Trusted Resources: Evidence & Education
Scientific literature and patient education texts
Insomnia and clinical pain in sickle cell disease patients
source: The Journal of Pain
year: 2017
authors: A. Tilton, P. Carroll, S. Lanzkron, K. Kiley, M. Smith, J. Smythe, J. Haythornthwaite, C. Campbell
summary/abstract:Chronic pain is one of several debilitating complications that arises in patients suffering from sickle cell disease with many patients reporting concurrent sleep disturbance. It is widely recognized that pain disrupts sleep, however little is known about how sleep affects pain in this population. The current analyses examined SCD patients’ calculated Insomnia Severity Index (ISI) scores and its prospective relationship to self-reported clinical pain over a 90 day electronic diary period, 3 months of weekly telephone calls, and one year of monthly telephone calls. Seventy-two African American SCD patients rated their average daily clinical pain (x=26.60/100, SD=20.84) and 64 of them remained in the study and completed the weekly and monthly calls (average clinical pain x=2.5/10, SD=1.7 and x=3.5/10, SD=1.9, respectively). Multivariate models predicting clinical pain at each time period controlled for education, sex, age, central sensitization (CS), depression, and chronic opioid therapy (COT). ISI independently predicted 7.5 % of the variance in clinical pain during the diary period. The overall model accounted for 76% of the total variance, with COT, CS, and ISI significant covariates in the model. ISI independently predicted 7.6% of the variance in clinical pain over the 3 months of weekly calls. Both COT and ISI were significant in this model, for which 65% of the total variance was accounted. Lastly, in the twelve month period of monthly calls, ISI independently predicted 9.2% of the variance in clinical pain during the final 12 months of observation, accounting for 66% of the variance. COT, ISI, and depression were significant for this final model. These data suggest that sleep has a significant and long-lasting influence on SCD pain and deserves further, in-depth investigation.
organization: Johns Hopkins University School of Medicine, Baltimore, MDDOI: 10.1016/j.jpain.2017.02.159
read more
Related Content
-
Beliefs about hydroxyurea in youth with sickle cell diseaseBackground: Hydroxyurea reduces complic...
-
Robert I. Liem, MD, MSRobert I. Liem is Associate Professor of...
-
Marina Cavazzana, MD, PhDMarina Cavazzana is a pediatrician, Prof...
-
Nociceptors Protect Sickle Cell Disease Mice From Vaso-Occlusive Episodes and Chronic Organ DamageSickle cell disease (SCD) is a common he...
-
National Sickle Cell Advocacy Day 2020 — Sickle Cell Disease Association of America – CANCELEDPlease join the Sickle Cell Disease Asso...
-
GBT launches ACCEL grants program to improve access to care for people with Sickle cell diseaseGlobal Blood Therapeutics, Inc. (GBT) to...
-
My medical school lesson was tinged with racism. Did that affect how I treated a sickle cell patient years later?The young woman was curled up in a ball....
To improve your experience on this site, we use cookies. This includes cookies essential for the basic functioning of our website, cookies for analytics purposes, and cookies enabling us to personalize site content. By clicking on 'Accept' or any content on this site, you agree that cookies can be placed. You may adjust your browser's cookie settings to suit your preferences. More Information
The cookie settings on this website are set to "allow cookies" to give you the best browsing experience possible. If you continue to use this website without changing your cookie settings or you click "Accept" below then you are consenting to this.