All Stories

  1. Agreement of PROMIS Preference (PROPr) scores generated from the PROMIS-29 + 2 and the PROMIS-16
  2. Commentary on “When (not) to rely on the reliable change index”.
  3. Comparison of the EQ-5D-5L and the patient-reported outcomes measurement information system preference score (PROPr) in the United States
  4. Development of a Web-Based Interactive Tool for Visualizing Breast Cancer Clinical Trial Tolerability Data
  5. A Health-Related Quality of Life Measure for Patients Who Undergo Minimally Invasive Glaucoma Surgery
  6. Support for a Single Underlying Dimension of Self-Reported Health in a Sample of Adults with Low Back Pain in the United States
  7. The PROMIS-16 reproduces the PROMIS-29 physical and mental health summary scores accurately in a probability-based internet panel
  8. Predictors of drop-out in a longitudinal survey of Amazon Mechanical Turk workers with low back pain (Preprint)
  9. Drop-out in a longitudinal survey of Amazon Mechanical Turk workers with low back pain: An observational study (Preprint)
  10. Development of short forms for screening children’s dental caries and urgent treatment needs using item response theory and machine learning methods
  11. Mapping of the PROMIS global health measure to the PROPr in the United States
  12. Associations of the Consumer Assessment of Healthcare Providers and Systems (CAHPS) Clinician and Group Survey Scores with Interventions and Site, Provider, and Patient Factors: A Systematic Review of the Evidence
  13. Comparison of patient-reported outcomes measurement information system (PROMIS®)-29 and PROMIS global physical and mental health scores
  14. Seeing the Light in Self-Reported Glare
  15. Data from Dynamic Risk Prediction of Treatment Discontinuation Using Patient-Reported Outcomes Data in the Phase III NSABP B-35 Trial
  16. Data from Dynamic Risk Prediction of Treatment Discontinuation Using Patient-Reported Outcomes Data in the Phase III NSABP B-35 Trial
  17. Supplementary Figure S1 from Dynamic Risk Prediction of Treatment Discontinuation Using Patient-Reported Outcomes Data in the Phase III NSABP B-35 Trial
  18. Supplementary Figure S1 from Dynamic Risk Prediction of Treatment Discontinuation Using Patient-Reported Outcomes Data in the Phase III NSABP B-35 Trial
  19. Supplementary Figure S2 from Dynamic Risk Prediction of Treatment Discontinuation Using Patient-Reported Outcomes Data in the Phase III NSABP B-35 Trial
  20. Supplementary Figure S2 from Dynamic Risk Prediction of Treatment Discontinuation Using Patient-Reported Outcomes Data in the Phase III NSABP B-35 Trial
  21. Supplementary Figure S3 from Dynamic Risk Prediction of Treatment Discontinuation Using Patient-Reported Outcomes Data in the Phase III NSABP B-35 Trial
  22. Supplementary Figure S3 from Dynamic Risk Prediction of Treatment Discontinuation Using Patient-Reported Outcomes Data in the Phase III NSABP B-35 Trial
  23. Supplementary Figure S4 from Dynamic Risk Prediction of Treatment Discontinuation Using Patient-Reported Outcomes Data in the Phase III NSABP B-35 Trial
  24. Supplementary Figure S4 from Dynamic Risk Prediction of Treatment Discontinuation Using Patient-Reported Outcomes Data in the Phase III NSABP B-35 Trial
  25. Supplementary Figure S5 from Dynamic Risk Prediction of Treatment Discontinuation Using Patient-Reported Outcomes Data in the Phase III NSABP B-35 Trial
  26. Supplementary Figure S5 from Dynamic Risk Prediction of Treatment Discontinuation Using Patient-Reported Outcomes Data in the Phase III NSABP B-35 Trial
  27. Supplementary Figure S6 from Dynamic Risk Prediction of Treatment Discontinuation Using Patient-Reported Outcomes Data in the Phase III NSABP B-35 Trial
  28. Supplementary Figure S6 from Dynamic Risk Prediction of Treatment Discontinuation Using Patient-Reported Outcomes Data in the Phase III NSABP B-35 Trial
  29. Supplementary Figure S7 from Dynamic Risk Prediction of Treatment Discontinuation Using Patient-Reported Outcomes Data in the Phase III NSABP B-35 Trial
  30. Supplementary Figure S7 from Dynamic Risk Prediction of Treatment Discontinuation Using Patient-Reported Outcomes Data in the Phase III NSABP B-35 Trial
  31. Supplementary Methods S1 from Dynamic Risk Prediction of Treatment Discontinuation Using Patient-Reported Outcomes Data in the Phase III NSABP B-35 Trial
  32. Supplementary Methods S1 from Dynamic Risk Prediction of Treatment Discontinuation Using Patient-Reported Outcomes Data in the Phase III NSABP B-35 Trial
  33. Supplementary Methods S2 from Dynamic Risk Prediction of Treatment Discontinuation Using Patient-Reported Outcomes Data in the Phase III NSABP B-35 Trial
  34. Supplementary Methods S2 from Dynamic Risk Prediction of Treatment Discontinuation Using Patient-Reported Outcomes Data in the Phase III NSABP B-35 Trial
  35. Supplementary Table S1 from Dynamic Risk Prediction of Treatment Discontinuation Using Patient-Reported Outcomes Data in the Phase III NSABP B-35 Trial
  36. Supplementary Table S1 from Dynamic Risk Prediction of Treatment Discontinuation Using Patient-Reported Outcomes Data in the Phase III NSABP B-35 Trial
  37. Supplementary Table S2 from Dynamic Risk Prediction of Treatment Discontinuation Using Patient-Reported Outcomes Data in the Phase III NSABP B-35 Trial
  38. Supplementary Table S2 from Dynamic Risk Prediction of Treatment Discontinuation Using Patient-Reported Outcomes Data in the Phase III NSABP B-35 Trial
  39. Supplementary Table S3 from Dynamic Risk Prediction of Treatment Discontinuation Using Patient-Reported Outcomes Data in the Phase III NSABP B-35 Trial
  40. Supplementary Table S3 from Dynamic Risk Prediction of Treatment Discontinuation Using Patient-Reported Outcomes Data in the Phase III NSABP B-35 Trial
  41. Supplementary Table S4 from Dynamic Risk Prediction of Treatment Discontinuation Using Patient-Reported Outcomes Data in the Phase III NSABP B-35 Trial
  42. Supplementary Table S4 from Dynamic Risk Prediction of Treatment Discontinuation Using Patient-Reported Outcomes Data in the Phase III NSABP B-35 Trial
  43. Performance of the Physical Functioning Activities of Daily Living Scale in the 2020 Medicare Health Outcomes Survey
  44. Are some ways of defining chronic low back pain more indicative of future back pain than others?
  45. Dynamic Risk Prediction of Treatment Discontinuation Using Patient-Reported Outcomes Data in the Phase III NSABP B-35 Trial
  46. Predictors of Pain Management Strategies in Adults with Low-Back Pain: A Secondary Analysis of Amazon Mechanical Turk Survey Data
  47. Embedding research study recruitment within the patient portal preCheck-in
  48. Effects of Excluding Those Who Report Having “Syndomitis” or “Chekalism” on Data Quality: Longitudinal Health Survey of a Sample From Amazon’s Mechanical Turk
