Right-to-left shunt in normal man determined by the use of tritium and krypton 85

1962 ◽  
Vol 17 (5) ◽  
pp. 778-782 ◽  
Author(s):  
K. Mellemgaard ◽  
N. A. Lassen ◽  
J. Georg

An aqueous solution of tritium and krypton 85 together with Evans blue dye was injected intravenously in twelve normal subjects during quiet breathing, during apnea, and during voluntary hyperventilation. Arterial blood was sampled within the first 30 sec after the injection to measure the recovery of the two gases. Blood-gas partition coefficients of the two gases at 37 C were determined experimentally and the ratio between them was found to be 3.8 in normal blood. Knowing this ratio it is possible to calculate the fraction of the arterial recovery due to a right-to-left shunt, and that due to alveolar back pressure. The shunt calculated from findings during quiet breathing is 0.26% of the cardiac output. Recoveries during apnea lead to a calculated shunt of identical size, whereas the shunt calculated from the experiments during hyperventilation amounts to only 0.11% of the cardiac output. Submitted on March 8, 1962

1961 ◽  
Vol 1 (04) ◽  
pp. 353-379
Author(s):  
Jacques Lammerant ◽  
Norman Veall ◽  
Michel De Visscher

Summary1. The technique for the measurement of cardiac output by external recording of the intracardiac flow of 131I labelled human serum albumin has been extended to provide a measure of the mean circulation time from right to left heart and hence a new approach to the estimation of the pulmonary blood volume.2. Values for the basal cardiac output in normal subjects and its variations with age are in good agreement with the previously published data of other workers.3. The pulmonary blood volume in normal man in the basal state was found to be 28.2 ± 0.6% of the total blood volume.4. There was no correlation between cardiac output and pulmonary blood volume in a series of normal subjects in the basal state.5. The increase in cardiac output during digestion was associated with a decrease in pulmonary blood volume equal to 6.3 ± 1.2% of the total blood volume, that is, about 280 ml.6. The increase in cardiac output during exercise was associated with a decrease in pulmonary blood volume equal to 4.5 ± 1.0% of the total blood volume, that is, about 200 ml.7. The increase in cardiac output attributed to alarm is not associated with a decrease in pulmonary blood volume, the latter may in fact be increased.8. The total blood volume is advocated as a standard of reference for studies of this type in normal subjects in preference to body weight or surface area.9. The significance of these results and the validity of the method are discussed.


1981 ◽  
Vol 51 (5) ◽  
pp. 1103-1107 ◽  
Author(s):  
P. W. Jones ◽  
W. French ◽  
M. L. Weissman ◽  
K. Wasserman

Cardiac output changes were induced by step changes of heart rate (HR) in six patients with cardiac pacemakers during monitoring of ventilation and gas exchange, breath-by-breath. Mean low HR was 48 beats/min; mean high HR was 82 beats/min. The change of oxygen uptake immediately after the HR change was used as an index of altered cardiac output. After HR increase, oxygen uptake (V02) rose by 34 +/- 20% (SD), and after HR decrease, Vo2 fell by 24 +/- 11%. There was no change in arterial blood pressure. After HR increase, ventilation increased, after a mean delay of 19 +/- 4 s; after HR reduction, ventilation fell, after a mean delay of 29 +/- 7 s. In the period between HR increase and the resulting increase in ventilation, end-tidal PCO2 (PETCO2) rose by 2.6 +/- 2.0 Torr, and in the period between HR decreases and the fall in ventilation, PETCO2 dropped by 2.9 +/- 2.2 Torr. The response time and end-tidal gas tension changes implicate the chemoreceptors in the reflex correction of blood gas disturbances that may result from imbalances between cardiac output and ventilation.


1973 ◽  
Vol 45 (6) ◽  
pp. 733-742 ◽  
Author(s):  
N. K. Hollenberg ◽  
D. F. Adams ◽  
P. Mendell ◽  
H. L. Abrams ◽  
J. P. Merrill

1. The renal vascular response to intravenously administered dopamine was assessed in normal man by selective renal arteriography and xenon washout. Infusion of 3 μg min−1 kg−1 induced renal vasodilatation with an increase in the cortical component of blood flow. Arterial blood pressure was not influenced and a systemic effect was not demonstrable. Lower doses did not induce a renal response. Increasing dosage raised arterial blood pressure and induced subjective symptoms, but did not result in a further increase in renal blood flow. 2. Renal vascular resistance increased with increasing age in the normal subjects. A significant inverse relationship was found between the initial vascular resistance and the renal vasodilator response to dopamine. It thus appears that the vascular effects of increasing age (nephrosclerosis) may limit the dilator response to dopamine. 3. It is concluded that dopamine is an effective renal cortical vasodilator when administered intravenously at doses which are free from other systemic cardiovascular effects. The dose-response relationship must be considered in attempts at reversal of conditions characterized by renal vasoconstriction.


