Information for Professionals
Information for Professionals
The ESRD Network of Texas provides, maintains and manages four areas of information and resources for the ESRD community. The Network is responsible for Information Management of both patient and facility data, Quality Improvement, Patient Services and Community Outreach for the state of Texas. The Network assists providers in establishing and maintaining dynamic, ongoing quality management and outcomes assessment programs through services and programs offered.
The Network develops and maintains criteria and standards that are reviewed and revised by the Medical Review Board, as necessary. The Criteria and Standards are used to guide the ESRD community in providing appropriate and quality care. Criteria and Standards are recommended practice standards within the Network and are utilized to:
- Create quality improvement studies
- Guide facility practice
- Provide standards for medical review decisions
- Provide standards for complaint/grievance investigations
The Network can provide facility staff with comparative outcome data, copies of state and federal guidelines, advice on QI projects and assistance with difficult patients, complaints/grievances and staff training or retraining. The Network staff can participate and facilitate specific improvement projects onsite upon request. The majority of Network support focuses on quality of care issues (such as hemodialysis adequacy, peritoneal dialysis and vascular access management), accurate and timely data collection (such as PAR, 2728, 2746 and 2744 forms), maintaining positive patient/staff relationships and providing useful information and resources to support ongoing quality of care throughout Texas.
Vocational Rehabilitation
Special Alerts
- FDA Proposes Withdrawal of Low Blood Pressure Drug (midodrine hydrochloride) - 08/17/10
- Coumadin 1 mg Tablet Blister Packs: Recall - 07/14/10
- Qualaquin (quinine sulfate): New Risk Management Plan due to potential for serious hematological reactions - 07/08/10
- FDA - LIFEPAK 20 and LIFEPAK 20e External Defibrillator/Monitors by Physio-Control Inc.: Class I Recall Due To Power Supply Failure 07/02/10
- FDA: Tamiflu: Counterfeit Product Sold on Internet - risk for those allergic to penicillins- 06/17/10
- FDA Recall of Defibtech DBP-2800 Battery Packs used in Lifeline AED and ReviveR AED - 06/14/10
- FDA Public Health Alert: Healthcare Professionals Warned Not To Use Certain Intravenous Metronidazole, Ondansetron, and Ciprofloxacin Due To Potential Contamination - 05/31/10

Professionals