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Remifentanil: raccolta di abstracts
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a cura di A. De Nicola
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Titolo
- Remifentanil-propofol anesthesia in vertebral disc operations: a
comparison with desflurane-N2O inhalation anesthesia. Effect on hemodynamics and recovery
- Autore
- Grundmann U; Risch A; Kleinschmidt S; Klatt R; Larsen R
- Address
- Klinik fur Anaesthesiologie und Intensivmedizin, Universitatskliniken des
Saarlandes, Homburg/Saar.
- Abstract
- OBJECTIVE: To ascertain whether there is a difference between total
intravenous anaesthesia with propofol (P) and remifentanil (R) and inhalational
anaesthesia with desflurane (D) and nitrous oxide (N) with regard to haemodynamic
reactions, recovery profile and postoperative analgesic demand in patients scheduled for
elective microsurgical vertebral disc resection. METHODS: 50 patients (ASA I-II, 18-65
years) were randomly assigned to receive total intravenous anaesthesia with propofol and
remifentanil or inhalational anaesthesia with desflurane and nitrous oxide. After
standardised induction of anaesthesia in both groups (1 microgram.kg-1 remifentanil, 1.5
mg.kg-1 propofol 0.1 mg.kg-1 cisatracurium), anaesthesia was maintained in the D/N group
with desflurane in 50% N2O. The patients of the P/R group received a constant infusion of
2 mg.kg-1.h-1 propofol and a constant infusion of 0.5 microgram.kg-1.min-1 remifentanil,
which was reduced after 15 min by 50%. The administration of desflurane and the infusion
of the anaesthetics were adjusted to maintain a surgical depth of anaesthesia. At the end
of surgery the anaesthetics were discontinued and early emergence from anaesthesia was
assessed by measuring time to spontaneous ventilation (VT > 4 ml/kg), tracheal
extubation, opening of the eyes and stating correct name and data of birth. The frequency
of analgesics and total demand for analgesics were determined using patient-controlled
analgesia and recorded for 2 h postoperatively. In addition the pain level of the patients
was measured on a visual analogue scale and the incidence of postoperative shivering,
nausea and vomiting was noted. RESULTS: Patients anaesthetised with desflurane responded
to tracheal intubation and skin incision with increasing blood pressure and showed higher
heart rates than patients anaesthetised with propofol and remifentanil, but there were no
other haemodynamic differences between the groups in response to surgical stimuli. There
were significantly shorter times to spontaneous ventilation (3.2 vs. 6.3 min), extubation
(3.8 vs. 9.5 min), eye opening (3.0 vs. 11.5 min) and giving name and date of birth (4.8
vs. 14.3 min) in patients anaesthetised with remifentanil and propofol than in those
receiving desflurane and nitrous oxide. In addition, patients anaesthetised with
remifentanil and propofol had a greater incidence of postoperative shivering. There were
no significant differences between the two groups in the patients' pain scores, analgesic
demand and incidence of nausea and vomiting. CONCLUSION: Patients anaesthetised with
propofol and remifentanil have significantly shorter emergence times than patients
anaesthetised with desflurane and nitrous oxide. The low incidence of postoperative pain
after microsurgical vertebral disc resections requires no large-scale analgesic therapy,
even after total intravenous anaesthesia including remifentanil.
- Titolo
- A randomized, blind comparison of remifentanil and alfentanil
during anesthesia for outpatient surgery.
- Autore
- Cartwright DP; Kvalsvik O; Cassuto J; Jansen JP; Wall C; Remy B; Knape
JT; Noronha D; Upadhyaya BK
- Giornale
- Anesth Analg, 85(5):1014-9 1997 Nov
- Abstract
- We compared remifentanil, an esterase-metabolized opioid, with alfentanil
as part of balanced anesthesia with at least 0.8% isoflurane during outpatient surgery in
a randomized, double-blind trial. One hundred two patients received remifentanil, and 99
patients received alfentanil. Patients who received remifentanil experienced significantly
fewer stress responses to surgical stimuli (52.9% and 65.7%, P < 0.05); significantly
fewer remifentanil patients responded to skin closure (11% and 22%, P < 0.05) than
patients who received alfentanil. Significantly more patients in the alfentanil group
required extra analgesia compared with the remifentanil group (P < 0.05). Time to
respond to verbal command was shorter for alfentanil than remifentanil (median 7 min vs 9
min), and times to spontaneous respiration (median 5 min vs 8 min), adequate respiratory
rate (median 6 min vs 9 min), and tracheal extubation (median 6 min vs 9 min) were
significantly shorter for alfentanil in comparison with remifentanil (P < 0.05).
