Volume 11 Number 1
March 2010
Editorial 2
Osteoradionecrosis - a review of prevention and management
Mary Burke and Michael Fenlon 3
Patients and carers views of a special care dentistry
general anaesthetic service
Louise Hopper and Lucy Szymkowiak 10
Establishing a procedure for managing poor standards of oral
care in vulnerable and dependent adults
Daniel Knibb 14
The Mental Capacity Act 2005: implications for primary care
dental services: a summary
D Mudie, S Berman and A Kaul 17
The Mental Capacity Act 2005: its significance for Special Care
Dentistry and patient care
A Kaul, D Mudie and S Berman 21
The Mental Capacity Act 2005: implementation within Special
Care Dental services
A Kaul, D Mudie and S Berman 25
Arthrogryposis Multiplex Congenita: dental findings and treatment
of an 8-year-old child
D E Emmanouil, T Roumani and G Petsi 32
Disability and cultural issues in research lessons learned
Mili Doshi, Mary Burke and Janice Fiske 37
Editorial
I am honoured to write an editorial for the Journal of Disability
and Oral Health. As a medical doctor with a disability, a past campaigner
for the rights of people with disabilities and a non-expert in oral
health, it is heartening to see a health journal refer repeatedly
in its editorials to both the rights of people with disabilities
to receive high quality healthcare and a recognition of the predominance
of the social over the medical model of disability.
My personal passion is access to healthcare. Previous editorials
have addressed the issue of access for people with disabilities.
I wish to address the issue of access for those in poverty. The
distance between inaccessibility for people in poverty versus with
disability is not great. In fact, they are inextricably linked with
reports consistently showing disabled people being hugely more likely
to end up in poverty than the general population (National Disability
Authority, Leonard Cheshire Disability).
Tudor Harts Inverse Care Law, which states that the need for healthcare
is inversely proportional to the provision of healthcare (or more
simply put, those who most need health services are least likely
to get them) sadly is persistently and consistently validated. It
is my contention that no matter how high its standards of healthcare
delivery, an inaccessible healthcare service can lay no claim to
being a quality service. It has been demonstrated that lack of access
results in patients being less likely to attend a physician, avail
of preventive or appropriate diagnostic and therapeutic services,
or bring their prescriptions for dispensing (Weinick et al., 1996;
Krauss et al., 1998; Newacheck et al., 1998; Baker et al., 2000;
Lasser et al., 2006). Prewitt identified continuous access to primary
care in inner cities as the primary approach to address health inequalities
(Prewitt, 1997).
Homeless people suffer from high levels of dental problems (Conte
et al., 2006). In Ireland, access to both primary care and dental
health services is dependant on having a medical card, a means-tested
way of accessing care. Yet in Dublin, it has been shown that 45%
of homeless people do not have medical cards (OCarroll and
OReilly, 2008). A specialised dental service had been set
up in Dublin to provide access to dental services for homeless people
was set up, yet it has not had an incumbent for some months for
lack of staffing. Thus in the specialised GP clinic we run, we frequently
come across homeless people with acute dental pain and no access
to any clinic (never mind those requiring non-acute dental treatment).
In the UK it has been reported that homeless people find it difficult
to access dental services (Dentistry; Homeless Link, 2009)
Even if you have a medical card in Ireland it can be difficult
to get a dentist to provide treatment. Reports indicate that the
case may be similar in the UK with cost deterring many patients
from accessing treatment (BBC News, 2007). Marmot, in reviewing
the evidence on the effect of having to pay out-of-pocket expenses
on the health of middle to low-income earners, comments that this
illustrates how health systems perpetuate injustice and social stratification
(Marmot and Shipley, 1996). Community and Personal Dental Services
offer a route for the provision of specialised services to hard
to reach groups such as homeless people. These services seek to
deliver services to where the patients feel comfortable. Hard to
reach groups find mainstream services difficult to access and intimidating.
It is not acceptable in a society that espouses social inclusion
that medical or dental care remains unavailable for all. As Martin
Luther King said: Of all the forms of inequality, injustice
in health is the most shocking and the most inhumane.
Dr Austin OCarroll
General Medical Practitioner, Dublin, Ireland
Baker DW, Shapiro MF, Schur CL. Health insurance and access to care
for symptomatic conditions. Arch Intern Med 2000; 160: 1269-1274.
BBC News, 2007. http://news.bbc.co.uk/2/hi/7041291.stm
Conte M, Broder HL, Jenkins G, Reed R, Janal MN. l Oral health,
related behaviors and oral health impacts among homeless adults.
J Public Health Dent 2006.
Dentistry. http://www.dentistry.co.uk/news/news_detail.php?id=2388
Homeless Link. Survey of Needs and Provision 2009. Homeless Link
London 2009. http://homeless.org.uk/sites/default/files/SNAP2009_Full_Report1.pdf
Krauss NA, Machlin S, Kass BL. Use of Health care Services, 1996.
