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1.
Am. j. obstet. gynecol ; 212(6)Jun. 2015. tab
Article in English | BIGG - GRADE guidelines | ID: biblio-965276

ABSTRACT

OBJECTIVE: We sought to provide evidence-based guidelines for the diagnosis and management of fetal anemia. METHODS: A systematic literature review was performed using MEDLINE, PubMed, EMBASE, and the Cochrane Library. The search was restricted to English-language articles published from 1966 through May 2014. Priority was given to articles reporting original research, in particular randomized controlled trials, although review articles and commentaries were consulted. Abstracts of research presented at symposia and scientific conferences were not considered adequate for inclusion. Evidence reports and published guidelines were also reviewed, and additional studies were located by reviewing bibliographies of identified articles. GRADE (Grading of Recommendations Assessment, Development, and Evaluation) methodology was used for defining the strength of recommendations and rating the quality of evidence. Consistent with US Preventive Task Force guidelines, references were evaluated for quality based on the highest level of evidence. RESULTS AND RECOMMENDATIONS: We recommend the following: (1) middle cerebral artery peak systolic velocity (MCA-PSV) measured by ultrasound Doppler interrogation be used as the primary technique to detect fetal anemia; (2) amniotic fluid delta OD450 not be used to diagnosis fetal anemia; (3) MCA-PSV assessment be reserved for those patients who are at risk of having an anemic fetus (proper technique for MCA-PSV evaluation includes assessment of the middle cerebral artery close to its origin, ideally at a zero degree angle without angle correction); (4) if a fetus is deemed at significant risk for severe fetal anemia (MCA greater than 1.5 multiples of the median or hydropic), fetal blood sampling be performed with preparation for an intrauterine transfusion, unless the pregnancy is at a gestational age when the risks associated with delivery are considered to be less than those associated with the procedure; (5) if a fetus is deemed at significant risk for severe fetal anemia, the patient be referred to a center with expertise in invasive fetal therapy; (6) MCA-PSV be considered to determine the timing of a second transfusion in fetuses with anemia, and, alternatively, a predicted decline in fetal hemoglobin may be used for timing the second procedure; and (7) pregnancies with a fetus at significant risk for fetal anemia be delivered at 37-38 weeks of gestation unless indications develop prior to this time.(AU)


Subject(s)
Humans , Fetal Nutrition Disorders/diagnosis , Fetal Nutrition Disorders/therapy , Blood Transfusion, Intrauterine , Hydrops Fetalis , Cordocentesis , Amniocentesis
2.
BJOG ; 122(13): 1740-7, 2015 Dec.
Article in English | MEDLINE | ID: mdl-25516497

ABSTRACT

OBJECTIVE: Smoking and pre-eclampsia (PE) are associated with increases in preterm birth, placental abruption and low birthweight. We evaluated the relationship between prenatal vitamin C and E (C/E) supplementation and perinatal outcomes by maternal self-reported smoking status focusing on outcomes known to be impacted by maternal smoking. DESIGN/SETTING/POPULATION: A secondary analysis of a multi-centre trial of vitamin C/E supplementation starting at 9-16 weeks in low-risk nulliparous women with singleton gestations. METHODS: We examined the effect of vitamin C/E by smoking status at randomisation using the Breslow-Day test for interaction. MAIN OUTCOME MEASURES: The trial's primary outcomes were PE and a composite outcome of pregnancy-associated hypertension (PAH) with serious adverse outcomes. Perinatal outcomes included preterm birth and abruption. RESULTS: There were no differences in baseline characteristics within subgroups (smokers versus nonsmokers) by vitamin supplementation status. The effect of prenatal vitamin C/E on the risk of PE (P = 0.66) or PAH composite outcome (P = 0.86) did not differ by smoking status. Vitamin C/E was protective for placental abruption in smokers (relative risk [RR] 0.09; 95% CI 0.00-0.87], but not in nonsmokers (RR 0.92; 95% CI 0.52-1.62) (P = 0.01), and for preterm birth in smokers (RR 0.76; 95% CI 0.58-0.99) but not in nonsmokers (RR 1.03; 95% CI 0.90-1.17) (P = 0.046). CONCLUSION: In this cohort of women, smoking was not associated with a reduction in PE or the composite outcome of PAH. Vitamin C/E supplementation appears to be associated with a reduction in placental abruption and preterm birth among smokers.


