Stratus CS 200 Acute Cardiac Care Troponin Analyzer Video
The Stratus® CS 200 Acute Care™ Cardiac Analyzer* delivers lab-quality Troponin I results for chest-pain patients with speed and efficiency at the point of care. It delivers the first result in as fast as 14 minutes to support rapid, informed decision making that may lead to better patient care. Clinicians may individually select and test multiple assays from a single sample, on a single run, and on a single instrument. Simple operation and advanced connectivity help to promote consistent results and efficient workflow.
- Perform critical serial testing with a guideline acceptable sensitive troponin I assay.
- Exclude pulmonary embolism with a clinically validated D-dimer** assay.
- Select tests based on patient need. Choose from seven individually packaged assays: TnI, hsCRP, NT-proBNP, myoglobin, CKMB, D-dimer, and ßhCG.
- Achieve lab-quality performance in a POC setting: whole blood samples and strong correlation to central lab analyzers.
- Expect consistent results. System automation helps to minimize steps and simplify operation for users at all skill levels.
Características e Benefícios
The Stratus CS 200 cardiac troponin analyzer* is easy to use, with rapid turnaround time, an intuitive touchscreen interface, and multiple cardiac assay offerings.
The analyzer delivers lab-quality results at the point of care and with the speed needed for cardiac patients. It offers a comprehensive cardiac menu, including guideline acceptable sensitive troponin I and D-dimer assays, and automatically spins whole blood into plasma for testing, thereby reducing the risk of biohazard exposure. The Stratus CS 200 system ensures results will be comparable to lab tests run on plasma samples.
Simple Steps for Fast and Consistent Results
- With the first result available in as fast as 14 minutes and subsequent results within 4 minutes, the Stratus CS 200 system allows for faster diagnosis of patients.
- The acute cardiac care system accepts whole blood samples in a collection tube; no sample preparation is required.
- Simply input sample and walk away—minimal operator involvement.
- A user-friendly touchscreen interface allows for easier navigation through the instrument’s screens.
- The bar-code reader eliminates the need for manual entry and reduces potential for error.
- Bidirectional connectivity feature with third-party data managers allows for the safe and secure transmission of results.
- Remote monitoring saves time by eliminating the need to walk to the analyzer to check when calibration is due.
- Ample memory allows storage of up to 50 patient results and up to 500 operator IDs.
Multiple cardiac assays are available to meet your point-of-care testing demands. Test cartridges are individually packaged, providing flexibility to select appropriate tests based on patient need. As many as four assays can be run simultaneously per patient sample on the Stratus CS 200 system*
Guideline Acceptable Sensitive Troponin I Assay
The cTnl assay meets the ESC/ACC Joint Committee recommendations of ≤10% CV at the 99th percentile of a normal population. The assay is used for the measurement of cardiac troponin I to aid in the diagnosis of AMI and in the risk stratification of patients with acute coronary syndromes (ACS).
D-dimer Assay (with Pulmonary Embolism Exclusion**)
D-dimer is a quantitative measurement of cross-linked fibrin degradation products (D-dimer) in human citrated or heparinized plasma. The D-dimer assay is intended for use in conjunction with a non-high clinical pretest probability (PTP) assessment model to exclude pulmonary embolism (PE) disease and as an aid in the diagnosis of venous thromboembolism (VTE) [deep vein thrombosis (DVT) or PE].
CKMB Mass Assay
CKMB is for the measurement of the MB isoenzyme of creatine kinase in heparinized whole blood/plasma. CKMB measurements can be used as an aid in diagnosing acute myocardial infarction.
Myoglobin measures myoglobin in heparinized whole blood /plasma. Myoglobin measurements can be used as an aid in diagnosing myocardial infarction.
NT-proBNP is a quantitative measurement of N-terminal pro-brain natriuretic peptide (NT-proBNP) in heparinized plasma. Measurements of NT-proBNP are used as an aid in the diagnosis of individuals suspected of having congestive heart failure (CHF). The test is further indicated for the risk stratification of patients with acute coronary syndrome and heart failure, resulting from left-ventricular dysfunction.
