| Journal of Hematology, ISSN 1927-1212 print, 1927-1220 online, Open Access |
| Article copyright, the authors; Journal compilation copyright, J Hematol and Elmer Press Inc |
| Journal website https://www.thejh.org |
Original Article
Volume 10, Number 2, April 2021, pages 46-52
Opioid Use in Adults With Sickle Cell Disease Hospitalized During Vaso-Occlusive Crisis: A Systematic Review
Table
| Author | Location | Study sample size | Age in years | Gender | Type of SCD |
|---|---|---|---|---|---|
| SCD: sickle cell disease; SC: sickle cell; HbSS: most severe form of SCD; HbSC: second most common form of SCD; HbSβ0: severe form of SCD. | |||||
| Al-Anazi et al, 2017 [33] | Saudi Arabia | 99 | Mean 26.9 | Males 47%, females 52% | Not specified |
| Ballas et al, 2010 [34] | USA and Canada | 299 | 18 - 59 | Male 49%, female 51% | SC α+ thalassemia, n = 298 |
| Desai et al, 2013 [35] | USA | 13 | 22 - 50 | Male 31%, female 69% | HbSS, n = 6; HbSβ0, n = 2; HbSC, n = 1 |
| Lagas et al, 2010 [36] | the Netherlands | 1 | 61 | Male 100% | HbSC, n = 1 |
| van Beers et al, 2007 [37] | the Netherlands | 19 | 20 - 42 | Male < 50%, female > 50% | HbSS, majority of sample |