scholarly journals Optimism Predicting Daily Pain Medication Use in Adolescents with Sickle Cell Disease

2007 ◽  
Vol 33 (3) ◽  
pp. 302-309 ◽  
Author(s):  
Laura Pence ◽  
Cecelia R. Valrie ◽  
Karen M. Gil ◽  
Rupa Redding-Lallinger ◽  
Charles Daeschner
Pain Practice ◽  
2015 ◽  
Vol 16 (6) ◽  
pp. 680-687 ◽  
Author(s):  
Lucia De Franceschi ◽  
Paolo Mura ◽  
Vittorio Schweiger ◽  
Elisa Vencato ◽  
Francesca Maria Quaglia ◽  
...  

Blood ◽  
2016 ◽  
Vol 128 (22) ◽  
pp. 4857-4857
Author(s):  
Samip Master ◽  
Shajadi Patan ◽  
Shashank Cingam ◽  
Runhua Shi ◽  
Richard Preston Mansour

Abstract Introduction: The chronic pain in sickle cell disease (SCD) arises from chronic bone damage as a consequence of bone marrow infraction during vaso-occulsive events. There are certain barriers to adequate pain management in adult patients with SCD, namely, limited knowledge among the clinicians, inadequate assessment, concerns about addiction, and biases against opioid use. We did retrospective analysis to investigate the average pain medication needed by adult patient with SCD. We also did analysis to see if there was a relation between plasma vitamin D level and amount of pain medication needed. Methods: We take care of approximately 300 active adult SCD at Hematology clinic at our institute. We did a retrospective analysis of 458 adult patients with SCD seen at our clinic between 2001 and 2016. We collected data on type of SCD, plasma 25 -hydroxyvitamin d level and amount of opioid pain medication in mg. To get uniform units of opiates, we converted all the different opiates into morphine. Results: The average morphine dose in a 24 hours period needed to manage chronic pain in an adult patient with SS type was 84 mg with standard deviation of 72, for SC type was 60 mg with standard deviation of 72 and for sickle beta thal type was 72 mg with standard deviation of 71. There were 4 patients with SS with hereditary persistence of hemoglobin F and average opiate dose in them was 84 mg. We obtained vitamin d level on 223 patients and out of them, 47 had vitamin d level of <4.2 ng/ml (lowest level reportable by our lab). We also found negative correlation between amount of pain medication and vitamin D level. The spearman correlation coefficient was -0.2 and p value was <0.01. Conclusion: Because we were unable to find any previous reports of the correlation of vitamin D levels and opiate use in an adult population with SCD, we believe that this is the first study to report this correlation. It also provides a rough estimate regarding average amount of opiates that an adult patient with SCD needs. This correlation between Vitamin D levels and opiate requirement supports our current practice of screening all patients for Vitamin D deficiency using 25hydroxy vitamin D levels and treating all patients who are found to be deficient. We do not know if this Vitamin D replacement will reduce pain, bone health or the amount of opiate medication needed in the future. Disclosures No relevant conflicts of interest to declare.


2016 ◽  
pp. jsw061 ◽  
Author(s):  
Cynthia W. Karlson ◽  
Anna M. Baker ◽  
Maggie H. Bromberg ◽  
Thomas David Elkin ◽  
Suvankar Majumdar ◽  
...  

1998 ◽  
Vol 5 (3) ◽  
pp. 185-203 ◽  
Author(s):  
Laura S. Porter ◽  
Karen M. Gil ◽  
Jan A. Sedway ◽  
Jawana Ready ◽  
Elizabeth Workman ◽  
...  

2017 ◽  
Vol 183 (2) ◽  
pp. 306-308
Author(s):  
Charles R. Jonassaint ◽  
Chaeryon Kang ◽  
Daniel M. Abrams ◽  
Jingyi J. Li ◽  
Jason Mao ◽  
...  

2017 ◽  
Vol 92 (2) ◽  
pp. 179-186 ◽  
Author(s):  
Charlotte F. J. van Tuijn ◽  
Joep W. R. Sins ◽  
Karin Fijnvandraat ◽  
Bart J. Biemond

2017 ◽  
Vol 65 (4) ◽  
pp. e26906 ◽  
Author(s):  
Andrea K. Morrison ◽  
Matthew P. Myrvik ◽  
David C. Brousseau ◽  
Amy L. Drendel ◽  
J. Paul Scott ◽  
...  

Blood ◽  
2012 ◽  
Vol 120 (21) ◽  
pp. 1016-1016
Author(s):  
Charlotte F.J. van Tuijn ◽  
Bart J. Biemond

Abstract Abstract 1016 Background and aims Sickle cell disease is characterised by frequent episodes of vaso-occlusive pain resulting in frequent health care utilisation and cumulating organ damage. Disease severity is often quantified by the number of hospital admissions. However, sickle cell patients frequently experience episodes of pain without health care utilisation. In the present study, we analysed whether daily self-reported sickle cell pain in adult patients is related to disease severity quantified by frequency of hospital admission or disease severity defined by genotype. Methods We conducted a prospective cohort study in order to analyse daily pain in adult sickle cell patients in a tertiary teaching hospital in the Netherlands. Patients were divided in having severe (HbSS/HbS-β0) or milder (HbSC/HbS-β+) disease according to genotype. Daily pain was assessed for a period of 6 months by the use of pain diaries. Pain intensity was measured with different validated pain assessment instruments (Visual Analog Scale (VAS), McGill Pain Questionnaire and Brief Pain Inventory). Daily pain scores were correlated with genotype and frequency of hospital admission. Results 110 consecutive outpatients with sickle cell disease were approached. 16 patients were excluded for different reasons (pregnancy, unable to fill in a diary or declined participation), 19 patients missed their appointments in the outpatient clinic and 26 patients completed less than a month of their diaries. 49 patients (mean age 33 years (SD 12.6); 67% female) completed at least two month of the diaries (response rate: 65%). No differences in disease severity according to genotype or age were observed between responders/non-responders. Pain was reported in 18% of the total 5016 patient-days. Overall median pain intensity was 3.6 (VAS). 41% of the patients reported pain in 5% or fewer diary days and 5% of all patients reported pain in more than 95% of the days. The frequency of hospital admission was unrelated to self-reported pain and no difference in daily pain was observed between patients with severe or milder disease according to genotype. Furthermore, lab results (hemoglobin and fetal hemoglobin levels, leukocyte counts, lactate dehydrogenase (LDH) and the presence of alfa-thalassemia) were not associated with daily pain. Conclusions Using daily pain diaries, adult sickle cell patients report pain in 18% of their total diary days. Interestingly, our patient population reported less daily pain in comparison to daily pain in adults reported previously (over 50%). Daily pain appeared to be unrelated to disease severity according to genotype or defined by frequency of hospital admission. Our results further stress that daily pain is an important problem in sickle cell patients and appears to be unrelated to the traditional definitions of disease severity. Disclosures: No relevant conflicts of interest to declare.


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