Sickle Cell Disease and Quality of Life: An Evaluation of Reporting of Patient-Reported Outcomes in Randomized Controlled Trials-Reference-Cited by-同舟云学术

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Sickle Cell Disease and Quality of Life: An Evaluation of Reporting of Patient-Reported Outcomes in Randomized Controlled Trials

Published:2022-09-03 Issue:5 Volume:46 Page:265-268
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Renner Abbey¹,Love Mitchell¹^ORCID,Garrett Elizabeth¹,Douglas Alexander¹,Kee Micah¹,Heigle Benjamin¹,Wise Audrey¹,Ottwell Ryan¹²^ORCID,Hartwell Micah¹³^ORCID,Vassar Matt¹³^ORCID

Affiliation:

1. Office of Medical Student Research, Oklahoma State University Center for Health Sciences, Tulsa, OK, USA

2. Department of Internal Medicine, University of Oklahoma, School of Community Medicine, Tulsa, OK, USA

3. Department of Psychiatry and Behavioral Sciences, Oklahoma State University Center for Health Sciences, Tulsa, OK, USA

Funder

Oklahoma State University Center for Health Sciences

Publisher

Informa UK Limited

Subject

Biochemistry (medical),Clinical Biochemistry,Genetics (clinical),Hematology

Link

https://www.tandfonline.com/doi/pdf/10.1080/03630269.2022.2121215

Reference20 articles.

1. Patient‐reported outcomes in sickle cell disease and association with clinical and psychosocial factors: Report from the sickle cell disease implementation consortium

2. The World Health Organization quality of life assessment (WHOQOL): Development and general psychometric properties

3. Depression, Suicidal Ideation, and Attempts in Black Patients With Sickle Cell Disease

4. Recent Advances in the Treatment of Sickle Cell Disease

5. Patient-reported outcomes in randomized clinical trials: development of ISOQOL reporting standards

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