Table 1

Summary of major differences in protocol

ECDC protocolDeviationsRationale
Patient inclusion and exclusion
  • All patients admitted to the ward before or at 08:00 and not discharged from the ward at the time of survey, including neonates on maternity and paediatric wards, will be included

  • 50% patients in acute wards and all intensive care unit patients

  • Only adults ≥18 years old admitted to the ward before or at 08:00 and not discharged from the ward at the time of survey will be included

  • Insufficient resources to sample every patient

Data collection processes
  • Composition of the team responsible for data collection varied from one hospital to another

  • The same data collectors will be collecting data for all hospitals in the PPS

  • To minimise variation and maximise consistency in classifying infections

  • Minimise the burden of data collection on participating hospitals

  • Total time frame for data collection for all wards of a single hospital did not exceed 2 to 3 weeks

  • Data to be collected during a one-off hospital visit (1–3 days)

  • Same data collectors used across all facilities

  • Smaller sample size

Patient data fields
  • McCabe score was employed to classify the severity of underlying medical conditions

  • No risk factor data will be collected

  • Insufficient resources to collect risk factor data

  • Antimicrobial use

  • No antimicrobial use data will be collected

  • Antimicrobial data already collected in annual point prevalence survey

Data validation
  • Recommended sample size at the national level was 750 patients in 25 hospitals

  • Records of 100% of patients identified as having an infection at the first hospital (up to a maximum of 40) and a random sample of 5% of those identified as not having an infection will be reviewed

  • Same data collectors used across all facilities

  • Pragmatic validation within existing resources

  • Validation team consisted was separate from the original data collection team

  • Validation team members will consist of the chief investigators who cross-check the data

  • Same data collectors used across all facilities

  •  Blinded data validation recommended

  • Validation team will not be blinded

  • Not practical for this study

  • ECDC, European Centres for Disease Control; PPS, point prevalence study.