Network


Latest external collaboration on country level. Dive into details by clicking on the dots.

Hotspot


Dive into the research topics where Caroline F. Anderson is active.

Publication


Featured researches published by Caroline F. Anderson.


Journal of the American College of Cardiology | 1986

Doppler echocardiographic studies of diastolic function in the human fetal heart: Changes during gestation

Kathryn L. Reed; David J. Sahn; Sarah Scagnelli; Caroline F. Anderson; Lewis Shenker

With the combined use of two-dimensional ultrasound and Doppler echocardiography, noninvasive examination of the human fetal heart and circulation has recently become possible. These techniques were employed to investigate diastolic atrioventricular valve flow in the fetal heart in 120 fetuses studied between 17 and 42 weeks of gestation. Two-dimensional ultrasound was used to examine fetal and intrauterine anatomy, and estimates of gestational age were made based on biparietal diameters and femur lengths. Doppler echocardiography was performed with a 3.5 or 5 MHz Doppler sector scanner. Flow velocity patterns were obtained through the tricuspid and mitral valves during diastole. Peak flow velocity during late diastole or atrial contraction (A) was compared with peak flow velocity during early diastole (E) in four groups of fetuses: Group 1, 17 to 24 weeks of gestation; Group 2, 25 to 30 weeks; Group 3, 31 to 36 weeks; and Group 4, 37 to 42 weeks. The ratio of A to E decreased significantly as gestational age advanced, from 1.56 +/- 0.06 (+/- SE) to 1.22 +/- 0.03 across the tricuspid valve (p less than 0.001) and from 1.55 +/- 0.04 to 1.22 +/- 0.06 across the mitral valve (p less than 0.001). In tricuspid valve measurements, peak flow velocity during early diastole increased from 26.3 +/- 2.0 cm/s in Group 1 to 36.5 +/- 1.7 cm/s in Group 4 (p less than 0.001), whereas peak flow velocity during atrial contraction did not change.(ABSTRACT TRUNCATED AT 250 WORDS)


Circulation | 1980

Qualitative real-time cross-sectional echocardiographic imaging of the human fetus during the second half of pregnancy.

L W Lange; David J. Sahn; Hugh D. Allen; Stanley J. Goldberg; Caroline F. Anderson; H Giles

In this study, we used high-resolution echocardiographic systems to investigate how early in pregnancy normal fetal cardiac anatomy could be noninvasively evaluated. Over a 2-year period, 84 of 88 fetuses were successfully imaged (27 were studied serially). Postnatal images of 73 were obtained during the newborn period. Estimated fetal age varied at initial examination from 19-41 weeks (mean 31 ± 0.5 weeks [± SEMI) of pregnancy. Estimated fetal weight using an ultrasound algorithm varied from 500-3100 g (mean 1580 ± 80 g [± SEMI). To evaluate fetal cardiac anatomy, we reproduced commonly used cross-sectional views of the heart. The four-chamber and the short-axis great artery views have been most successful for cardiac evaluation in the fetus. These views could be obtained in 96% and 95% of the patients, respectively. With these views, cardiac chamber and valve structures, as well as two great arteries, could be imaged in detail. The ascending and descending aorta, as well as the aortic arch and vessels to the arms and head, were visualized in 87% of examinations, and the inferior and superior venae cavae were visualized in 76%. In two of three RH fetuses, changes in cardiac chambers compatible with hydrops fetalis were demonstrated. We examined all fetuses after birth and verified clinically (or noninvasively) that no cardiac malformations were present. It appears, however, that the diagnosis of major congenital heart defects should be possible before birth.


American Journal of Obstetrics and Gynecology | 1987

Changes in intracardiac Doppler blood flow velocities in fetuses with absent umbilical artery diastolic flow

Kathryn L. Reed; Caroline F. Anderson; Lewis Shenker

Umbilical artery Doppler blood flow velocity studies were used to identify 14 fetuses with absent flow during diastole to determine the significance of absent umbilical artery diastolic flow. Outcomes of these fetuses were recorded, and the associated intracardiac Doppler changes were identified in 12 of them. Maximal and mean intracardiac flow velocities were measured, and volume flows through the right (tricuspid valve, pulmonary valve) and left (mitral valve, aortic valve) sides of the heart were compared. Ratios of intracardiac peak flow velocity in late diastole to peak flow velocity in early diastole were calculated. Eleven fetuses had intrauterine growth retardation, and four had multiple congenital anomalies. Fetuses with no diastolic flow in the umbilical artery had increased volume flow across the tricuspid and pulmonary valves compared with normal fetuses of similar weights. The ratio of right-sided to left-sided volume flow in the heart (2.15:1) was increased compared with values in normal fetuses (1.33:1, p less than 0.01). The ratio of late diastolic to early diastolic peak flow velocities across the mitral valve was decreased (p less than 0.01). Absent umbilical artery diastolic flow is associated with increased tricuspid and pulmonary valve volume flow and changes in mitral flow velocity patterns, which suggests that there are alterations in left ventricular function.


