Netherlands Heart Journal

, 19:470

Clinical and scientific progress related to the interface between cardiology and psychology: lessons learned from 35 years of experience at the Thoraxcenter of the Erasmus Medical Center in Rotterdam

Open AccessReview Article

DOI: 10.1007/s12471-011-0190-5

Cite this article as:
Erdman, R.A.M. & Pedersen, S.S. Neth Heart J (2011) 19: 470. doi:10.1007/s12471-011-0190-5


In November 1975, as the first in the Netherlands, a full-time psychologist was employed at the Department of Cardiology of the Thoraxcenter of the Erasmus Medical Center. This innovative decision was consistent with a view to treat the patient as a whole rather than the heart as a single body part in need of repair, combined with the understanding that the heart and mind interact to affect health. The present selective review addresses the broad range of contributions of 35 years of psychology to clinical cardiology and cardiovascular research with a focus on research, teaching, psychological screening and patient care. The review ends with lessons to be learned and challenges for the future with respect to improving the care and management of patients with heart disease in order to enhance secondary prevention and the role of behavioural and psychological factors in this endeavour.


Behavioural factorsCardiac psychologyHeart diseaseReview


Clinical treatment and understanding of medicine has benefited greatly from the holistic view of the human body [1]. In cardiology, major advances have been made by examining the interactions between heart and mind—that is to say, cardiovascular medicine entails the art of medicine that understands disease as more than the sum of its parts—which in essence reflects the bio-psychosocial model that we know and use today. In November 1975, as the first in the Netherlands, Professor Paul G. Hugenholtz—Head of Cardiology at the Erasmus Medical Center (MC) in Rotterdam—elected to employ a full-time psychologist in the Department of Cardiology of the Thoraxcenter. This innovative decision was consistent with his view to treat the patient as a whole rather than the heart as a single body part in need of repair, combined with the understanding that the heart and mind interact to affect health. This integrative understanding of cardiology also gave rise to a practical need for a standardised self-report questionnaire that could provide cardiologists with quantifiable information about the psychological well-being of cardiac patients. As such, he could be considered a pioneer in behavioural cardiology. The present selective review addresses the broad range of contributions of 35 years of psychology to clinical cardiology and cardiovascular research in the Erasmus MC.

Cardiac psychology is the field of health psychology that identifies psychosocial risk factors for the development of cardiovascular illness and lifestyle changes that may help prevent and heal heart disease. In this selective review we address questions, including: Have patients profited? Have cardiologists, nurses on the ward, and other healthcare professionals managing cardiac patients benefited? Has it from a scientific point of view led to groundbreaking results? What are the lessons to be learned?

Research in the field of cardiac psychology

Over the past 35 years, research in the field of cardiac psychology at the Erasmus MC has been diverse. A selection of these investigations includes:
  • Development and validation of psychological instruments for specific groups of heart patients [24].

  • Information provision for patients undergoing cardiac surgery [5].

  • Influence of early discharge of acute myocardial infarction (MI) patients on psychological morbidity [6].

  • Psychosocial and physical functioning after cardiac rehabilitation [7].

  • Psychological aspects of non-cardiac chest pain [8].

  • Secondary prevention, multifactorial smoking cessation programme in cardiac patients [9].

  • Psychosocial aspects in patients with congenital heart disease [10].

  • Patient- and physician-related factors explaining the delay prior to admission among acute myocardial infarction patients [11].

  • Effects of treating vital exhaustion in angioplasty patients on new coronary events [12].

  • The role of personality as a determinant of quality of life in heart transplantation recipients [13].

  • Web-based behavioural intervention in patients with an implantable cardioverter defibrillator (ICD) [14].

  • Risk of chronic anxiety in patients with an ICD [15].

  • Psychological morbidity and quality of life in patients with peripheral artery disease [16].

  • Anxiety in partners of ICD patients and the role of personality, shocks and ICD indication [17, 18].

  • Influence of personality and psychological distress on mortality in diverse groups of cardiac patients [19, 20].

Specific results deserve particular attention, since research in these patient groups is still ongoing at the Erasmus MC and because of their potential to influence patient care. These results relate to the impact of heart disease and treatment strategies on the emotional well-being and quality of life of patients, and the influence of psychological factors on morbidity and mortality. For this end, we have chosen to reflect on the results of patients with congenital heart disease and patients receiving state-of-the-art treatment, such as percutaneous coronary intervention (PCI) with drug-eluting stenting and ICD therapy. These last two patient groups have been the focus of cardiac psychology research in the Erasmus MC since 2001 and 2003, respectively.
  • A cohort study of 498 patients 15 years or younger at the time of surgical correction for congenital heart disease performed between 1968 and 1980 at the Erasmus MC and followed up for 10 years showed that these patients displayed scores in the psychological, deviant range compared with peers from a normative reference group (27% versus 10%) [21]. A second follow-up of 362 patients 20–46 years postsurgery indicated that the congenital patients had measurable impairments in their level of education, occupation, and physical functioning. Predictors for long-term psychopathology were female gender, low exercise capacity, physical restrictions imposed by physicians, and the level of patient-perceived restrictions imposed by the scar following open heart surgery [22].

