Comprehensive diagnosis of whole-body acid-base and fluid-electrolyte disorders using a mathematical model and whole-body base excess

Verfasser / Beitragende:
[Matthew Wolf]
Ort, Verlag, Jahr:
2015
Enthalten in:
Journal of Clinical Monitoring and Computing, 29/4(2015-08-01), 475-490
Format:
Artikel (online)
ID: 605510113
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024 7 0 |a 10.1007/s10877-014-9625-z  |2 doi 
035 |a (NATIONALLICENCE)springer-10.1007/s10877-014-9625-z 
100 1 |a Wolf  |D Matthew  |u Department of Pharmacology, Physiology and Neuroscience, School of Medicine, University of South Carolina, 29209, Columbia, SC, USA  |4 aut 
245 1 0 |a Comprehensive diagnosis of whole-body acid-base and fluid-electrolyte disorders using a mathematical model and whole-body base excess  |h [Elektronische Daten]  |c [Matthew Wolf] 
520 3 |a A mathematical model of whole-body acid-base and fluid-electrolyte balance was used to provide information leading to the diagnosis and fluid-therapy treatment in patients with complex acid-base disorders. Given a set of measured laboratory-chemistry values for a patient, a model of their unique, whole-body chemistry was created. This model predicted deficits or excesses in the masses of Na+, K+, Cl− and H2O as well as the plasma concentration of unknown or unmeasured species, such as ketoacids, in diabetes mellitus. The model further characterized the acid-base disorder by determining the patient's whole-body base excess and quantitatively partitioning it into ten components, each contributing to the overall disorder. The results of this study showed the importance of a complete set of laboratory measurements to obtain sufficient accuracy of the quantitative diagnosis; having only a minimal set, just pH and PCO2, led to a large scatter in the predicted results. A computer module was created that would allow a clinician to achieve this diagnosis at the bedside. This new diagnostic approach should prove to be valuable in the treatment of the critically ill. 
540 |a Springer Science+Business Media New York, 2014 
690 7 |a Acid-base balance  |2 nationallicence 
690 7 |a Fluid-electrolyte balance  |2 nationallicence 
690 7 |a Whole-body base excess  |2 nationallicence 
690 7 |a Metabolic acidosis  |2 nationallicence 
690 7 |a Bicarbonate space  |2 nationallicence 
690 7 |a Mathematical model  |2 nationallicence 
690 7 |a Atot : Electrical charge of plasma "weak” ions (mEq/lP)  |2 nationallicence 
690 7 |a ABS : Apparent bicarbonate space (lP/kg)  |2 nationallicence 
690 7 |a AG : Anion gap (mEq/lP)  |2 nationallicence 
690 7 |a AGadj : AG adjusted for albumin effect  |2 nationallicence 
690 7 |a AGc : AG corrected for albumin and Pi effects  |2 nationallicence 
690 7 |a Alb : Serum albumin  |2 nationallicence 
690 7 |a B : Blood  |2 nationallicence 
690 7 |a BE : Base excess (mEq/l)  |2 nationallicence 
690 7 |a BS : Bicarbonate space (lP/kg)  |2 nationallicence 
690 7 |a CIPE : Refers to cell-interstitial-plasma-erythrocyte model compartments  |2 nationallicence 
690 7 |a E : Erythrocyte  |2 nationallicence 
690 7 |a ECF : Extracellular fluid  |2 nationallicence 
690 7 |a Ht : Height (cm)  |2 nationallicence 
690 7 |a IPE : Refers to interstitial-plasma-erythrocyte model compartments  |2 nationallicence 
690 7 |a Hb : Hemoglobin  |2 nationallicence 
690 7 |a I : Interstitial  |2 nationallicence 
690 7 |a LBM : Lean body mass (kg)  |2 nationallicence 
690 7 |a M : Mass (mmol)  |2 nationallicence 
690 7 |a MZ : Mass times electrical valence (mEq)  |2 nationallicence 
690 7 |a P : Plasma  |2 nationallicence 
690 7 |a Pi− : Phosphate ions  |2 nationallicence 
690 7 |a SBE : Standard base excess (mEq/lB+ECF)  |2 nationallicence 
690 7 |a SID : Strong ion difference (mEq/lP)  |2 nationallicence 
690 7 |a SIG : Strong ion gap (mEq/lP)  |2 nationallicence 
690 7 |a QDV : Quantitative diagnostic variable  |2 nationallicence 
690 7 |a Wt : Weight (kg)  |2 nationallicence 
690 7 |a WBBE : Whole-body base excess (mEq/kg)  |2 nationallicence 
690 7 |a XA− : Net charge of undetermined or unmeasured ions in plasma (mEq/lP)  |2 nationallicence 
690 7 |a a : Arterial  |2 nationallicence 
690 7 |a v : Venous  |2 nationallicence 
690 7 |a [i] : Concentration of species i  |2 nationallicence 
690 7 |a Δ : Change  |2 nationallicence 
773 0 |t Journal of Clinical Monitoring and Computing  |d Springer Netherlands  |g 29/4(2015-08-01), 475-490  |x 1387-1307  |q 29:4<475  |1 2015  |2 29  |o 10877 
856 4 0 |u https://doi.org/10.1007/s10877-014-9625-z  |q text/html  |z Onlinezugriff via DOI 
898 |a BK010053  |b XK010053  |c XK010000 
900 7 |a Metadata rights reserved  |b Springer special CC-BY-NC licence  |2 nationallicence 
908 |D 1  |a research-article  |2 jats 
949 |B NATIONALLICENCE  |F NATIONALLICENCE  |b NL-springer 
950 |B NATIONALLICENCE  |P 856  |E 40  |u https://doi.org/10.1007/s10877-014-9625-z  |q text/html  |z Onlinezugriff via DOI 
950 |B NATIONALLICENCE  |P 100  |E 1-  |a Wolf  |D Matthew  |u Department of Pharmacology, Physiology and Neuroscience, School of Medicine, University of South Carolina, 29209, Columbia, SC, USA  |4 aut 
950 |B NATIONALLICENCE  |P 773  |E 0-  |t Journal of Clinical Monitoring and Computing  |d Springer Netherlands  |g 29/4(2015-08-01), 475-490  |x 1387-1307  |q 29:4<475  |1 2015  |2 29  |o 10877