Stat Profile Prime Plus is a comprehensive, whole blood critical care analyzer that combines blood gases, electrolytes, metabolites, CO-Oximetry, and 32 calculated results in a simple, compact analyzer. Prime Plus combines maintenance-free, component cartridge technology for sensors and reagents with patented, new, maintenance-free, and non-lysing whole blood CO-Oximetry technology.
Prime Plus results are produced rapidly, a complete test menu panel in about one minute, and are combined with bidirectional connectivity, a robust data management system, and comprehensive cybersecurity protection.
Urea (BUN), Creatinine and eGFR
Over 50% of patients admitted to the ICU will develop some stage of acute kidney injury (AKI).1 Stat Profile Prime Plus is the only blood gas analyzer to provide whole blood urea (BUN) and creatinine (plus eGFR) test options for rapid assessment of kidney function.
Ionized magnesium (iMg)
Disruptions in the balance of iMg, Na, K, and iCa can cause cardiac arrhythmias, reduced cardiac contraction, and cardiac arrest. Prime Plus is the only blood gas analyzer to provide a comprehensive profile of electrolytes including iMg.
Prime Plus incorporates a new, patented multi-wavelength optical system that scans a continuous spectrum of optical wavelengths to enable a comprehensive CO-Oximetry panel result without lysing the sample. The optical components in contact with blood are contained in the disposable sensor card.
CO-Oximetry test menu
O2Hb COHb MetHb HHb tHb
NovaNet bidirectional middleware for all Nova connected devices
NovaNet ensures timely, accurate capture of Nova analyzer test results for clinicians and managers to retrieve wherever and whenever needed. Also included is comprehensive cybersecurity protection and encryption that provides protection against attempts to access a hospital's network.
Liquid QC provides the only reliable test of analyzer performance
United States federal government regulations and many international government regulations have eliminated electronic equivalent QC and are requiring true
liquid QC.2
Automated QC complies with U.S. CLIA, German RiLiBAK, and other international QC requirements
QC cartridges contain a 30-day supply of liquid QC material. Controls are run automatically at user-selected intervals. Prime Plus quality controls:
Prime Plus provides an automated electronic quality monitoring supplement to liquid QC. SQM continuously monitors the status and performance of all analytical components (including sensors, reagents, calibrators, sample integrity, software, and electronics), providing real-time, sample-to-sample assurance of correct performance.
1. Mandelbaum T et al. Outcome of critically ill patients with acute kidney injury using the Akin criteria. Crit Care Med 2011;39:2259-2264.
2. Centers for Medicare and Medicard Services, Center for Clinical Standards and Quality/Survey and Certification Group. Policy clarification or acceptable control materials used when quality control (QC) is performed in laboratories. Baltimore, MD: CMS, April 8, 2016.
Critical Care Test Menu | Methodology |
pH | Direct ISE |
PCO2 | Severinghaus |
PO2 | Amperometric |
SO2% | Optical, reflectance |
Hematocrit | Conductivity/Na correction |
Na | Direct ISE |
K | Direct ISE |
Cl | Direct ISE |
iCa | Direct ISE |
iMg | Direct ISE |
Glucose | Enzyme/Amperometric |
Lactate | Enzyme/Amperometric |
Urea (BUN) | Enzyme/Amperometric |
Creat | Enzyme/Amperometric |
Calculated Tests
eGFR | A-aDO2 | iCa/iMg Ratio |
HCO3- | a/A | Normalized iCa |
TCO2 | PO2/FIO2 | Normalized iMg |
BE-ecf | Anion Gap | Osmolality |
BE-b | SBC | Hemoglobin |
A | Base Excess | O2 Saturation |
pH/PCO2/PO2 Corrected to Patient Temperature Respiratory Index (If % FIO2 value entered) Actual Bicarbonate Standard Bicarbonate |
CO-Oximetry Tests | |
HHb, deoxyhemoglobin | O2Hb, oxyhemoglobin |
MetHb, methemoglobin | COHb, carboxyhemoglobin |
tHb, total hemoglobin | SO2%, oxygen saturation |
Dimensions for Prime Plus, including CO-Oximetry and bidirectional connectivity:
Other Features
Full color, 10.1-inch touchscreen, multilingual, QC statistics, onboard data management, automatic sampler, integrated capillary adapter, optional barcode scanner, QC data storage, optional mobile cart with UPS
MicroSensor Card
60 µL Sample Volume
Electrical Power Requirement
< 90 Watts
Acceptable Samples
Whole blood (heparinized), arterial, venous, mixed venous
135 µL Sample draw requirement
Communication Protocols
ASTM, HL7, or POCT01-A2 connectivity formats
Certifications and Compliance: Nova Biomedical is certified to FDA Quality System Regulations and EN ISO 13485:2016 Complies to IVDD Tested according to: EN 61010-1:2010, EN 61010-2-101:2015, EN 60825-1/A1:2014.
Specifications current as of revision date.