Releases Saturday 23 September 2000
No 7263 Volume 321

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(1)  TOO FEW INTENSIVE CARE COTS FOR
NEWBORNS TO COPE WITH DEMAND

(2)  BABIES BORN TO DIABETIC MOTHERS FOUR
TIMES AS LIKELY TO DIE AS THOSE BORN TO
HEALTHY MOTHERS

(3)  FINDINGS OF GRIFFITHS REVIEW INTO
ALLEGATIONS OF RESEARCH MISCONDUCT
FUNDAMENTALLY FLAWED

(4)  TWINS ARE SIGNIFICANTLY LESS LIKELY TO
HAVE ASTHMA THAN SINGLETONS

(5)  ABRUPT WITHDRAWAL OF DRUGS TO PREPARE
FOR SURGERY CAN BE DANGEROUS
 


 
(1)  TOO FEW INTENSIVE CARE COTS FOR
NEWBORNS TO COPE WITH DEMAND

(National census of availability of neonatal intensive care)
http://bmj.com/cgi/content/full/321/7263/727

Demand for neonatal intensive care in the UK outstrips
supply, finds research in this week's BMJ.

Field and colleagues conducted a census on the availability of
neonatal intensive care in the UK's 37 largest regional
perinatal centres dealing with high risk births. The study ran
between April and June last year.

During the three months of the study, 309 transfers were
made, equivalent to over 1200 a year, of which 264 were
made before the baby had been born. Sixty five of these
transfers involved a multiple birth. The most common reason
given for the transfer was lack of neonatal beds, which
includes lack of appropriate staff and equipment even if the
bed is empty, rather than inability of the centre to provide the
service. Regions differed considerably in their ability to cope
with demand, with the highest numbers of transfers in Wales
with a rate of 5.24 per 1000 births, followed closely by the
South and West region, with a rate of 5.16, and the Trent
region with a rate of 3.52.

Most deliveries in the UK take place in district general
hospitals, but when delivery units are full or there are
complications, these hospitals will refer to perinatal units. But,
say the authors, the findings of this study indicate that they will
find considerable difficulty in obtaining a place. And
anecdotal evidence suggests the problem is growing, say the
authors.

Transfers will always be part of obstetrics, say the authors,
and there is no evidence to suggest that the health of either
mothers or their babies is compromised by these transfers.
But the psychological and financial burdens borne by the
families involved are considerable, they say. National
standards or targets set for the NHS, and a comprehensive
nationwide strategy to deal with high risk perinatal care are
needed to alleviate the "chaotic" situation.

Contacts:

Dr Janet Rennie, King's College Hospital, London

Professor Philip J Steer, Chelsea & Westminster Hospital,
London
Email: P.Steer{at}ic.ac.uk
 

(2)  BABIES BORN TO DIABETIC MOTHERS FOUR
TIMES AS LIKELY TO DIE AS THOSE BORN TO
HEALTHY MOTHERS

(Outcome of pregnancy in diabetic women in northeast
England and in Norway, 1994-97)
http://bmj.com/cgi/content/full/321/7263/730

The babies of diabetic mothers in northeast England are four
times as likely to die as those born to healthy mothers, finds a
study in this week's BMJ. The risk is six times higher in the
UK than it is in Norway, the research shows.

Hawthorne and colleagues compared the rates of death and
complications among babies born to diabetic and
non-diabetic mothers in northeastern England and Norway
between 1994 and 1997.

The babies of diabetic mothers were over four times as likely
to die as those born to non-diabetic mothers in the UK and
six times as likely to die as those born to non-diabetic
mothers in Norway. In Norway, just over 10 in every 1000
births to diabetic mothers resulted in death compared with
almost seven in every 1000 births to non-diabetic mothers.
Comparable figures in northeast England were almost 43 and
10 per 1000 births, respectively. The risk of having a baby
with birth defects was also 2.5 times as high in diabetic as in
non-diabetic women in northeast England, while no increase
was seen in Norway.

The differences are not explained by the way in which data
on diabetes and stillbirths are collected, say the authors, so
there must be other reasons for the differences.

Contacts:

Professor Rolf T Lie, Professor of Medical Statistics,
University of Bergen, Norway (available Tuesday 19 -
Thursday 21 September)
Email: rolv.lie{at}smis.uib.no

Professor L M Irgens, University of Bergen, Norway
 

(3)  FINDINGS OF GRIFFITHS REVIEW INTO
ALLEGATIONS OF RESEARCH MISCONDUCT
FUNDAMENTALLY FLAWED

(Investigating allegations of research misconduct: the vital
need for due process)
http://bmj.com/cgi/content/full/321/7263/752

(Commentary: Response from members of the Griffiths
inquiry)
http://bmj.com/cgi/content/full/321/7263/752#resp1

(Editorial: Inquiring into inquiries)
http://bmj.com/cgi/content/full/321/7263/715

"Almost every statement made about the design, conduct,
and reporting of the neonatal CNEP trial in the Griffiths
report was ill informed, misguided, or factually wrong,"
concludes a review of its findings in this week's BMJ.

The internal review chaired by Professor Rod Griffiths was
set up in February 1999 after several parents alleged that
their premature babies had been entered into a controlled trial
of a breathing support technique, known as continuous
negative extrathoracic pressure (CNEP), without their
consent. The resulting report was published in May this year.

