Biomedical subjects

D G Silverman

Publications and source records attributed to D G Silverman.

At least 73 records · Page 4Linked to original sources

PubMed1991

Effect of tetanus on subsequent neuromuscular monitoring in patients receiving vecuronium.

The current study evaluated the effects of tetanic stimulation on neuromuscular responses to serial train-of-four (TOF) and double-burst stimulation (DBS). For TOF monitoring (n = 13), a degree of neuromuscular blockade was achieved with an intravenous vecuronium infusion such that the ratio of fourth twitch (T4) to first twitch (T1), T4/T1, was stable at a value between 0.1 and 0.7. Four seconds after a 5-s, 50-Hz tetanic stimulus was delivered, TOF monitoring was resumed at 10-s intervals. Significant changes were noted for T1, T4, and T4/T1, with median increases of 38, 250, and 93%, respectively. The median times for T1, T4, and T4/T1 to return to within 10% of their pretetanic (baseline) values were 34, 43, and 34 s, respectively (P = nonsignificant [NS] among times to recovery). A 100-Hz tetanic stimulus induced 50, 300, and 178% median increases of T1, T4, and T4/T1, while corresponding values for recovery times were 53, 73, and 54 s. For DBS monitoring (n = 14), tetanic stimulation (50-Hz, 5-s) induced 38, 300, and 153% median increases of the DBS3,3 parameters (first response [D1], second response [D2], and their ratio [D2 not equal to D1], respectively). The posttetanic effects on D1, D2, and D2/D1 persisted for 43, 66, and 46 s, respectively. For DBS3,2, median posttetanic (50-Hz, 5-s) increases were 41, 275, and 176%, while corresponding times to recovery were 43, 43, and 43 s. Although the data indicate that the posttetanic percent increase was at least 10 times larger at greater degrees of blockade (T4/T1 = 0.1) than at lesser degrees (T4/T1 = 0.7), all T4/T1 and D2/D1 ratios returned to within 10% of baseline in 125 s or less after 5-s tetanic stimulation.

Adult↗

PubMed1991

Comparison of epidurally administered sufentanil, morphine, and sufentanil-morphine combination for postoperative analgesia.

Postoperative analgesia provided by epidurally administered sufentanil and/or morphine was evaluated in 45 patients recovering from major gynecologic surgery. At the first complaint of pain in the Postanesthesia Care Unit, patients received a single epidural bolus of 30 micrograms sufentanil (group A), 5 mg morphine (group B), or 30 micrograms sufentanil plus 3 mg morphine (group C) in a randomized blinded fashion. Analgesic efficacy was assessed throughout the 24-h study period with 10-cm visual analog scales. The need for additional postoperative analgesia (patient-controlled analgesia, 1 mg of morphine every 6 min as necessary) and the incidence of adverse effects were also assessed. Patients receiving sufentanil (groups A and C) had significantly faster onset of analgesia than did patients given morphine alone (group B, P less than 0.05). Group B subjects experienced the longest duration of analgesia (B vs A and C, P less than 0.05) and required significantly less patient-controlled analgesia (morphine) than patients in group A (P less than 0.05). No patient developed clinically significant respiratory depression or excessive sedation, and there were no intergroup differences in incidence of pruritus or nausea (P value not significant). The data indicate that a mixture of sufentanil and morphine provides either a more rapid onset of epidural analgesia or reduced patient-controlled analgesia narcotic requirement than respective doses of each agent administered alone.

Adult↗

PubMed1991

Epidural sufentanil for postoperative analgesia: dose-response in patients recovering from major gynecologic surgery.

