Section 25 Emergency Medicine and the Law
25.1 Mental health and the law: the Australasian and UK perspectives
Introduction
In the UK and Australasia, doctors in general are empowered by legislation to detain a mentally ill person who is in need of treatment. Mental illness, particularly its manifestation as self-harm, is a common ED presentation (in the UK, making up around 1–2% of new patient attendances, and up to 5% of attendances in Australasia), and emergency physicians require not only the clinical skills to distinguish between those who require psychiatric or medical intervention, but also a sound working knowledge of the mental health legislation and services relevant to the state where they practise. This ensures that patients with psychiatric illness are managed in the most appropriate way, with optimal utilization of mental health resources and with the best interests and rights of the patient and the community taken into consideration.
Whilst there are variations in mental health legislation between the UK, Australia and New Zealand, all legislation recognizes fundamental common principles that respect individual autonomy and employ least restrictive management practices. The World Health Organisation (WHO) advises 10 basic principles of mental healthcare law, including enshrining geographical, cultural and economic equity of access to mental health care, acceptable standards of clinical assessment, facilitating self-determination, minimizing restrictive treatment and enshrining regular and impartial decision-making and review of care.1 These themes are all present in Australasian and UK law, and awareness of such principles aids the clinician in delivering humane and ethical treatment for mentally unwell patients who seek emergency care.
Variations in practice
Mental health legislation in England and Wales
Mental Health Act
Detention of patients with mental illness
Section 2 of the Mental Health Act facilitates compulsory admission to hospital for assessment and treatment for up to 28 days. The application is usually made by an approved social worker or the patient’s nearest relative and requires two medical recommendations, usually from the patient’s general practitioner and the duty senior psychiatrist (who is approved under Section 12 of the Mental Health Act). In the ED, the responsibility for coordinating the procedure often lies with the emergency physician.
Section 3 of the Mental Health Act covers compulsory admission for treatment. Once again, recommendations must be made by two doctors, one of whom is usually the general practitioner and the other a psychiatrist approved under Section 12 of the Act. The application is usually made by an approved social worker or the patient’s nearest relative. Detention is for up to 6 months but can be renewed.
Section 4 of the Mental Health Act covers emergency admission for assessment and attempts to avoid delay in emergency situations when obtaining a second recommendation could be dangerous. It requires the recommendation of only one doctor, who may be any registered medical practitioner who must have seen the patient within the previous 24 h. The order lasts for 72 h. Application can be made by the patient’s nearest relative or an approved social worker. In practice, the application of Section 4 of the Mental Health Act rarely happens. Usually Section 2 or 3 is the preferred option.
Section 5 (2) – doctors holding power and Section 5 (4) – nurses holding power of the Act allow the detention of patients who are already admitted to hospital until a more formal Mental Health Act assessment can take place. Unfortunately, presence in the ED is not considered to constitute admission to hospital, and this section is, therefore, not applicable to the ED.
A new draft Mental Health Bill published in 2002 was opposed by professional and patient groups alike. It aimed to introduce a new legal framework for the compulsory treatment of people with mental disorders in hospitals and the community. The new procedure involved a single pathway in three stages: a preliminary examination, a period of formal assessment lasting up to 28 days and treatment under a Mental Health Act order. In order for the compulsory process to be used, four conditions needed to be satisfied: the patient must have a mental disorder, the disorder must warrant medical treatment, treatment must be necessary for the health and safety of the patient or others, and an appropriate treatment for the disorder must be available. The draft Bill made provision for treatment without consent as it is justified under the European Convention on Human Rights Article 8 (2) in the interests of public safety or to protect health or moral standards.
Mental Capacity Act
Emergency treatment
Treatment can be given to patients who lack capacity but several factors need to be considered:
Use of sedation or physical restraint
This is covered in detail elsewhere (Chapters 20.6 and 21.5). From the perspective of the mental health legislation, there are occasions where physical or pharmacological restraint is needed. Sedation or restraint must be the minimum that is necessary to prevent the patient from self-harming or harming others. Generally, a patient committed involuntarily is subject to treatment necessary for their care and control, and this may reasonably include the administration of sedative or antipsychotic medication as emergency treatment. Transporting these patients to a mental health service should be done by suitably trained medical or ambulance staff, and not delegated to police officers or other persons acting alone.
Mental health legislation in Australasia
In Australia mental health legislation is a state jurisdiction, and among the various states and territories there is considerable variation in the scope of mental health acts, and between definitions and applications of the various sections. Since the National Mental Health Strategy in 1992, there has been an effort in Australia to adopt a consistent approach between jurisdictions, with an emphasis on ensuring legislated review mechanisms and a broad spectrum of treatment modalities.2 Nevertheless, key differences apply between mental health acts and therefore specific issues should be referred to the Act relevant to the emergency physician’s practice location.
