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Value and limitations of the Continuous Glucose Monitoring System in the management of type 1 diabetes.

The CGMS (Continuous Glucose Monitoring System) is a portable device allowing continuous measuring of glucose. It provides recordings of at least 72 h, during which 288 measures/day are performed. Results are visualised in the form of a set of curves, illustrating the variations in blood glucose levels over time. The quality of the records has often been questioned by several authors. Some of the system's physiologically related limitations can be explained by the less than perfect coincidence of variations in glucose levels observed in the interstitial tissue, where CGMS measurings are done, and in the blood, where calibrations are performed. Other limitations, such as defects in accuracy or in reproducibility of tracings or premature curtailments of recordings, are due to technical weaknesses which were considerably improved during the past few years, particularly with regard to the quality of the electrodes providing a more stable signal over time. In clinical practice, CGMS is a tool for investigating the glycaemic patterns of diabetic patients in conjonction with SMBG. It allows the identification of overlooked hyper- or hypoglycaemia. Generally well accepted, it is a usefull tool to analyse the nocturnal period, or any situation where glucose checks are rare. The visual nature of its results provides a facilitating support in the discussion between the patient and the care-provider during consultations or educational sessions. CGMS utilisation was proposed for guiding treatment adjustment. At present, it is still difficult to state with certainty that this tool allows effective improvement in the metabolic control of patients with type 1 diabetes, in view of the paucity of controlled studies showing an impact on HbA1c values or on the frequency of hypoglycaemia, even if such a tendency emerges from most non-controlled intervention trials.

Blood Glucose↗

Analysing post-alarm data in a monitoring system in order to accept or reject the alarm.

In a disease monitoring system embracing several diseases and communities, alarms indicating a significant increase in disease incidence will frequently occur even though the false alarm rate has been set quite low. An approach is presented by which an alarm is determined as either confirmed or rejected according to data observed subsequent to the alarm. The suggested procedure is expected to weed out a substantial proportion (say about 75 per cent) of the false alarms at the expense of some delay in detecting a true alarm.

Cluster Analysis↗

Collection efficiency of particulate and xenon sampling in the international monitoring system of the comprehensive Nuclear-Test-Ban Treaty.

Low-level monitoring of atmospheric radioactivity requires sampling with high collection efficiency for the aerosols and gases of interest. The radionuclide station network of the International Monitoring System designed to detect very low-levels of airborne radionuclides will consist of 80 particulate and 40 noble gas stations. This paper reports on studies performed to select suitable filter material and to characterise the sampling efficiency of air inlet configurations of high-volume particulate samplers. It also considers the collection characteristics of automatic xenon sampling systems.

Journal Article↗

A monitoring system to detect increased rates of cancer incidence.

A new method for monitoring occurrences of rare health events is proposed. This proposed method is similar in principle to the sets technique but is shown to have much better expected time to alarm properties. This is illustrated for a number of hypothetical situations, and then both methods are applied to cancer mortality data. The proposed method will allow the use of large monitoring systems consisting of implementations of the method in a number of subregions (i.e., counties) of a larger region (i.e., state) independently, and still maintain reasonable expected times between false alarms.

Biometry↗

Productivity monitoring systems: their use in management planning, forecasting, and labor budgeting.

The productivity monitoring system (PMS) has long proved itself a useful and necessary management tool for controlling scarce and costly labor resources. Here, the reader is introduced to the use of the PMS within the hospital industry. The general concern with controlling productivity in hospitals is presented within the context of regulatory change and overall cost-consciousness, followed by a description of a successful PMS and the information it provides. Techniques and an example for using PMSs in workload forecasting are also provided.

Budgets↗

[A computer-assisted noninvasive monitoring system with graphic display of online determination of cardiovascular parameters].

