Willem Drenthen
University of Groningen
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Featured researches published by Willem Drenthen.
European Heart Journal | 2010
Willem Drenthen; E. Boersma; Ali Balci; Philip Moons; Jolien W. Roos-Hesselink; Barbara J.M. Mulder; Hubert W. Vliegen; Arie P.J. van Dijk; Adriaan A. Voors; Sing-Chien S-C. Yap; Dirk J. van Veldhuisen; Petronella G. Pieper
AIMS Data regarding pregnancy outcome in women with congenital heart disease (CHD) are limited. METHODS AND RESULTS In 1802 women with CHD, 1302 completed pregnancies were observed. Independent predictors of cardiac, obstetric, and neonatal complications were calculated using logistic regression. The most prevalent cardiac complications during pregnancy were arrhythmias (4.7%) and heart failure (1.6%). Factors independently associated with maternal cardiac complications were the presence of cyanotic heart disease (corrected/uncorrected) (P < 0.0001), the use of cardiac medication before pregnancy (P < 0.0001), and left heart obstruction (P < 0.0001). New characteristics were mechanical valve replacement (P = 0.0014), and systemic (P = 0.04) or pulmonary atrioventricular valve regurgitation related with the underlying (moderately) complex CHD (P = 0.03). A new risk score for cardiac complications is proposed. The most prevalent obstetric complications were hypertensive complications (12.2%). No correlation of maternal characteristics with adverse obstetric outcome was found. The most prevalent neonatal complications were premature birth (12%), small for gestational age (14%), and mortality (4%). Cyanotic heart disease (corrected/uncorrected) (P = 0.0003), mechanical valve replacement (P = 0.03), maternal smoking (P = 0.007), multiple gestation (P = 0.0014), and the use of cardiac medication (P = 0.0009) correlated with adverse neonatal outcome. CONCLUSION In our tertiary CHD cohort, cardiac, obstetric, and neonatal complications were frequently encountered, and (new) correlations of maternal baseline data with adverse outcome are reported. A new risk score for adverse cardiac complications is proposed, although prospective validation remains necessary.
Heart | 2014
Ali Balci; Krystyna M. Sollie-Szarynska; Antoinette G L van der Bijl; Titia P.E. Ruys; Barbara J.M. Mulder; Jolien W. Roos-Hesselink; Arie P.J. van Dijk; Elly M.C.J. Wajon; Hubert W. Vliegen; Willem Drenthen; Hans L. Hillege; Jan G. Aarnoudse; Dirk J. van Veldhuisen; Petronella G. Pieper
Objectives Adequate prepregnancy prediction of maternal cardiovascular and offspring risk is important for counselling and management of pregnancy in women with congenital heart disease (CHD). Therefore we performed a study to identify the optimal assessment strategy for estimating the risk of pregnancy in women with CHD. Methods In this prospective study, we determined the outcomes of 213 pregnancies in 203 women with CHD. The ZAHARA I (Zwangerschap bij Aangeboren HARtAfwijkingen I) and CARPREG (CARdiac disease in PREGnancy) risk scores were calculated for each pregnancy, as was the total number of cardiovascular (TPc) or offspring risk predictors (TPo) from these and other studies combined. Pregnancies were also classified according to the modified WHO classification of maternal cardiovascular risk and according to disease complexity (DC). Results Maternal cardiovascular events occurred during 22 pregnancies (10.3%). Offspring events occurred during 77 pregnancies in 81 children (37.3%). Cardiovascular and offspring event rates increased with higher risk scores, higher TPc or TPo, higher WHO class and greater DC. The highest area under the curve (AUC) for maternal cardiovascular risk was achieved by the WHO class (AUC: 0.77, p<0.0001). AUC for the ZAHARA I risk score was 0.71 (p=0.001), and for the CARPREG risk score 0.57 (p=0.32). All models performed insufficiently in predicting offspring events (AUC≤0.6). Conclusions The WHO classification is the best available risk assessment model for estimating cardiovascular risk in pregnant women with CHD. None of the offspring prediction models perform adequately in our cohort.
Circulation | 2013
Petronella G. Pieper; Ali Balci; Jan G. Aarnoudse; Marlies A.M. Kampman; Krystyna M. Sollie; Henk Groen; Barbara J.M. Mulder; Martijn A. Oudijk; Jolien W. Roos-Hesselink; Jérôme Cornette; Arie P.J. van Dijk; Marc Spaanderman; Willem Drenthen; Dirk J. van Veldhuisen
Background— Pregnant women with congenital heart disease (CHD) are susceptible to cardiovascular, obstetric, and offspring complications. In women with CHD, cardiac dysfunction may compromise uteroplacental flow and contribute to the increased incidence of obstetric and offspring events. Methods and Results— We performed a prospective multicenter cohort study of pregnant women with CHD and healthy pregnant women. We compared clinical, laboratory, echocardiographic, and uteroplacental Doppler flow (UDF) parameters at 20 and 32 weeks gestation, and pregnancy outcome. We related cardiovascular parameters to UDF parameters and pregnancy outcome in women with CHD. We included 209 women with CHD and 70 healthy women. Cardiovascular parameters (N-terminal pro-B-type natriuretic peptide, left and right ventricular function) differed between both groups. UDF parameters were impaired in CHD women (umbilical artery pulsatility and resistance index at 32 weeks in CHD versus healthy women, P=0.0085 and P=0.017). The following cardiovascular parameters prepregnancy and at 20 weeks gestation were associated with UDF (umbilical artery resistance index) at 32 weeks at multivariable analysis: (1) right ventricular function (tricuspid annular plane systolic excursion) (P=0.002), (2) high N-terminal pro-B-type natriuretic peptide (P=0.085), (3) systemic (P=0.001), and (4) pulmonary (P=0.045) atrioventricular valve regurgitation. Women with CHD had more obstetric (58.9% versus 32.9%, P<0.0001) and offspring events (35.4% versus 18.6%, P=0.008) than healthy women. Impaired UDF was associated with adverse obstetric and offspring outcome. Conclusions— UDF parameters are abnormal in pregnant women with CHD. Cardiovascular function is associated with an abnormal pattern of UDF. Compromised UDF may be a key factor in the high incidence of offspring and obstetric complications in this population.