Subject(s)
Abruptio Placentae/epidemiology , Hypertension, Pregnancy-Induced/epidemiology , Pre-Eclampsia/epidemiology , Premature Birth/epidemiology , Smoking/epidemiology , Vitamins/administration & dosage , Adolescent , Adult , Ascorbic Acid/administration & dosage , Dietary Supplements , Double-Blind Method , Female , Humans , Pregnancy , Vitamin E/administration & dosage , Young Adult
3.
BJOG ; 120(10): 1183-91, 2013 Sep.
Article in English | MEDLINE | ID: mdl-23331974

ABSTRACT

OBJECTIVE: To determine if change in maternal angiogenic biomarkers between the first and second trimesters predicts pre-eclampsia in low-risk nulliparous women. DESIGN: A nested case-control study of change in maternal plasma soluble Flt-1 (sFlt-1), soluble endoglin (sEng) and placenta growth factor (PlGF). We studied 158 pregnancies complicated by pre-eclampsia and 468 normotensive nonproteinuric controls. SETTING: A multicentre study in 16 academic medical centres in the USA. POPULATION: Low-risk nulliparous women. METHODS: Luminex assays for PlGF, sFlt-1 and sEng performed on maternal EDTA plasma collected at 9-12, 15-18 and 23-26 weeks of gestation. Rate of change of analyte between first and either early or late second trimester was calculated with and without adjustment for baseline clinical characteristics. MAIN OUTCOME MEASURES: Change in PlGF, sFlt-1 and sEng. RESULTS: Rates of change of PlGF, sEng and sFlt-1 between first and either early or late second trimesters were significantly different in women who developed pre-eclampsia, severe pre-eclampsia or early-onset pre-eclampsia compared with women who remained normotensive. Inclusion of clinical characteristics (race, body mass index and blood pressure at entry) increased sensitivity for detecting severe and particularly early-onset pre-eclampsia but not pre-eclampsia overall. Receiver operating characteristics curves for change from first to early second trimester in sEng, PlGF and sFlt-1 with clinical characteristics had areas under the curve of 0.88, 0.84 and 0.86, respectively, and for early-onset pre-eclampsia with sensitivities of 88% (95% CI 64-99), 77% (95% CI 50-93) and 77% (95% CI 50-93) for 80% specificity, respectively. Similar results were seen in the change from first to late second trimester. CONCLUSION: Change in angiogenic biomarkers between first and early second trimester combined with clinical characteristics has strong utility for predicting early-onset pre-eclampsia.


Subject(s)
Antigens, CD/blood , Pre-Eclampsia/blood , Pregnancy Proteins/blood , Pregnancy Trimester, First/blood , Pregnancy Trimester, Second/blood , Receptors, Cell Surface/blood , Vascular Endothelial Growth Factor Receptor-1/blood , Adult , Biomarkers/blood , Blood Pressure , Body Mass Index , Early Diagnosis , Endoglin , Female , Humans , Longitudinal Studies , Parity , Placenta Growth Factor , Pre-Eclampsia/diagnosis , Pre-Eclampsia/ethnology , Pregnancy , Risk Factors , Young Adult
4.
BJOG ; 119(13): 1617-23, 2012 Dec.
Article in English | MEDLINE | ID: mdl-23078336

ABSTRACT

OBJECTIVE: To determine whether vitamin D status is associated with recurrent preterm birth, and any interactions between vitamin D levels and fish consumption. DESIGN: A nested case-control study, using data from a randomised trial of omega-3 fatty acid supplementation to prevent recurrent preterm birth. SETTING: Fourteen academic health centres in the USA. POPULATION: Women with prior spontaneous preterm birth. METHODS: In 131 cases (preterm delivery at <35 weeks of gestation) and 134 term controls, we measured serum 25-hydroxyvitamin D [25(OH)D] concentrations by liquid chromatography-tandem mass spectrometry (LC-MS) from samples collected at baseline (16-22 weeks of gestation). Logistic regression models controlled for study centre, maternal age, race/ethnicity, number of prior preterm deliveries, smoking status, body mass index, and treatment. MAIN OUTCOME MEASURES: Recurrent preterm birth at <37 and <32 weeks of gestation. RESULTS: The median mid-gestation serum 25(OH)D concentration was 67 nmol/l, and 27% had concentrations of <50 nmol/l. Serum 25(OH)D concentration was not significantly associated with preterm birth (OR 1.33; 95% CI 0.48-3.70 for lowest versus highest quartiles). Likewise, comparing women with 25(OH)D concentrations of 50 nmol/l, or higher, with those with <50 nmol/l generated an odds ratio of 0.80 (95% CI 0.38-1.69). Contrary to our expectation, a negative correlation was observed between fish consumption and serum 25(OH)D concentration (-0.18, P < 0.01). CONCLUSIONS: In a cohort of women with a prior preterm birth, vitamin D status at mid-pregnancy was not associated with recurrent preterm birth.


