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1. |
Trust |
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Obstetrics & Gynecology,
Volume 99,
Issue 5, Part 1,
2002,
Page 681-682
John Queenan,
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ISSN:0029-7844
出版商:OVID
年代:2002
数据来源: OVID
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2. |
Roy M. Pitkin Award |
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Obstetrics & Gynecology,
Volume 99,
Issue 5, Part 1,
2002,
Page 683-683
James Scott,
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ISSN:0029-7844
出版商:OVID
年代:2002
数据来源: OVID
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3. |
Third‐Trimester Unexplained Intrauterine Fetal Death Is Associated With Inherited Thrombophilia |
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Obstetrics & Gynecology,
Volume 99,
Issue 5, Part 1,
2002,
Page 684-687
Ariel Many,
Ronit Elad,
Yuval Yaron,
Amiram Eldor,
Joseph Lessing,
Michael Kupferminc,
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摘要:
OBJECTIVETo determine the risk of thrombophilias in women with unexplained intrauterine fetal deaths (IUFD).METHODSAll women with IUFD at 27 weeks' gestation or greater were initially assessed during a period of 26 months. Subjects with multiple pregnancies, congenital anomalies, intrauterine infection, chorioamnionitis, immune hydrops, diabetes mellitus, previous thromboembolism, and severe hypertensive disease were excluded. The remaining 40 women with unexplained IUFD (study group) were matched for age and ethnicity with 80 healthy women who had at least one normal pregnancy (control group). All participants were tested at least 2 months after delivery for mutations of factor V Leiden, prothrombin gene, methylenetetrahydrofolate reductase, and for deficiencies of protein S, protein C, and antithrombin III. They were also tested and found to be negative for anticardiolipin antibodies.RESULTSThe gestational age at delivery and birth weight were significantly lower in the study group. The prevalence of inherited thrombophilias was 42.5% in the study group compared with 15% in the control group (odds ratio 2.8, 95% confidence interval 1.5, 5.3,P= .001). The prothrombin mutation and protein S deficiency rates were significantly higher in the study group (odds ratio 2.3, 95% confidence interval 1.3, 4.0, and odds ratio 3.2, 95% confidence interval 2.4, 4.1, respectively).CONCLUSIONThird-trimester IUFD is significantly associated with thrombophilias. These findings suggest that thrombophilia work-ups should be part of IUFD investigations and may have therapeutic and prognostic implications in future pregnancies.
ISSN:0029-7844
出版商:OVID
年代:2002
数据来源: OVID
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4. |
Neonatal Organ System Injury in Acute Birth Asphyxia Sufficient to Result in Neonatal Encephalopathy |
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Obstetrics & Gynecology,
Volume 99,
Issue 5, Part 1,
2002,
Page 688-691
Gary Hankins,
Sophia Koen,
Alfredo Gei,
Suzanne Lopez,
James Van Hook,
Garland Anderson,
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摘要:
OBJECTIVETo identify the proportion of major organ system injury in cases of acute intrapartum asphyxia that result in neonatal encephalopathy.METHODSA prospectively maintained database was cross-referenced using medical record coding to identify diagnoses of acute intrapartum asphyxia, acute birth asphyxia, or neonatal encephalopathy over a 6-year period. An acute intrapartum asphyxial antecedent was validated with emphasis on excluding long-standing or chronic conditions where injury likely occurred before presentation. Injury pattern was evaluated using routinely available laboratory and imaging tests.RESULTSForty-six cases of acute peripartum asphyxia sufficient to result in the diagnosis of neonatal encephalopathy were identified. Clinical central nervous system injury resulting in encephalopathy was present in 100% of cases as it was an entry criteria; of these, 49% had electroencephalogram and 40% had imaging studies diagnostic of acute injury. Liver injury based on elevated aspartate transaminase or alanine transaminase levels occurred in 80%. Heart injury, as defined by pressor or volume support beyond 2 hours of life or elevated cardiac enzymes, occurred in 78%. Renal injury, defined by an elevation of serum creatinine to greater than 1.0 mg/dL, persistent hematuria, persistent proteinuria, or clinical oliguria, occurred in 72%. An elevation in nucleated red blood cell counts exceeding 26 per 100 white blood cells occurred in 41%.CONCLUSIONUsing common diagnostic tests as markers of acute asphyxial injury, we noted that multiple organs suffer damage during an acute intrapartum asphyxial event sufficient to result in a neonatal encephalopathy.
