Data Collection System
Cross-source consensus on Data Collection System from 1 sources and 5 claims.
1 sources · 5 claims
Uses
Benefits
Other
Highlighted claims
- Registry data are collected online in hospitalisation and postdischarge follow-up phases. — Neonatal hypoxic-ischemic encephalopathy online registry in Shenzhen: protocol for a multicentre, prospective, open, observational cohort study
- Hospitalisation data are entered by data specialists into the Shenzhen specialised HIE database. — Neonatal hypoxic-ischemic encephalopathy online registry in Shenzhen: protocol for a multicentre, prospective, open, observational cohort study
- Postdischarge follow-up data are collected through a WeChat application with physician and guardian portals. — Neonatal hypoxic-ischemic encephalopathy online registry in Shenzhen: protocol for a multicentre, prospective, open, observational cohort study
- Each participating centre and patient receives a unique identification number. — Neonatal hypoxic-ischemic encephalopathy online registry in Shenzhen: protocol for a multicentre, prospective, open, observational cohort study
- Hospitalisation and follow-up records are interconnected and shared to reduce entry errors. — Neonatal hypoxic-ischemic encephalopathy online registry in Shenzhen: protocol for a multicentre, prospective, open, observational cohort study