To determine the lowest effective dose of epidural sufentanil given for analgesia, 41 patients undergoing elective abdominal gynecologic surgery during continuous epidural anesthesia (lidocaine 2%) were randomly assigned to one of four postoperative treatment groups. Patients received an epidural bolus of either 25 (group A), 40 (group B), 55 (group C), or 70 micrograms (group D) sufentanil in 10 mL of saline. They were evaluated for the next 8 h using a 10-cm visual analogue scale. Except for two individuals in group A, all patients achieved a visual analogue scale score of 1 cm or less during the study interval. The onset of analgesia was most rapid in the two higher dose groups (A vs C and D; P less than 0.05). Pairwise comparison between groups showed a significant difference in the time needed to achieve maximum pain relief between the lowest and highest treatment groups (A vs D; P less than 0.05). Duration of analgesia was also significantly longer in groups C and D than in group A (208.0 +/- 21.1 and 224.0 +/- 14.7 vs 140.0 +/- 10.7 min; P less than 0.05). There were no differences among groups with regard to mean respiratory rate, level of sedation, 24-h narcotic requirements, or incidence of nausea, vomiting, and pruritus (P = NS). A single patient in group D suffered profound respiratory depression within seconds of administration. We conclude that, in patients recovering from lower abdominal surgery, a single 40-55-micrograms epidural bolus of sufentanil provides 3-3.5 h of effective analgesia, and that larger doses are not warranted.

Abdomen↗

PubMed1991

Metoclopramide: an analgesic adjunct to patient-controlled analgesia.

This randomized, double-blind trial evaluated the effect of metoclopramide on the pain and analgesic requirements associated with prostaglandin-induced labor for second-trimester termination of pregnancy. After receiving intrauterine prostaglandin, seven women were given intravenous metoclopramide (10 mg), and eight received saline, concurrent with initiation of patient controlled analgesia (PCA). Group differences were assessed with serial visual analogue scale for pain, interval PCA-morphine consumption, and time to fetal delivery. The metoclopramide group used 54% less PCA morphine (24.1 vs 52.0 mg), had lower visual analogue scale scores, and interval morphine consumption at 2, 4, and 6 h after PCA had been initiated, as well as earlier delivery of the fetus when compared with the control group (P less than 0.05). We conclude that a single dose of metoclopramide reduces the pain and PCA-morphine requirements of patients undergoing prostaglandin-induced labor and may facilitate passage of the fetus. Metoclopramide may have a similar application in treating other types of gynecologic pain.

Abortion, Induced↗

PubMed1991

Visual assessment of train-of-four and double burst-induced fade at submaximal stimulating currents.

The influence of current intensity on visual assessment of fade in response to train-of-four (TOF) and two modes of double-burst stimulation (DBS) was determined to assess the utility of low-current neurostimulation. Each of 150 sets of assessments (in 51 patients) included a mechanographic TOF at 60 mA followed by visual assessments of TOF, DBS3,3 (two minitetanic bursts of three stimuli each), and DBS3,2 (a burst of three followed by a burst of two impulses) at 20, 30, 50, and 60 mA in random order. For the range of mechanographic TOF ratios between 0.41 and 0.70, visual assessment of TOF fade failed to identify fade in 33%, 36%, 44%, and 58% of cases at 20, 30, 50, and 60 mA, respectively. Corresponding false-negative rates for DBS3,3 were 11%, 17%, 36%, and 33%, and for DBS3,2 they were 6%, 6%, 17%, and 28%. Within each method, P less than 0.05 (by Mantel-Haenszel analysis) for a linear trend of increasing accuracy as current decreased. For the range between 0.41 and 0.70, quantitative assessment overestimated the actual ratio at all currents for TOF, at 30, 50, and 60 mA for DBS3,3, and at 50 and 60 mA for DBS3,2 (P less than 0.05 by Wilcoxon signed rank test). At each current tested, DBS was more sensitive in detecting fade visually than TOF. The accuracy of visual fade detection was not influenced significantly by level of observer training. In conclusion, visual assessment of fade by novice and expert observers is improved by testing at low currents.

Adolescent↗

PubMed1991

Time required for oral ranitidine to decrease gastric fluid acidity.

