Reproductive health in adults with congenital heart disease:a review on fertility, sexual health, assisted reproductive technology and contraception

Introduction: Due to the improved survival in individuals with congenital heart disease (CHD), considering their reproductive health has become more important. Currently, this topic is still underexplored. Areas covered: We discuss fertility, sexuality, assisted reproductive technology (ART), and contraception in adults with CHD. Expert opinion: Timely counseling regarding fertility, sexuality, pregnancy, and contraception is necessary, preferably during teenage years. Due to a lack of data, whether or not to perform ART in adults with CHD is almost always based on expert opinion and follow-up in an expert center is recommended. Future research is necessary to fill the gaps in knowledge on the risks and frequency of complications of ART in adults with CHD, but also to be able to differentiate the relative risks in the different types of CHD. Only then will we be able to counsel adults with CHD correctly and not unjustly deprive someone of a chance of pregnancy.</p

Incidence and Predictors of Maternal Cardiovascular Mortality and Severe Morbidity in the Netherlands: A Prospective Cohort Study

Objective: To assess incidence and possible risk factors of severe maternal morbidity and mortality from cardiovascular disease in the Netherlands. Design: A prospective population based cohort study. Setting: All 98 maternity units in the Netherlands. Population: All women delivering in the Netherlands between August 2004 and August 2006 (n = 371,021) Methods: Cases of severe maternal morbidity and mortality from cardiovascular disease were prospectively collected during a two-year period in the Netherlands. Women with cardiovascular complications during pregnancy or postpartum who were admitted to the ward, intensive care or coronary care unit were included. Cardiovascular morbidity was defined as cardiomyopathy, valvular disease, ischaemic heart disease, arrhythmias or aortic dissection. All women delivering in the same period served as a reference cohort. Main outcome measures: Incidence, case fatality rates and possible risk factors. Results: Incidence of severe maternal morbidity due to cardiovascular disease was 2.3 per 10,000 deliveries (84/358,874). Maternal mortality rate from cardiovascular disease was 3.0 per 100,000 deliveries (11/358,874). Case fatality rate in women with severe maternal morbidity due to cardiovascular disease was 13% (11/84). Case fatality rate was highes

Systematic review and meta-analysis of music interventions in hypertension treatment: A quest for answers

Background: Adverse effects, treatment resistance and high costs associated with pharmacological treatment of hypertension have led to growing interest in non-pharmacological complementary therapies such as music interventions. This meta-analysis aims to provide an overview of reported evidence on the effica

Cardiologist and cardiac surgeon view on decision-making in prosthetic aortic valve selection: does profession matter?

Cardiolog

Managing cardiac emergencies in pregnancy

A multidisciplinary, high-risk team should evaluate all pregnant women presenting with an acute cardiac event. Such events are potentially devastating if not recognised early and treated by experienced specialists. Management decisions are determined by the severity of the maternal condition and fetal viability. The management of most cardiac complications is similar in pregnant and non-pregnant women. There are n

Cardiologist and cardiac surgeon view on decision-making in prosthetic aortic valve selection: Does profession matter?

Aims Assess and compare among Dutch cardiothoracic surgeons and cardiologists: opinion on (1) patient involvement, (2) conveying risk in aortic valve selection, and (3) aortic valve preferences. Methods and results A survey among 117 cardiothoracic surgeons and cardiologists was conducted. Group responses were compared using the Mann-Whitney U test. Most respondents agreed that patients should be involved in decision-making, with surgeons leaning more toward patient involvement (always: 83 % versus 50 % respectively; p < 0.01) than cardiologists. Most respondents found that ideally doctors and patients should decide together, with cardiologists leaning more toward taking the lead compared with surgeons (p < 0.01). Major risks of the therapeutic options were usually discussed with patients, and less common complications to a lesser extent. A wide variation in valve preference was noted with cardiologists leaning more toward mechanical prostheses, while surgeons more often preferred bioprostheses (p < 0.05). Conclusion Patient involv

Combined cardiological and neurological abnormalities due to filamin A gene mutation

Background: Cardiac defects can be the presenting symptom in patients with mutations in the X-linked gene FLNA. Dysfunction of this gene is associated with cardiac abnormalities, especially in the left ventricular outflow tract, but can also cause a congenital malformation of the cerebral cortex. We noticed that some patients diagnosed at the neurogenetics clinic had first presented to a cardiologist, suggesting that earlier recognition may be possible if the diagnosis is suspected. Methods and results: From the Erasmus MC cerebral malformations database 24 patients were identified with cerebral bilateral periventricular nodular heterotopia (PNH) without other cerebral cortical malformations. In six of these patients, a pathogenic mutation in FLNA was present. In five a cardiac defect was also found in the outflow tract. Four had presented to a cardiologist before the cerebral abnormalities were diagnosed. Conclusions: The cardiological phenotype typically consists of aortic or mitral regurgitation, coarctation of the aorta or other left-sided cardiac malformations. Most patients in this category will not have a FLNA mutation, but the presence of neurological complaints, hyperlaxity of the skin or joints and/or a family history with similar cardiac or neurological problems in a possibly X-linked pattern may alert the clinician to the possibility of a FLNA mutation