2012 ◽  
Vol 113 (4) ◽  
pp. 541-548 ◽  
Author(s):  
Tracey L. Bryan ◽  
Sean van Diepen ◽  
Mohit Bhutani ◽  
Miriam Shanks ◽  
Robert C. Welsh ◽  
...  

The development of intrapulmonary shunts with increased cardiac output during exercise in healthy humans has been reported in several recent studies, but mechanisms governing their recruitment remain unclear. Dobutamine and dopamine are inotropes commonly used to augment cardiac output; however, both can increase venous admixture/shunt fraction (Qs/Qt). It is possible that, as with exercise, intrapulmonary shunts are recruited with increased cardiac output during dobutamine and/or dopamine infusion that may contribute to the observed increase in Qs/Qt. The purpose of this study was to examine how dobutamine and dopamine affect intrapulmonary shunt and gas exchange. Nine resting healthy subjects received serial infusions of dobutamine and dopamine at incremental doses under normoxic and hyperoxic (inspired O2fraction = 1.0) conditions. At each step, alveolar-to-arterial Po2difference (A-aDo2) and Qs/Qt were calculated from arterial blood gas samples, intrapulmonary shunt was evaluated using contrast echocardiography, and cardiac output was calculated by Doppler echocardiography. Both dobutamine and dopamine increased cardiac output and Qs/Qt. Intrapulmonary shunt developed in most subjects with both drugs and paralleled the increase in Qs/Qt. A-aDo2was unchanged due to a concurrent rise in mixed venous oxygen content. Hyperoxia consistently eliminated intrapulmonary shunt. These findings contribute to our present understanding of the mechanisms governing recruitment of these intrapulmonary shunts as well as their impact on gas exchange. In addition, given the deleterious effect on Qs/Qt and the risk of neurological complications with intrapulmonary shunts, these findings could have important implications for use of dobutamine and dopamine in the clinical setting.


1961 ◽  
Vol 16 (2) ◽  
pp. 321-325 ◽  
Author(s):  
Niels A. Lassen ◽  
K. Mellemgaard ◽  
J. Georg

A method is described for estimating right-to-left shunts through the determination of the recovery of intravenously injected tritium gas in the arterial blood. Tritiated water was used as an indicator of the dilution that would have occurred had no loss of tritium gas taken place in the alveoli. In normal man, average recovery values obtained were: 1.1% during normal respiration, 0.6% during hyperventilation, 0.9% during inspiratory apnea and 1.8% during expiratory apnea. In two patients with congenital heart disease large recovery values were found with right-to-left shunt, agreeing with the shunt estimates obtained using oxygen analysis. While no significant diffusion limitation at the alveolar membrane can be supposed to occur normally, a significant back pressure results from the gradually increasing alveolar tritium concentration. This factor is presumably responsible for the greater part of the recovery found in normal man, while a smaller part may be due to actual bypassing of the alveoli. On the basis of the experiments it is estimated that in normal man 0.3% of the blood entering the right side of the heart reaches the left side without passing air-filled alveoli. Submitted on November 5, 1960


1990 ◽  
Vol 69 (6) ◽  
pp. 2091-2096 ◽  
Author(s):  
B. L. Brizzee ◽  
B. R. Walker

Experiments were performed on conscious chronically instrumented rats to determine the contribution of peripheral V2-vasopressinergic receptors in any alteration of baroreceptor reflex (BRR) sensitivity on release from 1 wk of 30 degrees head-down tilt resulting from tail suspension. Initial experiments determined changes in plasma volume (PV) occurring over this period by use of the Evans Blue dye dilution technique. PV was determined immediately before tail suspension and on day 7 of the stimulus. PV, erythrocyte volume, and total blood volume were all significantly diminished on day 7, whereas hematocrit was unchanged. Other rats were instrumented with pulsed Doppler flow probes on the ascending aorta for determination of cardiac output and with arterial and venous catheters 7-10 days before study. Immediately before tail suspension, control cardiac output, mean arterial blood pressure, and heart rate values were determined. In addition, BRR sensitivity was estimated both before and after intravenous administration of a V2-receptor antagonist by assessing the slope of the pulse interval-mean arterial blood pressure relationship in response to a series of pressor doses of phenylephrine. BRR sensitivity was determined on the last day of head-down tilt, 1 min after release from tail suspension, and 10 min after administration of a specific V2-vasopressinergic antagonist. BRR sensitivity tended to fall on day 7 of tail suspension compared with control and was significantly increased after release. However, BRR sensitivity was not altered by intravenous V2 antagonist administration either before tail suspension or after release.(ABSTRACT TRUNCATED AT 250 WORDS)


