Erratum: Development of the NIH patient-reported outcomes measurement information system (PROMIS) Gastrointestinal Symptom Scales (American Journal of Gastroenterology (2014) 109 (1804-1814) DOI: 10.1038/ajg.2014.237);Development of the NIH patient-reported outcomes measurement information system (PROMIS) gastrointestinal symptom scales

American Journal of Gastroenterology

Volumn 109, Issue 11, 2014, Pages 1804-1814

  Spiegel, Brennan M R ^a,b,c   Hays, Ron D ^c,d   Bolus, Roger ^a   Melmed, Gil Y ^a   Chang, Lin ^d   Whitman, Cynthia ^a   Khanna, Puja P ^e   Paz, Sylvia H ^c   Hays, Tonya ^c   Reise, Steve ^f   Khanna, Dinesh ^e  

^a CEDARS SINAI MEDICAL CENTER   (United States)

^b VA GREATER LOS ANGELES HEALTHCARE SYSTEM   (United States)

^c UNIVERSITY OF CALIFORNIA   (United States)

^d UNIVERSITY OF CALIFORNIA   (United States)

^e UNIVERSITY OF MICHIGAN   (United States)

^f UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ABDOMINAL PAIN; ADULT; AGED; ARTICLE; BLOATING; CONSTIPATION; CONSTRUCT VALIDITY; CONTENT VALIDITY; CROSS-SECTIONAL STUDY; DIARRHEA; DYSPHAGIA; FECES INCONTINENCE; FEMALE; FLATULENCE; GASTROESOPHAGEAL REFLUX; GASTROINTESTINAL DISEASE; GASTROINTESTINAL SYMPTOM; HUMAN; INFLAMMATORY BOWEL DISEASE; INFORMATION PROCESSING; IRRITABLE COLON; MAJOR CLINICAL STUDY; MALE; NAMED INVENTORIES, QUESTIONNAIRES AND RATING SCALES; NATIONAL HEALTH ORGANIZATION; NAUSEA AND VOMITING; PATIENT REPORTED OUTCOME MEASUREMENT INFORMATION SYSTEM; RATING SCALE; RELIABILITY; SYSTEMIC SCLEROSIS; UNITED STATES; GASTROINTESTINAL DISEASES; INFORMATION SYSTEM; MIDDLE AGED; OUTCOME ASSESSMENT; PSYCHOMETRY; VERY ELDERLY;

ADULT; AGED; AGED, 80 AND OVER; FEMALE; FOCUS GROUPS; GASTROINTESTINAL DISEASES; HUMANS; INFORMATION SYSTEMS; MALE; MIDDLE AGED; NATIONAL INSTITUTES OF HEALTH (U.S.); PATIENT OUTCOME ASSESSMENT; PSYCHOMETRICS; UNITED STATES;

EID: 84909950426     PISSN: 00029270     EISSN: 15720241     Source Type: Journal    
DOI: 10.1038/ajg.2015.62     Document Type: Erratum

References (29)

