St Christophers
Malcolm Payne

Social care and social work are important in end-of-life care.

Malcolm Payne's blog focuses on developments in social care and social work that affect palliative and end-of-life care. It is part of the information work of St Christopher's Hospice, London.

Misys Charitable Foundation

Archive for the ‘confidentiality’ Category

Losing personal information in the iPad age

Wednesday, February 1st, 2012


Staff working for a care provider in the Isle of Man lost an unencrypted memory stick (encryption means you have to put in a password before you can get at the information on the stick) with lots of client/patient information on it. Nobody knows where it went. They have had to sign an undertaking with the Isle of Man and UK regulator for information security.

Within the undertaking Praxis have agreed that all memory sticks, laptops and similar devices will be encrypted, all staff will be trained in the company’s policy for the storage, use and disposal of personal information, information which is no longer relevant will be disposed of in a secure manner, compliance with data protection policies will be regularly monitored and lastly the company will take steps to ensure personal data is secure.

In the iPad age, information is becoming more mobile, and people take it for granted that they can work on stuff on their mobile phones, Blackberries and iPads wherever they are. That means stuff is going to get lost. I wonder how many health and social care memory sticks have been lost from handbags or pockets over the past year or two. And how many were encrypted – difficult because you have to remember and input the password every time you use it. But it’s still personal information and often in a hospice or social care agency it will be highly personal stuff. Are we thinking carefully enough about this?

Another organisation got hammered for losing membership aplication forms on a train.

Details on the web here: http://www.ico.gov.uk/news/latest_news/2012/action-taken-after-care-provider-lost-unencrypted-memory-stick-18012012.aspx

Thread informed consent through social work practice

Tuesday, November 15th, 2011


Back from an interesting conference last Friday run by the University of East Anglia and the journal Ethics and Social Welfare on Confidentiality and Collaboration. Some very thoughtful contributions from experienced people mainly from safeguarding. Of course, the worry in that field of practice is that people’s professional rules about confidentiality prevents them sharing concerns about children and vulnerable adults at risk of abuse and neglect. But the law and all professional codes of ethics and practice require disclosure of concerns to colleagues to prevent offences and risk to others. This is really not difficult. Is someone at risk? Then disclose your concerns; at least at the outset we are only talking about conversations with professional colleagues who have the same objectives of public safety and concern for the people we are trying to help.

However, my view of this emphasises the importance of ‘informed consent’ as the answer to many confidentiality problems. One contributor was right in saying that I think informed consent should be threaded through our practice; I thought this was a nice concept. After all, it is contained in most social work codes of ethics, but I don’t think it is emphasised enough in practice. See my Humanistic Social Work: Core Principles in Practice, (Palgrave Macmillan, UK; Lyceum, USA). Chapter 2 promotes informed consent as an important way of offering accountability to service users and professional colleagues as well as to agencies.

For Humanistic Social Work in the UK and Europe: http://www.palgrave.com/products/title.aspx?pid=497063

For Humanistic Social Work in the US: http://lyceumbooks.com/HumanisticSocialWork.htm

(You get some free chapter downloads from the US site).

Breaching confidentiality: fines to make you think twice

Monday, June 13th, 2011


Of course, you can’t make rules against people behaving stupidly, but it seems surprising that most health and social care professionals would fail to be aware that this was a no-no, but apparently not, and the Information Commissioner has started getting strict about people breaching confidentiality. A legal report tells us about a fine for an employee of a private injury claims service who got his nurse girlfriend to give him names of patients who were recently injured – he followed them up to try to get personal injury claims. The nurse’s PCT found out about it when patients complained about being contacted. The report ends:

in a statement released by the ICO last week, the Information Commissioner Christopher Graham said that “the ICO will always pursue prosecutions where individuals breach both their duty of confidentiality and the Data Protection Act. Those whose responsibilities include the custodianship of sensitive personal data should take note.”

http://www.macroberts.com/content/content_1484.html#page=1

Confidentiality guidelines for LAs

Wednesday, October 28th, 2009


The Standards Board for England has published guidance on what is confidential for local councillors and the like, which is clear and succinct; other people may find it useful. It says:

Information is confidential:

* if it is about something serious and not trivial
* if the nature of the information is sensitive or personal, for example it is a business secret
* if it is information that you would expect people would want to be private
* if it was divulged in a way which implied it should be kept confidential
* if disclosing the information would be detrimental to the person who wishes to keep it confidential.

The good thing about this formulation is the emphasis on thinking what the person (a normal reasonable person) would want, and thinking about what they implied rather than specifically stated. Not news, but it sets it out well.

The full guidance on the web: http://www.standardsforengland.gov.uk/Guidance/TheCodeofConduct/Guidance/Quickguides/DisclosingConfidentialInformation/

The Standards Board sets standards for how local councillors and other elected/quango people should behave and investigates complaints: on the web: http://www.standardsforengland.gov.uk/

Their links site gives links to the Boards for the other countries: http://www.standardsforengland.gov.uk/aboutus/Usefullinks/

Is not talking about your own death bad?

Friday, June 19th, 2009


Another element of the clinical review was the palliative care culture that we shuld talk about our deaths compared with the culture of some minority groups and the preferences of some individuals, never mind their ethnicity, not to talk about death. Does this mean that they cannot be helped so well? Is talking about your own death always good for you? Is not talking about your death always a bad thing?

Care for adults is less important than care for children

Friday, June 19th, 2009


Another day another clinical review. This one, led by the social work team, was mainly about issues in working with African people in a UK setting. As part of the discussion, though, an interesting exchange about the impact on families of people who don’t want to talk about their death.

