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. Does an “EZ” Survey Improve the Data Quality of the Consumer Assessment of Healthcare Providers and Systems (CAHPS®) Clinician and Group Survey 3.1?
  14. Comparison of patient-reported outcomes measurement information system (PROMIS®)-29 and PROMIS global physical and mental health scores
  15. Seeing the Light in Self-Reported Glare
  16. Data from Dynamic Risk Prediction of Treatment Discontinuation Using Patient-Reported Outcomes Data in the Phase III NSABP B-35 Trial
  17. Data 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 S1 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 S2 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 S3 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 S4 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 S5 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 S6 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 Figure S7 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 S1 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 Methods S2 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 S1 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 S2 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 S3 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. Supplementary Table S4 from Dynamic Risk Prediction of Treatment Discontinuation Using Patient-Reported Outcomes Data in the Phase III NSABP B-35 Trial
  44. Performance of the Physical Functioning Activities of Daily Living Scale in the 2020 Medicare Health Outcomes Survey
  45. Are some ways of defining chronic low back pain more indicative of future back pain than others?
  46. Dynamic Risk Prediction of Treatment Discontinuation Using Patient-Reported Outcomes Data in the Phase III NSABP B-35 Trial
  47. Predictors of Pain Management Strategies in Adults with Low-Back Pain: A Secondary Analysis of Amazon Mechanical Turk Survey Data
  48. Embedding research study recruitment within the patient portal preCheck-in
  49. Effects of Excluding Those Who Report Having “Syndomitis” or “Chekalism” on Data Quality: Longitudinal Health Survey of a Sample From Amazon’s Mechanical Turk
  50. How Well Do Seven Self-Report Measures Represent Underlying Back Pain Impact?
  51. Pediatric Inpatient Leaders, Views Changed with COVID-19: A Call to Re-engage in Quality Improvement
  52. Support for Use of Consumer Assessment of Healthcare Providers and Systems Communication Items Among Seriously Ill Patients
  53. Use of Patient Experience Scales Differs by Education and Asian Race/Ethnicity
  54. Shadow Coaching Improves Patient Experience for English-Preferring Patients but not for Spanish-Preferring Patients
  55. Minimally important changes do not always reflect minimally important change; moreover, there is no need for them
  56. 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)
  57. Telephone Outreach Enhances Recruitment of Underrepresented Seriously Ill Patients for an Advance Care Planning Pragmatic Trial
  58. Veteran knowledge, perceptions, and receipt of care following visits to VA emergency departments for ambulatory care sensitive conditions
  59. Current Postlaunch Implementation of State Mandates of Newborn Screening for Critical Congenital Heart Disease by Pulse Oximetry in U.S. States and Hospitals
  60. Vision-related quality of life compared to generic measures in retinoblastoma survivors
  61. Response to: “Criteria for determining if a treatment for pain works”
  62. Correction: Likely change indexes improve estimates of individual change on patient‑reported outcomes
  63. Toxicity Index, patient-reported outcomes, and persistence of breast cancer chemotherapy-associated side effects in NRG Oncology/NSABP B-30
  64. Follow-Up Shadow Coaching Improves Primary Care Provider-Patient Interactions and Maintains Improvements When Conducted Regularly: A Spline Model Analysis
  65. Poor Self-rated Mental Health and Medicare Beneficiaries’ Routine Care-Seeking
  66. A Systematic Review of Strategies to Enhance Response Rates and Representativeness of Patient Experience Surveys
  67. Simulation study comparing analytical methods for single-item longitudinal patient-reported outcomes data
  68. Comparing Data Collected on Amazon's Mechanical Turk to National Surveys
  69. Definitions of Chronic Low Back Pain from a Scoping Review, and Analyses of Narratives and Self-Reported Health of Adults with Low Back Pain
  70. Unpacking the impact of chronic pain as measured by the impact stratification score
  71. Comparison of Simple-Summated Scoring and Toxicity Index Scoring of Symptom Bother in the NSABP B-30 Clinical Trial
  72. Race and Ethnicity Differences in Walking and Associations with Neighborhood Perceptions among Older Adults in California
  73. Likely change indexes improve estimates of individual change on patient-reported outcomes
  74. A Patient Reported Outcome Ontology: Conceptual Issues and Challenges Addressed by the Patient-Reported Outcomes Measurement Information System® (PROMIS®)
  75. Cross-walking the National Institutes of Health Impact Stratification Score to the PEG
  76. Development, methodology, and adaptation of the Medicare Consumer Assessment of Healthcare Providers and Systems (CAHPS®) patient experience survey, 2007–2019
  77. Development and Evaluation of the Clinical Trial HEalth Knowledge and Beliefs Scale (CHEKS)
  78. Experiences of Sleep Problems Among Older Korean Immigrants
  79. Health‐related quality of life outcomes after neoadjuvant chemoradiotherapy for rectal cancer in NRG  Oncology/ NSABP R‐04
  80. Health-Related Quality of Life in Adolescent and Young Adult Retinoblastoma Survivors
  81. 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
  82. Analyses of Cross-Sectional Data to Link the PEG with the Patient Reported Outcomes Measurement and Information System (PROMIS®) Global Physical Health Scale
  83. 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’
  84. Investigating Perceptions of Teachers and School Nurses on Child and Adolescent Oral Health in Los Angeles County
  85. 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
  86. Survival After Severe COVID-19: Long-Term Outcomes of Patients Admitted to an Intensive Care Unit
  87. Health-Related Quality of Life Measurement in Public Health
  88. Perceptions of Teachers and School Nurses on Child and Adolescent Oral Health
  89. 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
  90. Content and Actionability of Recommendations to Providers After Shadow Coaching
  91. 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
  92. 2022 Update to state of the journal of patient-reported outcomes
  93. 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
  94. A Systematic Literature Review of Health-related Quality of Life Measures for Women with Hypoactive Sexual Desire Disorder and Female Sexual Interest/Arousal Disorder
  95. Using a Machine Learning Algorithm to Predict the Likelihood of Presence of Dental Caries among Children Aged 2 to 7
  96. Guidelines for Designing and Evaluating Feasibility Pilot Studies
  97. Assessing the Significance of Individual Change in 2 Samples of Patients in Treatment for Low Back Pain Using 5 Different Statistical Indicators
  98. Toxicity Index, Patient-Reported Outcomes, and Early Discontinuation of Endocrine Therapy for Breast Cancer Risk Reduction in NRG Oncology/NSABP B-35
  99. Patient-Reported Care Coordination is Associated with Better Performance on Clinical Care Measures
  100. Using CAHPS patient experience data for patient-centered medical home transformation
  101. Vision-Targeted Health-Related Quality-of-Life Survey for Evaluating Minimally Invasive Glaucoma Surgery
  102. Practices and changes associated with patient-centered medical home transformation
  103. Longitudinal Associations of PROMIS-29 Anxiety and Depression Symptoms With Low Back Pain Impact in a Sample of U.S. Military Service Members
  104. Methodological and Statistical Considerations for the National Children's Study
  105. Guest Editors’ Introduction to the Invited Special Section
  106. Development and validation of a patient experience of care survey for emergency departments
  107. Shadow Coaching Improves Patient Experience With Care, But Gains Erode Later
  108. Evaluation of PROMIS Preference Scoring System (PROPr) in Patients Undergoing Hemodialysis or Kidney Transplant
  109. Letter to the Editor: What Are the MCIDs for PROMIS, NDI, and ODI Instruments Among Patients With Spinal Conditions?
