7 research outputs found
Random effects model fit to the natural anti-RhD titer decline of donors in the absence of boostering.
<p>A jitter of 1.75 was applied to the titer change measurements to enhance interpretability of the data. For individual fits, the line ends at a donor’s maximum time of measurement. Note that for 5% of donors a small positive annual change is modelled due to measurement errors and since it is not possible to restrict the model to negative values.</p
Predicting anti-RhD titers in donors: Boostering response and decline rates are personal
<div><p>Background</p><p>Anti-RhD immunised donors provide anti-RhD immunoglobulins used for the prevention of rhesus disease. These donors are periodically hyper-immunised (boostered) to retain a high titer level of anti-RhD.</p><p>Study design and methods</p><p>We analysed anti-RhD donor records from 1998 to 2016, consisting of 30,116 anti-RhD titers from 755 donors, encompassing 3,372 booster events. Various models were fit to these data to allow describing the anti-RhD titers over time.</p><p>Results</p><p>A random effects model with a log-linear anti-RhD titer decline over time and a saturating titer response to boostering is shown to fit the data well. This model contains two general model parameters, relating timing and maximum of the booster effect, as well as two parameters characterizing the individual donor, namely how fast the booster effect saturates with current titer and the anti-RhD decline rate. The average individual log<sub>2</sub> decline is 0.55 per year, i.e. a 32% decline in absolute titer, with half of the donors declining between 13% and 41% per year. Their anti-RhD titer peaks around 26 days following a booster event. Boostering response reduces with higher titers at boostering; at median titer (log<sub>2</sub> 11) the mean increase per booster is log<sub>2</sub> 0.38, that is from an absolute titer of 2048 to 2665 (+30%), with half of all donors increasing between 16% and 65% in their titer.</p><p>Conclusion</p><p>The model describes anti-RhD titer change per individual with only four parameters, two of which are donor specific. This information can be used to enhance the blood bank’s immunisation programme, by deriving individualized immunization policies in which boostering is adjusted to the anticipated anti-RhD decline, effectiveness of boostering and titer levels required.</p></div
Four examples of model fits to individual donor titers observed over time.
<p><b>(</b>See <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0196382#pone.0196382.s006" target="_blank">S5 Fig</a> for the model fits for all individual donors).</p
Peak in anti-RhD titer gain after boostering.
<p>A jitter of 1.95 was applied on the measurements of both titer change and titer at boostering to enhance interpretability of the data. Individuals were not boostered in the 50 days preceding the booster of interest. Black circles denote the approximate peak in increase assumed at 26–50 days from boostering (see Step 2A results), when a donor was boostered only once. Blue crosses denote this increase when one or more boosters were given subsequent to the booster of interest. Our best model fit to all these data-points together (shown for <i>t</i> = 26) hence represents an overestimate of the titer gain from boostering once. Also shown is the fit dependence from our final model (see Step 3 in the main text, shown for an average individual and also for 26 days from boostering).</p
Cost-effectiveness frontier of DAA-treatment strategies among PWID compared to PegIFN/RBV<sup>a</sup>. Strategy 2: DAA/RBV (G2-3) & dual DAA (g1-4); 3: Dual DAA for all genotypes; 4: Dual DAA with a 3x higher treatment uptake.
<p>a The strategies that fall below the dashed blue line are strategies that fall bellow a willingness to pay threshold reflecting 1 GDP per head of the population, i.e., €38,255 for the Netherlands, and are considered highly cost-effective compared to PegIFN/RBV. However, scenarios are compared incrementally to identify the <i>most</i> cost-effective strategy. The most cost-effective strategy is shown on the “cost-effectiveness frontier”, the line that is closest to the X-axis.</p
Cumulative discounted costs, effects, and incremental cost-effectiveness ratios of four Hepatitis C treatment strategies in a declining epidemic and a stable HCV epidemic.
<p>Cumulative discounted costs, effects, and incremental cost-effectiveness ratios of four Hepatitis C treatment strategies in a declining epidemic and a stable HCV epidemic.</p
Base case demographics, annual transition probabilities, and SVR probabilities per treatment scenario.
<p>Base case demographics, annual transition probabilities, and SVR probabilities per treatment scenario.</p