Much of the discussion was about children, and the need to get a mother to acknowledge their impending death, so that they can work things out with their children and plan for the future. Although this is often an issue with African peoples, it also affects every ethnic group, and particularly younger patients. Nurses and social workers felt that this was an important issue to overcome for the sake of the children.

One colleague asked whether it was just as important for adults in the family. The view among nurses (no doctors present) was that their main priority was the patient, and whether adults, spouses and siblings for example, could talk with their patient about their position was that adult’s responsibility.

But social workers have, ethically, just as strong a responsibility for enabling family communication for everyone, including adults, and in general for the functioning of the family. As an advice worker pointed out, knowing that someone was dying is often crucial for securing the spouse or partner’s immigration status, and that, in turn, may well have an impact on children.

The point is a wider one, though. Should the assumption be, for a social worker and for other professionals, that another human being, just because they are an adult, is a lower priority for help than a child? You might think so when you compare the anxiety about deaths of children with the shrug of the shulders when it’s another old person who dies alone. What do you think?

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Professional Codes of Ethics and Practice

Thursday, March 12th, 2009


I have been redoing the Hospice’s policy on confidentiality, and this means I have looked at loads of codes of ethics and practice that might be relevant to palliative care and social work. So here is a listing of British ones; often these websites have extensive additional documentation as well as the codes. Any palliative care and social work agency ought to keep up to date on the codes that are relevant to their work; most of these have been updated within the last five years. You could also compare them, to see how they differ on points of interest.

Professional regulators
Care Councils
There are different councils, covering at the moment social workers, but eventually all social care employees, for each UK nation, but they have an agreed Code of Practice (which is currently being revised); the Code also covers social care employers, who have specific duties (which hospices should ensure that they comply with if they employ social workers)

http://www.gscc.org.uk/codes

General Medical Council

Guidance on Good Medical Practice; there are other more detailed documents on this website

http://www.gmc-uk.org/guidance/good_medical_practice/index.asp

Health Professions Council
This will be taking in psychologists and counsellors, but currently covers arts therapists, biomedical scientists, chiropodists/podiatrists, clinical scientists, dietitians, occupational therapists, operating department practitioners, orthoptists, paramedics, physiotherapists, prosthetists & orthotists, radiographers, speech & language therapists.
Standards of Conduct, Performance and Ethics May 2008

http://www.hpc-uk.org/aboutregistration/standards/standardsofconductperformanceandethics/

Nursing and Midwifery Council
The Code: Standards of Conduct, Performace and Ethics for Nurses and Midwives; adopted 1st May 2008

http://www.nmc-uk.org/aArticle.aspx?ArticleID=3056

Professional organisations
British Association of Social Workers
Code of Ethics; last revised in 2002

http://www.basw.co.uk/Default.aspx?tabid=64

British Association for Counselling and Psychotherapy

Ethical Framework for Good Practice in Counselling and Psychotherapy; the most recent revision is dated January 2009.

http://www.bacp.co.uk/admin/structure/files/pdf/566_ethical%20framework%20revised%202009.pdf

British Medical Association
Medical Ethics Today: The BMA’s Handbook of Ethics and Law is a substantial book, the second edition of which was published in 2004, and there are updates dated 2007.

http://www.bma.org.uk/ethics/MET2004.jsp

British Psychological Society
Code of Conduct and Ethical Guidelines; last republished in 2006

http://www.bps.org.uk/the-society/code-of-conduct/code-of-conduct_home.cfm

International Federation of Social Workers
Ethics in Social Work: Statement of Principles, is designed to be a framework within which national members of the Federation can devise their own guidelines. Their website also has links to national codes of ethics throughout the world

http://www.ifsw.org/en/f38000032.html

Choice about death

Thursday, February 19th, 2009


(18th February 2009; inserted later because I am away)

A colleague not in the palliative care world has recently been admitted to hospital with cancer and died after only a short admission; it seems that she did not want visits from work colleagues, and people are shocked that she did not seek treatment earlier. As I read the paper on the journey home, this connects in my mind with the commentary on Jade Goody, the reality tv star who has announced she is now suffering from terminal cervical cancer, and plans to get a lot of well-paid publicity from her impending marriage and death ‘in public’, as the paper puts it, to fund her children’s future.

That’s a legitimately personal choice. How people die, who they want alongside them as they do so and how they get themselves through the process ought not to be subject to others’ demands. I was always taught that you could invite who you like to your wedding and nobody was entitled to be aggrieved; is that the same as your death? You can be generous about who is allowed in, but why should you be?

Who rescues the rescuers?

Monday, February 2nd, 2009


Who rescues the rescuers, I ask? Sitting at home today, having decided it’s impossible to get to work in snow which is apparently the worst in London for 19 years, I see an RAC van stuck in the road outside my window, accompanied by another RAC van that has come to rescue it, only also to get stuck. I’ve often been caused to wonder who deals with the social workers who beat their children or neglect their elders. Yesterday, a nursing colleague who is in hospital has been plied with requests by her consultant to have a private room, on the grounds that she should have the privileges of a senior NHS staff member. Equality of access to health care?

Human rights should not depend on responsibilities

Monday, February 2nd, 2009


Jack Straw’s been making a speech about human rights again. The main point is to say that any charter of British Human Rights should include responsibilities as well as rights. I have problems with the communitarian view of the world. Basic human rightsdon;t come with responsibilities. A right to education for the whole of yur life (even up to the moment of death), say, or to life itself, or to healthcare treatment or (I know this isn’t in any charter) to palliative care, or indeed to having a social work service (and a decent one) which also isn’t in any charter are all things that go along with being a human being in a civilised society. They should not depend on whether we have done our duty to society, particularly some duty imagined in its own interest by some political party..

The speech at: http://www.justice.gov.uk/news/sp280109a.htm