Cochrane · intervention · CD009603

Interventions for the management of dry mouth: non‐pharmacological interventions

Furness, S, Bryan, G, McMillan, R, et al. · Cochrane Database of Systematic Reviews · 2013 · Cochrane Library

Oral HealthOral medicine and oral cancer3 versionsAMSTAR 2: not assessed
Full textEvery question was extracted from the full review (methods and results), not only its Summary of Findings table.
Questions
21
current version
GRADE rated
7
No studies
8
Included studies
9
as reported
No studies 8 · 38.1%Ungraded 6 · 28.6%Very low 2 · 9.5%Low 5 · 23.8%Moderate 0 · 0%High 0 · 0%

Ungraded means an effect was reported without a GRADE rating; it is not a gap. No studies means the review found nothing to answer the question. The six categories are a display order, not a score.

Review question

ElementPlanned (methods)Found (results)
PopulationPeople seeking treatment for symptoms of dry mouth (xerostomia) due to any cause (haemodialysis; hormonal disorders such as diabetes; autoimmune conditions such as Sjogren's Syndrome, systemic lupus erythematosus and rheumatoid arthritis; immune disorders such as AIDS and graft versus host disease; patients undergoing or having received radiotherapy; and medication-related xerostomia); participants must have had xerostomia at baseline366 adult participants randomised (9 RCTs); dry mouth due to radiotherapy for head and neck cancer (4 trials), Sjogren's Syndrome (3 trials), medication-related (1 trial) or mixed causes (1 trial); age range 12 to 77 years
InterventionNon-pharmacological interventions such as acupuncture, electrostimulation or low level laser therapy for the management of xerostomiaAcupuncture (n=153, 5 trials); Electrostimulation devices (n=101 in 2 placebo-controlled trials; 3 trials total including 1 uncontrolled); Powered toothbrush (1 trial)
ComparisonPlacebo / no treatment / another active non-systemic treatment such as topical salivary stimulants (comparisons with systemic treatments such as oral pilocarpine or cevimeline excluded)Placebo/sham acupuncture; Placebo/sham electrostimulation device; Manual toothbrush
OutcomesPrimary: xerostomia (dry mouth) short term (4 weeks after start of treatment) and longer term (3 months after end of treatment). Secondary: duration of effectiveness; quality of life; patient satisfaction with treatment; adverse events; salivary flow (unstimulated whole saliva UWS or stimulated whole saliva SWS); oral health assessmentMouth dryness (n=70); Unstimulated whole saliva end of treatment (n=71); Stimulated whole saliva end of treatment (n=71); Unstimulated whole saliva 12 months (n=54); Stimulated whole saliva 12 months (n=54); Adverse effects (narrative)
Study designsParallel group randomised controlled trials (cross-over studies excluded; trials comparing different frequencies of treatment included)Parallel-group RCT (n=9)
TimingShort term (4 weeks after start of treatment); longer term (3 months after end of treatment)End of treatment (4-6 weeks); 12-month (1 year) follow-up

Search date: 2013-04. Databases: The Cochrane Oral Health Group's Trials Register; The Cochrane Central Register of Controlled Trials (CENTRAL); MEDLINE via OVID; EMBASE via OVID; AMED via OVID; CINAHL via EBSCO; CANCERLIT via PubMed; meta Register of Controlled Clinical Trials; ClinicalTrials.gov; reference lists

Questions and results

Current version only

Acupuncture vs Placebo (sham acupuncture)

Population: Adults with dry mouth due to radiotherapy (head and neck cancer) or Sjogren's Syndrome
CD009603.PUB3 (current) · 10 questions
OutcomeEffectEvidenceStatus / GRADE
Duration of effectiveness
no estimate extracted0 studiesNo studies
Quality of life
no estimate extracted0 studiesNo studies
Stimulated whole saliva (SWS)
12 months (1 year follow-up)
MD 0.28 [0.09, 0.47]2 studies · 54 participantsLow
Downgraded: risk of bias, imprecision
Dry mouth (mouth dryness, different scales)
End of treatment (4-6 weeks)
SMD -0.34 [-0.81, 0.14]2 studies · 70 participantsLow
Downgraded: risk of bias, publication bias
Oral health assessment
no estimate extracted0 studiesNo studies
Unstimulated whole saliva (UWS)
12 months (1 year follow-up)
MD 0.06 [0.01, 0.11]2 studies · 54 participantsLow
Downgraded: risk of bias, imprecision
Patient satisfaction with treatment
no estimate extracted0 studiesNo studies
Adverse events
Acupuncture was associated with more adverse effects (tiny bruises and tiredness, mild and temporary); List 1998 noted significant eye discomfort; Pfister 2010 reported temporary increases in pain, minor bruising or…4 studiesUngraded
Unstimulated whole saliva (UWS)
End of treatment (4-6 weeks)
MD 0.02 [0, 0.04]3 studies · 71 participantsLow
Downgraded: risk of bias, inconsistency
Stimulated whole saliva (SWS)
End of treatment (4-6 weeks)
MD 0.19 [0.07, 0.31]3 studies · 71 participantsLow
Downgraded: risk of bias, inconsistency