ISSN:0029-7844
出版商:OVID
年代:2002
数据来源: OVID
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5. |
Persistence of Placenta Previa According to Gestational Age at Ultrasound Detection |
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Obstetrics & Gynecology,
Volume 99,
Issue 5, Part 1,
2002,
Page 692-697
Jodi Dashe,
Donald McIntire,
Ronald Ramus,
Rigoberto Santos-Ramos,
Diane Twickler,
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摘要:
OBJECTIVETo evaluate gestational age at ultrasound detection of placenta previa as a predictor of previa persistence until delivery, and to estimate the effects of previa type, parity, and prior cesarean delivery on previa persistence.METHODSThis was a retrospective cohort study of pregnancies with placenta previa detected during transabdominal or endovaginal ultrasound examination. Previa was categorized as complete if the placenta completely covered the internal cervical os or incomplete if the inferior placental edge partially covered or reached the margin of the os. Gestational age was grouped into 4-week intervals from 15 to 36 weeks. The outcome was cesarean delivery for persistent previa.RESULTSPrevia was detected during 940 ultrasound examinations in 714 pregnancies. Of those with placenta previa at 15–19 weeks, 20–23 weeks, 24–27 weeks, 28–31 weeks, and 32–35 weeks, previa persisted until delivery in 12%, 34%, 49%, 62%, and 73%, respectively. At each interval, complete previa was more likely to persist than incomplete previa, allP< .001. Prior cesarean delivery was an independent risk factor for persistent previa among women diagnosed with previa in the second trimester,P< .05. However, parity was not an independent risk factor for persistence at any gestational age interval after adjusting for prior cesarean delivery.CONCLUSIONGestational age at ultrasound detection of placenta previa may be used to predict likelihood of previa persistence. After midpregnancy, risk of persistence appears to be higher than previously reported. Type of placentation and prior cesarean delivery are important factors that modify the risk that previa will complicate delivery.
ISSN:0029-7844
出版商:OVID
年代:2002
数据来源: OVID
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6. |
Survival of Other Fetuses After a Fetal Death in Twin or Triplet Pregnancies |
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Obstetrics & Gynecology,
Volume 99,
Issue 5, Part 1,
2002,
Page 698-703
Courtney Johnson,
Jun Zhang,
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摘要:
OBJECTIVETo estimate the frequency of fetal death in multifetal pregnancies and the probability of survival to age 1 year for twins or triplets in which at least one fetal death occurred at 20 weeks' gestation or more.METHODSWe used the Matched Multiple Birth File from the US National Center for Health Statistics, which included 152,233 sets of twins and 5356 sets of triplets registered from 1995 to 1997. The Cox proportional hazards model was used to estimate the adjusted relative risk of death before age 1 year for remaining twins and triplets.RESULTSFetal death at 20 weeks' gestation or later was uncommon, occurring in 2.6% of twin and 4.3% of triplet gestations. After adjustment for confounders, the survival of the remaining fetuses was inversely related to the time of the first fetal demise. Same-sex twins were two times more likely than opposite-sex twins to die after an intrauterine demise at 25–32 weeks' gestation and were more than three times more likely to die after a death at 33 weeks' gestation or more.CONCLUSIONAfter a fetal death in a multifetal pregnancy at 20 weeks' gestation or later, the survival of the remaining fetuses is inversely related to the time the death occurred. Among twins, survival also depends on sex concordance, with opposite-sex twins more likely than same-sex twins to survive.