Remifentanil patients, however, showed significantly better recovery of psychomotor and
psychometric function between 30 and 90 min after surgery (P < 0.05). The incidences of
hypotension intraoperatively and shivering postoperatively were significantly higher with
remifentanil. No unexpected or serious adverse events were recorded with remifentanil;
however, one patient who received alfentanil experienced severe recurrent respiratory
depression after surgery. The metabolic profile of remifentanil allowed better
intraoperative analgesia without compromising recovery. IMPLICATIONS: The pharmacological
profile of remifentanil, a new opioid for use in anesthesia, suggests that rapid recovery
will occur after its use. This study of 200 outpatients shows that the differences
suggested from kinetic studies are not always borne out in clinical practice, although
later recovery variables did, in fact, favor remifentanil.
- Titolo
- Advances in anesthesiology in the 90's
- Autore
- Cartwright DP; Kvalsvik O; Cassuto J; Jansen JP; Wall C; Remy B; Knape
JT; Noronha D; Upadhyaya BK
- Giornale
- Orv Hetil, 85(5):1003-10 1998 Apr 26
- Abstract
- We compared remifentanil, an esterase-metabolized opioid, with alfentanil
as part of balanced anesthesia with at least 0.8% isoflurane during outpatient surgery in
a randomized, double-blind trial. One hundred two patients received remifentanil, and 99
patients received alfentanil. Patients who received remifentanil experienced significantly
fewer stress responses to surgical stimuli (52.9% and 65.7%, P < 0.05); significantly
fewer remifentanil patients responded to skin closure (11% and 22%, P < 0.05) than
patients who received alfentanil. Significantly more patients in the alfentanil group
required extra analgesia compared with the remifentanil group (P < 0.05). Time to
respond to verbal command was shorter for alfentanil than remifentanil (median 7 min vs 9
min), and times to spontaneous respiration (median 5 min vs 8 min), adequate respiratory
rate (median 6 min vs 9 min), and tracheal extubation (median 6 min vs 9 min) were
significantly shorter for alfentanil in comparison with remifentanil (P < 0.05).
Remifentanil patients, however, showed significantly better recovery of psychomotor and
psychometric function between 30 and 90 min after surgery (P < 0.05). The incidences of
hypotension intraoperatively and shivering postoperatively were significantly higher with
remifentanil. No unexpected or serious adverse events were recorded with remifentanil;
however, one patient who received alfentanil experienced severe recurrent respiratory
depression after surgery. The metabolic profile of remifentanil allowed better
intraoperative analgesia without compromising recovery. IMPLICATIONS: The pharmacological
profile of remifentanil, a new opioid for use in anesthesia, suggests that rapid recovery
will occur after its use. This study of 200 outpatients shows that the differences
suggested from kinetic studies are not always borne out in clinical practice, although
later recovery variables did, in fact, favor remifentanil.
- Titolo
- Rapid development of tolerance to analgesia during remifentanil
infusion in humans.
- Autore
- Vinik HR; Kissin I
- Giornale
- Anesth Analg, 85(6):1307-11 1998 Jun
- Abstract
- Studies in experimental animals have demonstrated a rapidly developing
acute tolerance to the analgesic effect of opioids administered by continuous i.v.
infusion. The aim of the present study was to determine whether acute tolerance plays an
important role in the analgesic effect of remifentanil provided by i.v. infusion to
humans. The analgesic effect of remifentanil, infused at a constant rate of 0.1 microg x
kg(-1) x min(-1) for 4 h, was evaluated by measuring pain tolerance with thermal (2
degrees C water) and mechanical (pressure) noxious stimulations in 13 paid volunteers. The
constant-rate infusion of remifentanil resulted in a threefold increase in pain tolerance
with both tests. After reaching its maximum in 60-90 min, the analgesic effect of
remifentanil began to decline despite the constant-rate infusion, and after 3 h of
infusion, it was only one fourth of the peak value. A comparative rate in the development
of acute tolerance measured in terms of time to 50% recovery during infusion was 129 +/-
27 min (mean +/- SD) with the cold water test and 138 +/- 39 min with the pressure test.