  49. How Well Do Seven Self-Report Measures Represent Underlying Back Pain Impact?
  50. Pediatric Inpatient Leaders, Views Changed with COVID-19: A Call to Re-engage in Quality Improvement
  51. Support for Use of Consumer Assessment of Healthcare Providers and Systems Communication Items Among Seriously Ill Patients
  52. Use of Patient Experience Scales Differs by Education and Asian Race/Ethnicity
  53. Shadow Coaching Improves Patient Experience for English-Preferring Patients but not for Spanish-Preferring Patients
  54. Minimally important changes do not always reflect minimally important change; moreover, there is no need for them
  55. Effects of Excluding Those Who Report Having “Syndomitis” or “Chekalism” on Data Quality: Longitudinal Health Survey of a Sample From Amazon’s Mechanical Turk (Preprint)
  56. Telephone Outreach Enhances Recruitment of Underrepresented Seriously Ill Patients for an Advance Care Planning Pragmatic Trial
  57. Veteran knowledge, perceptions, and receipt of care following visits to VA emergency departments for ambulatory care sensitive conditions
  58. Current Postlaunch Implementation of State Mandates of Newborn Screening for Critical Congenital Heart Disease by Pulse Oximetry in U.S. States and Hospitals
  59. Vision-related quality of life compared to generic measures in retinoblastoma survivors
  60. Response to: “Criteria for determining if a treatment for pain works”
  61. Correction: Likely change indexes improve estimates of individual change on patient‑reported outcomes
  62. Toxicity Index, patient-reported outcomes, and persistence of breast cancer chemotherapy-associated side effects in NRG Oncology/NSABP B-30
  63. Follow-Up Shadow Coaching Improves Primary Care Provider-Patient Interactions and Maintains Improvements When Conducted Regularly: A Spline Model Analysis
  64. Poor Self-rated Mental Health and Medicare Beneficiaries’ Routine Care-Seeking
  65. A Systematic Review of Strategies to Enhance Response Rates and Representativeness of Patient Experience Surveys
  66. Simulation study comparing analytical methods for single-item longitudinal patient-reported outcomes data
  67. Comparing Data Collected on Amazon's Mechanical Turk to National Surveys
  68. Definitions of Chronic Low Back Pain from a Scoping Review, and Analyses of Narratives and Self-Reported Health of Adults with Low Back Pain
  69. Unpacking the impact of chronic pain as measured by the impact stratification score
  70. Comparison of Simple-Summated Scoring and Toxicity Index Scoring of Symptom Bother in the NSABP B-30 Clinical Trial
  71. Race and Ethnicity Differences in Walking and Associations with Neighborhood Perceptions among Older Adults in California
  72. Likely change indexes improve estimates of individual change on patient-reported outcomes
  73. A Patient Reported Outcome Ontology: Conceptual Issues and Challenges Addressed by the Patient-Reported Outcomes Measurement Information System® (PROMIS®)
  74. Cross-walking the National Institutes of Health Impact Stratification Score to the PEG
  75. Development, methodology, and adaptation of the Medicare Consumer Assessment of Healthcare Providers and Systems (CAHPS®) patient experience survey, 2007–2019
  76. Development and Evaluation of the Clinical Trial HEalth Knowledge and Beliefs Scale (CHEKS)
  77. Experiences of Sleep Problems Among Older Korean Immigrants
  78. Health‐related quality of life outcomes after neoadjuvant chemoradiotherapy for rectal cancer in NRG  Oncology/ NSABP R‐04
  79. Health-Related Quality of Life in Adolescent and Young Adult Retinoblastoma Survivors
  80. Comparing the Recruitment of Research Participants With Chronic Low Back Pain Using Amazon Mechanical Turk With the Recruitment of Patients From Chiropractic Clinics: A Quasi-Experimental Study
  81. Analyses of Cross-Sectional Data to Link the PEG with the Patient Reported Outcomes Measurement and Information System (PROMIS®) Global Physical Health Scale
  82. Summary of the 2020 AHRQ research meeting on ‘advancing methods of implementing and evaluating patient experience improvement using consumer assessment of healthcare providers and systems (CAHPS®) surveys’
  83. Investigating Perceptions of Teachers and School Nurses on Child and Adolescent Oral Health in Los Angeles County
  84. Erratum to: Health-Related Quality of Life among United States Service Members with Low Back Pain Receiving Usual Care plus Chiropractic Care vs Usual Care Alone: Secondary Outcomes of a Pragmatic Clinical Trial
  85. Survival After Severe COVID-19: Long-Term Outcomes of Patients Admitted to an Intensive Care Unit
  86. Health-Related Quality of Life Measurement in Public Health
  87. Perceptions of Teachers and School Nurses on Child and Adolescent Oral Health
  88. Abstract PD5-04: Risk factors for long-term adjuvant chemotherapy toxicity using pre-treatment host factors and self-rated treatment bother (GP5) in a clinical trial population
  89. Content and Actionability of Recommendations to Providers After Shadow Coaching
  90. Health-Related Quality of Life Among United States Service Members with Low Back Pain Receiving Usual Care Plus Chiropractic Care Plus Usual Care vs Usual Care Alone: Secondary Outcomes of a Pragmatic Clinical Trial
  91. 2022 Update to state of the journal of patient-reported outcomes
  92. Patient Experience with In-Person and Telehealth Visits Before and During the COVID-19 Pandemic at a Large Integrated Health System in the United States
  93. A Systematic Literature Review of Health-related Quality of Life Measures for Women with Hypoactive Sexual Desire Disorder and Female Sexual Interest/Arousal Disorder
  94. Using a Machine Learning Algorithm to Predict the Likelihood of Presence of Dental Caries among Children Aged 2 to 7
  95. Guidelines for Designing and Evaluating Feasibility Pilot Studies
  96. Assessing the Significance of Individual Change in 2 Samples of Patients in Treatment for Low Back Pain Using 5 Different Statistical Indicators
  97. Toxicity Index, Patient-Reported Outcomes, and Early Discontinuation of Endocrine Therapy for Breast Cancer Risk Reduction in NRG Oncology/NSABP B-35
  98. Patient-Reported Care Coordination is Associated with Better Performance on Clinical Care Measures
  99. Using CAHPS patient experience data for patient-centered medical home transformation
  100. Vision-Targeted Health-Related Quality-of-Life Survey for Evaluating Minimally Invasive Glaucoma Surgery
  101. Practices and changes associated with patient-centered medical home transformation
  102. Longitudinal Associations of PROMIS-29 Anxiety and Depression Symptoms With Low Back Pain Impact in a Sample of U.S. Military Service Members
  103. Methodological and Statistical Considerations for the National Children's Study
  104. Guest Editors’ Introduction to the Invited Special Section
  105. Development and validation of a patient experience of care survey for emergency departments
  106. Shadow Coaching Improves Patient Experience With Care, But Gains Erode Later
  107. Evaluation of PROMIS Preference Scoring System (PROPr) in Patients Undergoing Hemodialysis or Kidney Transplant
  108. Letter to the Editor: What Are the MCIDs for PROMIS, NDI, and ODI Instruments Among Patients With Spinal Conditions?
  109. Applying the Toxicity Index to Patient-Reported Symptom Data: An Example Using the European Organization for Research and Treatment of Cancer Colorectal Cancer–Specific Quality of Life Questionnaire
  110. Crosswalking the Patient-Reported Outcomes Measurement Information System Physical Function, Pain Interference, and Pain Intensity Scores to the Roland-Morris Disability Questionnaire and the Oswestry Disability Index
  111. Measuring Gender Role Conflict, Internalized Stigma, and Racial and Sexual Identity in Behaviorally Bisexual Black Men
  112. Between-group minimally important change versus individual treatment responders
  113. Using Item Response Theory to Identify Responders to Treatment: Examples with the Patient-Reported Outcomes Measurement Information System (PROMIS®) Physical Function Scale and Emotional Distress Composite
  114. Support for the Reliability and Validity of the National Institutes of Health Impact Stratification Score in a Sample of Active-Duty U.S. Military Personnel with Low Back Pain
  115. Provider and coach perspectives on implementing shadow coaching to improve provider–patient interactions
  116. Gender Differences in Patients’ Experience of Care in the Emergency Department
  117. Analysis of Movement-Based Mind–Body Interventions to Guide the Implementation of Osteoarthritis Exercise Programs: A Descriptive Review of Randomized Controlled Trials
  118. Estimating Responders to Treatment Using Five Indices of Significant Individual Change
  119. Estimating Responders to Treatment Using Five Indices of Significant Individual Change
  120. Letter to the Editor. Patient self-rated health and rating of their spine surgeon
  121. Consumer Assessment of Healthcare Providers and Systems (CAHPS®) survey of experiences with ambulatory healthcare for Asians and non-Hispanic Whites in the United States
  122. Associations of Self-Reported Sleep Quality with Demographic and Other Characteristics in Older Korean Immigrants
  123. Between Group-Level Minimally Important Change and Individual Treatment Responders
  124. Efficacy of a patient decision aid for improving person-centered decision-making by older adults with obstructive sleep apnea
  125. Estimating Responders to Chiropractic Treatment on The Impact Stratification Score Using Five Indices of Significant Individual Change
  126. State of the Journal of Patient-Reported Outcomes
  127. Adjustment of Patient Experience Surveys for How People Respond
  128. Validation of a Brief Multi‐Dimensional Assessment of Dementia Severity
  129. Overlap of Depressive Symptoms with Health-Related Quality-of-Life Measures
  130. A protocol for chronic pain outcome measurement enhancement by linking PROMIS-29 scale to legacy measures and improving chronic pain stratification
  131. Involving older people with multimorbidity in decision-making about their primary healthcare: A Cochrane systematic review of interventions (abridged)
  132. Some Aspects of Patient Experience Assessed by Practices Undergoing Patient-Centered Medical Home Transformation Are Measured by CAHPS, Others Are Not
  133. Nationwide Qualitative Study of Practice Leader Perspectives on What It Takes to Transform into a Patient-Centered Medical Home
  134. Practice Leaders Report Targeting Several Types of Changes in Care Experienced by Patients During Patient-Centered Medical Home Transformation
  135. Depression Risk and Outcomes Among ASCVD Patients
  136. Psychometric Properties of the Altarum Consumer Engagement (ACE) Measure of Activation in Patients with Prediabetes
  137. Evaluating Treatment Tolerability in Cancer Clinical Trials Using the Toxicity Index
  138. Do the unlabeled response categories of the Minnesota Living with Heart Failure Questionnaire satisfy the monotonicity assumption of simple-summated scoring?
