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PubMed Journals Articles About "Medicines Medical Devices Bill Introduced" RSS

06:26 EDT 1st April 2020 | BioPortfolio

Medicines Medical Devices Bill Introduced PubMed articles on BioPortfolio. Our PubMed references draw on over 21 million records from the medical literature. Here you can see the latest Medicines Medical Devices Bill Introduced articles that have been published worldwide.

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Showing "Medicines Medical Devices Bill introduced" PubMed Articles 1–25 of 15,000+

Senate Bill 296/House Bill 2150.


Reporting adverse events related to medical devices: A single center experience from a tertiary academic hospital.

Intensive care units (ICU) rely on multiple technical resources with extensive use of different medical devices, such as ventilators, vital sign monitors, infusion, and injection pumps. This study explored how ICU nurses approach adverse events related to medical devices in a single tertiary center and identify their level of awareness of the national reporting system for adverse events related to medical devices beside their source for risk information updates. Totally, 297 nurses working in the ICU at Kin...

Allergic contact dermatitis caused by a glucose monitoring system: an emerging side effect of diabetes medical devices.

New medical devices for diabetes, such as insulin pumps and glucose sensors, have been introduced in the past few years to improve diagnosis, treatment and follow-up of diabetic patients. In particular, the conventional self-assessment blood glucose measurement by finger pricking significantly worsens the patient's quality of life because of painful hardening of the fingertips. For this reason, glucose sensors for flash and continuous monitoring of interstitial glucose levels are increasingly used. Unfortun...


Dispensing patterns of emergency medicines prescribed by Australian dentists from 1992 to 2018 - a pharmacoepidemiology study.

As the population ages, dentists are likely to encounter medical emergencies due to metabolic factors and polypharmacy. To date, there have been no documented studies in Australia that have analysed the prescription rate of Pharmaceutical Benefits Scheme (PBS)-funded emergency medicines for dentists. Therefore, this pharmacoepidemiology study aims to describe the dispensing patterns of emergency medicines as prescribed by dental practitioners, related to medicines covered by the Australian PBS system.

Cytokine Removal in Extracorporeal Blood Purification: An in vitro Study.

Cytokines are among the main target substances that have to be removed effectively in order to improve the patient's health status in the treatment of sepsis, septic shock, and liver diseases. Although there are various medical devices commercially available, the success of their clinical use is limited. The aim of this in vitro study was to compare 3 different medical devices with respect to their clearance for the cytokines interleukin-6 (IL-6), IL-8, IL-1β, and tumor necrosis factor alpha. The medical d...

Advanced Medical Care Program for the rapid introduction of health care technologies to the National Health Insurance system in Japan.

Japan's Advanced Medical Care Program (AMCP) seeks to facilitate patient access to promising health care technologies through National Health Insurance (NHI) coverage. This study aimed to examine AMCP's contribution to the accelerated introduction of new technologies through NHI coverage. AMCP-type B technologies registered May 2006-March 2019 were examined. To investigate the use of AMCP for NHI coverage, data from the AMCP website and from regulatory authority documents were used. Of 127 AMCP-type B techn...

Medical Devices in Obesity Treatment.

Obesity is increasing at an alarming rate and now poses a global threat to humankind. In recent years, we have seen the emergence of medical devices to combat the obesity epidemic. These therapeutic strategies are discussed in this review dividing them into gastric and duodenal therapies.

The Incidence and Nature of Adverse Medical Device Events in Dutch Hospitals: A Retrospective Patient Record Review Study.

Despite widespread use of medical devices and their increasing complexity, their contribution to unintended injury caused by healthcare (adverse events, AEs) remains relatively understudied. The aim of this study was to gain insight in the incidence and types of AEs involving medical devices (AMDEs).

Australian pharmacists: ready for increased non-prescription medicines reclassification.

Reclassification of medicines from prescription to non-prescription increases timely access to treatment, promotes self-management of minor ailments and relieves healthcare system burden. Previous research identified that Australia lagged behind the United Kingdom and New Zealand in medicines reclassification. This study aimed to identify Australian pharmacists' opinions on the current state of medicines reclassification; the prescription medicines consumers requested without prescription; the medicines pha...

Identifying the most effective essential medicines policies for quality use of medicines: A replicability study using three World Health Organisation data-sets.

Poor quality use of medicines (QUM) has adverse outcomes. Governments' implementation of essential medicines (EM) policies is often suboptimal and there is limited information on which policies are most effective.

Clinical Experience of Endoscopic Endonasal Approach in the Innovative Newly Developed Operating Room "Smart Cyber Operating Theater (SCOT)": A Technical Case Report.

When the medical devices and equipment in an operating room are connected to a network, vast amounts of data concerning the progress of the operation and the patient's condition can be comprehensively processed to improve the precision and safety of the surgical procedure. To make this possible, a next-generation networked operating room, "Smart Cyber Operating Theater" (SCOT), has been developed with medical-engineer cooperation, which integrates standalone medical devices using the "OPeLiNK" communication...

Feasibility study of use of rabbit blood to evaluate platelet activation by medical devices.

