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Monitoring Techniques >>
Despite the
impression by some clinicians that they can examine a patient and
predict whether they have an elevated abdominal pressure, the fact is
clinical judgment for this disorder is no better than the flip of a
coin. Several studies have
confirmed that even in the hands of a staff level academic surgeon,
abdominal exam is completely unreliable at determining the presence or
absence of an elevated intra-abdominal pressure.[1, 2] These authors
conclude that due to the inaccuracies of physical exam findings,
intra-abdominal pressures must be measured by an objective, reliable,
reproducible method at an interval that is frequent enough to detect
rising pressure and allow interventions to occur prior to the onset of
the highly mortal abdominal compartment syndrome.
Since clinical exam
is inaccurate, early detection of increasing intra-abdominal pressure
requires a reliable, reproducible method of measuring it.
To date, the most reliable method is via pressure transduction
through a catheter within the peritoneal cavity. Other
less invasive options include pressure transduction through a tube
placed in the stomach, bladder, or rectum.[1, 2] Of these options, Obeid
et al found bladder pressure to most closely reflect intraperitoneal
pressure and to be the most technically reliable.[3] Multiple other
authors confirm Obeids’ findings that bladder pressures most closely
tracks peritoneal pressures, whereas stomach pressures are less
reliable.[4-7] Bladder pressures taken through a Foley catheter
correlate very closely with pressures measured directly in the abdominal
cavity and are now considered to be the gold standard method of
monitoring intra-abdominal pressure by an international consensus
committee – the world society of abdominal compartment syndrome.[8]
Methods to measure bladder pressure
Manometry
One of the
original methods described to measure bladder pressure via the Foley
catheter is the manometry technique.[9-11] The formal method of
manometry requires a manometry tube that is placed inline between the
Foley and the drain tube. A
priming volume of fluid must be infused into the bladder to assure
adequate volume to fill the Foley and the manometry tube until
equilibrium is reached. It is an absolute requirement to vent this tube
to ambient air pressure to avoid inaccuracies that will be introduced by
an air-lock or siphon effect that can develop in the distal drain
tube.[12] One must also carefully pay attention to where they hold the
zero point, the angle of the manometer and avoidance of Foley kinking
during the measurement.[12] Once the measurement is completed the tube
is removed and the Foley is reconnected to the drain tube. Repeat
measurements require breaking the system again and reassembling the
vented manometry tube – a time consuming proposition. While this
technique is accurate, there are significant disadvantages due to the
need to recurrently open the system and the time requirements to obtain
the pressure (leading to infrequent data acquisition). Another
disadvantage is that the information is obtained in centimeters of water
and must be converted to mm Hg (divide by 1.36) if one is using any of
the current recommendations for intervention.
Manometry as is
often currently practiced (dumping the urine back into the patient,
holding the tube up and observing the height of the fluid column) is
fraught with error and should not be used to obtain an intra-abdominal
pressure measurement.[11, 12] This method introduces two major items
that can lead to error: inadequate volume of infusion to fill the
manometry column and siphon effect of the distal drain tube.[12] There
must be a volume of infusion not less than 30 ml to ensure the large
diameter foley drain tube can fill up to the
level of the true IAP in patients with any significant elevation
of pressures – failure to have adequate volume may lead to a falsely low
measurement of IAP.[12] Unless one pre-fills the system with saline,
there may not be an adequate volume of urine in the drain tube to
adequately fill the manometer. Another common source of error is the
siphon effect. Lifting the drain tube causes urine to run distally as
well as proximally back into the bladder. The distal fluid, if caught in
a loop of the drain tube, will create a hydrodynamic siphon and “pull”
the urine out of the bladder leading to a false elevation in the
measured IAP.[12] Since the clinical situation in which these patients
are having their IAP measured is always complex, these errors are often
overlooked and will lead to misleading data. As with the traditional
methods of manometry, additional errors can be introduced unless careful
attention is paid to the zero point, the angle of the manometer and
avoidance of Foley kinking during the measurement. For these reasons as
well as potential infectious complications discussed below, simply
lifting the urine drain tube and eyeballing the fluid column height
should not be relied upon since it may lead to significant inaccuracies.
