After reviewing the system data logs, the rapidpoint instrument in question was found to be functioning as intended.There were no system or sensor related error events in and around the time of the escalated samples.The qc performance was found to be stable throughout the use life of the installed cartridge.For this patient, the sensor raw responses were found to be typical and passed the system signal integrity check algorithms.The reported patient results appear to be accurate for the sample as they were presented for analysis.It is also noted that there were significant differences in sample times for the comparative results.The root cause for the alleged discrepancy in potassium results for this patient couldn't be determined.
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