<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">OJPsych</journal-id><journal-title-group><journal-title>Open Journal of Psychiatry</journal-title></journal-title-group><issn pub-type="epub">2161-7325</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/ojpsych.2022.121005</article-id><article-id pub-id-type="publisher-id">OJPsych-114342</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Biomedical&amp;Life Sciences</subject></subj-group></article-categories><title-group><article-title>
 
 
  A Case Report: Prolonged Psychosis Secondary to Use of Highly Concentrated Tetra Hydro Cannabinoid (THC) (DABS)
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Srinivas</surname><given-names>Dannaram</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Madhuri</surname><given-names>Pulluri</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Christina</surname><given-names>Regan</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib></contrib-group><aff id="aff1"><addr-line>Banner Thunderbird Medical Center, Department of Psychiatry, College of Medicine-Phoenix, University of Arizona, Glendale, Arizona, USA</addr-line></aff><pub-date pub-type="epub"><day>22</day><month>11</month><year>2021</year></pub-date><volume>12</volume><issue>01</issue><fpage>49</fpage><lpage>52</lpage><history><date date-type="received"><day>22,</day>	<month>October</month>	<year>2021</year></date><date date-type="rev-recd"><day>28,</day>	<month>December</month>	<year>2021</year>	</date><date date-type="accepted"><day>31,</day>	<month>December</month>	<year>2021</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
  The Association of Schizophrenia, psychosis, and Marijuana is decades old. Swedish Conscripts cohort study 
  [1] was one of the earlier studies which reported dose-dependent associations between Marijuana use and schizophrenia. This landmark study was substantiated in other countries through research and systematic reviews 
  [2], which further strengthened the dose-dependent association between Marijuana and Psychosis. The dose defined in these studies 
  [1] was based on the frequency of use that is more times used means more risk of developing schizophrenia and or related psychosis. The concept of using highly concentrated marijuana is relatively new, especially in the light of episodes lasting longer than anticipated with treatment resistance. There is not much data on how it will change the course of psychosis and affect the current diagnostic criteria for Substance-induced psychosis, Schizophreniform Psychosis, and schizophrenia. Based on these challenges, we report a case of Dabs or concentrated Tetra Hydro Cannabinoid (THC)-induced prolonged psychosis with tachycardia and treatment resistance on two separate occasions. Both inpatient admissions were triggered using concentrated Tetra Hydro Cannabinoid (THC).
 
</p></abstract><kwd-group><kwd>Schizophrenia</kwd><kwd> Psychosis</kwd><kwd> Marijuana</kwd><kwd> THC</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Case</title><p>A 23-year-old female with no previous psychiatric illness presented with Paranoid delusions that her mother is playing old movies to pass subliminal messages and sister is changing lights to reflect her mood. She reported that she heard planes flying over her house shooting. She also reported hearing derogatory comments made by random people and was feeling stressed and suicidal. The patient has been smoking marijuana since the age of 21, and symptoms started two weeks back since she started to smoke Marijuana Wax pens on average 16 times daily. The patient had a Blood Pressure of 117/85 and a Heart rate of 110. The urine Toxicology Screen was positive for marijuana. The patient was admitted and was started on Olanzapine, which was gradually increased to a dose of 20 mg with no response; then Fluphenazine 5 mg two times a day was added to which she responded and was discharged on day 18th.</p><p>Following discharge, the antipsychotics were discontinued over a few weeks as she was not psychotic anymore. After seven months patient presented with two weeks history of paranoid delusions and auditory hallucinations that Television and Electronic devices are talking to her after using marijuana wax pens for about two weeks. The patient had a Heart rate of 110 - 120, and Urine Toxicology Screen was positive for marijuana. The family was concerned, and after admission, she reported that she might be pregnant. Despite repeating the pregnancy test, she was not convinced. She remained paranoid about other patients, was anxious, and was guilty about using wax pens. The patient was started on Olanzapine 5 mg with no initial change in the severity of symptoms. Patient-reported depressed mood and tearful episodes due to distress associated with psychosis and frustration related to lack of improvement. Lithium was added with no immediate effect after a 20 day stays in the hospital. Prozac was started to address anxiety and depression, and Olanzapine gradually increased to 20 mg with some improvement. The patient continued to have Tachycardia with normal Blood pressure, Electrocardiogram was done twice, and no abnormality was found. Propranolol was added to address autonomic symptoms of anxiety.