An additional concern with lifting the urinary drain tube and dumping
large volumes of urine back into the patient is that of urinary tract
infections. Maki et al
demonstrated manipulation of the drainage tube such that it rises above
the level of the bladder (and dumps old urine back into the patients
bladder) is the single best predictor of catheter associated urinary
tract infection caused by handling the catheter (more predictive that
violating the sampling port or maintaining a closed system).[13, 14]
Maki et al feels that biofilm creep is the primary cause of CAUTI, but
concludes that “Infections in
which the biofilm does not play a pathogenetic role are probably caused
by mass transport of intraluminal contaminants into the bladder by
retrograde reflux of microbe-laden urine when a catheter or collection
system is moved or manipulated.”
In summary, manometry using homemade systems or done by simply lifting
the drain tube and eyeballing the level of urine is fraught with risks
of erroneous data acquisition unless a formal vented manometry tube is
placed in line and carefully attention to detail occurs.
As currently practiced, it also raises significant concerns
regarding an increased urinary tract infection rate.
Given other accurate and low risk options, this method should
likely remain of historical interest but not be routinely applied in a
modern ICU.
Self made systems assembled in the
ICU
Measuring bladder
pressure with a “home made” system is well described in the medical
literature [1, 2, 15-17]: A Foley catheter is placed and the bladder is
drained. An infusion system
consisting of a needle, IV tubing, syringe, pressure transducer,
stopcocks and saline bag are assembled and the needle is inserted into
the urine sampling port of the Foley catheter. The transducer is
attached to a monitor and zeroed. The drain tubing is then clamped and
50 to 100 ml of saline are infused into the bladder. After equilibration
of the pressure within the system, the mean bladder pressure is noted on
the monitor. Once noted, the system is disassembled and removed and the
drain tubing is unclamped. A similar system can be assembled using a
3-way Foley catheter. Instead of a needle inserted into the sampling
port, the Y-extension of a pediatric feeding tube is connected to the
irrigation port of the 3-way catheter and fluid infusion/pressure
transduction is conducted through this lumen.

Home Made
IAP monitors are not adequate for broad application in ICU's - due to
usability issues and reproducibility problems this will not become
a standard, routing method to measure IAP
Although ingenious
for development of a concept and cutting edge research, the above
processes have significant disadvantages when applied to routine ICU
monitoring. First of all, both home made systems require the staff to
collect up a number of scattered items and assemble them correctly, a
hassle which may reduce the likelihood that the pressure is even
measured until the disease
process is far progressed (i.e a compartment syndrome – which is a
surgical disease, rather than intra-abdominal hypertension which is a
medical problem). The former invades a sterile space with a needle or
Luer attachment (the urinary drain system) every time the procedure is
done (every 1 to 4 hours), while the later requires replacement of a
2-way catheter with a 3-way catheter. Both methods risk variations in
assembly and measurement making inter-observer variations in pressure
measurement a concern.[18] This variation should not be taken lightly –
it is well recognized by experts in the field and elimination of
variation is a cornerstone to monitoring fluid filled systems in the
ICU.[18-21] Finally – all these homemade systems suffer from the concept
of lack of “usability”.
Usability relates to the evaluation of human-technological interfaces to
assess how easy a technology is to use. It evaluate efficacy – i.e. does
the technology work when used properly – and it evaluates satisfaction –
i.e. did the user find the technology easy to use. Even a good idea – an
ingenious idea – that is difficult or un-satisfying to use (like home
made IAP monitoring systems) will never find its way into routine
practice – regardless of outcomes data since humans will simply not
adopt the idea because of lack of “usability”. The point here is that
due some of the usability issues surrounding homemade IAP monitoring,
very few medical institutions have adopted it routinely as a screening
and monitoring tool – resulting in frequent delays is diagnosis or
complete failures to diagnose intra-abdominal hypertension.

