Impact of individualized pain plan on the emergency management of children with sickle cell disease

Pediatric Blood and Cancer

Volumn 61, Issue 10, 2014, Pages 1747-1753

  Krishnamurti, Lakshmanan ^a   Smith Packard, Bethanny ^b   Gupta, Ashish ^c   Campbell, Mary ^a   Gunawardena, Sriya ^a   Saladino, Richard ^a  

^a CHILDREN S HOSPITAL OF PITTSBURGH   (United States)

^b GEISINGER HEALTH SYSTEM   (United States)

^c BROOKLYN HOSPITAL CENTER   (United States)

Author keywords

Hemoglobinopathies; Pain; Sickle cell anemia; Sickle cell disease

Indexed keywords

ADOLESCENT; ADULT; ALGORITHM; ANALGESIA; ARTICLE; CHILD; EMERGENCY CARE; EMERGENCY WARD; FACES PAIN SCALE; FEMALE; HEALTH CARE QUALITY; HEALTH CARE UTILIZATION; HOSPITAL READMISSION; HOSPITALIZATION; HUMAN; MAJOR CLINICAL STUDY; MALE; PAIN; PATIENT SATISFACTION; PERSONALIZED MEDICINE; PRIORITY JOURNAL; SICKLE CELL ANEMIA;

HEMOGLOBINOPATHIES; PAIN; SICKLE CELL ANEMIA; SICKLE CELL DISEASE;

ADOLESCENT; ALGORITHMS; ANEMIA, SICKLE CELL; CHILD; EMERGENCY SERVICE, HOSPITAL; FEMALE; HOSPITALIZATION; HUMANS; INDIVIDUALIZED MEDICINE; MALE; PAIN; PAIN MANAGEMENT; PATIENT SATISFACTION;

EID: 84908553242     PISSN: 15455009     EISSN: 15455017     Source Type: Journal    
DOI: 10.1002/pbc.25024     Document Type: Article

References (29)

1. Chiang EY, Frenette PS. Sickle cell vaso-occlusion. Hematol Oncol Clin North Am 2005; 19:771-784.
2. Stuart MJ, Nagel RL. Sickle-cell disease. Lancet 2004; 364:1343-1360.
3. Brousseau DC, Owens PL, Mosso AL, et al. Acute care utilization and rehospitalizations for sickle cell disease. JAMA 2007; 303:1288-1294.
4. Wethers DL. Sickle cell disease in childhood: Part II. Diagnosis and treatment of major complications and recent advances in treatment. Am Fam Physician 2000; 62:1309-1314.
5. Wethers DL. Sickle cell disease in childhood: Part I. Laboratory diagnosis, pathophysiology and health maintenance. Am Fam Physician 2000; 62:1013-1020, 1027-1028.
6. Wilson RE, Krishnamurti L, Kamat D. Management of sickle cell disease in primary care. Clin Pediatr 2003; 42:753-761.
7. Ballas SK. Pain management of sickle cell disease. Hematology Oncol Clin North Am 2005; 19:785-802.
8. Friedland LR, Pancioli AM, Duncan KM. Pediatric emergency department analgesic practice. Pediatr Emerg Care 1997; 13:103-106.
9. Brown DW. The dawn of healthy people 2020: A brief look back at its beginnings. Prevent Med 2009; 48:94-95.
10. Ballas SK. Current issues in sickle cell pain and its management. Hematology Am Soc Hematol Educ Program 2007; 1:97-105.
11. Aisiku IP, Penberthy LT, Smith WR, et al. Patient satisfaction in specialized versus nonspecialized adult sickle cell care centers: The PiSCES study. J Natl Med Assoc 2007; 99:886-890.
12. Ballas SK. Ethical issues in the management of sickle cell pain. Am J Hematol 2001; 68:127-132.
13. Jacob E, Miaskowski C, Savedra M, et al. Management of vaso-occlusive pain in children with sickle cell disease. J Pediatr Hematol Oncol 2003; 25:307-311.
14. Jacob E, Mueller BU. Pain experience of children with sickle cell disease who had prolonged hospitalizations for acute painful episodes. Pain Med 2008; 9:13-21.
15. Maxwell K, Streetly A, Bevan D. Experiences of hospital care and treatment-seeking behavior for pain from sickle cell disease: Qualitative study. West J Med 1999; 171:306-313.
16. Rupp T, Delaney KA. Inadequate analgesia in emergency medicine. Ann Emerg Med 2004; 43:494-503.
17. Benjamin LJ, Swinson GI, Nagel RL. Sickle cell anemia day hospital: An approach for the management of uncomplicated painful crises. Blood 2000; 95:1130-1136.
18. Adewoye AH, Nolan V, McMahon L, et al. Effectiveness of a dedicated day hospital for management of acute sickle cell pain. Haematologica 2007; 92:854-855.
19. Raphael JL, Kamdar A, Beavers MB, et al. Treatment of uncomplicated vaso-occlusive crises in children with sickle cell disease in a day hospital. Pediatr Blood Cancer 2008; 51:82-85.
20. Raphael JL, Kamdar A, Wang T, et al. Day hospital versus inpatient management of uncomplicated vaso-occlusive crises in children with sickle cell disease. Pediatr Blood Cancer 2008; 51:398-401.
21. Baiardini I, Braido F, Bonini M, et al. Why do doctors and patients not follow guidelines? Curr Opin Allergy Clin Immunol 2009; 9:228-233.
22. Cabana MD, Rand CS, Powe NR, et al. Why don't physicians follow clinical practice guidelines? A framework for improvement. JAMA 1999; 282:1458-1465.
23. Francke AL, Smit MC, de Veer AJ, et al. Factors influencing the implementation of clinical guidelines for health care professionals: A systematic meta-review. BMC Med Inform Decis Mak 2008; 8:38.
24. Magaret ND, Clark TA, Warden CR, et al. Patient satisfaction in the emergency department-A survey of pediatric patients and their parents. Acad Emerg Med 2002; 9:1379-1388.
25. Givens M, Rutherford C, Joshi G, et al. Impact of an emergency department pain management protocol on the pattern of visits by patients with sickle cell disease. J Emerg Med 2007; 32:239-243.
26. Ballas SK, Lusardi M. Hospital readmission for adult acute sickle cell painful episodes: Frequency, etiology, and prognostic significance. Am J Hematol 2005; 79:17-25.
27. Vichinsky E, Onyekwere O, Porter J, et al. A randomised comparison of deferasirox versus deferoxamine for the treatment of transfusional iron overload in sickle cell disease. Br J Haematol 2007; 136:501-508.
28. Platt OS, Thorington BD, Brambilla DJ, et al. Pain in sickle cell disease. Rates and risk factors. New Engl J Med 1991; 325:11-16.
29. Lattimer L, Haywood C, Jr. Lanzkron S, et al. Problematic hospital experiences among adult patients with sickle cell disease. J Health Care Poor Underserved 2010; 21:1114-1123.