Literature DB >> 15857743

Are there phases to the vaso-occlusive painful episode in sickle cell disease?

Eufemia Jacob1, Judith E Beyer, Christine Miaskowski, Marilyn Savedra, Marsha Treadwell, Lori Styles.   

Abstract

The purpose of this study was to describe the pain experience of children with sickle cell disease who were hospitalized for vaso-occlusive painful episodes. The pain experience, and signs and symptoms prior to admission and during hospitalization, are presented in the context of whether there is evidence to support the existence of phases to a vaso-occlusive painful episode. Children were interviewed about the onset of the painful episode and were asked to describe their pain from the day of admission to the day of discharge from the hospital. They were also observed for the absence or presence of signs and symptoms associated with the painful vaso-occlusive episode. Findings from this study provide some evidence to support previous observations related to changes during the evolution of painful episodes that may be occurring in phases (e.g., evolving, inflammatory, resolving), as previously described in adults and children. These phases had different names, although the concepts were similar.

Entities:  

Mesh:

Year:  2005        PMID: 15857743     DOI: 10.1016/j.jpainsymman.2004.07.006

Source DB:  PubMed          Journal:  J Pain Symptom Manage        ISSN: 0885-3924            Impact factor:   3.612


  18 in total

1.  Successful Aging with Sickle Cell Disease: Using Qualitative Methods to Inform Theory.

Authors:  Coretta M Jenerette; Gloria Lauderdale
Journal:  J Theory Constr Test       Date:  2008-04-01

2.  Facilitating pediatric patient-provider communications using wireless technology in children and adolescents with sickle cell disease.

Authors:  Eufemia Jacob; Carol Pavlish; Joana Duran; Jennifer Stinson; Mary Ann Lewis; Lonnie Zeltzer
Journal:  J Pediatr Health Care       Date:  2012-03-24       Impact factor: 1.812

3.  Usability testing of a Smartphone for accessing a web-based e-diary for self-monitoring of pain and symptoms in sickle cell disease.

Authors:  Eufemia Jacob; Jennifer Stinson; Joana Duran; Ankur Gupta; Mario Gerla; Mary Ann Lewis; Lonnie Zeltzer
Journal:  J Pediatr Hematol Oncol       Date:  2012-07       Impact factor: 1.289

4.  Remote monitoring of pain and symptoms using wireless technology in children and adolescents with sickle cell disease.

Authors:  Eufemia Jacob; Joana Duran; Jennifer Stinson; Mary Ann Lewis; Lonnie Zeltzer
Journal:  J Am Assoc Nurse Pract       Date:  2012-07-12       Impact factor: 1.165

5.  Barriers to care and quality of primary care services in children with sickle cell disease.

Authors:  Eufemia Jacob; Courtney Childress; Joana Duran Nathanson
Journal:  J Adv Nurs       Date:  2015-09-15       Impact factor: 3.187

6.  Benchmarking pain outcomes for children with sickle cell disease hospitalized in a tertiary referral pediatric hospital.

Authors:  Abi Vijenthira; Jennifer Stinson; Jeremy Friedman; Lori Palozzi; Anna Taddio; Dennis Scolnik; Charles Victor; Melanie Kirby-Allen; Fiona Campbell
Journal:  Pain Res Manag       Date:  2012 Jul-Aug       Impact factor: 3.037

7.  Health-related stigma in young adults with sickle cell disease.

Authors:  Coretta M Jenerette; Cheryl Brewer
Journal:  J Natl Med Assoc       Date:  2010-11       Impact factor: 1.798

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

Authors:  Diana J Wilkie; Bonnye Johnson; A Kyle Mack; Richard Labotka; Robert E Molokie
Journal:  Nurs Clin North Am       Date:  2010-09       Impact factor: 1.208

9.  Care seeking for pain in young adults with sickle cell disease.

Authors:  Coretta M Jenerette; Cheryl A Brewer; Kenneth I Ataga
Journal:  Pain Manag Nurs       Date:  2013-01-21       Impact factor: 1.929

Review 10.  Endothelin receptors and pain.

Authors:  Alla Khodorova; Jean-Pierre Montmayeur; Gary Strichartz
Journal:  J Pain       Date:  2009-01       Impact factor: 5.820

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