Pregnancy Outcomes in Women After Arterial Switch Operation for Transposition of the Great Arteries: Results From ROPAC (Registry of Pregnancy and Cardiac Disease) of the European Society of Cardiology EURObservational Research Programme.

Background In the past 3 decades, the arterial switch procedure has replaced the atrial switch procedure as treatment of choice for transposition of the great arteries. Although survival is superior after the arterial switch procedure, data on pregnancy outcomes are scarce and transposition of the great arteries after arterial switch is not yet included in the modified World Health Organization classification of maternal cardiovascular risk. Methods and Results The ROPAC (Registry of Pregnancy and Cardiac disease) is an international prospective registry of pregnant women with cardiac disease, part of the European Society of Cardiology EURObservational Research Programme. Pregnancy outcomes in all women after an arterial switch procedure for transposition of the great arteries are described. The primary end point was a major adverse cardiovascular event, defined as combined end point of maternal death, supraventricular or ventricular arrhythmias requiring treatment, heart failure, aortic dissection, endocarditis, ischemic coronary events, and thromboembolic events. Altogether, 41 pregnant women (mean age, 26.7±3.9 years) were included, and there was no maternal mortality. A major adverse cardiovascular event occurred in 2 women (4.9%): heart failure in one (2.4%) and ventricular tachycardia in another (2.4%). One woman experienced fetal loss, whereas no neonatal mortality was observed. Conclusions Women after an arterial switch procedure for transposition of the great arteries tolerate pregnancy well, with a favorable maternal and fetal outcome. During counseling, most women should be reassured that the risk of pregnancy is low. Classification as modified World Health Organization risk class II seems appropriate

The endocarditis team

Endocarditis is een ernstig ziektebeeld met een hoge mortaliteit en morbiditeit. In de klinische praktijk proberen we de behandeling van deze patiënten te verbeteren door goede en snelle diagnostiek en door tijdig adequate antibiotische en zo nodig chirurgische therapie te starten. In de nieuwste richtlijnen wordt het begrip ‘endocarditisteam’ geïntroduceerd als cruciaal onderdeel in de verbetering van de zorg voor patiënten met (een verdenking op) endocarditis. Er wordt gesteld dat endocarditis een multidisciplinaire aanpak vraagt omdat het een ziekte is met een grote variatie in presentatie, waarvoor expertise nodig is van verschillende specialisaties, en ook omdat patiënten in een vroege fase dienen te worden besproken in een chirurgisch team. Observationele studies tonen een belangrijke reductie in de mortaliteit van endocarditispatiënten die zijn besproken in een endocarditisteam.Dit artikel bespreekt de ervaringen met het opzetten van een endocarditisteam in twee verschillende regio’s in Nederland (Rotterdam-​Rijnmond en Groningen). Wat is belangrijk als het gaat om de structuur en functie van een endocarditisteam? Het opzetten van een endocarditisteam kan lastig zijn. Daarom geven we enkele praktische tips. Ten slotte wordt de toegevoegde waarde van een operationeel endocarditisteam geïllustreerd aan de hand van een casus.Endocarditis is a life-​threatening disease with high mortality and morbidity. In clinical practice, we try to improve the outcome of patients with endocarditis by implementing a better and faster diagnostic workup, a timely start of antimicrobial therapy and an early surgical intervention if required. In the most recent update of the guidelines for the management of patients with endocarditis, an Endocarditis team is put forward as crucial part in the improvement of care for patients with (suspected) endocarditis. They state that endocarditis requires a multidisciplinary approach since patients present with highly variable signs and symptoms, need a high-​standard of care from several medical specialists, and need to be discussed in a surgical team early in the course of the disease. Observational studies support this implementation by showing a marked decrease in mortality after dicussing endocarditis patients in an Endocarditis team. This article discusses the experience with the implementation of an Endocarditis team in two different regions of the Netherlands (Rotterdam-​Rijnmond and Groningen). Which aspects are important for the structure and function of an Endocarditis team? The setting up of an Endocarditis team can be difficult, therefore we provide some practical advice. Finally, an illustrative case is presented