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  • 1
    In: Fetal Diagnosis and Therapy, S. Karger AG, Vol. 47, No. 1 ( 2020), p. 45-53
    Abstract: 〈 b 〉 〈 i 〉 Objective: 〈 /i 〉 〈 /b 〉 To determine hemodynamic changes by Doppler ultrasound of the living fetus during 24 h after umbilical cord occlusion (UCO) in monochorionic diamniotic (MCDA) twin pregnancies. 〈 b 〉 〈 i 〉 Method: 〈 /i 〉 〈 /b 〉 We conducted a prospective observational study on fetuses undergoing UCO from 2015 to 2017. Doppler parameters peak systolic velocity (PSV) and umbilical pulsatility index (PI) were obtained in the middle cerebral artery (MCA), umbilical artery (UA) and ductus venosus (DV) before and right after UCO, and at 1, 3, 6, 12, and 24 h after. We used multiple of the median (MoM) to adjust for gestational age. Spaghetti plots visualized flow changes over time. Mixed model adjusting for paired longitudinal data compared the values at different time points. 〈 b 〉 〈 i 〉 Results: 〈 /i 〉 〈 /b 〉 A total of 16 women were included. MCA-PSV dropped within the first hour after surgery from 0.91 to 0.82 MoM ( 〈 i 〉 p 〈 /i 〉 = 0.08). MCA-PI and UA-PI increased in the first hour from 0.75 to 0.91 MoM ( 〈 i 〉 p 〈 /i 〉 = 0.02) and 0.94 to 0.98 MoM ( 〈 i 〉 p 〈 /i 〉 = 0.22), respectively. The DV-PIV increased to 1.14 MoM 3 h after surgery ( 〈 i 〉 p 〈 /i 〉 = 0.07). The spaghetti plots illustrated the small changes within the first hours and showed a stabilization of flow measurements near initial values 24 h after UCO. 〈 b 〉 〈 i 〉 Conclusion: 〈 /i 〉 〈 /b 〉 Within the first hours after UCO the circulation of the survivor twin undergoes small hemodynamic changes.
    Type of Medium: Online Resource
    ISSN: 1015-3837 , 1421-9964
    Language: English
    Publisher: S. Karger AG
    Publication Date: 2020
    detail.hit.zdb_id: 1482292-1
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  • 2
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    Online Resource
    S. Karger AG ; 2010
    In:  Fetal Diagnosis and Therapy Vol. 27, No. 1 ( 2010), p. 1-7
    In: Fetal Diagnosis and Therapy, S. Karger AG, Vol. 27, No. 1 ( 2010), p. 1-7
    Abstract: 〈 i 〉 Introduction: 〈 /i 〉 As a consequence of the introduction of effective screening methods, the number of invasive prenatal diagnostic procedures is steadily declining. The aim of this review is to summarize the risks related to these procedures. 〈 i 〉 Material and Methods: 〈 /i 〉 Review of the literature. 〈 i 〉 Results: 〈 /i 〉 Data from randomised controlled trials as well as from systematic reviews and a large national registry study are consistent with a procedure-related miscarriage rate of 0.5–1.0% for amniocentesis as well as for chorionic villus sampling (CVS). In single-center studies performance may be remarkably good due to very skilled operators, but these figures cannot be used for general counselling. Amniocentesis performed prior to 15 weeks had a significantly higher miscarriage rate than CVS and mid-trimester amniocentesis, and also increased the risk of talipes equinovarus. Amniocentesis should therefore not be performed before 15 + 0 weeks’ gestation. CVS on the other hand should not be performed before 10 weeks’ gestation due to a possible increase in risk of limb reduction defects. 〈 i 〉 Discussion: 〈 /i 〉 Experienced operators have a higher success rate and a lower complication rate. The decreasing number of prenatal invasive procedures calls for quality assurance and monitoring of operators’ performance.
