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 Published: 22/12/2005
 


Cartwright Improvements at National Women's

C
ontents

The Cartwright Report  was released  on 5 August 1988. This Report of the Cervical Cancer Inquiry into activities at National Women's Hospital focussed on carcinoma-in-situ (CIS) treatment and research that occurred at the hospital during the 1950s and up-until the early 1980s.

Although the report was very critical of National Women's, the recommendations in the report have provided a strong impetus for change within the hospital. There is now a new style of management at National Women's that supports a women-centred approach and quality systems are in place to ensure the services provided to women are appropriate.

In 1998, the General Manager carried out an audit of the hospital's performance in meeting the requirements and intent of the recommendations articulated by Judge Silvia Cartwright in her report. This audit outlined what has been implemented at National Women's as a result of the report. It also included recommendations for making further improvements to National Women's services.

Some of the changes that have taken place at National Women's in response to the Cartwright Report include:

Go back to Contentsproviding women-centred care
The Cartwright Report emphasised the need for the focus of the service to shift from the doctor to the patient. National Women's now has a mission statement that is based on providing women-centred care.

A comprehensive quality of service programme is now in place. This includes a full-time Quality of Service Manager whois responsible fo the development and review of policies. Hospital-wide plus service-based multidisciplinary quality forums  include a consumer representative and regular service audits. There is a focus on collaboration and liaison within the hospital as well as with other health services and community groups.

Treatment guidelines and protocols are developed using an evidence-based approach. Consumers are involved in the development of policies, guidelines and protocols to ensure a consumer perspective is included.

A Maori Health Advisor is based at the hospital as part of the Maori Health Service's vision to recognise the concept of Mana Wahine in the delivery and planning of women's health services at National Women's.

Go back to Contentsrespecting the rights of patients
In response to the Cartwright Report, legislation was passed in 1994 by the New Zealand government to establish the Office of the Health and Disability Commissioner. The first Commissioner developed a Code of Rights for Health and Disability Consumers and established a national advocacy service, which is independent of health care providers.

The Code outlines the rights of all consumers using a New Zealand health or disability service. The Code requires that people be treated with respect and dignity; receive treatment that is free from discrimination and of a satisfactory standard; be given information in a manner that is meaningful and can be understood; be informed about their condition, treatment options, risks and benefits, and other relevant details necessary to make decisions and give informed consent. People also have the right to have a support person with them, make a complaint and access an independent advocate. These rights also apply to teaching and research settings.

Advocates from the local independent Health Advocates trust are available  for women who are using, or who have used a National Women's service. They are also available to advise staff on matters relating to the Code of Rights.

Auckland Healthcare has developed a leaflet called `Your Rights' which is given to everyone using a National Women's service. This leaflet is based on the Code of Rights and is available in a range of languages. Copies of the actual Code of Rights and information about the advocacy service are also available throughout the hospital.

In keeping with the Code of Rights, staff at National Women's pay particular attention to obtaining informed consent before any treatment and procedures are carried out. A wide range of information is available to inform women about various conditions and treatment options as well as the different services provided by National Women's staff. 

Interpreters in a range of languages are available and can be organised for women who are in need of one. A Chinese Liaison Midwife  is employed to address the particular needs of Chinese-speaking women.

Staff also take particular care to respect the privacy of women at National Women's and to make sure information about each woman (and baby) is treated confidentially.

Code of Rights audits are carried out to check that the requirements in the Code are being adhered to and that staff have a good understanding of the rights of consumers using a health service.

A user-friendly complaints process is now in place. An information sheet outlines how complaints can be made and all complaints receive a prompt response. National Women's has a commitment to taking seriously all concerns and complaints and to making changes that will improve the service provided to women.

A process is also in place to assist women who want access to their clinical records. One of the antenatal clinics tried hand-held records so women were responsible for their own maternity records during pregnancy. Copies of the records can  be available for women to keep if they wish to, after their baby is born.

A women's health information unit has been established to provide information on a comprehensive range of health topics. In addition to pamphlets and posters, a range of other resources are available for people to use. These include research computer databases, the International Cochrane Library, the Internet, videos, reference books, journals, and CD-ROM health programmes. Anyone can use the Unit and information can be mailed out to people unable to visit. Unit staff are available to assist people needing information Monday-Friday 9am-7pm. Unit staff co-ordinate the development and review of on-site written information to ensure it is up-to-date, easily accessible and consumer-friendly.

An annual report is produced with detailed statistics about the services provided at National Women's. This information is available to the public.