  110. 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
  111. 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
  112. Measuring Gender Role Conflict, Internalized Stigma, and Racial and Sexual Identity in Behaviorally Bisexual Black Men
  113. Between-group minimally important change versus individual treatment responders
  114. 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
  115. 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
  116. Provider and coach perspectives on implementing shadow coaching to improve provider–patient interactions
  117. Gender Differences in Patients’ Experience of Care in the Emergency Department
  118. Analysis of Movement-Based Mind–Body Interventions to Guide the Implementation of Osteoarthritis Exercise Programs: A Descriptive Review of Randomized Controlled Trials
  119. Estimating Responders to Treatment Using Five Indices of Significant Individual Change
  120. Estimating Responders to Treatment Using Five Indices of Significant Individual Change
  121. Letter to the Editor. Patient self-rated health and rating of their spine surgeon
  122. Consumer Assessment of Healthcare Providers and Systems (CAHPS®) survey of experiences with ambulatory healthcare for Asians and non-Hispanic Whites in the United States
  123. Associations of Self-Reported Sleep Quality with Demographic and Other Characteristics in Older Korean Immigrants
  124. Between Group-Level Minimally Important Change and Individual Treatment Responders
  125. Efficacy of a patient decision aid for improving person-centered decision-making by older adults with obstructive sleep apnea
  126. Estimating Responders to Chiropractic Treatment on The Impact Stratification Score Using Five Indices of Significant Individual Change
  127. State of the Journal of Patient-Reported Outcomes
  128. Adjustment of Patient Experience Surveys for How People Respond
  129. Validation of a Brief Multi‐Dimensional Assessment of Dementia Severity
  130. Overlap of Depressive Symptoms with Health-Related Quality-of-Life Measures
  131. A protocol for chronic pain outcome measurement enhancement by linking PROMIS-29 scale to legacy measures and improving chronic pain stratification
  132. Involving older people with multimorbidity in decision-making about their primary healthcare: A Cochrane systematic review of interventions (abridged)
  133. Some Aspects of Patient Experience Assessed by Practices Undergoing Patient-Centered Medical Home Transformation Are Measured by CAHPS, Others Are Not
  134. Nationwide Qualitative Study of Practice Leader Perspectives on What It Takes to Transform into a Patient-Centered Medical Home
  135. Practice Leaders Report Targeting Several Types of Changes in Care Experienced by Patients During Patient-Centered Medical Home Transformation
  136. Depression Risk and Outcomes Among ASCVD Patients
  137. Psychometric Properties of the Altarum Consumer Engagement (ACE) Measure of Activation in Patients with Prediabetes
  138. Evaluating Treatment Tolerability in Cancer Clinical Trials Using the Toxicity Index
  139. Do the unlabeled response categories of the Minnesota Living with Heart Failure Questionnaire satisfy the monotonicity assumption of simple-summated scoring?
  140. Vascular access-specific health-related quality of life impacts among hemodialysis patients: qualitative development of the hemodialysis access-related quality of life (HARQ) instrument
  141. Evaluation of the Psychometric Properties of the Five Facet of Mindfulness Questionnaire
  142. Computerized adaptive testing and short form development for child and adolescent oral health patient‐reported outcomes measurement
  143. 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”
  144. A Review of Literature on Health-Related Quality of Life of Retinoblastoma Survivors
  145. Associations of Mail Survey Length and Layout With Response Rates
  146. Developing Children’s Oral Health Assessment Toolkits Using Machine Learning Algorithm
  147. Responsiveness of PROMIS® to change in chronic obstructive pulmonary disease
  148. Coping and Management Techniques Used by Chronic Low Back Pain Patients Receiving Treatment From Chiropractors
  149. Development of toolkits for detecting dental caries and caries experience among children using self‐report and parent report
  150. Surgeon Profiles for Intraoperative and Postoperative Use
  151. Population-Based Pragmatic Trial of Advance Care Planning in Primary Care in the University of California Health System
  152. Surgeon Awareness of the Relative Costs of Common Surgical Instruments
  153. Variation in Intraoperative and Postoperative Utilization for 3 Common General Surgery Procedures
  154. Development of a Program Promoting Person‐Centered Care of Older Adults with Sleep Apnea
  155. Differential item functioning of the CAHPS® In-Center Hemodialysis Survey
  156. Researching the Appropriateness of Care in the Complementary and Integrative Health Professions Part 3: Designing Instruments With Patient Input
  157. Experiences With Chiropractic Care for Patients With Low Back or Neck Pain
  158. The effects of survey version on patient experience scores and plan rankings
  159. Differences in Consumer Assessment of Healthcare Providers and Systems Clinician and Group Survey Scores by Recency of the Last Visit
  160. Association of Race with Outcome Expectancy for Positive Airway Pressure Therapy Among Older Veterans with Obstructive Sleep Apnea
  161. Group and Individual-level Change on Health-related Quality of Life in Chiropractic Patients With Chronic Low Back or Neck Pain
  162. PROMIS® Adult Health Profiles: Efficient Short-Form Measures of Seven Health Domains
  163. African American women's perceptions of the meaning of support groups for improving adherence to hypertension treatment: a conceptual model
  164. 0982 Decide2Rest: A Program for Promoting Person-centered Obstructive Sleep Apnea (OSA) Treatment
  165. 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
  166. Expanding the Patient’s Voice in Nephrology with Patient-Reported Outcomes
  167. Measurement Characteristics of the Knowledge Assessment of Renal Transplantation
  168. Development of a parents’ short form survey of their children's oral health
  169. The Social Economics of Adolescent Behavior and Measuring the Behavioral Culture of Schools
  170. The challenge of determining appropriate care in the era of patient-centered care and rising health care costs
  171. Using predicted Spanish preference to target bilingual mailings in a mail survey with telephone follow‐up
  172. Personalized Goal Attainment in Dementia Care: Measuring What Persons with Dementia and Their Caregivers Want
  173. Effect of Mobile Device–Supported Single-Patient Multi-crossover Trials on Treatment of Chronic Musculoskeletal Pain
  174. Hospital quality indicators are not unidimensional: A reanalysis of Lieberthal and Comer
  175. Development and Psychometric Evaluation of a Fatigability Index for Full-Time Wheelchair Users With Spinal Cord Injury
  176. A Composite Measure of Caregiver Burden in Dementia: The Dementia Burden Scale-Caregiver
  177. Associations of CAHPS Composites With Global Ratings of the Doctor Vary by Medicare Beneficiaries’ Health Status
  178. Cross-sectional validation of the PROMIS-Preference scoring system
  179. Characteristics of Chiropractic Patients Being Treated for Chronic Low Back and Neck Pain
  180. Estimation of a Preference-Based Summary Score for the Patient-Reported Outcomes Measurement Information System: The PROMIS®-Preference (PROPr) Scoring System
  181. Preferences of adults with spinal cord injury for widely used health-related quality of life and subjective well-being measures
  182. 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)
  183. Vascular Access-Specific HRQOL Impacts Among Hemodialysis Patients: The Hemodialysis Access-Related QOL (HARQ) Project Focus Group Results
  184. Evaluation of options for presenting health-states from PROMIS® item banks for valuation exercises
  185. Correlation of High Molecular Weight Von Willebrand Factor Multimer loss and Rotational Speed During Short Term Mechanical Circulatory Support
  186. Psychometric Properties of the Kidney Disease Quality of Life 36-Item Short-Form Survey (KDQOL-36) in the United States
  187. PROMIS®-29 v2.0 profile physical and mental health summary scores
  188. Short form development for oral health patient-reported outcome evaluation in children and adolescents
  189. Qualitative methods in the development of a parent survey of children’s oral health status
  190. Quantifying Magnitude of Group-Level Differences in Patient Experiences with Health Care
  191. Commentary: Copyright Restrictions Versus Open Access to Survey Instruments
  192. Development of the Autosomal Dominant Polycystic Kidney Disease Impact Scale: A New Health-Related Quality-of-Life Instrument
  193. Development and evaluation of a measure of patient-reported symptoms of Blepharitis
  194. Patient Experiences with Care Differ with Chronic Care Management in a Federally Qualified Community Health Center
  195. Methodological considerations in using patient reported measures in dialysis clinics
  196. Alternative Approaches to Addressing Non-Normal Distributions in the Application of IRT Models to Personality Measures
  197. Two-item PROMIS® global physical and mental health scales
  198. Differential item functioning by language on the PROMIS® physical functioning items for children and adolescents
  199. Examining colorectal cancer survivors’ surveillance patterns and experiences of care: a SEER-CAHPS study
  200. Functional disability and other health-related quality-of-life domains: points to consider for clinical trials in systemic sclerosis
  201. Selection of key health domains from PROMIS® for a generic preference-based scoring system
  202. A comparison of perceptions of quality of life among adults with spinal cord injury in the United States versus the United Kingdom
  203. Implementation of Practice Transformation: Patient Experience According to Practice Leaders
  204. Using Patient-Reported Measures in Dialysis Clinics
  205. 1240 Non-REM Parasomnias As The Presenting Symptom Of Narcolepsy Without Cataplexy
  206. 1190 OLDER ADULTS’ PREFERENCES FOR OBSTRUCTIVE SLEEP APNEA TREATMENT ELICITED FROM A PILOT DISCRETE CHOICE EXPERIMENT
  207. Depressive symptomatology and fall risk among community-dwelling older adults
  208. Receipt of Caregiving and Fall Risk in US Community-dwelling Older Adults
  209. Associations of Health-Related Quality of Life with Overall Quality of Life in the Patient Reported Outcomes Measurement Information System (PROMIS®) Project
  210. Patient-Reported Usability of Positive Airway Pressure Equipment Is Associated With Adherence in Older Adults
  211. Responsiveness to Change and Minimally Important Differences of the Patient-Reported Outcomes Measurement Information System Gastrointestinal Symptoms Scales
  212. Differential item functioning of the patient-reported outcomes information system (PROMIS®) pain interference item bank by language (Spanish versus English)