    Type of Medium: Online Resource
    ISSN: 1015-3837 , 1421-9964
    Language: English
    Publisher: S. Karger AG
    Publication Date: 2010
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  • 3
    In: Fetal Diagnosis and Therapy, S. Karger AG, Vol. 46, No. 1 ( 2019), p. 20-27
    Abstract: Introduction: We sought to assess the incidence of severe neurodevelopmental impairment (NDI) in monochorionic twins treated for twin-twin transfusion syndrome (TTTS) and compare it to the incidence in uncomplicated monochorionic twins. Material and Methods: We included TTTS pregnancies treated by fetoscopic selective laser coagulation (FSLC) or umbilical cord occlusion (UCO) in 2004–2015. Primary outcome was severe NDI defined as cerebral palsy, bilateral blindness or bilateral deafness (ICD-10 diagnoses), and severe cognitive and/or motor delay (assessed by the Ages and Stages Questionnaires [ASQ]). Results: A total of 124 children after TTTS and 98 controls were followed up at 25 months of age (SD 11.4). Severe NDI was found in 8.9% of the TTTS children (10.5% [9/86] after FSLC; 5.3% [2/38] after UCO) compared to 3.1% in the control group (p = 0.10). The odds ratio for severe NDI was 1.8 in cases versus controls (p = 0.37). The total ASQ score was significantly lower in the TTTS group than in controls (p = 0.03) after FSLC (p = 0.03) and after UCO (p = 0.14). Discussion: Children after TTTS appear to have a higher risk of severe NDI and score significantly lower on the ASQ compared to monochorionic twins from uncomplicated pregnancies.
    Type of Medium: Online Resource
    ISSN: 1015-3837 , 1421-9964
    Language: English
    Publisher: S. Karger AG
    Publication Date: 2019
    detail.hit.zdb_id: 1482292-1
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  • 4
    In: Fetal Diagnosis and Therapy, S. Karger AG, Vol. 41, No. 3 ( 2017), p. 209-214
    Abstract: 〈 b 〉 〈 i 〉 Introduction: 〈 /i 〉 〈 /b 〉 The aim was to investigate the parental decisions about prenatal screening and diagnosis among infants with trisomy 21 (T21) in a national cohort with high uptake of combined first-trimester screening (cFTS). 〈 b 〉 〈 i 〉 Material and Methods: 〈 /i 〉 〈 /b 〉 This was a nationwide population-based study including infants born in 2009-2012. Information from the cFTS, fetal karyotype results and pregnancy outcome was obtained from the Danish Fetal Medicine Database on all women with a cFTS risk assessment. Cut-off for referral for invasive testing was ≥1:300. Karyotype results from pregnancies with no cFTS were obtained from the Danish Cytogenetic Central Registry. 〈 b 〉 〈 i 〉 Results: 〈 /i 〉 〈 /b 〉 The uptake rate of cFTS was 91.6%, and 82.8% (8,032/9,704) of the screen-positive women opted for invasive testing. Overall, 82.2% (454/552) chose to terminate an affected pregnancy. In the 4-year period, 102 of 232,962 singletons were born alive with T21. The cFTS risk was true-positive, false-negative or not obtained in 21.6, 48.0 and 30.4%, respectively, of these pregnancies. 〈 b 〉 〈 i 〉 Discussion: 〈 /i 〉 〈 /b 〉 In this large national cohort, 4.4 per 10,000 live-born infants had T21. Of 102 infants with T21 from 2009 to 2012, 52.0% were born after the women had not opted for cFTS or were true-positive but declined invasive testing or termination, and 48.0% were born after a false-negative risk assessment.
