Correspondence
Anaesthesia, 2000, 55, pages 1213±1235
.
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studies confirmed the diagnosis. Sero-
logical testing was positive for CMV 1 Hahn A. Guillain±Barre Syndrome.
IgM antibodies in a dilution of 1 : 512,
indicating recent Cytomegalovirus
(CMV) infection. Other relevant serol-
ogy was negative.
References
factor (vWF). In type I VWD there is a
reduction in the amount of vWF in the
blood, in type 2 VWD normal levels of
vWF are found but it is functionally
abnormal, and in type 3 VWD there is a
severe deficiency in levels of vWF. VWF
is required for platelet adhesion to
damaged endothelium during the for-
mation of the platelet plug. It is also the
carrier protein for factor VIII. Defi-
ciency of vWF leads to prolonged
bleeding times and patients usually
present with abnormal bleeding condi-
tions such as menorrhagia or epistaxis
The haematological investigations are
used in VWD to determine both the
quantity and functional capacity of vWF
in the patient's plasma. The amount of
vWF is determined by measuring the
vWF:Ag level, whereas the Ricof level
is a measure of its functional activity.
The vWF:Ag level in the plasma can be
assayed directly and compared to a
reference curve of standard dilutions so
that a level . 50% is normal. Ricof
levels are determined by adding a
sample of the patient's plasma to
normal platelets and then adding the
antibiotic ristocetin. Ristocetin reacts
with vWF and the platelet membrane to
induce platelet aggregation. This inter-
action requires the presence of a func-
tional unit of the vWF known as the
ristocetin cofactor. Ristocetin-induced
aggregation follows a dose±response
curve dependent upon the amount of
functional vWF present. Thus, a `normal'
Ricof level is quoted as . 50%. Ristoce-
tin does not agglutinate the platelets in
many patients with VWD due to the
absence of the ristocetin cofactor. Thus in
Lancet 1998; 352: 635±41.
2
3
4
Stagno S, Whitley RJ. Herpesvirus
infections of Pregnancy. Part I.
Cytomegalovirus and Epstein-Barr
virus infections. New England Journal of
Medicine 1985; 313: 1270±4.
Treatment with intravenous immuno-
globulin (IvIG) was started immediately
on admission to hospital. By day 2 of her
illness, she required mechanical ventila-
tion for respiratory insufficiency. Despite
marked autonomic dysequilibrium, a
general anaesthetic was administered
uneventfully on day 7 for insertion of a
tracheostomy. Her illness reached a nadir
at around 10 days when she exhibited a
dense quadriparesis and retained only
minimal motor function of her extra-
ocular muscles. Three weeks following
ICU admission, a pregnancy test was per-
formed because of amenorrhoea. It was
positive and ultrasonography suggested a
fetal age of 9 weeks. In view of her
severity of illness, gestational age and
CMV status, she elected for termination
of pregnancy. This was carried out under
Simor AE, Ferro S. Campylobacter
jejuni infection occurring during
pregnancy. European Journal of Clinical
Microbiology & Infectious Diseases 1990; 9:
142±4.
Freij BJ, Sever JL. Herpes virus
infections in pregnancy: risks to
embryo, fetus, and neonate. Clinics in
Perinatology 1988; 15: 203±31.
Von Willebrand's disease and
neuroaxial anaesthesia
We would like to report the case of a
3-year-old primigravida woman with
2
von Willebrand's disease (VWD). Our
local consultant haematologist notified
us of her when she was 36 weeks
gestation. Apart from her von Will-
ebrand's disease she was apparently fit
and healthy and was enjoying an
uncomplicated pregnancy. Her labora-
tory results were as follows: von Will-
ebrand factor antigen (vWF:Ag) 28%
and Ricof level 42%. On the basis of
these results, the haematologist sug-
gested that an experienced anaesthetist
could perform epidural analgesia safely
as her risk of bleeding into the epidural
space was minimal. We, along with our
colleagues, were not sure of the validity
of this advice and were unfamiliar with
(another uneventful) general anaesthetic.
After 86 days in the intensive care unit,
the patient was discharged for further
care. Her recovery was slow and compli-
cated, but eventually of a good quality.
This case adds to the information
provided by Brooks et al. CMV is
causally implicated in 10±22% of GBS
[1]. It is a serious infection in the first
trimester: 5% of infected babies will
have early multiple disabilities and a
further 5% develop later handicaps [2].
These include microcephaly, mental
retardation and motor disorders.
Other triggers associated with GBS
e.g. Epstein±Barr virus, Varicella zoster
(
these laboratory results. We therefore VWD the Ricof level is often reduced. If
decided to determine the significance of the Ricof level is above 30% the risk of
the haematological investigations per- bleeding is not thought to be increased;
formed in patients with VWD and however, when below this level, especially
clarify the risk of bleeding associated if the level is , 10%, there is a significant
with regional analgesia. We felt that risk of bleeding.
virus, HIV, Campylobacter jejuni [1]) may
also have implications for the mother
and fetus. These range from trivial to
include congenital varicella, sepsis and
fetal death [2±4]. Consequently, for all
patients with GBS who may be preg-
nant, a thorough search for potential
causes should be carried out, since the
results may have significant consequences
for the management of both patients.
anaesthetists need to be aware of this
There does not seem to be any
disease and have an understanding of consensus on the Ricof level that is safe
how it is investigated in order to make for regional anaesthesia (Giangrande
valued judgements in the use of regional PLF, Oxford Haemophilia Centre, per-
techniques in the presence of possible sonal communication). We could only
I. Nesbitt
abnormal haemostasis.
find one case report in the literature that
Freeman Road Hospital,
Newcastle upon Tyne NE7 7DN,
UK
Von Willebrand's disease is an inher- described the use of an epidural in a
ited haematological disorder where patient with VWD. This obstetric
there is a deficiency of von Willebrand's patient had a Ricof level of 10% and
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q 2000 Blackwell Science Ltd