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The system combines the accuracy of a full-scale laboratory analyser with the flexibility of a mobile solution. Its compact design and low weight makes PATHFAST™ the ideal analysis system in situations wherever fast quantitative results (with full-scale lab quality) are required at the point of care. With the only high sensitive assay (hs-cTnl) conforming to ESC and IFCC guideline, its space-saving design and large degree of flexibility PATHFAST™ is also an ideal supplement or back-up system to central labs. It can be available at any time (24 hrs per day) without interfering with the processes of routine analysis.
PATHFAST™ provided fast, differential diagnosis while being easy to operate, install and network. High precision makes this analyser an adequate “satellite” of a full-scale lab on a cardiology, intensive care or emergency ward. Parallel processing enables the examination of six samples in only a few minutes from whole blood, serum or plasma.
Central laboratory results at point of care generated in a simple 3 step process with no additional reagents, buffer solutions or accessories required.
Whole blood, serum or plasma samples can be used as sample material
Quantitative measurement of 6 analyses in parallel
Operation is simple, no special skills are required
PATHFAST™ is a fully automatic immunoassay analyser, which combines the progressive chemiluminescence technology with the patented Magtration® technology.
Small sample volumes can be detected with high accuracy and precision. The device and the reagent strips provide optimum sensitivity.
Whole blood, plasma and serum are automatically identified and processed. The results are perfectly reproducible and correlate outstandingly with lab analyses.
PATHFAST™ B･R･A･H･M･S PCT is an immunoassay for the in vitro quantitative determination of Procalcitonin (PCT) concentration in whole blood, plasma or serum. PCT is used as a marker of host response to bacterial infection. PATHFAST™ B･R･A･H･M･S PCT is used as an aid in the early detection and differential diagnosis of clinically relevant bacterial infections, in the assessment of the degree of septic severity and in the risk stratification of the outcome of patients with systemic bacterial infection, sepsis, severe sepsis and septic shock.
PATHFAST™ Presepsin is a chemiluminescent enzyme immunoassay for the quantitative measurement of presepsin (sCD14-ST) concentration in whole blood or plasma. PATHFAST™ Presepsin is used as an aid in the diagnosis and prognosis of sepsis, in the assessment of the degree of septic severity and to aid in the risk stratification of critically ill septic patients. PATHFAST™ Presepsin improves the diagnosis and prognosis of sepsis defining its level of severity. It is a valid indicator of risk stratification in septic patients.
PATHFAST™ hs-cTnI is an immunoassay for the in vitro quantitative determination of cardiac Troponin I (cTnI) in human anticoagulated whole blood and plasma on the PATHFAST™ analyser. PATHFAST™ hs-cTnI can be used as an aid in the diagnosis of acute myocardial infarction and in the risk stratification of patients presenting with acute coronary syndromes. In addition to the diagnosis of AMI, detection of low cardiac troponin levels may make it possible to predict information (risk stratification) in terms of short- and long term mortality of patients.
PATHFAST™ NTproBNP is an immunoassay for the in vitro quantitative determination of N-terminal pro-B-type natriuretic peptide (NTproBNP) in anticoagulated whole blood and plasma on the PATHFAST™ analyser. PATHFASTTM NTproBNP can be used as an aid in the diagnosis in patients suspicious for congestive heart failure, the detection left ventricular dysfunction of and in the assessment of the severity of congestive heart failure (CHF). PATHFAST™ NTproBNP can also be used in the risk stratification in patients with acute coronary syndromes (ACS) and congestive heart failure and for monitoring the therapy in patients with left ventricular dysfunction.
PATHFAST™ D-Dimer is a chemiluminescent enzyme immunoassay for the quantitative measurement of D-Dimer concentration in whole blood or plasma. PATHFAST™ D-Dimer is used an aid in the diagnosis of activation processes of the coagulation system including deep vein thrombosis (DVT) and pulmonary embolism (PE). Plasmin-induced lysis of crosslinked fibrin results in the formation of D-dimer containing fibrin degradation fragments (XDP). D-dimer is a specific marker of the degradation of factor XIIIa- crosslinked fibrin and an indirect early marker of activation of coagulation and clot formation.
PATHFAST™ hsCRP is a product for in-vitro diagnostic use with the in vitro diagnostic system PATHFAST™ for the quantitative measurement of C-reactive protein (CRP) in human serum, heparinized or EDTA whole blood and plasma, also at low concentrations. C-reactive protein (CRP) is an acute phase -globulin with a molecular mass of approximately 118,000 daltons. CRP is highly conserved, composed of five identical cyclic globular subunits, and is classified as a member of the pentraxin superfamily of proteins. As elevated CRP values are always associated with pathological changes, the CRP assay provides useful information for the diagnosis, therapy, and monitoring of inflammatory conditions and associated diseases.
PATHFAST™ Myo is a product for in vitro diagnostic use with the in vitro diagnostic system PATHFAST™ for the quantitative measurement of Myoglobin in heparinized whole blood and plasma. The result obtained with the assay is used to assist in the diagnosis and especially in the exclusion of acute myocardial infarction.
PATHFAST™ CK-MB is a product for in vitro diagnostic use with the in vitro diagnostic system PATHFAST™ for the quantitative measurement of CK-MB in heparinized whole blood and plasma. The result obtained with the assay is used to assist in the diagnosis of acute myocardial infarction.
AB Scientific are exclusive distributors of PATHFAST™ for the UK & Ireland.
PATHFAST™ is an immunoanalyzer for the measurement of emergency parameters (High-Sensitivity Troponin) or sepsis biomarker PCT and Presepsin in less than 17 minutes out of whole blood, serum or plasma in central laboratory quality.
The PATHFAST™ system combines the accuracy of a full-scale lab analyser with the flexibility of a mobile solution. 6 tests can be tested per run and takes less than 17 minutes offering fast quantitative results at POCT 24/7.
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