96 related articles for article (PubMed ID: 26840856)
1. Palliative Care Teams as Advocates for Adults with Sickle Cell Disease.
Ajayi TA; Edmonds KP; Thornberry K; Atayee RA
J Palliat Med; 2016 Feb; 19(2):195-201. PubMed ID: 26840856
[TBL] [Abstract][Full Text] [Related]
2. Transitioning Adolescents and Young Adults With Sickle Cell Disease From Pediatric to Adult Health Care: Provider Perspectives.
Stollon NB; Paine CW; Lucas MS; Brumley LD; Poole ES; Peyton T; Grant AW; Jan S; Trachtenberg S; Zander M; Bonafide CP; Schwartz LA
J Pediatr Hematol Oncol; 2015 Nov; 37(8):577-83. PubMed ID: 26492583
[TBL] [Abstract][Full Text] [Related]
3. Adolescents with sickle cell disease in a rural community: are they ready to transition to adulthood?
Mennito S; Hletko P; Ebeling M; Amann LA; Roberts J
South Med J; 2014 Sep; 107(9):578-82. PubMed ID: 25188623
[TBL] [Abstract][Full Text] [Related]
4. Primary Care Providers' Comfort Levels in Caring for Patients with Sickle Cell Disease.
Whiteman LN; Haywood C; Lanzkron S; Strouse JJ; Feldman L; Stewart RW
South Med J; 2015 Sep; 108(9):531-6. PubMed ID: 26332477
[TBL] [Abstract][Full Text] [Related]
5. An Integrative Review: The Evolution of Provider Knowledge, Attitudes, Perceptions and Perceived Barriers to Caring for Patients with Sickle Cell Disease 1970-Now.
Reich J; Cantrell MA; Smeltzer SC
J Pediatr Hematol Oncol Nurs; 2023; 40(1):43-64. PubMed ID: 35854420
[TBL] [Abstract][Full Text] [Related]
6. Improving Clinician Attitudes of Respect and Trust for Persons With Sickle Cell Disease.
Haywood C; Williams-Reade J; Rushton C; Beach MC; Geller G
Hosp Pediatr; 2015 Jul; 5(7):377-84. PubMed ID: 26136312
[TBL] [Abstract][Full Text] [Related]
7. How sickle cell disease patients experience, understand and explain their pain: An Interpretative Phenomenological Analysis study.
Coleman B; Ellis-Caird H; McGowan J; Benjamin MJ
Br J Health Psychol; 2016 Feb; 21(1):190-203. PubMed ID: 26333530
[TBL] [Abstract][Full Text] [Related]
8. A primary care provider's guide to preventive and acute care management of adults and children with sickle cell disease.
Pack-Mabien A; Haynes J
J Am Acad Nurse Pract; 2009 May; 21(5):250-7. PubMed ID: 19432908
[TBL] [Abstract][Full Text] [Related]
9. Adults with sickle cell disease: an interdisciplinary approach to home care and self-care management with a case study.
Lee L; Askew R; Walker J; Stephen J; Robertson-Artwork A
Home Healthc Nurse; 2012 Mar; 30(3):172-83; quiz 183-5. PubMed ID: 22391660
[TBL] [Abstract][Full Text] [Related]
10. Palliative care teams on the prairie: composition, perceived challenges & opportunities.
Schrader SL; Nelson ML; Eidsness LM
S D Med; 2007 Apr; 60(4):147-9, 151-3. PubMed ID: 17555150
[TBL] [Abstract][Full Text] [Related]
11. Sickle cell hospital unit: a disease-specific model.
Adams-Graves P; Ostric EJ; Martin M; Richardson P; Lewis JB
J Healthc Manag; 2008; 53(5):305-15; discussion 316-7. PubMed ID: 18856136
[TBL] [Abstract][Full Text] [Related]
12. Assessing the quality of life of children with sickle cell anaemia using self-, parent-proxy, and health care professional-proxy reports.
Constantinou C; Payne N; Inusa B
Br J Health Psychol; 2015 May; 20(2):290-304. PubMed ID: 24758574
[TBL] [Abstract][Full Text] [Related]
13. End-of-life in adults with congenital heart disease: a call for early communication.
Tobler D; Greutmann M; Colman JM; Greutmann-Yantiri M; Librach LS; Kovacs AH
Int J Cardiol; 2012 Mar; 155(3):383-7. PubMed ID: 21094550
[TBL] [Abstract][Full Text] [Related]
14. Experiences of African Americans Living With Sickle Cell Disease.
Wickersham KE; Dawson RM; Becker KP; Everhart KC; Miles HS; Schultz BE; Tucker CM; Wright PJ; Jenerette CM
J Transcult Nurs; 2022 May; 33(3):334-345. PubMed ID: 35094624
[TBL] [Abstract][Full Text] [Related]
15. Development and evaluation of a palliative care curriculum for cystic fibrosis healthcare providers.
Linnemann RW; O'Malley PJ; Friedman D; Georgiopoulos AM; Buxton D; Altstein LL; Sicilian L; Lapey A; Sawicki GS; Moskowitz SM
J Cyst Fibros; 2016 Jan; 15(1):90-5. PubMed ID: 25817162
[TBL] [Abstract][Full Text] [Related]
16. Health related quality of life and perception of stigmatisation in adolescents living with sickle cell disease in Nigeria: A cross sectional study.
Adeyemo TA; Ojewunmi OO; Diaku-Akinwumi IN; Ayinde OC; Akanmu AS
Pediatr Blood Cancer; 2015 Jul; 62(7):1245-51. PubMed ID: 25810358
[TBL] [Abstract][Full Text] [Related]
17. Use of a depression and sleep impairment treatment guideline to improve quality of life for patients with sickle cell disease.
Simo SM; Siela D
Int J Palliat Nurs; 2018 May; 24(5):246-255. PubMed ID: 29792764
[TBL] [Abstract][Full Text] [Related]
18. Sickle cell disease patients with and without extremely high hospital use: pain, opioids, and coping.
Brown SE; Weisberg DF; Balf-Soran G; Sledge WH
J Pain Symptom Manage; 2015 Mar; 49(3):539-47. PubMed ID: 25057985
[TBL] [Abstract][Full Text] [Related]
19. Pain management in sickle cell disease: palliative care begins at birth?
Benjamin L
Hematology Am Soc Hematol Educ Program; 2008; ():466-74. PubMed ID: 19074128
[TBL] [Abstract][Full Text] [Related]
20. Pain management and quality of life in sickle cell disease.
Howard J; Thomas VJ; Rawle HM
Expert Rev Pharmacoecon Outcomes Res; 2009 Aug; 9(4):347-52. PubMed ID: 19670995
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]