This study documented gastric fluid acidity in ambulatory surgical patients 30-120 min after they had taken a 300-mg tablet of ranitidine, as changes specific to this relatively brief dose-to-sampling interval previously had not been delineated. At 20-120 min before outpatient surgery, ranitidine was given with 15 mL of water to 112 ASA physical status I-III adults without increased risk factors for aspiration of acidic gastric contents. After induction of general endotracheal anesthesia, the gastric fluid was aspirated. Volume and pH were compared with a reference group (pH = 1.6 +/- 1; n = 161) that did not receive an H2-antagonist or water. Of 40 patients sampled at 30-60 min after dosing, 26 had pH greater than or equal to 2.5; mean pH was 3.9 +/- 2 (P less than 0.05 vs reference by Wilcoxon signed rank and chi 2 tests). Beyond 90 min, 28 of 28 patients had a pH greater than or equal to 2.5, with a mean of 6.3 +/- 1. No significant differences were noted with respect to mean gastric volume. We conclude that in patients without additional risk factors, oral ranitidine consistently prevents acid production when it is administered more than 90 min before induction of anesthesia.

Administration, Oral↗

PubMed1991

New anesthetic approaches to gynecologic surgery.

This review relates how the introduction of the short-acting narcotic alfentanil and the short-acting sedative-hypnotic propofol have expanded our capabilities both for providing conscious sedation and for administering general anesthesia for short surgical procedures. The rapid onset and limited distribution of alfentanil enable it to provide intense intraoperative analgesia without prolonged respiratory depression. The rapid elimination of propofol permits rapid titration to effect and provides recovery times significantly faster than those following thiopental. The review then focuses on the combined use of opioids and sedatives for conscious sedation. Use of these agents in concert results in potentiation of beneficial, as well as untoward, effects. Their use requires careful titration and vigilant monitoring.

Alfentanil↗

PubMed1991

Nausea prophylaxis using transdermal scopolamine in the setting of patient-controlled analgesia.

We evaluated the effectiveness of transdermal scopolamine in patients receiving morphine via patient-controlled intravenous analgesia following intra-abdominal gynecologic surgery. Soon after arrival in the post-anesthesia recovery unit (time 0), patients were randomized either to receive or not receive a postauricular transdermal scopolamine patch. Nausea and vomiting were scored on a 0-3 scale at this time and at 2, 4, 6, and 24 hours. Patients were treated with droperidol as deemed necessary by the primary care nurse. Within 2-4 hours, transdermal scopolamine patients evidenced less nausea and vomiting and required less droperidol than their counterparts who did not receive transdermal scopolamine. A significant decline in the severity of nausea was noted in the transdermal scopolamine group between 2-24 hours; significant inter-group differences were noted for changes in nausea severity during the 0-6-hour and 0-24-hour intervals. Transdermal scopolamine patients evidenced a significant (P less than .05) decrease in the severity of vomiting during the first 2 hours, significantly different from the increase in the non-transdermal scopolamine patients. After the 4-hour assessment, no transdermal scopolamine patients required droperidol; nine doses were administered to the patients who were not given transdermal scopolamine (P less than .05). Thus, transdermal scopolamine therapy appears to be an effective means of treating the nausea and vomiting that are encountered after gynecologic surgery.

Administration, Cutaneous↗

PubMed1990

Stimulation with submaximal current for train-of-four monitoring.