</p><p>The patient was stable by the 38th day in the hospital, educated about the risk of recurrent psychosis with marijuana, and was recommended a Long-acting injectable antipsychotic due to the risk of non-compliance. The patient agreed and attained stability on day 45.</p></sec><sec id="s2"><title>2. Discussion</title><p>The legalization of Marijuana with commercialization and technical advancement in purification and production has increased Tetra Hydro Cannabinoid (THC) concentration over time. According to [<xref ref-type="bibr" rid="scirp.114342-ref3">3</xref>] MA ElSohly et al. Tetra Hydro Cannabinoid (THC) content in confiscated samples increased from 3% in 1980 to 12% in 2012. Adolescent ED visits due to Marijuana use increased in both males and females by 53.6% and 42.9%, respectively, from 2005 to 2010 [<xref ref-type="bibr" rid="scirp.114342-ref4">4</xref>]. Highly concentrated Marijuana in the form of Dabs with high Tetra Hydro Cannabinoid (THC) concentrations ranging from 23.7% to 75.9% [<xref ref-type="bibr" rid="scirp.114342-ref5">5</xref>] are available legally. One case of Neuro and Cardiotoxicity [<xref ref-type="bibr" rid="scirp.114342-ref6">6</xref>] and two cases of acute psychosis [<xref ref-type="bibr" rid="scirp.114342-ref7">7</xref>] were reported after use of concentrated Tetra Hydro Cannabinoid (THC) extract known as cannabis “wax,” “oil,” or “dabs.” Two acute psychotic episodes cases reported by [<xref ref-type="bibr" rid="scirp.114342-ref7">7</xref>] JM Pierre et al. responded to antipsychotics by Hospital Days 12 and 17, respectively.</p><p>According to [<xref ref-type="bibr" rid="scirp.114342-ref8">8</xref>] Wyatt et al. Neurotoxicity hypothesis, prolonged or repeated episodes of psychosis leave scars on the brain, possibly via changes in morphology, biochemical alterations, or damage to neuronal connections. This is one of the several mechanisms used to explain the association between the longer duration of untreated psychosis and poorer outcomes [<xref ref-type="bibr" rid="scirp.114342-ref9">9</xref>] [<xref ref-type="bibr" rid="scirp.114342-ref10">10</xref>] [<xref ref-type="bibr" rid="scirp.114342-ref11">11</xref>].<sup> </sup></p><p>This was backed by a mechanism that involves dopaminergic hyperactivity resulting [<xref ref-type="bibr" rid="scirp.114342-ref12">12</xref>] [<xref ref-type="bibr" rid="scirp.114342-ref13">13</xref>] in prolonged elevation of dopamine leading to a progressive decline in neural volume in regions with concentrated dopamine receptors. Dopaminergic agents and activity also induce neuronal apoptosis [<xref ref-type="bibr" rid="scirp.114342-ref14">14</xref>].</p><p>This time-tested evidence proved that the prognosis worsens with significant functional impairment when psychosis is prolonged, frequent, and resistant to antipsychotic treatment. The second case was reported by JM Pierre et al., and our case needed more than one antipsychotic to treat Tetra Hydro Cannabinoid (THC)-induced psychosis. Marijuana is one of the most abused substances with growing popularity in recent decades [<xref ref-type="bibr" rid="scirp.114342-ref15">15</xref>] primarily attributed due to legalization in most states [<xref ref-type="bibr" rid="scirp.114342-ref16">16</xref>]. This, along with an increase in concentration in refined forms, can pose new challenges for the field of medicine with its impact on Central Nervous System, Cardio Vascular System, and Psychiatry, as evident by the cases reported so far.</p></sec><sec id="s3"><title>3. Conclusion</title><p>The concept of using highly concentrated marijuana is relatively new, especially in the light of episodes lasting longer than anticipated with treatment resistance. There is not much data on how this will change the course of psychosis and affect the current diagnostic criteria for Substance-induced psychosis, Schizophreniform Psychosis, and schizophrenia. Evidence suggests that the prognosis worsens with significant functional impairment when psychosis is prolonged, frequent, and resistant to antipsychotic treatment. Based on these new diagnostic and management challenges, further research in this area is needed to inform new strategies to guide the assessment and management of psychotic disorders triggered by highly concentrated Tetra Hydro Cannabinoid (THC).</p></sec><sec id="s4"><title>Conflicts of Interest</title><p>The authors declare no conflicts of interest regarding the publication of this paper.</p></sec><sec id="s5"><title>Cite this paper</title><p>Dannaram, S., Pulluri, M. and Regan, C. (2022) A Case Report: Prolonged Psychosis Secondary to Use of Highly Concentrated Tetra Hydro Cannabinoid (THC) (DABS). Open Journal of Psychiatry, 12, 49-52. https://doi.org/10.4236/ojpsych.2022.121005</p></sec></body><back><ref-list><title>References</title><ref id="scirp.114342-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Zammit, S., Allebeck, P., Andreasson, S., Lundberg, I. and Lewis, G. (2002) Self Reported Cannabis Use as a Risk Factor for Schizophrenia in Swedish Conscripts of 1969: Historical Cohort Study. British Medical Journal, 325, Article No. 1199. https://doi.org/10.1136/bmj.325.7374.1199</mixed-citation></ref><ref id="scirp.114342-ref2"><label>2</label><mixed-citation publication-type="other" xlink:type="simple">Semple, D.M., McIntosh, A.M. and Lawrie, S.M. (2005) Cannabis as a Risk Factor for Psychosis: Systematic Review. 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