Electrostimulation (device) vs Placebo (sham/placebo device)

Population: Adults with dry mouth due to Sjogren's Syndrome
CD009603.PUB3 (current) · 8 questions
OutcomeEffectEvidenceStatus / GRADE
Dry mouth (xerostomia)
Neither trial reported usable dry mouth data; Talal 1992: 'patients using the active device experienced relief from six of the most common symptoms of xerostomia secondary to Sjogren's Syndrome, with two of these…NRUngraded
Oral health assessment
no estimate extracted0 studiesNo studies
Quality of life
no estimate extracted0 studiesNo studies
Adverse events
Wong 2003 stated 'no adverse effects were caused by Codetron'; Steller 1988 and Talal 1992 did not mention whether adverse effects occurredNRUngraded
Patient satisfaction with treatment
no estimate extracted0 studiesNo studies
Stimulated whole saliva (SWS)
End of treatment (4 weeks)
MD 0.16 [-0.05, 0.37]1 study · 24 participantsVery low
Downgraded: risk of bias, imprecision
Duration of effectiveness
no estimate extracted0 studiesNo studies
Unstimulated whole saliva (UWS)
End of treatment (4 weeks)
MD 0.02 [-0.12, 0.16]1 study · 24 participantsVery low
Downgraded: risk of bias, imprecision

Powered toothbrush vs Manual toothbrush

Population: Adults with medication-related dry mouth
CD009603.PUB3 (current) · 3 questions
OutcomeEffectEvidenceStatus / GRADE
Unstimulated whole saliva (UWS)
45 minutes after brushing
MD -0.07 [-0.74, 0.60]1 studyUngraded
Stimulated whole saliva (SWS)
5 minutes after brushing
MD -0.13 [-1.92, 1.66]1 studyUngraded
Dry mouth (xerostomia)
Papas 2006 used a VAS to measure mouth dryness but did not report dry mouth outcome data1 studyUngraded

Acupuncture vs Placebo (sham acupuncture)

Population: Adults with dry mouth due to radiotherapy (head and neck cancer) or Sjogren's Syndrome
CD009603.PUB2 · 10 questions
OutcomeEffectEvidenceStatus / GRADE
Unstimulated whole saliva (UWS)
12 months (1 year follow-up)
MD 0.06 [0.01, 0.11]2 studies · 54 participantsLow
Downgraded: risk of bias, imprecision
Stimulated whole saliva (SWS)
12 months (1 year follow-up)
MD 0.28 [0.09, 0.47]2 studies · 54 participantsLow
Downgraded: risk of bias, imprecision
Stimulated whole saliva (SWS)
End of treatment (4-6 weeks)
MD 0.19 [0.07, 0.31]3 studies · 71 participantsLow
Downgraded: risk of bias, inconsistency
Unstimulated whole saliva (UWS)
End of treatment (4-6 weeks)
MD 0.02 [0, 0.04]3 studies · 71 participantsLow
Downgraded: risk of bias, inconsistency
Patient satisfaction with treatment
no estimate extracted0 studiesNo studies
Adverse events
Acupuncture was associated with more adverse effects (tiny bruises and tiredness, mild and temporary); List 1998 noted significant eye discomfort; Pfister 2010 reported temporary increases in pain, minor bruising or…4 studiesUngraded
Duration of effectiveness
no estimate extracted0 studiesNo studies
Quality of life
no estimate extracted0 studiesNo studies
Oral health assessment
no estimate extracted0 studiesNo studies
Dry mouth (mouth dryness, different scales)
End of treatment (4-6 weeks)
SMD -0.34 [-0.81, 0.14]2 studies · 70 participantsLow
Downgraded: risk of bias, publication bias