The Australian and New Zealand mental health acts referred to in this chapter are the following:
Definition of mentally ill or mental illness
South Australia
In the South Australian Act mental illness means any illness or disorder of the mind.
Indigenous and cultural acknowledgement
Cultural differences in the understanding and experiences of mental illness can impact greatly on the ability to provide adequate care. Whilst there are some cursory references to acknowledging special cultural and linguistic needs when interpreting the various mental health acts, only the Northern Territory in Australia and the New Zealand Mental Health Acts make specific mention of indigenous people, who are known to be a particularly vulnerable group.3
Involuntary admission
New South Wales
For a mentally ill patient the certificate is valid for 5 days from the time of writing, whereas for a mentally disordered patient the certificate is valid for 1 day. Mentally disordered patients cannot be detained on the grounds of being mentally disordered on more than three occasions in any 1 month.
Tasmania
In Tasmania, an application for involuntary admission of a person may be made by close relative or guardians, or an ‘authorized officer’. A medical practitioner must then assess the person and, if satisfied that the criteria are met, make an order for admission and detention as an involuntary patient in an approved hospital. This initial order is valid for 72 h and gives authority for the patient to be taken to the hospital and detained, whereupon a psychiatric assessment must be carried out within 24 h and the initial order confirmed or discharged. A further order for the continuing detention of a person as an involuntary patient can be made if the appropriate criteria are met and after two doctors (at least one a psychiatrist and neither having written the initial order) have examined the patient. A continuing care order can be valid for up to 6 months.
Use of sedation or physical restraint
Queensland requires that restraint used for the protection of the patient or others can only be done on an ‘order’ but is permissible for the purposes of treatment if it is clinically appropriate. Tasmania permits its use, on the approval of the responsible medical officer, for the medical treatment or protection of the patient, other persons or property. Victoria permits the restraint of involuntary patients for the purposes of medical treatment and the prevention of injury or persistent property destruction. Victoria also allows the use of restraint by ambulance officers, police or doctors in order to safely transport the patient to a mental health service, but this must be documented in the recommendation schedule.
Prisoners with mental illness
The New Zealand Act states that prisoners with mental illness who require acute care can be transferred to a general hospital for involuntary psychiatric treatment, if the prison is unable to provide that care. Australian Acts in New South Wales, the Northern Territory and Victoria all include similar specific provisions for mentally ill prisoners to be able to access involuntary care in public hospitals if needed. The Victorian Act is most detailed in this matter, although in practice rarely relies on public hospitals due to the development of a stand alone forensic psychiatric hospital. Both Queensland and Western Australia enshrine the same principle of allowing prisoners access to general psychiatric treatment, although their legislation is less specific, whilst the Tasmanian, South Australian and ACT Acts do not mention prisoners at all. In all jurisdictions, there is significant overlap with other laws such as Crimes and Prisons Acts, which also mention health needs of prisoners.
Deaths
Controversies and future directions
United Kingdom
Australasia
1 World Health Organisation. Mental Health Care Law: Ten Basic Principles. Geneva: World Health Organisation, Division of Mental Health and Prevention of Substance Abuse, 1996.
2 Forrester K, Griffiths D. Essentials of law for health professionals, 2nd edn. Sydney: Elsevier, 2005.
3 Australian Human Rights and Equal Opportunity Commission. Human Rights and Mental Illness. In Report of the national inquiry into the human rights of people with mental illness. Canberra: Australian Government Publishing Service; 1993.
Mental Capacity Act. http://www.opsi.gov.uk/acts/acts2005/20050009.html, 2005.
Jones R. Mental Health Act manual, 8th edn. London: Sweet and Maxwell, 2002.
Jones R. Mental Capacity Act manual, 2nd edn. London: Sweet and Maxwell, 2007.
Wallace M. Health care and the law, 2nd edn, Sydney: The Law Book Company Ltd, 1995.
WHO. Resource Book on Mental Health, Human Rights and Legislation. Geneva: World Health Organisation, 2005.
25.2 The coroner: the Australasian and UK perspectives
Australasia
Introduction
The function of the coroner is to investigate and report the circumstances surrounding a person’s death. A coronial inquest is a public inquiry into one or more deaths conducted by a coroner within a court of law. Legislation in each Australian state and territory defines the powers of this office and the obligations of medical practitioners and the public towards it. The process effectively puts details concerning a death on the public record and is being increasingly used to provide information and recommendations for future injury prevention.
