A novel lozenge containing bupivacaine as topical alleviation of oral mucositis pain in patients with head and neck cancer: a pilot study

TY - JOUR

T1 - A novel lozenge containing bupivacaine as topical alleviation of oral mucositis pain in patients with head and neck cancer

T2 - a pilot study

AU - Mogensen, Stine

AU - Treldal, Charlotte

AU - Sveinsdóttir, Kolbrún

AU - Jensen, Kenneth

AU - Kristensen, Claus A

AU - Mogensen, Torben S

AU - Petersen, Janne

AU - Andersen, Ove

PY - 2016/9/1

Y1 - 2016/9/1

N2 - Introduction: Oral mucositis induces severe oral pain in head and neck cancer patients. There is at this point no effective pain treatment without considerable side effects. Objective: The aim of this pilot study was to investigate pain reduction in oral cavity and pharynx in patients with head and neck cancer (HNC) with oral mucositis, the location of anesthetic effect, and duration of pain relief, after a single-dose administration of a 25 mg bupivacaine lozenge. Methods: Ten patients with HNC suffering from oral mucositis pain were included. The patients assessed pain in the oral cavity and pharynx on a visual analogue scale (from 0 to 100 mm) at baseline and up to 3 hours after the lozenge was dissolved. Possible adverse events were registered. Results: The baseline pain was 51 mm (range: 30–73 mm) in the oral cavity and 58 mm (range: 35–70 mm) in the pharynx. When the lozenge was dissolved, both oral (227 mm; range: 23 to 252 mm; P 5 0.0003) and pharynx pain (220 mm; range: 23 to 245 mm; P 5 0.008) were significantly reduced. After 180 minutes, the mean reduction in pain was significant in the oral cavity (218 mm; range: 28 to 230 mm; P, 0.0001) but not in the pharynx (28 mm; range: 14 to 223 mm; P 5 0.12). No adverse events were observed. Conclusion: The results indicate that the bupivacaine lozenge has a clinically significant and long-lasting pain-relieving effect on pain because of oral mucositis in patients with HNC.

AB - Introduction: Oral mucositis induces severe oral pain in head and neck cancer patients. There is at this point no effective pain treatment without considerable side effects. Objective: The aim of this pilot study was to investigate pain reduction in oral cavity and pharynx in patients with head and neck cancer (HNC) with oral mucositis, the location of anesthetic effect, and duration of pain relief, after a single-dose administration of a 25 mg bupivacaine lozenge. Methods: Ten patients with HNC suffering from oral mucositis pain were included. The patients assessed pain in the oral cavity and pharynx on a visual analogue scale (from 0 to 100 mm) at baseline and up to 3 hours after the lozenge was dissolved. Possible adverse events were registered. Results: The baseline pain was 51 mm (range: 30–73 mm) in the oral cavity and 58 mm (range: 35–70 mm) in the pharynx. When the lozenge was dissolved, both oral (227 mm; range: 23 to 252 mm; P 5 0.0003) and pharynx pain (220 mm; range: 23 to 245 mm; P 5 0.008) were significantly reduced. After 180 minutes, the mean reduction in pain was significant in the oral cavity (218 mm; range: 28 to 230 mm; P, 0.0001) but not in the pharynx (28 mm; range: 14 to 223 mm; P 5 0.12). No adverse events were observed. Conclusion: The results indicate that the bupivacaine lozenge has a clinically significant and long-lasting pain-relieving effect on pain because of oral mucositis in patients with HNC.

U2 - 10.1097/PR9.0000000000000571

DO - 10.1097/PR9.0000000000000571

M3 - Journal article

SN - 2471-2531

VL - 1

SP - 1

EP - 5

JO - Pain Reports

JF - Pain Reports

IS - 3

M1 - e571

ER -