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Biomedical subjects

J N Martin

Publications and source records attributed to J N Martin.

At least 91 records · Page 5Linked to original sources
PubMed1996

Trauma in pregnancy: the role of interpersonal violence.

OBJECTIVE: Our purpose was to determine what role interpersonal violence as intentional injury plays in the pregnant trauma victim. STUDY DESIGN: We performed a retrospective review of medical records. RESULTS: During a 9-year period in a single university medical and trauma center, 203 pregnant women were treated for a physically traumatic event. Sixty-four women (31.5%) were victims of intentional injury, in most cases by the husband or boyfriend. Although the mean Injury Severity Score was higher in women with fetal death than in women with successful pregnancy outcomes (7.25 vs 1.74, respectively; p < 0.01), 5 of the 8 women with fetal losses incurred these despite an apparent absence of physical injury (maternal Injury Severity Score = 0). CONCLUSIONS: Interpersonal violence during pregnancy is a frequent and increasingly common cause of maternal injury. The inconsistent relationship between Injury Severity Score and serious fetal injury or death is underscored by the loss of 5 fetuses despite an Injury Severity Score of 0.

Accidents, Traffic↗
PubMed1996

Intrapartum amniotic fluid index. A poor diagnostic test for adverse perinatal outcome.

OBJECTIVE: To determine if an intrapartum amniotic fluid index (IAFI) < or = 5.0 cm, or any other level, is associated with abdominal delivery for fetal intolerance to labor or Apgar scores < 7 at one and five minutes. STUDY DESIGN: Prospectively IAFI was obtained in the latent phase of labor in 1,000 parturients at > 26 weeks. Receiver operating characteristic curves were utilized to determine if any IAFI could be utilized to predict adverse outcome among (1) the entire population, (2) complicated pregnancies, (3) uncomplicated pregnancies, (4) term, or (5) preterm gestation. RESULTS: The frequencies of abdominal delivery for suspected fetal intolerance and low Apgar scores were similar among patients with IAFI < or = 5.0 cm (n = 288) versus those with IAFI > 5.0 cm. All five receiver operating characteristic curves indicated that IAFI is a poor predictor of adverse outcomes. At all the discriminatory IAFIs (0-20 cm), the false positive rate was virtually identical to the true positive rate. CONCLUSION: IAFI appears to be a poor screening test for identifying those at risk for abdominal delivery for presumed fetal distress or for birth of an infant with low Apgar scores.

Amniotic Fluid↗
PubMed1995

Effect of older age on survival in human immunodeficiency virus (HIV) disease.

To evaluate the impact of older age (> 50 years old) on survival in late-stage human immunodeficiency virus (HIV) disease, the authors analyzed 846 HIV-infected patients at the San Francisco Veterans Affairs Medical Center from 1987 to 1992. The median age was 42 years with 171 (20.2%) subjects aged 50 or more years. Survival was measured from the date of initial lymphocyte testing (median CD4 count, 223 cells/mm3) until death or censoring. Compared with those aged less than 40 years, and after multivariate proportional hazards adjustment for other significant determinants of survival (CD4 percentage, CD8 count, hematocrit, and prior acquired immunodeficiency syndrome diagnosis), there was no difference in survival for those aged 40-49 years, but there was a trend toward decreased survival in those aged 50-59 years (relative hazard = 1.32, 95% confidence interval 0.90-1.94) and in those aged 60 or more years (relative hazard = 1.56, 95% confidence interval 0.99-2.46). The impact of older age on mortality in HIV disease is, however, less than the impact of age on overall mortality in the United States. Accordingly, while older HIV-infected patients do have a somewhat poorer survival, this risk need not be too highly emphasized in individual patients; older patients deserve aggressive management.

Adult↗
PubMed1995

Climatic factors and preeclampsia-related hypertensive disorders of pregnancy.

Seasonal variations of temperature and humidity are said to influence the incidence of hypertensive disorders of pregnancy. Pregnant women with hypertensive disorders of pregnancy were assessed on the basis of temperature and relative humidity at diagnosis. Temperature variations with constant high humidity do not influence the incidence of preeclampsia-eclampsia-related hypertensive disorders of pregnancy.

Eclampsia↗
PubMed1995

Delivery of the nonvertex second twin: breech extraction versus external cephalic version.