1964 ◽  
Vol 19 (6) ◽  
pp. 1145-1150 ◽  
Author(s):  
William R. Keatinge ◽  
Malcolm B. McIlroy ◽  
Alan Goldfien

A shower of ice-cold water (0@#X2013;2.5 C) over the chest caused large increases in systolic and diastolic arterial pressures, pulse pressure, and pulse rate in normal subjects. Cardiac output rose by 59 and 100% in the two subjects in whom it was measured. The changes in pressure were considerably larger than those caused by a cold pressor test or by anxiety. The changes appear to be due to sympathetic nervous reflexes to the heart and blood vessels rather than release of adrenal catecholamines, as plasma epinephrine did not increase and plasma norepinephrine rose only by 0.32 @#X00B5;g/liter. Hyperventilation and evidence of peripheral venoconstriction occurred during the showers, but neither voluntary hyperventilation nor increased venous return from a change in posture produced the changes in blood pressure seen during shower arterial blood pressure; cardiac output; catecholamines; sympathetic nervous reflexes; hyperventilation; peripheral venoconstriction Submitted on March 10, 1964


Blood ◽  
2016 ◽  
Vol 128 (22) ◽  
pp. 1462-1462 ◽  
Author(s):  
John-Paul Tung ◽  
Gabriela Simonova ◽  
Sara Diab ◽  
Kimble Dunster ◽  
Margaret Passmore ◽  
...  

Abstract Introduction Despite the introduction of risk reduction strategies, transfusion-related acute lung injury (TRALI) continues to be a significant cause of morbidity and mortality. TRALI development may be associated with the transfusion of anti-leucocyte antibodies or biological response modifiers (BRMs). Our group has previously developed a model in which the development of TRALI in lipopolysaccharide (LPS) treated sheep was precipitated by the transfusion of pooled supernatant from date-of-expiry (day (d) 42) packed red blood cell (PRBC) units. This work pre-dated the introduction of pre-storage leukodepletion of PRBCs in Australia, therefore we investigated whether TRALI would still develop in LPS-treated sheep transfused with supernatant from d42 leukodepleted PRBCs. Methods On either d2 (n=75 units) or d42 (n=113 units) of storage, leukodepleted PRBCs underwent dual centrifugation to obtain acellular supernatants. Two supernatant pools (d2 and d42) were then prepared by pooling and heat-treating (56°C for 30min) the supernatants. Levels of potential BRMs in the PRBC supernatant pools were characterised using cytometric bead array and ELISA. Instrumented sheep (n=14) were infused with LPS then transfused (10% v/v) with either d2 (n=7) or d42 (n=7) pooled PRBC supernatant. Two hours later sheep were euthanized and post-mortem lung samples were collected. Physiological data were recorded continuously and then averaged in 30 minute blocks for these preliminary analyses. Blood and broncoalveolar lavage (BAL) fluid samples were collected at specific intervals. Blood samples were used for arterial blood gas analyses, coagulation tests (ROTEM), platelet function tests (MultiPlate) and ELISAs. TRALI was defined by hypoxemia (PaO2/FiO2 < 300 on arterial blood gas) and histological evidence of pulmonary edema (by two blinded histopathological assessments of hematoxylin and eosin stained lung sections). Data were compared by group (sheep transfused with d2 PRBC supernatant vs. d42 PRBC supernatant) and by outcome (sheep who developed TRALI vs. those who did not) with either t-tests or 2-way ANOVAs as appropriate. Results and Discussion Storage duration of leukodepleted PRBC was associated with increased levels of the potential BRMs 5-HETE, 12-HETE, 15-HETE and IL-8, but not soluble CD40 ligand. Only 3 sheep developed TRALI: one transfused with d2 leukodepleted PRBC supernatant and two transfused with d42 leukodepleted PRBC supernatant corresponding to an incidence of 14% and 29% respectively. This indicated a reduced incidence of TRALI in the sheep model compared to previous data using supernatant from d42 non-leukodepleted PRBC which resulted in an incidence of 75% (Tung et al. Vox Sanguinis. 2011). Preliminary analyses of the physiological data revealed a number of differences. Heart rate (P<0.001), blood pressure (P=0.003), pulmonary artery pressure (P<0.001), cardiac output (P<0.001) and PaO2/FiO2 (P<0.001) were different between sheep transfused with either d2 or d42 PRBC supernatant. Heart rate (P<0.001), pulmonary artery pressure (P<0.001), pulse oximeter oxygen saturation (P=0.003), cardiac output (P<0.001) and PaO2/FiO2 (P<0.001) were different between sheep that developed TRALI and sheep that did not. However, given the complexity of these data, further analyses using mixed effects modelling are required to better understand these differences. Sheep transfused with d42 PRBC supernatant had reduced IL-1β lung gene expression and reduced ADP-induced platelet aggregation (both total and area under curve) compared to sheep transfused with d2 PRBC supernatant (P=0.047, 0.012 and 0.028 respectively). In addition, sheep that developed TRALI had worse lung histology scores as well as reduced collagen-induced platelet aggregation (both total and area under curve) compared to sheep who did not develop TRALI (P=0.024, 0.049 and 0.018 respectively). Conclusions Comparison of these results to previously published data from the sheep model is suggestive that pre-storage leukodepletion of PRBCs is associated with a reduced incidence of TRALI. Unsurprisingly, the development of TRALI was associated with worsened respiratory function (oxygen saturation and PaO2/FiO2) and lung histology scores, while changes in hemodynamics and platelet function were also observed. Disclosures Fraser: Fisher and Paykel Healthcare: Consultancy, Other: Provision of equipment for research use, Research Funding; De Motu Cordis: Equity Ownership, Membership on an entity's Board of Directors or advisory committees.