Subject(s)
Diet , Premature Birth/etiology , Prenatal Nutritional Physiological Phenomena , Seafood , Vitamin D Deficiency/complications , Vitamin D/analogs & derivatives , Adult , Biomarkers/blood , Case-Control Studies , Chromatography, Liquid , Diet Surveys , Female , Humans , Logistic Models , Mass Spectrometry , Pregnancy , Premature Birth/blood , Prospective Studies , Recurrence , Risk , Self Report , Vitamin D/blood , Vitamin D Deficiency/blood
5.
J Perinatol ; 28(2): 102-6, 2008 Feb.
Article in English | MEDLINE | ID: mdl-18046339

ABSTRACT

OBJECTIVE: We sought to compare two approaches to antenatal testing for their impact on the workforce. STUDY DESIGN: This is a prospective observational study of women who presented for antenatal testing. All women were given a survey upon presentation. As per hospital protocol, nonstress testing (NST) was performed semiweekly and biophysical profile (BPP) was performed weekly. The choice of testing was determined by the attending physician. chi2- and Student's t-tests were performed where appropriate. A P-value of <0.05 was considered significant. RESULT: A total of 195 women were surveyed. Among them, 94 women had an NST and 101 had a BPP. Overall, 59.2% were multiparous, 33.1% had to arrange for child care and 97.2% felt reassured by the testing. There were no differences in demographic characteristics, education, type of insurance or employment status between the groups. Women who had NSTs were more likely to lose time from work than those who had BPPs (218.4 versus 68.9 min; P<0.001). Of the women who had semiweekly NSTs, 80.6% would have preferred weekly testing. If the 94 women who received semiweekly testing had weekly testing, a total of 534.4 h would have been available for the workforce. CONCLUSION: Twice-weekly NST results in a significant increase in time lost from the workforce compared with weekly BPP.


Subject(s)
Employment , Fetal Monitoring/methods , Prenatal Care/methods , Adult , Amniotic Fluid , Female , Heart Rate, Fetal , Humans , Occupational Health , Pregnancy , Prospective Studies , Time
6.
J Perinatol ; 28(1): 67-70, 2008 Jan.
Article in English | MEDLINE | ID: mdl-18033305

ABSTRACT

OBJECTIVE: We sought to evaluate neonatal hearing assessment by the otoacoustic emission (OAE) test in very low birth weight (VLBW) infants exposed to antenatal steroids. STUDY DESIGN: This is a retrospective cohort study of infants <1500 g delivered between July 1998 and July 2004 who completed hearing screens on discharge. All screens were performed by the OAE. Only infants who failed or passed the exam were included in the analysis. Infants with a partial or an inadequate exam were excluded. Neonates exposed to antenatal steroids were then compared to unexposed infants for the results of their OAE. RESULT: A total of 68,000 deliveries were performed during the study period. There were 703 VLBW infants who had hearing exams, of which 548 (78%) passed the screen, 95 (14%) failed and 59 (8%) were indeterminate. Gestational age, birth weight, score for neonatal acute physiology and severe intraventricular hemorrhage were associated with a failed screen (P<0.01). Antenatal steroid exposure was not associated with a failed screen (odds ratio: 0.83 (95% confidence interval 0.5-1.4), P=0.43). CONCLUSION: In our population, antenatal steroids were not associated with a positive or negative effect on hearing assessment of VLBW infants.