  139. Vascular access-specific health-related quality of life impacts among hemodialysis patients: qualitative development of the hemodialysis access-related quality of life (HARQ) instrument
  140. Evaluation of the Psychometric Properties of the Five Facet of Mindfulness Questionnaire
  141. Computerized adaptive testing and short form development for child and adolescent oral health patient‐reported outcomes measurement
  142. Problems with analyses and interpretation of data in “use of the KDQOL-36™ for assessment of health-related quality of life among dialysis patients in the United States”
  143. A Review of Literature on Health-Related Quality of Life of Retinoblastoma Survivors
  144. Associations of Mail Survey Length and Layout With Response Rates
  145. Developing Children’s Oral Health Assessment Toolkits Using Machine Learning Algorithm
  146. Responsiveness of PROMIS® to change in chronic obstructive pulmonary disease
  147. Coping and Management Techniques Used by Chronic Low Back Pain Patients Receiving Treatment From Chiropractors
  148. Development of toolkits for detecting dental caries and caries experience among children using self‐report and parent report
  149. Surgeon Profiles for Intraoperative and Postoperative Use
  150. Population-Based Pragmatic Trial of Advance Care Planning in Primary Care in the University of California Health System
  151. Surgeon Awareness of the Relative Costs of Common Surgical Instruments
  152. Variation in Intraoperative and Postoperative Utilization for 3 Common General Surgery Procedures
  153. Development of a Program Promoting Person‐Centered Care of Older Adults with Sleep Apnea
  154. Differential item functioning of the CAHPS® In-Center Hemodialysis Survey
  155. Researching the Appropriateness of Care in the Complementary and Integrative Health Professions Part 3: Designing Instruments With Patient Input
  156. Experiences With Chiropractic Care for Patients With Low Back or Neck Pain
  157. The effects of survey version on patient experience scores and plan rankings
  158. Differences in Consumer Assessment of Healthcare Providers and Systems Clinician and Group Survey Scores by Recency of the Last Visit
  159. Association of Race with Outcome Expectancy for Positive Airway Pressure Therapy Among Older Veterans with Obstructive Sleep Apnea
  160. Group and Individual-level Change on Health-related Quality of Life in Chiropractic Patients With Chronic Low Back or Neck Pain
  161. PROMIS® Adult Health Profiles: Efficient Short-Form Measures of Seven Health Domains
  162. African American women's perceptions of the meaning of support groups for improving adherence to hypertension treatment: a conceptual model
  163. 0982 Decide2Rest: A Program for Promoting Person-centered Obstructive Sleep Apnea (OSA) Treatment
  164. Kidney Disease Quality of Life 36-Item Short Form Survey (KDQOL-36) Normative Values for the United States Dialysis Population and New Single Summary Score
  165. Expanding the Patient’s Voice in Nephrology with Patient-Reported Outcomes
  166. Measurement Characteristics of the Knowledge Assessment of Renal Transplantation
  167. Development of a parents’ short form survey of their children's oral health
  168. The Social Economics of Adolescent Behavior and Measuring the Behavioral Culture of Schools
  169. The challenge of determining appropriate care in the era of patient-centered care and rising health care costs
  170. Using predicted Spanish preference to target bilingual mailings in a mail survey with telephone follow‐up
  171. Personalized Goal Attainment in Dementia Care: Measuring What Persons with Dementia and Their Caregivers Want
  172. Effect of Mobile Device–Supported Single-Patient Multi-crossover Trials on Treatment of Chronic Musculoskeletal Pain
  173. Hospital quality indicators are not unidimensional: A reanalysis of Lieberthal and Comer
  174. Development and Psychometric Evaluation of a Fatigability Index for Full-Time Wheelchair Users With Spinal Cord Injury
  175. A Composite Measure of Caregiver Burden in Dementia: The Dementia Burden Scale-Caregiver
  176. Associations of CAHPS Composites With Global Ratings of the Doctor Vary by Medicare Beneficiaries’ Health Status
  177. Cross-sectional validation of the PROMIS-Preference scoring system
  178. Characteristics of Chiropractic Patients Being Treated for Chronic Low Back and Neck Pain
  179. Estimation of a Preference-Based Summary Score for the Patient-Reported Outcomes Measurement Information System: The PROMIS®-Preference (PROPr) Scoring System
  180. Preferences of adults with spinal cord injury for widely used health-related quality of life and subjective well-being measures
  181. Negligible impact of differential item functioning between Black and White dialysis patients on the Kidney Disease Quality of Life 36-item short form survey (KDQOLTM-36)
  182. Vascular Access-Specific HRQOL Impacts Among Hemodialysis Patients: The Hemodialysis Access-Related QOL (HARQ) Project Focus Group Results
  183. Evaluation of options for presenting health-states from PROMIS® item banks for valuation exercises
  184. Correlation of High Molecular Weight Von Willebrand Factor Multimer loss and Rotational Speed During Short Term Mechanical Circulatory Support
  185. Psychometric Properties of the Kidney Disease Quality of Life 36-Item Short-Form Survey (KDQOL-36) in the United States
  186. PROMIS®-29 v2.0 profile physical and mental health summary scores
  187. Short form development for oral health patient-reported outcome evaluation in children and adolescents
  188. Qualitative methods in the development of a parent survey of children’s oral health status
  189. Quantifying Magnitude of Group-Level Differences in Patient Experiences with Health Care
  190. Commentary: Copyright Restrictions Versus Open Access to Survey Instruments
  191. Development of the Autosomal Dominant Polycystic Kidney Disease Impact Scale: A New Health-Related Quality-of-Life Instrument
  192. Development and evaluation of a measure of patient-reported symptoms of Blepharitis
  193. Patient Experiences with Care Differ with Chronic Care Management in a Federally Qualified Community Health Center
  194. Methodological considerations in using patient reported measures in dialysis clinics
  195. Alternative Approaches to Addressing Non-Normal Distributions in the Application of IRT Models to Personality Measures
  196. Two-item PROMIS® global physical and mental health scales
  197. Differential item functioning by language on the PROMIS® physical functioning items for children and adolescents
  198. Examining colorectal cancer survivors’ surveillance patterns and experiences of care: a SEER-CAHPS study
  199. Functional disability and other health-related quality-of-life domains: points to consider for clinical trials in systemic sclerosis
  200. Selection of key health domains from PROMIS® for a generic preference-based scoring system
  201. A comparison of perceptions of quality of life among adults with spinal cord injury in the United States versus the United Kingdom
  202. Implementation of Practice Transformation: Patient Experience According to Practice Leaders
  203. Using Patient-Reported Measures in Dialysis Clinics
  204. 1240 Non-REM Parasomnias As The Presenting Symptom Of Narcolepsy Without Cataplexy
  205. 1190 OLDER ADULTS’ PREFERENCES FOR OBSTRUCTIVE SLEEP APNEA TREATMENT ELICITED FROM A PILOT DISCRETE CHOICE EXPERIMENT
  206. Depressive symptomatology and fall risk among community-dwelling older adults
  207. Receipt of Caregiving and Fall Risk in US Community-dwelling Older Adults
  208. Associations of Health-Related Quality of Life with Overall Quality of Life in the Patient Reported Outcomes Measurement Information System (PROMIS®) Project
  209. Patient-Reported Usability of Positive Airway Pressure Equipment Is Associated With Adherence in Older Adults
  210. Responsiveness to Change and Minimally Important Differences of the Patient-Reported Outcomes Measurement Information System Gastrointestinal Symptoms Scales
  211. Differential item functioning of the patient-reported outcomes information system (PROMIS®) pain interference item bank by language (Spanish versus English)
  212. Colorectal cancer survivors’ surveillance patterns and experiences of care: A SEER-CAHPS study.
  213. Assessment of the Psychometric Properties of a Questionnaire Assessing Patient-Reported Outcomes With Laser In Situ Keratomileusis (PROWL)
  214. Implementation and Sequencing of Practice Transformation in Urban Practices with Underserved Patients
  215. Symptoms and Satisfaction of Patients in the Patient-Reported Outcomes With Laser In Situ Keratomileusis (PROWL) Studies
  216. Patient and caregiver goals for dementia care
  217. Gastrointestinal symptom severity in irritable bowel syndrome, inflammatory bowel disease and the general population
  218. Perceived Effectiveness, Self-efficacy, and Social Support for Oral Appliance Therapy Among Older Veterans With Obstructive Sleep Apnea
  219. Development of a high-value care culture survey: a modified Delphi process and psychometric evaluation
  220. Responsiveness of 8 Patient-Reported Outcomes Measurement Information System (PROMIS) measures in a large, community-based cancer study cohort
  221. Patient-Reported oral health outcome measurement for children and adolescents
  222. Readability and Comprehension of the Geriatric Depression Scale and PROMIS® Physical Function Items in Older African Americans and Latinos
  223. The Costs of Fall-Related Injuries among Older Adults: Annual Per-Faller, Service Component, and Patient Out-of-Pocket Costs
  224. Change in Health-Related Quality-of-Life at Group and Individual Levels Over Time in Patients Treated for Chronic Myofascial Neck Pain
  225. Measurement equivalence of the Consumer Assessment of Healthcare Providers and Systems (CAHPS®) Medicare survey items between Whites and Asians
  226. Racial/Ethnic Disparities in Medicare Beneficiaries’ Care Coordination Experiences
  227. The challenge of measuring intra-individual change in fatigue during cancer treatment
  228. Claims-based Identification Methods and the Cost of Fall-related Injuries Among US Older Adults
  229. Orientation to the Caregiver Role Among Latinas of Mexican Origin
  230. Patient-Provider Communication With Older Adults About Sleep Apnea Diagnosis and Treatment
  231. Validity of PROMIS physical function measured in diverse clinical samples
  232. Using Linear Equating to Map PROMIS® Global Health Items and the PROMIS-29 V2.0 Profile Measure to the Health Utilities Index Mark 3
  233. Development and psychometric evaluation of a health-related quality of life instrument for individuals with adult-onset hearing loss
  234. Cancer registry-survey data linkages to measure patient-centered quality of care: SEER-MHOS and SEER-CAHPS.
  235. Measurement equivalence of the Consumer Assessment of Healthcare Providers and Systems (CAHPS) Medicare survey items between non-Hispanic whites and Asians.