We conclude that the development of tolerance should be included in the calculations for
target-controlled infusions. Implications: Our study shows that tolerance to analgesia
during remifentanil infusion is profound and develops very rapidly. The administration of
opioids during anesthesia based on target-controlled infusions should include corrections
for the development of tolerance.
- Titolo
- Remifentanil and propofol combination for awake craniotomy: case report
with pharmacokinetic simulations.
- Autore
- Johnson KB; Egan TD
- Giornale
- J Neurosurg Anesthesiol, 85(1):25-9 1998 Jan
- Abstract
- Remifentanil and propofol infusions were used to provide
neuroleptanalgesia during an awake craniotomy to resect a left frontoparietal glioblastoma
near the motor speech center. This operation presented anesthetic requirements ranging
from adequate analgesia during bone flap removal to an appropriate level of consciousness
during cortical speech mapping. We performed pharmacokinetic simulations to estimate the
effect site concentrations of propofol and remifentanil as the infusion rates were
modulated to meet the dynamic sedation and analgesic needs of the operation. Simulations
revealed that changes in infusion rates were quickly followed by changes in the effect
site concentrations which corresponded well with the desired changes in patient sedation
and analgesia. We propose that remifentanil and propofol in combination may be a useful
technique for awake craniotomy.
- Titolo
- Remifentanil versus alfentanil in a balanced anesthetic technique
for total abdominal hysterectomy.
- Autore
- Kovac AL; Azad SS; Steer P; Witkowski T; Batenhorst R; McNeal S
- Giornale
- J Clin Anesth, 85(7):532-41 1997 Nov
- Abstract
- STUDY OBJECTIVES: To compare the intraoperative effects and recovery
characteristics of remifentanil hydrochloride and alfentanil when administered as part of
balanced anesthesia, and to assess the effects of an additional remifentanil infusion
administered as analgesic pretreatment before removal of the uterus. DESIGN: Multicenter,
double-blind, randomized, parallel-group study. SETTING: Two university hospitals.
PATIENTS: 35 ASA physical status I, II, and III women scheduled for elective total
abdominal hysterectomy with general endotracheal anesthesia. INTERVENTIONS: Patients were
premedicated with midazolam 0.05 mg/kg intravenously (i.v.). Anesthesia was induced with
thiopental 2 mg/kg, vecuronium 0.15 mg/kg, and a single dose of opioid over 60 seconds
(Pump 1): remifentanil 2 micrograms/kg (Remi/Placebo and Remi/Remi groups) or alfentanil
50 micrograms/kg (Alf/Placebo group). Anesthesia was maintained with a nitrous
oxide/oxygen mixture (66:34 ratio) and a continuous opioid infusion: remifentanil 0.25
microgram/kg/min (Remi/Placebo and Remi/Remi) or alfentanil 0.5 microgram/kg/min
(Alf/Placebo). At skin incision, a second blinded drug infusion was also initiated (Pump
2): remifentanil 0.25 microgram/kg/min (Remi/Remi) or saline placebo (Remi/Placebo and
Alf/Placebo). Intraoperative responses were controlled with single doses of opioid and/or
rate titrations via Pump 1. Pump 2 was terminated on removal of the uterus. Pump 1 was
terminated at skin closure. MEASUREMENTS AND MAIN RESULTS: The mean (+/- SD) opioid
infusion rates administered for the duration of Pump 2 to suppress responses to removal of
the uterus were 0.49 +/- 0.27 microgram/kg/min, 1.99 +/- 1.34 micrograms/kg/min, and 0.49
+/- 0.07 microgram/kg/min for the Remi/Placebo, Alf/Placebo, and Remi/Remi groups,
respectively. At these rates, similar proportions of patients in the Remi/Placebo (67%)
and the Alf/Placebo (60%) groups had responses. Fewer patients had responses in the
Remi/Remi group (8%) compared with the Remi/Placebo and Alf/Placebo groups (p < 0.05).