Subject(s)
Hearing/drug effects , Infant, Very Low Birth Weight , Steroids/adverse effects , Case-Control Studies , Cohort Studies , Female , Gestational Age , Hearing Tests , Humans , Infant, Newborn , Infant, Premature , Pregnancy , Retrospective Studies
7.
Obstet Gynecol ; 98(5 Pt 1): 751-6, 2001 Nov.
Article in English | MEDLINE | ID: mdl-11704164

ABSTRACT

OBJECTIVE: To compare use of the Foley catheter for preinduction cervical ripening in an inpatient versus outpatient setting. METHODS: A randomized trial was conducted from May 1998 to December 1999. Women with a term gestation in the vertex presentation, a reactive nonstress test, an amniotic fluid index above the fifth percentile, and a Bishop score of no more than 5 were included. The primary outcome variable was a change in Bishop score. A Foley catheter with a 30-mL balloon was placed through the cervix on gentle traction in each group. The outpatient group was then discharged home with written instructions and returned in the morning for induction. The inpatient group was admitted to labor and delivery, with induction started upon extrusion of the Foley. RESULTS: Sixty-one women were randomized into the outpatient group, and 50 women into the inpatient group. Maternal age, gravidity, previous cesarean delivery, and gestational age did not differ between the groups. The median Bishop score at entry was 3.0 for each group (P =.97). The mean change in Bishop scores after catheter placement was not different between the inpatient and outpatient groups (3.0 versus 3.0; P =.74). The maximum dose of oxytocin, time of oxytocin, epidural rate, induction time, 1-minute and 5-minute Apgar scores, and cord pH were not significantly different. The outpatient group on average avoided 9.6 hours of hospitalization. There were no adverse events or maternal morbidity in either group. CONCLUSIONS: The Foley bulb is as effective in the outpatient as the inpatient setting for preinduction cervical ripening.


Subject(s)
Catheterization , Cervical Ripening , Labor, Induced , Adult , Ambulatory Care , Case-Control Studies , Female , Hospitalization/statistics & numerical data , Humans , Pregnancy , Prospective Studies , Time Factors
8.
Am J Obstet Gynecol ; 185(5): 1090-3, 2001 Nov.
Article in English | MEDLINE | ID: mdl-11717639

ABSTRACT

OBJECTIVE: Midtrimester premature rupture of membranes causes significant perinatal morbidity and death. No effective treatment exists. We investigated (1) whether a needle puncture in the fetal membranes could be sealed in vitro and (2) the optimal composition of the sealant to be used. STUDY DESIGN: Membranes from second trimester pregnancies (16-24 weeks of gestation) were stretched over a modified syringe with a 2.5-cm open diameter. The syringe was filled with 20 mL of second trimester amniotic fluid, and the membrane was punctured with a 20-gauge needle. Sealants were injected into the amniotic fluid. The primary outcome variable was time for leakage of amniotic fluid. Median times for leakage for the formulations were compared by Wilcoxon exact rank sum test. RESULTS: Platelets alone failed to seal the puncture site. All other formulations stopped leakage temporarily. Tisseel (Baxter Corp, Glendale, Calif) and cryoprecipitate/thrombin preparations led to more prolonged sealing of punctured amniotic membranes than platelets (P <.01) and were not significantly different from each other. CONCLUSION: Of the sealants tested in vitro, amniotic membranes are best sealed by a fibrin/thrombin-based sealant.


Subject(s)
Amnion/drug effects , Fetal Membranes, Premature Rupture/drug therapy , Fibrin Tissue Adhesive/therapeutic use , Thrombin/therapeutic use , Tissue Adhesives/therapeutic use , Amnion/metabolism , Amniotic Fluid/metabolism , Blood Platelets/physiology , Female , Humans , In Vitro Techniques , Injections , Permeability , Pregnancy , Pregnancy Trimester, Second , Punctures , Time Factors
9.
Am J Obstet Gynecol ; 184(7): 1431-4; discussion 1434-5, 2001 Jun.
Article in English | MEDLINE | ID: mdl-11408864