Reportable deaths
As an example, the Victorian Coroners Act 1985 defines a reportable death as one (1) where the body is in Victoria; (2) that occurred in Victoria; (3) the cause of which occurred in Victoria; (4) of a person who ordinarily resided in Victoria at the time of death; (5) that appears to have been unexpected, unnatural or violent, or to have resulted, directly or indirectly, from accident or injury; (6) that occurs during an anaesthetic; (7) that occurs as a result of an anaesthetic and is not due to natural causes; (8) that occurs in prescribed circumstances; (9) of a person who immediately before death was a person held in care; (10) of a person whose identity is unknown; (11) that occurs in Victoria where a notice under Section 19(1)(b) of the Registration of Births Deaths and Marriages Act 1959 has not been signed; or (12) that occurs at a place outside Victoria where the cause of death is not certified by a person who, under the law in force in that place, is authorized to certify that death.
Despite the seemingly straightforward definitions given in the various Acts, there are many instances where it may not be clear whether a death is reportable or not. Emergency physicians are often faced with situations where there is a paucity of information regarding the circumstances of an event, and where the cause of death may be difficult to deduce. Correlation between the clinical diagnoses recorded on death certificates and subsequent autopsies has been consistently shown to be poor. What exactly constitutes unexpected, unnatural or unknown is open to debate and may require some judgement. In all cases the coroner expects the doctor to act with common sense and integrity. If at all in doubt it is wise to discuss the circumstances with the coroner or assistant, and to seek advice. This conversation and the advice given must be recorded in the medical notes.
Expert opinion
The person selected by the coroner to give this opinion should possess postgraduate specialist medical qualifications and be broadly experienced in the relevant medical specialty. For events occurring in the ED, a senior emergency physician with over 5 years of experience is usually most appropriate. The specialist medical colleges may be requested to nominate such a person.
UK
History of the coroner
The history of the coroner’s office is an interesting reflection of events that shaped our civilization and is in constant evolution. The Shipman Inquiry is the most recent event that will shape the coroner’s role. The office of the coroner was established in 1194 and its primary function then was that of protection of the crown’s pecuniary interests in criminal proceedings. The coroner was involved when a death was sudden or unexpected or a body was found in the open; however, aside from the duty to ensure the arrest of anyone involved in homicide, the coroner held a significant role in the collection of the deceased’s chattels and collection of various fines.1
The Broderick committee was appointed in 1965 to review death certification in response to adverse publicity about inquests and pressures to improve death certification. Their report published in 1971 contained 114 recommendations, many of which were enacted. Table 25.2.1 lists the reasons the Broderick Committee considered the purpose of an inquest.2
Table 25.2.1 Reasons for an inquest (according to the Broderick Committee)
The current Coroners Act (1988) states that a coroner shall hold an inquest into a death when there is ‘… reasonable cause to suspect that the deceased has died a violent or unnatural death, has died a sudden death of which the cause is unknown, or has died in prison or in a such place or circumstances as to require an inquest under any Act’.3
Structure of the coroner system in the UK
Coroners are independent judicial officers who mostly have a legal background (some also have a medical background) and must possess at least 5 years of postqualification experience. They are responsible only to the Crown, this being an important safeguard for society; however, their administration is largely the responsibility of the Home Office. They must work within the laws and regulations that apply to them: The Coroners Act 1988, Coroners Rules 1984 and the Model Coroners Charter. There are approximately 148 coroner’s districts throughout England and Wales, and each district has a coroner and a deputy and possibly several assistant deputy coroners. Coroners are assisted in their duties by coroner’s officers, who are frequently police officers or ex-police officers, whose work is dedicated solely to coronial matters. This follows long-established practice and has probably arisen because of the significant proportion of cases in which police are the notifying agent. The nature of a coronial investigation also frequently requires a person to possess knowledge about legal matters and skill in information gathering. From a practical viewpoint, the coroner’s assistants may be responsible for performing such duties as attending the scene of a death, arranging transport of the body to the mortuary, notification of the next of kin and obtaining statements from relevant parties. Clearly, variation in the structure of the service between regions is inevitable and reflects the size, composition and workload within the district.4
Reportable deaths
There is no statutory obligation in the UK for a doctor or any member of the public to report certain deaths to the coroner. However, an ethical responsibility exists and it is recognized practice to do so in particular circumstances. A 1996 letter from the Deputy Chief Medical Statistician to all doctors outlined these circumstances (Table 25.2.2).5
Table 25.2.2 Circumstances in which a death should be reported to the coroner
Scotland
In Scotland, the role of death investigation is undertaken by the procurator fiscal’s office, which is also responsible for the investigation and prosecution of crime. The spectrum of deaths investigated is essentially the same as in England and Wales; however, more specific guidelines regarding deaths possibly related to medical mismanagement are provided (Table 25.2.3).