  213. Colorectal cancer survivors’ surveillance patterns and experiences of care: A SEER-CAHPS study.
  214. Assessment of the Psychometric Properties of a Questionnaire Assessing Patient-Reported Outcomes With Laser In Situ Keratomileusis (PROWL)
  215. Implementation and Sequencing of Practice Transformation in Urban Practices with Underserved Patients
  216. Symptoms and Satisfaction of Patients in the Patient-Reported Outcomes With Laser In Situ Keratomileusis (PROWL) Studies
  217. Patient and caregiver goals for dementia care
  218. Gastrointestinal symptom severity in irritable bowel syndrome, inflammatory bowel disease and the general population
  219. Perceived Effectiveness, Self-efficacy, and Social Support for Oral Appliance Therapy Among Older Veterans With Obstructive Sleep Apnea
  220. Development of a high-value care culture survey: a modified Delphi process and psychometric evaluation
  221. Responsiveness of 8 Patient-Reported Outcomes Measurement Information System (PROMIS) measures in a large, community-based cancer study cohort
  222. Patient-Reported oral health outcome measurement for children and adolescents
  223. Readability and Comprehension of the Geriatric Depression Scale and PROMIS® Physical Function Items in Older African Americans and Latinos
  224. The Costs of Fall-Related Injuries among Older Adults: Annual Per-Faller, Service Component, and Patient Out-of-Pocket Costs
  225. Change in Health-Related Quality-of-Life at Group and Individual Levels Over Time in Patients Treated for Chronic Myofascial Neck Pain
  226. Measurement equivalence of the Consumer Assessment of Healthcare Providers and Systems (CAHPS®) Medicare survey items between Whites and Asians
  227. Racial/Ethnic Disparities in Medicare Beneficiaries’ Care Coordination Experiences
  228. The challenge of measuring intra-individual change in fatigue during cancer treatment
  229. Claims-based Identification Methods and the Cost of Fall-related Injuries Among US Older Adults
  230. Orientation to the Caregiver Role Among Latinas of Mexican Origin
  231. Patient-Provider Communication With Older Adults About Sleep Apnea Diagnosis and Treatment
  232. Validity of PROMIS physical function measured in diverse clinical samples
  233. Using Linear Equating to Map PROMIS® Global Health Items and the PROMIS-29 V2.0 Profile Measure to the Health Utilities Index Mark 3
  234. Development and psychometric evaluation of a health-related quality of life instrument for individuals with adult-onset hearing loss
  235. Cancer registry-survey data linkages to measure patient-centered quality of care: SEER-MHOS and SEER-CAHPS.
  236. Measurement equivalence of the Consumer Assessment of Healthcare Providers and Systems (CAHPS) Medicare survey items between non-Hispanic whites and Asians.
  237. Best (but oft-forgotten) practices: expressing and interpreting associations and effect sizes in clinical outcome assessments
  238. Performance of the Medicare Consumer Assessment of Health Care Providers and Systems (CAHPS) Physical Functioning Items
  239. Less Use of Extreme Response Options by Asians to Standardized Care Scenarios May Explain Some Racial/Ethnic Differences in CAHPS Scores
  240. Possibilities for Shortening the CAHPS Clinician and Group Survey
  241. The Facilitators of and Barriers to Adherence to Hypertension Treatment Scale
  242. Scoring the SF-36 in Orthopaedics: A Brief Guide
  243. Confirmatory Factor Analysis of the Patient Reported Outcomes Measurement Information System (PROMIS) Adult Domain Framework Using Item Response Theory Scores
  244. The PROMIS of QALYs
  245. Case Study of an Unsustainable Community-Academic Partnership: Toward Core Standards for the Structure of Emerging Participatory Research
  246. Linking Physical and Mental Health Summary Scores from the Veterans RAND 12-Item Health Survey (VR-12) to the PROMIS® Global Health Scale
  247. Use of Internet panels to conduct surveys
  248. Use of CAHPS® patient experience survey data as part of a patient-centered medical home quality improvement initiative
  249. Reliability and construct validity of PROMIS® measures for patients with heart failure who undergo heart transplant
  250. Child and adolescent perceptions of oral health over the life course
  251. Development of the Usability of Sleep Apnea Equipment – Positive Airway Pressure (USE-PAP) questionnaire
  252. 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
  253. U.S. General Population Estimate for “Excellent” to “Poor” Self-Rated Health Item
  254. Corrigendum: Development of the NIH Patient-Reported Outcomes Measurement Information System (PROMIS) Gastrointestinal Symptom Scales
  255. The PREEMPT study - evaluating smartphone-assisted n-of-1 trials in patients with chronic pain: study protocol for a randomized controlled trial
  256. Unveiling SEER-CAHPS®: A New Data Resource for Quality of Care Research
  257. Methodological Considerations When Studying the Association between Patient-Reported Care Experiences and Mortality
  258. US Valuation of Health Outcomes Measured Using the PROMIS-29
  259. Should Health Care Providers be Accountable for Patients’ Care Experiences?
  260. Health-related quality of life in older adult survivors of selected cancers: Data from the SEER-MHOS linkage
  261. Development and Evaluation of the CAHPS (Consumer Assessment of Healthcare Providers and Systems) Survey for In-Center Hemodialysis Patients
  262. Development of the NIH Patient-Reported Outcomes Measurement Information System (PROMIS) Gastrointestinal Symptom Scales
  263. Construct Validity of the Patient-Reported Outcomes Measurement Information System Gastrointestinal Symptom Scales in Systemic Sclerosis
  264. Correlation of PROMIS scales and clinical measures among chronic obstructive pulmonary disease patients with and without exacerbations
  265. A Randomized Controlled Pilot Trial of the Functional Assessment Screening Tablet to Engage Patients at the Point of Care
  266. Post-traumatic stress symptoms in cancer survivors: relationship to the impact of cancer scale and other associated risk factors
  267. Development and Evaluation of a Measure to Assess Restorative Sleep
  268. Examining the Role of Patient Experience Surveys in Measuring Health Care Quality
  269. FRI0223 Development and Validation of Patient-Reported Outcomes Measurement Information System (PROMIS®) Gastrointestinal (GI) Symptom Scales in Systemic Sclerosis
  270. 113 * EXAMINING MODELS OF SPECIALIST HEALTHCARE SUPPORT TO CARE HOMES
  271. Evaluation of the Consumer Assessment of Healthcare Providers and Systems In-Center Hemodialysis Survey
  272. GERD Symptoms in the General Population: Prevalence and Severity Versus Care-Seeking Patients
  273. Evaluating the Psychometric Properties of the CAHPS Patient-Centered Medical Home Survey
  274. Overview of Classical Test Theory and Item Response Theory for the Quantitative Assessment of Items in Developing Patient-Reported Outcomes Measures
