FROM OTHER JOURNALS
We scan the Annals of Internal Medicine
(www.annals.org), New
England Journal of Medicine (www.nejm.org),
Journal of the American Medical Association (www.jama.ama-assn.org),
Lancet (www.thelancet.com),
British Medical Journal (www.bmj.com),
Canadian Medical Association Journal (www.cma.ca/cmaj), Journal
of Medical Ethics (www.jmedethics.com) and Eubios Journal of Asian and International Bioethics
(www.biol/tsukuba.ac) for
articles of interest to the medical ethics community. For this issue of the IJME
we reviewed the November 2003-January 2004 issues of these journals. Articles of
interest from the National Medical Journal of India, Monash Bioethics Review,
and Developing World Bioethics are abstracted as and when they become available.
If you come across an article that you feel should be included, please
forward it tommamdani@comcast.net
Need for local research
capacity
The following article persuasively points out why
research relevant for India will have to come from within.
Academic professionals in developing countries work
in isolation from primary care settings. Most have to contend with an enormous
load of teaching and clinical care. There is little continuing medical education
and even rarer access to recent biomedical information, with the pharmaceutical
industry filling the gap. Salaries of academic professionals are insufficient to
support a white- collar lifestyle. Most of them resort to private practice. This
further encroaches on scarce time. Therefore, few are involved in developing and
testing public health interventions. Strengthening centres of learning and
creating local capacity for conducting and monitoring research are critical for
the promotion of academic medicine in developing countries.
Bhutta Z.
Practising just medicine in an unjust world; initiatives to improve academic
medicine in developing countries must come from within. BMJ
2003;327:1000-1
Consent for tissue
samples
Most Indians are unaware of the research and teaching
value of tissue samples taken during surgery. Therefore, a separate consent is
not taken from Indian patients for such use of their tissues. Yet it is
important for the Indian medical profession to be aware of the attitudes of the
public. This issue will surface in India sooner or later.
The authors interviewed 100 healthy volunteers to
assess what types of tissue individuals would be prepared to donate for
research, what types of research would be acceptable, whether parents would
consent to the donation of a child's tissues, and whether their tissues could be
used for teaching. They discovered that one in five would not agree to donate
any tissue, perhaps reflecting recent negative publicity surrounding post mortem
organ retention and reports of medical malpractice/criminal behaviour. Donation
of some tissues such as the eye and brain were unacceptable, while
ovarian/testicular tissue was not, perhaps because patients were familiar with
egg and sperm donation for fertility treatments. The majority agreed to donate
in case of use for cancer research but fewer agreed for research in genetic
disorders or genetic cloning. A majority favoured some ongoing control over
tissues removed at surgery. Although a detailed ethical review in 1995 concluded
that a patient's consent to the removal of tissue implied consent to its
subsequent use for any ethically acceptable purpose, this view is not universal.
Educating the public in the principles and practice of medical research may
change this attitude.
Goodson ML et al. A study of public opinion on the
use of tissue samples from living subjects for clinical research. J Clin Pathol
2004;57:135-8
Need for relevant
research
Research is not an elite, academic endeavour that
drains scarce resources from daily clinical practice. Instead, it is essential
for creating practical and relevant health systems. That is the message of the
following article describing the WHO's plans for the next decade.
In November 2004, at an international summit
organised by the WHO on health research in Mexico, the overriding question will
be what research is needed to reach the Millennium Development Goals (MDGs) by
2015. This research must return to the values of Alma Ata-WHO's 1978 commitment
to primary health care. All countries should have a health research system that
drives health sector reform. Research should be applied to improve health equity
and must be conducted according to universal ethical standards. The results of
research should be accessible to all. Civil society has a vital-and so far
neglected-part to play in setting research priorities.
Mexico, 2004:
Research for global health and security [editorial]. Lancet
2003;362:2033.
Research on
children
Research on children is essential to prevent harm as
the following article states persuasively.
Children are a vulnerable group that needs
protection from the potential harm of participating in a drug study. Therefore,
few drugs are tested in children; paediatric prescribing largely involves
educated guesses about doses, safety and effectiveness. Lack of information
either deprives children of the benefits of drug therapy or exposes them to
unknown side-effects. The most common hindrances cited are ethical, technical
and logistic. To rectify this, the US has recently taken the lead in offering
incentives for including children in trials.
Matsui D et al. The trials
and tribulations of doing drug research in children. CMAJ
2003;169:1033
Concordance of patient and
physician
We cannot always match patient and physician in a
country as diverse as India. Yet, the following article may help physicians who
want to increase the level of satisfaction among their patients. This is
especially important when dealing with disadvantaged groups.
All patients are sensitive to the affective climate
of the medical encounter; however, because of historical and personal
experiences with discrimination, African-American patients may be especially
sensitive to interpersonal cues from their physician that convey a message of
caring, trustworthiness and partnership. To study this, the authors audiotaped
252 primary care visits monitoring whether communication was more patient-
centred than physician-centred. When both physician and patient were
African-American or both were white, the visit was about two minutes longer and
the patient's affect was more positive but, surprisingly, was not more
patient-centred. This positive affect may thus reflect factors such as mutual
liking and respect, a sense of social or racial group affiliation and enhanced
trustworthiness or positive expectations.
Cooper, LA et al.
