Management of salivary flow in head and neck cancer patients--a systematic review

Oral Oncol. 2008 Nov;44(11):1000-8. doi: 10.1016/j.oraloncology.2008.02.007. Epub 2008 May 16.

Abstract

Altered salivary flow is frequently observed as a result of head and neck cancer (HNC) treatment. Decreased salivation or xerostomia consequent to radiation therapy is the most frequently observed complication resulting in patient discomfort, tooth decay, periodontal disease, and dysphagia. Excessive salivary flow or sialorrhea can be equally troublesome to the patient and their caregivers. It is caused by tumor or treatment-related dysphagia, or due to altered anatomy from oncologic resections of the upper aerodigestive tract, especially the middle third of the mandible. Post-operative sialoceles and fistulas are other manifestations of abnormal salivary flow which interfere with wound healing. The management of excessive salivary flow in HNC patients is a less frequently discussed subject in medical literature. Complications related to salivary flow can cause increased morbidity and occasionally mortality related to HNC treatment. Consequently, the management of excessive salivary flow in the post-operative setting and for palliation has a great impact on overall outcome of surgical intervention and quality of life for the patient. Excessive salivary flow can be treated with aggressive wound care, pharmacologic inhibition, radiation, or surgery. A review of the literature focused on the management of excessive salivary flow in HNC patients is presented.

Publication types

  • Review
  • Systematic Review

MeSH terms

  • Antineoplastic Agents, Hormonal / therapeutic use
  • Botulinum Toxins / therapeutic use
  • Cholinergic Antagonists / therapeutic use
  • Head and Neck Neoplasms / therapy*
  • Humans
  • Octreotide / therapeutic use
  • Oral Fistula / etiology
  • Oral Fistula / therapy
  • Oral Surgical Procedures / methods
  • Radiotherapy Dosage
  • Salivary Glands / surgery
  • Sialorrhea / etiology
  • Sialorrhea / therapy*

Substances

  • Antineoplastic Agents, Hormonal
  • Cholinergic Antagonists
  • Botulinum Toxins
  • Octreotide