Riesgo de vasooclusión                                                                 Risk of vasoocclusion  

Anderson N, Bellot J, Senu-Oke O, Ballas SK. Characteristics of Acute Care Utilization of a Delaware Adult Sickle Cell Disease Patient Population. Popul Health Manag. 2013 Aug 21.

Jacob E, Mack AK, Savedra M, Van Cleve L, Wilkie DJ. Adolescent Pediatric Pain Tool for Multidimensional Measurement of Pain in Children and Adolescents. Pain Manag Nurs. 2013 Jul 16. pii: S1524-9042(13)00032-5. doi: 10.1016/j.pmn.2013.03.002.

Jacob E, Duran J, Stinson J, Lewis MA, Zeltzer L. Remote monitoring of pain and symptoms using wireless technology in children and adolescents with sickle cell disease. J Am Assoc Nurse Pract. 2013; 25(1):42-54. doi: 10.1111/j.1745-7599.2012.00754.x.

Jenerette C, Leak A. The role of oncology nurses in the care of adults with sickle cell disease. Clin J Oncol Nurs. 2012; 16(6):633-5. doi: 10.1188/12.CJON.633-635.

Jacob E, Stinson J, Duran J, Gupta A, Gerla M, Ann Lewis M, Zeltzer L. Usability testing of a Smartphone for accessing a web-based e-diary for self-monitoring of pain and symptoms in sickle cell disease. J Pediatr Hematol Oncol. 2012; 34(5):326-35.

Lambing A, Kachalsky E, Mueller ML. The dangers of iron overload: bring in the iron police. J Am Acad Nurse Pract. 2012; 24(4):175-83.

Jenerette CM, Valrie CR. The influence of maternal behaviors during childhood on self-efficacy in individuals with sickle cell disease. J Fam Nurs. 2010; 16(4):422-34.

Jayaram A, Nagel RW, Jasty R. Impact of clinical pathway on quality of care in sickle cell patients. J Pediatr Hematol Oncol. 2010; 32(7):537-9.

Taylor LE, Stotts NA, Humphreys J, Treadwell MJ, Miaskowski C. A review of the literature on the multiple dimensions of chronic pain in adults with sickle cell disease. J Pain Symptom Manage. 2010; 40(3):416-35.

Ninkovich GM, Miller SK, Alpert PT. Sickle-cell anemia and pulmonary hypertension. J Am Acad Nurse Pract. 2010; 22(4):198-204.

Jacob E, Sockrider MM, Dinu M, Acosta M, Mueller BU. Respiratory symptoms and acute painful episodes in sickle cell disease. J Pediatr Oncol Nurs. 2010; 27(1):33-9.

Granados R, Jacob E. Pain experience in hospitalized adults with sickle cell disease. Medsurg Nurs. 2009;18(3):161-7, 182.

Adegbola MA. Can heterogeneity of chronic sickle-cell disease pain be explained by genomics? A literature review. Biol Res Nurs. 2009; 11(1):81-97.

Riesgo de recurrencia / progresión de vasooclusión                       Risk of vasoocclusion recurrence / progression  

Wang WC, Dwan K. Blood transfusion for preventing primary and secondary stroke in people with sickle cell disease. Cochrane Database Syst Rev. 2013 Nov 14; 11:CD003146.

Jacob E, Mack AK, Savedra M, Van Cleve L, Wilkie DJ. Adolescent Pediatric Pain Tool for Multidimensional Measurement of Pain in Children and Adolescents. Pain Manag Nurs. 2013 Jul 16. pii: S1524-9042(13)00032-5. doi: 10.1016/j.pmn.2013.03.002. 

Jacob E, Pavlish C, Duran J, Stinson J, Lewis MA, Zeltzer L. Facilitating pediatric patient-provider communications using wireless technology in children and adolescents with sickle cell disease. J Pediatr Health Care. 2013; 27(4):284-92. doi: 10.1016/j.pedhc.2012.02.004. 

Lee L, Askew R, Walker J, Stephen J, Robertson-Artwork A. Adults with sickle  cell disease: an interdisciplinary approach to home care and self-care management with a case study. Home Healthc Nurse. 2012; 30(3):172-83.

Schiavenato M, Alvarez O. Pain assessment during a vaso-occlusive crisis in the pediatric and adolescent patient: rethinking practice. J Pediatr Oncol Nurs. 2013; 30(5):242-8. doi: 10.1177/1043454213494014. 

Tanabe P, Thornton VL, Martinovich Z, Todd KH, Wun T, Lyons JS. The Emergency Department Sickle Cell Assessment of Needs and Strengths (ED-SCANS): reliability and validity. Adv Emerg Nurs J. 2013; 35(2):143-53. doi: 10.1097/TME.0b013e31828ecbd5. 

Myers M, Eckes EJ. A novel approach to pain management in persons with sickle cell disease. Medsurg Nurs. 2012; 21(5):293-8. 

Tanabe P, Hafner JW, Martinovich Z, Artz N. Adult emergency department patients with sickle cell pain crisis: results from a quality improvement learning collaborative model to improve analgesic management. Acad Emerg Med. 2012; 19(4):430-8. 

Brown M. Managing the acutely ill adult with sickle cell disease. Br J Nurs. 2012; 21(2):90-6. 

Tangayi S, Anionwu E, Westerdale N, Johnson K. A skills framework for sickle  cell disease and thalassaemia. Nurs Times. 2011; 107(41):12-3. 

Jenerette CM, Brewer C, Leak AN. Self-care recommendations of middle-aged and older adults with sickle cell disease. Nurs Res Pract. 2011;2011:270594. 

Jenerette CM, Valrie CR. The influence of maternal behaviors during childhood on self-efficacy in individuals with sickle cell disease. J Fam Nurs. 2010; 16(4):422-34. 

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