  • In a consecutive cohort of 796 PCI patients treated with drug-eluting stenting between February 2005 and February 2006, 30.2% patients were depressed 4 weeks post index event, as assessed with the 2-item Patient Health Questionnaire (PHQ-2). Depressed patients had an almost 2-fold increased risk of a non-fatal MI or mortality at a mean follow-up period of 1.4 years independent of their demographic and clinical risk profile. When stratifying analyses by gender, depressive symptoms were associated with a more than 2-fold increased risk of adverse clinical events in men but not in women [23].

  • In a consecutive cohort of 371 patients implanted with an ICD between August 2003 and December 2008, the incidence of mortality was close to 3-fold higher in those with a distressed (Type D) personality and 2-fold higher in patients with high levels of ICD concerns adjusting for demographic and clinical characteristics including ICD shocks. Patients with clustering of both Type D personality and high levels of pre-implantation concerns (HR:3.86; 95%CI:1.64–9.10) had a close to 4-fold increased risk of mortality compared with patients with one or none of these risk markers in adjusted analysis. ICD shocks during the follow-up period was associated with a 3-fold risk of mortality [20].

Perhaps not surprisingly these results emphasise that despite state-of-the art treatment with new innovative techniques in clinical cardiology, after 35 years the psychological profile of the patient still matters. More importantly, psychological factors carry independent prognostic value, irrespective of and adjusting statistically for traditional biomedical risk factors, as also demonstrated by others (see Pedersen et al. for a further overview of the role of psychological factors in heart disease) [24]. Together with other research findings in the field of cardiac psychology [19, 23, 2527], these results indicate that it is necessary to screen patients for psychological risk markers in clinical cardiology practice, as neither this information nor a proxy is available from the patients’ medical records. The identification of this subset of high-risk patients would allow further intervention including optimisation of medical treatment but also adjunctive intervention of a psychosocial and behavioural nature. Accordingly, in a recent advisory the American Heart Association recommended that patients with heart disease be screened standardly for depression [28]. However, this recommendation has led to an ardent debate in the scientific community, since we do not know whether early screening and detection leads to improved clinical outcomes [29, 30]. Irrespectively, depression deserves treatment in its own right due to its influence on quality of life, patient well-being, and compliance, with standardised and validated screening tools being available as are treatment options to reduce the burden of depression [29].

Screening for psychological morbidity

In order to screen cardiac patients for psychological factors in a standardised and valid fashion, it is important to use validated and reliable instruments. This not only requires knowledge of test development but also knowledge of the procedures used to adapt into Dutch existing instruments that were developed abroad, both of which form part of the expertise of medical and clinical psychologists. Validation of instruments in the Dutch setting developed in another language is necessary, as there may be cross-cultural differences such that a particular item in a scale may not be relevant in a different language and cultural setting, which might jeopardise the validity and reliability of the entire instrument. Among others, in the Erasmus MC, we have developed and/or validated the disease-specific instruments the Heart Patients Psychological Questionnaire (HPPQ) [4], the ICD Patient Concerns questionnaire [2], the Minnesota Living with Heart Failure Questionnaire [3], and the Peripheral Artery Questionnaire [31, 32]. These instruments do not tap all psychological factors that have been associated with increased risk of morbidity and mortality in cardiac patients independent of traditional biomedical risk factors.

The HPPQ—in Dutch known as the Medisch Psychologische Vragenlijst voor Hartpatiënten (MPVH)—is a disease-specific measure that was developed in order to be able to identify cardiac patients with psychological morbidity at an early stage such that cardiologists can intervene and if warranted refer the patient to a psychologist or another mental health professional. The HPPQ comprises four subscales tapping into patient well-being, feelings of being disabled, despondency, and social inhibition. The scale was validated in a mixed cohort of 1649 cardiac patients. Research has shown that feelings of being disabled assessed at the time of the index MI predict death 8–10 years post-MI and also morbidity and mortality 4 years post-PCI independent of traditional biomedical risk factors [3335].

In 1998, the collaboration with Wijbenga and others led to the translation and validation of the Minnesota Living with Heart Failure Questionnaire in Dutch, enabling the identification of patients with heart failure with poor quality of life [3]. Poor quality of life, as assessed with the Minnesota Living with Heart Failure Questionnaire, has been shown to predict mortality in heart failure patients [25].

