| PATIENT EDUCATION AND COUNSELING | 卷:88 |
| Endometrial cancer survivors are unsatisfied with received information about diagnosis, treatment and follow-up: A study from the population-based PROFILES registry | |
| Article | |
| Nicolaije, Kim Agnes Helma1  Husson, Olga1  Ezendam, Nicole Paulina Maria1  Vos, Maria Caroline2  Kruitwagen, Rutgerus Franciscus Petrus Maria3,4  Lybeert, Marnix Lodewijk Maria5  van de Poll-Franse, Lonneke Veronique1  | |
| [1] Tilburg Univ, CoRPS Ctr Res Psychol Somat Dis, Dept Med Psychol & Neuropsychol, NL-5000 LE Tilburg, Netherlands | |
| [2] St Elizabeth Hosp, Dept Obstet & Gynecol, Tilburg, Netherlands | |
| [3] Maastricht Univ Med Ctr, Dept Gynecol, Maastricht, Netherlands | |
| [4] Maastricht Univ Med Ctr, GROW Sch Oncol & Dev Biol, Maastricht, Netherlands | |
| [5] Catharina Hosp, Dept Radiotherapy, Eindhoven, Netherlands | |
| 关键词: Endometrial cancer; Cancer survivors; Information provision; Information satisfaction; Population-based; PROFILES registry; | |
| DOI : 10.1016/j.pec.2012.05.002 | |
| 来源: Elsevier | |
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【 摘 要 】
Objective: To evaluate perceived level of and satisfaction with information received by endometrial cancer survivors, and to identify associations with socio-demographic and clinical characteristics. Methods: All patients diagnosed with endometrial cancer between 1998 and 2007, registered in the Eindhoven Cancer Registry, received a questionnaire including EORTC-QLQ-INFO25. Results: Seventy-seven percent responded (n = 742). Most patients indicated receiving quite a bit information about their disease and medical tests. However, most patients were not (54%) or a little (24%) informed about the cause of their disease, and possible side effects (36%; 27%). Especially information about additional help, rehabilitation, psychological assistance, and expected results on social and sexual life was lacking. Five percent was not or a little (36%) satisfied. Four percent found the information not or a little (35%) helpful. Fifteen percent preferred more information. Younger age, more recent diagnosis, radiotherapy, absence of comorbidities, having a partner, having received written information, and higher educational level were associated with higher perceived information receipt. Conclusion: Many endometrial cancer survivors are unsatisfied with received information. Several areas of information provision are experienced as insufficient. Practice implications: More patient-tailored information is probably needed to provide optimal information. Implementation of Survivorship Care Plans might be a way to achieve this. (C) 2012 Elsevier Ireland Ltd. All rights reserved.
【 授权许可】
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【 预 览 】
| Files | Size | Format | View |
|---|---|---|---|
| 10_1016_j_pec_2012_05_002.pdf | 389KB |
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