Health Information Personnel Practice Test

What type of data does a clinical registry collect?

1. Data on healthcare costs and revenues.

2. Data on specific health conditions or treatments to improve quality of care.

3. Data on medical supply inventories.

4. Data on hospital staffing levels.

The correct answer is: Data on specific health conditions or treatments to improve quality of care.

Clinical registries are specialized databases that collect detailed information about specific health conditions or treatments. The purpose of these registries is to gather data that can lead to enhanced understanding and management of these conditions, ultimately aiming to improve the quality of care provided to patients. This type of data typically includes information on patient demographics, treatment protocols, outcomes, and other clinically relevant factors. By aggregating this information, healthcare professionals and researchers can analyze trends, evaluate treatment efficacy, and identify areas for improvement in healthcare practices. Clinical registries play a crucial role in evidence-based medicine, allowing for the continuous monitoring of quality indicators and patient outcomes, leading to advancements in care standards and practices for particular conditions. The other options focus on different aspects of healthcare management that do not directly relate to the core function of a clinical registry. Data on healthcare costs and revenues pertains more to fiscal management rather than patient care quality. Medical supply inventories relate to resource management, and hospital staffing levels involve workforce management. While all these data types are valuable for overall healthcare operations, they do not capture the clinical and quality improvement focus characteristic of clinical registries.