OBJECTIVE: Our purpose was to compare the maternal and perinatal outcomes of twin gestations in which the nonvertex second twin was delivered by total breech extraction versus those delivered by external cephalic version. STUDY DESIGN: The intrapartum courses of 284 consecutive twin gestations were analyzed retrospectively. Once those with actual birth weight < 600 gm, unrecognized multifetal pregnancy, multiple congenital anomalies, cesarean delivery, and/or antepartum intrauterine fetal death were excluded, 23 mothers were delivered by total breech extraction and 21 underwent external cephalic version. RESULTS: The two groups were similar for mean (+/- SD) maternal age, gravidity, parity, gestational age at delivery, ultrasonographic estimate of birth weight for twin B, incidence of breech or transverse presentation for the second fetus, and actual birth weight of the first or second newborn. Suspected fetal distress that led to cesarean delivery occurred significantly more often in parturients who underwent attempted external version (4/21) than total breech extraction (0/23, p = 0.04). The incidence of eventual abdominal delivery was also significantly higher in patients who underwent attempted external cephalic version (10/21) rather than breech extraction (1/23, p = 0.001). For twin B the occurrence of low Apgar scores at 1 minute was significantly higher for infants after attempted external version (7/21) rather than breech extraction (1/23, p = 0.02), but the mean pH, number with Apgar scores < 7 at 5 minutes, and number of neonatal intensive care unit admissions were similar. No perinatal traumatic injury occurred in either group. CONCLUSION: On the basis of our experience, total breech extraction of the nonvertex second twin is preferable to external cephalic version because it appears to be associated with a significantly lower incidence of fetal distress and abdominal delivery with comparable neonatal outcome.

Adult↗
PubMed1995

Trial of labor after cesarean delivery with a lower-segment, vertical uterine incision: is it safe?

OBJECTIVE: Our purpose was to assess maternal and perinatal outcomes associated with a trial of labor and attempted vaginal birth after prior low-segment vertical cesarean delivery. STUDY DESIGN: During a 10-year period in a single tertiary hospital, all patients with a prior low-segment uterine incision (whether vertical or transverse) were considered candidates for a trial of labor in the absence of other contraindications or patient refusal. Among the 1137 women who underwent low-segment vertical cesarean delivery, 262 were subsequently delivered of 322 live-born infants, and 174 (54%) of them were identified retrospectively as having attempted vaginal birth. The maternal and perinatal outcomes of patients who did or did not undergo a trial of labor were analyzed and compared. RESULTS: No significant differences between the two patient groups were observed regarding demographic characteristics, antepartum complications, gestational age at delivery (mean 37.4 weeks), birth weight, and cord pH at delivery. Vaginal delivery was accomplished successfully in 144 of 174 (83%) patients who underwent a trial of labor. Abdominal delivery was necessary for 17 mothers with labor disorders and 13 with suspected fetal distress. Postpartum hemorrhage occurred more often in the trial of labor group (7/174 [4.0%] vs 2/148 [1.4%], p not significant), but endometritis developed significantly more often in patients with elective repeat cesarean delivery (16.9% vs 6.3%, p = 0.006). Rupture of the low-segment vertical cesarean scar occurred in 2 patients during a trial of labor (1.1%) versus none in the elective repeat cesarean group. Neither mother experienced fetal extrusion or adverse maternal or fetal sequelae. Frequency of serious neonatal complications (8.1% vs 10%) and neonatal mortality (1.7% vs 2.0%) were similar between groups. All neonatal deaths were a result of extreme prematurity or congenital anomalies. CONCLUSIONS: Our experience indicates that a mother with a prior low-segment vertical cesarean delivery can undertake a trial of labor with relative maternal-perinatal safety. The likelihood of successful outcome and the incidence of complications are comparable to those of published experience with a trial of labor after a previous low-segment transverse incision.

Cesarean Section↗
PubMed1995

Postpartum plasma exchange for atypical preeclampsia-eclampsia as HELLP (hemolysis, elevated liver enzymes, and low platelets) syndrome.

OBJECTIVE: Our purpose was to investigate the postpartum use of plasma exchange in patients considered to have atypical preeclampsia-eclampsia manifested as persistent HELLP (hemolysis, elevated liver enzymes, and low platelets) syndrome with or without evidence of other organ injury. STUDY DESIGN: During a 10-year period, 18 patients with HELLP syndrome were treated post partum with single or multiple plasma exchange with fresh-frozen plasma. Each patient was entered into the clinical trial either because of persistent evidence of atypical preeclampsia-eclampsia as HELLP syndrome > 72 hours after delivery (group 1) or with evidence of worsening HELLP syndrome at any time post partum in association with single- or multiple-organ injury (group 2). All procedures were performed with the IBM 2997 Cell Separator (IBM, Cobe Laboratories, Inc., Lakewood, Colo.) system. Maternal and perinatal outcomes were the main outcomes studied. RESULTS: In the absence of other disease conditions, the 9 patients in group 1 with persistent postpartum HELLP syndrome complicated only by severe clinical expressions of preeclampsia-eclampsia responded rapidly to one or two plasma exchange procedures with few complications and no maternal deaths. In contrast, in the 9 patients of group 2 with HELLP syndrome presentations complicated by other organ disease, the response to plasma exchange was variable and there were two deaths in this group. CONCLUSION: The current series of patients details the successful postpartum application of plasma exchange therapy for unremitting HELLP syndrome but reveals that a uniformly positive response to this therapy will not always be observed when there is additional single or multiple organ injury.

