claudia Buss, Michael C. Lu. (2011) The Contribution of Maternal Stress to Preterm Birth: Issues and Considerations. Clinics in Perinatology 38:3, 351-384
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    Steven L. Clark, Alan R. Fleischman. (2011) Term Pregnancy: Time for a Redefinition. Clinics in Perinatology 38:3, 557-564
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    William A. Engle. (2011) Morbidity and Mortality in Late Preterm and Early Term Newborns: A Continuum. Clinics in Perinatology 38:3, 493-516
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    Mark A. Klebanoff, Sarah A. Keim. (2011) Epidemiology: The Changing Face of Preterm Birth. Clinics in Perinatology 38:3, 339-350
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    Natalia Novikova, Catherine Cluver, Natalia Novikova. 2011. Induction of labour versus expectant management for pre-eclampsia at or near term. .
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    Catherine Y. Spong, Brian M. Mercer, Mary DʼAlton, Sarah Kilpatrick, Sean Blackwell, George Saade. (2011) Timing of Indicated Late-Preterm and Early-Term Birth. Obstetrics & Gynecology 118:2, Part 1, 323-333
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    Girija Natarajan, Sreedhar R Anne, Sanjeev Aggarwal. (2011) Outcomes of congenital heart disease in late preterm infants: double jeopardy?. Acta Paediatrica 100:8, 1104-1107
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    Ashwin Ramachandrappa, Eli S. Rosenberg, Scott Wagoner, Lucky Jain. (2011) Morbidity and Mortality in Late Preterm Infants with Severe Hypoxic Respiratory Failure on Extra-Corporeal Membrane Oxygenation. The Journal of Pediatrics 159:2, 192-198.e3
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    Robin H. Steinhorn. (2011) Every Week Matters. The Journal of Pediatrics 159:2, 177-178
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    Szu-Nian Yang, Lih-Jong Shen, Tao Ping, Yu-Chun Wang, Ching-Wen Chien. (2011) The delivery mode and seasonal variation are associated with the development of postpartum depression. Journal of Affective Disorders 132:1-2, 158-164
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    Claire A. Hoffmire, Patricia R. Chess, Taha Ben Saad, J. Christopher Glantz. (2011) Elective Delivery Before 39 Weeks: The Risk of Infant Admission to the Neonatal Intensive Care Unit. Maternal and Child Health Journal
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    George Saade. 2011. Management of the Subsequent Pregnancy. , 242-250.
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    Alan T. N. Tita, Mark Landon, Yinglei Lai, Catherine Y. Spong. (2011) Timing of Elective Repeat Cesarean Delivery at Term and Maternal Perioperative Outcomes. Obstetrics & Gynecology 117:6, 1437-1438
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    Beena D. Kamath, Michael P. Marcotte, Emily A. DeFranco. (2011) Neonatal morbidity after documented fetal lung maturity in late preterm and early term infants. American Journal of Obstetrics and Gynecology 204:6, 518.e1-518.e8
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    Gerson D. Hernandez, Lisa M. Korst, Thomas M. Goodwin, David A. Miller, Aaron B. Caughey, Joseph G. Ouzounian. (2011) Late pregnancy complications can affect risk estimates of elective induction of labor. Journal of Maternal-Fetal and Neonatal Medicine 24:6, 787-794
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    Eliza F. Chakravarty. (2011) Rheumatoid arthritis and pregnancy: Beyond smaller and preterm babies. Arthritis & Rheumatism 63:6, 1469-1471
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    Hiroyuki Tsuda, Yuichiro Takahashi, Shigenori Iwagaki, Yasushi Uchida, Ichiro Kawabata, Masahiro Hayakawa, Seiji Sumigama, Hiromi Hayakawa, Tomomi Kotani, Fumitaka Kikkawa. (2011) Amniotic lamellar body counts can predict the occurrence of respiratory distress syndrome as well as transient tachypnea of the newborn (TTN). Journal of Perinatal Medicine 39:3, 245-250
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    Kathleen Rice Simpson. (2011) Clinicians’ Guide to the Use of Oxytocin for Labor Induction and Augmentation. Journal of Midwifery & Women's Health 56:3, 214-221
