Releases Saturday 24 November 2001
No 7323 Volume 323

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(1)  NIGHT SHIFTS IMPAIR SURGICAL DEXTERITY

(2)  CONCERNS RAISED OVER POLICY TO ADD
FOLIC ACID TO FLOUR

(3)  MEASURES NEEDED TO REDUCE
BLOODBORNE INFECTIONS IN IRISH
PRISONS

(4)  PRE--ECLAMPSIA LINKED TO HEART DISEASE
LATER IN LIFE

(5)  GENETIC DIAGNOSIS "WILL HAVE FEW
SOCIAL CONSEQUENCES"
 


 

(1)  NIGHT SHIFTS IMPAIR SURGICAL DEXTERITY

(Laparoscopic performance after one night on call in a
surgical department: prospective study)
http://bmj.com/cgi/content/full/323/7323/1222

One night on call in a surgical department affects a
surgeon's ability to perform laparoscopy (examination
of the interior of the abdomen using a specialised
viewing instrument), finds a study in this week's BMJ.

All 14 surgeons (11 men and three women) in training
at teaching hospital in Denmark participated in the
study. A night shift started at 3.30pm and finished at
9am the following day. All trainees had similar, limited
experience in laparoscopic surgery.

Using a virtual reality surgical trainer, all participants
performed nine repetitions of six tasks. The
laparoscopic surgical skills of the 14 trainees were
assessed on the 10th repetition of the task, which was
performed during normal daytime working hours and
again at 9.30am after a night on call with impaired
sleep. The average total sleep time during the night on
call was 1.5 hours.

Surgeons showed impaired speed and accuracy in
simulated laparoscopic performance after a night on
call, suggesting that significant deficits in psychomotor
performance occur after 17 hours on call with disturbed
night sleep, say the authors. Factors connected with
surgical work, such as emergency workload, stress, and
emotional demands, may potentiate the effects of sleep
deprivation alone, they add.

"Further studies should determine how long it takes for
surgeons' laparoscopic performance to recover after an
extended period on duty and should be aimed at
developing and evaluating countermeasures that can
maximise alertness and reduce fatigue," they conclude.

Contact:

Teodor Grantcharov, Research Fellow, Aarhus
University, Kommunehospitalet, Aarhus, Denmark
Email: ttgrant{at}dadlnet.dk
 

(2)  CONCERNS RAISED OVER POLICY TO ADD
FOLIC ACID TO FLOUR

(Editorial: Fortification of flour with folic acid)
http://bmj.com/cgi/content/full/323/7323/1198

A UK Department of Health committee has now
recommended universal fortification of flour with folic
acid to reduce the level of neural tube defects. Yet
researchers in this week's BMJ warn that we need to
be cautious before introducing such a policy.

Although the benefits of supplementation are clear, the
possible harms of such a policy are not, as there is no
trial evidence of the efficacy and safety of the
intervention, write child health experts, Brian Wharton
and Ian Booth.

In the United States, a 19% reduction in the prevalence
of neural tube defects has been reported following folic
acid fortification of grain products. However, this
reduction is less than half that seen in England and
Wales in the 1980s without a fortification programme.
These data are hardly a substitute for a controlled field
trial, they argue.

Furthermore, mandatory and universal fortification does
not, at present, need the same trial evidence as for a
drug. Yet a drug is not given in imprecise doses to all
members of the population without choice or indication,
they add.

In 1998, 399 pregnancies in England and Wales were
affected by central nervous system malformation.
Although a field trial would not be easy, say the authors,
is it acceptable to increase the folic acid intake of 50
million people to prevent a third to two thirds of these
affected pregnancies before there is firm evidence of
efficacy and safety in people who are not pregnant?

Contacts:

Brian Wharton, Honorary Professor, Institute of Child
Health, University College London, UK
Email: bwharton{at}ich.ucl.ac.uk

Ian Booth, Professor of Paediatrics and Child Health,
Institute of Child Health, Birmingham, UK
Email: i.w.booth{at}bham.ac.uk
 

(3)  MEASURES NEEDED TO REDUCE
BLOODBORNE INFECTIONS IN IRISH
PRISONS

(Prevalence of antibodies to hepatitis B, hepatitis C,
and HIV and risk factors in entrants to Irish prisons)
http://bmj.com/cgi/content/full/323/7323/1209

There is an urgent need for increased infection control
and harm reduction measures to reduce the transmission
of hepatitis B and C viruses, and HIV in Irish prisons,
concludes a study in this week's BMJ.

Between 6 April and 1 May 1999, researchers visited
five prisons in the Republic of Ireland daily and
interviewed all those committed within the previous 48
hours. An oral fluid sample was collected to determine
the level of antibodies to hepatitis B and C viruses, and
HIV.