  236. Best (but oft-forgotten) practices: expressing and interpreting associations and effect sizes in clinical outcome assessments
  237. Performance of the Medicare Consumer Assessment of Health Care Providers and Systems (CAHPS) Physical Functioning Items
  238. Less Use of Extreme Response Options by Asians to Standardized Care Scenarios May Explain Some Racial/Ethnic Differences in CAHPS Scores
  239. Possibilities for Shortening the CAHPS Clinician and Group Survey
  240. The Facilitators of and Barriers to Adherence to Hypertension Treatment Scale
  241. Scoring the SF-36 in Orthopaedics: A Brief Guide
  242. Confirmatory Factor Analysis of the Patient Reported Outcomes Measurement Information System (PROMIS) Adult Domain Framework Using Item Response Theory Scores
  243. The PROMIS of QALYs
  244. Case Study of an Unsustainable Community-Academic Partnership: Toward Core Standards for the Structure of Emerging Participatory Research
  245. Linking Physical and Mental Health Summary Scores from the Veterans RAND 12-Item Health Survey (VR-12) to the PROMIS® Global Health Scale
  246. Use of Internet panels to conduct surveys
  247. Use of CAHPS® patient experience survey data as part of a patient-centered medical home quality improvement initiative
  248. Reliability and construct validity of PROMIS® measures for patients with heart failure who undergo heart transplant
  249. Child and adolescent perceptions of oral health over the life course
  250. Development of the Usability of Sleep Apnea Equipment – Positive Airway Pressure (USE-PAP) questionnaire
  251. How much do cancer-related symptoms contribute to health-related quality of life in lung and colorectal cancer patients? A report from the Cancer Care Outcomes Research and Surveillance (CanCORS) Consortium
  252. U.S. General Population Estimate for “Excellent” to “Poor” Self-Rated Health Item
  253. Corrigendum: Development of the NIH Patient-Reported Outcomes Measurement Information System (PROMIS) Gastrointestinal Symptom Scales
  254. The PREEMPT study - evaluating smartphone-assisted n-of-1 trials in patients with chronic pain: study protocol for a randomized controlled trial
  255. Unveiling SEER-CAHPS®: A New Data Resource for Quality of Care Research
  256. Methodological Considerations When Studying the Association between Patient-Reported Care Experiences and Mortality
  257. US Valuation of Health Outcomes Measured Using the PROMIS-29
  258. Should Health Care Providers be Accountable for Patients’ Care Experiences?
  259. Health-related quality of life in older adult survivors of selected cancers: Data from the SEER-MHOS linkage
  260. Development and Evaluation of the CAHPS (Consumer Assessment of Healthcare Providers and Systems) Survey for In-Center Hemodialysis Patients
  261. Development of the NIH Patient-Reported Outcomes Measurement Information System (PROMIS) Gastrointestinal Symptom Scales
  262. Construct Validity of the Patient-Reported Outcomes Measurement Information System Gastrointestinal Symptom Scales in Systemic Sclerosis
  263. Correlation of PROMIS scales and clinical measures among chronic obstructive pulmonary disease patients with and without exacerbations
  264. A Randomized Controlled Pilot Trial of the Functional Assessment Screening Tablet to Engage Patients at the Point of Care
  265. Post-traumatic stress symptoms in cancer survivors: relationship to the impact of cancer scale and other associated risk factors
  266. Development and Evaluation of a Measure to Assess Restorative Sleep
  267. Examining the Role of Patient Experience Surveys in Measuring Health Care Quality
  268. FRI0223 Development and Validation of Patient-Reported Outcomes Measurement Information System (PROMIS®) Gastrointestinal (GI) Symptom Scales in Systemic Sclerosis
  269. 113 * EXAMINING MODELS OF SPECIALIST HEALTHCARE SUPPORT TO CARE HOMES
  270. Evaluation of the Consumer Assessment of Healthcare Providers and Systems In-Center Hemodialysis Survey
  271. GERD Symptoms in the General Population: Prevalence and Severity Versus Care-Seeking Patients
  272. Evaluating the Psychometric Properties of the CAHPS Patient-Centered Medical Home Survey
  273. Overview of Classical Test Theory and Item Response Theory for the Quantitative Assessment of Items in Developing Patient-Reported Outcomes Measures
  274. Demographic Differences in Health Preferences in the United States
  275. Improving Diabetes Health Literacy by Animation
  276. Depressed or Not Depressed: Untangling Symptoms of Depression in Patients Hospitalized With Coronary Heart Disease
  277. Development of a Preference-Based Index From the National Eye Institute Visual Function Questionnaire–25
  278. Should Linking Replace Regression When Mapping from Profile-Based Measures to Preference-Based Measures?
  279. Development of an Online Library of Patient-Reported Outcome Measures in Gastroenterology: The GI-PRO Database
  280. Comparison of US Panel Vendors for Online Surveys
  281. Evaluation of a Care Coordination Measure for the Consumer Assessment of Healthcare Providers and Systems (CAHPS®) Medicare Survey
  282. Upper-Extremity and Mobility Subdomains From the Patient-Reported Outcomes Measurement Information System (PROMIS) Adult Physical Functioning Item Bank
  283. Specialties Differ in Which Aspects of Doctor Communication Predict Overall Physician Ratings
  284. Responsiveness and minimally important difference for the Patient-Reported Outcomes Measurement Information System (PROMIS) 20-item physical functioning short form in a prospective observational study of rheumatoid arthritis
  285. Use of imaging and biomarker tests for posttreatment care of early‐stage breast cancer survivors
  286. Associations of cancer and other chronic medical conditions with SF-6D preference-based scores in Medicare beneficiaries
  287. Don’t middle your MIDs: regression to the mean shrinks estimates of minimally important differences
  288. Evaluating the Content of the Communication Items in the CAHPS® Clinician and Group Survey and Supplemental Items with What High-Performing Physicians Say They Do
  289. Validity of Temporal Measures as Proxies for Measuring Acculturation in Asian Indian Survey Respondents
  290. Psychometric analyses of patient-reported outcome instruments for autosomal dominant polycystic kidney disease
  291. Introduction to patient-reported outcome item banks: issues in minority aging research
  292. Norming plans for the NIH Toolbox
  293. Vision assessment using the NIH Toolbox
  294. Development of a vision-targeted health-related quality of life item measure
  295. ISOQOL recommends minimum standards for patient-reported outcome measures used in patient-centered outcomes and comparative effectiveness research
  296. Associations of Sleep Disturbance Symptoms With Health-Related Quality of Life in Parkinson’s Disease
  297. Depression Screening: Utility of the Patient Health Questionnaire in Patients With Acute Coronary Syndrome
  298. Evaluation of the Patient-Reported Outcomes Information System (PROMIS®) Spanish-language physical functioning items
  299. Racial/Ethnic Disparities in Medicare Part D Experiences
  300. Can Hospital Cultural Competency Reduce Disparities in Patient Experiences With Care?
  301. A Field Experiment on the Impact of Physician-level Performance Data on Consumers’ Choice of Physician
  302. Adapting the PRO-CTCAE for Patient Reporting of Toxicity in Radiation Oncology
  303. Introduction
  304. Development and Evaluation of CAHPS Questions to Assess the Impact of Health Information Technology on Patient Experiences With Ambulatory Care
  305. Development of and Field Test Results for the CAHPS PCMH Survey
  306. Differences in CAHPS Reports and Ratings of Health Care Provided to Adults and Children
  307. Psychometric Properties of the Consumer Assessment of Healthcare Providers and Systems (CAHPS®) Clinician and Group Adult Visit Survey
  308. The Authors Respond
  309. Health-related quality of life in patients with interstitial cystitis/bladder pain syndrome and frequently associated comorbidities
  310. The Consumer Assessment of Healthcare Providers and Systems (CAHPS) Cultural Competence (CC) Item Set
  311. Evaluating Measurement Equivalence Across Race and Ethnicity on the CAHPS Cultural Competence Survey
  312. Moving towards culturally competent health systems: Organizational and market factors
  313. Development and Evaluation of CAHPS® Survey Items Assessing How Well Healthcare Providers Address Health Literacy
  314. Development of Items to Assess Patients’ Health Literacy Experiences at Hospitals for the Consumer Assessment of Healthcare Providers and Systems (CAHPS) Hospital Survey
  315. How Much Is Lost in Using Single Items?
  316. US general population norms for telephone administration of the SF-36v2
  317. A Randomized Controlled Study to Evaluate the Efficacy of Noninvasive Limb Cover for Chronic Phantom Limb Pain Among Veteran Amputees
  318. Development of a Prognostic Model for Six-Month Mortality in Older Adults With Declining Health
  319. Development of a Prognostic Model for 6-month Mortality in Older Adults With Declining Health (316-A)
  320. Cultural competency assessment tool for hospitals
  321. Are hot flashes associated with sleep disturbance during midlife? Results from the STRIDE cohort study
  322. Confirmatory Factor Analysis of the Motor Unified Parkinson’s Disease Rating Scale
  323. Feasibility and Construct Validity of PROMIS and “Legacy” Instruments in an Academic Scleroderma Clinic
  324. Advancing PROMIS’s methodology: results of the Third Patient-Reported Outcomes Measurement Information System (PROMIS®) Psychometric Summit
  325. Gender Differences in Multiple Underlying Dimensions of Health-related Quality of Life Are Associated with Sociodemographic and Socioeconomic Status
  326. The future of measuring patient-reported outcomes in rheumatology: Patient-Reported Outcomes Measurement Information System (PROMIS)
  327. Agreement about Identifying Patients Who Change over Time
  328. Content validity of patient-reported outcome measures: perspectives from a PROMIS meeting
  329. The Impact of a Filariasis Control Program on Lihir Island, Papua New Guinea
  330. Rasch analysis in the development of a simplified version of the national eye institute visual-function questionnaire-25 for utility estimation
  331. Asthma outcome measures
  332. Depression and the Health Care Experiences of Medicare Beneficiaries
  333. The impact of menopause on health-related quality of life: results from the STRIDE longitudinal study
  334. Minimally Important Differences of the UCLA Scleroderma Clinical Trial Consortium Gastrointestinal Tract Instrument
  335. Patient education integrated with acupuncture for relief of cancer-related fatigue randomized controlled feasibility study
  336. Fulvestrant (F) and letrozole (L) combination in second-line or more for estrogen receptor (ER)-positive (+) metastatic breast cancer (MBC): Efficacy and predictive factors of response.
