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1.
Neuroendocrinology ; 108(1): 26-36, 2019.
Article in English | MEDLINE | ID: mdl-30282083

ABSTRACT

Recently, the European Neuroendocrine Tumor Society (ENETS) held working sessions composed of members of the advisory board and other neuroendocrine neoplasm (NEN) experts to attempt to identify unmet needs in NENs in different locations or with advanced/poorly differentiated NENs. This report briefly summarizes the main proposed areas of unmet needs in patients with functional and nonfunctional pancreatic NENs.


Subject(s)
Biomedical Research/trends , Disease Management , Neuroendocrine Tumors , Pancreatic Neoplasms , Biomarkers, Tumor/metabolism , Humans , Neuroendocrine Tumors/diagnosis , Neuroendocrine Tumors/drug therapy , Neuroendocrine Tumors/metabolism , Pancreatic Neoplasms/diagnosis , Pancreatic Neoplasms/drug therapy , Pancreatic Neoplasms/metabolism , Prognosis
2.
Trials ; 10: 84, 2009 Sep 14.
Article in English | MEDLINE | ID: mdl-19751500

ABSTRACT

BACKGROUND: ICU stay is often associated with negative experiences for the individual patient. Many patients are disabled and their communication is restricted during the ICU stay. Specific information on procedures, sensations and coping behavior are thought to reduce anxiety on the ICU. Until now information programs to reduce anxiety were mainly delivered preoperatively, completely neglecting informational needs of non-elective ICU patients. METHODS: The trial is designed as a prospective multicenter randomized controlled trial in the cities of Marburg, Halle and Stuttgart. Elective and non-elective ICU patients will be included. The trial includes an intervention and a control group on the ICU. The control group receives a trivial conversation without any ICU-specific information. The intervention group receives an information program with specific procedural, sensory and coping information about their ICU stay. Both conversations take place in the ICU and are planned to take about 10 minutes. DISCUSSION: In contrast to former trials on information programs on the ICU-stay our intervention will take place in the ICU itself. This approach will ensure to compensate for memory effects due to anesthesia or preoperative stress. Further the results will be applicable to non-elective ICU-patients. TRIAL REGISTRATION: ClinicalTrials NCT00764933.


Subject(s)
Anxiety/prevention & control , Intensive Care Units , Clinical Protocols , Humans
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