Go back to Contentsimproving gynaecology services
During the Inquiry, the Judge discovered there were differing views within the hospital about cervical screening as well as the management and treatment provided to women with cervical abnormalities. The prevailing view was revealed to be out-of-step with international standards. There was an absence of effective peer review processes and treatment protocols to provide guidance to practitioners, and safeguards for patients. This was of particular concern because of National Women's role as a large teaching hospital. The Judge was also keen to see a specialist gynaecological service developed at National Women's to ensure women received good quality appropriate care.

At a national level, the National Cervical Screening Programme (NCSP) was established in 1989, in response to Silvia Cartwright's recommendation that a national population-based screening programme be implemented immediately. This programme is actively supported by National Women's and the Auckland-based part of the National Cervical Screening Register is managed by Auckland Healthcare.

The Auckland School of Medicine, which has an obstetrics and gynaecology department based at National Women's, teaches students about carcinoma in situ (CIS) according to internationally accepted standards. The medical school has also introduced ethics and patients rights into its curriculum.

The cases of all the women who received inappropriate management of their cervical abnormalities have been reviewed and appropriate treatment implemented where indicated. National Women's acknowledges the special duty of care owed to these women and has taken steps to ease their access to any further assessments and treatment at the hospital. A review of the clinical management of cervical dysplasia at National Women's from 1965-1988 has been carried out.

A specialist oncology service for the treatment of invasive cancer of the genital tract has been established at National Women's. Specialised training programmes are in place for staff working in this area as well as a peer review process. Competency standards and a professional development programme (PDP) have been developed for gynaecology nurses.

A national protocol has been developed for the management of women with abnormal cervical smears. National Women's has established a process for the development of evidence-based guidelines for the treatment of gynaecologic diseases to provide guidance for health professionals and to inform women. Information leaflets are also provided on various conditions and treatments so that women are able to make informed decisions about their care.

Following a colposcopy review a clinical nurse specialist was appointed to work with the medical staff within the Colposcopy Clinic. The clinic carries out colposcopies for women who have had an abnormal smear with dysplasia. The nurse also provides a smear-taking service in a clinic set up for women staff members.

The review of National Women's gynaecologic oncology services looked at ways to improve the service further and in particular, focus on the role of nurses in the service. This assessment of the service included contact with other New Zealand and overseas services.

Go back to Contentsusing an ethical approach to teaching and research
The Cartwright Inquiry revealed a lack of robust ethical review processes to ensure that research proposals and new treatments to be carried at National Women's were properly scrutinised. The hospital ethics committee that existed at the time was an in-house arrangement that failed to provide proper safeguards for research participants. Criticism was also directed at the Auckland School of Medicine for involving patients at National Women's in teaching situations without their consent.

All research carried out at National Women's must be approved by a North Health regional ethics committee. This is an accredited committee, with health professionals, researchers, lay, Maori and Pacific Islands members, that is independent of the hospital. Research proposals must include a consent form and patient information as well as meeting specific requirements before they are approved by the ethics committee.

Informed consent must be given and the official consent form signed by each participant before they are involved in a research project at National Women's. Participants are able to change their mind about being involved in a research study, and can withdraw at any time. Their health care is not affected if they withdraw from a study.

Auckland Healthcare has established a Research Development Office with two research co-ordinators to work with and advise staff involved with research activities. They are available to assist researchers at National Women's and provide information about the ethical and other approval processes that are required. They have set up an on-line manual and produce a monthly report of research activities. They also liaise with Maori Health Management to make sure Maori perspectives are addressed. There are approximately 480 research projects registered with the Research Development Office.

A display board has been set up in the main entrance of National Women's (outside the Women's Health Information Unit) to inform people about the research activities in the hospital. Leaflets about particular studies are also available. There continues to be a high level of interest in this display from members of the public.

Staff are required to obtain consent before involving a woman, or a baby in a teaching or training situation. Consent must also be obtained for situations where observers are present. Although National Women's is a teaching hospital, women have the right to refuse to participate in teaching. If a request to be involved with teaching is declined the care provided is not affected in any way.

Instead of practising on hospital patients, medical students are now taught vaginal and pelvic examinations through a gynaecological teaching associates (GTA) programme as a part of their training.

Go back to ContentsIn conclusion
National Women's has made significant changes in the years since the release of the Cartwright Report. The recommendations and the intent of the Report have been incorporated into the provision of services to women. When the care provided is disappointing or not in keeping with expectations, there are effective processes in place for people to complain and for feedback to be used in positive ways to improve the service. National Women's welcomes and encourages suggestions that will enhance the way we care for women.

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