  275. Demographic Differences in Health Preferences in the United States
  276. Improving Diabetes Health Literacy by Animation
  277. Depressed or Not Depressed: Untangling Symptoms of Depression in Patients Hospitalized With Coronary Heart Disease
  278. Development of a Preference-Based Index From the National Eye Institute Visual Function Questionnaire–25
  279. Should Linking Replace Regression When Mapping from Profile-Based Measures to Preference-Based Measures?
  280. Development of an Online Library of Patient-Reported Outcome Measures in Gastroenterology: The GI-PRO Database
  281. Comparison of US Panel Vendors for Online Surveys
  282. Evaluation of a Care Coordination Measure for the Consumer Assessment of Healthcare Providers and Systems (CAHPS®) Medicare Survey
  283. Upper-Extremity and Mobility Subdomains From the Patient-Reported Outcomes Measurement Information System (PROMIS) Adult Physical Functioning Item Bank
  284. Specialties Differ in Which Aspects of Doctor Communication Predict Overall Physician Ratings
  285. 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
  286. Use of imaging and biomarker tests for posttreatment care of early‐stage breast cancer survivors
  287. Associations of cancer and other chronic medical conditions with SF-6D preference-based scores in Medicare beneficiaries
  288. Don’t middle your MIDs: regression to the mean shrinks estimates of minimally important differences
  289. 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
  290. Validity of Temporal Measures as Proxies for Measuring Acculturation in Asian Indian Survey Respondents
  291. Psychometric analyses of patient-reported outcome instruments for autosomal dominant polycystic kidney disease
  292. Introduction to patient-reported outcome item banks: issues in minority aging research
  293. Norming plans for the NIH Toolbox
  294. Vision assessment using the NIH Toolbox
  295. Development of a vision-targeted health-related quality of life item measure
  296. ISOQOL recommends minimum standards for patient-reported outcome measures used in patient-centered outcomes and comparative effectiveness research
  297. Associations of Sleep Disturbance Symptoms With Health-Related Quality of Life in Parkinson’s Disease
  298. Depression Screening: Utility of the Patient Health Questionnaire in Patients With Acute Coronary Syndrome
  299. Evaluation of the Patient-Reported Outcomes Information System (PROMIS®) Spanish-language physical functioning items
  300. Racial/Ethnic Disparities in Medicare Part D Experiences
  301. Can Hospital Cultural Competency Reduce Disparities in Patient Experiences With Care?
  302. A Field Experiment on the Impact of Physician-level Performance Data on Consumers’ Choice of Physician
  303. Adapting the PRO-CTCAE for Patient Reporting of Toxicity in Radiation Oncology
  304. Introduction
  305. Development and Evaluation of CAHPS Questions to Assess the Impact of Health Information Technology on Patient Experiences With Ambulatory Care
  306. Development of and Field Test Results for the CAHPS PCMH Survey
  307. Differences in CAHPS Reports and Ratings of Health Care Provided to Adults and Children
  308. Psychometric Properties of the Consumer Assessment of Healthcare Providers and Systems (CAHPS®) Clinician and Group Adult Visit Survey
  309. The Authors Respond
  310. Health-related quality of life in patients with interstitial cystitis/bladder pain syndrome and frequently associated comorbidities
  311. The Consumer Assessment of Healthcare Providers and Systems (CAHPS) Cultural Competence (CC) Item Set
  312. Evaluating Measurement Equivalence Across Race and Ethnicity on the CAHPS Cultural Competence Survey
  313. Moving towards culturally competent health systems: Organizational and market factors
  314. Development and Evaluation of CAHPS® Survey Items Assessing How Well Healthcare Providers Address Health Literacy
  315. Development of Items to Assess Patients’ Health Literacy Experiences at Hospitals for the Consumer Assessment of Healthcare Providers and Systems (CAHPS) Hospital Survey
  316. How Much Is Lost in Using Single Items?
  317. US general population norms for telephone administration of the SF-36v2
  318. A Randomized Controlled Study to Evaluate the Efficacy of Noninvasive Limb Cover for Chronic Phantom Limb Pain Among Veteran Amputees
  319. Development of a Prognostic Model for Six-Month Mortality in Older Adults With Declining Health
  320. Development of a Prognostic Model for 6-month Mortality in Older Adults With Declining Health (316-A)
  321. Cultural competency assessment tool for hospitals
  322. Are hot flashes associated with sleep disturbance during midlife? Results from the STRIDE cohort study
  323. Confirmatory Factor Analysis of the Motor Unified Parkinson’s Disease Rating Scale
  324. Feasibility and Construct Validity of PROMIS and “Legacy” Instruments in an Academic Scleroderma Clinic
  325. Advancing PROMIS’s methodology: results of the Third Patient-Reported Outcomes Measurement Information System (PROMIS®) Psychometric Summit
  326. Gender Differences in Multiple Underlying Dimensions of Health-related Quality of Life Are Associated with Sociodemographic and Socioeconomic Status
  327. The future of measuring patient-reported outcomes in rheumatology: Patient-Reported Outcomes Measurement Information System (PROMIS)
  328. Agreement about Identifying Patients Who Change over Time
  329. Content validity of patient-reported outcome measures: perspectives from a PROMIS meeting
  330. The Impact of a Filariasis Control Program on Lihir Island, Papua New Guinea
  331. Rasch analysis in the development of a simplified version of the national eye institute visual-function questionnaire-25 for utility estimation
  332. Asthma outcome measures
  333. Depression and the Health Care Experiences of Medicare Beneficiaries
  334. The impact of menopause on health-related quality of life: results from the STRIDE longitudinal study
  335. Minimally Important Differences of the UCLA Scleroderma Clinical Trial Consortium Gastrointestinal Tract Instrument
  336. Patient education integrated with acupuncture for relief of cancer-related fatigue randomized controlled feasibility study
  337. 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.
  338. Using the Nominal Response Model to Evaluate Response Category Discrimination in the PROMIS Emotional Distress Item Pools
  339. Differential Item Functioning by Survey Language Among Older Hispanics Enrolled in Medicare Managed Care
  340. Five preference-based indexes in cataract and heart failure patients were not equally responsive to change
  341. Interpreting patient-reported outcome results: US FDA guidance and emerging methods
  342. Assessment of Quality of Cancer-Related Follow-Up Care From the Cancer Survivor's Perspective
  343. Health-related quality of life: The impact of diagnostic angiography
  344. Clinical correlates of health-related quality of life among opioid-dependent patients
  345. Prevalence and correlates of sleep disturbance in systemic sclerosis--results from the UCLA scleroderma quality of life study
  346. Health-related quality of life in adults reporting arthritis: analysis from the National Health Measurement Study
  347. Medical Student Attitudes toward Complementary, Alternative and Integrative Medicine
  348. Diagnostic accuracy and agreement across three depression assessment measures for Parkinson’s disease
  349. Medication Responsiveness of Motor Symptoms in a Population-Based Study of Parkinson Disease
  350. 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)
  351. Representativeness of the Patient-Reported Outcomes Measurement Information System Internet panel
  352. The Patient-Reported Outcomes Measurement Information System (PROMIS) developed and tested its first wave of adult self-reported health outcome item banks: 2005–2008
  353. Development of a culturally appropriate health-related quality of life measure for human immunodeficiency virus-infected children in Thailand
  354. Longitudinal Changes in Visual Acuity and Health-related Quality of Life
  355. Association of gastrointestinal involvement and depressive symptoms in patients with systemic sclerosis
  356. Differences in Child versus Parent Reports of the Child's Health-Related Quality of Life in Children with Epilepsy and Healthy Siblings
  357. 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
  358. A Comparison of Two Educational Methods on Immigrant Latinas Breast Cancer Knowledge and Screening Behaviors
  359. Quality indicators for multiple sclerosis
  360. The impact of next and back buttons on time to complete and measurement reliability in computer-based surveys
  361. Health state preferences are equivalent in the United States and Trinidad and Tobago
  362. Valuation of scleroderma and psoriatic arthritis health states by the general public
  363. Efficiency of static and computer adaptive short forms compared to full-length measures of depressive symptoms
  364. Associations of Eye Diseases and Symptoms with Self-Reported Physical and Mental Health
  365. Development of a New Patient-Based Measure of Pediatric Ambulatory Care
  366. Reliability and validity of the university of california, los angeles scleroderma clinical trial consortium gastrointestinal tract instrument
  367. Effects of Mode and Order of Administration on Generic Health-Related Quality of Life Scores
  368. 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
  369. Readability estimates for commonly used health-related quality of life surveys
  370. Health-Related Quality of Life Predicts Mortality in Patients With Advanced Chronic Liver Disease
  371. Development and preliminary evaluation of a quality of life measure targeted at dementia caregivers
  372. Development of physical and mental health summary scores from the patient-reported outcomes measurement information system (PROMIS) global items
  373. Impact of Cancer on Health-Related Quality of Life of Older Americans
  374. 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
  375. 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
  376. PMC69 MULTITRAIT-MULTIMETHOD ANALYSIS OF THREE GENERIC PREFERENCE-BASED HEALTH-RELATED QUALITY OF LIFE MEASURES IN THE NATIONAL HEALTH MEASUREMENT STUDY
  377. Adjusting for Subgroup Differences in Extreme Response Tendency in Ratings of Health Care: Impact on Disparity Estimates
  378. Expectations prior to epilepsy surgery: An exploratory comparison of men and women
  379. Evidence-based effect size estimation:An illustration using the case of acupuncture for cancer-related fatigue
  380. A Randomized Study of Scleroderma Health State Values: A Picture Is Worth a Thousand Words, and Quite a Few Utilities
  381. Work hour restrictions and internal medicine residents’ health-related quality of life
  382. Can Additional Patient Experience Items Improve the Reliability of and Add New Domains to the CAHPS®Hospital Survey?
