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Biomedical subjects

B Biber

Publications and source records attributed to B Biber.

At least 91 records · Page 5Linked to original sources

Successful vasoconstrictor therapy of anaphylactoid reactions during induction of anaesthesia. A report of two cases.

Anaphylactoid reactions were evoked during intravenous induction of anaesthesia in two patients on three occasions. In the first patient the reaction occurred during the first anaesthetic on propranolol and hydrochlorthiazide medication due to hypertension. Since the major target organ for the anaphylactoid reaction in this patient was the pulmonary circulation, the cardiovascular collapse at his first anaesthetic was misinterpreted as a nonspecific reaction to anaesthesia reinforced by the beta-receptor blocking therapy. At the second anaesthetic central haemodynamics, plasma adrenaline (A) and noradrenaline (NA) were measured. Following injection of thiopentone sudden decreases of mean arterial blood pressure (60%), cardiac output (60%), and systemic vascular resistance (20%) were observed. Thirty minutes later, still during circulatory shock, the concentration of A had increased whereas that of NA was normal. In the second patient the anaphylactogenic drug was supposed to be thiopentone, suxamethonium or alcuronium. In this patient, the fall in arterial blood pressure was associated with bronchospasm and the sudden appearance of peripheral oedema. In both cases initial resuscitation comprised volume replacement and beta 1-agonist therapy but the cardiovascular state was not normalized until vasoconstricting agents were infused.

Adult↗

Effects of hyperventilation and hypoventilation on stress-induced intestinal vasoconstriction.

The combined effects of defined changes in ventilation and stress-induced vasoconstriction were studied in the intestinal vascular bed in cats (n = 20) anaesthetized with fentanyl, nitrous oxide and diazepam. Intestinal reflex vasoconstriction was induced by stimulation either of the hypothalamic defence-alarm area or of somatic and visceral pain afferents. The volume-controlled ventilation was changed by altering the tidal volume, and stimulations were performed during either control conditions (Paco2 4.5-5.0 kPa), hyperventilation (Paco2 3.0-3.5 kPa) or hypoventilation (Paco2 6.5-7.5 kPa). The increase in intestinal vascular resistance (IVR) elicited by defence-alarm area stimulation was potentiated during hyperventilation (306 +/- 83% vs 198 +/- 62%; P less than 0.01) and attenuated during hypoventilation (176 +/- 62% vs 240 +/- 44%; P less than 0.05). The increase in IVR elicited by pain fibre stimulation was potentiated during hyperventilation (73 +/- 21% vs 54 +/- 19%; P less than 0.01), but not significantly changed during hypoventilation (47 +/- 19% vs 68 +/- 34% during control ventilation). Our data indicate that the ventilatory pattern can be decisive for the vasoconstrictor response during experimental stress. We suggest that remote neurogenic mechanisms account for the increased responsiveness during hyperventilation. The decreased responsiveness during hypoventilation, on the other hand, seems to correlate with the local vasodilator effects of carbon dioxide.

Animals↗

Halothane dissolved in fat as an intravenous anaesthetic to rats.

The anaesthetic properties of a halothane-in-fat solution given either as a single i.v. dose or as a continuous i.v. infusion were investigated in rats. 0.3 ml of a 5% solution of halothane in fat emulsion was injected i.v. into 15 awake rats. At the end of the 30 s injection, all rats had collapsed from the upright position and showed no response to a firmly applied tail clamp. Breathing usually became shallow and irregular just after injection. Two rats died. In the surviving rats, movement in response to clamping of the tail reappeared after some 30 s (range 15-90 s). The rats regained the upright position after about 100 s, and appeared fully awake about 3 min (range 2-5 min) after injection. Surviving rats behaved normally after the experiment, and gained in weight. They were killed 1-29 days later. The lungs, kidneys, heart, brain and liver had a normal macroscopic and microscopic appearance. In a second set of experiments (n = 9), a 10% solution of halothane was continuously infused i.v. (3.75 microliters min-1). The anaesthetic depth, as well as the mean arterial pressure, heart rate, respiratory rate and arterial PCO2 and PO2 were similar to values observed during inhalation of halothane in air at an inspired concentration of 1.1%. By doubling the infusion rate, MAP was reduced by 23%. It was easy to adjust anaethestic depth by changing the infusion rate and recovery was fast.

