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Updated: Aug 9, 2026

Drug-Induced Sleep Endoscopy (DISE) with Target Controlled Infusion (TCI) and Bispectral Analysis in Obstructive Sleep Apnea
Published on: December 6, 2016
Drug therapy for obstructive sleep apnoea in adults
I Smith1, T J Lasserson, J Wright
1Papworth Hospital, Respiratory Support and Sleep Centre,Papworth Everard, Cambridge, UK, CB3 8RE. ian.smith@papworth.nhs.uk
Drug therapies for obstructive sleep apnoea (OSA) show limited efficacy, with insufficient evidence for widespread recommendation. Further research is needed to determine long-term benefits and patient-specific treatments for this common sleep disorder.
Area of Science:
- Sleep Medicine
- Pharmacology
- Respiratory Medicine
Background:
- Continuous positive airways pressure (CPAP) is the standard treatment for moderate to severe obstructive sleep apnoea (OSA).
- CPAP is not universally tolerated, and its effectiveness in mild OSA is unproven.
- Drug therapy is being explored as an alternative for patients intolerant to CPAP or with mild to moderate OSA.
Purpose of the Study:
- To evaluate the effectiveness of various drug therapies in treating obstructive sleep apnoea (OSA).
- To identify potential alternative pharmacological treatments for patients with OSA.
Main Methods:
- Conducted systematic searches of the Cochrane Airways Group Specialised Register of trials.
- Included randomized, placebo-controlled trials of adult patients with confirmed OSA.
- Excluded trials using CPAP, mandibular devices, or oxygen therapy.
Main Results:
- Twenty-six trials involving 21 drugs and 394 participants were analyzed.
- Most studies were small with methodological limitations; diagnostic criteria were not always explicit.
- Six drugs showed some impact on OSA severity, and two improved daytime symptoms; notable reductions in apnoea-hypopnoea index (AHI) were observed with intranasal fluticasone, physostigmine, mirtazipine, and nasal lubricant.
Conclusions:
- Insufficient evidence currently supports the recommendation of drug therapy for OSA treatment.
- Short-term studies indicate potential benefits of certain agents in reducing AHI.
- Longer-term studies are required to assess the impact of drugs like fluticasone, mirtazipine, physostigmine, and nasal lubricant on daytime symptoms, and personalized drug-matching strategies need further investigation.
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