A study from
Madrid has found that 92% of people taking an HIV test could
obtain a valid result by testing themselves with the kind of fingerprick point-of-care
blood test used at clinics, without any instruction except the brochure the
test came with.
The Madrid study
also tested people’s ability to recognise positive, negative and invalid test
results when shown photos of typical tests. Just over 5% of negative test
results were interpreted incorrectly (2.7% as false-positive) and 3.6% of
positive test results were interpreted incorrectly (1.1% as false-negative).
Participants
were not told their actual test results till the very end of the testing
process. Nine out of 519 participants (1.7% or one in 58 participants) had HIV.
Out of these, eight had correctly interpreted a picture similar to what their
own test result looked like, while the ninth was uncertain whether the picture
closest to his own test result was positive or invalid.
After
self-testing, 84% of participants said they were more motivated to self-test
for HIV again.
- Another study in the same project assessed participants' knowledge of post-exposure prophylaxis (PEP) - see this report.
How the study was conducted
The study set up
three testing sites in five locations in the Madrid region – in Chueca, the
city’s central gay district, next to two railway stations, and in two
university campuses. The test sites were in tents; the researchers note
that the trial period, October 2009 to February 2010, was “a particularly cold
and rainy winter,” and suggest that tests taken in the comfort of people’s
homes might produce more reliable results.
The study was
carefully structured so that participants received no instruction from staff in
how to use the test. First, 313 out of
519 participants were given a brochure with written instructions and illustrations
on how to use the test. They then used the kit to test themselves with staff
observing but not helping, as if they were doing it unassisted at home. Another
207 participants were, for purposes of comparison, given help and advice when
needed.
The test used
was the Determine HIV1-2 antibody/p24 antigen blood test. It consists of
pricking a finger with a small lancet and squeezing two drops of blood into the
two test windows that detect HIV antibodies and p24 antigen. In the test kit
supplied to clinics, medics are supplied with a small glass capillary tube to
pick up a precise quantity of blood, but untrained participants found this very
difficult to use, and the instruction to deposit “two large drops of blood”
appeared to provide adequate results.
After being
asked about their experience of doing the test, participants then saw a
healthcare worker who, after providing HIV counselling required by Spanish law,
took a second confirmatory blood test using the same Determine test kit, only
this time using the capillary tube.
The Determine
test takes about 20 minutes to provide results. During this time, participants
were each shown six photos of various positive, negative and invalid test
results and asked to interpret them based on their reading of the brochure. A
variety of sets of six photos were used in order to generate a large data set.
Participants
were also asked to give feedback during this point on their experience of
taking the test and of interpreting the results, whether they were motivated to
self-test again and how much they might be prepared to pay if the Determine
test was sold over the counter. They also completed a paper questionnaire on
demographic factors and risk behaviour.
Finally and only
at the very end of the process, they were given the result from the
staff-administered test, with appropriate counselling and referral.
Results in detail
Recruitment was
entirely voluntary: participants simply walked into a testing tent. Fifty-six
per cent of participants were recruited at the single tent in Chueca. Despite
this being the ‘gay village’ only 29% of all test participants defined as gay
men; 34% were women. Forty-seven per cent of all participants had taken an HIV
test before, and 51% of those who performed the test unaided (not a significant
difference). A quarter of enquirers decided not to participate (19% of those who
tested unassisted). There were no demographic differences between those who
participated and those who decided not to.
Eight per cent
(25) of those who took the test unassisted produced an invalid result; gay men
were less than a third as likely to produce an invalid result as other
participants.
About five per
cent of participants interpreted at least one test result picture wrongly as
positive, negative or invalid when it in fact showed a different result. About
2.7% of participants wrongly identified invalid or negative results as
positive; 1.5% identified invalid results as negative and 1.1% identified a
positive result as negative. People over 30, compared with people under this
age, were twice as likely to interpret a test result wrongly and people not
born in Spain or with no university education somewhat more likely.
Ninety-three per
cent of participants who produced valid results and 80% who produced invalid
results said self-administering the test was “very easy” or “quite easy” and
98% of those who correctly identified all six test result photos and 77% who
made at least one mistake said interpreting photos was very or quite easy.
There were a
couple of individual cases where people experienced some psychological
distress: in one case the person felt dizzy after drawing blood and in the
second the person became frightened of the possibility of a positive result
after taking the test and while looking at the photos of results.
No-one said
after self-administering a test that it had decreased their interest in using
such a test again and 80% said it had increased their interest.
When asked how
much they might be prepared to pay for such a test, a third said ten to 19 euros, a quarter said 20 to 29 euros and one in five said €30.00 or more. The
OraQuick test is now on sale for $40.00 in the US, which at today’s exchange rate is about
€31.00 or £25.00. The researchers comment that, given the recent questions
about the validity of the p24 antigen test, it should probably not be included
in a blood test designed for home use, which might make it cheaper.
Implications
This study is
important partly because the blood test concerned has a shorter ‘window period’
than OraQuick, the HIV test using oral fluid sampling that has been approved
for home-testing use in the US and is now on sale over the counter. OraQuick
has a considerable window period. In
the trial that led to Oraquick's approval, 7% of people who really did have HIV
received false-negative results.
The window period for the Determine HIV
antibody/p24 antigen blood test, used in this study, is likely to be somewhat shorter.
As the
researchers say, “This is the first published study showing that a high
percentage of HIV-negative people are able to perform a blood-based
point-of-care test and read the results correctly.”
They urge
further research into self-testing in different populations and with different
kits.