Indian Journal of PsychiatryIndian Journal of Psychiatry
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 Table of Contents    
LETTERS TO EDITOR  
Year : 2015  |  Volume : 57  |  Issue : 3  |  Page : 329-330
Author's reply


1 Department of Psychopharmacology, National Institute of Mental Health and Neurosciences, Bengaluru, Karnataka, India
2 JSS Medical College and Hospital, JSS University, Mysore, Karnataka, India

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Date of Web Publication6-Oct-2015
 

How to cite this article:
Andrade C, Sathyanarayana Rao T S. Author's reply. Indian J Psychiatry 2015;57:329-30

How to cite this URL:
Andrade C, Sathyanarayana Rao T S. Author's reply. Indian J Psychiatry [serial online] 2015 [cited 2020 Jun 1];57:329-30. Available from: http://www.indianjpsychiatry.org/text.asp?2015/57/3/329/166628


Sir,

Srivastava et al.[1] describe a 65-year-old woman with recurrent major depressive disorder whose 3-year course of illness showed increasing refractoriness to antidepressant treatment, and whose index (fourth) episode was refractory to two antidepressants despite antipsychotic augmentation. She was subsequently treated with 4 twice-weekly intravenous infusions of ketamine (0.5 mg/kg) administered across 40 min under anesthesiological supervision. Treatment was associated with excellent response; the patient remitted, and remission was maintained with antidepressant monotherapy for at least the following year.

We have two observations related to the management of the case. The baseline Hamilton Rating Scale for Depression score was 17, indicating that depression was mild. Therefore, it could have been appropriate to consider more conventional and approved approaches before resorting to the experimental treatment ketamine. As an example, the patient could have been advised a trial with an antidepressant such as venlafaxine, mirtazapine, or dothiepin; and augmentation, if necessary, could have been accomplished with an atypical antipsychotic drug such as aripiprazole or olanzapine. Next, had ketamine eventually been considered necessary, it could have been more simply dosed by the intranasal route,[2] obviating the inconvenience and discomfort associated with venipuncture.

How is intranasal ketamine administered? Ketamine solution (50 mg/ml) is loaded into an aerosol canister that ejects 0.1 ml/spray. Therefore, each 0.1 ml dose from the aerosol will contain 5 mg of ketamine. In a hypothetical woman who weights 60 kg, a 0.5 mg/kg dose translates to a total requirement of 30 mg of ketamine, or 6 sprays. Administering these 6 sprays at approximately 7 min intervals will result in the total dose being dispensed across approximately 35−40 min.

At the time of administration of the spray, the patient will need to lie down; else, the dose sprayed into the nostril may run downward and out of the nose. The patient should also be instructed not to "sniff" and "pull" the contents of the spray deeper into the nose; else, it may be pulled into the throat and be swallowed (with subsequent poor absorption). Allowing the dose to remain in the nasal mucosa results in absorption into the rich nasal vascular bed and possible direct transmission to the brain along the olfactory pathways through the cribriform plate of the ethmoid bone.[2]

The patient can sit up and even move around once the sprayed dose has been absorbed, before the next spray in that session is due. General precautions that need to be observed, such as cardiovascular monitoring and posttreatment monitoring for 2−4 h, are as with intravenous ketamine protocols.

Intranasal ketamine has been studied in a randomized, placebo-controlled crossover trial,[3] and has been administered in adolescent and adults as maintenance therapy for years.[2],[4] Like intravenous ketamine infusion, intranasal ketamine is emphatically an experimental procedure that should not be lightly undertaken. However, it could prove to be a useful resource as an emergency procedure for patients who are suicidal. It may even be preferable over intravenous ketamine in patients with refractory depression. It is acknowledged, however, that intranasal ketamine has not been as well studied as intravenous ketamine infusion.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.

 
   References Top

1.
Srivastava S, Gangwar RS, Kumar A. Safety and efficacy of ketamine infusion in late onset depression, and conversion to treatment response. Indian J Psychiatry 2015;57:328-9.  Back to cited text no. 1
  Medknow Journal  
2.
Andrade C. Intranasal drug delivery in neuropsychiatry: Focus on intranasal ketamine for refractory depression. J Clin Psychiatry 2015;76:e628-31.  Back to cited text no. 2
    
3.
Lapidus KA, Levitch CF, Perez AM, Brallier JW, Parides MK, Soleimani L, et al. A randomized controlled trial of intranasal ketamine in major depressive disorder. Biol Psychiatry 2014;76:970-6.  Back to cited text no. 3
    
4.
Papolos DF, Teicher MH, Faedda GL, Murphy P, Mattis S. Clinical experience using intranasal ketamine in the treatment of pediatric bipolar disorder/fear of harm phenotype. J Affect Disord 2013;147:431-6.  Back to cited text no. 4
    

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Correspondence Address:
Chittaranjan Andrade
Department of Psychopharmacology, National Institute of Mental Health and Neurosciences, Bengaluru, Karnataka
India
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Source of Support: None, Conflict of Interest: None


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