  383. The Minimally Important Difference for the Fatigue Visual Analog Scale in Patients with Rheumatoid Arthritis Followed in an Academic Clinical Practice
  384. Prospective validation of the short form liver disease quality of life instrument
  385. Development of a fatigue and functional impact scale in anemic cancer patients receiving chemotherapy
  386. Survey Response Style and Differential Use of CAHPS Rating Scales by Hispanics
  387. Prospects and challenges in using patient-reported outcomes in clinical practice
  388. Self‐Reported Health Status of Vietnamese and Non‐Hispanic White Older Adults in California
  389. Access to Care for Youth with Special Health Care Needs in the Transition to Adulthood
  390. Bridging From the Picker Hospital Survey to the CAHPS® Hospital Survey
  391. Case Management and Health-Related Quality of Life Outcomes in a National Sample of Persons with HIV/AIDS
  392. Development and Psychometric Assessment of a Multidimensional Measure of Internalized HIV Stigma in a Sample of HIV-positive Adults
  393. Evaluating the SF-36 Health Survey (Version 2) in Older Vietnamese Americans
  394. Language and Regional Differences in Evaluations of Medicare Managed Care by Hispanics
  395. Recommended methods for determining responsiveness and minimally important differences for patient-reported outcomes
  396. How Do Proxy Responses and Proxy-Assisted Responses Differ from What Medicare Beneficiaries Might Have Reported about Their Health Care?
  397. Reports and Ratings of Care: Black and White Medicare Enrollees
  398. Adherence treatment factors in hypertensive African American women
  399. Evaluating Differential Item Functioning of the PRIME-MD Mood Module Among Impoverished Black and White Women in Primary Care
  400. 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
  401. Mode of Administration Is Important in US National Estimates of Health-Related Quality of Life
  402. US Norms for Six Generic Health-Related Quality-of-Life Indexes From the National Health Measurement Study
  403. Ethnic Variations in Dementia Caregiving Experiences
  404. Developing a Spanish-language Consumer Report for CAHPS® Health Plan Surveys
  405. What Is Sufficient Evidence for the Reliability and Validity of Patient-Reported Outcome Measures?
  406. Development of a preliminary scleroderma gastrointestinal tract 1.0 quality of life instrument
  407. Design and Evaluation of Fiber Tip Lenses for Fiber Optic Transmitter and Receiver Applications
  408. Precision of Health-Related Quality-of-Life Data Compared With Other Clinical Measures
  409. Correlated physical and mental health summary scores for the SF-36 and SF-12 Health Survey, V.1
  410. A comparison of three sets of criteria for determining the presence of differential item functioning using ordinal logistic regression
  411. Severity of Visual Field Loss and Health-related Quality of Life
  412. Applying item response theory to enhance health outcomes assessment
  413. The role of the bifactor model in resolving dimensionality issues in health outcomes measures
  414. Item Response Theory Analyses of Physical Functioning Items in the Medical Outcomes Study
  415. Psychometric Evaluation and Calibration of Health-Related Quality of Life Item Banks
  416. The Impact of HIV on Oral Health and Subsequent Use of Dental Services
  417. Reliability, validity, and minimally important differences of the SF-6D in systemic sclerosis
  418. IRT health outcomes data analysis project: an overview and summary
  419. Next steps for use of item response theory in the assessment of health outcomes
  420. Does Ambulatory Process of Care Predict Health-Related Quality of Life Outcomes for Patients with Chronic Disease?
  421. A Randomized Controlled Trial of Tai Chi for Tension Headaches
  422. HEALTH STATUS OF VIETNAMESE ELDERS COMPARED WITH NON-HISPANIC WHITES IN CALIFORNIA.
  423. Repeated measures analyses of dose timing of antiretroviral medication and its relationship to HIV virologic outcomes
  424. The SF-36 physical and mental health factors were confirmed in cancer and HIV/AIDS patients
  425. Physician Communication About the Cost and Acquisition of Newly Prescribed Medications
  426. A Practical Method to Calibrate Self-Reported Adherence to Antiretroviral Therapy
  427. A Comprehensive Evaluation of Survey Questions for Adherence to Antiretroviral Medications and Exploratory Analyses for Identifying Optimal Sets of Survey Questions
  428. Classical Test Theory and Item Response Theory Analyses of Multi-Item Scales Assessing Parents?? Perceptions of Their Children??s Dental Care
  429. Correction: Patients' Global Ratings of Their Health Care Are Not Associated with the Technical Quality of Their Care
  430. Impact of Severity and Bilaterality of Visual Impairment on Health-Related Quality of Life
  431. Comparison of Data Quality for Reports and Ratings of Ambulatory Care by African American and White Medicare Managed Care Enrollees
  432. Responsiveness and minimal important differences for patient reported outcomes
  433. Physician Communication When Prescribing New Medications
  434. Mitochondrial membrane depolarization in Drosophila apoptosis
  435. Changes in symptoms and health-related quality of life in a nationally representative sample of adults in treatment for HIV
  436. Psychometric Performance of the National Eye Institute Visual Function Questionnaire in Latinos and Non-Latinos
  437. Linguistic disparities in health care access and health status among older adults
  438. A Pilot Study of Health Beliefs and Attitudes Concerning Measures of Antiretroviral Adherence Among Prisoners Receiving Directly Observed Antiretroviral Therapy
  439. Variations in provider conceptions of integrative medicine
  440. Patients' Global Ratings of Their Health Care Are Not Associated with the Technical Quality of Their Care
  441. A test of knowledge about prostate cancer screening
  442. Health-related quality of life and patient reports about care outcomes in a multidisciplinary hospital intervention
  443. Minimally important difference in diffuse systemic sclerosis: results from the D-penicillamine study
  444. Application of Group-Level Item Response Models in the Evaluation of Consumer Reports About Health Plan Quality
  445. Repeated Measures Longitudinal Analyses of HIV Virologic Response as a Function of Percent Adherence, Dose Timing, Genotypic Sensitivity, and Other Factors
  446. The Effect of a Multidisciplinary Hospitalist/Physician and Advanced Practice Nurse Collaboration on Hospital Costs
  447. International Prevalence, Recognition, and Treatment of Cardiovascular Risk Factors in Outpatients With Atherothrombosis
  448. An Alternative Approach to Reducing the Costs of Patient Care? A Controlled Trial of the Multi-Disciplinary Doctor-Nurse Practitioner (MDNP) Model
  449. Variation in the Readability of Items Within Surveys
  450. Comparison of Mail and Telephone in Assessing Patient Experiences in Receiving Care from Medical Group Practices
  451. Clinical significance of patient-reported questionnaire data: another step toward consensus
  452. Assessment of the Equivalence of the Spanish and English Versions of the CAHPS® Hospital Survey on the Quality of Inpatient Care
  453. Development and Evaluation of the CAHPS® Hospital Survey
  454. Equivalence of Mail and Telephone Responses to the CAHPS® Hospital Survey
  455. Exploratory Factor Analyses of the CAHPS® Hospital Pilot Survey Responses across and within Medical, Surgical, and Obstetric Services
