ABSTRACT
OBJECTIVE: We evaluated the outcome of fetuses diagnosed with having congenital cystic adenomatoid malformation (CCAM) on ultrasonographic examination and managed conservatively. METHODS: A retrospective study of 19 cases of CCAM diagnosed antenatally in our hospital was conducted between 1990 and 2001. Complete clinical information was available for all patients, with a mean follow-up of 62 months. RESULTS: The median gestational age at which CCAM was diagnosed was 23 weeks and there were eight live births. With conservative postnatal management, seven neonates had no major complications and one developed bronchopneumonia. CONCLUSION: Taken together, the findings of the present study and a review of the literature strongly support the conservative management of selected neonates with CCAM.
Subject(s)
Cystic Adenomatoid Malformation of Lung, Congenital/diagnosis , Pregnancy Outcome , Abortion, Induced , Bronchopneumonia/etiology , Cystic Adenomatoid Malformation of Lung, Congenital/complications , Female , Follow-Up Studies , Gestational Age , Humans , Hydrops Fetalis/complications , Infant , Male , Mediastinal Diseases/complications , Polyhydramnios/complications , Pregnancy , Prenatal Diagnosis , Retrospective StudiesABSTRACT
The incidence of a normal live fetus and a partial molar placenta is extremely rare. Although triploidy is the most frequent association, a fetus with normal karyotype can survive in cases of partial molar pregnancy. We report a case of partial molar placenta in which a live female baby was delivered at 32 weeks gestation by a 30-year-old woman. At the 18th week, ultrasonographic examination revealed a normal fetus with a huge, multicystic placenta. Chromosomal evaluation by amniocentesis revealed a normal female karyotype (46,XX), and serial biometric measurement of the fetus showed normal growth during pregnancy. There were no obstetric complications until the 32nd gestational week when preterm rupture of the membranes occurred. The electronic fetal heart beat tracing showed a repeated sinusoid pattern and late deceleration after admission. The patient underwent emergency Caesarean section and delivered a 1551-g, anaemic female baby with an Apgar score of 1, 4 and 6 at 1, 5 and 10 min, respectively. The baby recovered within 2 weeks after respiratory support and transfusion of packed red blood cells. Although anaemia is one of the risk factors that jeopardize the fetus in the case of partial molar pregnancy, termination is not indicated when the fetus is normal and no complications have occurred.
Subject(s)
Anemia/congenital , Hydatidiform Mole , Pregnancy Complications, Neoplastic , Uterine Neoplasms , Adult , Female , Humans , Infant, Newborn , Infant, Premature , PregnancyABSTRACT
This prospective study was designed to determine whether there would be a higher incidence of congenital cardiovascular malformation (CCVM) in pregnant women with certain risk factors. Fetal echocardiography, from second trimester of term, was performed in 1,659 pregnant women with risk factors for CCVMs and 826 pregnant women without risk factors from March 1990 to April 1995. Two-dimensional imaging, fetal M mode measurements, Doppler waveform velocity and Doppler color flow mapping were used for fetal heart examination. During this period, 70 fetuses with major cardiovascular malformations were found. The prenatal detection rate was determined as 2.8% (70/2,485) in our study. The rate in the high-risk group, however, was 3.7% (61/1,659). Of all indications, fetal risk factors had the highest rate (9.3%, 46/494) of detected CCVMs. Maternal and familial indications could be excluded from the high-risk group as they did not show any increased incidence over the low-risk group. We suggest that fetal echocardiography is mandatory in the high-risk group, especially in cases with fetal and placental risk factors. Fetal cardiac screening in the hands of first-line sonographers has a major role in prenatal diagnosis of CCVMs in the low-risk group.
Subject(s)
Echocardiography/methods , Heart Defects, Congenital/diagnostic imaging , Ultrasonography, Prenatal/methods , Female , Heart Defects, Congenital/epidemiology , Humans , Incidence , Pregnancy , Prospective Studies , Risk Factors , TaiwanABSTRACT
The prenatal diagnosis of tetralogy of Fallot (TOF) can be difficult, as the routine sonographic four-chamber view may be normal before birth. Unlike the normal fetus, in which blood flows adjacent to the left side of the interventricular septum, on color Doppler mapping a fetus with TOF also demonstrates antegrade flow along the right side of the interventricular septum. This Y-shaped ventricular outflow passing through the dilated aortic tract is confluent at the level of the ventricular septal defect during the systolic phase. In the past 3 years, three cases of TOF have been diagnosed prenatally at the Chang Gung Memorial Hospital. In each case, the above picture was demonstrated. 2-Dimensional Doppler color flow mapping may be helpful in the prenatal diagnosis of TOF.
