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Truvada for HIV Pre-Exposure Prophylaxis (PreP)

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Truvada for HIV Pre-Exposure Prophylaxis (PreP)

Old 4th May 2018, 19:29
  #1 (permalink)  
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Join Date: Mar 2013
Location: Glasgow
Posts: 21
Truvada for HIV Pre-Exposure Prophylaxis (PreP)

Thought I'd share my experience to-date of applying for a Class 3 certificate whilst taking Truvada. I had my initial Class 3 in the middle of March. The AME had no idea what it was.

The guidelines the CAA eventually provided are as follows:

- Applicants should be assessed as unfit when starting/re-starting PreP. They should provide their AME with baseline blood tests for renal function, liver function and serum phosphate measured before starting PreP and repeated after 4 weeks.
- Four weeks after starting/re-starting AMEs should review applicants for side-effects and check the baseline and four week bloods for a fit assessment/issue of an unrestricted Class 1, Class 2, Class 3 or LAPL medical certificate.
- Blood monitoring should be required monthly for the first 3 months and then the period can be increased to 3-4 months thereafter. Blood results to be submitted to an AME for review.

I haven't received any information on what the guidelines are for those who are applying for initial medicals and have already been on PreP for some time. My case has been deferred to the CAA. I'll provide updates when I receive them. Although, I'm very tempted to stop taking it. It seems much more hassle than it's worth. I spoke to my sexual health consultant who was strongly of the opinion that these guidelines are excessive.
tcm1707 is offline  
Old 16th May 2018, 10:40
  #2 (permalink)  
Join Date: Sep 2002
Location: Windhoek
Posts: 124
I also use PreP (Truvada) however don't currently hold a Class 3 any longer but when I did the restrictions were similar, however in another region. The CAA uses the HIV protocol as a base-line as the med can be used for those starting ARVs if they have the Virus and then obviously for PEP and PreP. The 4 week restriction of grounded is normal due to some having debilitating side-effects initially (Cramping most common). I under go blood monitoring on 3 monthly intervals (discussing moving to 6 with my Doctor who is also an AME).

If the person is already on PreP at application then it depends on the CAA/AME if the person's GP has the records side-effects and of the blood monitoring at the required intervals (3 Months) then they would apply to the CAA medical board for an unrestricted certificate, if the Blood monitoring is not available and the person's GP did not monitor side effects or the initial blood test wasn't done, then the person will usually get the 4 week restriction whilst the monitoring can be done.

To explain from the CAA expectation - the AVMED panels look at the chances of incapacitation occurring and for a medical to be issued as unrestricted the likelihood of ATC incapacitation should be around 1% of the time the ATC is on position (a rather arbitrary and difficult number to prove but in theory it is the discussion that is held) if the medication has a likelihood to induce side-effects that could cause you to become incapacitated (this does not mean passing out and not being able to control but more needing to leave your position for a period whilst on duty- so this includes the likelihood of diarrhoea or stomach cramps causing you to have to leave your position even momentarily would count as such incapacitation case). Although these are normally manageable in most people the AME would have to monitor your reaction to the side effects and hence the 4 week grounding period. As with any medication (including Beta Blockers or any other meds that could cause major side effects) the Medical is usually temporary suspended while the AME monitors the applicants reaction to the med and the side effects.

As more information is gathered on these, A protocol may be developed by the AVMED panels or ICAO and this would then be used as a norm. Truvada is still relatively new (even your AME didn't know what it was) so the data to develop a protocol will be coming from persons like you and I who are doing the regular monitoring etc. In a few years (unfortunately yes years the process to get the data for a new protocol is rather lengthy) if it is determined that the majority of Medical holders did not experience debilitating side-effects in the 1st 4 weeks and that there is little difference in 3 month or 4 month or 6 month blood results or the ability for such intervals to still pick up major problems then a protocol may be issued that lessons the restrictions and also precludes these cases going to medical panel all the time, only if an applicant displays symptoms outside of the protocol -additional side-effects or blood results at a certain level etc). For this reason I would suggest you keep on the programme so that more data is collected at your CAA-AVMED to allow for future sharing of data, however if this interferes too much with your license then stopping would be easier.
Little One is offline  
Old 21st May 2018, 03:17
  #3 (permalink)  
Join Date: Apr 2006
Location: South of the Equator
Posts: 147
The FAA is actually quite progressive on this issue from my readings.

This would be unlike my home CAA that, when I enquired what might be the guidelines here (admittedly a couple of years ago), they said the question had never been asked, they had never thought about it and would not think about it until presented with an active case. How's that for helpful?
Water Wings is offline  

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