MEPS Research Findings No. 7. AHCPR Publication No. 99-0018. Rockville,
MD: Agency for Health Care Policy and Research. 1998
Lasser KE, Himmelstein DU, Woolhandler S. Access to Care, Health
Status, and Health Disparities in the United States and Canada:
Results of a Cross-National Population-Based Survey. Am J Pub Health
2006; 96: 1300-1307.
Leonard Cheshire Disability. Disability Poverty in the UK. Available
at http://www.lcdisability.org/?lid=6386
Marmot MG, Shipley MJ. Do socioeconomic differences in mortality
persist after retirement? 25-year follow-up of civil servants from
the first Whitehall study. BMJ 1996; 313: 1177-1180.
National Disability Authority. http://www.nda.ie/cntmgmtnew.nsf/0/877A60DB1411D35980257066005332F6?OpenDocument
Newacheck PW, Stoddard JJ, Hughes DC, et al. Health insurance and
access to primary care for children. N Engl J Med 1998; 338: 513-519.
OCarroll A, OReilly F. Health and Homelessness in Dublin:
has anything changed in the context of Irelands economic boom?
EJPH 2008; 8: 448-453.
Prewitt E. Inner City Health Care. American College of Physicians.
Ann Intern Med 1997; 127: 485-490.
Weinick RM, Zuvekas SH, Drilea SK. Access to Health CareSources
and Barriers,. (MEPS research findings No. 3, AH CPR publication
No. 98-0001.) Rockville, MD: Agency f or Health Care Policy and
Research 1996.
Osteoradionecrosis - a review of prevention and management
Mary Burke BDS FDS RCS(Eng)1 and Michael Fenlon MA PhD BDentSc
MGDS FDS RCS(Ed)2
1Guys and St Thomas NHS Foundation Trust, 2Kings
College London
Abstract
It has been long recognised that patients who receive radiotherapy
for cancer of the head and neck area are at risk of developing osteoradionecrosis
(ORN) of the jaws. Guidelines to reduce risk have been written,
based upon the evidence of many studies which have looked at the
incidence of ORN in different groups. Much of the research was carried
out over 20 years ago and more recent analysis of data and consideration
of the changes in radiotherapy raises the question as to whether
modifications to the guidance is now needed. There is a wide variation
in recommendations and a simpler, more unified approach to prevention
of ORN could be developed as well as research on recent management
techniques.
Clinical relevance: ORN is a serious condition which can adversely
affect quality of life and treatment outcome of patients who have
already suffered the trauma of oral cancer. Features include chronic
exposed bone which fails to heal, pain, fractures and fistulae.
The incidence is decreasing, probably as a result of improved radiotherapy
techniques. The general dental practitioner may play the greatest
role in prevention with regular oral health care.
Establishing a procedure for managing poor standards of oral
care in vulnerable and dependent adults
Daniel Knibb BDS MFDS RCS Eng, DSCD
Senior Dental Officer, Devon Primary Care Trust
(previously Community Dental Officer, Cardiff & Vale NHS Trust)
Abstract
Vulnerable adults who, for reasons of impairment or disability,
cannot achieve good oral hygiene for themselves may be dependent
on paid carers for their oral care. When this care falls below the
standard necessary to prevent oral disease, their oral and general
health may suffer. If standards fail to improve despite intervention
by the dental team and oral health continues to deteriorate, this
could be seen as neglect and thus become an issue that requires
liaison with the Safeguarding Adults team. This paper describes
the development of a local procedure which aims to establish proper
procedure in such cases, in the absence of national guidelines on
this subject.
The Mental Capacity Act 2005 Implications for primary
care dental services: a summary
D Mudie BDS LDS MCCD (RCS Eng) 1, S Berman BDS, MSc2, A Kaul BDS
MFGDP (UK), MFDS (RCS Eng) 2
1Senior Dental Officer, Adult Special Care; 2Deputy Head of Primary
Care Trust Dental Service, Wandsworth Teaching Primary Care Trust,
London, UK
ABSTRACT
The Mental Capacity Act 2005 for England and Wales came into force
in October 2007. Prior to its implementation, the law surrounding
the provision of care for people unable to give valid consent was
based on case law, notions of best practice, and the provision of
treatment that was deemed to be in the patients best interest.
The 2005 Act places the provision of care for such people within
a defined legislative framework supported by new systems and statutory
bodies.
The main provisions of the Act, and the changes in the landscape
around consent for the vulnerable adult, are discussed. The Act
defines capacity, sets out a test to assess it and describes the
responsibilities of those providing care for vulnerable adults.
It states the rights of these adults to be as fully engaged as possible
with the decision-making process. The application of the Capacity
Test is described, together with its implications for patient, carer
and clinician. In addition, the Act sets out who should be consulted
when decisions about treatment are to be made.
Clinicians must now act with due regard to the guidance published
in the Code of Practice which accompanies the Act. Special Care
dentists need a sound working knowledge of the Act, an understanding
of how it impacts on the provision of care for the vulnerable adults
they treat, and must ensure that they comply with their ethical
and legal responsibilities as they treat these patients.
