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Query: UMLS:C0344307 (
analgesia
)
28,200
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
The use of paravertebral
analgesia
in cattle is not always successful. Dissection studies in five cadavers indicated that there was a divergence in the courses of the dorsal and ventral branches of the lumbar nerves which can account for the unreliability of conventional techniques. An alternative more certain method of blocking the lumbar nerves is described.
Vet
Rec
1986 Sep 06
PMID:Bovine paravertebral analgesia: radiographic analysis and suggested method for improvement. 376 99
The management of a case of quadrilateral flexural contracture in a 10-year-old pony is described. The animal was restored to normal appearance and function through a combination of surgical desmotomy and management techniques; the importance of
analgesia
and exercise as adjuncts to surgery is emphasised. The aetiology and pathogenesis of the condition in the immature animal and the adult is compared and a possible association is made between this condition and palmar fibromatosis (Dupuytren's contracture) occurring in man.
Vet
Rec
1985 Jun 29
PMID:Case of quadrilateral flexural contracture in a 10-year-old pony. 402 32
Xylazine was used on 84 occasions to anaesthetise 34 steers, (17 Herefords and 17 Friesians) between 10 and 24 months of age with bodyweights ranging from 209 to 563 kg. Xylazine as a 2 per cent solution was injected intravenously; the mean dose for the Hereford steers was 0.228 mg/kg and for the Friesian steers 0.274 mg/kg. On 21 occasions xylazine only was used. On the other occasions the xylazine was supplemented with local or regional
analgesia
. The Hereford steers became recumbent after injection of xylazine more readily than the Friesian steers and took longer to recover. In addition the Hereford steers showed fewer reactions to surgical stimulation than the Friesians. It is concluded that xylazine should be supplemented with some form of effective
analgesia
whenever a surgical operation is performed.
Vet
Rec
1984 Jun 09
PMID:Observations following intravenous xylazine administration in steers. 646 20
A technique for needle liver biopsy in camels was developed. Xylazine, 15 mg/100 kg intravenously, was used for sedation and
analgesia
. A 1.2 mm X 7 cm Menghini needle was introduced anteroventrally through the ninth right intercostal space, 1 cm caudal to the ninth rib and 2 cm dorsal to the costal cartilage. The needle was directed toward the contralateral olecranon with the camel in sternal recumbency. A core of liver tissue between 1 and 2 cm long was obtained from 99 of 120 attempts in 23 animals. There were no adverse effects from the procedure and histological preservation of the tissue was excellent.
Vet
Rec
1982 Feb 27
PMID:Technique for liver biopsy in the dromedary camel. 707 22
The clinical efficacy of a combination of medetomidine, butorphanol and midazolam for anaesthesia in dogs, and its reversal by atipamezole, was evaluated in two experimental groups of four adult beagle dogs and compared with a control group of four dogs receiving only midazolam and butorphanol. The anaesthetic procedure was used for surgical procedures in another group of 14 dogs. After the injection of medetomidine, a rapid loss of coordination followed by mild sedation was observed. Anaesthesia was attained 2 +/- 1 minutes after the administration of butorphanol and midazolam and lasted 82 +/- 5 minutes, the dogs recovered 51 +/- 6 minutes later and there were no side effects.
Analgesia
and skeletal muscle relaxation were optimal throughout the period of anaesthesia. Statistically significant bradycardia and hypothermia were observed but there were no significant effects on respiratory function. After atipamezole the dogs recovered their normal posture, heart rate and body temperature in less than 20 minutes. In the control group, the short-lived light sedation was accompanied by inadequate
analgesia
and poor muscle relaxation. In the surgical group, no differences, except in drug requirements, were recorded in comparison with the experimental groups. Good
analgesia
and muscle relaxation, total absence of side effects and stability in vital body functions were observed. The injection of atipamezole was always effective, devoid of side effects and induced recovery in less than 20 minutes.
Vet
Rec
1993 Apr 03
PMID:Medetomidine-butorphanol-midazolam for anaesthesia in dogs and its reversal by atipamezole. 809 70
Forty dogs undergoing a variety of orthopaedic surgical procedures were randomly assigned to one of two analgesic protocols, receiving either pethidine at 2 mg/kg pre-operatively and 3 mg/kg postoperatively, or carprofen, a new non-steroidal anti-inflammatory drug at 4 mg/kg pre-operatively.
Analgesia
and sedation were assessed after the operations under double blind conditions using a discontinuous scoring system and a visual analogue scale. There was good agreement between the two scoring systems, and a statistical analysis of the visual analogue scores showed that carprofen provided slightly better pain relief than pethidine and produced less sedation. Carprofen provided good
analgesia
during the 18 hours the dogs were in hospital and no adverse side effects were observed.
Vet
Rec
1994 Feb 19
PMID:Postoperative analgesic and sedative effects of carprofen and pethidine in dogs. 817 93
Forty dogs undergoing a variety of surgical procedures were assigned randomly to one of two groups. All the animals were premedicated with acepromazine (0.05 mg/kg bodyweight) intramuscularly, and anaesthesia was induced with thiopentone sodium, or propofol in the case of lean animals, and maintained with halothane in an oxygen/nitrous oxide mixture using a non-rebreathing circuit. The dogs in group 1 were given papaveretum (0.2 mg/kg) slowly intravenously within 35 minutes of induction of anaesthesia and the dogs in group 2 were given carprofen (4 mg/kg) in the same way. The dogs were scored for sedation and pain by a trained theatre nurse, who did not know which group they belonged to, using a visual analogue scale, at 15, 30, 60, 120, 240 and 360 minutes after the halothane was switched off at the end of the procedure. Nine of the dogs were withdrawn from the trial (eight of them from the papaveretum group) because of inadequate pain relief and these animals were given pethidine (3 mg/kg intramuscularly) which produced adequate
analgesia
within 15 minutes in all but one case. Carprofen provided profound
analgesia
which was as effective and of longer duration than that produced by papaveretum, and was associated with significantly less postoperative sedation and a quicker return to the normal conscious state.