Anesthesia, Intravenous↗

Intravenous infusion of halothane dissolved in fat. Haemodynamic effects in dogs.

Eight harrier dogs received an i.v. infusion of halothane dissolved 1:9 in a fat emulsion for i.v. nutrition (Intralipid, Vitrum). The rate of infusion was adjusted to maintain end-tidal halothane concentrations of 0.7% and 1.4%. At 1.4%, mean arterial pressure decreased to 76 +/- 8 mmHg (10.1 +/- 1.0 kPa) (mean +/- s.e.mean) from a pre-infusion value of 122 +/- 6 mmHg (16.2 +/- 0.8 kPa) (P less than 0.01). The concomitant decrease in cardiac output was 39% and left ventricular maximum dp/dt decreased by 50% (P less than 0.01). Changes in systemic vascular resistance and pulmonary arterial pressure were small. The haemodynamic responses during halothane inhalation, to corresponding end-tidal concentrations, were similar. Arterial and mixed venous halothane concentration increased in proportion to end-tidal concentration. There were no changes in arterial PO2 during the halothane-in-fat infusion. Triglyceride concentrations in plasma increased 12-fold. Haemodynamic recovery after the infusion was fast. We conclude that the halothane-in-fat infusion caused a dose-dependent depression of myocardial contractility and arterial pressure, similar to that seen during inhalation, and that end-tidal concentration could be used for control of the infusion rate.

Anesthesia, Intravenous↗

Evidence for cardiac volume-receptor regulation of feline jejunal blood flow and fluid transport.

The aim of the study was to investigate the role of cardiac mechanoreceptors in the reflex regulation of intestinal blood flow and fluid transport. Feline cardiac mechanoreceptor activity was modified with two noninvasive techniques: positive-pressure ventilation (PPV) and inspiratory resistance breathing (IRB). A jejunal segment with intact vascular and nervous supply was isolated and exposed to cholera toxin as a model for intestinal secretion. The results revealed that PPV induced a pronounced intestinal vasoconstriction and a marked inhibition of choleraic secretion. IRB had the opposite effects. The responses were well correlated with changes in central blood volume and either markedly reduced or abolished by vagotomy, intestinal alpha-adrenoreceptor blockade, or postganglionic mesenteric denervation. The results indicate that cardiac mechanoreceptors with vagal afferents may mediate the observed reflex responses, and hence this receptor station may be of importance in the normal reflex control of intestinal hemodynamics and fluid transport.

Animals↗

Hemodynamic and hematologic changes in a standardized trauma-sepsis model in rats.

The aim of this report was to describe an experimental trauma-sepsis model in rats. Trauma consisted of laparotomy and sepsis was induced by intravenous infusion of different amounts (10(8)-10(10)) of live Escherichia coli. Three experimental series were performed. In the first series survival rates were studied up to 7 days after trauma-sepsis. In the second and third series pulse rate, intraarterial blood pressure, cardiac output, liver blood flow and hematologic changes were studied after 24 h. Cardiac output was determined by dye-dilution method and hepatic blood flow by 133Xe wash-out technique. Survival rates were decreased in a dose-related manner when the amount of bacteria administered was increased from 10(8) to 10(10). Twenty-four hours after trauma-sepsis, survival rate was 100% following E. coli 10(8), 69% following E. coli 10(9), and 23% following E. coli 10(10). After 7 days the corresponding figures were 85%, 31%, and 8%. A dose-related decrease was also observed for cardiac output and hepatic blood flow when the amount of bacteria was increased. Mean arterial blood pressure was unchanged. Platelet and white blood cell counts were reduced 24 h following trauma-sepsis, and these changes were also more pronounced when the amount of bacteria infused was increased. Thus, it was possible to demonstrate a graded response following increasing amounts of bacteria regarding survival rate, cardiac output, liver blood flow, and hematologic changes in three subsequent experimental series. A carefully standardized experimental model may be of value for studies of metabolic events following trauma and sepsis.

Animals↗

Muscular compartment pressure following reconstructive arterial surgery of the lower limbs.

