Literature DB >> 15253025

[Desire for information and participation in therapeutic decisions concerning severe diseases, in patients of a university hospital].

André Gulinelli1, Rubens K Aisawa, Sérgio N Konno, Christian V Morinaga, Wagner L Costardi, Rodrigo O Antonio, Rodrigo B Dumarco, Renata M Moino, Márcio Katz, Sandro Giavarotti, Allan P Z Skarbnik, Cyntia S Forcione, Toshio Chiba, Mílton A Martins.   

Abstract

BACKGROUND: The purpose of our study was to evaluate the desire of the patients on being informed about diagnosis of severe diseases, the desire to have their families informed about this situation and to participate in therapeutic decisions.
METHODS: 363 patients (outpatients and inpatients) of a General Internal Medicine division of a University Hospital were interviewed. The questionnaire contained specific questions on their desire to be informed of the diagnosis in case of cancer or AIDS and on their desire to have their families informed as well. Specific questions on whether they wanted to be informed of and participate of the therapeutic discussion process in case of abdominal tumors were also included.
RESULTS: 96.1% of men and 92.6% of women showed the desire of being informed in case of cancer diagnosis and 87.7% of men and 84.2% of women wanted to have their families informed, 94.2% of men and 91% of women wanted to know the diagnosis of AIDS. While 86% of women and 76.6% of men wanted be informed in the case of a diagnosis of an abdominal tumor, only 58.5% of women and 39.6% of men wanted to give their opinion about in the case of different therapeutic alternatives. The desire to participate in therapeutic decisions was significantly lower (p<0.05) in men, people older than 60 years and inpatients.
CONCLUSIONS: Our results showed that the great majority of the population that seeks for medical support in a Brazilian university hospital wishes to be informed on this health condition, even in case of serious illness. In addition, there are intense familiar bonds that make patients want to have their families also informed.

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Year:  2004        PMID: 15253025     DOI: 10.1590/s0104-42302004000100033

Source DB:  PubMed          Journal:  Rev Assoc Med Bras (1992)        ISSN: 0104-4230            Impact factor:   1.209


  4 in total

1.  Quality of life of chronic myeloid leukemia patients in Brazil: ability to work as a key factor.

Authors:  Nelson Hamerschlak; Carmino de Souza; Ana Lúcia Cornacchioni; Ricardo Pasquini; Daniel Tabak; Nelson Spector; Merula Steagall
Journal:  Support Care Cancer       Date:  2014-03-20       Impact factor: 3.603

2.  Considerations for the cross-cultural adaptation of an advance care planning guide for youth with cancer.

Authors:  Marina Noronha Ferraz de Arruda-Colli; Ursula Sansom-Daly; Manoel Antônio Dos Santos; Lori Wiener
Journal:  Clin Pract Pediatr Psychol       Date:  2018-12

3.  In the shadow of bad news - views of patients with acute leukaemia, myeloma or lung cancer about information, from diagnosis to cure or death.

Authors:  Lena Hoff; Ulf Tidefelt; Lars Thaning; Göran Hermerén
Journal:  BMC Palliat Care       Date:  2007-01-24       Impact factor: 3.234

Review 4.  The relation between deaf patients and the doctor.

Authors:  Neuma Chaveiro; Celmo Celeno Porto; Maria Alves Barbosa
Journal:  Braz J Otorhinolaryngol       Date:  2009 Jan-Feb
  4 in total

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