Patient-centered communication, ratings of care, and concordance of patient and
physician race. Ann Intern Med 2003;139:907-15
Palliative care for
AIDS
AIDS has devastated Africa and some predict a similar fate
for India. The bulk of resources have been allocated for prevention as
anti-retrovirals are still beyond the reach of the average patient. The best
that can be offered to an individual with AIDS is death with dignity. India can
learn and adapt the programme described here.
Uganda is the first and only African country that
has made palliative care for people in the terminal stages of AIDS and cancer a
part of its national health plan. Cheap, powdered morphine has been the keystone
of Uganda's affordable, modern palliative care movement, Hospice Uganda. The
Ugandan government agreed to make free morphine available when the Hospice was
established, and modified statutes to allow nurse specialists to prescribe
morphine. The hospice had to overcome fear and myths about morphine in the early
years. Hospice training includes lectures on practical and psychological factors
in pain management and symptom control, together with lectures on cultural
beliefs and the use of local remedies.
Ramsay S. Leading the way in
African home-based palliative care. Lancet 2003;362:1812-13.
The medical maze
All patients, irrespective of economic
class, find hospital stay bewildering and frightening. The NHS in the UK has
adopted some methods to make them less so. Can we in India adopt their
methods?
When a child develops a serious medical condition,
parents are rapidly thrown into a turmoil of shock and anxiety. Medical care can
be messy, is often painful, and the outcome may be uncertain. Parents may
suddenly have to hand over the responsibility for care of their children to
staff they hardly know. Witnessing the distress of one's sick child is one of
the hardest situations for parents to be in. They look at doctors and nurses as
helpers and companions in the fight against disease and death. Too often,
however, we fail in these compassionate roles. Some specialties such as
transplantation surgery and oncology have people who act as a link between the
medical team and family, and often guide a family through the medical system and
beyond throughout the patient's life. Many have a nursing background and have
now become a patient's and a family's advocate, giving practical and emotional
support in and out of hospital. The writer of this editorial describes the UK
National Health Service's Patient Advocacy and Liaison Service in each Trust
hospital, which employs on an average 2·5 full-time staff per hospital who
provide support, education, and an open ear for any concerns.
Wanted:
help through the jungle of hospital care [editorial]. Lancet
2003;362:1947
Direct advertising
We are
aware of the hazards of advertising of pharma-ceuticals but are not as familiar
with the hazards of aggressive advertising of preventive medical services which
include the latest in diagnostic tests. The following article from Australia may
be of relevance to us in India as well.
The growth in direct medical advertising of
diagnostic tests, such as virtual colonoscopy and heart scans, has occurred
without being widely debated in the community or within the profession. This is
in stark contrast to the recent vigorous debate on direct advertising of
pharmaceuticals to consumers. Some would say it is the consumer's right to
choose and buy in a free market and that medical advertising is adequately
controlled by legislation, such as the Trade Practices Act 1974, which prohibits
misleading or deceptive advertising. But medicine should be regulated by medical
associations based on medical principles and not by trade associations based on
trade principles.
Van Der Weyden MB. Marketing medicine. Med J Aust
2003;180: 97
Quality of care
We tend to
focus on the most sensational lapses of the health care system while ignoring
major issues such as access and distribution. The latter cause far more
preventable deaths. That is the message of the following article, which has
particular relevance for India as the health care industry begins to emulate its
counterparts in the West.
Safety is an essential goal for health care.
However, patients deserve far more than not to be harmed by their physicians.
Improving safety is vital, but it should not distract from the larger mission of
helping people maintain their health and cope with illness, of which safety is
only one component. The medical profession should focus on this larger purpose
and not on fragments.
Woolf SH. Patient safety is not enough: targeting
quality improvements to optimize the health of the population. Ann Int Med
2004;140:33-6
Doctored admissions
This
article, written in a wonderful anecdotal style, describes corruption in medical
entrance exams and the extent to which it is organised.
In what appears to be sound business tactics, the
players practically guarantee the student concerned marks good enough to ensure
entrance into a medical college-this by releasing most of the questions a few
hours before the actual examination. If something goes wrong and the questions
leaked do not actually appear in the question paper, not only is the money
refunded (no questions asked), but a 20% concession is offered at the next
appearance. The problem, as the writer points out, is that terms such as medical
ethics will be wasted on people who use unethical, illegal and devious routes to
get into medical colleges. Serving the poor will be the last thing on their
minds as they try to recover their investment and make a profit as
well.
Anand AC. Doctored admissions: are we sowing the right seed? Natl
Med J India 2003,16:328-30.
Abuse during
childbirth
Women giving birth are particularly vulnerable to
abuse by health care personnel, and perhaps more so in public hospitals. This
qualitative investigation documents factors facilitating violation of women's
reproductive rights during childbirth in Mexico. It is based on approximately
200 testimonies, and formal and 64 systematic direct observations in birth and
labour rooms in two large public hospitals. The issues raised here are
definitely applicable to India.
Three patterns of behaviour during childbirth are
identified, which result in violation of women's reproductive rights. Health
care personnel use their positions of power and control to intimidate women. The
report documents the use of coercion, threats and physical punishment to obtain
consent for the insertion of contraceptive devices. Women unaccustomed to
defending their rights accept the role they are forced into as hospital
patients. And public health institutions discourage women from pursuing formal
complaints.
Castro R, Erviti J. Violations of reproductive rights during
hospital births in Mexico. Health and Human Rights 2003;7:
90-110.