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Guidelines on the choice of agents and how best to step up treatment for various subgroups in hypertension (high blood pressure) have changed over time and differ between countries. A Comparison of International Guidelines on Goal Blood Pressure and Initial Therapy for Adults With Hypertension (adapted from JNC 8 guidelines [ 1 ] )
The Reference Information Model [9] (RIM) is the cornerstone of the HL7 Version 3 development process and an essential part of the HL7 V3 development methodology. RIM expresses the data content needed in a specific clinical or administrative context and provides an explicit representation of the semantic and lexical connections that exist ...
GIN has an International Guideline Library and registry, [7] one of the world's largest guideline libraries, [citation needed] containing regularly updated guidelines and publications of the GIN membership, as well as other guideline developers. The registry is open for all guideline developers to register their guidelines.
Prehypertension, also known as high normal blood pressure and borderline hypertensive (BH), [1] is a medical classification for cases where a person's blood pressure is elevated above optimal or normal, but not to the level considered hypertension (high blood pressure).
A descendant of one of Jack the Ripper's victims has demanded a new inquest into one of history's most notorious serial killers, after DNA evidence suggested the murderer was a Polish barber.. The ...
GLENDALE, Ariz. -- Penn State coach James Franklin said his No. 6 seed Nittany Lions were eager to "corral" No. 3 Boise State's prolific running back Ashton Jeanty entering their College Football ...
Later, she posted the video on TikTok, where it went viral, garnering 16.7 million views and more than 10,000 comments. One family decided to have a little extra fun with gifting this holiday season.
In the 1980s, the European Union began harmonising regulatory requirements. In 1989, Europe, Japan, and the United States began creating plans for harmonisation. The International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH) was created in April 1990 at a meeting in Brussels.