Intramuscular pressure in the anterior tibial compartment and calf circumference were measured daily during six days following reconstructive surgery for lower limb atherosclerosis in 31 patients. Both intramuscular pressure and calf circumference were significantly increased in the operated extremity from the first postoperative day. Maximum intramuscular pressure was found on the second postoperative day. No patient developed a compartment syndrome. Calf circumference increased more slowly and reached maximum on the fifth postoperative day. Following successful reconstructive arterial surgery intramuscular pressure and calf circumference increased most in patients undergoing dissection of the groin and leg, probably reflecting intraoperative damage of lymphatic vessels. In four patients where the reconstructive arterial surgery failed intramuscular pressure and calf circumference remained unchanged postoperatively despite dissection of the groin and leg. Thus, the present study suggests that both impaired lymphatic drainage and increased capillary filtration contribute to the development of increased intramuscular pressure and calf circumference following reconstructive arterial surgery of the leg.

Aged↗

Effects of hydralazine on liver blood flow in normovolemic dogs.

The effects on liver blood flow caused by hydralazine were studied in 14 dogs. Hepatic artery and femoral artery blood flow were estimated with an electromagnetic flow meter. Total hepatic blood flow (THBF) was measured by 133Xenon clearance. Cardiac output (CO) was determined by intravenous injection of Cardio-Green. After 0.2 mg/kg of hydralazine total hepatic blood flow increased by 57%. The hepatic artery blood flow increased by 82% and portal blood flow by 58%. Cardiac output increased by about 50%, while total peripheral vascular resistance decreased. The results further suggest that hydralazine increases portal blood flow. Also the ratio THBF : CO increased. These findings together indicate a hydralazine-induced redistribution of cardiac output with a relatively increased proportion provided to the liver.

Animals↗

Effect of intravenous dopamine infusion on intramural blood flow distribution and fluid absorption in the feline small intestine.

The aim of the study was to investigate the effects of dopamine on the intestinal mucosal blood flow and transport function. Dopamine was infused intravenously at 20 micrograms X kg-1 X min-1 in anesthetized cats. Total and intramural blood flow in an isolated jejunal segment was measured by a combined drop-flow and 85Kr clearance technique. Net fluid transport was recorded by two independent perfusion methods. Unidirectional sodium transport was estimated from luminal 22Na disappearance. Dopamine induced a pronounced mucosal vasodilatation up to 400% of control values. Concomitantly, net fluid and sodium absorption increased by 50%. The effect on sodium transport was due to a pronounced decrease in tissue-to-lumen sodium flux, a pattern similar to the one seen on alpha-adrenergic stimulation. The effect of dopamine on blood flow was unaffected by phentolamine, 1 mg X kg-1, whereas the absorptive response was abolished. The findings indicate that dopamine induces a mucosal vasodilation via one mechanism (possibly dopaminergic) and enhances fluid transport via another mechanism, probably alpha-adrenergic.

Animals↗

Improved blood flow and protein synthesis in the postischemic liver following infusion of dopamine.

To study the effects of dopamine on hepatic blood flow and protein synthesis in a condition with reduced liver blood flow, dopamine (5 micrograms X kg-1 X min-1) or saline was infused intravenously following a period of liver ischemia in rats. Hepatic blood flow was measured by xenon washout technique and protein synthesis by leucine incorporation into proteins in incubated liver slices. Blood flow and protein synthesis in the postischemic liver were restituted faster and more completely in dopamine-treated rats suggesting that dopamine infusion can be of beneficial effect on liver metabolism in situations with reduced hepatic blood flow.

Animals↗

Intestinal vascular responses to dopamine during fentanyl-nitrous oxide anaesthesia, supplemented with dixyrazin.

Intestinal haemodynamics in response to continuous i.v. administration of dopamine were investigated in cats anaesthetized with fentanyl-nitrous oxide either with or without supplement of dixyrazin. A dose-dependent vasodilatation was observed in the dopamine dose range 2.5-35 micrograms . kg-1 . min-1 and the subsequent maximal intestinal blood flow increase was 121%. No net intestinal vasoconstriction was evident even at the largest dopamine doses, although the vascular response reached a plateau at 17.5 micrograms . kg-1 . min-1. Control experiments during chloralose anaesthesia gave similar results. Changes in mean arterial pressure and heart rate were small. Renal blood flow was virtually unchanged at dopamine doses below 10 micrograms . kg-1 . min-1, while renal vasoconstriction was evident following dopamine doses above that level. The addition of i.v. dixyrazin (0.15-0.30 mg . kg-1) to the fentanyl-nitrous oxide anaesthesia substantially potentiated the intestinal vasodilator response to i.v. dopamine and the maximal blood flow increase was 183% at 10-15 micrograms . kg-1 . min-1. In vitro experiments using mesenteric resistance vessels from the rat demonstrated a dose-dependent relaxation to dopamine. At very large doses this response was counteracted, but not reversed into vasoconstriction by dopamine-induced alpha-adrenergic stimulation.

