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National Healthcare Disparities Report - LDI Health Economist

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Patient Centeredness<br />

Measures<br />

The <strong>National</strong> <strong><strong>Health</strong>care</strong> Quality <strong>Report</strong> (NHQR) and the <strong>National</strong> <strong><strong>Health</strong>care</strong> <strong>Disparities</strong> <strong>Report</strong> (NHDR)<br />

track several measures of patients’ experience of care. The reports also address the priority of ensuring that<br />

each person and family are engaged as partners in their care, found in the <strong>National</strong> Strategy for Quality<br />

Improvement in <strong>Health</strong> Care. v The rationale is that “[h]ealth care should give each individual patient and<br />

family an active role in their care. Care should adapt readily to individual and family circumstances, as well<br />

as to differing cultures, languages, disabilities, health literacy levels, and social backgrounds.” Examples of<br />

person-centered care could be ensuring that patients’ feedback on their preferences, desired outcomes, and<br />

experiences of care is integrated into care delivery and enabling patients to effectively manage their care.<br />

The NHDR has tracked a growing number of patient centeredness measures. Organized around the <strong>National</strong><br />

Strategy for Quality Improvement in <strong>Health</strong> Care (<strong>National</strong> Quality Strategy), the 2011 NHDR presents the<br />

following measures that relate to the goal to provide patient-centered care:<br />

Chapter 5<br />

n Adults and children who reported poor communication at the doctor’s office (composite).<br />

n Adults who reported poor communication with nurses and doctors at the hospital.<br />

n Provider’s involvement of the patient in making treatment decisions.<br />

This year, the NHDR includes an expanded section that deals with language and includes some contextual<br />

data on primary language spoken at hospitals in California and New Jersey. In addition, this chapter includes<br />

two supporting measures: whether language assistance was provided by the usual source of care and need for<br />

a translator.<br />

The last supporting measure deals with whether a provider sometimes or never asked for the patient’s help in<br />

making treatment decisions. This measure relates to the <strong>National</strong> Quality Strategy goal of patient<br />

engagement.<br />

Findings<br />

Patients’ Experience of Care—Adults<br />

Optimal health care requires good communication between patients and providers, yet barriers to providerpatient<br />

communication are common. To provide all patients with the best possible care, providers need to<br />

understand patients’ diverse health care needs and preferences and communicate clearly with patients about<br />

their care.<br />

v Available at www.healthcare.gov/center/reports/nationalqualitystrategy032011.pdf.<br />

<strong>National</strong> <strong><strong>Health</strong>care</strong> Quality <strong>Report</strong>, 2011<br />

165

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