Evaluation in volunteers of the VIA V-ABG automated bedside blood gas, chemistry and hematocrit monitor

Citation
Pl. Bailey et al., Evaluation in volunteers of the VIA V-ABG automated bedside blood gas, chemistry and hematocrit monitor, J CLIN M C, 14(5), 1998, pp. 339-346
Citations number
10
Categorie Soggetti
Aneshtesia & Intensive Care
Journal title
JOURNAL OF CLINICAL MONITORING AND COMPUTING
ISSN journal
13871307 → ACNP
Volume
14
Issue
5
Year of publication
1998
Pages
339 - 346
Database
ISI
SICI code
1387-1307(199807)14:5<339:EIVOTV>2.0.ZU;2-C
Abstract
Objective. To evaluate the VIA V-ABG (VIA Medical Corp.) point-of-care bloo d gas and chemistry monitor in healthy human volunteers, with particular em phasis on the measurement of blood gases. Methods. Experimental conditions were varied by intermittently subjecting volunteers to either isocapnic hyp ercapnia (end-tidal (ET), PETCO2 = 50 +/- 2 mmHg, ETPO2 = 130 +/- 5 mmHg) o r isocapnic hypoxia (PETCO2 = 42 +/- 2, PETO2 + 45 +/- 2 mmHg) in addition to room air breathing. Measurements by the VIA V-ABG device were compared w ith paired samples and measurements performed by two ABL Radiometers (505 a nd 500). Analysis of results includes bias and precision plots and comparis on of results with minimal performance criteria as established by CLIA. Res ults. Nineteen volunteers yielded 222 matched samples. The range of values were 7.32-7.61 for pH, 20.9-51.6 mmHg for PCO2, 27.9-184.5 mmHg for PO2, 13 1-141 mmol/l for Na, 3.1-4.1 mmol/l for K, and 30.0-50.4% for hematocrit. B ias and precision (+/- 2 sd) for pH was 0.01 and 0.03, for PCO2 was 0.4 and 4.8, for PO2 was 1.0 and 17.0, for Na was -0.3 and 5.2, for K was 0.1 and 0.2, and for Her was 2.0 and 5.4. Conclusions. Over the range of blood gas values assessed, blood gas measurements by the VIA V-ABC device were clinic ally acceptable and met minimal performance criteria utilizing current Medi care CLIA proficiency standards. Performance criteria were also met by the VIA V-ABG device for Na, K, and Hct measurements but the range of values wa s too narrow to allow characterization of clinical acceptability. The VIA V -ABG device appears to perform well compared with the results which have be en published for other point-of-care devices. Comparison between different studies investigating point-of-care devices is difficult due to several fac tors (range of values measured, comparison device, population studied, etc. ). Some of these instruments, including the VIA V-ABG device, may serve qui ts well as point-oi-care devices to perform certain tests at the bedside. W hether or not any of these devices can substitute for traditional laborator y blood gas and chemistry measurements remains an issue that is not adequat ely studied.