  337. Using the Nominal Response Model to Evaluate Response Category Discrimination in the PROMIS Emotional Distress Item Pools
  338. Differential Item Functioning by Survey Language Among Older Hispanics Enrolled in Medicare Managed Care
  339. Five preference-based indexes in cataract and heart failure patients were not equally responsive to change
  340. Interpreting patient-reported outcome results: US FDA guidance and emerging methods
  341. Assessment of Quality of Cancer-Related Follow-Up Care From the Cancer Survivor's Perspective
  342. Health-related quality of life: The impact of diagnostic angiography
  343. Clinical correlates of health-related quality of life among opioid-dependent patients
  344. Prevalence and correlates of sleep disturbance in systemic sclerosis--results from the UCLA scleroderma quality of life study
  345. Health-related quality of life in adults reporting arthritis: analysis from the National Health Measurement Study
  346. Medical Student Attitudes toward Complementary, Alternative and Integrative Medicine
  347. Diagnostic accuracy and agreement across three depression assessment measures for Parkinson’s disease
  348. Medication Responsiveness of Motor Symptoms in a Population-Based Study of Parkinson Disease
  349. Relative to the general US population, chronic diseases are associated with poorer health-related quality of life as measured by the Patient-Reported Outcomes Measurement Information System (PROMIS)
  350. Representativeness of the Patient-Reported Outcomes Measurement Information System Internet panel
  351. The Patient-Reported Outcomes Measurement Information System (PROMIS) developed and tested its first wave of adult self-reported health outcome item banks: 2005–2008
  352. Development of a culturally appropriate health-related quality of life measure for human immunodeficiency virus-infected children in Thailand
  353. Longitudinal Changes in Visual Acuity and Health-related Quality of Life
  354. Association of gastrointestinal involvement and depressive symptoms in patients with systemic sclerosis
  355. Differences in Child versus Parent Reports of the Child's Health-Related Quality of Life in Children with Epilepsy and Healthy Siblings
  356. Health-related Quality of Life of Thai children with HIV infection: a comparison of the Thai Quality of Life in Children (ThQLC) with the Pediatric Quality of Life Inventory™ version 4.0 (PedsQL™ 4.0) Generic Core Scales
  357. A Comparison of Two Educational Methods on Immigrant Latinas Breast Cancer Knowledge and Screening Behaviors
  358. Quality indicators for multiple sclerosis
  359. The impact of next and back buttons on time to complete and measurement reliability in computer-based surveys
  360. Health state preferences are equivalent in the United States and Trinidad and Tobago
  361. Valuation of scleroderma and psoriatic arthritis health states by the general public
  362. Efficiency of static and computer adaptive short forms compared to full-length measures of depressive symptoms
  363. Associations of Eye Diseases and Symptoms with Self-Reported Physical and Mental Health
  364. Development of a New Patient-Based Measure of Pediatric Ambulatory Care
  365. Reliability and validity of the university of california, los angeles scleroderma clinical trial consortium gastrointestinal tract instrument
  366. Effects of Mode and Order of Administration on Generic Health-Related Quality of Life Scores
  367. SF-36 includes less Parkinson Disease (PD)-targeted content but is more responsive to change than two PD-targeted health-related quality of life measures
  368. Readability estimates for commonly used health-related quality of life surveys
  369. Health-Related Quality of Life Predicts Mortality in Patients With Advanced Chronic Liver Disease
  370. Development and preliminary evaluation of a quality of life measure targeted at dementia caregivers
  371. Development of physical and mental health summary scores from the patient-reported outcomes measurement information system (PROMIS) global items
  372. Impact of Cancer on Health-Related Quality of Life of Older Americans
  373. Recommendations on Evidence Needed to Support Measurement Equivalence between Electronic and Paper-Based Patient-Reported Outcome (PRO) Measures: ISPOR ePRO Good Research Practices Task Force Report
  374. Predicting EuroQol (EQ-5D) scores from the patient-reported outcomes measurement information system (PROMIS) global items and domain item banks in a United States sample
  375. PMC69 MULTITRAIT-MULTIMETHOD ANALYSIS OF THREE GENERIC PREFERENCE-BASED HEALTH-RELATED QUALITY OF LIFE MEASURES IN THE NATIONAL HEALTH MEASUREMENT STUDY
  376. Adjusting for Subgroup Differences in Extreme Response Tendency in Ratings of Health Care: Impact on Disparity Estimates
  377. Expectations prior to epilepsy surgery: An exploratory comparison of men and women
  378. Evidence-based effect size estimation:An illustration using the case of acupuncture for cancer-related fatigue
  379. A Randomized Study of Scleroderma Health State Values: A Picture Is Worth a Thousand Words, and Quite a Few Utilities
  380. Work hour restrictions and internal medicine residents’ health-related quality of life
  381. Can Additional Patient Experience Items Improve the Reliability of and Add New Domains to the CAHPS®Hospital Survey?
  382. The Minimally Important Difference for the Fatigue Visual Analog Scale in Patients with Rheumatoid Arthritis Followed in an Academic Clinical Practice
  383. Prospective validation of the short form liver disease quality of life instrument
  384. Development of a fatigue and functional impact scale in anemic cancer patients receiving chemotherapy
  385. Survey Response Style and Differential Use of CAHPS Rating Scales by Hispanics
  386. Prospects and challenges in using patient-reported outcomes in clinical practice
  387. Self‐Reported Health Status of Vietnamese and Non‐Hispanic White Older Adults in California
  388. Access to Care for Youth with Special Health Care Needs in the Transition to Adulthood
  389. Bridging From the Picker Hospital Survey to the CAHPS® Hospital Survey
  390. Case Management and Health-Related Quality of Life Outcomes in a National Sample of Persons with HIV/AIDS
  391. Development and Psychometric Assessment of a Multidimensional Measure of Internalized HIV Stigma in a Sample of HIV-positive Adults
  392. Evaluating the SF-36 Health Survey (Version 2) in Older Vietnamese Americans
  393. Language and Regional Differences in Evaluations of Medicare Managed Care by Hispanics
  394. Recommended methods for determining responsiveness and minimally important differences for patient-reported outcomes
  395. How Do Proxy Responses and Proxy-Assisted Responses Differ from What Medicare Beneficiaries Might Have Reported about Their Health Care?
  396. Reports and Ratings of Care: Black and White Medicare Enrollees
  397. Adherence treatment factors in hypertensive African American women
  398. Evaluating Differential Item Functioning of the PRIME-MD Mood Module Among Impoverished Black and White Women in Primary Care
  399. Evaluation of the reliability and validity of the Medical Outcomes Study sleep scale in patients with painful diabetic peripheral neuropathy during an international clinical trial
  400. Mode of Administration Is Important in US National Estimates of Health-Related Quality of Life
  401. US Norms for Six Generic Health-Related Quality-of-Life Indexes From the National Health Measurement Study
  402. Ethnic Variations in Dementia Caregiving Experiences
  403. Developing a Spanish-language Consumer Report for CAHPS® Health Plan Surveys
  404. What Is Sufficient Evidence for the Reliability and Validity of Patient-Reported Outcome Measures?
  405. Development of a preliminary scleroderma gastrointestinal tract 1.0 quality of life instrument
  406. Design and Evaluation of Fiber Tip Lenses for Fiber Optic Transmitter and Receiver Applications
  407. Precision of Health-Related Quality-of-Life Data Compared With Other Clinical Measures
  408. Correlated physical and mental health summary scores for the SF-36 and SF-12 Health Survey, V.1
  409. A comparison of three sets of criteria for determining the presence of differential item functioning using ordinal logistic regression