The level of antibodies to hepatitis B, hepatitis C, and
HIV in prison entrants who had previously been
imprisoned was similar to that found in the recent
national survey of Irish prisoners. However, the level of
these antibodies was much lower in the third of prison
entrants who had never previously been in prison.

Only 7% of those entering prison for the first time had
ever injected drugs, compared with 40% of those
previously imprisoned. The most important predictor of
hepatitis antibodies was a history of injecting drugs, say
the authors. Tattooing in prison was also an
independent risk factor for hepatitis C infection in
prisoners who had never used injected drugs.

Unlike England and Wales, Ireland already has a
programme of proactive hepatitis B vaccination in
prisons. However, increased control measures, such as
offering hepatitis B immunisation to all prisoners during
committal procedures, could further reduce rates of
infection in Irish prisons, conclude the authors.

Contacts:

Jean Long, Lecturer in International Health, Trinity
College Centre for Health Sciences, Dublin, Republic of
Ireland
Email: jelong{at}tcd.ie

Shane Allwright, Senior Lecturer in Epidemiology,
Trinity College Centre for Health Sciences, Dublin,
Republic of Ireland
Email: sllwrght{at}tcd.ie
 

(4)  PRE--ECLAMPSIA LINKED TO HEART DISEASE
LATER IN LIFE

(Long term mortality of mothers and fathers after
pre-eclampsia: population based cohort study)
http://bmj.com/cgi/content/full/323/7323/1213

Genetic factors that increase the risk of cardiovascular
disease may also be linked to pre-eclampsia (a serious
condition that can develop during the second half of a
pregnancy), finds a study in this week's BMJ.

Researchers in Norway identified 626,272 mothers
whose first delivery was registered between 1967 and
1992. Mothers and fathers were divided into groups
based on whether the mother had pre-eclampsia during
the pregnancy and whether the birth was term or
preterm. Deaths from cardiovascular causes, cancer,
and stroke in both parents were followed through to
1992.

Women who had pre-eclampsia and a preterm delivery
had an eightfold higher risk of death from
cardiovascular disease compared with women who did
not have pre-eclampsia and whose pregnancies went to
term. The long term risk of death was no higher among
the fathers of the pre-eclamptic pregnancies than the
fathers of pregnancies in which pre-eclampsia did not
occur.

These findings are consistent with but do not prove the
hypothesis that the long term risk of death from
cardiovascular causes is associated with a maternal
genetic predisposition to pre-eclampsia, say the
authors.

"Although our results apply only to relatively young
women, the implications for the determination of the
causes of pre-eclampsia and eventually its prevention
may still be important," say the authors. With longer
follow up the pattern of risks may become clearer but
may also change. For instance, it is possible that the risk
of death in the long term changes with outcome in
subsequent pregnancies, they conclude.

Contact:

Lorentz Irgens, Professor, Medical Birth Registry of
Norway, University of Bergen, Haukeland Hospital,
Bergen, Norway
Email: lorentz.irgens{at}mfr.uib.no
 

(5)  GENETIC DIAGNOSIS "WILL HAVE FEW
SOCIAL CONSEQUENCES"

(Ethics of using preimplantation genetic diagnosis to
select a stem cell donor for an existing person)
http://bmj.com/cgi/content/full/323/7323/1240

Using preimplantation genetic diagnosis (PGD) to
choose a stem cell donor is unlikely to cause harm to
anyone and is likely to be beneficial to some, suggest
researchers in this week's BMJ.

Clinical Genetics Fellow, Robert Boyle, and Professor
of Medical Ethics, Julian Savulescu, argue that the
uptake of this procedure will have few social
consequences and is likely to be a reasonable use of
limited health resources.

Since the 1980s, over 2,500 cycles of PGD have been
performed worldwide. A common objection to using
the procedure for the benefit of a sibling is that children
conceived in this way are not valued in their own right.
The authors argue that psychological harm to the
offspring is unpredictable, unlikely to occur, and, even if
it did occur, unlikely to be so severe that it would be
better for that particular child never to have existed.

Moreover, selection of children on a much grander
scale is already commonplace. An estimated 18,000
amniocenteses take place annually in Britain, mainly to
detect chromosomal abnormalities such as Down
syndrome, they say.

Who is harmed by allowing PGD to be performed
solely for the benefit of a relative, they ask? Not the
couple who wish to produce an embryo. Nor the child
who would not otherwise have existed. Nor the person
who receives the stem cell transplant that might save his
or her life. We must avoid the trap of interfering with
individual liberty by preventing such procedures for no
good reason, simply out of the "genophobia" that grips
much of society today.

"Some people object to using PGD along with in vitro
fertilisation for any indication. But if these procedures
are acceptable, as they are in many countries, it is
reasonable to use them to both bring a new person into
the world and to help save an existing life," they
conclude.

Contact:

Robert Boyle, Paediatric Registrar, Department of
Paediatrics, Hillingdon Hospital, UK
Email:  BobBoyle{at}doctors.org.uk  


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