Your browser doesn't support javascript.
loading
The Perspective of a Breast Cancer Patient: A Survey Study Assessing Needs and Expectations.
Prakash, Amulya; Sardar, Muhammad; Shaikh, Nasreen; Inkollu, Sindhura; Danish, Mary; Sharon, David J; Goldberg, Shira.
Afiliação
  • Prakash A; Internal Medicine, Monmouth Medical Center, Long Branch, USA.
  • Sardar M; Internal Medicine, Monmouth Medical Center, Long Branch, USA.
  • Shaikh N; Internal Medicine, Monmouth Medical Center, Long Branch, USA.
  • Inkollu S; Internal Medicine, Monmouth Medical Center, Long Branch, USA.
  • Danish M; Oncology, Monmouth Medical Center, Long Branch, USA.
  • Sharon DJ; Oncology, Monmouth Medical Center, Leon Hess Cancer Center, Long Branch, USA.
  • Goldberg S; Hospice and Palliative Care, Monmouth Medical Center, Long Branch, USA.
Cureus ; 12(7): e9171, 2020 Jul 13.
Article em En | MEDLINE | ID: mdl-32766015
ABSTRACT
Background Patient satisfaction is one of the key indicators of health care quality. We aim to identify patient's needs and expectations in a breast cancer clinic to provide patient-centered care and better overall satisfactionMethods A 17-item survey was administered to 110 patients at a breast cancer clinic. The survey was designed after a thorough literature review and approved by an oncologist and a palliative care physician.  Results Self-reported knowledge about the disease was reported adequate by 90.9% of our patients yet only 55.45% of our patients could identify the stage of their cancer. More education was desired by 32.7% of patients including various treatment options (29%), common complications (24.5%), prognosis (26.3%) and risk factors (11.8%). The majority of our patients were having some form of cancer-related emotional stress and physical symptoms. The majority of our patients (57.27%) wanted their oncologist to address social/emotional issues and 25.45% felt the need for more focus on physical symptoms in their subsequent visits. End-of-life (EoL) care discussions were considered an integral component of overall care by 29% of our patients. Components of EoL care discussions that patients stated they could benefit from included prognosis (27.27%), life expectancy (29%), the treatment effect on the quality of life (22.7%), palliative care (9%), hospice (10.9%), advance directives (11.8%), and family involvement in medical decision-making (13.6%). There was a difference noted regarding their EoL care discussion based on the stage of cancer. Patients with early-stage disease wanted their oncologists to decide on the frequency of this discussion (72.7%). Patients with advanced disease wanted EoL care discussion to be done more frequently as initiated by them or their oncologist or if there's a change in the treatment plan.  Conclusions A discrepancy between self-reported and actual knowledge in breast cancer patients emphasizes the need for patient education. Most patients rely on their oncologists for their diagnosis-related emotional and social issues. Surprisingly, more than a quarter of our patients consider EoL care discussions important even though the majority of our patients were healthy and having stage I and II disease.
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article