  410. Severity of Visual Field Loss and Health-related Quality of Life
  411. Applying item response theory to enhance health outcomes assessment
  412. The role of the bifactor model in resolving dimensionality issues in health outcomes measures
  413. Item Response Theory Analyses of Physical Functioning Items in the Medical Outcomes Study
  414. Psychometric Evaluation and Calibration of Health-Related Quality of Life Item Banks
  415. The Impact of HIV on Oral Health and Subsequent Use of Dental Services
  416. Reliability, validity, and minimally important differences of the SF-6D in systemic sclerosis
  417. IRT health outcomes data analysis project: an overview and summary
  418. Next steps for use of item response theory in the assessment of health outcomes
  419. Does Ambulatory Process of Care Predict Health-Related Quality of Life Outcomes for Patients with Chronic Disease?
  420. A Randomized Controlled Trial of Tai Chi for Tension Headaches
  421. HEALTH STATUS OF VIETNAMESE ELDERS COMPARED WITH NON-HISPANIC WHITES IN CALIFORNIA.
  422. Repeated measures analyses of dose timing of antiretroviral medication and its relationship to HIV virologic outcomes
  423. The SF-36 physical and mental health factors were confirmed in cancer and HIV/AIDS patients
  424. Physician Communication About the Cost and Acquisition of Newly Prescribed Medications
  425. A Practical Method to Calibrate Self-Reported Adherence to Antiretroviral Therapy
  426. A Comprehensive Evaluation of Survey Questions for Adherence to Antiretroviral Medications and Exploratory Analyses for Identifying Optimal Sets of Survey Questions
  427. Classical Test Theory and Item Response Theory Analyses of Multi-Item Scales Assessing Parents?? Perceptions of Their Children??s Dental Care
  428. Correction: Patients' Global Ratings of Their Health Care Are Not Associated with the Technical Quality of Their Care
  429. Impact of Severity and Bilaterality of Visual Impairment on Health-Related Quality of Life
  430. Comparison of Data Quality for Reports and Ratings of Ambulatory Care by African American and White Medicare Managed Care Enrollees
  431. Responsiveness and minimal important differences for patient reported outcomes
  432. Physician Communication When Prescribing New Medications
  433. Mitochondrial membrane depolarization in Drosophila apoptosis
  434. Changes in symptoms and health-related quality of life in a nationally representative sample of adults in treatment for HIV
  435. Psychometric Performance of the National Eye Institute Visual Function Questionnaire in Latinos and Non-Latinos
  436. Linguistic disparities in health care access and health status among older adults
  437. A Pilot Study of Health Beliefs and Attitudes Concerning Measures of Antiretroviral Adherence Among Prisoners Receiving Directly Observed Antiretroviral Therapy
  438. Variations in provider conceptions of integrative medicine
  439. Patients' Global Ratings of Their Health Care Are Not Associated with the Technical Quality of Their Care
  440. A test of knowledge about prostate cancer screening
  441. Health-related quality of life and patient reports about care outcomes in a multidisciplinary hospital intervention
  442. Minimally important difference in diffuse systemic sclerosis: results from the D-penicillamine study
  443. Application of Group-Level Item Response Models in the Evaluation of Consumer Reports About Health Plan Quality
  444. Repeated Measures Longitudinal Analyses of HIV Virologic Response as a Function of Percent Adherence, Dose Timing, Genotypic Sensitivity, and Other Factors
  445. The Effect of a Multidisciplinary Hospitalist/Physician and Advanced Practice Nurse Collaboration on Hospital Costs
  446. International Prevalence, Recognition, and Treatment of Cardiovascular Risk Factors in Outpatients With Atherothrombosis
  447. An Alternative Approach to Reducing the Costs of Patient Care? A Controlled Trial of the Multi-Disciplinary Doctor-Nurse Practitioner (MDNP) Model
  448. Variation in the Readability of Items Within Surveys
  449. Comparison of Mail and Telephone in Assessing Patient Experiences in Receiving Care from Medical Group Practices
  450. Clinical significance of patient-reported questionnaire data: another step toward consensus
  451. Assessment of the Equivalence of the Spanish and English Versions of the CAHPS® Hospital Survey on the Quality of Inpatient Care
  452. Development and Evaluation of the CAHPS® Hospital Survey
  453. Equivalence of Mail and Telephone Responses to the CAHPS® Hospital Survey
  454. Exploratory Factor Analyses of the CAHPS® Hospital Pilot Survey Responses across and within Medical, Surgical, and Obstetric Services
  455. Methods Used to Streamline the CAHPS® Hospital Survey
  456. Patterns of Unit and Item Nonresponse in the CAHPS® Hospital Survey
  457. Review of the Literature on Survey Instruments Used to Collect Data on Hospital Patients' Perceptions of Care
  458. Do Medicaid and Commercial CAHPS Scores Correlate Within Plans?
  459. Application of Structural Equation Modeling to Health Outcomes Research
  460. Impact of Chronic Viral Hepatitis on Health-Related Quality of Life in HIV: Results from a Nationally Representative Sample
  461. A Self-Report Measure of Clinicians' Orientation toward Integrative Medicine
  462. Evaluating the Statistical Significance of Health-Related Quality-Of-Life Change in Individual Patients
  463. Creating a Crosswalk to Estimate AIDS Clinical Trials Group Quality of Life Scores in a Nationally Representative Sample of Persons in Care for HIV in the United States
  464. Imputation of SF-12 Health Scores for Respondents with Partially Missing Data
  465. Development of the 12-Item Expectations Regarding Aging Survey
  466. Impact of hepatitis C on health related quality of life: A systematic review and quantitative assessment
  467. Patients' Preferences for Technical versus Interpersonal Quality When Selecting a Primary Care Physician
  468. Effects of Testosterone Replacement in Human Immunodeficiency Virus-Infected Women with Weight Loss
  469. Estimating clinically significant differences in quality of life outcomes
  470. Effect of a Multidisciplinary Intervention on Communication and Collaboration Among Physicians and Nurses
  471. Psychometric properties of the Medical Outcomes Study Sleep measure
  472. The Effect of Socioeconomic Status on the Survival of People Receiving Care for HIV Infection in the United States
  473. The association of health-related quality of life with survival among persons with HIV infection in the united states
  474. Racial Differences in the Impact of Irritable Bowel Syndrome on Health-Related Quality of Life
  475. Are Physician-Derived Disease Severity Indices Associated with Health-Related Quality of Life in Patients with End-Stage Liver Disease?
  476. Physician Recognition of Cognitive Impairment: Evaluating the Need for Improvement
  477. Opposing inputs by Hedgehog and Brinker define a stripe ofhairyexpression in theDrosophilaleg imaginal disc
  478. The applicability of the Consumer Assessments of Health Plans Survey (CAHPS(R)) to Preferred Provider Organizations in the United States: a discussion of industry concerns
  479. Delays and Unmet Need for Health Care Among Adult Primary Care Patients in a Restructured Urban Public Health System
  480. Racial and ethnic differences in patients' preferences for initial care by specialists
  481. No Evidence of an Association between Transient HIV Viremia (“Blips”) and Lower Adherence to the Antiretroviral Medication Regimen
  482. Racial differences in health-related quality of life among hemodialysis patients
  483. How Many Patients Are Needed to Provide Reliable Evaluations of Individual Clinicians?
  484. Health plan effects on patient assessments of medicaid managed care among racial/ethnic minorities
  485. Methodological Challenges Associated with Patient Responses to Follow-up Longitudinal Surveys Regarding Quality of Care
  486. Psychometric Properties of the Consumer Assessment of Health Plans Study (CAHPS®) 2.0 Adult Core Survey
  487. Psychometric properties of the National Eye Institute–Refractive Error Quality of Life instrument
  488. Responsiveness of the National Eye Institute Refractive Error Quality of Life instrument to surgical correction of refractive error
  489. Associations of Presbyopia With Vision-Targeted Health-Related Quality of Life
  490. Reply
  491. Patient Reports and Ratings of Individual Physicians: An Evaluation of the DoctorGuide and Consumer Assessment of Health Plans Study Provider-Level Surveys
  492. Patterns of Coping Among Persons with HIV Infection: Configurations, Correlates, and Change
  493. Psychometric Properties of the Spanish Consumer Assessment of Health Plans Survey (CAHPS)
  494. Bias in Assessment of Health-Related Quality of Life in a Hemodialysis Population
  495. Race/Ethnicity, Language, and Patients' Assessments of Care in Medicaid Managed Care
  496. The Diverse Older HIV-Positive Population
  497. The Tripartite Model of Anxiety and Depression: Symptom Structure in Depressive and Hypertensive Patient Groups
  498. Knowledge of Antiretroviral Regimen Dosing and Adherence: A Longitudinal Study
  499. Correlates of Social Function: A Comparison of a Black and a White Sample of Older Persons in Los Angeles
  500. A guide for clinicians to compare the accuracy and precision of health-related quality-of-life data relative to other clinical measures
  501. Assessing the clinical significance of patient-reported outcomes: Examples drawn from a recent meeting of the drug information association (DIA)
  502. HIV Patients’ Experiences With Inpatient and Outpatient Care
  503. Health-related quality of life, depressive symptoms, anemia, and malnutrition at hemodialysis initiation
  504. Remembering a Life
  505. Use of the SF-36 and other health-related quality of life measures to assess persons with disabilities
  506. Do Older Adults Expect to Age Successfully? The Association Between Expectations Regarding Aging and Beliefs Regarding Healthcare Seeking Among Older Adults
  507. A prospective study of predictors of adherence to combination antiretroviral medication
  508. The Alcohol‐Related Problems Survey: Identifying Hazardous and Harmful Drinking in Older Primary Care Patients
  509. Patient preferences regarding antiretroviral therapy
  510. Effect of CAHPS Performance Information on Health Plan Choices by Iowa Medicaid Beneficiaries
  511. Development, Reliability, and Validity of the Expectations Regarding Aging (ERA-38) Survey
  512. Effects of CAHPS Health Plan Performance Information on Plan Choices by New Jersey Medicaid Beneficiaries
  513. Seizure Reduction and Quality of Life Improvements in People with Epilepsy
  514. Beyond alcoholism: identifying older, at-risk drinkers in primary care.
  515. Comparing the alcohol-related problems survey (ARPS) to traditional alcohol screening measures in elderly outpatients