ABSTRACT

OBJECTIVE: We evaluated a new device that uses the intrauterine pressure catheter to measure the maternal temperature in patients who are in labor. STUDY DESIGN: The study was conducted at two medical centers, Christiana Hospital in Newark, Delaware, and Saint Louis University/St Mary's Health Center in St Louis, Missouri, from September 1, 1997, to May 2, 1998. An intrauterine pressure catheter with a thermistor sensor in the tip was placed into the uterus after spontaneous rupture of membranes. The intrauterine, oral, and tympanic temperatures were simultaneously obtained immediately after insertion of the intrauterine pressure catheter and then hourly until delivery or the initiation of amnioinfusion. RESULTS: The study comprised 97 patients and 404 temperature readings with a temperature range of 34.7 degrees C to 40.7 degrees C. The normal mean +/- SD for the oral, tympanic, and intrauterine temperatures was 36.7 degrees C +/- 0.5 degrees C, 36.8 degrees C +/- 0.5 degrees C, and 37.3 degrees C +/- 0.4 degrees C, respectively. There was a linear relationship among the oral, tympanic, and intrauterine temperatures. All three methods showed a significant increase in mean body temperature after epidural anesthesia. CONCLUSION: The new device, the intrauterine pressure-temperature catheter, provides a convenient and accurate means of continuously measuring uterine temperature in patients who are in labor and require intrauterine monitoring.


Subject(s)
Body Temperature , Labor, Obstetric/physiology , Obstetrics/instrumentation , Uterus/physiology , Anesthesia, Epidural , Ear, Middle/physiology , Equipment Design , Female , Humans , Mouth/physiology , Pregnancy , Pressure , Sensitivity and Specificity , Transducers
10.
Am J Obstet Gynecol ; 184(6): 1097-9, 2001 May.
Article in English | MEDLINE | ID: mdl-11349168

ABSTRACT

OBJECTIVE: Our aim was to compare outcomes in women with a questionable history of incompetent cervix, followed up with early transvaginal ultrasonography, with outcomes in women who had early cerclage. STUDY DESIGN: Charts were reviewed and patients identified for incompetent cervix from our obstetric database from 1995 through 1997. We included women who had an unclear history of incompetent cervix as follows: second-trimester loss or termination, > or =3 first-trimester terminations, cone biopsy or loop electrosurgical excision, or exposure to diethylstilbestrol. The primary outcome variable was gestational age at delivery. RESULTS: A total of 106 women were included, 45 in the early cerclage group and 61 in the early transvaginal ultrasonography group. The mean gestational age at delivery was 35.1 weeks for the early cerclage group versus 36.1 weeks for the early transvaginal ultrasonography group. CONCLUSION: In women with an unclear history of incompetent cervix, early cerclage does not appear to offer significant benefit over early transvaginal ultrasonography.


Subject(s)
Cervix Uteri/diagnostic imaging , Uterine Cervical Incompetence/diagnostic imaging , Adult , Delivery, Obstetric , Female , Gestational Age , Humans , Pregnancy , Suture Techniques , Ultrasonography , Uterine Cervical Incompetence/surgery
11.
Am J Obstet Gynecol ; 184(3): 368-73, 2001 Feb.
Article in English | MEDLINE | ID: mdl-11228489

ABSTRACT

OBJECTIVE: We report our experience with a transvaginally applied intracervical fibrin sealant at <24 weeks' gestation. STUDY DESIGN: This is an observational study of a referred patient population, with preterm premature rupture of the membranes at <24 weeks' gestation. RESULTS: Twelve women consented to our protocol. The mean gestational age at preterm premature rupture of membranes was 19 weeks 4 days (range, 13-23 weeks); the mean gestational age at treatment was 20 weeks 5 days (range, 17-23 weeks). All women had a diminution in the amount of amniotic fluid leakage with an increase in amniotic fluid index. Among the 12 pregnancies (13 fetuses), there were 7 surviving neonates. Two women had apparent "resealing" of the membranes. CONCLUSION: Fibrin sealants in midtrimester rupture of the membranes may lead to improved outcomes and now warrant formal evaluation.


