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Ann
R
Coll
Surg
Engl
1997;
79:
206-209
Surgeons'
follow-up
practice
after
resection
of
colorectal
cancer
Judy
Mella
FRCS'
Research
Registrar
S
N
Datta
FRCS2
Senior
Surgical
SHO
Anne
Biffin
BSc3
Data
Manager
A
G
Radcliffe
MS
FRCS4
Consultant
Surgeon
R
J
C
Steele
MD
FRCS1
Reader
in
Surgery/Honorary
Consultant
Surgeon
J
D
Stamatakis
BSc
MS
FRCS2
Consultant
Surgeon
Audit
and
Epidemiology
Unit,
The
Royal
College
of
Surgeons
of
England,
London
Key
words:
Colorectal
cancer;
Follow-up
Consultant
surgeons
in
two
United
Kingdom
Health
Regions
were
invited
to
complete
a
questionnaire
on
details
of
their
personal
management
of
patients
with
colon
and
rectal
cancer,
with
particular
emphasis
on
follow-up. Replies
from
140
(94%)
were
analysed
by
the
surgeon's
subspecialty
of
colorectal
and
gastro-
intestinal
surgery
(group
1)
and
all
others
(group
2).
There
was
a
wide
variation
in
the
duration
of
follow-
up,
but
no
difference
between
the
two
groups.
More
group
1
surgeons
carried
out
investigations
as
a
routine
after
colonic
(P
<0.01)
and
rectal
(P
<0.01)
resection.
Colonoscopy
was
used
more
frequently
by
group
1
(P<0.0001)
and
barium
enema
by
group
2
surgeons
(P<0.05).
Investigations
to
detect
asympto-
matic
metastases
were
used
as
a
routine
by
33.3%
of
surgeons,
in
whom
there
was
no
concordance
over
the
choice
or
combination
of
tests
and
no
difference
between
the
two
groups
of
surgeons.
There
is
no
consensus
among
surgeons
as
to
the
ideal
duration,
intensity
and
method
of
follow-up
after
resection
for
colorectal
cancer
and
little
difference
between
the
practice
of
colorectal
and
gastrointestinal
surgeons
and
that
of
other
specialists,
except
in
the
use
of
colonoscopy
and
barium
enema.
These
results
reflect
the
continuing
lack
of
evidence
on
which
to
base
the
follow-up
of
patients
after
surgery
for
colorectal
cancer.
1
Queen's
Medical
Centre,
Nottingham
2
Bridgend
and
District
NHS
Trust,
Bridgend
3
Clinical
Effectiveness
Resource
Unit,
Llandough
NHS
Trust,
Penarth
4
Llandough
NHS
Trust,
Penarth
Correspondence
to:
Mr
J
D
Stamatakis,
Department
of
Surgery,
Princess
of
Wales
Hospital,
Bridgend
CF31
1RQ
It
has
been
suggested
that
intensive
follow-up
of
patients
after
surgery
for
colorectal
cancer
will
detect
recurrent
tumour
at
an
early,
asymptomatic
stage,
when
further
curative
treatment
might
be
possible
(1,2).
Outpatient
review
also
provides
the
opportunity
to
audit
the
results
of
treatment,
provide
psychological
support
for
the
cancer
patient
and
detect
metachronous
cancers.
This
study
investigates
how
surgeons
in
two
United
Kingdom
(UK)
Health
Regions,
Wales
and
Trent,
follow
up
patients
after
apparent
curative
surgery
for
colorectal
cancer.
The
methods
of
follow-up
by
colorectal
and
gastrointestinal
surgeons
is
compared
with
that
of
all
other
surgeons,
who
also
treat
colorectal
cancer
in
the
two
regions.
Methods
Consultant
surgeons
who
had
taken
part
in
The
Royal
College
of
Surgeons
of
England
Colorectal
Cancer
Audit
were
invited
to
complete
a
questionnaire
on
their
management
of
colorectal
cancer.
The
audit
was
held
in
two
UK
Health
Regions,
Wales
and
Trent.
In
all,
161
surgeons
in
the
two
regions
treated
patients
with
colorectal
cancer
during
the
12-month
audit.
Question-
naires
were
sent
to
149
of
this
group,
the
remainder
had
died,
retired
or
emigrated
during
the
study
period.
The
questionnaire
asked
for
details
on
the
length
of
outpatient
follow-up
after
curative
resection
of
colorectal
cancer.
Additional
information
was
requested
on
out-
patient
investigations
used
to
look
for
local
recurrence,
metachronous
tumours
and
systemic
metastasis.