Adolescent↗
PubMed1995

Corticosteroid-induced arrest of HELLP syndrome progression in a marginally-viable pregnancy.

Corticosteroid therapy in preterm pregnancy complicated by severe pre-eclampsia as HELLP syndrome temporarily stabilizes the HELLP syndrome. One such patient complicated by extreme prematurity was treated with long-term high-dose corticosteroid therapy. The HELLP syndrome was temporarily stabilized and additional in utero fetal maturation was gained.

Adrenal Cortex Hormones↗
PubMed1995

Amniotic fluid volume of third-trimester diamniotic twin pregnancies.

OBJECTIVE: To define the normal range of amniotic fluid (AF) volume in third-trimester diamniotic twin gestations. METHODS: The AF volume of third-trimester diamniotic twin pregnancies was measured prospectively. An AF sample was drawn from both amniotic cavities of diamniotic twins either for diagnosis of subclinical chorioamnionitis with preterm labor and/or assessment of fetal lung maturity. Actual AF volume was determined in each amniotic cavity by a dye-dilution technique. RESULTS: The AF volume of 45 diamniotic twin pregnancies of 27-38 weeks' gestation was assessed. The AF volume per amniotic sac ranged from 155-5430 mL, with a mean (+/- standard deviation) of 877 +/- 860 mL. The AF volume in individual amniotic cavities and the total of both cavities in a diamniotic twin pregnancy were unchanged across the entire gestational age range (27-38 weeks). Neither fetal positioning within the uterus (lower twin versus upper twin) nor fetal weight were determining factors in the AF volume variability (P = .846 and P = .726, respectively). Based on absolute volumetric differences between the larger- and smaller-sac AF volume, we observed that as the AF volume of the larger sacs increased proportionately (P < .001), the AF volume of the smaller sacs remained relatively constant across the entire range of differences (P = .687) between 27-38 weeks. CONCLUSIONS: The average AF volume of 877 mL for each diamniotic twin is similar to the AF volume reported for third-trimester singletons. The AF volumes of diamniotic twin gestations relate neither to fetal position nor fetal weight, but instead develop independently without relation to the other amniotic cavity. Ninety percent of the AF volumes were 215-2500 mL.

Adolescent↗
PubMed1995

A randomized study to assess the efficacy of the amniotic fluid index as a fetal admission test.

OBJECTIVE: To determine whether there is a difference in the incidence of abdominal delivery for presumed fetal distress in women who have an intrapartum fluid index assessment and those who do not. METHODS: Over a 7-month period, parturients at 26-42 weeks' gestation and in early labor were randomized to the study (measured amniotic fluid index [AFI] on admission) or a control group (no sonographic assessment of amniotic fluid [AF] volume). The labor and delivery staff were aware of the AFI results of the study subjects. All patients had continuous electronic fetal monitoring, and none had an abnormal tracing on admission. Student t test or chi 2 was used for statistical analysis. P < .05 was considered significant. RESULTS: The study (N = 447) and control groups (N = 436) had similar maternal demographics as well as medical and obstetric complications. In the study group, the incidence of abdominal delivery for fetal distress (29 of 447) was significantly higher than among controls (14 of 436) (P = .02; relative risk 1.3, 95% confidence interval 1.1-1.7). Among parturients who had abdominal delivery for fetal distress, the decision-to-incision times (mean +/- standard deviation) were similar for parturients who had undergone assessment of AFI and those who had not (38.5 +/- 14.7 versus 32.5 +/- 14.7 minutes, respectively; P = .47). Mean birth weight, incidence of low birth weight, macrosomia, Apgar scores less than 7, and the number of admissions to the neonatal intensive care unit were not significantly different in the two groups. CONCLUSIONS: Patients having an intrapartum assessment of AFI as a fetal admission test are significantly more likely to have abdominal delivery for presumed fetal distress. However, the decision-to-incision time is not decreased and the perinatal outcome is not improved if the status of AF volume is known for patients in early labor.

