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Dive into the research topics where Venny L. Kvalheim is active.

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Featured researches published by Venny L. Kvalheim.


Scandinavian Cardiovascular Journal | 2006

Mean arterial pressure about 40 mmHg during CPB is associated with cerebral ischemia in piglets

Oddbjørn Haugen; Marit Farstad; Venny L. Kvalheim; Stein-Erik Rynning; Stig Morten Hammersborg; Arve Mongstad; Paul Husby

Objective. To investigate if a mean arterial pressure below 50 mmHg during CPB may lead to cerebral ischemia. Material and methods. Piglets with low mean arterial pressure by nitroprusside (LP-group) (n = 6) were compared with piglets given norepinephrine to obtain high pressure (HP-group) (n = 6) during normothermic and hypothermic CPB. Intracranial pressure, flow and markers of cerebral energy metabolism (microdialysis) were recorded. Results. Mean arterial pressure differed significantly between the groups and stabilized about 40–45 mmHg in the LP-group. Cerebral perfusion pressure decreased to 21.3 (7.7) mmHg in the LP-group and increased to 51.8 (11.2) mmHg in the HP-group at 150 min of CPB (P < 0.001, between groups). During bypass the intracerebral glucose concentration decreased significantly in the LP-group. In this group the lactate/pyruvate ratio increased from 15.5 (5.3) to 64.5 (87.6) at 90 min and 45.0 (36.5) at 150 min (P < 0.05) with no such changes in the HP-group. Similarly the cerebral glycerol concentration increased significantly in the LP-group, whereas glycerol remained stable in the HP-group. Conclusion. Mean arterial pressure about 40 mmHg during CPB is associated with cerebral ischemia.


Acta Anaesthesiologica Scandinavica | 2010

Infusion of hypertonic saline/starch during cardiopulmonary bypass reduces fluid overload and may impact cardiac function.

Venny L. Kvalheim; M. Farstad; E. Steien; Arve Mongstad; B. A. Borge; P. M. Kvitting; Paul Husby

Objective: Peri‐operative fluid accumulation resulting in myocardial and pulmonary tissue edema is one possible mechanism behind post‐operative cardiopulmonary dysfunction. This study aimed to confirm an improvement of cardiopulmonary function by reducing fluid loading during an open‐heart surgery.


The Annals of Thoracic Surgery | 2015

Intraaortic counterpulsation during cardiopulmonary bypass impairs distal organ perfusion.

Steinar Lundemoen; Venny L. Kvalheim; Øyvind Sverre Svendsen; Arve Mongstad; Knut S. Andersen; Ketil Grong; Paul Husby

BACKGROUND Recent studies have focused on the use of fixed-rate intraaortic balloon pumping (IABP) during cardiopulmonary bypass (CPB) to achieve pulsatile flow. Because application of an IABP catheter may represent a functional obstruction within the descending aorta, we explored the effect of IABP-pulsed CPB-perfusion with special attention to perfusion above and below the IABP balloon. METHODS Sixteen animals received an IABP catheter that remained turned off position (NP group, n = 8) or was switched to an automatic mode of 80 beats/min during CPB (PP group, n = 8). Flow-data and pressure-data were obtained above and below the IABP balloon. Tissue perfusion was evaluated by microspheres. RESULTS IABP-pulsed CPB-perfusion, as assessed at 30 minutes on CPB, increased proximal mean aortic pressure (p < 0.05) and carotid artery blood flow (p < 0.001), but decreased distal mean aortic pressure (p < 0.001). The decrease of distal mean aortic pressure in the PP group was associated with a 75 % decrease (p < 0.001) of renal tissue perfusion. During nonpulsed perfusion the respective variables remained essentially unchanged compared with pre-CPB levels. CONCLUSIONS Using IABP as a surrogate to achieve pulsatile perfusion during CPB contributes significantly to lowered aortic pressure in the distal portion of aorta and impaired tissue perfusion of the kidneys. The results are focusing on effects that may contribute to organ dysfunction and acute kidney injury. Consequently, assessment of perfusion pressure distal to the balloon should be addressed whenever IABP is used during CPB.


Acta Anaesthesiologica Scandinavica | 2006

Reduced fluid gain during cardiopulmonary bypass in piglets using a continuous infusion of a hyperosmolar/hyperoncotic solution

M. Farstad; Oddbjørn Haugen; Venny L. Kvalheim; Stig Morten Hammersborg; S. E. Rynning; Arve Mongstad; Else Nygreen; Paul Husby

Background:  The aim of this study was to evaluate how a continuous infusion of a hyperosmolar/hyperoncotic solution influences fluid shifts and intracranial pressure during cardiopulmonary bypass in piglets.


Anesthesiology | 2013

Isoflurane in contrast to propofol promotes fluid extravasation during cardiopulmonary bypass in pigs.