Subject(s)
Fetal Diseases/diagnostic imaging , Tetralogy of Fallot/diagnostic imaging , Adult , Female , Humans , Pregnancy , Ultrasonography, Doppler, Color , Ultrasonography, PrenatalABSTRACT
By use of duplex Doppler ultrasonography, we preliminarily studied 30 normal pregnancies (control group) and 30 patients with preeclampsia (study group) before treatment. The peak systolic flow height to end diastolic flow height (S/D) ratio of the maternal right and left renal arteries of both groups were compared and analyzed. The results showed that there were no significant differences between the right and left renal arteries in either group, but unexpectedly the S/D ratio of the renal artery on both sides in preeclamptic patients was significantly lower than in normal pregnant women (mean +/- SD, 2.07 +/- .12 vs. 2.41 +/- .12, respectively, P < .001). The lower S/D ratio of the renal artery may reflect a decrease in renovascular resistance and an increase in renal perfusion. These findings were the reverse of what might be expected from an elevated vascular resistance and hypoperfusion model.
Subject(s)
Kidney/blood supply , Pre-Eclampsia/physiopathology , Renal Artery/physiopathology , Ultrasonography, Prenatal , Adult , Female , Humans , Pre-Eclampsia/diagnostic imaging , Pregnancy/physiology , Pregnancy Trimester, Third , Regional Blood Flow , Vascular ResistanceABSTRACT
Meconium peritonitis is usually the result of prenatal bowel obstruction with subsequent perforation, then the contents spread into the peritoneal cavity, which results in a sterile inflammatory reaction. The incidence ranges from 1/1500 to 1/2000, if without prenatal diagnosis and planned postnatal treatment, the mortality rate is as high as 62%. We describe three children, two with surgically, one with autoptically confirmed meconium peritonitis. All had abnormally prenatal ultrasonographic examinations. The first fetus showed a large 10 x 11 cm intra-abdominal mass with floating echogenic substances inside and with an echogenic rim. The second showed increased echogenicity with dilated bowel in abdominal cavity in one of the twin, and the third had an intra-abdominal cyst with several echogenic bands inside, fetal ascites was also noted. It is remarkable that the ultrasonographic findings were different in the three children. Two of the three children survived postoperation, one died 3 hours later after induction out at 31 weeks of gestational age due to multiple congenital anomalies.
Subject(s)
Meconium/diagnostic imaging , Peritonitis/diagnostic imaging , Ultrasonography, Prenatal , Adult , Female , Humans , Infant, Newborn , Male , PregnancyABSTRACT
Appropriate interpretation of monitored fetal growth throughout pregnancy in individual patients and populations is dependent upon the availability of adequate standards. Previously published standards either were based on small samples, data decades old or were characteristic of foreign subpopulations. We have reviewed the data on a series of 46,575 singleton live births at Chang Gung Memorial Hospital from 1979 to 1989. The ratio of males to females was 1.08. The fetal growth pattern in the third trimester of pregnancy approximates a sigmoid curve. Fetal growth was most rapid from the 32nd to the 37th week of gestation with an average increase of 240 g per week. The birth weight declined beyond 42 weeks' gestation. There were significantly greater weight gains amongst male fetuses as compared to female fetuses from the 34th to the 42nd week of gestation. The mean birth weight recorded at 40 weeks' gestation in male and female newborns was 3,381 g and 3,262 g, respectively. Comparing the birth weight of term pregnancies using our data, with those of a previous, two-decade old report (1945-1967) by Chen, we found that birth weight were slightly higher in this study. The derived fetal growth curves are useful for clinical, public health, and investigational purposes.