Electrostimulation (device) vs Placebo (sham/placebo device)

Population: Adults with dry mouth due to Sjogren's Syndrome
CD009603.PUB2 · 8 questions
OutcomeEffectEvidenceStatus / GRADE
Stimulated whole saliva (SWS)
End of treatment (4 weeks)
MD 0.16 [-0.05, 0.37]1 study · 24 participantsVery low
Downgraded: risk of bias, imprecision
Patient satisfaction with treatment
no estimate extracted0 studiesNo studies
Oral health assessment
no estimate extracted0 studiesNo studies
Adverse events
Wong 2003 stated 'no adverse effects were caused by Codetron'; Steller 1988 and Talal 1992 did not mention whether adverse effects occurredNRUngraded
Unstimulated whole saliva (UWS)
End of treatment (4 weeks)
MD 0.02 [-0.12, 0.16]1 study · 24 participantsVery low
Downgraded: risk of bias, imprecision
Duration of effectiveness
no estimate extracted0 studiesNo studies
Quality of life
no estimate extracted0 studiesNo studies
Dry mouth (xerostomia)
Neither trial reported usable dry mouth data; Talal 1992: 'patients using the active device experienced relief from six of the most common symptoms of xerostomia secondary to Sjogren's Syndrome, with two of these…NRUngraded

Powered toothbrush vs Manual toothbrush

Population: Adults with medication-related dry mouth
CD009603.PUB2 · 3 questions
OutcomeEffectEvidenceStatus / GRADE
Dry mouth (xerostomia)
Papas 2006 used a VAS to measure mouth dryness but did not report dry mouth outcome data1 studyUngraded
Stimulated whole saliva (SWS)
5 minutes after brushing
MD -0.13 [-1.92, 1.66]1 studyUngraded
Unstimulated whole saliva (UWS)
45 minutes after brushing
MD -0.07 [-0.74, 0.60]1 studyUngraded

Acupuncture vs Placebo / no treatment / another active non-systemic treatment (e.g. topical salivary stimulant)

Population: People seeking treatment for symptoms of dry mouth (xerostomia) due to any cause (e.g. haemodialysis, hormonal disorders such as diabetes, autoimmune conditions such as Sjogren's Syndrome/SLE/rheumatoid arthritis, immune disorders, radiotherapy, or medications)
CD009603 · 8 questions
OutcomeEffectEvidenceStatus / GRADE
Salivary flow - stimulated whole saliva (SWS)
no estimate extractedNRNo studies
Salivary flow - unstimulated whole saliva (UWS)
no estimate extractedNRNo studies
Dry mouth (xerostomia)
Short term (4 weeks after start of treatment); longer term (3 months after end of treatment)
no estimate extractedNRNo studies
Patient satisfaction with treatment
no estimate extractedNRNo studies
Duration of effectiveness
no estimate extractedNRNo studies
Quality of life
no estimate extractedNRNo studies
Oral health assessment
no estimate extractedNRNo studies
Adverse events
no estimate extractedNRNo studies

Electrostimulation vs Placebo / no treatment / another active non-systemic treatment (e.g. topical salivary stimulant)

Population: People seeking treatment for symptoms of dry mouth (xerostomia) due to any cause (e.g. haemodialysis, hormonal disorders such as diabetes, autoimmune conditions such as Sjogren's Syndrome/SLE/rheumatoid arthritis, immune disorders, radiotherapy, or medications)
CD009603 · 8 questions
OutcomeEffectEvidenceStatus / GRADE
Quality of life
no estimate extractedNRNo studies
Adverse events
no estimate extractedNRNo studies
Patient satisfaction with treatment
no estimate extractedNRNo studies
Salivary flow - stimulated whole saliva (SWS)
no estimate extractedNRNo studies
Oral health assessment
no estimate extractedNRNo studies
Dry mouth (xerostomia)
Short term (4 weeks after start of treatment); longer term (3 months after end of treatment)
no estimate extractedNRNo studies
Duration of effectiveness
no estimate extractedNRNo studies
Salivary flow - unstimulated whole saliva (UWS)
no estimate extractedNRNo studies