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BMJ. 2003 August 2; 327(7409): 242–243.
PMCID: PMC1126643

The impact of parental psychiatric disorder on children

Avoiding stigma, improving care
Paul Ramchandani, MRC training fellow in health services research
Alan Stein, professor of child and adolescent psychiatry

Four decades ago Michael Rutter in a seminal monograph highlighted risks to the development of children of parents with a psychiatric disorder.1 Since then a good deal of research has been focused on these children and their parents. However, policy to help and support these families has lagged behind. Two recent reports by national bodies in Australia and the United Kingdom have belatedly provided some important recommendations.2,3 None the less, much remains to be done both in policy terms and in the development of evidence based interventions.

Several common psychiatric disorders—including depression, anxiety, and eating disorders—affect adults of child rearing age. These disorders have been shown notably to impair social and psychological functioning, leading to difficulties in work and family life.4 In recent years recognition has increased of the potential impact that parental psychiatric disorder can have on a child. Several aspects of children's development can be affected, including their physical, cognitive, social, emotional, and behavioural development.5,6 Although a number of genetic and environmental mechanisms are important in linking parental psychiatric disorder to children's difficulties, there is good evidence that quality of parenting and family interaction are key mediating variables.5,6

Much of the focus of health policy in this area has been on the most severe mental illnesses and particularly on those parents who need to be admitted to hospital—usually those with schizophrenia or bipolar disorder.7 However, little attention has been paid to other disorders that are much more common.

To help children of parents with psychiatric disorder the children need to be identified first. This can be difficult. Patients in hospital are often not asked about whether they have children, and information about children is often not recorded in medical notes.8 Facilities for children to visit their parents in adult psychiatric hospitals are not routinely provided.9 It is harder still to identify those children whose parents have a disorder but who either do not require hospitalisation or are unknown to health services. Although examples of good practice do exist in some areas,10 serious deficiencies remain. The impact of parental psychiatric disorder on children is not included routinely in medical education, and training in the sensitive discussion of parenting issues is rarely dealt with. The enduring stigma that surrounds mental illness also contributes to difficulty in discussing these issues.11 Parents need to be comfortable disclosing their difficulties to their general practitioners or even to teachers when necessary. Overcoming this stigma and the other barriers is crucial. The importance of identifying and helping these children is of wider benefit than to the child alone—for example, child psychiatric problems continue into adulthood in an appreciable minority of cases,12 and the consequent increased health expenditure means that the whole community is affected. An opportunity for prevention exists.

Steps have been identified in two recent reports from organisations on two different continents—the Australian Infant, Child and Family Mental Health Association and the UK Royal College of Psychiatrists.2,3 The more extensive Australian report highlights the need for improved recognition of children of parents with mental illness, the need for better identification of problems in these children, and provision of help for those problems. In addition it calls for increased support for this group of parents in their parenting roles and highlights the specific steps that could be taken to achieve these aims. Implementing these recommendations will require changes in service provision—including closer working of primary care services and mental health services for adults and those for children, education of healthcare staff, and the challenging of stigma to enable parents to even discuss their parenting without the fear of having their children taken into care.

We believe that these service developments must be coupled with high quality health services research to monitor change and identify the most effective, efficient, and equitable way of providing treatment to this diverse group of children and families. These and other changes in the identification and treatment of children at risk will need to be introduced in a sensitive way. It would be easy to increase the stigmatisation facing parents with psychiatric problems, by seeming to adopt a language of blame. The message can and should be a positive one—parents with mental health problems and their children can be helped and deserve better.


Competing interests: None declared.


1. Rutter M. Children of sick parents: an environmental and psychiatric study. Maudsley Monographs. London: Oxford University Press, 1966.
2. Australian Infant Child, Adolescent and Family Mental Health Association. Principles and actions for services and people working with children of parents with a mental illness. (accessed 16 May 2003).
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