

In medicine,monitoring is the observation of a disease, condition or one or several medical parameters over time.
It can be performed by continuously measuring certain parameters by using amedical monitor (for example, by continuously measuringvital signs by a bedside monitor), and/or by repeatedly performingmedical tests (such asblood glucose monitoring with aglucose meter in people withdiabetes mellitus).
Transmitting data from a monitor to a distant monitoring station is known astelemetry orbiotelemetry.
Monitoring can be classified by the target of interest, including:

Monitoring ofvital parameters can include several of the ones mentioned above, and most commonly include at leastblood pressure andheart rate, and preferably alsopulse oximetry andrespiratory rate. Multimodal monitors that simultaneously measure and display the relevant vital parameters are commonly integrated into the bedside monitors incritical care units, and theanesthetic machines inoperating rooms. These allow for continuous monitoring of a patient, with medical staff being continuously informed of the changes in general condition of a patient. Some monitors can even warn of pending fatalcardiac conditions before visible signs are noticeable to clinical staff, such asatrial fibrillation orpremature ventricular contraction (PVC).
Amedical monitor orphysiological monitor is amedical device used for monitoring. It can consist of one or moresensors, processing components,display devices (which are sometimes in themselves called "monitors"), as well as communication links for displaying or recording the results elsewhere through a monitoring network.[citation needed]
Sensors of medical monitors includebiosensors and mechanical sensors. For example, photodiode is used in pulse oximetry, Pressure sensor used in Non Invasive blood pressure measurement.
The translating component of medical monitors is responsible for converting the signals from the sensors to a format that can be shown on the display device or transferred to an external display or recording device.
Physiological data are displayed continuously on aCRT,LED orLCD screen asdata channels along the time axis. They may be accompanied bynumerical readouts of computed parameters on the original data, such as maximum, minimum and average values, pulse and respiratory frequencies, and so on.[citation needed]
Besides the tracings of physiological parameters along time (X axis), digital medical displays have automatednumeric readouts of the peak and/or average parameters displayed on the screen.
Modern medical display devices commonly usedigital signal processing (DSP), which has the advantages ofminiaturization,portability, and multi-parameter displays that can track many different vital signs at once.[citation needed]
Oldanalog patient displays, in contrast, were based onoscilloscopes, and had one channel only, usually reserved for electrocardiographic monitoring (ECG). Therefore, medical monitors tended to be highly specialized. One monitor would track a patient'sblood pressure, while another would measurepulse oximetry, another the ECG. Later analog models had a second or third channel displayed on the same screen, usually to monitorrespiration movements andblood pressure. These machines were widely used and saved many lives, but they had several restrictions, including sensitivity toelectrical interference, base level fluctuations and absence of numeric readouts and alarms.[citation needed]
Several models of multi-parameter monitors are networkable, i.e., they can send their output to a central ICU monitoring station, where a single staff member can observe and respond to several bedside monitors simultaneously.Ambulatory telemetry can also be achieved by portable, battery-operated models which are carried by the patient and which transmit their data via awireless data connection.
Digital monitoring has created the possibility, which is being fully developed, of integrating the physiological data from the patient monitoring networks into the emerging hospitalelectronic health record and digital charting systems, using appropriatehealth care standards which have been developed for this purpose by organizations such asIEEE andHL7. This newer method of charting patient data reduces the likelihood of human documentation error and will eventually reduce overall paper consumption. In addition,automated ECG interpretation incorporates diagnostic codes automatically into the charts. Medical monitor'sembedded software can take care of the data coding according to these standards and send messages to the medical records application, which decodes them and incorporates the data into the adequate fields.
Long-distance connectivity can avail fortelemedicine, which involves provision ofclinical health care at a distance.
A medical monitor can also have the function to produce an alarm (such as using audible signals) to alert the staff when certain criteria are set, such as when some parameter exceeds of falls the level limits.
