2019
DOI: 10.1007/s00520-019-05023-5
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Assessing risk factors of falls in cancer patients with chemotherapy-induced peripheral neurotoxicity

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Cited by 22 publications
(17 citation statements)
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“…Chemotherapy-induced peripheral neuropathy (CIPN) is one of the most common chemotherapy-induced toxicities; it can manifest in symptoms such as paresthesia, hyperalgesia, and allodynia 2,3 . CIPN can persist long after chemotherapy completion with patients experiencing pain, sensory loss, poor dexterity, and gait disturbance that significantly worsen quality of life, impact daily functions, and increase fall risks [4][5][6][7] . Currently, there are very limited treatment options for CIPN; additional treatments are needed 8 .…”
Section: Introductionmentioning
confidence: 99%
“…Chemotherapy-induced peripheral neuropathy (CIPN) is one of the most common chemotherapy-induced toxicities; it can manifest in symptoms such as paresthesia, hyperalgesia, and allodynia 2,3 . CIPN can persist long after chemotherapy completion with patients experiencing pain, sensory loss, poor dexterity, and gait disturbance that significantly worsen quality of life, impact daily functions, and increase fall risks [4][5][6][7] . Currently, there are very limited treatment options for CIPN; additional treatments are needed 8 .…”
Section: Introductionmentioning
confidence: 99%
“…The chronic form of OXAIPN was defined as a clinical syndrome characterized by a dose-related, persistent (at least two subsequent cycles without a "symptoms free" interval), symmetrical distal painful or non-painful paresthesia and dysesthesia. 15 The incidence and severity of the chronic, cumulative OXAIPN was graded by means of the seven-item composite Total Neuropathy Score-clinical version (TNSc). 16 Briefly, TNSc classified the OXAIPN severity as grade I (scores 1-7); grade II (scores 8-14); grade III (scores 15-21); and grade IV (scores >21), as previously described.…”
Section: Methodsmentioning
confidence: 99%
“…grade 1 OXAIPN in two patients (8%), grade 2 in 19 patients (76%), and grade 3 neuropathy in 4 (16%) patients Worsening of pre-existing OXAIPN was documented in seven (28%) patients and was significantly associated with higher OXA delivered cumulative dose (P < .001). Median TNSc scores following treatment (10; range [4][5][6][7][8][9][10][11][12][13][14][15][16][17][18] were significantly increased (P < .001), when compared to the scores recorded at the end of first line treatment (8; range [2][3][4][5][6][7][8][9][10][11][12]. Rechallenging OXA appears to relatively worsen the severity of existing OXAIPN.…”
mentioning
confidence: 85%
“…Biomarker studies are currently underway to identify genetic predictors for neuropathy development [ 13 ]. Recognition of CIPN is important as approximately 17.2% of patients with CIPN is estimated to have fallen at the completion of chemotherapy [ 15 ]. Both pharmacologic and non-pharmacologic treatment options have been explored in prevention and treatment of CIPN.…”
Section: Multi-organ Compromisementioning
confidence: 99%