During anesthesia the cardiovascular system is usually assessed on the basis of heart rate and arterial pressure, although the most important hemodynamic measurement is that of flow. A method for the non-invasive measurement of cardiac output is based on thoracic electrical bio-impedance. The NCCOM3-R7 is a non-invasive cardiac output monitor that makes use of thoracic electrical bioimpedance, which has been shown to provide results comparable with thermodilution in various hemodynamic states both in animals and humans. A new on-line hemodynamic monitoring system has been developed using the non-invasive NCCOM3-R7 (BoMed) cardiac output monitor, a portable microcomputer (NEC Multispeed) in connection with a software package CDDP-1 (BoMed), a Dinamap automatic arterial pressure monitor (Critikon) and an additional 14" display. Every 16 heart beats the cardiac output monitor transfers 11 cardiodynamic parameters in ASCII-format to the microcomputer, where the data are stored. Using the CDDP-1 program the current cardiodynamic status of the patient is displayed numerically and graphically on the monitor screen. Mean arterial pressure is determined by Dinamap and the data must be entered manually in the menu. The program then calculates systemic vascular resistance and left ventricular work index, the CVP being set to 3 torr and PAOP to 6 torr. In the graphic display the current hemodynamic status is shown and the underlying situation is analyzed in terms of systemic vascular resistance and volume-dependent contractility. The reliability of this on-line monitoring system is demonstrated in a high-risk patient.(ABSTRACT TRUNCATED AT 250 WORDS)

Anesthesia, General↗

New 434 MHz interstitial hyperthermia system monitored by microwave radiometry: theoretical and experimental results.

A new complete microwave interstitial hyperthermia system monitored automatically by microwave radiometry and working at 434 MHz is described in this paper. This system, which includes a new radiometer with two internal temperature references, is detailed. All its characteristics for microwave heating and radiometry are presented. The new possibilities are shown through numerous experiments on acrylamide phantom and excised tissues, which have been carried out for different antennae implantation corresponding to the clinical situation. The clinic protocol, associate to the brachytherapy, imposes the use of semi-loop catheters. Coaxial antennae, inserted in these catheters, are not, therefore, positioned in a rectilinear manner but undergo a curve. So, models based on the FDTD formalism are developed to determine the theoretical power deposition. Owing to these models, the effects of this physical motive on radiation diagrams can be taken into account. The results of the power deposition are presented for two antennae. Thermal patterns can then be determined by the solution of the bioheat-transfer equation in the steady state. Also, the comparison of the results given by the new interstitial hyperthermia system with those obtained with the previous 915 MHz one shows an improvement of the thermal performances.

Electromagnetic Fields↗

A multiparameter wearable physiologic monitoring system for space and terrestrial applications.

A novel, unobtrusive and wearable, multiparameter ambulatory physiologic monitoring system for space and terrestrial applications, termed LifeGuard, is presented. The core element is a wearable monitor, the crew physiologic observation device (CPOD), that provides the capability to continuously record two standard electrocardiogram leads, respiration rate via impedance plethysmography, heart rate, hemoglobin oxygen saturation, ambient or body temperature, three axes of acceleration, and blood pressure. These parameters can be digitally recorded with high fidelity over a 9-h period with precise time stamps and user-defined event markers. Data can be continuously streamed to a base station using a built-in Bluetooth RF link or stored in 32 MB of on-board flash memory and downloaded to a personal computer using a serial port. The device is powered by two AAA batteries. The design, laboratory, and field testing of the wearable monitors are described.

Aerospace Medicine↗

Monitoring health care workers after smallpox vaccination: findings from the Hospital Smallpox Vaccination-Monitoring System.

BACKGROUND: The Advisory Committee on Immunization Practices and the Healthcare Infection Control Practices Advisory Committee recommended that hospitals establish on-site, daily assessments of health care workers vaccinated with smallpox vaccine. The Hospital Smallpox Vaccination Monitoring System (HSVMS) was 1 component of the smallpox vaccination plan to monitor adverse events on-site in hospitals. This report presents findings from February to August 2003. METHODS: All US institutions participating in the smallpox vaccination program were eligible to enroll in and use HSVMS through the Internet-based Centers for Disease Control Secure Data Network. RESULTS: Of the 730 enrolled vaccinees, 341 (47%) were nurses; 122 (17%) physicians; 75 (10%) laboratory, patient care, radiology, or other technicians; 39 (5%) administrators; 22 (3%) housekeepers; 21 (3%) physical or respiratory therapists; 20 (3%) infection control professionals; 19 (3%) safety or security staff; and 17 (2%) epidemiologists; and 54 (7%) were workers in other job categories. Most (86%) vaccinees had been previously vaccinated. Postvaccination signs and symptoms were frequent: itching (75.2%), pain at the vaccination site (31.6%), swollen or tender lymph nodes (26.4%), fatigue (26.2%), and headache (20.8%). Symptoms were highest during the first week after vaccination; symptoms were more frequently reported among vaccinees without previous vaccination. Adherence to recommended vaccination site care was reported in 2732 of 3091 (88.4%) follow-up visits among workers with patient contact. Of the 4379 days workers planned to work, during 31 (0.7 per 100) days, workers performed restricted activities, and, in 60 (1.4 per 100) days, workers were absent. CONCLUSIONS: Findings from HSVMS indicate that adherence to post-smallpox vaccination site care was high and that the number of days of work affected was low.