Animals↗

Modification by baroreceptor feedback of circulatory responses to noxious stimuli during anaesthesia in cats.

In eight cats anaesthetized with chloralose, the carotid sinus on one side was either exposed to systemic arterial pressure or perfused with a pump in order to control sinus pressure. Baroreceptor influences from the contralateral carotid sinus and from the aortic arch were interrupted by denervation. Arrangements were made for intermittent electric stimulation of pain fibres in somatic and visceral nerves with stimulation parameters chosen to elicit reproducible increases in arterial blood pressure and in skeletal muscle vascular resistance. The elicited increases in arterial pressure and muscle vascular resistance were both about 40% smaller when the carotid sinus was exposed to systemic arterial pressure in comparison with the experimental condition of a constant carotid sinus pressure. I.v. metoprolol (0.1-0.3 mg kg-1) reduced base-line arterial pressure, but did not attenuate the arterial blood pressure increase in response to pain stimulation. The baroreceptor modulation of the haemodynamic response to the pain stimulation was not affected by metoprolol.

Anesthesia, General↗

Measurement of cardiac stroke volume during cesarean section: a comparison between impedance cardiography and the dye dilution technique.

Simultaneous determination of cardiac stroke volume by impedance cardiography and the dye dilution technique was compared in ten women undergoing elective cesarean section performed under general or epidural anesthesia. The influence of delivery and the anesthetic procedures used on stroke volume determination by the two methods was evaluated and compared. The correlation coefficients for measurements performed before and during anesthesia showed little variation and were largely unchanged after delivery of the child (r = 0.90-0.97). Mean stroke volume determined by impedance cardiography was significantly (P less than 0.001) lower than mean stroke volume calculated from the dye dilution technique. However, there was no significant difference between the mean change in stroke volume determined by the two techniques during serial measurements. Impedance cardiography was found to be a safe, reliable, non-invasive technique for the measurement of changes in stroke volume during cesarean section. The ability of the impedance method to determine changes in stroke volume was unaffected by the anesthetic procedures employed or by delivery of the child.

Anesthesia, Epidural↗

Influence of dixyrazine on intestinal and renal vasoconstrictor responses during fentanyl-nitrous oxide anaesthesia.

In cats (n = 24) anaesthetized with fentanyl-nitrous oxide and diazepam, stimulation of the hypothalamic defence-alarm area (DA) or afferent activation of somatic pain fibres (SA), elicited a pronounced increase in intestinal (DA 297%, SA 107%) and renal (DA 214%, SA 90%) vascular resistance as well as a decrease in diuresis. These stress-related responses were markedly counteracted by dixyrazine (0.15-0.5 mg X kg-1 b.w.i.v.), especially in the kidney where the subsequent increase in vascular resistance to DA and SA stimulations amounted to only 25% and 13%, respectively, while diuresis increased. Corresponding data for stimulation-induced increases in intestinal vascular resistance after dixyrazine were DA 156% and SA 28%. Dixyrazine is suggested to act both through interaction with peripheral alpha-adrenergic mechanisms in control of vascular tone and through central nervous cardiovascular reflex depression. In man (n = 7), during a similar form of anaesthesia, portal vein blood flow (1137 +/- 177 ml) was measured by the continuous thermodilution method. Preportal tissue vascular resistance during surgery decreased significantly (11.3 vs 8.7 kPa X min X ml-1 X 10(-3] after i.v. dixyrazine (0.15 mg X kg-1 b.w.). A concomitant increase in oxygen uptake in preportal tissues occurred (19.9 ml min-1 vs 24.5 ml X min-1).

Aged↗

In vitro analysis of thermal transport in coronary sinus thermodilution catheters.

