Welcome, Guest. Please login or register.
April 25, 2024, 03:47:13 am

Login with username, password and session length


Members
  • Total Members: 37651
  • Latest: Toropi_
Stats
  • Total Posts: 773288
  • Total Topics: 66348
  • Online Today: 651
  • Online Ever: 5484
  • (June 18, 2021, 11:15:29 pm)
Users Online
Users: 0
Guests: 595
Total: 595

Welcome


Welcome to the POZ Community Forums, a round-the-clock discussion area for people with HIV/AIDS, their friends/family/caregivers, and others concerned about HIV/AIDS.  Click on the links below to browse our various forums; scroll down for a glance at the most recent posts; or join in the conversation yourself by registering on the left side of this page.

Privacy Warning:  Please realize that these forums are open to all, and are fully searchable via Google and other search engines. If you are HIV positive and disclose this in our forums, then it is almost the same thing as telling the whole world (or at least the World Wide Web). If this concerns you, then do not use a username or avatar that are self-identifying in any way. We do not allow the deletion of anything you post in these forums, so think before you post.

  • The information shared in these forums, by moderators and members, is designed to complement, not replace, the relationship between an individual and his/her own physician.

  • All members of these forums are, by default, not considered to be licensed medical providers. If otherwise, users must clearly define themselves as such.

  • Forums members must behave at all times with respect and honesty. Posting guidelines, including time-out and banning policies, have been established by the moderators of these forums. Click here for “Do I Have HIV?” posting guidelines. Click here for posting guidelines pertaining to all other POZ community forums.

  • We ask all forums members to provide references for health/medical/scientific information they provide, when it is not a personal experience being discussed. Please provide hyperlinks with full URLs or full citations of published works not available via the Internet. Additionally, all forums members must post information which are true and correct to their knowledge.

  • Product advertisement—including links; banners; editorial content; and clinical trial, study or survey participation—is strictly prohibited by forums members unless permission has been secured from POZ.

To change forums navigation language settings, click here (members only), Register now

Para cambiar sus preferencias de los foros en español, haz clic aquí (sólo miembros), Regístrate ahora

Finished Reading This? You can collapse this or any other box on this page by clicking the symbol in each box.

Author Topic: Most UK clinic staff now tell people about U=U, but not always in the same way  (Read 3534 times)

0 Members and 1 Guest are viewing this topic.

Offline Jim Allen

  • Administrator
  • Member
  • Posts: 22,388
  • Threads: @jim16309
    • Social Media: Threads
I'm posting this here as its a survey result, not scientific news as such.
Most UK clinic staff now tell people about U=U, but not always in the same way

In Full: http://www.aidsmap.com/page/3478750/
In short:

Quote
Two presentations at this month’s British HIV Association (BHIVA) conference in Bournemouth show that most specialist healthcare workers are now informing people with HIV that if their viral load becomes undetectable as a result of taking antiretroviral therapy (ART), they can no longer transmit the virus ('Undetectable equals untransmittable', or 'U=U').

However, the healthcare workers told the patients at different times – on diagnosis, after starting therapy, aonce they were undetectable – and also phrased the information in different ways. The inconsistent practice highlighted in BHIVA's survey of its members prompted the organisation to issue a public statement about U=U on World AIDS Day, 1 December, last year.  https://www.bhiva.org/BHIVA-encourages-universal-promotion-of-U-U

A survey conducted at the Mortimer Market Centre’s Bloomsbury HIV clinic in London found that most patients received the information with relief, but that a minority found the information confusing or even distressing. Patients also misunderstood, or developed inaccurate beliefs, about U=U too, such as believing the message covers breastfeeding, which it currently does not.

U=U resources for UK clinics
http://i-base.info/u-equals-u-resources/


The BHIVA survey


Quote
The 270 responses were anonymous so we don't know the staff roles of the respondents, although the majority are likely to be doctors working in HIV services.

Although only three respondents had never heard of U=U, answers differed extensively among the other 267 with regard to when they told patients and what they said.

Seven (2.75%) of the respondents said they discussed U=U “only if asked” and six (2.35%) said “I don’t”.

Among the others, although 69% of respondents said they discussed U=U when patients were diagnosed and 55% said “when they start treatment”, 48% said “when they become undetectable” and 38% said “when they are fully adherent”. Although these are not exclusive categories – so some clinicians could be discussing U=U on all four occasions – it does leave open the question of whether some clinicians only discuss it once they feel sure that patients are at no risk of transmitting HIV.