Health Personnel↗

A patient monitoring system designed as a platform for application development.

This paper presents a patient data monitoring system for use in critical care areas. The system incorporates design criteria from the Institute of Electrical and Electronic Engineers' (IEEE) proposed standards body (P1073), the Medical Information Bus (MIB) and from our design team. Existing hardware and software technology is utilized wherever possible to maintain cost effectiveness. A major design objective is providing a consistent environment in which to develop applications for critical patient care delivery. The system allows applications to be developed without specific knowledge of the configuration of the bedside environment. Therefore, investments in 'user' application development are shielded from changes in patient care delivery technology. The system has been in limited operation in a surgical intensive care unit for several months with prototype applications.

Computer Systems↗

In situ long-term monitoring system for radioactive contaminants.

A long-term in situ subsurface instrument for monitoring radioactive contaminant plumes, as an alternative to soil analysis, is described. A portable, laser-based reader optically stimulates luminescence from sensors, each containing an Al2O3:C dosemeter. The sensors, designed for placement at various subsurface locations around a waste site, are allowed to accumulate dose for a predetermined time that is based on the instrument's minimum detectable dose (MDD). The reader is then attached to the sensor by fibre optic cable to read the accumulated dose; an increase above natural background levels indicating the presence of leaked radioactivity. Based on an MDD of 5 microGy, it is shown that the sensor can measure soil concentrations of 1.85 Bq cm(-3) after an exposure time of 50 h for 137Cs and 67 h for 90Sr/90Y. Discrimination between beta and gamma radiation is possible using an end cap placed over one of the two paired sensors, allowing simultaneous measurement of 137Cs and 90Sr/90Y in a mixed field. The monitor system represents a substantial improvement over quarterly soil sampling because of a greatly increased measurement frequency and the ability to perform measurements reproducibly.

Dose-Response Relationship, Radiation↗

A comparison of intravascular pressure monitoring system contamination and patient bacteremia with use of 48- and 72-hour system change intervals.

OBJECTIVE: To determine the incidence of culture positivity in intravascular monitoring systems by comparing 48- versus 72-hour intervals for flush solution, stopcocks, and catheters on removal. DESIGN: Prospective, quasi-experimental, random assignment. SETTING: Intensive care units of a midwestern university medical center and a community hospital. PATIENTS: Seventy-six critically ill adult patients, ranging in age from 24 to 96 years (X = 61.6), requiring arterial or pulmonary artery catheters. OUTCOME MEASURE: Culture positivity of flush solution, stopcocks, or catheter tips. INTERVENTION: Data collection was initiated at designated change intervals of 48- or 72-hours; cultures were taken of flush solution and stopcocks; catheter tip cultures were obtained on catheter removal. RESULTS: Chi-square analyses indicated that increasing the change interval to 72 hours resulted in no significant difference in culture positivity of catheter tips. However, the difference between the 48- and 72-hour groups in culture-positivity rates of stopcocks from arterial catheters was significant (1, N = 82) = 6.86, p less than 0.01. CONCLUSIONS: Our results showed that increasing the change interval to 72 hours did not increase the risk of catheter-associated infection or catheter-associated bacteremia. Chi-square analysis did not show an association between culture-positive stopcocks, the incidence of culture-positive catheter tips, entries into the system, or catheter-related bacteremia and a change interval that was increased to 72 hours. Thus, increasing the change interval to 72 hours does not increase the risk of infection.