American Heart Journal | 1982

Prenatal ultrasound diagnosis of hypoplastic left heart syndrome in utero associated with hydrops fetalis

David J. Sahn; Lewis Shenker; Kathryn L. Reed; Lilliam M. Valdes-Cruz; Richard E. Sobonya; Caroline F. Anderson

Abstract Ultrasound is widely used in obstetrics as a screening technique for fetal size and maturity, placental structure and function, and for detection of fetal congenital malformations in complicated pregnancies. 1–3 Our own work on qualitative and quantitative fetal echocardiography 4,5 and the work of others 6 has suggested that high resolution ultrasound can be used to assess fetal heart rhythm and function, and can detect congenital heart malformations before birth. In this report, we delineate prenatal diagnosis of hypoplastic left heart syndrome in a fetus with signs of hydrops fetalis, who was found after cesarean section to have associated trisomy 13. Additionally, we diagnosed the ususual occurrence of an intraventricular thrombus within the hypoplastic left ventricular cavity. The fetal ultrasound evaluation was of major importance in the perinatal management of both mother and unborn child.


American Journal of Obstetrics and Gynecology | 1991

Significance of oligohydramnios complicating pregnancy

Lewis Shenker; Kathryn L. Reed; Caroline F. Anderson; Nydia A. Borjon

Oligohydramnios is a serious complication of pregnancy that is associated with a poor perinatal outcome. Eighty pregnancies complicated by oligohydramnios constitute the basis for this retrospective study. Forty patients had premature rupture of the membranes; of these, outcomes were good in 25. Twelve of 14 fetuses with oligohydramnios and intrauterine growth retardation survived. None of the nine fetuses with severe renal anomalies lived. None of the twins with twin-twin transfusion and oligohydramnios survived. Six pregnancies with oligohydramnios and premature separation of the placenta were identified; all of these resulted in fetal or neonatal death during the second trimester.


American Journal of Obstetrics and Gynecology | 1989

Fetal pericardial effusion

Lewis Shenker; Kathryn L. Reed; Caroline F. Anderson; William Kern

Forty-four fetuses with pericardial effusions have been identified by ultrasonographic examinations. The clinical histories and courses of these patients were reviewed. At least eight different clinical features accompanied and were probably responsible for the pericardial effusions. The most common cause of a fetal pericardial effusion was heart failure (13 fetuses). Fetal renal cystic dysplasia with oligohydramnios and other anomalies was present in six fetuses. Four of this group had microscopic evidence of pericarditis on postmortem examination. Fetal pericardial effusions are always a manifestation of another disease process often presenting as fetal hydrops. Some pericardial effusions are transient. The etiologic origin of fetal pericardial effusions differs from that in the child or adult.


Obstetrics & Gynecology | 1997

Umbilical venous velocity pulsations are related to atrial contraction pressure waveforms in fetal lambs

Kathryn L. Reed; David G. Chaffin; Caroline F. Anderson; Adam T. Newman

Objective To identify the source of umbilical venous velocity pulsations, times of transmission from the atrial contraction pressure waveform to velocity waves in the inferior vena cava, ductus venosus, intra-abdominal umbilical vein, and intra-amniotic umbilical vein were examined. Methods Five lamb fetuses at 125-135 dayss gestation were instrumented with solid satte pressure transducers in the inferior vena cava, fluid-filled catheters in the inferior vena cava and descending aorta, ad epicardial pacemakers. Three to 5 days postoperatively, inferior vena cava, ductus venosus, and umbilical vein velocities were examined with Doppler ultrasoound. Normal saline was administered until umbilical vein velocity pulsations developed (180 ± 60 mL). In three fetuses, premature atrial contractions were induced under baseline conditions and after umbilical vein velocity pulsations developed. Results Times of transmission from the atrial contraction pressure waveform until velocity decreases in the fetal venous system were significantly different in the inferior vena cava, ductus venosus, intra-abdominal umbilical vein, and intra-amniotic umbilical vein (P < .001). Times increased with the distnance from the atrium. Inferior vena cava pressure increased with fluid administration from 3.7 ± 4.7 mmHg to 9.3 ± 2.3 mmHg (P < .01). Time from increased pressure waveforms with induced premature atrial contractions to the nadir of subsequent umbilical vein velocity waves decreased from 0.123 ± 0.047 seconds before saline administration to 0.072 ± 0.039 seconds after saline administration (P < .001). Conclusion Transmission time of atrial pressure into the venous circulation increases with distance from the atrum and decreases with volume loading. Umbilical venous velocity pulsations derive from atrial pressure changes transmitted in a retrograde fashion.