Adult↗
PubMed1995

Acute tocolysis for suspected intrapartum fetal distress: maternal effects of terbutaline versus magnesium sulfate.

This study was undertaken to determine the maternal hemodynamic impact of terbutaline versus magnesium sulfate in the acute treatment of fetal distress prior to cesarean delivery. Forty-six women were prospectively randomized to receive 0.25 mg subcutaneous terbutaline or 4.0 g intravenous magnesium sulfate for in utero fetal resuscitation before cesarean delivery. There were no significant differences between groups in baseline mean arterial pressure, arterial pressure before and after induction of anesthesia, maternal heart rate, maternal oxygen saturation, estimated blood loss, and pre- and postoperative hematocrits. Magnesium sulfate-treated women received significantly more intraoperative intravenous fluids (2365 +/- 877 ml) than the terbutaline group (1624 +/- 564 ml; P < 0.001). However, mean urine output was significantly greater in the terbutaline group (88 +/- 42 ml/h) than in those treated with magnesium sulfate (61 +/- 26 ml/h; P < 0.03). Terbutaline, the superior agent for acute tocolysis, is not associated with an increase in maternal cardiovascular side effects during anesthesia.

Journal Article↗
PubMed1995

Sonographic assessment of birth weight among breech presentations.

The objective in this study was to determine whether there was a difference in the accuracy of sonographically determined birth weight estimate in fetuses presenting by the breech as compared to the vertex. Prospectively, 104 consecutive singleton fetuses presented by the breech presentation were identified who also had a sonographic estimate of birth weight within 72 h of delivery. The control group (n = 104) consisted of fetuses presenting by the vertex of women who had the following hospital number and who were of similar demographic characteristics; the birth weight estimate in the control group had to be within 100 g of that of the women with the breech fetus. The estimate of the birth weight was derived for both groups using seven published models. Prediction limits were calculated for an estimated vs. actual birth weight for parturients with breech presentation. Among the study group, the mean standardized absolute error was similar for the seven models (range 120 +/- 104 to 138 +/- 118 g/kg; p = 0.08). For six of the models, the mean standardized absolute error was significantly higher for fetuses in the breech presentation than for fetuses in vertex presentation (range 80 +/- 63 to 112 +/- 95 g/kg; p = 0.02 to < 0.0001). Prediction limit calculations indicate that 99% of the time the actual birth weight was between 1500 and 3999 g if the estimate of birth weight was 2400-2900 g. We conclude that, for fetuses in a breech presentation, the error with most models is significantly higher than for a singleton in the vertex position.

Abdomen↗
PubMed1995

Factors adversely affecting pregnancy outcome in the military.

This prospective study was undertaken to identify the significant risk factors associated with adverse pregnancy outcome in active-duty women. The deliveries of 300 consecutive pregnancies of active-duty women were assessed for maternal-fetal outcome. The risk factors evaluated were: marital status, parity, race, smoking and alcohol consumption while pregnant, maternal weight gain during pregnancy, maternal height, and educational level. Two-thirds of these women were junior enlisted personnel (rank E-4 or below) and worked under demanding job conditions over which they had little control. Increased age as a risk factor was associated with a significant increase in pregnancy-associated complications of cesarean birth, operative vaginal delivery, pregnancy-induced hypertension, preterm labor, maternal transport for fetal indications, intrauterine growth restriction, intrauterine fetal death, postpartum hemorrhage, placenta previa, and 5-minute Apgar scores < 7 (p = 0.039). In gravidas more than 65 inches in height with a weight gain more than 42 pounds, there was a significant increase in the complications of pregnancy (p = 0.022). Interactions of these risk factors yielded a significant age (p = 0.025), maternal height (p = 0.007), and height times weight gain interaction (p = 0.006) association with pregnancy complications. The risk factors of advancing maternal age and tall stature with a maternal weight gain of more than 42 pounds are associated with increased pregnancy complications of active-duty women.

Adult↗
PubMed1995

Management of the obstetric patient with thrombocytopenia.

Thrombocytopenia that complicates pregnancy can occur secondary to known maternal disease processes or may arise again during, and as a result of, gestation. A combination of maternal history, clinical presentation, and laboratory investigation usually leads the obstetrician to the proper diagnosis of the condition and, when necessary, dictates appropriate fetal intervention. Although the differential diagnosis of thrombocytopenia can be a frustrating and difficult exercise, especially in an emergent intrapartum environment, clinical persistence coupled with hematology consultation when appropriate usually will reward the provider and patient with the best chance to achieve optimal maternal-fetal outcome.