Data
for
colon
and
rectal
cancer
were
collected
separately.
Details
of
the
surgeon's
usual
practice
were
requested,
accepting
Follow-up
after
resection
of
colorectal
cancer
207
Table
1.
Duration
and
frequency
of
outpatient
follow-up
after
surgery
Rectum
Colon
Group
1
Group
2
Group
1
Group
2
No
appointment
0
0
0
0
One
appointment
then
discharge
1
(1.8)
2
(2.3)
1
(1.8)
2
(2.3)
One
appointment
then
see
as
required
3
(5.5)
7
(8.2)
5
(9.2)
9
(10.6)
Regular
outpatient
appointments
for
<
1
year
2
(3.7)
5
(5.9)
2
(3.7)
4
(4.7)
1-2
years
4
(7.4)
11
(12.9)
5
(9.2)
13
(15.2)
2-5
years
30
(55.6)
33
(38.9)
24
(44)
28
(33)
5-10
years
9
(16.7)
13
(15.3)
10
(18.5)
12
(14.1)
>
10
years
5
(9.3)
14
(16.5)
7
(12.9)
17
(20)
Number
of
surgeons
in
each
group,
percentage
in
parentheses,
group
1,
colorectal
and
gastrointestinal
surgeons,
group
2
all
other
surgeons
that,
for
a
few
patients,
follow-up
might
not
be
appropriate
because
of
frailty,
infirmity
or
other
reasons.
Data
collection
was
anonymous
but
surgeons
were
asked
if
they
had
a
subspecialty
within
general
surgery.
Answers
were
entered
onto
a
computer
database
(Epi
Info)
for
analysis.
Statistical
analysis
was
by
the
x2
test
with
Yates'
correction.
Results
Questionnaires
were
sent
to
149
consultant
surgeons
and
140
replied,
a
response
rate
of
94%.
The
data
for
colorectal
(n=14)
and
gastrointestinal
(n=40)
surgeons
have
been
combined
and
are
presented
as
group
1.
Of
the
remaining
86
surgeons,
22
considered
themselves
general
surgeons
with
no
subspecialty
interest.
Others
declared
subspecialty
interests
in
vascular
(n
=
28),
breast
(n
=
15),
endocrine
(n
=
5),
urology
(n=
11)
and
other
(n
=
5).
The
combined
data
of
these
86
surgeons
is
presented
as
group
2.
All
140
surgeons
reviewed
patients
at
least
once
after
discharge
from
hospital,
although
the
frequency
of
clinic
appointments
varied
from
once
to
lifelong
surveillance.
There
was
no
difference
in
appointment
practice
between
the
two
groups
of
surgeons
and
no
difference
in
the
outpatient
follow-up
of
colon
and
rectal
cancer
(Table
I).
There
were
differences
between
the
two
groups
of
surgeons
in
the
use
of
investigations
for
detecting
recurrence
or
metachronous
tumours
after
resection
of
colonic
cancer
(Table
II).
The
majority,
87%,
of
group
1
carried
out
investigations
compared
with
65.1%
of
group
2
(P<0.01).
Significant
differences
were
in
the
more
Table
III.
Combinations
of
tests
used
for
follow-up
of
rectal
cancer
Table
II.
Combinations
of
tests
used
for
follow-up
of
colon
cancer
according
to
surgeon's
declared
subspecialty
interest
Group
1
Group
2
Routine
tests*
47
(87)
56
(65.1)
Colonoscopy
and
CEA
7
(13)
1
(1.2)
Colonoscopy
alone
22
(40.8)
12
(14)
Barium
enema
1
(1.8)
10
(18.6)
Flexible
sigmoidoscopy
1
(1.8)
2
(2.3)
Colonoscopy
and
barium
enema
1
(1.8)
6
(7)
Colonoscopy
and
abdominal
ultrasound
1
(1.8)
3
(3.5)
Other
tests
used
by
two
or
fewer
surgeons
14
(26)
22
(25.6)
Group
1,
colorectal
and
gastrointestinal
surgeons,
group
2
all
others,
numbers
of
surgeons
with
percentage
in
parentheses
*P
<0.01
Barium
enema
±
other
tests,
P
<
0.05
Colonoscopy
±
other
tests,
P
<
0.0001
Routine
tests*
Colonoscopy
alone
Rigid
sigmoidoscopy
alone
Rigid
sigmoidoscopy
and
CEA
Rigid
and
flexible
sigmoidoscopy
Rigid
sigmoidoscopy
and
colonoscopy
Rigid
sigmoidoscopy,
colonoscopy
and
CEA
Rigid
and
flexible
sigmoidoscopy
and
CEA
Rigid
sigmoidoscopy
and
barium
enema
Rigid
sigmoidoscopy,
barium
enema
and
CEA
Other
tests
used
by
two
or
fewer
surgeons
Group
1
Group
2
52
(96.3)
65
(75.6)
3
(5.6)
6
(7)
9
(16.7)
13
(15.1)
1
(1.9)
3
(3.5)
3
(5.6)
2
(2.3)
6
(11.1)
3
(3.5)
4
(7.4)
0
1
(1.9)
4
(4.7)
0
6
(7)
2
(3.7)
1
(1.2)
23
(42.6)
27
(31.4)
*
P<0.01
Number
of
surgeons
with
percentage
in
parentheses
208
J
Mella
et
al.