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    Karna Murthy, William A. Grobman, Todd A. Lee, Jane L. Holl. (2011) Trends in induction of labor at early-term gestation. American Journal of Obstetrics and Gynecology 204:5, 435.e1-435.e6
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    G. Eric Knox, Kathleen Rice Simpson. (2011) Perinatal high reliability. American Journal of Obstetrics and Gynecology 204:5, 373-377
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    Samantha J. Lain, Charles S. Algert, Natasha Nassar, Jennifer R. Bowen, Christine L. Roberts. (2011) Incidence of Severe Adverse Neonatal Outcomes: Use of a Composite Indicator in a Population Cohort. Maternal and Child Health Journal
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    Steven L. Clark, Janet A. Meyers, Donna K. Frye, Jonathan A. Perlin. (2011) Patient safety in obstetrics–the Hospital Corporation of America experience. American Journal of Obstetrics and Gynecology 204:4, 283-287
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    J.M. Mhyre. (2011) What’s new in obstetric anesthesia?. International Journal of Obstetric Anesthesia 20:2, 149-159
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    Debra Bingham, Nan Strauss, Francine Coeytaux. (2011) Maternal mortality in the United States: a human rights failure. Contraception 83:3, 189-193
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    S. Marret. (2011) Ce que pensent les néonatalogistes des césariennes programmées « à terme ». Revue de médecine périnatale 3:1, 22-24
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    Kari Horowitz, Deborah Feldman, Brittany Stuart, Adam Borgida, Yu Ming Victor Fang, Victor Herson. (2011) Full-term neonatal intenstive care unit admission in an urban community hospital: the role of respiratory morbidity. Journal of Maternal-Fetal and Neonatal Medicine1-4
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    Alan T. N. Tita, Yinglei Lai, Mark B. Landon, Catherine Y. Spong, Kenneth J. Leveno, Michael W. Varner, Steve N. Caritis, Paul J. Meis, Ronald J. Wapner, Yoram Sorokin, Alan M. Peaceman, Mary J. OʼSullivan, Baha M. Sibai, John M. Thorp, Susan M. Ramin, Brian M. Mercer. (2011) Timing of Elective Repeat Cesarean Delivery at Term and Maternal Perioperative Outcomes. Obstetrics & Gynecology 117:2, Part 1, 280-286
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    JA Hutcheon, S Lisonkova, LA Magee, P Von Dadelszen, HL Woo, S Liu, KS Joseph. (2011) Optimal timing of delivery in pregnancies with pre-existing hypertension. BJOG: An International Journal of Obstetrics & Gynaecology 118:1, 49-54
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    Josje Langenveld, Kim Broekhuijsen, Gert-Jan van Baaren, Maria G van Pampus, Anton H van Kaam, Henk Groen, Martina Porath, Martijn A Oudijk, Kitty W Bloemenkamp, Christianne Groot, Erik van Beek, Marloes E van Huizen, Herman P Oosterbaan, Christine Willekes, Ella J Wijnen-Duvekot, Maureen T M Franssen, Denise A M Perquin, Jan M J Sporken, Mallory D Woiski, Henk A Bremer, Dimitri N M Papatsonis, Jozien T J Brons, Mesruwe Kaplan, Bas W A Nij Bijvanck, Ben-Willen J Mol, . (2011) Induction of labour versus expectant monitoring for gestational hypertension or mild pre-eclampsia between 34 and 37 weeks' gestation (HYPITAT-II): a multicentre, open-label randomised controlled trial. BMC Pregnancy and Childbirth 11:1, 50
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    E. Gillet, E. Martens, G. Martens, H. Cammu. (2011) Prelabour Caesarean Section following IVF/ICSI in Older-Term Nulliparous Women: Too Precious to Push?. Journal of Pregnancy 2011, 1-5
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    Ipek Gurol-Urganci, David A Cromwell, Leroy C Edozien, Chidimma Onwere, Tahir A Mahmood, Jan H van der Meulen. (2011) The timing of elective caesarean delivery between 2000 and 2009 in England. BMC Pregnancy and Childbirth 11:1, 43
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    Gordon C.S. Smith. 2011. Delivery after Previous Cesarean Section. , 1261-1268.