The present study evaluated responses to train-of-four (TOF) stimulation at a range of stimulating currents. Traditionally TOF has been applied with a supramaximal stimulus but this may be quite uncomfortable for the awake patient. In the first part of this study, 12 healthy volunteers quantified (by 10-cm visual analog scale) the discomfort associated with TOF stimulation at 20, 30, and 50 mA. The median VAS scores were 2, 3, and 6, respectively (P less than 0.05 for differences between each group). In the second part, single twitch and TOF responses were compared at 20, 30, and 50 mA in 64 postoperative and in 19 intraoperative patients who had ratios of the fourth to the first twitch (T4/T1) ranging from 0.15-1.03. In all patients, neuromuscular responses to nerve stimulation were recorded by a mechanogram, and the T4/T1 ratios were calculated. Although single twitch heights increased significantly as amperage was increased, there was no statistical difference in the T4/T1 ratios at the three different currents. The mean +/- SD T4/T1 ratios at 20, 30, and 50 mA were 0.795 +/- 0.247, 0.798 +/- 0.237, and 0.802 +/- 0.233, respectively (P = ns). It is concluded that TOF monitoring using a submaximal stimulus is more comfortable for the awake patient who is suspected of residual weakness, and that T4/T1 testing can be reliably accomplished intraoperatively as well as postoperatively using submaximal stimuli.

Anesthesiology↗

PubMed1990

A compartment model for fluorometric indication of tissue perfusion.

Sodium fluorescein is an in vivo blood perfusion indicator for soft tissue. When fluorescein dye is introduced into the blood, it distributes throughout the vasculature and the extravascular space. Incident light from an external source causes the dye to fluoresce, the level of which is monitored by a photodetector placed over the tissue. In this study, theoretical analysis incorporating a multicompartmental model for dye distribution is applied to describe the relationship among perfusion, dye kinetics, and fluorescence readings. Errors in calculating perfusion from fluorescence are related to dye concentrations and to measurement errors. These error sources are minimized by selecting the measurement time. The alternatives of measurement during wash-in or during wash-out of dye are compared, as well as the alternatives of introducing dye by bolus injection or by constant infusion. Compensation of wash-in measurements for differences in skin pigmentation is accomplished by the matching of skin optical properties between incident and fluorescing wavelengths. A laboratory study at 80 measurement sites (from ten graded perfusion canine flaps) demonstrated a correlation of wash-in and wash-out perfusion data ranging from 0.88 to 0.96 at typical levels of fluorescein in blood. Since wash-in can be completed in a matter of a few minutes, this is likely to be preferable in the clinical setting to wash-out which can take much longer to complete.

Animals↗

PubMed1990

Subjective responses to train-of-four and double burst stimulation in awake patients.

The present study was undertaken to determine whether the discomfort associated with the sequential bursts of stimuli comprising the two recommended forms of double burst stimulation (DBS) is comparable to that associated with the repetitive stimuli of train-of-four (TOF). Twenty-one unmedicated volunteers rated on a visual analog scale the discomfort associated with randomly applied DBS and TOF stimulations at 20, 30 and 50 mA. All participants were blinded to the mode of stimulation, as well as to the current intensity. At each amperage tested, TOF produced significantly less discomfort than either form of DBS (P less than 0.01). Stimulation at 50 mA produced median visual analog scale scores of 7.5, 7.0, and 5.0 for DBS3,2, DBS3,3, and TOF, respectively. At 30 mA the corresponding median visual analog scale scores were 4.5, 5.5, and 3.0, whereas at 20 mA the scores were 4.0, 4.5, and 2.0, respectively. Thus, DBS is more uncomfortable than TOF at each current tested; however, in light of reports of its higher sensitivity, DBS may be the preferred means of assessing neuromuscular function in the awake as well as the anesthetized patient when a force transducer and recorder are not readily available.

Adult↗

PubMed1990

Correlation of train-of-four and double burst stimulation ratios at varying amperages.