Dr Edmund Hey, a retired paediatrician from Newcastle
upon Tyne, and Dr Iain Chalmers, director of the UK
Cochrane Centre in Oxford, conducted their review on behalf
of the Medical Defence Union. In their swingeing critique the
authors raise serious doubts about the reliability of the report,
the review, and the appropriateness of the ensuing
recommendations.

The authors defend the trial's design, which, they claim, the
panel had failed to understand. They refute the allegation that
no external peer review had been conducted and they accuse
the panel of making "an unwarranted slur on the
professionalism and skill of all the nurses concerned." They
say that a consent document existed among the research
records for every child in the study. Assertions made by a
small number of parents about events up to 10 years ago
went unchecked, say the authors, yet now form the basis for
recommending major changes to the governance of clinical
research in the NHS.

"We can still agree that there has been a scandal, but suspect
that the scandal is what has been done to, not what was done
by, the medical and nursing staff in Stoke on Trent."

Responding to the criticisms, the members of the panel say
that Hey and Chalmers have completely misunderstood the
terms of reference of the investigation and have ignored the
main substance of the report. Constrained by the fact that
some of the issues and individuals involved are still being
legally investigated, they nevertheless claim that the consent
forms did not contain all the necessary information and that
there were discrepancies between the stated ages at which
babies were entered into the trial. Parental recall may indeed
be faulty, they agree, but add: "this does not mean that all
parents are wrong and all researchers are right."

An accompanying editorial by Richard Smith says that the
whole system of such inquiries needs to be re-evaluated, and
that their process, including the appointment of the members
and the purpose of the investigation, should be made clear
from the outset. "Inquiries should publish their material and
methods, check oral allegations against documentary
evidence, and send drafts of evidence accusing individuals to
those individuals, so that errors of fact can be corrected."

Contacts:

Dr Iain Chalmers, UK Cochrane Centre, Oxford.
Email:  ichalmers{at}cochrane.co.uk

Professor Rod Griffiths, NHS Executive, West Midlands
Regional Office, Birmingham.

Dr Richard Smith, Editor BMJ, London.
Email: pressoffice{at}bma.org.uk
 

(4)  TWINS ARE SIGNIFICANTLY LESS LIKELY TO
HAVE ASTHMA THAN SINGLETONS

(Reduced risk of hospital admission for childhood asthma
among Scottish twins: record linkage study)
http://bmj.com/cgi/content/full/321/7263/732

Twins run less risk of developing asthma than singletons,
reports a study in this week's BMJ.

Strachan and colleagues analysed the admission data for
respiratory illness of twins and singletons up to the age of 10
among Scottish hospitals. The study covered the years 1981
to 1994.

They found that twins�overall risk of admission for
respiratory disease was significantly lower than that of
singletons. Although twins were more likely to be admitted
for acute bronchitis and bronchiolitis, they were much less
likely than singletons to be admitted to hospital for asthma.

The authors conclude that the difference in admission rates
might have been exaggerated if the admission of one twin with
asthma led to preventive treatment of the other, but suggest
that this is unlikely to explain the large difference in admission
rates. Nor can birthweight explain the difference as low
birthweight is associated with increased risk of asthma, but
twins weigh less than singletons. Rather, they suggest that
twinship is a special case of the protective effect of large
families on allergies.

Contact:

Dr David Strachan, Department of Public Health Sciences, St
George's Hospital Medical School, London.
Email:  d.strachan{at}sghms.ac.uk
 

(5)  ABRUPT WITHDRAWAL OF DRUGS TO PREPARE
FOR SURGERY CAN BE DANGEROUS

(Editorial: The risks of interrupting drug treatment before
surgery)
http://bmj.com/cgi/content/full/321/7263/719

Abruptly stopping drug treatments before surgery can be
dangerous and increase the risk of postoperative
complications, suggests an editorial in this week's BMJ.

Surgery, particularly major abdominal surgery, affects the rate
at which stomach contents are emptied, so reducing the
absorption of drugs. Patients may therefore have to wait
several days before they can resume their normal medical
routine.

Noble and Kehlet cite research showing a significantly
increased risk of adverse outcomes among patients whose
drug regimens had been stopped before surgery. Patients
taking therapeutic drugs that were unrelated to their surgery
were three times as likely to have complications as those not
taking medicines. And the longer the duration of abstinence,
the higher was the complication rate.

Doctors need to ensure that drug treatments are resumed as
soon as possible, write the authors, by providing alternative
routes, medicines, and by reducing the need for opioid
anaesthesia. But the pharmaceutical industry also needs to do
more, they say. Guidance should be included in drug
information leaftlets and in national drug formularies to help
doctors provide alternative medicines and be aware of the
symptoms associated with sudden withdrawal from treatment.

"Such is the scale of the problem that failing to prevent the
consequences of drug withdrawal in the postoperative period
should possibly be considered equivalent to those medication
errors that have been called 'worse than a crime', "
conclude the authors.

Contact:

Dr David Noble, Department of Anaesthesia, Intensive Care
and Hyperbaric Medicine, Grampian University Hospitals,
Aberdeen, Scotland.
Email:  david.noble{at}arh.grampian.scot.nhs.uk
 


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