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Insomnia in patients with addictions: A safer way to break the cycle

Current Psychiatry. 2008 May;07(05):97-109
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Fight relapse by improving sleep with nonaddictive agents and behavior therapy.

Other sedating antidepressants such as mirtazapine and doxepin have not been studied in patients with substance use disorders.

Quetiapine is a second-generation antipsychotic with sedating properties. When quetiapine, 25 to 200 mg/d, was given to alcohol-dependent veterans with sleep complaints, they remained abstinent more days and had fewer hospitalizations than veterans not receiving quetiapine.25 Both groups had high rates of psychiatric comorbidity, and 90% had posttraumatic stress disorder. Improved abstinence was thought to result from improved sleep, but no sleep measures were included to test this hypothesis.

A recently published, randomized controlled pilot study reported significantly reduced drinking and craving in severely alcohol-dependent patients receiving quetiapine vs placebo, although sleep data were not included.26

Other options. Tricyclic antidepressants carry risks of cardiotoxicity and other side effects but can be useful when other options have not worked or patients have comorbidities such as neuropathic pain or migraine headaches. Combinations of agents also may be considered for treatment-resistant insomnia.

Nonprescription remedies such as antihistamines, valerian root extract (from the herb Valeriana officinalis), and melatonin are commonly used for sleep, although data are limited in substance-abusing patients.

Table 3

Noncontrolled sedating agents for treating insomnia
in patients with a history of substance abuse

AgentDose range (mg)TMAX (hr)T½ (hr)
Melatonin receptor agonist
Ramelteon80.5 to 1.51 to 2.6
Sedating anticonvulsant
Gabapentin300 to 1,5002 to 36 to 7
Sedating antidepressants
Amitriptyline25 to 1502 to 85 to 45
Doxepin25 to 1502 to 810 to 30
Mirtazapine7.5 to 451 to 320 to 40
Nefazodone50 to 15016 to 18*
Nortriptyline10 to 75§2 to 820 to 55
Trazodone25 to 3001 to 23 to 9
Sedating second-generation antipsychotic
Quetiapine25 to 1001.56
TMAX: time to reach maximal plasma concentrations; T½: elimination half-life (all values are approximate for any given individual)
* Including active metabolites
† Tricyclic antidepressants
‡ Antihistaminergic effects predominate at low doses (7.5 to 15 mg)
§ Can be titrated to morning serum level (50 to 150 mcg/mL) 12 hr after bedtime dose if no effect at lower doses
¶ Major metabolite, mCPP, has 14-hour half-life
Related resourcesDrug brand name
  • Amitriptyline • Elavil, Endep
  • Doxepin • Sinequan
  • Estazolam • ProSom
  • Eszopiclone • Lunesta
  • Flurazepam • Dalmane
  • Gabapentin • Neurontin
  • Methamphetamine • Desoxyn
  • Methylphenidate • Concerta, Ritalin, others
  • Mirtazapine • Remeron
  • Nefazodone • Serzone
  • Nortriptyline • Pamelor
  • Pregabalin • Lyrica
  • Quazepam • Doral
  • Quetiapine • Seroquel
  • Ramelteon • Rozerem
  • Temazepam • Restoril
  • Theophylline • Theo-24, others
  • Trazodone • Desyrel
  • Triazolam • Halcion
  • Zaleplon • Sonata
  • Zolpidem • Ambien, Ambien CR
Disclosure

Dr. Conroy and Dr. Arnedt report no financial relationship with any company whose products are mentioned in this article or with manufacturers of competing products. Dr. Brower is a consultant to Pfizer.

Acknowledgment

This work was supported by an NIH grant to Dr. Brower (2K24 AA00304).