Forth Valley Primary Care NHS Trust, Royal Scottish National Hospital, Larbert, Falkirk, Scotland FK5 4SD
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We wished to ascertain to what extent patients had given informed consent to their medications. Therefore, 68 long-term psychiatric in-patients were interviewed about their knowledge and attitudes towards their medications.
RESULTS
Two-thirds of patients did not know the purpose of their medication; one-tenth knew about the side-effects. Longer length of stay, older age and voluntary status were associated with less knowledge. Despite poor knowledge, most patients accepted their treatment. However, few realised that they had any choice.
CLINICAL IMPLICATIONS
The prevalence of true informed consent is low among this group and raises issues about patients' rights.
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The Department of Health and the Welsh Office (1993) defines consent to treatment as "the voluntary and continued permission of the patient to receive a particular treatment based on an adequate knowledge of the purpose, nature, likely effects and risks of that treatment including the likelihood of its success and any alternatives to it. Permission given under any unfair undue pressure is not consent." (our emphasis.) Voluntary permission assumes that patients realise that they have a choice and agree to treatment in the absence of duress. There is little published research on the knowledge patients have of their medications, or of their rights to refuse treatment. In one depot clinic, 48% of patients did not realise they had a choice about receiving treatment (Eastwood & Pugh, 1997). Long-term in-patients may be even less aware of their rights.
Adequate knowledge of the purpose of medication depends on the clinician explaining treatment and the patient's capacity to understand. Roth et al (1977) proposes five tests of capacity to consent, increasing in stringency from absence of refusal to full understanding of the information. Patients should be informed of any risks of treatment that a prudent person would regard as significant, as well as the risks of having no treatment.
In this study we assessed the nature and degree of informed consent in long-term psychiatric in-patients, with particular reference to these three criteria:
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Procedure
A semi-structured interview was undertaken in March 1998 by one interviewer
(N.B.). Subjects were asked about the purpose and side-effects (as defined by
the British National Formulary;
British Medical Association & Royal
Pharmaceutical Society of Great Britain, 1998) of their
medication, whether staff had explained their drug treatment, their
willingness to take their medications and their belief about their right to
refuse it. Comparisons between groups were made using two-tailed
2 or Fisher's exact tests. Data were analysed using SPSS
(Version 9 for PCs).
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View this table: [in a new window] | Table 1 . Characteristics of sample |
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View this table: [in a new window] | Table 2. Patient knowledge and attitudes, by legal status |
Patients were on a median of two preparations (range: 1-5); 55 (81%) were on oral antipsychotics, 24 (35%) on antidepressants, 22 (32%) on depot antipsychotics and 13 (19%) on lithium. Knowledge and attitudes were not associated with preparation (Table 3).
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View this table: [in a new window] | Table 3. Patient knowledge and attitudes, by type of medication |
Of the detained patients, 26 (74%) were on Form 9 (i.e. they were considered to have given informed consent to their medication) and nine (26%) were on Form 10 (i.e. unable or unwilling to consent).
Of the patients, 44 (65%) did not know the purpose of any of their
medications. Only 13 patients (19%) knew the purpose of all their medications.
Knowledge was greater in detained patients (Fisher's exact test,
P=0.001) and those who had been in-patients for less than 10 years
(
2=9.6, d.f.=1, P<0.002).
Fifty-five patients (81%) did not know of any side-effects of their
medications and only seven patients (10%) knew some side-effects of all their
medications. Knowledge was greater in those who had been inpatients for less
than 10 years (
2=4.0, d.f.=1, P<0.04).
Forty-five patients (66%) were willing to take all their medications; 12
patients (18%) were unwilling to take any of them. Willingness was greater in
females (
2=4.3, d.f.=1, P<0.04), those who had
been inpatients for more than 5 years (
2=6.9, d.f.=1,
P<0.0009) and voluntary patients (Fisher's exact test,
P=0.04).
Four (11%) of the detained patients wrongly thought they had the right to refuse medication and 27 (82%) of the informal patients thought they had no right to refuse medication.
Nine patients (13%) recalled staff explaining medication. This was not associated with age, gender, length of stay or legal status.
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Lack of knowledge about the right to refuse medication was the most striking result, with 82% of informal patients wrongly thinking they had no choice. This was independent of age, length of stay, legal status or gender. Informal patients in our study may be eluding the safeguards of regular drug review afforded by the Mental Health (Scotland) Act 1984 because their passive acceptance of medication is accepted as informed consent to treatment.
This study has some limitations: the sample is relatively small and from one institution; there may be confounding variables, such as IQ, which we did not study; many of the variables may interrelate, for example, age and length of stay; and we did not investigate compliance with treatment. These issues were not our main focus of interest. Is the sample representative of other long-term patients? Findings elsewhere suggest that it may be. In an American state hospital population, only 8.4% could correctly name at least one of their medications, its dose and intended effect (Geller, 1982). Olin and Olin (1975) found that only 8% of a state hospital population were fully informed concerning their voluntary admission.
There is evidence that psychiatric patients themselves wish for more information about medications (Macpherson et al, 1993, 1996), although we did not ask about this. Worries that increasing patients' knowledge would decrease their compliance have not been substantiated (Schnieden et al, 1991; Rogers et al, 1993).
Our findings raise difficult questions about current psychiatric practice. Are long-term psychiatric inpatients told enough about the risks and benefits of treatment? How, and to what extent, can the prevalence of informed consent be improved in this patient population? Are patients, especially voluntary ones, adequately informed of their rights, and are those rights adequately protected? Are there adverse effects from increasing informed consent? In the absence of conclusive research evidence, the psychiatric professions and all those concerned for patient welfare must debate these questions.
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