Table 25.2.3 Specific guidelines regarding deaths related to medical management in Scotland
Handling the body
Clothing removed from the deceased during resuscitation efforts should be set aside and preferably placed into individual paper bags. Any remaining clothing on the deceased should be left in situ.6 Blood taken during resuscitation attempts, regardless of whether it was processed or not, should not be discarded, but kept refrigerated and its existence indicated to the coroner. The examination of antemortem blood samples can provide valuable information, particularly with respect to electrolyte and glucose concentrations, drug concentrations and in deaths possibly attributable to anaphylaxis, tryptase assay.7
Information for families
The next-of-kin of the deceased must be informed that the death has been reported to the coroner and the requirement or reasons for doing so. It is important to inform them that police may be involved in the investigation of the death on behalf of the coroner, but that this does not imply a criminal wrong-doing. An information leaflet explaining the coroner’s work and rights of the next-of-kin is available from the Home Office8 and should be available in every ED to pass on to bereaved families. Another useful publication written for bereaved families provides information regarding postmortems and is available from the Royal College of Pathologists.9
Postmortems
The coroner may decide upon the initial report of a death that a postmortem is necessary in order to determine the cause of death or resolve an issue relevant to a coronial inquiry. In the year 2000, postmortem examinations were conducted in 62% of cases reported to the coroner, continuing a steady downward trend in the proportion of postmortems conducted out of reported cases.10 Having decided upon the necessity for a postmortem, the coroner directs a pathologist to conduct a postmortem. The Coroners Act states that, in fact, the coroner may ‘direct any legally qualified medical practitioner’ to conduct the postmortem; however, the Coroners Rules 1984 direct that they should be performed ‘whenever practicable by a pathologist with suitable qualifications and experience’, and, in practice, most are conducted by Home Office accredited forensic pathologists. Clearly, if the standard of medical care provided by the hospital in which the death occurred is in question, it is inappropriate for a pathologist employed by that hospital to conduct the postmortem.
The issue of tissue retention at autopsy has received recent worldwide attention. Rule 9 of the Coroners Rules 1984 is quite broad, allowing the pathologist to retain ‘material which in his opinion bears upon the cause of death, for such a period as the Coroner sees fit’. Guidelines issued by The Royal College of Pathologists11 recommend that, in coroner’s cases, clear protocols between the coroner and the pathologist should exist, and retention of tissues outside of the above-mentioned context should occur with the agreement of both the relatives of the deceased and the coroner.
Inquest
An inquest is a public hearing at which the identity of the deceased and how, when and where the deceased came by his/her death are to be determined. In the year 2000, only 12% of reported deaths proceeded to inquest, the remainder being examined ‘in chambers’. Inquests (or fatal accident inquiries in Scotland) are mandatory in certain prescribed circumstances, including deaths in prison or police custody, and deaths resulting from workplace incidents. In certain circumstances, inquests are held with a jury that is responsible for the final verdict.
1 Knapman P, Powers M. The law and practice on coroners. Chichester: Barry Rose, 1985.
2 Cordner S, Loff B. 800 years of coroners: have they a future? Lancet. 1994;344:799-801.
3 Coroners Act. (c.13), 1988. http://www.hmso.gov.uk.
4 Tarling R. Coroner Service Survey: A Research and Statistics Directorate Report. London: Home Office, 1998.
5 Dorries C. Coroner’s courtsa guide to law and practice. Chichester: Wiley, 1999.
6 Dimond B. Death in accident and emergency. Accident and Emergency Nursing. 1995;3:38-41.
7 Burton J, Rutty G. The hospital autopsy, 2nd edn. London: Arnold, 2001.
8 Home Office. When sudden death occurscoroners and inquests. London: Home Office, 2002.
9 The Royal College of Pathologists. Examination of the body after deathinformation about post-mortem examination for relatives. The Royal College of Pathologists, London, 2000. http://www.rcpath.org.
10 Allen R. Deaths reported to coroners England and Wales 2000. London: Home Office Research Development and Statistics Directorate, 2000.
11 The Royal College of Pathologists. Guidelines for the retention of tissues and organs at post-mortem examination. The Royal College of Pathologists, London, 2000. http://www.rcpath.org.
25.3 Consent and competence – the Australasian and UK perspectives
Consent
There is therefore a requirement that patients consent to treatment, provided they are competent to do so. In situations where an intervention is proposed, agreement of the patient should therefore be sought. The term ‘informed decision-making’ is preferred by some to ‘informed consent’ as it reflects consideration of patient autonomy.1 It is also important to consider consent as a two-way process, with an exchange of knowledge between a patient and a doctor.2 The concepts of competence, provision of adequate information and the voluntariness with which consent is given are crucial in the consideration of obtaining valid consent or seeking an informed decision. Technically, treatment without consent may be considered an assault. This makes it extremely important that consent is obtained before treatment starts.
Consent may be given in several ways: implied, verbal or written.
