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Systematic reviews frequently encounter trials that report incomplete survival data – a log-rank p-value but no Hazard Ratio, or probabilities without a directly computed NNT. ParCC bridges these gaps with two tools in the HR Converter module.
An older trial (published 2005) reports:
The paper does not report a Hazard Ratio, which you need for your meta-analysis.
When only summary log-rank statistics are available, the Peto method estimates:
\[\ln(HR) = \pm \frac{\sqrt{\chi^2}}{\sqrt{E/4}}\]
with a 95% confidence interval:
\[\ln(HR) \pm \frac{1.96}{\sqrt{E/4}}\]
where \(E\) is the total number of events.
If the paper reports only “log-rank p = 0.009”:
A Pharmacy & Therapeutics committee asks: “How many patients must we treat with Drug X to prevent one additional death?” The trial reports:
\[NNT = \left\lceil \frac{1}{ARR} \right\rceil = \left\lceil \frac{1}{p_{control} - p_{intervention}} \right\rceil\]
Interpretation: For every 17 patients treated with Drug X for 12 months, one additional death is prevented.
ParCC supports four ways to compute NNT:
| Input Mode | You provide | ParCC calculates |
|---|---|---|
| Direct ARR | Absolute risk reduction | NNT = ceil(1/ARR) |
| Two Probabilities | Control & intervention probabilities | ARR, then NNT |
| RR + Baseline | Relative Risk + control probability | ARR = p0 x (1 - RR), then NNT |
| OR + Baseline | Odds Ratio + control probability | Converts to probabilities via Zhang & Yu, then NNT |
When the intervention increases risk (ARR < 0), the result is reported as NNH (Number Needed to Harm) with an orange warning. This happens when testing safety endpoints rather than efficacy.
These binaries (installable software) and packages are in development.
They may not be fully stable and should be used with caution. We make no claims about them.
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