Concordance and children's use of medicinesBMJ 2003; 327 doi: https://doi.org/10.1136/bmj.327.7419.858 (Published 09 October 2003) Cite this as: BMJ 2003;327:858
- Emilio J Sanz, reader in clinical pharmacology ()1
- 1Department of Pharmacology, School of Medicine, University of La Laguna, 38071 La Laguna,Tenerife, Spain
Doctors are expected to encourage patients' involvement in treatment decisions, but what about children? This article considers the issues
Concordance is usually established between two people, doctor and patient, but the use of drugs in children always involves a third partner, the parents. Developing concordance with children in their health care raises several questions with no straightforward answers. For example, should children have a more active role in taking decisions about health and drugs than they currently do? Should greater emphasis be placed on informing parents about the disease and its treatment or on direct communication with their sick child? From what age should children be addressed directly about their illness? What is really relevant for them? Do children's and parents' perceptions about the usefulness and risks (efficacy), rules, and use of drugs coincide?
This article, based on qualitative studies of children's perceptions and attitudes to health, disease, and drug use, presents information that, though by no means providing the “right” answers to the above questions, might be useful when considering the options.
Most studies of patient compliance and the health education of children refer to the professional view and address compliance with drug use, usually related to specific disease treatment. Few address the general issue of how to improve compliance (or to create concordance). In spite of some outstanding systematic reviews from the Cochrane Consumers and Communication Group,1–3 few studies have examined patients' perspectives about drugs, and even fewer have studied children. Hopefully, the new Cochrane Qualitative Research Methods Group will address the topic.
Of particular value are several international studies supported by the European Union that compared healthy and asthmatic children in their knowledge, perceptions, and expectations about health, diseases, and treatment.4–6 The data presented in this article are based on those sources, and as such represent a review of the literature about children and drug treatment.
Drugs and children: the triangle of communication
The triangle of communication between health professionals, parents, and children has only recently gained attention in research; mainly in the social sciences and focused on children aged 7-11 years old. Most of the following statements apply only to this age group. Older children and adolescents are increasingly treated as grown ups and are gradually accommodated into the general characteristics of concordance for adults. Less research has been done with younger children, whose limited experience and understanding would seem to preclude more direct communication with them.
Paediatric consultations usually involve a doctor questioning the mother about her child's symptoms, examining the child, and giving advice to the mother. Children are normally left out of the communication loop and are addressed directly only for a more or less polite welcome and farewell. However, children are knowledgeable and overhear a great deal. Children often correct their mother's account or even ask the doctor directly, although the adults do not expect such behaviour.
Exploring the knowledge of healthy children about their diseases (using qualitative methods, with drawings from the children and semi-structured interviews) has generated a substantial body of knowledge. In most homes, drugs are spread all over the house, and children have ready access to them.7 But children are generally able to properly distinguish drugs from sweets or foodstuff and tend not to take them just for fun. They recognise that drugs have side effects, even though few children reported actually experiencing any, and know that taking drugs without being ill is dangerous and could even lead to death.8
Drugs are seen as aids to recovery, but the same value is normally given to other “health remedies,” such as staying at home or in bed, special foods or drinks, special clothes, and, often, special care such as presents and being pampered. Children up to 11 years old seldom attach a preventive value to drugs, and they find it hard to understand why someone should take drugs when “not actually being ill.” The mechanisms of action of drugs are seen as magic (especially for injections), and colours and tastes are not normally associated with particular indications or diseases (although this might be more relevant at younger ages). Children are familiar with the more commonly used drugs, often knowing them by their commercial names.
Quite a different picture is drawn by children with asthma. Their degree of autonomy in the use of drugs is considerable. Even children as young as 7 years old were able to give clear explanations about their disease and the drugs used and their main characteristics—how they work and when they should be taken and at which doses.
Living with asthma is mainly a process of negotiation—children with their environment (including peers, teachers, siblings, and friends); parents with the doctor, school teachers, and other family members (to ensure that “environmental requirements” are met at home, at school, on holidays, etc); and children with their parents, on one side trying to gain greater freedom and independence and on the other trying to control symptoms that might be dangerous.
