Limited external reproducibility restricts the use of medical record review for benchmarking

Dorthe O Klein1, Roger Rennenberg2, Rijk Gans3

  • 1Department of Clinical Epidemiology and Medical Technology Assessment, Maastricht UMC+, Maastricht, The Netherlands.

BMJ Open Quality
|June 18, 2019
PubMed
Abstract

Insights

Medical record review (MRR) shows moderate reproducibility for adverse events (AEs) and fair-to-poor agreement for preventability and contribution to death. Caution is advised when using MRR for hospital benchmarking.

Area of Science:

  • Healthcare Quality and Safety
  • Medical Informatics
  • Patient Outcomes Research

Background:

  • Medical record review (MRR) is a key method for assessing hospital quality and safety.
  • Increasing use of MRR for institutional comparison necessitates high external reproducibility.
  • This study investigates the external reproducibility of MRR for adverse event assessment.

Purpose of the Study:

  • To evaluate the external reproducibility of medical record review for adverse event assessment.
  • To determine the agreement in identifying adverse events, their preventability, and contribution to death.
  • To assess the reliability of MRR when used for inter-institutional comparisons.

Main Methods:

  • A sample of 40 medical records from deceased patients was randomly selected from two Dutch university medical centers.
  • External review committees assessed these records using the same methodology as internal committees.
  • Agreement was measured using overall and kappa statistics for adverse events, preventability, and contribution to death.

Main Results:

  • Moderate agreement (kappa=0.47) was found for the presence of adverse events.
  • Fair agreement (kappa=0.39) was observed for the preventability of adverse events.
  • Poor agreement (kappa=-0.109) was noted for the contribution of adverse events to patient death.

Conclusions:

  • While MRR is valuable for identifying general patient safety issues, its use for benchmarking requires caution.
  • The findings suggest limitations in the external reproducibility of MRR for specific adverse event characteristics.
  • Further research may be needed to refine MRR methods for reliable inter-institutional comparisons.

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