4.4 Article

Chronic Pain and Neuropathy Following Adjuvant Chemotherapy

期刊

PAIN MEDICINE
卷 19, 期 9, 页码 1813-1824

出版社

OXFORD UNIV PRESS
DOI: 10.1093/pm/pnx231

关键词

Chemotherapy-Induced Neuropathy; Pain; Oxaliplatin; Docetaxel; Quantitative Sensory Testing (QST); Psychological Functioning

资金

  1. Innovative Medicines Initiative Joint Undertaking, from the European Union's Seventh Framework Programme (FP7/2007-2013) [115007]
  2. EFPIA companies
  3. Radiumstationens Forskningsfond
  4. Danish Diabetes Academy - Novo Nordisk Foundation
  5. Astellas
  6. Region Midtjyllands Sundhedsvidenskabelige Forskningsfond
  7. Frits, Georg og Marie Cecilie Gluds Legat

向作者/读者索取更多资源

Objective. To determine symptoms and characteristics of chronic sensory neuropathy in patients treated with oxaliplatin and docetaxel, including patterns of somatosensory abnormalities, pain descriptors, and psychological functioning. Design. A retrospective cross-sectional study. Setting. A chronic pain research center. Subjects. Thirty-eight patients with chronic peripheral pain and/or dysesthesia following chemotherapy. Methods. Sensory profiles, psychological functioning, and quality of life were assessed using standardized questionnaires. In addition, standardized quantitative sensory testing and nerve conduction studies were carried out. Results. The sensory profiles and clinical symptoms were very similar in the two groups. Pricking, numbness, and burning were common descriptors in both groups, and the predominant finding was sensory loss to A beta-mediated sensory modalities with decreased mechanical and vibration detection thresholds. A high frequency of abnormalities in thermal sensory limen and the presence of paradoxical heat sensation seem to be sensitive markers of small fiber loss. Both groups had mainly sensory, axonal large fiber or mixed fiber polyneuropathy, which tended to be most severe in the oxaliplatin group. Conclusions. Both oxaliplatin-induced and docetaxel-induced polyneuropathies represent a significant problem that affects the daily life of the patients. Our results, defining the somatosensory phenotype, can improve the understanding of the pathophysiological mechanisms useful for future studies in the tailored treatment of prevention of chemotherapy- induced peripheral neuropathy and pain.

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