If the patient voluntarily presents to the emergency department then some degree of consent is implied. If a doctor says ‘put your arm out straight because I need to take some blood for a test’ then this may be taken as implied consent. However, this would not cover the insertion of an intercostal catheter, for instance, a much more invasive procedure. Such a procedure would usually need some explanation in order that the patient understood what was to be done before the consent was given. This would be verbal consent.
Competence
The patient must be competent to give the consent or to refuse.
Questions that may be of assistance in assessing competence are listed in Tables 25.3.1 and 25.3.2. Third parties, such as relatives, are unable to legally provide consent, although it is frequently assumed that they are. However, it is a long-established practice and frequently a useful exercise to involve relatives in the process of determining what the patient would have wanted in a particular circumstance. They may also provide valuable information during the process of competence assessment regarding a person’s set of values and beliefs, and usual behaviour, particularly if the patient appears to have elected a path at odds with a previously expressed wish or one that might appear imprudent or irrational. A list of people considered to have parental responsibility is provided in Table 25.3.3.
Comprehension |
Ask patient to recall and paraphrase information related to proposed treatment, including risks and benefits of treatment, alternative treatment and consequences of no treatment at all. Retest later to check for stability |
Belief |
Tell me what you really believe is wrong with your health now |
Do you believe that you need some kind of treatment? |
What is the treatment likely to do for you? |
Why do you think it will have that effect? |
What do you believe will happen if you are not treated? |
Why do you think the doctor has recommended this treatment for you? |
Weighing |
Tell me how you reached the decision to accept (reject) treatment |
What things were important to you in reaching the decision? |
How do you balance those things? |
Choice |
Have you decided whether to go along with your doctor’s suggestion for treatment? |
Can you tell me what your treatment decision is? |
Table 25.3.2 Simplified questions for assessing competence
What is your present physical condition? |
What is the treatment being recommended for you? |
What do you and the doctor think might happen to you if you decide to accept the treatment? |
What do you and your doctor think might happen if you decide not to accept the recommended treatment? |
What are the alternatives available (including no treatment) and what are the possible consequences of accepting each? |
Table 25.3.3 People considered to have parental responsibility
The child’s parents if married to each other at the time of conception or birth |
The child’s mother, but not the father, if they were not so married, unless the father has acquired parental responsibility via a court order or a parental responsibility agreement or the couple subsequently marry |
The child’s legally appointed guardian |
A person in whose favour the court has made a residence order concerning the child |
A local authority designated in a care order in respect of the child |
A local authority or other authorized person who holds an emergency protection order in respect of the child |
Patients may make an advance statement or living will detailing their wishes for medical treatment should they become incapacitated at a later date. This may take the form of a written document or witnessed oral statement. It is legally binding provided the patient is an adult and was competent at the time made and the statement clearly applies to the current circumstances.4 If doubt exists about its validity, a court ruling should be sought.
Patients who might not be able to consent
Patient disabled by drugs or alcohol
When a patient is temporarily disabled by drugs or alcohol the situation is less clear. In some Australian states persons who have committed serious assault may escape conviction because the law considers them incapable of forming the intention to commit the act. Legal and medical opinions do not always agree, especially in respect of ‘capacity’ and blood alcohol readings. The absolute legal position is unclear as to whether an intoxicated person can give consent, but there is no doubt that any doctor who acts in the best interest of the patient will always be on solid ground in the event of an action (see Box 25.3.1).
The emergency patient
There has been little written about the patient who requires emergency care but is temporarily incapable of providing consent. The overriding principle, however, is one of the ‘duty of care’ owed by the doctor to the patient. This duty is to provide appropriate care at a standard commensurate with the skill and experience of the doctor. There is also an obligation to explain to the patient what has been done as early as is reasonable in the recovery phase.
Unique considerations for the emergency department
In short, the emergency physician must frequently make complex decisions at short notice with little background information. In situations where decisions have been made on behalf a patient who is felt to be incompetent, it is important to document carefully the information available to the physician, and the possible diagnoses and their sequelae entertained at that time, and the reasons for the course taken. It is good practice also to seek the assistance and advice of a colleague where the competence of a patient is in doubt and significant interventions are deemed necessary. Factors to be considered when acting in the patient’s best interests without consent are listed in Table 25.3.4.
