Anesthesia and analgesia
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Anesthesia and analgesia · May 1998
Randomized Controlled Trial Clinical TrialThe optimal test dose of epinephrine for epidural injection with lidocaine solution in awake patients premedicated with oral clonidine.
We attempted to determine the optimal test dose of epinephrine for use with epidural anesthesia in awake patients premedicated with clonidine. Eighty-eight adult patients were randomized into two groups [oral premedication with clonidine 5 microg/kg (CLON) or no premedication (CONT)]. Before induction of general anesthesia, heart rate (HR) and blood pressure (BP) were measured for 3 min after the i.v. injection of 3 mL of 1.5% lidocaine containing epinephrine (0, 1.25, 2.5, 5, 7.5, or 15 microg) in a randomized, double-blind manner. We calculated 95% confidence intervals for the peak HR and BP increases induced by each dose of epinephrine. At 7.5 microg, epinephrine induced a significantly greater increase in HR and BP in CLON than in CONT. The 95% confidence interval for the HR change induced by 7.5 microg of epinephrine in CLON was nearly the same as the accepted standard dose of epinephrine (15 microg) in CONT. We conclude that premedication with clonidine enhances HR and BP responses to the i.v. administration of epinephrine-containing epidural test solutions. Consequently, 7.5 microg of epinephrine may be sufficient to enable detection of accidental injection into a blood vessel in awake patients premedicated with clonidine 5 microg/kg. ⋯ Clonidine, a commonly used preanesthetic medication, alters patients' cardiovascular responses to drugs such as epinephrine. Our randomized, double-blind study suggests that, in awake patients receiving oral clonidine premedication, 7.5 microg of epinephrine (half the usual dose) is adequate as an indicator of accidental injection into the epidural vessels during epidural anesthesia.
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Anesthesia and analgesia · May 1998
Comparative StudyComparison of the three-in-one and fascia iliaca compartment blocks in adults: clinical and radiographic analysis.
The 3-in-1 (Group 1) and fascia iliaca compartment (Group 2) blocks, two single-injection, anterior approach procedures used to simultaneously block the femoral, obturator, and lateral femoral cutaneous (LFC) nerves, were compared in 100 adults after lower limb surgery. Pain control, sensory and motor blockades, and radiographically visualized spread of local anesthetic solution were studied prospectively. Both approaches provided efficient pain control using 30 mL of 2% lidocaine with 1:200,000 epinephrine and 0.5% bupivacaine and 5 mL of contrast media (iopamidol). Complete lumbar plexus blockade was achieved in 18 (38%) Group 1 and 17 (34%) Group 2 patients (n = 50 patients per group). Sensory block of the femoral, obturator, genitofemoral, and LFC nerves was obtained in 90% and 88%, 52% and 38%, 38% and 34%, and 62% and 90% of the patients in Groups 1 and 2, respectively (P < 0.05). Sensory LFC blockade was obtained more rapidly for the patients in Group 2 (P < 0.05). Concurrent internal and external spread of the local anesthetic solution under the fascia iliaca and between the iliacus and psoas muscles was noted in 62 of the 92 block procedures analyzed radiographically. Isolated external spreads under the fascia iliaca and over the iliacus muscle were noted in 10% and 36% of the patients in Groups 1 and 2, respectively (P < 0.05). The local anesthetic solution reached the lumbar plexus in only five radiographs. We conclude that the fascia iliaca compartment block is more effective than the 3-in-1 block in producing simultaneous blockade of the LFC and femoral nerves in adults. After both procedures, blockade was obtained primarily by the spread of local anesthetic under the fascia iliaca and only rarely by contact with the lumbar plexus. ⋯ In adults, the two anterior approaches, 3-in-1 and fascia iliaca compartment blocks, provide effective postoperative analgesia. The fascia iliaca compartment technique provides faster and more consistent simultaneous blockade of the lateral femoral cutaneous and femoral nerves. Sensory block is caused by the spread of local anesthetic solution under the fascia iliaca and only rarely to the lumbar plexus.
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Anesthesia and analgesia · May 1998
Randomized Controlled Trial Clinical TrialTracheal intubation with rocuronium using the "timing principle".