Subject(s)
Fetal Membranes, Premature Rupture/therapy , Fibrin Tissue Adhesive/therapeutic use , Adult , Amniotic Fluid/diagnostic imaging , Amniotic Fluid/physiology , Bed Rest , Cervix Uteri/pathology , Female , Fetal Membranes, Premature Rupture/complications , Fibrin Tissue Adhesive/administration & dosage , Gestational Age , Humans , Oligohydramnios/complications , Pilot Projects , Pregnancy , Pregnancy Outcome , Ultrasonography
12.
Obstet Gynecol ; 97(4): 603-7, 2001 Apr.
Article in English | MEDLINE | ID: mdl-11275035

ABSTRACT

OBJECTIVE: To compare the efficacy of intravaginal misoprostol tablets with transcervical Foley catheter for preinduction cervical ripening. METHODS: Pregnant women who presented for induction of labor with unfavorable cervices (Bishop score less than 6) were assigned randomly to intravaginal misoprostol (50 microg tablet every 4 hours for a maximum of six doses) or 30-mL Foley catheter placed transcervically with maintenance of traction. RESULTS: Among 111 women, 53 were allocated to misoprostol and 58 to Foley bulb. Contractile abnormalities were more frequent in the misoprostol group (20.4%) than the Foley group (0%) (P <.001). No statistically significant differences were noted between groups in change in Bishop score, preinduction cervical ripening times, and total induction times. There were no statistically significant differences in mode of delivery or adverse neonatal outcomes. Uterine rupture occurred in one woman with two previous cesarean deliveries in the misoprostol group. CONCLUSION: Intravaginal misoprostol and transcervical Foley catheter are equivalent for cervical ripening. Uterine contractile abnormalities and meconium passage are more common with misoprostol.


Subject(s)
Catheterization , Cervical Ripening , Misoprostol/administration & dosage , Oxytocics/administration & dosage , Administration, Intravaginal , Adult , Cervical Ripening/drug effects , Delivery, Obstetric , Female , Humans , Labor, Induced/methods , Labor, Induced/standards , Pregnancy , Tablets , Treatment Outcome , Uterine Contraction/drug effects
13.
Am J Perinatol ; 16(7): 365-72, 1999.
Article in English | MEDLINE | ID: mdl-10614705

ABSTRACT

The risk of sepsis associated with neutropenia in infants born to mothers with preeclampsia remains controversial. The objective of this study is to investigate the incidence of culture-proven sepsis along with changes in the complete blood count in very-low-birth-weight infants born to mothers with preeclampsia. We conducted a retrospective cohort study of infants cared for at a single tertiary care neonatal intensive care unit during a 4-year period. Infants born to mothers with preeclampsia (n = 88) were compared to infants born to mothers without preeclampsia (n = 416) by univariate and multivariate analysis. Although infants born to mothers with preeclampsia had lower absolute neutrophil and platelet counts throughout the first week of life, they were no more likely to have a platelet count <100,000 /mm3, and only more likely to be neutropenic at 24 and 72 hr of life compared to infants born to mothers without preeclampsia. After controlling for potential confounding variables, there was no increase in the odds of culture proven sepsis in infants born to mothers with preeclampsia (odds ratio 1.6, 95% confidence intervals 0.7-3.6, p = 0.3) compared to those infants born to mothers without preeclampsia. We conclude that very-low-birth-weight infants born to mothers with preeclampsia are not at increased risk of culture proven sepsis despite a reduction in absolute neutrophils.


Subject(s)
Infant, Very Low Birth Weight , Pre-Eclampsia/complications , Sepsis/etiology , Analysis of Variance , Cohort Studies , Confidence Intervals , Female , Follow-Up Studies , Gestational Age , Humans , Incidence , Infant, Newborn , Infant, Small for Gestational Age/blood , Infant, Very Low Birth Weight/blood , Intensive Care, Neonatal , Leukocyte Count , Multivariate Analysis , Neutropenia/etiology , Neutrophils/pathology , Odds Ratio , Platelet Count , Pregnancy , Retrospective Studies , Risk Factors
14.
Am J Obstet Gynecol ; 180(1 Pt 1): 55-60, 1999 Jan.
Article in English | MEDLINE | ID: mdl-9914578

ABSTRACT

OBJECTIVE: The objective of this study was to compare intracervical prostaglandin E2 gel with insertion of a Foley bulb for efficacy in preinduction cervical ripening. STUDY DESIGN: Women who came to the hospital for induction of labor with a Bishop score

Subject(s)
Catheterization , Cervical Ripening/drug effects , Cervical Ripening/physiology , Dinoprostone/administration & dosage , Labor, Induced , Cervix Uteri , Dinoprostone/therapeutic use , Female , Gels , Humans , Pregnancy , Prospective Studies , Time Factors , Treatment Outcome , Uterine Contraction/drug effects , Uterine Contraction/physiology
15.
Obstet Gynecol ; 91(6): 1023-6, 1998 Jun.
Article in English | MEDLINE | ID: mdl-9611018

