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Featured researches published by J. Hall.


Critical Care Medicine | 2002

Crystalloid strong ion difference determines metabolic acid-base change during in vitro hemodilution.

Thomas J. Morgan; Balasubramanian Venkatesh; J. Hall

Objectives To determine the relationship between the strong ion difference (SID) of a diluting crystalloid and its metabolic acid-base effects on in vitro blood dilution. Design Prospective in vitro study. Setting University research laboratory. Subjects Normal human blood. Interventions Three solutions were prepared, each with [Na] = 140 mmol/L. [Cl−] for solutions 1, 2, and 3 was 120, 110, and 100 mmol/L, respectively, the other anion being HCO3−. SID values were thus 20, 30, and 40 mEq/L, respectively. Serial dilutions of well-oxygenated fresh venous blood were performed anaerobically by using each of solutions 1–3 as well as 0.9% saline (SID = 0 mEq/L) and Hartmanns solution (SID = −4 mEq/L). Measurements and Main Results Blood gas and electrolyte analyses were performed before and after each dilution. Apart from dilutions with solution 3 (crystalloid SID 40 mEq/L) during which plasma SID did not change, plasma SID decreased during hemodilution. In contrast, base excess increased during hemodilution with solutions 3 and 2 (crystalloid SID 40 mEq/L and 30 mEq/L, respectively) and decreased only with the remaining three solutions. The relationships between hemoglobin concentrations and both plasma SID and whole blood base excess throughout dilution were linear, with slopes proportional to the SID of the diluent in each case. Linear regression revealed that the SID of crystalloid producing a zero base excess/hemoglobin concentration slope during blood dilution (i.e., no change in metabolic acid-base status) is 23.7 mEq/L. Conclusions On in vitro hemodilution, there is a simple linear relationship between diluent crystalloid SID and the rate and direction of change of plasma SID and whole blood base excess. Direct extrapolation to in vivo situations such as acute normovolemic hemodilution and large volume correction of extracellular fluid deficits requires experimental confirmation.


Anaesthesia and Intensive Care | 2005

Evaluation of random plasma cortisol and the low dose corticotropin test as indicators of adrenal secretory capacity in critically ill patients: a prospective study.

Bala Venkatesh; R. H. Mortimer; B. Couchman; J. Hall


Intensive Care Medicine | 2004

Crystalloid strong ion difference determines metabolic acid–base change during acute normovolaemic haemodilution

Thomas J. Morgan; Balasubramanian Venkatesh; J. Hall


Anaesthesia and Intensive Care | 2004

Serum procalcitonin and C-reactive protein as markers of sepsis and outcome in patients with neurotrauma and subarachnoid haemorrhage

E. O'Connor; Bala Venkatesh; C. Mashongonyika; Jeffrey Lipman; J. Hall; Peter Thomas


Intensive Care Medicine | 2007

Evidence of altered cortisol metabolism in critically ill patients: a prospective study

Bala Venkatesh; Jeremy Cohen; Ingrid J. Hickman; Janelle Nisbet; Peter Thomas; Gregory Ward; J. Hall; John Prins


Anaesthesia and Intensive Care | 2009

Changes in serum procalcitonin and C-reactive protein following antimicrobial therapy as a guide to antibiotic duration in the critically ill: a prospective evaluation

Bala Venkatesh; P. Kennedy; Peter Kruger; David Looke; Mark Jones; J. Hall; G. R. Barruel


Critical Care and Resuscitation | 2001

Procalcitonin in critical illness.

O'Connor E; Balasubramanian Venkatesh; Jeffrey Lipman; Mashongonyika C; J. Hall


Anaesthesia and Intensive Care | 2007

Acid-base and bio-energetics during balanced versus unbalanced normovolaemic haemodilution.

Thomas J. Morgan; Bala Venkatesh; A. Beindorf; I Andrew; J. Hall


Intensive Care Medicine | 2005

Subcutaneous gas tensions closely track ileal mucosal gas tensions in a model of endotoxaemia without anaerobism.

Bala Venkatesh; Thomas J. Morgan; J. Hall; Zolton Endre; D. A. Willgoss


Critical Care and Resuscitation | 2003

Interpreting CSF lactic acidosis: effect of erythrocytes and air exposure.

Bala Venkatesh; Thomas J. Morgan; Robert J. Boots; J. Hall; D. Siebert

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Bala Venkatesh

University of Queensland

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Thomas J. Morgan

Mater Misericordiae Hospital

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D. A. Willgoss

University of Queensland

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Jeffrey Lipman

University of Queensland

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Mark Jones

University of Queensland

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Peter Thomas

Royal Brisbane and Women's Hospital

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David Looke

Princess Alexandra Hospital

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Glenda C. Gobe

University of Queensland

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Gregory Ward

University of Queensland

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