// Resources
Everything You Need to Get Started
// Frequently Asked Questions
What data leaves each site?
Only aggregate summary statistics — gradient vectors and Hessian matrices — are transmitted. No individual patient records, no row-level data. Each site retains full control of its patient data at all times.
How many communication rounds does PDA-OTA require?
PDA-OTA converges in a single communication round. The one-shot approach transmits local gradients and Hessians once, allowing the coordinating center to compute a pooled-equivalent estimate immediately.
How does PDA compare to standard meta-analysis?
Unlike traditional meta-analysis which aggregates study-level estimates with inherent information loss, PDA aggregates patient-level sufficient statistics. This yields estimates asymptotically equivalent to pooling all raw data — a fundamentally more powerful approach.
What statistical models are supported?
PDA currently supports linear regression (ODAL), logistic regression (ODAL), Cox proportional hazards (ODAC), Poisson regression (ODAP), self-controlled case series (SCCS), and quantile regression. Custom models can be implemented via the extensible API.
Is IRB approval required at each site?
IRB requirements vary by institution and study design. We recommend consulting with your local IRB. In many cases, the non-sharing of patient data simplifies the approval process compared to traditional multi-site data sharing agreements.
How do I set up a coordinating center?
The coordinating center runs the aggregation step using the PDA R package. Detailed setup instructions are available in our implementation guideline. The PDA server can also be deployed via the hosted PDA-OTA platform for streamlined coordination.
// Contact Us
Interested in Collaborating?
We welcome new institutional partners, methodological collaborations, and feedback from the research community.