Many potential problems exist with homemade IAP kits


Commercially available
intra-abdominal pressure monitoring devices
In an effort to
simplify and standardize bladder pressure measurement manufacturers have
developed systems that are simple and easy to use, allowing frequent
data acquisition so early interventions can be implemented.
The following devices are currently on the market.
AbViser Intra-abdominal pressure
monitoring device
The AbViser,
(Wolfe Tory Medical, Salt Lake City Utah –www.wolfetory.com) comes as a
kit containing a pre-assembled intra-abdominal pressure monitoring
system and pressure transducer. The kit adapts to any Foley catheter and
interfaces with any ICU monitor. This allows the kit to be immediately
integrated into an ICU without the need to change current catheters,
transducers or cabling. With a simple injection of saline the AbViser
valve automatically occludes the Foley drain tube and sterile saline is
infused into the bladder. Intra-abdominal pressure measurement can be
made in under 30 seconds. After a pressure measurement is obtained the
valve automatically opens and the fluid drains out into the collection
bag. The process, which requires very little time to conduct, can be
repeated any time a pressure measurement is necessary. Once the device
is attached, no further exposure of the sterile urinary system is
necessary so the risk of introducing infection or exposing nursing staff
to body fluids is avoided.[22]
Because no needles are used, there is no risk to the patient or
the nurse from a needle. Finally, as a pre-assembled system, the risk of variations in
assembly and measurement make inter-observer variations in pressure
measurement unlikely as demonstrated in a number of studies.[23-25]
Foley-manometer
The Foley
Manometer (Holtech Medical - www.holtech-medical.com) comes as a kit
containing a preassembled manometer that attaches in-line with the Foley
drain systems. This product has solved the problems with inaccuracies
due to the siphon effect by placing a vented port in the manometer so
the distal drain tube can be equilibrated to ambient air pressure.
Due to recent improvement in the product, it now infuses a fairly
small volume of urine into the patient, resulting in a risk of CAUTI
similar to that seen at baseline ICU patients.[26]
Speigelberg IAP monitor and CiMON
monitor
Available
in Europe are two catheters that can be inserted through the nostril
into the stomach where they measure gastric pressure as a surrogate for
intra-abdominal pressure. They interface with a separate monitor,
allowing continuous data that may be useful in the extremely complex
patient in whom continuous data might be warranted.
Summary:
Although commercially available products do cost more than a home-made
device they offer several major advantages: Ease and speed of data
acquisition leading to early and frequent monitoring of IAP (i.e. they
solve the usability conundrum that exists with home-made systems),
standardized reproducible measurements, manufacturing quality control
and sterility. The first
advantage is the usability issue related to speed and ease of data
acquisition. Many ICU’s do not
even measure IAP due to the difficulties in assembling their own
monitoring device. Those that do measure IAP tend to do so only late in
the disease process to confirm that the patient has abdominal
compartment syndrome – a very progressed form of abdominal hypertension
that is a surgical emergency. This delay in obtaining IAP measurements
prevents the clinicians from detecting the problem early when it is
still amenable to urgent medical interventions that can prevent the
abdominal compartment syndrome from developing. Pre-assembled devices
are able to provide data in seconds, completely eliminating the delays
and hassles surrounding homemade products and allowing the clinician to
obtain frequent data points and trend patients’ intra-abdominal
pressure. The second problem with homemade devices is the problems with
data reproducibility, quality control and sterility.
Because the devices are constructed in the ICU with no quality
control oversight and no testing that is mandatory for pre-assembled
products, there is a high chance of errors in assembly and even greater
chance of errors in data acquisition by different nurses with varying
degrees of experience obtaining this data. They are also not constructed
using sterile techniques. Pre-assembled sterile devices standardize pressure measurements
and are proven to provide reproducible data between many different
nurses.[27] This allows the clinician to trust and rely on the data
provided.
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