Trusted Resources: Evidence & Education
Scientific literature and patient education texts
Drepa-Opia: A Pilot Study to Determine the Predictive Factors of Morphine Use and Consumption in Hospitalized Adult Patients With Sickle Cell Disease
source: Hemoglobin
year: 2018
authors: Sabrie M, Cannas G, Tazarourte K, Poutrel S, Connes P, Hot A, Renoux C, Fattoum J, Joly P
summary/abstract:The aim of this study was to evaluate the clinical, biological and genetic factors that could be associated with the use and dose of morphine during hospitalization for vaso-occlussive crisis (VOC) in adults with sickle cell disease. Ninety-nine hospitalizations for acute VOC (58 sickle cell disease patients aged 18 to 60 years, one to six hospitalizations each) were recorded; we investigated the associations between qualitative and quantitative opioid requirements and several biological, clinical, epidemiological and genetic parameters. Visual analog pain scale (VAS) was the only independent predictor of the qualitative need for morphine (mean value of 8.5 vs. 6.1 for the 77 hospitalizations that required morphine). A higher total administered morphine dose, which relates mainly to the overall crisis severity, was associated with a lower hemoglobin (Hb) level at entry.
The mean daily morphine dose, which is more influenced by the individual sensitivity to morphine, was not influenced by the studied genetic parameters [sickle cell disease type, α-thalassemia (α-thal) status, UGT2B7 and ABCB1 genotypes] but a very slight negative association was found with the total bilirubin (BIL) level at entry. Our study demonstrated that physicians are often reluctant to prescribe morphine in sickle cell disease as a VAS of 6 corresponds to the usual threshold of administration in other instances. Total Hb at entry was also associated for the first time with higher total morphine consumption and could be used in a predictive VOC severity score. These results have to be confirmed and completed on larger cohorts.
organization: Services de Santé et Recherche sur la Performance (HESPER), France; Hospices Civils de Lyon, France; Communauté d'Universités et d'Establissments (COMUE) de Lyon, France; Laboratoire d'Excellence sur le Globule Rouge (Labex GR-Ex), France; Institut Universitaire de France, FranceDOI: 10.1080/03630269.2018.1529602
read more
Related Content
-
Lakshmanan Krishnamurti, MDDr. Krishnamurti graduated from the Arme...
-
Olugbenga Olowokure, MDDr. Olugbenga Olowokure is a hematologis...
-
Improving disease knowledge in 6- to 10-year-olds with sickle cell disease: A quasi-experimental studyBackground: Increasing knowledge and un...
-
Jazz’ Journey With Sickle Cellhttps://www.youtube.com/watch?v=OMC5wOyD...
-
Clinical and Genetic Predictors of Priapism in Sickle Cell Disease: Results From the Recipient Epidemiology and Dono...Introduction: Priapism is the persiste...
-
Rare Disease Day Symposium at the Quinnipiac Frank H. Netter MD School of MedicineSince 2015, the Frank H. Netter MD Schoo...
-
Here to Stay — Living With Sickle Cell DiseaseMy name is Noah Alexander Williams and I...
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.