The present study was undertaken to document the relationship between train-of-four (TOF) and double burst stimulation (DBS) at varying degrees of blockade, and to determine whether this relationship remained constant over a range of stimulating currents. The neuromuscular responses to the two most commonly employed modes of DBS stimulation, DBS3,3 and DBS3,2, and the responses to TOF nerve stimulation were recorded and compared at 20, 30, and 50 mA. Twenty-two consenting patients undergoing general anesthesia received a vecuronium infusion to achieve a TOF ratio within the range of 0.1-1.0. Train-of-four, DBS3,3, and DBS3,2 were delivered at 20, 30, and 50 mA in random sequence after a steady state of neuromuscular blockade was achieved. At a stimulating current of 50 mA, there was a significant linear correlation between DBS3,3 and TOF (P less than 0.0001; r = 0.98) over the range of blockade. Similarly, there was a high degree of correlation between DBS3,2 and TOF at 50 mA, as the increased "fade" associated with DBS3,2 was maintained throughout the spectrum of blockade (P less than 0.0001; r = 0.95). The high degrees of correlation were maintained at stimulating currents of 20 and 30 mA (P less than 0.0001). In conclusion, the present study revealed that there is a high degree of linear correlation between DBS and TOF, and that this mechanographic relationship is maintained over a wide range of stimulating currents during varying degrees of clinical neuromuscular blockade.

Adult↗

PubMed1990

Monitoring skin fluorescein delivery independent of skin pigmentation.

This study evaluated two changes in fluorometric assessment of fluorescein dye delivery: (1) monitoring the proportional, rather than the absolute, increase above the preinjection background reading at each site to obviate the effect of skin color and (2) employing gradual means of dye administration to facilitate monitoring uptake kinetics and to lessen the likelihood and severity of histamine-mediated reactions. In 15 beagles, background and postdye readings were obtained with the fiberoptic fluorometer at 27 pairs of matched light- and dark-skin sites of intact perfusion. After dye administration, the absolute increase in fluorescence at light sites averaged more than twice (approximately 225%) that at dark sites. However, the newly introduced proportional increase (PI) was independent of pigmentation. The PI of comparably perfused light and dark sites differed by an average of 3.9% (p greater than 0.05 for difference between PIdark and PIlight). This consistency was maintained after each of three methods of fluorescein administration. After the color independence of the PI was established, its relation to perfusion was assessed in nine 3 X 12 cm pedicle flaps of varied pigmentation. Background fluorometric readings were obtained at eight sites along the longitudinal axis of each flap. Dye was administered as a 20-minute 0.25 mg/kg/min infusion. The PI clearly delineated gradations in perfusion, correlating highly with more time-consuming kinetic indexes and accurately predicting viability. The pedicle row, last viable row (V1), and first nonviable row (N1) had mean PI values of 10.5 +/- 4.5, 4.2 +/- 2.6, and 0.1 +/- 0.1, respectively, at 25 minutes after the start of infusion (p less than 0.05 for pedicle vs V1, pedicle vs N1, and V1 vs N1).

Animals↗

PubMed1989

Perfusion washout: increasing a microvascular free flap tolerance to ischemia.

Thirty-five Sprague-Dawley rats were divided into control (non-exsanguinated) groups of 8 and 10 hr of ischemia, and exsanguinated groups of 8, 10, 14, 16, and 18 hr of ischemia. Free flaps based on the superficial inferior epigastric artery were anastomosed to the contralateral femoral vessels after their designated ischemia period. Reperfusion was assessed by measuring fluorescein uptake in the free flaps after clamp release. In the exsanguinated groups, 100 percent (5/5) of the 8-hr, 10-hr, and 14-hr ischemia groups survived; 80 percent (4/5) of the 16-hr ischemia group free flaps survived; and none (0/5) of the 18-hr ischemia flaps survived. In the control groups, 100 percent (5/5) of the 8-hr ischemia flaps survived, while none (0/5) of the control 10-hr ischemia flaps survived. Fluorescein uptake correlated well with flap survival. By exsanguinating an experimental microvascular free flap prior to its ischemia period, it is possible to dramatically increase flap tolerance to ischemia.

Animals↗

PubMed1989

An evaluation of morphine and oxymorphone administered via patient-controlled analgesia (PCA) or PCA plus basal infusion in postcesarean-delivery patients.