Table 25.3.4 Factors to be considered when acting in the patient’s best interests without consent
The patient’s own wishes and values (where these can be ascertained) including any advance statement |
Clinical judgement about the effectiveness of the proposed treatment, particularly in relation to other options |
Where there is more than one option, which option is least restrictive of the patient’s future choices |
The likelihood and extent of any degree of improvement in the patient’s condition if treatment is provided |
The views of the parents if the patient is a child |
The views of people close to the patient, especially close relatives, partners, carers or proxy decision-makers about what the patient is likely to see as beneficial |
Any knowledge of the patient’s religious, cultural and other non-medical views that might have an impact upon the patient’s wishes |
Controversies and future directions
1 Skene L, Nisselle P. High Court warns of the ‘retrospectoscope’ in informed consent cases: Rosenberg v. Percival. Medicine Today. 2001:79-82. October
2 Alderson P, Goodey C. Theories of consent. British Medical Journal. 1998;317:1313-1315.
3 Miller S, Marin D. Assessing capacity. Emergency Medicine Clinics of North America. 2000;18:233-242.
4 British Medical Association. Consent Tool Kit Card 9 Advance Statements
Annas GJ, Densberger JE. Competence to refuse medical treatment: autonomy vs. paternalism. Toledo Law Review. 1984;15:561-592.
Appelbaum P, Grisso T. Assessing patients’ capacities to consent to treatment. New England Journal of Medicine. 1988;319:1635-1658.
Biegler P, Stewart C. Assessing competence to refuse medical treatment. Medical Journal of Australia. 2001;174:522-525.
Breen K, Plueckhahn V, Cordner S., et al. Ethics Law and Medical Practice. Allen and Unwin, St: Leonard’s British Medical Association Consent Tool Kit Card 5 Assessment of Competence, 1997.
British Medical Association. Assessment of Mental Capacity. BMA and the Law Society, 1995. Chapter 10. On http://www.bma.org.uk
General Medical Council. 0–18 Years:. The General Medical Council, 2007. London, Sept
Medical Practitioners Board of Victoria. Medico-Legal Guidelines. Melbourne: Medical Practitioners Board of Victoria, 2006. March
Moskop J. Informed consent in the emergency department. Emergency Medicine Clinics of North America. 1999;17:327-339.
Oats L. The courts’ role in decisions about medical treatment. British Medical Journal. 2000;321:1282-1284.
Pownall M. Doctors should obtain informed consent for intimate body searches. British Medical Journal. 1999;318:1310A.
Savulescu J, Kerridge I. Competence and consent. Medical Journal of Australia. 2001;175:313-315.
World Medical Association Declaration on the Rights of the Patient. 2008. http://www.net/e/policy/17-he.html. Accessed Sept
World Medical Association International Code of Medical Ethics. 2008. http://www.wma.net/e/policy/17-ae.html. Accessed Sept
25.4 Privacy and confidentiality
Physical privacy
Patient privacy incidents occur frequently in an ED, risk factors being length of stay and absence of a walled cubicle. Patients who have their conversations overheard are more likely to withhold information and less likely to have their expectations of privacy met.5 Privacy and confidentiality are challenged by physical design, crowding, visitors, film crews, communication and other factors.6
Prior permission should be obtained from the patient to allow students, nurses, other medical officers to be present during history taking, examination and procedures. This applies both in public and private hospitals. Some aspects of privacy in healthcare in the ED relate to confidentiality while being assessed (being overheard, being seen, being exposed and being embarrassed), which relate to ED design, staff awareness, sensitivity and care. ED staff may be unaware how their routine behaviour may infringe on patient privacy.7
Staff bays are now often enclosed by glass screens to prevent others from hearing details on a patient’s history or to prevent patients from becoming unnecessarily alarmed by discussion of serious differential diagnoses, which may need to be excluded. Inappropriate or unprofessional comments by staff may also be heard.8
When the patient is an adolescent, privacy needs may exclude communication with a parent. An understanding of the relevant informed consent law relating to minors is required.9 The federal Privacy Act does not specify an age at which a child is considered of sufficient maturity to make his or her own privacy decisions. Doctors need to address each case individually, having regard to the child’s maturity, degree of autonomy, understanding of the circumstances and the sensitivity of the information being sought.3
It is only within the last 5 years that the almost universal ‘whiteboard’ has virtually disappeared. This was a popular and useful management tool in EDs, displaying the patients’ names, working diagnoses, locations and management plans. They were easily visible to anyone who came into the department. To preserve privacy and confidentiality, it was inevitable that they were withdrawn despite strong opposition from ED staff, claiming that this would lead to disruptions in patient care, coordination and flow. These problems did occur during the change-over period, but staff adapted well, and the advent of patient-tracking computer systems means that each monitor now provides more clinical information than the whiteboard ever did.
Police
If an injured patient is suspected of being a crime victim or perpetrator and may be a danger to that patient’s or another’s life, it is the doctor’s civic duty to inform police of the circumstances.11
Assistance is also given to help police identify missing or deceased persons.
Legislation
Confidentiality of health information has been the focus of legislation over recent years.
