CHPCN(C) study materials
CHPCN(C) study resources

CHPCN(C) flashcards

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32 cards. Read the term and the definition here. The deck at the top of this page is optional.

Health record definition
The primary legal and clinical record of a patient's care, maintained by the organization and containing documentation of assessments, interventions, and outcomes in paper or electronic form.
Quantitative record analysis
A review that checks whether required forms, signatures, dates, and fields are present and complete, without judging the clinical content of the documentation.
Qualitative record analysis
A review that evaluates whether documentation content supports the diagnosis, justifies the care provided, and reflects the patient's condition and response to treatment.
Record retention schedule
A policy and legislated framework specifying how long health records must be kept, typically based on time since last encounter and special rules for minors.
Addendum correction method
A dated, signed entry added to the record to correct or clarify earlier documentation; the original entry remains visible and is never obliterated or deleted.
Release of information
The authorized disclosure of health information to a requesting party, requiring verification of identity, valid consent or legal authority, and logging of the disclosure.
CHIM credential
The Certified Health Information Management designation awarded by the Canadian Health Information Management Association, demonstrating competence in health information practice.
Chart deficiency process
A tracking system that identifies incomplete records, notifies responsible clinicians, and monitors completion against timelines set in medical staff bylaws.
Discharge summary content
A record entry summarizing the reason for admission, significant findings, procedures performed, discharge diagnoses, medications, follow-up plan, and condition at discharge.
ICD-10-CA
Canada's classification system for diagnoses and morbidity, maintained by CIHI, used to code conditions in acute care and other reporting databases.
CCI
The Canadian Classification of Health Interventions, maintained by CIHI, used to code procedures and interventions performed during care episodes.
SNOMED CT
A comprehensive, multilingual clinical terminology with concepts and relationships that enables consistent recording and semantic exchange of clinical information across systems.
LOINC
A standard terminology for identifying laboratory tests and clinical observations, enabling comparable results to be exchanged between systems and laboratories.
HL7 FHIR
A modern health interoperability standard using resources and application programming interfaces to exchange clinical and administrative data between systems.
Data quality dimensions
Attributes used to assess data, commonly accuracy, completeness, consistency, timeliness, validity, and uniqueness, each measurable against defined thresholds.
Discharge Abstract Database
A CIHI national database containing abstracted clinical, demographic, and administrative data for inpatient hospital discharges, used for reporting and case mix.
Case Mix Group Plus
CIHI's inpatient grouping methodology that assigns discharges to clinically and resource-similar groups using coded diagnoses, interventions, and patient characteristics.
Personal health information
Identifiable information about an individual's physical or mental health, care received, or payment for care, in any format including paper, electronic, and verbal.
Circle of care
The principle allowing health information to be shared among providers currently involved in a patient's care, generally without additional express consent.
Implied consent
Consent inferred from the patient's circumstances and expectations, commonly applied to sharing information within the treating care team rather than outside it.
Lockbox request
A patient's request to restrict access to specific health information; clinicians must apply it while considering safety obligations and applicable legal requirements.
Privacy breach notification
The process of containing a breach, assessing risk of harm, and notifying affected individuals and the regulator where legislation sets notification thresholds.
Right of access
A patient's legal right to view and obtain copies of their health record, subject to limited exceptions such as significant harm or third-party information.
Minimum necessary principle
The rule that only the least amount of health information needed for a purpose should be collected, used, or disclosed, limiting unnecessary exposure.
Privacy impact assessment
A structured review conducted before a new system or data flow is implemented, identifying privacy risks and the safeguards needed to mitigate them.
PIPEDA
Canada's federal private-sector privacy law applying to personal information, including health information, collected during commercial activity, with provincial laws sometimes replacing it.
Semantic interoperability
The ability of systems to exchange data and interpret its meaning consistently, requiring shared terminologies and models rather than only matching message formats.
Data warehouse
A consolidated repository that integrates data from multiple source systems for reporting and analysis, supported by documented definitions and metadata.
Descriptive analytics
The analytics tier that summarizes what happened, using counts, rates, trends, and dashboards to describe past performance and current status.
Predictive analytics
The analytics tier that uses historical data and statistical or machine learning models to estimate the likelihood of future events such as readmission.
Length of stay indicator
A measure of days a patient spends in hospital, calculated from defined admission and discharge dates, with in-day and alternate level of care rules applied consistently.
Role-based access control
A security method granting system permissions according to a user's job role, combined with audit logging to detect inappropriate access to health information.