ISSN:0029-7844
出版商:OVID
年代:2002
数据来源: OVID
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7. |
A Randomized Controlled Trial of Early Oral Analgesia in Gynecologic Oncology Patients Undergoing Intra‐Abdominal Surgery |
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Obstetrics & Gynecology,
Volume 99,
Issue 5, Part 1,
2002,
Page 704-708
Michael Pearl,
Dayna McCauley,
Jill Thompson,
Linda Mahler,
Fidel Valea,
Eva Chalas,
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摘要:
OBJECTIVETo evaluate the safety and efficacy of early oral analgesia after intra-abdominal surgery in gynecologic oncology patients.METHODSOver a 2.5-year period, 227 gynecologic oncology patients undergoing intra-abdominal surgery were enrolled in a randomized controlled trial of early oral versus traditional parenteral analgesia. All patients initially received parenteral morphine via a patient-controlled analgesia (PCA) pump with a basal dose of 0.5 mg/h and a PCA dose of 1 mg with a 10-minute lockout. On the first postoperative day, all patients began a clear liquid diet, which was advanced as tolerated. Patients allocated to early oral analgesia were switched from parenteral to oral morphine. They received a scheduled dose of 20 mg every 4 hours with an additional dose of 10 mg every 2 hours as needed for breakthrough pain. Patients allocated to traditional parenteral analgesia continued to receive parenteral morphine via a PCA pump with basal and PCA doses. On the second postoperative day, the scheduled oral and basal parenteral doses were discontinued. The oral and parenteral PCA doses were continued until 24 hours before discharge, at which time the patient was switched to oxycodone 5 mg/ acetaminophen 325 mg.RESULTSThere were no significant differences among the groups in any demographic or clinical indices, including age, case distribution, surgery length, blood loss, time to return of bowel function, length of hospital stay, pain, sedation, and satisfaction scores, and incidence of nausea, vomiting, or major postoperative complications.CONCLUSIONSEarly oral analgesia in gynecologic oncology patients undergoing intra-abdominal surgery is safe and efficacious.
ISSN:0029-7844
出版商:OVID
年代:2002
数据来源: OVID
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8. |
Prolonged GnRH Agonist and Add‐Back Therapy for Symptomatic EndometriosisLong‐term Follow‐up |
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Obstetrics & Gynecology,
Volume 99,
Issue 5, Part 1,
2002,
Page 709-719
Eric Surrey,
Mark Hornstein,
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摘要:
OBJECTIVETo assess post-treatment effects in endometriosis patients of a 12-month course of GnRH agonist alone or with one of three “add-back” regimens.METHODSThis is a post-treatment follow-up analysis of a randomized, double-masked, placebo-controlled 52-week trial. All patients had received monthly leuprolide acetate and were randomized to one of four groups: A—daily placebo; B—daily norethindrone acetate 5 mg; C—daily norethindrone acetate 5 mg and conjugated equine estrogens 0.625 mg; and D—daily norethindrone acetate 5 mg and conjugated equine estrogens 1.25 mg. Of 201 patients enrolled in the initial trial, 123 completed at least 280 days of therapy and entered the follow-up period. Physical findings and symptoms were quantified, and lumbar spine bone mineral density was determined at intervals for up to 12 and 24 months post-therapy.RESULTSSymptom and pelvic examination scores remained significantly below baseline for at least 8 months after completion of therapy for all four groups (P< .05). Findings were not affected by endometriosis scores noted on screening laparoscopy. Mean bone mineral density values remained at or above baseline in all add-back groups. The significant mean loss in bone density in group A during therapy reversed slowly and had not returned to baseline at the final follow-up visit (P< .001).CONCLUSIONGnRH agonist and norethindrone acetate alone or combined with low-dose conjugated equine estrogens administered to symptomatic endometriosis patients for 12 months provides extended pain relief and bone mineral density preservation after completion of therapy.