1. Spiegel BM. Patient-reported outcomes in gastroenterology: clinical and research applications. J Neurogastroenterol Motil 2013; 19: 137-48.
2. Spiegel B, Khanna D, Bolus R et al. Understanding gastrointestinal distress: a framework for clinical practice. Am J Gastroenterol 2011; 106: 380-5.
3. Wagner EH, Austin BT, Davis C et al. Improving chronic illness care: translating evidence into action. Health Aff (Millwood) 2001; 20: 64-78.
4. Wagner EH, Austin BT, Von Korff M. Organizing care for patients with chronic illness. Milbank Q 1996; 74: 511-44.
5. Marshall S, Haywood K, Fitzpatrick R. Impact of patient-reported outcome measures on routine practice: a structured review. J Eval Clin Pract 2006; 12: 559-68.
6. Dobscha SK, Gerrity MS, Ward MF. Eff ectiveness of an intervention to improve primary care provider recognition of depression. Eff Clin Pract 2001; 4: 163-71.
7. Taenzer P, Bultz BD, Carlson LE e t al. Impact of computerized quality of life screening on physician behaviour and patient satisfaction in lung cancer outpatients. Psychooncology 2000; 9: 203-13.
8. Velikova G, Booth L, Smith AB et al. Measuring quality of life in routine oncology practice improves communication and patient well-being: a randomized controlled trial. J Clin Oncol 2004; 22: 714-24.
9. Brown RF, Butow PN, Dunn SM et al. Promoting patient participation and shortening cancer consultations: a randomised trial. Br J Cancer 2001; 85: 1273-9.
10. Cella D, Yount S, Rothrock N et al. The Patient-Reported Outcomes Measurement Information System (PROMIS): progress of an NIH Roadmap cooperative group during its first two years. Med Care 2007; 45: S3-S11.
11. Burke LB, Kennedy DL, Miskala PH et al. The use of patient-reported outcome measures in the evaluation of medical products for regulatory approval. Clin Pharmacol Ther 2008; 84: 281-3.
12. Khanna P, Agarwal N, Khanna D et al. Development of an online library of patient reported outcome measures in gastroenterology: the GI-PRO database. Am J Gastroenterol 2014; 109: 234-48.
13. Reeve BB, Hays RD, Bjorner JB et al. Psychometric evaluation and calibration of health-related quality of life item banks: plans for the Patient- Reported Outcomes Measurement Information System (PROMIS). Med Care 2007; 45: S22-31.
14. DeWalt DA, Rothrock N, Yount S et al. Evaluation of item candidates: the PROMIS qualitative item review. Med Care 2007; 45: S12-21.
15. Spiegel BM, Bolus R, Agarwal N et al. Measuring symptoms in the irritable bowel syndrome: development of a framework for clinical trials. Aliment Pharmacol Ther 2010; 32: 1275-91.
16. McLaughlin G. SMOG grading: a new readability formula. J Reading 1969; 12: 639-46.
17. Labus JS, Bolus R, Chang L et al. The Visceral Sensitivity Index: development and validation of a gastrointestinal symptom-specific anxiety scale. Aliment Pharmacol Ther 2004; 20: 89-97.
18. Labus JS, Mayer EA, Chang L et al. The central role of gastrointestinalspecific anxiety in irritable bowel syndrome: further validation of the visceral sensitivity index. Psychosom Med 2007; 69: 89-98.
19. Hays RD, Bjorner JB, Revicki DA et al. Development of physical and mental health summary scores from the patient-reported outcomes measurement information system (PROMIS) global items. Qual Life Res 2009; 18: 873-80.
20. Revicki DA, Wood M, Wiklund I et al. Reliability and validity of the Gastrointestinal Symptom Rating Scale in patients with gastroesophageal reflux disease. Qual Life Res 1998; 7: 75-83.
21. The EuroQol Group. EuroQol-A new facility for the measurement of health-related quality of life. Health Policy 1990; 16: 199-208.
22. Patrick DL, Drossman DA, Frederick IO et al. Quality of life in persons with irritable bowel syndrome: development and validation of a new measure . Dig Dis Sci 1998; 43: 400-11.
23. Drossman DA, Patrick DL, Whitehead WE et al. Further validation of the IBS-QOL: a disease-specific quality-of-life questionnaire. Am J Gastroenterol 2000; 95: 999-1007.
24. Irvine EJ, Zhou Q, Th ompson AK. The short inflammatory bowel disease questionnaire: a quality of life instrument for community physicians managing inflammatory bowel disease. CCRPT Investigators. Canadian Crohn's Relapse Prevention Trial. Am J Gastroenterol 1996; 91: 1571-8.
25. Irvine EJ. Development and subsequent refinement of the inflammatory bowel disease questionnaire: a quality-of-life instrument for adult patients with inflammatory bowel disease. J Pediatr Gastroenterol Nutr 1999; 28: S23-7.
26. Khanna D, Hays RD, Park GS et al. Development of a preliminary scleroderma gastrointestinal tract 1.0 quality of life instrument. Arthritis Rheum 2007; 57: 1280-6.
27. Spiegel BM, Bolus R, Harris LA et al. Characterizing abdominal pain in IBS: guidance for study inclusion criteria, outcome measurement and clinical practice. Aliment Pharmacol Ther 2010; 32: 1192-202.
28. Bae S, Allanore Y, Furst D et al. Associations between a sclerodermaspecific gastrointestinal instrument and objective tests of upper gastrointestinal involvements in systemic sclerosis. Clin Exp Rheumatol 2013; 31: 57-63.
29. Khanna D, Nagaraja V, Gladue H et al. Measuring response in the gastrointestinal tract in systemic sclerosis. Curr Opin Rheumatol 2013; 25: 700-6.