Hege Kristin Brekke; Stig Morten Hammersborg; Steinar Lundemoen; Arve Mongstad; Venny L. Kvalheim; Oddbjørn Haugen; Paul Husby

Background:A highly positive intraoperative fluid balance should be prevented as it negatively impacts patient outcome. Analysis of volume-kinetics has identified an increase in interstitial fluid volume after crystalloid fluid loading during isoflurane anesthesia. Isoflurane has also been associated with postoperative hypoxemia and may be associated with an increase in alveolar epithelial permeability, edema formation, and hindered oxygen exchange. In this article, the authors compare fluid extravasation rates before and during cardiopulmonary bypass (CPB) with isoflurane- versus propofol-based anesthesia. Methods:Fourteen pigs underwent 2 h of tepid CPB with propofol (P-group; n = 7) or isoflurane anesthesia (I-group; n = 7). Fluid requirements, plasma volume, colloid osmotic pressures in plasma and interstitial fluid, hematocrit levels, and total tissue water content were recorded, and fluid extravasation rates calculated. Results:Fluid extravasation rates increased in the I-group from the pre-CPB level of 0.27 (0.13) to 0.92 (0.36) ml·kg−1·min−1, but remained essentially unchanged in the P-group with significant between-group differences during CPB (pb = 0.002). The results are supported by corresponding changes in interstitial colloid osmotic pressure and total tissue water content. Conclusions:During CPB, isoflurane, in contrast to propofol, significantly contributes to a general increase in fluid shifts from the intravascular to the interstitial space with edema formation and a possible negative impact on postoperative organ function.


Scandinavian Cardiovascular Journal | 2008

Fluid overload during cardiopulmonary bypass is effectively reduced by a continuous infusion of hypertonic saline/dextran (HSD)

Venny L. Kvalheim; S. E. Rynning; Marit Farstad; Oddbjørn Haugen; Else Nygreen; Arve Mongstad; Paul Husby

Objective. Cardiopulmonary bypass (CPB) is associated with fluid overload. We examined how a continuous infusion of hypertonic saline/dextran (HSD) influenced fluid shifts during CPB. Materials and methods. Fourteen animals were randomized to a control-group (CT-group) or a hypertonic saline/dextran-group (HSD-group). Ringers solution was used as CPB-prime and as maintenance fluid at a rate of 5 ml/kg/h. In the HSD group, 1 ml/kg/h of the maintenance fluid was substituted with HSD. After 60 min of normothermic CPB, hypothermic CPB was initiated and continued for 90 min. Fluid was added to the CPB-circuit as needed to maintain a constant level in the venous reservoir. Fluid balance, plasma volume, total tissue water (TTW), intracranial pressure (ICP) and fluid extravasation rates (FER) were measured/calculated. Results. In the HSD-group the fluid need was reduced with 60% during CPB compared with the CT-group. FER was 0.38(0.06) ml/kg/min in the HSD-group and 0.74 (0.16) ml/kg/min in the CT-group. TTW was significantly lower in the heart and some of the visceral organs in the HSD-group. In this group ICP remained stable during CPB, whereas an increase was observed in the CT-group (p <0.01). Conclusions. A continuous infusion of HSD reduced the fluid extravasation rate and total fluid gain during CPB. TTW was reduced in the heart and some visceral organs. During CPB ICP remained normal in the HSD-group, whereas an increase was present in the CT-group. No adverse effects were observed.


Perfusion | 2008

A hyperosmolar-colloidal additive to the CPB-priming solution reduces fluid load and fluid extravasation during tepid CPB:

Venny L. Kvalheim; M. Farstad; Oddbjørn Haugen; Hege Kristin Brekke; Arve Mongstad; Else Nygreen; Paul Husby

Cardiopulmonary bypass(CPB) is associated with fluid overload. We hypothesized that fluid gain during CPB could be reduced by substituting parts of a crystalloid prime with 7.2% hypertonic saline and 6% poly(O-2-hydroxyethyl) starch solution (HyperHaes®). 14 animals were randomized to a control group (Group C) or to Group H. CPB-prime in Group C was Ringer’s solution. In group H, 4 ml/kg of Ringer’s solution was replaced by the hypertonic saline / hydroxyethyl starch solution. After 60 min stabilization, CPB was initiated and continued for 120 min. All animals were allowed drifting of normal temperature (39.0°C) to about 35.0°C. Fluid was added to the CPB circuit as needed to maintain a 300-ml level in the venous reservoir. Blood chemistry, hemodynamic parameters, fluid balance, plasma volume, fluid extravasation rate (FER), tissue water content and acid-base parameters were measured/calculated. Total fluid need during 120 min CPB was reduced by 60% when hypertonic saline/hydroxyethyl starch solution was added to the CPB prime (p<0.01). The reduction was related to a lowered FER. The effect was most pronounced during the first 30 min on CPB, with 0.6 (0.43) (Group H) compared with 1.5 (0.40) ml/kg/min (Group C) (p<0.01). Hemodynamics and laboratory parameters were similar in both groups. Serum concentrations of sodium and chloride increased to maximum levels of 148 (1.5) and 112 (1.6) mmol/l in Group H. To conclude: addition of 7.2% hypertonic saline and 6% poly(O-2-hydroxyethyl) starch solution to crystalloid CPB prime reduces fluid needs and FER during tepid CPB.


