What's new

The Corrona Rheumatoid Arthritis (RA) Registry was created in 2001 as an ongoing longitudinal clinical registry. Corrona* has a network of >250 participating academic and community rheumatologists at >100 participating practices (academic and private) in 35 states within USA.

Remember to stop by Booth #21 at ISPOR (May 23-25, 2016) in Washington D.C.to conduct your own search and enter to win prizes.

*The Consortium of Rheumatology Researchers of North America, Inc.

The Clalit Health Services (Clalit) computerized database is a combination of administrative and electronic medical records across an entire lifetime for more than half the population of Israel. Started in 1998, the database is complete for over 5 years and partial for over 2 decades.

View our database listing to see all 263 databases we have profiled from 36 countries.

Come visit DGI at ISPOR (May 23-25, 2016 - Booth #21). Stop by to conduct your own database search and enter a drawing for FREE Access.

Read our latest newsletter talking about enhancements made to B.R.I.D.G.E. over the past few months including:

- Additional fields when exporting search results to a spreadsheet

- Easier navigation of results

- Brand new citations page

The Alaska Cancer Registry (ACR) is an incidence only, population-based cancer surveillance system funded by the Centers for Disease Control and Prevention (CDC). ACR collects data on all newly diagnosed cases of cancer. Read more about ACR in our resource by logging in or signing up.

Maccabi Healthcare Services (MHS) has established an automated registry of women diagnosed or treated for infertility. The MHS Infertility Registry was initiated in 2004, but data are available since 1998. As of November 2015, a total of 71,193 members have been identified, out of which 97,810 were active members of MHS in October 2014. Read more about the 9th Maccabi profile in our resource by logging in or signing up.

Subscribers can now view profiles for The University of Massachusetts Minimum Data Set (MDS) and the Korea National Cancer Incidence Database (KNCI DB).

If you haven’t done so already, make sure you view our updated tutorials and sample set, and see our complete database listing with all 260 profiles.

The University of Massachusetts Minimum Data Set (MDS) consists of a comprehensive clinical record of all long-stay residents of nursing homes receiving any Centers for Medicare and Medicaid Services (CMS) MediCare funds in the United States and Territories.

View our database listing to see all 259 databases we have profiled.

In our ongoing effort to describe more population healthcare databases, we now have profiles from 36 countries.

Our newest profile, the Malta Congenital Anomalies Register (MCAR) captures major birth defect data from all hospitals on the Maltese Islands via case report forms on an active and passive basis. Over the 2003-2012 period, out of 40,493 live births, a total of 1,184 babies with major congenital anomalies were registered with MCAR.

The Youth Risk Behavior Survey (YRBS) monitors six high priority health risk behaviors that contribute markedly to the leading causes of death, disability, and social problems among youth and adults in the United States. YRBS data are representative of all public and private school students in grades 9-12 in the 50 states and the District of Columbia.

Read more by logging in or signing up.