The mean total opioid doses used during maintenance were 84.6 micrograms/kg
(Remi/Placebo), 393 micrograms/kg (Alf/Placebo), and 68.7 micrograms/kg (Remi/Remi).
Awakening times were significantly shorter (p < 0.05) in the remifentanil population
compared with the alfentanil population, but discharge times were similar. More patients
received naloxone to reverse opioid effects in the alfentanil population (60%) than in the
remifentanil population (20%) (p < 0.05). CONCLUSIONS: A mean remifentanil infusion of
0.49 microgram/kg/min is as effective as a mean alfentanil infusion of 1.99
micrograms/kg/min in suppressing intraoperative responses. Doubling of the remifentanil
infusion to 0.5 microgram/kg/min before the major stress event improves suppression of
responses and lowers intraoperative use of remifentanil without prolonging recovery times.
Remifentanil allows faster awakening times than alfentanil, but preemptive administration
of postoperative analgesics is recommended to facilitate discharge.
- Titolo
- Use of remifentanil in patients breathing spontaneously during
monitored anesthesia care and in the management of acute postoperative care
- Autore
- Kovac AL; Azad SS; Steer P; Witkowski T; Batenhorst R; McNeal S
- Giornale
- Anesthesiology, 85(7):1124-6 1998 Apr
- Abstract
- STUDY OBJECTIVES: To compare the intraoperative effects and recovery
characteristics of remifentanil hydrochloride and alfentanil when administered as part of
balanced anesthesia, and to assess the effects of an additional remifentanil infusion
administered as analgesic pretreatment before removal of the uterus. DESIGN: Multicenter,
double-blind, randomized, parallel-group study. SETTING: Two university hospitals.
PATIENTS: 35 ASA physical status I, II, and III women scheduled for elective total
abdominal hysterectomy with general endotracheal anesthesia. INTERVENTIONS: Patients were
premedicated with midazolam 0.05 mg/kg intravenously (i.v.). Anesthesia was induced with
thiopental 2 mg/kg, vecuronium 0.15 mg/kg, and a single dose of opioid over 60 seconds
(Pump 1): remifentanil 2 micrograms/kg (Remi/Placebo and Remi/Remi groups) or alfentanil
50 micrograms/kg (Alf/Placebo group). Anesthesia was maintained with a nitrous
oxide/oxygen mixture (66:34 ratio) and a continuous opioid infusion: remifentanil 0.25
microgram/kg/min (Remi/Placebo and Remi/Remi) or alfentanil 0.5 microgram/kg/min
(Alf/Placebo). At skin incision, a second blinded drug infusion was also initiated (Pump
2): remifentanil 0.25 microgram/kg/min (Remi/Remi) or saline placebo (Remi/Placebo and
Alf/Placebo). Intraoperative responses were controlled with single doses of opioid and/or
rate titrations via Pump 1. Pump 2 was terminated on removal of the uterus. Pump 1 was
terminated at skin closure. MEASUREMENTS AND MAIN RESULTS: The mean (+/- SD) opioid
infusion rates administered for the duration of Pump 2 to suppress responses to removal of
the uterus were 0.49 +/- 0.27 microgram/kg/min, 1.99 +/- 1.34 micrograms/kg/min, and 0.49
+/- 0.07 microgram/kg/min for the Remi/Placebo, Alf/Placebo, and Remi/Remi groups,
respectively. At these rates, similar proportions of patients in the Remi/Placebo (67%)
and the Alf/Placebo (60%) groups had responses. Fewer patients had responses in the
Remi/Remi group (8%) compared with the Remi/Placebo and Alf/Placebo groups (p < 0.05).
The mean total opioid doses used during maintenance were 84.6 micrograms/kg
(Remi/Placebo), 393 micrograms/kg (Alf/Placebo), and 68.7 micrograms/kg (Remi/Remi).