Adult↗

Therapeutic concordance of two portable monitors and two routine automatic oral anticoagulant monitoring systems using as reference the manual prothrombin time technique.

Two models of capillary blood prothrombin time (PT) monitoring systems were evaluated for analytical performance and then compared with two routine PT systems using the reference manual technique and a high-sensitivity thromboplastin. Two sets of 60 and 80 plasmas were analyzed from anticoagulated patients stabilized over 3 months in an INR range 2-3.5 for therapy. Capillary PT determination was performed in two portable monitors, CoaguChek S and CoaguChek PT (Roche Diagnostics), and plasma automatic methods were Neoplastine/STA (Diagnostics Stago) and PT-FibrinogenHsPlus/ACL7000 (Instrumental Laboratories). Thromboplastin Bilbao (TBi), an in-house high-sensitivity rabbit thromboplastin (ISI=1.08), recommended as the reference reagent by an External Spanish Oral Anticoagulant Quality Assessment, was used in the PT manual technique. The two monitors' coefficients of correlation with the reference system were 0.74 for CoaguChek S and 0.81 for CoaguChek PT. The automatic routine systems showed a correlation of 0.92 (Neoplastine/STA) and 0.91 (PT-FbHsPlus/ACL7000). Clinical agreement expressed as the percentage of simple correlation ranged between 75.0% (CoaguChek S) and 88.9% (Neoplastine/STA). The systems having the best kappa index with the manual technique were CoaguChek PT (71.9%) and the Neoplastine/STA system (73%). The routine PT management systems exhibited better correlation and percentage of concordance when using the TBi/manual technique than did the portable monitors, which moreover performed unequally in this regard.

Anticoagulants↗

Performance evaluation of the MiniMed continuous glucose monitoring system during patient home use.

BACKGROUND: The recent availability of a continuous glucose monitor offers the opportunity to match the demands of intensive diabetes management with a period of equally intensive blood glucose monitoring. The present study evaluates the performance of the MiniMed continuous glucose monitoring system (CGMS) in patients with diabetes during home use. METHODS: Performance data and demographic information were obtained from 135 patients who were (mean +/- SD) 40.5+/-14.5 years old, had an average duration of diabetes of 18.0+/-9.8 years, 50% were female, 90% were Caucasian, and 87% of whom had been diagnosed with type 1 diabetes. Patients were selected by their physician, trained on the use of the CGMS and wore the device at home for 3 days or more. The performance of the CGMS was evaluated against blood glucose measurements obtained using each patient's home blood glucose meter. Evaluation statistics included correlation, linear regression, mean difference and percent absolute difference scores, and Clarke error grid analysis. RESULTS: The CGMS values were compared to 2477 SMBG tests (r = 0.91, slope = 0.93, intercept = 14.5 mg/dL, mean absolute difference = 18.0%+/-19.8%). Clarke error grid analysis showed 96.2% of the data pairs falling within the clinically acceptable regions (zones A and B). CONCLUSIONS: These results demonstrate the agreement of the CGMS to blood glucose meter values, under conditions of home use, in patients selected by their physicians as candidates for continuous monitoring. The detailed glucose information provided by the CGMS should make successful management of diabetes more easily achieved.

Adult↗

Evaluation of a continuous glucose monitoring system for use in dogs, cats, and horses.

OBJECTIVE: To evaluate a continuous glucose monitoring system (CGMS) for use in dogs, cats, and horses. DESIGN: Prospective clinical study. Animals-7 horses, 3 cats, and 4 dogs that were clinically normal and 1 horse, 2 cats, and 3 dogs with diabetes mellitus. PROCEDURE: Interstitial glucose concentrations were monitored and recorded every 5 minutes by use of a CGMS. Interstitial glucose concentrations were compared with whole blood glucose concentrations as determined by a point-of-care glucose meter. Interstitial glucose concentrations were also monitored in 2 clinically normal horses after oral and i.v. administration of glucose. RESULTS: There was a positive correlation between interstitial and whole blood glucose concentrations for clinically normal dogs, cats, and horses and those with diabetes mellitus. Events such as feeding, glucose or insulin administration, restraint, and transport to the clinic were recorded by the owner or clinician and could be identified on the graph and associated with time of occurrence. CONCLUSIONS AND CLINICAL RELEVANCE: Our data indicate that use of CGMS is valid for dogs, cats, and horses. This system alleviated the need for multiple blood samples and the stress associated with obtaining those samples. Because hospitalization was not required, information obtained from the CGMS provided a more accurate assessment of the animal's glucose concentrations for an extended period, compared with measurement of blood glucose concentrations. Use of the CGMS will promote the diagnostic and research potential of serial glucose monitoring.