    Type of Medium: Online Resource
    ISSN: 1015-3837 , 1421-9964
    Language: English
    Publisher: S. Karger AG
    Publication Date: 2017
    detail.hit.zdb_id: 1482292-1
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  • 5
    In: Fetal Diagnosis and Therapy, S. Karger AG, Vol. 45, No. 6 ( 2019), p. 424-429
    Abstract: 〈 b 〉 〈 i 〉 Aim: 〈 /i 〉 〈 /b 〉 To examine the performance of the combined First Trimester Screening (cFTS) algorithm when outliers of 4 risk parameters (maternal age, nuchal translucency (NT) thickness, PAPP-A and β-hCG) were included in the classification of “high-risk”. 〈 b 〉 〈 i 〉 Methods: 〈 /i 〉 〈 /b 〉 A retrospective analysis of singleton pregnancies undergoing cFTS between 2008 and 2011 in Denmark. Abnormal karyotypes were classified as trisomy 21 (T21), trisomy 13 (T13) and trisomy 18 (T18), sex chromosome aberrations and atypical abnormal karyotypes. 〈 b 〉 〈 i 〉 Results: 〈 /i 〉 〈 /b 〉 cFTS was completed in 193,638 pregnancies. In 10,205 (5.3%) cases, cytogenetic or molecular analysis was performed pre- or postnatally. An abnormal karyotype was seen in 1,122 (11.0%). The algorithm identified 87% of T21, 80% of T13, 75% of T18, 79% of sex chromosome aberrations and 35% of atypical abnormal karyotypes. Additional classification of a single risk parameter outlier (low PAPP-A or free β-hCG ( & #x3c; 0.2 MoMs), high β-hCG (≥5.0 MoMs), maternal age ≥45 years or NT ≥3.5 mm) as being at high-risk would have improved detection rates to 88, 80, 81, 81 and 37% respectively. The screen positive rate increased from 4.4 to 4.8%. 〈 b 〉 〈 i 〉 Discussion: 〈 /i 〉 〈 /b 〉 Addition of outliers of the 4 parameters used in cFTS algorithm will lead to a statistically significant increase in detection rates for chromosomal abnormality.
    Type of Medium: Online Resource
    ISSN: 1015-3837 , 1421-9964
    Language: English
    Publisher: S. Karger AG
    Publication Date: 2019
    detail.hit.zdb_id: 1482292-1
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  • 6
    In: Fetal Diagnosis and Therapy, S. Karger AG, Vol. 46, No. 4 ( 2019), p. 257-265
    Abstract: 〈 b 〉 〈 i 〉 Introduction: 〈 /i 〉 〈 /b 〉 The false-positive rate in the prediction of fetal anemia is 10–15%. We investigated if a new, noninvasive MRI method used as a supplement to ultrasound could improve the prediction. 〈 b 〉 〈 i 〉 Methods: 〈 /i 〉 〈 /b 〉 Fetuses suspected of anemia and controls were scanned in a 1.5-tesla MRI scanner 1–4 times during pregnancy. Cases were scanned before and after intrauterine blood transfusion with a T1-mapping MRI sequence in a cross-section of the umbilical vein. 〈 b 〉 〈 i 〉 Results: 〈 /i 〉 〈 /b 〉 Inclusion of 8 cases and 11 controls resulted in 10 case scans (2 cases were included twice) and 33 control scans. In controls, the T1 relaxation time was 1,005–1,391 ms; in cases with severe anemia, 1,505–1,595 ms, moderate anemia 1,503–1,525 ms, and no/mild anemia 1,245–1,410 ms. After blood transfusions, values dropped to 1,123–1,288 ms. The mean value in moderate and severe anemic cases was 275 ms higher than in controls (95% CI 210–341 ms, 〈 i 〉 p 〈 /i 〉 & #x3c; 0.0001), and after blood transfusion it was comparable to controls (3 ms, 95% CI –62 to 68 ms, 〈 i 〉 p 〈 /i 〉 = 0.934). A 1,450-ms cut-off would have identified all cases in need of blood transfusion with no false-positive cases. 〈 b 〉 〈 i 〉 Conclusions: 〈 /i 〉 〈 /b 〉 Our findings indicate a potential for this new MRI method to improve the prediction of fetal anemia as a supplement to ultrasound.