The analgesic efficacy and adverse effects of morphine and oxymorphone in 32 patients who received traditional patient-controlled analgesia (PCA) following cesarean delivery were compared with those in 32 other patients receiving the same agents via PCA plus basal opioid infusion (PCA + BI). All patients were operated upon during epidural anesthesia with 2% lidocaine and 1:200,000 epinephrine to achieve a T4 sensory level. Upon first complaint of pain in the recovery room, patients were given a titrated iv loading dose of the assigned opioid until comfortable and were then provided with a programmable PCA device. Group I (PCA) consisted of two subsets in which incremental boluses of morphine (1.8 mg, n = 16) or oxymorphone (0.3 mg, n = 16) could be self-administered via conventional PCA. Patients in group II (PCA + BI) received a basal infusion of morphine (0.6 mg/hour, n = 16) or oxymorphone (0.1 mg/hour, n = 16) in addition to self-administered boluses of 1.8 and 0.3 mg, respectively. Patients were evaluated for 24 h following initiation of analgesic therapy, and 10-cm visual analog scales (VAS) were utilized at selected intervals to assess pain at rest, pain during movement, and satisfaction with therapy. The level of sedation and incidence of nausea/vomiting and pruritus were also recorded. Patients utilizing PCA + BI noted significant reductions in resting pain scores with oxymorphone and decreased pain during movement with both opioids when compared with individuals using PCA alone (P less than 0.05). There were no significant differences between treatment groups in 24-h dose requirements or patient satisfaction with therapy (P = ns).(ABSTRACT TRUNCATED AT 250 WORDS)

Cesarean Section↗

PubMed1989

The effects of a topical PGE2 analogue on global flap ischemia in rats.

The present study evaluated the ability of DHV-PGE2ME, a topically effective 16-vinyl prostaglandin E2 analogue, to improve the tolerance of skin flaps to a period of ischemia. DHV-PGE2ME and placebo were applied to bilateral island flaps on 70 anesthetized rats; then the vascular pedicle of each flap was clamped for 10 hours. Treated flaps evidenced significantly better reperfusion, as documented by quantification of fluorescein dye delivery at 90 minutes after clamp release, and they had significantly greater ultimate viability (p less than 0.05, by ANOVA). While less than 3 percent of untreated flaps survived, those treated with 1.75 and 17.5 microgram/cm2 of drug evidenced 76 and 86 percent survival, respectively. Treatment of a given flap did not affect its contralateral mate, since there was no evidence of a systemic effect. Especially since its effect can be limited to the site of application, DHV-PGE2ME should be valuable for the treatment of compromised perfusion in a variety of settings.

Administration, Topical↗

PubMed1989

Fluorometric evaluation of large and small intestinal ischaemia in the horse.

Arteriovenous (ischaemic strangulating obstruction, ISO) and venous obstructions (haemorrhagic strangulating obstruction, HSO) were created for 70 min in the small intestine of eight anaesthetised horses, and ISO was created in four horses for 2 h and four horses for 3 h at the sternal and diaphragmatic flexures of the large colon. Five minutes following release of the occlusions, sodium fluorescein 20 per cent (0.5 mg/kg bodyweight intravenously) was administered. Serial quantitative measurements of serosal surface fluorescence of the injured segments and a control segment were made at 2, 10, 15, 20 and 30 mins using a fibreoptic perfusion fluorometer. Significant differences in fluorescence were seen in small intestine segments between HSO vs control, ISO vs HSO, but not ISO vs control segments. In the large colon, significant differences were seen between the fluorescence in the ischaemic 3 h ventral colon and control segments, and a trend for difference in fluorescence between the 2 and 3 h ischaemic segments. Differences in fluorescence between 2 vs 3 h dorsal colon segments and 2 or 3 h dorsal colon vs control segments were not significant.

Analysis of Variance↗

PubMed1989

Cocaine use and acute rupture of ectopic pregnancies.

The hemodynamic changes associated with ingestion of cocaine may precipitate rupture of ectopic pregnancy. Two cases are presented in which this association was suspected. We believe this to be the first report of this clinical entity, representing a risk factor that should be identified in patients with suspected ectopic pregnancy.

Adult↗