Issue 101
Sudden infant death and dummies
This paper was set up to examine the
association between use of a dummy (pacifier) during sleep and the
risk of sudden infant death syndrome (SIDS) in relation to other
risk factors.
It was a population based
case-control study set in seven counties in California. Mothers or
carers of 185 infants whose deaths were attributed to SIDS and 312
randomly selected controls matched for race or ethnicity and age
were chosen. The study looked at the use of a dummy during sleep
determined through interviews.
The study found that the adjusted
odds ratio for SIDS associated with using a dummy during the last
sleep was 0.08. The use of a dummy was associated with a reduction
in risk in every category of socio-demographic characteristics and
risk factors examined.
The reduced risk associated with use
seemed to be greater with adverse sleep conditions (such as sleeping
prone or on one side and sleeping with a mother who smoked),
although the observed interactions were not significant.
In addition, use of a dummy may
reduce the impact of other risk factors for SIDS, especially those
related to adverse sleep environment. For example, infants who did
not use a dummy and slept prone or on their sides (v on their back)
had an increased risk of SIDS (odds ratio: 2.61).
In infants who used dummies, there
was no increased risk associated with sleeping position (OR = 0.66).
While cosleeping with a mother who smoked was also associated with
increased risk of SIDS among infants who did not use a dummy
(OR=4.5), There was no association among those who did (OR=1.1)
The study concluded that use of a
dummy seems to reduce the risk of SIDS and possibly reduces the
influence of known risk factors in the sleep environment.
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NICE calls for wider use of statins
Treatment with statins should be
considered in patients with clinical evidence of cardiovascular
disease and in people with a 20% or greater risk of developing the
disease within 10 years. This was the recommended guidance to the
NHS in England and Wales published in January 2006, which will make
an additional 3.3 million people eligible for these drugs.
The National Institute for Health
and Clinical Excellence (NICE), the body that advises on the use of
treatments by the NHS, reviewed all available studies on the
efficacy and cost effectiveness of statins. NICE recommends use of
statins in adults with clinical evidence of cardiovascular disease
and in the primary prevention of the disease for adults with a 20%
or greater 10 year risk than average of developing it.
Previous guidance recommended the
use of statins in patients with a 30% risk and in people who already
had symptoms of the disease. Lowering the risk threshold for statins
will more than double the number of people who can be prescribed the
drugs on the NHS, from the current two million in England and Wales.
The guidance recommended that
treatment should usually be started with a low cost statin drug,
taking into account the required daily dose and product price per
dose. NICE estimated that the net cost to the NHS of increasing
provision of the drugs would be about £8.5m a year.
David Barnett, the chairman of the
independent appraisal committee that developed the guidance for
NICE, said, "In terms of potential impact, this guidance is arguably
one of the most significant to have come out of NICE since it
started over six years ago.
It offers clear guidance about which
patients should be started on treatment with a statin and how
doctors should go about it." He added that lifestyle changes to
reduce cardiovascular disease, such as stopping smoking, should also
be considered when starting treatment with statins.
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Depression in older people in primary care
The IMPACT trial was conducted at 18
diverse primary care clinics across the United States. The 1801
study participants were self referred or referred by their doctor,
or identified by systematic depression screening. Patients were aged
60 or older and met criteria for major depression or dysthymia, or
both, according to the structured clinical interview for DSM-IV axis
I disorders
(After a structured baseline
interview, patients were randomised to IMPACT collaborative care or
usual care. The aim of the study was to determine the long term
effectiveness of collaborative care management for depression in
late life.
The study was a
two arm, randomised, clinical trial; with an intervention for
one year and follow-up two years.
It took place in
18 primary care clinics in eight US healthcare
organisations.
There were
1801 primary care patients aged 60 and older with major depression,
dysthymia, or both.
Intervention Patients were randomly assigned to a 12 month
collaborative care intervention (IMPACT) or usual care for
depression. Teams including a depression care manager, primary care
doctor, and psychiatrist offered education, behavioural activation,
antidepressants, a brief, behaviour based psychotherapy (problem
solving treatment), and relapse prevention geared to each patient’s
needs and preferences.
The main outcome
measure was conducted by interviews in person at baseline and
by telephone at each subsequent follow-up. They measured depression
(SCL-20), overall functional impairment and quality of life (SF-12),
physical functioning (PCS-12), depression treatment, and
satisfaction with care.
Overall the
IMPACT patients fared significantly (P < 0.05) better than controls
regarding continuation of antidepressant treatment, depressive
symptoms, remission of depression, physical functioning, quality of
life, self efficacy, and satisfaction with care at 18 and 24 months.
One year after IMPACT resources were
withdrawn, a significant difference in SCL-20 scores (0.23, P <
0.0001) favouring IMPACT patients remained.
It appeared that
the tailored collaborative care actively engages older adults
in treatment for depression and delivers substantial and persistent
long term benefits. These include less depression, better physical
functioning, and an enhanced quality of life.
The IMPACT model may show the way to
less depression and healthier lives for older adults.
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