2014
DOI: 10.1002/alr.21282
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A new model for collection of clinical outcomes data in patients with chronic rhinosinusitis

Abstract: Quality of life data can be effectively collected from CRS patients in both the private and academic practice setting. The addition of an online data collection tool can significantly increase response rates, and allow a comprehensive capture of meaningful clinical outcomes. Such a model is not difficult to implement and has increasing relevance as payers begin to request outcome data from providers.

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Cited by 14 publications
(26 citation statements)
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“…The validated SNOT‐22 questionnaire is a commonly used tool to quantify CRS symptom burden in both the clinical and research settings . As a patient‐reported outcome measure, understanding the clinical relevance of changes in the SNOT‐22 score requires knowledge of the MCID.…”
Section: Discussionmentioning
confidence: 99%
“…The validated SNOT‐22 questionnaire is a commonly used tool to quantify CRS symptom burden in both the clinical and research settings . As a patient‐reported outcome measure, understanding the clinical relevance of changes in the SNOT‐22 score requires knowledge of the MCID.…”
Section: Discussionmentioning
confidence: 99%
“…As treatment decisions in the CRS population are largely symptom driven, accurate measurement of patient‐reported outcomes through the use of both disease‐specific and GHRQOL instruments remains critical in the assessment of medical and surgical interventions . Today more than in years past, patients are expecting a high QOL into their later years .…”
Section: Discussionmentioning
confidence: 99%
“…Patients were asked to complete the 22‐item Sinonasal Outcomes Test (SNOT‐22) and the EuroQol 5‐Dimension Health Assessment (EQ‐5D) questionnaires on the day of surgery (baseline) and at 12 and 24 months postoperatively. Data collection was performed by electronic survey, mail, or phone in a Health Insurance Portability and Accountability Act compliant manner as discussed previously . Institutional review board approval was obtained from the Human Studies Committee of the Massachusetts Eye and Ear Infirmary (protocol 201247‐15).…”
Section: Methodsmentioning
confidence: 99%
“…Data collection was performed by mail, phone, or electronic survey in a Health Insurance Portability and Accountability Act–compliant manner. An online survey firm (DataStar, Waltham, MA) was employed to create and administer an Internet‐based system for patients to securely enter their responses to QOL questionnaires …”
Section: Methodsmentioning
confidence: 99%