  456. Methods Used to Streamline the CAHPS® Hospital Survey
  457. Patterns of Unit and Item Nonresponse in the CAHPS® Hospital Survey
  458. Review of the Literature on Survey Instruments Used to Collect Data on Hospital Patients' Perceptions of Care
  459. Do Medicaid and Commercial CAHPS Scores Correlate Within Plans?
  460. Application of Structural Equation Modeling to Health Outcomes Research
  461. Impact of Chronic Viral Hepatitis on Health-Related Quality of Life in HIV: Results from a Nationally Representative Sample
  462. A Self-Report Measure of Clinicians' Orientation toward Integrative Medicine
  463. Evaluating the Statistical Significance of Health-Related Quality-Of-Life Change in Individual Patients
  464. 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
  465. Imputation of SF-12 Health Scores for Respondents with Partially Missing Data
  466. Development of the 12-Item Expectations Regarding Aging Survey
  467. Impact of hepatitis C on health related quality of life: A systematic review and quantitative assessment
  468. Patients' Preferences for Technical versus Interpersonal Quality When Selecting a Primary Care Physician
  469. Effects of Testosterone Replacement in Human Immunodeficiency Virus-Infected Women with Weight Loss
  470. Estimating clinically significant differences in quality of life outcomes
  471. Effect of a Multidisciplinary Intervention on Communication and Collaboration Among Physicians and Nurses
  472. Psychometric properties of the Medical Outcomes Study Sleep measure
  473. The Effect of Socioeconomic Status on the Survival of People Receiving Care for HIV Infection in the United States
  474. The association of health-related quality of life with survival among persons with HIV infection in the united states
  475. Racial Differences in the Impact of Irritable Bowel Syndrome on Health-Related Quality of Life
  476. Are Physician-Derived Disease Severity Indices Associated with Health-Related Quality of Life in Patients with End-Stage Liver Disease?
  477. Physician Recognition of Cognitive Impairment: Evaluating the Need for Improvement
  478. Opposing inputs by Hedgehog and Brinker define a stripe ofhairyexpression in theDrosophilaleg imaginal disc
  479. 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
  480. Delays and Unmet Need for Health Care Among Adult Primary Care Patients in a Restructured Urban Public Health System
  481. Racial and ethnic differences in patients' preferences for initial care by specialists
  482. No Evidence of an Association between Transient HIV Viremia (“Blips”) and Lower Adherence to the Antiretroviral Medication Regimen
  483. Racial differences in health-related quality of life among hemodialysis patients
  484. How Many Patients Are Needed to Provide Reliable Evaluations of Individual Clinicians?
  485. Health plan effects on patient assessments of medicaid managed care among racial/ethnic minorities
  486. Methodological Challenges Associated with Patient Responses to Follow-up Longitudinal Surveys Regarding Quality of Care
  487. Psychometric Properties of the Consumer Assessment of Health Plans Study (CAHPS®) 2.0 Adult Core Survey
  488. Psychometric properties of the National Eye Institute–Refractive Error Quality of Life instrument
  489. Responsiveness of the National Eye Institute Refractive Error Quality of Life instrument to surgical correction of refractive error
  490. Associations of Presbyopia With Vision-Targeted Health-Related Quality of Life
  491. Reply
  492. Patient Reports and Ratings of Individual Physicians: An Evaluation of the DoctorGuide and Consumer Assessment of Health Plans Study Provider-Level Surveys
  493. Patterns of Coping Among Persons with HIV Infection: Configurations, Correlates, and Change
  494. Psychometric Properties of the Spanish Consumer Assessment of Health Plans Survey (CAHPS)
  495. Bias in Assessment of Health-Related Quality of Life in a Hemodialysis Population
  496. Race/Ethnicity, Language, and Patients' Assessments of Care in Medicaid Managed Care
  497. The Diverse Older HIV-Positive Population
  498. The Tripartite Model of Anxiety and Depression: Symptom Structure in Depressive and Hypertensive Patient Groups
  499. Knowledge of Antiretroviral Regimen Dosing and Adherence: A Longitudinal Study
  500. Correlates of Social Function: A Comparison of a Black and a White Sample of Older Persons in Los Angeles
  501. A guide for clinicians to compare the accuracy and precision of health-related quality-of-life data relative to other clinical measures
  502. Assessing the clinical significance of patient-reported outcomes: Examples drawn from a recent meeting of the drug information association (DIA)
  503. HIV Patients’ Experiences With Inpatient and Outpatient Care
  504. Health-related quality of life, depressive symptoms, anemia, and malnutrition at hemodialysis initiation
  505. Remembering a Life
  506. Use of the SF-36 and other health-related quality of life measures to assess persons with disabilities
  507. Do Older Adults Expect to Age Successfully? The Association Between Expectations Regarding Aging and Beliefs Regarding Healthcare Seeking Among Older Adults
  508. A prospective study of predictors of adherence to combination antiretroviral medication
  509. The Alcohol‐Related Problems Survey: Identifying Hazardous and Harmful Drinking in Older Primary Care Patients
  510. Patient preferences regarding antiretroviral therapy
  511. Effect of CAHPS Performance Information on Health Plan Choices by Iowa Medicaid Beneficiaries
  512. Development, Reliability, and Validity of the Expectations Regarding Aging (ERA-38) Survey
  513. Effects of CAHPS Health Plan Performance Information on Plan Choices by New Jersey Medicaid Beneficiaries
  514. Seizure Reduction and Quality of Life Improvements in People with Epilepsy
  515. Beyond alcoholism: identifying older, at-risk drinkers in primary care.
  516. Comparing the alcohol-related problems survey (ARPS) to traditional alcohol screening measures in elderly outpatients
  517. Patients Using Chiropractors in North America
  518. How well do clinicians estimate patients’ adherence to combination antiretroviral therapy?
  519. Patient, clinician, and population perspectives on determining the clinical significance of quality-of-life scores
  520. Similar Effectiveness of Paroxetine, Fluoxetine, and Sertraline in Primary Care
  521. Factors related to agreement between self-reported and conventional Expanded Disability Status Scale (EDSS) scores
  522. IMPROVEMENT IN EMOTIONAL WELL-BEING AND RELATIONSHIPS OF USERS OF SILDENAFIL
  523. QL3: PSYCHOMETRIC PERFORMANCE OF THE MEDICAL OUTCOMES STUDY SLEEP SCALE IN THE US GENERAL POPULATION
  524. Expectations Regarding Aging Among Older Adults and Physicians Who Care for Older Adults
  525. Development of the 25-list-item National Eye Institute Visual Function Questionnaire
  526. Responsiveness of the smoking cessation quality of life (SCQoL) questionnaire
  527. A Comparison Study of Multiple Measures of Adherence to HIV Protease Inhibitors
  528. Associations of Symptoms and Health-Related Quality of Life: Findings from a National Study of Persons with HIV Infection