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    Ashwin Ramachandrappa, Lucky Jain. 2011. The late preterm infant. , 629-642.
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    Richard J. Martin, Avroy A. Fanaroff, Michele C. Walsh. 2011. Epidemiology and perinatal services. , 19-32.
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    Waldemar A. Carlo. 2011. Overview of Mortality and Morbidity. , 532-532.e5.
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    Elizabeth Bates, Dwight J. Rouse, Merry Lynn Mann, Victoria Chapman, Waldemar A. Carlo, Alan T. N. Tita. (2010) Neonatal Outcomes After Demonstrated Fetal Lung Maturity Before 39 Weeks of Gestation. Obstetrics & Gynecology 116:6, 1288-1295
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    Diane M Ashton. (2010) Elective delivery at less than 39 weeks. Current Opinion in Obstetrics and Gynecology 22:6, 506-510
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    Van Leung-Pineda, Ann M Gronowski. (2010) Biomarker tests for fetal lung maturity. Biomarkers in Medicine 4:6, 849-857
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    Marian F. MacDorman, Eugene Declercq, Jun Zhang. (2010) Obstetrical Intervention and the Singleton Preterm Birth Rate in the United States From 1991–2006. American Journal of Public Health 100:11, 2241-2247
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    Steven L. Clark, Donna R. Frye, Janet A. Meyers, Michael A. Belfort, Gary A. Dildy, Shalece Kofford, Jane Englebright, Jonathan A. Perlin. (2010) Reduction in elective delivery at <39 weeks of gestation: comparative effectiveness of 3 approaches to change and the impact on neonatal intensive care admission and stillbirth. American Journal of Obstetrics and Gynecology 203:5, 449.e1-449.e6
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    Douglas H. Kirkpatrick, Ronald T. Burkman. (2010) Does Standardization of Care Through Clinical Guidelines Improve Outcomes and Reduce Medical Liability?. Obstetrics & Gynecology 116:5, 1022-1026
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    David G. Grenache, Andrew R. Wilson, Gilad A. Gross, Ann M. Gronowski. (2010) Clinical and laboratory trends in fetal lung maturity testing. Clinica Chimica Acta 411:21-22, 1746-1749
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    Rany Al-Agha, Brendan T. Kinsley, Francis M. Finucane, Sharon Murray, Sean Daly, Michael Foley, Sam Coulter Smith, Richard G. Firth. (2010) Caesarean section and macrosomia increase transient tachypnoea of the newborn in type 1 diabetes pregnancies. Diabetes Research and Clinical Practice 89:3, e46-e48
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    Ravi M. Patel, Lucky Jain. (2010) Delivery After Previous Cesarean: Short-Term Perinatal Outcomes. Seminars in Perinatology 34:4, 272-280
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    Mona T. Lydon-Rochelle, Alison G. Cahill, Catherine Y. Spong. (2010) Birth After Previous Cesarean Delivery: Short-Term Maternal Outcomes. Seminars in Perinatology 34:4, 249-257
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    Elizabeth G. Livingston, Yanling Huo, Kunjal Patel, Susan B. Brogly, Ruth Tuomala, Gwendolyn B. Scott, Arlene Bardeguez, Alice Stek, Jennifer S. Read. (2010) Mode of Delivery and Infant Respiratory Morbidity Among Infants Born to HIV-1-Infected Women. Obstetrics & Gynecology 116:2, Part 1, 335-343
