Administration

 

External Advisory Committee

 

Internal Advisory Committee

 

Research Support Facilities

 

Research Centers

Facilities

 

Integrated Research Information Support Services (IRISS)

 

Common Instrumentation Areas (CIAS)

 

Animal Resource Center

(ARC)

 

Behavioral Testing Facility

(BTF)

  Office of the Assistant Dean for Research and Graduate Studies
  Scientific Human Resources Development Unit (SHRDU)

Centers

 
 

RRC Data Core

RRC HIV Laboratory Core

RRC Pilot Projects

 
 

CMBN  NGCF

 

 

  Cell and Molecular Biology  Center (CMBC)

 

MCBC Optical Imaging Facility

MCBC Protein and Nucleic Acid Core

 MCBC Pilot Projects

 

 

Publications

 

Upcoming Events

 

Collaborations: SNRP/CEA  and NIH Links

 

Data Core

The HIV Data Core

 

   

The Registry is a large-scale prospective database made up of information gathered from HIV-infected participants who visit our local health service facilities (University Hospital, Immunology Clinic). This registry became operational in early 1992 and currently boasts 1,900 patients registered as of September of 1997. The registry’s overall goal is to study key elements associated with the progression and manifestation of HIV infection disease on the island of Puerto Rico. Information on risk behavior history, sociodemographic factors, immunological markers, lab values, presence of clinical conditions, psychological stress factors and institutional profile is collected through an initial interview. Follow-up interview are conducted at six-month intervals.

María Gómez Ph.D. Coordinator

Tel:  787-787-8710 ó 787-787-8722

 

mgomez@caribe.net

In the HIV Central Registry, the most important component of the Retrovirus Research Center, emphasis has been stressed for the improvement of quality strategies and data management. Novel approaches, as discussed with Dr. Janet Saint Lawrence, are proven to be essential for the accomplishment of the Registry’s objective.
A research strategy has been implemented for all patients with an unknown status through a matching program with PASET database and the systemic use of the Immunologic Clinic and the Hospital records. This has permitted us to detect an rectify errors within the socio-demographic module, decrease the rate of patients without and identified risk from approximately 18% to 7%, update mortality data of 175 patients, verify systematically the death certificates of AIDS patients and identify the number of patients that are not actually in the initial baseline data bank. In addition, 203 patients have completed new pilot tests conducted with small samples (as the Beck Depression Inventory and the Derogates Stress Scale), which have been incorporated in the data collection.

     

Team Members

 

Miriam Velázquez, MSPH
Ms. Gisela Cestero
Wanda Marín 
Magaly Torres, BBA

Glenda L. Ortiz

Doriz Báez

Angel Mayor

Heidy Ortiz

Johanna Maysonet

 

Robert Hunter, MD

Eddy Ríos, Ph.D.

José Rivera Del Río, MD

DianaFernández, MSPH

Wanda Figueroa, MD

     
     
     

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Contacting Mrs. Ivonne Amill Assistant Director

Recent change: October 18, 2007

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