  529. Does physician gender affect satisfaction of men and women visiting the emergency department?
  530. Racial differences in the impact of irritable bowel syndrome (IBS) on health-related quality of life (HRQOL)
  531. IN RE ALCOHOL USE IN OLDER ADULTS
  532. The RAND-36 measure of health-related quality of life
  533. A Review of Health-Related Quality-of-Life Measures in Stroke
  534. COMPARISON OF THE ROST AND THE CAGE ALCOHOL SCREENING INSTRUMENTS IN YOUNG ADULTS
  535. Medical Care
  536. USING DATA TO ENHANCE THE EXPERT PANEL PROCESS
  537. Confirmatory factor analysis of the Consumer Assessment of Health Plans Study (CAHPS) 1.0 core survey.
  538. Electroacupuncture for Control of Myeloablative Chemotherapy–Induced Emesis
  539. Identifying a Short Functional Disability Screen for Older Persons
  540. Physical and Role Functioning Among Persons With HIV
  541. The Concept of Clinically Meaningful Difference in Health-Related Quality of Life Research
  542. Development of subscales from the symptoms/problems and effects of kidney disease scales of the kidney disease quality of life instrument
  543. Item Response Theory and Health Outcomes Measurement in the 21st Century
  544. The impact of irritable bowel syndrome on health-related quality of life
  545. Effects of Incentive Size and Timing on Response Rates to a Follow-Up Wave of a Longitudinal Mailed Survey
  546. Coping, Conflictual Social Interactions, Social Support, and Mood Among HIV-Infected Persons
  547. Review: The Newspaper Indian: Native American Identity in the Press, 1820-90, by John Coward
  548. Self-Study from Web-Based and Printed Guideline Materials
  549. Access to Medical Care Reported by Asians and Pacific Islanders in a West Coast Physician Group Association
  550. Development of a Health-Related Quality of Life Measure for Peripheral Neuropathy
  551. 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
  552. Using a criterion standard to validate the Alcohol-Related Problems Survey (ARPS): A screening measure to identify harmful and hazardous drinking in older persons
  553. Quality of life measures in epilepsy: How well can they detect change over time?
  554. Evaluating the Equivalence of Health Care Ratings by Whites and Hispanics
  555. Testosterone Replacement and Resistance Exercise in HIV-Infected Men With Weight Loss and Low Testosterone Levels
  556. Impact of Psychiatric Conditions on Health-Related Quality of Life in Persons With HIV Infection
  557. A Comparative Review of Generic Quality-of-Life Instruments
  558. Ethnic and Racial Differences in Long-Term Survival From Hospitalization for HIV Infection
  559. Health Status Measurement Performance and Health Status Differences by Age, Ethnicity, and Gender: Assessment in the Medical Outcomes Study
  560. The Role of Peer-Reviewed Journals in Science
  561. Development of the Smoking Cessation quality of life questionnaire
  562. Are latinos less satisfied with communication by health care providers?
  563. The influence of gatekeeping and utilization review on patient satisfaction
  564. Drinking Habits Among Older Persons: Findings from the NHANES I Epidemiologic Follow-up Study (1982-84)
  565. Review: Fly a Cell!
  566. Psychometric Properties of the CAHPS™ 1.0 Survey Measures
  567. Special Issues Addressed in the CAHPS™ Survey of Medicare Managed Care Beneficiaries
  568. Special Issues in Assessing Care of Medicaid Recipients
  569. A New Paradigm for Alcohol Use in Older Persons
  570. Associations of clinical parameters with health-related quality of life in hospitalized persons with HIV disease
  571. 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
  572. Psychometric Properties of the National Eye Institute Visual Function Questionnaire (NEI-VFQ)
  573. Effects of Testosterone Replacement with a Nongenital, Transdermal System, Androderm, in Human Immunodeficiency Virus-Infected Men with Low Testosterone Levels
  574. A COMPARISON OF SELF-REPORTED UTILIZATION OF OPHTHALMIC CARE FOR DIABETES IN MANAGED CARE VERSUS FEE-FORSERVICE
  575. The UCLA Prostate Cancer Index
  576. Member Ratings of Health Care Provided by 48 Physician Groups
  577. Does Dissatisfaction with Access to Specialists Affect the Desire to Leave a Managed Care Plan?
  578. Reliability of an Arabic Version of the RAND-36 Health Survey and its Equivalence to the US-English Version
  579. The Prospective Effect of Access to Medical Care on Health-Related Quality-of-Life Outcomes in Patients with Symptomatic HIV Disease
  580. Constitutional Symptoms and Health-Related Quality of Life in Patients with Symptomatic HIV Disease
  581. The Dose-Response Relation of Intrathecal Fentanyl for Labor Analgesia 
  582. The Structure of Satisfaction with Pharmacy Services
  583. Debating Survey Approaches
  584. 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
  585. Euphausiids as intermediate hosts of <i>Anisakis simplex</i> in the St. Lawrence estuary
  586. It Performance Turnaround: The Outsourcing Alternative
  587. Adjusting for Attrition in School-Based Samples
  588. Primary care physicians' satisfaction with quality of care in California capitated medical groups
  589. Assessing health and quality of life outcomes in dialysis: A report on an institute of medicine workshop
  590. Reliability and Validity of Self-Report CD4 Counts in Persons Hospitalized with HIV Disease
  591. Comparison of a generic to disease-targeted health-related quality-of-life measures for multiple sclerosis
  592. A Randomized Trial of Office-Based Screening for Common Problems in Older Persons
  593. The Impact of Blurred Vision on Functioning and Well-being
  594. Sedation and analgesia for colonoscopy: patient tolerance, pain, and cardiorespiratory parameters
  595. Understanding Changes in Health Status
  596. Access to Community-Based Medical Services and Number of Hospitalizations Among Patients with HIV Disease: Are They Related?
  597. Quality assurance in capitated physician groups. Where is the emphasis?
  598. A comparison of health-related quality of life in patients with epilepsy, diabetes and multiple sclerosis
  599. Teenagers and alcohol misuse in the United States: by any definition, it's a big problem
  600. A review of health-related quality-of-life measures used in end-stage renal disease
  601. Long-term Care Residents' Preferences for Health States on the Quality of Well-Being Scale
  602. Alcohol-related problems in older persons. Determinants, consequences, and screening
  603. Associations between drug use and deviant behavior in teenagers
  604. WHAT IS ADOLESCENT ALCOHOL MISUSE IN THE UNITED STATES ACCORDING TO THE EXPERTS?
  605. Physician implementation of and patient adherence to recommendations from comprehensive geriatric assessment
  606. Medical education and health for all
  607. Bedside charting of pain levels in hospitalized patients with cancer: A randomized controlled trial
  608. Preferential targeting of oxidative base damage to interucleosomal DNA
  609. Outcomes in 248 patients who had diagnostic evaluations for epilepsy surgery
  610. Development of the Quality of Life in Epilepsy Inventory
  611. A Cost and Value Analysis of Two Interventions with Incontinent Nursing Home Residents
  612. Managed Care and Capitation in California: How Do Physicians at Financial Risk Control Their Own Utilization?
  613. The Relationship of Neuropsychological Functioning to Quality of Life in Epilepsy
  614. Validation of a new measure of diarrhea
  615. The relationship between visual acuity and functioning and well-being among diabetics
  616. Access to Medical Care and Health-Related Quality of Life for Low-Income Persons with Symptomatic Human Immunodeficiency Virus
  617. A health-related quality of life measure for multiple sclerosis
  618. Comparing Outcomes and Charges for Patients with Acute Myocardial Infarction in Three Community Hospitals: an Approach for Assessing "Value"
  619. Personal and psychosocial risk factors for physical and mental health outcomes and course of depression among depressed patients.
  620. Response burden, reliability, and validity of the CAGE, Short MAST, and AUDIT alcohol screening measures
  621. Feasibility and Accuracy of a Postcard Diary System for Tracking Healthcare Utilization of Community-Dwelling Older Persons
  622. Agreement between self reports and proxy reports of quality of life in epilepsy patients
  623. Directions for future research
  624. Derivation and Properties of a Brief Health Status Assessment Instrument for Use in HIV Disease
  625. Outcome assessment for epilepsy surgery: The impact of measuring health-related quality of life
  626. Quality-of-life outcomes in men treated for localized prostate cancer
  627. Measuring Physical Function in Community-Dwelling Older Persons: A Comparison of Self-Administered, Interviewer-Administered, and Performance-Based Measures
  628. Functioning and Well-being Outcomes of Patients With Depression Compared With Chronic General Medical Illnesses
  629. Perceptions of Intoxication and Impairment at Arrest among Adults Convicted of Driving under the Influence of Alcohol
  630. Development of the Kidney Disease Quality of Life (KDQOLTM) Instrument
  631. Predictors of Patient Refusal to Participate in Ambulatory-based Comprehensive Geriatric Assessment
  632. The impact of patient adherence on health outcomes for patients with chronic disease in the medical outcomes study
  633. The benefits and pitfalls of health services research funded by proprietary firms
  634. A Perceived Health Index for Use in Persons With Advanced HIV Disease: Derivation, Reliability, and Validity
  635. A short-form measure of dentists' job satisfaction
  636. Long-term functioning and well-being outcomes associated with physical activity and exercise in patients with chronic conditions in the medical outcomes study
  637. The Effect of Oral Support on Sucking Efficiency in Preterm Infants
  638. Quality of Life of Epilepsy Surgery Patients as Compared with Outpatients with Hypertension, Diabetes, Heart Disease, and/or Depressive Symptoms
  639. THE IMPACT OF RESPONSE OPTIONS AND LOCATION IN A MICROCOMPUTER INTERVIEW ON DRINKING DRIVERS' ALCOHOL USE SELF-REPORTS