The Privacy Act 19881 applied only to the Australian Commonwealth public sector, but steps were taken early on to introduce it to the private sector, resulting in the Privacy Amendment (Private Sector) Act 2000 becoming law to cover the private (and public) health sector in December 2001.2
In New Zealand, the Privacy Act was enacted in 1993 and was used to develop the Health Network Code of Practice and Health Information Privacy Code 1994, which was further modified by the Health Information Standards Organisation in 2005.5
National privacy principles
The Privacy Act offers privacy protection to patients, while balancing this with the need for health service providers to share information, where necessary, for the provision of quality healthcare. The National Privacy Principles (NPPs) applicable to hospitals are summarized in Table 25.4.1.
Table 25.4.1 National Privacy Principles (applicable to hospitals)
NPP1 | Collection |
Only collect information necessary to deliver the health service | |
Obtain consent (this may not be possible with some emergency department patients, in which case, consent is implied) | |
NPP2 | Use and disclosure |
Explain how the information will be used | |
To whom the information may be disclosed, e.g. other treating clinicians and health carers, pathology, radiology and pharmacy | |
By law, to courts, when subpoenaed | |
NPP3 | Data quality |
Set standards to keep information accurate, complete and up to date | |
NPP4 | Data security |
Protect and secure from loss, misuse and unauthorized access | |
NPP5 | Openness |
Explain how health information is handled | |
NPP6 | Access and correction |
Gives patients right of access to their own records and the right to correct it | |
NPP7 | Identifiers |
Hospital must have its own identifier such as a Unit Record number, and must not use | |
Commonwealth identifiers such as Medicare or Veteran Affairs numbers | |
NPP8 | Anonymity |
Where lawful or practicable, patients must have the option of using health services without identifying themselves | |
NPP9 | Transborder data flows |
Obligations regarding transfer of health information to another country | |
NPP10 | Sensitive information |
Health information is sensitive information and must not be collected or disclosed without the patient’s consent, except when required by law or under certain specified limited circumstances, such as serious or imminent threat to life or health, medical defence, for research relevant to public health or safety (preferably de-identified) | |
Includes racial or ethnic origin, religious beliefs, sexual preferences or criminal record |
NPP1
When collecting demographic data, this is best done by providing a patient with documents to complete, rather than asking patients at an open desk in a waiting room. Triage should be performed in a private area. Taking of family histories can be done without their consent, as this helps in diagnosis, and is part of good clinical practice.
NPP4
Patient records must not be left within reach of, or viewed by, others.
Patient details on a computer screen should not be visible to other patients or visitors. Screen savers are useful if the screen is unattended. Computerized patient data must only be accessible to authorized personnel by password-protected access.10
NPP6
Patients do have a right to access opinion as well as factual material, including a specialist’s report, whether or not the report states that it is not to be shown to the patient without the patient’s consent.3 Patients are not obliged to give their reason for requesting access. Patients do not have immediate right to investigation results. The doctor ordering the tests must be given the opportunity to assess and discuss the results; otherwise there is the risk of misinterpretation.
NPP8
In some settings such as counselling in HIV/AIDS or sexual health, there are instances where anonymity is requested and granted. In the case of public or private hospital EDs, for providing a safe health service, and for billing and rebate purposes, doctors are required to record the identity of the patient.3
NPP10
The original 10th NPP was titled ‘Sensitive Information’. In some revisions of this principle, it has been split into NPP10 ‘Limits on Use of Personal Information’ and NPP11 ‘Limits on Disclosure of Personal Information’. The Federal Privacy Act 1988 has recently been amended to permit disclosure of genetic information to an at-risk relative when there is a serious (although not necessarily imminent) threat to the person’s life, health or safety. It applies only to doctors and other health professionals in the private sector and does not cover those in state public hospitals or Commonwealth government agencies.12,13 Why this is so needs further consideration.
New Zealand
New Zealand implemented its Privacy Act in 1993, with 12 principles that are similar to the Australian NPPs.4 The Privacy Act has 12 information privacy principles:
In 2005, the Ministry of Health released the Health Information Strategy for New Zealand,4 with an emphasis on security of electronic data, and maintenance of trust in, and integrity of, communication. They developed a Privacy, Authentication and Security (PAS) guide, which brought all the existing relevant documents together.14
Implementation
Most hospitals now provide brochures to patients on arrival, outlining these privacy issues. These are important whether the hospital is public or private.15,16 ED staff must be aware that some patients will require more detailed explanation before they are prepared to reveal all relevant information, and a sensitive approach is needed. Complaints about alleged breaches of privacy may be made and, if necessary, may be referred to the state health ombudsman or the state or federal privacy commissioner.