  516. Patients Using Chiropractors in North America
  517. How well do clinicians estimate patients’ adherence to combination antiretroviral therapy?
  518. Patient, clinician, and population perspectives on determining the clinical significance of quality-of-life scores
  519. Similar Effectiveness of Paroxetine, Fluoxetine, and Sertraline in Primary Care
  520. Factors related to agreement between self-reported and conventional Expanded Disability Status Scale (EDSS) scores
  521. IMPROVEMENT IN EMOTIONAL WELL-BEING AND RELATIONSHIPS OF USERS OF SILDENAFIL
  522. QL3: PSYCHOMETRIC PERFORMANCE OF THE MEDICAL OUTCOMES STUDY SLEEP SCALE IN THE US GENERAL POPULATION
  523. Expectations Regarding Aging Among Older Adults and Physicians Who Care for Older Adults
  524. Development of the 25-list-item National Eye Institute Visual Function Questionnaire
  525. Responsiveness of the smoking cessation quality of life (SCQoL) questionnaire
  526. A Comparison Study of Multiple Measures of Adherence to HIV Protease Inhibitors
  527. Associations of Symptoms and Health-Related Quality of Life: Findings from a National Study of Persons with HIV Infection
  528. Does physician gender affect satisfaction of men and women visiting the emergency department?
  529. Racial differences in the impact of irritable bowel syndrome (IBS) on health-related quality of life (HRQOL)
  530. IN RE ALCOHOL USE IN OLDER ADULTS
  531. The RAND-36 measure of health-related quality of life
  532. A Review of Health-Related Quality-of-Life Measures in Stroke
  533. COMPARISON OF THE ROST AND THE CAGE ALCOHOL SCREENING INSTRUMENTS IN YOUNG ADULTS
  534. Medical Care
  535. USING DATA TO ENHANCE THE EXPERT PANEL PROCESS
  536. Confirmatory factor analysis of the Consumer Assessment of Health Plans Study (CAHPS) 1.0 core survey.
  537. Electroacupuncture for Control of Myeloablative Chemotherapy–Induced Emesis
  538. Identifying a Short Functional Disability Screen for Older Persons
  539. Physical and Role Functioning Among Persons With HIV
  540. The Concept of Clinically Meaningful Difference in Health-Related Quality of Life Research
  541. Development of subscales from the symptoms/problems and effects of kidney disease scales of the kidney disease quality of life instrument
  542. Item Response Theory and Health Outcomes Measurement in the 21st Century
  543. The impact of irritable bowel syndrome on health-related quality of life
  544. Effects of Incentive Size and Timing on Response Rates to a Follow-Up Wave of a Longitudinal Mailed Survey
  545. Coping, Conflictual Social Interactions, Social Support, and Mood Among HIV-Infected Persons
  546. Review: The Newspaper Indian: Native American Identity in the Press, 1820-90, by John Coward
  547. Self-Study from Web-Based and Printed Guideline Materials
  548. Access to Medical Care Reported by Asians and Pacific Islanders in a West Coast Physician Group Association
  549. Development of a Health-Related Quality of Life Measure for Peripheral Neuropathy
  550. Health-related quality of life in patients with human immunodeficiency virus infection in the United States: results from the HIV cost and services utilization study
  551. Using a criterion standard to validate the Alcohol-Related Problems Survey (ARPS): A screening measure to identify harmful and hazardous drinking in older persons
  552. Quality of life measures in epilepsy: How well can they detect change over time?
  553. Evaluating the Equivalence of Health Care Ratings by Whites and Hispanics
  554. Testosterone Replacement and Resistance Exercise in HIV-Infected Men With Weight Loss and Low Testosterone Levels
  555. Impact of Psychiatric Conditions on Health-Related Quality of Life in Persons With HIV Infection
  556. A Comparative Review of Generic Quality-of-Life Instruments
  557. Ethnic and Racial Differences in Long-Term Survival From Hospitalization for HIV Infection
  558. Health Status Measurement Performance and Health Status Differences by Age, Ethnicity, and Gender: Assessment in the Medical Outcomes Study
  559. The Role of Peer-Reviewed Journals in Science
  560. Development of the Smoking Cessation quality of life questionnaire
  561. Are latinos less satisfied with communication by health care providers?
  562. The influence of gatekeeping and utilization review on patient satisfaction
  563. Drinking Habits Among Older Persons: Findings from the NHANES I Epidemiologic Follow-up Study (1982-84)
  564. Review: Fly a Cell!
  565. Psychometric Properties of the CAHPS™ 1.0 Survey Measures
  566. Special Issues Addressed in the CAHPS™ Survey of Medicare Managed Care Beneficiaries
  567. Special Issues in Assessing Care of Medicaid Recipients
  568. A New Paradigm for Alcohol Use in Older Persons
  569. Associations of clinical parameters with health-related quality of life in hospitalized persons with HIV disease
  570. An International Comparison of the Reliability and Responsiveness of the Duke Health Profile for Measuring Health-Related Quality of Life of Patients Treated With Alprostadil for Erectile Dysfunction
  571. Psychometric Properties of the National Eye Institute Visual Function Questionnaire (NEI-VFQ)
  572. Effects of Testosterone Replacement with a Nongenital, Transdermal System, Androderm, in Human Immunodeficiency Virus-Infected Men with Low Testosterone Levels
  573. A COMPARISON OF SELF-REPORTED UTILIZATION OF OPHTHALMIC CARE FOR DIABETES IN MANAGED CARE VERSUS FEE-FORSERVICE
  574. The UCLA Prostate Cancer Index
  575. Member Ratings of Health Care Provided by 48 Physician Groups
  576. Does Dissatisfaction with Access to Specialists Affect the Desire to Leave a Managed Care Plan?
  577. Reliability of an Arabic Version of the RAND-36 Health Survey and its Equivalence to the US-English Version
  578. The Prospective Effect of Access to Medical Care on Health-Related Quality-of-Life Outcomes in Patients with Symptomatic HIV Disease
  579. Constitutional Symptoms and Health-Related Quality of Life in Patients with Symptomatic HIV Disease
  580. The Dose-Response Relation of Intrathecal Fentanyl for Labor Analgesia 
  581. The Structure of Satisfaction with Pharmacy Services
  582. Debating Survey Approaches
  583. Capelin (<i>Mallotus villosus</i>) and herring (<i>Clupea harengus</i>) as paratenic hosts of <i>Anisakis simplex,</i> a parasite of beluga (<i>Delphinapterus leucas</i>) in the St. Lawrence estuary
  584. Euphausiids as intermediate hosts of <i>Anisakis simplex</i> in the St. Lawrence estuary
  585. It Performance Turnaround: The Outsourcing Alternative
  586. Adjusting for Attrition in School-Based Samples
  587. Primary care physicians' satisfaction with quality of care in California capitated medical groups
  588. Assessing health and quality of life outcomes in dialysis: A report on an institute of medicine workshop
  589. Reliability and Validity of Self-Report CD4 Counts in Persons Hospitalized with HIV Disease
  590. Comparison of a generic to disease-targeted health-related quality-of-life measures for multiple sclerosis
  591. A Randomized Trial of Office-Based Screening for Common Problems in Older Persons
  592. The Impact of Blurred Vision on Functioning and Well-being
  593. Sedation and analgesia for colonoscopy: patient tolerance, pain, and cardiorespiratory parameters
  594. Understanding Changes in Health Status
  595. Access to Community-Based Medical Services and Number of Hospitalizations Among Patients with HIV Disease: Are They Related?
  596. Quality assurance in capitated physician groups. Where is the emphasis?
  597. A comparison of health-related quality of life in patients with epilepsy, diabetes and multiple sclerosis
  598. Teenagers and alcohol misuse in the United States: by any definition, it's a big problem
  599. A review of health-related quality-of-life measures used in end-stage renal disease
  600. Long-term Care Residents' Preferences for Health States on the Quality of Well-Being Scale
  601. Alcohol-related problems in older persons. Determinants, consequences, and screening
  602. Associations between drug use and deviant behavior in teenagers
  603. WHAT IS ADOLESCENT ALCOHOL MISUSE IN THE UNITED STATES ACCORDING TO THE EXPERTS?
  604. Physician implementation of and patient adherence to recommendations from comprehensive geriatric assessment
  605. Medical education and health for all
  606. Bedside charting of pain levels in hospitalized patients with cancer: A randomized controlled trial
  607. Preferential targeting of oxidative base damage to interucleosomal DNA
  608. Outcomes in 248 patients who had diagnostic evaluations for epilepsy surgery
  609. Development of the Quality of Life in Epilepsy Inventory
  610. A Cost and Value Analysis of Two Interventions with Incontinent Nursing Home Residents
  611. Managed Care and Capitation in California: How Do Physicians at Financial Risk Control Their Own Utilization?
  612. The Relationship of Neuropsychological Functioning to Quality of Life in Epilepsy
  613. Validation of a new measure of diarrhea
  614. The relationship between visual acuity and functioning and well-being among diabetics
  615. Access to Medical Care and Health-Related Quality of Life for Low-Income Persons with Symptomatic Human Immunodeficiency Virus
  616. A health-related quality of life measure for multiple sclerosis
  617. Comparing Outcomes and Charges for Patients with Acute Myocardial Infarction in Three Community Hospitals: an Approach for Assessing "Value"
  618. Personal and psychosocial risk factors for physical and mental health outcomes and course of depression among depressed patients.