Vet
Rec
1993 Sep 04
PMID:Comparison of the postoperative analgesic and sedative effects of carprofen and papaveretum in the dog. 823 40
Horses undergoing surgery were randomly assigned to one of three groups to receive phenylbutazone at 4 mg/kg (n = 72), flunixin at 1 mg/kg (n = 68) or carprofen at 0.7 mg/kg (n = 63) by slow intravenous injection at the end of surgery, just before they were disconnected from halothane. Pain was assessed by either of two resident surgical clinicians (who did not know which non-steroidal anti-inflammatory drug had been given) when the horses first stood up, two and four hours later and the next morning. If repeated doses of analgesic drugs were given the time was recorded and taken as an end point for the study. The presence or absence of side effects was also recorded. In the three groups there was no significant difference between the types of surgery performed, the numbers of horses requiring further
analgesia
or the pain scores at any time. In the horses needing further
analgesia
there was a significant difference in the time after surgery at which the further
analgesia
was given between those in the flunixin group, 12.8 +/- 4.3 hours (mean +/- sd) and those in the phenylbutazone group, 8.4 +/- 4.6 hours; the carprofen group had an intermediate interval of 11.7 +/- 6.9 hours. Significantly fewer of the horses that received butorphanol during surgery needed further
analgesia
than of those that did not receive any opioid.
Vet
Rec
1993 Oct 02
PMID:Postoperative analgesia using phenylbutazone, flunixin or carprofen in horses. 823 75
Seventy-two healthy dogs required sedation and
analgesia
for a variety of procedures causing discomfort or pain. They were treated either with the alpha 2-agonist medetomidine at 40 micrograms/kg (15 intravenously and 17 intramuscularly), or 80 micrograms/kg (15 intravenously and 15 intramuscularly) or with xylazine plus l-methadone (1.0 mg)(10 intravenously). The levels of sedation,
analgesia
and safety were compared clinically and by measurements of the effects on the electrocardiogram (ECG) and blood gases, body temperature, haematology and clinical chemistry. Sedation was achieved reliably with both medetomidine and xylazine plus l-methadone but its onset, depth and duration were influenced by the dose and route of administration. In the medetomidine-treated dogs, intravenous administration resulted in more rapid sedation and the effects of the higher dose were deeper and longer lasting. The small dogs receiving 40 micrograms/kg may have been underdosed. The initial analgesic effects in response to a pin prick to the body surface were sufficient and similar for both drugs, except for the intramuscular dose of 40 micrograms/kg medetomidine.
Analgesia
for the clinical procedures was less reliable with medetomidine and was not always adequate even at the high dose, but xylazine plus l-methadone assured
analgesia
in almost every case. Medetomidine resulted in marked bradycardia, lasting as long as the sedation and the ECG revealed a sinus arrhythmia with sinoatrial and atrioventricular blocks grade I and II as a sign of interference with transduction. The bradycardia with xylazine plus l-methadone was less pronounced. A decrease in respiratory rate accompanying sedation had no influence on blood gases and blood acidity in the dogs treated with medetomidine but caused a respiratory acidosis with xylazine plus l-methadone. Body temperature decreased with all treatments for the duration of the period of sedation. Blood glucose concentration increased to a similar extent in all treatment groups, but all other haematological and clinicochemical variables remained unchanged. Treatment with the specific alpha 2 antagonist, atipamezole, reversed the sedation and cardiovascular and pulmonary effects due to medetomidine within minutes.
Vet
Rec
1996 Feb 10
PMID:Clinical comparison of medetomidine with xylazine/l-methadone in dogs. 865 Sep 15
This study evaluated the quality of anaesthesia and the cardiorespiratory effects induced by the combination of medetomidine with either ketamine, propofol or fentanyl. Medetomidine premedication (1000 or 1500 micrograms/m2 body surface area) was followed by intravenous induction of anaesthesia with ketamine (3.0 mg/kg), propofol (2.0 mg/kg) or fentanyl (2.0 micrograms/kg) in bitches undergoing elective ovariohysterectomy. Anaesthesia was prolonged by incremental doses of the induction agents as necessary. The mean (sem) overall doses (including induction) were 0.09 (0.01) mg/kg/min for ketamine, 0.06 (0.01) mg/kg/min for propofol and 0.07 (0.005) microgram/kg/min for fentanyl during procedures which lasted 88 (6) minutes, 72 (3) minutes and 79 (7) minutes, respectively. At the end of the procedure, medetomidine was antagonised with atipamezole. The quality of anaesthesia, heart rate and arterial blood pressure were recorded continuously and arterial blood gases were measured at intervals. At the end of the procedure, the animals received 10 micrograms/kg buprenorphine intramuscularly for postoperative
analgesia
. From the adequacy of anaesthesia, the lack of significant adverse side effects and the reliable and rapid recovery it is concluded that, in healthy dogs anaesthetised with ketamine or propofol, medetomidine is a satisfactory sedative-analgesic premedicant. The differences in haemodynamics and the quality of recovery suggest that the combination of medetomidine with propofol provided the better quality anaesthesia. The combination of medetomidine with fentanyl was unsuitable for obtaining surgical anaesthesia in spontaneously breathing animals owing to the severity of the respiratory depression at dosages needed for general anaesthesia.
Vet
Rec
1997 May 24
PMID:Medetomidine as a premedicant for ketamine, propofol or fentanyl anaesthesia in dogs. 918 10
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