Subject(s)
Birth Weight , Adult , Female , Gestational Age , Humans , Infant, Newborn , Male , Pregnancy , Sex Factors , TaiwanABSTRACT
Severe preeclampsia affects placental function and causes fetal compromise. It is necessary to deliver the fetus at an appropriate time in order to minimize fetal mortality and morbidity. Cordocentesis was performed in 9 patients with severe preeclampsia (group 1) and 10 patients with other pregnancy complications (group 2). Intrauterine growth retardation occurred in 5 patients in group 1 and in only one patient in group 2. Blood gas parameters including pH, pO2 and O2 saturation were significantly lower for group 1, while pCO2 was significantly higher, as compared to group 2. For patients in group 1, non-invasive fetal surveillance successfully identified 5 patients with fetal compromise, who required immediate termination of pregnancy. All 5 of these patients had abnormal fetal blood gas analyses by cordocentesis. Fetal blood gas analysis was abnormal in 2 additional fetuses among the remaining 4 patients who exhibited normal findings by non-invasive methods of fetal surveillance. These results suggest that cordocentesis is useful in identifying fetal compromise (fetal hypoxia/acidosis) prior to the onset of labor in high-risk patients, such as preeclampsia associated with intrauterine growth retardation.
Subject(s)
Fetal Blood/chemistry , Fetal Diseases/diagnosis , Pre-Eclampsia/blood , Prenatal Diagnosis , Acidosis/diagnosis , Bicarbonates/blood , Carbon Dioxide/blood , Female , Humans , Hydrogen-Ion Concentration , Hypoxia/diagnosis , Oxygen/blood , PregnancyABSTRACT
Listeria monocytogenes, an uncommon perinatal infection in human, has been reported to be correlated with abortion, premature labor, intrauterine fetal sepsis, intrauterine fetal death and neonatal infections. Reported here was the first case of perinatal listeriosis complicated with Listeria monocytogenes chorioamnionitis at 33 weeks' gestation in Taiwan. The transabdominal amniocentesis in this particular case confirmed the diagnosis. An live premature male fetus was delivered by emergency cesarean section on the next day of hospitalization due to acute fetal distress. The acute ill baby developed signs of meningitis on the following day. Blood culture of Listeriosis monocytogenes indicated early onset neonatal listeriosis. Brain sonography showed hydrocephalus after a one-month period antibiotic treatment, he was lost to follow-up one month later. A review of the literature is presented to describe the clinical, epidemiological and pathological findings and to highlight their variable presentations and procedures for management. Thus it is of great importance for obstetricians to include listeriosis as a differential diagnosis in cases of fever of unknown origin during pregnancy. Promptly obtaining proper cultures and instituting appropriate antibiotics therapy is emphasized.
Subject(s)
Chorioamnionitis/therapy , Fetal Diseases/therapy , Listeriosis/therapy , Pregnancy Complications, Infectious/therapy , Adult , Chorioamnionitis/diagnosis , Chorioamnionitis/etiology , Female , Fetal Diseases/diagnosis , Fetal Diseases/etiology , Humans , Infant, Newborn , Listeriosis/diagnosis , Listeriosis/etiology , Male , PregnancyABSTRACT
This study assesses the relative risks of first trimester transcervical chorionic villus sampling (CVS) versus midtrimester amniocentesis performed between April 1986 and March 1988. The most common indication for prenatal diagnosis was advanced maternal age. We discovered 5.1% chromosomal aberrations in CVS compared to 1.0% in amniocentesis. Bleeding was the most frequent early complication, and only 1 case had major hemorrhage with subsequent spontaneous abortion. The fetal loss rate (gestational age less than 28 weeks) was 4.5% in CVS versus 1.2% in amniocentesis, which was not significantly different from the background fetal loss rate reported in normal pregnancies after an 8-week gestational age. Three cases of fetal loss after CVS were probably procedure-related; 1 case had spontaneous abortion and 2 cases had chorioamnionitis. Therefore, we considered that the causal relationship between CVS and the infection was highly probable. The clinical pregnancy outcome indicated that there were no differences in overall perinatal mortality, Apgar score, body weight, body length, gestational age at delivery, intrauterine growth retardation, placenta weight and placental disorders between the CVS group and the amniocentesis group. The pregnancies did not reveal any specific effects of the prenatal diagnostic procedure, but a long-term pediatric follow-up is needed.