Electronic medical records training 92591

Electronic medical records training 92591 professional#

A 'Maintenance of Certification Program' encourages board certified physicians to continue learning and self-evaluating throughout their medical career. MOC - He does not participate in the Medicare Maintenance of Certification Program.Million Hearts is a national initiative that encourages health care professionals to report and perform well on activities related to heart health in an effort to prevent heart attacks and strokes. MHI - He does not commit to heart health through the Million Hearts initiative.Electronic health records are important because they may improve a health care professional's ability to make well-informed treatment decisions.

The Electronic Health Records (EHR) Incentive Program encourages health care professionals to use certified EHR technology in ways that may improve health care.

EHR - He does not use electronic health records (EHR).

Electronic medical records training 92591 professional#

Quality measures can show how well a health care professional provides care to people with Medicare. The Physician Quality Reporting System (PQRS) is a Medicare program encouraging health care professionals and group practices to report information on their quality of care. PQRS - He does not report Quality Measures (PQRS).eRx - He does not participate in the Medicare Electronic Prescribing (eRx) Incentive Program.NPPES Last Update: Thursday, January 16, 2014.NPI Enumeration Date: Friday, February 13, 2009.Dennis Miller graduated from medical school in 1997. degree have attained the ability to become licensed as osteopathic physicians who have equivalent rights, privileges, and responsibilities as physicians with a Doctor of Medicine degree (M.D.). or DO) is a professional doctoral degree for physicians and surgeons offered by medical schools in the United States. There were no adverse patient effects and no clinically significant delay in the procedure.Doctor of Osteopathic Medicine (D.O. The delivery catheter and guide wire were removed as a single unit. The sensor was deployed without incident, however resistance was felt when removing the guide wire out of the delivery catheter. The guide wire was inserted into the lower left lobe of the pulmonary artery. It was reported that the procedure was to place a cardiomems sensor using a hitorque command 18 guide wire. It should be noted that per electronic instructions for use (ifu), high torque command 18 guide wire for pta: this hi-torque guide wire is intended to facilitate the placement of balloon dilatation. There is no indication of a product quality issue with respect to the design, manufacture, or labeling of the device. A review of the electronic lot history record and similar incident query for this product was not performed since the lot number was not reported and the device was not returned for analysis. It is likely that during the procedure the delivery device or guide wire became damaged due to manipulation resulting in the difficulty to remove. The investigation determined the reported difficulty to remove appear to be related to operational circumstances of the procedure. The guide wire may also be used to reach and cross a target lesion, provide a pathway within the vessel structure, facilitate the substitution of one diagnostic or interventional device for another, and to distinguish the vasculature.ДЄlthough it was reported that the physician used the device in the wrong the anatomy, the reported violation of the ifu did not caused or contribute to the reported complaint. This guide wire may also be used with compatible stent devices during therapeutic procedures. It should be noted that per electronic instructions for use (ifu), high torque command 18 guide wire for pta: this hi-torque guide wire is intended to facilitate the placement of balloon dilatation catheters during percutaneous transluminal angioplasty (pta), in arteries such as the femoral, popliteal and infra-popliteal arteries. Product performance engineering reviewed the reported information however, the device was not returned for evaluation.ДЄ review of the electronic lot history record and similar incident query for this product was not performed since the lot number was not reported and the device was not returned for analysis.