Table
IV.
Investigations
carried
out
as
a
routine
for
asymptomatic
metastatic
disease
Group
I
Group
2
Liver
function
tests
13
(24)
13
(15.1)
Ultrasound
liver
15
(27.8)
17
(19.8)
CEA
12
(22.2)
15
(17.4)
Chest
radiographs
4
(7.4)
4
(4.6)
Thoracic
CT
3
(5.5)
1
(1.2)
Liver
CT
3
(5.5)
2
(2.3)
Pelvic
CT
(rectal
cancer
only)
5
(9.2)
2
(2.3)
Group
1,
colorectal
and
gastrointestinal
surgeons,
group
2
all
others,
numbers
of
surgeons
with
percentage
in
parentheses
frequent
use
of
colonoscopy,
with
or
without
other
investigations,
by
group
1
(57.4%
vs
25.6%,
P<0.0001)
and
the
more
frequent
use
of
barium
enema
by group
2
(18.6%
vs
3.7%, P<0.05).
There
was
no
apparent
agreement
between
and
within
groups
about
which
combination
of
tests
might
be
the
most
effective
(Table
II).
Follow-up
practice
for
colon
cancer
by
26%
of
group
1
and
25.6%
of
group
2
surgeons
was
either
unique
or
in
common
with
one
other
surgeon.
The
results
for
rectal
cancer
are
given
in
Table
III.
More
surgeons
in
group
1
carried
out
routine
investiga-
tions
compared
with
those
in
group
2
(96.3%
vs
75.6%,
P
<0.01).
However,
unlike
colonic
cancer,
there
was
no
difference
between
the
two
groups
in
the
methods
of
investigation.
The
follow-up
practice
for
rectal
cancer
by
42.6%
of
group
1
and
31.4%
of
group
2
surgeons
was
either
unique
or
in
common
with
one
other
surgeon.
Routine
investigation
for
asymptomatic
metastases
was
carried
out
by
47
(33.5%)
of
surgeons.
These
employed
various
combinations
of
the
following:
liver
function
tests
(26
surgeons),
liver
ultrasound
(32
surgeons),
carcinoma
embryonic
antigen
(CEA)
levels
(27
surgeons),
chest
radiographs
(eight
surgeons),
thoracic
computed
tomo-
graphy
(CT)
(four
surgeons),
liver
CT
(five
surgeons)
and
pelvic
CT
(five
surgeons).
There
was
no
difference
between
group
1
and
group
2
surgeons
in
the
use
of
any
of
these
tests.
Discussion
The
results
of
this
study
emphasise
the
lack
of
a
consensus
among
surgeons
in
two
UK
Health
Regions
over
surveillance
strategy
after
surgery
for
colorectal
cancer.
The
lack
of
conformity
is
equally
true
for
colorectal
and
gastrointestinal
surgeons
(group
1),
when
compared
with
all
other
'non-abdominal'
surgeons
(group
2).
There
are
some
differences
between
the
two
groups.
More
patients
with
rectal
or
colonic
cancer,
treated
by
group
1
surgeons,
were
found
to
undergo
investigation
for
local
recurrence
and
metachronous
tumour.
This
may
be
because
of
a
greater
commitment
to
audit
in
their
field
of
interest
by
colorectal
and
gastrointestinal
surgeons.
There
was
also
a
difference
between
specialist
and
non-specialist
surgeons
in
the
use
of
colonoscopy
and
barium
enema.
This
may
reflect
the
involvement
and
easier
access
of
colorectal
and
gastrointestinal
surgeons
to
endoscopy.
Whether
these
differences
in
practice
result
in
better
outcome
for
the
individual
patient
is
not
known.