CardioPhase® hsCRP Assay
Measurement of CRP is useful for the detection and evaluation of infection, tissue injury, inflammatory disorders, and associated diseases. High-sensitivity CRP (hsCRP) measurements may be used as an independent risk marker for the identification of individuals at risk for future cardiovascular disease. Measurements of hsCRP, when used in conjunction with traditional clinical laboratory evaluation of acute coronary syndromes, may be useful as an independent marker of prognosis for recurrent events, in patients with stable coronary disease or acute coronary syndromes.
Quantitative βhCG Assay
Running STAT βhCG ensures that clinicians know of any potential pregnancies in their cardiac patients, and can recommend the most appropriate diagnostic assessments for those patients.
Stratus CS 200 System* and Assay Specifications
Troponin I Assay
0.03–50 μg/L (30–50,000 ng/L)
0.3–150 μg/L (ng/mL)
6–5000 μg/L (ng/mL) FEU
1–900 μg/L (ng/mL)
0.5–1250 IU/L (mIU/mL)
<0.03 μg/L (<30 ng/L)
6.0 μg/L FEU
10% at 0.06 μg/L (10% at 60 ng/L)
4.0% at 3.7 μg/L
4.4% at 96.6 pg/mL
4.1% at 412 μg/L
6.8% at 1.16 mg/L
3.4% at 56 μg/L; 4.6% at 142 μg/L†
2.5% at 27.1 IU/L‡
Please refer to the assay package inserts for more detailed information.
Qualified Collection Tube Types
Becton Dickinson 13 x 75 mm green Hemogard® tube, 4.0 mL draw (lithium or sodium heparin)
Becton Dickinson 13 x 75 mm lt blue Hemogard tube, 4.5 mL draw (3.2% sodium citrate)
Sarstedt Monovette® tube 13 x 65 mm orange, 2.6 mL draw (lithium heparin)
Sarstedt Monovette tube 13 x 65 mm blue, 2.9 mL draw (sodium citrate)
Microprocessor-verified between 18,000 and 22,000 rpm
115 VAC: 103–127 volt range, 47–63 Hz, ~1.5 amp, and 400 watts maximum power
230 VAC: 207–253 volt range, 47–63 Hz, ~0.8 amp, and 400 watts maximum power
Circuit: Separate, dedicated line with hot, neutral, and isolated ground in its own conduit
Receptacle: Hospital-grade receptacle accessible to the 2.7 m (9 ft) power cord upon arrival of the instrument
Patient ID and/or sample ID scannable using universal bar-code reader
Sample collection-time entry
Stores up to 500 operator IDs; locks out unauthorized operators
Notification of TestPak lot expiration
Password protection of advanced setup functions
Last 50 patient results stored for later transmission
Bidirectional connectivity through network connection
Compatible with Conworx POCcelerator™ System
Unidirectional connectivity through serial port
Instrument: 18 in. H x 28 in. W x 23 in. D (46 cm H x 71 cm W x 58 cm D)
Operating clearance: 20 in. H x 31 in. W x 24 in. D (51 cm H x 79 cm W x 61 cm D)
Service clearance: 37 in. H x 39 in. W x 34 in. D (94 cm H x 99 cm W x 86 cm D)
Optional workstation: 39.25 in. H x 30 in. W x 27.25 in. D (99.7 cm H x 76.2 cm W x 69.2 cm D)
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*Not available for sale in the U.S. Product availability varies by country.
**Exclusion of PE in conjunction with non-high PTP model at point of care.
†Upper end of reference range = 82 μg/L
‡Total precision measured with Bio-Rad Control Liquichek™ Level 2. Liquichek is a trademark of Bio-Rad.
The products/features (mentioned herein) are not commercially available in all countries. Due to regulatory reasons their future availability cannot be guaranteed. Please contact your local Siemens organization for further details.