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February
1999
Labor Epidural Analgesia Without an Intravascular "Test
Dose"
Norris MC, Fogel ST, Dalman H, Borrenpohl S, Hoppe W, Riley A.
Anesthesiology 1998;88:1495-1501.
Commentary by Dr.
Dwane
Return to the Current Literature
Review Front Page
[ see abstract below ]
The most common life threatening problems with epidurals
occur as a result of where malpositioned epidural catheters come to rest:
most commonly, intravascularly (IV), to a lesser extent, intrathecally
(IT), and, rarely, in the subdural space. We employ many different safety
steps to define these inadvertent misplacements. These tests are chosen
to cause the least physiological impairment of the parturient, and to
ensure the clearest endpoint.
In this study, Norris et al performed epidurals on 1029 parturients, placing
catheters as either part of combined spinal/epidural blocks, or as continuous
lumbar epidurals. Once placed, the catheters were tested by simple aspiration
for the return of blood or cerebrospinal fluid. Sixty IV placements and
4 IT placements were identified and managed appropriately. Aspiration-negative
catheters were then injected with 2 mL of 0.25% bupivacaine or 0.2% ropivacaine
to rule out IT placement. Before the epidural catheters were used they
were tested by injecting 10-15 mL of local anesthetic with or without
opioid, in divided doses.
All 4 IT catheters in the study were identified by aspiration and only
2 additional IV catheters that were not identified by aspiration were
subsequently detected. This false-negative rate compares favorably with
those of both Doppler testing and the epinephrine test dose.
Although there were no false-negative tests using aspiration to identify
IT placement, even this study protocol specified a small dose of epidural
local anesthetic to rule out IT placement. Notably, one patient was felt
to have had a subdural placement of the catheter, having a negative (for
blood or CSF) aspiration test, no analgesia with 2 cc of local anesthetic
but with two 5 mL doses of 0.25% bupivacaine producing analgesia, hypotension,
and a sensory level to T2. This complication would not have been detected
by other safety steps except incremental injection of the local anesthetic
dose. Also, because of the lack of sensitivity of this aspiration test
if used when manipulating epidural catheters known to be intravenously
placed, the authors recommend the immediate replacement of a known IV
catheter rather than attempting epidural catheter manipulation.
In summary, this study demonstrates that simple aspiration through the
multiport epidural catheter is as reliable as the Doppler test or epinephrine
test dose in detecting intravenous catheter placement. No safety maneuver
of itself is 100% reliable. Therefore the use of a secondary safety test
coupled with incremental injection of local anesthetic doses is still
necessary to insure patient safety.
Note: This study applies to currently used concentrations of local anesthetics
for obstetrical analgesia. The use of aspiration alone with epidurals
for operative obstetrical anesthesia still requires examination. For a
discussion of safety steps for epidural injection of local anesthetics,
please see: Mulroy MF, Norris MC, Liu SS. Safety steps for epidural injection
of local anesthetics: Review of the Literature and Recommendations. Anesth
Analg. 1997.85:1346-1356.
Return to the Current
Literature Review Front Page
ABSTRACT
BACKGROUND:
This study prospectively evaluated the ability of aspiration to detect intravascular
placement of multiple-orifice epidural catheters.
METHODS: Multiple-orifice,
20-gauge epidural catheters were inserted in 1,029 laboring women. Catheters
were observed and aspirated for blood or cerebrospinal fluid before they
were tested with 2 ml local anesthetic. If the results of this test were
negative (no spinal anesthesia), the authors induced and maintained labor
analgesia with a dilute local anesthetic and opioid solution. Patients with
bilateral sensory change and effective labor analgesia had a "positive"
epidural catheter. Women with unilateral block, inadequate analgesia despite
some sensory change or those who delivered before being adequately assessed
had "equivocal" catheters. Patients with neither analgesia nor sensory change
had "negative" catheters.
RESULTS: Aspiration
and observation identified 60 intravenously placed catheters. Six catheters,
which were placed initially in a blood vessel, were withdrawn until aspiration
was negative, and then the anesthetic was infused. Four of these catheters
were positive and two were still positioned intravascularly. Two other catheters
may have been intravenously placed despite negative results of aspiration.
The incidence of false-negative results of aspiration was 0 to 2 of 1,085
(upper limit of 95% CI, 0.2% to 0.4%). No patient showed any signs or symptoms
of local anesthetic toxicity.
CONCLUSIONS: Under the
conditions of this study, which include using multiple- orifice catheters
and dilute solutions of local anesthetic and opioid, aspiration and incremental
drug injection alone safeguard against the risks of intravenously positioned
local anesthetics. These results should not be extrapolated to other clinical
settings without further study.
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