Similarly, in 2005 we adapted and validated the ICD Patient Concerns questionnaire (ICDC) to the Dutch setting [2], which was developed in the UK to tap patient concerns about the ICD giving a shock [36]. Recently, in a cohort of ICD patients from the EMC, we have shown that patient concerns, as assessed with the ICDC, predict mortality with the associated odds being 2-fold [20].

With these developments at least two goals can be reached. First, in the diagnosis and treatment of patients with heart disease, the cardiologist has the opportunity to use disease-specific self-report questionnaires representing the patient perspective. Such screening allows for the early identification of patients at high risk for cardiovascular morbidity and mortality, but may also aid in clinical decision-making pointing to patients who may need more aggressive or adjunctive treatment [37]. Dependent on the patient’s psychological profile, level of psychological morbidity, and health status, it may be necessary to refer the patient to a medical psychologist. This healthcare professional is knowledgeable about heart disease, the impact of treatment options (e.g. living with an ICD) on patients, but also how to treat psychological morbidity taking into account the patient’s social situation (e.g. not having a partner), such that the intervention is tailored to the individual. Due to the possibility of early intervention, this is not only likely to improve patient care but also survival. Second, it makes for a more complete and holistic approach to the clinical management of patients with heart disease. With the information provided by the questionnaires completed by patients, the cardiologist will have a better understanding of the psychological profile of the patient, which is likely to enhance patient-doctor communication, patient satisfaction and perhaps even patient adherence with treatment advice. Psychological morbidity, such as depression, has been shown to reduce adherence to cardiac rehabilitation and lifestyle advice in cardiac patients [38].

Cardiac rehabilitation

The time when the benefits of cardiac rehabilitation still had to be proven is luckily in the past. Today healthcare professionals involved in the care and treatment of cardiac patients are increasingly recognising that an MI, bypass operation, heart transplantation, or the receipt of one or multiple ICD shocks may be associated with psychological consequences. In 1975 this was not the case, and scepticism towards cardiac rehabilitation was pervasive across the country. Together with the various Rehabilitation Committees of the Dutch Heart Foundation, the Rotterdam rehabilitation programme Capri served as a pioneer to promote cardiac rehabilitation. Scientific publications on the usefulness and effect of rehabilitation led to further evolvement of cardiac rehabilitation programmes [7, 39, 40]. Today’s cardiac rehabilitation comprises a series of modules, including physical training, stress management, smoking cessation, dietary advice, and relaxation therapy that are targeted towards the needs of the individual patient. Following an acute cardiac event, cardiac patients today have the possibility of receiving professional assistance that is geared towards increasing physical activity and exercise tolerance, dealing with feelings of anxiety and depression, activating social support, and promoting social re-integration [41]. This is a far cry from what was available in 1975. Nevertheless, we are not quite there yet. So far, the assumption has been that one size fits all, while there is an indication that subsets of patients, such as women, older patients, and depressed patients, may warrant specialised and more individually tailored cardiac rehabilitation [42]. Moreover, there is a great disparity in the percentage of patients attending cardiac rehabilitation across Europe and a large number of patients who do not meet the lifestyle targets set out for cardiovascular disease prevention [43].


Interview techniques and patient-doctor communication are, in our experience, not topics that the average cardiologist tends to consciously think about on a daily basis. Nevertheless, patient complaints lodged with the complaints committee of hospitals tend to a great extent to be attributable to poor patient-doctor communication, commonly leaving the patient with a feeling of not being listened to, misunderstood, and even mistreated. In order to enhance the quality of the consultation between patient and cardiologist, in the Erasmus MC at least one conversation between the intern and the patient is recorded on camera during the intern’s training and is discussed with a psychologist (the first author). The intern will learn about the basic do’s and don’ts of conversational techniques. Don’ts include starting the consult with a detailed cardiac history (usually serves to make the intern feel at ease), using medical terminology unnecessarily, posing suggestive questions, forcing a change in lifestyle (forcing does not help), displaying no empathy in situations that are difficult to the patient, writing down too much or looking at the computer screen instead of maintaining the relation with the patient by means of eye contact, forgetting to ask the patient if he has any further questions or if something is not clear at the end of the consult. When looking at the recording together with the psychologist, the intern is usually worried about potential criticism. However, it helps to say that the consult with the psychologist is meant as a learning opportunity and nothing else, and that the recording and what will be discussed will remain confidential. This instils in the intern a feeling of being in a safe and protective setting, which in turn enhances openness and facilitates discussion, while providing a way to learn from one’s own mistakes and the possibility of becoming a better doctor. Throughout his or her career - when dealing with patients—the cardiologist is faced with the challenge of keeping a balance between these softer sides of patient care and the more technical aspects of clinical cardiology.

Patient care

Perhaps the most important remaining question is whether patient care has improved as a result of the addition of a psychologist to the interdisciplinary team managing patients with heart disease? The answer to this question is not straightforward, but the presence of such expertise makes it possible for cardiologists and cardiovascular nurses to:
  • Consult the psychologist if a patient is emotionally distraught while admitted in the unit and needs psychological counselling.