ISSN:0029-7844
出版商:OVID
年代:2002
数据来源: OVID
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9. |
Meeting the Needs of Young Women With Secondary Amenorrhea and Spontaneous Premature Ovarian Failure |
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Obstetrics & Gynecology,
Volume 99,
Issue 5, Part 1,
2002,
Page 720-725
Nahrain Alzubaidi,
Heather Chapin,
Vien Vanderhoof,
Karim Calis,
Lawrence Nelson,
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摘要:
OBJECTIVETo investigate the experiences of young women with spontaneous premature ovarian failure with regard to the initial presenting symptom, promptness of diagnosis, and patient education.METHODSWe asked 50 patients previously diagnosed with spontaneous premature ovarian failure to participate in a structured interview survey consisting of 38 true-or-false, multiple-choice, and open-ended questions.RESULTSDisturbance in menstrual pattern was the most common initial symptom in the 48 women who completed the interview (44 of 48, 92%). Over half of the 44 women who presented with this complaint reported visiting a clinician's office three or more times before laboratory testing was performed to determine the diagnosis. Over half of them reported seeing three or more different clinicians before diagnosis. In 25% of women it took longer than 5 years for the diagnosis of premature ovarian failure to be established. Patients who spent more than 5 minutes with the clinician discussing the diagnosis were significantly more likely to be satisfied with the manner in which they were informed (P< .001). Ninety percent of participants were college graduates, and 40% had graduate degrees.CONCLUSIONWomen with spontaneous premature ovarian failure perceived a need for more aggressive evaluation of secondary amenorrhea and oligomenorrhea. Loss of menstrual regularity can be a sign of ovarian insufficiency, and the associated estrogen deficiency is a well-established risk factor for osteoporosis.
ISSN:0029-7844
出版商:OVID
年代:2002
数据来源: OVID
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10. |
The Association Between Serum Estradiol Level and Hearing Sensitivity in Postmenopausal Women |
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Obstetrics & Gynecology,
Volume 99,
Issue 5, Part 1,
2002,
Page 726-730
Sung Kim,
Byung Kang,
Hee Chae,
Chung Kim,
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摘要:
OBJECTIVETo estimate whether hearing sensitivity in postmenopausal women is associated with serum estradiol level or bone mineral density.METHODSSerum estradiol level, bone mineral densities of the lumbar vertebrae and femoral neck, and hearing sensitivity were measured in 1830 postmenopausal women. Serum estradiol level was measured by radioimmunoassay, and dual energy x-ray absorptiometry was used to measure bone mineral densities of the lumbar vertebrae and femoral neck. Hearing sensitivity was evaluated by pure tone audiometry. Age, serum estradiol level, bone mineral densities of the lumbar vertebrae and femoral neck, and the proportion of women on hormone replacement therapy were analyzed in women with and without hearing loss.RESULTSOn univariate analysis, significant differences were found in mean age, serum estradiol level, bone mineral densities of the lumbar vertebrae and femoral neck, and the proportion of women on hormone replacement therapy between the two groups (mean ± standard deviation, 59.4 ± 5.6 versus 56.9 ± 4.7 years,P< .001; 8.4 ± 3.8 versus. 9.9 ± 8.7 pg/mL,P< .001; 0.85 ± 0.14 versus 0.88 ± 0.15 g/cm2,P< .01; 0.65 ± 0.10 versus 0.68 ± 0.10 g/cm2,P< .005; 0.006% versus 0.03%,P< .05, respectively). On multiple logistic regression analysis, significant association was found between age and hearing loss and between serum estradiol level and hearing loss (P< .001,P= .02, respectively).CONCLUSIONThis study suggests that a lower level of serum estradiol possibly impedes hearing sensitivity in postmenopausal women.
ISSN:0029-7844
出版商:OVID
年代:2002
数据来源: OVID
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