Doctors play a part in these complex negotiations, but are by no means at the centre of it. Parents' attitudes to the disease (whether they see it as a chronic disease or as repetitive crises) influence their children's knowledge and perceptions. Children with asthma use their drugs alone most of the time, keep their drugs as their own property, remind their parents for refills, and can adjust the frequency and intensity of inhalations. They are alone, or only with other children, on most of the occasions when a crisis occurs. They quickly look for help but show good management of the initial steps.
Though a common chronic disease, asthma has its own peculiarities and might be different from other chronic diseases in childhood, such as diabetes and epilepsy. It is impossible to address all those differences in this article but Bluebond-Langner's descriptions of the “private world of dying children”9 is useful in revealing the attitudes of children at the other end of the spectrum of illness.
These studies show there is much room for improvement in doctors' direct communication with children. Children with a chronic disease will often be directly responsible for their drugs and treatment, and, even for occasional illnesses, children might wish to take some responsibility for treatment, overseen by their parents.
Ten guiding principles for teaching children and adolescents about medicines
Children, as users of medicines, have a right to appropriate information about their medicines that reflects the child's health status, capabilities, and culture
Children want to know. Healthcare providers and health educators should communicate directly with children about their medicines
Children's interest in medicines should be encouraged, and they should be taught how to ask questions of healthcare providers, parents, and other care givers about medicines and other therapies
Children learn by example. The actions of parents and other care givers should show children appropriate use of medicines
Children, their parents, and their healthcare providers should negotiate the gradual transfer of responsibility for medicine use in ways that respect parental responsibilities and the health status and capabilities of the child
Children's medicine education should take into account what children want to know about medicines, as well as what health professionals think children should know
Children should receive basic information about medicines and their proper use as a part of school health education
Children's medicine education should include information about the general use and misuse of medicines, as well as about the specific medicines the child is using
Children have a right to information that will enable them to avoid poisoning through the misuse of medicines
Children asked to participate in clinical trials (after parents consent) have a right to receive appropriate information to promote their understanding before assent and participation.
The principles were developed by the Division of Information Development, United States Pharmacopeia (http://www.usp.org/), as a result of the open conference “Children and medicines: information isn't just for grownups” held in Washington, DC, in 1996
Exploring the communication between parents and children in relation to health and drug use is difficult.10 The above mentioned studies revealed remarkable discrepancies between children's perceptions of their autonomy in the use of drugs and the autonomy “reported” or “conceded” by the parents. Children tend to be happy taking care of their own drugs (even if mother is putting the syrup on the spoon) and report “taking the medicines by themselves” but not on their own decision
Developing concordance with children
Concordance in health care with children is multi-faceted: drugs are part of the picture, but equally important are the special food, the special care, and love (see figure). The same should apply with adults. Communicating health decisions is not only giving technical advice on drugs, it involves the whole world of the patient. For these reasons, the notion of compliance represents a very restricted view of reality. Concordance needs to accommodate all these other factors as well, and the first of these is the communication that children offer to their healthcare providers.
Several years ago, “ten guiding principles for teaching children and adolescents about medicines” were developed (see box).11 Currently, through national and local activities and websites, many organisations are following up with the initiative of empowering patients to “ask questions” and thereby participate actively with their healthcare providers.
Etymologically, concordance comes from the Latin “concordare,” and that from “con-corde” (literally, with the same heart). Applying concordance means trying to get two people's hearts to beat in unison. Concordance implies not only the best technical solution to the problem (the body), but also the best approach to the disease and how to live with it (the mind, the heart, the soul, the psyche). Perhaps the change is too deep to be taken at once, but the strategies and philosophy behind the concepts are appealing.
Having the same “heart” as a child is a challenge: clinicians have to come down from their exalted position to the ground, to discover the meaning of children's lives and play. This requires more stamina and flexibility from health professionals, but children always give a full heart when they feel they are being taken seriously. Concordance with children is demanding but most rewarding.
Paediatric consultations traditionally involve a two way conversation between doctor and parent, with the child having a purely passive role
However, children are familiar with the concept of illness and treatments and are capable of taking a more active role
In particular, children with asthma are often highly autonomous, taking responsibility for treating their condition and taking care of their drugs
Achieving concordance with children means more than just achieving the best technical solution to an illness (the body), but also the best approach to the disease and how to live with it (the mind, the heart, the soul, the psyche)
Competing interests None declared.