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    Dariusz Sagan, Andrzej Semczuk, Elżbieta Lampka. (2010) Combination chemotherapy for Hodgkin's lymphoma during pregnancy: Favorable outcome for mother and child. Journal of Obstetrics and Gynaecology Research 36:4, 882-886
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    T. Michael O'Shea, Mark A. Klebanoff, Caroline Signore. (2010) Delivery After Previous Cesarean: Long-Term Outcomes in the Child. Seminars in Perinatology 34:4, 281-292
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    Alan R. Fleischman, Motoko Oinuma, Steven L. Clark. (2010) Rethinking the Definition of “Term Pregnancy”. Obstetrics & Gynecology 116:1, 136-139
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    Alan T.N. Tita, Luisa A. Wetta, Elizabeth Bates, Amy Doss, Jamie L. Erwin. (2010) Discussion: ‘Infant death among Ohio residents’ by Donovan et al. American Journal of Obstetrics and Gynecology 203:1, e8-e9
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    Edward F. Donovan, John Besl, John Paulson, Barbara Rose, Jay Iams. (2010) Infant death among Ohio resident infants born at 32 to 41 weeks of gestation. American Journal of Obstetrics and Gynecology 203:1, 58.e1-58.e5
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    Caroline Signore. (2010) No Time for Complacency. Obstetrics & Gynecology 116:1, 4-6
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    Christopher J. Robinson, Margaret S. Villers, Donna D. Johnson, Kit N. Simpson. (2010) Timing of elective repeat cesarean delivery at term and neonatal outcomes: a cost analysis. American Journal of Obstetrics and Gynecology 202:6, 632.e1-632.e6
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    Jennifer L. Bailit, Kimberly D. Gregory, Uma M. Reddy, Victor H. Gonzalez-Quintero, Judith U. Hibbard, Mildred M. Ramirez, D. Ware Branch, Ronald Burkman, Shoshana Haberman, Christos G. Hatjis, Matthew K. Hoffman, Michelle Kominiarek, Helain J. Landy, Lee A. Learman, James Troendle, Paul Van Veldhuisen, Isabelle Wilkins, Liping Sun, Jun Zhang. (2010) Maternal and neonatal outcomes by labor onset type and gestational age. American Journal of Obstetrics and Gynecology 202:3, 245.e1-245.e12
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    (2010) A statewide initiative to reduce inappropriate scheduled births at 360/7–386/7 weeks' gestation. American Journal of Obstetrics and Gynecology 202:3, 243.e1-243.e8
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    Freke A. Wilmink, Chantal W.P.M. Hukkelhoven, Simone Lunshof, Ben Willem J. Mol, Joris A.M. van der Post, Dimitri N.M. Papatsonis. (2010) Neonatal outcome following elective cesarean section beyond 37 weeks of gestation: a 7-year retrospective analysis of a national registry. American Journal of Obstetrics and Gynecology 202:3, 250.e1-250.e8
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    Richard L Nelson, Sylvia E Furner, Matthew Westercamp, Cindy Farquhar, Richard L Nelson. 2010. Cesarean delivery for the prevention of anal incontinence. .
