Literature DB >> 20804884

Sickle cell disease: an opportunity for palliative care across the life span.

Diana J Wilkie1, Bonnye Johnson, A Kyle Mack, Richard Labotka, Robert E Molokie.   

Abstract

Sickle cell disease is a chronic illness that affects patients physically and emotionally and can do so at an early age. An ecological model of palliative care that involves improved communication among the health care team, patients, and their families can be beneficial. Open and honest communication regarding advance care planning, disease management, relief of pain and other symptoms, and bereavement and grief are all important for the patient, family, and health care team. Given the multiple acute and chronic complications of sickle cell disease, an approach to care that is holistic and comprehensive may help to improve a patient's biologic function and the perceived health, functional status, and quality of life of the patient and family.
Copyright © 2010 Elsevier Ltd. All rights reserved.

Entities:  

Mesh:

Year:  2010        PMID: 20804884      PMCID: PMC2932707          DOI: 10.1016/j.cnur.2010.03.003

Source DB:  PubMed          Journal:  Nurs Clin North Am        ISSN: 0029-6465            Impact factor:   1.208


  83 in total

Review 1.  Secondary iron overload.

Authors:  J P Kushner; J P Porter; N F Olivieri
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2001

Review 2.  The promise of a good death.

Authors:  E J Emanuel; L L Emanuel
Journal:  Lancet       Date:  1998-05       Impact factor: 79.321

Review 3.  Leg ulcers in sickle cell disease.

Authors:  J R Eckman
Journal:  Hematol Oncol Clin North Am       Date:  1996-12       Impact factor: 3.722

4.  Pain management in sickle cell disease: palliative care begins at birth?

Authors:  Lennette Benjamin
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2008

5.  Discontinuing penicillin prophylaxis in children with sickle cell anemia. Prophylactic Penicillin Study II.

Authors:  J M Falletta; G M Woods; J I Verter; G R Buchanan; C H Pegelow; R V Iyer; S T Miller; C T Holbrook; T R Kinney; E Vichinsky
Journal:  J Pediatr       Date:  1995-11       Impact factor: 4.406

6.  Incidence of invasive pneumococcal disease among individuals with sickle cell disease before and after the introduction of the pneumococcal conjugate vaccine.

Authors:  Natasha B Halasa; Sadhna M Shankar; Thomas R Talbot; Patrick G Arbogast; Ed F Mitchel; Winfred C Wang; William Schaffner; Allen S Craig; Marie R Griffin
Journal:  Clin Infect Dis       Date:  2007-04-18       Impact factor: 9.079

7.  Pain management and symptoms of substance dependence among patients with sickle cell disease.

Authors:  James Elander; Joanne Lusher; David Bevan; Paul Telfer
Journal:  Soc Sci Med       Date:  2003-11       Impact factor: 4.634

8.  Priapism associated with the sickle cell hemoglobinopathies: prevalence, natural history and sequelae.

Authors:  J E Fowler; M Koshy; M Strub; S K Chinn
Journal:  J Urol       Date:  1991-01       Impact factor: 7.450

9.  Variations in pain, sleep, and activity during hospitalization in children with cancer.

Authors:  Eufemia Jacob; Joy Hesselgrave; Gennaro Sambuco; Marilyn Hockenberry
Journal:  J Pediatr Oncol Nurs       Date:  2007 Jul-Aug       Impact factor: 1.636

10.  An Ethical Argument for Integrated Palliative Care.

Authors:  Shay Beider
Journal:  Evid Based Complement Alternat Med       Date:  2005-04-27       Impact factor: 2.629

View more
  8 in total

1.  A QST-based Pain Phenotype in Adults With Sickle Cell Disease: Sensitivity and Specificity of Quality Descriptors.

Authors:  Brenda W Dyal; Miriam O Ezenwa; Saunjoo L Yoon; Roger B Fillingim; Yingwei Yao; Judith M Schlaeger; Marie L Suarez; Zaijie J Wang; Robert E Molokie; Diana J Wilkie
Journal:  Pain Pract       Date:  2019-10-18       Impact factor: 3.183

2.  Differences in Sensory Pain, Expectation, and Satisfaction Reported by Outpatients with Cancer or Sickle Cell Disease.

Authors:  Miriam O Ezenwa; Robert E Molokie; Zaijie Jim Wang; Yingwei Yao; Marie L Suarez; Brenda Dyal; Khulud Abudawood; Diana J Wilkie
Journal:  Pain Manag Nurs       Date:  2018-03-01       Impact factor: 1.929

3.  A Mixed-Methods Study of Pain-related Quality of Life in Sickle Cell Vaso-Occlusive Crises.

Authors:  Richard J Lin; Arthur T Evans; Kerri Wakeman; Michelle Unterbrink
Journal:  Hemoglobin       Date:  2015-06-26       Impact factor: 0.849

4.  Tract specific analysis in patients with sickle cell disease.

Authors:  Yaqiong Chai; Julie Coloigner; Xiaoping Qu; Soyoung Choi; Adam Bush; Matt Borzage; Chau Vu; Natasha Lepore; John Wood
Journal:  Proc SPIE Int Soc Opt Eng       Date:  2015-12-22

5.  Pattern of referral of noncancer patients to palliative care in the eastern province of saudi arabia.

Authors:  Hafez M Ghanem; Rawabi M Shaikh; Ahmad M Abou Alia; Amani S Al-Zayir; Samy A Alsirafy
Journal:  Indian J Palliat Care       Date:  2011-09

Review 6.  A biopsychosocial model for the management of patients with sickle-cell disease transitioning to adult medical care.

Authors:  Lori E Crosby; Charles T Quinn; Karen A Kalinyak
Journal:  Adv Ther       Date:  2015-04-02       Impact factor: 3.845

7.  Quality of care in sickle cell disease: Cross-sectional study and development of a measure for adults reporting on ambulatory and emergency department care.

Authors:  Christian T Evensen; Marsha J Treadwell; San Keller; Roger Levine; Kathryn L Hassell; Ellen M Werner; Wally R Smith
Journal:  Medicine (Baltimore)       Date:  2016-08       Impact factor: 1.889

8.  Outcome of cranial surgery in Nigerian patients with hemoglobinopathies: A retrospective study.

Authors:  Oluwakemi A Badejo; Olusola K Idowu; James A Balogun; Wuraola A Shokunbi; Simbo D Amanor-Boadu; Matthew T Shokunbi
Journal:  Surg Neurol Int       Date:  2019-02-06
  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.