It is important to ascertain platelet responses to blood-contacting medical devices as part of a complete hemocompatibility evaluation. Nevertheless, researchers often face the problem of insufficient quantities of human blood for evaluation of platelet activation by actual medical devices. If animal blood can replace human blood to evaluate platelet activation by medical devices, testing will be smoother and will aid for quality control of related products. Therefore, in this study, we exposed representati...

Effectiveness of autoclaving in sterilizing reusable medical devices in healthcare facilities.

Medical devices are sterilized before being used for invasive clinical procedures such as surgery, to prevent pathogen transfer. Failure to sterilize medical devices properly presents a risk of healthcare-associated infections. Studies and reports have indicated that inadequately sterilized medical devices are one of the causes of a higher rate of healthcare-associated infections in developing countries. Steam sterilization (autoclaving) is the most widely used method for sterilization and is considered the...

Commentary: Medical Devices and Pressure Injuries in the Very Young: Evidence to Support Offloading Pressure From Medical Devices, Skin Assessment, and Reducing Moisture to Lower Nasal Pressure Injury Rates.

Nurse-led medicines' monitoring in care homes, implementing the Adverse Drug Reaction (ADRe) Profile improvement initiative for mental health medicines: An observational and interview study.

Preventable adverse effects of medicines often pass unnoticed, but lead to real harm.

Experiences With Counterfeit Aesthetic Medical Devices and Injectables: A National Survey.

Counterfeit medical devices and injectables have recently garnered interest in the field of aesthetics. Unlike their original counterparts, these counterfeit products have neither been tested nor verified using certified quality control measures.

Sleep assessment devices: types, market analysis, and a critical view on accuracy and validation.

: Sleep assessment devices are essential for the detection, diagnosis, and monitoring of sleep disorders. This paper provides a state-of-the-art review and comparison of sleep assessment devices and a market analysis.: Hardware devices are classified into contact and contactless devices. For each group, the underlying technologies are presented, paying special attention to their limitations. A systematic literature review has been carried out by comparing the most important validation studies of sleep track...

Association Between Vaccine Exemption Policy Change in California and Adverse Event Reporting.

California Senate Bill 277 (SB277) eliminated non-medical immunization exemptions. Since its introduction on February 19, 2015, the rate of medical exemptions in the state has increased. Filing a report to Vaccine Adverse Event Reporting System (VAERS) may be perceived as helpful in applying for a medical exemption. Our objective was to describe trends in reporting to VAERS from California coincident with introduction of SB277.

Inappropriate use of medicines and associated factors in Brazil: an approach from a national household survey.

This article aims to describe the inappropriate use of medicines in the Brazilian urban population and to identify associated factors. We conducted a data analysis of a household survey carried out in Brazil in 2013-14. The sampling plan was done by clusters with representativeness of the urban population and large regions of the country, according to gender and age domains. For this analysis, we considered a sample of adults (≥20 years) who reported having chronic non-communicable diseases, medical ind...

Effect on Treatment Adherence of Distributing Essential Medicines at No Charge: The CLEAN Meds Randomized Clinical Trial.

Nonadherence to treatment with medicines is common globally, even for life-saving treatments. Cost is one important barrier to access, and only some jurisdictions provide medicines at no charge to patients.

Integrated Security, Safety, and Privacy Risk Assessment Framework for Medical Devices.

The substantial improvements and innovations in communication networks and bio-medical technologies have led to the adoption of networked medical devices. Due to such developments, medical devices have made phenomenal strides in the course of the last half-century. However, the prolific amalgamation of technology and medical devices is constantly generating novel attack vectors. As these devices are no longer standalone systems and are network-connected, the attack surface has increased profoundly. Numerous...

Isobornyl Acrylate.

Multidisciplinary collaboration between several European dermatology departments has identified isobornyl acrylate (IBOA; CAS 5888-33-5), once deemed a low-risk sensitizer, as a major culprit contact allergen in glucose sensors and insulin pumps, medical devices used by diabetes patients worldwide. Although the patch test modalities of IBOA have been fairly well characterized, intriguing questions remain. For example, its cross-reactive profile to other acrylates remains to be determined, and the striking o...

Could the publication of new european guidelines change practices in France?

The use of predictive biomarkers in the diagnosis and prediction of the efficacy of targeted therapies for the individualized management of patients is generally based on the use of in vitro medical diagnosis devices that are now covered by the guidelines 90/385/EEC, 93/42/EEC and 98/42/EEC. On 25 May 2017, the European Parliament and Council Regulations 2017/745 and 2017/746 of 5 April 2017, related to medical devices and in vitro medical diagnosis devices, respectively, were published, disrupting years of...

Taking Privacy to a New Level: Texas Lowers Reporting Threshold for Security Breaches.

Federal requirements have not changed, but starting Jan. 1, breach notification requirements will become even more stringent for Texas physicians or medical entities. The Texas Legislature dropped the threshold for breach reporting from 500 patients to 250. House Bill 4390 also requires medical entities to report breaches to the Texas attorney general's office within 60 days of the breach.

Extra-medical use of antipsychotics: What can be learnt from experiences with other prescription medicines?


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