The continuous thermodilution technique for measuring blood flow in the range 50-300 ml/min was evaluated in vitro. Experiments indicated that thermotransport within the catheter from the indicator line to the mixing thermistor exists. The resulting error in calculated thermodilution flow will increase with increasing flow rate. A correction factor for thermal transport, Ft, obtained from a blood circulation model was incorporated in a modified formula for calculation of thermodilution flow. Flows derived with the standard Ganz formula were significantly lower than timed volumetric flows, whereas flows obtained with the modified formula agreed with volumetric flow. The coefficient of variation for four consecutive measurements was 3.4%.

Blood Flow Velocity↗

Portal blood flow in man during surgery, measured by a modification of the continuous thermodilution method.

The continuous thermodilution method was applied to measurement of peroperative portal venous blood flow in man in relation to hepatic surgery during steady-state enflurane nitrous oxide anaesthesia. Portal-vein catheterization through the umbilical vein for cytostatic administration and blood flow measurements was successful in 14 out of 17 patients with primary or secondary liver tumours. Mean portal blood flow was 1195 +/- 179 ml X min-1 (mean +/- SEM), corresponding to 17.6 +/- 2.9 ml X min-1 X kg-1 body weight. Mean oxygen consumption in the prehepatic splanchnic area was 0.27 +/- 0.04 ml X min-1 X kg-1. No significant complications were associated with the catheterization or flow recording procedures. The described method offers possibilities for haemodynamic and pharmacokinetic investigations in man.

Catheterization↗

Long-term beta-receptor blockade--adrenergic and metabolic response to surgery and neurolept anaesthesia.

Twenty-six patients on chronic (greater than 3 months) beta-receptor blocking therapy due to ischaemic heart disease and/or hypertension were randomly distributed to a 4-day gradual withdrawal (n = 13) or a continuation of ordinary therapy until a planned cholecystectomy under neurolept anaesthesia (n = 13). Plasma-adrenaline, -noradrenaline, -potassium, -glycerol, -FFA, -insulin and b-glucose were determined perioperatively. The metabolic response to surgery was as expected with hyperglycaemia and depressed insulin levels, which did not differ significantly between the two groups of patients. Plasma-catecholamines showed the highest mean values during emergence from anaesthesia. Plasma-adrenaline and -potassium were constantly highest in the beta-receptor-blocked patients, who also showed indices of a relatively depressed lipolysis compared to patients in whom beta-receptor blockers had been withdrawn. These discrepancies between withdrawal versus continuation of preoperative beta-receptor blockade seemed to be of small clinical importance and did not oppose the present view that beta-receptor blockers should generally be continued during surgery. However, findings in individual patients suggest that beta-receptor blockade may maintain hypoglycaemia in catabolic patients.

Adrenergic beta-Antagonists↗

beta-Receptor blockade and neurolept anaesthesia. Withdrawal vs continuation of long-term therapy in gall-bladder and carotid artery surgery.

Forty-eight chronically (greater than 3 months) beta-receptor-blocked patients with ischaemic heart disease and/or hypertension were studied on 49 occasions after random distribution to a 4-day, gradual preoperative withdrawal (n = 26) or a continuation (n = 23) of beta-receptor blockers. The patients were scheduled for either a cholecystectomy (n = 28) or a carotid thrombendarterectomy (n = 21) under neurolept anaesthesia. Three patients were excluded from the randomized part of the study due to complications (tachycardia, hypertension, severe angina) after therapy withdrawal. In subgroups, central haemodynamics (beta-receptor blockers withdrawn n = 6, continued n = 8) and creatinine-kinase B (beta-receptor blockers withdrawn n = 9, continued n = 11) were studied. Withdrawal of beta-receptor blockers was associated with high heart rates, supraventricular tachyarrhythmias and a hyperkinetic circulation during pain stimuli. Significantly more postoperative ECG changes (P less than 0.02) indicative of myocardial ischaemia were found than in beta-receptor blocked patients. These patients had low heart rates but also pronounced increases in pulmonary capillary wedge pressures, which in single patients could be associated with myocardial damage. These results imply that beta-receptor blockers should be continued before surgery and that a concomitant vasodilatatory therapy is likely to avoid the drawbacks of an increased cardiac afterload.

Adrenergic beta-Antagonists↗