Positive Outlook – Nov-2

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Positive Outlook – Issue 8.0 – Nov 2014

CDC HIV/AIDS Science Facts:
CDC Releases Revised HIV Testing Recommendations in Healthcare Settings

Effective September 2006, CDC has revised its recommendations for HIV testing in healthcare settings. The Revised Recommendations for HIV Testing of Adults, Adolescents, and Pregnant Women in Healthcare Settings aim to make HIV testing a routine part of medical care in addition to expanding the gains made in diagnosing HIV infection among pregnant women. The Recommendations replace CDC’s 1993 Recommendations for HIV Testing Services for Inpatients and Outpatients in Acute-Care Settings and they update portions of CDC’s 2001 Revised Guidelines for HIV Counseling, Testing, and Referral and Revised Recommendations for HIV Screening of Pregnant Women.

What is different about the new Recommendations?
Key differences in the Recommendations for patients in all healthcare settings are:

HIV screening (another term for broad-based testing) for patients ages 13 to 64 in all healthcare settings after the patient is notified that testing will be performed unless the patient declines (opt-out screening).
HIV testing of people at high risk for HIV infection at least once a year.
Screening should be incorporated into the general consent for medical care; separate written consent is not recommended
Prevention counseling should not be required with HIV diagnostic testing or as part of HIV screening programs in healthcare settings.

Additional key differences in the Recommendations for pregnant women in healthcare settings are:

Including HIV screening in the routine panel of prenatal screening tests for all pregnant women, unless the patient declines (opt-out screening).
Repeat screening in the third trimester in certain jurisdictions with elevated rates of HIV infection among pregnant women.

The Recommendations emphasize the importance of voluntary testing. Various constituencies have expressed concern that eliminating the recommendation for separate informed consent for an HIV test could result in some patients being tested for HIV without their knowledge. Others have asserted that requiring separate, written informed consent is a barrier that makes HIV screening difficult to conduct in healthcare settings, and that removing this requirement would make widespread HIV screening feasible.

Concerns have also been expressed over the lack of HIV prevention counseling in conjunction with HIV testing. CDC continues to support prevention counseling as an intervention to help people reduce their risks for HIV, but recognizes it can become a barrier to HIV testing in busy healthcare settings.

CDC still recommends that patients receive information about HIV testing, HIV infection, and the meaning of test results.

Why did CDC revise the Recommendations?
There are several compelling reasons why CDC has revised the Recommendations.

An estimated one-fourth of the approximately 1 million persons in this country who are living with HIV do not know they are infected. That’s approximately 250,000 persons who could be spreading HIV to their partners unknowingly. As HIV screening becomes a more routine aspect of medical care, more people will know they are infected with HIV.
People living with HIV can receive effective treatment, resulting in improved health and extended life, if their HIV infection is diagnosed earlier. Currently, many people learn of their HIV infection only after they have developed symptoms (in a large study of HIV-infected persons, 65% reported they were first tested for HIV because of illness)
Most people, after finding out they have HIV, adopt behaviors that reduce HIV transmission. Routine HIV testing may help protect the partners of persons who are living with HIV but do not know it. In theory, new sexually transmitted HIV infections could be reduced more than 30% per year if all HIV-infected persons knew of their infection and adopted changes in behavior similar to those of persons already aware of their infection.
Routine HIV testing may reduce the stigma associated with an HIV test offered based on the healthcare provider’s perception (or knowledge) of risk. When every person gets offered an HIV test at some point in his or her health care, it should take controversy and judgment out of the test and make it a normal part of taking care of oneself.
Providers reported that requirements for pre-test counseling and written informed consent were not feasible in emergency rooms and other busy healthcare settings.

For whom are the Recommendations intended?
The Recommendations are intended for healthcare providers in both the public and private sectors. These include healthcare workers in hospital emergency departments, inpatient services (including labor and delivery), correctional health care facilities, clinics including substance abuse treatment, public health, community, pediatric and adolescent, prenatal, and mental health, and other primary care settings.

These Recommendations address HIV testing in healthcare settings only. They do not change existing CDC guidelines on HIV counseling, testing, and referral for persons at high risk for HIV who receive testing in nonclinical settings (e.g., at community-based organizations.)

How did CDC develop the Recommendations?
These Recommendations are the culmination of a lengthy and deliberate process that began in 1999 when the Institute of Medicine (IOM) recommended adopting a national policy of universal testing of pregnant women with patient notification (opt-out screening), eliminating requirements for extensive pretest counseling, and eliminating requirements for explicit written consent for HIV testing. Adoption of the IOM recommendations led to increased prenatal screening, and, combined with appropriate medical care, contributed to a dramatic 95% decline in perinatally acquired AIDS cases. CDC began exploring the feasibility of adopting a similar policy for the general public, which could bring about reductions in sexually transmitted HIV. Between 1999 and 2006, CDC involved healthcare providers, representatives from professional associations and community organizations, researchers, public health officials, and persons living with HIV to research and refine the Recommendations in order to expand HIV testing, especially in high-volume, high-prevalence acute-care settings. Through this process, CDC has tried to involve persons most likely to be affected by the Recommendations and ensure the resulting Recommendations are ethical and fair and would achieve their stated goals.

Conclusion
CDC believes that the adoption of voluntary, HIV screening in healthcare settings will foster the earlier detection of HIV infection, help healthcare workers identify and counsel persons with previously unrecognized HIV infection and link them to clinical and prevention services, and further reduce sexual and perinatal transmission of HIV in the United States.

For more information . . .
CDC HIV/AIDS
http://www.cdc.gov/hiv
CDC HIV/AIDS resources

CDC-INFO
1-800-232-4636
Information about personal risk and where to get an HIV test

CDC National HIV Testing Resources
http://www.hivtest.org
Location of HIV testing sites

CDC National Prevention Information
Network (NPIN)
1-800-458-5231
http://www.cdcnpin.org
CDC resources, technical assistance, and publications

AIDSinfo
1-800-448-0440
http://www.aidsinfo.nih.gov
Resources on HIV/AIDS treatment and
clinical trials