Some 12% said they had discussed U=U with patients of unknown HIV status, often to encourage testing.

Thirty-seven per cent said they used the term “zero risk” or “no risk”. But 22% preferred using the phrase “next to zero”, 11% “negligible,” 10% “virtually impossible”, and 8.3% “extremely low”.

The Prevention Access campaign that promotes the U=U message warns against the use of ambiguous terms such as “negligible”, as they are “often misconstrued as still a risk to take into consideration in sexual and reproductive health decisions.”

The BHIVA statement says: “We recommend consistent and unambiguous terminology when discussing U=U such as 'no risk' or 'zero risk' of sexual transmission of HIV, avoiding terms like 'negligible risk' and 'minimal risk'."

Eighty-five per cent said they still recommended that people disclose their HIV to sexual partners if they are undetectable, but many added comments such as “yes, but I no longer tell them they have to”, or “not always if they’re out having fun, but disclosure is important in a long-term relationship.”

Fifty-six per cent of respondents said they still advised patients to use condoms, but many added phrases such as “yes, to avoid STIs or pregnancy” or “yes, if in a non-exclusive relationship”. Nearly a quarter said they no longer advised patients they had to use condoms, while 12% said they were not sure what to say.

While 71% told patients U=U did not apply to breastfeeding, 8% said it did and 21% were not sure: if clinicians are this uncertain, it is not surprising that patients are as well.


The Bloomsbury Clinic survey

Quote
The Bloomsbury Clinic survey canvassed 81 patients and 31 healthcare workers for their knowledge and opinions.

Eleven of the Bloomsbury Clinic patients were women and 12 were heterosexual men; the other 58 were gay/bisexual men. All of them were taking ART.

Sixty-eight per cent (55 individuals) had heard of U=U and 30% (24 patients) had heard about it at the clinic. However, although 80% agreed with the statement “being undetectable for six months means no sexual transmission”, which is correct, 58% also agreed with the statement “being undetectable for six months means HIV can’t be passed to a baby, including through breastfeeding”, which isn’t.

Seventy-nine per cent said that knowing or learning about U=U had had a positive impact on them.

When asked specifically about the most positive consequence of knowing, there was an interesting difference between heterosexual patients and the gay/bisexual men. For the gay men the most frequently mentioned positive impact – cited by 56% – was that it made disclosure and dating easier and made them feel more confident.

For heterosexuals, the most positive impacts were individual and medical rather than social; 47% said that U=U had helped them decide to start taking ART and served as an incentive to keep taking it regularly.

There were, however, eleven patients (14%) who had negative reactions. Some people had experienced bad reactions to ART and were unsure that U=U compensated for these in improving their quality of life. Some people simply found the news confusing or needed more convincing. One patient was strongly opposed to spreading the U=U message





Fifteen doctors, six health advisors, five nurses, four psychologists and one patient rep answered the clinicians' survey. Eighty-seven per cent (i.e. all but four) of the staff said they had discussed U=U with patients. Only 35% felt that all or most of their patients knew about U=U, compared with 68% of patients actually knowing about it.

In general, though, it was interesting how congruent the responses from the 31 healthcare workers were with patients’ responses. The clinicians estimated that 77% of their patients had a positive response to U=U and 14% a negative one, which almost exactly matches the patient figures of 79% positive and 14% negative.

Teasing these reactions apart a bit more, the clinicians reported 70% of their patients reacting with relief, 37% with confusion, 33% with disbelief, and 3% with anger – this 3% representing the one person quoted above. The clinicians tended to overestimate the impact of U=U on disclosure and dating, and underestimated its impact on whether to take and adhere to treatment.

HIV 101 - Everything you need to know
HIV 101
Read more about Testing here:
HIV Testing
Read about Treatment-as-Prevention (TasP) here:
HIV TasP
You can read about HIV prevention here:
HIV prevention
Read about PEP and PrEP here
PEP and PrEP

My Instagram
Threads

 


Terms of Membership for these forums
 

© 2024 Smart + Strong. All Rights Reserved.   terms of use and your privacy
Smart + Strong® is a registered trademark of CDM Publishing, LLC.