  640. Short-Form Measures of Physician and Employee Judgments About Hospital Quality
  641. Do Response Options Influence Self-Reports of Alcohol Use?
  642. State-of-the-art SAW channelizer for EW receiver application
  643. EVIDENCE FOR THE FORMATION OF MULTIPLE TYPES OF ACETALDEHYDE-HAEMOGLOBIN ADDUCTS
  644. International use, application and performance of health-related quality of life instruments
  645. Psychometric considerations in evaluating health-related quality of life measures
  646. Change in self-reported functioning in older persons entering a residential care facility
  647. Recall of recommendations and adherence to advice among patients with chronic medical conditions
  648. Health-related quality of life in osteoporosis clinical trials urinary calcium loss
  649. Occupational stress, life stress and mental health among dentists
  650. Response times for the CAGE, short-MAST, AUDIT, and JELLINEK alcohol scales
  651. The ?states versus weights? dilemma in quality of life measurement
  652. Donation and retrieval of cadaveric organs in Australia
  653. Aboriginal Health and Society
  654. The Swedish Health-Related Quality of Life Survey (SWED-QUAL)
  655. Do depressed patients in different treatment settings have different levels of well-being and functioning?
  656. Measuring Functioning and Health in the Very Old
  657. Physicians' characteristics influence patients' adherence to medical treatment: Results from the Medical Outcomes Study.
  658. Value of functional status as a predictor of mortality: Results of a prospective study
  659. OLD AND NEW MMPI-DERIVED SCALES AND THE SHORT-MAST AS SCREENING TOOLS FOR ALCOHOL DISORDER
  660. Antecedents of adherence to medical recommendations: Results from the medical outcomes study
  661. Stepping through the drug use sequence: Longitudinal scalogram analysis of initiation and regular use.
  662. Psychotherapist-patient sexual contact after termination of treatment
  663. A Microcomputer Assessment System (MAS) for administering computer-based surveys: Preliminary results from administration to clients at an impaired-driver treatment program
  664. Benefits and Obstacles of Health Status Assessment in Ambulatory Settings
  665. A Health-Related Quality of Life Instrument for Patients Evaluated for Epilepsy Surgery
  666. Improving task comprehension in the measurement of health state preferences
  667. On becoming involved with drugs: Modeling adolescent drug use over time.
  668. Antecedents of drinking among young adolescents with different alcohol use histories.
  669. Multitrait-Multimethod Analysis of Health-Related Quality-of-Life Measures
  670. Development of an Instrument to Measure Job Satisfaction Among Dentists
  671. Hospital Quality Trends
  672. Marital Status, Social Support, and Health Transitions in Chronic Disease Patients
  673. The Functional Status of Patients
  674. Hierarchical Measures of Physical Function in Ambulatory Geriatrics
  675. Physician-Patient Communication and Adherence
  676. 5. Response to Questionnaire
  677. 6. The PJHQ Questionnaire Exploratory Factor Analysis and Empirical Scale Construction
  678. 7. Further Evaluations of the PJHQ Scales
  679. Peer Cluster Theory and Adolescent Drug Use: A Reanalysis
  680. ROC: Estimation of the Area Under a Receiver Operating Characteristic Curve
  681. The Detection of Depression and the Financing of Medical Care-Reply
  682. Beyond internal consistency reliability: Rationale and user’s guide for Multitrait Analysis Program on the microcomputer
  683. How Generalizable Are Adolescents' Beliefs About Pro-Drug Pressures and Resistance Self-Efficacy?1
  684. Longitudinal scalogram analysis: A methodology and microcomputer program for Guttman scale analysis of longitudinal data
  685. Distinguishing Depression From Functional Impairment in the Medical Outcomes Study-Reply
  686. Beliefs About Resistance Self-Efficacy and Drug Prevalence: Do They Really Affect Drug Use?
  687. Guttman Scale Analysis of Longitudinal Data: A Methodology and Drug Use Applications
  688. Detection of depressive disorder for patients receiving prepaid or fee-for-service care. Results from the Medical Outcomes Study
  689. Robustness of a model of exercise
  690. A Five-Item Measure of Socially Desirable Response Set
  691. Methodological issues in adherence to cancer control regimens
  692. Functional status and well-being of patients with chronic conditions. Results from the Medical Outcomes Study
  693. The functioning and well-being of depressed patients. Results from the Medical Outcomes Study
  694. ALPHA2: An Alternative SAS Program For Estimating Internal Consistency Reliability
  695. Training the creative arts therapist: Identity with integration
  696. The Quality Of Patients' Ratings
  697. X.EXE: A Program for Simplifying EQS Input
  698. The MOS Short-form General Health Survey
  699. Methods For Measuring Patient Satisfaction With Specific Medical Encounters
  700. Reliability and validity of drug use items differing in the nature of their response options.
  701. A microcomputer program for analyzing multitrait-multimethod matrices
  702. A Short-Form Measure of Loneliness
  703. Computer Program Exchange
  704. Professional Satisfaction and Client Outcomes
  705. The Importance of Considering Alternative Structural Equation Models in Evaluation Research
  706. Problem behavior theory and adolescent alcohol use
  707. Structural-equation models of current drug use: Are appropriate models so simple(x)?
  708. Inhibition of Liver Lipogenesis by Dietary Polyunsaturated Fat in Severely Diabetic Rats
  709. Multistage Path Models of Adolescent Alcohol and Drug Use: A Reanalysis
  710. My Medical Care Is Better Than Yours
  711. Book Review : Computer Program Exchange
  712. Book Review : Computer Program Exchange
  713. Relationship of physicians' nonverbal communication skill to patient satisfaction, appointment noncompliance, and physician workload.
  714. Lambda: A Basic Program for Calculating Random Data Eigenvalues
  715. Validity of self-reports of alcohol and other drug use: A multitrait-multimethod assessment.
  716. Fetal Alcohol Syndrome and Fetal Alcohol Effects
  717. The myth and reality of supervisory development
  718. Covariation among health-related behaviors
  719. Validity of five MMPI alcoholism scales: A critique and reanalysis
  720. A study of the reliability and validity of the holmes alcoholism scale
  721. 1218 A FAMILIAL X-LINKED MENTAL RETARDATION SYNDROME ASSOCIATED WITH MULTIPLE CONGENITAL ANOMALIES, MEGALOGENITALIA AND A FRAGILE X CHROMOSOME
  722. Honesty Requiring a Self-Initiated Response
  723. Posterior Resection of Selected Rectal Tumors
  724. Numerical Technique for the Convolution of Piecewise Polynomial Functions
  725. A direct and exact method for computing the transfer function of the optimum smoothing filter
  726. Renal Glycosuria, Aminoaciduria, and Proximal Renal Tubular Acidosis in Association with Membranous Glomerulonephritis.
  727. Two reviews: Motivating economic achievement motivation through the work itself
  728. Two reviews: Motivation through the work itself
  729. Harmony in Modern Counterpoint
  730. Immediate and delayed reactions to interpersonal disagreements: Some effects of the type of issue and order of response
  731. Psychology of the Scientist: III. Introduction to “Passages from the ‘Idea Books’ of Clark L. Hull”
  732. Splanchnic hematocrit in the dog determined from simultaneously measured splanchnic plasma and red cell volumes
  733. Direct Determination of Available Phosphoric Acid by Titration of Ammonium Phosphomolybdate
  734. Properties of firefly pyrophosphatase
  735. A preliminary determination of the functional relationship of effective reaction potential (sER) to the ordinal number of Vincentized extinction reactions (n).
  736. A non-profit/municipality/corporate partnership: an innovative model for collecting end-of-life electronics