Screening for symptom burden and supportive needs of patients with glioblastoma and brain metastases and their caregivers in relation to their use of specialized palliative care

被引:21
|
作者
Seekatz, Bettina [1 ,2 ]
Lukasczik, Matthias [2 ]
Loehr, Mario [3 ]
Ehrmann, Katja [1 ,2 ]
Schuler, Michael [2 ]
Kessler, Almuth F. [3 ]
Neuderth, Silke [4 ]
Ernestus, Ralf-Ingo [3 ]
van Oorschot, Birgitt [1 ]
机构
[1] Univ Hosp Wurzburg, Interdisciplinary Ctr Palliat Med, Wurzburg, Germany
[2] Univ Wurzburg, Dept Med Psychol Med Sociol & Rehabil Sci, Wurzburg, Germany
[3] Univ Hosp Wurzburg, Dept Neurosurg, Wurzburg, Germany
[4] Univ Appl Sci Wurzburg Schweinfurt, Fac Appl Social Sci, Wurzburg, Germany
关键词
Palliative care; Glioblastoma; Brain metastases; Caregivers; Symptomscreening; Supportive care needs; OF-THE-LITERATURE; CANCER-PATIENTS; DISTRESS THERMOMETER; ASSESSMENT SCALE; VALIDATION; TUMORS; LIFE; IDENTIFICATION; PROJECT;
D O I
10.1007/s00520-017-3687-7
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose Patients with brain tumors have a high symptom burden and multiple supportive needs. Needs of caregivers are often unattended. This study aims to determine screening-based symptom burden and supportive needs of patients and caregivers with regard to the use of specialized palliative care (SPC). Methods Seventy-nine patients with glioblastoma and brain metastases and 46 caregivers were screened with standardized questionnaires following diagnosis and 2 months later. The screening assessed symptom burden, quality of life (QoL), distress, and supportive needs. Results The most relevant symptoms were drowsiness, tiredness, and low well-being (53-58%). The most prevalent patient supportive needs were the need for information about available resources, the illness, and possible lifestyle changes (50-56%). The most prevalent caregiver needs were information about the illness, lifestyle changes, and about available resources (56-74%). Patients who received SCP and their caregivers had higher symptom burden and supportive needs than those without SPC. They reported moderate improvement in pain, distress, and QoL, while patients without SPC also improved their QoL, but had small to moderate deteriorations in pain, drowsiness, nauseas, well-being, and other problems. Distress of caregivers with SPC improved with moderate to large effect sizes but still was on a high level and remained stable for those without SPC. Conclusions Symptom burden and supportive needs were high, but even more caregivers than patients expressed high distress and supportive needs. SPC appears to reach the target group, both patients and caregivers with elevated symptom burden. Targeted interventions are needed to improve tiredness and drowsiness.
引用
收藏
页码:2761 / 2770
页数:10
相关论文
共 46 条
  • [41] The impact of automated screening with Edmonton Symptom Assessment System (ESAS) on health-related quality of life, supportive care needs, and patient satisfaction with care in 268 ambulatory cancer patients
    Diplock, Benjamin D.
    McGarragle, Kaitlin M. C.
    Mueller, Willem A.
    Haddad, Sana
    Ehrlich, Rachel
    Yoon, Dong-Hyun A.
    Cao, Xingshan
    Al-Allaq, Yaseen
    Karanicolas, Paul
    Fitch, Margaret I.
    Myers, Jeff
    Mitchell, Alex J.
    Ellis, Janet W. M.
    SUPPORTIVE CARE IN CANCER, 2019, 27 (01) : 209 - 218
  • [42] Determining the cut-off value for the Minimal Documentation System (MIDOS2) screening tool to initiate specialized palliative care based on patient's subjective need for palliative support and symptom burden in inpatients with advanced cancer
    Heinzelmann, Anna
    Tewes, Mitra
    Mueller, Sandy
    Sure, Ulrich
    Herrmann, Ken
    Schadendorf, Dirk
    Warnecke, Eva
    Rausch, Raya
    Skoda, Eva-Maria
    Salvador Comino, Maria Rosa
    JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY, 2024, 150 (07)
  • [43] Care needs level in long-term care insurance system and family caregivers' self-perceived time-dependent burden in patients with home palliative care for cancer: a cross-sectional study
    Otsuki, Naoko
    Yamamoto, Ryohei
    Sakaguchi, Yukihiro
    Masukawa, Kento
    Morita, Tatsuya
    Kizawa, Yoshiyuki
    Tsuneto, Satoru
    Shima, Yasuo
    Fukui, Sakiko
    Miyashita, Mitsunori
    SUPPORTIVE CARE IN CANCER, 2022, 30 (02) : 1587 - 1596
  • [44] Care needs level in long-term care insurance system and family caregivers’ self-perceived time-dependent burden in patients with home palliative care for cancer: a cross-sectional study
    Naoko Otsuki
    Ryohei Yamamoto
    Yukihiro Sakaguchi
    Kento Masukawa
    Tatsuya Morita
    Yoshiyuki Kizawa
    Satoru Tsuneto
    Yasuo Shima
    Sakiko Fukui
    Mitsunori Miyashita
    Supportive Care in Cancer, 2022, 30 : 1587 - 1596
  • [45] Patient-Reported Symptom Burden and Supportive Care Needs of Patients With Stage II-III Colorectal Cancer During and After Adjuvant Systemic Treatment: A Real-World Evidence Study
    Cuthbert, Colleen A.
    O'Sullivan, Dylan E.
    Boyne, Devon J.
    Brenner, Darren R.
    Cheung, Winson Y.
    JCO ONCOLOGY PRACTICE, 2023, 19 (03) : 142 - +
  • [46] Use of Nursing Support Among Nurses for Caregiver Burden in Family Caregivers of Terminally Ill Patients with Cancer in Palliative Care Units in Japan: Multisite Cross-Sectional Study
    Kajiwara, Kohei
    Kobayashi, Masamitsu
    Nakano, Kimiko
    Kanno, Yusuke
    Morikawa, Miharu
    Matsuda, Yoshinobu
    Kako, Jun
    PALLIATIVE MEDICINE REPORTS, 2024, 5 (01): : 425 - 429