    Type of Medium: Online Resource
    ISSN: 1015-3837 , 1421-9964
    Language: English
    Publisher: S. Karger AG
    Publication Date: 2019
    detail.hit.zdb_id: 1482292-1
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  • 7
    In: Fetal Diagnosis and Therapy, S. Karger AG, Vol. 44, No. 1 ( 2018), p. 65-71
    Abstract: 〈 b 〉 〈 i 〉 Introduction: 〈 /i 〉 〈 /b 〉 Ultrasound-guided bipolar umbilical cord occlusion (UCO) is used in complicated monochorionic multiple pregnancies in Denmark. The aim of this study was to assess a learning curve in the procedure of UCO. 〈 b 〉 〈 i 〉 Materials and Methods: 〈 /i 〉 〈 /b 〉 One hundred and two monochorionic pregnancies treated with UCO at Rigshospitalet, Denmark between 2004 and 2015 were included. The procedures were divided into period 1 (2004-2009) and period 2 (2010-2015) to determine a learning curve. Primary outcome measure was survival rate. Secondary outcome measures were time from operation to fetal loss and gestational age (GA) at delivery. 〈 b 〉 〈 i 〉 Results: 〈 /i 〉 〈 /b 〉 Period 1 included 59 cases. The median GA at procedure was 19.9 weeks (range 16.7-25.9) and at delivery 34.7 weeks (range 24.3-40.3). Period 2 included 43 cases. The median GA at procedure was 20.7 weeks (range 16.7-27.6) and at delivery 37.3 weeks (range 29.1-40.3). Survival rate increased from 78% (period 1) to 95% (period 2) ( 〈 i 〉 p 〈 /i 〉 = 0.02). GA at delivery increased as well. Fetal death within 48 h after surgery decreased from 4 (period 1) to 0 (period 2). 〈 b 〉 〈 i 〉 Discussion: 〈 /i 〉 〈 /b 〉 Our results suggest a learning curve in the procedure of UCO with improved outcome on all measures.
    Type of Medium: Online Resource
    ISSN: 1015-3837 , 1421-9964
    Language: English
    Publisher: S. Karger AG
    Publication Date: 2018
    detail.hit.zdb_id: 1482292-1
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  • 8
    In: Fetal Diagnosis and Therapy, S. Karger AG, Vol. 29, No. 3 ( 2011), p. 216-223
    Abstract: 〈 i 〉 Objectives: 〈 /i 〉 To investigate if a cervical length (CL) cutoff of 15 mm is relevant to use in women with threatened preterm labor. 〈 i 〉 Methods: 〈 /i 〉 From 2006 to 2009, 146 women with singleton pregnancies were admitted with threatened preterm labor between 23 and 33+6 weeks of gestation at Copenhagen University Hospital. Transvaginal sonographic measurement of CL was carried out on admission. Outcome measures were spontaneous delivery within 48 h, within 7 days and delivery before 34 weeks according to a CL cutoff of 15 mm. 〈 i 〉 Results: 〈 /i 〉 CL was 〈 15 mm in 36 women (24.7%) and ≧15 mm in 110 women (75.3%). Spontaneous delivery occurred within 48 h or 7 days of presentation and before 34 weeks in 25, 38.9 and 50.0% of women with CL 〈 15 mm and 3.6, 9.1 and 11.8% of women with CL ≧15 mm, respectively. The 15-mm CL cutoff had a sensitivity, false positive rate and negative predictive value for delivery within 48 h of 69.0, 20.3 and 96.4%, and within 7 days of 58.3, 18.1 and 90.9%. Women with CL 〈 15 mm had odds of delivery within 7 days of 6.4 (95% CI 2.5–16.2). 〈 i 〉 Conclusion: 〈 /i 〉 Although a 15-mm CL defines a group of women at high risk of spontaneous preterm delivery, 10 out of 110 women (9.1%) with a CL ≧15 mm deliver within 7 days.