  • Prior to discharge, refer the patient via the psychologist to a healthcare professional with the same expertise in the area where the patient lives.

  • Provide more optimal after care in the outpatient clinic with a cardiac psychologist onboard who is knowledgeable not only about psychological issues but also the somatic condition, including the latest treatment possibilities in clinical cardiology and the potential impact of such treatments on the patient.

In addition, the expertise of the psychologist may exert its influence on patient care in more subtle and indirect ways that are not necessarily visible or consciously acknowledged in daily clinical practice. From that point of view all of the aspects discussed here are woven together and form more than the sum of their parts in terms of improving the quality of patient care (Fig. 1).
Fig. 1

The role of the psychologist in improving the quality of patient care

Cardiac psychology—future challenges

Despite the progress made in the field of cardiac psychology since the decision to employ a full-time psychologist at the Department of Cardiology in the Erasmus MC 35 years ago, there are several imminent challenges that need clinical and scientific attention, which are outlined in Table 1.
Table 1

Challenges ahead for the field of cardiac psychology that may help enhance the quality of patient care



• Incorporating screening for psychological risk markers and health status as part of standard clinical practice

• Psychological factors and health status predict prognosis independent of traditional biomedical risk factors [20, 25, 44] and cannot be derived from other proxy measures available in clinical practice

• The incorporation of patient-reported health status in clinical practice can help in treatment decision-making [45] and health status can be used as a performance measure of the quality of care [37]

• In 2003, behavioural and psychological factors were introduced for the first time in the official European guidelines on cardiovascular disease prevention [46], but little has changed in clinical practice

• Development and improvement of disease-specific self-report questionnaires

• These measures aid to identify vulnerable and high-risk patients in clinical research and practice [29]

• Implementation and fine-tuning of behavioural interventions

• Evidence from large-scale intervention trials targeting depression is mixed with respect to influencing prognosis [47]

• The assumption that one size fits all and that we are able to influence cardiovascular endpoints might be some of the explanations for the failure of these trials, with stepped collaborative care being more successful [29, 48]

• Further enhancement of secondary prevention programmes, such as cardiac rehabilitation

• Cardiac rehabilitation is an effective means to reduce morbidity and mortality

• However, there is an indication that one size fits all does not hold, with subsets of patients, such as women, older patients, and depressed patients, warranting specialised and more individually tailored cardiac rehabilitation [42]

• There is a great disparity in the percentage of patients attending cardiac rehabilitation across Europe [49] and a large number of patients who do not meet the lifestyle targets set out for cardiovascular disease prevention [43]

• Development of genetic counselling programmes for patients and their families with a risk of familiar heart disease

• Screening, waiting for and learning of the outcome may lead to distress in subsets of patients [50]

• No such programmes are currently available for patients and their families at the cardiology department

In essence all of these challenges relate to the inclusion of the patient perspective (i.e., asking the patient to rate how he or she feels) in the care and management of patients with heart disease with the objective of enhancing the quality of care that we give to patients. The value of behavioural and psychological factors was recognised by the European Society of Cardiology guidelines on cardiovascular disease prevention in 2003 [46]. Continued efforts need to be made to increase the incorporation of these psychosocial factors in clinical practice. For example, consider how a patient would feel if he/she had heart disease and knew that being depressed would influence prognosis, would that patient not want to be screened for depression similar to screening for ‘traditional risk factors’ such as blood pressure, cholesterol levels, and blood glucose levels? Ignorance may be bliss, but knowing about the patient’s psychological risk profile would provide the opportunities for integrative interventions and care. Already 35 years ago, the importance of the psychological profile of the patient in recovery and disease progression was recognised; the time now seems ripe for implementing what we have learnt to optimise cardiovascular care, particularly in high-risk patients. The major challenge for the future lies in the implementation of early psychological screening and assessment of behavioural and emotional problems, and treatment of these problems in cardiac patients, in particular with respect to availability of the necessary infrastructure, logistics, and staff.


We would like to thank Professor Dr. Felix Zijlstra, Professor Dr. Maarten Simoons, Dr. Liesbeth Utens—the Erasmus MC—and Professor dr. Willem Kop, CoRPS—Center of Research on Psychology in Somatic diseases, Tilburg University, for their helpful comments to a previous draft of this article.

Open Access

This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.

Copyright information

© The Author(s) 2011

Authors and Affiliations

  1. 1.Department of Cardiology, ThoraxcenterErasmus Medical CenterRotterdamthe Netherlands
  2. 2.Department of Medical Psychology and PsychotherapyErasmus Medical CenterRotterdamthe Netherlands
  3. 3.CoRPS—Center of Research on Psychology in Somatic diseasesTilburg UniversityTilburgthe Netherlands