- 128 Views
- Uploaded on
- Presentation posted in: General

Thoughts on Simplifying the Estimation of HIV Incidence

Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author.While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server.

- - - - - - - - - - - - - - - - - - - - - - - - - - E N D - - - - - - - - - - - - - - - - - - - - - - - - - -

Thoughts on Simplifying the Estimation of HIV Incidence

John Hargrove, Alex Welte, Paul Mostert [and others]

Estimates of incident(new) cases are important in the assessment of changes in an epidemic, identifying “hot spots” and in gauging the effects of interventions

HIV incidence most accurately estimated vialongitudinal studies – but these are lengthy, expensive, logistically challenging.

Do provide a “gold standard” against which to judge other estimates of HIV incidence

An alternative way of estimating incidence, involving none of the disadvantages of a longitudinal study, would be to use a single chemical test that can be used to estimate the proportions of recentvslong-established HIV infections in cross-sectional surveys

Idea: identify HIV test where measured outcome not simply +/- but rather a graded response increasing steadily over a long period

One such assay is the BED-CEIA developed by CDCGraph shows result for a seroconverting client taken from the ZVITAMBO study carried out in Zimbabwe[14,110 post partum women followed up at 6-wk, 3-mo, then every 3-mo to two years]

The idea is to calibrate the BED assay to estimate the “average” time [or “window”] taken for a person’s BED optical density [OD] to increase to a given OD cutoff

In cross-sectional surveys proportion of HIV positive people with BED < cut-off allows us to calculate the proportion of new infections – and thus the incidence.

Estimation of the window period is thus central to the successful application of the BED

Data from commercial seroconversion panels withaccurately known times of seroconversion indicate

Problem 1.

Delay (~25 days) between sero-conversion and the onset of then increase in BED optical density

Window period (W)

W'

Date of

seroconversion

Sero-

negative

Sero-

positive

Date of

infection

Extrapolated time when OD = baseline

D1

D2

Baseline OD = 0.0476

Problem 2: Considerable variability between clients in a real population. No prospect of using BED to identify individual recent infections. Idea only to estimate population incidence

Problem 3: Often have limited follow-up: of 353 seroconverters in ZVITAMBO, 167 only produced a single HIV positive sample,

Problem 4: The available data for a given client quite often do not span the OD cut-off. The proportion that fail to do so varies with the chosen cut-off. Failure to span increases the uncertainty in estimating the time at which the OD cut-off is crossed

Problem 5: There is a large variation (27 – 656 days) in the time (t0) elapsing between last negative and first positive HIV tests. The degree of uncertainty in the timing of seroconversion increases with increasing t0

We need to consider how variation in samples per client, t0 , and failure to span the cut-off affect our estimate of the window period.

How to approach problem?Scatter-plot of the data?Makes no use of the information of the trend for individual clients and ignores the fact that the sequential points for that client are not independent.

Alternative which uses trend in BED OD is suggested by an approximately linear relationship between square root of OD and time-since-last-negative HIV test (t).Allows a regression approach taking out variance due to t and to difference between clients

Gives consistent results; in that results independent of whether we insist on minimum of 3, 4 or 5 samples per client; and on value of t0 between 75 and 180 days

Are we even using the right transformation?And should we be using the time of last negative HIV test as the origin

Try instead to do a preliminary estimate of the time when OD starts to increase by fitting a quadratic polynomial to the data. Then use this estimate as the origin.

Seems to suggest that the true relationship may actually be a power function.What it really were? What would we see if we plotted OD vs time since-last negative

Examples of times when HIV -ve tests might have been taken

Our problem is that we do not know when seroconversion occurred.

We only know the time of the last HIV negative test.

And the greater the delay between last negative and first positive tests the greater the uncertainty

For zero offset the window is UNDER-estimated; for 100-day offset it is OVER-estimated

This approach to window estimation is clearly not optimal since the window estimate changes with the timing of the last HIV-negative testBut can we do any better?

If OD increases as a power function fit:or equivalently where a and b are constants, t is the time since the last negative and t0isthe estimated time of seroconversion.

We use the data to estimate a,b and t0 by non-linear regression

For the generated data [without noise] this approach gives the correct window – regardless of the time of the last negative test

But for real data in 40% of 61 cases the time of seroconversion was estimated to be before the time of the last negative test or after the time of the first positive.

[Work in progress]

Turnbull survival analysis different approach suggested by Paul Mostert (Stellenbosch Statistics Department).This is a slightly more sophisticated variant of the Kaplan Meier survival analysis. Works on the basis that the (unknown) times of: i) seroconversion ii) OD cut-off each lie between two known timesThe times of the two events are quantified using interval censoring

Turnbull window estimatesRunsAll data (red; 183 d)2: Excluding max OD < 0.8 (purple; 141 d)3: Excluding min OD > 0.8 (green; 210 d)4: Excluding 2 and 3 (blue; 163 d)

The window length is estimated using a non-parametric survival technique which makes no assumptions about any parametric models and underlying distributions. . No interpolation is used to obtain the cut-off time where the BED OD reaches 0.8 or the seroconversion time point. Only time points that will define the interval boundaries were used, which means that time points more than four for a specific women were not fully utilised. However, time points as few as two per women could be used in this estimation of window length.

Conclusion

There is still no general agreement on how best to estimate the window for methods like the BED. Fortunately most of those described seem to give fairly similar answers – though it’s not clear to what extent this is happening by chance.