Clinical Protocols↗
PubMed1995

The laboratory evaluation of hypertensive gravidas.

A number of laboratory tests are available for the evaluation of the hypertensive gravida. These tests can be used to either predict and/or prognosticate between preeclampsia and other hypertensive disorders of pregnancy. These laboratory tests were evaluated based on published experience with special attention to its ability to facilitate identification of the patient with preeclampsia apart from other hypertensive disorders that co-exist with and occur as a complication of pregnancy. Hypocalciuria and increased cellular plasma fibronectin seem to be good tests to differentiate preeclampsia from chronic hypertension. The management of preeclampsia with its increased risk of perinatal morbidity and mortality renders this differentiation clinically very important. Hyperuricemia, proteinuria, increased serum beta-thromboglobulin concentration, abnormal red blood cell morphology with increased hemoglobin/hematocrit, and increased serum iron individually and collectively reflect the severity of preeclampsia. Platelets and total serum lactate dehydrogenase are the best tests to reflect the severity of HELLP syndrome. Circulating hCG and serum thromboglobulin seem to be the most promising future predictors for preeclampsia.

Diagnosis, Differential↗
PubMed1995

Accuracy of ultrasonography in evaluating amniotic fluid volume at less than 24 weeks' gestation.

The purpose of this investigation was to evaluate the accuracy of common sonographic techniques in assessing the amniotic fluid volume in pregnancies of less than 24 weeks' gestation. Patients at less than 24 weeks' gestation undergoing an amniocentesis for the placement of prostaglandin F2 alpha for termination (because of genetic or fetal anomalies, or both) were assessed for amniotic fluid volume. All fetuses were alive at the time of prostaglandin instillation. The amniotic fluid index and two-diameter pocket were used to determine the amniotic fluid volume. Prior to the prostaglandin instillation, the amniotic fluid volume was determined with para-aminohippurate using a diazo dye reaction with spectrophotometric analysis. The amniotic fluid volume was determined in 21 pregnancies between 15 and 24 weeks' gestation, yielding volumes ranging from 189 to 1840 ml. Using published standards for amniotic fluid volume in singleton pregnancies, oligohydramnios was present in three gestations, the volume was found to be normal in 15, and hydramnios complicated three pregnancies. The two-diameter pocket identified the amniotic fluid volumes correctly more often (18 of 21 [85.7%]) than the amniotic fluid index (10 of 21 [47.6%]) (P = 0.02). Normal amniotic fluid volume was identified in nine of 15 (60%) pregnancies by the amniotic fluid index and in 14 of 15 (93.3%) by the two-diameter pocket (P = not significant). Abnormal amniotic fluid volumes, oligohydramnios, and hydramnios were recognized more often by the two-diameter pocket (66.7%) than by the amniotic fluid index (1 of 6 [16.7%], P = not significant).

Abortion, Induced↗
PubMed1995

Intrapartum amniotic fluid index for predicting fetal acidemia. Results of receiver operating characteristic curve analysis.

OBJECTIVE: The objective of this study was to determine if the discriminatory intrapartum amniotic fluid index can reliably predict respiratory or metabolic acidosis in the newborn. STUDY DESIGN: Among 256 parturients at 37 weeks' gestation or more, the intrapartum amniotic fluid index was obtained in early labor, and umbilical arterial blood gas analysis was performed within 30 minutes of delivery. The mean (+/- SD) amniotic fluid indices in labor among newborns with no acidosis versus those with respiratory or metabolic acidosis were compared. A receiver operating characteristic curve was used to determine the best discriminatory intrapartum amniotic fluid index for respiratory and metabolic acidosis. RESULTS: Statistical analysis revealed that the mean intrapartum amniotic fluid index among 12 newborns with respiratory acidosis and 26 with metabolic acidosis was significantly lower than the mean index in 218 newborns without fetal acidemia. Despite the differences in the mean intrapartum amniotic fluid index in the three groups analyzed, the receiver operating characteristic curve indicated that an intrapartum amniotic fluid index alone is a poor test for predicting acidosis (respiratory or metabolic) in the neonate. CONCLUSION: The mean intrapartum amniotic fluid index in labor among newborns with respiratory or metabolic acidosis was significantly lower than that among nonacidotic newborns. The receiver operating characteristic curve indicated that the intrapartum amniotic fluid index cannot reliably distinguish nonacidotic infants from those with respiratory or metabolic acidosis.

Acidosis↗