Articles: analgesia.
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Stereotact Funct Neurosurg · Jan 1991
Case ReportsPercutaneous retroperitoneal stimulation of the sacral plexus. Initial report and technical note.
A new percutaneous approach to stimulate the sacral plexus for the treatment of pain is described. The percutaneous electrode is inserted under fluoroscopy through the chosen dorsal and ventral sacral foramen and is advanced into the retroperitoneal layer where the plexus lies. The electrode, can be advanced several centimeters and lies in close proximity to the branches of the sacral plexus. ⋯ We report our initial experience with a new approach to stimulation of the peripheral nervous structures. That is stimulation of the sacral plexus through electrodes implanted percutaneously along the plexus in the retroperitoneal area. This initial report is not meant to give clinical results of this methodology, but simply to point to another route to apply electrical stimulation safely to various parts of the nervous system.
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Stereotact Funct Neurosurg · Jan 1991
How do geometric factors influence epidural spinal cord stimulation? A quantitative analysis by computer modeling.
Effects of both anatomic and electrode geometry on the recruitment of rostrocaudal fibers in the spinal cord were investigated by computer simulation of epidural spinal cord stimulation. A three-dimensional model was used, representing the geometry and electrical conductivity of the spinal cord and surrounding tissues, in combination with a model representing the electrical properties of a myelinated nerve fiber. Recruitment contours in the dorsal columns were calculated at various spinal geometries as a function of electrode position, combination and area. ⋯ Recruitment areas resulting from different contact combinations of a mediodorsal array were almost identical. It was shown that perception threshold largely depends on both dorsal cerebrospinal fluid width and fiber size. The usual bipolar contact separation appeared to approximate the theoretically optimal value, resulting in maximum fiber recruitment at minimum stimulus.
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J Pain Symptom Manage · Jan 1991
Randomized Controlled Trial Comparative Study Clinical TrialEvaluation of patient-controlled analgesia (PCA) versus PCA plus continuous infusion in postoperative cancer patients.
The benefits of two dosing methods, patient-controlled analgesia (PCA) with morphine sulfate (MS) alone and PCA plus continuous infusion of morphine sulfate (PCA + CI) were clinically evaluated in a randomized, single-blinded study of 30 adult abdominal surgery patients. Doses were adjusted based on pain and sedation ratings. Respirations, pulse, blood pressure, pain and sedation ratings were assessed. ⋯ There seems to be a trend for the PCA + CI group to have less fluctuation in sedation between days and better pain control (as demonstrated by verbal and visual analog pain scores) on the third postoperative day. Statistical significance was not found, however. PCA plus continuous infusion of MS may be a beneficial approach to the management of postoperative pain in selected patients; studies to identify these patients need to be done.
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Anesthesia and analgesia · Jan 1991
Randomized Controlled Trial Clinical TrialEpidural morphine with butorphanol for postoperative analgesia after cesarean delivery.
Epidural morphine has been used more and more to provide long-lasting postoperative analgesia after cesarean delivery. However, the incidence of pruritus (20%-93%) and nausea (17%-60%) detract from the usefulness of epidural morphine. The purpose of this study was to evaluate, in 30 patients having epidural anesthesia for cesarean delivery, the analgesic efficacy and side effects when a combination of epidural morphine, a mu-receptor agonist, and butorphanol, a mu-receptor antagonist and kappa-receptor agonist, was administered. ⋯ Patients were monitored for 24 h after administration of the study medications. There were no significant differences between the groups in visual analogue pain scores, time to first analgesic request, respiratory rate, or Trieger dot test performance in the 24 h immediately after these epidural injections. There were three patients in group 1 and one patient in group 2 who experienced oxygen saturations less than 90%. (No patients in group 3 developed an oxygen saturation less than 92%.) The patients in group 3 did not require treatment for pruritus or nausea, a response significantly different (P less than 0.001 and P less than 0.05, respectively) from group 1 or group 2.(ABSTRACT TRUNCATED AT 250 WORDS)
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Ann Fr Anesth Reanim · Jan 1991
Randomized Controlled Trial Comparative Study Clinical Trial[Evaluation of obstetrical pain by a questionnaire of adjectives. Comparison of 2 epidural analgesia protocols].
A French version of the McGill pain questionnaire, the "Questionnaire Douleur Saint Antoine" (QDSA), was assessed prospectively by comparing two epidural analgesia protocols using bupivacaine. One hundred women in labour who asked for epidural analgesia were randomly allocated to two groups and received either 0.25% or 0.5% bupivacaine (mean initial doses 32.5 and 50 mg respectively) with adrenaline 1 in 200,000. All the patients were then instructed to trigger a patient controlled analgesia (PCA) device for top-up doses of 0.25% bupivacaine with adrenaline 1 in 400,000 once they became aware of pain returning. ⋯ On the other hand, the affective part of the score was only correlated with the level of anxiety and behaviour. The sensory part of this score was the only one to show a difference between the different initial doses given to the patients. The results obtained with this series of patients underline the value of a multidimensional assessment of labour pain.