An entirely new scope is opened with mobile carried monitors, even such in sub-skin carriage. This class of monitors delivers information gathered in body-area networking (BAN) to e.g.smart phones and implementedautonomous agents.
Monitoring of clinical parameters is primarily intended to detect changes (or absence of changes) in the clinical status of an individual. For example, the parameter ofoxygen saturation is usually monitored to detect changes inrespiratory capability of an individual.
When monitoring a clinical parameters, differences between test results (or values of a continuously monitored parameter after a time interval) can reflect either (or both) an actual change in the status of the condition or atest-retest variability of the test method.
In practice, the possibility that a difference is due to test-retest variability can almost certainly be excluded if the difference is larger than a predefined "critical difference". This "critical difference" (CD) is calculated as:[2]
, where:[2]
For example, if a patient has a hemoglobin level of 100 g/L, the analytical variation (CVa) is 1.8% and the intra-individual variabilityCVi is 2.2%, then the critical difference is 8.1 g/L. Thus, for changes of less than 8 g/L since a previous test, the possibility that the change is completely caused by test-retest variability may need to be considered in addition to considering effects of, for example, diseases or treatments.
| Sodium | 3% |
| Potassium | 14% |
| Chloride | 4% |
| Urea | 30% |
| Creatinine | 14% |
| Calcium | 5% |
| Albumin | 8% |
| Fasting glucose | 15% |
| Amylase | 30% |
| Carcinoembryonic antigen | 69% |
| C-reactive protein | 43%[3] |
| Glycated hemoglobin | 21% |
| Hemoglobin | 8% |
| Erythrocytes | 10% |
| Leukocytes | 32% |
| Platelets | 25% |
| Unless otherwise specified, then reference for critical values isFraser 1989[2] | |
Critical differences for other tests include early morning urinary albumin concentration, with a critical difference of 40%.[2]
In a clinical laboratory, adelta check is alaboratory quality control method that compares a current test result with previous test results of the same person, and detects whether there is a substantial difference, as can be defined as a critical difference as per previous section, or defined by other pre-defined criteria. If the difference exceeds the pre-defined criteria, the result is reported only after manual confirmation by laboratory personnel, in order to exclude a laboratory error as a cause of the difference.[4] In order to flag samples as deviating from previously, the exact cutoff values are chosen to give a balance betweensensitivity and the risk of being overwhelmed by false-positive flags.[5] This balance, in turn, depends on the different kinds of clinical situations where the cutoffs are used, and hence, different cutoffs are often used at different departments even in the same hospital.[5]
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The development of new techniques for monitoring is an advanced and developing field insmart medicine, biomedical-aidedintegrative medicine,alternative medicine,self-tailoredpreventive medicine andpredictive medicine that emphasizes monitoring of comprehensive medical data of patients, people at risk and healthy people using advanced, smart, minimallyinvasivebiomedical devices,biosensors,lab-on-a-chip (in the futurenanomedicine[6][7] devices likenanorobots) and advancedcomputerizedmedical diagnosis and early warning tools over a short clinical interview anddrug prescription.
Asbiomedical research,nanotechnology andnutrigenomics advances, realizing the human body'sself-healing capabilities and the growing awareness of the limitations ofmedical intervention by chemicaldrugs-only approach of old school medical treatment, new researches that shows the enormous damage medications can cause,[8][9] researchers are working to fulfill the need for a comprehensive further study and personal continuousclinical monitoring of health conditions while keeping legacy medical intervention as a last resort.
In many medical problems, drugs offer temporary relief of symptoms while theroot of a medical problem remains unknown without enough data of all ourbiological systems[10]. Our body is equipped with sub-systems for the purpose of maintaining balance and self healing functions. Intervention without sufficient data might damage those healing sub systems.[10] Monitoring medicine fills the gap to prevent diagnosis errors and can assist in future medical research by analyzing alldata of many patients.

The development cycle in medicine is extremely long, up to 20 years, because of the need for U.S.Food and Drug Administration (FDA) approvals, therefore many of monitoring medicine solutions are not available today in conventional medicine.

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