ABSTRACT

OBJECTIVE: To determine fellowship satisfaction through a survey of maternal-fetal medicine fellows. METHODS: We constructed a survey using multiple choice, Likert scale, ordinal, and categorical scale questions. The questions focused on faculty involvement, mentorship, research time and productivity, education, fellowship selection, ultimate goals of fellows, and satisfaction. We sent the survey in two mailings to all maternal-fetal medicine fellows during April and May 1996. RESULTS: One hundred thirty-eight surveys were mailed, and 136 were returned (98.5% return rate). Twenty-seven percent of fellows did not believe they would complete their thesis by the end of their fellowship. No statistically significant relationship was noted between the fellows' predicted thesis completion and the availability of funding, support for statistical analysis, the presence of animal research facilities, age, number of dependents, or year of fellowship. The presence of a mentor on the maternal-fetal medicine faculty increased the likelihood of thesis completion from 52.3% to 83.5% (P < .001). Similarly, the presence of a faculty advisor increased the likelihood of thesis completion from 58.9% to 83.5% (P = .001). Thirty-two percent of the respondents did not have a mentor on the faculty, and 41% did not have a faculty advisor. Forty percent indicated that they were too involved in clinical pursuits to perform research. This group was significantly more likely to believe that their theses would not be completed (63% versus 80%, P = .029). Overall, 22% of the fellows would not recommend their fellowships. Fellows with a mentor (88.2% versus 55.8%; P < .001) or faculty advisor (87.3% versus 64.9%; P = .002) were more likely than those without to recommend their fellowship. CONCLUSION: A mentor or faculty advisor plays a significant role in the training of maternal-fetal medicine fellows and is associated with a higher incidence of satisfaction with the fellowship program, thesis completion, and entrance into academic practice.


Subject(s)
Career Choice , Fellowships and Scholarships , Mentors , Obstetrics/education , Academic Dissertations as Topic , Adult , Attitude of Health Personnel , Data Collection , Female , Humans , Job Satisfaction , Male
16.
Am J Perinatol ; 15(3): 177-81, 1998 Mar.
Article in English | MEDLINE | ID: mdl-9572373

ABSTRACT

To determine whether hospital admission and parenteral tocolysis of patients with threatened preterm labor results in a decreased preterm delivery rate and improved perinatal outcome, we performed a prospective cohort study comparing tocolytic treatment versus no tocolytic treatment. Women between 20 and 37 weeks' gestation who presented with at least eight uterine contractions per hour and a cervical examination <2 cm dilated, <80% effaced, and no cervical change over a 2-hr period were entered into the study. Exclusion criteria included cervical change, multiple gestation, chorioamnionitis, rupture of membranes, placenta previa or abruption, undiagnosed vaginal bleeding, and prior tocolytic therapy in the current pregnancy. Seventy-five patients were admitted to the hospital for tocolysis (tocolysis cohort) and 81 were observed and discharged to home (observation cohort). There was no significant difference in mean gestational age at delivery, mean birth weight, or in preterm delivery rate between the two cohorts. Four of the eight women in the observation cohort who delivered preterm had a history of preterm delivery. We conclude that discharging women with preterm contractions without objective evidence of labor does not result in an increase in preterm births. More importantly, tocolysis did not decrease the preterm delivery rate in this cohort.


Subject(s)
Obstetric Labor, Premature/prevention & control , Pregnancy Outcome , Tocolysis , Adult , Birth Weight , Female , Humans , Magnesium Sulfate/therapeutic use , Pregnancy , Prospective Studies , Terbutaline/therapeutic use , Tocolytic Agents/therapeutic use , Treatment Outcome
18.
Am J Perinatol ; 14(8): 449-56, 1997 Sep.
Article in English | MEDLINE | ID: mdl-9376004