American Journal of Obstetrics and Gynecology | 1988

Fetal cardiac Doppler flow studies in prenatal diagnosis of heart disease

Lewis Shenker; Kathryn L. Reed; Gerald R. Marx; Richard L. Donnerstein; Hugh D. Allen; Caroline F. Anderson

The prenatal diagnosis of fetal cardiac disease has become increasingly accurate as the technology of ultrasound has improved. Although two-dimensional real-time ultrasound remains the primary method of diagnosis, Doppler blood flow velocity estimates can provide valuable pathophysiologic information to support the anatomic diagnosis. We present six cases in which Doppler studies contributed to the accuracy of the diagnosis of fetal heart disease, including tetralogy of Fallot, right and left ventricular hypoplasia, atrioventricular canal defect, double-outlet right ventricle, and pulmonic stenosis. Velocities in these cases are compared with those in normal fetuses. If Doppler flow velocities are not consistent with the observed morphologic changes, further observations are indicated. Inasmuch as most anatomical heart lesions result in altered flow patterns, Doppler investigations of intracardiac and extracardiac flow should be a routine component of the fetal echocardiogram when structural abnormalities are found.


American Journal of Obstetrics and Gynecology | 1991

Doppler flow velocities in single umbilical arteries

Norman B. Duerbeck; Marcello Pietrantoni; Kathryn L. Reed; Caroline F. Anderson; Lewis Shenker

Fetal compromise has been associated with an umbilical artery waveform pattern of low or absent diastolic velocity relative to systolic velocity. Fetuses with single umbilical arteries have an increased risk of major malformations, mortality, retarded fetal growth, and prematurity. In this study Doppler flow velocities were obtained in 13 fetuses (four twin fetuses and nine singletons) with a single umbilical artery. Five (38%) fetuses, consisting of four singletons and one twin, had anomalies. Six (46%) fetuses were small for gestational age, including two twin fetuses and three singleton fetuses with anomalies. Three (23%) of the 13 systolic-to-diastolic velocity ratios were abnormally high. Whereas this is a higher rate of abnormal ratios than the reported 2% to 3% in control populations, it is interesting to note that 77% of fetuses with single umbilical arteries had normal systolic-to-diastolic ratios.


American Journal of Obstetrics and Gynecology | 2000

Changes in umbilical venous velocities with physiologic perturbations

Kathryn L. Reed; Caroline F. Anderson

OBJECTIVE The purpose of this study was to determine the direction of transmission of umbilical venous Doppler flow velocity changes in human fetuses. STUDY DESIGN Strip chart recordings of simultaneously measured umbilical arterial and venous velocities were examined at two sites in the umbilical cord, one near the fetus (proximal) and one near the placenta (distal). Fetuses with venous pulsations or breathing episodes were included. At both locations time from venous pulsation to arterial systole was measured in fetuses with venous pulsations and duration of phase delay between arterial diastolic velocity minimum and venous velocity minimum was measured in fetuses with breathing episodes. RESULTS In 21 fetuses with venous pulsations the pulsations occurred earlier in the cardiac cycle at proximal sites (0.12 +/- 0.04 second before systole) and later at distal sites (0.02 +/- 0.04 second before systole;P <.001). Phase delays in venous velocities in the 5 fetuses with breathing episodes were also longer at distal sites than at proximal sites (P <.011). CONCLUSION Changes in umbilical venous velocities occurred earlier at sites that were closer to the fetus. These findings suggest that changes in umbilical venous velocities originate in the fetal venous system and are transmitted to, rather than from, the placenta.

Collaboration


Dive into the Caroline F. Anderson's collaboration.

Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar

Gerald R. Marx

Boston Children's Hospital

View shared research outputs
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar

L W Lange

University of Arizona

View shared research outputs
Researchain Logo
Decentralizing Knowledge