Animals↗

The use of a continuous glucose monitoring system in hypoglycemic disorders.

OBJECTIVE: To evaluate the use of a continuous glucose monitoring system (CGMS) in the evaluation and treatment of infants and children with hypoglycemic disorders. METHODS: Patients with hypoglycemic disorders wore the CGMS device in the Pediatric Clinic Research Center during their evaluation and treatment. Capillary blood glucose (CBG) values were obtained at least 3 times each day and entered into the device for calibration purposes. We evaluated the number of hypoglycemic episodes below 3.3 mmol/l (60 mg/dl) detected by CGMS compared to CBG values and characterized episodes by their duration and intensity. RESULTS: Five patients with hypoglycemic disorders were included in the study. There were a total of 13,369 sensor points, 343 paired sensor and CBG data points, and 57 days included. A total of 180 episodes of hypoglycemia occurred in these five patients, with an average duration of 55 +/- 13 minutes. Using a cut-off of 3.3 mmol/l (60 mg/dl) for hypoglycemia, the sensor had a sensitivity of 65.4%, specificity of 90.6%, and false positive rate of 42.9%. The positive and negative predictive values were 57.1% and 93.2%, respectively. CONCLUSION: CGMS is a useful adjunct in the diagnosis and evaluation of hypoglycemia, and for documentation of euglycemia in these patients following therapy.

Adolescent↗

[Indication of CGMS (Continuous Glucose Monitoring System) in the functionnal investigations of adult type 1 diabetic patients].

The Minimed CGMS (Continuous Glucose Monitoring System) is a holter-style electroenzymatic sensor allowing 3-days continuous monitoring of interstitial glucose fluctuations. This device gathers wide informations about the fluctuations of glucose over the day, in a more detailed (288 measurements) but less accurate way than those obtained from glucose self-monitoring. Its utilisation has been proposed for the analysis of nocturnal glucose control, to detect asymptomatic hypoglycemia or dawn phenomenon, and could be useful in the adjustment of type 1 diabetes therapy. Thus, its use could contribute to an improvement in glucose control, especially in patients with low compliance to self-monitoring. CGMS graphs can be used as an individual teaching support, or illustrate characteristic situations during collective educational sessions. The period chosen for the CGMS record, the duration of the record and the instructions given to the patients are of major importance to obtain accurate and reproductive graphs, that can be used in clinical practice.

Adult↗

Correlates of postpartum smoking relapse. Results from the Pregnancy Risk Assessment Monitoring System (PRAMS).

BACKGROUND: Using population-based data from the Pregnancy Risk Assessment Monitoring System (PRAMS), this study examines the prevalence and intensity of smoking before, during, and after pregnancy, and identifies correlates of postpartum smoking relapse. METHODS: Women who delivered live births in 1996 responded to a mailed questionnaire approximately 2 to 6 months after delivery (N =17,378). Data from 10 states participating in PRAMS were included in the study, and the overall participation rate was 75%. Analyses were adjusted for survey design and sampling strategy. Logistic regression analysis identified independent correlates of smoking relapse. RESULTS: Overall, 25.6% of women reported cigarette smoking before pregnancy. Among women who smoked before pregnancy, 44.5% quit during pregnancy. Among women who quit during pregnancy, half relapsed by the time of the survey. Independent correlates associated with increased risk of postpartum relapse included African American race/ethnicity, multiparity, high maternal weight gain, late or no prenatal care, and stressful life events. CONCLUSIONS: Correlates of postpartum smoking relapse identified by this study may contribute to the development of effective and targeted interventions to maintain long-term smoking cessation.

Adult↗