1979 ◽  
Vol 47 (1) ◽  
pp. 112-118 ◽  
Author(s):  
T. V. Santiago ◽  
J. Johnson ◽  
D. J. Riley ◽  
N. H. Edelman

The effects of analgesic doses of morphine on ventilation, arterial blood gas tensions, chemical control of breathing, and the ventilatory response to exercise were studied in six normal subjects. After administration of 0.2 mg/kg morphine, resting ventilation decreased primarily because of a reduction of tidal volume. Ventilatory responses to carbon dioxide and hypoxia were significantly reduced to one-half and one-third of control, respectively. Ventilatory responses at any given level of exercise were significantly reduced after morphine. However, since oxygen consumption during exercise was similarly reduced after morphine, the relationship between ventilation and metabolic rate during steady-state exercise was not altered by the drug. In addition, morphine prolonged the attainment of steady-state ventilation in four of the six subjects, similar to that reported for chemodenervated subjects. The findings suggest that blunting of chemoreception for hypoxia and hypercapnia has no effect upon the link between metabolic rate and ventilation during steady-state exercise, but the hypoxia chemoreflex may be involved in determining the dynamic characteristics of the response.


1989 ◽  
Vol 67 (6) ◽  
pp. 2627-2630 ◽  
Author(s):  
R. Dal Negro ◽  
L. Allegra

Twenty-eight asymptomatic asthmatics and 28 healthy volunteers were challenged with ultrasonically nebulized distilled water (UNDW). Blood gas composition was monitored transcutaneously (PtCO2 and PtcCO2) over 42 min (20 min for electrode stability, 3 min base line, 5 min during UNDW, and 14 min after UNDW). Flow-volume curves were recorded before and 15 min after UNDW. Forced expiratory volume in 1 s and expiratory flows decreased in asthmatics but not in normal subjects after UNDW. Mean base-line PtCO2 and PtcCO2 were comparable in the two groups. UNDW in normal subjects produced no significant changes in mean PtcCO2 and PtCO2. In asthmatics, the UNDW-induced decrease in mean PtcCO2 was greater and longer lasting, accompanied by a prolonged decrease in mean PtCO2. PtcCO2 and PtCO2 trends showed highly significant differences compared with healthy volunteers (P less than 0.001). Arterial blood gas measurements validated these changes. UNDW in asymptomatic asthmatics gives rise to a greater and more prolonged hyperventilation than in normal subjects and to gas-exchange abnormalities presumably reflecting a ventilation-perfusion mismatching.


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