Impact of clinical registries on quality of patient care and health outcomes: protocol for a systematic review.

ABSTRACT:

Introduction

Many developed countries have regional and national clinical registries aimed at improving health outcomes of patients diagnosed with particular diseases or cared for in particular healthcare settings. Clinical quality registries (CQRs) are clinical registries established with the purpose of monitoring quality of care and providing feedback to improve health outcomes. The aim of this systematic review is to understand the impact of CQRs on (1) mortality/survival; (2) measures of outcome that reflect a process or outcome of healthcare; (3) healthcare utilisation and (4) costs.

Methods and analysis

The PRISMA-P methodology, checklist and standard strategy using predefined inclusion and exclusion criteria and structured data abstraction tools will be followed. A se

SUBMITTER: Hoque DM 

PROVIDER: S-EPMC4853981 | biostudies-literature | 2016 Apr

REPOSITORIES: biostudies-literature