Literature DB >> 26626003

The illness of women and men with sickle cell disease: a Grounded Theory study.

Rosa Cândida Cordeiro1, Silvia Lúcia Ferreira2, Ane Caroline da Cruz Santos2.   

Abstract

OBJECTIVE: To understand the meanings given by women and men with sickle cell disease on the illness experience.
METHOD: Analytical study with a qualitative approach, conducted with 17 adults with sickle cell disease using the Theory Based on Data, or Grounded Theory, as theoretical-methodological referential. Data were collected between the years of 2012 and 2013, in an individual in-depth interview. All the interviews were recorded and analyzed according to the Grounded Theory comparative analysis technique.
RESULTS: Data show four categories which group the experience of illness, the feelings experienced and the path to living with sickle cell disease.
CONCLUSIONS: It was possible to understand that the experience was built by a process in which these people redefined the meaning of their lives, applying new directions to life and to care regarding the experience of the illness. In the context of chronic disease, the nurse's care is also seen in this study as a foundation, providing attention, directions, and guidance through the required confrontations. Understanding the experience lived by these people, it is possible to enlarge the dimensions and the essence of nursing care required throughout life.

Entities:  

Mesh:

Year:  2015        PMID: 26626003      PMCID: PMC4664012          DOI: 10.1590/0104-1169.0594.2656

Source DB:  PubMed          Journal:  Rev Lat Am Enfermagem        ISSN: 0104-1169


  13 in total

1.  Consolidated criteria for reporting qualitative research (COREQ): a 32-item checklist for interviews and focus groups.

Authors:  Allison Tong; Peter Sainsbury; Jonathan Craig
Journal:  Int J Qual Health Care       Date:  2007-09-14       Impact factor: 2.038

2.  Grounded theory--conceptual and operational aspects: a method possible to be applied in nursing research.

Authors:  Claudia de Carvalho Dantas; Joséte Luzia Leite; Suzinara Beatriz Soares de Lima; Marluci Andrade Conceição Stipp
Journal:  Rev Lat Am Enfermagem       Date:  2009 Jul-Aug

3.  The impact of gender roles on health.

Authors:  María del Pilar Sánchez-López; Isabel Cuellar-Flores; Virginia Dresch
Journal:  Women Health       Date:  2012

Review 4.  Psychosocial treatments in pain management of sickle cell disease.

Authors:  LeKisha Y Edwards; Christopher L Edwards
Journal:  J Natl Med Assoc       Date:  2010-11       Impact factor: 1.798

5.  Attitudes toward patients with sickle cell disease in a multicenter sample of emergency department providers.

Authors:  Caroline E Freiermuth; Carlton Haywood; Susan Silva; David M Cline; Mariam Kayle; Dori Sullivan; Victoria Thornton; Paula Tanabe
Journal:  Adv Emerg Nurs J       Date:  2014 Oct-Dec

6.  Perceived discrimination in health care is associated with a greater burden of pain in sickle cell disease.

Authors:  Carlton Haywood; Marie Diener-West; John Strouse; C Patrick Carroll; Shawn Bediako; Sophie Lanzkron; Jennifer Haythornthwaite; Gladys Onojobi; Mary Catherine Beach
Journal:  J Pain Symptom Manage       Date:  2014-04-15       Impact factor: 3.612

7.  Voices of Adults Living with Sickle Cell Disease Pain.

Authors:  Maxine A Adegbola; Donelle M Barnes; Jakki G Opollo; Keela Herr; Jennifer Gray; Ann Marie McCarthy
Journal:  J Natl Black Nurses Assoc       Date:  2012-12

8.  Perceived discrimination, patient trust, and adherence to medical recommendations among persons with sickle cell disease.

Authors:  Carlton Haywood; Sophie Lanzkron; Shawn Bediako; John J Strouse; Jennifer Haythornthwaite; C Patrick Carroll; Marie Diener-West; Gladys Onojobi; Mary Catherine Beach
Journal:  J Gen Intern Med       Date:  2014-09-10       Impact factor: 5.128

9.  Knowledge of family health program practitioners in Brazil about sickle cell disease: a descriptive, cross-sectional study.

Authors:  Ludmila M X Gomes; Magda M Vieira; Tatiana C Reis; Thiago L A Barbosa; Antônio P Caldeira
Journal:  BMC Fam Pract       Date:  2011-08-19       Impact factor: 2.497

10.  Sickle Cell Disease: quality of life in patients with hemoglobin SS and SC disorders.

Authors:  Sônia Aparecida Dos Santos Pereira; Stela Brener; Clareci Silva Cardoso; Anna Bárbara de Freitas Carneiro Proietti
Journal:  Rev Bras Hematol Hemoter       Date:  2013
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