| Literature DB >> 24814100 |
Kathleen A Griffith1, Susan G Dorsey, Cynthia L Renn, Shijun Zhu, Mary E Johantgen, David R Cornblath, Andreas A Argyriou, Guido Cavaletti, Ingemar S J Merkies, Paola Alberti, Tjeerd J Postma, Emanuela Rossi, Barbara Frigeni, Jordi Bruna, Roser Velasco, Haralabos P Kalofonos, Dimitri Psimaras, Damien Ricard, Andrea Pace, Edvina Galie, Chiara Briani, Chiara Dalla Torre, Catharina G Faber, Roy I Lalisang, Willem Boogerd, Dieta Brandsma, Susanne Koeppen, Joerg Hense, Dawn J Storey, Simon Kerrigan, Angelo Schenone, Sabrina Fabbri, Maria Grazia Valsecchi.
Abstract
Chemotherapy-induced peripheral neuropathy (CIPN) lacks standardized clinical measurement. The objective of the current secondary analysis was to examine data from the CIPN Outcomes Standardization (CI-PeriNomS) study for associations between clinical examinations and neurophysiological abnormalities. Logistic regression estimated the strength of associations of vibration, pin, and monofilament examinations with lower limb sensory and motor amplitudes. Examinations were classified as normal (0), moderately abnormal (1), or severely abnormal (2). Among 218 participants, those with class 1 upper extremity (UE) and classes 1 or 2 lower extremity (LE) monofilament abnormality were 2.79 (95% confidence interval [CI]: 1.28-6.07), 3.49 (95%CI: 1.61-7.55), and 4.42 (95%CI: 1.35-14.46) times more likely to have abnormal sural nerve amplitudes, respectively, compared to individuals with normal examinations. Likewise, those with class 2 UE and classes 1 or 2 LE vibration abnormality were 8.65 (95%CI: 1.81-41.42), 2.54 (95%CI: 1.19-5.41), and 7.47 (95%CI: 2.49-22.40) times more likely to have abnormal sural nerve amplitudes, respectively, compared to participants with normal examinations. Abnormalities in vibration and monofilament examinations are associated with abnormal sural nerve amplitudes and are useful in identifying CIPN.Entities:
Keywords: assessment; chemotherapy; neurophysiology; peripheral neuropathy
Mesh:
Year: 2014 PMID: 24814100 PMCID: PMC4175057 DOI: 10.1111/jns5.12064
Source DB: PubMed Journal: J Peripher Nerv Syst ISSN: 1085-9489 Impact factor: 3.494