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This document analyzes the ability to match known patients to their health records using publicly available data in Washington State, discussing implications on privacy and data sharing in healthcare.
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How to fill out Matching Known Patients to Health Records in Washington State Data

01
Gather all relevant patient information including names, dates of birth, social security numbers, and any unique identifiers.
02
Access the health records database where the known patients' information is stored.
03
Use the search functionality to input the gathered patient information to locate existing records.
04
Cross-check the searched records with your patient information for accuracy and completeness.
05
Match entries based on common identifiers, ensuring to resolve any discrepancies in data.
06
Document the matched records systematically, noting any patients that could not be matched.
07
Review the matched data to ensure compliance with privacy regulations.

Who needs Matching Known Patients to Health Records in Washington State Data?

01
Healthcare providers and hospitals for accurate patient identification.
02
Public health agencies for accurate data collection and tracking.
03
Insurance companies for processing claims and ensuring proper coverage.
04
Researchers studying health trends and outcomes related to specific patient groups.
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Here are some common methods and techniques of data collection in healthcare research: Surveys and Questionnaires: Clinical Interviews: Observations: Medical Records Review: Clinical Trials: Biological Sampling: Focus Groups: Secondary Data Analysis:
The HIPAA Breach Notification Rule requires healthcare organizations to report breaches that compromise the confidentiality, integrity, or availability of protected health information. Incidents that are considered reportable breaches include: Hacking or IT incidents. Unauthorized access or disclosure of PHI.
Here are some common methods and techniques of data collection in healthcare research: Surveys and Questionnaires: Clinical Interviews: Observations: Medical Records Review: Clinical Trials: Biological Sampling: Focus Groups: Secondary Data Analysis:
Some common data collection methods include surveys, interviews, observations, focus groups, experiments, and secondary data analysis.
Electronic copies will be sent to you via your DOH Public Records customer portal unless requested otherwise. Per WAC 246-08-990(7), requestors are required to pay fees for copies in advance of receiving records.
Examples include data about how long patients stay in hospital, what they are diagnosed with, and some basic demographic information such as age, gender and ethnicity.
6. What is involved in collecting data – six steps to success Step 1: Identify issues and/or opportunities for collecting data. Step 2: Select issue(s) and/or opportunity(ies) and set goals. Step 3: Plan an approach and methods. Step 4: Collect data. Step 5: Analyze and interpret data. Step 6: Act on results.
The list below provides the most common data collection methods: 1) Focus Groups, 2) Interviews, 3) Observations, and 4) Surveys. This data collection method involves face-to-face interactions between the researcher/moderator and respondents.

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Matching Known Patients to Health Records involves the process of aligning patient identity with their corresponding health records within Washington State's health data systems. This ensures that patient information is accurate and can be reliably traced, allowing for effective healthcare delivery.
Healthcare providers, facilities, and organizations that handle patient health information in Washington State are required to file Matching Known Patients to Health Records. This includes hospitals, clinics, and any entity that maintains health records.
To fill out the Matching Known Patients to Health Records, healthcare entities should collect patient identification details such as name, date of birth, gender, and other relevant identifiers. This data should then be entered into the designated health record system as per the state's guidelines and templates.
The purpose is to ensure that health records accurately reflect the identity of patients, thereby enhancing the quality of patient care, reducing errors, and improving health data interoperability across various healthcare systems.
The information that must be reported typically includes patient demographic details like full name, date of birth, address, unique identification numbers, and any additional factors that may assist in accurately matching health records to known patients.
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