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1.
Am J Perinatol ; 31(9): 795-8, 2014 Oct.
Article in English | MEDLINE | ID: mdl-24338114

ABSTRACT

OBJECTIVE: The aim of the study was to examine pregnancy outcomes of healthy nulliparous women aged ≥ 40 years at delivery. STUDY DESIGN: The study included 53,480 nulliparous women aged 20 to 29 or ≥ 40 years delivering singleton infants, enrolled in a pregnancy risk assessment program between July 1, 2006, and August 1, 2011. Women reporting medical disorders, tobacco use, or conception with assistive reproductive technology were excluded. Data were grouped by body mass (obese or nonobese) and age (20-29 or ≥ 40 years). Pregnancy outcomes were compared within each body mass group for women aged 20 to 29 years versus ≥ 40 years and between obese and nonobese women aged ≥ 40 years. RESULTS: Within each body mass group, nulliparous women aged ≥ 40 years delivered at a significantly lower gestational age and had a greater incidence of cesarean delivery, gestational diabetes, preterm birth, and both low and very low birth weight infants, compared with controls aged 20 to 29 years. For women aged ≥ 40 years, obesity was associated with higher rates of adverse pregnancy outcomes. CONCLUSION: In healthy women, both advanced maternal age and obesity negatively influence pregnancy outcomes. Women who delay pregnancy until age 40+ years may modify their risk for cesarean section, preterm birth, and low-birth-weight infants by reducing their weight to nonobese levels before conception.


Subject(s)
Body Mass Index , Diabetes, Gestational/epidemiology , Maternal Age , Obesity/epidemiology , Pregnancy Outcome , Premature Birth/epidemiology , Adult , Body Weight , Cesarean Section , Female , Gestational Age , Humans , Incidence , Infant, Low Birth Weight , Infant, Newborn , Infant, Very Low Birth Weight , Middle Aged , Parity , Pregnancy , United States/epidemiology , Young Adult
2.
Am J Obstet Gynecol ; 205(3): 269.e1-6, 2011 Sep.
Article in English | MEDLINE | ID: mdl-22071060

ABSTRACT

OBJECTIVE: The purpose of this study was to determine the role of previous term delivery on the rate of recurrent preterm birth in women with previous spontaneous preterm delivery (SPTD) who receive 17-alphahydroxyprogesterone caproate (17P) therapy. STUDY DESIGN: Women with singleton gestations who were receiving 17P therapy were studied. Rates of recurrent SPTD were compared for 1 or ≥2 SPTD with and without a previous term delivery. RESULTS: Five thousand one hundred two women had 1 previous SPTD, and 2217 women had ≥2 SPTDs. In women with 1 previous SPTD, a previous term delivery had lower rates of SPTD at <35 weeks (8.4% vs 11.2%; P = .002) and preterm delivery at <32 weeks (4.7% vs 6.2%; P = .027) compared with those women with no such history. No differences were found for SPTD at <35 weeks with ≥2 SPTDs. CONCLUSION: In patients who received 17P therapy with 1 previous SPTD, a previous term delivery confers a reduction in risk of preterm delivery at <37, <35, and <32 weeks' gestation; such reduction is not evident with ≥2 previous SPTDs.


Subject(s)
Hydroxyprogesterones/therapeutic use , Premature Birth/prevention & control , Progestins/therapeutic use , 17 alpha-Hydroxyprogesterone Caproate , Adult , Female , Humans , Infant, Newborn , Infant, Premature , Pregnancy , Retrospective Studies , Risk , Secondary Prevention , Term Birth
3.
Am J Obstet Gynecol ; 205(3): 275.e1-5, 2011 Sep.
Article in English | MEDLINE | ID: mdl-22071063

ABSTRACT

OBJECTIVE: We sought to compare rates of recurrent spontaneous preterm birth (SPTB) in women receiving 17-α-hydroxyprogesterone caproate (17P) with prior SPTB due to preterm labor (PTL) vs preterm premature rupture of membranes (PPROM). STUDY DESIGN: Women with singleton gestation having 1 prior SPTB enrolled at 16-24.9 weeks' gestation for weekly outpatient 17P administration were identified from a database. Rates of recurrent SPTB were compared between those with prior SPTB due to PTL or PPROM overall and by gestational age at prior SPTB. RESULTS: Records from 2123 women were analyzed. The prior PTL group vs the prior PPROM group experienced higher rates of recurrent SPTB at <37 weeks (29.7% vs 22.9%, P = .004), <35 weeks (14.0% vs 9.1%, P = .004), and <32 weeks (5.9% vs 3.3%, P = .024), respectively. CONCLUSION: Reason and gestational age of prior SPTB influence the likelihood of recurrent SPTB in women receiving 17P prophylaxis.