Congenital Heart Disease | 2008
Willem Drenthen; Elke S. Hoendermis; Philip Moons; Karst Y. Heida; Jolien W. Roos-Hesselink; Barbara J.M. Mulder; Arie P.J. van Dijk; Hubert W. Vliegen; Krystyna M. Sollie; Rolf M.F. Berger; A. Titia Lely; Mary M. Canobbio; Petronella G. Pieper
OBJECTIVES To investigate the age at menarche, the prevalence of menstrual cycle (interval) disorders, and determinants in women with congenital heart disease (CHD). DESIGN Using two CHD registries, 1802 (82%) of the 2196 women with CHD contacted (aged 18-58 years) provided written informed consent. After exclusion of patients with genetic disorders known to be associated with menstrual cycle disorders, 1593 eligible patients remained. Interviews by telephone and reviews of medical records were conducted. RESULTS Overall, the age at menarche was slightly increased in women with CHD (13.3 vs. 13.1 years in the general population), mainly attributable to an increased prevalence of primary amenorrhea (n = 147; 9.2%). Other menstrual cycle disorders were documented: secondary amenorrhea (n = 181, 11.4%), polymenorrhea (n = 103, 6.5%), oligomenorrhea (n = 90, 5.6%), and menorrhagia (n = 117, 6.5%). The occurrence of these disorders also depended on the presence of cyanotic heart disease, surgical status, the number of surgical interventions, and the severity of CHD. DISCUSSION Menstrual cycle disturbances, in particular primary amenorrhea, were frequently observed in this population. Patients with complex (cyanotic) heart disease needing repeated surgical interventions prior to menarche are especially at risk.
The Cardiology | 2008
Willem Drenthen; Petronella G. Pieper; Karin van der Tuuk; Jolien W. Roos-Hesselink; Elke S. Hoendermis; Adriaan A. Voors; Barbara J.M. Mulder; Arie P.J. van Dijk; Sing C. Yap; Hubert W. Vliegen; Philip Moons; Tjark Ebels; Dirk J. van Veldhuisen
Objectives: To investigate outcome of pregnancy and fertility in women with double outlet right ventricle (DORV). Methods: Using 2 congenital heart disease registries, 21 female patients with DORV (aged 18–39 years) were retrospectively identified. Detailed recordings of each patient and their completed (>20 weeks gestation) pregnancies were recorded. Results: Overall, 10 patients had 19 pregnancies, including 3 spontaneous miscarriages (16%). During the 16 live birth pregnancies, primarily (serious) noncardiac complications were observed, e.g. premature labor/delivery (n = 7 and n = 3, respectively), small for gestational age (n = 4), preeclampsia (n = 2) and recurrence of congenital heart disease (n = 2). Except for postpartum endocarditis and deterioration of subpulmonary obstruction, only mild cardiac complication pregnancies were recorded. Two women with children reported secondary female infertility. Several menstrual cycle disorders were reported: secondary amenorrhea (n = 4), primary amenorrhea (n = 3) and oligomenorrhea (n = 2). Conclusion: Successful pregnancy in women with DORV is possible. Primarily noncardiac complications were observed and only few (minor) cardiac complications. Infertility and menstrual cycle disorders appear to be more prevalent.
The Cardiology | 2008
Elke S. Hoendermis; Willem Drenthen; Krystyna M. Sollie; Rudolphus Berger
Truncus arteriosus, a rare and complex congenital heart disease, is hallmarked by a single great vessel (truncus) that arises over a large ventricular septal defect and provides both the pulmonary and systemic circulation. Pregnancy reports after repair for truncus arteriosus are scarce. Therefore, the maternal and offspring outcomes are unknown. We report the outcome of a pregnancy in an 18-year-old woman with repaired truncus arteriosus. Despite severe and symptomatic deterioration of truncal valve regurgitation, she successfully delivered a healthy child, and the valve function recovered within 2 weeks postpartum.
International Journal of Cardiology | 2008
Sing-Chien Yap; Willem Drenthen; Petronella G. Pieper; Philip Moons; Barbara J.M. Mulder; Bianca Mostert; Hubert W. Vliegen; Arie P.J. van Dijk; Folkert J. Meijboom; Eric A.P. Steegers; Jolien W. Roos-Hesselink
European Heart Journal | 2005
Willem Drenthen; Petronella G. Pieper; Martine Ploeg; Adriaan A. Voors; Jolien W. Roos-Hesselink; Barbara J.M. Mulder; Hubert W. Vliegen; Krystyna M. Sollie; Tjark Ebels; Dirk J. van Veldhuisen
European Heart Journal | 2007
Sing-Chien Yap; Jolien W. Roos-Hesselink; Elke S. Hoendermis; Werner Budts; Hubert W. Vliegen; Barbara J.M. Mulder; Arie P.J. van Dijk; Martin J. Schalij; Willem Drenthen
European Heart Journal | 2005
Willem Drenthen; Petronella G. Pieper; Karin van der Tuuk; Jolien W. Roos-Hesselink; Adriaan A. Voors; Bianca Mostert; Barbara J.M. Mulder; Philip Moons; Tjark Ebels; Dirk J. van Veldhuisen