  619. Response burden, reliability, and validity of the CAGE, Short MAST, and AUDIT alcohol screening measures
  620. Feasibility and Accuracy of a Postcard Diary System for Tracking Healthcare Utilization of Community-Dwelling Older Persons
  621. Agreement between self reports and proxy reports of quality of life in epilepsy patients
  622. Directions for future research
  623. Derivation and Properties of a Brief Health Status Assessment Instrument for Use in HIV Disease
  624. Outcome assessment for epilepsy surgery: The impact of measuring health-related quality of life
  625. Quality-of-life outcomes in men treated for localized prostate cancer
  626. Measuring Physical Function in Community-Dwelling Older Persons: A Comparison of Self-Administered, Interviewer-Administered, and Performance-Based Measures
  627. Functioning and Well-being Outcomes of Patients With Depression Compared With Chronic General Medical Illnesses
  628. Perceptions of Intoxication and Impairment at Arrest among Adults Convicted of Driving under the Influence of Alcohol
  629. Development of the Kidney Disease Quality of Life (KDQOLTM) Instrument
  630. Predictors of Patient Refusal to Participate in Ambulatory-based Comprehensive Geriatric Assessment
  631. The impact of patient adherence on health outcomes for patients with chronic disease in the medical outcomes study
  632. The benefits and pitfalls of health services research funded by proprietary firms
  633. A Perceived Health Index for Use in Persons With Advanced HIV Disease: Derivation, Reliability, and Validity
  634. A short-form measure of dentists' job satisfaction
  635. Long-term functioning and well-being outcomes associated with physical activity and exercise in patients with chronic conditions in the medical outcomes study
  636. The Effect of Oral Support on Sucking Efficiency in Preterm Infants
  637. Quality of Life of Epilepsy Surgery Patients as Compared with Outpatients with Hypertension, Diabetes, Heart Disease, and/or Depressive Symptoms
  638. THE IMPACT OF RESPONSE OPTIONS AND LOCATION IN A MICROCOMPUTER INTERVIEW ON DRINKING DRIVERS' ALCOHOL USE SELF-REPORTS
  639. Short-Form Measures of Physician and Employee Judgments About Hospital Quality
  640. Do Response Options Influence Self-Reports of Alcohol Use?
  641. State-of-the-art SAW channelizer for EW receiver application
  642. EVIDENCE FOR THE FORMATION OF MULTIPLE TYPES OF ACETALDEHYDE-HAEMOGLOBIN ADDUCTS
  643. International use, application and performance of health-related quality of life instruments
  644. Psychometric considerations in evaluating health-related quality of life measures
  645. Change in self-reported functioning in older persons entering a residential care facility
  646. Recall of recommendations and adherence to advice among patients with chronic medical conditions
  647. Health-related quality of life in osteoporosis clinical trials urinary calcium loss
  648. Occupational stress, life stress and mental health among dentists
  649. Response times for the CAGE, short-MAST, AUDIT, and JELLINEK alcohol scales
  650. The ?states versus weights? dilemma in quality of life measurement
  651. Donation and retrieval of cadaveric organs in Australia
  652. Aboriginal Health and Society
  653. The Swedish Health-Related Quality of Life Survey (SWED-QUAL)
  654. Do depressed patients in different treatment settings have different levels of well-being and functioning?
  655. Measuring Functioning and Health in the Very Old
  656. Physicians' characteristics influence patients' adherence to medical treatment: Results from the Medical Outcomes Study.
  657. Value of functional status as a predictor of mortality: Results of a prospective study
  658. OLD AND NEW MMPI-DERIVED SCALES AND THE SHORT-MAST AS SCREENING TOOLS FOR ALCOHOL DISORDER
  659. Antecedents of adherence to medical recommendations: Results from the medical outcomes study
  660. Stepping through the drug use sequence: Longitudinal scalogram analysis of initiation and regular use.
  661. Psychotherapist-patient sexual contact after termination of treatment
  662. A Microcomputer Assessment System (MAS) for administering computer-based surveys: Preliminary results from administration to clients at an impaired-driver treatment program
  663. Benefits and Obstacles of Health Status Assessment in Ambulatory Settings
  664. A Health-Related Quality of Life Instrument for Patients Evaluated for Epilepsy Surgery
  665. Improving task comprehension in the measurement of health state preferences
  666. On becoming involved with drugs: Modeling adolescent drug use over time.
  667. Antecedents of drinking among young adolescents with different alcohol use histories.
  668. Multitrait-Multimethod Analysis of Health-Related Quality-of-Life Measures
  669. Development of an Instrument to Measure Job Satisfaction Among Dentists
  670. Hospital Quality Trends
  671. Marital Status, Social Support, and Health Transitions in Chronic Disease Patients
  672. The Functional Status of Patients
  673. Hierarchical Measures of Physical Function in Ambulatory Geriatrics
  674. Physician-Patient Communication and Adherence
  675. 5. Response to Questionnaire
  676. 6. The PJHQ Questionnaire Exploratory Factor Analysis and Empirical Scale Construction
  677. 7. Further Evaluations of the PJHQ Scales
  678. Peer Cluster Theory and Adolescent Drug Use: A Reanalysis
  679. ROC: Estimation of the Area Under a Receiver Operating Characteristic Curve
  680. The Detection of Depression and the Financing of Medical Care-Reply
  681. Beyond internal consistency reliability: Rationale and user’s guide for Multitrait Analysis Program on the microcomputer
  682. How Generalizable Are Adolescents' Beliefs About Pro-Drug Pressures and Resistance Self-Efficacy?1
  683. Longitudinal scalogram analysis: A methodology and microcomputer program for Guttman scale analysis of longitudinal data
  684. Distinguishing Depression From Functional Impairment in the Medical Outcomes Study-Reply
  685. Beliefs About Resistance Self-Efficacy and Drug Prevalence: Do They Really Affect Drug Use?
  686. Guttman Scale Analysis of Longitudinal Data: A Methodology and Drug Use Applications
  687. Detection of depressive disorder for patients receiving prepaid or fee-for-service care. Results from the Medical Outcomes Study
  688. Robustness of a model of exercise
  689. A Five-Item Measure of Socially Desirable Response Set
  690. Methodological issues in adherence to cancer control regimens
  691. Functional status and well-being of patients with chronic conditions. Results from the Medical Outcomes Study
  692. The functioning and well-being of depressed patients. Results from the Medical Outcomes Study
  693. ALPHA2: An Alternative SAS Program For Estimating Internal Consistency Reliability
  694. Training the creative arts therapist: Identity with integration
  695. The Quality Of Patients' Ratings
  696. X.EXE: A Program for Simplifying EQS Input
  697. The MOS Short-form General Health Survey
  698. Methods For Measuring Patient Satisfaction With Specific Medical Encounters
  699. Reliability and validity of drug use items differing in the nature of their response options.
  700. A microcomputer program for analyzing multitrait-multimethod matrices
  701. A Short-Form Measure of Loneliness
  702. Computer Program Exchange
  703. Professional Satisfaction and Client Outcomes
  704. The Importance of Considering Alternative Structural Equation Models in Evaluation Research
  705. Problem behavior theory and adolescent alcohol use
  706. Structural-equation models of current drug use: Are appropriate models so simple(x)?
  707. Inhibition of Liver Lipogenesis by Dietary Polyunsaturated Fat in Severely Diabetic Rats
  708. Multistage Path Models of Adolescent Alcohol and Drug Use: A Reanalysis
  709. My Medical Care Is Better Than Yours
  710. Book Review : Computer Program Exchange
  711. Book Review : Computer Program Exchange
  712. Relationship of physicians' nonverbal communication skill to patient satisfaction, appointment noncompliance, and physician workload.
  713. Lambda: A Basic Program for Calculating Random Data Eigenvalues
  714. Validity of self-reports of alcohol and other drug use: A multitrait-multimethod assessment.
  715. Fetal Alcohol Syndrome and Fetal Alcohol Effects
  716. The myth and reality of supervisory development
  717. Covariation among health-related behaviors
  718. Validity of five MMPI alcoholism scales: A critique and reanalysis
  719. A study of the reliability and validity of the holmes alcoholism scale
  720. 1218 A FAMILIAL X-LINKED MENTAL RETARDATION SYNDROME ASSOCIATED WITH MULTIPLE CONGENITAL ANOMALIES, MEGALOGENITALIA AND A FRAGILE X CHROMOSOME
  721. Honesty Requiring a Self-Initiated Response
  722. Posterior Resection of Selected Rectal Tumors
  723. Numerical Technique for the Convolution of Piecewise Polynomial Functions
  724. A direct and exact method for computing the transfer function of the optimum smoothing filter
  725. Renal Glycosuria, Aminoaciduria, and Proximal Renal Tubular Acidosis in Association with Membranous Glomerulonephritis.
  726. Two reviews: Motivating economic achievement motivation through the work itself
  727. Two reviews: Motivation through the work itself
  728. Harmony in Modern Counterpoint
  729. Immediate and delayed reactions to interpersonal disagreements: Some effects of the type of issue and order of response
  730. Psychology of the Scientist: III. Introduction to “Passages from the ‘Idea Books’ of Clark L. Hull”
  731. Splanchnic hematocrit in the dog determined from simultaneously measured splanchnic plasma and red cell volumes
  732. Direct Determination of Available Phosphoric Acid by Titration of Ammonium Phosphomolybdate
  733. Properties of firefly pyrophosphatase
  734. A preliminary determination of the functional relationship of effective reaction potential (sER) to the ordinal number of Vincentized extinction reactions (n).
  735. A non-profit/municipality/corporate partnership: an innovative model for collecting end-of-life electronics