Awakening times were significantly shorter (p < 0.05) in the remifentanil population
compared with the alfentanil population, but discharge times were similar. More patients
received naloxone to reverse opioid effects in the alfentanil population (60%) than in the
remifentanil population (20%) (p < 0.05). CONCLUSIONS: A mean remifentanil infusion of
0.49 microgram/kg/min is as effective as a mean alfentanil infusion of 1.99
micrograms/kg/min in suppressing intraoperative responses. Doubling of the remifentanil
infusion to 0.5 microgram/kg/min before the major stress event improves suppression of
responses and lowers intraoperative use of remifentanil without prolonging recovery times.
Remifentanil allows faster awakening times than alfentanil, but preemptive administration
of postoperative analgesics is recommended to facilitate discharge.
- Titolo
- Effect of continuous spinal remifentanil infusion on behaviour
and spinal glutamate release evoked by subcutaneous formalin in the rat.
- Autore
- Buerkle H; Marsala M; Yaksh TL
- Giornale
- Br J Anaesth, 85(3):348-53 1998 Mar
- Abstract
- Injection of formalin into the hind paw of the rat evokes a biphasic
nociceptive behavioural response, which is considered to be an animal model of
postoperative pain in humans. The initial response (phase 1) is caused by activation of
peripheral nociceptors and is followed by a second phase attributed to ongoing activity in
primary afferents and increased sensitivity of dorsal horn neurones. The latter effect is
thought to result from glutamate-mediated N-methyl-D-aspartate receptor activation. In
studies to date it has been difficult to discriminate mechanisms underlying phase 1 and
phase 2 events because of the long-lasting half-times of intrathecally administered
opioids. To further understanding of the opioid pharmacology of the two different phases
of the formalin test, we have studied behavioural activity and spinal glutamate release
after intrathecal administration of remifentanil, a new short-lasting mu opioid.
Intrathecal remifentanil 3 micrograms microliter-1 min-1 delivered during phase 1
inhibited behavioural response during phase 1 (100%), but did not abolish subsequent phase
2 behavioural activity completely (67 (12) %). Intrathecal remifentanil administered
separately in phase 1 and phase 2 revealed a similar ED50 (0.2 microgram microliter-1
min-1) for inhibition of the behavioural responses. In vivo, spinal microdialysis showed
incomplete reduction in glutamate concentrations in response to intrathecal remifentanil
administration; this in turn inhibited phase 1 behavioural responses. Therefore we contend
that supramaximal doses of intrathecal remifentanil sufficient to inhibit phase 1 activity
still permitted sufficient glutamate release to allow spinal facilitation. Incomplete
suppression of spinal excitatory neurotransmitter release by intrathecal opioids is
consistent with spinal wind-up that is triggered during phase 1 and results in phase 2
afferent drive. This might reflect one of the mechanisms underlying post-operative pain.
- Titolo
- Future applications for TCI systems.
- Autore
- Buerkle H; Marsala M; Yaksh TL
- Giornale
- Anaesthesia, 85(3):56-60 1998 Apr
- Abstract
- Infusion pumps incorporating 'Diprifusor' for the administration of
propofol by target controlled infusion are now commercially available and are becoming
more widely used. This paper considers possible future applications of target controlled
infusion and summarises results obtained using prototype systems as a component of other
control techniques and with other drugs. These include studies with patient-controlled
systems for the administration of analgesia or sedation and a closed loop control system
for the administration of propofol. Among currently available analgesic drugs, alfentanil
and remifentanil are considered to be the most suitable for administration by target
controlled infusion, but commercial systems for these agents are not yet available.
- Titolo
- Effect of remifentanil on respiratory burst of human neutrophilic
granulocytes in vitro
- Autore
- Jaeger K; Andr´e M; Scheinichen D; Heine J; Kleine HD; Leuwer M;
Piepenbrock S
- Giornale
- Anaesthesiol Reanim, 85(5):121-4 1997
- Abstract
- Recovery chances for severely ill patients have been significantly
improved by the progress of intensive care medicine. The success of any therapy, however,
is still jeopardized by postoperative infections and septic complications. In the early
stage of bacterial infections polymorphonuclear leukocytes (PMNL) play a decisive role.