ABSTRACT

Sophisticated neonatal transport has improved the safety of transporting preterm infants, but may not substitute for the benefits of in utero transport. To describe gestational age trends and assess differences in complications between maternal (in utero) and neonatal transports, we analyzed maternal and neonatal transports, over 3 years, to the only tertiary center in the region. Those who delivered between 24 and 34 weeks' gestation were included in the analysis. Gestational age trends for each complication are described, showing, in general, decreasing morbidity with gestational age in both groups. These trends were usually parallel, but not equal. A significantly greater mean neonatal intensive care unit (p = 0.003) and total length of stay (p = 0.006) as well as longer ventilator time (p = 0.01) and oxygen therapy exposure (p = 0.018) were noted in those transported neonatally. The incidence of respiratory distress syndrome (p < 0.001), bronchopulmonary dysplasia (p = 0.027), intraventricular hemorrhage (p = 0.041), intraventricular hemorrhage grades III and IV (p = 0.008), patent ductus arteriosus (p = 0.032), and mortality (p = 0.001) were all significantly greater among the neonatal transports. The differences were not significant for retinopathy of prematurity, hyperbilirubinemia, necrotizing enterocolitis, periventricular leukomalacia, and culture proven sepsis. Specialized neonatal transport and advanced neonatology techniques have not removed the significant advantage of decreased morbidity, mortality, and length of hospital intervention resulting from maternal (in utero) transport.


Subject(s)
Delivery, Obstetric , Infant Mortality , Patient Transfer , Pregnancy Complications , Pregnancy Outcome , Adult , Female , Gestational Age , Humans , Incidence , Infant, Newborn , Infant, Premature , Male , Morbidity , Pregnancy
19.
Br J Obstet Gynaecol ; 104(6): 743-5, 1997 Jun.
Article in English | MEDLINE | ID: mdl-9197883

ABSTRACT

Glycocalicin has been found to be a marker of increased platelet turnover, while interleukin-6 may be increased in response to thrombocytopenia. We used these markers to study the pathophysiology of thrombocytopenia in newborn infants. Cord blood platelet counts were obtained from 499 infants. Thrombocytopenic infants (< 100,000/mm3) and a control group had ELISA assays for interleukin-6 and glycocalicin performed. The mean levels of glycocalicin and interleukin-6 were elevated in cord blood of thrombocytopaenic infants. Infants with intrauterine growth restriction and thrombocytopaenia had no detectable glycocalicin in their plasma, despite elevated levels of interleukin-6. This probably reflects impaired thrombopoiesis in these infants.


Subject(s)
Blood Platelets/metabolism , Interleukin-6/blood , Platelet Aggregation Inhibitors/metabolism , Platelet Count , Platelet Glycoprotein GPIb-IX Complex/metabolism , Thrombocytopenia/immunology , Thrombocytopenia/metabolism , Case-Control Studies , Enzyme-Linked Immunosorbent Assay , Fetal Blood/chemistry , Fetal Growth Retardation/complications , Gestational Age , Humans , Infant, Newborn , Thrombocytopenia/etiology
20.
Am J Perinatol ; 14(5): 249-51, 1997 May.
Article in English | MEDLINE | ID: mdl-9259937

ABSTRACT

In the third trimester, the amniotic fluid index (AFI) may be affected by maternal fluid status. As the ambient temperature increases, there is an increase in insensible fluid loss and the potential for dehydration. We hypothesize that as temperature increases there would be a concomitant decrease in AFI. From June 11 to August 16, 1993, during a period of unusual high heat, 42 women with singleton pregnancies between 27 and 40 weeks' gestation undergoing serial antenatal testing had AFI determinations recorded at least weekly. The daily high ambient temperature in our urban area was subsequently obtained. A 2-, 3-, and 4-day mean temperature prior to the test date was compared to AFI using a Spearman-rank Correlation. The daily high temperature ranged from 71 to 104 degrees F and AFI values ranged from 1.7 to 24.7 cm during the study period. There was a significant correlation between the 2-, 3-, and 4-day mean temperature and AFI, with the 4-day mean being the most significant (r = 0.31, p < 0.001). Fluctuations in ambient temperature are inversely correlated to changes in AFI. This relationship should be taken into account when interpreting the AFI as a measure of fetal well-being.


Subject(s)
Amniotic Fluid/physiology , Body Temperature , Adult , Dehydration/diagnosis , Dehydration/etiology , Female , Follow-Up Studies , Gestational Age , Humans , Pregnancy , Pregnancy Trimester, Third , Retrospective Studies , Risk Factors
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