Subject(s)
Fetal Membranes, Premature Rupture/prevention & control , Gestational Age , Hydroxyprogesterones/therapeutic use , Premature Birth/prevention & control , Progestins/therapeutic use , 17 alpha-Hydroxyprogesterone Caproate , Adult , Age Factors , Female , Fetal Membranes, Premature Rupture/drug therapy , Fetal Membranes, Premature Rupture/etiology , Humans , Infant, Newborn , Infant, Premature , Pregnancy , Premature Birth/drug therapy , Premature Birth/etiology , Secondary Prevention
4.
Am J Obstet Gynecol ; 204(1): 44.e1-5, 2011 Jan.
Article in English | MEDLINE | ID: mdl-20934682

ABSTRACT

OBJECTIVE: To examine the frequency of elective delivery and neonatal outcomes in women with stable mild gestational hypertension delivering late preterm. STUDY DESIGN: The frequency of elective delivery between 1995 and 2007 at gestational age of 34°(/)7-366(/)7 weeks (late preterm), 37°(/)7-376(/)7 weeks, and ≥38°(/)7 weeks, as well as neonatal outcomes, were studied in singleton gestation with mild gestational hypertension without proteinuria from a large national database. RESULTS: One thousand eight hundred fifty-eight patients were studied: 607 (33%) were delivered for maternal/fetal reasons and 1251 (67%) were electively delivered. Among the 1251 women delivered electively, 25.5% were late preterm, 24.4% at 37°(/)7-376(/)7 weeks and 50.1% at ≥38°(/)7 weeks' gestation. Neonatal intensive care unit admission, ventilatory assistance, and respiratory distress syndrome were more common in late-preterm infants. There was no maternal/perinatal mortality. CONCLUSION: We found that 25.5% of patients with stable mild gestational hypertension, without any maternal or fetal complication, had iatrogenic elective late-preterm delivery. This practice also was associated with increased rates of neonatal complications and neonatal length of stay.


Subject(s)
Delivery, Obstetric/methods , Hypertension, Pregnancy-Induced , Premature Birth , Adolescent , Adult , Delivery, Obstetric/adverse effects , Female , Gestational Age , Humans , Infant, Newborn , Infant, Premature , Intensive Care Units, Neonatal , Middle Aged , Pregnancy , Respiration, Artificial/statistics & numerical data , Respiratory Distress Syndrome, Newborn/etiology , Retrospective Studies , Young Adult
5.
Am J Perinatol ; 27(4): 343-8, 2010 Apr.
Article in English | MEDLINE | ID: mdl-20013580

ABSTRACT

We sought to identify maternal or clinical characteristics of women likely to develop preterm labor (PTL) at <34 weeks' gestation while receiving 17 alpha-hydroxyprogesterone caproate (17P) prophylaxis. Current singleton gestations with prior preterm delivery enrolled for outpatient 17P administration at <27 weeks' gestation were identified ( N = 1177). Maternal and clinical characteristics were compared between women hospitalized and diagnosed with PTL at <34 weeks' gestation (PTL group, N = 270) and those without PTL (No PTL group, N = 660). PTL at <34 weeks' gestation occurred in 270/1177 (22.9%) of patients receiving 17P prophylaxis (mean gestational age at diagnosis was 28.3 +/- 4.0 weeks). Recurrent preterm delivery occurred in 73.3% of women with PTL at <34 weeks. Maternal age, marital status, race, tobacco use, cerclage, gestational age at start of 17P, and Medicaid status were similar between the groups. Women developing PTL at <34 weeks were more likely to have >1 prior preterm delivery than those without PTL (35.2% versus 25.9%, P = 0.006, odds ratio [95% confidence interval] 1.5 [1.1, 2.1]). Women receiving 17P prophylaxis remain at increased risk for PTL and preterm birth. Patient education and surveillance for PTL symptoms may be warranted in women with a history of more than one prior preterm delivery.


Subject(s)
17-alpha-Hydroxyprogesterone/administration & dosage , Obstetric Labor, Premature/chemically induced , Pregnancy Outcome , Pregnancy, High-Risk , Premature Birth/prevention & control , Adult , Cohort Studies , Dose-Response Relationship, Drug , Drug Administration Schedule , Female , Fetal Monitoring/methods , Follow-Up Studies , Gestational Age , Humans , Infant, Newborn , Obstetric Labor, Premature/epidemiology , Obstetric Labor, Premature/prevention & control , Pregnancy , Probability , Recurrence , Retrospective Studies , Risk Assessment
6.
Am J Perinatol ; 26(2): 123-8, 2009 Feb.
Article in English | MEDLINE | ID: mdl-18850519

ABSTRACT

We compared neonatal outcomes from singleton pregnancies in women hospitalized with preterm labor (PTL) at 32 0/7 to 34 6/7 weeks managed with and without acute tocolysis. Women enrolled for outpatient surveillance who were hospitalized and diagnosed with PTL between 32 0/7; to 34 6/7 weeks' gestation without conditions necessitating interventional delivery during hospitalization were identified ( N = 2921). Patients with contraindications to pregnancy prolongation were excluded ( N = 168). Data were compared between patients whose clinical management included tocolysis ( N = 2342) and patients in whom tocolysis was not utilized ( N = 411). The incidence of preterm birth (77.9% versus 48.1%), low birth weight (48.9% versus 16.7%), neonatal intensive care unit admission (41.4% versus 16.2%), and nursery length of stay > 7 days (28.0% versus 9.7%) were all higher in women not receiving acute tocolysis compared with the acute tocolysis group (all P < 0.001). Using acute tocolysis to prolong pregnancy in patients hospitalized with PTL at 32 0/7 to 34 6/7 weeks' gestation is associated with improved neonatal outcomes.


Subject(s)
Obstetric Labor, Premature/epidemiology , Obstetric Labor, Premature/prevention & control , Pregnancy Outcome , Tocolysis , Adolescent , Adult , Female , Gestational Age , Humans , Incidence , Infant, Newborn , Pregnancy
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