The Mental Capacity Act 2005: its significance for Special Care
Dentistry and patient care
A Kaul BDS MFGDP (UK), MFDS (RCS Eng) 1, D Mudie BDS LDS MCCD (RCS
Eng) 1 and S Berman BDS, MSc2,
1Senior Dental Officer, Adult Special Care; 2Deputy Head of Primary
Care Trust Dental Service, Wandsworth Teaching Primary Care Trust,
London, UK
ABSTRACT
The Mental Capacity Act 2005 came into force for both England and
Wales, and was fully implemented by October 2007 (for Scotland separate
legislation exists, which is the Adults with Incapacity Act 2000).
Since this time, many Primary Care Trusts in England and Wales have
developed guidance on implementing the legislation. However, there
has been very little written about the day to day challenges faced
by the healthcare professionals who must abide by the Act, and its
accompanying Code of Practice.
Within Adult Special Care Dentistry, a significant portion of the
caseload can consist of vulnerable adults who lack decision-making
capacity, or whose decision-making capacity may be in doubt; in
these situations, the Mental Capacity Act will be of particular
relevance. Composite scenarios based on the authors experiences
are presented to illustrate some of the challenges that may be faced
by the clinician, along with their impact on patient assessment,
and oral health care provision. The Act emphasises the need for
effective communication within the multi-disciplinary care environment
which surrounds many of these potentially vulnerable adults.
It is important to raise awareness of the Act and the Code of Practice
amongst all members of the care team, including those who provide
informal care, and support for the patient, and most importantly,
the patients themselves.
The Mental Capacity Act 2005: implementation within Special
Care Dental services
A Kaul BDS MFGDP (UK), MFDS (RCS Eng) 1, D Mudie BDS LDS MCCD (RCS
Eng) 1 and S Berman BDS MSc2
1Senior Dental Officer, Adult Special Care; 2Deputy Head of Primary
Care Trust Dental Service, Wandsworth Teaching Primary Care Trust,
London, UK
Abstract
There are certain patient groups within Special Care Dentistry
for whom the Mental Capacity Act 2005 will have particular relevance.
Once the principles and legal implications of the Mental Capacity
Act (MCA) have been understood, the dental team must apply and integrate
these principles into their patient assessment and oral health care
plans. Implementation of the Act will involve raising awareness
amongst patients, family, friends and others who provide care for
vulnerable adults.
Factors that may affect capacity are discussed including how they
may impact on the delivery of oral healthcare, and some of the challenges
which clinicians may face in assessing capacity. The importance
of the Capacity Test and the Best Interest Checklist, along with
their documentation is discussed.
The role of the Independent Mental Capacity Advocacy Service (IMCAS)
and the situations when they may be required are outlined, with
particular reference to what may be defined as serious medical treatment
within the context of special care dentistry.
Arthrogryposis Multiplex Congenita: dental findings and treatment
of an 8-year-old child
D E Emmanouil DDS MSc PhD, T Roumani DDS MSc and G Petsi DDS
Dept. of Paediatric Dentistry, School of Dentistry, University
of Athens, Greece
Abstract
This report describes a case of Arthrogryposis Multiplex Congenita
(AMC) with limited mouth opening and dental caries. Conservative
dental treatment and physiotherapy exercises were prescribed. The
aim of this case report is to describe the method and difficulties
in the dental care of this patient and outline the importance of
a preventive programme.
Disability and cultural issues in research lessons learned
Mili Doshi BDS MFDS RCS (Eng) MSc1, Mary Burke BDS FDS RCS (Eng)
2 and Janice Fiske MBE BDS MPhil FDSRCS (Eng) 3
1Senior Dental Officer, Tower Hamlets Community Dental Service,
2Associate Specialist in Special Care Dentistry, Guys and
St Thomas NHS Foundation Trust, 3Senior Lecturer/Consultant
in Special Care Dentistry, King's College London
Abstract
Aim: To discuss the disability and cultural issues, which need
to be considered during the planning and implementation of a study
to investigate the oral health of young adults with a learning disability
and from a minority ethnic group.
Design: A study of the oral health of Bangladeshi young adults with
a learning disability is used as an example, to highlight the barriers
identified in the research process for this group. These barriers
included: access, culture, language and literacy, consent, communication
and co-operation. The paper highlights the approach required to
gain co-operation for access to the study population via day centres;
the development of an oral health questionnaire relevant to the
particular ethnic community; and translation requirements. It also
describes how support was given during a structured, informed consent
process and the use of props, photographs and scales used to support
and aid understanding.
Results: A participation rate of 98% was obtained in the study and
80% of individuals appeared to enjoy participating. The results
showed participants were very aware of oral health and their social
implications indicating that the approach used facilitated understanding
and communication.
Conclusion: By considering and adapting the research process to
meet the needs of people with a disability and from an ethnic minority
background, the study was acceptable to their needs and participation
levels were high.
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