NAHQ CPHQ Exam Dumps - Actual Questions Answers

The most significant limitation of the sampling methodology in which a hospital collects patient satisfaction data by mailing surveys to discharged patients is the potential non-representativeness of the respondents. This can lead to biased results because:

Response Bias: The patients who choose to respond to the survey may have different experiences or opinions compared to those who do not respond. For example, individuals with very positive or very negative experiences may be more motivated to complete and return the survey, while those with neutral experiences may not bother to respond. This creates a response bias.

Nonresponse Bias: If a significant portion of the patient population does not respond to the survey, the data collected may not accurately reflect the overall patient satisfaction. This can result in an overestimation or underestimation of patient satisfaction levels, leading to incorrect conclusions and potentially flawed quality improvement strategies.

Sampling Bias: Since the survey is voluntary, there is no guarantee that the sample of respondents is representative of the entire discharged patient population. Factors such as age, literacy, socioeconomic status, and health condition might influence who responds, further skewing the results.

Impact on Data Validity: The lack of representativeness can compromise the validity of the findings. Decision-makers relying on these survey results may implement changes based on incomplete or biased information, which might not address the needs or concerns of the broader patient population.

Sharing external audit results with leadership involves ensuring compliance with privacy regulations, particularly the Health Insurance Portability and Accountability Act (HIPAA), which protects patient health information (PHI).

Option A (Acquire authorization from external auditors to share): Auditors may have confidentiality agreements, but sharing results internally with leadership typically does not require their authorization, as leadership is part of the covered entity.

Option B (Remove patient identifiers): This is the correct answer. The NAHQ CPHQ study guide states, “To share medical record audit results internally, patient identifiers must be removed to comply with HIPAA and protect PHI” (Domain 1). De-identification ensures privacy while allowing leadership to review aggregate findings.

Option C (Classify sections with protected health information as confidential): Classifying PHI as confidential is standard, but it does not address sharing results, which requires de-identification for broader dissemination.

Option D (Obtain specific patient consent): Consent is not required for internal quality improvement activities, as they fall under HIPAA’s healthcare operations exemption, provided PHI is protected.

CPHQ Objective Reference: Domain 1: Patient Safety, Objective 1.8, “Ensure compliance with privacy regulations in quality activities,” emphasizes de-identification for sharing audit results. The NAHQ study guide notes, “Removing patient identifiers allows safe sharing of audit data for quality improvement” (Domain 1).

Rationale: De-identifying audit results ensures HIPAA compliance, enabling safe sharing with leadership, aligning with CPHQ’s patient safety and privacy principles.

Social determinants of health (SDOH) are non-medical factors (e.g., housing, education, income) that influence health outcomes. Collecting SDOH data helps providers understand and address these factors to improve care.

Option A (This evaluates connections between the disease and the living conditions): This is the correct answer. NAHQ CPHQ study materials state that SDOH data is collected to identify how factors like housing instability or food insecurity impact diseases (e.g., asthma exacerbations in poor living conditions), enabling tailored interventions to improve outcomes.

Option B (This information is needed to meet a new quality metric): While SDOH data may contribute to quality metrics, the primary purpose is to understand health impacts, not just compliance with metrics.

Option C (This is a result of an update to the electronic medical record system): EMR updates may facilitate SDOH data collection, but they are a tool, not the purpose of the data collection.

Option D (This information facilitates the patient’s application for state resources): SDOH data may support resource referrals, but the primary goal is to evaluate health impacts, not solely to secure resources.