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    Pisake Lumbiganon, Malinee Laopaiboon, A Metin Gülmezoglu, João Paulo Souza, Surasak Taneepanichskul, Pang Ruyan, Deepika Eranjanie Attygalle, Naveen Shrestha, Rintaro Mori, Nguyen Duc Hinh, Hoang Thi Bang, Tung Rathavy, Kang Chuyun, Kannitha Cheang, Mario Festin, Venus Udomprasertgul, Maria Julieta V Germar, Gao Yanqiu, Malabika Roy, Guillermo Carroli, Katherine Ba-Thike, Ekaterina Filatova, José Villar. (2010) Method of delivery and pregnancy outcomes in Asia: the WHO global survey on maternal and perinatal health 2007–08. The Lancet 375:9713, 490-499
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    J.A. Stockman. (2010) Timing of Elective Repeat Cesarean Delivery at Term and Neonatal Outcomes. Yearbook of Pediatrics 2010, 440-441
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    D.H. Chestnut. (2010) Elective caesarean section increases the risk of respiratory morbidity of the newborn. Yearbook of Anesthesiology and Pain Management 2010, 299-300
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    D.H. Chestnut. (2010) Timing of Elective Repeat Cesarean Delivery at Term and Neonatal Outcomes. Yearbook of Anesthesiology and Pain Management 2010, 300-301
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    H. M. Gardiner. (2009) Head start for heart babies: perspectives on neurodevelopmental outcome. Ultrasound in Obstetrics and Gynecology 34:6, 616-617
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    Elliott K Main. (2009) New perinatal quality measures from the National Quality Forum, the Joint Commission and the Leapfrog Group. Current Opinion in Obstetrics and Gynecology 21:6, 532-540
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    Ida Sue Baron, Kristine Erickson, Margot D. Ahronovich, Kelly Coulehan, Robin Baker, Fern R. Litman. (2009) Visuospatial and verbal fluency relative deficits in ‘complicated’ late-preterm preschool children. Early Human Development 85:12, 751-754
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    Robert L. Goldenberg, Elizabeth M. McClure, Anand Bhattacharya, Tina D. Groat, Pamela J. Stahl. (2009) Women’s Perceptions Regarding the Safety of Births at Various Gestational Ages. Obstetrics & Gynecology 114:6, 1254-1258
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    Terrie E Inder, Steve M Liao. (2009) Late preterm infants: not so near to term. Pediatric Health 3:5, 417-419
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    Koji Matsuo, Koichiro Shimoya, Tadashi Kimura. (2009) Elective cesarean delivery at 38 weeks' gestation: Is the timing too early?. Journal of Perinatal Medicine 37:5, 569-569
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    Vicki FLENADY, Julie MacPHAIL, Glenn GARDENER, Yogesh CHADHA, Kassam MAHOMED, Alexander HEAZELL, Ruth FRETTS, Frederik FRØEN. (2009) Detection and management of decreased fetal movements in Australia and New Zealand: A survey of obstetric practice. Australian and New Zealand Journal of Obstetrics and Gynaecology 49:4, 358-363
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    (2009) Even at Term, Timing Of Cesarean Is Linked To Adverse Outcomes. Perspectives on Sexual and Reproductive Health 41:2, 130-131
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    M. A. Kominiarek. (2009) Infants Born Late Preterm: Indications and Recommendations for Obstetric Care. NeoReviews 10:6, e295-e302
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    Lokesh Guglani, Rita M Ryan, Satyan Lakshminrusimha. (2009) Risk factors and management of transient tachypnea of the newborn. Pediatric Health 3:3, 251-260
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    Ashwin Ramachandrappa, Lucky Jain. (2009) Health Issues of the Late Preterm Infant. Pediatric Clinics of North America 56:3, 565-577
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    Methodius G Tuuli, Anthony O Odibo. (2009) Neonatal outcomes in relation to timing of repeat cesarean delivery at term. Women's Health 5:3, 239-242
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    (2009) Timing of Elective Repeat Cesarean Delivery at Term. New England Journal of Medicine 360:15, 1570-1571
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    Greene, Michael F., . (2009) Making Small Risks Even Smaller. New England Journal of Medicine 360:2, 183-184
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    J.S. Dungan. (2009) Timing of Elective Repeat Cesarean Delivery at Term and Neonatal Outcomes. Yearbook of Obstetrics, Gynecology and Women's Health 2009, 92-95
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    A.A. Fanaroff. (2009) Timing of Elective Repeat Cesarean Delivery at Term and Neonatal Outcomes. Yearbook of Neonatal and Perinatal Medicine 2009, 50-54
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