Complaints and non-compliance
Doctors are advised to obtain their own independent legal advice and notify their medical indemnity/insurance company, if they are investigated by the privacy commissioner as the result of a complaint that privacy may have been breached. Monetary fines or imprisonment may result from non-compliance.17
Retrospectivity
In general, the principles apply to information collected on or after 21 December 2001 in Australia but may apply before then, if referred to, used or disclosed later. If compliance poses an unreasonable administrative burden or expense, then a summary is an option. This refers to NPP 5, 6, 7 and 9.3 There is no obligation by a doctor to provide access to information which is not in use collected prior to 21 December 2001.
State, territory and New Zealand privacy laws
New South Wales has 15 health privacy principles, which came into effect on 1 September 2004. They are a more detailed expansion of the NPPs.18 In Victoria, the Health Records Act 2001 came into operation on 1 July 2002, and this becomes the relevant date for ‘old’ versus ‘new’ information.19 In Queensland, there is no separate privacy law. Queensland Health requires compliance with the 10 NPPs.20 In Western Australia, there is currently no legislative privacy regimen, but an Information Privacy Bill was introduced in March 2007.14 South Australia has a Code of Fair Information Practice based on the NPPs.21 Tasmania has superseded its previous privacy principles with the Personal Information and Protection Act 2004.22 The Northern Territory has a Health Information Privacy website issued in March 2002.23 The Australian Capital Territory uses a slightly amended version of the Federal Privacy Act, which is administered by the Federal Privacy Commissioner on behalf of the ACT government.24
New Zealand implemented its Privacy Act in 1993, with 12 principles that are similar to the Australian NPPs.4 In 2005, the Ministry of Health released the Health Information Strategy for New Zealand,4 with an emphasis on security of electronic data, and maintenance of trust in, and integrity of, communication. They developed a PAS guide, which brought all the existing relevant documents together.25
1 Office of the Federal Privacy Commissioner. National Privacy Principles. The Privacy Act, 1988. http://www.privacy.gov.au.
2 Office of the Federal Privacy Commissioner. Guidelines on Privacy in the Private Health Sector, 2001. http://www.privacy.gov.au/publications/hg_01.html. 9 Nov (Accessed Sept. 2008.)
3 Phelps K, Mudge T. Privacy resource handbook. Canberra: Australian Medical Association, 2002.
4 Health Information Standards Organisation. Health Information Strategy for New Zealand, 2005. http://www.moh.govt.nz.
5 Karro J, Dent AW, Farish S. Patient perceptions of privacy infringements in an emergency department. Emergency Medicine of Australasia. 2005;17:117-123.
6 Geiderman JM, Moskop JC, Derse AR. Privacy and confidentiality in emergency medicine: obligations and challenges. Emergency Medical Clinics of North America. 2006;24:633-656.
7 Knopp RK, Satterlee PA. Confidentiality in the ED. Emergency Medical Clinics of North America. 1999;17:385-396.
8 Olsen JC, Sabin BR. ED patient perceptions of privacy and confidentiality. Journal of Emergency Medicine. 2003;25:329-333.
9 Baren JM. Ethical dilemmas in the care of minors in the ED. Emergency Clinics of North America, 24. 2006, 619-631.
10 Privacy Legislation and Notifiable Infectious Diseases. Melbourne: Department of Human Services, 2002. June http://www.dhs.vic.gov.au/phd/
11 Frampton A. Some legal and ethical issues surrounding breaking patient confidentiality. Emergency Medicine Journal. 2005;22:84-86.
12 Otlowski MFA. Disclosure of genetic information to at-risk relatives. Medical Journal of Australia. 2007;187:398-399.
13 Skene L. Patient’s rights or family responsibilities? Two approaches to genetic testing. Medical Law Review. 1998;6:1-41.
14 Information Privacy Bill. March. Western Australia Legislative Assembly, 2007.
15 Treatment of Patient. Information at Epworth Hospital, 2001.
16 Know your rights and responsibilities. Private patients hospital charter. Commonwealth of Australia. 2006.
17 Privacy an ongoing concern. Pamela Burton, Legal Counsel. Federal AMA, Australian Medicine, 2001. 18 Mar
18 Health Records and Information Privacy Act. Office of the New South Wales Privacy Commissioner, 2002.
19 Information to Private Health Service Providers. Health Services Commissioner, Victoria, 2004. http://www.health.vic.gov.au/hsc/. April
20 Queensland Government Information Standard (IS42A). Queensland Department of Health, 2001. Sep
21 Code of Fair Information Practice. South Australian Department of Health. http://www.publications.health.sa.gov.au/ainfo/1/.
22 Personal Information and Protection Act. Tasmanian Ombudsman, 2004. http://www.thelaw.tas.gov.au.
23 Northern Territory Government. Health Information Privacy website. http://www.nt.gov.au/health/org-supp/legal/privacy/health.
24 Health Records (Privacy and Access) Act. Australian Capital Territory, 1997.
25 The Privacy, Authentication and Security Guide. Ministry of Health, 2005. New Zealand