A
more
uniform
follow-up
practice
is
reported
by
specialist
surgeons
in
the
United
States
of
America
(3).
In
a
survey
of
the
American
Society
of
Colon
and
Rectal
Surgeons,
more
than
75%
of
respondents
follow-up
their
patients
every
3-6
months
for
the
first
2
years,
with
80%
doing
CEA
assays
every
3
months
for
3
years.
However,
there
was
considerable
variation
in
the
use
of
investiga-
tions
such
as
colonoscopy,
chest
radiographs,
CT
scanning
and
liver
function
tests.
Evidence
to
support
individual
practice
was
not
discussed
in
this
survey.
These
variations
reflect
a
lack
of published
evidence
on
which
to
base
clinical
practice.
No
prospective,
random-
ised,
controlled
trial
of
follow-up
versus
minimal
surveillance
has
been
carried
out,
although
the
protocol
for
such
a
study
has
been
drawn
up
(4).
Meta-analysis
has
been
used
in
an
attempt
to
define
any
benefit
from
postoperative
surveillance.
The
results
from
seven
studies,
each
comparing
the
outcome
of
two
follow-up
programmes,
of
varying
intensity,
after
surgery
for
colorectal
cancer,
have
been
analysed
(5).
However,
none
of
these
studies
were
randomised.
In
three,
patients
undergoing
intensive
follow-up
were
compared
with
contemporary
controls
who
elected
to
opt
out
of
post-
operative
surveillance.
In
the
remaining
four
studies,
patients
were
compared
with
historic
controls.
The
meta-
analysis
showed
no
increase
in
5-year
survival
of
patients
undergoing
intensive
follow-up
unless
CEA
levels
were
measured.
However,
the
authors
highlighted
the
poor
quality
of
the
data
available
and
were
unable
to
give
an
unequivocal
answer
about
the
value
of
intensive
follow-
up.
Although
published
studies
neither
support
nor
disprove
routine
follow-up
as
a
means
to
improve
survival,
a
special
case
may
be
made
for
the
detection
of
metastatic
liver
disease.
There
is
good
evidence
that
1-3%
of
all
patients
with
colorectal
cancer
may
benefit
from
resection
of
liver
metastases
(6).
For
a
common
disease,
this
small
percentage
translates
into
a
significant
number
of
cases
and
supports
a
follow-up
strategy
that
includes
liver
imaging
for
metachronous
metastases.
In
the
present
survey,
only
26.4%
of
surgeons
use
ultrasound
or
computed
tomography
to
screen
for
asymptomatic
liver
disease.
It
was
disappointing
to
find
that
there
has
been
no
real
change
in
surgeons'
follow-up
practice
since
a
report
from
Wales
and
the
South-West
of
England
almost
10
years
ago
(7).
The
continued
lack
of
evidence
on
which
to
base
clinical
practice
is
one
reason
for
the
persistent
wide
variation
in
follow-up.
Until
such
evidence
is
available,
there
will
be
continuing
diversity
in
surgeons'
follow-up
activity.
Studies
are
needed
on
audit
of
cancer
care,
as
highlighted
by
the
Calman-Hine
Report
(8),
psychologi-
cal
support
for
the
patient,
screening
for
metachronous
tumours
and
survival,
before
standards
for
follow-up
can
be
defined.
Follow-up
after
resection
of
colorectal
cancer
209
The
authors
wish
to
thank
the
general
surgeons
of
Wales
and
Trent
who
took
part
in
the
audit
and
completed
questionnaires.
We
also
thank
the
Clinical
Effectiveness
Support
Unit
(Wales)
for
data
processing
and
the
Welsh
Office
and
Department
of
Health
for
financial
support.
References
1
Eckart
VF,
Stamm
H,
Kanzler
G,
Bernhard
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Improved
survival
after
colorectal
cancer
in
patients
complying
with
a
postoperative
endoscopic
surveillance
programme.
Endoscopy
1994;
26:
523-7.
2
Ovaska
J,
Jarvinen
H,
Kujari
H,
Perttila
I,
Mecklin
J-P.
Follow-up
of
patients
operated
on
for
colorectal
cancer.
Am
J
Surg
1990;
159:
593-6.
3
Vernava
AM,
Longo
WE,
Virgo
KS,
Coplin
MA,
Wade
TP,
Johnson
FE.
Current
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strategies
after
resection
of
colon
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Dis
Colon
Rectum
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37:
573-83.
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Kronberg
0,
Fenger
C,
Deichgraber
E,
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