Guest guest Posted March 24, 2006 Report Share Posted March 24, 2006 This is admittedly just my back yard...but a surprising place for this kind of invasive behavior to begin? Probably not. Bush et al. can be as secretive as they want, stonewalling all information and FOIAs etc., with an INJustice Dept. full of liars, thieves and torturers doing their level best to cover their crimes up while snooping into the private lives of Quakers. So....why not elsewhere in the world? An article from Housing Works. M. ** http://www.hwadvocacy.com/update/archives/2006/03/beyond_extreme.html March 21, 2006 BEYOND EXTREME Frieden bill demands near-total DOH access to patient records, ignores patient consent for HIV testing FRIEDEN'S BILL: Some language is worse than he ever suggested A bill that NYC health commissioner Dr. Tom Frieden is putting before Albany lawmakers to change state HIV-testing and medical privacy laws is far broader in its call for DOH access to patient histories than the health commissioner has ever indicated. The bill, which Housing Works obtained this afternoon, appears to demand that virtually any provider of healthcare or other services for people with HIV/AIDS turn over any information on a patient that is requested by the health department. It also requires Medicaid and the AIDS Drug Assistance Program (ADAP) to share with the health department any patient's current or former HIV-medication history. In addition, the bill suggests that providers don't need to obtain explicit consent from patients before giving an HIV testbut merely inform patients they will be given a test. Click here for the bill and here for its memo of support. " It's sad and infuriating to learn that this bill embodies some of the very worst and most extreme provisions that the comissioner has been saying all along he wouldn't endorse, " said Housing Works president King this afternoon. " I feel vindicated in my distrust of the health department under Frieden, " King continued. " And I hope that community groups that have been unsure about his proposals will now join us in opposition when they read the extreme measures here that Frieden is trying to write into law. " The bill calls for alarming changes in three areas: ACCESS TO PRIVATE PATIENT FILES: For months, written and oral presentations from the DOH have asserted that the department wanted merely the authority to contact HIV-care providers (and, in some cases, patients) based on a limited amount of treatment information it already obtains from the state, including individual patient CD4-counts, viral loads and resistance profiles. But the actual bill reads that " The commissioner...may require a health facility or health-care provider...to provide additional information [italics ours] concerning a[n HIV] case. " The bill then extends that requirement to HIV COBRA case-management programs; other PWHA-serving case-management programs; HIV special-needs plans (SNPs); and the AIDS Drug Assistance Program (ADAP). The language is alarming, because the broadness of " additional information " could encompass anything from further medical details to particulars of the person's sexual or drug-using history. Further, the number of agencies beholden to the law encompass nearly the entire array of programs relied upon by low-income New Yorkers living with HIV/AIDS. Requiring such information from COBRA case-management programs, in particular, puts dozens of nonprofit community-based programs that have spent years building up trust with their clients in the position of having to open client files to government watchdogs. In addition, the bill makes no mention of appropriating new funding to help groups provide such information for the health department. ACCESS TO PATIENT MEDICATION HISTORIES: Page 2 of the bill states: " A medical assistance program...shall disclose to the commissioner...upon request...information concerning pharmaceutical claims made by or on behalf of individuals [in such a program]...Such information shall be limited to antiretroviral drugs... " Moreover, the bill makes no mention of appropriating funding to help Medicaid or ADAP, which is cash starved, provide such records. DEFINITION OF INFORMED CONSENT FOR HIV-TESTING: The bill strongly suggests that a provider giving an HIV-test doesn't need explicit permission from the patienteven an oral oneto give the test. The bill reads: " In order for there to be informed consent, the person ordering the test shall at a minimum advise the protected individual that an HIV-related test is being performed. " This is very similar to a provider-education publication on HIV-testing the DOH put out recently that suggests providers tell patients they will be given an HIV test and then ask, " Do you have any questions? " rather than explicitly asking, " Is that OK with you? " or " Do you consent to that? " " That publication read like they were trying to ram HIV tests down people's throats without their permission, " said King. " And now it's clear from the bill that they're trying to write that violation of people's rights into the actual law. " Housing Works will provide further analysis of and community reaction to the bill later in the week. Meanwhile, HW hopes that making the bill available here will give people time to brief themselves on it before tomorrow (Wednesday) night's first of several open community meetings with the DOH. The forum takes place 6-8pm in the Repertory Theater at Hostos Community College in the Bronx (click the link for directions). Quote Link to comment Share on other sites More sharing options...
Recommended Posts
Join the conversation
You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.