Contracting role of graduated compression stockings
in prevention of perioperative venous thromboembolism
Joseph Shalhoub*
Imperial Vascular Unit, Imperial College Healthcare NHS Trust, St Mary’s Hospital, London, UK
*Correspondence to: Joseph Shalhoub, Imperial Vascular Unit, Imperial College Healthcare NHS Trust, St Mary’s Hospital, Praed Street, London W2 1NY, UK
(e-mail: j.shalhoub@imperial.ac.uk)
There can be no doubt that the prevention of venous
thromboembolism (VTE) is a healthcare need and priority
1
.
The issue remains in sharp focus in surgery, with the
implementation of VTE risk assessment, and the use of
mechanical and pharmacological thromboprophylaxis. These
measures have been further enhanced through education and
dissemination, and have been reinforced through key clinical
guidelines
2,3
and incentivization
4
.
There was a 15 per cent reduction in hospital-associated VTE
deaths (within 90 days of admission) in the UK between 2010 and
2017
5
, with concurrent falls in pulmonary embolism-related
mortality among European countries
6
. This is likely to be more
impressive considering that improved awareness and imaging are
likely to have increased the diagnosis of VTE, resulting in a further
reduction in the case fatality rate. The factors responsible for this
reduction are likely to be multifactorial. This can be attributed to
a long list of varied and important factors, including (but not
limited to) prehabilitation, systematic VTE risk assessment
(including computer-aided assessment
7
), enhanced recovery with
early mobilization, patient hydration, use of advanced minimally
invasive surgical techniques resulting in a reduction in the
systemic inflammatory response (both magnitude and duration),
and of course thromboprophylaxis.
Given the number of relevant factors at play, it is challenging to
know which are dominant, and this also applies when considering
mechanical and pharmacological thromboprophylaxis. Much of
the evidence underpinning perioperative thromboprophylaxis
is dated and may not reflect modern surgical practice.
Furthermore, these studies, for the most part, used mechanical
thromboprophylaxis alone or pharmacological thromboprophylaxis
alone, with little evidence relating to the use of both mechanical
and pharmacological strategies
8
. Many studies were funded by
stocking manufacturers
9
. It was for these and a number of other
reasons that doubt was cast over the evidence that formed the
basis of recommendations for mechanical thromboprophylaxis,
particularly the use of graduated compression stockings
(GCS)
9,10
. What should be considered is whether, in
individuals receiving pharmacological thromboprophylaxis,
GCS further reduce the VTE risk.
The first CLOTS trial
11
randomized 2518 patients admitted
to hospital following an acute stroke to receive either routine
care including thigh-length GCS, or routine care with avoidance
of GCS. Not only was there no significant reduction in
symptomatic or asymptomatic deep vein thrombosis (DVT),
complications of skin breaks, ulcers, blisters, and skin necrosis
were significantly more common in the GCS arm of the trial
12
.
A subsequent RCT
12
included individuals in critical care
who were receiving pharmacological thromboprophylaxis and
were randomized to receive either additional intermittent
pneumatic compression (991 patients) or no additional
intermittent pneumatic compression (1012). The addition of
intermittent pneumatic compression did not result in a lower
incidence of proximal lower limb DVT than pharmacological
thromboprophylaxis alone
12
. These studies generated further
uncertainty around the role of mechanical thromboprophylaxis
in medical inpatient and critical care settings, respectively.
What does this mean for the surgical patient? In 2007, an RCT
13
of individuals undergoing hip surgery was published. This
compared postoperative VTE or sudden death between those
randomized to a combination of fondaparinux and compression
stockings (395 patients, 19 DVT events) or to fondaparinux alone
(400 patients, 22 DVT events), and concluded ‘the addition of
graduated compression stockings to fondaparinux appears to
offer no additional benefit over the use of fondaparinux alone’
13
.
This trial set the scene for the large UK National Institute for
Health Research (NIHR)-funded GAPS (Graduated compression
stockings as an Adjunct to Pharmacoprophylaxis in Surgery) trial.
GAPS aimed to elucidate the role of GCS in individuals undergoing
elective surgery who were assessed as being at moderate or high
risk of VTE, and who were receiving prophylactic-dose low
molecular weight heparin (LMWH)
14
. The primary outcome,
imaging-confirmed lower limb DVT with or without symptoms, or
pulmonary embolism with symptoms within 90 days of surgery,
occurred in 16 of 937 patients (1.7 per cent) in the LMWH-alone
group compared with 13 of 921 (1.4 per cent) in the LMWH and
GCS group. LMWH alone was confirmed to be statistically
non-inferior (non-inferiority margin of 3.5 per cent risk difference)
to the combination of LMWH and GCS in this surgical patient
group
15,16
. Considering this subgroup of elective surgical patients,
removing the cost of purchasing GCS and of the nursing time
required to apply them, it has been estimated conservatively that
more than £60 million (approximately €70 million [exchange
rate date 11th May 2022]) per annum could be liberated from
National Health Service budgets in England alone on a recurring
basis
14
. This estimate did not consider the costs of treating
complications related to GCS such as those reported by the CLOTS
Received: April 24, 2022. Accepted: April 27, 2022
© The Author(s) 2022. Published by Oxford University Press on behalf of BJS Society Ltd. All rights reserved.
For permissions, please e-mail: journals.permissions@oup.com
BJS, 2022, 109, 669–670
https://doi.org/10.1093/bjs/znac157
Advance Access Publication Date: 20 May 2022
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