Acta Anaesthesiologica Scandinavica | 2005

Low arterial pressure during cardiopulmonary bypass in piglets does not decrease fluid leakage

Oddbjørn Haugen; M. Farstad; Venny L. Kvalheim; S. E. Rynning; Arve Mongstad; Paul Husby

Background:  Cardiopulmonary bypass (CPB) is associated with increased fluid filtration occasionally leading to post‐operative organ dysfunction. One of the factors determining fluid filtration is the capillary hydrostatic pressure which depends on arterial pressure, venous pressure and pre‐ to post‐capillary resistance ratio. The purpose of this study was to assess whether lowering of the mean arterial pressure and/or the central venous pressure could reduce fluid extravasation during normothermic and hypothermic CPB.


Perfusion | 2007

Intraoperative fluid balance during cardiopulmonary bypass: effects of different mean arterial pressures

Oddbjørn Haugen; Marit Farstad; Venny L. Kvalheim; Stig Morten Hammersborg; Paul Husby

Financial support . This study was financially supported by The Western Norway Regional Health Authority, The Norwegian Council on Cardiovascular Diseases, Faculty of Medicine, University of Bergen and The Frank Mohn Foundation, Norway. Introduction. This study investigated whether two levels of mean arterial pressure (MAP) during cardiopulmonary bypass did influence per-operative fluid shifts. Methods. Sixteen pigs underwent 60 minutes of normothermic cardiopulmonary bypass (CPB) followed by 90 minutes of hypothermic CPB. Eight animals had a MAP of 60—80 mmHg by norepinephrine (HP group). Another 8 animals had a MAP of 40—45 mmHg by phentolamine (LP group). Blood chemistry, plasma/interstitial colloid osmotic pressures, plasma volume, fluid balance, fluid extravasation rate and tissue water content were measured or calculated. Results. The plasma volume was significantly lower in the HP group compared with the LP group after 60 minutes of CPB. Net fluid balance was 0.18 (0.05) ml·kg - 1·min - 1 in the HP group and 0.21 ml·kg - 1·min - 1 in the LP group (P > 0.05) while fluid extravasation rate was 1.18 (0.5) and 1.13 (0.4) ml·kg - 1·min - 1 in the HP group and the LP group during CPB (P > 0.05). Conclusion. Net fluid balance and fluid extravasation rate were similar in the animals with elevated and with lowered MAP during CPB. Perfusion (2007) 22, 273—278.


Perfusion | 2018

Is the use of hydroxyethyl starch as priming solution during cardiac surgery advisable? A randomized, single-center trial:

Øyvind Sverre Svendsen; Marit Farstad; Arve Mongstad; Rune Haaverstad; Paul Husby; Venny L. Kvalheim

Introduction: The use of cardiopulmonary bypass (CPB) leads to increased fluid filtration and edema. The use of artificial colloids to counteract fluid extravasation during cardiac surgery is controversial. Beneficial effects on global fluid loading, leading to better cardiac performance and hemodynamics, have been claimed. However, renal function and coagulation may be adversely affected, with unfavorable impact on outcome following cardiac surgery. Methods: Forty patients were randomly allocated to study groups receiving either acetated Ringer’s solution (CT group) or hydroxyethyl starch (HES group, Tetraspan®) as CPB priming solution. Fluid balance, bleeding and hemodynamics, including cardiac output, were followed postoperatively. The occurrence of acute kidney injury was closely registered. Results: Two patients were excluded from further analyzes due to surgical complications. Fluid accumulation was attenuated in the HES group (3374 (883) ml) compared with the CT group (4328 (1469) ml) (p=0.024). The reduced perioperative fluid accumulation was accompanied by an increased cardiac index immediately after surgery (2.7 (0.4) L/min/m2 in the HES group and 2.1 (0.3) L/min/m2 in the CT group (p<0.001)). No increase in bleeding could be demonstrated in the HES group. Three patients, all of them in the HES group, experienced acute kidney injury postoperatively. Conclusions: CPB priming with HES solution lowers fluid loading during bypass and improves cardiac function in the early postoperative period. The manifestation of acute kidney injury exclusively in the HES group of patients raises doubts about the use of HES products in conjunction with cardiac surgery. (https://clinicaltrials.gov/ct2/show/NCT01511120)

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Paul Husby

Haukeland University Hospital

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Arve Mongstad

Haukeland University Hospital

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Oddbjørn Haugen

Haukeland University Hospital

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Marit Farstad

Haukeland University Hospital

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M. Farstad

Haukeland University Hospital

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Steinar Lundemoen

Haukeland University Hospital

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Bjørg Elvevoll

Haukeland University Hospital

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Else Nygreen

Haukeland University Hospital

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