Perceived need for information of patients with haematological malignancies: a literature review

被引:28
作者
Rood, Janneke A. J. [1 ,2 ]
Eeltink, Corien M. [3 ]
van Zuuren, Florence J. [4 ]
Verdonck-de Leeuw, Irma M. [5 ]
Huijgens, Peter C. [3 ]
机构
[1] Vrije Univ Amsterdam, Med Ctr, Dept Haematol, Alkmaar, Netherlands
[2] Med Ctr, Dept Internal Med, Alkmaar, Netherlands
[3] Vrije Univ Amsterdam, Med Ctr, Dept Haematol Pk 2 Br 018, NL-1007 MB Amsterdam, Netherlands
[4] Univ Amsterdam, Dept Clin Psychol, NL-1018 WB Amsterdam, Netherlands
[5] Vrije Univ Amsterdam, Dept Clin Psychol 1D116, Amsterdam, Netherlands
关键词
haematological malignancies; information need; leukaemia; lymphoma; multiple myeloma; QUALITY-OF-LIFE; CANCER-PATIENTS; LYMPHOMA SURVIVORS; DECISION-MAKING; SEEKING BEHAVIOR; RADIATION; EDUCATION; OLDER; PRIORITIES; PROVISION;
D O I
10.1111/jocn.12630
中图分类号
R47 [护理学];
学科分类号
1011 ;
摘要
Aims and objectives. To provide insight into the perceived need for information of patients with haematological malignancies. Background. Providing timely and accurate information to patients diagnosed with a haematological malignancy is a challenge in clinical practice; treatment often has to start promptly, with little time to inform patients. Design. Literature review. Methods. A comprehensive literature search was conducted from all available literature to May 2013 in the databases: Cumulative Index to Nursing and Allied Health Literature, PsycINFO and PubMed (Medline). Relevant studies were reviewed regarding the perceived need for information on various topics, sources of information and satisfaction with information provided. Results. The initial search revealed 215 articles, fourteen of which were relevant. Patients need basic information on the disease (diagnosis and diagnostics), treatment (various treatment options, side effects and duration), prognosis (curability and prolonging life) and all other topics (recovery, self-care and psychosocial functioning). Need for detailed information varied between studies. Patients expressed a higher need for medical than for psychosocial information. Patients preferred to receive information from their doctors the most, followed by nurses. Most studies described patients' satisfaction with the information provided. Conclusion. Based on the limited number of data available, medical information is for patients of higher priority compared to psychosocial information. Patients need basic information on diagnosis, treatment, prognosis and all other topics. Need for detailed information varied between studies. Patients were satisfied with the provided information, preferably offered by doctors and nurses. Relevance to clinical practice. The perceived need for information and satisfaction with the information provided differs strongly between patients. In clinical practice, more attention is needed for information tailored to the patient, taking into account important moderating factors such as age, type of cancer, time since diagnosis, treatment modality and coping style.
引用
收藏
页码:353 / 369
页数:17
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