    Type of Medium: Online Resource
    ISSN: 1015-3837 , 1421-9964
    Language: English
    Publisher: S. Karger AG
    Publication Date: 2011
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  • 9
    In: Fetal Diagnosis and Therapy, S. Karger AG, Vol. 48, No. 4 ( 2021), p. 304-312
    Abstract: 〈 b 〉 〈 i 〉 Objective: 〈 /i 〉 〈 /b 〉 The study aimed to investigate the association between placental growth factor (PlGF) and adverse obstetric outcomes in a mixed-risk cohort of pregnant women screened for preeclampsia (PE) in the first trimester. 〈 b 〉 〈 i 〉 Methods: 〈 /i 〉 〈 /b 〉 We included women with singleton pregnancies screened for PE between April 2014 and September 2016. Outcome data were retrieved from the New South Wales Perinatal Data Collection (NSW PDC) by linkage to the prenatal cohort. Adverse outcomes were defined as spontaneous preterm birth (sPTB) before 37-week gestation, birth weight (BW) below the 3rd centile, PE, gestational hypertension (GH), stillbirth, and neonatal death. 〈 b 〉 〈 i 〉 Results: 〈 /i 〉 〈 /b 〉 The cohort consisted of 11,758 women. PlGF multiple of the median (MoM) was significantly associated with maternal sociodemographic characteristics (particularly smoking status and parity) and all biomarkers used in the PE first trimester screening model (notably pregnancy-associated plasma protein A MoM and uterine artery pulsatility index [PI] MoM). Low levels of PlGF ( & #x3c;0.3 MoM and & #x3c;0.5 MoM) were independently associated with sPTB, low BW, PE, GH, and a composite adverse pregnancy outcome score, with odds ratios between 1.81 and 4.44 on multivariable logistic regression analyses. 〈 b 〉 〈 i 〉 Conclusions: 〈 /i 〉 〈 /b 〉 Low PlGF MoM levels are independently associated with PE and a range of other adverse pregnancy outcomes. Inclusion of PlGF should be considered in future models screening for adverse pregnancy outcomes in the first trimester.
    Type of Medium: Online Resource
    ISSN: 1015-3837 , 1421-9964
    Language: English
    Publisher: S. Karger AG
    Publication Date: 2021
    detail.hit.zdb_id: 1482292-1
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  • 10
    Online Resource
    Online Resource
    S. Karger AG ; 2020
    In:  Fetal Diagnosis and Therapy Vol. 47, No. 3 ( 2020), p. 228-236
    In: Fetal Diagnosis and Therapy, S. Karger AG, Vol. 47, No. 3 ( 2020), p. 228-236
    Abstract: 〈 b 〉 〈 i 〉 Objective: 〈 /i 〉 〈 /b 〉 The aim of this work was to investigate the association between maternal and fetal characteristics and the fetal fraction at 8–14 weeks’ gestation, with emphasis on the change in the fetal fraction upon repeat sampling. 〈 b 〉 〈 i 〉 Method: 〈 /i 〉 〈 /b 〉 One sample for cell-free DNA (cfDNA) testing was collected at the same time as the biochemical markers for combined first trimester screening (visit 1) and another at the nuchal translucency scan (visit 2). Chromosome-selective cfDNA analysis was performed on frozen plasma. 〈 b 〉 〈 i 〉 Results: 〈 /i 〉 〈 /b 〉 Overall, 321 women were included at visit 1, and 307 had a repeat blood sampling. A fetal fraction was obtained in 532 samples (238 samples with repeat fetal fraction). The fetal fraction decreased with maternal BMI ( 〈 i 〉 p 〈 /i 〉 & #x3c; 0.001), was lower in Asian women ( 〈 i 〉 p 〈 /i 〉 = 0.03), and increased with β-hCG levels ( 〈 i 〉 p 〈 /i 〉 & #x3c; 0.001) and gestational age ( 〈 i 〉 p 〈 /i 〉 = 0.04). Before 10 weeks’ gestation, the fetal fraction was lower ( 〈 i 〉 p 〈 /i 〉 = 0.02), as was the probability of a sufficient fetal fraction ( 〈 i 〉 p 〈 /i 〉 = 0.03) after adjustment for maternal BMI. Asian women had a higher increase in fetal fraction upon repeat sampling ( 〈 i 〉 p 〈 /i 〉 & #x3c; 0.001). 〈 b 〉 〈 i 〉 Conclusion: 〈 /i 〉 〈 /b 〉 Before 10 weeks’ gestation, the fetal fraction is significantly lower but seems to increase more rapidly compared to later gestations. Presently, combined first trimester screening with cfDNA testing should not include samples before 10 weeks’ gestation.
    Type of Medium: Online Resource
    ISSN: 1015-3837 , 1421-9964
    Language: English
    Publisher: S. Karger AG
    Publication Date: 2020
    detail.hit.zdb_id: 1482292-1
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