We compared the endotracheal intubating conditions after rocuronium, using the "timing principle," with those after succinylcholine. The timing principle entails administration of a single bolus dose of nondepolarizing muscle relaxant, followed by an induction drug at the onset of clinical weakness. Forty-five patients were randomly assigned to three groups. Patients allocated to Groups 1 and 2 received rocuronium 0.6 mg/kg. At the onset of clinical weakness (onset of ptosis), anesthesia was induced with thiopental 4-6 mg/kg; intubation was accomplished after 45 s in Group 1 and after 60 s in Group 2. Patients in Group 3 received vecuronium (0.01 mg/kg) 3 min before the administration of thiopental and succinylcholine 1.5 mg/kg, and their tracheas were intubated 60 s later by a blind anesthesiologist. Intubating conditions were assessed according to a grading scale and were either good (5 patients in Groups 1 and 2, 4 patients in Group 3) or excellent (10 patients in Groups 1 + 2, 11 patients in Group 3) in all patients. Patients were interviewed postoperatively, and all were satisfied with the induction of anesthesia. We conclude that rocuronium 0.6 mg/kg provides good to excellent intubating conditions 45 and 60 s after the induction of anesthesia using the timing principle. ⋯ We compared the ease with which a breathing tube could be placed in patients using three techniques. The standard technique (succinylcholine) was compared with two others in which a muscle-relaxing drug (rocuronium) was administered just before the anesthetic drug (so-called timing principle). No difference among the techniques was observed.
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Anesthesia and analgesia · May 1998
Randomized Controlled Trial Comparative Study Clinical TrialQuantifying oral analgesic consumption using a novel method and comparison with patient-controlled intravenous analgesic consumption.
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Anesthesia and analgesia · May 1998
Tests to evaluate intravenous placement of epidural catheters in laboring women: a prospective clinical study.
We prospectively evaluated the diagnostic accuracy of an epinephrine-containing epidural test dose (EpiTD) as a marker of intravascular injection in 209 unmedicated laboring women. Maternal heart rate (MHR) was continuously monitored and recorded on a strip chart. A tocodynamometer monitored uterine activity. A lumbar epidural catheter was placed and aspirated. If aspiration was positive for blood or cerebrospinal fluid (CSF), the catheter was replaced. In uterine diastole and with stable MHR, 198 patients received an EpiTD (epinephrine 15 microg plus lidocaine 45 mg) via the catheter. MHR and the generated HR strip were observed. A positive EpiTD was defined as a sudden increase in MHR of 10 bpm more than the resting MHR, within one minute after the injection, with a fast acceleratory phase of more than 1 bpm. Absence of a tachycardiac response suggested a negative EpiTD. If the tachycardiac response was deemed equivocal or a uterine contraction followed the EpiTD injection within 1 min, the EpiTD was invalidated and repeated. Catheter aspiration was repeated, and the catheter was removed if aspiration was positive. All patients with negative EpiTD and aspiration received 6-12 mL of epidural bupivacaine 0.25% with or without fentanyl 50 microg. Absence of analgesia without signs or symptoms of systemic toxicity after a maximum of bupivacaine 30 mg defined failed epidural analgesia. All patients with positive EpiTD and negative aspiration received 5 mL of lidocaine 2% epidurally as a second test dose (Lido100TD). The presence of tinnitus and/or metallic taste defined a positive Lido100TD. There were 176 true negatives, 0 false negatives, 14 true positives, and 8 false positives. The sensitivity of EpiTD was 100%, the specificity 96%, the negative predictive value 100%, and the positive predictive value 63%. The prevalence of negative tests was 88%, and the prevalence of positive tests was 12%. The overall accuracy of an EpiTD was 95.5%. We conclude that EpiTD is a reliable test to identify i.v. catheters during the performance of lumbar epidural analgesia in laboring patients. ⋯ Catheters inserted for epidural analgesia in laboring patients may accidentally enter a blood vessel. Local anesthetics injected through these catheters may cause seizures and cardiac arrest. In this study, we concluded that injecting a small amount of epinephrine before injecting a local anesthetic frequently helps to identify these misplaced catheters. Few catheters may actually be in the correct place even after responses to epinephrine.