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Index/Order Form of Materials Please note - Pain Resource Center ...

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13. Zempsky, W. T., Loiselle, K. A., McKay, K., Lee. B. H., Hagstrom, J. N., & Schechter, N. L. (2010). Do children with sicklecell disease receive disparate care for pain in the emergency department? The Journal <strong>of</strong> Emergency Medicine, 39(5), 691-695.DOI:10.1016/j.jemermed.2009.06.003.14. Mousa, S. A., Al Momen, A., Al Sayegh, F., Al Jaouni, S., Nasrullah, Z., Al Saeed, H., et al. (2010). Management <strong>of</strong> painfulvaso-occlusive crisis <strong>of</strong> sickle-cell anemia: Consensus opinion. Clinical and Applied Thrombosis/Hemostasis, 16(4), 365-376.DOI: 10.1177/1076029609352661.15. Dampier, C., Lieff, S., LeBeau, P. Rhee, S., McMurray, M., Rogers, Z., et al. (2010). Health-related quality <strong>of</strong> life in childrenwith sickle cell disease: A report from the comprehensive sickle cell centers clinical trial consortium. Pediatric Blood Cancer,55, 485-494. DOI 10.1002/pbc.22497.16. Odesina, V., Bellini, S., Leger, R., Bona, R., Delaney, C., Andemariam, B., et al. (2010). Evidence-based sickle cell painmanagement in the emergency department, Advanced Emergency Nursing Journal, 32(2), 102-111.DOI: 10.1097/TME.0b013e3181da588c.17. Solomon, L. R. (2010). <strong>Pain</strong> management in adults with sickle cell disease in a medical center emergency department. Journal<strong>of</strong> the National Medical Association, 102(1), 1025-1032.18. Taylor, L. E. V., Stotts, N. A., Humphreys, J., Treadwell, M. J., & Miaskowski, C. (2010). A review <strong>of</strong> the literature on themultiple dimensions <strong>of</strong> chronic pain in adults with sickle cell disease. Journal <strong>of</strong> <strong>Pain</strong> and Symptom Management, 40(3), 416-435. DOI:10.1016/j.jpainsymman.2009.12.027.19. Wilkie, D. J., Molokie, R., Boyd-Seal, D., Suarez, M. L., Kim, Y. O., Zong, S., et al. (2010). Patient-reported outcomes:Descriptors <strong>of</strong> nociceptive and neuropathic pain and barriers to effective pain management in adult outpatients with sickle celldisease. Journal <strong>of</strong> the National Medical Association, 102(1), 18-27.20. Sickle Cell Anemia: A Mother’s Perspective What Every Parent Should Know- Lipscome, M & Chamberlin, M. (2010). CreateSpace. ISBN: 978-1456450670Website: https://www.createspace.com/350928121. Miscola, P. Sorrentino, F., Scaramucci, L., de Fabritiis, P., Cianciulli, P. (2009). <strong>Pain</strong> syndromes in sickle cell disease: Anupdate. <strong>Pain</strong> Medicine, 10(3), 470-480. DOI:10.1111/j.1526-4637.2009.00601.x22. Cotton, S., Grossoehme, D., Rosenthan, S. L., McGrady, M. E., Roberts, Y. H., Hines, J., et al. (2009). Religious/spiritualcoping in adolescents with sickle cell disease: A pilot study. Journal <strong>of</strong> Pediatric Hematology Oncology, 31(5), 313-318.DOI:10.1097/MPH.0b013e31819e40e3.23. Howard, J., Thomas, V. J., & Rawle, H. M. (2009). <strong>Pain</strong> management and quality <strong>of</strong> life in sickle cell disease. Expert ReviewsPharmacoeconomics Outcomes, Research, 9(4), 347-352. DOI:10.1586/ERP.09.32.24. McClellan, C. B., Schatz, J. C., Puffer, E., Sanchez, C. E., Stancil, M. T., & Roberts, C. W. (2009). Use <strong>of</strong> handheld wirelesstechnology for a home-based sickle cell pain management protocol. Journal <strong>of</strong> Pediatric Psychology, 34(5), 564-573.DOI:10.1093/jpepsy/jsn121.25. Huang, Y-C., Harraz, A. M., Shindel, A. W., & Lue, T. F. (2009). Evaluation and management <strong>of</strong> priapism: 2009 update. NatureReviews/Urology, 6, 263-271. DOI:10.1038/nrurol.2009.50.26. O’Connell-Edwards, C. F., Edwards, C. L., Pearce, M., Wachholtz, A. B., Wood, M., Muhammad, M., et al. (2009). Religiouscoping and pain associated with sickle cell disease: Exploration <strong>of</strong> a non-linear model. Journal <strong>of</strong> African American Studies, 13,1-13. DOI 10.1007/s12111-008-9063-4.27. Field, J. J., Knight-Perry, J. E., & DeBaun, M. R. (2009). Acute pain in children and adults with sickle cell disease:Management in the absence <strong>of</strong> evidence-based guidelines. Current Opinion in Hematology, 16, 173-178.DOI:10.1097/MOH.0b013e328329e16728. Mann-Jiles, V. & Morris, D. L. (2009). Quality <strong>of</strong> life <strong>of</strong> adult patients with sickle cell disease. Journal <strong>of</strong> the AmericanAcademy <strong>of</strong> Nurse Practitioners, 21, 349-349. DOI:10.1111/j.1745-7599.2009.00416.x.29. Benjamin, L. (2008). <strong>Pain</strong> management in sickle cell disease: Palliative care begins at birth? Hematology/the EducationProgram <strong>of</strong> the American Society <strong>of</strong> Hematology, 466-474.73

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