blood exposure in mouth
Answered by
University of Washington
Seattle - WA
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and I have been exposed. He placed a call to the powers that be
in infection control (assumed to be an infectious disease
specialist) and loaded me with Combivar (SP) and another drug
I think is AZT (which my guy is allergic to).
I just want to know if I have the 1/1000 chance that is
cited in all the studies published or if I have better odds.
These drugs are tough to take but I'm 1/2 way home. If indeed
they do reduce transmission by some 80% I'll stick with them.
I was also wondering when I should follow up with a test.
I will follow up. However, if you'd
please.. Are you saying that swallowing *** or any other
body fluid is about the same risk as swallowing blood?
Is it true that saliva inhibits the HIV virus?
Is an exposure in the mouth less than unprotected vaginal sex?
When should I follow up? I was refered to my Primary Doc not
a disease specialist. Is it imperitive that I see her now or
can I wait until I finish the meds ( I already have an appt in
a couple weeks). I understand if you can not answer questions
regarding treatment.
Thanks Doc, your words are reassuring to me. You have provided
some relief to a lot of people ...thanks again...
Saliva inhibits HIV. Mouth exposure or swallowing is much lower risk than unprotected vaginal sex.
People on PEP should be seen at least once during treatment, usually a couple of times, to check for side effects and general assessment. Ask your provider what s/he recommends; or if s/he isn't up to speed on PEP, ask for referral to someone who is.
Glad to help. Take care-- HHH, MD
Good luck - I hope your a-ok, I think you will be!
but it appears that there is a different make up of the
virus in milk vs blood. I just hope we are not comparing
apples to oranges. Doc, this is not a challenge to what
you posted, I'm just frightened.
Conf Retrovir Opportunistic Infect 2004 Feb 8-11; 11:(abstract no. 93)
Edwards B, Ghosh M, Sabbaj S, Rhodes A, Decker D, Goepfert P, Aldrovandi G; Univ. of Alabama at Birmingham, USA and 2Childrens' Hosp. Los Angeles, CA, USA
BACKGROUND:
Transmission of HIV via breast milk is a significant source of pediatric infection, yet the majority of infants do not acquire infection through this route. This latter finding may be due to the low levels of HIV RNA in breast milk compared with plasma. We therefore hypothesized that the magnitude and quality of T cells in breast milk are different than the peripheral blood compartment as an explanation for the lower viral load in the former compartment.
CONCLUSIONS: T cells found in the breast milk compartment express a highly activated/effector phenotype that preferentially migrate to this area. These findings may not be specific for HIV, as other antigen responses also appear increased in breast milk. Nevertheless, our data are consistent with the hypothesis that increased numbers of activated HIV-specific CD8+ T cells result in lower viral RNA levels in the breast milk than peripheral blood compartments