After PMNL activation, the production of oxygen radicals during the respiratory burst (RB)
denature the phagocytosed micro-organisms. Remifentanil is a new opioid which has been
safely administered to various patient groups and shows pharmacokinetic advantages in
comparison to the already established opioids. As some intravenous anaesthetics can
influence PMNL functions, we analysed, by flow cytometry, the in vitro influence of
clinically relevant remifentanil concentrations on the respiratory burst. In our study
remifentanil had no influence on the respiratory burst of human PMNL in vitro, regardless
of the RB triggering agents chosen.
- Titolo
- The role of newer opioids in geriatric anesthesia.
- Autore
- Shafer SL
- Giornale
- Acta Anaesthesiol Belg, 49(2):91-103 1998
- Abstract
- The unique features of remifentanil are its rapid clearance and rapid
ke0, resulting in a rapid onset and offset of drug effect. It is tempting to speculate
that these characteristics will make remifentanil an easy drug to titrate, and that
clinicians will not need to consider patient covariates such as advanced age when choosing
a dosing regimen. However, the rapid onset of drug effect may be accompanied by rapid
onset of adverse events such as apnea and muscle rigidity. The rapid offset of drug effect
can result in patients who are in severe pain at a time when the anesthesiologist is ill
equipped to deal the problem, for example when the patient is in transit to the recovery
room. It is thus important that when treating elderly patients anesthesiologists
understand the proper dose adjustment required for the elderly. By adjusting the bolus and
infusion doses, the anesthesiologist can hope to avoid the peaks and valleys that might
expose these patients to risk. When the proper adjustment is made, the variability in
remifentanil pharmacokinetics is considerably less than for any other intravenous opioid.
This makes remifentanil the most predictable opioid for treatment of the elderly.
- Titolo
- Remifentanil
- Autore
- Shafer SL
- Giornale
- Anaesthesia, 49(2):409 1998 Apr
- Abstract
- The unique features of remifentanil are its rapid clearance and rapid
ke0, resulting in a rapid onset and offset of drug effect. It is tempting to speculate
that these characteristics will make remifentanil an easy drug to titrate, and that
clinicians will not need to consider patient covariates such as advanced age when choosing
a dosing regimen. However, the rapid onset of drug effect may be accompanied by rapid
onset of adverse events such as apnea and muscle rigidity. The rapid offset of drug effect
can result in patients who are in severe pain at a time when the anesthesiologist is ill
equipped to deal the problem, for example when the patient is in transit to the recovery
room. It is thus important that when treating elderly patients anesthesiologists
understand the proper dose adjustment required for the elderly. By adjusting the bolus and
infusion doses, the anesthesiologist can hope to avoid the peaks and valleys that might
expose these patients to risk. When the proper adjustment is made, the variability in
remifentanil pharmacokinetics is considerably less than for any other intravenous opioid.
This makes remifentanil the most predictable opioid for treatment of the elderly.
- Titolo
- Nalbuphine and pruritus
- Autore
- Shafer SL
- Giornale
- Anaesthesia, 49(2):1023 1997 Oct
- Abstract
- The unique features of remifentanil are its rapid clearance and rapid
ke0, resulting in a rapid onset and offset of drug effect. It is tempting to speculate
that these characteristics will make remifentanil an easy drug to titrate, and that
clinicians will not need to consider patient covariates such as advanced age when choosing
a dosing regimen. However, the rapid onset of drug effect may be accompanied by rapid
onset of adverse events such as apnea and muscle rigidity. The rapid offset of drug effect
can result in patients who are in severe pain at a time when the anesthesiologist is ill
equipped to deal the problem, for example when the patient is in transit to the recovery
room. It is thus important that when treating elderly patients anesthesiologists
understand the proper dose adjustment required for the elderly. By adjusting the bolus and
infusion doses, the anesthesiologist can hope to avoid the peaks and valleys that might
expose these patients to risk. When the proper adjustment is made, the variability in
remifentanil pharmacokinetics is considerably less than for any other intravenous opioid.
This makes remifentanil the most predictable opioid for treatment of the elderly.
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